LipidBank - Long chain alcohol

No	Structure	COMMON NAME	NAME	DATA No	INFORMANT	SYMBOL	FORMULA	MOL.WT(ave)	Download	BIOOGICAL ACTIVITY	PHYSICAL AND CHEMICAL PROPERTIES						SPECTRAL DATA					CHROMATOGRAM DATA	SOURCE	CHEMICAL SYNTHESIS	METABOLISM	GENETIC INFORMATION	NOTE	REFERENCES
No	Structure	COMMON NAME	NAME	DATA No	INFORMANT	SYMBOL	FORMULA	MOL.WT(ave)	Download	BIOOGICAL ACTIVITY	MELTING POINT	BOILING POINT	DENSITY	REFRACTIVE INDEX	OPTICAL ROTATION	SOLUBILITY	UV SPECTRA	IR SPECTRA	NMR SPECTRA	MASS SPECTRA	OTHER SPECTRA	CHROMATOGRAM DATA	SOURCE	CHEMICAL SYNTHESIS	METABOLISM	GENETIC INFORMATION	NOTE	REFERENCES
1			3,6,8-dodecatrien-1-ol	DLL0001	Yasushi Kawakami		C₁₂H₂₀O	180.287		This compound induce trail-following behavior in the subterranean termite (Ref. 0001)									(Ref. 0001)				Trail-following pheromon of subterranean termites					[0001]
2		Ceryl alcohol	1-hexacosanol	DLL0002	Yasushi Kawakami		C₂₆H₅₆O₂	400.722		Promotion of the maturation of central neurons (neulite outgrowth)(Ref. 0002) An inhibitory effect on insulin secretion stimulated by glucose in rats(Ref. 0003)	80(Ref. 0003)												Chinese insect wax and many other waxes.(Ref. 0004)					[0002] / [0003] / [0004]
3		Montanyl alcohol	1-octacosanol	DLL0003	Yasushi Kawakami		C₂₈H₅₈O	410.760		Depress the serum triglycerol level and enhance the concentration of serum fatty acids The addition of octacosanol (10 g/kg diet) to the high-fat diet led to a significant reduction (p < 0.05) in the perirenal adipose tissue weight (Ref. 0008)	82.6-82.9C (Ref. 0005)(Ref. 0007)							(Ref. 0006)			X-lay (Ref. 0005)		Wheat wax (Ref. 0005) Cassia javanica Linn. (Leguminosae) (Ref. 0007) Hypericum perforatum L. (Ref. 0006)					[0005] / [0006] / [0007] / [0008]
4		plaunotol	7-hydroxymethyl-3,11,15-trimethyl-2,6,10,14-hexadecatetraen-1-ol	DLL0004	Yasushi Kawakami		C₂₀H₃₄O₂	306.483		Antipeptic ulcer substance(Ref. 0009) (Ref. 0010)(Ref. 0011),(Ref. 0012)								(Ref. 0009)	(Ref. 0009)	(Ref. 0009>		(Ref. 0009)	Croton sublyratus Kurz(Ref. 0009)	(Ref. 0009)	The hydroxyl group at 1-position of plaunotol is oxidized to carboxyl group (1-carboxylic plaunotol), and then methyl group at 16-position is oxidized by w-oxidation enzymes to dicarboxylic acid. (Ref. 0035) The conjugated plaunotol or 1-carboxylic plaunotol is excreted into bile. (Ref. 0035)			[0009] / [0010] / [0011] / [0012] / [0035]
5		falcarindiol	1,9-heptadecadien-4,6-diyn-3,8-diol	DLL0005	Yasushi Kawakami		C₁₇H₂₄O₂	260.371		Antifungal activity (Ref. 0015)(Ref. 0016)(Ref. 0018)							(Ref. 0017)	(Ref. 0015)(Ref. 0017)(Ref. 0019)	(Ref. 0015)(Ref. 0017)	(Ref. 0015)		TLC(Ref. 0018)	Apium graveolens L.(Ref. 0013) Root of Peucedanum oreoselinum (Ref. 0014) Carrot root (Ref. 0016)(Ref. 0017) G. littoralis (Ref. 0015) Elder (Aegopodium podagraria L.) (Ref. 0018)	(Ref. 0019)(Ref. 0020)				[0013] / [0014] / [0015] / [0016] / [0017] / [0018] / [0019] / [0020]
6		Melissyl alcohol, Myricyl alcohol	1-triacontanol	DLL0006	Yasushi Kawakami		C₃₀H₆₂O	438.813		Plant growth stimulant (Ref. 0023) Stimulation of ATPase activity in barley (Hardeum valgare) root plasma membrane (Ref. 0024) (Ref. 0025) Decrease in the number of thymus cell of mice by intraperitoneally injection	86.5C(Ref. 0021)									(Ref. 0023)		GLC(Ref. 0022)	Alfalfa(Medicago sativa L.)	(Ref. 0021)				[0021] / [0022] / [0023] / [0024] / [0025]
7		Bombykol	10,12-hexadecadien-1-ol,(10E,12Z)-form	DLL0007	Yasushi Kawakami		C₁₆H₃₀O	238.409		Sex pheromone of the silk worm moth,Bombyx mori.		B.P.₀_.₀₀₅130-133C(Ref. 0028) B.P.₀_.₀₀₅115-130C(Ref. 0029)		[n]=1.4835(Ref. 0028)			(Ref. 0027)(Ref. 0028)	(Ref. 0030)	(Ref. 0029)(Ref. 0030)	(Ref. 0030)			Sex pheromone of the silk worm moth (Ref. 0031)(Ref. 0032)(Ref. 0033)(Ref. 0034)	(Ref. 0027)(Ref. 0028)(Ref. 0030)				[0027] / [0028] / [0029] / [0030] / [0031] / [0032] / [0033] / [0034]
8		Behenyl alcohol	1-docosanol	DLL0008	Yasushi Kawakami		C₂₂H₄₆O	326.600		This compound exerts a substantial inhibitory effect on replication of certain viruses. (Ref. 0074)(Ref. 0075)(Ref. 0076)(Ref. 0077)(Ref. 0078)	M_p 70.8C(Ref. 0061) M_p 80C(Ref. 0073)											(Ref. 0073)		(Ref. 0061)				[0061] / [0073] / [0074] / [0075] / [0076] / [0077] / [0078]
9			14-methyl-1-hexadecanol	DLL0009	Yasushi Kawakami		C₁₇H₃₆O	256.467		This compound markedly prolonged the life-span of Ehrlich ascites carcinoma or S180 fibrosarcoma implanted mice without acute toxic side-effects.(Ref. 0077)													Sheep cutaneous wax					[0077]
10			14-methyl-1-pentadecanol	DLL0010	Yasushi Kawakami		C₁₆H₃₄O	242.441		This compound markedly prolonged the life-span of Ehrlich ascites carcinoma or S180 fibrosarcoma implanted mice without acute toxic side-effects.(Ref. 0077)									(Ref. 0077)	(Ref. 0077)			Sheep cutaneous wax					[0077]
11		persin	(Z,Z)-1-(acetoxy)-2-hydroxy-12,15-heneicosadien-4-one	DLL0011	Yasushi Kawakami		C₂₃H₄₀O₄	380.561		This compound causes necrosis of the acinar epithelium of the lacting mammary gland and the myocardium.(Ref. 0051) This compound is shown to be antifungal for unripe avocado fruits.(Ref. 0081)					(Ref. 0051)(Ref. 0080)		(Ref. 0051)	(Ref. 0051)(Ref. 0080)	(Ref. 0051)(Ref. 0080)	(Ref. 0051)(Ref. 0080)			This compound was isolated from avocado leaves.(Ref. 0051)	(Ref. 0051)				[0051] / [0080] / [0081]
12		vasculyne		DLL0012	Yasushi Kawakami		C₄₃H₇₄O₂	623.046		This compound shows a cytotoxicity profile toward the melanoma and colon tumor cell-lines (NCI 60-cell antitumor screen)					[a]_D -24 (c 0.25,CDCl₃)(Ref. 0054)		(Ref. 0054)	(Ref. 0054)	(Ref. 0054)	(Ref. 0054)			This compound was isolated from the Marine Sponge Cribrochalina vasculum .(Ref. 0054)					[0054]
13		depdecin	(2R,3S,4S,5E,7S,8S,9R)-2,9-dihydroxy-3,4,7,8-diepoxy-undeca-5,10-diene	DLL0013	Yasushi Kawakami		C₁₁H₁₆O₄	212.242		This compound exhibits anti-angiogenic activity in an in vivo assay system involving the chorioallantoic membrane of growing chick embryo.(Ref. 0101) This compound exhibits the growth-inhibitory activity against ras/srt NIH3T3 cells.(Ref. 0102)					[a] -35.8 (c 0.52,CH₃OH) (Ref. 0102)		(Ref. 0102)	(Ref. 0102)	(Ref. 0102)	(Ref. 0102)	HOHAHA (Ref. 0102) HMBC spectrum of HMQC (Ref. 0102)	TLC (Ref. 0102)	This compound was isolated from the fungus Alternaria brassicicola.(Ref. 0102)					[0101] / [0102]
14		gummiferol	14-O-acetyl-8,9(E)-10,11(E)-diepoxy-12(E)-en-2,4,6-triyn-tetradecan-1-ol	DLL0014	Yasushi Kawakami		C₁₆H₁₄O₅	286.279		This compound exhibits significant cytotoxic activity against the KB human cell line and broad cytotoxic spectrum against other human cancer cell lines					[a] -170 (c=0.2 MeOH) (Ref. 0055)		(Ref. 0055)	(Ref. 0055)	(Ref. 0055)	(Ref. 0055)			This compound was isolated from the leaves of Adenia gummifera.					[0055]
15			10-propyl-5,9-tridecadienyl-1-ol	DLL0015	Yasushi Kawakami					The acetate form of this compound is sexual pheromone secreted by the female of Pectinophora gossypiella saunders (pink bollworm moth ). (Ref. 0144)		110-120/0.08mmHg (Ref. 0144) 110-120/0.4mm(Ref. 0146)		n 1.4715(Ref. 0144)(Ref. 0146)			(Ref. 0144)	(Ref. 0144)(Ref. 0146)	(Ref. 0144)(Ref. 0146)	(Ref. 0144)			The acetate form of this compound was isolated from virgin female pink bellworm moth.(Ref. 0144)	(Ref. 0144)(Ref. 0145)(Ref. 0146)				[0144] / [0145] / [0146]
16			13-tetradecen-2,4-diyn-1-ol	DLL0016	Yasushi Kawakami		C₁₄H₂₀O	204.308		This compound exhibited ichthyotoxicity and inhibits the growth of some bacteria and fungi.(Ref. 0147)							(Ref. 0147)	(Ref. 0147)	(Ref. 0147)	(Ref. 0147)			This compound was isolated from hermatypic corals,Montipora mollis and Pectinia lactuca.(Ref. 0147)					[0147]
17		gemcadiol	2,2,9,9-tetra-methyl-decan-1,10-diol	DLL0017	Yasushi Kawakami		C₁₄H₃₀O₂	230.387		This compound is effective in reducing serum cholesterol and triglyceride levels. This compound has toxic properties for rodents,dogs and monkeys together with teratology studies in rats and rabbits.
18			(3S,8E)-1,3-dihydroxy-8-decen-5-one	DLL0018	Yasushi Kawakami	IC201	C₁₀H₁₈O₂	170.249		This compound is effective in retarding growth of the solid tumor of Ehrlich carcinoma.(Ref. 0107) The addition of this compound to P3889D₁ cell culture enhanced the release of interleukin 1. (Ref. 0058)					[a] =+23(c=1.05,CHCl₃)(Ref. 0106) [a]:+26 (Ref. 0060)		(Ref. 0106)	(Ref. 0106)(Ref. 0057)	(Ref. 0106)(Ref. 0107)(Ref. 0057)(Ref. 0060)	(Ref. 0106)		(Ref. 0107)	This compound was isolated from cultured broth of Streptomyces fimbriatus (Ref. 0106) and Streptomyces cirratus.(Ref. 0107)					[0057] / [0058] / [0060] / [0106] / [0107]
19		Panaxynol	1,9(Z)-heptadecadien-4,6-diyn-3-ol	DLL0019	Yasushi Kawakami		C₁₇H₂₄O	244.372		This compound shows a growth-inhibitory activity against ML-1 cells,B-16 cells,L-929 cells,MRC-5 cells,Mesothelial cells.(Ref. 0064) This compound inhibits the formation of thromboxane B₂ in human platelets.(Ref. 0088)				n 1.5018 (Ref. 0085)			(Ref. 0088)	(Ref. 0085)(Ref. 0088)	(Ref. 0037)(Ref. 0085)(Ref. 0088)(Ref. 0089)			(Ref. 0084)	This compound was isolated from red ginseng.(Ref. 0064) This compound was isolated from Saposhnikoviae radix(fangfeng,root of Saposhnikovia divaricata Schischk.,Umbelliferae)(Ref. 0088)	(Ref. 0085)				[0037] / [0064] / [0084] / [0085] / [0088] / [0089]
20			5,7-dodecadien-1-ol	DLL0020	Yasushi Kawakami		C₁₂H₂₂O	182.302		This compound captures male Malacosoma disstria.(Ref. 0108)		90-91/0.05torr(Ref. 0108)		n1.4865(Ref. 0108)				(Ref. 0108)(Ref. 0110)	(Ref. 0108)(Ref. 0110)	(Ref. 0108)		GLC(Ref. 0108)	This compound is a principal compound of the sex pheromone of forest tent caterpillar,Malacosoma disstria.(Ref. 0108)	(Ref. 0108)(Ref. 0110)				[0108] / [0110]
21			11-dodecen-1-ol	DLL0021	Yasushi Kawakami		C₁₂H₂₄O	184.318		Acetate form of this compound shows attractive activity to male moth,Diparopsis castanea.(Ref. 0111)										(Ref. 0111)		GC (Ref. 0111)	This compound is female sex pheromone of the red bollworm moth,Diparopsis castanea.(Ref. 0111)					[0111]
22			2,9-heptadecadien-4,6-diyn-1,8-diol	DLL0022	Yasushi Kawakami		C₁₇H₂₄O₂	260.371		This compound exhibits significant antibiotic activity against the Gram-positive bacteria Staphylococcus aureus and Bacillus subtilis.(Ref. 0083)					[a] +270,c=0.7,CHCl₃ (Ref. 0083)		(Ref. 0083)	(Ref. 0083)	(Ref. 0083)	(Ref. 0083)			This compound was isolated from Bupleurum salicifolium.(Ref. 0083)					[0083]
23			7,11-hexadecadien-1-ol	DLL0023	Yasushi Kawakami		C₁₆H₃₀O	238.409		The acetate form of this compound is attractive to male pink bollworm moths.(Ref. 0165)		118/0.2mm(Ref. 0162)		n¹⁶_D 1.4715 (Ref. 0162)				(Ref. 0162)	(Ref. 0162)			GLC(Ref. 0162)	The acetate form of this compound is sex pheromone of pink bollworm moth,Pectinophora gossypiella.(Ref. 0165)	(Ref. 0162) (Ref. 0163) (Ref. 0164)				[0162] / [0163] / [0164] / [0165]
24			9-dodecen-1-ol	DLL0024	Yasushi Kawakami		C₁₂H₂₄O	184.318		The acetate form of this compound is sex pheromone of the European pine shoot moth,Rhyacinoia buoliana.(Ref. 0089)(Ref. 0092)		83/0.01(Ref. 0085)						(Ref. 0058)(Ref. 0085)	(Ref. 0058)			GC(Ref. 0058)	The acetate form of this compound was isolated from European pine shoot moth,Rhyacionia buoliana.(Ref. 0089)(Ref. 0092)	(Ref. 0058) (Ref. 0085)				[0058] / [0085] / [0089] / [0092]
25			10-dodecen-1-ol	DLL0025	Yasushi Kawakami		C₁₂H₂₄O	184.318		Acetate form of this compound is sex attractant for Cosmopterix victor Stringer.(Ref. 0113)		91-92(0.02mmHg)(Ref. 0112)		D 1.4519(23C)(Ref. 0112)				(Ref. 0112)	(Ref. 0112)					(Ref. 0112)				[0112] / [0113]
26			(E,Z)-7,9-dodecadien-1-ol	DLL0026	Yasushi Kawakami		C₁₂H₂₂O	182.302		This compound is the sex pheromone of the grapevine moth,Lobesia botrana.(Ref. 0115)(Ref. 0116)								(Ref. 0114)	(Ref. 0114)	(Ref. 0114)(Ref. 0115)(Ref. 0116)		GC(Ref. 0115)(Ref. 0116)	This compound was isolated from Lobesia botrana.(Ref. 0115)	(Ref. 0114)				[0114] / [0115] / [0116]
27		panaxytriol	1-heptadecen-4,6-diyn-3,9,10-triol	DLL0027	Yasushi Kawakami		C₁₇H₂₆O₃	278.387		This compound shows a growth-inhibitory activity against MK-1 cells,B16 cells,L929 cells,SW620 cells,Hela cells,K562 cells.(Ref. 0062)(Ref. 0064)(Ref. 0090)	m.p. 68-72 C (Ref. 0062)				[a] -25.4 (Ref. 0084)		(Ref. 0062)(Ref. 0084)	(Ref. 0062)(Ref. 0084)	(Ref. 0062)(Ref. 0084)(Ref. 0037)(Ref. 0090)	(Ref. 0062)(Ref. 0084)		RIC(Ref. 0052)(Ref. 0084)	This compound was isolated from red ginseng.(Ref. 0062)					[0037] / [0052] / [0062] / [0064] / [0084] / [0090]
28		panaxydol	9,10-epoxy-1-heptadecen-4,6-diyn-3-ol	DLL0028	Yasushi Kawakami		C₁₇H₂₄O₂	260.371		This compound shows the growth-inhibitory activity against MK-1 cells,B-16 cells,L-929 cells,MRC-5 cells,Mesothekiak cells,(Ref. 0064),MK-1 cells,Hela cells,(Ref. 0086),Leukemia cells.(Ref. 0087) This compound shows cytotoxic activity against L1210 cells.(Ref. 0090)					[a]_D -19.5 (MeOH,c=0.6) (Ref. 0087)	(Ref. 0064)		(Ref. 0087)(Ref. 0084)(Ref. 0091)	(Ref. 0087)(Ref. 0084)(Ref. 0090)(Ref. 0091)(Ref. 0051)	(Ref. 0087)(Ref. 0091)			This compound was isolated from Panax ginseng.(Ref. 0086)(Ref. 0064)	(Ref. 0091)				[0051] / [0064] / [0084] / [0086] / [0087] / [0090] / [0091]
29			1,9(Z),16-heptadecatrien-4,6-diyn-3,8-diol	DLL0029	Yasushi Kawakami		C₁₇H₂₂O₂	258.355		This compound exhibits cytotoxic activity against Hep-G2,A-431,H-4							(Ref. 0100)	(Ref. 0100)	(Ref. 0100)	(Ref. 0100)		(Ref. 0099)	This compound was isolated from the leaves of Dendropanax arboreus (Araliacesa) from Monteverde,Costa Rica (Ref. 0099) or Artemesia borealis (Asteraceae) (Ref. 0100).					[0099] / [0100]
30			9-hexadecen-1-ol	DLL0030	Yasushi Kawakami		C₁₆H₃₂O	240.425		This compouns is attractant for Bumblebees.(Ref. 0158)		137-138C (0.03) (Ref. 0085)						(Ref. 0085)					This compound was isolated from male bumblebees,Bombus lapidarius.(Ref. 0158)	(Ref. 0085)				[0085] / [0158]
31			7(R)-methyl-6(E)-nonen-3-ol	DLL0031	Yasushi Kawakami		C₁₀H₂₀O	156.265		The acetate form of this compound is aggregation pheromone produced by the male sequare-necked grain beetle (Cathartus quadricollis) (Ref. 0072)		Bp₁₈:99-102C (Ref. 0050)		n=1.4489 (Ref. 0050)	[a]=-10.8 (Ref. 0050)			(Ref. 0071) (Ref. 0050)	(Ref. 0071) (Ref. 0050)	(Ref. 0071)		GC (Ref. 0050)	The acetate form of this compound is aggregation pheromone produced by the male sequare-necked grain beetle (Cathartus quadricollis) (Ref. 0072)	(Ref. 0071)(Ref. 0036)(Ref. 0037)(Ref. 0050)				[0036] / [0037] / [0050] / [0071] / [0072]
32			3-methyl-6-(1-methyl ethyl)-3,9-decadien-1-ol	DLL0032	Yasushi Kawakami		C₁₄H₂₄O	208.340		Sex pheromone-activity in California red scale (Aonidiella aurantii) (Ref. 0038)								(Ref. 0039)	(Ref. 0038)(Ref. 0039)			GLC (Ref. 0038)(Ref. 0039)	Sex pheromone of California red scale (Aonidiella aurantii) (Ref. 0038)	(Ref. 0038)(Ref. 0039)(Ref. 0040)(Ref. 0041)(Ref. 0042)				[0038] / [0039] / [0040] / [0041] / [0042]
33			3,5-dodecadien-1-ol	DLL0033	Yasushi Kawakami		C₁₂H₂₂O	182.302		This compound and acetate form of this compound attract the one Phyllonorycter sp.,Chionodes lugubrella (Pack.),Pyrausta fodinalis (Led.),Notocelia purpurissatana Heinr.,Phaneta alterana Heinr. (Ref. 0097) This compound is ""trail-following pheromones""among certain termites. (Ref. 0093)(Ref. 0094)(Ref. 0096)							(Ref. 0098)	(Ref. 0098)	(Ref. 0098)	(Ref. 0098)			This compound was isolated from root of Cyperus Iria L. (Ref. 0098)	(Ref. 0093)				[0093] / [0094] / [0096] / [0097] / [0098]
34			14-methyl-8-hexadecen-1-ol	DLL0034	Yasushi Kawakami		C₁₇H₃₄O	254.451		This compound shows sex attractant activity in female dermestid beetle.(Ref. 0043)		Bp ₀_.₀₃ 108-109 (S)-(E) (Ref. 0044) BP ₀_.₁ 150-151 (S)-(Z) (Ref. 0045)		n 1.4584 (S)-(E) (Ref. 0044) n 1.4568 (S)-(Z) (Ref. 0045)	[a]²⁵&_p +5.52 (S)-(E) (Ref. 0044) [a]²⁵&_p +5.76 (S)-(Z) (Ref. 0045)			(Ref. 0043)(Ref. 0044)(Ref. 0045)	(Ref. 0043)(Ref. 0045)	(Ref. 0043)(Ref. 0045)			Sex attractant of a female dermestid beetle (Trogoderma inclusum) (Ref. 0043)	(Ref. 0043)(Ref. 0044)(Ref. 0045)				[0043] / [0044] / [0045]
35			10-methyl-1-dodecanol	DLL0035	Yasushi Kawakami		C₁₃H₂₈O	200.361		The acetate form of this compound has Sex attractant activity in smaller tea tortrix moth (Adoxophes sp.) <(R)-form> (Ref. 0049)		B_p.₀_.₀₄ 84-86 B_p.₀_.₂₅ 125-135(Ref. 0046)			[a] -5.19 (Ref. 0047)			(Ref. 0047)	(Ref. 0047) (Ref. 0048)	(Ref. 0047)			The acetate form of this compound is female sex pheromone of the smaller tea tortrix moth (Adoxophyes sp.) <(R)-form> (Ref. 0049)	(Ref. 0046) (Ref. 0047) (Ref. 0048)				[0046] / [0047] / [0048] / [0049]
36			(3S,7S)-dimethyl-trideca-2-ol	DLL0036	Yasushi Kawakami		C₁₅H₃₂O	228.414		This compound is minor component of the sex pheromone of European pine sawfly Neodiprion sertifer.(Ref. 0082)		90C (0.07mmHg)		n 1.4485	[a] -14.2 (c 1.0 hexane)				(Ref. 0082)				This comound was isolated from female of Neodiprion sertifer.(Ref. 0082)	(Ref. 0082)				[0082]
37		panaxydol chlorohydrine	10-chloro-3,9-dihydroxyheptadeca-1-en-4,6-diyne	DLL0037	Yasushi Kawakami		C₁₇H₂₅ClO₂	296.832		This compound shows cytotoxic activity against L1210 cells.(Ref. 0053)					[a] -5.2 (c=0.3,CHCl₃) (Ref. 0052)		(Ref. 0053)(Ref. 0052)	(Ref. 0053)(Ref. 0052)	(Ref. 0053)(Ref. 0051)(Ref. 0052)(Ref. 0091)	(Ref. 0052)		(Ref. 0052)	This compound was isolated from Korean Ginseng root.(Ref. 0053) This compound is formed by the aqueous hydrochloric acid treatment of panaxydol.(Ref. 0052)	(Ref. 0091)				[0051] / [0052] / [0053] / [0091]
38			(3S,7S)-dimethyl-tetradeca-2-ol	DLL0038	Yasushi Kawakami		C₁₆H₃₄O	242.441		This compound is minor component of the sex pheromone of European pine sawfly Neodiprion sertifer.(Ref. 0082)		100C (0.07mmHg)		n 1.4501	[a] -13.5 (c 1.0 hexane)				(Ref. 0082)				This compound was isolated from female of Neodoprion sertifer.(Ref. 0082)	(Ref. 0082)				[0082]
39			(S)-(-)-3-(9-hydroxynonyl)-1-cyclopentene	DLL0039	Yasushi Kawakami		C₁₄H₂₆O	210.356		The acetate form of this compound is insect pheromone for red-bonded leaf roller and European corn borer					[a]-70.70.4(Ref. 0056)(acetate form)				(Ref. 0056)(acetate form)	(Ref. 0056)(acetate form)				(Ref. 0056)				[0056]
40			(R)-(+)-3-(9-hydroxynonyl)-1-cyclopentene	DLL0040	Yasushi Kawakami		C₁₄H₂₆O	210.356		The acetate form of this compound is insect pheromone for red-bonded leaf roller					[a]+70.80.7(Ref. 0056)(acetate form)				(Ref. 0056)(acetate form)	(Ref. 0056)(acetate form)				(Ref. 0056)				[0056]
41			1-tetradecanol	DLL0041	Yasushi Kawakami		C₁₄H₃₀O	214.387			38,0(Ref. 0151)								(Ref. 0150)				This compound is major component of Blue Inlet wax derived from the pollen of the Lodgepole pine (Pinus contorta).(Ref. 0149)					[0149] / [0150] / [0151]
42			5-decen-1-ol	DLL0042	Yasushi Kawakami		C₁₀H₂₀O	156.265		Sex pheromone of Peach Twing Moth (Anorsia lineatella) (Ref. 0063)		Bp ₁₄:100120 (Ref. 0065) Bp ₀_.₁₅:8385 (Ref. 0066)						(Ref. 0065) (Ref. 0066)	(Ref. 0065) (Ref. 0066)	(Ref. 0066)		GC (Ref. 0066)	Sex pheromone of Peach Twing Moth (Anorsia lineatella) (Ref. 0063)	(Ref. 0065) (Ref. 0066) (Ref. 0067)				[0063] / [0065] / [0066] / [0067]
43			(7E)-decen-1-ol	DLL0043	Yasushi Kawakami		C₁₀H₂₀O	156.265		The cis isomer of this compound shows a weeker lowering attraction-inhibition for male B.pinicolella. (Ref. 0070)		b.p. 92(7mm)(Ref. 0068) b.p. 75(0.02mm)(Ref. 0069)	d 0.8520(Ref. 0068)	n=1.4518(Ref. 0068) n=1.4496(Ref. 0069)				(Ref. 0069)	(Ref. 0069)				This compoound was isolated from the sea squirt,Halacynthia roretzi v. Drasche.(Ref. 0068)	(Ref. 0068) (Ref. 0069)				[0068] / [0069] / [0070]
44			(3S,7S)-dimethyl-hexadeca-2-ol	DLL0044	Yasushi Kawakami		C₁₈H₃₈O	270.494		This compound is minor component of the sex pheromone of European pine sawfly Neodiprion sertifer.(Ref. 0082)		130C (0.07 mmHg)		n 1.4520	[a] -12.1 (c 0.8 hexane)				(Ref. 0082)				This compound was isolated from female of Neodoprion sertifer.(Ref. 0082)	(Ref. 0082)				[0082]
45			(8Z)-dodecen-1-ol	DLL0045	Yasushi Kawakami		C₁₂H₂₄O	184.318		The acetate form of this compound attracts Grapholitha molesta and Grapholitha packrdi.(Ref. 0103)(Ref. 0104)		99-100/1.1mm (Ref. 0105)		n 1.4552 (Ref. 0105)				(Ref. 0105)	(Ref. 0105)			GLC(Ref. 0105)	This compound was isolated as a male sex attractant of moth,Grapholitha molesta.(Ref. 0103)(Ref. 0104)	(Ref. 0104)(Ref. 0105)				[0103] / [0104] / [0105]
46			(8E,10E)-dodecadien-1-ol	DLL0046	Yasushi Kawakami		C₁₂H₂₂O	182.302		This compound is sex pheromone of Carpocaspa pomonella.(Ref. 0117) This compound is a sex attractant of the codling moth,Laspeyresia pomonella.(Ref. 0118)	29-30(Ref. 0119)	89-90(0.2mmHg)(Ref. 0119)						(Ref. 0120)	(Ref. 0119)(Ref. 0120)	(Ref. 0120)		GC(Ref. 0117)(Ref. 0118)	This compound was isolated from virgin female Carpocaspa pomonella.(Ref. 0117)(Ref. 0119) This compound was isolated from codling moth,Laspeyresia pomonella.(Ref. 0118)	(Ref. 0118)(Ref. 0119)(Ref. 0120)				[0117] / [0118] / [0119] / [0120]
47			(Z,Z)-3,13-octadecadien-1-ol	DLL0047	Yasushi Kawakami		C₁₈H₃₄O	266.462		The acetate form of this compound is sex attractant of male peachtree borer,Sanninoidea exitiosa.(Ref. 0154)		133-135C/0.45mmHg (Ref. 0153)		n 1.4670 (Ref. 0153)				(Ref. 0153)	(Ref. 0153)			TLC(Ref. 0153) GLC(Ref. 0153)	This compound was isolated from the female peachtree borer ,Sannioidea exitiosa.(Ref. 0154)	(Ref. 0152) (Ref. 0153) (Ref. 0154) (Ref. 0155) (Ref. 0156)				[0152] / [0153] / [0154] / [0155] / [0156]
48			(E,Z)-3,13-octadecadien-1-ol	DLL0048	Yasushi Kawakami		C₁₈H₃₄O	266.462		The acetate form of this compound is sex attractant of male lesser peachtree borer,Synanthedon pictipes.(Ref. 0154)		125-130C/0.15mmHg (Ref. 0153)		n 1.4660 (Ref. 0153)				(Ref. 0153)	(Ref. 0153)			TLC(Ref. 0153) GLC(Ref. 0153)	This compound was isolated from female lesser peachtree borer,Synanthedon pictipes.(Ref. 0154)					[0153] / [0154]
49			(7E)-dodecen-1-ol	DLL0049	Yasushi Kawakami		C₁₂H₂₄O	184.318		This compound was identified as sex pheromone of the False Codling Moth,Argyroploce leucotreta.(Ref. 0122)	78-81(0.06mm)(Ref. 0124)			n 1.4538(Ref. 0121) n 1.4521(Ref. 0124)			(Ref. 0121)	(Ref. 0121)					This compound was identified as sex pheromone of the False Codling Moth,Argyroploce leucotreta.(Ref. 0122)	(Ref. 0121)<0123>>				[0121] / [0122] / [0124]
50			9-pentadecen-1-ol	DLL0050	Yasushi Kawakami		C₁₅H₃₀O	226.398		This compound inhibits the attraction of male moth induced by sex pheromone trap.(Ref. 0159) The acetate form of this compound attracts male A.orona moths.(Ref. 0160)(Ref. 0161)		141-142/1.9mmHg (Ref. 0157) 108-111/0.01 Torr (Ref. 0085)						(Ref. 0085)	(Ref. 0157)					(Ref. 0157) (Ref. 0085)				[0085] / [0157] / [0159] / [0160] / [0161]
51			(11Z)-eicosen-1-ol	DLL0051	Yasushi Kawakami		C₂₀H₄₀O	296.531		This compound is as active as natural pheromone from the sting.(Ref. 0127) This compound is stings pheromone of honey bee,Apis mellifera L.(HYMENOPTERA,APIDAE)(Ref. 0128)	25-26C (Ref. 0126)							(Ref. 0126)	(Ref. 0127)(Ref. 0128)	(Ref. 0127)(Ref. 0128)		GLC(Ref. 0126)(Ref. 0127)(Ref. 0128)	This compound was isolated from worker honey bees.(Ref. 0127) This compound was identified from thoracic gland of male carpenter bees (Xylocopa spp.)(Ref. 0128)	(Ref. 0125)(Ref. 0126)				[0125] / [0126] / [0127] / [0128]
52			(Z)-11-heptadecen-1-ol	DLL0052	Yasushi Kawakami		C₁₇H₃₄O	254.451		Acetate form of this compound is female sex pheromone components of Mamestra brassicae.(Ref. 0130)(Ref. 0131)													This compound was found in Ostrinia nubilalis and Bombyx moxi as the sex pheromone.(Ref. 0129) This compound was found from pheromone glands of cabbage armyworm,Mamesta brassicae.(Ref. 0130)	(Ref. 0131)(Acetate form of this compound)				[0129] / [0130] / [0131]
53			(E,Z)-6-11-hexadecadien-1-ol	DLL0053	Yasushi Kawakami		C₁₆H₃₀O	238.409		Mixture of Acetate form of this compound and aldehyde form of this compound elicite electroantennogram reaction in male Antheraea pernyi .(Ref. 0132)								(Ref. 0133)				GC(Ref. 0132)	The acetate form of this compound was found as sex pheromone components of the female saturniid moth Antheraea pernyi (lepidoptera:Saturniidae)(Ref. 0132)(Ref. 0133)	(Ref. 0133)				[0132] / [0133]
54			(Z,Z)-6,11-hexadecadien-1-ol	DLL0054	Yasushi Kawakami		C₁₆H₃₀O	238.409		Acetate form of this compound is sex pheromone of Eudia pavonia.(Ref. 0134)								(Ref. 0134)	(Ref. 0134)				Acetate form of this compound was sex pheromone of Eudia pavonia.(Ref. 0134)	Acetate form(Ref. 0134)				[0134]
55			(Z)-7-hexadecen-1-ol	DLL0055	Yasushi Kawakami		C₁₆H₃₂O	240.425		Acetate form of this compound is sex attractant for the male pink ballworm moth,Pectinophora gossipiella.(Ref. 0136)(Ref. 0138)		Acetate form of this compound is 100-104C(0.001mm)(Ref. 0136) Acetate form of this compound is 121.5-124.5C(0.08-0.14mm)(Ref. 0136)		Acetate form of this compound is n 1.4484 (Ref. 0136)				(Ref. 0138)Acetate form of this compound	(Ref. 0138)Acetate form of this compound	(Ref. 0138)Acetate form of this compound		GC of acetate form of this compound (Ref. 0138)	This compound was identified from extracts of worker heads of stingless bee.(Scaptotrigona postica)(Ref. 0137) This compound was found from extracts of heads of male Bombus agrorum.(Ref. 0139)	(Ref. 0136) (Ref. 0138)(Acetate form)				[0136] / [0137] / [0138] / [0139]
56			(Z)-11-hexadecen-1-ol	DLL0056	Yasushi Kawakami		C₁₆H₃₂O	240.425		This compound is sex pheromone of the Clover Cutworm Moth,Scotogramma trifolii.(Ref. 0140) The acetate form of this compound attracts male moth.(Ref. 0141) The acetate form of this compound is a major component of the bertha armyworm sex pheromone.(Ref. 0143)		140C (0.15 torr)(Ref. 0142)						(Ref. 0142)	(Ref. 0142)			(Ref. 0140)	This compound was isolated from an extracts of female abdominal tips of Scotogramma trifolii.(Ref. 0140) The acetate form of this compound was isolated from diamondback moth. (Lepidoptera : Platellidae)(Ref. 0141) The acetate form of this compound was isolated from the Bertha armywoorm ,Mamestra Configurate.(Ref. 0143)	(Ref. 0141) (Ref. 0142)				[0140] / [0141] / [0142] / [0143]
57			(E,Z)-2,13-octadecadien-1-ol	DLL0057	Yasushi Kawakami		C₁₈H₃₄O	266.462		The acetate form of this compound attracts males of grape root borer.(Ref. 0148)										(Ref. 0148)			The acetate form of this compound was identified from ovipositor extracts of the grape root borer.(Ref. 0148)	Acetate form of this compound (Ref. 0148)				[0148]

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AUTHOR	:	Boudouy,R.
TITLE	:	SYNTHESE STEREOSELECTIVE D'UNE COMPOSANTE DE LA PHEROMONE SEXUELLE DE ""L'ECAILLE ROUGE DE CALIFORNIE"":L'ACETATE D'ISOPROPENYL-6 METHYL-3 DECADIENE-3,9 YLE (3Z,6R)
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AUTHOR	:	Rossi,R.,Carpita,A.
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AUTHOR	:	Mori,K.
TITLE	:	ABSOLUTE CONFIGURATIONS OF (-)-14-METHYLHEXADEC-8-cis-EN -1-OL AND METHYL (-)-14-METHYLHEXADEC-8-cis-ENOATE,THE SEX PHEROMONE OF FEMALE DERMESTID BEETLE
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AUTHOR	:	Philip,E.,S.
TITLE	:	Syntheses of the Stereoisomers of the Sex Pheromones of the Southern Corn Rootworm and Lesser Tea Tortrix
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AUTHOR	:	Hans,J.,B.,Rosa,T.,S.,F.,Nelson,F.,Otto,V.
TITLE	:	Synyhese der Enantiomeren von 10-Methyldodecylacetat und 12-Methyltetradecylacetat, chiralen Pheromonkomponenten von Adoxophyes-Arten (Lepidoptera: Tortricidae)
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AUTHOR	:	Mats,H.,Hans-erik,H.
TITLE	:	Synthesis of (R)-and (S)-10-Methl-1-dodecyl Acetate,Sex Pheromone Components of the Smaller Tea Tortrix Moth (Adoxophyes sp.),from Chiral Synthons Prepared via Asymmetric Synthesis
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AUTHOR	:	Tamaki,Y.,Noguchi,H.,Sugie,H.,Santo,R.,Karlya,A.
TITLE	:	Minor Coponents of the Female Sex-Attractant Pheromone of the Smaller Tea Tortrix Moth (Lepidoptera:Tortricidae):Isolation and Identification
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AUTHOR	:	Mori,K.,Puapoomchareon,P.
TITLE	:	Synthesis of the Enantiomers of (E)-1-Ethyl-5-methyl-4-heptenyl Acetate (Quadrilure),the Aggregation Pherioomone of Cathartus quadricollis
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AUTHOR	:	Peter,B.,Oelrichs,Jack,C.,Ng,Alan,A.,Seawright,Lothar,Schaffeler,John,K.Macleod
TITLE	:	Isolation and Identification of a Compound From Avocado (Persea americana )Leaves Which Causes Necrosis of the Acinar Epithelium of the Lacting Mammary Gland and the Myocardium
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AUTHOR	:	Kitagawa, I., Taniyama, T., Shibuya, H., Noda, T., and Yoshikawa, M.
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AUTHOR	:	Ahn,B.,Z.,Kim,S.,I.,Lee,Y.,H.
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AUTHOR	:	Dai, J. R., Hallock, Y. F., Cardellina, J. H., 2nd, and Boyd, M. R.
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AUTHOR	:	Walter,K.,S.,Wuthier,D.
TITLE	:	(3S,8E)-1,3-Dihydroxy-8-decen-5-on,ein Stoffwechselprodukt von Streptomyces fimbriatus
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AUTHOR	:	F.,Szurdoki,L.,Novak,Cs.,Szantay,E.,B.,Gacs,M.,Toth
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AUTHOR	:	Fitzgerald, J. E., Petrere, J. A., McGuire, E. J., and de la Iglesia, F. A.
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AUTHOR	:	Matsunaga, H., Katano, M., Yamamoto, H., Mori, M., and Takata, K.
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AUTHOR	:	Matsunaga, H., Katano, M., Yamamoto, H., Fujito, H., Mori, M., and Takata, K.
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TITLE	:	Isolation of 7-Decen-1-ol from an Ascidian
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AUTHOR	:	Svirskaya,P.,I.,Leznoff,C.,C.,Weatherston,J.,Laing,J.,E.
TITLE	:	Syntheses of Trans Alken-1-ols as Candidates for Insect Sex Attractants
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AUTHOR	:	Proesner,E.
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AUTHOR	:	Pierce,Jr.,H.,D.,Poerce,A.,M.,Johnston,B.,D.,Oehlschlager,A.,C.,Borden,J.,H.
TITLE	:	AGGREGATION PHEROMONE OF SQUARE-NECKED GRAIN BEETLE,Cathartus quadricollis (GUER.)
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AUTHOR	:	Joseph,Kalish
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AUTHOR	:	Katz, D. H., Marcelletti, J. F., Khalil, M. H., Pope, L. E., and Katz, L. R.
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AUTHOR	:	Katz, D. H., Marcelletti, J. F., Pope, L. E., Khalil, M. H., Katz, L. R., and McFadden, R.
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AUTHOR	:	Hedenstrom,E.,Hogberg,H.,E.,Wassgren,A.,B.,Bergstrom,G.,Lofqvist,J.,Hansson,B.,Anderbrant,O.
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AUTHOR	:	Estevez-Braun, A., Estevez-Reyes, R., Moujir, L. M., Ravelo, A. G., and Gonzalez, A. G.
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AUTHOR	:	H.,J.,Bestmann,W.,Stransky,O.,Vostrowsky,P.,Range
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AUTHOR	:	Matsunaga, H., Saita, T., Nagumo, F., Mori, M., and Katano, M.
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AUTHOR	:	Smith, R. G., Daterman, G. E., Daves, G. D., Jr., McMurtrey, K. D., and Roelofs, W. L.
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AUTHOR	:	Poplawski,J.,Wrobel,J.,T.,Glinka,T.
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AUTHOR	:	Reed,D.,W.,Chisholm,M.,D.
TITLE	:	ATTRACTION OF MOTH SPECIES OF TORTRICIDAE,GELECHIIDAE,GEOMETRIDAE,DREPANIDAE,PYRALIDAE, AND GRACILLAROODAE FAMILIES TO FIELD TRAPS BAITED WITH CONJUGATED DIENES
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AUTHOR	:	Iwamura,J.,Komaki,K.,Komai,K.,Hirao,N.
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AUTHOR	:	Setzer, W. N., Green, T. J., Whitaker, K. W., Moriarity, D. M., Yancey, C. A., Lawton, R. O., and Bates, R. B.
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AUTHOR	:	Wang,Y.,Toyota,M.,Krause,F.,Hamburger,M.,Hostettmann,K.
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AUTHOR	:	Oikawa, T., Onozawa, C., Inose, M., and Sasaki, M.
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AUTHOR	:	Roelofs,W.,L.,Comeau,A.,Selle,R.
TITLE	:	Sex Pheromone of the Oriental Fruit Moth
JOURNAL	:	Nature
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AUTHOR	:	Holan,G.,O'Keefe,D.,F.
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AUTHOR	:	Mori,K.,Uchida,M.,Matsui,M.
TITLE	:	SYNTHESIS OF ALIPHATIC INSECT PHEROMONES FROM ALICYCLIC STARTING MATERIALS
JOURNAL	:	Tetrahedron
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AUTHOR	:	Keller,S.,W.,Wuthier,D.
TITLE	:	122.Stoffwechselprodukte von Mikroorganismen (3S,8E)-1,3-Dihydroxy-8-decen-5-one,ein Stoffwechselprodukt von Streptomyces fimbriatus (Millard und Burr 1926)
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AUTHOR	:	Mizutani, S., Odai, H., Masuda, T., Iijima, M., Osono, M., Hamada, M., Naganawa, H., Ishizuka, M., and Takeuchi, T.
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AUTHOR	:	Rossi,R.
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AUTHOR	:	Chisholm,M.,D.,Underhill,E.,W.,Steck,W.,Slessor,K.,N.,Grant,G.,G.
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AUTHOR	:	Ando,T.,Yoshida,S.,Tatsuki,S.,Takahashi,N.
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AUTHOR	:	Polina,I.,S.,Clifford,C.,L.,
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AUTHOR	:	Descoius,C.,Samain,D.,Cassou,B.,L.,Gallois,M
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[0115]

AUTHOR	:	Buser, H. R., Rauscher, S., and Arn, H.
TITLE	:	Sex pheromone of Lobesia botrana: (E,Z)-7,9-dodecadienyl acetate in the female grape vine moth PubMed ID:4281209
JOURNAL	:	Z Naturforsch [C].
VOL	:	29 PAGE : 781-783 (1974)

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[0116]

AUTHOR	:	Buser, H. R., and Arn, H.
TITLE	:	Analysis of insect pheromones by quadrupole mass fragmentography and high-resolution gas chromatography PubMed ID:1150795
JOURNAL	:	J Chromatogr.
VOL	:	106 PAGE : 83-95 (1975)

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[0117]

AUTHOR	:	McDonough,L.,M.,Gorge,D.,A.,Butt,B.,A.,Jacobson,M.,Johnson,G.,R.
TITLE	:	Isolation of a Sex Pheromone of the Codling Moth.
JOURNAL	:	J.Econ.ntomol.
VOL	:	62 PAGE : 62-65 (1969)

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[0118]

AUTHOR	:	Roerofs,W.,Comeau,A.,Hill,A.,Milicevic,G.
TITLE	:	Sex Attractant of the codling Moth:Characterization with Electroantennogram Technique.
JOURNAL	:	Science(Washington D.C.)
VOL	:	174 PAGE : 297-299 (1971)

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[0119]

AUTHOR	:	Descoins,C.,Henrick,C.,A.
TITLE	:	STEREOSELECTIVE SYNTHESIS OF A SEX ATTRACTANT OF THE CODLING MOTH.
JOURNAL	:	Tetrahedron lett.
VOL	:	30 PAGE : 2999-3002 (1972)

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[0120]

AUTHOR	:	Yamada,S.,Ohsawa,H.,Suzuki,T.,Takayama,H.
TITLE	:	Stereoselective Synthesis of (E)-,(E,Z)-,and (E,E)-Conjugated Dienes via Alkylation of 3-Sulfolenes as the Key Step.
JOURNAL	:	J.Org.Chem.
VOL	:	51 PAGE : 4934-4940 (1986)

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[0121]

AUTHOR	:	Leznoff,C.,C.,Fyles,T.,M.,Weatherston,J.
TITLE	:	The use of polymer supports in organic synthesis. VIII. solid phase syntheses of insect sex attractants.
JOURNAL	:	Can.J.Chem.
VOL	:	55 PAGE : 1143-1153 (1977)

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[0122]

AUTHOR	:	Read,J.,S.,Warren,F.,L.
TITLE	:	Identification of the Sex Pheromone of the False Codling Moth,Argyroploce leucotreta.
JOURNAL	:	J.Chem.Soc.,Chem.Commun.
VOL	:	PAGE : 792-793 (1968)

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[0123]

AUTHOR	:	Brown,H.,C.,Molander,G.,A.
TITLE	:	Vinylic Organoboranes. 2. Improved Procedures for the Protonolysis of Alkenyldialkylboranes Providing a Simplified Stereospecific Synthesis of (Z)-Alkenes.
JOURNAL	:	c
VOL	:	51 PAGE : 4512-4514 (1986)

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[0124]

AUTHOR	:	Green, N., Jacobson, M., Henneberry, T. J., and Kishaba, A. N.
TITLE	:	Insect sex attractants. VI. 7-dodecen-1-ol acetates and congeners PubMed ID:6037038
JOURNAL	:	J Med Chem.
VOL	:	10 PAGE : 533-535 (1967)

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[0125]

AUTHOR	:	Shani,A.
TITLE	:	AN EFFICIENT SYNTHESIS OF MUSCALURE FROM JOJOBA OIL OR OLEYL ALCOHOL.
JOURNAL	:	Journal of Chemical Ecology
VOL	:	5 PAGE : 557-563 (1979)

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[0126]

AUTHOR	:	Kobayashi,A.,Sugawara,F.,Yamashita,K.
TITLE	:	Stereoselective Synthesis of (Z)-11- and (E)-11-Eicosenyl Acetate.
JOURNAL	:	Agric.Biol.Chem.
VOL	:	42 PAGE : 1973-1974 (1978)

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[0127]

AUTHOR	:	Pickett,J.A.,Williams,I.,H.,Martin,A.,P.
TITLE	:	(Z)-11-EICOSEN-1-OL,AN IMPORTANT NEW PHEROMONAL COMPONENT FROM THE STING OF THE HONEY BEE,Apis mellifera L.(HYMENOPTERA,APIDAE).
JOURNAL	:	Journal of Chemical Ecology
VOL	:	8 PAGE : 163-175 (1982)

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[0128]

AUTHOR	:	Andersen,J.,F.,Buchmann,S.,L.,Weisleder,D.,Plattner,R.,D.,Minckley,R.,L.
TITLE	:	IDENTIFICATION OF THORACIC GLAND CONSTITUENTS FROM MALE Xylocopa spp. LATREILLE (Hymenoptera:Anthophoridae) FROM ARIZONA.
JOURNAL	:	Journal of Chemical Ecology
VOL	:	14 PAGE : 1153-1162 (1988)

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[0129]

AUTHOR	:	Attygalle,A.,B.,Herrig,M.,Vostrowsky,O.,Bestmann,H.,J.
TITLE	:	TECHNIQUE FOR INJECTING INTACT GLANDS FOR ANALYSIS OF SEX PHEROMONES OF LEPIDOPTERA BY CAPILLARY GAS CHROMATOGRAPHY:Reinvestigation of Pheromone Complex of Mamestra brassicae.
JOURNAL	:	Journal of Chemical Ecology
VOL	:	13 PAGE : 1299-1311 (1987)

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[0130]

AUTHOR	:	Den Otter,C.,J.,Van Der Haagen,M.,M.
TITLE	:	SEX PHEROMONE ATTRACTANTS AND INHIBITORS IN THE CABBAGE ARMYWORM,MAMESTRA BRASSICAE L.(LEP.:NOCTUIDAE):ELECTROPHYSIOLOGICAL DISCRIMINATION.
JOURNAL	:	Insect Sci.Applic.
VOL	:	10 PAGE : 235-242 (1989)

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[0131]

AUTHOR	:	Novak,L.,Toth,M.,Balla,J.,Szantay,Cs.
TITLE	:	SEX PHEROMONE OF THE CABBAGE ARMYWORM,MAMESTRA BRASSICAE:ISOLATION,IDENTIFICATION AND STEREOCONTROLLED SYNTHESIS.
JOURNAL	:	Acta Chimica Academiae Scientiarum Hungaricae
VOL	:	102 PAGE : 135-140 (1979)

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[0132]

AUTHOR	:	Bestmann,H.,J.,Attygalle,A.,B.,Brosche,T.,Erler,J.,Platz,H.,Schwarz,J.,Vostrowsky,O.,Hong,W.,C.
TITLE	:	Identification of Three Sex Pheromone Components of the Female Saturniid Moth Antheraea pernyi (Lepidoptera:Saturniidae).
JOURNAL	:	Z.Naturforsch.
VOL	:	42 PAGE : 631-636 (1987)

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[0133]

AUTHOR	:	Kochansky,J.,P.,Carde,R.,T.,Taschenberg,E.,F.,Roelofs,W.,L.
TITLE	:	RHYTHMS OF MALE Antheraea polyphemus Attraction and Female Attractiveness,and an Improved Pheromonate Synthesis.
JOURNAL	:	J.Chem.Ecol.
VOL	:	3 PAGE : 419-427 (1977)

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[0134]

AUTHOR	:	Ducoux,J.,P.,Menez,P.,L.,Kunesch,N.
TITLE	:	An Efficient and Stereoselective Synthesis of Insect Pheromones by Way of Nickel-catalyzed Grignard Reactions.Syntheses of Gossyplure and Pheromonws of Eudia panovia and Drosophila melanogaster.
JOURNAL	:	Tetrahedron
VOL	:	48 PAGE : 6403-6412 (1992)

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[0135]

AUTHOR	:	Bestmann,H.,J.,Koschatzky,K.,H.,Vostrowsky,O.
TITLE	:
JOURNAL	:	Liebigs Ann. Chem.
VOL	:	PAGE : 1478- (1982)

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[0136]

AUTHOR	:	Green, N., Jacobson, M., and Keller, J. C.
TITLE	:	Hexalure, an insect sex attractant discovered by empirical screening PubMed ID:5801774
JOURNAL	:	Experientia.
VOL	:	25 PAGE : 682-683 (1969)

[TOP]

[0137]

AUTHOR	:	Engels,E.,Engels,W.,Schroder,W.,Francke,W.
TITLE	:	INTRANIDAL WORKER REACTIONS TO VOLATILE COMPOUNDS IDENTIFIED FROM CEPHALIC SECRETIONS IN THE STINGLESS BEE,Scaptotrigona postica (HYMENOPTERA, MELIPONINAE).
JOURNAL	:	Journal of Chemical Ecology
VOL	:	13 PAGE : 371-385 (1987)

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[0138]

AUTHOR	:	Subramanian,G.,B.,V.,Sharma,R.
TITLE	:	A short synthesis of hexalure from aleuritic acid.
JOURNAL	:	Chemistry and Industry
VOL	:	17 PAGE : 664-665 (1988)

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[0139]

AUTHOR	:	Baraabas,A.,Botar,A.,A.,Gocan,A.,Popovici,N.,Hodosan,F.
TITLE	:	¹³C NMR OF SOME INSECT ATTRACTANTS AND RELATED COMPOUNDS.
JOURNAL	:	Tetrahedron
VOL	:	34 PAGE : 2191-2194 (1978)

[TOP]

[0140]

AUTHOR	:	Underhill,E.,W.,Steck,W.,F.,Chisholm,M.,D.
TITLE	:	Sex Pheromone of the Clover Cutworm Moth,Scotogramma trifolii:Isolation,Identification and Field Studies.
JOURNAL	:	Environmental Entomology
VOL	:	5 PAGE : 307-310 (1975)

[TOP]

[0141]

AUTHOR	:	Tamali,Y.,Kawasaki,K.,Yamada,H.,Koshihara,T.,Osaki,N.,Ando,T.,Yoshida,S.,Kakinohara,H.
TITLE	:	(Z)-11-Hexadecenal and (Z)-11-Hexadecennyl Acetate:Sex Pheromone Components of the Diamondback Moth (Lepidoptera : Plutellidae).
JOURNAL	:	Appl.Ent.Zool.
VOL	:	12 PAGE : 208-210 (1977)

[TOP]

[0142]

AUTHOR	:	Bestmann,H.,J.,Kantardjiew,I.,Rosel,P.,Stransky,W.,Vostrowsky,O.
TITLE	:	Synthese von 1-substituierten (Z)-11-Alkenen.
JOURNAL	:	Chem.Ber.
VOL	:	111 PAGE : 248-253 (1978)

[TOP]

[0143]

AUTHOR	:	Chisholm,M.,D.,Steck.W.,F.,Arthur,A.,P.,Underhill,E.,W.
TITLE	:	EVIDENCE FOR CIS-11-HEXADECEN-1-OL ACETATE AS A MAJOR COMPONENT OF THE SEX PHEROMONE OF THE BERTHA ARMYWORM,MAMESTRA CONFIGURATA (LEPIDOPTERA : NOCTUIDAE).
JOURNAL	:	Can.Ent.
VOL	:	107 PAGE : 361-366 (1975)

[TOP]

[0144]

AUTHOR	:	William,A.,Jones,M.Jacobson,Dial,F.,Martin
TITLE	:	Sex Attractant of the Pink Bollworm Moth: Isolation , Identification , and Synthesis.
JOURNAL	:	SCIENCE
VOL	:	152 PAGE : 1516-1517 (1966)

[TOP]

[0145]

AUTHOR	:	J.,Kossanyi,B.,Furth,J.,P.,Morizur
TITLE	:	INSECT CHEMISTRY.APPLICATION OF THE NORRISH TYPE-I REACTION TO THE SYNTHESIS OF PROPYLURE,THE SEXUAL PHEROMONE OF Pectinophora gossypiella Saundere.
JOURNAL	:	Tetrahedron Letters
VOL	:	36 PAGE : 3459-3462 (1973)

[TOP]

[0146]

AUTHOR	:	G.Pattenden
TITLE	:	A Synthesis of Propylure,Sex Attractant of the Pink Bollworm Moth.
JOURNAL	:	Journal of Chem. Soc.
VOL	:	PAGE : 2385-2388 (1968)

[TOP]

[0147]

AUTHOR	:	T.,Higa,J.,Tanaka,T.,Kohagura,T.,Wauke
TITLE	:	Bioactive Polyacetylenes from Stony Corals.
JOURNAL	:	CHEMISTRY LETTERS
VOL	:	PAGE : 145-148 (1990)

[TOP]

[0148]

AUTHOR	:	M.,Schwarz,J.,A.,Klun,B.,A.,Leonhardt,D.,T.,Johnson
TITLE	:	(E,Z)-2,13-OCTADECADIEN-1-OL ACETATE . A NEW PHEROMONE STRUCTURE FOR SESIID MOTHS.
JOURNAL	:	Tetrahedron Letters
VOL	:	24 PAGE : 1007-1010 (1983)

[TOP]

[0149]

AUTHOR	:	K.,R.,Adams,R.,Bonnett
TITLE	:	Blue Inlet Wax.
JOURNAL	:	NATURE
VOL	:	223 PAGE : 943-944 (1969)

[TOP]

[0150]

AUTHOR	:	R.,Rossi
TITLE	:	INSECT PHEROMONE COMPONENTS.
JOURNAL	:	Tetrahedron
VOL	:	38 PAGE : 639-644 (1982)

[TOP]

[0151]

AUTHOR	:	A.,Watanabe
TITLE	:	Synthesis and Physical Properties of Normal Higher Promary Alcohols. IV. Thermal and X-Ray Studies on the Polymorphism of the Alcohols of Even Carbon Numbers from Dodecanol to Tetratriacontanol.
JOURNAL	:	Bull.Chem.Soc.
VOL	:	34 PAGE : 1728-1734 (1961)

[TOP]

[0152]

AUTHOR	:	M.,Uchida,K.,Nakagawa,K.,Mori
TITLE	:	Stereoselective Synthesis of (Z,Z)-3,13-Octadecadienyl acetate ,the Attractant for Smaller Clear Wing Moth.
JOURNAL	:	Agric. Biol. Chem.
VOL	:	43 PAGE : 1919-1922 (1979)

[TOP]

[0153]

AUTHOR	:	M.,Uchida,K.,Mori,M.,Matsui
TITLE	:	Synthesis of (Z,Z)-3,13-Octadecadienyl Acetate and Its (E,Z)-Isomer,the Attractant for the Cherrytree Borer.
JOURNAL	:	Agric.Biol.Chem.
VOL	:	42 PAGE : 1067-1070 (1978)

[TOP]

[0154]

AUTHOR	:	J.,H.,Tumlinson,C.,E.,Yonce,R.,E.,Doolittle,R.,R.,Heath,C.,R.,Gentry,E.,R.,Mitchell
TITLE	:	Sex Pheromone and Reproductive Isolation of the Lesser Peachtree Borer and the Peachtree Borer.
JOURNAL	:	Science
VOL	:	185 PAGE : 614-616 (1974)

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[0155]

AUTHOR	:	P.,Vinczer,G.,Baan,L.,Novak,C.,Szantay
TITLE	:	A NOVEL STEREOCONTROLLED SYNTHESIS OF (Z,Z)-3-13-OCTADECADIEN-1-YL ACETATE, THE SEX PHEROMONE OF SYNANTHEDON SPECIES.
JOURNAL	:	Tetrahedron Letters
VOL	:	25 PAGE : 2701-2704 (1984)

[TOP]

[0156]

AUTHOR	:	T.,Ebata,K.,Mori
TITLE	:	A Convenient Synthesis of a Mixture of (Z,Z)-3,13-Octadecadienyl Acetate and Its (E,Z)-Isomer,the Attractant for the Cherrytree Borer.
JOURNAL	:	Agric.Biol.Chem.
VOL	:	43 PAGE : 1567-1570 (1979)

[TOP]

[0157]

AUTHOR	:	M.,Horiike,M.,Tanouchi,C.,Hirano
TITLE	:	A Convenient Method for Synthesizing (Z)-Alkenols and Acetates.
JOURNAL	:	Agric.Biol.Chem.
VOL	:	44 PAGE : 257-261 (1980)

[TOP]

[0158]

AUTHOR	:	D.,H.,Calam
TITLE	:	Species and Sex-specific Compounds from the Heads of Male Bumblebees (Bombus spp.). PubMed << 5765060>>
JOURNAL	:	NATURE
VOL	:	221 PAGE : 856-857 (1969)

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[0159]

AUTHOR	:	C.,Hirano,M.,Tanouchi,M.,Horiike
TITLE	:	Inhinitory Effect of (Z)-9-Alkenols and (Z)-9-Alkenyl Acetates on Attraction of Male Spodoptera litura to the Synthetic Sex Pheromone.
JOURNAL	:	Appl.Ent.Zool.
VOL	:	15 PAGE : 502-503 (1980)

[TOP]

[0160]

AUTHOR	:	S.,Voerman,A.,K.,Minks,E.,A.,Goewie
TITLE	:	SPECIFICITY OF THE PHEROMONE SYSTEM OF Adoxophyes orama AND Clepsis spectrana.
JOURNAL	:	J.Chem.Ecol.
VOL	:	1 PAGE : 423-429 (1975)

[TOP]

[0161]

AUTHOR	:	S.,Voerman,A.,K.,Minks,N.,W.,H.,Houx
TITLE	:	Sex Pheromones of Summerfruit Tortrix Moth,Adoxophyes orana : Investigations on Compounds Modifying Their Attractancy.
JOURNAL	:	ENVIRONMENTAL ENTOMOLOGY
VOL	:	PAGE : 701-704 (1974)

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[0162]

AUTHOR	:	K.,Mori,M.,Tokunaga,M.,Matsui
TITLE	:	STEREOSELECTIVE SYNTHESIS OF THE PINK BOLLWORM SEX PHEROMONE,(Z,Z)7,11-HEXADECADIENYL ACETATE AND ITS (Z,E)-ISOMER.
JOURNAL	:	Tetrahedron
VOL	:	31 PAGE : 1846-1848 (1975)

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[0163]

AUTHOR	:	K.,Mori,M.,Tominaga,M.,Matsui
TITLE	:	Synthesis of the Pink Bollworm Sex Pheromone,7-cis ,11cis-Hexadecadienyl Acetate and Its 11-trans Isomer.
JOURNAL	:	Agr.Biol.Chem.
VOL	:	38 PAGE : 1551-1552 (1974)

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[0164]

AUTHOR	:	K.,.W.,Vick,H.,C.,F.,Su,L.,L.,Sower,P.,G.,Mahany,P.,C.,Drummond
TITLE	:	(Z-E)-7,11-hexadecadien-1-ol Acetate : The Sex Pheromone of the Angoumois Grain Moth,Sitotroga cerealella.
JOURNAL	:	Experientia
VOL	:	30 PAGE : 17-18 (1974)

[TOP]

[0165]

AUTHOR	:	H.,E.,Hummel,L.,K.,Gaston,H.,H.,Shorey,R.,S.,Kaae,K.,L.,Byrne
TITLE	:
JOURNAL	:	Sience
VOL	:	181 PAGE : 873- (1973)

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