InChI=1S/C16H26O3/c1- 12(9- 10- 14- 16(3,4) 19- 14) 7- 6- 8- 13(2) 11- 15(17) 18- 5/h7,11,14H,6,8- 10H2,1- 5H3/b12- 7+,13- 11+/t14- /m1/s1 |
QVJMXSGZTCGLHZ-HONBPKQLSA-N |
COC(=O)\C=C(/C)CC\C=C(/C)CC[C@H]1OC1(C)C |
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animal metabolite
Any eukaryotic metabolite produced during a metabolic reaction in animals that include diverse creatures from sponges, insects to mammals.
(via juvenile hormone )
hormone
Originally referring to an endogenous compound that is formed in specialized organ or group of cells and carried to another organ or group of cells, in the same organism, upon which it has a specific regulatory function, the term is now commonly used to include non-endogenous, semi-synthetic and fully synthetic analogues of such compounds.
(via juvenile hormone )
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View more via ChEBI Ontology
methyl (2E,6E)-9-[(2R)-3,3-dimethyloxiran-2-yl]-3,7-dimethylnona-2,6-dienoate
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(+)-Juvenile hormone III
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ChemIDplus
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(10R)-Juvenile hormone III
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ChemIDplus
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JH III
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ChemIDplus
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Juvenile hormone 3
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ChemIDplus
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juvenile hormone III
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UniProt
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Methyl (2E,6E)-(10R)-10,11-epoxy-3,7,11-trimethyl-2,6-dodecadienoate
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ChemIDplus
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Methyl (R-(E,E))-9-(3,3-dimethyloxiranyl)-3,7-dimethyl-2,6-nonadienoate
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ChemIDplus
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Methyl 10,11-epoxy-3,7,11-trimethyl-trans,trans-(10R)-2,6-dodecadienoate
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ChemIDplus
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Methyl 10,11-epoxy-3,7,11-trimethyl-trans,trans-2,6-dodecadienoate
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ChemIDplus
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Methyl R-(+)-10,11-epoxyfarnesate
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ChemIDplus
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22963-93-5
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CAS Registry Number
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KEGG COMPOUND
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22963-93-5
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CAS Registry Number
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ChemIDplus
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4453965
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Reaxys Registry Number
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Reaxys
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22664054
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PubMed citation
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Europe PMC
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23034815
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PubMed citation
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Europe PMC
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23121109
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PubMed citation
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Europe PMC
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24657668
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PubMed citation
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Europe PMC
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