Details
Stereochemistry | ABSOLUTE |
Molecular Formula | C15H24O2 |
Molecular Weight | 236.3499 |
Optical Activity | UNSPECIFIED |
Defined Stereocenters | 5 / 5 |
E/Z Centers | 0 |
Charge | 0 |
SHOW SMILES / InChI
SMILES
C[C@@H]1[C@H](O)C[C@@H](O)C2=CC[C@H](C[C@]12C)C(C)=C
InChI
InChIKey=BXXSHQYDJWZXPB-OKNSCYNVSA-N
InChI=1S/C15H24O2/c1-9(2)11-5-6-12-14(17)7-13(16)10(3)15(12,4)8-11/h6,10-11,13-14,16-17H,1,5,7-8H2,2-4H3/t10-,11-,13-,14-,15-/m1/s1
Approval Year
PubMed
Title | Date | PubMed |
---|---|---|
Differential induction of sesquiterpene metabolism in tobacco cell suspension cultures by methyl jasmonate and fungal elicitor. | 2000 Sep 15 |
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Cloning, heterologous expression, and functional characterization of 5-epi-aristolochene-1,3-dihydroxylase from tobacco (Nicotiana tabacum). | 2001 Sep 15 |
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Probing sesquiterpene hydroxylase activities in a coupled assay with terpene synthases. | 2003 Jan 15 |
|
Kinetic and molecular analysis of 5-epiaristolochene 1,3-dihydroxylase, a cytochrome P450 enzyme catalyzing successive hydroxylations of sesquiterpenes. | 2005 Feb 4 |
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1O869T5P54
Created by
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CAPSIDIOL
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37208-05-2
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DTXSID50190703
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161937
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28283
Created by
admin on Sat Dec 16 07:42:40 GMT 2023 , Edited by admin on Sat Dec 16 07:42:40 GMT 2023
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SUBSTANCE RECORD