Details
| Stereochemistry | ACHIRAL |
| Molecular Formula | C15H16O4 |
| Molecular Weight | 260.2851 |
| Optical Activity | NONE |
| Defined Stereocenters | 0 / 0 |
| E/Z Centers | 0 |
| Charge | 0 |
SHOW SMILES / InChI
SMILES
CC(C)C1=C2C=C(C)C=C(O)C2=C(C=O)C(O)=C1O
InChI
InChIKey=WWHRTLINNBKCGL-UHFFFAOYSA-N
InChI=1S/C15H16O4/c1-7(2)12-9-4-8(3)5-11(17)13(9)10(6-16)14(18)15(12)19/h4-7,17-19H,1-3H3
| Molecular Formula | C15H16O4 |
| Molecular Weight | 260.2851 |
| Charge | 0 |
| Count |
|
| Stereochemistry | ACHIRAL |
| Additional Stereochemistry | No |
| Defined Stereocenters | 0 / 0 |
| E/Z Centers | 0 |
| Optical Activity | NONE |
Approval Year
PubMed
| Title | Date | PubMed |
|---|---|---|
| The cyclization of farnesyl diphosphate and nerolidyl diphosphate by a purified recombinant delta-cadinene synthase. | 2001 Apr |
|
| 8-Hydroxy-(+)-delta-cadinene is a precursor to hemigossypol in Gossypium hirsutum. | 2003 Sep |
|
| The peroxidative coupling of hemigossypol to (+)- and (-)-gossypol in cottonseed extracts. | 2006 Feb |
|
| Increased terpenoid accumulation in cotton (Gossypium hirsutum) foliage is a general wound response. | 2008 Apr |
|
| Stereoselective coupling of hemigossypol to form (+)-gossypol in moco cotton is mediated by a dirigent protein. | 2008 Dec |
Patents
| Substance Class |
Chemical
Created
by
admin
on
Edited
Fri Dec 15 17:58:46 GMT 2023
by
admin
on
Fri Dec 15 17:58:46 GMT 2023
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| Record UNII |
A7A75KAZ73
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| Record Status |
Validated (UNII)
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| Record Version |
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40817-07-0
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DTXSID60193806
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admin on Fri Dec 15 17:58:46 GMT 2023 , Edited by admin on Fri Dec 15 17:58:46 GMT 2023
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115300
Created by
admin on Fri Dec 15 17:58:46 GMT 2023 , Edited by admin on Fri Dec 15 17:58:46 GMT 2023
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A7A75KAZ73
Created by
admin on Fri Dec 15 17:58:46 GMT 2023 , Edited by admin on Fri Dec 15 17:58:46 GMT 2023
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PRIMARY |