Details
| Stereochemistry | ACHIRAL |
| Molecular Formula | C15H14O4 |
| Molecular Weight | 258.2693 |
| Optical Activity | NONE |
| Defined Stereocenters | 0 / 0 |
| E/Z Centers | 0 |
| Charge | 0 |
SHOW SMILES / InChI
SMILES
OC(=O)C1=C(CCC2=CC=C(O)C=C2)C=CC=C1O
InChI
InChIKey=GFSQDOUEUWXRSL-UHFFFAOYSA-N
InChI=1S/C15H14O4/c16-12-8-5-10(6-9-12)4-7-11-2-1-3-13(17)14(11)15(18)19/h1-3,5-6,8-9,16-17H,4,7H2,(H,18,19)
Approval Year
PubMed
| Title | Date | PubMed |
|---|---|---|
| Evolutionarily conserved regulatory mechanisms of abscisic acid signaling in land plants: characterization of ABSCISIC ACID INSENSITIVE1-like type 2C protein phosphatase in the liverwort Marchantia polymorpha. | 2010-03 |
|
| [Chemical constituents of fresh celery]. | 2009-06 |
|
| Directed ortho-metalation of unprotected benzoic acids. Methodology and regioselective synthesis of useful contiguously 3- and 6-substituted 2-methoxybenzoic acid building blocks. | 2006-02-16 |
|
| Inhibition of endothelial cell functions by novel potential cancer chemopreventive agents. | 2004-12-03 |
|
| Stilbenecarboxylate biosynthesis: a new function in the family of chalcone synthase-related proteins. | 2003-02 |
|
| The biological and structural similarity between lunularic acid and abscisic acid. | 2002-04 |
Patents
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Preferred Name | English | ||
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| Code System | Code | Type | Description | ||
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9ZQ3FYV21C
Created by
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DTXSID40177826
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161413
Created by
admin on Mon Mar 31 21:22:23 GMT 2025 , Edited by admin on Mon Mar 31 21:22:23 GMT 2025
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Lunularic acid
Created by
admin on Mon Mar 31 21:22:23 GMT 2025 , Edited by admin on Mon Mar 31 21:22:23 GMT 2025
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m6936
Created by
admin on Mon Mar 31 21:22:23 GMT 2025 , Edited by admin on Mon Mar 31 21:22:23 GMT 2025
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23255-59-6
Created by
admin on Mon Mar 31 21:22:23 GMT 2025 , Edited by admin on Mon Mar 31 21:22:23 GMT 2025
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SUBSTANCE RECORD
