Details
| Stereochemistry | ACHIRAL |
| Molecular Formula | C10H8O4 |
| Molecular Weight | 192.1681 |
| Optical Activity | NONE |
| Defined Stereocenters | 0 / 0 |
| E/Z Centers | 0 |
| Charge | 0 |
SHOW SMILES / InChI
SMILES
CC1=CC(=O)C2=C(O1)C=C(O)C=C2O
InChI
InChIKey=NCUJRUDLFCGVOE-UHFFFAOYSA-N
InChI=1S/C10H8O4/c1-5-2-7(12)10-8(13)3-6(11)4-9(10)14-5/h2-4,11,13H,1H3
| Molecular Formula | C10H8O4 |
| Molecular Weight | 192.1681 |
| 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 |
|---|---|---|
| Ceramide and Cerebroside from the stem bark of Ficus mucuso (Moraceae). | 2010-12 |
|
| Engineered biosynthesis of plant polyketides: structure-based and precursor-directed approach. | 2010 |
|
| Chrotacumines A-D, chromone alkaloids from Dysoxylum acutangulum. | 2009-10 |
|
| [Study on chemical constituents from roots of Saussurea lappa]. | 2009-05 |
|
| Structure-based engineering of a plant type III polyketide synthase: formation of an unnatural nonaketide naphthopyrone. | 2007-05-09 |
|
| Crystallization and preliminary crystallographic analysis of a novel plant type III polyketide synthase that produces pentaketide chromone. | 2006-09-01 |
|
| [Study on the constituents from Neonauclea sessilifolia]. | 2002-12 |
|
| Anti-AIDS agents, 10. Acacetin-7-O-beta-D-galactopyranoside, an anti-HIV principle from Chrysanthemum morifolium and a structure-activity correlation with some related flavonoids. | 1994-01 |
| Substance Class |
Chemical
Created
by
admin
on
Edited
Mon Mar 31 19:31:47 GMT 2025
by
admin
on
Mon Mar 31 19:31:47 GMT 2025
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| Record UNII |
M0KFC1Q5JC
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| Record Status |
Validated (UNII)
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| Record Version |
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DTXSID80143828
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