Details
| Stereochemistry | ACHIRAL |
| Molecular Formula | C22H14O6 |
| Molecular Weight | 374.343 |
| Optical Activity | NONE |
| Defined Stereocenters | 0 / 0 |
| E/Z Centers | 0 |
| Charge | 0 |
SHOW SMILES / InChI
SMILES
CC1=CC2=C(C(=O)C=C(C2=O)C3=C(C)C=C4C(=O)C=CC(=O)C4=C3O)C(O)=C1
InChI
InChIKey=WRFTYMHHWSAKSK-UHFFFAOYSA-N
InChI=1S/C22H14O6/c1-9-5-12-19(16(25)6-9)17(26)8-13(21(12)27)18-10(2)7-11-14(23)3-4-15(24)20(11)22(18)28/h3-8,25,28H,1-2H3
| Molecular Formula | C22H14O6 |
| Molecular Weight | 374.343 |
| 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 |
|---|---|---|
| Antitubercular and antibacterial activity of quinonoid natural products against multi-drug resistant clinical isolates. | 2014-07 |
|
| Antimycobacterial activity of diospyrin derivatives and a structural analogue of diospyrin against Mycobacterium tuberculosis in vitro. | 2003-02 |
|
| Inhibition of drug-sensitive and drug-resistant strains of Mycobacterium tuberculosis by diospyrin, isolated from Euclea natalensis. | 2001-12 |
|
| Effects of atovaquone and diospyrin-based drugs on the cellular ATP of Pneumocystis carinii f. sp. carinii. | 2000-03 |
|
| Effects of atovaquone and diospyrin-based drugs on ubiquinone biosynthesis in Pneumocystis carinii organisms. | 2000-01 |
Patents
| Substance Class |
Chemical
Created
by
admin
on
Edited
Mon Mar 31 18:39:50 GMT 2025
by
admin
on
Mon Mar 31 18:39:50 GMT 2025
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| Record UNII |
O0IQZ8B2R7
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| Record Status |
Validated (UNII)
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| Record Version |
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O0IQZ8B2R7
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DTXSID30182429
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28164-57-0
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208730
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