Details
| Stereochemistry | ACHIRAL |
| Molecular Formula | C20H18O6 |
| Molecular Weight | 354.3533 |
| Optical Activity | NONE |
| Defined Stereocenters | 0 / 0 |
| E/Z Centers | 0 |
| Charge | 0 |
SHOW SMILES / InChI
SMILES
CC(C)=CCC1=CC(=CC=C1O)C2=C(O)C(=O)C3=C(O)C=C(O)C=C3O2
InChI
InChIKey=PGCKDCPTJAQQSQ-UHFFFAOYSA-N
InChI=1S/C20H18O6/c1-10(2)3-4-11-7-12(5-6-14(11)22)20-19(25)18(24)17-15(23)8-13(21)9-16(17)26-20/h3,5-9,21-23,25H,4H2,1-2H3
| Molecular Formula | C20H18O6 |
| Molecular Weight | 354.3533 |
| Charge | 0 |
| Count |
|
| Stereochemistry | ACHIRAL |
| Additional Stereochemistry | No |
| Defined Stereocenters | 0 / 0 |
| E/Z Centers | 0 |
| Optical Activity | NONE |
Approval Year
| Substance Class |
Chemical
Created
by
admin
on
Edited
Mon Mar 31 22:55:22 GMT 2025
by
admin
on
Mon Mar 31 22:55:22 GMT 2025
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| Record UNII |
355E7H7EHH
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| Record Status |
Validated (UNII)
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| Record Version |
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94805-83-1
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admin on Mon Mar 31 22:55:22 GMT 2025 , Edited by admin on Mon Mar 31 22:55:22 GMT 2025
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5318585
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admin on Mon Mar 31 22:55:22 GMT 2025 , Edited by admin on Mon Mar 31 22:55:22 GMT 2025
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DTXSID801317129
Created by
admin on Mon Mar 31 22:55:22 GMT 2025 , Edited by admin on Mon Mar 31 22:55:22 GMT 2025
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355E7H7EHH
Created by
admin on Mon Mar 31 22:55:22 GMT 2025 , Edited by admin on Mon Mar 31 22:55:22 GMT 2025
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| Related Record | Type | Details | ||
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PARENT -> CONSTITUENT ALWAYS PRESENT |
ISOLICOFLAVONOL showed antibacterial activity against MSSAs (strains FDA 209P and Smith) and MRSAs(strains K3 and ST 28) (MICs1.56?25 ug/ml). This compound exhibited antimicrobial activity against Micrococcus luteus ATCC 9341 and Bacillus subtilis PCI 219 (MICs3.13?25 ug/ml) but not against Klebsiella pneumoniae PCI 602 and Pseudomonas aeruginosa IFO 3445.
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