Details
| Stereochemistry | ACHIRAL |
| Molecular Formula | C23H17ClF4N2O5S |
| Molecular Weight | 544.903 |
| Optical Activity | NONE |
| Defined Stereocenters | 0 / 0 |
| E/Z Centers | 0 |
| Charge | 0 |
SHOW SMILES / InChI
SMILES
CC1=CC(=CC=C1NC(=O)COC2=CC=C(Cl)C=C2C(=O)C3=CC(=CC(F)=C3)C(F)(F)F)S(N)(=O)=O
InChI
InChIKey=PNJKKJNQGSBNDN-UHFFFAOYSA-N
InChI=1S/C23H17ClF4N2O5S/c1-12-6-17(36(29,33)34)3-4-19(12)30-21(31)11-35-20-5-2-15(24)10-18(20)22(32)13-7-14(23(26,27)28)9-16(25)8-13/h2-10H,11H2,1H3,(H,30,31)(H2,29,33,34)
| Molecular Formula | C23H17ClF4N2O5S |
| Molecular Weight | 544.903 |
| 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 |
|---|---|---|
| Structure-activity relationship studies of novel benzophenones leading to the discovery of a potent, next generation HIV nonnucleoside reverse transcriptase inhibitor. | 2006-01-26 |
|
| Novel benzophenones as non-nucleoside reverse transcriptase inhibitors of HIV-1. | 2004-02-26 |
Patents
| Substance Class |
Chemical
Created
by
admin
on
Edited
Mon Mar 31 22:05:09 GMT 2025
by
admin
on
Mon Mar 31 22:05:09 GMT 2025
|
| Record UNII |
2Q35E4D937
|
| Record Status |
Validated (UNII)
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| Record Version |
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Common Name | English | ||
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Preferred Name | English |
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486517
Created by
admin on Mon Mar 31 22:05:09 GMT 2025 , Edited by admin on Mon Mar 31 22:05:09 GMT 2025
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329936-49-4
Created by
admin on Mon Mar 31 22:05:09 GMT 2025 , Edited by admin on Mon Mar 31 22:05:09 GMT 2025
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2Q35E4D937
Created by
admin on Mon Mar 31 22:05:09 GMT 2025 , Edited by admin on Mon Mar 31 22:05:09 GMT 2025
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PRIMARY |
| Related Record | Type | Details | ||
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