Details
| Stereochemistry | ACHIRAL |
| Molecular Formula | C14H12N2O2S2 |
| Molecular Weight | 304.387 |
| Optical Activity | NONE |
| Defined Stereocenters | 0 / 0 |
| E/Z Centers | 0 |
| Charge | 0 |
SHOW SMILES / InChI
SMILES
NC(=O)C1=CC=CC=C1SSC2=CC=CC=C2C(N)=O
InChI
InChIKey=OEEHSSKRJOGQMP-UHFFFAOYSA-N
InChI=1S/C14H12N2O2S2/c15-13(17)9-5-1-3-7-11(9)19-20-12-8-4-2-6-10(12)14(16)18/h1-8H,(H2,15,17)(H2,16,18)
Approval Year
PubMed
| Title | Date | PubMed |
|---|---|---|
| New anti-HIV agents and targets. | 2002-11 |
|
| New developments in anti-HIV chemotherapy. | 2002-07-18 |
|
| Functional reconstitution of lost activity of chemically cross-linked or mutant moloney murine leukemia virus nucleocapsid proteins by trans-complementation. | 2001-12 |
|
| New developments in anti-HIV chemotherapy. | 2001-11 |
|
| 2,2'-Dithiobisbenzamides and 2-benzisothiazolones, two new classes of antiretroviral agents: SAR and mechanistic considerations. | 1997-05 |
|
| A new class of anti-HIV-1 agents targeted toward the nucleocapsid protein NCp7: the 2,2'-dithiobisbenzamides. | 1997-03 |
|
| The human immunodeficiency virus type 1 (HIV-1) nucleocapsid protein zinc ejection activity of disulfide benzamides and benzisothiazolones: correlation with anti-HIV and virucidal activities. | 1997-02 |
|
| Synthesis and antibacterial activity of 2,2'-dithiobis(benzamide) derivatives against Mycobacterium species. | 1985-12 |
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219-766-4
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DTXSID8062494
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72552
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2527-57-3
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9X53S9RZ6B
Created by
admin on Mon Mar 31 18:51:50 GMT 2025 , Edited by admin on Mon Mar 31 18:51:50 GMT 2025
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SUBSTANCE RECORD