Details
| Stereochemistry | ACHIRAL |
| Molecular Formula | C7H6N2O2 |
| Molecular Weight | 150.1347 |
| Optical Activity | NONE |
| Defined Stereocenters | 0 / 0 |
| E/Z Centers | 0 |
| Charge | 0 |
SHOW SMILES / InChI
SMILES
NC(=O)C1=CC(=CC=C1)N=O
InChI
InChIKey=OZUBORKYZRYLSQ-UHFFFAOYSA-N
InChI=1S/C7H6N2O2/c8-7(10)5-2-1-3-6(4-5)9-11/h1-4H,(H2,8,10)
| Molecular Formula | C7H6N2O2 |
| Molecular Weight | 150.1347 |
| 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 |
|---|---|---|
| Inhibition of HIV-1 infectivity by zinc-ejecting aromatic C-nitroso compounds. | 1993 Feb 4 |
|
| Inhibition of the replication of native and 3'-azido-2',3'-dideoxythymidine (AZT)-resistant simian immunodeficiency virus (SIV) by 3-nitrosobenzamide. | 1993 Jul 12 |
|
| Anti-HIV agents that selectively target retroviral nucleocapsid protein zinc fingers without affecting cellular zinc finger proteins. | 1998 Apr 23 |
|
| Anti-cancer action of 4-iodo-3-nitrobenzamide in combination with buthionine sulfoximine: inactivation of poly(ADP-ribose) polymerase and tumor glycolysis and the appearance of a poly(ADP-ribose) polymerase protease. | 2002 Feb 1 |
|
| A copper-containing oxidase catalyzes C-nitrosation in nitrosobenzamide biosynthesis. | 2010 Sep |
Patents
| Substance Class |
Chemical
Created
by
admin
on
Edited
Sat Dec 16 02:03:19 GMT 2023
by
admin
on
Sat Dec 16 02:03:19 GMT 2023
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| Record UNII |
9JL5O473RB
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| Record Status |
Validated (UNII)
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| Record Version |
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m7990
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674195
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144189-66-2
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1679
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9JL5O473RB
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DTXSID50162642
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admin on Sat Dec 16 02:03:19 GMT 2023 , Edited by admin on Sat Dec 16 02:03:19 GMT 2023
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