182149-25-3

Basic information

• Product Name: N,N''-[DITHIOBIS(O-PHENYLENECARBONYL)]BIS-L-ISOLEUCINE
• Synonyms: N,N''-[DITHIOBIS(O-PHENYLENECARBONYL)]BIS-L-ISOLEUCINE
• CAS NO: 182149-25-3
• Molecular Formula: C₂₆H₃₂N₂O₆S₂
• Molecular Weight: 0
• Mol File: 182149-25-3.mol
• Article Data: 4

Chemical Properties

• Appearance: /
• CAS DataBase Reference: N,N''-[DITHIOBIS(O-PHENYLENECARBONYL)]BIS-L-ISOLEUCINE(CAS DataBase Reference)
• NIST Chemistry Reference: N,N''-[DITHIOBIS(O-PHENYLENECARBONYL)]BIS-L-ISOLEUCINE(182149-25-3)
• EPA Substance Registry System: N,N''-[DITHIOBIS(O-PHENYLENECARBONYL)]BIS-L-ISOLEUCINE(182149-25-3)

Safety Data

• Hazardous Substances Data: 182149-25-3(Hazardous Substances Data)

Upstream product

• 19602-82-5 2,2'-dithiodibenzoic acid dichloride 
• 73-32-5 L-isoleucine 
• 16874-08-1 L-Isoleucin-tert-butylester 
• 119-80-2 2,2'-dithiobenzoic acid 
• 181861-32-5 (2S,3S)-2-{2-[2-((1S,2S)-1-tert-Butoxycarbonyl-2-methyl-butylcarbamoyl)-phenyldisulfanyl]-benzoylamino}-3-methyl-pentanoic acid tert-butyl ester 

Downstream Products

• 177785-47-6 (2S,3S)-3-methyl-2-(3-oxo-3H-benzo[d]isothiazol-2-yl)pentanoic acid 

Relevant articles and documents

Thiolesters and uses thereof

This invention pertains to the discovery of a novel family of thiolesters and uses thereof. Also provided for are viricidal compounds and pharmaceutical formulations comprising these novel thiolesters. The invention also provides thiolester-inactivated vi

A new class of anti-HIV-1 agents targeted toward the nucleocapsid protein NCp7: The 2,2'-dithiobisbenzamides

As part of the National Cancer Institute's Drug Screening Program, a new class of antiretrovirals active against the human immunodeficiency virus HIV-1 has been identified, and the HIV-1 nucleocapsid protein NCp7 was proposed as the target of antiviral action. The 2,2'-dithiobis-[4'-(sulfamoyl)benzanilide] (3x) and the 2,2'-dithiobis(5-acetylamino)benzamide (10) represented the prototypic lead structures. A wide variety of 2,2'-dithiobisbenzamides were prepared and tested for anti-HIV-1 activity, cytotoxicity, and their ability to extrude zinc from the zinc fingers for NCp7. The structure-activity relationships demonstrated that the ability to extrude zinc from NCp7 resided in the 2,2'-dithiobisbenzamide core structure. The 3,3' and the 4,4' isomers were inactive. While many analogs based upon the core structure retained the zinc extrusion activity, the best overall anti-HIV-1 activity was only found in a narrow set of derivatives possessing carboxylic acid, carboxamide, or phenylsulfonamide functional groups. These functional groups were more important for reducing cytotoxicity than improving antiviral potency or activity vs NCp7. All of the compounds with antiviral activity also extruded zinc from NCp7. From this study several classes of low μM anti-HIV agents with simple chemical structures were identified as possible chemotherapeutic agents for the treatment of AIDS.