862179-60-0

Basic information

• Product Name: imidazole-1-carbothioic acid O-[2-(6-amino-purin-9-yl)-5-(tert-butyl-diphenyl-silanyloxymethyl)-tetrahydro-furan-3-yl] ester
• Synonyms: imidazole-1-carbothioic acid O-[2-(6-amino-purin-9-yl)-5-(tert-butyl-diphenyl-silanyloxymethyl)-tetrahydro-furan-3-yl] ester
• CAS NO: 862179-60-0
• Molecular Weight: 599.789
• Mol File: 862179-60-0.mol
• Article Data: 1

Chemical Properties

• CAS DataBase Reference: imidazole-1-carbothioic acid O-[2-(6-amino-purin-9-yl)-5-(tert-butyl-diphenyl-silanyloxymethyl)-tetrahydro-furan-3-yl] ester(CAS DataBase Reference)
• NIST Chemistry Reference: imidazole-1-carbothioic acid O-[2-(6-amino-purin-9-yl)-5-(tert-butyl-diphenyl-silanyloxymethyl)-tetrahydro-furan-3-yl] ester(862179-60-0)
• EPA Substance Registry System: imidazole-1-carbothioic acid O-[2-(6-amino-purin-9-yl)-5-(tert-butyl-diphenyl-silanyloxymethyl)-tetrahydro-furan-3-yl] ester(862179-60-0)

Safety Data

• Hazardous Substances Data: 862179-60-0(Hazardous Substances Data)

Upstream product

• 6160-65-2 1,1'-Thiocarbonyldiimidazole 
• 862179-59-7 5'-O-(tert-butyldiphenylsilyl)-3'-deoxy-adenosine 
• 58-61-7 adenosine 
• 58479-61-1 tert-butylchlorodiphenylsilane 
• 116285-72-4 9-((2R,3R,5S)-3-((tert-butyldimethylsilyl)oxy)-5-(((tert-butyldimethylsilyl)oxy)methyl)tetrahydrofuran-2-yl)-9H-purin-6-amine 
• 73-03-0 cordycepin 
• 65109-11-7 2',5'-bis-O-(tert-butyldimethylsilyl)adenosine 
• 862179-57-5 imidazole-1-carbothioic acid O-[5-(6-amino-purin-9-yl)-4-(tert-butyl-dimethyl-silanyloxy)-2-(tert-butyl-dimethyl-silanyloxymethyl)-tetrahydro-furan-3-yl] ester 

Downstream Products

• 4097-22-7 2',3'-Dideoxyadenosine 

Relevant articles and documents

Deoxyribosyl analogues of methionyl and isoleucyl sulfamate adenylates as inhibitors of methionyl-tRNA and isoleucyl-tRNA synthetases

2′-Deoxy, 3′-deoxy, and 2′,3′-dideoxyribosyl surrogates of isoleucyl and methionyl sulfamate adenylates have been investigated to identify the pharmacophoric importance of the ribose group for the inhibition of Escherichia coli methionyl-tRNA (MRS) and isoleucyl-tRNA (IRS) synthetases. Molecular modeling of 2′,3′-dideoxyribosyl Met-NHSO2-AMP (9) with the crystal structure of E. coli MRS revealed that the lack of the two hydroxyl groups on ribose was compensated by the formation of an extra hydrogen bond between the ring oxygen and His24, resulting in a small activity reduction.