≥99% for sensitive chromatographic and analytical workflows requiring minimal baseline interference.
Protected from light,Store at -80°C Ships Dry ice packs + Cold packs Check lot-specific COA for exact specifications.
SDS, COA, datasheet, and spec sheet available for download. Lot-specific COA accessible via lot number lookup.
Cited in 0 peer-reviewed publications across chromatography, organic synthesis, and cross-coupling reactions.
HCV-IN-31 (compound 4) is a HCV inhibitor, with an EC 50 /EC 95 of 15.7 μM for HCV replicon
Form:Solid
IC50& Target:EC50/EC95: 15.7 μM (HCV replicon)
| Sonrisas canónicas | CC1(C(C(OC1N2C=NC3=C(N=C(N=C32)N)NC)CO)O)F |
|---|---|
| IUPAC Name | (2R,3R,4R,5R)-5-[2-amino-6-(methylamino)purin-9-yl]-4-fluoro-2-(hydroxymethyl)-4-methyloxolan-3-ol |
| InChIKey | HPINXBYYNVDDEB-GSWPYSDESA-N |
| INCHI | 1S/C12H17FN6O3/c1-12(13)7(21)5(3-20)22-10(12)19-4-16-6-8(15-2)17-11(14)18-9(6)19/h4-5,7,10,20-21H,3H2,1-2H3,(H3,14,15,17,18)/t5-,7-,10-,12-/m1/s1 |
| PubChem CID | 122510185 |
| Peso molecular | 312.30 |
Comprehensive hazard, handling, storage, and regulatory compliance document.
Download SDS →Lot-specific quality data. Enter your lot number to retrieve the exact COA.
Look up COA →Full quality attributes and acceptance criteria for this grade.
View spec sheet →Taxonomy Tree
| Kingdom | Organic compounds |
|---|---|
| Superclass | Organoheterocyclic compounds |
| Clase | Imidazopyrimidines |
| Subclass | Purines and purine derivatives |
| Intermediate Tree Nodes | 6-aminopurines |
| Direct Parent | 6-alkylaminopurines |
| Alternative Parents | Secondary alkylarylamines Pyrimidines and pyrimidine derivatives N-substituted imidazoles Monosaccharides Imidolactams Tetrahydrofurans Imidazolines Heteroaromatic compounds Secondary alcohols Fluorohydrins Propargyl-type 1,3-dipolar organic compounds Oxacyclic compounds Formamidines Dialkylamines Carboximidamides Azacyclic compounds Primary amines Organopnictogen compounds Organofluorides Hydrocarbon derivatives Alkyl fluorides |
| Molecular Framework | Aromatic heteropolycyclic compounds |
| Substituents | 6-alkylaminopurine - Secondary aliphatic/aromatic amine - Imidolactam - Pyrimidine - N-substituted imidazole - Monosaccharide - Heteroaromatic compound - Tetrahydrofuran - 2-imidazoline - Azole - Secondary alcohol - Halohydrin - Fluorohydrin - Formamidine - Oxacycle - Azacycle - Organic 1,3-dipolar compound - Propargyl-type 1,3-dipolar organic compound - Carboximidamide - Secondary amine - Secondary aliphatic amine - Amidine - Organic nitrogen compound - Organic oxygen compound - Organopnictogen compound - Hydrocarbon derivative - Primary amine - Organooxygen compound - Organonitrogen compound - Organofluoride - Organohalogen compound - Amine - Alkyl halide - Alkyl fluoride - Alcohol - Aromatic heteropolycyclic compound |
| Descripción | This compound belongs to the class of organic compounds known as 6-alkylaminopurines. These are compounds that contain an alkylamine group attached at the 6-position of a purine. Purine is a bicyclic aromatic compound made up of a pyrimidine ring fused to an imidazole ring. |
| External Descriptors | Not available |
| Solubilidad | DMSO : 60 mg/mL (192.12 mM; Need ultrasonic) |
|---|
