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2',3'-DIDEOXYCYTIDINE

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Name: 2',3'-DIDEOXYCYTIDINE
CAS: 7481-89-2
Synonyms: 4-AMINO-1-[(2R,5S)-5-(HYDROXYMETHYL)TETRAHYDRO-2-FURANYL]-2(1H)-PYRIMIDINONE ; DIDEOXYCYTIDINE ; CYTIDINE, 2',3'-DIDEOXY- ; 1-(2,3-DIDEOXY-BETA-D-RIBOFURANOSYL)CYTOSINE ; 2',3-DIDEOXYCYTIDINE ; RO 24-2027/000 ; BETA-D-2',3'-DIDEOXYCYTIDINE ; 2',3'-DIDEOXYCYTIDINE ; ZALCITABINE ; DDC ; 4-AMINO-1-((2R,5S)-5-(HYDROXYMETHYL)TETRAHYDROFURAN-2-YL)PYRIMIDIN-2(1H)-ONE ; HIVID ; 4-AMINO-1-[(2R,5S)-5-(HYDROXYMETHYL)OXOLAN-2-YL]-1,2-DIHYDROPYRIMIDIN-2-ONE ; 2′,3′-DIDEOXYCYTIDINE ; 1-(2',3'-DIDEOXY-BETA-RIBOFURANOSYL)CYTOSINE
MDL.: MFCD00012188
H bond acceptor: 6
H bond donor: 2
Smile: c1cn(c(=O)nc1N)[C@H]2CC[C@H](O2)CO
InChi: InChI=1S/C9H13N3O3/c10-7-3-4-12(9(14)11-7)8-2-1-6(5-13)15-8/h3-4,6,8,13H,1-2,5H2,(H2,10,11,14)/t6-,8+/m0/s1
InChiKey: InChIKey=WREGKURFCTUGRC-POYBYMJQSA-N

Property

Melting Point: 217-218 DEG C(LIT)/209°C
Comments: ASSAY METHOD: HPLC
BIOCHEM/PHYSIOL ACTIONS: DDCYD INHIBITS THE IN VITRO INFECTIVITY AND CYTOPATHIC EFFECTS OF HUMAN TLYMPHOTROPIC VIRUS TYPE III/LYMPHADENOPATHY-ASSOCIATED VIRUS (HTLV-III/LAV)
BIOCHEM/PHYSIOL ACTIONS: INFECTION OF NIH SWISS 3T3 CELLS BY 334C MURINE LEUKEMIA VIRUS IS INHIBITED BY 50 MICROMOLE DDCYD WITHOUT EFFECTING CELL GROWTH
RTECS: HA3870000
STORAGE TEMPERATURE: 2-8 DEG C
UNSPSC: 12352200
WGK: 3

Safety information

Symbol: GHS08 GHS08
Signal word: Warning
Hazard statements: H351
Precautionary statements: P281
hazard symbol: Xn
Risk Code: R:40
Safe Code: S:22-36
WGK Germany: 3

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