Home Categories API Adenine 9-&#946;-<SC>D</SC>-arabinofuranoside
A0969012

Adenine 9-&#946;-<SC>D</SC>-arabinofuranoside , 99% , 5536-17-4

Synonym(s):
9-β-D-Arabinofuranosyladenine;Ara-A;Vidarabine

CAS NO.:5536-17-4

Empirical Formula: C10H13N5O4

Molecular Weight: 267.25

MDL number: MFCD00005752

EINECS: 226-893-9

Pack Size Price Stock Quantity
1G RMB47.20 In Stock
5G RMB126.40 In Stock
25G RMB408.80 In Stock
others     Enquire
Update time: 2022-07-08

PRODUCT Properties

Melting point: 260-265 °C (dec.)
alpha  D27 -5° (c = 0.25)
Boiling point: 410.43°C (rough estimate)
Density  1.3382 (rough estimate)
refractive index  1.7610 (estimate)
storage temp.  -20°C
solubility  DMSO (Slightly, Heated)
pka pKa 3.55(H2O t=20 I=0.1 (KCl)) (Uncertain);11.4 (Uncertain)
form  Powder
color  White to Off-white
Water Solubility  Soluble in DMF (10 mg/ml), 0.5 M HCl (50 mg/ml), DMSO (53 mg/ml at 25°C), ethanol (<1 mg/ml at 25°C), and water (3 mg/ml at 25°C).
Merck  13,10039
BRN  624881
InChIKey OIRDTQYFTABQOQ-UHTZMRCNSA-N
LogP -0.755 (est)

Description and Uses

Vidarabine (adenine arabinoside) is the stereoisomer of adenosine. This analog of a purine nucleoside exhibits selective activity against the herpes virus. The ribose residue is replaced with an arabinose residue. Like acyclovir, it turns into mono-, di-, and triphosphate in cells infected by a virus, thus inhibiting DNA polymerase, and correspondingly preventing DNA synthesis of the virus approximately 20–40 times more than in “host” cells. It is easily metabolized to a less active, yet nonetheless antiviral compound—arabinosylhypoxanthine. It has been successfully used for herpetic encephalitis, and for complicated shingles. It is used in the form of eye drops for herpetic keratoconjuctivitis. A synonym of this drug is Vira-A.

antifungal;Antiviral;Adenosine antimetabolite.

Safety

Symbol(GHS) 
GHS08
Signal word  Warning
Hazard statements  H361d
Precautionary statements  P201-P202-P280-P308+P313-P405-P501
Hazard Codes  Xn,Xi
Risk Statements  63-36/37/38
Safety Statements  36/37-36-26
RIDADR  2811
WGK Germany  3
RTECS  AU6200000
10-23
TSCA  Yes
HazardClass  6.1(a)
PackingGroup  II
HS Code  29349990
Toxicity LD50 in mice (mg/kg): 4677 i.p.; >7950 orally (Kurtz)

RELATED PRODUCTS