Adenine 9-β-<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 |
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 |
F | 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) |