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Abacavir Related CoMpound D

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Abacavir Related CoMpound D Basic information

Product Name:
Abacavir Related CoMpound D
Synonyms:
  • Abacavir EP Imp B
  • Abacavir Related CoMpound D
  • N6-Cyclopropyl-9-{(1R,4S)-4-[(2,5-diamino-6-chloropyrimidin-4-yloxy)methyl]cyclopent-2-enyl}-9H-purine-2,6-diamine
  • Abacavir 5'-4-Chloro-6-methylpyrimidine-2,5-diamine
  • Abacavir Impurity 2(Abacavir EP Impurity B)
  • Abacavir EP Impurity B
  • O-Pyrimidine Derivative Abacavir (USP)
  • 6-(Cyclopropylamino)-9-[(1R,4S)-4-[[(2,5-diamino-6-chloropyrimidin-4-yl)oxy]methyl]cyclopent-2-enyl]-9H-purine-2-amine
CAS:
1443421-69-9
MF:
C18H21ClN10O
MW:
428.88
Mol File:
1443421-69-9.mol
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Abacavir Related CoMpound D Chemical Properties

Boiling point:
830.1±75.0 °C(Predicted)
Density 
1.90±0.1 g/cm3(Predicted)
storage temp. 
2-8°C
pka
4.86±0.10(Predicted)
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Safety Information

WGK Germany 
3
HS Code 
2933599550
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Abacavir Related CoMpound D Usage And Synthesis

Uses

Abacavir 5’-4-Chloro-6-methylpyrimidine-2,5-diamine (Abacavir EP Impurity B) is a degradation product of Abacavir Sulfate (A105000). Abacavir is a carbocyclic 2''-deoxyguanosine nucleoside reverse transcriptase inhibitor and an anti-HIV drug used to treat HIV infection (1). Intracellular enzymes convert Abacavir to its active form, carbovir-triphosphate (CBV-TP), which then selectively inhibits HIV reverse transcriptase by incorporating into viral DNA (2). Abacavir is metabolized in the liver by uridine diphosphate glucuronyltransferase and alcohol dehydrogenase resulting in inactive glucuronide and carboxylate metabolites, respectively.

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