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Abacavir

Abacavir Structure
CAS No.
136470-78-5
Chemical Name:
Abacavir
Synonyms
CS-107;1592u89;Abacavir;Abacavir >Abacavir(base);Abacavir Tablet;Abacavir, ≥ 98.0%;Abacavir USP/EP/BP;Abacavir Standard;Abacavir (see A105000)
CBNumber:
CB5698138
Molecular Formula:
C14H18N6O
Molecular Weight:
286.33
MOL File:
136470-78-5.mol
MSDS File:
SDS
Modify Date:
2024/4/16 18:29:06

Abacavir Properties

Melting point 165°
alpha D20 -59.7°; 43620 -127.8°; 36520 -218.1° (c = 0.15 in methanol)
Boiling point 636.0±65.0 °C(Predicted)
Density 1.70±0.1 g/cm3(Predicted)
storage temp. Sealed in dry,2-8°C
solubility DMSO (Slightly, Heated), Methanol (Slightly)
pka 5.01(at 25℃)
form Solid
color Off-White to Pale Beige
Merck 14,1
BCS Class 3
CAS DataBase Reference 136470-78-5(CAS DataBase Reference)
EPA Substance Registry System 2-Cyclopentene-1-methanol, 4-[2-amino-6-(cyclopropylamino)-9H-purin-9-yl]-, (1S,4R)- (136470-78-5)

SAFETY

Risk and Safety Statements

Symbol(GHS) 
GHS08
Signal word  Danger
Hazard statements  H361-H317-H334-H341
Precautionary statements  P501-P261-P272-P202-P201-P280-P284-P302+P352-P308+P313-P362+P364-P304+P340-P333+P313-P405
RTECS  GY5979200
HS Code  2933.99.7500
NFPA 704
0
2 0

Abacavir price More Price(2)

Manufacturer Product number Product description CAS number Packaging Price Updated Buy
TCI Chemicals (India) A2694 Abacavir 136470-78-5 1G ₹6000 2022-05-26 Buy
TCI Chemicals (India) A2694 Abacavir 136470-78-5 5G ₹17800 2022-05-26 Buy
Product number Packaging Price Buy
A2694 1G ₹6000 Buy
A2694 5G ₹17800 Buy

Abacavir Chemical Properties,Uses,Production

Description

The drug is extensively metabolized via stepwise phosphorylation to 5′-mono-, di-, and triphosphate. Abacavir is well absorbed (>75%) and penetrates the CNS. The drug can be taken without regard to meals. The drug does not show any clinically significant drug–drug interactions. Abacavir has been reported to produce life-threatening hypersensitivity reactions. The major use of abacavir appears to be in combination with other nucleoside RT inhibitors. A fixed-combination product has recently been approved by the U.S. FDA consisting of 300 mg of ABC, 150 mg of 3TC, and 300 mg of ZDV (Trizivar). The combination has been shown to be superior to other combinations in reducing viral load as well as to show improvement in CD4 cell count.

Uses

Abacavir is a commonly used nucleoside analogue with potent antiviral activity against HIV-1. - See more at: http://www.selleckchem.com/products/abacavir-sulfate.html#sthash.lApvcTNO.dpuf

Indications

Abacavir (Ziagen) is a guanosine nucleoside analogue indicated for the therapy of HIV-1 infection in adults and children. It is used as part of a multidrug regimen and is available in a fixed-dose combination with zidovudine and lamivudine (Trizivir). It is also used for postexposure HIV infection prophylaxis.

Antimicrobial activity

Abacavir has activity against HIV-1, HIV-2 and human T-cell lymphotrophic virus type-1 (HTLV-1).

Acquired resistance

Resistance is associated with specific changes in codons 184 with 65, 74 or 115 in the HIV reverse transcriptase codon region.

General Description

Abacavir is a nucleoside reverse transcriptase inhibitorNRTI that has been approved for use in combination therapiesfor the treatment of HIV and AIDS. Once in the tissues,it is metabolized by stepwise phosphorylation to themonophosphate, diphosphate, and triphosphate. Abacavir ishighly bioavailable (>75%) and is effective by the oralroute. It penetrates the blood-brain barrier efficiently.Abacavir has been reported to produce life-threatening hypersensitivityreactions in some patients.

Pharmaceutical Applications

A synthetic analog of guanine formulated for oral use.

Pharmacokinetics

Oral absorption: 83%
Cmax 300 mg oral, twice daily: 3.0 ± 0.89 mg/L
600 mg once daily: 4.26 mg/L
Plasma half-life: 1.5 h
Volume of distribution: 0.8 L/kg
Plasma protein binding: c. 49%
Absorption
After oral administration abacavir sulfate undergoes rapid and extensive absorption unaffected by food.
Distribution
It penetrates well into the cerebrospinal fluid (CSF) and is an NRTI of choice if this characteristic is thought desirable. Good penetration into the male genital tract has been observed. The drug is secreted into human breast milk.
Metabolism
It is primarily metabolized in the liver, mainly by alcohol dehydrogenase and glucuronidation.
Excretion
Around 83% of the dose is eliminated in the urine, <2% as unchanged drug; the remainder is excreted in the feces. Dose adjustment is unnecessary in renal impairment. It can be used in moderate hepatic impairment, but is contraindicated if dysfunction is severe.

Clinical Use

Treatment of HIV infection in adults and children (in combination with other antiretroviral drugs)

Side effects

Life-threatening hypersensitivity reactions occur in 5–8% of all individuals, necessitating discontinuation of the drug. Typically patients present within the first 6 weeks of starting treatment with fever, rash or other symptoms that worsen in severity with continued drug exposure. Hypersensitivity is associated with carriage of the major histocompatibility complex class I allele HLA-B57*01 and screening for this allele can significantly reduce the incidence of this effect.
Current or recent (within the preceding 6 months) use of abacavir has been associated with a risk of myocardial infarction, but studies have yielded conflicting data.

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Abacavir Spectrum

1592u89 [(1s,4r)-4-[2-amino-6-(cyclopropylamino)purin-9-yl]-1-cyclopent-2-enyl]methanol [(1S,4R)-4-(2-AMINO-6-CYCLOPROPYLAMINO-PURIN-9-YL)-CYCLOPENT-2-ENYL]-METHANOL 2-Cyclopentene-1-methanol, 4-[2-amino-6-(cyclopropylamino)-9H-purin-9-yl]-, (1S,4R)- 2-Cyclopentene-1-methanol, 4-[2-amino-6-(cyclopropylamino)-9H-purin-9-yl]-, (1S-cis)- (+/-)-4-[2-amino-6-(cyclopropylamino)-9h-purin-9-yl]-2-cyclopentene-1-methanol Abacavir Abacavir (see A105000) Abacavir-(1R,trans)-isoMer Abacavir-5'-tert-butyl ether (1S-cis)-4-[2-AMino-6-(cyclopropylaMino)-9H-purin-9-yl]-2-cyclopentene-1-Methanol Abacavir(base) [(1S,4R)-4-[2-amino-6-(cyclopropylamino)-9-purinyl]-1-cyclopent-2-enyl]methanol CS-107 [(1S,4R)-4-[2-amino-6-(cyclopropylamino)purin-9-yl]cyclopent-2-en-1-yl]methanol Abacavir > ({(1S,4R)-4-[2-amino-6-(cyclopropylamino)-9H-Purin-9- yl]cyclopent-2-en-l-yl} methanol) Abacavir USP/EP/BP Abacavir (1.0 mg/mL in Methanol) {(1S,4R)-4-[2-amino-6-(cyclopropylamino)-9Hpurin-9-yl]cyclopent-2-en-1-yl}methanol abacavir D5Q: What is abacavir D5 Q: What is the CAS Number of abacavir D5 Abacavir Tablet Abacavir Standard Abacavir Manufacturer/High quality/Best price/In stock CAS NO.136470-78-5 ((1S,4R)-4-(2-Amino-6-(cyclopropylamino)-9H-purin-9-yl)cyclopent-2-en-1-yl)methanol[Abacavir Abacavir, ≥ 98.0% Abacavir-d4 5’-4-Chloro-6-methylpyrimidine-2,5-diamine 136470-78-5 C14H18N6O Heterocycles Bases & Related Reagents Inhibitors Intermediates & Fine Chemicals Nucleotides Pharmaceuticals