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Abacavir sulfate

SIGMA/SML0089 - ≥98% (HPLC)

Synonym: (1S,4R)-4-[2-Amino-6-(cyclopropylamino)-9H-purin-9-yl]-2-cyclopentene-1-methanol sulfate; ABC; Abacavir Hemisulfate

CAS Number: 188062-50-2
Empirical Formula (Hill Notation): C14H18N6O · 0.5 H2SO4
Molecular Weight: 335.37
MDL Number: MFCD04112763
Linear Formula: C14H18N6O · 0.5 H2SO4
Product Type: Chemical

Catalog Number PKG Qty. Price Quantity
45-SML0089-10MG 10 mg
$114.00
1/EA
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45-SML0089-50MG 50 mg
$459.00
1/EA
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This picture is provided solely for illustration purposes. Optical properties of the actual product may deviate. Relevant product information is printed on labeled products and other accompanying or available information material. This image depicts SKU: SML0089-50MG

 

assay ≥98% (HPLC)
color white to tan
form powder
InChI 1S/2C14H18N6O.H2O4S/c2*15-14-18-12(17-9-2-3-9)11-13(19-14)20(7-16-11)10-4-1-8(5-10)6-21;1-5(2,3)4/h2*1,4,7-10,21H,2-3,5-6H2,(H3,15,17,18,19);(H2,1,2,3,4)/t2*8-,10+;/m11./s1
InChI key WMHSRBZIJNQHKT-FFKFEZPRSA-N
optical activity [α]/D -30 to -40°, c = 0.5 in methanol
originator GlaxoSmithKline
Quality Level 100 
SMILES string OS(O)(=O)=O.Nc1nc(NC2CC2)c3ncn([C@@H]4C[C@H](CO)C=C4)c3n1.Nc5nc(NC6CC6)c7ncn([C@@H]8C[C@H](CO)C=C8)c7n5
solubility H2O: ≥17 mg/mL
storage temp. 2-8°C
Application: Abacavir sulfate has been used as a compound to validate the P19C5 gastrulation in mouse. It has also been used to induces chromosomal double-strand breaks (DSBs) and kills adult T cell leukemia (ATL) cells.
Application: Abacavir sulfate has been used in the cytotoxicity to test its tumour promoting activity U937 cells.
Biochem/physiol Actions: Abacavir incorporated in the cells is converted to triphosphate containing guanine analog carbovir (CBV) and it favors the generation of higher double stranded breaks (DSBs).
Biochem/physiol Actions: Abacavir sulfate is a Nucleoside analog reverse transcriptase inhibitor (NRTI); guanosine analog used to treat HIV and AIDS.
Features and Benefits: This compound is a featured product for ADME Tox research. Click here  to discover more featured ADME Tox products. Learn more about bioactive small molecules for other areas of research at sigma.com/discover-bsm .
Features and Benefits: This compound was developed by GlaxoSmithKline . To browse the list of other pharma-developed compounds and Approved Drugs/Drug Candidates, click here .
General description: Abacavir exhibits antiviral activity. It is associated with myocardial infarction and fatal hypersensitivity reaction (HSR).
Packaging: 10 mg in glass bottle
Packaging: 50 mg in poly bottle
Purity ≥98% (HPLC)
Storage Temp. 2-8°C
UNSPSC 12352200

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