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Abacavir Lopinavir Methylene Conjugation

N° de SZ CAT:SZ-A049053
Número CASNA
Mol.F.C52H66N10O6
Peso Molecular927.2
Status de FaturaUnder Synthesis

Nome Químico: (S)-N-((2S,4S,5S)-4-(((6-(Cyclopropylamino)-9-((1R,4S)-4-(hydroxymethyl)cyclopent-2-en-1-yl)-9H-purin-2-yl)amino)methoxy)-5-(2-(2,6-dimethylphenoxy)acetamido)-1,6-diphenylhexan-2-yl)-3-methyl-2-(2-oxotetrahydropyrimidin-1(2H)-yl)butanamide

Shipping Temperature: Ambient

HSN Code: 38229010

Country of Origin: India

Sorrisos: O=C([C@@H](N1C(NCCC1)=O)C(C)C)N[C@H](C[C@H](OCNC2=NC(N([C@H]3C=C[C@@H](CO)C3)C=N4)=C4C(NC5CC5)=N2)[C@@H](NC(COC6=C(C)C=CC=C6C)=O)CC7=CC=CC=C7)CC8=CC=CC=C8

Abacavir Lopinavir Methylene Conjugation is chemically (S)-N-((2S,4S,5S)-4-(((6-(Cyclopropylamino)-9-((1R,4S)-4-(hydroxymethyl)cyclopent-2-en-1-yl)-9H-purin-2-yl)amino)methoxy)-5-(2-(2,6-dimethylphenoxy)acetamido)-1,6-diphenylhexan-2-yl)-3-methyl-2-(2-oxotetrahydropyrimidin-1(2H)-yl)butanamide. Abacavir Lopinavir Methylene Conjugation is supplied with detailed characterization data compliant with regulatory guideline. Abacavir Lopinavir Methylene Conjugation can be used for the analytical method development, method validation (AMV), Quality Controlled (QC) application for Abbreviated New Drug Application (ANDA) or during commercial production of Abacavir.

The product can be used as reference standards and further traceability against pharmacopeial standards (USP or EP) can be provided based on feasibility. SynZeal products are for analytical purpose only and not for human use.

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