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Volumn 54, Issue 8, 2011, Pages 418-425
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The syntheses and in vitro biotransformation studies of [ 14C]apixaban, a highly potent, selective, efficacious and orally bioavailable inhibitor of blood coagulation Factor Xa
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Author keywords
ADME; apixaban; Factor Xa; hepatocytes; microsomes
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Indexed keywords
BLOOD;
COAGULATION;
ADME;
APIXABAN;
BIOAVAILABLE;
BLOOD COAGULATION;
COAGULATION FACTOR;
FACTOR XA;
HEPATOCYTES;
IN-VITRO;
MICROSOME;
POTENT INHIBITOR;
SYNTHESIS (CHEMICAL);
1 (4 METHOXYPHENYL) 6 [4 (2 OXOPIPERIDIN 1 YL)PHENYL] 4,5,6,7 TETRAHYDRO 1H PYRAZOLO[3,4 C]PYRIDINE 3 CARBOXAMIDE C 14;
1 (4 METHOXYPHENYL) 7 OXO 6 [4 (2 OXOPIPERIDIN 1 YL)PHENYL] 4,5,6,7 TETRAHYDRO 1H PYRAZOLO[3,4 C]PYRIDINE 3 CARBOXAMIDE C 14;
APIXABAN;
APIXABAN C 14;
BLOOD CLOTTING FACTOR 10A INHIBITOR;
CARBON 14;
UNCLASSIFIED DRUG;
ANIMAL CELL;
ARTICLE;
CONTROLLED STUDY;
DRUG EFFICACY;
DRUG METABOLISM;
DRUG POTENCY;
DRUG PURIFICATION;
DRUG SELECTIVITY;
DRUG STRUCTURE;
DRUG SYNTHESIS;
DRUG TRANSFORMATION;
HUMAN;
HUMAN CELL;
IN VITRO STUDY;
ISOTOPE LABELING;
LIVER CELL;
LIVER MICROSOME;
NONHUMAN;
RAT;
REPRODUCIBILITY;
TECHNIQUE;
RATTUS;
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EID: 79960676834
PISSN: 03624803
EISSN: 10991344
Source Type: Journal
DOI: 10.1002/jlcr.1890 Document Type: Article |
Times cited : (8)
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References (5)
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