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rdf:type |
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lifeskim:mentions |
umls-concept:C0010622,
umls-concept:C0010798,
umls-concept:C0014431,
umls-concept:C0025519,
umls-concept:C0031327,
umls-concept:C0379528,
umls-concept:C0796517,
umls-concept:C1261322,
umls-concept:C1566327,
umls-concept:C1999216,
umls-concept:C2603343
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pubmed:issue |
7
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pubmed:dateCreated |
2009-6-18
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pubmed:abstractText |
BMS-299897 is a gamma-secretase inhibitor that was effective in reducing amyloid beta-peptide (A beta) in transgenic mice and guinea pigs. Therefore, pharmacokinetic and drug metabolism studies were conducted in animals to support its clinical development. The compound appeared to have low to intermediate total body clearance and was orally bioavailable (24-100%). The oral absorption of BMS-299897 from solid dosage forms appeared to be dissolution rate-limited. BMS-299897 was distributed into extravascular space (V(ss) >or= 1.3 l kg(-1)), including brain (brain-to-plasma ratio = 0.13-0.50). BMS-299897 appeared to be a P-glycoprotein (P-gp) substrate as the brain-to-plasma ratio was two-fold higher in the mdr1a knockout mouse as compared with the wild-type. Apparent autoinduction by BMS-299897 was observed in murine and rat efficacy and toxicity studies. In vitro, BMS-299897 was a weaker inducer of cytochrome P450 3A4 (CYP3A4) and a weaker transactivator of human pregnane X receptor (hPXR) as compared with rifampicin. Induction of human UGT1A and UGT2B was evaluated in primary human hepatocytes, but the results were inconclusive. A low potential for autoinduction in humans was predicted at a clinical dose of 250 mg and the prediction was consistent with the findings from a clinical multiple-dose study with BMS-299897 in probable Alzheimer's patients.
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pubmed:language |
eng
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pubmed:journal |
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pubmed:citationSubset |
IM
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pubmed:chemical |
http://linkedlifedata.com/resource/pubmed/chemical/4-(2-((1R)-1-(((4-chlorophenyl)sulfo...,
http://linkedlifedata.com/resource/pubmed/chemical/Amyloid Precursor Protein Secretases,
http://linkedlifedata.com/resource/pubmed/chemical/Amyloid beta-Peptides,
http://linkedlifedata.com/resource/pubmed/chemical/Antibiotics, Antitubercular,
http://linkedlifedata.com/resource/pubmed/chemical/Butyric Acids,
http://linkedlifedata.com/resource/pubmed/chemical/CYP3A4 protein, human,
http://linkedlifedata.com/resource/pubmed/chemical/Cyp3a41 protein, mouse,
http://linkedlifedata.com/resource/pubmed/chemical/Cytochrome P-450 CYP3A,
http://linkedlifedata.com/resource/pubmed/chemical/Cytochrome P-450 Enzyme System,
http://linkedlifedata.com/resource/pubmed/chemical/Hydrocarbons, Halogenated,
http://linkedlifedata.com/resource/pubmed/chemical/P-Glycoprotein,
http://linkedlifedata.com/resource/pubmed/chemical/Receptors, Steroid,
http://linkedlifedata.com/resource/pubmed/chemical/Rifampin,
http://linkedlifedata.com/resource/pubmed/chemical/cytochrome P-450 3A4, rat,
http://linkedlifedata.com/resource/pubmed/chemical/pregnane X receptor
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pubmed:status |
MEDLINE
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pubmed:month |
Jul
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pubmed:issn |
1366-5928
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pubmed:author |
pubmed-author:AndersonJ JJJ,
pubmed-author:BartenD MDM,
pubmed-author:BoultonD WDW,
pubmed-author:FlintO POP,
pubmed-author:HanselS BSB,
pubmed-author:KrishnaRR,
pubmed-author:LubinskiJJ,
pubmed-author:PursleyJ MJM,
pubmed-author:SantoneK SKS,
pubmed-author:ThakurAA,
pubmed-author:WangJJ,
pubmed-author:WarshawskyLL,
pubmed-author:YaoMM,
pubmed-author:ZhengMM
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pubmed:issnType |
Electronic
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pubmed:volume |
39
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pubmed:owner |
NLM
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pubmed:authorsComplete |
Y
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pubmed:pagination |
544-55
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pubmed:dateRevised |
2010-11-18
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pubmed:meshHeading |
pubmed-meshheading:19480557-Adult,
pubmed-meshheading:19480557-Amyloid Precursor Protein Secretases,
pubmed-meshheading:19480557-Amyloid beta-Peptides,
pubmed-meshheading:19480557-Animals,
pubmed-meshheading:19480557-Antibiotics, Antitubercular,
pubmed-meshheading:19480557-Biological Availability,
pubmed-meshheading:19480557-Brain,
pubmed-meshheading:19480557-Butyric Acids,
pubmed-meshheading:19480557-Cells, Cultured,
pubmed-meshheading:19480557-Cytochrome P-450 CYP3A,
pubmed-meshheading:19480557-Cytochrome P-450 Enzyme System,
pubmed-meshheading:19480557-Dogs,
pubmed-meshheading:19480557-Enzyme Induction,
pubmed-meshheading:19480557-Female,
pubmed-meshheading:19480557-Guinea Pigs,
pubmed-meshheading:19480557-Hepatocytes,
pubmed-meshheading:19480557-Humans,
pubmed-meshheading:19480557-Hydrocarbons, Halogenated,
pubmed-meshheading:19480557-Male,
pubmed-meshheading:19480557-Mice,
pubmed-meshheading:19480557-Mice, Knockout,
pubmed-meshheading:19480557-P-Glycoprotein,
pubmed-meshheading:19480557-Rats,
pubmed-meshheading:19480557-Rats, Sprague-Dawley,
pubmed-meshheading:19480557-Receptors, Steroid,
pubmed-meshheading:19480557-Rifampin,
pubmed-meshheading:19480557-Species Specificity
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pubmed:year |
2009
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pubmed:articleTitle |
Studies on the pharmacokinetics and metabolism of a gamma-secretase inhibitor BMS-299897, and exploratory investigation of CYP enzyme induction.
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pubmed:affiliation |
Metabolism and Pharmacokinetics, Bristol-Myers Squibb Research and Development, Wallingford, CT, USA. Ming.Zheng@bms.com
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pubmed:publicationType |
Journal Article,
Comparative Study,
Research Support, Non-U.S. Gov't
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