Effects of diltiazem, a moderate inhibitor of CYP3A4, on the pharmacokinetics of tamsulosin in different CYP2D6 genotypes
활용도 Analysis
논문 Analysis
연구자 Analysis
저자
변지영
이윤정
김영훈
김세형
이충민
배정우
장춘곤
이석용
최창익
제어번호
106053014
학술지명
Archives of Pharmacal Research
권호사항
Vol.
41
No.
5
[
2018
]
발행처
대한약학회
발행처 URL
http://www.psk.or.kr
자료유형
학술저널
수록면
564-570
(
7쪽)
언어
English
출판년도
2018
등재정보
KCI등재
소장기관
부산대학교 중앙도서관
숙명여자대학교 중앙도서관
영남대학교 중앙도서관
영남대학교 중앙도서관
중앙대학교 서울캠퍼스 중앙도서관
중앙대학교 서울캠퍼스 중앙도서관
중앙대학교 서울캠퍼스 중앙도서관
판매처
'
Effects of diltiazem, a moderate inhibitor of CYP3A4, on the pharmacokinetics of tamsulosin in different CYP2D6 genotypes' 의 참고문헌
Tamsulosin exposure is significantly increased by the CYP2D6*10/*10 genotype
Semiphysiologically based pharmacokinetic models for the inhibition of midazolam clearance by diltiazem and its major metabolite
Role of small intestinal cytochromes p450 in the bioavailability of oral nifedipine
Radioreceptor assay analysis of tamsulosin and terazosin pharmacokinetics
Power and sample size calculations for studies involving linear regression
Polymorphic cytochrome P450 enzymes (CYPs) and their role in personalized therapy
Pharmacokinetics and pharmacodynamics of tamsulosin in its modifiedrelease and oral controlled absorption system formulations
Pharmacokinetic interaction of finasteride with tamsulosin hydrochloride: an open-label, randomized, 3-period crossover study in healthy Chinese male volunteers
Pharmacogenetic prediction of individual variability in drug response based on CYP2D6, CYP2C9 and CYP2C19 genetic polymorphisms
PCR-based genotyping for duplicated and deleted CYP2D6 genes
Inhibition of human intestinal wall metabolism by macrolide antibiotics: effect of clarithromycin on cytochrome P450 3A4/5 activity and expression
Impact of genetic polymorphisms in CYP2C9 and CYP2C19 on the pharmacokinetics of clinically used drugs
Identification of cytochrome P450 isozymes involved in metabolism of the alpha1-adrenoceptor blocker tamsulosin in human liver microsomes
Genetic analysis of the Chinese cytochrome P4502D locus: characterization of variant CYP2D6 genes present in subjects with diminished capacity for debrisoquine hydroxylation
Efficacy of low-dose tamsulosin on lower urinary tract symptoms suggestive of benign prostatic hyperplasia: a nonblind multicentre Korean study
Efficacy of low-dose tamsulosin in chinese patients with symptomatic benign prostatic hyperplasia
Effects of the CYP2D6*10 allele on the pharmacokinetics of atomoxetine and its metabolites
Effects of tamsulosin metabolites at alpha-1 adrenoceptor subtypes
Effects of strong CYP2D6 and 3A4 inhibitors, paroxetine and ketoconazole, on the pharmacokinetics and cardiovascular safety of tamsulosin
Effect of the CYP2D6*10 allele on the pharmacokinetics of clomiphene and its active metabolites
Effect of tamsulosin on the pharmacokinetics of dutasteride in Chinese male healthy volunteers
Effect of concomitant administration of cimetidine hydrochloride on the pharmacokinetic and safety profile of tamsulosin hydrochloride 0.4 mg in healthy subjects
Effect of Cytochrome P450 polymorphism on the action and metabolism of selective serotonin reuptake inhibitors
Drugs for treatment of benign prostatic hyperplasia: affinity comparison at cloned alpha 1-adrenoceptor subtypes and in human prostate
Drug interactions with calcium channel blockers: possible involvement of metaboliteintermediate complexation with CYP3A
Dose of midazolam should be reduced during diltiazem and verapamil treatments
Disposition of the selective alpha1A-adrenoceptor antagonist tamsulosin in humans: comparison with data from interspecies scaling
Diltiazem: a review of its pharmacological properties and therapeutic efficacy
Diltiazem increases blood concentrations of cyclized cyclosporine metabolites resulting in different cyclosporine metabolite patterns in stable male and female renal allograft recipients
Diltiazem enhances the effects of triazolam by inhibiting its metabolism
Determination of in vivo absorption, metabolism, and transport of drugs by the human intestinal wall and liver with a novel perfusion technique
Desacetyl-diltiazem displays severalfold higher affinity to CYP2D6 compared with CYP3A4
Comparison of tamsulosin and finasteride for lower urinary tract symptoms associated with benign prostatic hyperplasia in Korean patients
Clinical application of pharmacogenomics
CYP2D6 polymorphism in a Mexican American population
CYP2D6 is involved in O-demethylation of diltiazem. An in vitro study with transfected human liver cells
Boehringer Ingelheim Pharmaceuticals Incorporated, Ridgefield
Alpha1-, alpha2- and beta-adrenoceptors in the urinary bladder, urethra and prostate
Absorption, metabolism and excretion of tamsulosin hydrochloride in man
'
Effects of diltiazem, a moderate inhibitor of CYP3A4, on the pharmacokinetics of tamsulosin in different CYP2D6 genotypes'
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