Results 31 to 40 of about 6,916 (201)
Interactions of antiretroviral drugs with the SLC22A1 (OCT1) drug transporter [PDF]
The SLC22A1 influx transporter is expressed on the basolateral membrane of hepatocytes and is involved in the excretion of numerous cations. Inhibition of SLC22A1 by several antiretrovirals, such as the protease inhibitor darunavir, has not previously been determined.
Moss, Darren M. +3 more
openaire +3 more sources
The substrate specificity of recombinant human mitochondrial intermediate peptidase (hMIP) using a synthetic support‐bound FRET peptide library is presented.
M.F.M. Marcondes +6 more
doaj +1 more source
Drug-Drug Interactions at Organic Cation Transporter 1
The interaction between drugs and various transporters is one of the decisive factors that affect the pharmacokinetics and pharmacodynamics of drugs. The organic cation transporter 1 (OCT1) is a member of the Solute Carrier 22A (SLC22A) family that plays
Shiwei Zhou +5 more
doaj +1 more source
Role of OCT1 in hepatocellular carcinoma.
Hepatocellular carcinoma (HCC) is one of the most commonly diagnosed cancers causing death worldwide. It is difficult to detect at an early stage and most patients with advanced HCC rarely achieve satisfying therapeutic results. Accordingly, researchers have been trying to find new biomarkers for diagnosis and new methods of treatment.
Li,Jingguo, Yang,Zhengyi, Tuo,Biguang
openaire +3 more sources
Ro 31-8220 is a potent protein kinase C (PKC) inhibitor belonging to the chemical class of bisindolylmaleimides (BIMs). Various PKC-independent effects of Ro 31-8220 have however been demonstrated, including inhibition of the ATP-binding cassette drug ...
Abdullah Mayati +6 more
doaj +1 more source
Background Esophageal squamous cell carcinoma (ESCC) is a highly malignant neoplasm. DNA-damaging drugs, such as cisplatin (CDDP) and 5-fluorouracil (5-FU), are most frequently used in preoperative chemotherapy for ESCC.
Masahiro Izutsu +9 more
doaj +1 more source
The organic cation transporter OCT1 (SLC22A1) mediates uptake and metabolism of the active tramadol metabolite (+)O-desmethyltramadol in the liver. In this study, the influence of OCT1 genetic polymorphisms on pharmacokinetics and analgesic efficacy of ...
Tzvetkov, Mladen Vassilev +14 more
core +1 more source
Combined and independent effects of OCT1 and CYP2D6 on the cellular disposition of drugs
The organic cation transporter 1 (OCT1) mediates the cell uptake and cytochrome P450 2D6 (CYP2D6) the metabolism of many cationic substrates. Activities of OCT1 and CYP2D6 are affected by enormous genetic variation and frequent drug-drug interactions.
Lukas Gebauer +3 more
openaire +3 more sources
OCT1-target neural gene PFN2 promotes tumor growth in androgen receptor-negative prostate cancer
Androgen and androgen receptor (AR) targeted therapies are the main treatment for most prostate cancer (PC) patients. Although AR signaling inhibitors are effective, tumors can evade this treatment by transforming to an AR-negative PC via lineage ...
Daisuke Obinata +11 more
doaj +1 more source
PHARMACOGENETICS OF ORGANIC CATION TRANSPORTERS
This article describes basic information about the classification, structure, substrate specificity and expression of organic cation transporters. The pharmacokinetic and pharmacogenetic aspects of transporters are discussed in more detail, as well as ...
V. A. Evteev +3 more
doaj +1 more source

