Proteins > Solute carrier organic anion transporter family member 1A1
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Solute carrier organic anion transporter family member 1A1
A solute carrier organic anion transporter family member 1A1 that is encoded in the genome of rat. [OMA:P46720, PRO:DNx]
Synonyms
Organic anion-transporting polypeptide 1;
OATP-1;
Sodium-independent organic anion transporter 1;
Solute carrier family 21 member 1
Research
Bioassay Publications (18)
Timeframe | Studies on this Protein(%) | All Drugs % |
pre-1990 | 0 (0.00) | 18.7374 |
1990's | 13 (72.22) | 18.2507 |
2000's | 5 (27.78) | 29.6817 |
2010's | 0 (0.00) | 24.3611 |
2020's | 0 (0.00) | 2.80 |
Compounds (35)
Drugs with Inhibition Measurements
Drugs with Other Measurements
Polyspecific substrate uptake by the hepatic organic anion transporter Oatp1 in stably transfected CHO cells.The American journal of physiology, , Volume: 276, Issue:4, 1999
The modified dipeptide, enalapril, an angiotensin-converting enzyme inhibitor, is transported by the rat liver organic anion transport protein.Hepatology (Baltimore, Md.), , Volume: 28, Issue:5, 1998
Expression cloning of a rat liver Na(+)-independent organic anion transporter.Proceedings of the National Academy of Sciences of the United States of America, , Jan-04, Volume: 91, Issue:1, 1994
[no title available],
Characterization of the efflux transport of 17beta-estradiol-D-17beta-glucuronide from the brain across the blood-brain barrier.The Journal of pharmacology and experimental therapeutics, , Volume: 298, Issue:1, 2001
Polyspecific substrate uptake by the hepatic organic anion transporter Oatp1 in stably transfected CHO cells.The American journal of physiology, , Volume: 276, Issue:4, 1999
The modified dipeptide, enalapril, an angiotensin-converting enzyme inhibitor, is transported by the rat liver organic anion transport protein.Hepatology (Baltimore, Md.), , Volume: 28, Issue:5, 1998
Organic anion transporting polypeptide mediates organic anion/HCO3- exchange.The Journal of biological chemistry, , Oct-17, Volume: 272, Issue:42, 1997
Estradiol 17 beta-D-glucuronide is a high-affinity substrate for oatp organic anion transporter.The American journal of physiology, , Volume: 270, Issue:2 Pt 2, 1996
Functional characterization of the basolateral rat liver organic anion transporting polypeptide.Hepatology (Baltimore, Md.), , Volume: 20, Issue:2, 1994
Polyspecific substrate uptake by the hepatic organic anion transporter Oatp1 in stably transfected CHO cells.The American journal of physiology, , Volume: 276, Issue:4, 1999
Polyspecific drug and steroid clearance by an organic anion transporter of mammalian liver.The Journal of pharmacology and experimental therapeutics, , Volume: 276, Issue:3, 1996
Estradiol 17 beta-D-glucuronide is a high-affinity substrate for oatp organic anion transporter.The American journal of physiology, , Volume: 270, Issue:2 Pt 2, 1996
Comparative inhibitory effects of different compounds on rat oatpl (slc21a1)- and Oatp2 (Slc21a5)-mediated transport.Pharmaceutical research, , Volume: 19, Issue:2, 2002
Characterization of the efflux transport of 17beta-estradiol-D-17beta-glucuronide from the brain across the blood-brain barrier.The Journal of pharmacology and experimental therapeutics, , Volume: 298, Issue:1, 2001
Polyspecific substrate uptake by the hepatic organic anion transporter Oatp1 in stably transfected CHO cells.The American journal of physiology, , Volume: 276, Issue:4, 1999
Contribution of organic anion transporting polypeptide to uptake of its possible substrates into rat hepatocytes.The Journal of pharmacology and experimental therapeutics, , Volume: 288, Issue:2, 1999
Transport of temocaprilat into rat hepatocytes: role of organic anion transporting polypeptide.The Journal of pharmacology and experimental therapeutics, , Volume: 287, Issue:1, 1998
Estradiol 17 beta-D-glucuronide is a high-affinity substrate for oatp organic anion transporter.The American journal of physiology, , Volume: 270, Issue:2 Pt 2, 1996
Polyspecific drug and steroid clearance by an organic anion transporter of mammalian liver.The Journal of pharmacology and experimental therapeutics, , Volume: 276, Issue:3, 1996