Title : Interaction of human organic anion transporter polypeptides 1B1 and 1B3 with antineoplastic compounds.

Pub. Date : 2015 Mar 6

PMID : 25618019






6 Functional Relationships(s)
Download
Sentence
Compound Name
Protein Name
Organism
1 OATP1B3 showed highly significant interactions with a variety of antineoplastic compounds including chlorambucil, mitoxantrone, vinblastine, vincristine, paclitaxel and etoposide, with Ki values of 40.6 muM, 3.2 muM, 15.9 muM, 30.6 muM, 1.8 muM and 13.5 muM, respectively. Etoposide latexin Homo sapiens
2 OATP1B3 showed highly significant interactions with a variety of antineoplastic compounds including chlorambucil, mitoxantrone, vinblastine, vincristine, paclitaxel and etoposide, with Ki values of 40.6 muM, 3.2 muM, 15.9 muM, 30.6 muM, 1.8 muM and 13.5 muM, respectively. Etoposide latexin Homo sapiens
3 OATP1B3 showed highly significant interactions with a variety of antineoplastic compounds including chlorambucil, mitoxantrone, vinblastine, vincristine, paclitaxel and etoposide, with Ki values of 40.6 muM, 3.2 muM, 15.9 muM, 30.6 muM, 1.8 muM and 13.5 muM, respectively. Etoposide latexin Homo sapiens
4 OATP1B3 showed highly significant interactions with a variety of antineoplastic compounds including chlorambucil, mitoxantrone, vinblastine, vincristine, paclitaxel and etoposide, with Ki values of 40.6 muM, 3.2 muM, 15.9 muM, 30.6 muM, 1.8 muM and 13.5 muM, respectively. Etoposide latexin Homo sapiens
5 OATP1B3 showed highly significant interactions with a variety of antineoplastic compounds including chlorambucil, mitoxantrone, vinblastine, vincristine, paclitaxel and etoposide, with Ki values of 40.6 muM, 3.2 muM, 15.9 muM, 30.6 muM, 1.8 muM and 13.5 muM, respectively. Etoposide latexin Homo sapiens
6 OATP1B3 showed highly significant interactions with a variety of antineoplastic compounds including chlorambucil, mitoxantrone, vinblastine, vincristine, paclitaxel and etoposide, with Ki values of 40.6 muM, 3.2 muM, 15.9 muM, 30.6 muM, 1.8 muM and 13.5 muM, respectively. Etoposide latexin Homo sapiens