Co-Target(s) Information
Target General Information | Top | ||||
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Target ID | T70680 | Target Info | |||
Target Name | Solute carrier family 22 member 8 (SLC22A8) | ||||
Synonyms |
hROAT1; hPAHT; hOAT1; Solute carrier family 22 member 6; SLC22A8; SLC22A6; Renal organic anion transporter 1; PAHT; PAH transporter; OAT1
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Target Type | Successful Target | ||||
Gene Name | SLC22A8 | ||||
Biochemical Class | Major facilitator superfamily | ||||
UniProt ID |
Co-Targets of This Target | Top | |||||
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Co-Target Name | Carbonic anhydrase II (CA-II) | Successful Target | ||||
UniProt ID | CAH2_HUMAN | |||||
Gene Name | CA2 | |||||
Synonyms |
Carbonic anhydrase C; Carbonic anhydrase 2; Carbonate dehydratase II; CAC
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Representative Drug(s) | Probenecid | Drug Info | Ki = 431 nM | [1] | ||
Co-Target Name | Carbonic anhydrase IX (CA-IX) | Clinical trial Target | ||||
UniProt ID | CAH9_HUMAN | |||||
Gene Name | CA9 | |||||
Synonyms |
Renal cell carcinoma-associated antigen G250; RCC-associated antigen G250; PMW1; P54/58N; Membrane antigen MN; MN; G250 antigen (MN/CA IX/G250); G250; Carbonic anhydrase 9; Carbonate dehydratase IX; CAIX
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Representative Drug(s) | Probenecid | Drug Info | Ki = 360 nM | [2] |
References | Top | ||||
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REF 1 | Exploring new Probenecid-based carbonic anhydrase inhibitors: Synthesis, biological evaluation and docking studies. Bioorg Med Chem. 2015 Sep 1;23(17):5311-8. | ||||
REF 2 | Selective inhibition of human carbonic anhydrases by novel amide derivatives of probenecid: synthesis, biological evaluation and molecular modelling studies. Bioorg Med Chem. 2014 Aug 1;22(15):3982-8. |
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