Target Gene Table
VIS IDVirusEnsembl IDGene TypeTarget GeneOncogeneTumor Suppressor GeneNCBI IDUniprot ID
TVIS10006400HBVENSG00000006071.16protein_codingABCC8NoNo6833Q09428
TVIS10014476HBVENSG00000006071.16protein_codingABCC8NoNo6833Q09428
TVIS20010586HPVENSG00000006071.16protein_codingABCC8NoNo6833Q09428
TVIS44004571HTLV-1ENSG00000006071.16protein_codingABCC8NoNo6833Q09428
TVIS44020396HTLV-1ENSG00000006071.16protein_codingABCC8NoNo6833Q09428
TCGA Plot Options
Drug Information
GeneABCC8
DrugBank IDDB00731
Drug NameNateglinide
Target IDBE0000207
UniProt IDQ09428
Regulation Typeinhibitor
PubMed IDs10773014; 11716850; 12196472; 12604678; 12764427; 11728565
CitationsHu S, Wang S, Fanelli B, Bell PA, Dunning BE, Geisse S, Schmitz R, Boettcher BR: Pancreatic beta-cell K(ATP) channel activity and membrane-binding studies with nateglinide: A comparison with sulfonylureas and repaglinide. J Pharmacol Exp Ther. 2000 May;293(2):444-52.@@Sunaga Y, Gonoi T, Shibasaki T, Ichikawa K, Kusama H, Yano H, Seino S: The effects of mitiglinide (KAD-1229), a new anti-diabetic drug, on ATP-sensitive K+ channels and insulin secretion: comparison with the sulfonylureas and nateglinide. Eur J Pharmacol. 2001 Nov 9;431(1):119-25.@@Hansen AM, Christensen IT, Hansen JB, Carr RD, Ashcroft FM, Wahl P: Differential interactions of nateglinide and repaglinide on the human beta-cell sulphonylurea receptor 1. Diabetes. 2002 Sep;51(9):2789-95.@@Chachin M, Yamada M, Fujita A, Matsuoka T, Matsushita K, Kurachi Y: Nateglinide, a D-phenylalanine derivative lacking either a sulfonylurea or benzamido moiety, specifically inhibits pancreatic beta-cell-type K(ATP) channels. J Pharmacol Exp Ther. 2003 Mar;304(3):1025-32.@@Norman P, Rabasseda X: Nateglinide: A structurally novel, short-acting, hypoglycemic agent. Drugs Today (Barc). 2001 Jun;37(6):411-426.@@Dornhorst A: Insulinotropic meglitinide analogues. Lancet. 2001 Nov 17;358(9294):1709-16.
GroupsApproved; Investigational
Direct ClassificationPhenylalanine and derivatives
SMILESCC(C)[C@H]1CC[C@@H](CC1)C(=O)N[C@H](CC1=CC=CC=C1)C(O)=O
PathwaysNateglinide Action Pathway
PharmGKBPA450600
ChEMBLCHEMBL783