Target Gene Table
VIS IDVirusEnsembl IDGene TypeTarget GeneOncogeneTumor Suppressor GeneNCBI IDUniprot ID
TVIS30031807HIVENSG00000151067.23protein_codingCACNA1CNoNo775A0A0A0MR67
A0A0A0MSA1
F5H522
Q13936
Q5V9X9
TVIS30031808HIVENSG00000151067.23protein_codingCACNA1CNoNo775A0A0A0MR67
A0A0A0MSA1
F5H522
Q13936
Q5V9X9
TVIS30031809HIVENSG00000151067.23protein_codingCACNA1CNoNo775A0A0A0MR67
A0A0A0MSA1
F5H522
Q13936
Q5V9X9
TVIS30031810HIVENSG00000151067.23protein_codingCACNA1CNoNo775A0A0A0MR67
A0A0A0MSA1
F5H522
Q13936
Q5V9X9
TVIS30031811HIVENSG00000151067.23protein_codingCACNA1CNoNo775A0A0A0MR67
A0A0A0MSA1
F5H522
Q13936
Q5V9X9
TVIS20001122HPVENSG00000151067.23protein_codingCACNA1CNoNo775A0A0A0MR67
A0A0A0MSA1
F5H522
Q13936
Q5V9X9
TVIS20003482HPVENSG00000151067.23protein_codingCACNA1CNoNo775A0A0A0MR67
A0A0A0MSA1
F5H522
Q13936
Q5V9X9
TVIS20002454HPVENSG00000151067.23protein_codingCACNA1CNoNo775A0A0A0MR67
A0A0A0MSA1
F5H522
Q13936
Q5V9X9
TVIS20011267HPVENSG00000151067.23protein_codingCACNA1CNoNo775A0A0A0MR67
A0A0A0MSA1
F5H522
Q13936
Q5V9X9
TVIS20014481HPVENSG00000151067.23protein_codingCACNA1CNoNo775A0A0A0MR67
A0A0A0MSA1
F5H522
Q13936
Q5V9X9
TCGA Plot Options
Drug Information
GeneCACNA1C
DrugBank IDDB09227
Drug NameBarnidipine
Target IDBE0000430
UniProt IDQ13936
Regulation Typeantagonist
PubMed IDs7760349; 19416978; 11022040
CitationsKwan YW, Bangalore R, Lakitsh M, Glossmann H, Kass RS: Inhibition of cardiac L-type calcium channels by quaternary amlodipine: implications for pharmacokinetics and access to dihydropyridine binding site. J Mol Cell Cardiol. 1995 Jan;27(1):253-62.@@Tikhonov DB, Zhorov BS: Structural model for dihydropyridine binding to L-type calcium channels. J Biol Chem. 2009 Jul 10;284(28):19006-17. doi: 10.1074/jbc.M109.011296. Epub 2009 May 5.@@Yamaguchi S, Okamura Y, Nagao T, Adachi-Akahane S: Serine residue in the IIIS5-S6 linker of the L-type Ca2+ channel alpha 1C subunit is the critical determinant of the action of dihydropyridine Ca2+ channel agonists. J Biol Chem. 2000 Dec 29;275(52):41504-11. doi: 10.1074/jbc.M007165200.
GroupsExperimental
Direct ClassificationDihydropyridinecarboxylic acids and derivatives
SMILESCOC(=O)C1=C(C)NC(C)=C([C@H]1C1=CC(=CC=C1)[N+]([O-])=O)C(=O)O[C@H]1CCN(CC2=CC=CC=C2)C1
Pathways
PharmGKB
ChEMBLCHEMBL2103761