Reaction Details |
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Target | Potassium voltage-gated channel subfamily A member 1 |
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Ligand | BDBM50279106 |
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Substrate/Competitor | n/a |
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Meas. Tech. | ChEMBL_1758559 (CHEMBL4193567) |
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IC50 | 250±n/a nM |
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Citation | Zidar, N; ?ula, A; Toma?i?, T; Rogers, M; Kirby, RW; Tytgat, J; Peigneur, S; Kikelj, D; Ila?, J; Ma?i?, LP Clathrodin, hymenidin and oroidin, and their synthetic analogues as inhibitors of the voltage-gated potassium channels. Eur J Med Chem139:232-241 (2017) [PubMed] Article |
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More Info.: | Get all data from this article, Assay Method |
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Potassium voltage-gated channel subfamily A member 1 |
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Name: | Potassium voltage-gated channel subfamily A member 1 |
Synonyms: | KCNA1 | KCNA1_HUMAN | Potassium (voltage dependent) | Potassium voltage-gated channel subfamily A member 1 | Voltage-gated potassium channel | Voltage-gated potassium channel subfamily A member 1/beta-1 | Voltage-gated potassium channel subunit Kv1.1 |
Type: | Enzyme Catalytic Domain |
Mol. Mass.: | 56451.30 |
Organism: | Homo sapiens (Human) |
Description: | Potassium (voltage dependent) 0 0::Q09470 |
Residue: | 495 |
Sequence: | MTVMSGENVDEASAAPGHPQDGSYPRQADHDDHECCERVVINISGLRFETQLKTLAQFPN
TLLGNPKKRMRYFDPLRNEYFFDRNRPSFDAILYYYQSGGRLRRPVNVPLDMFSEEIKFY
ELGEEAMEKFREDEGFIKEEERPLPEKEYQRQVWLLFEYPESSGPARVIAIVSVMVILIS
IVIFCLETLPELKDDKDFTGTVHRIDNTTVIYNSNIFTDPFFIVETLCIIWFSFELVVRF
FACPSKTDFFKNIMNFIDIVAIIPYFITLGTEIAEQEGNQKGEQATSLAILRVIRLVRVF
RIFKLSRHSKGLQILGQTLKASMRELGLLIFFLFIGVILFSSAVYFAEAEEAESHFSSIP
DAFWWAVVSMTTVGYGDMYPVTIGGKIVGSLCAIAGVLTIALPVPVIVSNFNYFYHRETE
GEEQAQLLHVSSPNLASDSDLSRRSSSTMSKSEYMEIEEDMNNSIAHYRQVNIRTANCTT
ANQNCVNKSKLLTDV
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BDBM50279106 |
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n/a |
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Name | BDBM50279106 |
Synonyms: | 4-(4-phenoxybutoxy)-7H-furo[3,2-g]chromen-7-one | 5-(4-phenoxybutoxy)psoralen | CHEMBL444449 |
Type | Small organic molecule |
Emp. Form. | C21H18O5 |
Mol. Mass. | 350.3646 |
SMILES | O=c1ccc2c(OCCCCOc3ccccc3)c3ccoc3cc2o1 |
Structure |
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