Reaction Details |
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Target | Potassium voltage-gated channel subfamily A member 3 |
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Ligand | BDBM50099583 |
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Substrate/Competitor | n/a |
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Meas. Tech. | ChEMBL_214954 (CHEMBL821183) |
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IC50 | 86±n/a nM |
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Citation | Coghlan, MJ; Carroll, WA; Gopalakrishnan, M Recent developments in the biology and medicinal chemistry of potassium channel modulators: update from a decade of progress. J Med Chem44:1627-53 (2001) [PubMed] |
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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 3 |
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Name: | Potassium voltage-gated channel subfamily A member 3 |
Synonyms: | HGK5 | HLK3 | HPCN3 | HuKIII | KCNA3 | KCNA3_HUMAN | Potassium voltage-gated channel subfamily A member 3 | Voltage-gated potassium channel | Voltage-gated potassium channel subunit Kv1.3 |
Type: | PROTEIN |
Mol. Mass.: | 63835.47 |
Organism: | Homo sapiens (Human) |
Description: | ChEMBL_1513935 |
Residue: | 575 |
Sequence: | MDERLSLLRSPPPPSARHRAHPPQRPASSGGAHTLVNHGYAEPAAGRELPPDMTVVPGDH
LLEPEVADGGGAPPQGGCGGGGCDRYEPLPPSLPAAGEQDCCGERVVINISGLRFETQLK
TLCQFPETLLGDPKRRMRYFDPLRNEYFFDRNRPSFDAILYYYQSGGRIRRPVNVPIDIF
SEEIRFYQLGEEAMEKFREDEGFLREEERPLPRRDFQRQVWLLFEYPESSGPARGIAIVS
VLVILISIVIFCLETLPEFRDEKDYPASTSQDSFEAAGNSTSGSRAGASSFSDPFFVVET
LCIIWFSFELLVRFFACPSKATFSRNIMNLIDIVAIIPYFITLGTELAERQGNGQQAMSL
AILRVIRLVRVFRIFKLSRHSKGLQILGQTLKASMRELGLLIFFLFIGVILFSSAVYFAE
ADDPTSGFSSIPDAFWWAVVTMTTVGYGDMHPVTIGGKIVGSLCAIAGVLTIALPVPVIV
SNFNYFYHRETEGEEQSQYMHVGSCQHLSSSAEELRKARSNSTLSKSEYMVIEEGGMNHS
AFPQTPFKTGNSTATCTTNNNPNSCVNIKKIFTDV
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BDBM50099583 |
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n/a |
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Name | BDBM50099583 |
Synonyms: | 5-isopropenyloxy-1b,3a,10b-trimethyl-2,3-di(methylcarbonyloxy)-5a-(1-methylcarbonyloxyethyl)-14-methylene-1a-methyloxycarbonyl-8-oxo-1a,1b,2,3,3a,3b,4,5,5a,6,8,10a,10b,11,12,12a,12b,13,14,14a-icosahydrooxireno[3',2':7,8]chryseno[2,1-c]oxepin-4-ylaceta | CHEMBL290227 |
Type | Small organic molecule |
Emp. Form. | C41H54O14 |
Mol. Mass. | 770.8591 |
SMILES | COC(=O)[C@@]12O[C@@H]1C(=C)CC1[C@@H]3CC[C@@]4(C)[C@@H]5C=CC(=O)OC[C@]5([C@@H](C)OC(C)=O)[C@@H](OC(C)=C)[C@@H](OC(C)=O)[C@@H]4[C@@]3(C)[C@H](OC(C)=O)[C@H](OC(C)=O)[C@@]21C |c:18| |
Structure |
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