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TargetEndothelin-1 receptor
LigandBDBM50029770
Substrate/Competitorn/a
Meas. Tech.ChEMBL_63217 (CHEMBL674069)
IC50 4000±n/a nM
Citation Stein, PDFloyd, DMBisaha, SDickey, JGirotra, RNGougoutas, JZKozlowski, MLee, VGLiu, ECMalley, MF Discovery and structure-activity relationships of sulfonamide ETA-selective antagonists. J Med Chem38:1344-54 (1995) [PubMed]
More Info.:Get all data from this article,  Assay Method
 
Endothelin-1 receptor
Name:Endothelin-1 receptor
Synonyms:EDNRA_RAT | ENDOTHELIN A | Ednra | Endothelin receptor | Endothelin-1 receptor
Type:Enzyme Catalytic Domain
Mol. Mass.:48256.91
Organism:RAT
Description:ENDOTHELIN A EDNRA RAT::P26684
Residue:426
Sequence:
MGVLCFLASFWLALVGGAIADNAERYSANLSSHVEDFTPFPGTEFNFLGTTLQPPNLALP
SNGSMHGYCPQQTKITTAFKYINTVISCTIFIVGMVGNATLLRIIYQNKCMRNGPNALIA
SLALGDLIYVVIDLPINVFKLLAGRWPFDHNDFGVFLCKLFPFLQKSSVGITVLNLCALS
VDRYRAVASWSRVQGIGIPLITAIEIVSIWILSFILAIPEAIGFVMVPFEYKGEQHRTCM
LNATTKFMEFYQDVKDWWLFGFYFCMPLVCTAIFYTLMTCEMLNRRNGSLRIALSEHLKQ
RREVAKTVFCLVVIFALCWFPLHLSRILKKTVYDEMDKNRCELLSFLLLMDYIGINLATM
NSCINPIALYFVSKKFKNCFQSCLCCCCHQSKSLMTSVPMNGTSIQWKNQEQNHNTERSS
HKDSMN
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  Blast E-value cutoff:
BDBM50029770
n/a
NameBDBM50029770
Synonyms:4-amino-N-(5-methyl-isoxazol-3-yl)-benzenesulfonamide | 4-amino-N-(5-methylisoxazol-3-yl)benzenesulfonamide | ACETYLSULFAMETHOXAZOLE | BACTRIM | CHEMBL443 | COTRIM | GANTANOL | GANTANOL-DS | RO 4-2130 | SEPTRA | SULFAMETHOPRIM | SULFAMETHOPRIM-DS | SULFAMETHOXAZOLE SODIUM | SULFATRIM | SULFATRIM-DS | SULFATRIM-SS | SULMEPRIM | SULPHAMETHOXAZOLE | TRIMETH/SULFA | UROBAK
TypeSmall organic molecule
Emp. Form.C10H11N3O3S
Mol. Mass.253.278
SMILESCc1cc(NS(=O)(=O)c2ccc(N)cc2)no1
Structure
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