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TargetEndothelin receptor type B
LigandBDBM50068720
Substrate/Competitorn/a
Meas. Tech.ChEMBL_64185 (CHEMBL878144)
Ki 940±n/a nM
Citation Murugesan, NGu, ZStein, PDBisaha, SSpergel, SGirotra, RLee, VGLloyd, JMisra, RNSchmidt, JMathur, AStratton, LKelly, YFBird, EWaldron, TLiu, ECZhang, RLee, HSerafino, RAbboa-Offei, BMathers, PGiancarli, MSeymour, AAWebb, MLHunt, JT Biphenylsulfonamide endothelin antagonists: structure-activity relationships of a series of mono- and disubstituted analogues and pharmacology of the orally active endothelin antagonist 2'-amino-N- (3,4-dimethyl-5-isoxazolyl)-4'-(2-methylpropyl)[1, 1'-biphenyl]-2-sulfonamide (BMS-187308). J Med Chem41:5198-218 (1999) [PubMed]  Article
More Info.:Get all data from this article,  Assay Method
 
Endothelin receptor type B
Name:Endothelin receptor type B
Synonyms:EDNRB_RAT | ENDOTHELIN B | ET-B | Ednrb | Endothelin receptor | Endothelin receptor non-selective type
Type:Enzyme Catalytic Domain
Mol. Mass.:49483.43
Organism:RAT
Description:ENDOTHELIN B EDNRB RAT::P21451
Residue:442
Sequence:
MQSSASRCGRALVALLLACGLLGVWGEKRGFPPAQATPSLLGTKEVMTPPTKTSWTRGSN
SSLMRSSAPAEVTKGGRVAGVPPRSFPPPCQRKIEINKTFKYINTIVSCLVFVLGIIGNS
TLLRIIYKNKCMRNGPNILIASLALGDLLHIIIDIPINAYKLLAGDWPFGAEMCKLVPFI
QKASVGITVLSLCALSIDRYRAVASWSRIKGIGVPKWTAVEIVLIWVVSVVLAVPEAIGF
DVITSDYKGKPLRVCMLNPFQKTAFMQFYKTAKDWWLFSFYFCLPLAITAIFYTLMTCEM
LRKKSGMQIALNDHLKQRREVAKTVFCLVLVFALCWLPLHLSRILKLTLYDQSNPQRCEL
LSFLLVLDYIGINMASLNSCINPIALYLVSKRFKNCFKSCLCCWCQTFEEKQSLEEKQSC
LKFKANDHGYDNFRSSNKYSSS
Blast this sequence in BindingDB or PDB
  Blast E-value cutoff:
BDBM50068720
n/a
NameBDBM50068720
Synonyms:6-Hydroxy-4'-isobutyl-biphenyl-2-sulfonic acid (3,4-dimethyl-isoxazol-5-yl)-amide | CHEMBL421955
TypeSmall organic molecule
Emp. Form.C21H24N2O4S
Mol. Mass.400.491
SMILESCC(C)Cc1ccc(cc1)-c1c(O)cccc1S(=O)(=O)Nc1onc(C)c1C
Structure
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