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TargetEDNRB
LigandBDBM50284011
Substrate/Competitorn/a
Meas. Tech.ChEMBL_64030
IC50 1100±n/a nM
Citation Cody, WLHe, JXDePue, PLRapundalo, STHingorani, GPDudley, DTHill, KEReynolds, EEDoherty, AM Structure-activity relationships in a series of monocyclic endothelin analogues Bioorg Med Chem Lett4:567-572 (1994)    Article
More Info.:Get all data from this article,  Assay Method
 
EDNRB
Name:Endothelin receptor
Synonyms:ENDOTHELIN B | ET-B | 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
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  Blast E-value cutoff:
BDBM50284011
NameBDBM50284011
Synonyms:CHEMBL438768 | Trp-Ile-Ile-Asp-Leu-Hisc(Cys-Ser-Asp-Lys-Glu-Val-Tyr-Phe-Cys)
TypeSmall organic molecule
Emp. Form.C86H121N19O24S2
Mol. Mass.1869.124
SMILESCC[C@H](C)[C@H](NC(=O)[C@H](CC(O)=O)NC(=O)[C@H](CC(C)C)NC(=O)[C@H](Cc1cnc[nH]1)NC(=O)[C@H]1CSSC[C@H](N)C(=O)N[C@@H](CO)C(=O)N[C@H](CC(O)=O)C(=O)N[C@@H](CCCCN)C(=O)N[C@H](CCC(O)=O)C(=O)N[C@@H](C(C)C)C(=O)N[C@H](Cc2ccc(O)cc2)C(=O)N[C@@H](Cc2ccccc2)C(=O)N1)C(=O)N[C@@H]([C@@H](C)CC)C(=O)N[C@@H](Cc1c[nH]c2ccccc12)C(O)=O
Structure
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