Reaction Details |
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Target | Endothelin receptor type B |
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Ligand | BDBM50000558 |
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Substrate/Competitor | n/a |
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Meas. Tech. | ChEBML_63192 |
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IC50 | 1.6±n/a nM |
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Citation | Cody, WL; Doherty, AM; He, JX; DePue, PL; Rapundalo, ST; Hingorani, GA; Major, TC; Panek, RL; Dudley, DT; Haleen, SJ Design of a functional hexapeptide antagonist of endothelin. J Med Chem35:3301-3 (1992) [PubMed] |
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More Info.: | Get all data from this article, Assay Method |
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Endothelin receptor type B |
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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
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BDBM50000558 |
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n/a |
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Name | BDBM50000558 |
Synonyms: | CHEMBL437472 | ET-1 | Endothelin -1 | Endothelin 1, ET-1 | Endothelin derivative | Endothelin-1 | c(Cys-Ser-c(Cys-Ser-Ser-Leu-Met-Asp-Lys-Gln-Cys)-Val-Tyr-Phe-Cys)-His-Leu-Asp-Ile-Ile-Trp |
Type | Small organic molecule |
Emp. Form. | C109H159N25O32S5 |
Mol. Mass. | 2491.902 |
SMILES | CC[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]2CSSC[C@@H](NC(=O)[C@H](CCC(O)=O)NC(=O)[C@H](CCCCN)NC(=O)[C@@H](CC(O)=O)NC(=O)[C@H](CCSC)NC(=O)[C@@H](CC(C)C)NC(=O)[C@H](CO)NC(=O)[C@@H](CO)NC2=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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