Ki Summary

Reaction Details

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Target

5-hydroxytryptamine receptor 2B

Ligand

BDBM30704

Substrate

n/a

2.3±n/a nM

Comments

PDSP_1209

Citation

McKenna, DJ; Peroutka, SJ Differentiation of 5-hydroxytryptamine2 receptor subtypes using 125I-R-(-)2,5-dimethoxy-4-iodo-phenylisopropylamine and 3H-ketanserin. J Neurosci 9:3482-90 (1989) [PubMed]

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Target

Name:

5-hydroxytryptamine receptor 2B

Synonyms:

5-HT2B | 5-hydroxytryptamine 2B receptor | HTR2B

Type:

Enzyme Catalytic Domain

Mol. Mass.:

15564.62

Organism:

BOVINE

Description:

Q8MI09

Residue:

137

Sequence:

KPPQRLTWLTVSTVFQRDETPCSSPEKVAMLDGFHKDKTLPNASADILMRRMSTVGKKSVQTISNEQRASKVLGIVFFLFLLMWCPFFITNVTLVLCDSCNQTTLNMLLEIFVWIGYVSSGVNPLVYTLFNKTFRDA

Inhibitor

Name:

BDBM30704

Synonyms:

(phenylmethyl) N-[[(6aR,9S,10aR)-4,7-dimethyl-6,6a,8,9,10,10a-hexahydroindolo[4,3-fg]quinoline-9-yl]methyl]carbamate | CHEMBL19215 | METERGOLINE | MLS000069437 | N-[[(6aR,9S,10aR)-4,7-dimethyl-6,6a,8,9,10,10a-hexahydroindolo[4,3-fg]quinoline-9-yl]methyl]carbamic acid (phenylmethyl) ester | N-[[(6aR,9S,10aR)-4,7-dimethyl-6,6a,8,9,10,10a-hexahydroindolo[4,3-fg]quinoline-9-yl]methyl]carbamic acid benzyl ester | SMR000059050 | benzyl N-[[(6aR,9S,10aR)-4,7-dimethyl-6,6a,8,9,10,10a-hexahydroindolo[4,3-fg]quinoline-9-yl]methyl]carbamate | cid_28693

Type:

Small organic molecule

Emp. Form.:

C25H29N3O2

Mol. Mass.:

403.5167

SMILES:

CN1C[C@H](CNC(=O)OCc2ccccc2)C[C@H]2[C@H]1Cc1cn(C)c3cccc2c13

Structure: