Ki Summary

Reaction Details

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Target

5-hydroxytryptamine receptor 4

Ligand

BDBM50288588

Substrate/Competitor

n/a

Meas. Tech.

ChEBML_3344

>1000±n/a nM

Citation

Fancelli, D; Caccia, C; Fornaretto, M; McArthur, R; Severino, D; Vaghi, F; Varasi, M Serotoninergic 5-HT3 and 5-HT4 receptor activities of dihydrobenzofuran carboxylic acid derivatives Bioorg Med Chem Lett6:263-266 (1996) Article

More Info.:

Get all data from this article, Assay Method

5-hydroxytryptamine receptor 4

Name:

5-hydroxytryptamine receptor 4

Synonyms:

5-HT-4 | 5-HT4 | 5-HT4L | 5-HT4S | 5-hydroxytryptamine receptor 4 | 5HT4R_RAT | Htr4 | Serotonin (5-HT) receptor | Serotonin 4 (5-HT4) receptor

Type:

Enzyme Catalytic Domain

Mol. Mass.:

46117.31

Organism:

RAT

Description:

5-HT4 HTR4 RAT::Q62758

Residue:

406

Sequence:

MDRLDANVSSNEGFGSVEKVVLLTFFAMVILMAILGNLLVMVAVCRDRQLRKIKTNYFIV
SLAFADLLVSVLVNAFGAIELVQDIWFYGEMFCLVRTSLDVLLTTASIFHLCCISLDRYY
AICCQPLVYRNKMTPLRIALMLGGCWVIPMFISFLPIMQGWNNIGIVDVIEKRKFNHNSN
STFCVFMVNKPYAITCSVVAFYIPFLLMVLAYYRIYVTAKEHAQQIQMLQRAGATSESRP
QTADQHSTHRMRTETKAAKTLCVIMGCFCFCWAPFFVTNIVDPFIDYTVPEKVWTAFLWL
GYINSGLNPFLYAFLNKSFRRAFLIILCCDDERYKRPPILGQTVPCSTTTINGSTHVLRD
TVECGGQWESRCHLTATSPLVAAQPVIRRPQDNDLEDSCSLKRSQS

BDBM50288588

n/a

Name

BDBM50288588

Synonyms:

2-(4-amino-2,3-dihydrobenzo[b]furan-7-ylcarboxamido)-(2R)-4-azabicyclo[2.2.2]octane | CHEMBL312898

Type

Small organic molecule

Emp. Form.

C16H21N3O2

Mol. Mass.

287.3568

SMILES

Nc1ccc(C(=O)N[C@H]2CN3CCC2CC3)c2OCCc12 |wD:8.7,(8.09,-10.5,;8.15,-8.96,;6.84,-8.16,;6.91,-6.61,;8.27,-5.92,;8.33,-4.38,;7.04,-3.56,;9.69,-3.65,;9.75,-2.13,;11.12,-1.42,;11.18,.11,;9.88,.95,;8.5,.22,;8.43,-1.32,;9.25,-.14,;9.91,-.78,;9.56,-6.73,;11.03,-6.32,;11.9,-7.59,;10.94,-8.8,;9.5,-8.27,)|

Structure