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TargetChemerin-like receptor 1
LigandBDBM50603318
Substrate/Competitorn/a
Meas. Tech.ChEMBL_2243619 (CHEMBL5157829)
IC50 14±n/a nM
Citation Imaizumi, TOtsubo, SMaemoto, MKobayashi, AKomai, MTakada, HSakaida, YOtsubo, N Discovery and mechanistic study of thiazole-4-acylsulfonamide derivatives as potent and orally active ChemR23 inhibitors with a long-acting effect in cynomolgus monkeys. Bioorg Med Chem56:0 (2022) [PubMed]  Article
More Info.:Get all data from this article,  Assay Method
 
Chemerin-like receptor 1
Name:Chemerin-like receptor 1
Synonyms:CHEMR23 | CHEMR23 | CMKLR1 | CML1_HUMAN | Chemokine-like receptor 1 | DEZ | G-protein coupled receptor ChemR23 | G-protein coupled receptor DEZ
Type:PROTEIN
Mol. Mass.:42333.62
Organism:Homo sapiens (Human)
Description:ChEMBL_100822
Residue:373
Sequence:
MRMEDEDYNTSISYGDEYPDYLDSIVVLEDLSPLEARVTRIFLVVVYSIVCFLGILGNGL
VIIIATFKMKKTVNMVWFLNLAVADFLFNVFLPIHITYAAMDYHWVFGTAMCKISNFLLI
HNMFTSVFLLTIISSDRCISVLLPVWSQNHRSVRLAYMACMVIWVLAFFLSSPSLVFRDT
ANLHGKISCFNNFSLSTPGSSSWPTHSQMDPVGYSRHMVVTVTRFLCGFLVPVLIITACY
LTIVCKLQRNRLAKTKKPFKIIVTIIITFFLCWCPYHTLNLLELHHTAMPGSVFSLGLPL
ATALAIANSCMNPILYVFMGQDFKKFKVALFSRLVNALSEDTGHSSYPSHRSFTKMSSMN
ERTSMNERETGML
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  Blast E-value cutoff:
BDBM50603318
n/a
NameBDBM50603318
Synonyms:CHEMBL5183004
TypeSmall organic molecule
Emp. Form.C82H109ClN12O18S3
Mol. Mass.1682.46
SMILES[H][C@]12CS[C@@H](CCCCC(=O)NCCOCCOCCOCCOCCC(=O)NCCC(=O)N3Cc4ccccc4-c4nnn(CCOCCOCCOCCOCCOCCOCCNC(=O)c5ccc(Cl)cc5-c5ccc(cc5)[C@@H](C)N(CC5CC5)c5nc(C(=O)NS(=O)(=O)C6CC6)c(s5)C5CC5)c4-c4ccccc34)[C@@]1([H])NC(=O)N2 |r|
Structure
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