Reaction Details |
| Report a problem with these data |
Target | Histamine H1 receptor |
---|
Ligand | BDBM50449038 |
---|
Substrate/Competitor | n/a |
---|
Meas. Tech. | ChEBML_1690603 |
---|
Ki | <100±n/a nM |
---|
Citation | Pensa, AV; Cinelli, MA; Li, H; Chreifi, G; Mukherjee, P; Roman, LJ; Martásek, P; Poulos, TL; Silverman, RB Hydrophilic, Potent, and Selective 7-Substituted 2-Aminoquinolines as Improved Human Neuronal Nitric Oxide Synthase Inhibitors. J Med Chem60:7146-7165 (2017) [PubMed] Article |
---|
More Info.: | Get all data from this article, Assay Method |
---|
|
Histamine H1 receptor |
---|
Name: | Histamine H1 receptor |
Synonyms: | H1R | HH1R | HISTAMINE H1 | HRH1 | HRH1_HUMAN |
Type: | G Protein-Coupled Receptor (GPCR) |
Mol. Mass.: | 55808.72 |
Organism: | Homo sapiens (Human) |
Description: | Cell pellets from SK-N-MC cells transfected with human H1 receptor were used in binding assay. |
Residue: | 487 |
Sequence: | MSLPNSSCLLEDKMCEGNKTTMASPQLMPLVVVLSTICLVTVGLNLLVLYAVRSERKLHT
VGNLYIVSLSVADLIVGAVVMPMNILYLLMSKWSLGRPLCLFWLSMDYVASTASIFSVFI
LCIDRYRSVQQPLRYLKYRTKTRASATILGAWFLSFLWVIPILGWNHFMQQTSVRREDKC
ETDFYDVTWFKVMTAIINFYLPTLLMLWFYAKIYKAVRQHCQHRELINRSLPSFSEIKLR
PENPKGDAKKPGKESPWEVLKRKPKDAGGGSVLKSPSQTPKEMKSPVVFSQEDDREVDKL
YCFPLDIVHMQAAAEGSSRDYVAVNRSHGQLKTDEQGLNTHGASEISEDQMLGDSQSFSR
TDSDTTTETAPGKGKLRSGSNTGLDYIKFTWKRLRSHSRQYVSGLHMNRERKAAKQLGFI
MAAFILCWIPYFIFFMVIAFCKNCCNEHLHMFTIWLGYINSTLNPLIYPLCNENFKKTFK
RILHIRS
|
|
|
BDBM50449038 |
---|
n/a |
---|
Name | BDBM50449038 |
Synonyms: | CHEMBL3126204 | US9212144, 15 (Ex. 17) |
Type | Small organic molecule |
Emp. Form. | C19H20ClN3 |
Mol. Mass. | 325.835 |
SMILES | Nc1ccc2ccc(CCNCCc3cccc(Cl)c3)cc2n1 |
Structure |
|