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Compile Data Set for Download or QSAR

Found 3 hits Enz. Inhib. hit(s) with Target = 'Calcitonin gene-related peptide type 1 receptor' and Ligand = 'BDBM50224414'   
Target/Host
(Institution)
LigandTarget/Host
Links
Ligand
Links
Trg + Lig
Links
Ki
nM
ΔG°
kJ/mole
IC50
nM
Kd
nM
EC50/IC50
nM
koff
s-1
kon
M-1s-1
pHTemp
°C
Calcitonin gene-related peptide type 1 receptor


(Homo sapiens (Human))
BDBM50224414
PNG
(4-(2-oxo-2,3-dihydro-1H-imidazo[4,5-b]pyridin-1-yl...)
Show SMILES O=C(N[C@@H]1CC[C@H](CNC1=O)c1ccccc1)N1CCC(CC1)n1c2cccnc2[nH]c1=O
Show InChI InChI=1S/C24H28N6O3/c31-22-19(9-8-17(15-26-22)16-5-2-1-3-6-16)27-23(32)29-13-10-18(11-14-29)30-20-7-4-12-25-21(20)28-24(30)33/h1-7,12,17-19H,8-11,13-15H2,(H,26,31)(H,27,32)(H,25,28,33)/t17-,19-/m1/s1
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PubMed
83n/an/an/an/an/an/an/an/a



Merck Research Laboratories

Curated by ChEMBL


Assay Description
Displacement of [125I]CGPR from human CL receptor expressed in HEK293 cells


J Med Chem 50: 5564-7 (2007)


Article DOI: 10.1021/jm070668p
BindingDB Entry DOI: 10.7270/Q28C9W02
More data for this
Ligand-Target Pair
Calcitonin gene-related peptide type 1 receptor


(Homo sapiens (Human))
BDBM50224414
PNG
(4-(2-oxo-2,3-dihydro-1H-imidazo[4,5-b]pyridin-1-yl...)
Show SMILES O=C(N[C@@H]1CC[C@H](CNC1=O)c1ccccc1)N1CCC(CC1)n1c2cccnc2[nH]c1=O
Show InChI InChI=1S/C24H28N6O3/c31-22-19(9-8-17(15-26-22)16-5-2-1-3-6-16)27-23(32)29-13-10-18(11-14-29)30-20-7-4-12-25-21(20)28-24(30)33/h1-7,12,17-19H,8-11,13-15H2,(H,26,31)(H,27,32)(H,25,28,33)/t17-,19-/m1/s1
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antibodypedia
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PC cid
PC sid
UniChem

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Article
PubMed
n/an/a 520n/an/an/an/an/an/a



Merck Research Laboratories

Curated by ChEMBL


Assay Description
Antagonist activity at human CL receptor expressed in E10 cells assessed as CGRP-stimulated cAMP production


J Med Chem 50: 5564-7 (2007)


Article DOI: 10.1021/jm070668p
BindingDB Entry DOI: 10.7270/Q28C9W02
More data for this
Ligand-Target Pair
Calcitonin gene-related peptide type 1 receptor


(Homo sapiens (Human))
BDBM50224414
PNG
(4-(2-oxo-2,3-dihydro-1H-imidazo[4,5-b]pyridin-1-yl...)
Show SMILES O=C(N[C@@H]1CC[C@H](CNC1=O)c1ccccc1)N1CCC(CC1)n1c2cccnc2[nH]c1=O
Show InChI InChI=1S/C24H28N6O3/c31-22-19(9-8-17(15-26-22)16-5-2-1-3-6-16)27-23(32)29-13-10-18(11-14-29)30-20-7-4-12-25-21(20)28-24(30)33/h1-7,12,17-19H,8-11,13-15H2,(H,26,31)(H,27,32)(H,25,28,33)/t17-,19-/m1/s1
PDB

UniProtKB/SwissProt

antibodypedia
GoogleScholar
AffyNet 
CHEMBL
PC cid
PC sid
UniChem

Similars

Article
PubMed
n/an/a 700n/an/an/an/an/an/a



Merck Research Laboratories

Curated by ChEMBL


Assay Description
Antagonist activity at human CL receptor expressed in E10 cells assessed as CGRP-stimulated cAMP production in presence of 50% human serum


J Med Chem 50: 5564-7 (2007)


Article DOI: 10.1021/jm070668p
BindingDB Entry DOI: 10.7270/Q28C9W02
More data for this
Ligand-Target Pair