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Compile Data Set for Download or QSAR

Found 2 hits Enz. Inhib. hit(s) with Target = 'Retinoic acid receptor RXR-alpha' and Ligand = 'BDBM50218432'   
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
Retinoic acid receptor RXR-alpha


(Homo sapiens (Human))
BDBM50218432
PNG
(4-(2-cyano-5,7,7,10,10-pentamethyl-7,8,9,10-tetrah...)
Show SMILES CN1c2ccc(cc2N=C(c2ccc(C(O)=O)c(F)c2)c2cc3c(cc12)C(C)(C)CCC3(C)C)C#N |t:9|
Show InChI InChI=1S/C30H28FN3O2/c1-29(2)10-11-30(3,4)22-15-26-20(14-21(22)29)27(18-7-8-19(28(35)36)23(31)13-18)33-24-12-17(16-32)6-9-25(24)34(26)5/h6-9,12-15H,10-11H2,1-5H3,(H,35,36)
PDB
MMDB

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



Tsukuba Research Institute

Curated by ChEMBL


Assay Description
Inhibition of 9-cis-retinoic acid-induced RXRalpha transactivation


Bioorg Med Chem Lett 17: 4804-7 (2007)


Article DOI: 10.1016/j.bmcl.2007.06.080
BindingDB Entry DOI: 10.7270/Q2ZS2W7W
More data for this
Ligand-Target Pair
Retinoic acid receptor RXR-alpha


(Homo sapiens (Human))
BDBM50218432
PNG
(4-(2-cyano-5,7,7,10,10-pentamethyl-7,8,9,10-tetrah...)
Show SMILES CN1c2ccc(cc2N=C(c2ccc(C(O)=O)c(F)c2)c2cc3c(cc12)C(C)(C)CCC3(C)C)C#N |t:9|
Show InChI InChI=1S/C30H28FN3O2/c1-29(2)10-11-30(3,4)22-15-26-20(14-21(22)29)27(18-7-8-19(28(35)36)23(31)13-18)33-24-12-17(16-32)6-9-25(24)34(26)5/h6-9,12-15H,10-11H2,1-5H3,(H,35,36)
PDB
MMDB

NCI pathway
Reactome pathway
KEGG

UniProtKB/SwissProt

B.MOAD
DrugBank
antibodypedia
GoogleScholar
AffyNet 
CHEMBL
PC cid
PC sid
UniChem

Patents


Similars

Article
PubMed
n/an/a 1.20E+3n/an/an/an/an/an/a



Tsukuba Research Institute

Curated by ChEMBL


Assay Description
Inhibition of LG100268-induced RXRalpha transactivation


Bioorg Med Chem Lett 17: 4804-7 (2007)


Article DOI: 10.1016/j.bmcl.2007.06.080
BindingDB Entry DOI: 10.7270/Q2ZS2W7W
More data for this
Ligand-Target Pair