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BDBM50534330 CHEMBL4520899

SMILES: OC1=C(Sc2ccccc2Cl)C(=O)NC(C1)(c1ccsc1)c1ccc(cc1)N1CCCCC1

InChI Key: InChIKey=OSCRHRYASAHIKU-UHFFFAOYSA-N

Data: 3 IC50

Find this compound or compounds like it in BindingDB or PDB:
   Substructure
Similarity at least:  must be >=0.5
Exact match

Activity Spreadsheet -- Enzyme Inhibition Constant Data from BindingDB

Found 3 hits for monomerid = 50534330   
Target/Host
(Institution)
LigandTarget/Host
Links
Ligand
Links
Trg + Lig
Links
Ki
nM
ΔG°
kcal/mole
IC50
nM
Kd
nM
EC50
nM
koff
s-1
kon
M-1s-1
pHTemp
°C
L-lactate dehydrogenase B chain


(Homo sapiens (Human))
BDBM50534330
PNG
(CHEMBL4520899)
Show SMILES OC1=C(Sc2ccccc2Cl)C(=O)NC(C1)(c1ccsc1)c1ccc(cc1)N1CCCCC1
Show InChI InChI=1S/C26H25ClN2O2S2/c27-21-6-2-3-7-23(21)33-24-22(30)16-26(28-25(24)31,19-12-15-32-17-19)18-8-10-20(11-9-18)29-13-4-1-5-14-29/h2-3,6-12,15,17,30H,1,4-5,13-14,16H2,(H,28,31)
PDB
MMDB

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PC cid
PC sid
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Article
PubMed
n/an/a 49n/an/an/an/an/an/a



Genentech

Curated by ChEMBL


Assay Description
Inhibition of human recombinant carboxy-terminal His-tagged LDHB by UV endpoint assay


ACS Med Chem Lett 7: 896-901 (2016)


Article DOI: 10.1021/acsmedchemlett.6b00190
More data for this
Ligand-Target Pair
L-lactate dehydrogenase A chain


(Homo sapiens (Human))
BDBM50534330
PNG
(CHEMBL4520899)
Show SMILES OC1=C(Sc2ccccc2Cl)C(=O)NC(C1)(c1ccsc1)c1ccc(cc1)N1CCCCC1
Show InChI InChI=1S/C26H25ClN2O2S2/c27-21-6-2-3-7-23(21)33-24-22(30)16-26(28-25(24)31,19-12-15-32-17-19)18-8-10-20(11-9-18)29-13-4-1-5-14-29/h2-3,6-12,15,17,30H,1,4-5,13-14,16H2,(H,28,31)
PDB
MMDB

Reactome pathway
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UniProtKB/SwissProt
UniProtKB/TrEMBL

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antibodypedia
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PC cid
PC sid
UniChem
Article
PubMed
n/an/a 670n/an/an/an/an/an/a



Genentech

Curated by ChEMBL


Assay Description
Inhibition of LDHA in human MiPaca2 cells assessed as inhibition of lactate production


ACS Med Chem Lett 7: 896-901 (2016)


Article DOI: 10.1021/acsmedchemlett.6b00190
More data for this
Ligand-Target Pair
L-lactate dehydrogenase A chain


(Homo sapiens (Human))
BDBM50534330
PNG
(CHEMBL4520899)
Show SMILES OC1=C(Sc2ccccc2Cl)C(=O)NC(C1)(c1ccsc1)c1ccc(cc1)N1CCCCC1
Show InChI InChI=1S/C26H25ClN2O2S2/c27-21-6-2-3-7-23(21)33-24-22(30)16-26(28-25(24)31,19-12-15-32-17-19)18-8-10-20(11-9-18)29-13-4-1-5-14-29/h2-3,6-12,15,17,30H,1,4-5,13-14,16H2,(H,28,31)
PDB
MMDB

Reactome pathway
KEGG

UniProtKB/SwissProt
UniProtKB/TrEMBL

B.MOAD
DrugBank
antibodypedia
GoogleScholar
PC cid
PC sid
UniChem
Article
PubMed
n/an/a 9n/an/an/an/an/an/a



Genentech

Curated by ChEMBL


Assay Description
Inhibition of human recombinant carboxy-terminal His-tagged LDHA by UV endpoint assay


ACS Med Chem Lett 7: 896-901 (2016)


Article DOI: 10.1021/acsmedchemlett.6b00190
More data for this
Ligand-Target Pair