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BDBM50279669 CHEMBL4167266

SMILES: Nc1ccc2COB(O)c2c1

InChI Key: InChIKey=USCKQKQTFCBECF-UHFFFAOYSA-N

Data: 4 KI

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 5 hits for monomerid = 50279669   
Target/Host
(Institution)
LigandTarget/Host
Links
Ligand
Links
Trg + Lig
Links
Ki
nM
ΔG°
kcal/mole
IC50
nM
Kd
nM
EC50/IC50
nM
koff
s-1
kon
M-1s-1
pHTemp
°C
Carbonic Anhydrase 2 (Can2)


(Cryptococcus neoformans var. grubii (Filobasidiell...)
BDBM50279669
PNG
(CHEMBL4167266)
Show SMILES Nc1ccc2COB(O)c2c1
Show InChI InChI=1S/C7H8BNO2/c9-6-2-1-5-4-11-8(10)7(5)3-6/h1-3,10H,4,9H2
PDB
MMDB

UniProtKB/TrEMBL

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MCE
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Article
PubMed
93n/an/an/an/an/an/an/an/a



University of Montpellier

Curated by ChEMBL


Assay Description
Inhibition of Cryptococcus neoformans Can2 incubated for 15 mins prior to testing by stopped flow CO2 hydrase assay


ACS Med Chem Lett 8: 1194-1198 (2017)


Article DOI: 10.1021/acsmedchemlett.7b00369
BindingDB Entry DOI: 10.7270/Q2SN0CHK
More data for this
Ligand-Target Pair
Carbonic anhydrase


(Candida glabrata)
BDBM50279669
PNG
(CHEMBL4167266)
Show SMILES Nc1ccc2COB(O)c2c1
Show InChI InChI=1S/C7H8BNO2/c9-6-2-1-5-4-11-8(10)7(5)3-6/h1-3,10H,4,9H2
KEGG

UniProtKB/TrEMBL

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MCE
PC cid
PC sid
UniChem

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Article
PubMed
244n/an/an/an/an/an/an/an/a



University of Montpellier

Curated by ChEMBL


Assay Description
Evaluated for the inhibition of dihydrofolate reductase from L1210 mouse leukemia cells


ACS Med Chem Lett 8: 1194-1198 (2017)


Article DOI: 10.1021/acsmedchemlett.7b00369
BindingDB Entry DOI: 10.7270/Q2SN0CHK
More data for this
Ligand-Target Pair
Carbonic anhydrase 2


(Homo sapiens (Human))
BDBM50279669
PNG
(CHEMBL4167266)
Show SMILES Nc1ccc2COB(O)c2c1
Show InChI InChI=1S/C7H8BNO2/c9-6-2-1-5-4-11-8(10)7(5)3-6/h1-3,10H,4,9H2
PDB
MMDB

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590n/an/an/an/an/an/an/an/a


TBA



Citation and Details
More data for this
Ligand-Target Pair
Carbonic anhydrase 2


(Homo sapiens (Human))
BDBM50279669
PNG
(CHEMBL4167266)
Show SMILES Nc1ccc2COB(O)c2c1
Show InChI InChI=1S/C7H8BNO2/c9-6-2-1-5-4-11-8(10)7(5)3-6/h1-3,10H,4,9H2
PDB
MMDB

Reactome pathway
KEGG

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MCE
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Article
PubMed
590n/an/an/an/an/an/an/an/a



University of Montpellier

Curated by ChEMBL


Assay Description
Inhibitory activity against human liver Dihydrodipicolinate reductase (DHPR)


ACS Med Chem Lett 8: 1194-1198 (2017)


Article DOI: 10.1021/acsmedchemlett.7b00369
BindingDB Entry DOI: 10.7270/Q2SN0CHK
More data for this
Ligand-Target Pair
Carbonic anhydrase


(Homo sapiens (Human))
BDBM50279669
PNG
(CHEMBL4167266)
Show SMILES Nc1ccc2COB(O)c2c1
Show InChI InChI=1S/C7H8BNO2/c9-6-2-1-5-4-11-8(10)7(5)3-6/h1-3,10H,4,9H2
PDB
MMDB

NCI pathway
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Article
PubMed
9.44E+3n/an/an/an/an/an/an/an/a



University of Montpellier

Curated by ChEMBL


Assay Description
Inhibition of human carbonic anhydrase-1 incubated for 15 mins prior to testing by stopped flow CO2 hydrase assay


ACS Med Chem Lett 8: 1194-1198 (2017)


Article DOI: 10.1021/acsmedchemlett.7b00369
BindingDB Entry DOI: 10.7270/Q2SN0CHK
More data for this
Ligand-Target Pair