BDBM50094936 CHEMBL86473::Vanadate

SMILES: O[V](=O)=O

InChI Key: InChIKey=XDBSEZHMWGHVIL-UHFFFAOYSA-M

Data: 5 KI  6 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 11 hits for monomerid = 50094936   

Target/Host (Institution)	Ligand	Target/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	pH	Temp °C
Carbonic anhydrase 2 (Homo sapiens (Human))	BDBM50094936 (CHEMBL86473 | Vanadate) Show SMILES O[V](=O)=O Show InChI InChI=1S/H2O.2O.V/h1H2;;;/q;;;+1/p-1	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt UniProtKB/TrEMBL B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Patents Similars	Article PubMed	1.16E+7	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
Universit£ degli Studi di Firenze Curated by ChEMBL					Assay Description Inhibitory activity against human Carbonic anhydrase II				Bioorg Med Chem Lett 15: 567-71 (2005) Article DOI: 10.1016/j.bmcl.2004.11.056 BindingDB Entry DOI: 10.7270/Q22R3SDV
					More data for this Ligand-Target Pair
Carbonic anhydrase 1 (Homo sapiens (Human))	BDBM50094936 (CHEMBL86473 | Vanadate) Show SMILES O[V](=O)=O Show InChI InChI=1S/H2O.2O.V/h1H2;;;/q;;;+1/p-1	PDB MMDB NCI pathway Reactome pathway KEGG UniProtKB/SwissProt UniProtKB/TrEMBL B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Patents Similars	Article PubMed	2.25E+7	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
Universit£ degli Studi di Firenze Curated by ChEMBL					Assay Description Inhibitory activity against human Carbonic anhydrase I				Bioorg Med Chem Lett 15: 567-71 (2005) Article DOI: 10.1016/j.bmcl.2004.11.056 BindingDB Entry DOI: 10.7270/Q22R3SDV
					More data for this Ligand-Target Pair
Carbonic anhydrase 5A, mitochondrial (Homo sapiens (Human))	BDBM50094936 (CHEMBL86473 | Vanadate) Show SMILES O[V](=O)=O Show InChI InChI=1S/H2O.2O.V/h1H2;;;/q;;;+1/p-1	Reactome pathway KEGG UniProtKB/SwissProt DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Patents Similars	Article PubMed	3.86E+7	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
Universit£ degli Studi di Firenze Curated by ChEMBL					Assay Description Inhibitory activity against human Carbonic anhydrase V				Bioorg Med Chem Lett 15: 567-71 (2005) Article DOI: 10.1016/j.bmcl.2004.11.056 BindingDB Entry DOI: 10.7270/Q22R3SDV
					More data for this Ligand-Target Pair
Carbonic anhydrase 9 (Homo sapiens (Human))	BDBM50094936 (CHEMBL86473 | Vanadate) Show SMILES O[V](=O)=O Show InChI InChI=1S/H2O.2O.V/h1H2;;;/q;;;+1/p-1	PDB MMDB NCI pathway Reactome pathway KEGG UniProtKB/SwissProt UniProtKB/TrEMBL B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Patents Similars	Article PubMed	4.26E+7	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
Universit£ degli Studi di Firenze Curated by ChEMBL					Assay Description Inhibitory activity against human Carbonic anhydrase IX				Bioorg Med Chem Lett 15: 567-71 (2005) Article DOI: 10.1016/j.bmcl.2004.11.056 BindingDB Entry DOI: 10.7270/Q22R3SDV
					More data for this Ligand-Target Pair
Carbonic anhydrase 4 (Homo sapiens (Human))	BDBM50094936 (CHEMBL86473 | Vanadate) Show SMILES O[V](=O)=O Show InChI InChI=1S/H2O.2O.V/h1H2;;;/q;;;+1/p-1	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Patents Similars	Article PubMed	4.48E+7	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
Universit£ degli Studi di Firenze Curated by ChEMBL					Assay Description Inhibitory activity against human Carbonic anhydrase IV				Bioorg Med Chem Lett 15: 567-71 (2005) Article DOI: 10.1016/j.bmcl.2004.11.056 BindingDB Entry DOI: 10.7270/Q22R3SDV
					More data for this Ligand-Target Pair
Tyrosine-protein phosphatase non-receptor type 1 (Homo sapiens (Human))	BDBM50094936 (CHEMBL86473 | Vanadate) Show SMILES O[V](=O)=O Show InChI InChI=1S/H2O.2O.V/h1H2;;;/q;;;+1/p-1	PDB MMDB NCI pathway Reactome pathway KEGG UniProtKB/SwissProt UniProtKB/TrEMBL B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Patents Similars	PubMed	n/a	n/a	3.81E+4	n/a	n/a	n/a	n/a	n/a	n/a
Taisho Pharmaceutical Co., Ltd Curated by ChEMBL					Assay Description The compound was evaluated for its inhibitory activity towards Protein tyrosine phosphatase of PTP-S2				Bioorg Med Chem Lett 10: 2657-60 (2000) BindingDB Entry DOI: 10.7270/Q2MK6C54
					More data for this Ligand-Target Pair
Tyrosine-protein phosphatase non-receptor type 1 (Homo sapiens (Human))	BDBM50094936 (CHEMBL86473 | Vanadate) Show SMILES O[V](=O)=O Show InChI InChI=1S/H2O.2O.V/h1H2;;;/q;;;+1/p-1	PDB MMDB NCI pathway Reactome pathway KEGG UniProtKB/SwissProt UniProtKB/TrEMBL B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Patents Similars	PubMed	n/a	n/a	>1.00E+6	n/a	n/a	n/a	n/a	n/a	n/a
Taisho Pharmaceutical Co., Ltd Curated by ChEMBL					Assay Description The compound was evaluated for its inhibitory activity towards Protein tyrosine phosphatase of PTP1B				Bioorg Med Chem Lett 10: 2657-60 (2000) BindingDB Entry DOI: 10.7270/Q2MK6C54
					More data for this Ligand-Target Pair
Tyrosine-protein phosphatase non-receptor type 1 (Homo sapiens (Human))	BDBM50094936 (CHEMBL86473 | Vanadate) Show SMILES O[V](=O)=O Show InChI InChI=1S/H2O.2O.V/h1H2;;;/q;;;+1/p-1	PDB MMDB NCI pathway Reactome pathway KEGG UniProtKB/SwissProt UniProtKB/TrEMBL B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Patents Similars	PubMed	n/a	n/a	3.02E+4	n/a	n/a	n/a	n/a	n/a	n/a
Taisho Pharmaceutical Co., Ltd Curated by ChEMBL					Assay Description The compound was evaluated for its inhibitory activity towards Protein tyrosine phosphatase of PP2A				Bioorg Med Chem Lett 10: 2657-60 (2000) BindingDB Entry DOI: 10.7270/Q2MK6C54
					More data for this Ligand-Target Pair
Tyrosine-protein phosphatase non-receptor type 1 (Homo sapiens (Human))	BDBM50094936 (CHEMBL86473 | Vanadate) Show SMILES O[V](=O)=O Show InChI InChI=1S/H2O.2O.V/h1H2;;;/q;;;+1/p-1	PDB MMDB NCI pathway Reactome pathway KEGG UniProtKB/SwissProt UniProtKB/TrEMBL B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Patents Similars	PubMed	n/a	n/a	3.08E+4	n/a	n/a	n/a	n/a	n/a	n/a
Taisho Pharmaceutical Co., Ltd Curated by ChEMBL					Assay Description The compound was evaluated for its inhibitory activity towards Protein tyrosine phosphatase of PP1				Bioorg Med Chem Lett 10: 2657-60 (2000) BindingDB Entry DOI: 10.7270/Q2MK6C54
					More data for this Ligand-Target Pair
Tyrosine-protein phosphatase non-receptor type 1 (Homo sapiens (Human))	BDBM50094936 (CHEMBL86473 | Vanadate) Show SMILES O[V](=O)=O Show InChI InChI=1S/H2O.2O.V/h1H2;;;/q;;;+1/p-1	PDB MMDB NCI pathway Reactome pathway KEGG UniProtKB/SwissProt UniProtKB/TrEMBL B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Patents Similars	PubMed	n/a	n/a	>1.00E+6	n/a	n/a	n/a	n/a	n/a	n/a
Taisho Pharmaceutical Co., Ltd Curated by ChEMBL					Assay Description The compound was evaluated for its inhibitory activity towards Protein tyrosine phosphatase of LAR				Bioorg Med Chem Lett 10: 2657-60 (2000) BindingDB Entry DOI: 10.7270/Q2MK6C54
					More data for this Ligand-Target Pair
Receptor-type tyrosine-protein phosphatase C (Homo sapiens (Human))	BDBM50094936 (CHEMBL86473 | Vanadate) Show SMILES O[V](=O)=O Show InChI InChI=1S/H2O.2O.V/h1H2;;;/q;;;+1/p-1	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Patents Similars	PubMed	n/a	n/a	3.42E+4	n/a	n/a	n/a	n/a	n/a	n/a
Taisho Pharmaceutical Co., Ltd Curated by ChEMBL					Assay Description The compound was evaluated for its inhibitory activity towards Protein tyrosine phosphatase of CD45				Bioorg Med Chem Lett 10: 2657-60 (2000) BindingDB Entry DOI: 10.7270/Q2MK6C54
					More data for this Ligand-Target Pair