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Compile Data Set for Download or QSAR

Found 409 hits Enz. Inhib. hit(s) with Target = 'tyrosine-protein phosphatase non-receptor type 5 isoform a' AND taxid = 9606   
Target
(Institution)
LigandTarget
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
tyrosine-protein phosphatase non-receptor type 5 isoform a


(Homo sapiens)
BDBM50103445
PNG
(CHEMBL3398243)
Show SMILES FC(F)(F)c1ccc2SSSSSc2c1
Show InChI InChI=1S/C7H3F3S5/c8-7(9,10)4-1-2-5-6(3-4)12-14-15-13-11-5/h1-3H
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PubMed
109n/an/an/an/an/an/an/an/a



Department of Chemistry, Yale University, New Haven, CT 06520, United States.

Curated by ChEMBL


Assay Description
Inhibition of STEP (unknown origin) in absence of GSH by p-nitrophenyl phosphate hydrolysis assay


Citation and Details
More data for this
Ligand-Target Pair
tyrosine-protein phosphatase non-receptor type 5 isoform a


(Homo sapiens)
BDBM50067512
PNG
(CHEMBL3401893)
Show SMILES Nc1cc(cc2SSSSSc12)C(F)(F)F
Show InChI InChI=1S/C7H4F3NS5/c8-7(9,10)3-1-4(11)6-5(2-3)12-14-16-15-13-6/h1-2H,11H2
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PubMed
115n/an/an/an/an/an/an/an/a



Department of Chemistry, Yale University, New Haven, CT 06520, United States.

Curated by ChEMBL


Assay Description
Inhibition of STEP (unknown origin) in absence of GSH by p-nitrophenyl phosphate hydrolysis assay


Citation and Details
More data for this
Ligand-Target Pair
tyrosine-protein phosphatase non-receptor type 5 isoform a


(Homo sapiens)
BDBM50103444
PNG
(CHEMBL3398244)
Show SMILES Cl.Cc1cc(N)c2SSSSSc2c1
Show InChI InChI=1S/C7H7NS5.ClH/c1-4-2-5(8)7-6(3-4)9-11-13-12-10-7;/h2-3H,8H2,1H3;1H
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116n/an/an/an/an/an/an/an/a



Department of Chemistry, Yale University, New Haven, CT 06520, United States.

Curated by ChEMBL


Assay Description
Inhibition of STEP (unknown origin) in absence of GSH by p-nitrophenyl phosphate hydrolysis assay


Citation and Details
More data for this
Ligand-Target Pair
tyrosine-protein phosphatase non-receptor type 5 isoform a


(Homo sapiens)
BDBM50103448
PNG
(CHEMBL3398247)
Show SMILES CC(=O)Nc1cc(cc2SSSSSc12)C(F)(F)F
Show InChI InChI=1S/C9H6F3NOS5/c1-4(14)13-6-2-5(9(10,11)12)3-7-8(6)16-18-19-17-15-7/h2-3H,1H3,(H,13,14)
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123n/an/an/an/an/an/an/an/a



Department of Chemistry, Yale University, New Haven, CT 06520, United States.

Curated by ChEMBL


Assay Description
Inhibition of STEP (unknown origin) in absence of GSH by p-nitrophenyl phosphate hydrolysis assay


Citation and Details
More data for this
Ligand-Target Pair
tyrosine-protein phosphatase non-receptor type 5 isoform a


(Homo sapiens)
BDBM50103447
PNG
(CHEMBL3398250)
Show SMILES Cl.Cl.Nc1cc(cc2SSSc3c(N)cc(cc3SSSc12)C(F)(F)F)C(F)(F)F
Show InChI InChI=1S/C14H8F6N2S6.2ClH/c15-13(16,17)5-1-7(21)11-9(3-5)23-28-26-12-8(22)2-6(14(18,19)20)4-10(12)24-27-25-11;;/h1-4H,21-22H2;2*1H
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124n/an/an/an/an/an/an/an/a



Department of Chemistry, Yale University, New Haven, CT 06520, United States.

Curated by ChEMBL


Assay Description
Inhibition of STEP (unknown origin) in absence of GSH by p-nitrophenyl phosphate hydrolysis assay


Citation and Details
More data for this
Ligand-Target Pair
tyrosine-protein phosphatase non-receptor type 5 isoform a


(Homo sapiens)
BDBM50103450
PNG
(CHEMBL3398249)
Show SMILES FC(F)(F)c1cc(NCc2ccccc2)c2SSSSSc2c1
Show InChI InChI=1S/C14H10F3NS5/c15-14(16,17)10-6-11(18-8-9-4-2-1-3-5-9)13-12(7-10)19-21-23-22-20-13/h1-7,18H,8H2
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175n/an/an/an/an/an/an/an/a



Department of Chemistry, Yale University, New Haven, CT 06520, United States.

Curated by ChEMBL


Assay Description
Inhibition of STEP (unknown origin) in absence of GSH by p-nitrophenyl phosphate hydrolysis assay


Citation and Details
More data for this
Ligand-Target Pair
tyrosine-protein phosphatase non-receptor type 5 isoform a


(Homo sapiens)
BDBM50103443
PNG
(CHEMBL3398245)
Show SMILES Cl.Nc1cccc2SSSSSc12
Show InChI InChI=1S/C6H5NS5.ClH/c7-4-2-1-3-5-6(4)9-11-12-10-8-5;/h1-3H,7H2;1H
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183n/an/an/an/an/an/an/an/a



Department of Chemistry, Yale University, New Haven, CT 06520, United States.

Curated by ChEMBL


Assay Description
Inhibition of STEP (unknown origin) in absence of GSH by p-nitrophenyl phosphate hydrolysis assay


Citation and Details
More data for this
Ligand-Target Pair
tyrosine-protein phosphatase non-receptor type 5 isoform a


(Homo sapiens)
BDBM50103446
PNG
(CHEMBL3398251)
Show SMILES [O-][N+](=O)c1cc(cc2SSSc12)C(F)(F)F
Show InChI InChI=1S/C7H2F3NO2S3/c8-7(9,10)3-1-4(11(12)13)6-5(2-3)14-16-15-6/h1-2H
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210n/an/an/an/an/an/an/an/a



Department of Chemistry, Yale University, New Haven, CT 06520, United States.

Curated by ChEMBL


Assay Description
Inhibition of STEP (unknown origin) in absence of GSH by p-nitrophenyl phosphate hydrolysis assay


Citation and Details
More data for this
Ligand-Target Pair
tyrosine-protein phosphatase non-receptor type 5 isoform a


(Homo sapiens)
BDBM50103449
PNG
(CHEMBL3398248)
Show SMILES CCNc1cc(cc2SSSSSc12)C(F)(F)F
Show InChI InChI=1S/C9H8F3NS5/c1-2-13-6-3-5(9(10,11)12)4-7-8(6)15-17-18-16-14-7/h3-4,13H,2H2,1H3
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230n/an/an/an/an/an/an/an/a



Department of Chemistry, Yale University, New Haven, CT 06520, United States.

Curated by ChEMBL


Assay Description
Inhibition of STEP (unknown origin) in absence of GSH by p-nitrophenyl phosphate hydrolysis assay


Citation and Details
More data for this
Ligand-Target Pair
tyrosine-protein phosphatase non-receptor type 5 isoform a


(Homo sapiens)
BDBM50067504
PNG
(CHEMBL3398246)
Show SMILES FC(F)(F)C(=O)Nc1cc(cc2SSSSSc12)C(F)(F)F
Show InChI InChI=1S/C9H3F6NOS5/c10-8(11,12)3-1-4(16-7(17)9(13,14)15)6-5(2-3)18-20-22-21-19-6/h1-2H,(H,16,17)
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PubMed
235n/an/an/an/an/an/an/an/a



Department of Chemistry, Yale University, New Haven, CT 06520, United States.

Curated by ChEMBL


Assay Description
Inhibition of STEP (unknown origin) in absence of GSH by p-nitrophenyl phosphate hydrolysis assay


Citation and Details
More data for this
Ligand-Target Pair
tyrosine-protein phosphatase non-receptor type 5 isoform a


(Homo sapiens)
BDBM50441296
PNG
(CHEMBL2431665 | CHEMBL2431667)
Show SMILES O[C@@H](c1cccc(c1)-c1ccc(cc1)C(=O)P(O)(O)O)c1ccc(Cl)c(Cl)c1
Show InChI InChI=1S/C20H17Cl2O5P/c21-17-9-8-16(11-18(17)22)19(23)15-3-1-2-14(10-15)12-4-6-13(7-5-12)20(24)28(25,26)27/h1-11,19,23,25-28H/t19-/m0/s1
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PubMed
7.80E+3n/an/an/an/an/an/an/an/a



Yale University

Curated by ChEMBL


Assay Description
Inhibition of human STEP using pNPP as substrate after 5 mins by spectrophotometric plate reader analysis


Citation and Details
More data for this
Ligand-Target Pair
tyrosine-protein phosphatase non-receptor type 5 isoform a


(Homo sapiens)
BDBM50441302
PNG
(CHEMBL2431688)
Show SMILES OP(O)(O)C(=O)c1ccc(cc1)-c1cccc(Cc2ccc(Cl)c(Cl)c2)c1
Show InChI InChI=1S/C20H17Cl2O4P/c21-18-9-4-14(12-19(18)22)10-13-2-1-3-17(11-13)15-5-7-16(8-6-15)20(23)27(24,25)26/h1-9,11-12,24-27H,10H2
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PubMed
8.30E+3n/an/an/an/an/an/an/an/a



Yale University

Curated by ChEMBL


Assay Description
Inhibition of human STEP using pNPP as substrate after 5 mins by spectrophotometric plate reader analysis


Citation and Details
More data for this
Ligand-Target Pair
tyrosine-protein phosphatase non-receptor type 5 isoform a


(Homo sapiens)
BDBM50441297
PNG
(CHEMBL2431664 | CHEMBL2431666)
Show SMILES O[C@H](c1cccc(c1)-c1ccc(cc1)C(=O)P(O)(O)O)c1ccc(Cl)c(Cl)c1
Show InChI InChI=1S/C20H17Cl2O5P/c21-17-9-8-16(11-18(17)22)19(23)15-3-1-2-14(10-15)12-4-6-13(7-5-12)20(24)28(25,26)27/h1-11,19,23,25-28H/t19-/m1/s1
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8.90E+3n/an/an/an/an/an/an/an/a



Yale University

Curated by ChEMBL


Assay Description
Inhibition of human STEP using pNPP as substrate after 5 mins by spectrophotometric plate reader analysis


Citation and Details
More data for this
Ligand-Target Pair
tyrosine-protein phosphatase non-receptor type 5 isoform a


(Homo sapiens)
BDBM50441304
PNG
(CHEMBL2431686)
Show SMILES OP(O)(=O)C(F)(F)c1ccc(cc1)-c1cccc(Cc2ccc(Cl)c(Cl)c2)c1
Show InChI InChI=1S/C20H15Cl2F2O3P/c21-18-9-4-14(12-19(18)22)10-13-2-1-3-16(11-13)15-5-7-17(8-6-15)20(23,24)28(25,26)27/h1-9,11-12H,10H2,(H2,25,26,27)
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9.60E+3n/an/an/an/an/an/an/an/a



Yale University

Curated by ChEMBL


Assay Description
Inhibition of human STEP using pNPP as substrate after 5 mins by spectrophotometric plate reader analysis


Citation and Details
More data for this
Ligand-Target Pair
tyrosine-protein phosphatase non-receptor type 5 isoform a


(Homo sapiens)
BDBM50441303
PNG
(CHEMBL2431687)
Show SMILES OC(c1cccc(c1)-c1ccc(cc1)C(F)(F)P(O)(O)=O)c1ccc(Cl)c(Cl)c1
Show InChI InChI=1S/C20H15Cl2F2O4P/c21-17-9-6-15(11-18(17)22)19(25)14-3-1-2-13(10-14)12-4-7-16(8-5-12)20(23,24)29(26,27)28/h1-11,19,25H,(H2,26,27,28)
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PubMed
1.60E+4n/an/an/an/an/an/an/an/a



Yale University

Curated by ChEMBL


Assay Description
Inhibition of human STEP using pNPP as substrate after 5 mins by spectrophotometric plate reader analysis


Citation and Details
More data for this
Ligand-Target Pair
tyrosine-protein phosphatase non-receptor type 5 isoform a


(Homo sapiens)
BDBM50441305
PNG
(CHEMBL2431685)
Show SMILES OP(O)(=O)C(F)(F)c1ccc(cc1)-c1cccc(Cc2ccc(Cl)cc2)c1
Show InChI InChI=1S/C20H16ClF2O3P/c21-19-10-4-14(5-11-19)12-15-2-1-3-17(13-15)16-6-8-18(9-7-16)20(22,23)27(24,25)26/h1-11,13H,12H2,(H2,24,25,26)
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1.90E+4n/an/an/an/an/an/an/an/a



Yale University

Curated by ChEMBL


Assay Description
Inhibition of human STEP using pNPP as substrate after 5 mins by spectrophotometric plate reader analysis


Citation and Details
More data for this
Ligand-Target Pair
tyrosine-protein phosphatase non-receptor type 5 isoform a


(Homo sapiens)
BDBM50441298
PNG
(CHEMBL2431708)
Show SMILES Oc1c(cccc1-c1cccc(c1)C(F)(F)P(O)(O)=O)C1CCCCC1
Show InChI InChI=1S/C19H21F2O4P/c20-19(21,26(23,24)25)15-9-4-8-14(12-15)17-11-5-10-16(18(17)22)13-6-2-1-3-7-13/h4-5,8-13,22H,1-3,6-7H2,(H2,23,24,25)
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2.00E+4n/an/an/an/an/an/an/an/a



Yale University

Curated by ChEMBL


Assay Description
Inhibition of human STEP using pNPP as substrate after 5 mins by spectrophotometric plate reader analysis


Citation and Details
More data for this
Ligand-Target Pair
tyrosine-protein phosphatase non-receptor type 5 isoform a


(Homo sapiens)
BDBM50441322
PNG
(CHEMBL2431707)
Show SMILES Oc1c(cccc1-c1cccc(c1)C(F)(F)P(O)(O)=O)C1CCCC1
Show InChI InChI=1S/C18H19F2O4P/c19-18(20,25(22,23)24)14-8-3-7-13(11-14)16-10-4-9-15(17(16)21)12-5-1-2-6-12/h3-4,7-12,21H,1-2,5-6H2,(H2,22,23,24)
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2.50E+4n/an/an/an/an/an/an/an/a



Yale University

Curated by ChEMBL


Assay Description
Inhibition of human STEP using pNPP as substrate after 5 mins by spectrophotometric plate reader analysis


Citation and Details
More data for this
Ligand-Target Pair
tyrosine-protein phosphatase non-receptor type 5 isoform a


(Homo sapiens)
BDBM50441306
PNG
(CHEMBL2431684)
Show SMILES OP(O)(=O)C(F)(F)c1ccc(cc1)-c1cccc(Cc2ccc(F)cc2)c1
Show InChI InChI=1S/C20H16F3O3P/c21-19-10-4-14(5-11-19)12-15-2-1-3-17(13-15)16-6-8-18(9-7-16)20(22,23)27(24,25)26/h1-11,13H,12H2,(H2,24,25,26)
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3.50E+4n/an/an/an/an/an/an/an/a



Yale University

Curated by ChEMBL


Assay Description
Inhibition of human STEP using pNPP as substrate after 5 mins by spectrophotometric plate reader analysis


Citation and Details
More data for this
Ligand-Target Pair
tyrosine-protein phosphatase non-receptor type 5 isoform a


(Homo sapiens)
BDBM50441320
PNG
(CHEMBL2431670)
Show SMILES Oc1c(cccc1-c1cccc(c1)C(=O)P(O)(O)O)C1CCCCC1
Show InChI InChI=1S/C19H23O5P/c20-18-16(13-6-2-1-3-7-13)10-5-11-17(18)14-8-4-9-15(12-14)19(21)25(22,23)24/h4-5,8-13,20,22-25H,1-3,6-7H2
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3.60E+4n/an/an/an/an/an/an/an/a



Yale University

Curated by ChEMBL


Assay Description
Inhibition of human STEP using pNPP as substrate after 5 mins by spectrophotometric plate reader analysis


Citation and Details
More data for this
Ligand-Target Pair
tyrosine-protein phosphatase non-receptor type 5 isoform a


(Homo sapiens)
BDBM50441323
PNG
(CHEMBL2431706)
Show SMILES Oc1c(cccc1-c1cccc(c1)C(F)(F)P(O)(O)=O)C1CCC1
Show InChI InChI=1S/C17H17F2O4P/c18-17(19,24(21,22)23)13-7-2-6-12(10-13)15-9-3-8-14(16(15)20)11-4-1-5-11/h2-3,6-11,20H,1,4-5H2,(H2,21,22,23)
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4.50E+4n/an/an/an/an/an/an/an/a



Yale University

Curated by ChEMBL


Assay Description
Inhibition of human STEP using pNPP as substrate after 5 mins by spectrophotometric plate reader analysis


Citation and Details
More data for this
Ligand-Target Pair
tyrosine-protein phosphatase non-receptor type 5 isoform a


(Homo sapiens)
BDBM50441321
PNG
(CHEMBL2431669)
Show SMILES Oc1c(cccc1-c1cccc(c1)C(F)(F)P(O)(O)=O)C1CCCCCC1
Show InChI InChI=1S/C20H23F2O4P/c21-20(22,27(24,25)26)16-10-5-9-15(13-16)18-12-6-11-17(19(18)23)14-7-3-1-2-4-8-14/h5-6,9-14,23H,1-4,7-8H2,(H2,24,25,26)
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PubMed
6.20E+4n/an/an/an/an/an/an/an/a



Yale University

Curated by ChEMBL


Assay Description
Inhibition of human STEP using pNPP as substrate after 5 mins by spectrophotometric plate reader analysis


Citation and Details
More data for this
Ligand-Target Pair
tyrosine-protein phosphatase non-receptor type 5 isoform a


(Homo sapiens)
BDBM50441324
PNG
(CHEMBL2431705)
Show SMILES CC(C)(C)c1cccc(c1O)-c1cccc(c1)C(F)(F)P(O)(O)=O
Show InChI InChI=1S/C17H19F2O4P/c1-16(2,3)14-9-5-8-13(15(14)20)11-6-4-7-12(10-11)17(18,19)24(21,22)23/h4-10,20H,1-3H3,(H2,21,22,23)
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PubMed
6.30E+4n/an/an/an/an/an/an/an/a



Yale University

Curated by ChEMBL


Assay Description
Inhibition of human STEP using pNPP as substrate after 5 mins by spectrophotometric plate reader analysis


Citation and Details
More data for this
Ligand-Target Pair
tyrosine-protein phosphatase non-receptor type 5 isoform a


(Homo sapiens)
BDBM50441327
PNG
(CHEMBL2431702)
Show SMILES CC(C)c1cccc(c1O)-c1cccc(c1)C(F)(F)P(O)(O)=O
Show InChI InChI=1S/C16H17F2O4P/c1-10(2)13-7-4-8-14(15(13)19)11-5-3-6-12(9-11)16(17,18)23(20,21)22/h3-10,19H,1-2H3,(H2,20,21,22)
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6.90E+4n/an/an/an/an/an/an/an/a



Yale University

Curated by ChEMBL


Assay Description
Inhibition of human STEP using pNPP as substrate after 5 mins by spectrophotometric plate reader analysis


Citation and Details
More data for this
Ligand-Target Pair
tyrosine-protein phosphatase non-receptor type 5 isoform a


(Homo sapiens)
BDBM50441307
PNG
(CHEMBL2431683)
Show SMILES OP(O)(=O)C(F)(F)c1ccc(cc1)-c1cccc(Cc2ccccc2)c1
Show InChI InChI=1S/C20H17F2O3P/c21-20(22,26(23,24)25)19-11-9-17(10-12-19)18-8-4-7-16(14-18)13-15-5-2-1-3-6-15/h1-12,14H,13H2,(H2,23,24,25)
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7.30E+4n/an/an/an/an/an/an/an/a



Yale University

Curated by ChEMBL


Assay Description
Inhibition of human STEP using pNPP as substrate after 5 mins by spectrophotometric plate reader analysis


Citation and Details
More data for this
Ligand-Target Pair
tyrosine-protein phosphatase non-receptor type 5 isoform a


(Homo sapiens)
BDBM50441330
PNG
(CHEMBL2431699)
Show SMILES CC(C)c1cccc(c1)-c1cccc(c1)C(F)(F)P(O)(O)=O
Show InChI InChI=1S/C16H17F2O3P/c1-11(2)12-5-3-6-13(9-12)14-7-4-8-15(10-14)16(17,18)22(19,20)21/h3-11H,1-2H3,(H2,19,20,21)
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8.10E+4n/an/an/an/an/an/an/an/a



Yale University

Curated by ChEMBL


Assay Description
Inhibition of human STEP using pNPP as substrate after 5 mins by spectrophotometric plate reader analysis


Citation and Details
More data for this
Ligand-Target Pair
tyrosine-protein phosphatase non-receptor type 5 isoform a


(Homo sapiens)
BDBM50441310
PNG
(CHEMBL2431680)
Show SMILES CC(O)c1cccc(c1)-c1ccc(cc1)C(F)(F)P(O)(O)=O
Show InChI InChI=1S/C15H15F2O4P/c1-10(18)12-3-2-4-13(9-12)11-5-7-14(8-6-11)15(16,17)22(19,20)21/h2-10,18H,1H3,(H2,19,20,21)
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8.80E+4n/an/an/an/an/an/an/an/a



Yale University

Curated by ChEMBL


Assay Description
Inhibition of human STEP using pNPP as substrate after 5 mins by spectrophotometric plate reader analysis


Citation and Details
More data for this
Ligand-Target Pair
tyrosine-protein phosphatase non-receptor type 5 isoform a


(Homo sapiens)
BDBM50441297
PNG
(CHEMBL2431664 | CHEMBL2431666)
Show SMILES O[C@H](c1cccc(c1)-c1ccc(cc1)C(=O)P(O)(O)O)c1ccc(Cl)c(Cl)c1
Show InChI InChI=1S/C20H17Cl2O5P/c21-17-9-8-16(11-18(17)22)19(23)15-3-1-2-14(10-15)12-4-6-13(7-5-12)20(24)28(25,26)27/h1-11,19,23,25-28H/t19-/m1/s1
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8.80E+4n/an/an/an/an/an/an/an/a



Yale University

Curated by ChEMBL


Assay Description
Inhibition of human STEP using pNPP as substrate after 5 mins by spectrophotometric plate reader analysis


Citation and Details
More data for this
Ligand-Target Pair
tyrosine-protein phosphatase non-receptor type 5 isoform a


(Homo sapiens)
BDBM50441296
PNG
(CHEMBL2431665 | CHEMBL2431667)
Show SMILES O[C@@H](c1cccc(c1)-c1ccc(cc1)C(=O)P(O)(O)O)c1ccc(Cl)c(Cl)c1
Show InChI InChI=1S/C20H17Cl2O5P/c21-17-9-8-16(11-18(17)22)19(23)15-3-1-2-14(10-15)12-4-6-13(7-5-12)20(24)28(25,26)27/h1-11,19,23,25-28H/t19-/m0/s1
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9.30E+4n/an/an/an/an/an/an/an/a



Yale University

Curated by ChEMBL


Assay Description
Inhibition of human STEP using pNPP as substrate after 5 mins by spectrophotometric plate reader analysis


Citation and Details
More data for this
Ligand-Target Pair
tyrosine-protein phosphatase non-receptor type 5 isoform a


(Homo sapiens)
BDBM50441326
PNG
(CHEMBL2431703)
Show SMILES CC(C)c1ccc(O)c(c1)-c1cccc(c1)C(F)(F)P(O)(O)=O
Show InChI InChI=1S/C16H17F2O4P/c1-10(2)11-6-7-15(19)14(9-11)12-4-3-5-13(8-12)16(17,18)23(20,21)22/h3-10,19H,1-2H3,(H2,20,21,22)
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9.50E+4n/an/an/an/an/an/an/an/a



Yale University

Curated by ChEMBL


Assay Description
Inhibition of human STEP using pNPP as substrate after 5 mins by spectrophotometric plate reader analysis


Citation and Details
More data for this
Ligand-Target Pair
tyrosine-protein phosphatase non-receptor type 5 isoform a


(Homo sapiens)
BDBM50441299
PNG
(CHEMBL2431668)
Show SMILES OC(c1cccc(c1)-c1ccc(CP(O)(O)=O)cc1)c1ccc(Cl)c(Cl)c1
Show InChI InChI=1S/C20H17Cl2O4P/c21-18-9-8-17(11-19(18)22)20(23)16-3-1-2-15(10-16)14-6-4-13(5-7-14)12-27(24,25)26/h1-11,20,23H,12H2,(H2,24,25,26)
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9.70E+4n/an/an/an/an/an/an/an/a



Yale University

Curated by ChEMBL


Assay Description
Inhibition of human STEP using pNPP as substrate after 5 mins by spectrophotometric plate reader analysis


Citation and Details
More data for this
Ligand-Target Pair
tyrosine-protein phosphatase non-receptor type 5 isoform a


(Homo sapiens)
BDBM50441308
PNG
(CHEMBL2431682)
Show SMILES OP(O)(=O)C(F)(F)c1ccc(cc1)-c1cccc(Nc2ccccc2)c1
Show InChI InChI=1S/C19H16F2NO3P/c20-19(21,26(23,24)25)16-11-9-14(10-12-16)15-5-4-8-18(13-15)22-17-6-2-1-3-7-17/h1-13,22H,(H2,23,24,25)
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1.12E+5n/an/an/an/an/an/an/an/a



Yale University

Curated by ChEMBL


Assay Description
Inhibition of human STEP using pNPP as substrate after 5 mins by spectrophotometric plate reader analysis


Citation and Details
More data for this
Ligand-Target Pair
tyrosine-protein phosphatase non-receptor type 5 isoform a


(Homo sapiens)
BDBM50441311
PNG
(CHEMBL2431679)
Show SMILES CS(=O)(=O)Nc1cccc(c1)-c1ccc(cc1)C(F)(F)P(O)(O)=O
Show InChI InChI=1S/C14H14F2NO5PS/c1-24(21,22)17-13-4-2-3-11(9-13)10-5-7-12(8-6-10)14(15,16)23(18,19)20/h2-9,17H,1H3,(H2,18,19,20)
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1.13E+5n/an/an/an/an/an/an/an/a



Yale University

Curated by ChEMBL


Assay Description
Inhibition of human STEP using pNPP as substrate after 5 mins by spectrophotometric plate reader analysis


Citation and Details
More data for this
Ligand-Target Pair
tyrosine-protein phosphatase non-receptor type 5 isoform a


(Homo sapiens)
BDBM50075308
PNG
((Biphenyl-4-yl-difluoro-methyl)-phosphonic acid | ...)
Show SMILES OP(O)(=O)C(F)(F)c1ccc(cc1)-c1ccccc1
Show InChI InChI=1S/C13H11F2O3P/c14-13(15,19(16,17)18)12-8-6-11(7-9-12)10-4-2-1-3-5-10/h1-9H,(H2,16,17,18)
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1.20E+5n/an/an/an/an/an/an/an/a



Yale University

Curated by ChEMBL


Assay Description
Inhibition of human STEP using pNPP as substrate after 5 mins by spectrophotometric plate reader analysis


Citation and Details
More data for this
Ligand-Target Pair
tyrosine-protein phosphatase non-receptor type 5 isoform a


(Homo sapiens)
BDBM50441325
PNG
(CHEMBL2431704)
Show SMILES CCc1cccc(c1O)-c1cccc(c1)C(F)(F)P(O)(O)=O
Show InChI InChI=1S/C15H15F2O4P/c1-2-10-5-4-8-13(14(10)18)11-6-3-7-12(9-11)15(16,17)22(19,20)21/h3-9,18H,2H2,1H3,(H2,19,20,21)
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1.24E+5n/an/an/an/an/an/an/an/a



Yale University

Curated by ChEMBL


Assay Description
Inhibition of human STEP using pNPP as substrate after 5 mins by spectrophotometric plate reader analysis


Citation and Details
More data for this
Ligand-Target Pair
tyrosine-protein phosphatase non-receptor type 5 isoform a


(Homo sapiens)
BDBM50441314
PNG
(CHEMBL2431676)
Show SMILES CC(C)c1cccc(c1)-c1ccc(cc1)C(F)(F)P(O)(O)=O
Show InChI InChI=1S/C16H17F2O3P/c1-11(2)13-4-3-5-14(10-13)12-6-8-15(9-7-12)16(17,18)22(19,20)21/h3-11H,1-2H3,(H2,19,20,21)
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1.32E+5n/an/an/an/an/an/an/an/a



Yale University

Curated by ChEMBL


Assay Description
Inhibition of human STEP using pNPP as substrate after 5 mins by spectrophotometric plate reader analysis


Citation and Details
More data for this
Ligand-Target Pair
tyrosine-protein phosphatase non-receptor type 5 isoform a


(Homo sapiens)
BDBM50441331
PNG
(CHEMBL2431698)
Show SMILES Cc1cccc(c1)-c1cccc(c1)C(F)(F)P(O)(O)=O
Show InChI InChI=1S/C14H13F2O3P/c1-10-4-2-5-11(8-10)12-6-3-7-13(9-12)14(15,16)20(17,18)19/h2-9H,1H3,(H2,17,18,19)
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1.37E+5n/an/an/an/an/an/an/an/a



Yale University

Curated by ChEMBL


Assay Description
Inhibition of human STEP using pNPP as substrate after 5 mins by spectrophotometric plate reader analysis


Citation and Details
More data for this
Ligand-Target Pair
tyrosine-protein phosphatase non-receptor type 5 isoform a


(Homo sapiens)
BDBM50441329
PNG
(CHEMBL2431700)
Show SMILES Oc1ccccc1-c1cccc(c1)C(F)(F)P(O)(O)=O
Show InChI InChI=1S/C13H11F2O4P/c14-13(15,20(17,18)19)10-5-3-4-9(8-10)11-6-1-2-7-12(11)16/h1-8,16H,(H2,17,18,19)
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1.68E+5n/an/an/an/an/an/an/an/a



Yale University

Curated by ChEMBL


Assay Description
Inhibition of human STEP using pNPP as substrate after 5 mins by spectrophotometric plate reader analysis


Citation and Details
More data for this
Ligand-Target Pair
tyrosine-protein phosphatase non-receptor type 5 isoform a


(Homo sapiens)
BDBM50441313
PNG
(CHEMBL2431677)
Show SMILES CC(C)c1ccc(cc1)-c1ccc(cc1)C(F)(F)P(O)(O)=O
Show InChI InChI=1S/C16H17F2O3P/c1-11(2)12-3-5-13(6-4-12)14-7-9-15(10-8-14)16(17,18)22(19,20)21/h3-11H,1-2H3,(H2,19,20,21)
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1.85E+5n/an/an/an/an/an/an/an/a



Yale University

Curated by ChEMBL


Assay Description
Inhibition of human STEP using pNPP as substrate after 5 mins by spectrophotometric plate reader analysis


Citation and Details
More data for this
Ligand-Target Pair
tyrosine-protein phosphatase non-receptor type 5 isoform a


(Homo sapiens)
BDBM50441316
PNG
(CHEMBL2431674)
Show SMILES CC(C)Oc1cccc(c1)-c1ccc(cc1)C(F)(F)P(O)(O)=O
Show InChI InChI=1S/C16H17F2O4P/c1-11(2)22-15-5-3-4-13(10-15)12-6-8-14(9-7-12)16(17,18)23(19,20)21/h3-11H,1-2H3,(H2,19,20,21)
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2.00E+5n/an/an/an/an/an/an/an/a



Yale University

Curated by ChEMBL


Assay Description
Inhibition of human STEP using pNPP as substrate after 5 mins by spectrophotometric plate reader analysis


Citation and Details
More data for this
Ligand-Target Pair
tyrosine-protein phosphatase non-receptor type 5 isoform a


(Homo sapiens)
BDBM50441333
PNG
(CHEMBL2431696)
Show SMILES Cc1ccc(cc1)-c1cccc(c1)C(F)(F)P(O)(O)=O
Show InChI InChI=1S/C14H13F2O3P/c1-10-5-7-11(8-6-10)12-3-2-4-13(9-12)14(15,16)20(17,18)19/h2-9H,1H3,(H2,17,18,19)
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2.05E+5n/an/an/an/an/an/an/an/a



Yale University

Curated by ChEMBL


Assay Description
Inhibition of human STEP using pNPP as substrate after 5 mins by spectrophotometric plate reader analysis


Citation and Details
More data for this
Ligand-Target Pair
tyrosine-protein phosphatase non-receptor type 5 isoform a


(Homo sapiens)
BDBM50441332
PNG
(CHEMBL2431697)
Show SMILES CC(C)c1ccc(cc1)-c1cccc(c1)C(F)(F)P(O)(O)=O
Show InChI InChI=1S/C16H17F2O3P/c1-11(2)12-6-8-13(9-7-12)14-4-3-5-15(10-14)16(17,18)22(19,20)21/h3-11H,1-2H3,(H2,19,20,21)
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2.22E+5n/an/an/an/an/an/an/an/a



Yale University

Curated by ChEMBL


Assay Description
Inhibition of human STEP using pNPP as substrate after 5 mins by spectrophotometric plate reader analysis


Citation and Details
More data for this
Ligand-Target Pair
tyrosine-protein phosphatase non-receptor type 5 isoform a


(Homo sapiens)
BDBM50441315
PNG
(CHEMBL2431675)
Show SMILES CC(C)Oc1ccc(cc1)-c1ccc(cc1)C(F)(F)P(O)(O)=O
Show InChI InChI=1S/C16H17F2O4P/c1-11(2)22-15-9-5-13(6-10-15)12-3-7-14(8-4-12)16(17,18)23(19,20)21/h3-11H,1-2H3,(H2,19,20,21)
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2.31E+5n/an/an/an/an/an/an/an/a



Yale University

Curated by ChEMBL


Assay Description
Inhibition of human STEP using pNPP as substrate after 5 mins by spectrophotometric plate reader analysis


Citation and Details
More data for this
Ligand-Target Pair
tyrosine-protein phosphatase non-receptor type 5 isoform a


(Homo sapiens)
BDBM50441328
PNG
(CHEMBL2431701)
Show SMILES COc1ccccc1-c1cccc(c1)C(F)(F)P(O)(O)=O
Show InChI InChI=1S/C14H13F2O4P/c1-20-13-8-3-2-7-12(13)10-5-4-6-11(9-10)14(15,16)21(17,18)19/h2-9H,1H3,(H2,17,18,19)
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2.71E+5n/an/an/an/an/an/an/an/a



Yale University

Curated by ChEMBL


Assay Description
Inhibition of human STEP using pNPP as substrate after 5 mins by spectrophotometric plate reader analysis


Citation and Details
More data for this
Ligand-Target Pair
tyrosine-protein phosphatase non-receptor type 5 isoform a


(Homo sapiens)
BDBM50121106
PNG
(1,1'-biphenyl-3-yl(difluoro)methylphosphonate)
Show SMILES [O-]P([O-])(=O)C(F)(F)c1cccc(c1)-c1ccccc1
Show InChI InChI=1S/C13H11F2O3P/c14-13(15,19(16,17)18)12-8-4-7-11(9-12)10-5-2-1-3-6-10/h1-9H,(H2,16,17,18)/p-2
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3.37E+5n/an/an/an/an/an/an/an/a



Yale University

Curated by ChEMBL


Assay Description
Inhibition of human STEP using pNPP as substrate after 5 mins by spectrophotometric plate reader analysis


Citation and Details
More data for this
Ligand-Target Pair
tyrosine-protein phosphatase non-receptor type 5 isoform a


(Homo sapiens)
BDBM50441319
PNG
(CHEMBL2431671)
Show SMILES OP(O)(=O)C(F)(F)c1ccc(cc1)-c1ccccc1C#N
Show InChI InChI=1S/C14H10F2NO3P/c15-14(16,21(18,19)20)12-7-5-10(6-8-12)13-4-2-1-3-11(13)9-17/h1-8H,(H2,18,19,20)
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3.75E+5n/an/an/an/an/an/an/an/a



Yale University

Curated by ChEMBL


Assay Description
Inhibition of human STEP using pNPP as substrate after 5 mins by spectrophotometric plate reader analysis


Citation and Details
More data for this
Ligand-Target Pair
tyrosine-protein phosphatase non-receptor type 5 isoform a


(Homo sapiens)
BDBM50441318
PNG
(CHEMBL2431672)
Show SMILES OP(O)(=O)C(F)(F)c1ccc(cc1)-c1cccc(c1)C#N
Show InChI InChI=1S/C14H10F2NO3P/c15-14(16,21(18,19)20)13-6-4-11(5-7-13)12-3-1-2-10(8-12)9-17/h1-8H,(H2,18,19,20)
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4.00E+5n/an/an/an/an/an/an/an/a



Yale University

Curated by ChEMBL


Assay Description
Inhibition of human STEP using pNPP as substrate after 5 mins by spectrophotometric plate reader analysis


Citation and Details
More data for this
Ligand-Target Pair
tyrosine-protein phosphatase non-receptor type 5 isoform a


(Homo sapiens)
BDBM50441309
PNG
(CHEMBL2431681)
Show SMILES CC(O)c1ccc(cc1)-c1ccc(cc1)C(F)(F)P(O)(O)=O
Show InChI InChI=1S/C15H15F2O4P/c1-10(18)11-2-4-12(5-3-11)13-6-8-14(9-7-13)15(16,17)22(19,20)21/h2-10,18H,1H3,(H2,19,20,21)
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PubMed
4.50E+5n/an/an/an/an/an/an/an/a



Yale University

Curated by ChEMBL


Assay Description
Inhibition of human STEP using pNPP as substrate after 5 mins by spectrophotometric plate reader analysis


Citation and Details
More data for this
Ligand-Target Pair
tyrosine-protein phosphatase non-receptor type 5 isoform a


(Homo sapiens)
BDBM50441317
PNG
(CHEMBL2431673)
Show SMILES OP(O)(=O)C(F)(F)c1ccc(cc1)-c1ccc(cc1)C#N
Show InChI InChI=1S/C14H10F2NO3P/c15-14(16,21(18,19)20)13-7-5-12(6-8-13)11-3-1-10(9-17)2-4-11/h1-8H,(H2,18,19,20)
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6.17E+5n/an/an/an/an/an/an/an/a



Yale University

Curated by ChEMBL


Assay Description
Inhibition of human STEP using pNPP as substrate after 5 mins by spectrophotometric plate reader analysis


Citation and Details
More data for this
Ligand-Target Pair
tyrosine-protein phosphatase non-receptor type 5 isoform a


(Homo sapiens)
BDBM50441312
PNG
(CHEMBL2431678)
Show SMILES CS(=O)(=O)Nc1ccccc1-c1ccc(cc1)C(F)(F)P(O)(O)=O
Show InChI InChI=1S/C14H14F2NO5PS/c1-24(21,22)17-13-5-3-2-4-12(13)10-6-8-11(9-7-10)14(15,16)23(18,19)20/h2-9,17H,1H3,(H2,18,19,20)
PDB
MMDB

KEGG

UniProtKB/SwissProt

B.MOAD
antibodypedia
GoogleScholar
AffyNet 
CHEMBL
PC cid
PC sid
UniChem
AffyNet 
Article
PubMed
6.73E+5n/an/an/an/an/an/an/an/a



Yale University

Curated by ChEMBL


Assay Description
Inhibition of human STEP using pNPP as substrate after 5 mins by spectrophotometric plate reader analysis


Citation and Details
More data for this
Ligand-Target Pair
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