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PubMed code 1992118

Compile data set for download or QSAR
Found 5 hits of Enzyme Inhibition Constant Data   
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
Dihydrofolate reductase


(Homo sapiens (human))
BDBM18050
PNG
(2-[(4-{[(2,4-diaminopteridin-6-yl)methyl](methyl)a...)
Show SMILES CN(Cc1cnc2nc(N)nc(N)c2n1)c1ccc(cc1)C(=O)N[C@@H](CCC(O)=O)C(O)=O
Show InChI InChI=1S/C20H22N8O5/c1-28(9-11-8-23-17-15(24-11)16(21)26-20(22)27-17)12-4-2-10(3-5-12)18(31)25-13(19(32)33)6-7-14(29)30/h2-5,8,13H,6-7,9H2,1H3,(H,25,31)(H,29,30)(H,32,33)(H4,21,22,23,26,27)/t13-/m0/s1
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n/an/a 25n/an/an/an/an/an/a



Institute

Curated by ChEMBL


Assay Description
Ability to inhibit purified Dihydrofolate reductase from human leukemic lymphoblasts was determined spectrophotometrically at 340 nM.


Citation and Details
More data for this
Ligand-Target Pair
3D
3D Structure (crystal)
Dihydrofolate reductase


(Homo sapiens (human))
BDBM50367055
PNG
(4-Aminofolic acid | 4-Aminopteroic acid | AMINOPTE...)
Show SMILES Nc1nc(N)c2nc(CNc3ccc(cc3)C(=O)N[C@@H](CCC(O)=O)C(O)=O)cnc2n1
Show InChI InChI=1S/C19H20N8O5/c20-15-14-16(27-19(21)26-15)23-8-11(24-14)7-22-10-3-1-9(2-4-10)17(30)25-12(18(31)32)5-6-13(28)29/h1-4,8,12,22H,5-7H2,(H,25,30)(H,28,29)(H,31,32)(H4,20,21,23,26,27)/t12-/m0/s1
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n/an/a 25n/an/an/an/an/an/a



Institute

Curated by ChEMBL


Assay Description
Ability to inhibit purified Dihydrofolate reductase from human leukemic lymphoblasts was determined spectrophotometrically at 340 nM.


Citation and Details
More data for this
Ligand-Target Pair
Dihydrofolate reductase


(Homo sapiens (human))
BDBM50010924
PNG
(2-{4-[(2,4-Diamino-pteridin-6-ylmethyl)-methyl-ami...)
Show SMILES CN(Cc1cnc2nc(N)nc(N)c2n1)c1ccc(cc1)C(=O)NC(CC(=C)C(O)=O)C(O)=O
Show InChI InChI=1S/C21H22N8O5/c1-10(19(31)32)7-14(20(33)34)26-18(30)11-3-5-13(6-4-11)29(2)9-12-8-24-17-15(25-12)16(22)27-21(23)28-17/h3-6,8,14H,1,7,9H2,2H3,(H,26,30)(H,31,32)(H,33,34)(H4,22,23,24,27,28)
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n/an/a 44n/an/an/an/an/an/a



Institute

Curated by ChEMBL


Assay Description
Ability to inhibit purified Dihydrofolate reductase from human leukemic lymphoblasts was determined spectrophotometrically at 340 nM.


Citation and Details
More data for this
Ligand-Target Pair
Dihydrofolate reductase


(Homo sapiens (human))
BDBM50010927
PNG
(2-Cyano-4-{4-[(2,4-diamino-pteridin-6-ylmethyl)-me...)
Show SMILES CN(Cc1cnc2nc(N)nc(N)c2n1)c1ccc(cc1)C(=O)NC(CC(C#N)C(O)=O)C(O)=O
Show InChI InChI=1S/C21H21N9O5/c1-30(9-12-8-25-17-15(26-12)16(23)28-21(24)29-17)13-4-2-10(3-5-13)18(31)27-14(20(34)35)6-11(7-22)19(32)33/h2-5,8,11,14H,6,9H2,1H3,(H,27,31)(H,32,33)(H,34,35)(H4,23,24,25,28,29)
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n/an/a 57n/an/an/an/an/an/a



Institute

Curated by ChEMBL


Assay Description
Ability to inhibit purified Dihydrofolate reductase from human leukemic lymphoblasts was determined spectrophotometrically at 340 nM.


Citation and Details
More data for this
Ligand-Target Pair
Dihydrofolate reductase


(Homo sapiens (human))
BDBM50010925
PNG
(2-{4-[(2,4-Diamino-pteridin-6-ylmethyl)-amino]-ben...)
Show SMILES Nc1nc(N)c2nc(CNc3ccc(cc3)C(=O)NC(CC(=C)C(O)=O)C(O)=O)cnc2n1
Show InChI InChI=1S/C20H20N8O5/c1-9(18(30)31)6-13(19(32)33)26-17(29)10-2-4-11(5-3-10)23-7-12-8-24-16-14(25-12)15(21)27-20(22)28-16/h2-5,8,13,23H,1,6-7H2,(H,26,29)(H,30,31)(H,32,33)(H4,21,22,24,27,28)
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PubMed
n/an/a 88n/an/an/an/an/an/a



Institute

Curated by ChEMBL


Assay Description
Ability to inhibit purified Dihydrofolate reductase from human leukemic lymphoblasts was determined spectrophotometrically at 340 nM.


Citation and Details
More data for this
Ligand-Target Pair
* indicates data uncertainty>20%