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15 molecules are shown

Wt: 669.6
BDBM8089
Wt: 666.8
BDBM8098
Wt: 651.7
BDBM8101
Wt: 656.8
BDBM8108
Wt: 561.6
BDBM50071549
Wt: 622.1
BDBM50076291
Wt: 751.8
BDBM50076293
Wt: 650.1
BDBM50076294
Wt: 649.1
BDBM50076285
Wt: 698.1
BDBM50076286
Wt: 709.8
BDBM50076287
Wt: 695.8
BDBM50076288
Wt: 799.8
BDBM50076289
Wt: 691.7
BDBM50076290
Wt: 619.0
BDBM50297442

Activity Spreadsheet -- Enzyme Inhibition Constant Data from BindingDB

Found 34 hits for monomerid = 8089,8098,8101,8108,50071549,50076291,50076293,50076294,50076285,50076286,50076287,50076288,50076289,50076290,50297442   
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
Cathepsin D


(Homo sapiens (human))
BDBM50076285
PNG
(1-Acetyl-piperidine-4-carboxylic acid (2-benzo[1,3...)
Show SMILES CC(=O)N1CCC(CC1)C(=O)N(CCc1ccc2OCOc2c1)C[C@H](O)[C@H](Cc1ccccc1)NC(=O)CNc1cccc(Cl)c1
Show InChI InChI=1S/C35H41ClN4O6/c1-24(41)39-16-13-27(14-17-39)35(44)40(15-12-26-10-11-32-33(19-26)46-23-45-32)22-31(42)30(18-25-6-3-2-4-7-25)38-34(43)21-37-29-9-5-8-28(36)20-29/h2-11,19-20,27,30-31,37,42H,12-18,21-23H2,1H3,(H,38,43)/t30-,31-/m0/s1
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1.30n/an/an/an/an/an/an/an/a



University of California

Curated by ChEMBL


Assay Description
Compound was tested for the inhibitory activity against human liver cathepsin D


J Med Chem 42: 1428-40 (1999)


Article DOI: 10.1021/jm980641t
BindingDB Entry DOI: 10.7270/Q2MS3RZX
More data for this
Ligand-Target Pair
Cathepsin D


(Homo sapiens (human))
BDBM50076294
PNG
(1-Acetyl-piperidine-4-carboxylic acid (2-benzo[1,3...)
Show SMILES CC(=O)N1CCC(CC1)C(=O)N(CCc1ccc2OCOc2c1)C[C@H](O)[C@H](Cc1ccccc1)NC(=O)COc1cccc(Cl)c1
Show InChI InChI=1S/C35H40ClN3O7/c1-24(40)38-16-13-27(14-17-38)35(43)39(15-12-26-10-11-32-33(19-26)46-23-45-32)21-31(41)30(18-25-6-3-2-4-7-25)37-34(42)22-44-29-9-5-8-28(36)20-29/h2-11,19-20,27,30-31,41H,12-18,21-23H2,1H3,(H,37,42)/t30-,31-/m0/s1
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1.90n/an/an/an/an/an/an/an/a



University of California

Curated by ChEMBL


Assay Description
Compound was tested for the inhibitory activity against human liver cathepsin D


J Med Chem 42: 1428-40 (1999)


Article DOI: 10.1021/jm980641t
BindingDB Entry DOI: 10.7270/Q2MS3RZX
More data for this
Ligand-Target Pair
Plasmepsin 2


(Plasmodium falciparum)
BDBM50076291
PNG
(1-Methyl-piperidine-4-carboxylic acid (2-benzo[1,3...)
Show SMILES CN1CCC(CC1)C(=O)N(CCc1ccc2OCOc2c1)C[C@H](O)[C@H](Cc1ccccc1)NC(=O)COc1cccc(Cl)c1
Show InChI InChI=1S/C34H40ClN3O6/c1-37-15-13-26(14-16-37)34(41)38(17-12-25-10-11-31-32(19-25)44-23-43-31)21-30(39)29(18-24-6-3-2-4-7-24)36-33(40)22-42-28-9-5-8-27(35)20-28/h2-11,19-20,26,29-30,39H,12-18,21-23H2,1H3,(H,36,40)/t29-,30-/m0/s1
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2n/an/an/an/an/an/an/an/a



University of California

Curated by ChEMBL


Assay Description
Inhibitory activity against Plasmepsin 2


J Med Chem 42: 1428-40 (1999)


Article DOI: 10.1021/jm980641t
BindingDB Entry DOI: 10.7270/Q2MS3RZX
More data for this
Ligand-Target Pair
3D
3D Structure (docked)
Plasmepsin 2


(Plasmodium falciparum)
BDBM50076285
PNG
(1-Acetyl-piperidine-4-carboxylic acid (2-benzo[1,3...)
Show SMILES CC(=O)N1CCC(CC1)C(=O)N(CCc1ccc2OCOc2c1)C[C@H](O)[C@H](Cc1ccccc1)NC(=O)CNc1cccc(Cl)c1
Show InChI InChI=1S/C35H41ClN4O6/c1-24(41)39-16-13-27(14-17-39)35(44)40(15-12-26-10-11-32-33(19-26)46-23-45-32)22-31(42)30(18-25-6-3-2-4-7-25)38-34(43)21-37-29-9-5-8-28(36)20-29/h2-11,19-20,27,30-31,37,42H,12-18,21-23H2,1H3,(H,38,43)/t30-,31-/m0/s1
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3n/an/an/an/an/an/an/an/a



University of California

Curated by ChEMBL


Assay Description
Inhibitory activity against Plasmepsin 2


J Med Chem 42: 1428-40 (1999)


Article DOI: 10.1021/jm980641t
BindingDB Entry DOI: 10.7270/Q2MS3RZX
More data for this
Ligand-Target Pair
3D
3D Structure (docked)
Plasmepsin 2


(Plasmodium falciparum)
BDBM50076294
PNG
(1-Acetyl-piperidine-4-carboxylic acid (2-benzo[1,3...)
Show SMILES CC(=O)N1CCC(CC1)C(=O)N(CCc1ccc2OCOc2c1)C[C@H](O)[C@H](Cc1ccccc1)NC(=O)COc1cccc(Cl)c1
Show InChI InChI=1S/C35H40ClN3O7/c1-24(40)38-16-13-27(14-17-38)35(43)39(15-12-26-10-11-32-33(19-26)46-23-45-32)21-31(41)30(18-25-6-3-2-4-7-25)37-34(42)22-44-29-9-5-8-28(36)20-29/h2-11,19-20,27,30-31,41H,12-18,21-23H2,1H3,(H,37,42)/t30-,31-/m0/s1
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4n/an/an/an/an/an/an/an/a



University of California

Curated by ChEMBL


Assay Description
Inhibitory activity against Plasmepsin 2


J Med Chem 42: 1428-40 (1999)


Article DOI: 10.1021/jm980641t
BindingDB Entry DOI: 10.7270/Q2MS3RZX
More data for this
Ligand-Target Pair
3D
3D Structure (docked)
Plasmepsin 2


(Plasmodium falciparum)
BDBM50076287
PNG
(1-Methyl-piperidine-4-carboxylic acid [(2S,3S)-3-(...)
Show SMILES COc1ccc(CCN(C[C@H](O)[C@H](Cc2ccccc2)NC(=O)c2cc(OC)c(OCc3ccccc3)c(OC)c2)C(=O)C2CCN(C)CC2)cc1
Show InChI InChI=1S/C42H51N3O7/c1-44-22-20-33(21-23-44)42(48)45(24-19-30-15-17-35(49-2)18-16-30)28-37(46)36(25-31-11-7-5-8-12-31)43-41(47)34-26-38(50-3)40(39(27-34)51-4)52-29-32-13-9-6-10-14-32/h5-18,26-27,33,36-37,46H,19-25,28-29H2,1-4H3,(H,43,47)/t36-,37-/m0/s1
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4.10n/an/an/an/an/an/an/an/a



University of California

Curated by ChEMBL


Assay Description
Inhibitory activity against Plasmepsin 2


J Med Chem 42: 1428-40 (1999)


Article DOI: 10.1021/jm980641t
BindingDB Entry DOI: 10.7270/Q2MS3RZX
More data for this
Ligand-Target Pair
3D
3D Structure (docked)
Cathepsin D


(Homo sapiens (human))
BDBM50076293
PNG
(1-Acetyl-piperidine-4-carboxylic acid (2-benzo[1,3...)
Show SMILES COc1cc(cc(OC)c1OCc1ccccc1)C(=O)N[C@@H](Cc1ccccc1)[C@@H](O)CN(CCc1ccc2OCOc2c1)C(=O)C1CCN(CC1)C(C)=O
Show InChI InChI=1S/C43H49N3O9/c1-29(47)45-20-17-33(18-21-45)43(50)46(19-16-31-14-15-37-38(23-31)55-28-54-37)26-36(48)35(22-30-10-6-4-7-11-30)44-42(49)34-24-39(51-2)41(40(25-34)52-3)53-27-32-12-8-5-9-13-32/h4-15,23-25,33,35-36,48H,16-22,26-28H2,1-3H3,(H,44,49)/t35-,36-/m0/s1
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4.30n/an/an/an/an/an/an/an/a



University of California

Curated by ChEMBL


Assay Description
Compound was tested for the inhibitory activity against human liver cathepsin D


J Med Chem 42: 1428-40 (1999)


Article DOI: 10.1021/jm980641t
BindingDB Entry DOI: 10.7270/Q2MS3RZX
More data for this
Ligand-Target Pair
Plasmepsin 2


(Plasmodium falciparum)
BDBM50076293
PNG
(1-Acetyl-piperidine-4-carboxylic acid (2-benzo[1,3...)
Show SMILES COc1cc(cc(OC)c1OCc1ccccc1)C(=O)N[C@@H](Cc1ccccc1)[C@@H](O)CN(CCc1ccc2OCOc2c1)C(=O)C1CCN(CC1)C(C)=O
Show InChI InChI=1S/C43H49N3O9/c1-29(47)45-20-17-33(18-21-45)43(50)46(19-16-31-14-15-37-38(23-31)55-28-54-37)26-36(48)35(22-30-10-6-4-7-11-30)44-42(49)34-24-39(51-2)41(40(25-34)52-3)53-27-32-12-8-5-9-13-32/h4-15,23-25,33,35-36,48H,16-22,26-28H2,1-3H3,(H,44,49)/t35-,36-/m0/s1
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4.80n/an/an/an/an/an/an/an/a



University of California

Curated by ChEMBL


Assay Description
Inhibitory activity against Plasmepsin 2


J Med Chem 42: 1428-40 (1999)


Article DOI: 10.1021/jm980641t
BindingDB Entry DOI: 10.7270/Q2MS3RZX
More data for this
Ligand-Target Pair
3D
3D Structure (docked)
Cathepsin D


(Homo sapiens (human))
BDBM50076291
PNG
(1-Methyl-piperidine-4-carboxylic acid (2-benzo[1,3...)
Show SMILES CN1CCC(CC1)C(=O)N(CCc1ccc2OCOc2c1)C[C@H](O)[C@H](Cc1ccccc1)NC(=O)COc1cccc(Cl)c1
Show InChI InChI=1S/C34H40ClN3O6/c1-37-15-13-26(14-16-37)34(41)38(17-12-25-10-11-31-32(19-25)44-23-43-31)21-30(39)29(18-24-6-3-2-4-7-24)36-33(40)22-42-28-9-5-8-27(35)20-28/h2-11,19-20,26,29-30,39H,12-18,21-23H2,1H3,(H,36,40)/t29-,30-/m0/s1
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5.80n/an/an/an/an/an/an/an/a



University of California

Curated by ChEMBL


Assay Description
Compound was tested for the inhibitory activity against human liver cathepsin D


J Med Chem 42: 1428-40 (1999)


Article DOI: 10.1021/jm980641t
BindingDB Entry DOI: 10.7270/Q2MS3RZX
More data for this
Ligand-Target Pair
Plasmepsin 2


(Plasmodium falciparum)
BDBM50076288
PNG
(CHEMBL284955 | Piperidine-4-carboxylic acid [(2S,3...)
Show SMILES COc1ccc(CCN(C[C@H](O)[C@H](Cc2ccccc2)NC(=O)c2cc(OC)c(OCc3ccccc3)c(OC)c2)C(=O)C2CCNCC2)cc1
Show InChI InChI=1S/C41H49N3O7/c1-48-34-16-14-29(15-17-34)20-23-44(41(47)32-18-21-42-22-19-32)27-36(45)35(24-30-10-6-4-7-11-30)43-40(46)33-25-37(49-2)39(38(26-33)50-3)51-28-31-12-8-5-9-13-31/h4-17,25-26,32,35-36,42,45H,18-24,27-28H2,1-3H3,(H,43,46)/t35-,36-/m0/s1
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9n/an/an/an/an/an/an/an/a



University of California

Curated by ChEMBL


Assay Description
Inhibitory activity against Plasmepsin 2


J Med Chem 42: 1428-40 (1999)


Article DOI: 10.1021/jm980641t
BindingDB Entry DOI: 10.7270/Q2MS3RZX
More data for this
Ligand-Target Pair
3D
3D Structure (docked)
Plasmepsin I


(Plasmodium falciparum)
BDBM8108
PNG
((2S)-N-[(2S,3S)-4-{[(1S)-2-[4-(2H-1,3-benzodioxol-...)
Show SMILES CC(C)[C@H](NC(=O)C1CCCCC1)C(=O)N[C@@H](Cc1ccccc1)[C@@H](O)CN[C@@H](Cc1ccc(cc1)-c1ccc2OCOc2c1)C(N)=O
Show InChI InChI=1S/C38H48N4O6/c1-24(2)35(42-37(45)28-11-7-4-8-12-28)38(46)41-30(19-25-9-5-3-6-10-25)32(43)22-40-31(36(39)44)20-26-13-15-27(16-14-26)29-17-18-33-34(21-29)48-23-47-33/h3,5-6,9-10,13-18,21,24,28,30-32,35,40,43H,4,7-8,11-12,19-20,22-23H2,1-2H3,(H2,39,44)(H,41,46)(H,42,45)/t30-,31-,32-,35-/m0/s1
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12n/an/an/an/an/an/an/an/a



Uppsala University



Assay Description
Enzyme activities were assayed by monitoring the hydrolysis of substrate in the presence or absence of inhibitor compounds. The hydrolysis was record...


J Comb Chem 5: 456-64 (2003)


Article DOI: 10.1021/cc0301014
BindingDB Entry DOI: 10.7270/Q27S7KZZ
More data for this
Ligand-Target Pair
Cathepsin D


(Homo sapiens (human))
BDBM50076286
PNG
(CHEMBL34051 | N-(2-Benzo[1,3]dioxol-5-yl-ethyl)-N-...)
Show SMILES O[C@@H](CN(CCc1ccc2OCOc2c1)C(=O)CCN1C(=O)c2ccccc2C1=O)[C@H](Cc1ccccc1)NC(=O)COc1cccc(Cl)c1
Show InChI InChI=1S/C38H36ClN3O8/c39-27-9-6-10-28(21-27)48-23-35(44)40-31(19-25-7-2-1-3-8-25)32(43)22-41(17-15-26-13-14-33-34(20-26)50-24-49-33)36(45)16-18-42-37(46)29-11-4-5-12-30(29)38(42)47/h1-14,20-21,31-32,43H,15-19,22-24H2,(H,40,44)/t31-,32-/m0/s1
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15n/an/an/an/an/an/an/an/a



University of California

Curated by ChEMBL


Assay Description
Compound was tested for the inhibitory activity against human liver cathepsin D


J Med Chem 42: 1428-40 (1999)


Article DOI: 10.1021/jm980641t
BindingDB Entry DOI: 10.7270/Q2MS3RZX
More data for this
Ligand-Target Pair
Plasmepsin I


(Plasmodium falciparum)
BDBM8101
PNG
((2S)-N-[(2S,3S)-4-{[(1S)-2-[4-(2H-1,3-benzodioxol-...)
Show SMILES CC(C)[C@H](NC(=O)c1ccccn1)C(=O)N[C@@H](Cc1ccccc1)[C@@H](O)CN[C@@H](Cc1ccc(cc1)-c1ccc2OCOc2c1)C(N)=O
Show InChI InChI=1S/C37H41N5O6/c1-23(2)34(42-36(45)28-10-6-7-17-39-28)37(46)41-29(18-24-8-4-3-5-9-24)31(43)21-40-30(35(38)44)19-25-11-13-26(14-12-25)27-15-16-32-33(20-27)48-22-47-32/h3-17,20,23,29-31,34,40,43H,18-19,21-22H2,1-2H3,(H2,38,44)(H,41,46)(H,42,45)/t29-,30-,31-,34-/m0/s1
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23n/an/an/an/an/an/an/an/a



Uppsala University



Assay Description
Enzyme activities were assayed by monitoring the hydrolysis of substrate in the presence or absence of inhibitor compounds. The hydrolysis was record...


J Comb Chem 5: 456-64 (2003)


Article DOI: 10.1021/cc0301014
BindingDB Entry DOI: 10.7270/Q27S7KZZ
More data for this
Ligand-Target Pair
Plasmepsin I


(Plasmodium falciparum)
BDBM8098
PNG
((2S)-N-[(2S,3S)-4-{[(1S)-1-carbamoyl-2-(4-phenylph...)
Show SMILES COc1cccc(C(=O)N[C@@H](C(C)C)C(=O)N[C@@H](Cc2ccccc2)[C@@H](O)CN[C@@H](Cc2ccc(cc2)-c2ccccc2)C(N)=O)c1OC
Show InChI InChI=1S/C39H46N4O6/c1-25(2)35(43-38(46)30-16-11-17-34(48-3)36(30)49-4)39(47)42-31(22-26-12-7-5-8-13-26)33(44)24-41-32(37(40)45)23-27-18-20-29(21-19-27)28-14-9-6-10-15-28/h5-21,25,31-33,35,41,44H,22-24H2,1-4H3,(H2,40,45)(H,42,47)(H,43,46)/t31-,32-,33-,35-/m0/s1
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24n/an/an/an/an/an/an/an/a



Uppsala University



Assay Description
Enzyme activities were assayed by monitoring the hydrolysis of substrate in the presence or absence of inhibitor compounds. The hydrolysis was record...


J Comb Chem 5: 456-64 (2003)


Article DOI: 10.1021/cc0301014
BindingDB Entry DOI: 10.7270/Q27S7KZZ
More data for this
Ligand-Target Pair
3D
3D Structure (docked)
Plasmepsin 2


(Plasmodium falciparum)
BDBM8101
PNG
((2S)-N-[(2S,3S)-4-{[(1S)-2-[4-(2H-1,3-benzodioxol-...)
Show SMILES CC(C)[C@H](NC(=O)c1ccccn1)C(=O)N[C@@H](Cc1ccccc1)[C@@H](O)CN[C@@H](Cc1ccc(cc1)-c1ccc2OCOc2c1)C(N)=O
Show InChI InChI=1S/C37H41N5O6/c1-23(2)34(42-36(45)28-10-6-7-17-39-28)37(46)41-29(18-24-8-4-3-5-9-24)31(43)21-40-30(35(38)44)19-25-11-13-26(14-12-25)27-15-16-32-33(20-27)48-22-47-32/h3-17,20,23,29-31,34,40,43H,18-19,21-22H2,1-2H3,(H2,38,44)(H,41,46)(H,42,45)/t29-,30-,31-,34-/m0/s1
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52n/an/an/an/an/an/an/an/a



Uppsala University



Assay Description
Enzyme activities were assayed by monitoring the hydrolysis of substrate in the presence or absence of inhibitor compounds. The hydrolysis was record...


J Comb Chem 5: 456-64 (2003)


Article DOI: 10.1021/cc0301014
BindingDB Entry DOI: 10.7270/Q27S7KZZ
More data for this
Ligand-Target Pair
3D
3D Structure (docked)
Cathepsin D


(Homo sapiens (human))
BDBM50076287
PNG
(1-Methyl-piperidine-4-carboxylic acid [(2S,3S)-3-(...)
Show SMILES COc1ccc(CCN(C[C@H](O)[C@H](Cc2ccccc2)NC(=O)c2cc(OC)c(OCc3ccccc3)c(OC)c2)C(=O)C2CCN(C)CC2)cc1
Show InChI InChI=1S/C42H51N3O7/c1-44-22-20-33(21-23-44)42(48)45(24-19-30-15-17-35(49-2)18-16-30)28-37(46)36(25-31-11-7-5-8-12-31)43-41(47)34-26-38(50-3)40(39(27-34)51-4)52-29-32-13-9-6-10-14-32/h5-18,26-27,33,36-37,46H,19-25,28-29H2,1-4H3,(H,43,47)/t36-,37-/m0/s1
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58n/an/an/an/an/an/an/an/a



University of California

Curated by ChEMBL


Assay Description
Compound was tested for the inhibitory activity against human liver cathepsin D


J Med Chem 42: 1428-40 (1999)


Article DOI: 10.1021/jm980641t
BindingDB Entry DOI: 10.7270/Q2MS3RZX
More data for this
Ligand-Target Pair
Cathepsin D


(Homo sapiens (human))
BDBM50076288
PNG
(CHEMBL284955 | Piperidine-4-carboxylic acid [(2S,3...)
Show SMILES COc1ccc(CCN(C[C@H](O)[C@H](Cc2ccccc2)NC(=O)c2cc(OC)c(OCc3ccccc3)c(OC)c2)C(=O)C2CCNCC2)cc1
Show InChI InChI=1S/C41H49N3O7/c1-48-34-16-14-29(15-17-34)20-23-44(41(47)32-18-21-42-22-19-32)27-36(45)35(24-30-10-6-4-7-11-30)43-40(46)33-25-37(49-2)39(38(26-33)50-3)51-28-31-12-8-5-9-13-31/h4-17,25-26,32,35-36,42,45H,18-24,27-28H2,1-3H3,(H,43,46)/t35-,36-/m0/s1
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71n/an/an/an/an/an/an/an/a



University of California

Curated by ChEMBL


Assay Description
Compound was tested for the inhibitory activity against human liver cathepsin D


J Med Chem 42: 1428-40 (1999)


Article DOI: 10.1021/jm980641t
BindingDB Entry DOI: 10.7270/Q2MS3RZX
More data for this
Ligand-Target Pair
Plasmepsin 2


(Plasmodium falciparum)
BDBM50076289
PNG
(CHEMBL32997 | N-((1S,2S)-3-{(2-Benzo[1,3]dioxol-5-...)
Show SMILES COc1cc(cc(OC)c1OCc1ccccc1)C(=O)N[C@@H](Cc1ccccc1)[C@@H](O)CN(CCc1ccc2OCOc2c1)C(=O)CCN1C(=O)c2ccccc2C1=O
Show InChI InChI=1S/C46H45N3O10/c1-55-40-25-33(26-41(56-2)43(40)57-28-32-13-7-4-8-14-32)44(52)47-36(23-30-11-5-3-6-12-30)37(50)27-48(21-19-31-17-18-38-39(24-31)59-29-58-38)42(51)20-22-49-45(53)34-15-9-10-16-35(34)46(49)54/h3-18,24-26,36-37,50H,19-23,27-29H2,1-2H3,(H,47,52)/t36-,37-/m0/s1
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100n/an/an/an/an/an/an/an/a



University of California

Curated by ChEMBL


Assay Description
Inhibitory activity against Plasmepsin 2


J Med Chem 42: 1428-40 (1999)


Article DOI: 10.1021/jm980641t
BindingDB Entry DOI: 10.7270/Q2MS3RZX
More data for this
Ligand-Target Pair
3D
3D Structure (docked)
Plasmepsin 2


(Plasmodium falciparum)
BDBM8108
PNG
((2S)-N-[(2S,3S)-4-{[(1S)-2-[4-(2H-1,3-benzodioxol-...)
Show SMILES CC(C)[C@H](NC(=O)C1CCCCC1)C(=O)N[C@@H](Cc1ccccc1)[C@@H](O)CN[C@@H](Cc1ccc(cc1)-c1ccc2OCOc2c1)C(N)=O
Show InChI InChI=1S/C38H48N4O6/c1-24(2)35(42-37(45)28-11-7-4-8-12-28)38(46)41-30(19-25-9-5-3-6-10-25)32(43)22-40-31(36(39)44)20-26-13-15-27(16-14-26)29-17-18-33-34(21-29)48-23-47-33/h3,5-6,9-10,13-18,21,24,28,30-32,35,40,43H,4,7-8,11-12,19-20,22-23H2,1-2H3,(H2,39,44)(H,41,46)(H,42,45)/t30-,31-,32-,35-/m0/s1
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110n/an/an/an/an/an/an/an/a



Uppsala University



Assay Description
Enzyme activities were assayed by monitoring the hydrolysis of substrate in the presence or absence of inhibitor compounds. The hydrolysis was record...


J Comb Chem 5: 456-64 (2003)


Article DOI: 10.1021/cc0301014
BindingDB Entry DOI: 10.7270/Q27S7KZZ
More data for this
Ligand-Target Pair
3D
3D Structure (docked)
Plasmepsin 2


(Plasmodium falciparum)
BDBM8098
PNG
((2S)-N-[(2S,3S)-4-{[(1S)-1-carbamoyl-2-(4-phenylph...)
Show SMILES COc1cccc(C(=O)N[C@@H](C(C)C)C(=O)N[C@@H](Cc2ccccc2)[C@@H](O)CN[C@@H](Cc2ccc(cc2)-c2ccccc2)C(N)=O)c1OC
Show InChI InChI=1S/C39H46N4O6/c1-25(2)35(43-38(46)30-16-11-17-34(48-3)36(30)49-4)39(47)42-31(22-26-12-7-5-8-13-26)33(44)24-41-32(37(40)45)23-27-18-20-29(21-19-27)28-14-9-6-10-15-28/h5-21,25,31-33,35,41,44H,22-24H2,1-4H3,(H2,40,45)(H,42,47)(H,43,46)/t31-,32-,33-,35-/m0/s1
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110 -9.39n/an/an/an/an/a4.522



Uppsala University



Assay Description
Enzyme activities were assayed by monitoring the hydrolysis of substrate in the presence or absence of inhibitor compounds. The hydrolysis was record...


J Comb Chem 5: 456-64 (2003)


Article DOI: 10.1021/cc0301014
BindingDB Entry DOI: 10.7270/Q27S7KZZ
More data for this
Ligand-Target Pair
3D
3D Structure (docked)
Plasmepsin I


(Plasmodium falciparum)
BDBM8089
PNG
((2S)-N-[(2S,3S)-4-{[(1S)-2-(4-bromophenyl)-1-carba...)
Show SMILES COc1cccc(C(=O)N[C@@H](C(C)C)C(=O)N[C@@H](Cc2ccccc2)[C@@H](O)CN[C@@H](Cc2ccc(Br)cc2)C(N)=O)c1OC
Show InChI InChI=1S/C33H41BrN4O6/c1-20(2)29(38-32(41)24-11-8-12-28(43-3)30(24)44-4)33(42)37-25(17-21-9-6-5-7-10-21)27(39)19-36-26(31(35)40)18-22-13-15-23(34)16-14-22/h5-16,20,25-27,29,36,39H,17-19H2,1-4H3,(H2,35,40)(H,37,42)(H,38,41)/t25-,26-,27-,29-/m0/s1
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180n/an/an/an/an/an/an/an/a



Uppsala University



Assay Description
Enzyme activities were assayed by monitoring the hydrolysis of substrate in the presence or absence of inhibitor compounds. The hydrolysis was record...


J Comb Chem 5: 456-64 (2003)


Article DOI: 10.1021/cc0301014
BindingDB Entry DOI: 10.7270/Q27S7KZZ
More data for this
Ligand-Target Pair
3D
3D Structure (docked)
Plasmepsin 2


(Plasmodium falciparum)
BDBM50076286
PNG
(CHEMBL34051 | N-(2-Benzo[1,3]dioxol-5-yl-ethyl)-N-...)
Show SMILES O[C@@H](CN(CCc1ccc2OCOc2c1)C(=O)CCN1C(=O)c2ccccc2C1=O)[C@H](Cc1ccccc1)NC(=O)COc1cccc(Cl)c1
Show InChI InChI=1S/C38H36ClN3O8/c39-27-9-6-10-28(21-27)48-23-35(44)40-31(19-25-7-2-1-3-8-25)32(43)22-41(17-15-26-13-14-33-34(20-26)50-24-49-33)36(45)16-18-42-37(46)29-11-4-5-12-30(29)38(42)47/h1-14,20-21,31-32,43H,15-19,22-24H2,(H,40,44)/t31-,32-/m0/s1
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220n/an/an/an/an/an/an/an/a



University of California

Curated by ChEMBL


Assay Description
Inhibitory activity against Plasmepsin 2


J Med Chem 42: 1428-40 (1999)


Article DOI: 10.1021/jm980641t
BindingDB Entry DOI: 10.7270/Q2MS3RZX
More data for this
Ligand-Target Pair
3D
3D Structure (docked)
Plasmepsin 2


(Plasmodium falciparum)
BDBM50076290
PNG
(CHEMBL284151 | N-(2-Benzo[1,3]dioxol-5-yl-ethyl)-N...)
Show SMILES Cc1ccc(C)c(OCC(=O)N[C@@H](Cc2ccccc2)[C@@H](O)CN(CCc2ccc3OCOc3c2)C(=O)CCN2C(=O)c3ccccc3C2=O)c1
Show InChI InChI=1S/C40H41N3O8/c1-26-12-13-27(2)35(20-26)49-24-37(45)41-32(21-28-8-4-3-5-9-28)33(44)23-42(18-16-29-14-15-34-36(22-29)51-25-50-34)38(46)17-19-43-39(47)30-10-6-7-11-31(30)40(43)48/h3-15,20,22,32-33,44H,16-19,21,23-25H2,1-2H3,(H,41,45)/t32-,33-/m0/s1
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300n/an/an/an/an/an/an/an/a



University of California

Curated by ChEMBL


Assay Description
Inhibitory activity against Plasmepsin 2


J Med Chem 42: 1428-40 (1999)


Article DOI: 10.1021/jm980641t
BindingDB Entry DOI: 10.7270/Q2MS3RZX
More data for this
Ligand-Target Pair
3D
3D Structure (docked)
Cathepsin D


(Homo sapiens (human))
BDBM8098
PNG
((2S)-N-[(2S,3S)-4-{[(1S)-1-carbamoyl-2-(4-phenylph...)
Show SMILES COc1cccc(C(=O)N[C@@H](C(C)C)C(=O)N[C@@H](Cc2ccccc2)[C@@H](O)CN[C@@H](Cc2ccc(cc2)-c2ccccc2)C(N)=O)c1OC
Show InChI InChI=1S/C39H46N4O6/c1-25(2)35(43-38(46)30-16-11-17-34(48-3)36(30)49-4)39(47)42-31(22-26-12-7-5-8-13-26)33(44)24-41-32(37(40)45)23-27-18-20-29(21-19-27)28-14-9-6-10-15-28/h5-21,25,31-33,35,41,44H,22-24H2,1-4H3,(H2,40,45)(H,42,47)(H,43,46)/t31-,32-,33-,35-/m0/s1
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570n/an/an/an/an/an/an/an/a



Uppsala University



Assay Description
Enzyme activities were assayed by monitoring the hydrolysis of substrate in the presence or absence of inhibitor compounds. The hydrolysis was record...


J Comb Chem 5: 456-64 (2003)


Article DOI: 10.1021/cc0301014
BindingDB Entry DOI: 10.7270/Q27S7KZZ
More data for this
Ligand-Target Pair
Plasmepsin 2


(Plasmodium falciparum)
BDBM50071549
PNG
(CHEMBL309056 | N-[(S)-(1-Benzyl-3-butylcarbamoyl-2...)
Show SMILES CCCCNC(=O)CC(O)C(Cc1ccccc1)NC(=O)[C@@H](NC(=O)c1ccc(OC)cc1OC)c1ccccc1
Show InChI InChI=1S/C32H39N3O6/c1-4-5-18-33-29(37)21-27(36)26(19-22-12-8-6-9-13-22)34-32(39)30(23-14-10-7-11-15-23)35-31(38)25-17-16-24(40-2)20-28(25)41-3/h6-17,20,26-27,30,36H,4-5,18-19,21H2,1-3H3,(H,33,37)(H,34,39)(H,35,38)/t26?,27?,30-/m0/s1
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590n/an/an/an/an/an/an/an/a



Pharmacopeia, Inc.

Curated by ChEMBL


Assay Description
In vitro inhibition of plasmepsin-2 from Plasmodium falciparum.


Bioorg Med Chem Lett 8: 2315-20 (1999)


Article DOI: 10.1016/s0960-894x(98)00419-3
BindingDB Entry DOI: 10.7270/Q2SN09G9
More data for this
Ligand-Target Pair
3D
3D Structure (docked)
Plasmepsin 2


(Plasmodium falciparum)
BDBM8089
PNG
((2S)-N-[(2S,3S)-4-{[(1S)-2-(4-bromophenyl)-1-carba...)
Show SMILES COc1cccc(C(=O)N[C@@H](C(C)C)C(=O)N[C@@H](Cc2ccccc2)[C@@H](O)CN[C@@H](Cc2ccc(Br)cc2)C(N)=O)c1OC
Show InChI InChI=1S/C33H41BrN4O6/c1-20(2)29(38-32(41)24-11-8-12-28(43-3)30(24)44-4)33(42)37-25(17-21-9-6-5-7-10-21)27(39)19-36-26(31(35)40)18-22-13-15-23(34)16-14-22/h5-16,20,25-27,29,36,39H,17-19H2,1-4H3,(H2,35,40)(H,37,42)(H,38,41)/t25-,26-,27-,29-/m0/s1
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810 -8.22n/an/an/an/an/a4.522



Uppsala University



Assay Description
Enzyme activities were assayed by monitoring the hydrolysis of substrate in the presence or absence of inhibitor compounds. The hydrolysis was record...


J Comb Chem 5: 456-64 (2003)


Article DOI: 10.1021/cc0301014
BindingDB Entry DOI: 10.7270/Q27S7KZZ
More data for this
Ligand-Target Pair
3D
3D Structure (docked)
Cathepsin D


(Homo sapiens (human))
BDBM8101
PNG
((2S)-N-[(2S,3S)-4-{[(1S)-2-[4-(2H-1,3-benzodioxol-...)
Show SMILES CC(C)[C@H](NC(=O)c1ccccn1)C(=O)N[C@@H](Cc1ccccc1)[C@@H](O)CN[C@@H](Cc1ccc(cc1)-c1ccc2OCOc2c1)C(N)=O
Show InChI InChI=1S/C37H41N5O6/c1-23(2)34(42-36(45)28-10-6-7-17-39-28)37(46)41-29(18-24-8-4-3-5-9-24)31(43)21-40-30(35(38)44)19-25-11-13-26(14-12-25)27-15-16-32-33(20-27)48-22-47-32/h3-17,20,23,29-31,34,40,43H,18-19,21-22H2,1-2H3,(H2,38,44)(H,41,46)(H,42,45)/t29-,30-,31-,34-/m0/s1
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1.90E+3n/an/an/an/an/an/an/an/a



Uppsala University



Assay Description
Enzyme activities were assayed by monitoring the hydrolysis of substrate in the presence or absence of inhibitor compounds. The hydrolysis was record...


J Comb Chem 5: 456-64 (2003)


Article DOI: 10.1021/cc0301014
BindingDB Entry DOI: 10.7270/Q27S7KZZ
More data for this
Ligand-Target Pair
Cathepsin D


(Homo sapiens (human))
BDBM50071549
PNG
(CHEMBL309056 | N-[(S)-(1-Benzyl-3-butylcarbamoyl-2...)
Show SMILES CCCCNC(=O)CC(O)C(Cc1ccccc1)NC(=O)[C@@H](NC(=O)c1ccc(OC)cc1OC)c1ccccc1
Show InChI InChI=1S/C32H39N3O6/c1-4-5-18-33-29(37)21-27(36)26(19-22-12-8-6-9-13-22)34-32(39)30(23-14-10-7-11-15-23)35-31(38)25-17-16-24(40-2)20-28(25)41-3/h6-17,20,26-27,30,36H,4-5,18-19,21H2,1-3H3,(H,33,37)(H,34,39)(H,35,38)/t26?,27?,30-/m0/s1
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2.10E+3n/an/an/an/an/an/an/an/a



Pharmacopeia, Inc.

Curated by ChEMBL


Assay Description
Inhibitory activity against cathepsin D


Bioorg Med Chem Lett 8: 2315-20 (1999)


Article DOI: 10.1016/s0960-894x(98)00419-3
BindingDB Entry DOI: 10.7270/Q2SN09G9
More data for this
Ligand-Target Pair
Cathepsin D


(Homo sapiens (human))
BDBM8089
PNG
((2S)-N-[(2S,3S)-4-{[(1S)-2-(4-bromophenyl)-1-carba...)
Show SMILES COc1cccc(C(=O)N[C@@H](C(C)C)C(=O)N[C@@H](Cc2ccccc2)[C@@H](O)CN[C@@H](Cc2ccc(Br)cc2)C(N)=O)c1OC
Show InChI InChI=1S/C33H41BrN4O6/c1-20(2)29(38-32(41)24-11-8-12-28(43-3)30(24)44-4)33(42)37-25(17-21-9-6-5-7-10-21)27(39)19-36-26(31(35)40)18-22-13-15-23(34)16-14-22/h5-16,20,25-27,29,36,39H,17-19H2,1-4H3,(H2,35,40)(H,37,42)(H,38,41)/t25-,26-,27-,29-/m0/s1
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>2.90E+3n/an/an/an/an/an/an/an/a



Uppsala University



Assay Description
Enzyme activities were assayed by monitoring the hydrolysis of substrate in the presence or absence of inhibitor compounds. The hydrolysis was record...


J Comb Chem 5: 456-64 (2003)


Article DOI: 10.1021/cc0301014
BindingDB Entry DOI: 10.7270/Q27S7KZZ
More data for this
Ligand-Target Pair
Cathepsin D


(Homo sapiens (human))
BDBM8108
PNG
((2S)-N-[(2S,3S)-4-{[(1S)-2-[4-(2H-1,3-benzodioxol-...)
Show SMILES CC(C)[C@H](NC(=O)C1CCCCC1)C(=O)N[C@@H](Cc1ccccc1)[C@@H](O)CN[C@@H](Cc1ccc(cc1)-c1ccc2OCOc2c1)C(N)=O
Show InChI InChI=1S/C38H48N4O6/c1-24(2)35(42-37(45)28-11-7-4-8-12-28)38(46)41-30(19-25-9-5-3-6-10-25)32(43)22-40-31(36(39)44)20-26-13-15-27(16-14-26)29-17-18-33-34(21-29)48-23-47-33/h3,5-6,9-10,13-18,21,24,28,30-32,35,40,43H,4,7-8,11-12,19-20,22-23H2,1-2H3,(H2,39,44)(H,41,46)(H,42,45)/t30-,31-,32-,35-/m0/s1
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3.30E+3n/an/an/an/an/an/an/an/a



Uppsala University



Assay Description
Enzyme activities were assayed by monitoring the hydrolysis of substrate in the presence or absence of inhibitor compounds. The hydrolysis was record...


J Comb Chem 5: 456-64 (2003)


Article DOI: 10.1021/cc0301014
BindingDB Entry DOI: 10.7270/Q27S7KZZ
More data for this
Ligand-Target Pair
Cathepsin D


(Homo sapiens (human))
BDBM50071549
PNG
(CHEMBL309056 | N-[(S)-(1-Benzyl-3-butylcarbamoyl-2...)
Show SMILES CCCCNC(=O)CC(O)C(Cc1ccccc1)NC(=O)[C@@H](NC(=O)c1ccc(OC)cc1OC)c1ccccc1
Show InChI InChI=1S/C32H39N3O6/c1-4-5-18-33-29(37)21-27(36)26(19-22-12-8-6-9-13-22)34-32(39)30(23-14-10-7-11-15-23)35-31(38)25-17-16-24(40-2)20-28(25)41-3/h6-17,20,26-27,30,36H,4-5,18-19,21H2,1-3H3,(H,33,37)(H,34,39)(H,35,38)/t26?,27?,30-/m0/s1
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6.20E+3n/an/an/an/an/an/an/an/a



Pharmacopeia, Inc.

Curated by ChEMBL


Assay Description
Inhibitory activity against cathepsin D


Bioorg Med Chem Lett 8: 2315-20 (1999)


Article DOI: 10.1016/s0960-894x(98)00419-3
BindingDB Entry DOI: 10.7270/Q2SN09G9
More data for this
Ligand-Target Pair
Plasmepsin 2


(Plasmodium falciparum)
BDBM50071549
PNG
(CHEMBL309056 | N-[(S)-(1-Benzyl-3-butylcarbamoyl-2...)
Show SMILES CCCCNC(=O)CC(O)C(Cc1ccccc1)NC(=O)[C@@H](NC(=O)c1ccc(OC)cc1OC)c1ccccc1
Show InChI InChI=1S/C32H39N3O6/c1-4-5-18-33-29(37)21-27(36)26(19-22-12-8-6-9-13-22)34-32(39)30(23-14-10-7-11-15-23)35-31(38)25-17-16-24(40-2)20-28(25)41-3/h6-17,20,26-27,30,36H,4-5,18-19,21H2,1-3H3,(H,33,37)(H,34,39)(H,35,38)/t26?,27?,30-/m0/s1
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>3.00E+4n/an/an/an/an/an/an/an/a



Pharmacopeia, Inc.

Curated by ChEMBL


Assay Description
In vitro inhibition of plasmepsin-2 from Plasmodium falciparum.


Bioorg Med Chem Lett 8: 2315-20 (1999)


Article DOI: 10.1016/s0960-894x(98)00419-3
BindingDB Entry DOI: 10.7270/Q2SN09G9
More data for this
Ligand-Target Pair
3D
3D Structure (docked)
Plasmepsin 2


(Plasmodium falciparum)
BDBM50297442
PNG
(CHEMBL555902 | N-((2S,3R,4R,5S)-5-(2-chloro-4-fluo...)
Show SMILES O[C@@H]([C@H](O)[C@H](Cc1ccccc1)NC(=O)c1ccc(F)cc1Cl)[C@H](Cc1ccccc1)NC(=O)c1ccc2OCCOc2c1
Show InChI InChI=1S/C34H32ClFN2O6/c35-26-20-24(36)12-13-25(26)34(42)38-28(18-22-9-5-2-6-10-22)32(40)31(39)27(17-21-7-3-1-4-8-21)37-33(41)23-11-14-29-30(19-23)44-16-15-43-29/h1-14,19-20,27-28,31-32,39-40H,15-18H2,(H,37,41)(H,38,42)/t27-,28-,31+,32+/m0/s1
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n/an/a 1.18E+4n/an/an/an/an/an/a



National University of Singapore

Curated by ChEMBL


Assay Description
Inhibition of Plasmodium falciparum plasmepsin-2 in fluorescence microplate assay


Bioorg Med Chem Lett 19: 3945-8 (2009)


Article DOI: 10.1016/j.bmcl.2009.03.041
BindingDB Entry DOI: 10.7270/Q2TD9XD5
More data for this
Ligand-Target Pair
3D
3D Structure (docked)
Plasmepsin I


(Plasmodium falciparum)
BDBM50297442
PNG
(CHEMBL555902 | N-((2S,3R,4R,5S)-5-(2-chloro-4-fluo...)
Show SMILES O[C@@H]([C@H](O)[C@H](Cc1ccccc1)NC(=O)c1ccc(F)cc1Cl)[C@H](Cc1ccccc1)NC(=O)c1ccc2OCCOc2c1
Show InChI InChI=1S/C34H32ClFN2O6/c35-26-20-24(36)12-13-25(26)34(42)38-28(18-22-9-5-2-6-10-22)32(40)31(39)27(17-21-7-3-1-4-8-21)37-33(41)23-11-14-29-30(19-23)44-16-15-43-29/h1-14,19-20,27-28,31-32,39-40H,15-18H2,(H,37,41)(H,38,42)/t27-,28-,31+,32+/m0/s1
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n/an/a>2.50E+4n/an/an/an/an/an/a



National University of Singapore

Curated by ChEMBL


Assay Description
Inhibition of Plasmodium falciparum plasmepsin-1 in fluorescence microplate assay


Bioorg Med Chem Lett 19: 3945-8 (2009)


Article DOI: 10.1016/j.bmcl.2009.03.041
BindingDB Entry DOI: 10.7270/Q2TD9XD5
More data for this
Ligand-Target Pair