BindingDB logo
myBDB logout
Compile Data Set for Download or QSAR

Found 10 hits with Last Name = 'pore' and Initial = 'v'   
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
Cholesterol side-chain cleavage enzyme, mitochondrial


(Rattus norvegicus)
BDBM50335519
PNG
((S)-3,6-Diamino-hexanoic acid {(3S,9S,12S,15S)-3-(...)
Show SMILES CN[C@H](CC(C)C)C(=O)N[C@@H]1[C@H](O)c2ccc(Oc3cc4cc(Oc5ccc(cc5Cl)[C@@H](O)[C@@H]5NC(=O)[C@H](NC(=O)[C@@H]4NC(=O)[C@H](CC(N)=O)NC1=O)c1ccc(O)c(c1)-c1c(O)cc(O)cc1[C@H](NC5=O)C(O)=O)c3O[C@@H]1O[C@H](CO)[C@@H](O)[C@H](O)[C@H]1O[C@H]1C[C@](C)(N)[C@H](O)[C@H](C)O1)c(Cl)c2 |r|
Show InChI InChI=1S/C66H75Cl2N9O24/c1-23(2)12-34(71-5)58(88)76-49-51(83)26-7-10-38(32(67)14-26)97-40-16-28-17-41(55(40)101-65-56(54(86)53(85)42(22-78)99-65)100-44-21-66(4,70)57(87)24(3)96-44)98-39-11-8-27(15-33(39)68)52(84)50-63(93)75-48(64(94)95)31-18-29(79)19-37(81)45(31)30-13-25(6-9-36(30)80)46(60(90)77-50)74-61(91)47(28)73-59(89)35(20-43(69)82)72-62(49)92/h6-11,13-19,23-24,34-35,42,44,46-54,56-57,65,71,78-81,83-87H,12,20-22,70H2,1-5H3,(H2,69,82)(H,72,92)(H,73,89)(H,74,91)(H,75,93)(H,76,88)(H,77,90)(H,94,95)/t24-,34+,35-,42+,44-,46+,47+,48-,49+,50-,51+,52+,53+,54-,56+,57+,65-,66-/m0/s1
Reactome pathway
KEGG

UniProtKB/SwissProt

GoogleScholar
AffyNet 
Purchase

CHEMBL
DrugBank
MCE
PC cid
PC sid
UniChem

Patents


Similars

PubMed
n/an/a 41.4n/an/an/an/an/an/a



National Chemical Laboratory

Curated by ChEMBL


Assay Description
Antibacterial activity against gram positive bacteria Enterococcus faecalis was determined by twofold Micro-broth dilution assay


Bioorg Med Chem Lett 14: 773-7 (2004)


BindingDB Entry DOI: 10.7270/Q2FJ2JZ3
More data for this
Ligand-Target Pair
Cholesterol side-chain cleavage enzyme, mitochondrial


(Rattus norvegicus)
BDBM50103513
PNG
(CHEBI:17076 | Chemform | Gerox | NSC-14083 | Strep...)
Show SMILES CN[C@H]1[C@H](O)[C@@H](O)[C@H](CO)O[C@H]1O[C@H]1[C@H](O[C@H]2[C@H](O)[C@@H](O)[C@H](NC(N)=N)[C@@H](O)[C@@H]2NC(N)=N)O[C@@H](C)[C@]1(O)C=O
Show InChI InChI=1S/C21H39N7O12/c1-5-21(36,4-30)16(40-17-9(26-2)13(34)10(31)6(3-29)38-17)18(37-5)39-15-8(28-20(24)25)11(32)7(27-19(22)23)12(33)14(15)35/h4-18,26,29,31-36H,3H2,1-2H3,(H4,22,23,27)(H4,24,25,28)/t5-,6-,7+,8-,9-,10-,11+,12-,13-,14+,15+,16-,17-,18-,21+/m0/s1
Reactome pathway
KEGG

UniProtKB/SwissProt

GoogleScholar
AffyNet 
Purchase

DrugBank
MCE
KEGG
PC cid
PC sid
PDB
UniChem

Similars

PubMed
n/an/a 2.23E+3n/an/an/an/an/an/a



National Chemical Laboratory

Curated by ChEMBL


Assay Description
Antibacterial activity against gram positive bacteria Enterococcus faecalis was determined by twofold Micro-broth dilution assay


Bioorg Med Chem Lett 14: 773-7 (2004)


BindingDB Entry DOI: 10.7270/Q2FJ2JZ3
More data for this
Ligand-Target Pair
Cholesterol side-chain cleavage enzyme, mitochondrial


(Rattus norvegicus)
BDBM50221769
PNG
(CHEMBL166184)
Show SMILES [H][C@@]1(CC[C@@]2([H])[C@]3([H])CC[C@]4([H])C[C@H](O)CC[C@]4(C)[C@@]3([H])C[C@H](O)[C@]12C)[C@H](C)CCC(=O)N[C@@H](CO)[C@@H](O)c1ccc(cc1)[N+]([O-])=O
Show InChI InChI=1S/C33H50N2O7/c1-19(4-13-30(39)34-28(18-36)31(40)20-5-8-22(9-6-20)35(41)42)25-11-12-26-24-10-7-21-16-23(37)14-15-32(21,2)27(24)17-29(38)33(25,26)3/h5-6,8-9,19,21,23-29,31,36-38,40H,4,7,10-18H2,1-3H3,(H,34,39)/t19-,21-,23-,24+,25-,26+,27+,28+,29+,31+,32+,33-/m1/s1
Reactome pathway
KEGG

UniProtKB/SwissProt

GoogleScholar
AffyNet 
CHEMBL
PC cid
PC sid
UniChem

Similars

PubMed
n/an/a 1.70E+4n/an/an/an/an/an/a



National Chemical Laboratory

Curated by ChEMBL


Assay Description
Antibacterial activity against gram positive bacteria Enterococcus faecalis was determined by twofold Micro-broth dilution assay


Bioorg Med Chem Lett 14: 773-7 (2004)


BindingDB Entry DOI: 10.7270/Q2FJ2JZ3
More data for this
Ligand-Target Pair
Cholesterol side-chain cleavage enzyme, mitochondrial


(Rattus norvegicus)
BDBM50221777
PNG
(CHEMBL352932)
Show SMILES [H][C@@]1(CC[C@@]2([H])[C@]3([H])CC[C@]4([H])C[C@H](O)CC[C@]4(C)[C@@]3([H])C[C@H](O)[C@]12C)[C@H](C)CCC(=O)N[C@H](CO)[C@H](O)c1ccc(cc1)[N+]([O-])=O
Show InChI InChI=1S/C33H50N2O7/c1-19(4-13-30(39)34-28(18-36)31(40)20-5-8-22(9-6-20)35(41)42)25-11-12-26-24-10-7-21-16-23(37)14-15-32(21,2)27(24)17-29(38)33(25,26)3/h5-6,8-9,19,21,23-29,31,36-38,40H,4,7,10-18H2,1-3H3,(H,34,39)/t19-,21-,23-,24+,25-,26+,27+,28-,29+,31-,32+,33-/m1/s1
Reactome pathway
KEGG

UniProtKB/SwissProt

GoogleScholar
AffyNet 
CHEMBL
PC cid
PC sid
UniChem

Similars

PubMed
n/an/a 2.55E+4n/an/an/an/an/an/a



National Chemical Laboratory

Curated by ChEMBL


Assay Description
Antibacterial activity against gram positive bacteria Enterococcus faecalis was determined by twofold Micro-broth dilution assay


Bioorg Med Chem Lett 14: 773-7 (2004)


BindingDB Entry DOI: 10.7270/Q2FJ2JZ3
More data for this
Ligand-Target Pair
Cholesterol side-chain cleavage enzyme, mitochondrial


(Rattus norvegicus)
BDBM50221774
PNG
(CHEMBL353406)
Show SMILES [H][C@@]1(CC[C@@]2([H])[C@]3([H])C(O)C[C@]4([H])C[C@H](O)CC[C@]4(C)[C@@]3([H])C[C@H](O)[C@]12C)[C@H](C)CCC(=O)N[C@@H](CO)[C@@H](O)c1ccccc1
Show InChI InChI=1S/C33H51NO6/c1-19(9-12-29(39)34-26(18-35)31(40)20-7-5-4-6-8-20)23-10-11-24-30-25(17-28(38)33(23,24)3)32(2)14-13-22(36)15-21(32)16-27(30)37/h4-8,19,21-28,30-31,35-38,40H,9-18H2,1-3H3,(H,34,39)/t19-,21+,22-,23-,24+,25+,26+,27?,28+,30+,31+,32+,33-/m1/s1
Reactome pathway
KEGG

UniProtKB/SwissProt

GoogleScholar
AffyNet 
CHEMBL
PC cid
PC sid
UniChem

Similars

PubMed
n/an/a 7.17E+4n/an/an/an/an/an/a



National Chemical Laboratory

Curated by ChEMBL


Assay Description
Antibacterial activity against gram positive bacteria Enterococcus faecalis was determined by twofold Micro-broth dilution assay


Bioorg Med Chem Lett 14: 773-7 (2004)


BindingDB Entry DOI: 10.7270/Q2FJ2JZ3
More data for this
Ligand-Target Pair
Cholesterol side-chain cleavage enzyme, mitochondrial


(Rattus norvegicus)
BDBM50221746
PNG
(CHEMBL354064)
Show SMILES [H][C@@]1(CC[C@@]2([H])[C@]3([H])C(O)C[C@]4([H])C[C@H](O)CC[C@]4(C)[C@@]3([H])C[C@H](O)[C@]12C)[C@H](C)CCC(=O)N[C@H](CO)[C@H](O)c1ccc(cc1)[N+]([O-])=O
Show InChI InChI=1S/C33H50N2O8/c1-18(4-11-29(40)34-26(17-36)31(41)19-5-7-21(8-6-19)35(42)43)23-9-10-24-30-25(16-28(39)33(23,24)3)32(2)13-12-22(37)14-20(32)15-27(30)38/h5-8,18,20,22-28,30-31,36-39,41H,4,9-17H2,1-3H3,(H,34,40)/t18-,20+,22-,23-,24+,25+,26-,27?,28+,30+,31-,32+,33-/m1/s1
Reactome pathway
KEGG

UniProtKB/SwissProt

GoogleScholar
AffyNet 
CHEMBL
PC cid
PC sid
UniChem

Patents


Similars

PubMed
n/an/a 9.95E+4n/an/an/an/an/an/a



National Chemical Laboratory

Curated by ChEMBL


Assay Description
Antibacterial activity against gram positive bacteria Enterococcus faecalis was determined by twofold Micro-broth dilution assay


Bioorg Med Chem Lett 14: 773-7 (2004)


BindingDB Entry DOI: 10.7270/Q2FJ2JZ3
More data for this
Ligand-Target Pair
Cholesterol side-chain cleavage enzyme, mitochondrial


(Rattus norvegicus)
BDBM50221744
PNG
(CHEMBL349656)
Show SMILES [H][C@@]1(CC[C@@]2([H])[C@]3([H])C(O)C[C@]4([H])C[C@H](O)CC[C@]4(C)[C@@]3([H])C[C@H](O)[C@]12C)[C@H](C)CCC(=O)N[C@H](CO)[C@H](O)c1ccccc1
Show InChI InChI=1S/C33H51NO6/c1-19(9-12-29(39)34-26(18-35)31(40)20-7-5-4-6-8-20)23-10-11-24-30-25(17-28(38)33(23,24)3)32(2)14-13-22(36)15-21(32)16-27(30)37/h4-8,19,21-28,30-31,35-38,40H,9-18H2,1-3H3,(H,34,39)/t19-,21+,22-,23-,24+,25+,26-,27?,28+,30+,31-,32+,33-/m1/s1
Reactome pathway
KEGG

UniProtKB/SwissProt

GoogleScholar
AffyNet 
CHEMBL
PC cid
PC sid
UniChem

Similars

PubMed
n/an/a 1.07E+5n/an/an/an/an/an/a



National Chemical Laboratory

Curated by ChEMBL


Assay Description
Antibacterial activity against gram positive bacteria Enterococcus faecalis was determined by twofold Micro-broth dilution assay


Bioorg Med Chem Lett 14: 773-7 (2004)


BindingDB Entry DOI: 10.7270/Q2FJ2JZ3
More data for this
Ligand-Target Pair
Cholesterol side-chain cleavage enzyme, mitochondrial


(Rattus norvegicus)
BDBM50221745
PNG
(CHEMBL350726)
Show SMILES [H][C@@]1(CC[C@@]2([H])[C@]3([H])CC[C@]4([H])C[C@H](O)CC[C@]4(C)[C@@]3([H])C[C@H](O)[C@]12C)[C@H](C)CCC(=O)N[C@H](CO)[C@H](O)c1ccccc1
Show InChI InChI=1S/C33H51NO5/c1-20(9-14-30(38)34-28(19-35)31(39)21-7-5-4-6-8-21)25-12-13-26-24-11-10-22-17-23(36)15-16-32(22,2)27(24)18-29(37)33(25,26)3/h4-8,20,22-29,31,35-37,39H,9-19H2,1-3H3,(H,34,38)/t20-,22-,23-,24+,25-,26+,27+,28-,29+,31-,32+,33-/m1/s1
Reactome pathway
KEGG

UniProtKB/SwissProt

GoogleScholar
AffyNet 
CHEMBL
PC cid
PC sid
UniChem

Patents


Similars

PubMed
n/an/a 1.10E+5n/an/an/an/an/an/a



National Chemical Laboratory

Curated by ChEMBL


Assay Description
Antibacterial activity against gram positive bacteria Enterococcus faecalis was determined by twofold Micro-broth dilution assay


Bioorg Med Chem Lett 14: 773-7 (2004)


BindingDB Entry DOI: 10.7270/Q2FJ2JZ3
More data for this
Ligand-Target Pair
Cholesterol side-chain cleavage enzyme, mitochondrial


(Rattus norvegicus)
BDBM50221743
PNG
(CHEMBL352152)
Show SMILES [H][C@@]1(CC[C@@]2([H])[C@]3([H])C(O)C[C@]4([H])C[C@H](O)CC[C@]4(C)[C@@]3([H])C[C@H](O)[C@]12C)[C@H](C)CCC(=O)N[C@@H](CO)[C@@H](O)c1ccc(cc1)[N+]([O-])=O
Show InChI InChI=1S/C33H50N2O8/c1-18(4-11-29(40)34-26(17-36)31(41)19-5-7-21(8-6-19)35(42)43)23-9-10-24-30-25(16-28(39)33(23,24)3)32(2)13-12-22(37)14-20(32)15-27(30)38/h5-8,18,20,22-28,30-31,36-39,41H,4,9-17H2,1-3H3,(H,34,40)/t18-,20+,22-,23-,24+,25+,26+,27?,28+,30+,31+,32+,33-/m1/s1
Reactome pathway
KEGG

UniProtKB/SwissProt

GoogleScholar
AffyNet 
CHEMBL
PC cid
PC sid
UniChem

Patents


Similars

PubMed
n/an/a>4.14E+5n/an/an/an/an/an/a



National Chemical Laboratory

Curated by ChEMBL


Assay Description
Antibacterial activity against gram positive bacteria Enterococcus faecalis was determined by twofold Micro-broth dilution assay


Bioorg Med Chem Lett 14: 773-7 (2004)


BindingDB Entry DOI: 10.7270/Q2FJ2JZ3
More data for this
Ligand-Target Pair
Cholesterol side-chain cleavage enzyme, mitochondrial


(Rattus norvegicus)
BDBM50221775
PNG
(CHEMBL164621)
Show SMILES [H][C@@]1(CC[C@@]2([H])[C@]3([H])CC[C@]4([H])C[C@H](O)CC[C@]4(C)[C@@]3([H])C[C@H](O)[C@]12C)[C@H](C)CCC(=O)N[C@@H](CO)[C@@H](O)c1ccccc1
Show InChI InChI=1S/C33H51NO5/c1-20(9-14-30(38)34-28(19-35)31(39)21-7-5-4-6-8-21)25-12-13-26-24-11-10-22-17-23(36)15-16-32(22,2)27(24)18-29(37)33(25,26)3/h4-8,20,22-29,31,35-37,39H,9-19H2,1-3H3,(H,34,38)/t20-,22-,23-,24+,25-,26+,27+,28+,29+,31+,32+,33-/m1/s1
Reactome pathway
KEGG

UniProtKB/SwissProt

GoogleScholar
AffyNet 
CHEMBL
PC cid
PC sid
UniChem

Similars

PubMed
n/an/a>4.61E+5n/an/an/an/an/an/a



National Chemical Laboratory

Curated by ChEMBL


Assay Description
Antibacterial activity against gram positive bacteria Enterococcus faecalis was determined by twofold Micro-broth dilution assay


Bioorg Med Chem Lett 14: 773-7 (2004)


BindingDB Entry DOI: 10.7270/Q2FJ2JZ3
More data for this
Ligand-Target Pair