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BDBM50094709 CHEMBL3589349

SMILES: OC(=O)CCCCCCC(=O)Nc1ccc(OS(=O)(=O)C2CC3OC2C(=C3c2ccc(O)cc2)c2ccc(O)cc2)cc1

InChI Key: InChIKey=IMGAXPLXFWWHLA-ZKCZORBVSA-N

Data: 2 KI  4 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 6 hits for monomerid = 50094709   
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
Estrogen receptor


(Homo sapiens (Human))
BDBM50094709
PNG
(CHEMBL3589349)
Show SMILES OC(=O)CCCCCCC(=O)Nc1ccc(OS(=O)(=O)C2CC3OC2C(=C3c2ccc(O)cc2)c2ccc(O)cc2)cc1 |c:26|
Show InChI InChI=1S/C60H93N17O17S2.C40H48N2O6/c1-4-31(2)48(63)59(93)75-42-30-96-95-29-41-51(85)66-27-47(82)76-23-9-13-43(76)58(92)70-36(12-5-7-21-61)52(86)71-38(25-33-15-17-34(79)18-16-33)54(88)73-40(28-78)55(89)68-35(49(64)83)11-6-8-22-65-46(81)20-19-37(69-56(42)90)53(87)72-39(26-45(62)80)60(94)77-24-10-14-44(77)57(91)67-32(3)50(84)74-41;1-41(2)17-15-27-22-34(44-6)36-24-30(27)31(41)19-25-9-12-29(13-10-25)47-40-38-28(23-37(45-7)39(40)46-8)16-18-42(3,4)32(38)20-26-11-14-33(43-5)35(21-26)48-36/h15-18,31-32,35-44,48,78-79H,4-14,19-30,61,63H2,1-3H3,(H2,62,80)(H2,64,83)(H,65,81)(H,66,85)(H,67,91)(H,68,89)(H,69,90)(H,70,92)(H,71,86)(H,72,87)(H,73,88)(H,74,84)(H,75,93);9-14,21-24,31-32H,15-20H2,1-8H3/q;+2/t31-,32-,35-,36-,37-,38-,39-,40-,41-,42-,43-,44-,48-;31-,32+/m00/s1
PDB

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PubMed
25n/an/an/an/an/an/an/an/a



Key Laboratory of Combinatorial Biosynthesis and Drug Discovery (Wuhan University)

Curated by ChEMBL


Assay Description
Binding affinity to human ER-alpha ligand binding domain after 2 hrs by competitive fluorometric binding assay


J Med Chem 58: 4550-72 (2015)


Article DOI: 10.1021/acs.jmedchem.5b00099
BindingDB Entry DOI: 10.7270/Q2Z321CF
More data for this
Ligand-Target Pair
Estradiol receptor beta (ERβ)


(Homo sapiens (Human))
BDBM50094709
PNG
(CHEMBL3589349)
Show SMILES OC(=O)CCCCCCC(=O)Nc1ccc(OS(=O)(=O)C2CC3OC2C(=C3c2ccc(O)cc2)c2ccc(O)cc2)cc1 |c:26|
Show InChI InChI=1S/C60H93N17O17S2.C40H48N2O6/c1-4-31(2)48(63)59(93)75-42-30-96-95-29-41-51(85)66-27-47(82)76-23-9-13-43(76)58(92)70-36(12-5-7-21-61)52(86)71-38(25-33-15-17-34(79)18-16-33)54(88)73-40(28-78)55(89)68-35(49(64)83)11-6-8-22-65-46(81)20-19-37(69-56(42)90)53(87)72-39(26-45(62)80)60(94)77-24-10-14-44(77)57(91)67-32(3)50(84)74-41;1-41(2)17-15-27-22-34(44-6)36-24-30(27)31(41)19-25-9-12-29(13-10-25)47-40-38-28(23-37(45-7)39(40)46-8)16-18-42(3,4)32(38)20-26-11-14-33(43-5)35(21-26)48-36/h15-18,31-32,35-44,48,78-79H,4-14,19-30,61,63H2,1-3H3,(H2,62,80)(H2,64,83)(H,65,81)(H,66,85)(H,67,91)(H,68,89)(H,69,90)(H,70,92)(H,71,86)(H,72,87)(H,73,88)(H,74,84)(H,75,93);9-14,21-24,31-32H,15-20H2,1-8H3/q;+2/t31-,32-,35-,36-,37-,38-,39-,40-,41-,42-,43-,44-,48-;31-,32+/m00/s1
PDB

UniProtKB/SwissProt
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antibodypedia
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Article
PubMed
773n/an/an/an/an/an/an/an/a



Key Laboratory of Combinatorial Biosynthesis and Drug Discovery (Wuhan University)

Curated by ChEMBL


Assay Description
Binding affinity to human ER-beta ligand binding domain after 2 hrs by competitive fluorometric binding assay


J Med Chem 58: 4550-72 (2015)


Article DOI: 10.1021/acs.jmedchem.5b00099
BindingDB Entry DOI: 10.7270/Q2Z321CF
More data for this
Ligand-Target Pair
Estradiol receptor beta (ERβ)


(Homo sapiens (Human))
BDBM50094709
PNG
(CHEMBL3589349)
Show SMILES OC(=O)CCCCCCC(=O)Nc1ccc(OS(=O)(=O)C2CC3OC2C(=C3c2ccc(O)cc2)c2ccc(O)cc2)cc1 |c:26|
Show InChI InChI=1S/C60H93N17O17S2.C40H48N2O6/c1-4-31(2)48(63)59(93)75-42-30-96-95-29-41-51(85)66-27-47(82)76-23-9-13-43(76)58(92)70-36(12-5-7-21-61)52(86)71-38(25-33-15-17-34(79)18-16-33)54(88)73-40(28-78)55(89)68-35(49(64)83)11-6-8-22-65-46(81)20-19-37(69-56(42)90)53(87)72-39(26-45(62)80)60(94)77-24-10-14-44(77)57(91)67-32(3)50(84)74-41;1-41(2)17-15-27-22-34(44-6)36-24-30(27)31(41)19-25-9-12-29(13-10-25)47-40-38-28(23-37(45-7)39(40)46-8)16-18-42(3,4)32(38)20-26-11-14-33(43-5)35(21-26)48-36/h15-18,31-32,35-44,48,78-79H,4-14,19-30,61,63H2,1-3H3,(H2,62,80)(H2,64,83)(H,65,81)(H,66,85)(H,67,91)(H,68,89)(H,69,90)(H,70,92)(H,71,86)(H,72,87)(H,73,88)(H,74,84)(H,75,93);9-14,21-24,31-32H,15-20H2,1-8H3/q;+2/t31-,32-,35-,36-,37-,38-,39-,40-,41-,42-,43-,44-,48-;31-,32+/m00/s1
PDB

UniProtKB/SwissProt
UniProtKB/TrEMBL

antibodypedia
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CHEMBL
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PC sid
UniChem

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Article
PubMed
n/an/a 160n/an/an/an/an/an/a



Key Laboratory of Combinatorial Biosynthesis and Drug Discovery (Wuhan University)

Curated by ChEMBL


Assay Description
Antagonist activity at ER-beta (unknown origin) transfected in HEK293T cells assessed as inhibition of transcriptional activity after 24 hrs by lucif...


J Med Chem 58: 4550-72 (2015)


Article DOI: 10.1021/acs.jmedchem.5b00099
BindingDB Entry DOI: 10.7270/Q2Z321CF
More data for this
Ligand-Target Pair
Cereblon/Histone deacetylase 6


(Homo sapiens (Human))
BDBM50094709
PNG
(CHEMBL3589349)
Show SMILES OC(=O)CCCCCCC(=O)Nc1ccc(OS(=O)(=O)C2CC3OC2C(=C3c2ccc(O)cc2)c2ccc(O)cc2)cc1 |c:26|
Show InChI InChI=1S/C60H93N17O17S2.C40H48N2O6/c1-4-31(2)48(63)59(93)75-42-30-96-95-29-41-51(85)66-27-47(82)76-23-9-13-43(76)58(92)70-36(12-5-7-21-61)52(86)71-38(25-33-15-17-34(79)18-16-33)54(88)73-40(28-78)55(89)68-35(49(64)83)11-6-8-22-65-46(81)20-19-37(69-56(42)90)53(87)72-39(26-45(62)80)60(94)77-24-10-14-44(77)57(91)67-32(3)50(84)74-41;1-41(2)17-15-27-22-34(44-6)36-24-30(27)31(41)19-25-9-12-29(13-10-25)47-40-38-28(23-37(45-7)39(40)46-8)16-18-42(3,4)32(38)20-26-11-14-33(43-5)35(21-26)48-36/h15-18,31-32,35-44,48,78-79H,4-14,19-30,61,63H2,1-3H3,(H2,62,80)(H2,64,83)(H,65,81)(H,66,85)(H,67,91)(H,68,89)(H,69,90)(H,70,92)(H,71,86)(H,72,87)(H,73,88)(H,74,84)(H,75,93);9-14,21-24,31-32H,15-20H2,1-8H3/q;+2/t31-,32-,35-,36-,37-,38-,39-,40-,41-,42-,43-,44-,48-;31-,32+/m00/s1
PDB
MMDB

NCI pathway
Reactome pathway
KEGG

UniProtKB/SwissProt
UniProtKB/TrEMBL

B.MOAD
DrugBank
antibodypedia
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CHEMBL
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Article
PubMed
n/an/a 8.34E+3n/an/an/an/an/an/a



Key Laboratory of Combinatorial Biosynthesis and Drug Discovery (Wuhan University)

Curated by ChEMBL


Assay Description
Inhibition of human recombinant HDAC6 after 15 mins by fluorogenic assay


J Med Chem 58: 4550-72 (2015)


Article DOI: 10.1021/acs.jmedchem.5b00099
BindingDB Entry DOI: 10.7270/Q2Z321CF
More data for this
Ligand-Target Pair
Histone deacetylase 1


(Homo sapiens (Human))
BDBM50094709
PNG
(CHEMBL3589349)
Show SMILES OC(=O)CCCCCCC(=O)Nc1ccc(OS(=O)(=O)C2CC3OC2C(=C3c2ccc(O)cc2)c2ccc(O)cc2)cc1 |c:26|
Show InChI InChI=1S/C60H93N17O17S2.C40H48N2O6/c1-4-31(2)48(63)59(93)75-42-30-96-95-29-41-51(85)66-27-47(82)76-23-9-13-43(76)58(92)70-36(12-5-7-21-61)52(86)71-38(25-33-15-17-34(79)18-16-33)54(88)73-40(28-78)55(89)68-35(49(64)83)11-6-8-22-65-46(81)20-19-37(69-56(42)90)53(87)72-39(26-45(62)80)60(94)77-24-10-14-44(77)57(91)67-32(3)50(84)74-41;1-41(2)17-15-27-22-34(44-6)36-24-30(27)31(41)19-25-9-12-29(13-10-25)47-40-38-28(23-37(45-7)39(40)46-8)16-18-42(3,4)32(38)20-26-11-14-33(43-5)35(21-26)48-36/h15-18,31-32,35-44,48,78-79H,4-14,19-30,61,63H2,1-3H3,(H2,62,80)(H2,64,83)(H,65,81)(H,66,85)(H,67,91)(H,68,89)(H,69,90)(H,70,92)(H,71,86)(H,72,87)(H,73,88)(H,74,84)(H,75,93);9-14,21-24,31-32H,15-20H2,1-8H3/q;+2/t31-,32-,35-,36-,37-,38-,39-,40-,41-,42-,43-,44-,48-;31-,32+/m00/s1
PDB
MMDB

NCI pathway
Reactome pathway
KEGG

UniProtKB/SwissProt
UniProtKB/TrEMBL

B.MOAD
DrugBank
antibodypedia
GoogleScholar
AffyNet 
CHEMBL
PC cid
PC sid
UniChem

Similars

Article
PubMed
n/an/a 107n/an/an/an/an/an/a



Key Laboratory of Combinatorial Biosynthesis and Drug Discovery (Wuhan University)

Curated by ChEMBL


Assay Description
Inhibition of human recombinant HDAC1 after 15 mins by fluorogenic assay


J Med Chem 58: 4550-72 (2015)


Article DOI: 10.1021/acs.jmedchem.5b00099
BindingDB Entry DOI: 10.7270/Q2Z321CF
More data for this
Ligand-Target Pair
Estrogen receptor


(Homo sapiens (Human))
BDBM50094709
PNG
(CHEMBL3589349)
Show SMILES OC(=O)CCCCCCC(=O)Nc1ccc(OS(=O)(=O)C2CC3OC2C(=C3c2ccc(O)cc2)c2ccc(O)cc2)cc1 |c:26|
Show InChI InChI=1S/C60H93N17O17S2.C40H48N2O6/c1-4-31(2)48(63)59(93)75-42-30-96-95-29-41-51(85)66-27-47(82)76-23-9-13-43(76)58(92)70-36(12-5-7-21-61)52(86)71-38(25-33-15-17-34(79)18-16-33)54(88)73-40(28-78)55(89)68-35(49(64)83)11-6-8-22-65-46(81)20-19-37(69-56(42)90)53(87)72-39(26-45(62)80)60(94)77-24-10-14-44(77)57(91)67-32(3)50(84)74-41;1-41(2)17-15-27-22-34(44-6)36-24-30(27)31(41)19-25-9-12-29(13-10-25)47-40-38-28(23-37(45-7)39(40)46-8)16-18-42(3,4)32(38)20-26-11-14-33(43-5)35(21-26)48-36/h15-18,31-32,35-44,48,78-79H,4-14,19-30,61,63H2,1-3H3,(H2,62,80)(H2,64,83)(H,65,81)(H,66,85)(H,67,91)(H,68,89)(H,69,90)(H,70,92)(H,71,86)(H,72,87)(H,73,88)(H,74,84)(H,75,93);9-14,21-24,31-32H,15-20H2,1-8H3/q;+2/t31-,32-,35-,36-,37-,38-,39-,40-,41-,42-,43-,44-,48-;31-,32+/m00/s1
PDB

UniProtKB/SwissProt
UniProtKB/TrEMBL

antibodypedia
GoogleScholar
AffyNet 
CHEMBL
PC cid
PC sid
UniChem

Similars

Article
PubMed
n/an/a 50n/an/an/an/an/an/a



Key Laboratory of Combinatorial Biosynthesis and Drug Discovery (Wuhan University)

Curated by ChEMBL


Assay Description
Antagonist activity at ER-alpha (unknown origin) transfected in HEK293T cells assessed as inhibition of transcriptional activity after 24 hrs by luci...


J Med Chem 58: 4550-72 (2015)


Article DOI: 10.1021/acs.jmedchem.5b00099
BindingDB Entry DOI: 10.7270/Q2Z321CF
More data for this
Ligand-Target Pair