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BDBM104500 US8575114, I-12

SMILES: Cc1cc2nn(Cc3cc(ccc3Cl)[C@@H]3O[C@H](CO)[C@@H](O)[C@H](O)[C@H]3O)c(=O)n2cc1Cl

InChI Key: InChIKey=LIKSGJKEDNKMAF-FTWQHDNSSA-N

Data: 10 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 10 hits for monomerid = 104500   
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
Sodium/glucose cotransporter 2


(Homo sapiens (Human))
BDBM104500
PNG
(US8575114, I-12)
Show SMILES Cc1cc2nn(Cc3cc(ccc3Cl)[C@@H]3O[C@H](CO)[C@@H](O)[C@H](O)[C@H]3O)c(=O)n2cc1Cl |r|
Show InChI InChI=1S/C20H21Cl2N3O6/c1-9-4-15-23-25(20(30)24(15)7-13(9)22)6-11-5-10(2-3-12(11)21)19-18(29)17(28)16(27)14(8-26)31-19/h2-5,7,14,16-19,26-29H,6,8H2,1H3/t14-,16-,17+,18-,19+/m1/s1
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US Patent
n/an/a 36.6n/an/an/an/an/an/a



Albany Molecular Research, Inc.

US Patent


Assay Description
The inhibitory activity of the compounds of this invention against the SGLT-1 or SGLT-2 transporters.


US Patent US8575114 (2013)


BindingDB Entry DOI: 10.7270/Q23B5XTT
More data for this
Ligand-Target Pair
Sodium/glucose cotransporter 1 (SGLT1)


(Homo sapiens (Human))
BDBM104500
PNG
(US8575114, I-12)
Show SMILES Cc1cc2nn(Cc3cc(ccc3Cl)[C@@H]3O[C@H](CO)[C@@H](O)[C@H](O)[C@H]3O)c(=O)n2cc1Cl |r|
Show InChI InChI=1S/C20H21Cl2N3O6/c1-9-4-15-23-25(20(30)24(15)7-13(9)22)6-11-5-10(2-3-12(11)21)19-18(29)17(28)16(27)14(8-26)31-19/h2-5,7,14,16-19,26-29H,6,8H2,1H3/t14-,16-,17+,18-,19+/m1/s1
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US Patent
n/an/a>9.00E+4n/an/an/an/an/an/a



Albany Molecular Research, Inc.

US Patent


Assay Description
The inhibitory activity of the compounds of this invention against the SGLT-1 or SGLT-2 transporters.


US Patent US8575114 (2013)


BindingDB Entry DOI: 10.7270/Q23B5XTT
More data for this
Ligand-Target Pair
Sodium/glucose cotransporter 2


(Homo sapiens (Human))
BDBM104500
PNG
(US8575114, I-12)
Show SMILES Cc1cc2nn(Cc3cc(ccc3Cl)[C@@H]3O[C@H](CO)[C@@H](O)[C@H](O)[C@H]3O)c(=O)n2cc1Cl |r|
Show InChI InChI=1S/C20H21Cl2N3O6/c1-9-4-15-23-25(20(30)24(15)7-13(9)22)6-11-5-10(2-3-12(11)21)19-18(29)17(28)16(27)14(8-26)31-19/h2-5,7,14,16-19,26-29H,6,8H2,1H3/t14-,16-,17+,18-,19+/m1/s1
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Article
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n/an/a 33n/an/an/an/an/an/a



AMRI

Curated by ChEMBL


Assay Description
Inhibition of human SGLT2 expressed in CHOK1 cells assessed as inhibition of [14C]-AMG uptake after 3 hrs by microbeta scintillation counting analysi...


Bioorg Med Chem 22: 3414-22 (2014)


Article DOI: 10.1016/j.bmc.2014.04.036
BindingDB Entry DOI: 10.7270/Q2H70HCT
More data for this
Ligand-Target Pair
Sodium/glucose cotransporter 1 (SGLT1)


(Homo sapiens (Human))
BDBM104500
PNG
(US8575114, I-12)
Show SMILES Cc1cc2nn(Cc3cc(ccc3Cl)[C@@H]3O[C@H](CO)[C@@H](O)[C@H](O)[C@H]3O)c(=O)n2cc1Cl |r|
Show InChI InChI=1S/C20H21Cl2N3O6/c1-9-4-15-23-25(20(30)24(15)7-13(9)22)6-11-5-10(2-3-12(11)21)19-18(29)17(28)16(27)14(8-26)31-19/h2-5,7,14,16-19,26-29H,6,8H2,1H3/t14-,16-,17+,18-,19+/m1/s1
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n/an/a>9.00E+4n/an/an/an/an/an/a



AMRI

Curated by ChEMBL


Assay Description
Inhibition of human SGLT1 expressed in CHOK1 cells assessed as inhibition of [14C]-AMG uptake after 3 hrs by microbeta scintillation counting analysi...


Bioorg Med Chem 22: 3414-22 (2014)


Article DOI: 10.1016/j.bmc.2014.04.036
BindingDB Entry DOI: 10.7270/Q2H70HCT
More data for this
Ligand-Target Pair
Cytochrome P450 3A4


(Homo sapiens (Human))
BDBM104500
PNG
(US8575114, I-12)
Show SMILES Cc1cc2nn(Cc3cc(ccc3Cl)[C@@H]3O[C@H](CO)[C@@H](O)[C@H](O)[C@H]3O)c(=O)n2cc1Cl |r|
Show InChI InChI=1S/C20H21Cl2N3O6/c1-9-4-15-23-25(20(30)24(15)7-13(9)22)6-11-5-10(2-3-12(11)21)19-18(29)17(28)16(27)14(8-26)31-19/h2-5,7,14,16-19,26-29H,6,8H2,1H3/t14-,16-,17+,18-,19+/m1/s1
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n/an/a>1.10E+4n/an/an/an/an/an/a



AMRI

Curated by ChEMBL


Assay Description
Inhibition of CYP3A4 (unknown origin)


Bioorg Med Chem 22: 3414-22 (2014)


Article DOI: 10.1016/j.bmc.2014.04.036
BindingDB Entry DOI: 10.7270/Q2H70HCT
More data for this
Ligand-Target Pair
Cytochrome P450 2B6


(Homo sapiens (Human))
BDBM104500
PNG
(US8575114, I-12)
Show SMILES Cc1cc2nn(Cc3cc(ccc3Cl)[C@@H]3O[C@H](CO)[C@@H](O)[C@H](O)[C@H]3O)c(=O)n2cc1Cl |r|
Show InChI InChI=1S/C20H21Cl2N3O6/c1-9-4-15-23-25(20(30)24(15)7-13(9)22)6-11-5-10(2-3-12(11)21)19-18(29)17(28)16(27)14(8-26)31-19/h2-5,7,14,16-19,26-29H,6,8H2,1H3/t14-,16-,17+,18-,19+/m1/s1
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n/an/a>1.10E+4n/an/an/an/an/an/a



AMRI

Curated by ChEMBL


Assay Description
Inhibition of CYP2B6 (unknown origin)


Bioorg Med Chem 22: 3414-22 (2014)


Article DOI: 10.1016/j.bmc.2014.04.036
BindingDB Entry DOI: 10.7270/Q2H70HCT
More data for this
Ligand-Target Pair
Cytochrome P450 2C9


(Homo sapiens (Human))
BDBM104500
PNG
(US8575114, I-12)
Show SMILES Cc1cc2nn(Cc3cc(ccc3Cl)[C@@H]3O[C@H](CO)[C@@H](O)[C@H](O)[C@H]3O)c(=O)n2cc1Cl |r|
Show InChI InChI=1S/C20H21Cl2N3O6/c1-9-4-15-23-25(20(30)24(15)7-13(9)22)6-11-5-10(2-3-12(11)21)19-18(29)17(28)16(27)14(8-26)31-19/h2-5,7,14,16-19,26-29H,6,8H2,1H3/t14-,16-,17+,18-,19+/m1/s1
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n/an/a>1.10E+4n/an/an/an/an/an/a



AMRI

Curated by ChEMBL


Assay Description
Inhibition of CYP2C9 (unknown origin)


Bioorg Med Chem 22: 3414-22 (2014)


Article DOI: 10.1016/j.bmc.2014.04.036
BindingDB Entry DOI: 10.7270/Q2H70HCT
More data for this
Ligand-Target Pair
Cytochrome P450 2C19


(Homo sapiens (Human))
BDBM104500
PNG
(US8575114, I-12)
Show SMILES Cc1cc2nn(Cc3cc(ccc3Cl)[C@@H]3O[C@H](CO)[C@@H](O)[C@H](O)[C@H]3O)c(=O)n2cc1Cl |r|
Show InChI InChI=1S/C20H21Cl2N3O6/c1-9-4-15-23-25(20(30)24(15)7-13(9)22)6-11-5-10(2-3-12(11)21)19-18(29)17(28)16(27)14(8-26)31-19/h2-5,7,14,16-19,26-29H,6,8H2,1H3/t14-,16-,17+,18-,19+/m1/s1
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n/an/a>1.10E+4n/an/an/an/an/an/a



AMRI

Curated by ChEMBL


Assay Description
Inhibition of CYP2C19 (unknown origin)


Bioorg Med Chem 22: 3414-22 (2014)


Article DOI: 10.1016/j.bmc.2014.04.036
BindingDB Entry DOI: 10.7270/Q2H70HCT
More data for this
Ligand-Target Pair
Cytochrome P450 2D6


(Homo sapiens (Human))
BDBM104500
PNG
(US8575114, I-12)
Show SMILES Cc1cc2nn(Cc3cc(ccc3Cl)[C@@H]3O[C@H](CO)[C@@H](O)[C@H](O)[C@H]3O)c(=O)n2cc1Cl |r|
Show InChI InChI=1S/C20H21Cl2N3O6/c1-9-4-15-23-25(20(30)24(15)7-13(9)22)6-11-5-10(2-3-12(11)21)19-18(29)17(28)16(27)14(8-26)31-19/h2-5,7,14,16-19,26-29H,6,8H2,1H3/t14-,16-,17+,18-,19+/m1/s1
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n/an/a>1.10E+4n/an/an/an/an/an/a



AMRI

Curated by ChEMBL


Assay Description
Inhibition of CYP2D6 (unknown origin)


Bioorg Med Chem 22: 3414-22 (2014)


Article DOI: 10.1016/j.bmc.2014.04.036
BindingDB Entry DOI: 10.7270/Q2H70HCT
More data for this
Ligand-Target Pair
Cytochrome P450 1A


(Homo sapiens (Human))
BDBM104500
PNG
(US8575114, I-12)
Show SMILES Cc1cc2nn(Cc3cc(ccc3Cl)[C@@H]3O[C@H](CO)[C@@H](O)[C@H](O)[C@H]3O)c(=O)n2cc1Cl |r|
Show InChI InChI=1S/C20H21Cl2N3O6/c1-9-4-15-23-25(20(30)24(15)7-13(9)22)6-11-5-10(2-3-12(11)21)19-18(29)17(28)16(27)14(8-26)31-19/h2-5,7,14,16-19,26-29H,6,8H2,1H3/t14-,16-,17+,18-,19+/m1/s1
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n/an/a>1.10E+4n/an/an/an/an/an/a



AMRI

Curated by ChEMBL


Assay Description
Inhibition of CYP1A2 (unknown origin)


Bioorg Med Chem 22: 3414-22 (2014)


Article DOI: 10.1016/j.bmc.2014.04.036
BindingDB Entry DOI: 10.7270/Q2H70HCT
More data for this
Ligand-Target Pair