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BDBM3227 1-{[2,6-dihydroxy-4-({[(3R,4R)-4-[(4-hydroxybenzene)amido]pyrrolidin-3-yl]oxy}carbonyl)phenyl]carbonyl}naphthalene-2-carboxylic acid::Modified Benzophenone Ring, Balanol Analog 27::trans-3-(4-Hydroxybenzamido)-4-[3,5-dihydroxy-4-(2-carboxy-1-naphthylcarbonyl)benzoyloxy]pyrrolidine

SMILES: OC(=O)c1ccc2ccccc2c1C(=O)c1c(O)cc(cc1O)C(=O)O[C@@H]1CNC[C@H]1NC(=O)c1ccc(O)cc1

InChI Key: InChIKey=CTBULQFIIOEIHV-ZJSXRUAMSA-N

Data: 4 IC50

Find this compound or compounds like it in BindingDB or PDB:
   Substructure
Similarity at least:  must be >=0.5
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Activity Spreadsheet -- Enzyme Inhibition Constant Data from BindingDB

Found 4 hits for monomerid = 3227   
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
Protein kinase C alpha type


(Homo sapiens (Human))
BDBM3227
PNG
(1-{[2,6-dihydroxy-4-({[(3R,4R)-4-[(4-hydroxybenzen...)
Show SMILES OC(=O)c1ccc2ccccc2c1C(=O)c1c(O)cc(cc1O)C(=O)O[C@@H]1CNC[C@H]1NC(=O)c1ccc(O)cc1 |r|
Show InChI InChI=1S/C30H24N2O9/c33-18-8-5-16(6-9-18)28(37)32-21-13-31-14-24(21)41-30(40)17-11-22(34)26(23(35)12-17)27(36)25-19-4-2-1-3-15(19)7-10-20(25)29(38)39/h1-12,21,24,31,33-35H,13-14H2,(H,32,37)(H,38,39)/t21-,24-/m1/s1
PDB
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PC cid
PC sid
UniChem

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Article
PubMed
n/an/a 7.80E+3n/an/an/an/an/an/a



Sphinx Laboratories



Assay Description
PKC was assayed by quantitating the incorporation of 32P from [gamma-32P]ATP into histone type IIIs.


J Med Chem 45: 2624-43 (2002)


Article DOI: 10.1021/jm020018f
BindingDB Entry DOI: 10.7270/Q2BG2M50
More data for this
Ligand-Target Pair
cAMP-Dependent Protein Kinase (PKA)


(Bos taurus (bovine))
BDBM3227
PNG
(1-{[2,6-dihydroxy-4-({[(3R,4R)-4-[(4-hydroxybenzen...)
Show SMILES OC(=O)c1ccc2ccccc2c1C(=O)c1c(O)cc(cc1O)C(=O)O[C@@H]1CNC[C@H]1NC(=O)c1ccc(O)cc1 |r|
Show InChI InChI=1S/C30H24N2O9/c33-18-8-5-16(6-9-18)28(37)32-21-13-31-14-24(21)41-30(40)17-11-22(34)26(23(35)12-17)27(36)25-19-4-2-1-3-15(19)7-10-20(25)29(38)39/h1-12,21,24,31,33-35H,13-14H2,(H,32,37)(H,38,39)/t21-,24-/m1/s1
PDB

UniProtKB/SwissProt

GoogleScholar
AffyNet 
PC cid
PC sid
UniChem

Similars

Article
PubMed
n/an/a 330n/an/an/an/an/an/a



Sphinx Laboratories



Assay Description
The activity of PKA, activated by cAMP, is measured by its ability to transfer phosphate from [gamma-32P]ATP to histone.


J Med Chem 45: 2624-43 (2002)


Article DOI: 10.1021/jm020018f
BindingDB Entry DOI: 10.7270/Q2BG2M50
More data for this
Ligand-Target Pair
Protein kinase C, epsilon


(Homo sapiens (Human))
BDBM3227
PNG
(1-{[2,6-dihydroxy-4-({[(3R,4R)-4-[(4-hydroxybenzen...)
Show SMILES OC(=O)c1ccc2ccccc2c1C(=O)c1c(O)cc(cc1O)C(=O)O[C@@H]1CNC[C@H]1NC(=O)c1ccc(O)cc1 |r|
Show InChI InChI=1S/C30H24N2O9/c33-18-8-5-16(6-9-18)28(37)32-21-13-31-14-24(21)41-30(40)17-11-22(34)26(23(35)12-17)27(36)25-19-4-2-1-3-15(19)7-10-20(25)29(38)39/h1-12,21,24,31,33-35H,13-14H2,(H,32,37)(H,38,39)/t21-,24-/m1/s1
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PC sid
UniChem

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Article
PubMed
n/an/a 4.60E+3n/an/an/an/an/an/a



Sphinx Laboratories



Assay Description
PKC was assayed by quantitating the incorporation of 32P from [gamma-32P]ATP into histone type IIIs.


J Med Chem 45: 2624-43 (2002)


Article DOI: 10.1021/jm020018f
BindingDB Entry DOI: 10.7270/Q2BG2M50
More data for this
Ligand-Target Pair
PKC alpha and beta-2


(Homo sapiens (Human))
BDBM3227
PNG
(1-{[2,6-dihydroxy-4-({[(3R,4R)-4-[(4-hydroxybenzen...)
Show SMILES OC(=O)c1ccc2ccccc2c1C(=O)c1c(O)cc(cc1O)C(=O)O[C@@H]1CNC[C@H]1NC(=O)c1ccc(O)cc1 |r|
Show InChI InChI=1S/C30H24N2O9/c33-18-8-5-16(6-9-18)28(37)32-21-13-31-14-24(21)41-30(40)17-11-22(34)26(23(35)12-17)27(36)25-19-4-2-1-3-15(19)7-10-20(25)29(38)39/h1-12,21,24,31,33-35H,13-14H2,(H,32,37)(H,38,39)/t21-,24-/m1/s1
PDB
MMDB

NCI pathway
Reactome pathway
KEGG

UniProtKB/SwissProt

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

Similars

Article
PubMed
n/an/a 8.00E+3n/an/an/an/an/an/a



Sphinx Laboratories



Assay Description
PKC was assayed by quantitating the incorporation of 32P from [gamma-32P]ATP into histone type IIIs.


J Med Chem 45: 2624-43 (2002)


Article DOI: 10.1021/jm020018f
BindingDB Entry DOI: 10.7270/Q2BG2M50
More data for this
Ligand-Target Pair