KAEMPFEROL 3-O-D-GALACTOSIDE

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Molecule Category Free-form
UNII 7CKD5ET5SP
Source Gaulton A, Kale N, van Westen GJ, Bellis LJ, Bento AP, Davies M, Hersey A, Papadatos G, Forster M, Wege P, Overington JP. A large-scale crop protection bioassay data set. Sci Data. 2015 Jul 7;2:150032. Read more ...

Structure

InChI Key JPUKWEQWGBDDQB-HBDJNLTOSA-N
Smiles OC[C@H]1OC(OC2=C(Oc3cc(O)cc(O)c3C2=O)c4ccc(O)cc4)[C@H](O)[C@@H](O)[C@H]1O
InChI
InChI=1S/C21H20O11/c22-7-13-15(26)17(28)18(29)21(31-13)32-20-16(27)14-11(25)5-10(24)6-12(14)30-19(20)8-1-3-9(23)4-2-8/h1-6,13,15,17-18,21-26,28-29H,7H2/t13-,15+,17+,18-,21?/m1/s1

Physicochemical Descriptors

Property Name Value
Molecular Formula C21H20O11
Molecular Weight 448.38
AlogP -0.06
Hydrogen Bond Acceptor 11.0
Hydrogen Bond Donor 7.0
Number of Rotational Bond 4.0
Polar Surface Area 186.36
Molecular species ACID
Aromatic Rings 2.0
Heavy Atoms 32.0

Pharmacology

Targets EC50(nM) IC50(nM) Kd(nM) Ki(nM) Inhibition(%)
Enzyme Hydrolase
- 12 - - -
EC50(nM) IC50(nM) Kd(nM) Ki(nM) Inhibition(%)
Homo sapiens
- 12 - - -

Cross References

Resources Reference
ChEMBL CHEMBL2297279
FDA SRS 7CKD5ET5SP
PubChem 5488283
SureChEMBL SCHEMBL572288
CONTENTS