(2S)-N-{(1S)-2-AMINO-1-[4-(1,1-DIOXIDO-3-OXO-2,3-DIHYDROISOTHIAZOL-5-YL)BENZYL]-2-OXOETHYL}-3-PHENYL-2-[(PHENYLACETYL)AMINO]PROPANAMIDE

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Molecule Category Free-form
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 JZINOMQSKFFHFP-ZEQRLZLVSA-N
Smiles NC(=O)[C@H](Cc1ccc(cc1)C2=CC(=O)NS2(=O)=O)NC(=O)[C@H](Cc3ccccc3)NC(=O)Cc4ccccc4
InChI
InChI=1S/C29H28N4O6S/c30-28(36)23(15-21-11-13-22(14-12-21)25-18-27(35)33-40(25,38)39)32-29(37)24(16-19-7-3-1-4-8-19)31-26(34)17-20-9-5-2-6-10-20/h1-14,18,23-24H,15-17H2,(H2,30,36)(H,31,34)(H,32,37)(H,33,35)/t23-,24-/m0/s1

Physicochemical Descriptors

Property Name Value
Molecular Formula C29H28N4O6S
Molecular Weight 560.62
AlogP 1.77
Hydrogen Bond Acceptor 6.0
Hydrogen Bond Donor 4.0
Number of Rotational Bond 11.0
Polar Surface Area 172.91
Molecular species ACID
Aromatic Rings 3.0
Heavy Atoms 40.0

Pharmacology

Targets EC50(nM) IC50(nM) Kd(nM) Ki(nM) Inhibition(%)
Enzyme Phosphatase Protein Phosphatase Tyrosine protein phosphatase
- 1000000 - - -
EC50(nM) IC50(nM) Kd(nM) Ki(nM) Inhibition(%)
Homo sapiens
- 1000000 - - -

Cross References

Resources Reference
ChEMBL CHEMBL2297020
PubChem 58746618
SureChEMBL SCHEMBL5892857
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