(R)-2-((4E,6E)-(2S,3S)-3-Acetylamino-7-biphenyl-4-yl-2,6-dimethyl-hepta-4,6-dienoylamino)-propionic acid

ID: ALA98309

Chembl Id: CHEMBL98309

PubChem CID: 44330451

Max Phase: Preclinical

Molecular Formula: C26H30N2O4

Molecular Weight: 434.54

Molecule Type: Small molecule

Associated Items:

Names and Identifiers

Canonical SMILES:  CC(=O)N[C@@H](/C=C/C(C)=C/c1ccc(-c2ccccc2)cc1)[C@H](C)C(=O)N[C@H](C)C(=O)O

Standard InChI:  InChI=1S/C26H30N2O4/c1-17(16-21-11-13-23(14-12-21)22-8-6-5-7-9-22)10-15-24(28-20(4)29)18(2)25(30)27-19(3)26(31)32/h5-16,18-19,24H,1-4H3,(H,27,30)(H,28,29)(H,31,32)/b15-10+,17-16+/t18-,19+,24-/m0/s1

Standard InChI Key:  AQMMABVSCIIRQI-NJFSSMHLSA-N

Associated Targets(Human)

PPM1B Tchem Protein phosphatase 2C beta (71 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID

Associated Targets(non-human)

PPP2CA Serine/threonine protein phosphatase 2A, catalytic subunit, alpha isoform (49 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID

Molecule Features

Natural Product: NoOral: NoChemical Probe: NoParenteral: No
Molecule Type: Small moleculeTopical: NoFirst In Class: NoBlack Box: No
Chirality: NoAvailability: NoProdrug: No

Drug Indications

MESH IDMESH Heading EFO IDsEFO TermsMax Phase for IndicationReferences

Mechanisms of Action

Mechanism of ActionAction Typetarget IDTarget NameTarget TypeTarget OrganismBinding Site NameReferences

Calculated Properties

Molecular Weight: 434.54Molecular Weight (Monoisotopic): 434.2206AlogP: 4.04#Rotatable Bonds: 9
Polar Surface Area: 95.50Molecular Species: ACIDHBA: 3HBD: 3
#RO5 Violations: HBA (Lipinski): 6HBD (Lipinski): 3#RO5 Violations (Lipinski):
CX Acidic pKa: 3.87CX Basic pKa: CX LogP: 3.73CX LogD: 0.50
Aromatic Rings: 2Heavy Atoms: 32QED Weighted: 0.52Np Likeness Score: 0.20

References

1. Gulledge BM, Aggen JB, Eng H, Sweimeh K, Chamberlin AR..  (2003)  Microcystin analogues comprised only of Adda and a single additional amino acid retain moderate activity as PP1/PP2A inhibitors.,  13  (17): [PMID:14611855] [10.1016/s0960-894x(03)00588-2]

Source