(S)-2-[2-(2-Guanidino-acetylamino)-acetylamino]-3-(4-phenylethynyl-phenyl)-propionic acid methyl ester

ID: ALA429868

Chembl Id: CHEMBL429868

PubChem CID: 11281972

Max Phase: Preclinical

Molecular Formula: C23H25N5O4

Molecular Weight: 435.48

Molecule Type: Protein

Associated Items:

Names and Identifiers

Canonical SMILES:  COC(=O)[C@H](Cc1ccc(C#Cc2ccccc2)cc1)NC(=O)CNC(=O)CN=C(N)N

Standard InChI:  InChI=1S/C23H25N5O4/c1-32-22(31)19(28-21(30)15-26-20(29)14-27-23(24)25)13-18-11-9-17(10-12-18)8-7-16-5-3-2-4-6-16/h2-6,9-12,19H,13-15H2,1H3,(H,26,29)(H,28,30)(H4,24,25,27)/t19-/m0/s1

Standard InChI Key:  PZRSPVXDDCJCBQ-IBGZPJMESA-N

Associated Targets(non-human)

Il2ra Interleukin-2 receptor alpha chain (47 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID

Molecule Features

Natural Product: NoOral: NoChemical Probe: NoParenteral: No
Molecule Type: ProteinTopical: 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: 435.48Molecular Weight (Monoisotopic): 435.1907AlogP: -0.32#Rotatable Bonds: 8
Polar Surface Area: 148.90Molecular Species: BASEHBA: 5HBD: 4
#RO5 Violations: HBA (Lipinski): 9HBD (Lipinski): 6#RO5 Violations (Lipinski): 1
CX Acidic pKa: 11.71CX Basic pKa: 10.32CX LogP: 0.60CX LogD: -1.55
Aromatic Rings: 2Heavy Atoms: 32QED Weighted: 0.19Np Likeness Score: -0.23

References

1. Raimundo BC, Oslob JD, Braisted AC, Hyde J, McDowell RS, Randal M, Waal ND, Wilkinson J, Yu CH, Arkin MR..  (2004)  Integrating fragment assembly and biophysical methods in the chemical advancement of small-molecule antagonists of IL-2: an approach for inhibiting protein-protein interactions.,  47  (12): [PMID:15163192] [10.1021/jm049967u]

Source