ID: ALA166018

Max Phase: Preclinical

Molecular Formula: C31H25N3O5

Molecular Weight: 519.56

Molecule Type: Small molecule

Associated Items:

Representations

Canonical SMILES:  CC(=O)Nc1cccc(-c2ccc(C(=O)N3CCc4c([nH]c5ccccc45)C3c3ccc4c(c3)OCO4)o2)c1

Standard InChI:  InChI=1S/C31H25N3O5/c1-18(35)32-21-6-4-5-19(15-21)25-11-12-27(39-25)31(36)34-14-13-23-22-7-2-3-8-24(22)33-29(23)30(34)20-9-10-26-28(16-20)38-17-37-26/h2-12,15-16,30,33H,13-14,17H2,1H3,(H,32,35)

Standard InChI Key:  FATPWUGVUTWOQJ-UHFFFAOYSA-N

Associated Targets(Human)

PDE5A Tclin Phosphodiesterase 5A (5113 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

Properties

Molecular Weight: 519.56Molecular Weight (Monoisotopic): 519.1794AlogP: 5.90#Rotatable Bonds: 4
Polar Surface Area: 96.80Molecular Species: NEUTRALHBA: 5HBD: 2
#RO5 Violations: 2HBA (Lipinski): 8HBD (Lipinski): 2#RO5 Violations (Lipinski): 2
CX Acidic pKa: CX Basic pKa: CX LogP: 4.33CX LogD: 4.33
Aromatic Rings: 5Heavy Atoms: 39QED Weighted: 0.31Np Likeness Score: -0.85

References

1. Sui Z, Guan J, Macielag MJ, Jiang W, Qiu Y, Kraft P, Bhattacharjee S, John TM, Craig E, Haynes-Johnson D, Clancy J..  (2003)  Synthesis and biological activities of novel beta-carbolines as PDE5 inhibitors.,  13  (4): [PMID:12639576] [10.1016/s0960-894x(02)01036-3]
2. Beato A, Gori A, Boucherle B, Peuchmaur M, Haudecoeur R..  (2021)  β-Carboline as a Privileged Scaffold for Multitarget Strategies in Alzheimer's Disease Therapy.,  64  (3.0): [PMID:33528252] [10.1021/acs.jmedchem.0c01887]

Source