ID: ALA5273421

Max Phase: Preclinical

Molecular Formula: C32H39NO3

Molecular Weight: 485.67

Associated Items:

Representations

Canonical SMILES:  CCCCCCCCCCCC1=C(O)C(=O)C2=C(Nc3ccccc3C2c2ccc(C)c(C)c2)C1=O

Standard InChI:  InChI=1S/C32H39NO3/c1-4-5-6-7-8-9-10-11-12-16-25-30(34)29-28(32(36)31(25)35)27(23-19-18-21(2)22(3)20-23)24-15-13-14-17-26(24)33-29/h13-15,17-20,27,33,35H,4-12,16H2,1-3H3

Standard InChI Key:  JLYGVVIIOSDZRW-UHFFFAOYSA-N

Associated Targets(Human)

MCF7 126967 Activities

Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID

Associated Targets(non-human)

J774.A1 2436 Activities

Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID

H9c2 3506 Activities

Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID

Mitogen-activated protein kinase 1 and 3 (ERK2 and ERK1) 27 Activities

Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID

Molecule Features

Natural Product: NoOral: NoChemical Probe: NoParenteral: No
Molecule Type: Topical: 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: 485.67Molecular Weight (Monoisotopic): 485.2930AlogP: 8.00#Rotatable Bonds: 11
Polar Surface Area: 66.40Molecular Species: ACIDHBA: 4HBD: 2
#RO5 Violations: 1HBA (Lipinski): 4HBD (Lipinski): 2#RO5 Violations (Lipinski): 1
CX Acidic pKa: 5.94CX Basic pKa: CX LogP: 8.71CX LogD: 7.24
Aromatic Rings: 2Heavy Atoms: 36QED Weighted: 0.25Np Likeness Score: 0.37

References

1. Martín-Acosta P, Cuadrado I, González-Cofrade L, Pestano R, Hortelano S, de Las Heras B, Estévez-Braun A..  (2023)  Synthesis of Quinoline and Dihydroquinoline Embelin Derivatives as Cardioprotective Agents.,  86  (2.0): [PMID:36749898] [10.1021/acs.jnatprod.2c00924]

Source