ID: ALA4793174

Max Phase: Preclinical

Molecular Formula: C32H27N7O4

Molecular Weight: 573.61

Molecule Type: Unknown

Associated Items:

Representations

Canonical SMILES:  CCOc1nc2cccc(C(=O)NCc3ccc4c(c3)OCO4)c2n1Cc1ccc(-c2ccccc2-c2nnn[nH]2)cc1

Standard InChI:  InChI=1S/C32H27N7O4/c1-2-41-32-34-26-9-5-8-25(31(40)33-17-21-12-15-27-28(16-21)43-19-42-27)29(26)39(32)18-20-10-13-22(14-11-20)23-6-3-4-7-24(23)30-35-37-38-36-30/h3-16H,2,17-19H2,1H3,(H,33,40)(H,35,36,37,38)

Standard InChI Key:  ZPMBCTZDTLYROO-UHFFFAOYSA-N

Associated Targets(Human)

NEDD8-activating enzyme E1 regulatory subunit 121 Activities

Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID

A549 127892 Activities

Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID

Molecule Features

Natural Product: NoOral: NoChemical Probe: NoParenteral: No
Molecule Type: UnknownTopical: 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: 573.61Molecular Weight (Monoisotopic): 573.2125AlogP: 4.99#Rotatable Bonds: 9
Polar Surface Area: 129.07Molecular Species: ACIDHBA: 9HBD: 2
#RO5 Violations: 1HBA (Lipinski): 11HBD (Lipinski): 2#RO5 Violations (Lipinski): 2
CX Acidic pKa: 4.23CX Basic pKa: 1.91CX LogP: 5.44CX LogD: 3.84
Aromatic Rings: 6Heavy Atoms: 43QED Weighted: 0.25Np Likeness Score: -1.19

References

1. Chen X,Yang X,Mao F,Wei J,Xu Y,Li B,Zhu J,Ni S,Jia L,Li J.  (2021)  Development of novel benzimidazole-derived neddylation inhibitors for suppressing tumor growth invitro and invivo.,  210  [PMID:33129593] [10.1016/j.ejmech.2020.112964]

Source