ID: ALA575101

Max Phase: Preclinical

Molecular Formula: C26H26ClNO4

Molecular Weight: 415.49

Molecule Type: Small molecule

Associated Items:

Representations

Canonical SMILES:  COc1ccc2c(c1OC)C(c1ccccc1)N1CCc3cc4c(cc3C1C2)OCO4.Cl

Standard InChI:  InChI=1S/C26H25NO4.ClH/c1-28-21-9-8-18-12-20-19-14-23-22(30-15-31-23)13-17(19)10-11-27(20)25(24(18)26(21)29-2)16-6-4-3-5-7-16;/h3-9,13-14,20,25H,10-12,15H2,1-2H3;1H

Standard InChI Key:  KPDKWIQWFCGORL-UHFFFAOYSA-N

Associated Targets(Human)

Ras-related C3 botulinum toxin substrate 1 221 Activities

Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID

Cell division control protein 42 homolog 123 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: 415.49Molecular Weight (Monoisotopic): 415.1784AlogP: 4.68#Rotatable Bonds: 3
Polar Surface Area: 40.16Molecular Species: NEUTRALHBA: 5HBD: 0
#RO5 Violations: 0HBA (Lipinski): 5HBD (Lipinski): 0#RO5 Violations (Lipinski): 0
CX Acidic pKa: CX Basic pKa: 5.62CX LogP: 4.87CX LogD: 4.86
Aromatic Rings: 3Heavy Atoms: 31QED Weighted: 0.62Np Likeness Score: 0.63

References

1. Beausoleil E, Chauvignac C, Taverne T, Lacombe S, Pognante L, Leblond B, Pallares D, Oliveira CD, Bachelot F, Carton R, Peillon H, Coutadeur S, Picard V, Lambeng N, Désiré L, Schweighoffer F..  (2009)  Structure-activity relationship of isoform selective inhibitors of Rac1/1b GTPase nucleotide binding.,  19  (19): [PMID:19716293] [10.1016/j.bmcl.2009.08.037]

Source