ID: ALA2070260

Max Phase: Preclinical

Molecular Formula: C24H26BrN3O3

Molecular Weight: 484.39

Molecule Type: Small molecule

Associated Items:

Representations

Canonical SMILES:  CCCCCCn1cc(COc2ccc(C(=O)/C=C/c3ccc(Br)cc3)c(O)c2)nn1

Standard InChI:  InChI=1S/C24H26BrN3O3/c1-2-3-4-5-14-28-16-20(26-27-28)17-31-21-11-12-22(24(30)15-21)23(29)13-8-18-6-9-19(25)10-7-18/h6-13,15-16,30H,2-5,14,17H2,1H3/b13-8+

Standard InChI Key:  SESSKLXWMJLTNZ-MDWZMJQESA-N

Associated Targets(non-human)

Mycolicibacterium aurum 354 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: 484.39Molecular Weight (Monoisotopic): 483.1158AlogP: 5.80#Rotatable Bonds: 11
Polar Surface Area: 77.24Molecular Species: NEUTRALHBA: 6HBD: 1
#RO5 Violations: 1HBA (Lipinski): 6HBD (Lipinski): 1#RO5 Violations (Lipinski): 1
CX Acidic pKa: 7.09CX Basic pKa: CX LogP: 6.91CX LogD: 6.44
Aromatic Rings: 3Heavy Atoms: 31QED Weighted: 0.21Np Likeness Score: -0.74

References

1. Anand N, Singh P, Sharma A, Tiwari S, Singh V, Singh DK, Srivastava KK, Singh BN, Tripathi RP..  (2012)  Synthesis and evaluation of small libraries of triazolylmethoxy chalcones, flavanones and 2-aminopyrimidines as inhibitors of mycobacterial FAS-II and PknG.,  20  (17): [PMID:22854194] [10.1016/j.bmc.2012.07.009]

Source