ID: ALA2391386

Max Phase: Preclinical

Molecular Formula: C27H39N3

Molecular Weight: 405.63

Molecule Type: Small molecule

Associated Items:

Representations

Canonical SMILES:  CCCCCCCCCCCCN(Cc1nc2ccccc2[nH]1)c1ccc(C)cc1

Standard InChI:  InChI=1S/C27H39N3/c1-3-4-5-6-7-8-9-10-11-14-21-30(24-19-17-23(2)18-20-24)22-27-28-25-15-12-13-16-26(25)29-27/h12-13,15-20H,3-11,14,21-22H2,1-2H3,(H,28,29)

Standard InChI Key:  KELCQTYJEGNJNT-UHFFFAOYSA-N

Associated Targets(non-human)

Aspergillus flavus 8875 Activities

Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID

Saccharomyces cerevisiae 19171 Activities

Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID

Cyberlindnera jadinii 900 Activities

Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID

Candida 1648 Activities

Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID

Candida albicans 78123 Activities

Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID

Salmonella typhi 4293 Activities

Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID

Pseudomonas aeruginosa 123386 Activities

Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID

Escherichia coli 133304 Activities

Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID

Bacillus 868 Activities

Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID

Micrococcus luteus 7463 Activities

Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID

Bacillus subtilis 32866 Activities

Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID

Staphylococcus aureus 210822 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: 405.63Molecular Weight (Monoisotopic): 405.3144AlogP: 7.80#Rotatable Bonds: 14
Polar Surface Area: 31.92Molecular Species: NEUTRALHBA: 2HBD: 1
#RO5 Violations: 1HBA (Lipinski): 3HBD (Lipinski): 1#RO5 Violations (Lipinski): 1
CX Acidic pKa: 11.47CX Basic pKa: 5.05CX LogP: 8.56CX LogD: 8.56
Aromatic Rings: 3Heavy Atoms: 30QED Weighted: 0.28Np Likeness Score: -1.06

References

1. Zhang HZ, Damu GL, Cai GX, Zhou CH..  (2013)  Design, synthesis and antimicrobial evaluation of novel benzimidazole type of Fluconazole analogues and their synergistic effects with Chloromycin, Norfloxacin and Fluconazole.,  64  [PMID:23644216] [10.1016/j.ejmech.2013.03.049]

Source