ID: ALA2401882

Max Phase: Preclinical

Molecular Formula: C15H17BrF2N4O2

Molecular Weight: 403.23

Molecule Type: Small molecule

Associated Items:

Representations

Canonical SMILES:  Cc1ncc([N+](=O)[O-])n1CCN(CCBr)Cc1ccc(F)cc1F

Standard InChI:  InChI=1S/C15H17BrF2N4O2/c1-11-19-9-15(22(23)24)21(11)7-6-20(5-4-16)10-12-2-3-13(17)8-14(12)18/h2-3,8-9H,4-7,10H2,1H3

Standard InChI Key:  YTPNHBFCIIBAMV-UHFFFAOYSA-N

Associated Targets(non-human)

Candida 1648 Activities

Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID

Candida albicans 78123 Activities

Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID

Proteus vulgaris 5823 Activities

Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID

Pseudomonas aeruginosa 123386 Activities

Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID

Shigella dysenteriae 933 Activities

Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID

Escherichia coli 133304 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: 403.23Molecular Weight (Monoisotopic): 402.0503AlogP: 3.28#Rotatable Bonds: 8
Polar Surface Area: 64.20Molecular Species: NEUTRALHBA: 5HBD: 0
#RO5 Violations: 0HBA (Lipinski): 6HBD (Lipinski): 0#RO5 Violations (Lipinski): 0
CX Acidic pKa: CX Basic pKa: 5.90CX LogP: 3.11CX LogD: 3.10
Aromatic Rings: 2Heavy Atoms: 24QED Weighted: 0.39Np Likeness Score: -2.08

References

1. Zhang L, Chang JJ, Zhang SL, Damu GL, Geng RX, Zhou CH..  (2013)  Synthesis and bioactive evaluation of novel hybrids of metronidazole and berberine as new type of antimicrobial agents and their transportation behavior by human serum albumin.,  21  (14): [PMID:23743440] [10.1016/j.bmc.2013.05.007]

Source