ID: ALA2425264

Max Phase: Preclinical

Molecular Formula: C48H30Br3N3O6

Molecular Weight: 984.50

Molecule Type: Small molecule

Associated Items:

Representations

Canonical SMILES:  O=C(/C=C/c1ccc(Oc2nc(Oc3ccc(/C=C/C(=O)c4ccc(Br)cc4)cc3)nc(Oc3ccc(/C=C/C(=O)c4ccc(Br)cc4)cc3)n2)cc1)c1ccc(Br)cc1

Standard InChI:  InChI=1S/C48H30Br3N3O6/c49-37-16-10-34(11-17-37)43(55)28-7-31-1-22-40(23-2-31)58-46-52-47(59-41-24-3-32(4-25-41)8-29-44(56)35-12-18-38(50)19-13-35)54-48(53-46)60-42-26-5-33(6-27-42)9-30-45(57)36-14-20-39(51)21-15-36/h1-30H/b28-7+,29-8+,30-9+

Standard InChI Key:  HFBQVRMQACHONS-RVDOLHKDSA-N

Associated Targets(non-human)

Proteus vulgaris 5823 Activities

Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID

Staphylococcus aureus 210822 Activities

Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID

Pectobacterium carotovorum 295 Activities

Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID

Alternaria 24 Activities

Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID

Curvularia 47 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: 984.50Molecular Weight (Monoisotopic): 980.9685AlogP: 13.22#Rotatable Bonds: 15
Polar Surface Area: 117.57Molecular Species: NEUTRALHBA: 9HBD: 0
#RO5 Violations: 2HBA (Lipinski): 9HBD (Lipinski): 0#RO5 Violations (Lipinski): 2
CX Acidic pKa: CX Basic pKa: CX LogP: 14.45CX LogD: 14.45
Aromatic Rings: 7Heavy Atoms: 60QED Weighted: 0.07Np Likeness Score: -0.22

References

1. Khan FG, Yadav MV, Sagar AD.  (2013)  Synthesis, characterization, and antimicrobial evaluation of novel trichalcones containing core s-triazine moiety,  [10.1007/s00044-013-0837-4]

Source