ID: ALA3353613

Max Phase: Preclinical

Molecular Formula: C31H50F9N7O6

Molecular Weight: 445.70

Molecule Type: Small molecule

Associated Items:

Representations

Canonical SMILES:  N=C(N)NCCCCCCCCNCCCCCCCCNC(=N)NCc1ccccc1.O=C(O)C(F)(F)F.O=C(O)C(F)(F)F.O=C(O)C(F)(F)F

Standard InChI:  InChI=1S/C25H47N7.3C2HF3O2/c26-24(27)30-20-14-7-3-1-5-12-18-29-19-13-6-2-4-8-15-21-31-25(28)32-22-23-16-10-9-11-17-23;3*3-2(4,5)1(6)7/h9-11,16-17,29H,1-8,12-15,18-22H2,(H4,26,27,30)(H3,28,31,32);3*(H,6,7)

Standard InChI Key:  JVLSOTRMGCFKDV-UHFFFAOYSA-N

Associated Targets(non-human)

Escherichia coli 133304 Activities

Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID

Aeromonas hydrophila 292 Activities

Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID

Acinetobacter baumannii 41033 Activities

Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID

Klebsiella pneumoniae 43867 Activities

Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID

Pseudomonas aeruginosa 123386 Activities

Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID

Bacillus subtilis 32866 Activities

Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID

Enterococcus faecalis 29875 Activities

Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID

Staphylococcus epidermidis 22802 Activities

Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID

Streptococcus pyogenes 16140 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: 445.70Molecular Weight (Monoisotopic): 445.3893AlogP: 4.05#Rotatable Bonds: 20
Polar Surface Area: 121.84Molecular Species: BASEHBA: 3HBD: 7
#RO5 Violations: 1HBA (Lipinski): 7HBD (Lipinski): 8#RO5 Violations (Lipinski): 1
CX Acidic pKa: CX Basic pKa: 12.63CX LogP: 4.26CX LogD: -3.54
Aromatic Rings: 1Heavy Atoms: 32QED Weighted: 0.09Np Likeness Score: -0.02

References

1. Maccari G, Sanfilippo S, De Luca F, Deodato D, Casian A, Dasso Lang MC, Zamperini C, Dreassi E, Rossolini GM, Docquier JD, Botta M..  (2014)  Synthesis of linear and cyclic guazatine derivatives endowed with antibacterial activity.,  24  (23): [PMID:25455183] [10.1016/j.bmcl.2014.09.081]

Source