ID: ALA4583313

Max Phase: Preclinical

Molecular Formula: C35H76N14O

Molecular Weight: 709.09

Molecule Type: Unknown

Associated Items:

Representations

Canonical SMILES:  CCNC(=N)NCCCCCCN(CCCCCCNC(=N)N)C(=O)N(CCCCCCNC(=N)NCC)CCCCCCNC(=N)NCC

Standard InChI:  InChI=1S/C35H76N14O/c1-4-41-32(38)45-24-16-8-12-20-28-48(27-19-11-7-15-23-44-31(36)37)35(50)49(29-21-13-9-17-25-46-33(39)42-5-2)30-22-14-10-18-26-47-34(40)43-6-3/h4-30H2,1-3H3,(H4,36,37,44)(H3,38,41,45)(H3,39,42,46)(H3,40,43,47)

Standard InChI Key:  MXAMOYXHKGZNSY-UHFFFAOYSA-N

Associated Targets(non-human)

Bacillus spizizenii 1898 Activities

Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID

Enterococcus faecalis 29875 Activities

Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID

Staphylococcus aureus 210822 Activities

Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID

Streptococcus pyogenes 16140 Activities

Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID

Acinetobacter baumannii 41033 Activities

Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID

Escherichia coli 133304 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

Molecule Features

Natural Product: NoOral: NoChemical Probe: NoParenteral: No
Molecule Type: UnknownTopical: 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: 709.09Molecular Weight (Monoisotopic): 708.6327AlogP: 3.84#Rotatable Bonds: 31
Polar Surface Area: 229.18Molecular Species: BASEHBA: 5HBD: 12
#RO5 Violations: 2HBA (Lipinski): 15HBD (Lipinski): 13#RO5 Violations (Lipinski): 3
CX Acidic pKa: CX Basic pKa: 12.85CX LogP: 2.78CX LogD: -6.88
Aromatic Rings: 0Heavy Atoms: 50QED Weighted: 0.03Np Likeness Score: -0.06

References

1. Pasero C, D'Agostino I, De Luca F, Zamperini C, Deodato D, Truglio GI, Sannio F, Del Prete R, Ferraro T, Visaggio D, Mancini A, Guglielmi MB, Visca P, Docquier JD, Botta M..  (2018)  Alkyl-guanidine Compounds as Potent Broad-Spectrum Antibacterial Agents: Chemical Library Extension and Biological Characterization.,  61  (20): [PMID:30265809] [10.1021/acs.jmedchem.8b00619]

Source