ID: ALA2431747

Max Phase: Preclinical

Molecular Formula: C30H62N4O6

Molecular Weight: 574.85

Molecule Type: Small molecule

Associated Items:

Representations

Canonical SMILES:  CCCCCCCCCO[C@@H]1[C@@H](N)[C@@H](O[C@H]2[C@H](O)[C@@H](OCCCCCCCCC)[C@H](N)C[C@@H]2N)O[C@H](CN)[C@H]1O

Standard InChI:  InChI=1S/C30H62N4O6/c1-3-5-7-9-11-13-15-17-37-27-21(32)19-22(33)28(26(27)36)40-30-24(34)29(25(35)23(20-31)39-30)38-18-16-14-12-10-8-6-4-2/h21-30,35-36H,3-20,31-34H2,1-2H3/t21-,22+,23-,24-,25-,26-,27+,28-,29-,30-/m1/s1

Standard InChI Key:  PPBOFDZGLKCMEV-QKOPAVOMSA-N

Associated Targets(non-human)

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

Acinetobacter lwoffii 550 Activities

Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID

Staphylococcus aureus 210822 Activities

Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID

J774 3120 Activities

Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID

Mus musculus 284745 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: 574.85Molecular Weight (Monoisotopic): 574.4669AlogP: 2.43#Rotatable Bonds: 21
Polar Surface Area: 181.46Molecular Species: BASEHBA: 10HBD: 6
#RO5 Violations: 2HBA (Lipinski): 10HBD (Lipinski): 10#RO5 Violations (Lipinski): 2
CX Acidic pKa: 12.81CX Basic pKa: 9.54CX LogP: 3.09CX LogD: -1.63
Aromatic Rings: 0Heavy Atoms: 40QED Weighted: 0.11Np Likeness Score: 1.03

References

1. Zimmermann L, Bussière A, Ouberai M, Baussanne I, Jolivalt C, Mingeot-Leclercq MP, Décout JL..  (2013)  Tuning the antibacterial activity of amphiphilic neamine derivatives and comparison to paromamine homologues.,  56  (19): [PMID:24083676] [10.1021/jm401148j]
2. Zimmermann L, Das I, Désiré J, Sautrey G, Barros R S V, El Khoury M, Mingeot-Leclercq MP, Décout JL..  (2016)  New Broad-Spectrum Antibacterial Amphiphilic Aminoglycosides Active against Resistant Bacteria: From Neamine Derivatives to Smaller Neosamine Analogues.,  59  (20): [PMID:27690420] [10.1021/acs.jmedchem.6b00818]
3. Zimmermann L, Kempf J, Briée F, Swain J, Mingeot-Leclercq MP, Décout JL..  (2018)  Broad-spectrum antibacterial amphiphilic aminoglycosides: A new focus on the structure of the lipophilic groups extends the series of active dialkyl neamines.,  157  [PMID:30282323] [10.1016/j.ejmech.2018.08.022]

Source