ID: ALA570170

Max Phase: Preclinical

Molecular Formula: C22H39ClN2

Molecular Weight: 330.56

Molecule Type: Small molecule

Associated Items:

Representations

Synonyms (1): SQ-109
Synonyms from Alternative Forms(1):

    Canonical SMILES:  CC(C)=CCC/C(C)=C/CNCCNC1C2CC3CC(C2)CC1C3.Cl

    Standard InChI:  InChI=1S/C22H38N2.ClH/c1-16(2)5-4-6-17(3)7-8-23-9-10-24-22-20-12-18-11-19(14-20)15-21(22)13-18;/h5,7,18-24H,4,6,8-15H2,1-3H3;1H/b17-7+;

    Standard InChI Key:  RZHMMKGXUDVQCD-VYYXIRCESA-N

    Associated Targets(non-human)

    Elizabethkingia meningoseptica 23 Activities

    Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID

    Klebsiella pneumoniae 43867 Activities

    Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID

    Klebsiella oxytoca 929 Activities

    Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID

    Escherichia coli 133304 Activities

    Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID

    Staphylococcus aureus 210822 Activities

    Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID

    Staphylococcus xylosus 41 Activities

    Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID

    Prescottella equi 132 Activities

    Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID

    Bacillus subtilis 32866 Activities

    Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID

    Aspergillus flavus 8875 Activities

    Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID

    Penicillium sp. 198 Activities

    Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID

    Rhizomucor 96 Activities

    Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID

    Scopulariopsis 18 Activities

    Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID

    Sporothrix schenckii 1580 Activities

    Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID

    Fusarium sp. 88 Activities

    Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID

    Aspergillus fumigatus 16427 Activities

    Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID

    Candida parapsilosis 8521 Activities

    Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID

    Pichia kudriavzevii 7448 Activities

    Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID

    Candida albicans 78123 Activities

    Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID

    Trichosporon asahii 679 Activities

    Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID

    Candida tropicalis 8381 Activities

    Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID

    Cyberlindnera jadinii 900 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: 330.56Molecular Weight (Monoisotopic): 330.3035AlogP: 4.68#Rotatable Bonds: 9
    Polar Surface Area: 24.06Molecular Species: BASEHBA: 2HBD: 2
    #RO5 Violations: 0HBA (Lipinski): 2HBD (Lipinski): 2#RO5 Violations (Lipinski): 0
    CX Acidic pKa: CX Basic pKa: 10.24CX LogP: 4.64CX LogD: 1.87
    Aromatic Rings: 0Heavy Atoms: 24QED Weighted: 0.47Np Likeness Score: 0.85

    References

    1. Onajole OK, Belewa XV, Coovadia Y, Govender T, Kruger HG, Maguire GEM, Naidu D, Somai B, Singh N, Govender P.  (2011)  SQ109 analogues as potential antimicrobial candidates,  20  (8): [10.1007/s00044-010-9490-3]

    Source