ID: ALA1257352

Max Phase: Preclinical

Molecular Formula: C18H34N4O

Molecular Weight: 322.50

Molecule Type: Small molecule

Associated Items:

Representations

Canonical SMILES:  CC[C@@H](O)CCCCC/C=C\CCCCCCCc1nnn[nH]1

Standard InChI:  InChI=1S/C18H34N4O/c1-2-17(23)15-13-11-9-7-5-3-4-6-8-10-12-14-16-18-19-21-22-20-18/h3,5,17,23H,2,4,6-16H2,1H3,(H,19,20,21,22)/b5-3-/t17-/m1/s1

Standard InChI Key:  CBCHRXJIOQGZNV-MAVJXHJTSA-N

Associated Targets(non-human)

Mannheimia haemolytica 42 Activities

Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID

Pasteurella multocida 1166 Activities

Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID

Actinobacillus pleuropneumoniae 73 Activities

Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID

Histophilus somni 12 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: 322.50Molecular Weight (Monoisotopic): 322.2733AlogP: 4.36#Rotatable Bonds: 15
Polar Surface Area: 74.69Molecular Species: ACIDHBA: 4HBD: 2
#RO5 Violations: 0HBA (Lipinski): 5HBD (Lipinski): 2#RO5 Violations (Lipinski): 0
CX Acidic pKa: 5.08CX Basic pKa: CX LogP: 4.97CX LogD: 3.44
Aromatic Rings: 1Heavy Atoms: 23QED Weighted: 0.37Np Likeness Score: 0.16

References

1. Watanabe T, Kurata I, Hayashi C, Igarashi M, Sawa R, Takahashi Y, Akamatsu Y..  (2010)  The synthesis of paleic acid, an antimicrobial agent effective against Mannheimia and Pasteurella, and its structurally related derivatives.,  20  (19): [PMID:20728353] [10.1016/j.bmcl.2010.07.115]

Source