15-(2-ethyl-1,3-dioxolan-2-yl)pentadec-9-enoic acid

ID: ALA1257230

Chembl Id: CHEMBL1257230

PubChem CID: 52943700

Max Phase: Preclinical

Molecular Formula: C20H36O4

Molecular Weight: 340.50

Molecule Type: Small molecule

Associated Items:

Names and Identifiers

Canonical SMILES:  CCC1(CCCCC/C=C\CCCCCCCC(=O)O)OCCO1

Standard InChI:  InChI=1S/C20H36O4/c1-2-20(23-17-18-24-20)16-14-12-10-8-6-4-3-5-7-9-11-13-15-19(21)22/h4,6H,2-3,5,7-18H2,1H3,(H,21,22)/b6-4-

Standard InChI Key:  SNYNQQPKEZCABD-XQRVVYSFSA-N

Alternative Forms

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

Calculated Properties

Molecular Weight: 340.50Molecular Weight (Monoisotopic): 340.2614AlogP: 5.46#Rotatable Bonds: 15
Polar Surface Area: 55.76Molecular Species: ACIDHBA: 3HBD: 1
#RO5 Violations: 1HBA (Lipinski): 4HBD (Lipinski): 1#RO5 Violations (Lipinski): 1
CX Acidic pKa: 4.99CX Basic pKa: CX LogP: 5.86CX LogD: 3.48
Aromatic Rings: Heavy Atoms: 24QED Weighted: 0.32Np Likeness Score: 0.99

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