ID: ALA2229028

Max Phase: Preclinical

Molecular Formula: C23H32ClNO5

Molecular Weight: 437.96

Molecule Type: Small molecule

Associated Items:

Representations

Canonical SMILES:  O=C1CCCCCCCCCC/C(=N/OC(=O)COc2ccc(Cl)cc2)CCCO1

Standard InChI:  InChI=1S/C23H32ClNO5/c24-19-13-15-21(16-14-19)29-18-23(27)30-25-20-10-7-5-3-1-2-4-6-8-12-22(26)28-17-9-11-20/h13-16H,1-12,17-18H2/b25-20-

Standard InChI Key:  CJHLOJDZYWIXST-QQTULTPQSA-N

Associated Targets(non-human)

Amaranthus tricolor 65 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: 437.96Molecular Weight (Monoisotopic): 437.1969AlogP: 5.86#Rotatable Bonds: 4
Polar Surface Area: 74.19Molecular Species: NEUTRALHBA: 6HBD: 0
#RO5 Violations: 1HBA (Lipinski): 6HBD (Lipinski): 0#RO5 Violations (Lipinski): 1
CX Acidic pKa: CX Basic pKa: 1.27CX LogP: 6.13CX LogD: 6.13
Aromatic Rings: 1Heavy Atoms: 30QED Weighted: 0.33Np Likeness Score: -0.41

References

1. Meng XQ, Zhang JJ, Liang XM, Zhu WJ, Dong YH, Wu XM, Huang JX, Rui CH, Fan XL, Chen FH, Wang DQ..  (2009)  Synthesis and herbicidal activity of 12-(aryloxyacyloxyimino)-1,15-pentadecanlactone derivatives.,  57  (2): [PMID:19117417] [10.1021/jf802649w]

Source