ID: ALA2229025

Max Phase: Preclinical

Molecular Formula: C24H33Cl2NO5

Molecular Weight: 486.44

Molecule Type: Small molecule

Associated Items:

Representations

Canonical SMILES:  CC1CCC(=NOC(=O)COc2ccc(Cl)cc2Cl)CCCCCCCCCCC(=O)O1

Standard InChI:  InChI=1S/C24H33Cl2NO5/c1-18-12-14-20(10-8-6-4-2-3-5-7-9-11-23(28)31-18)27-32-24(29)17-30-22-15-13-19(25)16-21(22)26/h13,15-16,18H,2-12,14,17H2,1H3

Standard InChI Key:  RXUXVDBJRMZOBN-UHFFFAOYSA-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: 486.44Molecular Weight (Monoisotopic): 485.1736AlogP: 6.90#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: 0.98CX LogP: 7.15CX LogD: 7.15
Aromatic Rings: 1Heavy Atoms: 32QED Weighted: 0.26Np Likeness Score: -0.27

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