ID: ALA2229034

Max Phase: Preclinical

Molecular Formula: C23H33NO5

Molecular Weight: 403.52

Molecule Type: Small molecule

Associated Items:

Representations

Canonical SMILES:  O=C1CCCCCCCCCCC(=NOC(=O)COc2ccccc2)CCCO1

Standard InChI:  InChI=1S/C23H33NO5/c25-22-17-11-6-4-2-1-3-5-8-13-20(14-12-18-27-22)24-29-23(26)19-28-21-15-9-7-10-16-21/h7,9-10,15-16H,1-6,8,11-14,17-19H2

Standard InChI Key:  KLDTZWSFXGRWDS-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: 403.52Molecular Weight (Monoisotopic): 403.2359AlogP: 5.20#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: 1.68CX LogP: 5.53CX LogD: 5.53
Aromatic Rings: 1Heavy Atoms: 29QED Weighted: 0.39Np 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