1-(3,5-dichloro-2,4,6-trimethoxyphenyl)heptan-1-one

ID: ALA3594289

Chembl Id: CHEMBL3594289

PubChem CID: 122182555

Max Phase: Preclinical

Molecular Formula: C16H22Cl2O4

Molecular Weight: 349.25

Molecule Type: Small molecule

Associated Items:

Names and Identifiers

Canonical SMILES:  CCCCCCC(=O)c1c(OC)c(Cl)c(OC)c(Cl)c1OC

Standard InChI:  InChI=1S/C16H22Cl2O4/c1-5-6-7-8-9-10(19)11-14(20-2)12(17)16(22-4)13(18)15(11)21-3/h5-9H2,1-4H3

Standard InChI Key:  XKQUCFJJLAEQHI-UHFFFAOYSA-N

Alternative Forms

  1. Parent:

    ALA3594289

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Associated Targets(Human)

Jurkat (10389 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID

Associated Targets(non-human)

Drosophila (190 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: 349.25Molecular Weight (Monoisotopic): 348.0895AlogP: 5.17#Rotatable Bonds: 9
Polar Surface Area: 44.76Molecular Species: NEUTRALHBA: 4HBD:
#RO5 Violations: 1HBA (Lipinski): 4HBD (Lipinski): #RO5 Violations (Lipinski): 1
CX Acidic pKa: CX Basic pKa: CX LogP: 4.74CX LogD: 4.74
Aromatic Rings: 1Heavy Atoms: 22QED Weighted: 0.46Np Likeness Score: 0.49

References

1. Nguyen VH, Kikuchi H, Kubohara Y, Takahashi K, Katou Y, Oshima Y..  (2015)  Development of novel DIF-1 derivatives that selectively suppress innate immune responses.,  23  (15): [PMID:26122773] [10.1016/j.bmc.2015.06.027]

Source