3-Isopropyl-7-methyl-8-(4-methyl-3-oxo-pentyl)-[1,2]naphthoquinone

ID: ALA328722

Chembl Id: CHEMBL328722

Cas Number: 250691-57-7

PubChem CID: 11771368

Max Phase: Preclinical

Molecular Formula: C20H24O3

Molecular Weight: 312.41

Molecule Type: Small molecule

Associated Items:

Names and Identifiers

Canonical SMILES:  Cc1ccc2c(c1CCC(=O)C(C)C)C(=O)C(=O)C(C(C)C)=C2

Standard InChI:  InChI=1S/C20H24O3/c1-11(2)16-10-14-7-6-13(5)15(8-9-17(21)12(3)4)18(14)20(23)19(16)22/h6-7,10-12H,8-9H2,1-5H3

Standard InChI Key:  KDNPHTQAHFLSCY-UHFFFAOYSA-N

Alternative Forms

  1. Parent:

Associated Targets(Human)

HL-60 (67320 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
SPC-A4 (17 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
SGC-7901 (2773 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID

Associated Targets(non-human)

P388 (20296 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID

Molecule Features

Natural Product: YesOral: 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: 312.41Molecular Weight (Monoisotopic): 312.1725AlogP: 3.96#Rotatable Bonds: 5
Polar Surface Area: 51.21Molecular Species: NEUTRALHBA: 3HBD:
#RO5 Violations: HBA (Lipinski): 3HBD (Lipinski): #RO5 Violations (Lipinski):
CX Acidic pKa: CX Basic pKa: CX LogP: 5.50CX LogD: 5.50
Aromatic Rings: 1Heavy Atoms: 23QED Weighted: 0.77Np Likeness Score: 1.46

References

1. Zhang JS, Ding J, Tang QM, Li M, Zhao M, Lu LJ, Chen LJ, Yuan ST..  (1999)  Synthesis and antitumour activity of novel diterpenequinone salvicine and the analogs.,  (18): [PMID:10509925] [10.1016/s0960-894x(99)00472-2]

Source