ID: ALA4575866

Max Phase: Preclinical

Molecular Formula: C26H27ClN4O4

Molecular Weight: 494.98

Molecule Type: Unknown

Associated Items:

Representations

Canonical SMILES:  CCCOC(=O)N1CCN(C(=O)c2ccc3c(Cl)cc(-c4ccc(C(=O)NC)cc4)nc3c2)CC1

Standard InChI:  InChI=1S/C26H27ClN4O4/c1-3-14-35-26(34)31-12-10-30(11-13-31)25(33)19-8-9-20-21(27)16-22(29-23(20)15-19)17-4-6-18(7-5-17)24(32)28-2/h4-9,15-16H,3,10-14H2,1-2H3,(H,28,32)

Standard InChI Key:  PWXZDAKDUSEPIY-UHFFFAOYSA-N

Associated Targets(Human)

Histone-lysine N-methyltransferase SMYD3 260 Activities

Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID

Molecule Features

Natural Product: NoOral: NoChemical Probe: NoParenteral: No
Molecule Type: UnknownTopical: 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: 494.98Molecular Weight (Monoisotopic): 494.1721AlogP: 4.22#Rotatable Bonds: 5
Polar Surface Area: 91.84Molecular Species: NEUTRALHBA: 5HBD: 1
#RO5 Violations: 0HBA (Lipinski): 8HBD (Lipinski): 1#RO5 Violations (Lipinski): 0
CX Acidic pKa: CX Basic pKa: 1.13CX LogP: 3.71CX LogD: 3.71
Aromatic Rings: 3Heavy Atoms: 35QED Weighted: 0.57Np Likeness Score: -1.32

References

1. Huang C, Liew SS, Lin GR, Poulsen A, Ang MJY, Chia BCS, Chew SY, Kwek ZP, Wee JLK, Ong EH, Retna P, Baburajendran N, Li R, Yu W, Koh-Stenta X, Ngo A, Manesh S, Fulwood J, Ke Z, Chung HH, Sepramaniam S, Chew XH, Dinie N, Lee MA, Chew YS, Low CB, Pendharkar V, Manoharan V, Vuddagiri S, Sangthongpitag K, Joy J, Matter A, Hill J, Keller TH, Foo K..  (2019)  Discovery of Irreversible Inhibitors Targeting Histone Methyltransferase, SMYD3.,  10  (6): [PMID:31223458] [10.1021/acsmedchemlett.9b00170]

Source