ID: ALA490230

Max Phase: Preclinical

Molecular Formula: C17H26N4O4

Molecular Weight: 350.42

Molecule Type: Small molecule

Associated Items:

Representations

Canonical SMILES:  CN(C)c1ccc(/C=C/NNC(=O)CCCCCC(=O)NO)c(O)c1

Standard InChI:  InChI=1S/C17H26N4O4/c1-21(2)14-9-8-13(15(22)12-14)10-11-18-19-16(23)6-4-3-5-7-17(24)20-25/h8-12,18,22,25H,3-7H2,1-2H3,(H,19,23)(H,20,24)/b11-10+

Standard InChI Key:  RCSMLUPKYWMMSO-ZHACJKMWSA-N

Associated Targets(Human)

MM1.S 1111 Activities

Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID

Associated Targets(non-human)

Plasmodium falciparum 966862 Activities

Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID

Histone deacetylase 41 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: 350.42Molecular Weight (Monoisotopic): 350.1954AlogP: 1.51#Rotatable Bonds: 10
Polar Surface Area: 113.93Molecular Species: NEUTRALHBA: 6HBD: 5
#RO5 Violations: 0HBA (Lipinski): 8HBD (Lipinski): 5#RO5 Violations (Lipinski): 0
CX Acidic pKa: 8.79CX Basic pKa: 3.83CX LogP: 1.16CX LogD: 1.14
Aromatic Rings: 1Heavy Atoms: 25QED Weighted: 0.25Np Likeness Score: -0.38

References

1. Patel V, Mazitschek R, Coleman B, Nguyen C, Urgaonkar S, Cortese J, Barker RH, Greenberg E, Tang W, Bradner JE, Schreiber SL, Duraisingh MT, Wirth DF, Clardy J..  (2009)  Identification and characterization of small molecule inhibitors of a class I histone deacetylase from Plasmodium falciparum.,  52  (8): [PMID:19317450] [10.1021/jm801654y]

Source