N-(4-(((2,4-Diaminoquinazolin-6-yl)amino)methyl)phenethyl)-3,5-dimethoxybenzamide

ID: ALA4209975

Chembl Id: CHEMBL4209975

PubChem CID: 141483003

Max Phase: Preclinical

Molecular Formula: C26H28N6O3

Molecular Weight: 472.55

Molecule Type: Small molecule

Associated Items:

Names and Identifiers

Canonical SMILES:  COc1cc(OC)cc(C(=O)NCCc2ccc(CNc3ccc4nc(N)nc(N)c4c3)cc2)c1

Standard InChI:  InChI=1S/C26H28N6O3/c1-34-20-11-18(12-21(14-20)35-2)25(33)29-10-9-16-3-5-17(6-4-16)15-30-19-7-8-23-22(13-19)24(27)32-26(28)31-23/h3-8,11-14,30H,9-10,15H2,1-2H3,(H,29,33)(H4,27,28,31,32)

Standard InChI Key:  SWKMIEHYUOCXBW-UHFFFAOYSA-N

Alternative Forms

  1. Parent:

    ALA4209975

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Associated Targets(non-human)

Cysteine protease falcipain-2 (149 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Dihydrofolate reductase (1810 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: 472.55Molecular Weight (Monoisotopic): 472.2223AlogP: 3.40#Rotatable Bonds: 9
Polar Surface Area: 137.41Molecular Species: NEUTRALHBA: 8HBD: 4
#RO5 Violations: HBA (Lipinski): 9HBD (Lipinski): 6#RO5 Violations (Lipinski): 1
CX Acidic pKa: CX Basic pKa: 7.71CX LogP: 3.01CX LogD: 2.71
Aromatic Rings: 4Heavy Atoms: 35QED Weighted: 0.29Np Likeness Score: -1.00

References

1. Chen W, Huang Z, Wang W, Mao F, Guan L, Tang Y, Jiang H, Li J, Huang J, Jiang L, Zhu J..  (2017)  Discovery of new antimalarial agents: Second-generation dual inhibitors against FP-2 and PfDHFR via fragments assembely.,  25  (24): [PMID:29111368] [10.1016/j.bmc.2017.10.017]

Source