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

ID: ALA4207059

Chembl Id: CHEMBL4207059

PubChem CID: 141482985

Max Phase: Preclinical

Molecular Formula: C24H23FN6O

Molecular Weight: 430.49

Molecule Type: Small molecule

Associated Items:

Names and Identifiers

Canonical SMILES:  Nc1nc(N)c2cc(NCc3ccc(CCNC(=O)c4cccc(F)c4)cc3)ccc2n1

Standard InChI:  InChI=1S/C24H23FN6O/c25-18-3-1-2-17(12-18)23(32)28-11-10-15-4-6-16(7-5-15)14-29-19-8-9-21-20(13-19)22(26)31-24(27)30-21/h1-9,12-13,29H,10-11,14H2,(H,28,32)(H4,26,27,30,31)

Standard InChI Key:  SXTABGSSQYSTFD-UHFFFAOYSA-N

Alternative Forms

  1. Parent:

    ALA4207059

    ---

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: 430.49Molecular Weight (Monoisotopic): 430.1917AlogP: 3.52#Rotatable Bonds: 7
Polar Surface Area: 118.95Molecular Species: NEUTRALHBA: 6HBD: 4
#RO5 Violations: HBA (Lipinski): 7HBD (Lipinski): 6#RO5 Violations (Lipinski): 1
CX Acidic pKa: CX Basic pKa: 7.41CX LogP: 3.47CX LogD: 3.17
Aromatic Rings: 4Heavy Atoms: 32QED Weighted: 0.36Np Likeness Score: -1.43

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