ID: ALA5314304

Max Phase: Preclinical

Molecular Formula: C19H34N4O

Molecular Weight: 334.51

Associated Items:

Representations

Canonical SMILES:  CN1CCN(C2(CNC(=O)[C@H]3CC34CCNCC4)CCCC2)CC1

Standard InChI:  InChI=1S/C19H34N4O/c1-22-10-12-23(13-11-22)19(4-2-3-5-19)15-21-17(24)16-14-18(16)6-8-20-9-7-18/h16,20H,2-15H2,1H3,(H,21,24)/t16-/m1/s1

Standard InChI Key:  QGJFJPSIPRZAIH-MRXNPFEDSA-N

Associated Targets(non-human)

Plasmodium falciparum 966862 Activities

Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID

Molecule Features

Natural Product: NoOral: NoChemical Probe: NoParenteral: No
Molecule Type: Topical: 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: 334.51Molecular Weight (Monoisotopic): 334.2733AlogP: 1.05#Rotatable Bonds: 4
Polar Surface Area: 47.61Molecular Species: BASEHBA: 4HBD: 2
#RO5 Violations: 0HBA (Lipinski): 5HBD (Lipinski): 2#RO5 Violations (Lipinski): 0
CX Acidic pKa: CX Basic pKa: 10.03CX LogP: 0.56CX LogD: -2.70
Aromatic Rings: 0Heavy Atoms: 24QED Weighted: 0.81Np Likeness Score: -0.49

References

1. Bosc N, Felix E, Gardner JMF, Mills J, Timmerman M, Asveld D, Rensen K, Mukherjee P, Das R, Chenu E, Besson D, Burrows JN, Duffy J, Laleu B, Guantai EM, Leach AR..  (2023)  MAIP: An Open-Source Tool to Enrich High-Throughput Screening Output and Identify Novel, Druglike Molecules with Antimalarial Activity.,  14  (12): [PMID:38116432] [10.1021/acsmedchemlett.3c00369]

Source

Source(1):