ID: ALA512991

Max Phase: Preclinical

Molecular Formula: C21H16Cl2N4O2S

Molecular Weight: 459.36

Molecule Type: Small molecule

Associated Items:

Representations

Canonical SMILES:  O=C1S/C(=N\c2ccccc2Cl)N(CCCNc2ccnc3cc(Cl)ccc23)C1=O

Standard InChI:  InChI=1S/C21H16Cl2N4O2S/c22-13-6-7-14-16(8-10-25-18(14)12-13)24-9-3-11-27-19(28)20(29)30-21(27)26-17-5-2-1-4-15(17)23/h1-2,4-8,10,12H,3,9,11H2,(H,24,25)/b26-21-

Standard InChI Key:  FCTXSEMBMMUDFB-QLYXXIJNSA-N

Associated Targets(non-human)

Plasmodium falciparum 966862 Activities

Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID

Histidine-rich protein 528 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: 459.36Molecular Weight (Monoisotopic): 458.0371AlogP: 5.13#Rotatable Bonds: 6
Polar Surface Area: 74.66Molecular Species: NEUTRALHBA: 6HBD: 1
#RO5 Violations: 1HBA (Lipinski): 6HBD (Lipinski): 1#RO5 Violations (Lipinski): 1
CX Acidic pKa: CX Basic pKa: 7.31CX LogP: 5.19CX LogD: 4.95
Aromatic Rings: 3Heavy Atoms: 30QED Weighted: 0.41Np Likeness Score: -1.65

References

1. Sunduru N, Srivastava K, Rajakumar S, Puri SK, Saxena JK, Chauhan PM..  (2009)  Synthesis of novel thiourea, thiazolidinedione and thioparabanic acid derivatives of 4-aminoquinoline as potent antimalarials.,  19  (9): [PMID:19339178] [10.1016/j.bmcl.2009.03.026]

Source