ID: ALA4062505

Max Phase: Preclinical

Molecular Formula: C20H25N3O5S2

Molecular Weight: 451.57

Molecule Type: Small molecule

Associated Items:

Representations

Canonical SMILES:  CC(C)(C)C1CCN(S(=O)(=O)c2ccc(NC(=O)c3ccc([N+](=O)[O-])s3)cc2)CC1

Standard InChI:  InChI=1S/C20H25N3O5S2/c1-20(2,3)14-10-12-22(13-11-14)30(27,28)16-6-4-15(5-7-16)21-19(24)17-8-9-18(29-17)23(25)26/h4-9,14H,10-13H2,1-3H3,(H,21,24)

Standard InChI Key:  LXXJCYWGAGIGNV-UHFFFAOYSA-N

Associated Targets(Human)

IMR-90 216 Activities

Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID

Associated Targets(non-human)

Trypanosoma brucei 78846 Activities

Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID

Leishmania amazonensis 3813 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: 451.57Molecular Weight (Monoisotopic): 451.1236AlogP: 4.36#Rotatable Bonds: 5
Polar Surface Area: 109.62Molecular Species: NEUTRALHBA: 6HBD: 1
#RO5 Violations: 0HBA (Lipinski): 8HBD (Lipinski): 1#RO5 Violations (Lipinski): 0
CX Acidic pKa: 12.51CX Basic pKa: CX LogP: 4.31CX LogD: 4.31
Aromatic Rings: 2Heavy Atoms: 30QED Weighted: 0.54Np Likeness Score: -2.15

References

1. Hackler A, Patrick SL, Kahney EW, Flaherty DP, Sharlow ER, Morris JC, Golden JE..  (2017)  Antiparasitic lethality of sulfonamidebenzamides in kinetoplastids.,  27  (4): [PMID:28119024] [10.1016/j.bmcl.2017.01.043]

Source