ID: ALA134616

Max Phase: Preclinical

Molecular Formula: C16H10F3N3O4S

Molecular Weight: 397.33

Molecule Type: Small molecule

Associated Items:

Representations

Canonical SMILES:  COC(=O)Nc1nc2cc(C(=O)c3cc(C(=O)C(F)(F)F)cs3)ccc2[nH]1

Standard InChI:  InChI=1S/C16H10F3N3O4S/c1-26-15(25)22-14-20-9-3-2-7(4-10(9)21-14)12(23)11-5-8(6-27-11)13(24)16(17,18)19/h2-6H,1H3,(H2,20,21,22,25)

Standard InChI Key:  RZXMCOSXLCPHLU-UHFFFAOYSA-N

Associated Targets(non-human)

Tubulin alpha chain 497 Activities

Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID

B16 5829 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: 397.33Molecular Weight (Monoisotopic): 397.0344AlogP: 3.78#Rotatable Bonds: 4
Polar Surface Area: 101.15Molecular Species: NEUTRALHBA: 6HBD: 2
#RO5 Violations: 0HBA (Lipinski): 7HBD (Lipinski): 2#RO5 Violations (Lipinski): 0
CX Acidic pKa: 9.11CX Basic pKa: 3.34CX LogP: 3.86CX LogD: 3.86
Aromatic Rings: 3Heavy Atoms: 27QED Weighted: 0.65Np Likeness Score: -1.16

References

1. Kruse LI, Ladd DL, Harrsch PB, McCabe FL, Mong SM, Faucette L, Johnson R..  (1989)  Synthesis, tubulin binding, antineoplastic evaluation, and structure-activity relationship of oncodazole analogues.,  32  (2): [PMID:2913301] [10.1021/jm00122a020]

Source