ID: ALA4633352

Max Phase: Preclinical

Molecular Formula: C22H24FN5O4S

Molecular Weight: 473.53

Molecule Type: Unknown

Associated Items:

Representations

Canonical SMILES:  CCn1cc(C(=O)O)c(=O)c2cc(F)c(N3CCN(C/C(=N/OC)c4cccs4)CC3)nc21

Standard InChI:  InChI=1S/C22H24FN5O4S/c1-3-27-12-15(22(30)31)19(29)14-11-16(23)21(24-20(14)27)28-8-6-26(7-9-28)13-17(25-32-2)18-5-4-10-33-18/h4-5,10-12H,3,6-9,13H2,1-2H3,(H,30,31)/b25-17-

Standard InChI Key:  CLVCLLWAWQYJBW-UQQQWYQISA-N

Associated Targets(Human)

MCF7 126967 Activities

Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID

SK-MEL3 228 Activities

Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID

A-431 6446 Activities

Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID

EJ 302 Activities

Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID

SW480 6023 Activities

Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID

Molecule Features

Natural Product: NoOral: NoChemical Probe: NoParenteral: No
Molecule Type: UnknownTopical: 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: 473.53Molecular Weight (Monoisotopic): 473.1533AlogP: 2.49#Rotatable Bonds: 7
Polar Surface Area: 100.26Molecular Species: ACIDHBA: 9HBD: 1
#RO5 Violations: 0HBA (Lipinski): 9HBD (Lipinski): 1#RO5 Violations (Lipinski): 0
CX Acidic pKa: 5.44CX Basic pKa: 4.71CX LogP: 2.93CX LogD: 1.26
Aromatic Rings: 3Heavy Atoms: 33QED Weighted: 0.42Np Likeness Score: -1.49

References

1. Gao F, Zhang X, Wang T, Xiao J..  (2019)  Quinolone hybrids and their anti-cancer activities: An overview.,  165  [PMID:30660827] [10.1016/j.ejmech.2019.01.017]

Source