ID: ALA5281158

Max Phase: Preclinical

Molecular Formula: C15H15ClN4O3S

Molecular Weight: 366.83

Associated Items:

Representations

Canonical SMILES:  O=C(Cc1ccnc(NS(=O)(=O)C2CC2)n1)Nc1cccc(Cl)c1

Standard InChI:  InChI=1S/C15H15ClN4O3S/c16-10-2-1-3-11(8-10)18-14(21)9-12-6-7-17-15(19-12)20-24(22,23)13-4-5-13/h1-3,6-8,13H,4-5,9H2,(H,18,21)(H,17,19,20)

Standard InChI Key:  BDEBKUWUURJGSE-UHFFFAOYSA-N

Associated Targets(Human)

Jurkat E6.1 134 Activities

Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID

CTP synthase 1 39 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: 366.83Molecular Weight (Monoisotopic): 366.0553AlogP: 2.22#Rotatable Bonds: 6
Polar Surface Area: 101.05Molecular Species: ACIDHBA: 5HBD: 2
#RO5 Violations: 0HBA (Lipinski): 7HBD (Lipinski): 2#RO5 Violations (Lipinski): 0
CX Acidic pKa: 6.46CX Basic pKa: CX LogP: 1.93CX LogD: 1.25
Aromatic Rings: 2Heavy Atoms: 24QED Weighted: 0.82Np Likeness Score: -2.10

References

1. Novak A, Laughton D, Lane R, Blackham E, Thomas J, Chatzopoulou E, Wrigglesworth J, Quddus A, Ahmed S, Cousin D, Duffy L, Dubois N, Unitt J, Orban K, Browne E, Ward M, Mycock D, Ieva M, Bland N, George P, Bourne T, Asnagli H, Birch L, Jones G..  (2022)  Discovery and Optimization of Potent and Orally Available CTP Synthetase Inhibitors for Use in Treatment of Diseases Driven by Aberrant Immune Cell Proliferation.,  65  (24.0): [PMID:36449304] [10.1021/acs.jmedchem.2c01446]

Source