ID: ALA5288393

Max Phase: Preclinical

Molecular Formula: C19H25N3O4S2

Molecular Weight: 423.56

Associated Items:

Representations

Canonical SMILES:  CCCOc1ccc(NC(=O)C(C)(C)c2csc(NS(=O)(=O)C3CC3)n2)cc1

Standard InChI:  InChI=1S/C19H25N3O4S2/c1-4-11-26-14-7-5-13(6-8-14)20-17(23)19(2,3)16-12-27-18(21-16)22-28(24,25)15-9-10-15/h5-8,12,15H,4,9-11H2,1-3H3,(H,20,23)(H,21,22)

Standard InChI Key:  BOEWQRNBSGZWMC-UHFFFAOYSA-N

Associated Targets(Human)

CTP synthase 1 39 Activities

Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID

Jurkat E6.1 134 Activities

Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID

CTP synthase 2 4 Activities

Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID

Associated Targets(non-human)

CTP synthase 2 4 Activities

Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID

CTP synthase 2 4 Activities

Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID

CTP synthase 1 4 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: 423.56Molecular Weight (Monoisotopic): 423.1286AlogP: 3.75#Rotatable Bonds: 9
Polar Surface Area: 97.39Molecular Species: ACIDHBA: 6HBD: 2
#RO5 Violations: 0HBA (Lipinski): 7HBD (Lipinski): 2#RO5 Violations (Lipinski): 0
CX Acidic pKa: 6.47CX Basic pKa: CX LogP: 3.74CX LogD: 3.06
Aromatic Rings: 2Heavy Atoms: 28QED Weighted: 0.64Np Likeness Score: -1.67

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