ID: ALA4442032

Max Phase: Preclinical

Molecular Formula: C21H23N5O4

Molecular Weight: 409.45

Molecule Type: Unknown

Associated Items:

Representations

Canonical SMILES:  Nc1nc2[nH]cc(Cc3ccc(C(=O)NC4CCCCC4C(=O)O)cc3)c2c(=O)[nH]1

Standard InChI:  InChI=1S/C21H23N5O4/c22-21-25-17-16(19(28)26-21)13(10-23-17)9-11-5-7-12(8-6-11)18(27)24-15-4-2-1-3-14(15)20(29)30/h5-8,10,14-15H,1-4,9H2,(H,24,27)(H,29,30)(H4,22,23,25,26,28)

Standard InChI Key:  WBBNOYZOZAGYRQ-UHFFFAOYSA-N

Associated Targets(Human)

TYMS Tclin Thymidylate synthase (1651 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID

Associated Targets(non-human)

Bifunctional dihydrofolate reductase-thymidylate synthase (81 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: 409.45Molecular Weight (Monoisotopic): 409.1750AlogP: 1.80#Rotatable Bonds: 5
Polar Surface Area: 153.96Molecular Species: ACIDHBA: 5HBD: 5
#RO5 Violations: 0HBA (Lipinski): 9HBD (Lipinski): 6#RO5 Violations (Lipinski): 1
CX Acidic pKa: 4.20CX Basic pKa: 3.29CX LogP: 1.69CX LogD: -1.06
Aromatic Rings: 3Heavy Atoms: 30QED Weighted: 0.43Np Likeness Score: -0.17

References

1. Czyzyk DJ, Valhondo M, Deiana L, Tirado-Rives J, Jorgensen WL, Anderson KS..  (2019)  Structure activity relationship towards design of cryptosporidium specific thymidylate synthase inhibitors.,  183  [PMID:31536894] [10.1016/j.ejmech.2019.111673]

Source