ID: ALA5197263

Max Phase: Preclinical

Molecular Formula: C20H19ClF4N6O4

Molecular Weight: 518.86

Associated Items:

Representations

Canonical SMILES:  CCn1c(CO)nn(-c2nc(O[C@@H](C)C(F)(F)F)c(C(=O)Nc3c(Cl)ccnc3C)cc2F)c1=O

Standard InChI:  InChI=1S/C20H19ClF4N6O4/c1-4-30-14(8-32)29-31(19(30)34)16-13(22)7-11(18(28-16)35-10(3)20(23,24)25)17(33)27-15-9(2)26-6-5-12(15)21/h5-7,10,32H,4,8H2,1-3H3,(H,27,33)/t10-/m0/s1

Standard InChI Key:  OIFTVPMDTTWOSI-JTQLQIEISA-N

Associated Targets(Human)

Dihydroorotate dehydrogenase 2737 Activities

Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID

MOLM-13 2241 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: 518.86Molecular Weight (Monoisotopic): 518.1092AlogP: 3.02#Rotatable Bonds: 7
Polar Surface Area: 124.16Molecular Species: NEUTRALHBA: 9HBD: 2
#RO5 Violations: 1HBA (Lipinski): 10HBD (Lipinski): 2#RO5 Violations (Lipinski): 1
CX Acidic pKa: 12.90CX Basic pKa: 4.31CX LogP: 3.02CX LogD: 3.02
Aromatic Rings: 3Heavy Atoms: 35QED Weighted: 0.46Np Likeness Score: -1.19

References

1. Cisar JS, Pietsch C, DeRatt LG, Jacoby E, Kazmi F, Keohane C, Legenski K, Matico R, Shaffer P, Simonnet Y, Tanner A, Wang CY, Wang W, Attar R, Edwards JP, Kuduk SD..  (2022)  N-Heterocyclic 3-Pyridyl Carboxamide Inhibitors of DHODH for the Treatment of Acute Myelogenous Leukemia.,  65  (16.0): [PMID:35925768] [10.1021/acs.jmedchem.2c00788]

Source