ID: ALA5209113

Max Phase: Preclinical

Molecular Formula: C20H18ClF5N6O5

Molecular Weight: 552.84

Associated Items:

Representations

Canonical SMILES:  CCn1c(CO)nn(-c2nc(O[C@@H](C)C(F)(F)F)c(C(=O)Nc3c(F)cnc(OC)c3Cl)cc2F)c1=O

Standard InChI:  InChI=1S/C20H18ClF5N6O5/c1-4-31-12(7-33)30-32(19(31)35)15-10(22)5-9(17(29-15)37-8(2)20(24,25)26)16(34)28-14-11(23)6-27-18(36-3)13(14)21/h5-6,8,33H,4,7H2,1-3H3,(H,27,28,34)/t8-/m0/s1

Standard InChI Key:  HURVWBMKBFRRLF-QMMMGPOBSA-N

Associated Targets(Human)

DHODH Tclin 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: 552.84Molecular Weight (Monoisotopic): 552.0947AlogP: 2.86#Rotatable Bonds: 8
Polar Surface Area: 133.39Molecular Species: NEUTRALHBA: 10HBD: 2
#RO5 Violations: 1HBA (Lipinski): 11HBD (Lipinski): 2#RO5 Violations (Lipinski): 2
CX Acidic pKa: 11.27CX Basic pKa: 0.60CX LogP: 3.47CX LogD: 3.47
Aromatic Rings: 3Heavy Atoms: 37QED Weighted: 0.41Np Likeness Score: -1.07

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