ID: ALA5176109

Max Phase: Preclinical

Molecular Formula: C19H16ClF5N6O4

Molecular Weight: 522.82

Associated Items:

Representations

Canonical SMILES:  CCn1c(CO)nn(-c2nc(O[C@@H](C)C(F)(F)F)c(C(=O)Nc3c(F)cncc3Cl)cc2F)c1=O

Standard InChI:  InChI=1S/C19H16ClF5N6O4/c1-3-30-13(7-32)29-31(18(30)34)15-11(21)4-9(17(28-15)35-8(2)19(23,24)25)16(33)27-14-10(20)5-26-6-12(14)22/h4-6,8,32H,3,7H2,1-2H3,(H,26,27,33)/t8-/m0/s1

Standard InChI Key:  KNGXLDIJPBNUBM-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: 522.82Molecular Weight (Monoisotopic): 522.0842AlogP: 2.85#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: 11.37CX Basic pKa: 1.81CX LogP: 3.03CX LogD: 3.03
Aromatic Rings: 3Heavy Atoms: 35QED Weighted: 0.46Np Likeness Score: -1.15

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