ID: ALA5176043

Max Phase: Preclinical

Molecular Formula: C19H19N5O3

Molecular Weight: 365.39

Associated Items:

Representations

Canonical SMILES:  CCNC(=O)c1cnc(-c2cncc(Oc3ncccc3OCC)c2)nc1

Standard InChI:  InChI=1S/C19H19N5O3/c1-3-21-18(25)14-10-23-17(24-11-14)13-8-15(12-20-9-13)27-19-16(26-4-2)6-5-7-22-19/h5-12H,3-4H2,1-2H3,(H,21,25)

Standard InChI Key:  GDVFYAPTMWNIKT-UHFFFAOYSA-N

Associated Targets(Human)

Diacylglycerol O-acyltransferase 2 347 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: 365.39Molecular Weight (Monoisotopic): 365.1488AlogP: 2.87#Rotatable Bonds: 7
Polar Surface Area: 99.12Molecular Species: NEUTRALHBA: 7HBD: 1
#RO5 Violations: 0HBA (Lipinski): 8HBD (Lipinski): 1#RO5 Violations (Lipinski): 0
CX Acidic pKa: 13.09CX Basic pKa: 3.23CX LogP: 1.53CX LogD: 1.53
Aromatic Rings: 3Heavy Atoms: 27QED Weighted: 0.69Np Likeness Score: -1.59

References

1. Futatsugi K, Cabral S, Kung DW, Huard K, Lee E, Boehm M, Bauman J, Clark RW, Coffey SB, Crowley C, Dechert-Schmitt AM, Dowling MS, Dullea R, Gosset JR, Kalgutkar AS, Kou K, Li Q, Lian Y, Loria PM, Londregan AT, Niosi M, Orozco C, Pettersen JC, Pfefferkorn JA, Polivkova J, Ross TT, Sharma R, Stock IA, Tesz G, Wisniewska H, Goodwin B, Price DA..  (2022)  Discovery of Ervogastat (PF-06865571): A Potent and Selective Inhibitor of Diacylglycerol Acyltransferase 2 for the Treatment of Non-alcoholic Steatohepatitis.,  65  (22.0): [PMID:36322383] [10.1021/acs.jmedchem.2c01200]

Source