ChemicalBook--->CAS DataBase List--->1244639-78-8

1244639-78-8

1244639-78-8 Structure

1244639-78-8 Structure
IdentificationBack Directory
[Name]

VU 0364739 hydrochloride
[CAS]

1244639-78-8
[Synonyms]

VU 0364739 HYDROCHLORIDE
2-Naphthalenecarboxamide, N-[2-[1-(3-fluorophenyl)-4-oxo-1,3,8-triazaspiro[4.5]dec-8-yl]ethyl]-
[Molecular Formula]

C26H27FN4O2
[MOL File]

1244639-78-8.mol
[Molecular Weight]

446.52
Chemical PropertiesBack Directory
[solubility ]

DMSO: Sparingly soluble: 1-10 mg/ml
[form ]

Solid
[color ]

Off-white to light yellow
Hazard InformationBack Directory
[Uses]

VU 0364739 Hydrochloride is a selective, small molecule inhibitor of phopholipase D2.
[References]

[1] ROBERT R. LAVIERI. Design, Synthesis, and Biological Evaluation of Halogenated N-(2-(4-Oxo-1-phenyl-1,3,8-triazaspiro[4.5]decan-8-yl)ethyl)benzamides: Discovery of an Isoform-Selective Small Molecule Phospholipase D2 Inhibitor[J]. Journal of Medicinal Chemistry, 2010, 53 18: 6706-6719. DOI: 10.1021/jm100814g
[2] THOMAS P. MATHEWS. Human Phospholipase D Activity Transiently Regulates Pyrimidine Biosynthesis in Malignant Gliomas[J]. ACS Chemical Biology, 2015, 10 5: 1258-1268. DOI: 10.1021/cb500772c
[3] HANS JÖRG LEIS  Werner W. Phospholipase D1 activity is crucial for cytosolic phospholipase A2 –dependent prostaglandin E2 formation in murine osteoblastic MC3T3-E1 cells[J]. Prostaglandins, leukotrienes, and essential fatty acids, 2023, 198: Article 102592. DOI: 10.1016/j.plefa.2023.102592
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