ChemicalBook--->CAS DataBase List--->2173134-00-2

2173134-00-2

2173134-00-2 Structure

2173134-00-2 Structure
IdentificationBack Directory
[Name]

vanin-1 inhibitor
[CAS]

2173134-00-2
[Synonyms]

VUN34002
vanin-1 inhibitor
Vanin-1 inhibitor 1
VUN34002(vanin-1 inhibitor)
8-Oxa-2-azaspiro[4.5]dec-2-yl[2-[(2-pyrazinylmethyl)amino]-5-pyrimidinyl]methanone
Methanone, 8-oxa-2-azaspiro[4.5]dec-2-yl[2-[(2-pyrazinylmethyl)amino]-5-pyrimidinyl]-
[Molecular Formula]

C18H22N6O2
[MDL Number]

MFCD32201155
[MOL File]

2173134-00-2.mol
[Molecular Weight]

354.41
Chemical PropertiesBack Directory
[Boiling point ]

617.9±65.0 °C(Predicted)
[density ]

1.34±0.1 g/cm3(Predicted)
[storage temp. ]

Store at -20°C
[solubility ]

DMSO: 125 mg/mL (352.70 mM)
[form ]

Solid
[pka]

1.77±0.10(Predicted)
[color ]

White to off-white
[InChI]

1S/C18H22N6O2/c25-16(24-6-1-18(13-24)2-7-26-8-3-18)14-9-21-17(22-10-14)23-12-15-11-19-4-5-20-15/h4-5,9-11H,1-3,6-8,12-13H2,(H,21,22,23)
[InChIKey]

VGRLXWFIXGZRMS-UHFFFAOYSA-N
[SMILES]

O=C(C1=CN=C(N=C1)NCC2=CN=CC=N2)N3CCC4(C3)CCOCC4
Safety DataBack Directory
[WGK Germany ]

WGK 3
[Storage Class]

11 - Combustible Solids
Hazard InformationBack Directory
[Uses]

PFI-653 (Vanin-1-IN-1, compound 3) is a vanin-1 inhibitor that binds to plasma vanin-1 from mouse, rat, dog, and human. Vanin-1 is a cell surface-associated inositol (GPi) -anchored protein that plays important roles in metabolism and inflammation. PFI-653 inhibits vanin-1 from different species with IC50s of 6.85 nM (human recombinant plasma vanin-1), 9.0 nM (human plasma vanin-1), 24.5 nM (mouse recombinant vanin-1), and 53.4 nM (mouse plasma vanin-1)[1][2].
[Biological Activity]

PFI-653 is a cell permeablepotentand selective inhibitor of Vanin-1 (Vascular non-inflammatory molecule-1) enzyme.
[in vivo]

After a single intravenous injection (2 mg/kg) in rats, PFI-653 (compound 3) has a low clearance rate, a steady-state volume of distribution of 0.84 L/kg, and an effective half-life of 0.5 hours. After oral administration (10 mg/kg), PFI-653 exhibits rapid and almost complete absorption, with a bioavailability of 96%[1].

[storage]

Store at -20°C
[References]

[1] Casimiro-Garcia A, et al. Discovery of a Series of Pyrimidine Carboxamides as Inhibitors of Vanin-1. J Med Chem. 2022 Jan 13;65 (1) :757-784. DOI:10.1021/acs.jmedchem.1c01849
[2] Agustin Casimiro-Garcia, et al. Novel pyrimidine carboxamides as inhibitors of vanin-1 enzyme. WO2018011681A1.
Spectrum DetailBack Directory
[Spectrum Detail]

vanin-1 inhibitor(2173134-00-2)1HNMR
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