Home Other Building Blocks 4H-Pyrido[1,2-a]pyrimidin-4-one

4H-Pyrido[1,2-a]pyrimidin-4-one

CAS No.:
23443-10-9
Catalog Number:
AG002N9I
Molecular Formula:
C8H6N2O
Molecular Weight:
146.1460
Pack Size
Purity
Availability
Location
Price(USD)
Quantity
  
250mg
98%
In Stock USA
United States
$125
- +
1g
98%
In Stock USA
United States
$307
- +
5g
98%
In Stock USA
United States
$1063
- +
10g
98%
In Stock USA
United States
$1875
- +
Product Description
Catalog Number:
AG002N9I
Chemical Name:
4H-Pyrido[1,2-a]pyrimidin-4-one
CAS Number:
23443-10-9
Molecular Formula:
C8H6N2O
Molecular Weight:
146.1460
MDL Number:
MFCD07434961
IUPAC Name:
pyrido[1,2-a]pyrimidin-4-one
InChI:
InChI=1S/C8H6N2O/c11-8-4-5-9-7-3-1-2-6-10(7)8/h1-6H
InChI Key:
NYJWYCAHJRGKMI-UHFFFAOYSA-N
SMILES:
O=c1ccnc2n1cccc2
NSC Number:
607398
Properties
Complexity:
310  
Compound Is Canonicalized:
Yes
Covalently-Bonded Unit Count:
1  
Defined Atom Stereocenter Count:
0
Defined Bond Stereocenter Count:
0
Exact Mass:
146.048g/mol
Formal Charge:
0
Heavy Atom Count:
11  
Hydrogen Bond Acceptor Count:
2  
Hydrogen Bond Donor Count:
0
Isotope Atom Count:
0
Molecular Weight:
146.149g/mol
Monoisotopic Mass:
146.048g/mol
Rotatable Bond Count:
0
Topological Polar Surface Area:
32.7A^2
Undefined Atom Stereocenter Count:
0
Undefined Bond Stereocenter Count:
0
XLogP3:
0.2  
Literature
Title Journal
Fused bicycles as arylketone bioisosteres leading to potent, orally active thiadiazole H3 antagonists. Bioorganic & medicinal chemistry letters 20120501
Suzuki-Miyaura cross-coupling reactions of halo derivatives of 4H-pyrido[1,2-a]pyrimidin-4-ones. Organic & biomolecular chemistry 20111007
Synthesis and antiproliferative activity of novel diaryl ureas possessing a 4H-pyrido[1,2-a]pyrimidin-4-one group. Archiv der Pharmazie 20100101
Anti-ischaemic activity of an antioxidant aldose reductase inhibitor on diabetic and non-diabetic rat hearts. The Journal of pharmacy and pharmacology 20100101
MexAB-OprM specific efflux pump inhibitors in Pseudomonas aeruginosa. Part 7: highly soluble and in vivo active quaternary ammonium analogue D13-9001, a potential preclinical candidate. Bioorganic & medicinal chemistry 20071115
Pyrido[1,2-a]pyrimidin-4-one derivatives as a novel class of selective aldose reductase inhibitors exhibiting antioxidant activity. Journal of medicinal chemistry 20071004
MexAB-OprM specific efflux pump inhibitors in Pseudomonas aeruginosa. Part 6: exploration of aromatic substituents. Bioorganic & medicinal chemistry 20061215
MexAB-OprM specific efflux pump inhibitors in Pseudomonas aeruginosa. Part 5: Carbon-substituted analogues at the C-2 position. Bioorganic & medicinal chemistry 20060315
Isocyanate acting as a carbonyl precursor: pyridyl group-assisted formation of 4H-pyrido[1,2-a]pyrimidin-4-ones from ketimines and isocyanates. Organic & biomolecular chemistry 20060121
Synthesis and biological activities of flavonoid derivatives as A3 adenosine receptor antagonists. Journal of medicinal chemistry 19960607
Properties