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150450-42-3

150450-42-3 | 4-Quinazolinamine, N-(1,3-benzodioxol-5-ylmethyl)-6-methoxy-

CAS No: 150450-42-3 Catalog No: AG001MMT MDL No:

Product Description

Catalog Number:
AG001MMT
Chemical Name:
4-Quinazolinamine, N-(1,3-benzodioxol-5-ylmethyl)-6-methoxy-
CAS Number:
150450-42-3
Molecular Formula:
C17H15N3O3
Molecular Weight:
309.3193
IUPAC Name:
N-(1,3-benzodioxol-5-ylmethyl)-6-methoxyquinazolin-4-amine
InChI:
InChI=1S/C17H15N3O3/c1-21-12-3-4-14-13(7-12)17(20-9-19-14)18-8-11-2-5-15-16(6-11)23-10-22-15/h2-7,9H,8,10H2,1H3,(H,18,19,20)
InChI Key:
GZQGUYVURISNFJ-UHFFFAOYSA-N
SMILES:
COc1ccc2c(c1)c(ncn2)NCc1ccc2c(c1)OCO2

Properties

Complexity:
397  
Compound Is Canonicalized:
Yes
Covalently-Bonded Unit Count:
1  
Defined Atom Stereocenter Count:
0
Defined Bond Stereocenter Count:
0
Exact Mass:
309.111g/mol
Formal Charge:
0
Heavy Atom Count:
23  
Hydrogen Bond Acceptor Count:
6  
Hydrogen Bond Donor Count:
1  
Isotope Atom Count:
0
Molecular Weight:
309.325g/mol
Monoisotopic Mass:
309.111g/mol
Rotatable Bond Count:
4  
Topological Polar Surface Area:
65.5A^2
Undefined Atom Stereocenter Count:
0
Undefined Bond Stereocenter Count:
0
XLogP3:
3.1  

Literature

Title Journal
Cyclic GMP protects endothelial progenitors from oxidative stress. Angiogenesis 20110901
Inhibition of cGMP-dependent protein kinases potently decreases neutrophil spontaneous apoptosis. Biochemical and biophysical research communications 20020927
Immunopharmacological potential of selective phosphodiesterase inhibition. II. Evidence for the involvement of an inhibitory-kappaB/nuclear factor-kappaB-sensitive pathway in alveolar epithelial cells. The Journal of pharmacology and experimental therapeutics 20020201
Caffeine eliminates gamma-ray-induced G2-phase delay in human tumor cells but not in normal cells. Radiation research 20020101
Role of cyclic nucleotides in vasodilations of the rat thoracic aorta induced by adenosine analogues. British journal of pharmacology 20010701

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