Home Aminos 2,4-Diaminoquinazoline

2,4-Diaminoquinazoline

CAS No.:
1899-48-5
Catalog Number:
AG002E3Z
Molecular Formula:
C8H8N4
Molecular Weight:
160.1759
Pack Size
Purity
Availability
Location
Price(USD)
Quantity
  
1g
98%
1 week
United States
$30
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Product Description
Catalog Number:
AG002E3Z
Chemical Name:
2,4-Diaminoquinazoline
CAS Number:
1899-48-5
Molecular Formula:
C8H8N4
Molecular Weight:
160.1759
MDL Number:
MFCD00236032
IUPAC Name:
quinazoline-2,4-diamine
InChI:
InChI=1S/C8H8N4/c9-7-5-3-1-2-4-6(5)11-8(10)12-7/h1-4H,(H4,9,10,11,12)
InChI Key:
XELRMPRLCPFTBH-UHFFFAOYSA-N
SMILES:
Nc1nc2ccccc2c(n1)N
UNII:
R3UB0T78EL
NSC Number:
403373
Properties
Complexity:
161  
Compound Is Canonicalized:
Yes
Covalently-Bonded Unit Count:
1  
Defined Atom Stereocenter Count:
0
Defined Bond Stereocenter Count:
0
Exact Mass:
160.075g/mol
Formal Charge:
0
Heavy Atom Count:
12  
Hydrogen Bond Acceptor Count:
4  
Hydrogen Bond Donor Count:
2  
Isotope Atom Count:
0
Molecular Weight:
160.18g/mol
Monoisotopic Mass:
160.075g/mol
Rotatable Bond Count:
0
Topological Polar Surface Area:
77.8A^2
Undefined Atom Stereocenter Count:
0
Undefined Bond Stereocenter Count:
0
XLogP3:
1  
Literature
Title Journal
Stimulation of host immune defenses by a small molecule protects C. elegans from bacterial infection. PLoS genetics 20120601
Discovery and optimization of 2,4-diaminoquinazoline derivatives as a new class of potent dengue virus inhibitors. Journal of medicinal chemistry 20120412
Synthesis of 2,4-diaminoquinazolines and tricyclic quinazolines by cascade reductive cyclization of methyl N-cyano-2-nitrobenzimidates. The Journal of organic chemistry 20120316
Design, synthesis, and biological evaluation of new diaminoquinazolines as β-catenin/Tcf4 pathway inhibitors. Journal of medicinal chemistry 20120209
Structure-based design of new DHFR-based antibacterial agents: 7-aryl-2,4-diaminoquinazolines. Bioorganic & medicinal chemistry letters 20110915
New insights into the structural requirements for pro-apoptotic agents based on 2,4-diaminoquinazoline, 2,4-diaminopyrido[2,3-d]pyrimidine and 2,4-diaminopyrimidine derivatives. European journal of medicinal chemistry 20110901
Importazole, a small molecule inhibitor of the transport receptor importin-β. ACS chemical biology 20110715
The contribution of mouse models to understanding the pathogenesis of spinal muscular atrophy. Disease models & mechanisms 20110701
Synthesis and biological evaluation of 2,4-diaminoquinazoline derivatives as novel heat shock protein 90 inhibitors. Bioorganic & medicinal chemistry letters 20110315
Computational perspectives into plasmepsins structure-function relationship: implications to inhibitors design. Journal of tropical medicine 20110101
Utility of survival motor neuron ELISA for spinal muscular atrophy clinical and preclinical analyses. PloS one 20110101
Spinal muscular atrophy. Orphanet journal of rare diseases 20110101
Synthesis of highly functionalized 2,4-diaminoquinazolines as anticancer and anti-HIV agents. Bioorganic & medicinal chemistry letters 20100801
Synthesis and characterization of potent inhibitors of Trypanosoma cruzi dihydrofolate reductase. Bioorganic & medicinal chemistry 20100601
Effects of 2,4-diaminoquinazoline derivatives on SMN expression and phenotype in a mouse model for spinal muscular atrophy. Human molecular genetics 20100201
Development and validation of a cytochrome c-coupled assay for pteridine reductase 1 and dihydrofolate reductase. Analytical biochemistry 20100115
Binding modes of 2,4-diaminoquinazoline and 2,4-diaminopteridine analogs to P. falciparum dihydrofolate reductase enzyme: Molecular docking studies. Indian journal of pharmaceutical sciences 20100101
Mouse survival motor neuron alleles that mimic SMN2 splicing and are inducible rescue embryonic lethality early in development but not late. PloS one 20100101
N-(3,4-dimethoxyphenethyl)-4-(6,7-dimethoxy-3,4-dihydroisoquinolin-2[1H]-yl)-6,7-dimethoxyquinazolin-2-amine (CP-100,356) as a 'chemical knock-out equivalent' to assess the impact of efflux transporters on oral drug absorption in the rat. Journal of pharmaceutical sciences 20091201
2,4-Diamino-quinazolines as inhibitors of beta-catenin/Tcf-4 pathway: Potential treatment for colorectal cancer. Bioorganic & medicinal chemistry letters 20090901
N9-substituted 2,4-diaminoquinazolines: synthesis and biological evaluation of lipophilic inhibitors of pneumocystis carinii and toxoplasma gondii dihydrofolate reductase. Journal of medicinal chemistry 20081009
Potent CCR4 antagonists: synthesis, evaluation, and docking study of 2,4-diaminoquinazolines. Bioorganic & medicinal chemistry 20080901
Discovery of potent CCR4 antagonists: Synthesis and structure-activity relationship study of 2,4-diaminoquinazolines. Bioorganic & medicinal chemistry 20080715
Synthesis and biological evaluation of novel 2,4-diaminoquinazoline derivatives as SMN2 promoter activators for the potential treatment of spinal muscular atrophy. Journal of medicinal chemistry 20080214
Binding of an aminoacridine derivative to a GAAA RNA tetraloop. Bioorganic & medicinal chemistry letters 20041206
A novel method of synthesis of 2,4-diamino-6-arylmethylquinazolines using palladium(0)-catalyzed organozinc chemistry. The Journal of organic chemistry 20011102
Traceless solid-phase synthesis of 2,4-diaminoquinazolines. Organic letters 20010222
Solid-phase synthesis of 2,4-diaminoquinazoline libraries. Journal of combinatorial chemistry 20010101
Inhibitors of protein-RNA complexation that target the RNA: specific recognition of human immunodeficiency virus type 1 TAR RNA by small organic molecules. Biochemistry 19981006
Selective inhibitors of Candida albicans dihydrofolate reductase: activity and selectivity of 5-(arylthio)-2,4-diaminoquinazolines. Journal of medicinal chemistry 19950901
2,4-Diamino-5-substituted-quinazolines as inhibitors of a human dihydrofolate reductase with a site-directed mutation at position 22 and of the dihydrofolate reductases from Pneumocystis carinii and Toxoplasma gondii. Journal of medicinal chemistry 19950303
Assays to detect and characterize human immunodeficiency virus type 1 (HIV-1) receptor antagonists, compounds that inhibit binding of the HIV-1 surface glycoprotein, gp120, to the CD4 receptor on human T lymphocytes. Antimicrobial agents and chemotherapy 19940901
Properties