Home Aminos 2-Bromo-4-[(6,7-dimethoxyquinazolin-4-yl)amino]phenol

2-Bromo-4-[(6,7-dimethoxyquinazolin-4-yl)amino]phenol

CAS No.:
211555-04-3
Catalog Number:
AG00BF57
Molecular Formula:
C16H14BrN3O3
Molecular Weight:
376.2047
Pack Size
Purity
Availability
Location
Price(USD)
Quantity
  
5mg
≥98%
1 week
United States
$147
- +
10mg
≥98%
1 week
United States
$201
- +
25mg
≥98%
1 week
United States
$396
- +
50mg
99%
1 week
United States
$683
- +
Product Description
Catalog Number:
AG00BF57
Chemical Name:
2-Bromo-4-[(6,7-dimethoxyquinazolin-4-yl)amino]phenol
CAS Number:
211555-04-3
Molecular Formula:
C16H14BrN3O3
Molecular Weight:
376.2047
MDL Number:
MFCD02179366
IUPAC Name:
2-bromo-4-[(6,7-dimethoxyquinazolin-4-yl)amino]phenol
InChI:
InChI=1S/C16H14BrN3O3/c1-22-14-6-10-12(7-15(14)23-2)18-8-19-16(10)20-9-3-4-13(21)11(17)5-9/h3-8,21H,1-2H3,(H,18,19,20)
InChI Key:
CBIAKDAYHRWZCU-UHFFFAOYSA-N
SMILES:
COc1cc2c(ncnc2cc1OC)Nc1ccc(c(c1)Br)O
Properties
Complexity:
390  
Compound Is Canonicalized:
Yes
Covalently-Bonded Unit Count:
1  
Defined Atom Stereocenter Count:
0
Defined Bond Stereocenter Count:
0
Exact Mass:
375.022g/mol
Formal Charge:
0
Heavy Atom Count:
23  
Hydrogen Bond Acceptor Count:
6  
Hydrogen Bond Donor Count:
2  
Isotope Atom Count:
0
Molecular Weight:
376.21g/mol
Monoisotopic Mass:
375.022g/mol
Rotatable Bond Count:
4  
Topological Polar Surface Area:
76.5A^2
Undefined Atom Stereocenter Count:
0
Undefined Bond Stereocenter Count:
0
XLogP3:
3.7  
Literature
Title Journal
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Janus kinase 3 is expressed in erythrocytes, phosphorylated upon energy depletion and involved in the regulation of suicidal erythrocyte death. Cellular physiology and biochemistry : international journal of experimental cellular physiology, biochemistry, and pharmacology 20110101
Differential regulation of proliferation and differentiation in neural precursor cells by the Jak pathway. Stem cells (Dayton, Ohio) 20101001
A novel indole-3-propanamide exerts its immunosuppressive activity by inhibiting JAK3 in T cells. The Journal of pharmacology and experimental therapeutics 20091101
The specificity of JAK3 kinase inhibitors. Blood 20080215
Oncogenic tyrosine kinase NPM/ALK induces activation of the rapamycin-sensitive mTOR signaling pathway. Oncogene 20070816
Jak3- and JNK-dependent vascular endothelial growth factor expression in cutaneous T-cell lymphoma. Leukemia 20061001
Interplay between epidermal growth factor receptor and Janus kinase 3 regulates polychlorinated biphenyl-induced matrix metalloproteinase-3 expression and transendothelial migration of tumor cells. Molecular cancer research : MCR 20060601
The JAK3 inhibitor WHI-P154 prevents PDGF-evoked process outgrowth in human neural precursor cells. Journal of neurochemistry 20060401
JAK inhibitors AG-490 and WHI-P154 decrease IFN-gamma-induced iNOS expression and NO production in macrophages. Mediators of inflammation 20060101
Inhibition of ALK enzymatic activity in T-cell lymphoma cells induces apoptosis and suppresses proliferation and STAT3 phosphorylation independently of Jak3. Laboratory investigation; a journal of technical methods and pathology 20051201
Inhibition of the antigen-induced activation of rodent mast cells by putative Janus kinase 3 inhibitors WHI-P131 and WHI-P154 in a Janus kinase 3-independent manner. British journal of pharmacology 20050701
IL-4-dependent CD86 expression requires JAK/STAT6 activation and is negatively regulated by PKCdelta. Cellular signalling 20040201
Prevention of organ allograft rejection by a specific Janus kinase 3 inhibitor. Science (New York, N.Y.) 20031031
Suppression of early T-cell-receptor-triggered cellular activation by the Janus kinase 3 inhibitor WHI-P-154. Transplantation 20030615
Augmentation of mast cell bactericidal activity by the anti-leukemic drug, 4-(3'bromo-4'-hydroxylphenyl)-amino-6,7-dimethoxyquinazoline. Leukemia & lymphoma 20020601
Regulation of IGF-I mRNA and signal transducers and activators of transcription-3 and -5 (Stat-3 and -5) by GH in C2C12 myoblasts. Endocrinology 20020201
4-[3-Bromo-4-hydroxyphenyl)amino]-6,7-dimethoxyquinazolin-1-ium chloride methanol solvate and 4-[(3-hydroxyphenyl)amino]-6,7-dimethoxy-1-quinazolinium chloride. Acta crystallographica. Section C, Crystal structure communications 20010101
Tyrosine kinase inhibitors against EGF receptor-positive malignancies. Methods in molecular biology (Clifton, N.J.) 20010101
Properties