123129
2-氨基噻唑
97%
别名:
2-噻唑胺
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关于此项目
经验公式（希尔记法）:
C3H4N2S
化学文摘社编号:
分子量:
100.14
UNSPSC Code:
12352100
NACRES:
NA.22
PubChem Substance ID:
EC Number:
202-511-6
Beilstein/REAXYS Number:
105738
MDL number:
Assay:
97%
InChI
1S/C3H4N2S/c4-3-5-1-2-6-3/h1-2H,(H2,4,5)
InChI key
RAIPHJJURHTUIC-UHFFFAOYSA-N
SMILES string
Nc1nccs1
assay
97%
mp
91-93 °C (lit.)
solubility
1 M HCl: soluble 50 mg/mL, clear (dark yellow-brown)
Quality Level
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Application
2-氨基噻唑用于合成 2-氨基噻唑修饰硅胶 。在超声辐射介导下与 2-氯苯甲酸进行 Ulmann 偶联 。
Biochem/physiol Actions
2-氨基噻唑是有效的细胞周期蛋白依赖性激酶 5 抑制剂，是治疗阿尔茨海默病和其他神经退行性疾病的治疗药物。
signalword
Warning
hcodes
Hazard Classifications
Acute Tox. 4 Oral
存储类别
11 - Combustible Solids
wgk
WGK 3
flash_point_f
Not applicable
flash_point_c
Not applicable
ppe
dust mask type N95 (US), Eyeshields, Faceshields, Gloves
Xin Cao et al.
Bioorganic & medicinal chemistry, 16(11), 5890-5898 (2008-05-20)
Because both c-Src and iNOS are key regulatory enzymes in tumorigenesis, a new series of 4-heteroarylamino-3-quinolinecarbonitriles as potent dual inhibitors of both enzymes were designed, prepared, and evaluated for blocking multiple signaling pathways in cancer therapy. All compounds were evaluated
Synthetic Communications, 37, 1853-1853 (2007)
Christopher J Helal et al.
Bioorganic & medicinal chemistry letters, 14(22), 5521-5525 (2004-10-16)
High-throughput screening with cyclin-dependent kinase 5 (cdk5)/p25 led to the discovery of N-(5-isopropyl-thiazol-2-yl)isobutyramide (1). This compound is an equipotent inhibitor of cdk5 and cyclin-dependent kinase 2 (cdk2)/cyclin E (IC(50)=ca. 320nM). Parallel and directed synthesis techniques were utilized to explore the
Meredeth A McGowan et al.
Organic letters, 14(6), 1432-1435 (2012-03-08)
A method for the Pd-catalyzed coupling of 2-aminothiazole derivatives with aryl bromides and triflates is described. Significantly, for this class of nucleophiles, the coupling exhibits a broad substrate scope and proceeds with a reasonable catalyst loading. Furthermore, an interesting effect
Synthesis of chiral polyaminothiazoles.
Sergey Arutyunyan et al.
Journal of combinatorial chemistry, 12(3), 315-317 (2010-03-12)
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