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(4-chloro-benzyl)-guanidine; hydrochloride is a chemical compound with the molecular formula C8H10ClN3. It is a derivative of guanidine, an organic compound with the structure H2N-C(=NH)-NH2, and features a 4-chloro-benzyl group attached to the guanidine moiety. The hydrochloride salt form of (4-chloro-benzyl)-guanidine; hydrochloride is obtained by combining the base with hydrochloric acid, resulting in the addition of a chloride ion and a proton to the molecule. (4-chloro-benzyl)-guanidine; hydrochloride is often used in pharmaceutical applications, particularly as an intermediate in the synthesis of various drugs, due to its potential to form stable complexes with other molecules. It is important to note that the properties and reactivity of (4-chloro-benzyl)-guanidine; hydrochloride can vary depending on the specific context and conditions in which it is used.

1129-76-6

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1129-76-6 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1129-76-6 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 1,1,2 and 9 respectively; the second part has 2 digits, 7 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 1129-76:
(6*1)+(5*1)+(4*2)+(3*9)+(2*7)+(1*6)=66
66 % 10 = 6
So 1129-76-6 is a valid CAS Registry Number.

1129-76-6Upstream product

1129-76-6Relevant academic research and scientific papers

INHIBITION OF CELL PROLIFERATION

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Page/Page column 47; 58; 59; 73, (2008/06/13)

The disclosed modulators of Rb:Raf-1 interactions are potent, selective disruptors of Rb:Raf-1 binding, with IC50 values ranging from 80 nM to 500 nM. Further, these compounds are surprisingly effective in inhibiting a wide variety of cancer cells, including osteosarcoma, epithelial lung carcinoma, non small cell lung carcinoma, three different pancreatic cancer cell lines, two different glioblastoma cell lines, metastatic breast cancer, melanoma, and prostate cancer. Moreover, the disclosed compounds effectively disrupt angiogenesis and significantly inhibited tumors in nude mice derived from human epithelial lung carcinoma tumors. Accordingly, the disclosed compounds, pharmaceutical compositions comprising the compounds, methods of inhibiting cell proliferation, methods of treating subjects with cancer, and methods of preparing the disclosed compounds are provided.

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