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(2-benzo[1,3]dioxol-5-yl-ethyl)-benzyl-amine is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

68104-29-0

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68104-29-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 68104-29-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,8,1,0 and 4 respectively; the second part has 2 digits, 2 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 68104-29:
(7*6)+(6*8)+(5*1)+(4*0)+(3*4)+(2*2)+(1*9)=120
120 % 10 = 0
So 68104-29-0 is a valid CAS Registry Number.

68104-29-0Relevant academic research and scientific papers

TRNA SYNTHETASE INHIBITORS

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Paragraph 00165-00167; 00221, (2019/07/30)

Disclosed herein are secondary amine compounds that inhibit tRNA synthetase. The compounds of the invention are useful in inhibiting tRNA synthetase in Gram-negative bacteria and are useful in killing Gram-negative bacteria. The secondary amine compounds of the invention are also useful in the treatment of tuberculosis.

Synthesis and structure-activity relationships of berberine analogues as a novel class of low-density-lipoprotein receptor up-regulators

Yang, Peng,Song, Dan-Qing,Li, Ying-Hong,Kong, Wei-Jia,Wang, Yan-Xiang,Gao, Li-Mei,Liu, Shu-Yu,Cao, Rui-Qiang,Jiang, Jian-Dong

scheme or table, p. 4675 - 4677 (2009/04/06)

Berberine (BBR, 1) is a novel cholesterol-lowering agent that up-regulates low-density-lipoprotein receptor (LDLR) expression through a mechanism different from that of statins. Because of the unique mode of action and good safety record, BBR provoked our

Synthesis and antihyperglycemic evaluation of various protoberberine derivatives

Bian, Xiaoli,He, Langchong,Yang, Guangde

, p. 1380 - 1383 (2007/10/03)

Various berberine derivatives (2-17) were synthesized and their antihyperglycemic activities were evaluated in a model of β-cell-membrane chromatography and a model of alloxan-induced diabetes mice. The results indicated that compounds 5 and 14 exhibited antihyperglycemic activity. Their structure-activity relationships were discussed.

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