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(R)-(4-benzyloxyphenyl)(tert-butoxycarbonylamino)acetic acid methyl ester is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

342898-56-0

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342898-56-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 342898-56-0 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 3,4,2,8,9 and 8 respectively; the second part has 2 digits, 5 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 342898-56:
(8*3)+(7*4)+(6*2)+(5*8)+(4*9)+(3*8)+(2*5)+(1*6)=180
180 % 10 = 0
So 342898-56-0 is a valid CAS Registry Number.

342898-56-0Relevant academic research and scientific papers

Novel 2-[(benzylamino)methyl]pyrrolidine-3,4-diol derivatives as α-mannosidase inhibitors and with antitumor activities against hematological and solid malignancies

Bello, Claudia,Cea, Michele,Bello, Giovanna Dal,Garuti, Anna,Rocco, Ilaria,Cirmena, Gabriella,Moran, Eva,Nahimana, Aimable,Duchosal, Michel A.,Fruscione, Floriana,Pronzato, Paolo,Grossi, Francesco,Patrone, Franco,Ballestrero, Alberto,Dupuis, Marc,Sordat, Bernard,Nencioni, Alessio,Vogel, Pierre

experimental part, p. 3320 - 3334 (2010/07/05)

Novel α-mannosidase inhibitors of the type (2R,3R,4S)-2-({[(1R)-2-hydroxy-1-arylethyl]amino}methyl)pyrrolidine-3,4-diol have been prepared and assayed for their anticancer activities. Compound 30 with the aryl group = 4-trifluoromethylbiphenyl inhibits the proliferation of primary cells and cell lines of different origins, irrespective of Bcl-2 expression levels, inducing a G2/Mcell cycle arrest and by modification of genes involved in cell cycle progression and survival.

Derivatives of Dihydroxypyrrolidine as Anti-Cancer Compounds

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Page/Page column 11; 20, (2009/06/27)

The present invention relates to derivatives of dihydroxypyrrolidine useful in the treatment of cancer. The invention further relates to a process for making the compounds. The compounds are inhibitors of α mannosidase, and possibly, also inhibit nicotina

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