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1-(2,3,4,6-tetra-O-benzyl-1-deoxy-β-D-glucopyranos-1-yl)-2,3-dihydro-1H-indole is a complex organic compound that features a 1H-indole core with a 2,3-dihydro substitution. The molecule is further characterized by a tetra-O-benzyl-1-deoxy-β-D-glucopyranosyl group attached to the indole nitrogen. This group consists of a β-D-glucopyranose sugar moiety with all four hydroxyl groups (at positions 2, 3, 4, and 6) protected by benzyl groups, and a 1-deoxy modification, which means the first carbon of the sugar ring lacks an oxygen atom. This chemical structure is significant in the field of organic synthesis, particularly in the preparation of complex carbohydrates and glycoconjugates, and may have applications in medicinal chemistry due to its potential interactions with biological targets.

4132-33-6

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4132-33-6 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 4132-33-6 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 4,1,3 and 2 respectively; the second part has 2 digits, 3 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 4132-33:
(6*4)+(5*1)+(4*3)+(3*2)+(2*3)+(1*3)=56
56 % 10 = 6
So 4132-33-6 is a valid CAS Registry Number.

4132-33-6Relevant academic research and scientific papers

Synthesis and antiproliferative evaluation of glucosylated pyrazole analogs of K252c

Douara, Bachir,Esvan, Yannick J.,Pereira, Elisabeth,Giraud, Francis,Volodina, Yulia L.,Kaluzhny, Dmitry N.,Shtil, Alexander A.,Anizon, Fabrice,Moreau, Pascale

, p. 892 - 901 (2018)

Pyrazole analogs of the staurosporine aglycon K252c were recently described as potent inhibitors of the three Pim protein kinase isoforms. To evaluate the impact of the introduction of a sugar moiety on the biological activities of this heterocyclic scaffold, four new glucosylated pyrazole analogs of K252c were synthesized. Their biological evaluation demonstrated that most active compounds 11 and 19 substituted by a β-D-glucosyl moiety at N12 or N13 positions exhibited antiproliferative activities toward HCT116 cells.

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