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tert-butyl N-[(2S)-2-amino-4-methylpentyl]carbamate is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

1217317-66-2

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1217317-66-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1217317-66-2 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,2,1,7,3,1 and 7 respectively; the second part has 2 digits, 6 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 1217317-66:
(9*1)+(8*2)+(7*1)+(6*7)+(5*3)+(4*1)+(3*7)+(2*6)+(1*6)=132
132 % 10 = 2
So 1217317-66-2 is a valid CAS Registry Number.

1217317-66-2Downstream Products

1217317-66-2Relevant academic research and scientific papers

COMBINATIONS AND DOSING REGIMES TO TREAT RB-POSITIVE TUMORS

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Page/Page column 123, (2016/06/01)

This invention directed to methods for treating select RB-positive cancers and other Rb- positive abnormal cellular proliferative disorders using CDK4/6 inhibitors in specific dosing and combination or alternation regimes. In one aspect, treatments of select RB-positive cancers are disclosed using specific CDK4/6 inhibitors in combination or alternation with another chemotherapeutic, for example, an additional kinase inhibitor, PD-1 inhibitor, or BCL-2 inhibitor, or combination thereof.

TRANSIENT PROTECTION OF NORMAL CELLS DURING CHEMOTHERAPY

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Page/Page column 131; 132, (2014/09/29)

This invention is in the area of improved compounds, compositions and methods of transiently protecting healthy cells, and in particular hematopoietic stem and progenitor cells (HSPC) as well as renal cells, from damage associated with DNA damaging chemotherapeutic agents. In one aspect, improved protection of healthy cells is disclosed using disclosed compounds that act as highly selective and short, transiently-acting cyclin-dependent kinase 4/6 (CDK 4/6) inhibitors when administered to subjects undergoing DNA damaging chemotherapeutic regimens for the treatment of proliferative disorders.

CDK INHIBITORS

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Paragraph 0250, (2013/09/26)

Compounds of formulae I, II or III, and pharmaceutically acceptable salts thereof, are useful as CDK inhibitors.

Parallel synthesis of an oligomeric imidazole-4, 5-dicarboxamide library

Xu, Zhigang,DiCesare, John C.,Baures, Paul W.

supporting information; experimental part, p. 248 - 254 (2010/08/19)

A library of oligomeric compounds was synthesized based on the imidazole-4, 5-dicarboxylic acid scaffold along with amino acid esters and chiral diamines derived from amino acids. The final compounds incorporate nonpolar amino acids (Leu, Phe, Trp), polar amino acids (Ser, Asp, Arg), and neutral amino acids (Gly, Ala), and were designed to be useful in screening for inhibitors of protein-protein interactions. Many of the protected and deprotected oligomers show evidence of conformational isomers persistent at room temperature in aqueous solution. A total of 317 final oligomers, out of 441 targeted compounds, were obtained in high analytical purity and of sufficient quantity to submit them for high-throughput screening as part of the NIH Roadmap.

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