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(2E,6E)-2,6-bis(thiophene-3-methylene)cyclohexanone is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

1360119-52-3

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1360119-52-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1360119-52-3 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,3,6,0,1,1 and 9 respectively; the second part has 2 digits, 5 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 1360119-52:
(9*1)+(8*3)+(7*6)+(6*0)+(5*1)+(4*1)+(3*9)+(2*5)+(1*2)=123
123 % 10 = 3
So 1360119-52-3 is a valid CAS Registry Number.

1360119-52-3Downstream Products

1360119-52-3Relevant academic research and scientific papers

Ag/P-Stereogenic Phosphine-Catalyzed Enantioselective 1,3-Dipolar Cycloadditions: A Method to Optically Active Pyrrolidines

Zhi, Mengna,Gan, Zhenjie,Ma, Rong,Cui, Hao,Li, Er-Qing,Duan, Zheng,Mathey, Fran?ois

, (2019)

A Ag/P-stereogenic phosphine-complex-catalyzed 1,3-dipolar cycloaddition of azomethine ylides with electron-deficient olefins is reported. In this reaction, highly functionalized pyrrolines with a spiro-quaternary stereogenic center were obtained in good yields (up to 99%) with excellent levels of diastereo-(up to >20:1 dr) and enantioselectivities (up to >99% ee). The chirality of adducts was controlled predominantly by the P-stereogenic phosphines.

Synthesis and evaluation of curcumin-related compounds for anticancer activity

Wei, Xingchuan,Du, Zhi-Yun,Zheng, Xi,Cui, Xiao-Xing,Conney, Allan H.,Zhang, Kun

experimental part, p. 235 - 245 (2012/08/28)

Sixty-one curcumin-related compounds were synthesized and evaluated for their anticancer activity toward cultured prostate cancer PC-3 cells, pancreas cancer Panc-1 cells and colon cancer HT-29 cells. Inhibitory effects of these compounds on the growth of PC-3, Panc-1 and HT-29 cells were determined by the MTT assay. Compounds E10, F10, FN1 and FN2 exhibited exceptionally potent inhibitory effects on the growth of cultured PC-3, Panc-1 and HT-29 cells. The IC50 for these compounds was lower than 1 μM in all three cell lines. E10 was 72-, 46- and 117-fold more active than curcumin for inhibiting the growth of PC-3, Panc-1 and HT-29 cells, respectively. F10 was 69-, 34- and 72-fold more active than curcumin for inhibiting the growth of PC-3, Panc-1 and HT-29 cells, respectively. FN1 and FN2 had about the same inhibitory effect as E10 and F10 toward Panc-1 cells but were less active than E10 and F10 toward PC-3 and HT-29 cells. The active compounds were potent stimulators of apoptosis. The present study indicates that E10, F10, FN1 and FN2 may have useful anticancer activity.

CURCUMIN ANALOGS AND METHODS OF USE THEREOF

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Page/Page column 20; 28-29, (2012/03/09)

Curcumin analogs and methods of use thereof are provided.

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