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125354-13-4

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125354-13-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 125354-13-4 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,2,5,3,5 and 4 respectively; the second part has 2 digits, 1 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 125354-13:
(8*1)+(7*2)+(6*5)+(5*3)+(4*5)+(3*4)+(2*1)+(1*3)=104
104 % 10 = 4
So 125354-13-4 is a valid CAS Registry Number.

125354-13-4Downstream Products

125354-13-4Relevant articles and documents

Taxol Structure-Activity Relationships: Synthesis and Biological Evaluation of 10-Deoxytaxol

Chen, Shu-Hui,Fairchild, Craig,Mamber, Stephen W.,Farina, Vittorio

, p. 2927 - 2928 (2007/10/02)

10-Deoxytaxol 2 was prepared from taxol (1) in four steps via the intermediate dienone 5b; the key reaction in the sequence is a Yarovenko reagent-mediated dehydration at the C-10 hydroxyl group.Compound 2 was found to possess comparable antitumor activity with respect to taxol.This confirms that the functional group at C-10 in taxol is not involved in receptor binding.

Relationships between the structure of taxol analogues and their antimitotic activity

Gueritte-Voegelein,Guenard,Lavelle,Le Goff,Mangatal,Potier

, p. 992 - 998 (2007/10/02)

A variety of synthetic analogues of taxol, a naturally occurring antitumor diterpene, were examined for their potency to inhibit microtubule disassembly. For some of the compounds, the in vitro cytotoxic properties showed a good correlation with the tubulin assay. This structure-activity relationship study shows that inhibition of microtubule disassembly is quite sensitive to the configuration at C-2' and C-3'. A correlation between the conformation of the side chain at C-13 and the activity is suggested. Of all the compounds examined, one of the most potent in inhibiting microtubule disassembly and in inhibiting murine P388 leukemic cells, N-debenzoyl-N-tert-(butoxycarbonyl)-10-deacetyltaxol, named taxotere, was selected for evaluation as a potential anticancer agent.

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