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N'-tert-Butyl-N-((E)-4,8-dimethyl-nona-3,7-dienyl)-N-methyl-formamidine is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

1026396-93-9

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1026396-93-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1026396-93-9 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,0,2,6,3,9 and 6 respectively; the second part has 2 digits, 9 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 1026396-93:
(9*1)+(8*0)+(7*2)+(6*6)+(5*3)+(4*9)+(3*6)+(2*9)+(1*3)=149
149 % 10 = 9
So 1026396-93-9 is a valid CAS Registry Number.

1026396-93-9Downstream Products

1026396-93-9Relevant academic research and scientific papers

Inhibition of geranylgeranyl diphosphate synthase by bisphosphonates and diphosphates: A potential route to new bone antiresorption and antiparasitic agents

Szabo, Christina M.,Matsumura, Yoshihiro,Fukura, Sayaka,Martin, Michael B.,Sanders, John M.,Sengupta, Suraj,Cieslak, John A.,Loftus, Timothy C.,Lea, Christopher R.,Lee, Hyung-Jae,Koohang, Ali,Coates, Robert M.,Sagami, Hiroshi,Oldfield, Eric

, p. 2185 - 2196 (2007/10/03)

We report the inhibition of a human recombinant geranylgeranyl diphosphate synthase (GGPPSase) by 23 bisphosphonates and six azaprenyl diphosphates. The IC50 values range from 140 nM to 690 μM. None of the nitrogen-containing bisphosphonates that inhibit farnesyl diphosphate synthase were effective in inhibiting the GGPPSase enzyme. Using threedimensional quantitative structure-activity relationship/comparative molecular field analysis (CoMFA) methods, we find a good correlation between experimental and predicted activity: R2 = 0.938, Rcv2 = 0.900, Rbs2 = 0.938, and F-test = 86.8. To test the predictive utility of the CoMFA approach, we used three training sets of 25 compounds each to generate models to predict three test sets of three compounds. The rms pIC50 error for the nine predictions was 0.39. We also investigated the pharmacophore of these GGPPSase inhibitors using the Catalyst method. The results demonstrated that Catalyst predicted the pIC50 values for the nine test set compounds with an rms error of 0.28 (R2 between experimental and predicted activity of 0.948).

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