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4-(4-benzyloxy-phenyl)-3-tert-butoxycarbonylamino-butyric acid methyl ester is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

127106-65-4

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127106-65-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 127106-65-4 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,2,7,1,0 and 6 respectively; the second part has 2 digits, 6 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 127106-65:
(8*1)+(7*2)+(6*7)+(5*1)+(4*0)+(3*6)+(2*6)+(1*5)=104
104 % 10 = 4
So 127106-65-4 is a valid CAS Registry Number.

127106-65-4Relevant academic research and scientific papers

Synthesis and initial pharmacology of dual-targeting ligands for putative complexes of integrin αvβ3 and PAR2

Dockendorff, Chris,Gandhi, Disha M.,Hernandez, Irene,Holyst, Trudy,Majewski, Mark W.,Rosas, Ricardo,Wang, Zhengli,Weiler, Hartmut,Zhu, Jieqing

, p. 940 - 949 (2020/09/21)

Unpublished data from our labs led us to hypothesize that activated protein C (aPC) may initiate an anti-inflammatory signal in endothelial cells by modulating both the integrin αVβ3 and protease-activated receptor 2 (PAR2), which may exist in close proxi

α- and β-Substituted phosphonate analogs of LPA as autotaxin inhibitors

Cui, Peng,McCalmont, William F.,Tomsig, Jose L.,Lynch, Kevin R.,Macdonald, Timothy L.

, p. 2212 - 2225 (2008/09/21)

Autotaxin (ATX) is an attractive pharmacological target due to its lysophospholipase D activity which leads to the production of lysophosphatidic acid (LPA). Blockage of ATX produced LPA by small molecules could be a potential anticancer chemotherapy. In our previous study, we have identified the two β-hydroxy phosphonate analogs of LPA (compounds f17 and f18) as ATX inhibitors. With this work, we investigated α- and β-substituted phosphonate analogs of LPA and evaluated them for ATX inhibitory activity. The stereochemistry of β-hydroxy phosphonates was also studied.

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