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(S)-4-tert-butyl 1-((R)-2-(pent-4-enamido)-3-phenylpropyl)-2-allylsuccinate is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

1395847-83-2

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1395847-83-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1395847-83-2 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,3,9,5,8,4 and 7 respectively; the second part has 2 digits, 8 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 1395847-83:
(9*1)+(8*3)+(7*9)+(6*5)+(5*8)+(4*4)+(3*7)+(2*8)+(1*3)=222
222 % 10 = 2
So 1395847-83-2 is a valid CAS Registry Number.

1395847-83-2Relevant academic research and scientific papers

SONIC HEDGEHOG MODULATORS

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Paragraph 0877; 0886; 1241, (2014/04/17)

Sonic Hedgehog modulators and methods of use thereof are provided for.

Macrocyclic hedgehog pathway inhibitors: Optimization of cellular activity and mode of action studies

Dockendorff, Chris,Nagiec, Marek M.,Weiwer, Michel,Buhrlage, Sara,Ting, Amal,Nag, Partha P.,Germain, Andrew,Kim, Han-Je,Youngsaye, Willmen,Scherer, Christina,Bennion, Melissa,Xue, Linlong,Stanton, Benjamin Z.,Lewis, Timothy A.,MacPherson, Lawrence,Palmer, Michelle,Foley, Michael A.,Perez, Jose R.,Schreiber, Stuart L.

supporting information, p. 808 - 813 (2013/01/15)

Macrocyclic Hedgehog (Hh) pathway inhibitors have been discovered with improved potency and maximal inhibition relative to the previously reported macrocycle robotnikinin. Analogues were prepared using a modular and efficient build-couple-pair (BCP) approach, with a ring-closing metathesis step to form the macrocyclic ring. Varying the position of the macrocycle nitrogen and oxygen atoms provided inhibitors with improved activity in cellular assays; the most potent analogue was 29 (BRD-6851), with an IC50 of 0.4 μM against C3H10T1/2 cells undergoing Hh-induced activation, as measured by Gli1 transcription and alkaline phosphatase induction. Studies with Patched knockout (Ptch-/-) cells and competition studies with the Smoothened (Smo) agonists SAG and purmorphamine demonstrate that in contrast to robotnikinin, select analogues are Smo antagonists.

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