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(R)-2-(benzyloxy)-1-((3aR,5S,6aR)-2,2-dimethyltetrahydrofuro[2,3-d][1,3]dioxol-5-yl)ethan-1-ol is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

78784-99-3

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78784-99-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 78784-99-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,8,7,8 and 4 respectively; the second part has 2 digits, 9 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 78784-99:
(7*7)+(6*8)+(5*7)+(4*8)+(3*4)+(2*9)+(1*9)=203
203 % 10 = 3
So 78784-99-3 is a valid CAS Registry Number.

78784-99-3Relevant academic research and scientific papers

TLR7 AGONISTS

-

, (2021/05/28)

The present invention relates to TLR7 agonists according to Formula I and their use in the treatment of diseases such as cancer and infectious disease.

Design, synthesis and SAR of potent statine-based BACE-1 inhibitors: Exploration of P1 phenoxy and benzyloxy residues

Baeck, Marcus,Nyhlen, Jonas,Kvarnstroem, Ingemar,Appelgren, Sara,Borkakoti, Neera,Jansson, Katarina,Lindberg, Jimmy,Nystroem, Susanne,Hallberg, Anders,Rosenquist, Asa,Samuelsson, Bertil

experimental part, p. 9471 - 9486 (2009/04/11)

Several BACE-1 inhibitors with low nanomolar level activities, encompassing a statine-based core structure with phenyloxymethyl- and benzyloxymethyl residues in the P1 position, are presented. The novel P1 modification introduced to allow the facile exploration of the S1 binding pocket of BACE-1, delivered highly promising inhibitors.

Design and synthesis of potent inhibitors of the malaria aspartyl proteases plasmepsin I and II. Use of solid-phase synthesis to explore novel statine motifs

Johansson, Per-Ola,Chen, Yantao,Belfrage, Anna Karin,Blackman, Michael J.,Kvarnstr?m, Ingemar,Jansson, Katarina,Vrang, Lotta,Hamelink, Elizabeth,Hallberg, Anders,Rosenquist, ?sa,Samuelsson, Bertil

, p. 3353 - 3366 (2007/10/03)

Picomolar to low nanomolar inhibitors of the two aspartic proteases plasmepsin (Plm) I and II, from the malaria parasite Plasmodium falciparum, have been identified from sets of libraries containing novel statine-like templates modified at the amino and c

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