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(R)-3-hydroxymethyl-5-phenyl-1,3-dihydro-benzo[e][1,4]diazepin-2-one is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

896746-84-2

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896746-84-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 896746-84-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 8,9,6,7,4 and 6 respectively; the second part has 2 digits, 8 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 896746-84:
(8*8)+(7*9)+(6*6)+(5*7)+(4*4)+(3*6)+(2*8)+(1*4)=252
252 % 10 = 2
So 896746-84-2 is a valid CAS Registry Number.

896746-84-2Downstream Products

896746-84-2Relevant academic research and scientific papers

Novel peptidomimetic cysteine protease inhibitors as potential antimalarial agents

Micale, Nicola,Kozikowski, Alan P.,Ettari, Roberta,Grasso, Silvana,Zappalà, Maria,Jeong, Jong-Jin,Kumar, Ajay,Hanspal, Manjit,Chishti, Athar H.

, p. 3064 - 3067 (2006)

The synthesis of a new class of peptidomimetics 1a-j, based on a 1,4-benzodiazepine scaffold and on a C-terminal aspartyl aldehyde building block, is described. Compounds 1a-j provided significant inhibitory activity against falcipains 2A and 2B (FP-2A an

Synthesis and biological evaluation of novel peptidomimetics as rhodesain inhibitors

Ettari, Roberta,Previti, Santo,Cosconati, Sandro,Kesselring, Jochen,Schirmeister, Tanja,Grasso, Silvana,Zappalà, Maria

, p. 1184 - 1191 (2016/10/09)

Novel rhodesain inhibitors were developed by combining an enantiomerically pure 3-bromoisoxazoline warhead with a 1,4-benzodiazepine scaffold as specific recognition moiety. All compounds were proven to inhibit rhodesain with K i values in the low-micromolar range. Their activity towards rhodesain was found to be coupled to an in vitro antitrypanosomal activity, with IC50 values ranging from the mid-micromolar to a low-micromolar value for the most active rhodesain inhibitor (R,S,S)-3. All compounds showed a good selectivity against the target enzyme since all of them were proven to be poor inhibitors of human cathepsin L.

NMR characterization and conformational analysis of a potent papain-family cathepsin L-like cysteine protease inhibitor with different behaviour in polar and apolar media

Rotondo, Archimede,Ettari, Roberta,Zappalà, Maria,De Micheli, Carlo,Rotondo, Enrico

, p. 337 - 343 (2015/01/16)

We recently reported the synthesis, of a potent papain-family cathepsin L-like cysteine protease inhibitor, as new lead compound for the development of new drugs that can be used as antiprotozoal agents. The investigation of its conformational profile is

Development of peptidomimetics with a vinyl sulfone warhead as irreversible falcipain-2 inhibitors

Ettari, Roberta,Nizi, Emanuela,Di Francesco, Maria Emilia,Dude, Marie-Adrienne,Pradel, Gabriele,Vi?ík, Radim,Schirmeister, Tanja,Micale, Nicola,Grasso, Silvana,Zappalà, Maria

, p. 988 - 996 (2008/09/19)

This paper describes the synthesis of a new class of peptidomimetic cysteine protease inhibitors based on a 1,4-benzodiazepine scaffold and on an electrophilic vinyl sulfone moiety. The former was introduced internally to a peptide sequence that mimics th

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