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20777-79-1

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20777-79-1 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 20777-79-1 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,0,7,7 and 7 respectively; the second part has 2 digits, 7 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 20777-79:
(7*2)+(6*0)+(5*7)+(4*7)+(3*7)+(2*7)+(1*9)=121
121 % 10 = 1
So 20777-79-1 is a valid CAS Registry Number.

20777-79-1Relevant articles and documents

Design, synthesis, and in vitro evaluation of aza-peptide aldehydes and ketones as novel and selective protease inhibitors

Border, Sarah E.,Caffrey, Conor R.,Corrigan, Thomas S.,Do?an Ekici, ?zlem,Fajtova, Pavla,Hadad, Christopher M.,Kasper, Kayla Q.,Lotti Diaz, Leilani M.,McElroy, Craig A.,Ratigan, Steven C.,Salvesen, Guy S.,Sojka, Daniel

, p. 1387 - 1402 (2020/07/13)

Aza-peptide aldehydes and ketones are a new class of reversible protease inhibitors that are specific for the proteasome and clan CD cysteine proteases. We designed and synthesised aza-Leu derivatives that were specific for the chymotrypsin-like active si

Aza-peptide epoxides: A new class of inhibitors selective for clan CD cysteine proteases

Asgian, Juliana L.,James, Karen Ellis,Li, Zhao Zhao,Carter, Wendy,Barrett, Alan J.,Mikolajczyk, Jowita,Salvesen, Guy S.,Powers, James C.

, p. 4958 - 4960 (2007/10/03)

Aza-peptide epoxides, a new class of irreversible protease inhibitors, are specific for the clan CD cysteine proteases. The inhibitors have second-order rate constants up to 105 M-1 s-1, with the most potent epoxides having the S,S stereochemistry. The aza-Asn derivatives are effective legumain inhibitors, while the aza-Asp epoxides were specific for caspases. The inhibitors have little or no inhibition with other proteases such as chymotrypsin, papain, or cathepsin B.

Synthesis and inhibiting activities of 1-peptidyl-2-haloacetyl hydrazines toward cathepsin B and calpains

Giordano, C,Calabretta, R,Gallina, C,Consalvi, V,Scandurra, R,et al.

, p. 297 - 311 (2007/10/02)

Twenty-four 1-peptidyl-2-haloacetyl hydrazines which can be considered azapeptide halomethanes were synthesized and tested as models of cathepsin B, calpain I and calpain II inhibitors.Reagents designed for cathepsin B inactivation include Z-Tyr, Z-Tyr(I)

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