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Val-Glu(OBzl)-OBzl is a tripeptide derivative, consisting of two amino acids, valine (Val) and glutamic acid (Glu), with a benzyl (OBzl) protecting group on the side chain of glutamic acid and a terminal benzyl ester group. This chemical structure is significant in peptide chemistry, as the benzyl protecting groups are used to prevent unwanted side reactions, such as hydrolysis or racemization, during peptide synthesis. The terminal benzyl ester group can also serve as a protecting group for the carboxylic acid functionality, which is crucial for subsequent coupling reactions in peptide chain elongation. The synthesis and manipulation of such protected peptides are essential for the development of pharmaceuticals and the study of protein structure and function.

3062-13-3

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3062-13-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 3062-13-3 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 3,0,6 and 2 respectively; the second part has 2 digits, 1 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 3062-13:
(6*3)+(5*0)+(4*6)+(3*2)+(2*1)+(1*3)=53
53 % 10 = 3
So 3062-13-3 is a valid CAS Registry Number.

3062-13-3Relevant academic research and scientific papers

Amino acids and peptides. XVII. Synthesis of peptides related to N-terminal portion of fibrin alpha-chain and their inhibitory effect on fibrinogen/thrombin clotting.

Kawasaki,Tsuji,Hirase,Miyano,Inouye,Iwamoto

, p. 525 - 528 (2007/10/02)

Various peptides related to N-terminal portion of fibrin alpha-chain were synthesized by the solution method and the solid-phase method, and their inhibitory effect on fibrinogen/thrombin clotting was examined. Extension of peptide chain from N-terminal t

N-acyl peptide, processes for their preparation and pharmaceutical compositions thereof

-

, (2008/06/13)

N-acylpeptides are disclosed of the formula: STR1 wherein R1 is alkanoyloxy or alkenoyloxy; R2 is alkyl or alkenyl; R3 and R4 are each lower alkyl, hydroxy(lower)alkyl, ar(lower)alkyl, esterified carboxy(lower)alkyl, carboxy(lower)alkyl, protected amino(lower)alkyl or amino(lower)alkyl; R5 is hydrogen, hydroxy(lower)alkyl, protected amino(lower)alkyl, amino(lower)alkyl, carboxy(lower)alkyl or esterified carboxy(lower)alkyl; R6 is carboxy, esterified carboxy or sulfo(lower)alkyl; A1, A2 and A3 are each bond or lower alkylene; and m and n are each an integer of 0 or 1; or its pharmaceutically acceptable salt. These compounds have anti-complementary activity and fibrinolytic activity, and are useful as therapeutic agents for immune-complex diseases or autoimmune diseases such as nephritis, rheumatic diseases, systemic lupus erythematosus, etc. and thrombosis such as cerebral apoplexy, coronary insufficiency, pulmonary embolism, etc.

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