Welcome to LookChem.com Sign In|Join Free
  • or
Z-Orn-OBn, also known as N-benzyloxycarbonyl-L-ornithine, is a chemical compound with the molecular formula C14H22N2O4. It is a derivative of the amino acid L-ornithine, where the carboxylic acid group is protected by a benzyloxycarbonyl (Z) group, and the amino group is also protected by a benzyl group. Z-Orn-OBn is commonly used in peptide synthesis as a building block, particularly in solid-phase peptide synthesis (SPPS), due to its stability and ease of coupling. The Z group serves as a temporary protecting group that can be removed under mild acidic conditions, allowing for the subsequent addition of other amino acids to form longer peptide chains. Z-Orn-OBn is also used in research to study the properties and interactions of peptides and proteins.

98512-07-3

Post Buying Request

98512-07-3 Suppliers

Recommended suppliers

  • Product
  • FOB Price
  • Min.Order
  • Supply Ability
  • Supplier
  • Contact Supplier

98512-07-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 98512-07-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 9,8,5,1 and 2 respectively; the second part has 2 digits, 0 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 98512-07:
(7*9)+(6*8)+(5*5)+(4*1)+(3*2)+(2*0)+(1*7)=153
153 % 10 = 3
So 98512-07-3 is a valid CAS Registry Number.

98512-07-3Relevant academic research and scientific papers

NG-aminoguanidines from primary amines and the preparation of nitric oxide synthase inhibitors

Martin, Nathaniel I.,Beeson, William T.,Woodward, Joshua J.,Marletta, Michael A.

, p. 924 - 931 (2008/09/20)

A concise, general, and high-yielding method for the preparation of N G-aminoguanidines from primary amines is reported. Using available and readily prepared materials, primary amines are converted to protected N G-aminoguanidines in a one-pot procedure. The method has been successfully applied to a number of examples including the syntheses of four nitric oxide synthase (NOS) inhibitors. The inhibitors prepared were investigated as competitive inhibitors and as mechanistic inactivators of the inducible isoform of NOS (iNOS). In addition, one of the four inhibitors prepared, NG-amino-NG-2,2,2-trifluoroethyl-L-arginine 19, displays the unique ability to both inhibit NO formation and prevent NADPH consumption by iNOS without irreversible inactivation of the enzyme.

Synthesis and evaluation of peptidic maleimides as transglutaminase inhibitors

Halim, Dany,Caron, Karine,Keillor, Jeffrey W.

, p. 305 - 308 (2007/10/03)

A series of novel transglutaminase inhibitors was prepared, based on the scaffold of a commonly used peptide substrate and bearing an electrophilic maleimide group. These compounds were evaluated in vitro and shown to lead to irreversible inactivation of tissue transglutaminase. Comparison with inhibitors studied previously provides insight into the steric environment of the enzyme active site.

Post a RFQ

Enter 15 to 2000 letters.Word count: 0 letters

Attach files(File Format: Jpeg, Jpg, Gif, Png, PDF, PPT, Zip, Rar,Word or Excel Maximum File Size: 3MB)

1 Customer Service

What can I do for you?
Get Best Price

Get Best Price for 98512-07-3