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Home  > (5S,8S,14S,17S,20S)-14,17-Dibenzyl-5-carbamoyl-20-(carboxymethyl)-8-isobutyl-15-methyl-7,10,13,16,19,22-hexaoxo-2-thia-6,9,12,15,18,21-hexaazapentacosan-25-oic acid

AD78422

106128-89-6 | (5S,8S,14S,17S,20S)-14,17-Dibenzyl-5-carbamoyl-20-(carboxymethyl)-8-isobutyl-15-methyl-7,10,13,16,19,22-hexaoxo-2-thia-6,9,12,15,18,21-hexaazapentacosan-25-oic acid

Packsize Purity Availability Price Discounted Price    Quantity
1mg in stock $337.00 $236.00 -   +
5mg in stock $1,170.00 $819.00 -   +
10mg in stock $2,004.00 $1,403.00 -   +
25mg in stock $4,227.00 $2,959.00 -   +

*All products are for research use only and not intended for human or animal use.

*All prices are in USD.

Description
Catalog Number: AD78422
Chemical Name: (5S,8S,14S,17S,20S)-14,17-Dibenzyl-5-carbamoyl-20-(carboxymethyl)-8-isobutyl-15-methyl-7,10,13,16,19,22-hexaoxo-2-thia-6,9,12,15,18,21-hexaazapentacosan-25-oic acid
CAS Number: 106128-89-6
Molecular Formula: C40H55N7O11S
Molecular Weight: 841.97
MDL Number: MFCD00076799
SMILES: CSCC[C@@H](C(=O)N)NC(=O)[C@@H](NC(=O)CNC(=O)[C@@H](N(C(=O)[C@@H](NC(=O)[C@@H](NC(=O)CCC(=O)O)CC(=O)O)Cc1ccccc1)C)Cc1ccccc1)CC(C)C

 

Upstream Synthesis Route
  • The compound (5S,8S,14S,17S,20S)-14,17-Dibenzyl-5-carbamoyl-20-(carboxymethyl)-8-isobutyl-15-methyl-7,10,13,16,19,22-hexaoxo-2-thia-6,9,12,15,18,21-hexaazapentacosan-25-oic acid plays a crucial role in chemical synthesis, particularly in peptide chemistry. Due to its complex structure and specific functional groups, this compound is commonly used as a building block in peptide synthesis to introduce unique side chains and functionalities into peptides. Its multifunctional nature allows for precise manipulation during peptide assembly, enabling the creation of novel peptide sequences with tailored properties. Additionally, the presence of the carboxymethyl and carbamoyl groups in this compound facilitates conjugation reactions with other molecules, expanding its utility in the preparation of peptide conjugates and bioconjugates for various research and therapeutic applications.
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