3422-91-1

Upstream product

• 2432-99-7 11-aminoundecanoic acid 
• 501-53-1 benzyl chloroformate 
• 163358-15-4 3-(11-benzyloxycarbonylamino-n-undecanoyl)-4(S)-(phenylmethyl)-2-oxazolidinone 
• 90719-32-7 (S)-4-Benzyl-2-oxazolidinone 
• 3282-30-2 pivaloyl chloride 

Downstream Products

• 114255-94-6 N-<2-O-<2-acetamido-1,5-anhydro-6-O-(11-benzyloxycarbonylaminoundecanoyl)-2,3-dideoxy-D-glucitol-3-yl>-D-lactoyl>-L-alanyl-D-isoglutamine methyl ester 
• 150671-88-8 N¹-<11-<(Benzyloxycarbonyl)amino>undecanoyl>-N⁴,N⁸-bis(toluol-4-sulfonyl)spermidin 
• 98603-11-3 methyl 11-benzyloxycarbonylaminoundecanoate 
• 189131-85-9 11-{[(benzyloxy)carbonyl](methyl)amino}undecanoic acid 
• 1638743-08-4 benzyl (1R,2R,7S,8aR)-1,2-di-tert-butoxyoctahydroindolizin-7-yl decane-1,10-diylbiscarbamate 
• 1638743-07-3 benzyl (11-azido-11-oxoundecyl)carbamate 
• 1037297-70-3 C₈₇H₁₁₆N₂O₁₃ 
• 111637-14-0 Benzyloxycarbonyl-tris-ω-amino-undecansaeure-thiophenylester 
• 101121-13-5 Benzyloxycarbonyl-bis-ω-amino-undecansaeure-hydrazid 
• 735224-83-6 ω-Amino-undecansaeure-thiophenylester 
• 3611-30-1 S-benzyl-N-{11-[(S-benzyl-N-benzyloxycarbonyl-L-cysteinyl)-amino]-undecanoyl}-L-cysteine benzyl ester 
• 150672-05-2 (RS)-N¹-<11-<alanyl>amino>undecanoyl>-N⁴,N⁸-bis(toluol-4-sulfonyl)spermidin 
• 150672-02-9 (RS)-N¹-<11-<alanyl>amino>undecanoyl>-N⁴,N⁸-bis(toluol-4-sulfonyl)spermidin 
• 150672-00-7 (RS)-N¹-<11-<amino>undecanoyl>-N⁴,N⁸-bis(toluol-4-sulfonyl)spermidin 

Relevant academic research and scientific papers

COMPOUND OR SALT THEREOF, NATURAL KILLER T CELL ACTIVATOR, AND PHARMACEUTICAL COMPOSITION

The invention provides a compound or a salt thereof capable of activating natural killer T cell, a natural killer T cell activating agent containing such a compound or a salt thereof, and a pharmaceutical composition. The compound of the invention is a co

Synthesis of biotin and fluorescein labeled (-)-lentiginosine

The important proapoptotic activity of (-)-lentiginosine, the enantiomer of a natural glycosidase inhibitor, associated with its low cytotoxicity, suggests the study of the unknown receptor responsible for the triggering of the proapoptotic cascade. To th

ALIPHATIC PYRAZINOYLGUANIDINE SODIUM CHANNEL BLOCKERS WITH BETA AGONIST ACTIVITY

The present invention provides sodium channel blockers possessing beta-adrenergic receptor agonist activity.

Benzyl and tert-butyl carbamate derivatives of 1,ω-amino acids as simple yet efficient gelators

We report the synthesis and a study of the gelation properties of a series of N-protected long-chain amino acids. Especially, benzyl and tert-butyl carbamate derivatives of 11-aminoundecanoic acid in their deprotonated form can gelate polar organic solvents and water at very low concentration (less than 5 mM). This is explained by the contribution of multiple forces-H-bond, van der Waals and ionic interactions-in the gel aggregate formation and stabilization, which is confirmed by the experimental data. Among the series of compounds investigated, only a dimer of 11-aminoundecanoic acid is capable of gelating toluene, which stems from the increased number of hydrogen bonding sites in the main aliphatic chain.

Substituted N-carboxyalkylpeptidyl derivatives as antidegenerative agents

Novel N-carboxyalkylpeptidyl compounds represented by the formula which are found to be useful inhibitors of matrix metalloendoproteinases which degrade major components of articular cartilage and basement membranes causing degenerative diseases such as a

Synthetic Analogues of Low-Molecular-Weight Acyl-polyamine Spider Toxins

Low-molecular-weight spider and wasp toxins are selective inhibitors of glutamate receptors of the central nervous system and consist of a polyamine backbone and one or several carboxylic acids and/or amino acids linked by a peptide-like bond.The syntheses of twelve analogues of spider and wasp toxins are described (10a-c, 15a-c, 20a-c, 25a-c) having the general structure of acyl, arylacyl, or heteroarylacyl -> DL-alanyl -> ω-aminoacyl -> N1-spermidine, with variation in the acyl and the ω-aminoacyl part.

Glucosamine derivatives

Compounds of the following formula and their physiologically acceptable salts are novel and have excellent immunostimulatory activity: STR1