84759-63-7

Upstream product

• 13122-89-9 (S)-methyl 2-((S)-2-(tert-butoxycarbonylamino)-3-phenylpropanamido)-3-phenylpropanoate 
• 2577-90-4 methyl (2S)-2-amino-3-phenylpropanoate 
• 2666-93-5 (S)-Leu-OMe 
• 13122-90-2 Boc-Phe-Phe-OH 
• 64152-76-7 methyl (S)-2-((S)-2-(tert-butoxycarbonylamino)-3-phenylpropanamido)-4-methylpentanoate 
• 13734-34-4 N-tert-butoxycarbonyl-L-phenylalanine 
• 68835-84-7 L-phenylalanyl-L-leucine methyl ester trifluoroacetate 
• 42267-16-3 (d,l)-phenylserine ethyl ester hydrochloride 
• 84759-52-4 ^tBOC-(S)-Phe-ΔPhe-(S)-Leu-OMe 
• 7517-19-3 methyl (L)-leucinate hydrochloride 
• 110694-57-0 Boc-Phe-(β-OH)Phe-OH 
• 110697-93-3 Boc-Phe-Phe-azlactone 

Downstream Products

• 1590380-85-0 C₄₁H₅₄N₄O₁₀ 
• 1590380-89-4 C₃₂H₃₆N₄O₇ 
• 1590380-66-7 C₄₁H₄₇N₅O₇ 
• 1590380-67-8 C₃₄H₄₁N₅O₇ 
• 1590380-68-9 C₃₅H₄₁N₅O₈ 
• 1590380-93-0 C₃₈H₄₈N₆O₈ 
• 1590380-70-3 C₃₃H₄₀N₆O₆*C₂HF₃O₂ 

Relevant academic research and scientific papers

On the Role of Chirality in Guiding the Self-Assembly of Peptides

Homochirality in peptides is crucial in sustaining “like–like” intermolecular interactions that allow the formation of assemblies and aggregates and is ultimately responsible for the resulting material properties. With the help of a series of stereoisomer

NOVEL SHORT-CHAIN PEPTIDES AS KAPPA (κ) OPIOID RECEPTORS (KOR) AGONIST

The present invention relates to novel short-chain peptides of the general formula (I), which are selective and peripherally acting KOR agonist, their tautomeric forms, their enantiomers, their diastereoisomers, their stereoisomers, their pharmaceutically

Furan-based locked Z -vinylogous γ-amino acid stabilizing protein α-turn in water-soluble cyclic α3γ tetrapeptides

Described here is the design, synthesis, and conformational analysis of cyclic tetrapeptides (CTPs) with α3γ architecture containing a furan-based locked Z-vinylogous amino acid (Vaa). This unnatural amino acid locks into a γ-turn that induces

SYNTHESIS OF CHIRAL OLIGOPEPTIDES BY MEANS OF CATALYTIC ASYMMETRIC HYDROGENATION OF DEHYDROPEPTIDES

Asymmetric hydrogenation of Ac-ΔTyr(Ac)-(S)-Ala-Gly-OMe (6), Ac-ΔTyr(Ac)-(R)-Ala-Gly-(S)-Phe-OMe (7), Ac-ΔPhe-NH-CH(R)-CH2-OCH2Ph (10), HCO-ΔPhe-(S)-Leu-OMe (16), X-AA-ΔPhe-AA'-OMe ( 5: X=tBOC, CBZ, CF3CO; AA, AA'= α-amino acid ), and t

SYNTHESIS OF CHIRAL TRIPEPTIDES BY ASYMMETRIC HYDROGENATION OF DEHYDROPEPTIDES. REMARKABLE EFFECTS OF N-PROTECTING GROUPS ON STEREOSELECTIVITY AND REACTIVITY

Dehydrotripeptides, X-CH(Ri)-ΔPhe-CH(Rk)COOMe (3: X = tBOC-NH, CBZ-NH, CF3CONH and N3), were employed for the asymmetric hydrogenation catalyzed by chiral rhodium complexes and it was found that tBOC-3 brought a