104347-81-1

Upstream product

• 1161-13-3 N-Cbz-L-Phe 
• 105500-29-6 N²-(benzyloxycarbonyl)-N¹,N¹-dimethyl-L-phenylalanin-amid 
• 124-40-3 dimethyl amine 
• 2578-84-9 N-benzyloxycarbonyl-L-phenylalanine p-nitrophenyl ester 

Downstream Products

• 96574-62-8 L-phenylalanyl-L-phenylalanine dimethylamide 
• 121638-08-2 2,8-Bis<(N-carbonyl-Gly-Phe-NMe2)-Pro-D-Ala-NH>epindolidione 
• 128302-57-8 C₅₆H₆₆N₁₄O₁₂ 
• 128302-52-3 C₅₈H₆₆N₁₄O₁₂ 
• 128326-89-6 C₆₄H₇₈N₁₄O₁₂ 
• 128302-56-7 C₆₂H₇₄N₁₄O₁₂ 
• 128302-56-7 C₆₂H₇₄N₁₄O₁₂ 
• 104347-82-2 Boc-D-Arg(NO₂)-Phe-N(CH₃)2 
• 104347-79-7 Tyr-D-Arg-Phe-N(CH₃)2 
• 104347-83-3 Boc-Tyr-D-Arg(NO₂)-Phe-N(CH₃)2 
• 96574-33-3 N^2.2-<(R)-N^2.1-benzoyl-2-phenyl-2-allylglycyl>-L-phenylalanyl-L-phenylalanine dimethylamide 
• 96574-33-3 N^2.2-<(S)-N^2.1-benzoyl-2-phenyl-2-allylglycyl>-L-phenylalanyl-L-phenylalanine dimethylamide 
• 95525-87-4 N^2.2-<(R)-N^2.1-benzoyl-2-phenylalanyl>-L-phenylalanyl-L-phenylalanine dimethylamide 
• 95525-88-5 N^2.2-<(S)-N^2.1-benzoyl-2-phenylalanyl>-L-phenylalanyl-L-phenylalanine dimethylamide 

Relevant academic research and scientific papers

Synthesis and Conformational Analysis of Epindolidione-Derived Peptide Models for β-Sheet Formation

Synthesis of 2,8-diaminoepindolidione (2,8-diaminodibenzonaphthyridine-6,12(5,11H)-dione) in 19percent yield from p-nitroaniline is reported, as well as further conversion to 2,8-bis(Boc-L-Pro-Xxx)epindolidione (Xxx=Gly, D-Ala) and then to 2,8-bis(OC(Yyy-Zzz-NMe2)-L-Pro-Xxx)epindolidione (Yyy=Gly, L-Ala, D-Ala; Zzz=Gly, L-Phe, D-Phe).The β-turn-forming tendencies of the series 2,8-bis(X-L-Pro-D-Ala)epindolidione, where X=Ac, Boc, and COGlyOEt, are assigned from 1H NMR evidence.

Tumor retarding (1-benzyl-ethylenediamine)-platin (II)-complexes

There are described (1-benzylethylenediamine)-platin(II)-complexes of the general formula: STR1 wherein the radicals R1, R2, R3, and R4 are the same or different and are hydrogen, a C1 -C6