• CAS#159857-90-6
  • NameCbz-Phe-(Alloc)Lys-PAB-PNP
  • For reserach use only and not for human use!

Product Details

High quality purity >99% Cbz-Phe-(Alloc)Lys-PAB-PNP 159857-90-6 for sale

  • Molecular Formula:C41H43N5O11
  • Molecular Weight:781.819

159857-90-6 Relevant articles

CONJUGATE COMPOUNDS

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Page/Page column 78, (2014/06/24)

The invention relates to sphingoglycolip...

Design, synthesis, and antitumor activity of 4-halocolchicines and their pro-drugs activated by cathepsin B

Yasobu, Naoko,Kitajima, Mariko,Kogure, Noriyuki,Shishido, Yoshiyuki,Matsuzaki, Takeshi,Nagaoka, Masato,Takayama, Hiromitsu

scheme or table, p. 348 - 352 (2011/07/09)

Novel colchicine derivatives possessing ...

Cathepsin B-sensitive dipeptide prodrugs. 1. A model study of structural requirements for efficient release of doxorubicin

Dubowchik, Gene M.,Firestone, Raymond A.

, p. 3343 - 3346 (2007/10/03)

A series of lysosomal protease-sensitive...

159857-90-6 Process route

4-Nitrophenyl chloroformate
7693-46-1

4-Nitrophenyl chloroformate

N-Cbz-Phe-Lys(ε-Alloc)-4-aminobenzyl alcohol
159857-89-3

N-Cbz-Phe-Lys(ε-Alloc)-4-aminobenzyl alcohol

N-Cbz-Phe-Lys(ε-Alloc)-4-aminobenzyl 4-nitrophenyl carbonate
159857-90-6

N-Cbz-Phe-Lys(ε-Alloc)-4-aminobenzyl 4-nitrophenyl carbonate

Conditions
Conditions Yield
With pyridine; In tetrahydrofuran;
95%
With pyridine; In tetrahydrofuran; at 0 - 20 ℃;
71%
With pyridine; In dichloromethane; Ambient temperature;
N-(benzyloxycarbonyl)-phenylalanine-N-hydroxysuccinimide ester
3397-32-8

N-(benzyloxycarbonyl)-phenylalanine-N-hydroxysuccinimide ester

N-Cbz-Phe-Lys(ε-Alloc)-4-aminobenzyl 4-nitrophenyl carbonate
159857-90-6

N-Cbz-Phe-Lys(ε-Alloc)-4-aminobenzyl 4-nitrophenyl carbonate

Conditions
Conditions Yield
Multi-step reaction with 3 steps
1: NaHCO3 / 1,2-dimethoxy-ethane; H2O / Ambient temperature
2: 2-ethoxy-1-ethoxycarbonyl-1,2-dihydroquinoline / tetrahydrofuran / Ambient temperature
3: pyridine / CH2Cl2 / Ambient temperature
With pyridine; sodium hydrogencarbonate; N-ethoxycarbonyl-2-ethoxy-1,2-dihydroquinoline; In tetrahydrofuran; 1,2-dimethoxyethane; dichloromethane; water;
Multi-step reaction with 3 steps
1: sodium hydrogencarbonate / 1,2-dimethoxyethane; water
2: 4-methyl-morpholine; benzotriazol-1-ol; 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride / tetrahydrofuran
3: pyridine / tetrahydrofuran
With 4-methyl-morpholine; pyridine; sodium hydrogencarbonate; benzotriazol-1-ol; 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride; In tetrahydrofuran; 1,2-dimethoxyethane; water;
Multi-step reaction with 3 steps
1: sodium hydrogencarbonate / water; 1,2-dimethoxyethane
2: benzotriazol-1-ol; N-(3-dimethylaminopropyl)-N-ethylcarbodiimide; 4-methyl-morpholine / 4 h / 20 °C / Inert atmosphere; Cooling with ice
3: pyridine / tetrahydrofuran / 0 - 20 °C
With 4-methyl-morpholine; pyridine; sodium hydrogencarbonate; benzotriazol-1-ol; N-(3-dimethylaminopropyl)-N-ethylcarbodiimide; In tetrahydrofuran; 1,2-dimethoxyethane; water;

159857-90-6 Upstream products

  • 7693-46-1
    7693-46-1

    4-Nitrophenyl chloroformate

  • 159857-89-3
    159857-89-3

    N-Cbz-Phe-Lys(ε-Alloc)-4-aminobenzyl alcohol

  • 3397-32-8
    3397-32-8

    N-(benzyloxycarbonyl)-phenylalanine-N-hydroxysuccinimide ester

  • 623-04-1
    623-04-1

    4-aminobenzenemethanol

159857-90-6 Downstream products

  • 1279111-12-4
    1279111-12-4

    C55H60FN5O13

  • 1279111-11-3
    1279111-11-3

    C55H61N5O13

  • 71448-16-3
    71448-16-3

    Cbz-L-Phe-L-Lys-OH

  • 1613320-97-0
    1613320-97-0

    (2S,3S,4R)-1-O-(α-D-galactopyranosyl)-4-O-(hexacosanoyl)-2-[N-Cbz-Phe-Lys(ε-Alloc)-((4-aminobenzyloxy)carbonyl)amino]octadecane-1,3,4-triol

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