• CAS#72103-53-8
  • NameTuftsin
  • For reserach use only and not for human use!

Product Details

MF: C25H48N8O10

Cost-effective and customizable Tuftsin 72103-53-8 factory

  • Molecular Formula:C25H48N8O10
  • Molecular Weight:620.70
  • PSA:289.78000 
  • LogP:0.53410 

TUFTSIN ACETATE SALT(Cas 72103-53-8) Usage

General Description

Tuftsin acetate salt is a synthetic derivative of the naturally occurring tetrapeptide tuftsin. It is a white to off-white powder with the chemical formula C22H33N7O7. Tuftsin acetate salt has been studied for its potential immunomodulatory and anti-tumor effects. It has been shown to enhance the activity of immune cells, such as macrophages and natural killer cells, and to increase the production of tumor necrosis factor alpha (TNF-α), which plays a key role in the body's immune response to cancer. Tuftsin acetate salt is currently being investigated for its potential as a therapeutic agent in cancer treatment and other immune-related disorders.

InChI:InChI=1/C21H40N8O6.C2H4O2/c1-12(30)16(23)18(32)27-13(6-2-3-9-22)19(33)29-11-5-8-15(29)17(31)28-14(20(34)35)7-4-10-26-21(24)25;1-2(3)4/h12-16,30H,2-11,22-23H2,1H3,(H,27,32)(H,28,31)(H,34,35)(H4,24,25,26);1H3,(H,3,4)

72103-53-8 Relevant articles

Synthesis of Tuftsin Using Picolyl Ester Method.

Dasgupta, S.,Chauhan, V. S.

, p. 1138 - 1141 (2007/10/02)

A convenient and quick synthesis of tuft...

72103-53-8 Process route

acetic acid
64-19-7,77671-22-8

acetic acid

N-t-butoxycarbonyl-O-benzyl-L-threonyl-N<sup>ε</sup>-benzyloxycarbonyl-L-lysyl-L-prolyl-N<sup>ω</sup>-nitro-L-arginine 4-picolyl ester
109277-03-4

N-t-butoxycarbonyl-O-benzyl-L-threonyl-Nε-benzyloxycarbonyl-L-lysyl-L-prolyl-Nω-nitro-L-arginine 4-picolyl ester

tuftsin
72103-53-8,104240-42-8,109277-04-5,111610-67-4

tuftsin

Conditions
Conditions Yield
With hydrogen; palladium on activated charcoal; In methanol; for 12h; Ambient temperature;
53%
N-benzyloxycarbonyl-L-threonyl-N<sup>ε</sup>-benzyloxycarbonyl-L-lysyl-L-prolyl-N<sup>ω</sup>-nitro-L-arginine 4-picolyl ester
109333-59-7

N-benzyloxycarbonyl-L-threonyl-Nε-benzyloxycarbonyl-L-lysyl-L-prolyl-Nω-nitro-L-arginine 4-picolyl ester

trifluoroacetic acid
76-05-1

trifluoroacetic acid

tuftsin
72103-53-8,104240-42-8,109277-04-5,111610-67-4

tuftsin

Conditions
Conditions Yield
With hydrogen; palladium on activated charcoal; Yield given. Multistep reaction; 1) methanol, acetic acid, 16hr, 2) 30 min;

72103-53-8 Upstream products

  • 64-19-7
    64-19-7

    acetic acid

  • 109277-03-4
    109277-03-4

    N-t-butoxycarbonyl-O-benzyl-L-threonyl-Nε-benzyloxycarbonyl-L-lysyl-L-prolyl-Nω-nitro-L-arginine 4-picolyl ester

  • 109333-59-7
    109333-59-7

    N-benzyloxycarbonyl-L-threonyl-Nε-benzyloxycarbonyl-L-lysyl-L-prolyl-Nω-nitro-L-arginine 4-picolyl ester

  • 76-05-1
    76-05-1

    trifluoroacetic acid

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