Peptides & Peptide Synthesis Products

Boc-His(Dnp)-OH·IPA

Boc-His(Dnp)-OH·IPA
$20.00
$20.00
Boc-His(Dnp)-OH·IPA, Catalog No: 48059
N-alpha-Boc-N-tau-(2,4-dinitrophenyl)-L-histidine isopropyl alcohol complex, CAS: 25024-53-7, MW: 481.5, Formula: C17H19N5O8 · C3H8O
Catalog No: 48059
N-alpha-Boc-N-tau-(2,4-dinitrophenyl)-L-histidine isopropyl alcohol complex, CAS: 25024-53-7, MW: 481.5, Formula: C17H19N5O8 · C3H8O
Description

Details

N-alpha-Boc-N-tau-(2,4-dinitrophenyl)-L-histidine isopropyl alcohol complex
Additional Information

Additional Information

Catalog Number 48059
CAS 25024-53-7
M.W. 481.5
Formula C17H19N5O8 · C3H8O
IUPAC Name (2S)-3-[1-(2,4-dinitrophenyl)imidazol-4-yl]-2-[(2-methylpropan-2-yl)oxycarbonylamino]propanoic acid
Synonym N-alpha-Boc-N-tau-(2,4-dinitrophenyl)-L-histidine isopropyl alcohol complex
Also Known As
  • (2S)-3-[1-(2,4-dinitrophenyl)imidazol-4-yl]-2-[(2-methylpropan-2-yl)oxycarbonylamino]propanoic acid
  • (2S)-2-(tert-butoxycarbonylamino)-3-[1-(2,4-dinitrophenyl)imidazol-4-yl]propanoic acid
  • (2S)-2-[(tert-butoxy-oxomethyl)amino]-3-[1-(2,4-dinitrophenyl)-4-imidazolyl]propanoic acid
  • (2S)-2-(tert-butoxycarbonylamino)-3-[1-(2,4-dinitrophenyl)imidazol-4-yl]propionic acid
  • 25024-53-7
  • 95485-28-2
  • ST067128
  • 15287_FLUKA
  • Boc-His(Dnp)-OH
  • Nalpha-Boc-N(im)-2,4-dinitrophenyl-L-histidine
  • EINECS 246-569-0
  • L-Histidine, N-((1,1-dimethylethoxy)carbonyl)-1-(2,4-dinitrophenyl)-
  • N-((1,1-Dimethylethoxy)carbonyl)-1-(2,4-dinitrophenyl)-L-histidine
  • N-(tert-Butoxycarbonyl)-1-(2,4-dinitrophenyl)-L-histidine
InChIKey KPGVUOQMOHGHEW-LBPRGKRZSA-N
InChI InChI=1S/C17H19N5O8/c1-17(2,3)30-16(25)19-12(15(23)24)6-10-8-20(9-18-10)13-5-4-11(21(26)27)7-14(13)22(28)29/h4-5,7-9,12H,6H2,1-3H3,(H,19,25)(H,23,24)/t12-/m0/s1
SMILES CC(C)(C)OC(=O)N[C@@H](CC1=CN(C=N1)C2=C(C=C(C=C2)[N+](=O)[O-])[N+](=O)[O-])C(=O)O
Cited Uses

Details

1. Giustiniano M et al, "Amino Acid Derivatives as New Zinc Binding Groups for the Design of Selective Matrix Metalloproteinase Inhibitors", Journal of Amino Acids, 2013() pp.178381 (2013).
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3. Lee YJ et al, "pH-Sensitive Polymeric Micelle-based pH Probe for Detecting and Imaging Acidic Biological Environments", Biomacromolecules, 13(9) pp.2945-2951 (2012 Sep 10).
4. Khoo KK et al, "Lactam-stabilized helical analogues of the analgesic ?-conotoxin KIIIA", Journal of medicinal chemistry, 54(21) pp.7558-7566 (2011 Nov 10).
5. Ferguson AL et al, "An Experimental and Computational Investigation of Spontaneous Lasso Formation in Microcin J25", Biophysical Journal, 99(9) pp.3056-3065 (2010 Nov 3).
6. Allahverdi A et al, "The effects of histone H4 tail acetylations on cation-induced chromatin folding and self-association", Nucleic Acids Research, 39(5) pp.1680-1691 (2011 Mar).
7. Samant MP et al, "Iterative Approach to the Discovery of Novel Degarelix Analogues: Substitutions at Positions 3, 7 and 8. Part II", Journal of medicinal chemistry, 48(15) pp.4851-4860 (2005 Jul 28).
8. Hackeng TM et al, "Total chemical synthesis of human matrix Gla protein", Protein Science : A Publication of the Protein Society, 10(4) pp.864-870 (2001 Apr).
9. Miranda LP et al, "Accelerated chemical synthesis of peptides and small proteins", Proceedings of the National Academy of Sciences of the United States of America, 96(4) pp.1181-1186 (1999 Feb 16).
10. Hackeng TM et al, "Total chemical synthesis of enzymatically active human type II secretory phospholipase A2", Proceedings of the National Academy of Sciences of the United States of America, 94(15) pp.7845-7850 (1997 Jul 22).
11. Cosand WL et al, "Concept of internal structural controls for evaluation of inactive synthetic peptide analogs: synthesis of [Orn13,14]apamin and its guanidination to an apamin derivative with full neurotoxic activity.", Proceedings of the National Academy of Sciences of the United States of America, 74(7) pp.2771-2775 (1977 Jul).
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