Peptides & Peptide Synthesis Products

Boc-Pro-OH

Boc-Pro-OH

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Boc-Pro-OH, Catalog No: 48095
(2S)-1-[(2-methylpropan-2-yl)oxycarbonyl]pyrrolidine-2-carboxylic acid, CAS: 15761-39-4, MW: 215.25, Formula: C10H17NO4
Catalog No: 48095
(2S)-1-[(2-methylpropan-2-yl)oxycarbonyl]pyrrolidine-2-carboxylic acid, CAS: 15761-39-4, MW: 215.25, Formula: C10H17NO4
Description

Details

(2S)-1-[(2-methylpropan-2-yl)oxycarbonyl]pyrrolidine-2-carboxylic acid
Additional Information

Additional Information

Catalog Number 48095
CAS 15761-39-4
M.W. 215.25
Formula C10H17NO4
IUPAC Name (2S)-1-[(2-methylpropan-2-yl)oxycarbonyl]pyrrolidine-2-carboxylic acid
Synonym No
Also Known As
  • (2S)-1-[(2-methylpropan-2-yl)oxycarbonyl]pyrrolidine-2-carboxylic acid
  • (2S)-1-tert-butoxycarbonylpyrrolidine-2-carboxylic acid
  • (2S)-1-(tert-butoxy-oxomethyl)-2-pyrrolidinecarboxylic acid
  • (2S)-1-tert-butoxycarbonylproline
  • BB_NC-1899
  • 15490_FLUKA
  • UPCMLD00WGW001:001
  • NCGC00165407-01
  • ST5307216
  • 1,2-Pyrrolidinedicarboxylic acid, 1-(1,1-dimethylethyl) ester, (2S)-
  • 1,2-Pyrrolidinedicarboxylic acid, 1-(1,1-dimethylethyl) ester, (S)- (9CI)
  • 1,2-Pyrrolidinedicarboxylic acid, 1-tert-butyl ester, L- (8CI)
  • 1-(tert-Butyl) hydrogen (S)-pyrrolidine-1,2-dicarboxylate
  • EINECS 239-848-3
  • NSC 164660
  • 134570_ALDRICH
  • Boc-L-proline
  • Boc-Pro-OH
InChIKey ZQEBQGAAWMOMAI-ZETCQYMHSA-N
InChI InChI=1S/C10H17NO4/c1-10(2,3)15-9(14)11-6-4-5-7(11)8(12)13/h7H,4-6H2,1-3H3,(H,12,13)/t7-/m0/s1
SMILES CC(C)(C)OC(=O)N1CCC[C@H]1C(=O)O
Cited Uses

Details

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11. Ekoue-Kovi K et al, "Synthesis and antimalarial activity of new 4-amino-7-chloroquinolyl amides, sulfonamides, ureas and thioureas", Bioorganic & medicinal chemistry, 17(1) pp.270-283 (2009 Jan 1).
12. You L et al, "Anion transport properties of amine and amide-sidechained peptides are affected by charge and phospholipid composition", Organic & biomolecular chemistry, 6(16) pp.2914-2923 (2008 Aug 21).
13. You L et al, "Carboxylate Anion Diminishes Chloride Transport through a Synthetic, Self-Assembled Transmembrane Pore", Chemistry (Weinheim an der Bergstrasse, Germany), 14(1) pp.382-396 (2008).
14. Vartak A et al, "Allosteric Modulation of the Dopamine Receptor by Conformationally Constrained Type VI ?-Turn Peptidomimetics of Pro-Leu-Gly-NH2", Journal of medicinal chemistry, 50(26) pp.6725-6729 (2007 Dec 27).
15. Fisher A et al, "Design and Synthesis of Photoaffinity Labeling Ligands of the l-Prolyl-l-leucyl-glycinmide Binding Site Involved in the Allosteric Modulation of the Dopamine Receptor", Journal of medicinal chemistry, 49(1) pp.307-317 (2006 Jan 12).
16. Abiko T et al, "Synthesis of [I-NaI3]] thymopoietin II and examination of its immunological effect on the uremic T-lymphocytes.", Mediators of Inflammation, 9(3-4) pp.201-206 (2000).
17. Lynas J et al, "Peptidyl inverse esters of p-methoxybenzoic acid: a novel class of potent inactivator of the serine proteases.", Biochemical Journal, 325(Pt 3) pp.609-616 (1997 Aug 1).
18. Perczel A et al, "Quantitative analysis of cyclic beta-turn models.", Protein Science : A Publication of the Protein Society, 1(3) pp.378-395 (1992 Mar).
19. Foreman JC et al, "Structure-activity relationships for some substance P-related peptides that cause wheal and flare reactions in human skin.", The Journal of Physiology, 335() pp.449-465 (1983 Feb).
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