Peptides & Peptide Synthesis Products

Boc-Trp-OH

Boc-Trp-OH
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Boc-Trp-OH, Catalog No: 48115
(2S)-3-(1H-indol-3-yl)-2-[(2-methylpropan-2-yl)oxycarbonylamino]propanoic acid, CAS: 13139-14-5, MW: 304.34, Formula: C16H20N2O4
Catalog No: 48115
(2S)-3-(1H-indol-3-yl)-2-[(2-methylpropan-2-yl)oxycarbonylamino]propanoic acid, CAS: 13139-14-5, MW: 304.34, Formula: C16H20N2O4
Description

Details

(2S)-3-(1H-indol-3-yl)-2-[(2-methylpropan-2-yl)oxycarbonylamino]propanoic acid
Additional Information

Additional Information

Catalog Number 48115
CAS 13139-14-5
M.W. 304.34
Formula C16H20N2O4
IUPAC Name (2S)-3-(1H-indol-3-yl)-2-[(2-methylpropan-2-yl)oxycarbonylamino]propanoic acid
Synonym No
Also Known As
  • (2S)-3-(1H-indol-3-yl)-2-[(2-methylpropan-2-yl)oxycarbonylamino]propanoic acid
  • (2S)-2-(tert-butoxycarbonylamino)-3-(1H-indol-3-yl)propanoic acid
  • (2S)-2-[(tert-butoxy-oxomethyl)amino]-3-(1H-indol-3-yl)propanoic acid
  • (2S)-2-(tert-butoxycarbonylamino)-3-(1H-indol-3-yl)propionic acid
  • 118552-56-0
  • 15512_FLUKA
  • Boc-Trp-OH
  • Nalpha-(tert-Butoxycarbonyl)-L-tryptophan
  • Nalpha-Boc-L-tryptophan
  • EINECS 236-072-7
  • L-Tryptophan, N-((1,1-dimethylethoxy)carbonyl)-
  • N-((1,1-Dimethylethoxy)carbonyl)-L-tryptophan
  • N-((tert-Butoxy)carbonyl)-L-tryptophan
  • NSC 334306
  • Tryptophan, N-carboxy-, N-tert-butyl ester, L- (8CI)
  • NCGC00166098-01
InChIKey NFVNYBJCJGKVQK-ZDUSSCGKSA-N
InChI InChI=1S/C16H20N2O4/c1-16(2,3)22-15(21)18-13(14(19)20)8-10-9-17-12-7-5-4-6-11(10)12/h4-7,9,13,17H,8H2,1-3H3,(H,18,21)(H,19,20)/t13-/m0/s1
SMILES CC(C)(C)OC(=O)N[C@@H](CC1=CNC2=CC=CC=C21)C(=O)O
Cited Uses

Details

1. 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).
2. Tiefenbrunn TK et al, "Chemical synthesis and biotinylation of the thrombospondin domain TSR2", Protein Science : A Publication of the Protein Society, 18(5) pp.970-979 (2009 May).
3. Horne WS et al, "Probing the Bioactive Conformation of an Archetypal Natural Product HDAC Inhibitor Using Conformationally Homogeneous Triazole-Modified Cyclic Tetrapeptides", Angewandte Chemie (International ed. in English), 48(26) pp.4718-4724 (2009).
4. 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).
5. Salvadori S et al, "Role of Benzimidazole (Bid) in the δ Opioid Agonist Pseudopeptide H-Dmt-Tic-NH-CH2-Bid (UFP-502)", Bioorganic & medicinal chemistry, 16(6) pp.3032-3038 (2008 Mar 15).
6. Myers MC et al, "Identification and Synthesis of a Unique Thiocarbazate Cathepsin L Inhibitor", Bioorganic & medicinal chemistry letters, 18(1) pp.210-214 (2008 Jan 1).
7. Kullmann W et al, "Protease-catalyzed peptide bond formation: application to synthesis of the COOH-terminal octapeptide of cholecystokinin.", Proceedings of the National Academy of Sciences of the United States of America, 79(9) pp.2840-2844 (1982 May).
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