- Description
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Details
Nα-Fmoc-Nγ-Boc-L-2,4-diaminobutyric acid - Additional Information
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Additional Information
Catalog Number 47256 CAS 125238-99-5 M.W. 440.49 Formula C24H28N2O6 IUPAC Name (2S)-2-(9H-fluoren-9-ylmethoxycarbonylamino)-4-[(2-methylpropan-2-yl)oxycarbonylamino]butanoic acid Synonym Nα-Fmoc-Nγ-Boc-L-2,4-diaminobutyric acid Also Known As - (2S)-2-(9H-fluoren-9-ylmethoxycarbonylamino)-4-[(2-methylpropan-2-yl)oxycarbonylamino]butanoic acid
- (2S)-4-(tert-butoxycarbonylamino)-2-(9H-fluoren-9-ylmethoxycarbonylamino)butanoic acid
- (2S)-4-[(tert-butoxy-oxomethyl)amino]-2-[(9H-fluoren-9-ylmethoxy-oxomethyl)amino]butanoic acid
- (2S)-4-(tert-butoxycarbonylamino)-2-(9H-fluoren-9-ylmethoxycarbonylamino)butyric acid
- Nalpha-Fmoc-Ngamma-Boc-L-2,4-diaminobutyric acid
- 86971_FLUKA
- Fmoc-Dab(Boc)-OH
InChIKey LIWKOFAHRLBNMG-FQEVSTJZSA-N InChI InChI=1S/C24H28N2O6/c1-24(2,3)32-22(29)25-13-12-20(21(27)28)26-23(30)31-14-19-17-10-6-4-8-15(17)16-9-5-7-11-18(16)19/h4-11,19-20H,12-14H2,1-3H3,(H,25,29)(H,26,30)(H,27,28)/t20-/m0/s1 SMILES CC(C)(C)OC(=O)NCC[C@@H](C(=O)O)NC(=O)OCC1C2=CC=CC=C2C3=CC=CC=C13 - Cited Uses
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Details
1. Azad MA et al, "Significant Accumulation of Polymyxin in Single Renal Tubular Cells: A Medicinal Chemistry and Triple Correlative Microscopy Approach", Analytical Chemistry, 87(3) pp.1590-1595 (2015/02/03 00:00).2. Hu HY et al, "In Vivo Imaging of Mouse Tumors by a Lipidated Cathepsin S Substrate", Angewandte Chemie (International Ed. in English), 53(29) pp.7669-7673 (2014/07/14 00:00).3. Deris ZZ et al, "Probing the Penetration of Antimicrobial Polymyxin Lipopeptides into Gram-Negative Bacteria", Bioconjugate Chemistry, 25(4) pp.750-760 (2014/04/16 00:00).4. Blankson GA et al, "Macrocyclic biphenyl tetraoxazoles: Synthesis, evaluation as G-quadruplex stabilizers and cytotoxic activity", Bioorganic & medicinal chemistry, 21(15) pp.4511-4520 (2013/08/01 00:00).5. Tsai SM et al, "Unanticipated differences between α- and γ-diaminobutyric acid-linked hairpin polyamide-alkylator conjugates", Nucleic Acids Research, 35(1) pp.307-316 (2007/01/01 00:00).6. Kelly JA et al, "Structure–activity studies with high-affinity inhibitors of pyroglutamyl-peptidase II", Biochemical Journal, 389(Pt 2) pp.569-576 (2005/07/15 00:00). - Reviews
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Peptides & Peptide Synthesis Products