- Description
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Details
2,6-bis[(2-methylpropan-2-yl)oxycarbonylamino]hexanoic acid - Additional Information
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Additional Information
Catalog Number 48071 CAS 2483-46-7 M.W. 346.42 Formula C16H30N2O6 IUPAC Name 2,6-bis[(2-methylpropan-2-yl)oxycarbonylamino]hexanoic acid Synonym No Also Known As - 2,6-bis[(2-methylpropan-2-yl)oxycarbonylamino]hexanoic acid
- 2,6-bis(tert-butoxycarbonylamino)hexanoic acid
- 2,6-bis[(tert-butoxy-oxomethyl)amino]hexanoic acid
- 2483-46-7
- NSC164052
InChIKey FBVSXKMMQOZUNU-UHFFFAOYSA-N InChI InChI=1S/C16H30N2O6/c1-15(2,3)23-13(21)17-10-8-7-9-11(12(19)20)18-14(22)24-16(4,5)6/h11H,7-10H2,1-6H3,(H,17,21)(H,18,22)(H,19,20) SMILES CC(C)(C)OC(=O)NCCCCC(C(=O)O)NC(=O)OC(C)(C)C - Cited Uses
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Details
1. Grünberg J et al, "DOTA-Functionalized Polylysine: A High Number of DOTA Chelates Positively Influences the Biodistribution of Enzymatic Conjugated Anti-Tumor Antibody chCE7agl", PLoS ONE, 8(4) pp.e60350 ().2. Waruna Jinadasa RG et al, "Syntheses and Cellular Investigations of 173-, 152- and 131-Amino Acid Derivatives of Chlorin e6", Journal of medicinal chemistry, 54(21) pp.7464-7476 (2011 Nov 10).3. Olive C et al, "A Lipid Core Peptide Construct Containing a Conserved Region Determinant of the Group A Streptococcal M Protein Elicits Heterologous Opsonic Antibodies", Infection and Immunity, 70(5) pp.2734-2738 (2002 May). - Reviews
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Peptides & Peptide Synthesis Products