1160760-08-6
1160760-08-6
Chemical Structure
Fmoc-Asp(OtBu)-OH-13C4,15N
- CAS No.: 1160760-08-6
- Formula:C1913C4H2515NO6
- Molecular Weight:416.41
IUPAC Name: (S)-2-((((9H-fluoren-9-yl)methoxy)carbonyl)amino-15N)-4-(tert-butoxy)-4-oxobutanoic-1,2,3,4-13C4 acid
InChIKey: FODJWPHPWBKDON-LJRMHOJXSA-N
SMILES: O=[13C]([13CH2][13C@H]([15NH]C(OCC1C2=C(C3=C1C=CC=C3)C=CC=C2)=O)[13C](O)=O)OC(C)(C)C
Biological Activity: Fmoc-Asp(OtBu)-OH-13C4,15N is the 13C and 15N labeled Fmoc-Asp(OtBu)-OH[1]. Fmoc-Asp(OtBu)-OH (4-tert-Butyl N-(fluoren-9-ylmethoxycarbonyl)-L-aspartate) is a aspartate derivative containing amine protecting group Fmoc. Fmoc-Asp(OtBu)-OH can be used for peptide synthesis[2].
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Fmoc-Asp(OtBu)-OH-13C4,15N | Fmoc-Asp(OtBu)-OH-13C4,15N is the 13C and 15N labeled Fmoc-Asp(OtBu)-OH. Fmoc-Asp(OtBu)-OH (4-tert-Butyl N-(fluoren-9-ylmethoxycarbonyl)-L-aspartate) is a aspartate derivative containing amine protecting group Fmoc. Fmoc-Asp(OtBu)-OH can be used for peptide synthesis. | |||||||||||||||||||||
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References
- [1]. Russak EM, et al. Impact of Deuterium Substitution on the Pharmacokinetics of Pharmaceuticals. Ann Pharmacother. 2019 Feb;53(2):211-216. [Content Brief]
- [2]. Esquivel J B, et al. Chiral HPLC separation of protected amino acids. Journal of liquid chromatography & related technologies, 1998, 21(6): 777-791.
