1217442-29-9
1217442-29-9
Chemical Structure
Fmoc-Ile-OH-13C6,15N
Synonym(s): Fmoc-L-isoleucine-13C6,15N
- CAS No.: 1217442-29-9
- Formula:C1513C6H2315NO4
- Molecular Weight:360.36
IUPAC Name: (((9H-fluoren-9-yl)methoxy)carbonyl)-L-isoleucine-13C6-15N
InChIKey: QXVFEIPAZSXRGM-HJECYYBSSA-N
SMILES: [13CH3][13CH2][13C@@H]([13C@@H]([13C](O)=O)[15NH]C(OCC1C2=C(C3=C1C=CC=C3)C=CC=C2)=O)[13CH3]
Biological Activity: Fmoc-Ile-OH-13C6,15N is the 13C and 15N labeled Fmoc-Ile-OH[1]. Fmoc-Ile-OH is an isoleucine derivative[2].
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Fmoc-Ile-OH-13C6,15N | 99.90% | Fmoc-Ile-OH-13C6,15N is the 13C and 15N labeled Fmoc-Ile-OH. Fmoc-Ile-OH is an isoleucine derivative. | ||||||||||||||||||||
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Fmoc-Ile-OH-15N | 95.14% | Fmoc-Ile-OH-15N is the 15N labeled Fmoc-Ile-OH. | ||||||||||||||||||||
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Fmoc-Ile-OH | 99.96% | Fmoc-Ile-OH is an isoleucine derivative. | ||||||||||||||||||||
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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]. Luckose F, et al. Effects of amino acid derivatives on physical, mental, and physiological activities. Crit Rev Food Sci Nutr. 2015;55(13):1793-1144. [Content Brief]
