122996-47-8

122996-47-8 structure

Name	Fmoc-(2S,4R)-(-)-4-t-butoxypyrrolidine-2-carboxylic acid
Synonyms	Fmoc-Hyp(tBu) (2S,4R)-1-(((9H-Fluoren-9-yl)methoxy)carbonyl)-4-(tert-butoxy)pyrrolidine-2-carboxylic acid Fmoc-Hyp(OtBu)-OH FMOC-O-T-BUTYL-L-HYDROXYPROLINE FMOC-HYDROXYPROLINE(TBU)-OH FMOC-L-HYP(TBU)-OH Fmoc-4-tert-butoxy-L-proline (4R)-1-[(9H-Fluoren-9-ylmethoxy)carbonyl]-4-[(2-methyl-2-propanyl)oxy]-L-proline FMOC-O-T-BUTYL-L-4-HYDROXYPROLINE 1,2-Pyrrolidinedicarboxylic acid, 4-(1,1-dimethylethoxy)-, 1-(9H-fluoren-9-ylmethyl) ester, (2S,4R)- Fmoc-Hyp(tBu)-OH MFCD00065655 FMOC-HYP(TBU)-OHMIN FMOC-HYP(BUT)-OH

Description	Fmoc-Hyp(tBu)-OH is a proline derivative[1].
Related Catalog	Research Areas >> Others Signaling Pathways >> Others >> Others
In Vitro	Amino acids and amino acid derivatives have been commercially used as ergogenic supplements. They influence the secretion of anabolic hormones, supply of fuel during exercise, mental performance during stress related tasks and prevent exercise induced muscle damage. They are recognized to be beneficial as ergogenic dietary substances[1].
References	[1]. 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.

Personal Protective Equipment	Eyeshields;Gloves;type N95 (US);type P1 (EN143) respirator filter
Hazard Codes	Xi
Safety Phrases	22-24/25
RIDADR	NONH for all modes of transport
WGK Germany	3