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Solubility & Handling
| Storage instructions | Room temperature |
| Solubility overview | Soluble in water (50 mM), and in DMSO (100 mM) |
| Important | This product is for RESEARCH USE ONLY and is not intended for therapeutic or diagnostic use. Not for human or veterinary use |
Chemical Data
| Chemical name | (2S)-2-[(2S)-2-hydroxypropanamido]-3-(d5)phenylpropanoic acid |
| Chemical structure |  |
| Molecular Formula | C12H10D5NO4 |
| SMILES | [2H]c1c(C[C@H](NC(=O)[C@H](C)O)C(=O)O)c([2H])c([2H])c([2H])c1[2H] |
| InChi | InChI=1S/C12H15NO4/c1-8(14)11(15)13-10(12(16)17)7-9-5-3-2-4-6-9/h2-6,8,10,14H,7H2,1H3,(H,13,15)(H,16,17)/t8-,10-/m0/s1/i2D,3D,4D,5D,6D |
References for Lac-Phe-d5 (N-lactoyl-phenylalanine-d5)
References are publications that support the biological activity of the product
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An exercise-inducible metabolite that suppresses feeding and obesity.
Li VL et al (2022) Nature 606 : 785-790 -
N-lactoyl-amino acids are ubiquitous metabolites that originate from CNDP2-mediated reverse proteolysis of lactate and amino acids.
Jansen RS et al (2015) Proceedings of the National Academy of Sciences of the United States of America 112 : 6601-6
Deuterated Lac-Phe (N-lactoyl-phenylalanine)
Understanding purity and quality - a guide for life scientists
