Glycine-15N
- Product Name
- Glycine-15N
- CAS No.
- 7299-33-4
- Chemical Name
- Glycine-15N
- Synonyms
- GLYCINE-15N;[15N]GLYCINE;H-[15N]GLY-OH;[15N]-L-GLYCINE;15N,98%-Glycine;Glycine (1?N, 98%);Nitrogen-15 glycine;2-azanylacetic acid;2-azanylethanoic acid;Glycine-15N
- CBNumber
- CB4494014
- Molecular Formula
- C2H5NO2
- Formula Weight
- 76.08
- MOL File
- 7299-33-4.mol
Glycine-15N Property
- Melting point:
- 240 °C (dec.)(lit.)
- storage temp.
- Keep in dark place,Sealed in dry,Room Temperature
- solubility
- Aqueous Base (Slightly, Sonicated, Heated), Water (Sparingly)
- form
- Solid
- color
- White to Off-White
- BRN
- 1853034
- InChIKey
- DHMQDGOQFOQNFH-LBPDFUHNSA-N
- CAS Number Unlabeled
- 56-40-6
- CAS Number Unlabeled
- 56-40-6
Safety
- WGK Germany
- 3
- HS Code
- 28459000
N-Bromosuccinimide Price
- Product number
- 299294
- Product name
- Glycine-15N
- Purity
- 98 atom %
- Packaging
- 250mg
- Price
- $117
- Updated
- 2025/07/31
- Product number
- 299294
- Product name
- Glycine-15N
- Purity
- 98 atom %
- Packaging
- 1g
- Price
- $237.5
- Updated
- 2025/07/31
- Product number
- 451331
- Product name
- Glycine-15N
- Packaging
- 10mg
- Price
- $319
- Updated
- 2021/12/16
- Product number
- G615989
- Product name
- Glycine-15N
- Packaging
- 100mg
- Price
- $120
- Updated
- 2021/12/16
- Product number
- N1092
- Product name
- Glycine-15N
- Packaging
- 1g
- Price
- $495
- Updated
- 2021/12/16
Glycine-15N Chemical Properties,Usage,Production
Chemical Properties
White powder
Uses
Glycine-15N is the labelled form of Glycine (G615990). Glycine is a non-essential amino acid for human development. Glycine is an inhibitory neurotransmitter in spinal cord, allosteric regulator of NMDA receptors.
Biological Activity
Glycine-15N is the 15N-labeled Glycine. Glycine is an inhibitory neurotransmitter in the CNS and also acts as a co-agonist along with glutamate, facilitating an excitatory potential at the glutaminergic N-methyl-D-aspartic acid (NMDA) receptors[1].
IC 50
NMDA Receptor
References
[1] EDWARD M RUSSAK Edward M B. Impact of Deuterium Substitution on the Pharmacokinetics of Pharmaceuticals.[J]. Annals of Pharmacotherapy, 2019, 53 2: 211-216. DOI:10.1177/1060028018797110.
[2] W. GREENAWAY F. R W. A convenient synthesis of creatine-15N from glycine-15N via sarcosine-15N[J]. Journal of labelled compounds & radiopharmaceuticals, 1978, 14 4: 611-615. DOI:10.1002/jlcr.2580140417.
[3] HE J, ZHANG X, HE Q, et al. Synthesis of 15N-labeled heterocycles via the cleavage of C–N bonds of anilines and glycine-15N†[J]. Chemical Communications, 2021, 44: 5442-5445. DOI:10.1039/D1CC01734A.
[4] T P STEIN. Measurement of protein synthesis rates with [15N]glycine.[J]. American Journal of Physiology, 1980, 239 4: E294-E300. DOI:10.1152/ajpendo.1980.239.4.E294.
[5] MOSTAFA OTHMAN. Millimeter-Sized Clusters of Triple Cation Perovskite Enables Highly Efficient and Reproducible Roll-to-Roll Fabricated Inverted Perovskite Solar Cells[J]. Advanced Functional Materials, 2021, 32 12. DOI:10.1002/adfm.202110700.
Glycine-15N Preparation Products And Raw materials
Raw materials
Preparation Products
Glycine-15N Suppliers
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