17343-07-6
Chemical Structure
H-Gly-Gly-Tyr-OH
Synonym(s): Gly-Gly-Tyr
- CAS No.: 17343-07-6
- Formula:C13H17N3O5
- Molecular Weight:295.29
IUPAC Name: ethyl 1-benzyl-2,5-dimethyl-1H-pyrrole-3-carboxylate
InChIKey: INLIXXRWNUKVCF-JTQLQIEISA-N
SMILES: C1=CC(=CC=C1C[C@@H](C(=O)O)NC(=O)CNC(=O)CN)O
Biological Activity: H-Gly-Gly-Tyr-OH is a tripeptide that plays an important role in various biochemical applications. H-Gly-Gly-Tyr-OH can be used in the fields of pharmaceuticals and biochemistry[1][2].
| Cat. No. | Product Name | Purity | Description | Pricing | |||||||||||||||||||
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
|
|
H-Gly-Gly-Tyr-OH | 99.93% | H-Gly-Gly-Tyr-OH is a tripeptide that plays an important role in various biochemical applications. H-Gly-Gly-Tyr-OH can be used in the fields of pharmaceuticals and biochemistry. | ||||||||||||||||||||
|
loading...
/
|
|||||||||||||||||||||||
- [1]. Klochkov V V, et al. Spatial structures of tripeptides glycylglycyl-l-histidine and glycylglycyl-l-tyrosine based on residual dipolar couplings and quantum-chemical computations[J]. Mendeleev Communications, 2011, 21(2): 72-74.
- [2]. Serov N Y, et al. Complex structures, formation thermodynamics and substitution reaction kinetics in the copper (II)–glycylglycyl-l-tyrosine–l/d-histidine systems[J]. Polyhedron, 2022, 228: 116176.
Keywords