Molecular structure of 4-Hydroxy-L-phenylglycine, CAS Number: 32462-30-9
4-Hydroxy-L-phenylglycine (CAS 32462-30-9)
Application:
4-Hydroxy-L-phenylglycine is a carnitine palmitoyltransferase-1 inhibitor
CAS Number:
32462-30-9
Purity:
≥99%
Molecular Weight:
167.16
Molecular Formula:
C8H9NO3
For Research Use Only. Not Intended for Diagnostic or Therapeutic Use.
* Refer to Certificate of Analysis for lot specific data.
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SDS & Certificate of Analysis
4-Hydroxy-L-phenylglycine is a non-proteinogenic amino acid. It is involved in the synthesis of various important compounds, including antibiotics and other bioactive molecules. This amino acid plays a role in the formation of peptide bonds and is an building block for the production of complex organic molecules. 4-Hydroxy-L-phenylglycine is a key intermediate in the synthesis of many biologically active compounds, making it an important molecule in the field of biochemistry. 4-Hydroxy-L-phenylglycine is an important molecule in biochemistry due to its role in the synthesis of biologically active compounds.
4-Hydroxy-L-phenylglycine (CAS 32462-30-9) References
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- In silico analysis of the adenylation domains of the freestanding enzymes belonging to the eucaryotic nonribosomal peptide synthetase-like family. | Di Vincenzo, L., et al. 2005. FEBS J. 272: 929-41. PMID: 15691327
- Phenylglycine as a novel P2 scaffold in hepatitis C virus NS3 protease inhibitors. | Ortqvist, P., et al. 2007. Bioorg Med Chem. 15: 1448-74. PMID: 17113777
- Improved P2 phenylglycine-based hepatitis C virus NS3 protease inhibitors with alkenylic prime-side substituents. | Lampa, A., et al. 2010. Bioorg Med Chem. 18: 5413-24. PMID: 20541424
- Aromatic C-methyltransferases with antipodal stereoselectivity for structurally diverse phenolic amino acids catalyze the methylation step in the biosynthesis of the actinomycin chromophore. | Crnovcić, I., et al. 2010. Biochemistry. 49: 9698-705. PMID: 20945860
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- Comparative Physiological and Metabolic Analysis Reveals a Complex Mechanism Involved in Drought Tolerance in Chickpea (Cicer arietinum L.) Induced by PGPR and PGRs. | Khan, N., et al. 2019. Sci Rep. 9: 2097. PMID: 30765803
- Macrophages rely on extracellular serine to suppress aberrant cytokine production. | Kurita, K., et al. 2021. Sci Rep. 11: 11137. PMID: 34045514
- Cellular Metabolomics Profiles Associated With Drug Chemosensitivity in AML. | Stockard, B., et al. 2021. Front Oncol. 11: 678008. PMID: 34178663
- Improved l-phenylglycine synthesis by introducing an engineered cofactor self-sufficient system. | Wang, P., et al. 2022. Synth Syst Biotechnol. 7: 513-521. PMID: 35024478
- N-acetyloxfenicine strongly induces mitohormesis in mice as well as in insects. | Matsumura, T., et al. 2023. FEBS Lett. 597: 288-297. PMID: 36527170
- Azobenzene-Based Amino Acids for the Photocontrol of Coiled-Coil Peptides. | Crone, NSA., et al. 2023. Bioconjug Chem. 34: 345-357. PMID: 36705971
Inhibitor of:
ACAD-12, ACADVL, ACOT10, ACOT3, ACOT6, ACSF4, ACSL6, ACSM2A, ACSM2B, ACSM4, ACSM5, ACSVL2, Carnitine Acetyltransferase, CPTI-M, CPTII, CROT, ECH1, ECHDC2, ECHDC3, ECHS1, FATP-1, HADHSC, and MCAD.Activator of:
CDV.Ordering Information
| Product Name | Catalog # | UNIT | Price | Qty | FAVORITES | |
4-Hydroxy-L-phenylglycine, 5 g | sc-254680A | 5 g | $82.00 | |||
4-Hydroxy-L-phenylglycine, 10 g | sc-254680 | 10 g | $109.00 |