33965-47-8
Chemical Structure
H-D-Phe(4-Cl)OMe.HCl
- CAS No.: 33965-47-8
- Formula:C10H13Cl2NO2
- Molecular Weight:250.12
IUPAC Name: H-D-Phe(4-Cl)OMe.HCl
InChIKey: GCBCWTWQAFLKJG-SBSPUUFOSA-N
SMILES: N[C@H](CC1=CC=C(Cl)C=C1)C(OC)=O.[H]Cl
Biological Activity: H-D-Phe(4-Cl)OMe.HCl is a phenylalanine derivative[1].
| Cat. No. | Product Name | Purity | Description | Pricing | |||||||||||||||||||
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H-D-Phe(4-Cl)OMe.HCl | 99.28% | H-D-Phe(4-Cl)OMe.HCl is a phenylalanine derivative. | ||||||||||||||||||||
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PCPA methyl ester hydrochloride | 99.89% | PCPA methyl ester hydrochloride (4-Chloro-DL-phenylalanine methyl ester hydrochloride), a reversible tryptophan hydroxylase inhibitor, is a serotonin (5-HT) synthesis inhibitor. PCPA methyl ester hydrochloride crosses the blood brain barrier and reduces 5-HT central availability. | ||||||||||||||||||||
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Fenclonine | 99.98% | Fenclonine is a selective and irreversible tryptophan hydroxylase inhibitor, which is a rate-limiting enzyme in the biosynthesis of serotonin. Fenclonine can be used in carcinoid syndrome research. | ||||||||||||||||||||
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D-Phe-OMe monohydrochloride | D-Phe-OMe monohydrochloride is a phenylalanine derivative. | |||||||||||||||||||||
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H-Tyr-OMe | 99.92% | H-Tyr-OMe is an amino acid derivative and also a coordinating ligand for CuII ions. H-Tyr-OMe can serve as a surface functionalization reagent for carbon dots, and is used to prepare fluorescent probes for biothiol sensing. H-Tyr-OMe is oxidized to quinone under the catalysis of Tyrosinase via its phenolic hydroxyl group, which quenches the fluorescence of carbon dots. H-Tyr-OMe contains potential coordination sites, including carboxyl, amino and phenolic hydroxyl groups. | ||||||||||||||||||||
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H-Tyr-OMe.HCl | 99.47% | H-Tyr-OMe.HCl is an amino acid derivative and also a coordinating ligand for CuII ions. H-Tyr-OMe.HCl can serve as a surface functionalization reagent for carbon dots, and is used to prepare fluorescent probes for biothiol sensing. H-Tyr-OMe.HCl is oxidized to quinone under the catalysis of Tyrosinase via its phenolic hydroxyl group, which quenches the fluorescence of carbon dots. H-Tyr-OMe.HCl contains potential coordination sites, including carboxyl, amino and phenolic hydroxyl groups. | ||||||||||||||||||||
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H-D-Phe(4-Cl)-OH (Standard) | ≥98% | H-D-Phe(4-Cl)-OH (Standard) is the analytical standard of H-D-Phe(4-Cl)-OH. This product is intended for research and analytical applications. H-D-Phe(4-Cl)-OH is a phenylalanine derivative. | ||||||||||||||||||||
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4-Chloro-L-phenylalanine | 99.96% | 4-Chloro-L-phenylalanine (L-PCPA) is a tryptophan hydroxylase inhibitor targeting TPH1 and TPH2, with the activity of blocking serotonin biosynthesis. 4-Chloro-L-phenylalanine reduces the levels of serotonin and its metabolites in the brain without impairing the survival of serotonergic neurons. 4-Chloro-L-phenylalanine enhances anhedonic, depression-like and anxiety-like behaviors in mice with depleted noradrenergic and dopaminergic neurons. 4-Chloro-L-phenylalanine acts as a decarboxylation substrate for aromatic L-amino acid decarboxylase from Bacillus atrophaeus. 4-Chloro-L-phenylalanine can be used in studies related to Parkinson's disease. | ||||||||||||||||||||
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(S)-Methyl 2-amino-3-(3-hydroxyphenyl)propanoate hydrochloride | 99.82% | (S)-Methyl 2-amino-3-(3-hydroxyphenyl)propanoate hydrochloride is a phenylalanine derivative. | ||||||||||||||||||||
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Methyl 4-iodo-L-phenylalaninate hydrochloride | Methyl 4-iodo-L-phenylalaninate hydrochloride is a Phenylalaninate derivative. Methyl 4-iodo-L-phenylalaninate hydrochloride can be used for the preparation of factor XI modulators used in the research of thrombotic and thromboembolic. Methyl 4-iodo-L-phenylalaninate hydrochloride can also be used for the synthesis of compounds for the research of amyloid-related diseases, such as Alzheimer’s disease. | |||||||||||||||||||||
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Fenclonine hydrochloride | 98.60% | Fenclonine hydrochloride is a selective and irreversible tryptophan hydroxylase inhibitor, which is a rate-limiting enzyme in the biosynthesis of serotonin. Fenclonine hydrochloride can be used in carcinoid syndrome research. | ||||||||||||||||||||
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