33965-47-8

H-D-Phe(4-Cl)OMe.HCl Chemical Structure
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
HY-W011931
H-D-Phe(4-Cl)OMe.HCl 99.28% H-D-Phe(4-Cl)OMe.HCl is a phenylalanine derivative.
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HY-101456
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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HY-B1368
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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HY-I0924A
D-Phe-OMe monohydrochloride D-Phe-OMe monohydrochloride is a phenylalanine derivative.
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HY-W007671
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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HY-W012228
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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HY-W012485R
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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HY-W019599
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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HY-W040441
(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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HY-W091734
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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HY-W772850
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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References