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ALPHA-METHYL-L-P-TYROSINE

ALPHA-METHYL-L-P-TYROSINE Structure
CAS No.
672-87-7
Chemical Name:
ALPHA-METHYL-L-P-TYROSINE
Synonyms
METYROSINE;Metirosine;Demser;α-Methyl-L-tyrosine;α-Methyl-L-tyrosine;AMPT;L-AMPT;L-α-MT;α-Me-Tyr-OH;Α-ME-TYR-OH
CBNumber:
CB2480716
Molecular Formula:
C10H13NO3
Molecular Weight:
195.22
MOL File:
672-87-7.mol
MSDS File:
SDS
Modify Date:
2023/6/26 8:28:19

ALPHA-METHYL-L-P-TYROSINE Properties

Melting point 320-340°C dec.
Boiling point 383.7±32.0 °C(Predicted)
Density 1.283±0.06 g/cm3(Predicted)
storage temp. -20°C
solubility Aqueous Acid (Slightly)
form Powder
pka pKa 2.7 (Uncertain);10.1 (Uncertain)
color White to pale yellow
Merck 13,6183
BRN 2368400
InChIKey NHTGHBARYWONDQ-JTQLQIEISA-N
CAS DataBase Reference 672-87-7(CAS DataBase Reference)

SAFETY

Risk and Safety Statements

Symbol(GHS) 
GHS07
Signal word  Warning
Hazard statements  H315-H319
Precautionary statements  P261-P281-P305+P351+P338
Risk Statements  22-38-40-48/20/22
Safety Statements  22-24/25
WGK Germany  3
TSCA  No
HS Code  2922504500
NFPA 704
0
2 0

ALPHA-METHYL-L-P-TYROSINE price More Price(4)

Manufacturer Product number Product description CAS number Packaging Price Updated Buy
Sigma-Aldrich(India) M8131 α-Methyl-L-tyrosine ≥98% (TLC) 672-87-7 100MG ₹9200 2022-06-14 Buy
Sigma-Aldrich(India) M8131 α-Methyl-L-tyrosine ≥98% (TLC) 672-87-7 250MG ₹19940 2022-06-14 Buy
Sigma-Aldrich(India) M8131 α-Methyl-L-tyrosine ≥98% (TLC) 672-87-7 1G ₹64210 2022-06-14 Buy
Sigma-Aldrich(India) M8131 α-Methyl-L-tyrosine ≥98% (TLC) 672-87-7 5G ₹219290 2022-06-14 Buy
Product number Packaging Price Buy
M8131 100MG ₹9200 Buy
M8131 250MG ₹19940 Buy
M8131 1G ₹64210 Buy
M8131 5G ₹219290 Buy

ALPHA-METHYL-L-P-TYROSINE Chemical Properties,Uses,Production

Chemical Properties

White Solid

Uses

A tyrosine hydroxylase inhibitor. An antihypertensive in pheochromocytoma

Uses

Metyrosine is the α-methyl derivative of tyrosine. It competitively inhibits tyrosine hydroxylase action, thus reducing the formation of epinephrine and norepinephrine. It is used for treating patients with pheochromocytoma, in cases where a rise in the level of catecholamines is observed.

Definition

ChEBI: An L-tyrosine derivative that consists of L-tyrosine bering an additional methyl substituent at position 2. An inhibitor of the enzyme tyrosine 3-monooxygenase, and consequently of the synthesis of catecholamines. It is us d to control the symptoms of excessive sympathetic stimulation in patients with pheochromocytoma.

General Description

Metyrosine (α-Methyl-L-tyrosine, Demser). Althoughinhibition of any of the three enzymes involved in CA biosynthesisshould decrease CAs, inhibitors of the first andthe rate-limiting enzyme TH would be the most effective.As such, metyrosine is a much more effective competitiveinhibitor of E and NE production than agents that inhibitany of the other enzymes involved in CA biosynthesis. Itis often possible to “fool” the enzymes into accepting astructurally similar and unnatural substrate such as metyrosine.Metyrosine differs structurally from tyrosine onlyin the presence of an α-methyl group . It is oneexample of a CA-biosynthesis inhibitor in clinical use.Although metyrosine is used as a racemic mixture, it is the (-)isomer that possesses the inhibitory activity.Metyrosine, which is given orally in dosages ranging from 1 to 4 g/day, is used principally for the preoperative managementof pheochromocytoma, chromaffin cell tumorsthat produce large amounts of NE and E. Although theseadrenal medullary tumors are often benign, patients frequentlysuffer hypertensive episodes. Metyrosine reducesthe frequency and severity of these episodes by significantlylowering CA production (35%–80%). The drug ispolar (log P=0.73) and excreted mainly unchanged in theurine. Because of its limited solubility in water caused byintramolecular bonding of the zwitterions, crystalluria is apotential serious side effect. It can be minimized by maintaininga daily urine volume of more than 2 L. Inhibitors ofCA synthesis have limited clinical utility because suchagents nonspecifically inhibit the formation of all CAs andresult in many side effects. Sedation is the most commonside effect of this drug.
A similar example is the use of α-methyl-m-tyrosine inthe treatment of shock. It differs structurally from metyrosineonly in the presence of m-OH instead of p-OH inmetyrosine. This unnatural amino acid is accepted by the enzymesof the biosynthetic pathway and converted tometaraminol (an α-agonist).

Synthesis

Metyrosine, (?)|á-methyltyrosine (12.3.11), is synthesized in a few different ways, the simplest of which is the synthesis from 4-methoxybenzylacetone, which is reacted with potassium cyanide in the presence of ammonium carbonate to give the hydantoin (12.3.9). Treating this with hydrogen iodide removes the methyl-protecting group on the phenyl hydroxyl group and the product (12.3.10) is hydrolyzed by barium hydroxide into a racemic mixture of |á-methyl-D,L-tyrosine, from which the desired L-isomer is isolated (12.3.11) [83¨C86].

Synthesis_672-87-7

ALPHA-METHYL-L-P-TYROSINE Preparation Products And Raw materials

Raw materials

Preparation Products

Global( 184)Suppliers
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Apicore Pharmaceuticals Pvt Ltd +91-2662267177 +91-2662267166 Gujarat, India 181 58 Inquiry
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Pharmaffiliates Analytics and Synthetics P. Ltd +91-172-5066494 Haryana, India 6773 58 Inquiry
SynZeal Research Pvt Ltd +1 226-802-2078 Gujarat, India 6522 58 Inquiry
CLEARSYNTH LABS LTD. +91-22-45045900 Hyderabad, India 6351 58 Inquiry
SUVEN PHARMACEUTICALS LTD +91-40-2354-1142 New Delhi, India 15 58 Inquiry
RAKS PHARMA PVT LTD +91 891 3081555 New Delhi, India 65 58 Inquiry
BIOPHORE INDIA PHARMACEUTICALS PVT LTD +91-4047474545 New Delhi, India 105 58 Inquiry
Henan Tianfu Chemical Co.,Ltd. +86-0371-55170693 +86-19937530512 China 21669 55 Inquiry
L-2-METHYL-3-[4-HYDROXYPHENYL]-ALANINE 2-Methyl-L-Tyrosine L-ALPHA-METHYLTYROSINE, 98% AMPT,Metyrosine, -Methyl-L-Tyr A-METHYL-L-TYROSINE L-2-Me-Tyr-OH ALPHA-METHYL-L-P-TRYOSINE (S)-alpha-Methyl-4-hydroxy phenylalanine, (S)-a-Methyltyrosine (>98%, >98%ee) H-alpha-Me-L-Tyr-OH L-2-Methyl-3-(4-hydroxyphenyl)alanine, L-AMPT L-α-Methyltyrosine α-Methyl-L-tyrosine, L-2-Methyl-3-(4-hydroxyphenyl)alanine, L-AMPT (S)-3-(2-Methyl-4-hydroxyphenyl)-2-aminopropionic acid a-Methyl-L-p-tyrosineDiscontinued L-AMPT L-α-Methylrosine Metyrosine (200 mg) L-2-Me-Tyr-OH α-Methyl-L-tyrosine (S)-2-(4-Hydroxybenzyl)-2-aMinopropanoic Acid (S)-α-Methyltyrosine L(-)-Metyrosine L-Metyrosine L-α-Methyl-p-tyrosine L-α-MT (S)-alpha-Methyltyrosine, 98%, 98% ee (S)-alpha-Methyltyrosine, 98% ee, 98% (S)-2-AMINO-2-METHYL-3-(4'-HYDROXYPHENYL)PROPANOIC ACID AMPT ALPHA-METHYLTYROSINE ALPHA-METHYL-L-P-TYROSINE ALPHA-METHYL-L-TYR ALPHA-METHYL-L-TYROSINE A-METHYL-L-P-TYROSINE H-(ME)TYR-OH (S)-a-Methyltyrosine α-Me-Tyr-OH α-Methyl-L-p-tyrosine (S)-α-Methyltyrosine, 98% ee (2S)-2-amino-3-(4-hydroxyphenyl)-2-methylpropanoic acid α-Me-L-Tyr-OH Α-ME-TYR-OH Alpha-Methyl-Tyr-OH L-alfa-Me-Tyr-OH L-Tyrosine, α-methyl- ALPHA-METHYL-L-P-TYROSINE USP/EP/BP Metyrosine (Metirosine) α-Methyltyrosine Metyrosine D3 L-Tyrosine, a-methyl- Metyrosine (1443205) L-α-Methyltyrosine A-METHYL-L-TYR METYROSINE Metirosine α-Methyl-L-tyrosine Demser α-Methyl-L-tyrosine