L-Methionine(H-Met-OH) - Moligand™, 10mM in Water , CAS No.63-68-3

CAS: 63-68-3 Cat. No.: L425234 Formula: C5H11NO2S Molecular Weight: 149.21 Beilstein Registry Number: 1722294 EC Number: 200-562-9
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GRADE & PURITY Moligand™ ? Moligand™ — Aladdin's line of ligands and bioactive small molecules. Use for receptor, pathway, and binding studies needing defined small-molecule tools. 10mM in Water
Synonyms
(35S)Methionine|carbon-11 methionine|L-2-Amino-4methylthiobutyric acid|METHIONINE [II]|L-Methionin|L-Methionine-34S|L-Methioninum|Methionine [USAN:USP:INN:BAN]|(2S)-2-amino-4-(methylsulfanyl)butanoic acid|METHIONINE (EP MONOGRAPH)|Methioninum|Hmet|L-METHIONINE [USP-RS]|L-Methionine,(S)|methionine|L-a-Amino-g-methylthiobutyric acid|METHIONINE [MART.]|L-alpha-Amino-gamma-methylmercaptobutyric acid|2-Amino-4-methylthiobutanoate|h-Met-oh|L(-)-Methionin|L-Methionine (H-Met-OH)|(S)-2-Amino-4-(methylmercapto)butyric acid|2-Amino-4-methylthiobutanoic acid (S)-|L-methionine|METHIONINE (II)|METHIONINE [HSDB]|Acimethin|meritonin|(S)-methionine|L-Homocysteine, S-methyl-|L-Lobamine|Methionine (USAN:USP:INN:BAN)|Methionine [USAN:INN]|METHIONINE, L-|L-METHIONINE [JAN]|METHIONINE (USP MONOGRAPH)|METHIONINE [EP MONOGRAPH]|methioninum racemicum|METHIONINE [INCI]|Methioninum [INN-Latin]|(2S)-2-amino-4-(methylsulfanyl)butanoate|L-Met|METHIONINE [USAN]|Methionine (USP)|A-amino-g-methylmercaptobutyrate|G-methylthio-a-aminobutyrate|IS_METHIONINE-METHYL-D3|(S)-(+)-Methionine|L(-)-Amino-gamma-methylthiobutyric acid|L-Methionine (JP17)|Methionine, L- (8CI)|gamma-Methylthio-alpha-aminobutyric acid|Metionina [DCIT]|(S)-2-amino-4-(methylthio)butyric acid|L-2-Amino-4-(methylthio)butanoic acid|L-alpha-Amino-gamma-methylthiobutyric acid|L-gamma-Methylthio-alpha-aminobutyric acid|C-11 Methionine|Methioninum (INN-Latin)|Butanoic acid, 2-amino-4-(methylthio)-, (S)-|METHIONINE [MI]|(S)-2-Amino-4-(methylthio)butanoic acid|l-2-Amino-4-(methylthio)butyric acid|Methionine (VAN)|METHIONINE [VANDF]|metionina|C-11 Met|Cymethion|racemic methionine|Methionine (L-Methionine)|S-Methyl-L-homocysteine|L-a-amino-g-methylthiobutyrate|Neo-methidin|(L)-Methionine|METHIONINE (MART.)|L-(-)-Methionine|g-Methylthio-a-aminobutyric acid|L-Methionine Z (TN)|Toxin WAR|Liquimeth|(2S)-2-Amino-4-methylsulfanylbutanoic acid|(2S)-2-amino-4-methylsulfanyl-butanoic acid|a-Amino-g-methylmercaptobutyric acid|Toxin WAR (Bacillus thuringiensis strain PS205C)|(R)-2-Amino-4-(methylmercapto)butyric acid|2-Amino-4-(methylthio)butyrate|met|Methilanin|3h-l-methionine|L-METHIONINE [FCC]
Storage
Protected from light,Store at -80°C
Shipped In
Dry ice packs + Cold packs
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Size
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Price
Qty
1ml
L425234-1ml
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Overview

L-Methionine is an essential amino acid for human development, hepatoprotectant, acetominophen poisoning antidote, and urinary acidifier.
An essential amino acid

Specifications

Synonyms
(35S)Methionine | carbon-11 methionine | L-2-Amino-4methylthiobutyric acid | METHIONINE [II] | L-Methionin | L-Methionine-34S | L-Methioninum | Methionine [USAN:USP:INN:BAN] | (2S)-2-amino-4-(methylsulfanyl)butanoic acid | METHIONINE (EP MONOGRAPH) | Methioninum | Hmet | L-METHIONINE [USP-RS] | L-Methionine,(S) | methionine | L-a-Amino-g- Show more
Specifications & Purity
Moligand™, 10mM in Water
Biochemical and Physiological Mechanisms
Methionine is an essential amino acid which acts a precursor for transmethylation and transsulphuration. In proteins, L-methionine is the biologically active form.The adenosylation of methionine results in the formation of S-adenosyl-L-methionine (SAM), w
Storage
Protected from light,Store at -80°C
Shipped In
Dry ice packs + Cold packs
This product requires cold chain shipping. Ground and other economy services are not available.
Grade
Moligand™
Names and Identifiers
Pubchem Sid
Canonical Smiles
CSCC[C@H](N)C(O)=O
IUPAC Name
(2S)-2-amino-4-methylsulfanylbutanoic acid
InChIKey
FFEARJCKVFRZRR-BYPYZUCNSA-N
INCHI
1S/C5H11NO2S/c1-9-3-2-4(6)5(7)8/h4H,2-3,6H2,1H3,(H,7,8)/t4-/m0/s1
Isomeric SMILES
CSCC[C@@H](C(=O)O)N
WGK Germany
1
RTECS
PD0457000
Molecular Weight
149.21
Beilstein
1722294
Reaxy-Rn
1722294
Reaxys-RN_link_address
https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=1722294&ln=

Advanced Data

Taxonomic Classification

Taxonomy Tree

KingdomOrganic compounds
SuperclassOrganic acids and derivatives
ClassCarboxylic acids and derivatives
SubclassAmino acids, peptides, and analogues
Intermediate Tree Nodes Amino acids and derivatives - Alpha amino acids and derivatives
Direct ParentMethionine and derivatives
Alternative Parents L-alpha-amino acids  Thia fatty acids  Amino acids  Sulfenyl compounds  Monocarboxylic acids and derivatives  Dialkylthioethers  Carboxylic acids  Organopnictogen compounds  Organic oxides  Monoalkylamines  Hydrocarbon derivatives  Carbonyl compounds  
Molecular FrameworkAliphatic acyclic compounds
Substituents Methionine or derivatives - Alpha-amino acid - L-alpha-amino acid - Thia fatty acid - Fatty acid - Fatty acyl - Amino acid - Carboxylic acid - Monocarboxylic acid or derivatives - Thioether - Sulfenyl compound - Dialkylthioether - Amine - Organic oxygen compound - Primary amine - Organosulfur compound - Organooxygen compound - Organonitrogen compound - Organic nitrogen compound - Primary aliphatic amine - Carbonyl group - Organopnictogen compound - Organic oxide - Hydrocarbon derivative - Aliphatic acyclic compound
DescriptionThis compound belongs to the class of organic compounds known as methionine and derivatives. These are compounds containing methionine or a derivative thereof resulting from reaction of methionine at the amino group or the carboxy group, or from the replacement of any hydrogen of glycine by a heteroatom.
External Descriptors Common amino acids
3D Structure
Interactive Chemical Structure Model





Associated Targets(Human)
F2 Tclin Thrombin (11687 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
ESR1 Tclin Estrogen receptor alpha (17718 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
PGR Tclin Progesterone receptor (8562 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
CHRM2 Tclin Muscarinic acetylcholine receptor M2 (10671 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
HTR1A Tclin Serotonin 1a (5-HT1a) receptor (14969 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
ADRA2A Tclin Alpha-2a adrenergic receptor (9450 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
AR Tclin Androgen Receptor (11781 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
CHRM1 Tclin Muscarinic acetylcholine receptor M1 (12690 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
GABRA1 Tclin GABA receptor alpha-1 subunit (399 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
MAOA Tclin Monoamine oxidase A (11911 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
DRD1 Tclin Dopamine D1 receptor (9720 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
ACHE Tclin Acetylcholinesterase (18204 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
PTGS1 Tclin Cyclooxygenase-1 (9233 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
SLC6A2 Tclin Norepinephrine transporter (10102 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
ADORA1 Tclin Adenosine A1 receptor (17603 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
SLC6A4 Tclin Serotonin transporter (12625 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
ADRA1A Tclin Alpha-1a adrenergic receptor (8359 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
OPRM1 Tclin Mu opioid receptor (19785 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
DRD3 Tclin Dopamine D3 receptor (14368 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
SLC6A3 Tclin Dopamine transporter (10535 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
PDE3A Tclin Phosphodiesterase 3A (3309 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
HTR2B Tclin Serotonin 2b (5-HT2b) receptor (10323 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
TBXA2R Tclin Thromboxane A2 receptor (5717 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
PDE4A Tclin Phosphodiesterase 4A (1943 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
HRH3 Tclin Histamine H3 receptor (10389 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
FASN Tchem Fatty acid synthase (3390 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Homo sapiens (32628 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
SLC7A5 Tchem L-type amino acid transporter 1 (388 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Associated Targets(non-human)
Mat1a S-adenosylmethionine synthetase alpha and beta forms (31 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Mat2a S-adenosylmethionine synthetase gamma form (83 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Hdac6 Histone deacetylase 6 (222 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Pkm Pyruvate kinase isozymes M1/M2 (66 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Ggt1 Gamma-glutamyltranspeptidase 1 (36 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Pyricularia grisea (1253 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Oryza sativa (2923 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
luxS S-ribosylhomocysteine lyase (12 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
rep Replicase polyprotein 1ab (378 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Slc16a10 Monocarboxylate transporter 10 (73 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Mat1a S-adenosylmethionine synthetase (MAT 1 and MAT 2) (155 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Slc1a5 Amino acid transporter (271 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Mechanisms of Action
Certificates (CoA,COO,BSE/TSE and Analysis Chart)
C of A & Other Certificates(BSE/TSE, COO):
Analytical Chart:
Chemical and Physical Properties
SensitivityLight sensitive.
Specific Rotation[α]24° (C=8,HCl (1+1))
Melt Point(°C)280-282°C
Molecular Weight149.210 g/mol
XLogP3-1.900
Hydrogen Bond Donor Count2
Hydrogen Bond Acceptor Count4
Rotatable Bond Count4
Exact Mass149.051 Da
Monoisotopic Mass149.051 Da
Topological Polar Surface Area88.600 Ų
Heavy Atom Count9
Formal Charge0
Complexity97.000
Isotope Atom Count0
Defined Atom Stereocenter Count1
Undefined Atom Stereocenter Count0
Defined Bond Stereocenter Count0
Undefined Bond Stereocenter Count0
The total count of all stereochemical bonds0
Covalently-Bonded Unit Count1
Documents & Articles
Functions and Significance of Common Physiological and Biochemical Indices in Animals and Plants
Methionine: Biological Roles and Key Points for Research Application
Review of the Principles, Methods, and Application Considerations for Superoxide Dismutase Activity Determination
β-Acyloxy Alkenyl Amides (AAAs): A New Approach to Amide Bond and Peptide Bond Construction Worth Attention
Silicon Reagent-Assisted Peptide Synthesis: Research Progress and Methodological Value of Peptide Bond Formation from Unprotected Substrates
From Analytical Instrument to Synthetic Platform: A New Strategy for Reconstructing Automated Flow Solid-Phase Peptide Synthesis with Standard Analytical HPLC
Roles of One-Carbon Metabolism Enzymes in Oxidative Stress and Epigenetic Regulation in Cardiovascular Diseases
The Research Potential of the MAT-SAM Axis in Drug Targeting and Metabolic Intervention
Progress in Research on the S-Adenosylmethionine Cycle and Regulatory Mechanisms of Methyltransfer Reactions
Low-Racemization Control in Peptide Synthesis: An Inverse N→C Peptide Synthesis Strategy via Activated α-Aminoesters
Methods and Applications for the Determination of Amino Acid Content and Composition
Analysis of Hydrolyzed Pearl as a Cosmetic Raw Material: Preparation Process, Active Components, and Skincare Formulation Applications
Regulatory Mechanisms, Research Methods, and Modification-Omics Analysis of Protein Post-Translational Modifications
Mechanistic Basis of Acetyl Hexapeptide-8 in the Management of Expression Lines: SNARE Complex Interference, Constraints on Percutaneous Delivery, and Combination Strategies
Structural Characteristics of Ergothioneine, OCTN1-Mediated Uptake by Skin Cells, and Antioxidant Mechanisms
Regulatory Mechanisms of 5mC DNA Methylation
How Does MTAP Deletion Create a Therapeutic Window for PRMT5 Inhibition? — Mechanistic Basis from MTA Accumulation to MTA-Cooperative PRMT5 Inhibitors
Citations of This Product
Solution Calculators
Reviews

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