Se-(Methyl)seleno-L-cysteine - ≥98%(HPLC)(T) , CAS No.26046-90-2

CAS: 26046-90-2 Cat. No.: S161277 Peso molecular: 182.08 Número EC: 684-218-7 PubChem CID: 147004
Disponible para pedir
GRADE & PURITY ≥98%(HPLC)(T)
Synonyms
methyl-L-selenocysteine | (2R)-2-amino-3-methylselanylpropanoic acid | 2-Amino-3-methylselenyl propionic acid | DB12697 | Lopac0_000799 | Methylseleno-L-cysteine | Se-(Methyl)selenocysteine hydrochloride | Se-Methyl-L-selenocysteine | (R)-2-Amino-3-(methy
Storage
Store at -20°C,Argon charged
Shipped In
Ice chest + Ice pads
 ·  off list, applied to all prices below.
Size
Estado
Price
Qty
10mg
S161277-10mg
3
9,90US$
50mg
S161277-50mg
3
29,90US$
100mg
S161277-100mg
3
47,90US$
250mg
S161277-250mg
2
109,90US$
1g
S161277-1g
2
339,90US$
Enter a quantity for the sizes you want to add.
🧪

Why this grade

≥98%(HPLC)(T) for sensitive chromatographic and analytical workflows requiring minimal baseline interference.

🌡

Storage & shipping

Store at -20°C,Argon charged Ships Ice chest + Ice pads Check lot-specific COA for exact specifications.

📋

Quality documents

SDS, COA, datasheet, and spec sheet available for download. Lot-specific COA accessible via lot number lookup.

📚

Literature proof

Cited in 2 peer-reviewed publications across chromatography, organic synthesis, and cross-coupling reactions.

Specifications

Sinónimos
methyl-L-selenocysteine | (2R)-2-amino-3-methylselanylpropanoic acid | 2-Amino-3-methylselenyl propionic acid | DB12697 | Lopac0_000799 | Methylseleno-L-cysteine | Se-(Methyl)selenocysteine hydrochloride | Se-Methyl-L-selenocysteine | (R)-2-Amino-3-(methy
Especificaciones y pureza
≥98%(HPLC)(T)
Mecanismos bioquímicos y fisiológicos
Seleno-amino acid. Induces apoptosis through caspase activation. Inhibits DMBA-induced mammary tumors. Potentiates antitumour activity and selectivity of chemotherapeutic agents. Shows chemopreventive effects in vivo.
Condiciones de almacenamiento de almacenamiento
Store at -20°C, Argon charged
Enviado en
Ice chest + Ice pads
Este producto requiere envío en cadena de frío. Los servicios terrestres y otros servicios económicos no están disponibles.
Nota
Wherever possible, you should prepare and use solutions on the same day. However, if you need to make up stock solutions in advance, we recommend that you store the solution as aliquots in tightly sealed vials at -20°C. Generally, these will be useable for up to one month. Before use, and prior to opening the vial we recommend that you allow your product to equilibrate to room temperature for at least 1 hour. Need more advice on solubility, usage and handling? Please visit our frequently asked questions (FAQ) page for more details.
Pureza
≥98%(HPLC)(T)
Nombres e identificadores
Pubchem Sid504757306
Pubchem Sid Urlhttps://pubchem.ncbi.nlm.nih.gov/substance/504757306
Sonrisas canónicasC[Se]CC(C(=O)O)N
IUPAC Name(2R)-2-amino-3-methylselanylpropanoic acid
InChIKeyXDSSPSLGNGIIHP-VKHMYHEASA-N
INCHI1S/C4H9NO2Se/c1-8-2-3(5)4(6)7/h3H,2,5H2,1H3,(H,6,7)/t3-/m0/s1
Isómeros SMILES C[Se]C[C@@H](C(=O)O)N
CAS alternativo 863394-07-4
PubChem CID 147004
Peso molecular 182.08

Documentation

📋 Safety Data Sheet (SDS)

Comprehensive hazard, handling, storage, and regulatory compliance document.

Download SDS →

✅ Certificate of Analysis (COA)

Lot-specific quality data. Enter your lot number to retrieve the exact COA.

Look up COA →

📊 Datasheet

Quick-reference summary of product specifications and applications.

View datasheet →

🔬 Specification Sheet

Full quality attributes and acceptance criteria for this grade.

View spec sheet →

Advanced Data

Taxonomic Classification

Taxonomy Tree

KingdomOrganic compounds
SuperclassOrganic acids and derivatives
ClaseCarboxylic acids and derivatives
SubclassAmino acids, peptides, and analogues
Intermediate Tree Nodes Amino acids and derivatives - Alpha amino acids and derivatives - Alpha amino acids
Direct ParentL-alpha-amino acids
Alternative Parents Amino acids  Selenoethers  Monocarboxylic acids and derivatives  Carboxylic acids  Organopnictogen compounds  Organic oxides  Monoalkylamines  Hydrocarbon derivatives  Carbonyl compounds  
Molecular FrameworkAliphatic acyclic compounds
Substituents L-alpha-amino acid - Amino acid - Carboxylic acid - Monocarboxylic acid or derivatives - Selenoether - Amine - Hydrocarbon derivative - Organic oxide - Organopnictogen compound - Primary amine - Organoselenium compound - Organooxygen compound - Organonitrogen compound - Organic oxygen compound - Primary aliphatic amine - Organic nitrogen compound - Carbonyl group - Aliphatic acyclic compound
DescripciónThis compound belongs to the class of organic compounds known as l-alpha-amino acids. These are alpha amino acids which have the L-configuration of the alpha-carbon atom.
External Descriptors non-proteinogenic L-alpha-amino acid - Se-methylselenocysteine - L-selenocysteine derivative
Estructura 3D
Modelo de Estructura Química Interactiva





Objetivos asociados (humanos)
APP Tclin Amyloid-beta A4 protein (8510 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
KYAT1 Tbio Kynurenine--oxoglutarate transaminase I (96 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
A-375 (9258 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Hs68 (138 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
MCF7 (126967 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
HEK293 (82097 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
SW-620 (52400 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
EHMT2 Tchem Histone-lysine N-methyltransferase, H3 lysine-9 specific 3 (93046 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
ATAD5 Tbio ATPase family AAA domain-containing protein 5 (122566 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
ATXN2 Tbio Ataxin-2 (54410 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
RGS4 Tchem Regulator of G-protein signaling 4 (13867 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Objetivos asociados (no humanos)
Hdac6 Histone deacetylase 6 (222 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Saccharomyces cerevisiae (19171 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Mycolicibacterium smegmatis (8003 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
V79 (1637 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
rep Replicase polyprotein 1ab (378 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Nfe2l2 Nuclear factor erythroid 2-related factor 2 (214 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Mecanismos de acción
Certificados (CoA, COO, BSE/TSE y tabla de análisis)
C of A & Other Certificates(BSE/TSE, COO):
Analytical Chart:

Find and download the COA for your product by matching the lot number on the packaging.

25 results found

Lot NumberCertificate TypeFechaArticulo
B2628653Certificate of AnalysisJan 27, 2026 S161277
B2628654Certificate of AnalysisJan 27, 2026 S161277
B2628655Certificate of AnalysisJan 27, 2026 S161277
B2628656Certificate of AnalysisJan 27, 2026 S161277
G2530441Certificate of AnalysisJun 20, 2025 S161277
G2530440Certificate of AnalysisJun 20, 2025 S161277
G2530433Certificate of AnalysisJun 20, 2025 S161277
G2530442Certificate of AnalysisJun 20, 2025 S161277
G2530450Certificate of AnalysisJun 20, 2025 S161277
I2504032Certificate of AnalysisJun 20, 2025 S161277
L2412597Certificate of AnalysisNov 27, 2024 S161277
L2412598Certificate of AnalysisNov 27, 2024 S161277
F2516029Certificate of AnalysisNov 27, 2024 S161277
L2412599Certificate of AnalysisNov 27, 2024 S161277
L2412600Certificate of AnalysisNov 27, 2024 S161277
J2414408Certificate of AnalysisMay 11, 2024 S161277
E2428430Certificate of AnalysisMay 11, 2024 S161277
E2428410Certificate of AnalysisMay 11, 2024 S161277
E2428409Certificate of AnalysisMay 11, 2024 S161277
E2428400Certificate of AnalysisMay 11, 2024 S161277
A2329656Certificate of AnalysisJan 03, 2023 S161277
A2329699Certificate of AnalysisJan 03, 2023 S161277
A2329697Certificate of AnalysisJan 03, 2023 S161277
A2329669Certificate of AnalysisJan 03, 2023 S161277
A2329657Certificate of AnalysisJan 03, 2023 S161277

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Propiedades químicas y físicas
Punto de fusión (°C)177 °C(dec.)
Peso molecular182.090 g/mol
XLogP3
Hydrogen Bond Donor Count2
Hydrogen Bond Acceptor Count3
Rotatable Bond Count3
Exact Mass182.98 Da
Monoisotopic Mass182.98 Da
Topological Polar Surface Area63.300 Ų
Heavy Atom Count8
Formal Charge0
Complexity86.100
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
Citations of This Product
Referencias
1. Furong Wang, Min Yan, Ting Zhang, Zhen Tian, Xinxin Niu, Zimeng Guo, Xian Wang, Xiaoben Li, Wei Song, Yan'e Luo, Yahong Yuan, Tianli Yue.  (2024)  Insight into sodium selenite-induced metabolic reprogramming in response to main seleno-amino acid enrichment in Saccharomyces cerevisiae using metabolomics.  Food Bioscience,      [PMID:] [10.1016/j.fbio.2024.103997]
2. Xiao-Xia Zhou, Quanzhi Xiao, Kena Zhang, Yan Gao, Jie Zhang, Liping Fang, Bing Yan, Fangbai Li.  (2024)  Quantitatively Tracking the Speciation and Dynamics of Selenium Nanoparticles in Rice Plants.  ANALYTICAL CHEMISTRY,      [PMID:39361821] [10.1021/acs.analchem.4c04032]
Calculadoras de soluciones
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