L-Cysteine - Moligand™, ≥99% , CAS No.52-90-4

Name: L-Cysteine - Moligand™, ≥99% , CAS No.52-90-4
Brand: Aladdin Scientific
SKU: C108237
Availability: InStock

CAS: 52-90-4 Cat. No.: C108237 Formule: C₃H₇NO₂S Poids moléculaire: 121.16 Beilstein Registry Number: 4506 Numéro CE: 200-158-2

1655 Citations COA

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L-Cysteine - Moligand™, ≥99% CAS No(52-90-4) by Aladdin Scientific

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DISPONIBLE À COMMANDE

QUALITÉ & PURETÉ Moligand™ ? ≥99%

Synonyms

Storage

Protected from light,Room temperature,Argon charged,Desiccated

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Fiche de spécifications

Vue d’ensemble Spécifications Noms et identifiants Documentation Données avancées Taxonomic Classification Structure 3D Cibles associées (humaines) Cibles associées (non humaines) Mécanismes d'action Certificats (CoA, COO, BSE/TSE et tableau d'analyse) Propriétés chimiques et physiques FAQ et articles Citations of This Product Calculateurs de solution Avis

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Pourquoi cette qualité

Moligand™, ≥99% Moligand™ pour les flux de travail chromatographiques et analytiques sensibles nécessitant une interférence de ligne de base minimale.

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Stockage & expédition

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Documents qualité

SDS, COA, fiche technique et fiche de spécifications disponibles au téléchargement. COA spécifique au lot accessible via la recherche par numéro de lot.

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Preuve documentaire

Cité dans 1655 publications à comité de lecture couvrant la chromatographie, la synthèse organique et les réactions de couplage croisé.

Vue d’ensemble

L-cysteine is a sulfur-containing non-essential amino acid.Its ability to reduce colitis symptoms is being assessed for potential use in treating inflammatory bowel disease (IBD).

Naturally occurring non-essential amino acid.

A non-essential amino acid.

L-cysteine can be used as a cysteine source to prepare L-cysteine functionalized gold nanoparticles for use as probes in the colorimetric detection of Hg2+ in aqueous solution.

Spécifications

Synonymes

Spécifications et pureté

Moligand™, ≥99%

Mécanismes biochimiques et physiologiques

NMDA glutamatergic receptor agonist.

Conditions de stockage de stockage

Protected from light,Room temperature,Argon charged,Desiccated

Expédié en

Normal

Grade

Moligand™

Pureté

≥99%

Noms et identifiants

Pubchem Sid

508810639

Pubchem Sid Url

https://pubchem.ncbi.nlm.nih.gov/substance/508810639

Sourires canoniques

C(C(C(=O)O)N)S

IUPAC Name

(2R)-2-amino-3-sulfanylpropanoic acid

InChIKey

XUJNEKJLAYXESH-REOHCLBHSA-N

INCHI

1S/C3H7NO2S/c4-2(1-7)3(5)6/h2,7H,1,4H2,(H,5,6)/t2-/m0/s1

Isomères SMILES

C([C@@H](C(=O)O)N)S

Poids moléculaire

121.16

Beilstein

4506

Reaxy-Rn

1721406

Reaxys-RN_link_address

https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=1721406&ln=

Documentation

📋 Fiche de données de sécurité (FDS)

Document complet couvrant les dangers, la manipulation, le stockage et la conformité réglementaire.

<<<<<<< HEAD Télécharger la SDS → ======= Télécharger la SDS → >>>>>>> release248-p3

✅ Certificat d'analyse (COA)

Données qualité spécifiques au lot. Saisissez votre numéro de lot pour récupérer le COA exact.

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📊 Fiche technique

Résumé de référence rapide des spécifications et applications du produit.

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🔬 Fiche de spécifications

Attributs de qualité complets et critères d'acceptation pour cette qualité.

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Données avancées

Taxonomic Classification

Taxonomy Tree

Kingdom Organic compounds
- Superclass Organic acids and derivatives
  - Classe Carboxylic acids and derivatives
    - Subclass Amino acids, peptides, and analogues
      - Level5 Amino acids and derivatives
        Level6 Alpha amino acids and derivatives
        Level7 Cysteine and derivatives

Kingdom	Organic compounds
Superclass	Organic acids and derivatives
Classe	Carboxylic acids and derivatives
Subclass	Amino acids, peptides, and analogues
Intermediate Tree Nodes	Amino acids and derivatives - Alpha amino acids and derivatives
Direct Parent	Cysteine and derivatives
Alternative Parents	L-alpha-amino acids Amino acids Monocarboxylic acids and derivatives Carboxylic acids Alkylthiols Organopnictogen compounds Organic oxides Monoalkylamines Hydrocarbon derivatives Carbonyl compounds
Molecular Framework	Aliphatic acyclic compounds
Substituents	Cysteine or derivatives - Alpha-amino acid - L-alpha-amino acid - Amino acid - Alkylthiol - Carboxylic acid - Monocarboxylic acid or derivatives - Organic oxygen compound - Primary amine - Organosulfur compound - Organooxygen compound - Organonitrogen compound - Organic nitrogen compound - Primary aliphatic amine - Carbonyl group - Amine - Hydrocarbon derivative - Organopnictogen compound - Organic oxide - Aliphatic acyclic compound
Description	This compound belongs to the class of organic compounds known as cysteine and derivatives. These are compounds containing cysteine or a derivative thereof resulting from reaction of cysteine 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
1. Djoumbou Feunang Y, Eisner R, Knox C, Chepelev L, Hastings J, Owen G, Fahy E, Steinbeck C, Subramanian S, Bolton E, Greiner R, and Wishart DS. ClassyFire: Automated Chemical Classification With A Comprehensive, Computable Taxonomy. Journal of Cheminformatics, 2016, 8:61. DOI: 10.1186/s13321-016-0174-y

Structure 3D

Cibles associées (humaines)

F2 Tclin Thrombin (11687 Activities)

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ESR1 Tclin Estrogen receptor alpha (17718 Activities)

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PGR Tclin Progesterone receptor (8562 Activities)

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CHRM2 Tclin Muscarinic acetylcholine receptor M2 (10671 Activities)

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HTR1A Tclin Serotonin 1a (5-HT1a) receptor (14969 Activities)

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ADRA2A Tclin Alpha-2a adrenergic receptor (9450 Activities)

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AR Tclin Androgen Receptor (11781 Activities)

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CHRM1 Tclin Muscarinic acetylcholine receptor M1 (12690 Activities)

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MAOA Tclin Monoamine oxidase A (11911 Activities)

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DRD1 Tclin Dopamine D1 receptor (9720 Activities)

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ACHE Tclin Acetylcholinesterase (18204 Activities)

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PTGS1 Tclin Cyclooxygenase-1 (9233 Activities)

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SLC6A2 Tclin Norepinephrine transporter (10102 Activities)

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SLC6A4 Tclin Serotonin transporter (12625 Activities)

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ADRA1A Tclin Alpha-1a adrenergic receptor (8359 Activities)

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OPRM1 Tclin Mu opioid receptor (19785 Activities)

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DRD3 Tclin Dopamine D3 receptor (14368 Activities)

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SLC6A3 Tclin Dopamine transporter (10535 Activities)

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PDE3A Tclin Phosphodiesterase 3A (3309 Activities)

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HTR2B Tclin Serotonin 2b (5-HT2b) receptor (10323 Activities)

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TBXA2R Tclin Thromboxane A2 receptor (5717 Activities)

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PDE4A Tclin Phosphodiesterase 4A (1943 Activities)

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ADORA3 Tchem Adenosine A3 receptor (15931 Activities)

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GSTM1 Tbio Glutathione S-transferase Mu 1 (61 Activities)

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HRH3 Tclin Histamine H3 receptor (10389 Activities)

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CPA1 Tchem Carboxypeptidase A1 (146 Activities)

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KDR Tclin Vascular endothelial growth factor receptor 2 (20924 Activities)

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SLC1A1 Tchem Excitatory amino acid transporter 3 (527 Activities)

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SLC1A3 Tchem Excitatory amino acid transporter 1 (586 Activities)

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GSTK1 Tchem Glutathione S-transferase kappa 1 (56 Activities)

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Homo sapiens (32628 Activities)

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HeLa (62764 Activities)

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KIF11 Tchem Kinesin-like protein 1 (1720 Activities)

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SLC7A11 Tchem Cystine/glutamate transporter (150 Activities)

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SLC36A1 Tchem Proton-coupled amino acid transporter 1 (102 Activities)

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Cibles associées (non humaines)

Hdac6 Histone deacetylase 6 (222 Activities)

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Pkm Pyruvate kinase isozymes M1/M2 (66 Activities)

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Mus musculus (284745 Activities)

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Rattus norvegicus (775804 Activities)

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H9c2 (3506 Activities)

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rep Replicase polyprotein 1ab (378 Activities)

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Slc16a10 Monocarboxylate transporter 10 (73 Activities)

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cAMP-specific 3',5'-cyclic phosphodiesterase 4B (18 Activities)

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spt Serine palmitoyltransferase (15 Activities)

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Slc1a5 Amino acid transporter (271 Activities)

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SARS-CoV-2 (38078 Activities)

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Mécanismes d'action

Certificats (CoA, COO, BSE/TSE et tableau d'analyse)

C of A & Other Certificates(BSE/TSE, COO):

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80 results found

Lot Number	Certificate Type	Date	Article
K2602210	Certificate of Analysis	Oct 22, 2026	C108237
K2602211	Certificate of Analysis	Oct 22, 2026	C108237
K2602212	Certificate of Analysis	Oct 22, 2026	C108237
K2602213	Certificate of Analysis	Oct 22, 2026	C108237
K2602214	Certificate of Analysis	Oct 22, 2026	C108237
A2606082	Certificate of Analysis	Sep 22, 2026	C108237
L2517263	Certificate of Analysis	Sep 21, 2026	C108237
L2517250	Certificate of Analysis	Sep 21, 2026	C108237
L2517252	Certificate of Analysis	Sep 21, 2026	C108237
L2517253	Certificate of Analysis	Sep 21, 2026	C108237
F2405157	Certificate of Analysis	Sep 01, 2026	C108237
I2512236	Certificate of Analysis	Jul 14, 2026	C108237
L2420659	Certificate of Analysis	Jul 03, 2026	C108237
B2628482	Certificate of Analysis	Feb 07, 2026	C108237
J2613161	Certificate of Analysis	Feb 07, 2026	C108237
B2628476	Certificate of Analysis	Feb 07, 2026	C108237
B2628475	Certificate of Analysis	Feb 07, 2026	C108237
B2628481	Certificate of Analysis	Feb 07, 2026	C108237
B2628480	Certificate of Analysis	Feb 07, 2026	C108237
F2427075	Certificate of Analysis	Jan 20, 2026	C108237
F2415174	Certificate of Analysis	Dec 12, 2025	C108237
L2517251	Certificate of Analysis	Dec 09, 2025	C108237
H2624060	Certificate of Analysis	Dec 09, 2025	C108237
L2517254	Certificate of Analysis	Dec 09, 2025	C108237
A2404897	Certificate of Analysis	Jul 14, 2025	C108237
K2505010	Certificate of Analysis	Jun 21, 2025	C108237
F2527332	Certificate of Analysis	Jun 21, 2025	C108237
I2512235	Certificate of Analysis	Jun 21, 2025	C108237
I2512135	Certificate of Analysis	Jun 21, 2025	C108237
I2512133	Certificate of Analysis	Jun 21, 2025	C108237
F2527337	Certificate of Analysis	Jun 21, 2025	C108237
F2527336	Certificate of Analysis	Jun 21, 2025	C108237
F2527326	Certificate of Analysis	Jun 21, 2025	C108237
F2527316	Certificate of Analysis	Jun 21, 2025	C108237
F2527279	Certificate of Analysis	Jun 21, 2025	C108237
F2415171	Certificate of Analysis	Apr 18, 2025	C108237
F2426270	Certificate of Analysis	Apr 08, 2025	C108237
F2415200	Certificate of Analysis	Mar 04, 2025	C108237
F2415178	Certificate of Analysis	Mar 04, 2025	C108237
F2527048	Certificate of Analysis	Dec 13, 2024	C108237
C2525068	Certificate of Analysis	Dec 13, 2024	C108237
L2420661	Certificate of Analysis	Dec 13, 2024	C108237
L2420658	Certificate of Analysis	Dec 13, 2024	C108237
L2420656	Certificate of Analysis	Dec 13, 2024	C108237
A2404210	Certificate of Analysis	Oct 23, 2024	C108237
A2404898	Certificate of Analysis	Oct 23, 2024	C108237
K2427240	Certificate of Analysis	Oct 23, 2024	C108237
G2219341	Certificate of Analysis	Oct 23, 2024	C108237
G2219359	Certificate of Analysis	Oct 23, 2024	C108237
D2115213	Certificate of Analysis	Oct 18, 2024	C108237
G2430050	Certificate of Analysis	Aug 01, 2024	C108237
J2412430	Certificate of Analysis	Jun 27, 2024	C108237
J2412429	Certificate of Analysis	Jun 27, 2024	C108237
F2415179	Certificate of Analysis	Jun 06, 2024	C108237
J2415162	Certificate of Analysis	Jun 06, 2024	C108237
G2412020	Certificate of Analysis	Jun 06, 2024	C108237
G2219340	Certificate of Analysis	Jan 12, 2024	C108237
F2222304	Certificate of Analysis	Jan 12, 2024	C108237
F2222307	Certificate of Analysis	Jan 12, 2024	C108237
B2422140	Certificate of Analysis	Dec 23, 2023	C108237
D2409026	Certificate of Analysis	Dec 23, 2023	C108237
E2413023	Certificate of Analysis	Dec 23, 2023	C108237
A2015103	Certificate of Analysis	Nov 20, 2023	C108237
E2317676	Certificate of Analysis	Apr 21, 2023	C108237
E2317844	Certificate of Analysis	Apr 21, 2023	C108237
E2317833	Certificate of Analysis	Apr 21, 2023	C108237
E2317684	Certificate of Analysis	Apr 21, 2023	C108237
E2317683	Certificate of Analysis	Apr 21, 2023	C108237
E2317682	Certificate of Analysis	Apr 21, 2023	C108237
E2317677	Certificate of Analysis	Apr 21, 2023	C108237
J2218533	Certificate of Analysis	Oct 12, 2022	C108237
J2218537	Certificate of Analysis	Oct 12, 2022	C108237
J2218536	Certificate of Analysis	Oct 12, 2022	C108237
J2218504	Certificate of Analysis	Oct 12, 2022	C108237
G2219336	Certificate of Analysis	Jul 05, 2022	C108237
G2219365	Certificate of Analysis	Jul 05, 2022	C108237
F2222306	Certificate of Analysis	Jun 15, 2022	C108237
F2222302	Certificate of Analysis	Jun 15, 2022	C108237
F2222308	Certificate of Analysis	Jun 15, 2022	C108237
F2110031	Certificate of Analysis	Jun 16, 2021	C108237

Propriétés chimiques et physiques

Solubilité	Soluble in water, alcohol, acetic acid and aqueous ammonia. Insoluble in ether, acetone, ethyl acetate, benzene, carbon disulfide and carbon tetrachloride
Sensibilité	Light & Air sensitive
Rotation spécifique [α]	8.8 ° (C=8, 1mol/L HCl)
Point de fusion (°C)	220°C
Poids moléculaire	121.160 g/mol
XLogP3	-2.500
Hydrogen Bond Donor Count	3
Hydrogen Bond Acceptor Count	4
Rotatable Bond Count	2
Exact Mass	121.02 Da
Monoisotopic Mass	121.02 Da
Topological Polar Surface Area	64.300 Å²
Heavy Atom Count	7
Formal Charge	0
Complexity	75.300
Isotope Atom Count	0
Defined Atom Stereocenter Count	1
Undefined Atom Stereocenter Count	0
Defined Bond Stereocenter Count	0
Undefined Bond Stereocenter Count	0
The total count of all stereochemical bonds	0
Covalently-Bonded Unit Count	1

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Polypeptide Fluorinated groups

The Logic of Biomimetic Peptide Action in Skin: Sequence and Conformation, Skin Delivery, Stability, and Target Matching

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liposomes Cell-Penetrating Peptides biomimetic peptides sequence mimicry signaling peptides stratum corneum delivery lipidation proteolytic stability cellular target matching extracellular matrix regulation

How Arbutin Regulates Melanin Production: α/β Anomeric Configuration and Tyrosinase Action

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Melanin Arbutin

Structural Characteristics of Ergothioneine, OCTN1-Mediated Uptake by Skin Cells, and Antioxidant Mechanisms

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L-ergothioneine EGT

Why Proximity to Cysteine Does Not Necessarily Lead to Covalent Bond Formation: Warhead Reactivity, Reaction Geometry, and Target-Site Microenvironment

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Cysteine Covalent Inhibition

Electron Transfer and Nucleophilic Reactions of Benzoquinones: Effects of the Conjugated Dicarbonyl Structure, Substituents, and Medium

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Carbonyl Conjugation

Structure–Reactivity Relationships of Naphthoquinone Compounds: Structural Control of Electron Transfer and Nucleophilic Addition

Categories: Technical Articles: Reagent Chemistry, Synthesis & Bioscience Guides

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Naphthoquinone

L-Cysteine: Properties, Applications & Lab Use Guide

Categories: Technical Articles: Reagent Chemistry, Synthesis & Bioscience Guides

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cell culture Amino acids thiol compounds Antioxidants L-Cysteine

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L-Cysteine - Moligand™, Animal Free, for cell culture, ≥98% , CAS No.52-90-4

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L-Cysteine - Moligand™, ≥99% , CAS No.52-90-4

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