L-Alanina - Moligand™, ≥99% , sodium-coupled neutral amino acid transporter 1;sodium-coupled neutral amino acid transporter 2;sodium-coupled neutral amino acid transporter 4, CAS No.56-41-7, sodium-coupled neutral amino acid transporter 1;sodium-coupled neutral amino acid transporter 2;sodium-coupled neutral amino acid transporter 4

Name: L-Alanina - Moligand™, ≥99% , sodium-coupled neutral amino acid transporter 1;sodium-coupled neutral amino acid transporter 2;sodium-coupled neutral amino acid transporter 4, CAS No.56-41-7, sodium-coupled neutral amino acid transporter 1;sodium-coupled neutral amino acid transporter 2;sodium-coupled neutral amino acid transporter 4
Brand: Aladdin Scientific
SKU: A108263
Availability: InStock

CAS: 56-41-7 Cat. No.: A108263 Fórmula: C₃H₇NO₂ Peso molecular: 89.09 Beilstein Registry Number: 1720248 Número CE: 200-273-8

466 Citations COA

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GRAU & PUREZA Moligand™ ? ≥99%

Synonyms

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Folha de especificações

Visão geral Especificações Nomes e identificadores Documentação Dados avançados Taxonomic Classification Estrutura 3D Alvos associados (humanos) Alvos associados (não humanos) Mecanismos de ação Certificados（CoA,COO,BSE/TSE e Mapa de Análise) Propriedades químicas e físicas FAQs e artigos Citations of This Product Calculadoras de soluções Revisões

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Por que este grau

Moligand™, ≥99% Moligand™ para fluxos de trabalho cromatográficos e analíticos sensíveis que exigem interferência mínima da linha de base.

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Armazenamento e envio

Dessecado Envio Normal. Consulte o COA específico do lote para obter as especificações exatas.

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SDS, COA, ficha técnica e folha de especificações disponíveis para download. COA específico do lote acessível por meio de pesquisa por número de lote.

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Comprovação documental

Citado em 466 publicações revisadas por pares nas áreas de cromatografia, síntese orgânica e reações de acoplamento cruzado.

Visão geral

A L-Alanina é um aminoácido não essencial que desempenha um papel fundamental no ciclo da glucose-alanina entre o tecido muscular e o fígado. Nos tecidos que degradam os aminoácidos, como o músculo, os grupos amino são agrupados como glutamato por reacções de transaminação. O grupo amino do glutamato é transferido para o piruvato através da alanina aminotransferase, formando alanina e α-cetoglutarato. A alanina passa para o sangue e é transportada para o fígado. Esta reação é invertida no fígado, onde o piruvato pode ser utilizado na gluconeogénese para formar glucose, que pode regressar a outros tecidos através do sistema circulatório.
Um aminoácido não essencial que desempenha um papel fundamental no ciclo da glucose-alanina

Especificações

Sinónimos

Especificações e pureza

Moligand™, ≥99%

Mecanismos bioquímicos e fisiológicos

Agonista do recetor inibitório da glicina.

Condições de armazenamento de armazenamento

Dessecado

Enviado em

Normal

Grau

Moligand™

Mecanismo de ação

sodium-coupled neutral amino acid transporter 1;sodium-coupled neutral amino acid transporter 2;sodium-coupled neutral amino acid transporter 4

Pureza

≥99%

Nomes e identificadores

Pubchem Sid

508810622

Sorrisos canónicos

CC(C(=O)O)N

IUPAC Name

(2S)-2-aminopropanoic acid

InChIKey

QNAYBMKLOCPYGJ-REOHCLBHSA-N

INCHI

1S/C3H7NO2/c1-2(4)3(5)6/h2H,4H2,1H3,(H,5,6)/t2-/m0/s1

SMILES isoméricas

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

WGK Alemanha

RTECS

AY2990000

CAS alternativo

56-41-7,18875-37-1,25191-17-7,77160-91-9,25191-17-7

Termos de entrada MeSH

Abuf\u00e8ne;Alanine;Alanine, L Isomer;Alanine, L-Isomer;L Alanine;L-Alanine;L-Isomer Alanine

Peso molecular

89.09

Beilstein

1720248

Reaxy-Rn

635807

Reaxys-RN_link_address

https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=635807&ln=

Documentação

📋 Ficha de dados de segurança (FDS)

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📊 Ficha técnica

Resumo de referência rápida das especificações e aplicações do produto.

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Dados avançados

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 Alanine 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	Alanine and derivatives
Alternative Parents	L-alpha-amino acids Amino acids Monocarboxylic acids and derivatives Carboxylic acids Organopnictogen compounds Organic oxides Monoalkylamines Hydrocarbon derivatives Carbonyl compounds
Molecular Framework	Aliphatic acyclic compounds
Substituents	Alanine or derivatives - Alpha-amino acid - L-alpha-amino acid - Amino acid - Carboxylic acid - Monocarboxylic acid or derivatives - Hydrocarbon derivative - Organic oxygen compound - Primary amine - Organooxygen compound - Organonitrogen compound - Organic nitrogen compound - Primary aliphatic amine - Carbonyl group - Amine - Organopnictogen compound - Organic oxide - Aliphatic acyclic compound
Descrição	This compound belongs to the class of organic compounds known as alanine and derivatives. These are compounds containing alanine or a derivative thereof resulting from reaction of alanine 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

Estrutura 3D

Alvos associados (humanos)

SLC38A2 Tbio Sodium-coupled neutral amino acid transporter 2 (0 Activities)

Discover Target: SLC38A2

Activity Type	Activity Value -log(M)	Mechanism of Action	Activity Reference	Publications (PubMed IDs)

SLC38A1 Tbio Sodium-coupled neutral amino acid transporter 1 (0 Activities)

Discover Target: SLC38A1

Activity Type	Activity Value -log(M)	Mechanism of Action	Activity Reference	Publications (PubMed IDs)

SLC38A4 Tbio Sodium-coupled neutral amino acid transporter 4 (0 Activities)

Discover Target: SLC38A4

Activity Type	Activity Value -log(M)	Mechanism of Action	Activity Reference	Publications (PubMed IDs)

GPRC6A Tchem G-protein coupled receptor family C group 6 member A (0 Activities)

Discover Target: GPRC6A

Activity Type	Activity Value -log(M)	Mechanism of Action	Activity Reference	Publications (PubMed IDs)

F2 Tclin Thrombin (11687 Activities)

Discover Target: F2

Activity Type	Relation	Activity value	Units	Action Type	Journal	PubMed Id	doi	Assay Aladdin ID

CA2 Tclin Carbonic anhydrase II (17698 Activities)

Discover Target: CA2

Activity Type	Relation	Activity value	Units	Action Type	Journal	PubMed Id	doi	Assay Aladdin ID

ESR1 Tclin Estrogen receptor alpha (17718 Activities)

Discover Target: ESR1

Activity Type	Relation	Activity value	Units	Action Type	Journal	PubMed Id	doi	Assay Aladdin ID

PGR Tclin Progesterone receptor (8562 Activities)

Discover Target: PGR

Activity Type	Relation	Activity value	Units	Action Type	Journal	PubMed Id	doi	Assay Aladdin ID

CHRM2 Tclin Muscarinic acetylcholine receptor M2 (10671 Activities)

Discover Target: CHRM2

Activity Type	Relation	Activity value	Units	Action Type	Journal	PubMed Id	doi	Assay Aladdin ID

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

Discover Target: HTR1A

Activity Type	Relation	Activity value	Units	Action Type	Journal	PubMed Id	doi	Assay Aladdin ID

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

Discover Target: ADRA2A

Activity Type	Relation	Activity value	Units	Action Type	Journal	PubMed Id	doi	Assay Aladdin ID

AR Tclin Androgen Receptor (11781 Activities)

Discover Target: AR

Activity Type	Relation	Activity value	Units	Action Type	Journal	PubMed Id	doi	Assay Aladdin ID

CHRM1 Tclin Muscarinic acetylcholine receptor M1 (12690 Activities)

Discover Target: CHRM1

Activity Type	Relation	Activity value	Units	Action Type	Journal	PubMed Id	doi	Assay Aladdin ID

GABRA1 Tclin GABA receptor alpha-1 subunit (399 Activities)

Discover Target: GABRA1

Activity Type	Relation	Activity value	Units	Action Type	Journal	PubMed Id	doi	Assay Aladdin ID

MAOA Tclin Monoamine oxidase A (11911 Activities)

Discover Target: MAOA

Activity Type	Relation	Activity value	Units	Action Type	Journal	PubMed Id	doi	Assay Aladdin ID

DRD1 Tclin Dopamine D1 receptor (9720 Activities)

Discover Target: DRD1

Activity Type	Relation	Activity value	Units	Action Type	Journal	PubMed Id	doi	Assay Aladdin ID

ACHE Tclin Acetylcholinesterase (18204 Activities)

Discover Target: ACHE

Activity Type	Relation	Activity value	Units	Action Type	Journal	PubMed Id	doi	Assay Aladdin ID

PTGS1 Tclin Cyclooxygenase-1 (9233 Activities)

Discover Target: PTGS1

Activity Type	Relation	Activity value	Units	Action Type	Journal	PubMed Id	doi	Assay Aladdin ID

SLC6A2 Tclin Norepinephrine transporter (10102 Activities)

Discover Target: SLC6A2

Activity Type	Relation	Activity value	Units	Action Type	Journal	PubMed Id	doi	Assay Aladdin ID

SLC6A4 Tclin Serotonin transporter (12625 Activities)

Discover Target: SLC6A4

Activity Type	Relation	Activity value	Units	Action Type	Journal	PubMed Id	doi	Assay Aladdin ID

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

Discover Target: ADRA1A

Activity Type	Relation	Activity value	Units	Action Type	Journal	PubMed Id	doi	Assay Aladdin ID

OPRM1 Tclin Mu opioid receptor (19785 Activities)

Discover Target: OPRM1

Activity Type	Relation	Activity value	Units	Action Type	Journal	PubMed Id	doi	Assay Aladdin ID

DRD3 Tclin Dopamine D3 receptor (14368 Activities)

Discover Target: DRD3

Activity Type	Relation	Activity value	Units	Action Type	Journal	PubMed Id	doi	Assay Aladdin ID

SLC6A3 Tclin Dopamine transporter (10535 Activities)

Discover Target: SLC6A3

Activity Type	Relation	Activity value	Units	Action Type	Journal	PubMed Id	doi	Assay Aladdin ID

GRIN1 Tclin Glutamate (NMDA) receptor subunit zeta 1 (122 Activities)

Discover Target: GRIN1

Activity Type	Relation	Activity value	Units	Action Type	Journal	PubMed Id	doi	Assay Aladdin ID

KCNH2 Tclin HERG (29587 Activities)

Discover Target: KCNH2

Activity Type	Relation	Activity value	Units	Action Type	Journal	PubMed Id	doi	Assay Aladdin ID

PDE3A Tclin Phosphodiesterase 3A (3309 Activities)

Discover Target: PDE3A

Activity Type	Relation	Activity value	Units	Action Type	Journal	PubMed Id	doi	Assay Aladdin ID

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

Discover Target: HTR2B

Activity Type	Relation	Activity value	Units	Action Type	Journal	PubMed Id	doi	Assay Aladdin ID

TBXA2R Tclin Thromboxane A2 receptor (5717 Activities)

Discover Target: TBXA2R

Activity Type	Relation	Activity value	Units	Action Type	Journal	PubMed Id	doi	Assay Aladdin ID

PDE4A Tclin Phosphodiesterase 4A (1943 Activities)

Discover Target: PDE4A

Activity Type	Relation	Activity value	Units	Action Type	Journal	PubMed Id	doi	Assay Aladdin ID

ADORA3 Tchem Adenosine A3 receptor (15931 Activities)

Discover Target: ADORA3

Activity Type	Relation	Activity value	Units	Action Type	Journal	PubMed Id	doi	Assay Aladdin ID

CA1 Tclin Carbonic anhydrase I (13240 Activities)

Discover Target: CA1

Activity Type	Relation	Activity value	Units	Action Type	Journal	PubMed Id	doi	Assay Aladdin ID

HRH3 Tclin Histamine H3 receptor (10389 Activities)

Discover Target: HRH3

Activity Type	Relation	Activity value	Units	Action Type	Journal	PubMed Id	doi	Assay Aladdin ID

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

Discover Target: KDR

Activity Type	Relation	Activity value	Units	Action Type	Journal	PubMed Id	doi	Assay Aladdin ID

CYP2D6 Tclin Cytochrome P450 2D6 (33882 Activities)

Discover Target: CYP2D6

Activity Type	Relation	Activity value	Units	Action Type	Journal	PubMed Id	doi	Assay Aladdin ID

CYP1A2 Tchem Cytochrome P450 1A2 (26471 Activities)

Discover Target: CYP1A2

Activity Type	Relation	Activity value	Units	Action Type	Journal	PubMed Id	doi	Assay Aladdin ID

CYP2C9 Tchem Cytochrome P450 2C9 (32119 Activities)

Discover Target: CYP2C9

Activity Type	Relation	Activity value	Units	Action Type	Journal	PubMed Id	doi	Assay Aladdin ID

CYP2C19 Tchem Cytochrome P450 2C19 (29246 Activities)

Discover Target: CYP2C19

Activity Type	Relation	Activity value	Units	Action Type	Journal	PubMed Id	doi	Assay Aladdin ID

CYP3A4 Tclin Cytochrome P450 3A4 (53859 Activities)

Discover Target: CYP3A4

Activity Type	Relation	Activity value	Units	Action Type	Journal	PubMed Id	doi	Assay Aladdin ID

FFAR3 Tchem Free fatty acid receptor 3 (304 Activities)

Discover Target: FFAR3

Activity Type	Relation	Activity value	Units	Action Type	Journal	PubMed Id	doi	Assay Aladdin ID

APEX1 Tchem DNA-(apurinic or apyrimidinic site) lyase (38016 Activities)

Discover Target: APEX1

Activity Type	Relation	Activity value	Units	Action Type	Journal	PubMed Id	doi	Assay Aladdin ID

TDP1 Tchem Tyrosyl-DNA phosphodiesterase 1 (345557 Activities)

Discover Target: TDP1

Activity Type	Relation	Activity value	Units	Action Type	Journal	PubMed Id	doi	Assay Aladdin ID

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

Discover Target: SLC36A1

Activity Type	Relation	Activity value	Units	Action Type	Journal	PubMed Id	doi	Assay Aladdin ID

Alvos associados (não humanos)

alr Alanine racemase (2 Activities)

Discover Target: alr

Activity Type	Relation	Activity value	Units	Action Type	Journal	PubMed Id	doi	Assay Aladdin ID

CA4 Carbonic anhydrase IV (1713 Activities)

Discover Target: CA4

Activity Type	Relation	Activity value	Units	Action Type	Journal	PubMed Id	doi	Assay Aladdin ID

Hdac6 Histone deacetylase 6 (222 Activities)

Discover Target: Hdac6

Activity Type	Relation	Activity value	Units	Action Type	Journal	PubMed Id	doi	Assay Aladdin ID

Pkm Pyruvate kinase isozymes M1/M2 (66 Activities)

Discover Target: Pkm

Activity Type	Relation	Activity value	Units	Action Type	Journal	PubMed Id	doi	Assay Aladdin ID

Escherichia coli (133304 Activities)

Explore this target

Activity Type	Relation	Activity value	Units	Action Type	Journal	PubMed Id	doi	Assay Aladdin ID

Canis familiaris (36305 Activities)

Explore this target

Activity Type	Relation	Activity value	Units	Action Type	Journal	PubMed Id	doi	Assay Aladdin ID

rep Replicase polyprotein 1ab (378 Activities)

Discover Target: rep

Activity Type	Relation	Activity value	Units	Action Type	Journal	PubMed Id	doi	Assay Aladdin ID

Slc16a10 Monocarboxylate transporter 10 (73 Activities)

Discover Target: Slc16a10

Activity Type	Relation	Activity value	Units	Action Type	Journal	PubMed Id	doi	Assay Aladdin ID

Slc1a5 Amino acid transporter (271 Activities)

Discover Target: Slc1a5

Activity Type	Relation	Activity value	Units	Action Type	Journal	PubMed Id	doi	Assay Aladdin ID

SARS-CoV-2 (38078 Activities)

Explore this target

Activity Type	Relation	Activity value	Units	Action Type	Journal	PubMed Id	doi	Assay Aladdin ID

Mecanismos de ação

Certificados（CoA,COO,BSE/TSE e Mapa de Análise)

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.

41 results found

Lot Number	Certificate Type	Data	Item
A2305096	Certificate of Analysis	Sep 22, 2026	A108263
G2610193	Certificate of Analysis	Jun 12, 2026	A108263
G2610192	Certificate of Analysis	Jun 12, 2026	A108263
G2610191	Certificate of Analysis	Jun 12, 2026	A108263
G2610190	Certificate of Analysis	Jun 12, 2026	A108263
G2610189	Certificate of Analysis	Jun 12, 2026	A108263
G2203019	Certificate of Analysis	Apr 03, 2026	A108263
F2603016	Certificate of Analysis	Feb 27, 2026	A108263
C2612260	Certificate of Analysis	Feb 27, 2026	A108263
C2612261	Certificate of Analysis	Feb 27, 2026	A108263
C2612262	Certificate of Analysis	Feb 27, 2026	A108263
C2612263	Certificate of Analysis	Feb 27, 2026	A108263
C2612264	Certificate of Analysis	Feb 27, 2026	A108263
D2503242	Certificate of Analysis	Mar 22, 2025	A108263
D2503252	Certificate of Analysis	Mar 22, 2025	A108263
D2503243	Certificate of Analysis	Mar 22, 2025	A108263
K2507049	Certificate of Analysis	Mar 22, 2025	A108263
K2519071	Certificate of Analysis	Mar 22, 2025	A108263
D2503240	Certificate of Analysis	Mar 22, 2025	A108263
D2503241	Certificate of Analysis	Mar 22, 2025	A108263
A2509478	Certificate of Analysis	Dec 27, 2024	A108263
A2509479	Certificate of Analysis	Dec 27, 2024	A108263
A2509483	Certificate of Analysis	Dec 27, 2024	A108263
A2509484	Certificate of Analysis	Dec 27, 2024	A108263
A2509488	Certificate of Analysis	Dec 27, 2024	A108263
H2414471	Certificate of Analysis	Jul 29, 2024	A108263
C2421108	Certificate of Analysis	Apr 09, 2024	A108263
C2427111	Certificate of Analysis	Mar 14, 2024	A108263
C2427110	Certificate of Analysis	Mar 14, 2024	A108263
C2427109	Certificate of Analysis	Mar 14, 2024	A108263
C2427112	Certificate of Analysis	Mar 14, 2024	A108263
F2328204	Certificate of Analysis	Jun 09, 2023	A108263
F2328201	Certificate of Analysis	Jun 09, 2023	A108263
F2328196	Certificate of Analysis	Jun 09, 2023	A108263
J2312101	Certificate of Analysis	Jun 09, 2023	A108263
J2312102	Certificate of Analysis	Jun 09, 2023	A108263
G2203018	Certificate of Analysis	Jun 08, 2022	A108263
G2203020	Certificate of Analysis	Jun 08, 2022	A108263
G2203021	Certificate of Analysis	Jun 08, 2022	A108263
G2203022	Certificate of Analysis	Jun 08, 2022	A108263
F2306042	Certificate of Analysis	Jun 08, 2022	A108263

Propriedades químicas e físicas

Solubilidade	Soluble in water and cold ethanol. Slightly soluble in pyridine. Insoluble in ether and acetone.
Rotação específica [α]	14 ° (C=10, HCl)
Ponto de fusão (°C)	314-316°C
Peso molecular	89.090 g/mol
XLogP3	-3.000
Hydrogen Bond Donor Count	2
Hydrogen Bond Acceptor Count	3
Rotatable Bond Count	1
Exact Mass	89.0477 Da
Monoisotopic Mass	89.0477 Da
Topological Polar Surface Area	63.300 Å²
Heavy Atom Count	6
Formal Charge	0
Complexity	61.800
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

FAQs e artigos

Bio-based Chemicals: From Platform Molecules to Application Scenarios — Trend Insights and Aladdin’s Product Portfolio

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

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Bio-based Chemicals Biobased materials

Key Enzymes in Amino Acid Metabolism: A Mechanistic Framework and Research Applications

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

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metabolic flux amino acid metabolism key enzymes aminotransferases glutamate dehydrogenase branched-chain amino acid metabolism threonine metabolism D-amino acids stable isotope tracing compartmentalization

β-Acyloxy Alkenyl Amides (AAAs): A New Approach to Amide Bond and Peptide Bond Construction Worth Attention

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

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AAAs β-Acyloxy Alkenyl Amides

Silicon Reagent-Assisted Peptide Synthesis: Research Progress and Methodological Value of Peptide Bond Formation from Unprotected Substrates

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

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Peptide synthesis

From Analytical Instrument to Synthetic Platform: A New Strategy for Reconstructing Automated Flow Solid-Phase Peptide Synthesis with Standard Analytical HPLC

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

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HPLC Peptide synthesis coupling reagent Analytical Instrument

Reassessing Trimethylaluminum: Method Design and Experimental Value of One-Pot Peptide Elongation from Unprotected Amino Acids

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

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Trimethylaluminum Unprotected amino acids One pot method for peptide chain elongation

Technical Comparison and Method Selection for Hydroxyproline Determination

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

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High-performance liquid chromatography colorimetry hydroxyproline collagen quantification LC-MS/MS acid hydrolysis method comparison fibrosis assessment

Methods and Applications for the Determination of Amino Acid Content and Composition

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

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Amino acids Mass spectrometry High-performance liquid chromatography Derivatization free amino acids total amino acids amino acid composition ninhydrin

Porous Graphitic Carbon (PGC) Chromatography Columns: Creating New Selectivity for Challenging Separations through Molecular Shape and the π-Electron Cloud on the Graphitic Surface

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

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High-performance liquid chromatography Porous Graphitic Carbon

Analysis of Amino Acid-Based Surfactants: Basic Structure, Performance Origins, Category Selection, and Applications in Personal Care Formulations

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

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Amino acids Amino Acid-Based Surfactants

Analysis of Hydrolyzed Pearl as a Cosmetic Raw Material: Preparation Process, Active Components, and Skincare Formulation Applications

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

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Hydrolyzed Pearl

Moisturizing Mechanism of Polyglutamic Acid: From the γ-Glutamyl Structure to Hydration Networks and Surface Film-Forming Behavior

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

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cosmetics Polyglutamic Acid

Mechanisms by Which Fructan-Rich Ophiopogon japonicus Tuberous Root Extract Supports Skin Moisturization and Barrier Function

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

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Ophiopogon japonicus Root Extract Ophiopogon polysaccharides

Multilevel Moisturizing Mechanisms of Sodium Hyaluronate and Its Derivatives: Molecular Weight Modulation, Crosslinking, Acetylation, and Major Sites of Action

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

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Hyaluronic acid Sodium Hyaluronate HA

Catalytic Mechanisms of the Aminotransferase Family and Regulation of Amino Acid Metabolism

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

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amino acid metabolism aminotransferases alanine aminotransferase aspartate aminotransferase branched-chain amino acid aminotransferase pyridoxal 5′-phosphate

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Revisões

📚 Citações por aplicação

Other applications241

Organic synthesis — reaction medium197

Extraction & workup solvent120

Drug / compound screening94

Spectroscopy sample preparation98

Cell proliferation5

Nanoparticle / material biocompatibility15

Electrochemistry & battery electrolyte39

Crystallization & recrystallization6

Chromatography (HPLC / GC / TLC)28

Cytotoxicity screening15

Industrial & non-pharma application5

Cancer cell line characterization3

Polymer synthesis & polymerization15

Controlled-release & nanoparticle carrier11

Cell viability11

IC50 determination2

Cross-coupling reactions1

Ver todas as 466 citações →

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Produtos Relacionados

L-Alanine - Animal Free, USP, JP, Moligand™, Ph.Eur., for cell culture, ≥98.5% , sodium-coupled neutral amino acid transporter 1;sodium-coupled neutral amino acid transporter 2;sodium-coupled neutral amino acid transporter 4, CAS No.56-41-7

L-Alanine - Moligand™, 10mM in Water , sodium-coupled neutral amino acid transporter 1;sodium-coupled neutral amino acid transporter 2;sodium-coupled neutral amino acid transporter 4, CAS No.56-41-7

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Documentação

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