Name: Glycine - Moligand™, for electrophoresis, ≥99% , CAS No.56-40-6
Brand: Aladdin Scientific
SKU: A110752
Availability: InStock

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

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Stockage & expédition

Room temperature Expédition Normal. Consultez le COA spécifique au lot pour les spécifications exactes.

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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 1156 publications à comité de lecture couvrant la chromatographie, la synthèse organique et les réactions de couplage croisé.

Spécifications

Synonymes

Spécifications et pureté

Moligand™, for electrophoresis, ≥99%

Mécanismes biochimiques et physiologiques

Glycine is a non essential amino acid. Calcium influx through the cell membrane is mediated by glycine gated channels. Glycine participates in the synthesis of porphyrins, purines, and serines. It can also serve as a competitive agonist for binding glutam

Conditions de stockage de stockage

Room temperature

Expédié en

Normal

Grade

Moligand™, Suitable for electrophoresis

Pureté

≥99%

Noms et identifiants

Pubchem Sid

508814788

Sourires canoniques

C(C(=O)O)N

IUPAC Name

2-aminoacetic acid

InChIKey

DHMQDGOQFOQNFH-UHFFFAOYSA-N

INCHI

1S/C2H5NO2/c3-1-2(4)5/h1,3H2,(H,4,5)

Isomères SMILES

C(C(=O)O)N

WGK Allemagne

RTECS

MB7600000

Poids moléculaire

75.07

Beilstein

635782

Reaxy-Rn

635782

Reaxys-RN_link_address

https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=635782&ln=

Documentation

📋 Fiche de données de sécurité (FDS)

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

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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 Alpha amino acids

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	Alpha amino acids
Alternative Parents	Amino acids Monocarboxylic acids and derivatives Carboxylic acids Organopnictogen compounds Organic oxides Monoalkylamines Hydrocarbon derivatives Carbonyl compounds
Molecular Framework	Aliphatic acyclic compounds
Substituents	Alpha-amino acid - Amino acid - Carboxylic acid - Monocarboxylic acid or derivatives - Organic nitrogen compound - Organic oxide - Hydrocarbon derivative - Primary amine - Organooxygen compound - Organonitrogen compound - Organopnictogen compound - Primary aliphatic amine - Organic oxygen compound - Carbonyl group - Amine - Aliphatic acyclic compound
Description	This compound belongs to the class of organic compounds known as alpha amino acids. These are amino acids in which the amino group is attached to the carbon atom immediately adjacent to the carboxylate group (alpha carbon).
External Descriptors	Common amino acids - 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)

GPRC6A Tchem G-protein coupled receptor family C group 6 member A (1 Activities)

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

PDE5A Tclin Phosphodiesterase 5A (5113 Activities)

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EGFR Tclin Epidermal growth factor receptor erbB1 (33727 Activities)

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F2 Tclin Thrombin (11687 Activities)

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CA2 Tclin Carbonic anhydrase II (17698 Activities)

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ESR1 Tclin Estrogen receptor alpha (17718 Activities)

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HMGCR Tclin HMG-CoA reductase (2475 Activities)

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

NR3C1 Tclin Glucocorticoid receptor (14987 Activities)

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

INSR Tclin Insulin receptor (5558 Activities)

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

PGR Tclin Progesterone receptor (8562 Activities)

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

ADRB2 Tclin Beta-2 adrenergic receptor (11824 Activities)

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

CHRM2 Tclin Muscarinic acetylcholine receptor M2 (10671 Activities)

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

ADRB1 Tclin Beta-1 adrenergic receptor (6630 Activities)

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

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

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

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

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

AR Tclin Androgen Receptor (11781 Activities)

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

CHRM1 Tclin Muscarinic acetylcholine receptor M1 (12690 Activities)

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

ACE Tclin Angiotensin-converting enzyme (1423 Activities)

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

DRD2 Tclin Dopamine D2 receptor (23596 Activities)

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

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

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

MAOA Tclin Monoamine oxidase A (11911 Activities)

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

CNR1 Tclin Cannabinoid CB1 receptor (20913 Activities)

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

DRD1 Tclin Dopamine D1 receptor (9720 Activities)

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

DRD4 Tchem Dopamine D4 receptor (7907 Activities)

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

ACHE Tclin Acetylcholinesterase (18204 Activities)

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

PTGS1 Tclin Cyclooxygenase-1 (9233 Activities)

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

SLC6A2 Tclin Norepinephrine transporter (10102 Activities)

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

HRH2 Tclin Histamine H2 receptor (5428 Activities)

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

ADRA1D Tclin Alpha-1d adrenergic receptor (4171 Activities)

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

HTR1B Tclin Serotonin 1b (5-HT1b) receptor (2801 Activities)

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

HTR2A Tclin Serotonin 2a (5-HT2a) receptor (14758 Activities)

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

HTR2C Tclin Serotonin 2c (5-HT2c) receptor (11471 Activities)

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

SLC6A1 Tclin GABA transporter 1 (308 Activities)

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

ADORA1 Tclin Adenosine A1 receptor (17603 Activities)

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

CALCR Tclin Calcitonin receptor (2215 Activities)

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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)

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

PTGS2 Tclin Cyclooxygenase-2 (13999 Activities)

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

HRH1 Tclin Histamine H1 receptor (7573 Activities)

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

ADRA1B Tclin Alpha-1b adrenergic receptor (2912 Activities)

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

OPRM1 Tclin Mu opioid receptor (19785 Activities)

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

DRD3 Tclin Dopamine D3 receptor (14368 Activities)

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

AVPR1A Tclin Vasopressin V1a receptor (5412 Activities)

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

OPRD1 Tclin Delta opioid receptor (15096 Activities)

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

OPRK1 Tclin Kappa opioid receptor (16155 Activities)

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

HTR3A Tclin Serotonin 3a (5-HT3a) receptor (3366 Activities)

Discover Target: HTR3A

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)

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

KCNH2 Tclin HERG (29587 Activities)

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

HTR4 Tclin Serotonin 4 (5-HT4) receptor (2068 Activities)

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

PDE3A Tclin Phosphodiesterase 3A (3309 Activities)

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

Cibles associées (non humaines)

Agtr2 Angiotensin II type 2 (AT-2) receptor (803 Activities)

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

Mc4r Melanocortin receptor 4 (1205 Activities)

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

Ltc4s Leukotriene C4 synthase (1 Activities)

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

Sigmar1 Sigma opioid receptor (160 Activities)

Discover Target: Sigmar1

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

Npy1r Neuropeptide Y receptor type 1 (8 Activities)

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

Cckar Cholecystokinin A receptor (90 Activities)

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

Nos2 Nitric oxide synthase, inducible (3573 Activities)

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

Mapk1 MAP kinase ERK2 (650 Activities)

Discover Target: Mapk1

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

Slc6a9 Glycine transporter 1 (255 Activities)

Discover Target: Slc6a9

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

Hdac6 Histone deacetylase 6 (222 Activities)

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

Mmp9 Matrix metalloproteinase 9 (38 Activities)

Discover Target: Mmp9

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

Glra1 Glycine receptor subunit alpha-1 (65 Activities)

Discover Target: Glra1

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

Mus musculus (284745 Activities)

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

Rattus norvegicus (775804 Activities)

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

Slc6a11 GABA transporter 4 (930 Activities)

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

rep Replicase polyprotein 1ab (378 Activities)

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

Chrna3 Neuronal acetylcholine receptor; alpha3/beta4 (1368 Activities)

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

Grin1 Glutamate NMDA receptor (6467 Activities)

Discover Target: Grin1

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

Grin1 Glutamate NMDA receptor; Grin1/Grin2b (1028 Activities)

Discover Target: Grin1

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

Grin1 Glutamate NMDA receptor; Grin1/Grin2a (798 Activities)

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

Grin1 Glutamate NMDA receptor; Grin1/Grin2c (1127 Activities)

Discover Target: Grin1

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

Glra2 Glycine receptor (1745 Activities)

Discover Target: Glra2

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)

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

Mécanismes d'action

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

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

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51 results found

Lot Number	Certificate Type	Date	Article
K2602202	Certificate of Analysis	Oct 21, 2026	A110752
K2602201	Certificate of Analysis	Oct 21, 2026	A110752
K2602200	Certificate of Analysis	Oct 21, 2026	A110752
K2602199	Certificate of Analysis	Oct 21, 2026	A110752
K2520284	Certificate of Analysis	Nov 14, 2025	A110752
K2520286	Certificate of Analysis	Nov 14, 2025	A110752
K2520285	Certificate of Analysis	Nov 14, 2025	A110752
L2116214	Certificate of Analysis	Sep 17, 2025	A110752
F2516150	Certificate of Analysis	May 26, 2025	A110752
F2516210	Certificate of Analysis	May 26, 2025	A110752
F2516211	Certificate of Analysis	May 26, 2025	A110752
F2516212	Certificate of Analysis	May 26, 2025	A110752
C2620146	Certificate of Analysis	May 26, 2025	A110752
E2509510	Certificate of Analysis	Mar 01, 2025	A110752
E2509509	Certificate of Analysis	Mar 01, 2025	A110752
E2507232	Certificate of Analysis	Mar 01, 2025	A110752
E2507231	Certificate of Analysis	Mar 01, 2025	A110752
B2105071	Certificate of Analysis	Dec 13, 2024	A110752
A2510281	Certificate of Analysis	Nov 13, 2024	A110752
A2510280	Certificate of Analysis	Nov 13, 2024	A110752
A2510267	Certificate of Analysis	Nov 13, 2024	A110752
J2418450	Certificate of Analysis	Oct 10, 2024	A110752
J2418451	Certificate of Analysis	Oct 10, 2024	A110752
J2418452	Certificate of Analysis	Oct 10, 2024	A110752
J2418456	Certificate of Analysis	Oct 10, 2024	A110752
F2401013	Certificate of Analysis	May 11, 2024	A110752
F2401020	Certificate of Analysis	May 11, 2024	A110752
F2401025	Certificate of Analysis	May 11, 2024	A110752
F2401029	Certificate of Analysis	May 11, 2024	A110752
A2419097	Certificate of Analysis	Jan 08, 2024	A110752
A2419096	Certificate of Analysis	Jan 08, 2024	A110752
A2419099	Certificate of Analysis	Jan 08, 2024	A110752
A2419098	Certificate of Analysis	Jan 08, 2024	A110752
J2326014	Certificate of Analysis	Oct 11, 2023	A110752
E2311254	Certificate of Analysis	Apr 25, 2023	A110752
E2311253	Certificate of Analysis	Apr 25, 2023	A110752
E2311252	Certificate of Analysis	Apr 25, 2023	A110752
E2311214	Certificate of Analysis	Apr 25, 2023	A110752
E2311213	Certificate of Analysis	Apr 25, 2023	A110752
B2308205	Certificate of Analysis	Jan 04, 2023	A110752
B2308204	Certificate of Analysis	Jan 04, 2023	A110752
B2308202	Certificate of Analysis	Jan 04, 2023	A110752
B2308201	Certificate of Analysis	Jan 04, 2023	A110752
I2214113	Certificate of Analysis	Jul 13, 2022	A110752
I2214114	Certificate of Analysis	Jul 13, 2022	A110752
I2214115	Certificate of Analysis	Jul 13, 2022	A110752
I2214116	Certificate of Analysis	Jul 13, 2022	A110752
F2216077	Certificate of Analysis	May 30, 2022	A110752
F2216062	Certificate of Analysis	May 30, 2022	A110752
F2216079	Certificate of Analysis	May 30, 2022	A110752
L2214689	Certificate of Analysis	Nov 27, 2021	A110752

Propriétés chimiques et physiques

Solubilité	Easy to dissolve in water, solubility in water: 25g/100ml at 25 ℃; 39.1g/100ml at 50 ℃; 54.4g/100ml at 75 ℃; At 100 ℃, it is 67.2g/100ml. Extremely insoluble in ethanol, approximately 0.06g dissolved in 100g of anhydrous ethanol. Almost insoluble in aceto
Point de fusion (°C)	240 °C
Poids moléculaire	75.070 g/mol
XLogP3	-3.200
Hydrogen Bond Donor Count	2
Hydrogen Bond Acceptor Count	3
Rotatable Bond Count	1
Exact Mass	75.032 Da
Monoisotopic Mass	75.032 Da
Topological Polar Surface Area	63.300 Å²
Heavy Atom Count	5
Formal Charge	0
Complexity	42.900
Isotope Atom Count	0
Defined Atom Stereocenter Count	0
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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Nitrogen-containing heterocycles Polycyclic aromatic compounds aromatic compounds Chemiluminescence immunoassay

Chymosin: A Review of Molecular Features, Coagulation Kinetics, and Activity Evaluation

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chymosin rennin aspartic protease κ-casein Phe105–Met106 glycomacropeptide casein micelle coagulation kinetics milk-clotting activity cheese

dsDNase-Mediated Hydrolysis of Double-Stranded DNA: Enzymatic Characteristics, Methodological Strategies, and Bioanalytical Applications

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Biopharmaceuticals double-stranded deoxyribonuclease dsDNase dsDNA hydrolysis nucleic-acid removal sample pretreatment contamination control

Glutaraldehyde-mediated Microbial Inactivation: Chemical Mechanisms, Determinants, and Key Validation Considerations

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Glutaraldehyde Microbial Inactivation Dialdehyde Crosslinking Protein Fixation Biofilm Spores Viruses Inactivation Verification Neutralizer Residue Control

Invertebrate Oxygen Carrier Proteins in Immunology and Vaccine Research

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vaccine antigen presentation innate immunity Invertebrate Oxygen Carrier Protein Hemocyanin Carrier Protein Adjuvant

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

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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

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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

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HPLC Peptide synthesis coupling reagent Analytical Instrument

The Methodological Value of DSC: Building NHS-Type Activated Intermediates and Deciding When to Use Them

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DSC N,N′-disuccinimidyl carbonate

Progress in Research on the S-Adenosylmethionine Cycle and Regulatory Mechanisms of Methyltransfer Reactions

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methyl donor one-carbon metabolism Methionine Cycle Epigenetic Regulation S-Adenosylmethionine SAM cycle Methyl-transfer reactions S-adenosylhomocysteine

Technical Comparison and Method Selection for Hydroxyproline Determination

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

The Positioning of pNPP in ALP Testing: Quantitative Detection Logic, Application Scenarios, and Selection Criteria

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pNPP ALP activity assays Chromogenic Substrate

Tyramide Signal Amplification in In Situ Fluorescence Detection

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HRP TSA tyramide signal amplification in situ fluorescence detection multiplex immunofluorescence FFPE FISH

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

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

Experimental Selection of SEM-Cl: From O/N-SEM Protection and Directed Functionalization of N-Heterocycles to the Introduction of Protected C1 Fragments

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2-(Trimethylsilyl)ethoxymethyl chloride SEM-Cl

Experimental Evaluation of Triphosgene in Organic Synthesis: Understanding Its Selection Logic Through Reaction Tasks

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Organic synthesis Triphosgene

Experimental Assessment of Fmoc Introduction Routes: Impurity Profile Differences, Raw Material Carryover, and Quality Control

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Polypeptide Amino acids Fmoc

From Functional Groups to Experimental Decision-Making: Protein Crosslinker Selection and Experimental Essentials

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Functional Groups Crosslinkers

Perovskite Oxides for Energy and Environmental Catalysis: How Oxygen Vacancies, B-Site Metals, and the Metal–Oxygen Bond Network Regulate Reaction Performance

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perovskite perovskite oxides oxide

Application Differences Among Glutaraldehyde, Paraformaldehyde, and Formalin in Tissue and Cell Sample Fixation

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Immunohistochemistry Antigen Retrieval Immunofluorescence Paraformaldehyde Formaldehyde Cell fixation Glutaraldehyde Tissue Fixation Formalin Aldehyde Fixative Electron Microscopy Samples Tissue Morphology

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

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High-performance liquid chromatography Porous Graphitic Carbon

Practical Guide to TSA Tyramide Signal Amplification: How to Select Reagents, Optimize the Workflow, and Reduce Background When Detection Signals Are Weak for Low-Abundance Targets

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ICC IHC Immunohistochemistry Horseradish peroxidase In situ hybridization TSA tyramide signal amplification Fluorescence In Situ Hybridization

Performance Sources and Formulation Applications of Enzyme-Based Ingredients in Daily Chemical Products: Fermentation Transformation, Enzymatic Reactions, and Application Principles

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Enzyme Enzymes

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

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Amino acids Amino Acid-Based Surfactants

Mechanistic Analysis of Topical Glutathione in Skincare: Cellular Redox Regulation, Skin Delivery Challenges, and SLN-Based Delivery Strategies

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glutathione Cellular redox

If the DNA Sequence Remains Unchanged, Why Does Gene Expression Change? Core Mechanisms and Research Methods of Epigenetic Regulation

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DNA Epigenetics gene expression

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

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Hydrolyzed Pearl

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

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cosmetics Polyglutamic Acid

How Do Collagen Peptides Act on the Skin? From Surface Hydration and Percutaneous Delivery to Fibroblasts and Collagen Homeostasis

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skin care collagen peptide

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Exosomes Skincare

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

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Ophiopogon japonicus Root Extract Ophiopogon polysaccharides

How Cyclization Changes Peptide Behavior: Conformational Preorganization, Skin Delivery, and Integrin Binding, Using Cyclopeptide-5 as an Example

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Polypeptide Skincare

How Does Collagen Tripeptide Act on the Skin: Stratum Corneum Delivery, Matrix Protection, and Regulation of Collagen Homeostasis

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Extracellular matrix Fibroblasts stratum corneum delivery collagen tripeptide (CTP) Gly–X–Y sequence stratum corneum hydration matrix protection collagen homeostasis

What Determines Collagen Function: From Triple-Helix Formation to Hierarchical Assembly, Crosslink Maturation, and Dynamic Remodeling

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Collagen

What Is “Plant Collagen”? Distinguishing Ingredient Types, Structural Differences, Production Methods, and Skincare Effects

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Plant Collagen

The Combination Logic of Palmitoyl Tripeptide-1 and Palmitoyl Pentapeptide-4: Skin Delivery, Matrix Signaling, and Regulation of Collagen Homeostasis

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peptide palmitoyl chain

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

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L-ergothioneine EGT

Differences Between Animal-Derived Collagen and Recombinant Collagen in Skincare: Sequence and Structure, Safety, Skin Effects, and Evidence Evaluation

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Animal-Derived Collagen Recombinant Human Collagen Recombinant Humanized Collagen Triple Helix Immunogenicity Skin Repair Transepidermal Water Loss

Copper Tripeptide GHK-Cu and Skin Repair: From Copper Coordination Chemistry to Extracellular Matrix Remodeling

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Extracellular matrix Skin Repair ECM GHK-Cu

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Produits apparentés

Glycine - Moligand™, ACS, ≥98.5% , CAS No.56-40-6

Glycine - Moligand™, ≥99% , CAS No.56-40-6

Acide amino-acétique - Moligand™, pour la biologie moléculaire, ≥99%(NT) , CAS No.56-40-6

Glycine - PharmPure™,USP,BP,Ph.Eur.,≥99% , sodium-coupled neutral amino acid transporter 4;Agonist of GluN1;Agonist of GluN2A;Agonist of GluN2B;Agonist of GluN2C;Agonist of GluN2D;Agonist of GPRC6 receptor, CAS No.56-40-6

Glycine - Moligand™, 0.3M in water(pH3.0±0.2) , CAS No.56-40-6

1,3,5-Tris(4'-fluorobiphenyl-4-yl)benzene - ≥97% , CAS No.372956-40-6

Aminoacetic acid - Moligand™, 10mM in Water , CAS No.56-40-6

Aminoacetic acid - Moligand™, analytical standard , Agonist of GluN1;Agonist of GluN2A;Agonist of GluN2B;Agonist of GluN2C;Agonist of GluN2D;Agonist of GPRC6 receptor, CAS No.56-40-6

Glycine - UltraBio™, Suitable for molecular biology, Ultra pure, ≥99%(NT) , CAS No.56-40-6

Glycine - UltraBio™, Ultra pure, ≥99%(T) , CAS No.56-40-6

Glycine - Moligand™, for synthesis , CAS No.56-40-6

Glycine - Moligand™, for electrophoresis, ≥99% , CAS No.56-40-6

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Glycine - Moligand™, for electrophoresis, ≥99% , CAS No.56-40-6

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