Adénosine - Moligand™, pour culture cellulaire, ≥99.5%(HPLC) , CAS No.58-61-7

CAS: 58-61-7 Cat. No.: A108806 Formule: C10H13N5O4 Poids moléculaire: 267.24 Beilstein Registry Number: 93029 Numéro CE: 200-389-9
DISPONIBLE À COMMANDE
QUALITÉ & PURETÉ Moligand™ ? Moligand™ — Aladdin's line of ligands and bioactive small molecules. Use for receptor, pathway, and binding studies needing defined small-molecule tools. for Cell culture ? Cell-culture grade — low endotoxin and contaminants to support viable cell growth. Use in mammalian/other cell culture media and supplements. ≥99.5%(HPLC)
Synonyms
Adenine riboside | 9-beta-D-Ribofuranosidoadenine | 9-beta-D-Ribofuranosyl-9H-purin-6-amine | beta-D-Ribofuranoside, adenine-9 | beta-D-Adenosine | Nucleocardyl | 9-beta-D-Ribofuranosyladenine | adenosine | (2R,3R,4S,5R)-2-(6-Aminopurin-9-yl)-5-(hydroxyme
Storage
Stocker à 2-8°C, chargé d'argon
Shipped In
Glace humide
★
Taille
Allemagne (EU)
USA*
Prix
Qté
5g
A108806-5g
—
9 En stock
11,19€
25g
A108806-25g
—
3 En stock
21,61€
100g
A108806-100g
—
3 En stock
51,98€
Enter a quantity for the sizes you want to add.
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Pourquoi cette qualité

Moligand™, pour culture cellulaire, ≥99.5%(HPLC) Moligand™,pour la culture cellulaire pour les flux de travail chromatographiques et analytiques sensibles nécessitant une interférence de ligne de base minimale.

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Stockage & expédition

Stocker à 2-8°C, chargé d'argon Expédition Glace humide. 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 139 publications à comité de lecture couvrant la chromatographie, la synthèse organique et les réactions de couplage croisé.

Spécifications

Synonymes
Adenine riboside | 9-beta-D-Ribofuranosidoadenine | 9-beta-D-Ribofuranosyl-9H-purin-6-amine | beta-D-Ribofuranoside, adenine-9 | beta-D-Adenosine | Nucleocardyl | 9-beta-D-Ribofuranosyladenine | adenosine | (2R,3R,4S,5R)-2-(6-Aminopurin-9-yl)-5-(hydroxyme
Spécifications et pureté
Moligand™, pour culture cellulaire, ≥99.5%(HPLC)
Conditions de stockage de stockage
Stocker à 2-8°C, chargé d'argon
Expédié en
Glace humide
Grade
Moligand™, pour la culture cellulaire
Pureté
≥99.5%(HPLC)
Noms et identifiants
Pubchem Sid
Pubchem Sid Url
https://pubchem.ncbi.nlm.nih.gov/substance/488183412
Sourires canoniques
C1=NC(=C2C(=N1)N(C=N2)C3C(C(C(O3)CO)O)O)N
IUPAC Name
(2R,3R,4S,5R)-2-(6-aminopurin-9-yl)-5-(hydroxymethyl)oxolane-3,4-diol
InChIKey
OIRDTQYFTABQOQ-KQYNXXCUSA-N
INCHI
1S/C10H13N5O4/c11-8-5-9(13-2-12-8)15(3-14-5)10-7(18)6(17)4(1-16)19-10/h2-4,6-7,10,16-18H,1H2,(H2,11,12,13)/t4-,6-,7-,10-/m1/s1
Isomères SMILES
C1=NC(=C2C(=N1)N(C=N2)[C@H]3[C@@H]([C@@H]([C@H](O3)CO)O)O)N
WGK Allemagne
2
RTECS
AU7175000
Poids moléculaire
267.24
Beilstein
93029
Reaxy-Rn
1224871
Reaxys-RN_link_address
https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=1224871&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.

Rechercher le COA →

📊 Fiche technique

Résumé de référence rapide des spécifications et applications du produit.

Voir la fiche technique →

🔬 Fiche de spécifications

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

Voir la fiche de spécifications →

Données avancées

Taxonomic Classification

Taxonomy Tree

KingdomOrganic compounds
SuperclassNucleosides, nucleotides, and analogues
ClassePurine nucleosides
SubclassNot available
Intermediate Tree Nodes Not available
Direct ParentPurine nucleosides
Alternative Parents Glycosylamines  Pentoses  6-aminopurines  Aminopyrimidines and derivatives  N-substituted imidazoles  Imidolactams  Tetrahydrofurans  Heteroaromatic compounds  Secondary alcohols  Oxacyclic compounds  Azacyclic compounds  Primary amines  Primary alcohols  Organopnictogen compounds  Hydrocarbon derivatives  
Molecular FrameworkAromatic heteropolycyclic compounds
Substituents Purine nucleoside - Glycosyl compound - N-glycosyl compound - 6-aminopurine - Pentose monosaccharide - Imidazopyrimidine - Purine - Aminopyrimidine - Monosaccharide - N-substituted imidazole - Pyrimidine - Imidolactam - Tetrahydrofuran - Azole - Imidazole - Heteroaromatic compound - Secondary alcohol - Organoheterocyclic compound - Azacycle - Oxacycle - Organic oxygen compound - Organic nitrogen compound - Alcohol - Organonitrogen compound - Hydrocarbon derivative - Organopnictogen compound - Organooxygen compound - Amine - Primary alcohol - Primary amine - Aromatic heteropolycyclic compound
DescriptionThis compound belongs to the class of organic compounds known as purine nucleosides. These are compounds comprising a purine base attached to a ribosyl or deoxyribosyl moiety.
External Descriptors Ribonucleosides
Structure 3D
Modèle de structure chimique interactif





Cibles associées (humaines)
TRPM4 Tchem Transient receptor potential cation channel subfamily M member 4 (1 Activities)
Activity TypeActivity Value -log(M)Mechanism of ActionActivity ReferencePublications (PubMed IDs)
ADORA2A Tclin Adenosine receptor A2a (3 Activities)
Activity TypeActivity Value -log(M)Mechanism of ActionActivity ReferencePublications (PubMed IDs)
ADORA2B Tclin Adenosine receptor A2b (2 Activities)
Activity TypeActivity Value -log(M)Mechanism of ActionActivity ReferencePublications (PubMed IDs)
ADORA1 Tclin Adenosine receptor A1 (4 Activities)
Activity TypeActivity Value -log(M)Mechanism of ActionActivity ReferencePublications (PubMed IDs)
ADORA3 Tchem Adenosine receptor A3 (3 Activities)
Activity TypeActivity Value -log(M)Mechanism of ActionActivity ReferencePublications (PubMed IDs)
ABL1 Tclin Tyrosine-protein kinase ABL (18331 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
EGFR Tclin Epidermal growth factor receptor erbB1 (33727 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
ADA Tclin Adenosine deaminase (129 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
NR3C1 Tclin Glucocorticoid receptor (14987 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
INSR Tclin Insulin receptor (5558 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
PGR Tclin Progesterone receptor (8562 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
ADRB2 Tclin Beta-2 adrenergic receptor (11824 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
CHRM2 Tclin Muscarinic acetylcholine receptor M2 (10671 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
ADRB1 Tclin Beta-1 adrenergic receptor (6630 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
IMPDH2 Tclin Inosine-5'-monophosphate dehydrogenase 2 (1326 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
DRD2 Tclin Dopamine D2 receptor (23596 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
GABRA1 Tclin GABA receptor alpha-1 subunit (399 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
IMPDH1 Tclin Inosine-5'-monophosphate dehydrogenase 1 (221 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
MAOA Tclin Monoamine oxidase A (11911 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
CNR1 Tclin Cannabinoid CB1 receptor (20913 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
DRD1 Tclin Dopamine D1 receptor (9720 Activities)
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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
HRH2 Tclin Histamine H2 receptor (5428 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
HTR2A Tclin Serotonin 2a (5-HT2a) receptor (14758 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
HTR2C Tclin Serotonin 2c (5-HT2c) receptor (11471 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
AVPR2 Tclin Vasopressin V2 receptor (2912 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
ADORA1 Tclin Adenosine A1 receptor (17603 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
AGTR1 Tclin Type-1 angiotensin II receptor (5176 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
PTGS2 Tclin Cyclooxygenase-2 (13999 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
HRH1 Tclin Histamine H1 receptor (7573 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
AVPR1A Tclin Vasopressin V1a receptor (5412 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
OPRD1 Tclin Delta opioid receptor (15096 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
OPRK1 Tclin Kappa opioid receptor (16155 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
HTR3A Tclin Serotonin 3a (5-HT3a) receptor (3366 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
SLC6A3 Tclin Dopamine transporter (10535 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
GRIN1 Tclin Glutamate (NMDA) receptor subunit zeta 1 (122 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
KCNH2 Tclin HERG (29587 Activities)
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PDE3A Tclin Phosphodiesterase 3A (3309 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
SLC29A1 Tclin Equilibrative nucleoside transporter 1 (1711 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
ERBB2 Tclin Receptor protein-tyrosine kinase erbB-2 (7851 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
PDGFRB Tclin Platelet-derived growth factor receptor beta (5195 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
ADRA2B Tclin Alpha-2b adrenergic receptor (4412 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
ADRA2C Tclin Alpha-2c adrenergic receptor (4876 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
CHRM3 Tclin Muscarinic acetylcholine receptor M3 (7750 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
HTR2B Tclin Serotonin 2b (5-HT2b) receptor (10323 Activities)
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TBXA2R Tclin Thromboxane A2 receptor (5717 Activities)
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Cckar Cholecystokinin A receptor (90 Activities)
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Pde4d Phosphodiesterase 4D (4 Activities)
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Aplnr Apelin receptor (201 Activities)
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Adcy5 Adenylate cyclase type V (89 Activities)
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Prkcb Protein kinase C beta (2 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Mapk1 MAP kinase ERK2 (650 Activities)
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Hdac6 Histone deacetylase 6 (222 Activities)
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Fgfr3 Fibroblast growth factor receptor 3 (21 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Pnp Purine nucleoside phosphorylase (4 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
AT1 Adenosine transporter 1 (37 Activities)
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Eimeria tenella (990 Activities)
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Trichomonas vaginalis (2376 Activities)
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Human alphaherpesvirus 2 (4932 Activities)
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CHO-K1-BH4 (29 Activities)
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J774.A1 (2436 Activities)
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Luciferin 4-monooxygenase (66902 Activities)
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rep Replicase polyprotein 1ab (378 Activities)
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Mécanismes d'action
Certificats (CoA, COO, BSE/TSE et tableau d'analyse)
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31 results found

Lot NumberCertificate TypeDateArticle
K2603809K2603809Certificate of AnalysisOct 28, 2026 A108806
K2603808K2603808Certificate of AnalysisOct 28, 2026 A108806
K2603807K2603807Certificate of AnalysisOct 28, 2026 A108806
K2603806K2603806Certificate of AnalysisOct 28, 2026 A108806
H2624588H2624588Certificate of AnalysisAug 18, 2026 A108806
H2624587H2624587Certificate of AnalysisAug 18, 2026 A108806
H2607290H2607290Certificate of AnalysisMar 24, 2026 A108806
H2607289H2607289Certificate of AnalysisMar 24, 2026 A108806
D2603151D2603151Certificate of AnalysisMar 24, 2026 A108806
D2603152D2603152Certificate of AnalysisMar 24, 2026 A108806
D2603153D2603153Certificate of AnalysisMar 24, 2026 A108806
K2507228K2507228Certificate of AnalysisOct 24, 2025 A108806
K2507227K2507227Certificate of AnalysisOct 24, 2025 A108806
K2507226K2507226Certificate of AnalysisOct 24, 2025 A108806
B2526108B2526108Certificate of AnalysisFeb 07, 2025 A108806
B2526254B2526254Certificate of AnalysisFeb 07, 2025 A108806
B2526103B2526103Certificate of AnalysisFeb 07, 2025 A108806
G2404078G2404078Certificate of AnalysisJun 22, 2024 A108806
G2404079G2404079Certificate of AnalysisJun 22, 2024 A108806
I2320077I2320077Certificate of AnalysisAug 31, 2023 A108806
I2320073I2320073Certificate of AnalysisAug 31, 2023 A108806
I2320075I2320075Certificate of AnalysisAug 31, 2023 A108806
E23181245E23181245Certificate of AnalysisFeb 04, 2023 A108806
E23181241E23181241Certificate of AnalysisFeb 04, 2023 A108806
E23181243E23181243Certificate of AnalysisFeb 04, 2023 A108806
E23181249E23181249Certificate of AnalysisFeb 04, 2023 A108806
E23181248E23181248Certificate of AnalysisFeb 04, 2023 A108806
E23181244E23181244Certificate of AnalysisFeb 04, 2023 A108806
I2224013I2224013Certificate of AnalysisJul 15, 2022 A108806
I2224012I2224012Certificate of AnalysisJul 15, 2022 A108806
I2224011I2224011Certificate of AnalysisJul 15, 2022 A108806
Propriétés chimiques et physiques
SensibilitéAir sensitive
Rotation spécifique [α]-70 ° (C=2, 5% NaOH)
Point de fusion (°C)234-236°C
Poids moléculaire267.240 g/mol
XLogP3-1.100
Hydrogen Bond Donor Count4
Hydrogen Bond Acceptor Count8
Rotatable Bond Count2
Exact Mass267.097 Da
Monoisotopic Mass267.097 Da
Topological Polar Surface Area140.000 Ų
Heavy Atom Count19
Formal Charge0
Complexity335.000
Isotope Atom Count0
Defined Atom Stereocenter Count4
Undefined Atom Stereocenter Count0
Defined Bond Stereocenter Count0
Undefined Bond Stereocenter Count0
The total count of all stereochemical bonds0
Covalently-Bonded Unit Count1
FAQ et articles
For Cell Culture
A Panoramic Guide to Purines and Research Reagent Selection: Structural Hierarchy, Classification Map, Three Metabolic Pathways, and Typical Applications
Functional Systems of Nucleoside Metabolism-Related Enzymes in Drug Response and Disease Biology
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
Coupling Activators, Nucleoside Building Blocks, and Modification Design in Oligonucleotide Chemical Synthesis: Their Effects on Synthetic Efficiency, Purity, and Product Properties
Porous Graphitic Carbon (PGC) Chromatography Columns: Creating New Selectivity for Challenging Separations through Molecular Shape and the π-Electron Cloud on the Graphitic Surface
GPCR/G Protein Signal Transduction Mechanisms and Disease Research
Neuronal Signal Transduction Mechanisms and Disease Research
Analysis of Hydrolyzed Pearl as a Cosmetic Raw Material: Preparation Process, Active Components, and Skincare Formulation Applications
Anti-Photoaging Potential of Artemia Extract: UV-Induced Damage Cascades, HSP70-Related Stress Protection, and GP4G Metabolic Insights
Mechanisms by Which PDRN Participates in Skin Repair: A2A Receptor-Related Signaling, Nucleotide Salvage, and Extracellular Matrix Remodeling
Glycosidic Bond Structure and Cleavage Mechanisms—Chemical and Enzymatic Cleavage of O-, N-, S-, and C-Glycosides
From Tumor Sequencing to “One Patient, One Drug”: Machine-Learning-Assisted Design of V940 Individualized Neoantigen mRNA and the Phase III Breakthrough in Melanoma
Citations of This Product
Calculateurs de solution
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