[³⁵S]ADPβS - Moligand™ , Agonist of P2Y 1 receptor, CAS No.S614028, Agonist of P2Y 1 receptor

CAS: S614028 Cat. No.: S614028 PubChem CID: 73755052
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GRADE & PURITY Moligand™ ? Moligand™ — Aladdin's line of ligands and bioactive small molecules. Use for receptor, pathway, and binding studies needing defined small-molecule tools.
Storage
Room temperature
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Size
Deutschland (EU)
USA*
Price
Qty
5mg
S614028-5mg
Auf Bestellung · 8–12 Wochen
694,10€
25mg
S614028-25mg
Auf Bestellung · 8–12 Wochen
1.488,09€
Enter a quantity for the sizes you want to add.
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Why this grade

Moligand™ Moligand™ for sensitive chromatographic and analytical workflows requiring minimal baseline interference.

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Storage & shipping

Room temperature Ships Check lot-specific COA for exact specifications.

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Quality documents

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

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Literature proof

Cited in 0 peer-reviewed publications across chromatography, organic synthesis, and cross-coupling reactions.

Specifications

Spezifikationen & Reinheit
Moligand™
Storage
Room temperature
Note
Moligand™
Aktionsart
AGONIST
Mechanismus der Wirkung
Agonist of P2Y 1 receptor
Namen und Kennungen
Kanonisches LächelnO[C@@H]1[C@@H](COP(=O)(OP(=[35S])(O)O)O)O[C@H]([C@@H]1O)n1cnc2c1ncnc2N
IUPAC Name[({[(2R,3S,4R,5R)-5-(6-amino-9H-purin-9-yl)-3,4-dihydroxyoxolan-2-yl]methoxy}(hydroxy)phosphoryl)oxy](sulfanylidene)phosphonous acid
InChIKeyHCIKUKNAJRJFOW-JWNXZZODSA-N
INCHI1S/C10H15N5O9P2S/c11-8-5-9(13-2-12-8)15(3-14-5)10-7(17)6(16)4(23-10)1-22-25(18,19)24-26(20,21)27/h2-4,6-7,10,16-17H,1H2,(H,18,19)(H2,11,12,13)(H2,20,21,27)/t4-,6-,7-,10-/m1/s1/i27+3
Isomere SMILES C1=NC(=C2C(=N1)N(C=N2)[C@H]3[C@@H]([C@@H]([C@H](O3)COP(=O)(O)OP(=[35S])(O)O)O)O)N
PubChem CID 73755052

Documentation

📋 Safety Data Sheet (SDS)

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

Download SDS →

✅ Certificate of Analysis (COA)

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

Look up COA →

📊 Datasheet

Quick-reference summary of product specifications and applications.

View datasheet →

🔬 Specification Sheet

Full quality attributes and acceptance criteria for this grade.

View spec sheet →

Advanced Data

Taxonomic Classification

Taxonomy Tree

KingdomOrganic compounds
SuperclassNucleosides, nucleotides, and analogues
KlassePurine nucleotides
SubclassPurine ribonucleotides
Intermediate Tree Nodes Not available
Direct ParentPurine ribonucleoside monophosphates
Alternative Parents Pentose phosphates  Glycosylamines  6-aminopurines  Monosaccharide phosphates  Monoalkyl phosphates  Aminopyrimidines and derivatives  Organic thiophosphoric acids and derivatives  N-substituted imidazoles  Imidolactams  Heteroaromatic compounds  Oxolanes  1,2-diols  Secondary alcohols  Oxacyclic compounds  Azacyclic compounds  Organic oxides  Hydrocarbon derivatives  Primary amines  
Molecular FrameworkAromatic heteropolycyclic compounds
Substituents Purine ribonucleoside monophosphate - Pentose phosphate - Pentose-5-phosphate - Glycosyl compound - N-glycosyl compound - 6-aminopurine - Monosaccharide phosphate - Pentose monosaccharide - Imidazopyrimidine - Purine - Aminopyrimidine - Monoalkyl phosphate - Alkyl phosphate - Pyrimidine - Organic thiophosphoric acid or derivatives - Imidolactam - Monosaccharide - Phosphoric acid ester - N-substituted imidazole - Organic phosphoric acid derivative - Azole - Imidazole - Heteroaromatic compound - Oxolane - Secondary alcohol - 1,2-diol - Azacycle - Organoheterocyclic compound - Oxacycle - Primary amine - Alcohol - Hydrocarbon derivative - Organic oxide - Organic oxygen compound - Organic nitrogen compound - Organonitrogen compound - Organooxygen compound - Amine - Aromatic heteropolycyclic compound
BeschreibungThis compound belongs to the class of organic compounds known as purine ribonucleoside monophosphates. These are nucleotides consisting of a purine base linked to a ribose to which one monophosphate group is attached.
External Descriptors Not available
3D-Struktur
Interaktives chemisches Strukturmodell





Zugehörige Ziele (menschlich)
P2RY1 Tchem P2Y purinoceptor 1 (0 Activities)
Activity TypeActivity Value -log(M)Mechanism of ActionActivity ReferencePublications (PubMed IDs)
Zertifikate (CoA, COO, BSE/TSE und Analyse-Diagramm)
C of A & Other Certificates(BSE/TSE, COO):
Analytical Chart:
Lösungsrechner
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