Adenosine 3′-monophosphate , CAS No.84-21-9

CAS: 84-21-9 Cat. No.: A329610 Formula: C₁₀H₁₄N₅O₇P Peso molecolare: 347.22 Beilstein Registry Number: 54478 Numero EC: 201-521-8 PubChem CID: 41211

Synonyms

BDBM50395135 | 3'-ADENYLIC ACID [MI] | Q27103969 | (-)-3'-ADENYLIC ACID | 3'-AMP, 3'-Adenylic acid | Adenosine 3'-monophosphate | 4-26-00-03607 (Beilstein Handbook Reference) | Adenosine 3'-monophosphate, from yeast | PD070003 | C01367 | [(2R,3S,4R,5R)-5-

Storage

Store at -20°C

Shipped In

Ice chest + Ice pads

Panoramica

"Adenosine 3′-monophosphate" is a specific nucleotide, and its structure and properties can be deduced from its name. The term "adenosine" in the name refers to the nucleoside portion of the molecule, which consists of adenine, a nitrogenous base, attached to a ribose sugar. Adenine is one of the four bases found in DNA and RNA, and it pairs with thymine in DNA or uracil in RNA. The "3′-monophosphate" part of the name indicates that there is a single phosphate group attached to the 3′ carbon of the ribose sugar. This distinguishes it from other nucleotides that may have the phosphate group attached to a different carbon or that may have more than one phosphate group. Phosphates are key parts of nucleotides, contributing to their ability to form polymers like DNA and RNA. The phosphate group links nucleotides together in these structures by forming phosphodiester bonds with the sugars. In summary, "Adenosine 3′-monophosphate" is a nucleotide that consists of an adenine base, a ribose sugar, and a single phosphate group. These components are key to the molecule′s role in biological systems, particularly in the formation of nucleic acids.

Specifications

Sinonimi

BDBM50395135 | 3'-ADENYLIC ACID [MI] | Q27103969 | (-)-3'-ADENYLIC ACID | 3'-AMP, 3'-Adenylic acid | Adenosine 3'-monophosphate | 4-26-00-03607 (Beilstein Handbook Reference) | Adenosine 3'-monophosphate, from yeast | PD070003 | C01367 | [(2R,3S,4R,5R)-5-

Fonte

from yeast

Condizioni di conservazione di stoccaggio

Store at -20°C

Spedito in

Ice chest + Ice pads

Questo prodotto richiede spedizione a catena fredda. I servizi di terra e altri servizi economici non sono disponibili.

Proprietà del prodotto

• pKa: pKa: 1.84 (Predicted), pKa: 3.82 (Predicted)

Nomi e identificatori

• Sorrisi canonici: C1=NC(=C2C(=N1)N(C=N2)C3C(C(C(O3)CO)OP(=O)(O)O)O)N
• IUPAC Name: [(2R,3S,4R,5R)-5-(6-aminopurin-9-yl)-4-hydroxy-2-(hydroxymethyl)oxolan-3-yl] dihydrogen phosphate
• InChIKey: LNQVTSROQXJCDD-KQYNXXCUSA-N
• INCHI: 1S/C10H14N5O7P/c11-8-5-9(13-2-12-8)15(3-14-5)10-6(17)7(4(1-16)21-10)22-23(18,19)20/h2-4,6-7,10,16-17H,1H2,(H2,11,12,13)(H2,18,19,20)/t4-,6-,7-,10-/m1/s1
• Isomeri SMILES: C1=NC(=C2C(=N1)N(C=N2)[C@H]3[C@@H]([C@@H]([C@H](O3)CO)OP(=O)(O)O)O)N
• WGK Germania: 3
• PubChem CID: 41211
• Peso molecolare: 347.22
• Beilstein: 54478

Taxonomic Classification

Taxonomy Tree

• Kingdom Organic compounds
  • Superclass Nucleosides, nucleotides, and analogues
    • Classe Ribonucleoside 3'-phosphates

• Kingdom: Organic compounds
• Superclass: Nucleosides, nucleotides, and analogues
• Classe: Ribonucleoside 3'-phosphates
• Subclass: Not available
• Intermediate Tree Nodes: Not available
• Direct Parent: Ribonucleoside 3'-phosphates
• Alternative Parents: Pentose phosphates Glycosylamines 6-aminopurines Monosaccharide phosphates Aminopyrimidines and derivatives Monoalkyl phosphates Imidolactams N-substituted imidazoles Tetrahydrofurans Heteroaromatic compounds Secondary alcohols Oxacyclic compounds Azacyclic compounds Primary alcohols Hydrocarbon derivatives Primary amines Organic oxides Organopnictogen compounds
• Molecular Framework: Aromatic heteropolycyclic compounds
• Substituents: Pentose phosphate - Ribonucleoside 3'-phosphate - Glycosyl compound - N-glycosyl compound - 6-aminopurine - Pentose monosaccharide - Monosaccharide phosphate - Purine - Imidazopyrimidine - Aminopyrimidine - Monoalkyl phosphate - Organic phosphoric acid derivative - Phosphoric acid ester - N-substituted imidazole - Monosaccharide - Pyrimidine - Imidolactam - Alkyl phosphate - Heteroaromatic compound - Tetrahydrofuran - Azole - Imidazole - Secondary alcohol - Oxacycle - Azacycle - Organoheterocyclic compound - Primary amine - Amine - Alcohol - Organic nitrogen compound - Hydrocarbon derivative - Organic oxide - Organopnictogen compound - Organic oxygen compound - Primary alcohol - Organooxygen compound - Organonitrogen compound - Aromatic heteropolycyclic compound
• Descrizione: This compound belongs to the class of organic compounds known as ribonucleoside 3'-phosphates. These are ribonucleosides that contain a phosphate group attached to the C-3 carbon of the ribose or deoxyribose moiety. The nucleobases here are limited to purine, pyrimidine, and pyridine derivatives.
• External Descriptors: purine ribonucleoside 3'-monophosphate - adenosine 3'-phosphate

Data sources

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

Obiettivi associati (umani)

ADORA1 Tclin Adenosine A1 receptor (17603 Activities)

Discover Target: ADORA1

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

Meccanismi d'azione

Proprietà chimiche e fisiche

• Solubilità: Soluble in 1 N NH4OH (50 mg/ml), and water (0.5 mg/ml at 15° C).
• Indice di rifrazione: n20D~1.91 (Predicted)
• Punto di ebollizione (°C): 815.5° C at 760 mmHg
• Punto di fusione (°C): 197.2° C (dec.)
• Peso molecolare: 347.220 g/mol
• XLogP3: -2.700
• Hydrogen Bond Donor Count: 5
• Hydrogen Bond Acceptor Count: 11
• Rotatable Bond Count: 4
• Exact Mass: 347.063 Da
• Monoisotopic Mass: 347.063 Da
• Topological Polar Surface Area: 186.000 Ų
• Heavy Atom Count: 23
• Formal Charge: 0
• Complexity: 481.000
• Isotope Atom Count: 0
• Defined Atom Stereocenter Count: 4
• 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