Guanosine-5'-triphosphate disodium salt - ≥98% , CAS No.56001-37-7

CAS: 56001-37-7 Cat. No.: G419147 Peso molecular: 567.15 Beilstein Registry Number: 4113439 Número EC: 259-940-7 PubChem CID: 135465086

GRADE & PURITY ≥98%

Synonyms

Guanosine 5'-triphosphate disodium salt|56001-37-7|GUANOSINE-5'-TRIPHOSPHATE DISODIUM SALT|Guanosine-5'-triphosphoric aicd disodium salt|disodium;[[(2R,3S,4R,5R)-5-(2-amino-6-oxo-3H-purin-9-yl)-3,4-dihydroxyoxolan-2-yl]methoxy-oxidophosphoryl] phosphono p

Storage

Protected from light,Store at -20°C,Argon charged

Shipped In

Ice chest + Ice pads

Descripción general

Guanosine-5'-triphosphate disodium salt is a phosphoryl donor in protein synthesis and in signal transduction.
A phosphoryl donor in protein synthesis and signal transduction.

Specifications

Sinónimos

Guanosine 5'-triphosphate disodium salt | 56001-37-7 | GUANOSINE-5'-TRIPHOSPHATE DISODIUM SALT | Guanosine-5'-triphosphoric aicd disodium salt | disodium;[[(2R, 3S, 4R, 5R)-5-(2-amino-6-oxo-3H-purin-9-yl)-3, 4-dihydroxyoxolan-2-yl]methoxy-oxidophosphoryl] phosphono p

Especificaciones y pureza

≥98%

Condiciones de almacenamiento de almacenamiento

Protected from light, Store at -20°C, Argon charged

Enviado en

Ice chest + Ice pads

Este producto requiere envío en cadena de frío. Los servicios terrestres y otros servicios económicos no están disponibles.

Pureza

≥98%

Nombres e identificadores

• Pubchem Sid: 504773348
• Pubchem Sid Url: https://pubchem.ncbi.nlm.nih.gov/substance/504773348
• Sonrisas canónicas: C1=NC2=C(N1C3C(C(C(O3)COP(=O)([O-])OP(=O)([O-])OP(=O)(O)O)O)O)N=C(NC2=O)N.[Na+].[Na+]
• IUPAC Name: disodium;[[(2R,3S,4R,5R)-5-(2-amino-6-oxo-1H-purin-9-yl)-3,4-dihydroxyoxolan-2-yl]methoxy-oxidophosphoryl] phosphono phosphate
• InChIKey: FIZIYLKEXVIRHJ-LGVAUZIVSA-L
• INCHI: 1S/C10H16N5O14P3.2Na/c11-10-13-7-4(8(18)14-10)12-2-15(7)9-6(17)5(16)3(27-9)1-26-31(22,23)29-32(24,25)28-30(19,20)21;;/h2-3,5-6,9,16-17H,1H2,(H,22,23)(H,24,25)(H2,19,20,21)(H3,11,13,14,18);;/q;2*+1/p-2/t3-,5-,6-,9-;;/m1../s1
• Isómeros SMILES: C1=NC2=C(N1[C@H]3[C@@H]([C@@H]([C@H](O3)COP(=O)([O-])OP(=O)([O-])OP(=O)(O)O)O)O)N=C(NC2=O)N.[Na+].[Na+]
• PubChem CID: 135465086
• Peso molecular: 567.15
• Beilstein: 4113439

Taxonomic Classification

Taxonomy Tree

• Kingdom Organic compounds
  • Superclass Nucleosides, nucleotides, and analogues
    • Clase Purine nucleotides
      • Subclass Purine ribonucleotides

• Kingdom: Organic compounds
• Superclass: Nucleosides, nucleotides, and analogues
• Clase: Purine nucleotides
• Subclass: Purine ribonucleotides
• Intermediate Tree Nodes: Not available
• Direct Parent: Purine ribonucleoside triphosphates
• Alternative Parents: Purine ribonucleoside monophosphates Pentose phosphates Glycosylamines 6-oxopurines Hypoxanthines Monosaccharide phosphates Pyrimidones Aminopyrimidines and derivatives Alkyl phosphates N-substituted imidazoles Tetrahydrofurans Vinylogous amides Heteroaromatic compounds Secondary alcohols 1,2-diols Azacyclic compounds Oxacyclic compounds Hydrocarbon derivatives Organic zwitterions Primary amines Organopnictogen compounds Organic sodium salts Organic oxides
• Molecular Framework: Aromatic heteropolycyclic compounds
• Substituents: Purine ribonucleoside triphosphate - Purine ribonucleoside monophosphate - Pentose phosphate - Pentose-5-phosphate - Glycosyl compound - N-glycosyl compound - 6-oxopurine - Hypoxanthine - Monosaccharide phosphate - Pentose monosaccharide - Imidazopyrimidine - Purine - Aminopyrimidine - Pyrimidone - Alkyl phosphate - Phosphoric acid ester - Organic phosphoric acid derivative - N-substituted imidazole - Pyrimidine - Monosaccharide - Azole - Imidazole - Heteroaromatic compound - Vinylogous amide - Tetrahydrofuran - Secondary alcohol - 1,2-diol - Organoheterocyclic compound - Oxacycle - Azacycle - Organic alkali metal salt - Amine - Organic sodium salt - Organonitrogen compound - Alcohol - Organic nitrogen compound - Hydrocarbon derivative - Organic oxide - Organopnictogen compound - Organooxygen compound - Organic salt - Organic zwitterion - Primary amine - Organic oxygen compound - Aromatic heteropolycyclic compound
• Descripción: This compound belongs to the class of organic compounds known as purine ribonucleoside triphosphates. These are purine ribobucleotides with a triphosphate group linked to the ribose moiety.
• External Descriptors: Not available

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

Propiedades químicas y físicas

• Sensibilidad: Heat sensitive；Moisture sensitive；Light sensitive
• Peso molecular: 567.140 g/mol
• Hydrogen Bond Donor Count: 6
• Hydrogen Bond Acceptor Count: 16
• Rotatable Bond Count: 8
• Exact Mass: 566.955 Da
• Monoisotopic Mass: 566.955 Da
• Topological Polar Surface Area: 300.000 Ų
• Heavy Atom Count: 34
• Formal Charge: 0
• Complexity: 910.000
• 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: 3

XLogP3

Referencias

1. Ting Zeng, Jie Yin, Ziwen Liu, Zhaoxing Li, Yu Zhang, Yang Lv, Mei-Ling Lu, Min Luo, Meirong Chen, Yibei Xiao.  (2023)  Mechanistic insights into transposon cleavage and integration by TnsB of ShCAST system.  Cell Reports,      [PMID:37379212] [10.1016/j.celrep.2023.112698]

2. Ying Ding, Qingyan Jia, Yongmei Wen, Weimin Liu, Jiechao Ge, Jiasheng Wu, Hongyan Zhang, Pengfei Wang.  (2018)  New detection method for nucleoside triphosphates based on carbon dots: The distance-dependent singlet oxygen trapping.  ANALYTICA CHIMICA ACTA,      [PMID:30119732] [10.1016/j.aca.2018.05.024]

3. Qu Fei, Mao Beibei, Xue Fangfang, Xia Lian, You Jinmao, Song Cuihua.  (2018)  Photoinduced electron transfer from polymer-templated Ag nanoclusters to G-quadruplex-hemin complexes for the construction of versatile biosensors and logic gate applications.  ANALYTICAL AND BIOANALYTICAL CHEMISTRY,  410  (8): (2211-2219).  [PMID:29387952] [10.1007/s00216-018-0887-z]

4. Qinqin Sun, Fei Yan, Bin Su.  (2018)  Label-free electrochemical biosensors based on 3,3′,5,5′-tetramethylbenzidine responsive isoporous silica-micelle membrane.  BIOSENSORS & BIOELECTRONICS,      [PMID:29412936] [10.1016/j.bios.2018.01.026]

5. Fan Huahua, Wang Runjia, Zhang Li, Liu Minghua.  (2025)  Amplified circularly polarized luminescence in assembly of terpyridine-ZnII and GTP induced by silver(I) ion.  Science China-Chemistry,      [PMID:] [10.1007/s11426-024-2571-3]

6. Yiming Yang, Junlei Liu, Wenying Li, Yueqing Zheng, Wei Xu.  (2024)  Colorimetric/fluorescent dual-mode assay for antioxidant capacity of gallnuts based on CuCo nanozyme and AIE luminogen.  TALANTA,      [PMID:38878507] [10.1016/j.talanta.2024.126345]

7. Jie Lv, Shuangling Wang, Cong Zhang, Yulong Lin, Yan Fu, Meng Li.  (2020)  ATP induced alteration in the peroxidase-like properties of hollow Prussian blue nanocubes: a platform for alkaline phosphatase detection.  ANALYST,  145  (14): (5032-5040).  [PMID:32658942] [10.1039/D0AN00405G]

8. Haoran Zheng, Jiayu Guo, Han Wang, Yurou Wang, Wenxiang Zhou, Ke Liu, Qiang Ma, Yanfei Qi.  (2025)  A zeolitic imidazolate framework-90 enhanced ultrasensitive ATP sensing platform with HCR and CRISPR-Cas12a dual signal amplification for live bacteria detection.  JOURNAL OF HAZARDOUS MATERIALS,      [PMID:40378737] [10.1016/j.jhazmat.2025.138612]