Agmatine Sulfate - 10mM in Water , CAS No.2482-00-0

CAS: 2482-00-0 Cat. No.: A422852 Formula: C₅H₁₄N₄·H₂SO₄ Peso molecolare: 228.27 Beilstein Registry Number: 3918807 Numero EC: 219-617-3

GRADE & PURITY 10mM in Water

Synonyms

1-(4-Aminobutyl)guanidine sulfate(Chunks or pellets) | AS-15375 | SR-01000075244-1 | (4-Aminobutyl)guanidine sulfate | AI3-51851 | (4-Aminobutyl)guanidinium sulphate | NIH-11035 | A 7127 | SY033517 | 4-Guanidinobutylamine sulphate salt | FT-0600398 | Guan

Storage

Store at -80°C

Shipped In

Dry ice packs + Cold packs

Specifications

Sinonimi

1-(4-Aminobutyl)guanidine sulfate(Chunks or pellets) | AS-15375 | SR-01000075244-1 | (4-Aminobutyl)guanidine sulfate | AI3-51851 | (4-Aminobutyl)guanidinium sulphate | NIH-11035 | A 7127 | SY033517 | 4-Guanidinobutylamine sulphate salt | FT-0600398 | Guan

Specifiche e purezza

10mM in Water

Meccanismi biochimici e fisiologici

Putative endogenous neurotransmitter at imidazoline receptors; displaces clonidine at α2-adrenergic and at imidazoline receptors; blocks NMDA-activated ion channels in hippocampal neurons.

Condizioni di conservazione di stoccaggio

Store at -80°C

Spedito in

Dry ice packs + Cold packs

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

Tipo di azione

INHIBITOR

Nomi e identificatori

• Pubchem Sid: 528774101
• Pubchem Sid Url: https://pubchem.ncbi.nlm.nih.gov/substance/528774101
• Sorrisi canonici: C(CCN=C(N)N)CN.OS(=O)(=O)O
• IUPAC Name: 2-(4-aminobutyl)guanidine;sulfuric acid
• InChIKey: PTAYFGHRDOMJGC-UHFFFAOYSA-N
• INCHI: 1S/C5H14N4.H2O4S/c6-3-1-2-4-9-5(7)8;1-5(2,3)4/h1-4,6H2,(H4,7,8,9);(H2,1,2,3,4)
• Isomeri SMILES: C(CCN=C(N)N)CN.OS(=O)(=O)O
• WGK Germania: 3
• Peso molecolare: 228.27
• Beilstein: 3918807
• Reaxy-Rn: 19474094
• Reaxys-RN_link_address: https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=19474094&ln=

Taxonomic Classification

Taxonomy Tree

• Kingdom Organic compounds
  • Superclass Organic acids and derivatives
    • Classe Organic sulfuric acids and derivatives
      • Subclass Organic sulfuric acids

• Kingdom: Organic compounds
• Superclass: Organic acids and derivatives
• Classe: Organic sulfuric acids and derivatives
• Subclass: Organic sulfuric acids
• Intermediate Tree Nodes: Not available
• Direct Parent: Organic sulfuric acids
• Alternative Parents: Guanidines Propargyl-type 1,3-dipolar organic compounds Carboximidamides Organopnictogen compounds Organic oxides Monoalkylamines Hydrocarbon derivatives
• Molecular Framework: Aliphatic acyclic compounds
• Substituents: Sulfuric acid - Guanidine - Organic 1,3-dipolar compound - Propargyl-type 1,3-dipolar organic compound - Carboximidamide - Organic nitrogen compound - Organic oxygen compound - Organopnictogen compound - Organic oxide - Hydrocarbon derivative - Primary amine - Organonitrogen compound - Primary aliphatic amine - Amine - Aliphatic acyclic compound
• Descrizione: This compound belongs to the class of organic compounds known as organic sulfuric acids. These are organic compounds containing the sulfuric acid functional group, with the generic structure HOS(=O)(=O)OH.
• 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

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Meccanismi d'azione

Proprietà chimiche e fisiche

• Punto di fusione (°C): 234-238°C
• Peso molecolare: 228.270 g/mol
• Hydrogen Bond Donor Count: 5
• Hydrogen Bond Acceptor Count: 6
• Rotatable Bond Count: 4
• Exact Mass: 228.089 Da
• Monoisotopic Mass: 228.089 Da
• Topological Polar Surface Area: 173.000 Ų
• Heavy Atom Count: 14
• Formal Charge: 0
• Complexity: 166.000
• 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: 2

XLogP3

Riferimenti

1. Hongjie Hui, Yajun Bai, Tai-Ping Fan, Xiaohui Zheng, Yujie Cai.  (2020)  Biosynthesis of Putrescine from L-arginine Using Engineered Escherichia coli Whole Cells.  Catalysts,  10  (9): (947).  [PMID:] [10.3390/catal10090947]

2. Salman Riaz, Min Liu, Zhenwu Zhong, Hongyu Mi, Weizhi Zheng, Yi Xiao, Ying Qi, Muhammad Salik Qureshi, Shayan Umar, Yahong Xie.  (2024)  Enhancing efficiency and stability in carbon-based perovskite solar cells through dual-interface modification.  JOURNAL OF POWER SOURCES,      [PMID:] [10.1016/j.jpowsour.2024.236133]