N1,N11-Diethylnorspermine tetrahydrochloride - ≥98% , CAS No.156886-85-0

CAS: 156886-85-0 Cat. No.: N287060 Molecular Weight: 390.27 PubChem CID: 11501988

GRADE & PURITY ≥98%

Synonyms

SR-01000597988-1 | J-004628 | N,N''-BIS[3-(ETHYLAMINO)PROPYL]PROPANE-1,3-DIAMINE TETRAHYDROCHLORIDE | DENSPM (tetrahydrochloride) | Diethylnorspermine tetrahydrochloride | MS-26493 | N-ethyl-N'-[3-[3-(ethylamino)propylamino]propyl]propane-1,3-diamine;tetr

Storage

Store at -20°C

Shipped In

Ice chest + Ice pads

Overview

Product Describtion:

N1,N11-Diethylnorspermine tetrahydrochloride (DENSPM tetrahydrochloride) potently induces SSAT (spermidine/spermine N1-acetyltransferase) mRNA and effectively stabilizes SSAT enzyme activity.

Specifications

Synonyms

SR-01000597988-1 | J-004628 | N, N''-BIS[3-(ETHYLAMINO)PROPYL]PROPANE-1, 3-DIAMINE TETRAHYDROCHLORIDE | DENSPM (tetrahydrochloride) | Diethylnorspermine tetrahydrochloride | MS-26493 | N-ethyl-N'-[3-[3-(ethylamino)propylamino]propyl]propane-1, 3-diamine;tetr

Specifications & Purity

≥98%

Biochemical and Physiological Mechanisms

Highly potent inducer of spermidine/spermine N1-acetyltransferase, able to increase enzyme activity 200-1000 fold.

Storage

Store at -20°C

Shipped In

Ice chest + Ice pads

This product requires cold chain shipping. Ground and other economy services are not available.

Action Type

ACTIVATOR

Purity

≥98%

Names and Identifiers

• Canonical Smiles: CCNCCCNCCCNCCCNCC.Cl.Cl.Cl.Cl
• IUPAC Name: N-ethyl-N'-[3-[3-(ethylamino)propylamino]propyl]propane-1,3-diamine;tetrahydrochloride
• InChIKey: LAWBSOKBIROCQP-UHFFFAOYSA-N
• INCHI: 1S/C13H32N4.4ClH/c1-3-14-8-5-10-16-12-7-13-17-11-6-9-15-4-2;;;;/h14-17H,3-13H2,1-2H3;4*1H
• Isomeric SMILES: CCNCCCNCCCNCCCNCC.Cl.Cl.Cl.Cl
• PubChem CID: 11501988
• Molecular Weight: 390.27

Taxonomic Classification

Taxonomy Tree

• Kingdom Organic compounds
  • Superclass Organic nitrogen compounds
    • Class Organonitrogen compounds
      • Subclass Amines
        • Level5 Secondary amines
          • Level6 Dialkylamines

• Kingdom: Organic compounds
• Superclass: Organic nitrogen compounds
• Class: Organonitrogen compounds
• Subclass: Amines
• Intermediate Tree Nodes: Secondary amines
• Direct Parent: Dialkylamines
• Alternative Parents: Hydrochlorides Hydrocarbon derivatives
• Molecular Framework: Aliphatic acyclic compounds
• Substituents: Secondary aliphatic amine - Hydrocarbon derivative - Hydrochloride - Aliphatic acyclic compound
• Description: This compound belongs to the class of organic compounds known as dialkylamines. These are organic compounds containing a dialkylamine group, characterized by two alkyl groups bonded to the amino nitrogen.
• 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

Chemical and Physical Properties

• Solubility: Solvent:water, Max Conc. mg/mL: 39.03, Max Conc. mM: 100
• Sensitivity: Moisture sensitive.
• Molecular Weight: 390.300 g/mol
• Hydrogen Bond Donor Count: 8
• Hydrogen Bond Acceptor Count: 4
• Rotatable Bond Count: 14
• Exact Mass: 390.166 Da
• Monoisotopic Mass: 388.169 Da
• Topological Polar Surface Area: 48.100 Ų
• Heavy Atom Count: 21
• Formal Charge: 0
• Complexity: 117.000
• 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: 5

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