N,N'-Bis(3-aminopropyl)-1,4-butanediamine Tetrahydrochloride - 10mM in Water , CAS No.306-67-2

CAS: 306-67-2 Cat. No.: N423174 Peso molecular: 348.18 Número EC: 206-189-8 PubChem CID: 9384

GRADE & PURITY 10mM in Water

Synonyms

SR-01000075473 | 9CI1570O48 | NSC 69852 | 1,4-Bis(aminopropyl)butanediamine tetrahydrochloride | N,N'-BIS(3-AMINOPROPYL)-1,4-BUTANEDIAMINE, TETRAHYDROCHLORIDE | Spermine tetra hydrochloride | Spermine tetrahydrochloride, certified reference material, Trac

Storage

Store at -80°C

Shipped In

Dry ice packs + Cold packs

Descripción general

Mixed NMDA agonist/antagonist at the polyamine site. Neuroprotective effects have been observed at high concentrations (1 mM), while neurotoxicity is observed at lower concentrations. It enhances agonist effectiveness at the strychnine-insensitive glycine site. Plays a role in cellular proliferation and differentiation; inhibits neuronal nitric oxide synthase (nNOS). Mixed NMDA agonist/antagonist at the polyamine site. Plays a role in cellular proliferation and differentiation; inhibits neuronal nitric oxide synthase (nNOS).

Specifications

Sinónimos

SR-01000075473 | 9CI1570O48 | NSC 69852 | 1, 4-Bis(aminopropyl)butanediamine tetrahydrochloride | N, N'-BIS(3-AMINOPROPYL)-1, 4-BUTANEDIAMINE, TETRAHYDROCHLORIDE | Spermine tetra hydrochloride | Spermine tetrahydrochloride, certified reference material, Trac

Especificaciones y pureza

10mM in Water

Mecanismos bioquímicos y fisiológicos

Mixed NMDA agonist/antagonist at the polyamine site. Neuroprotective effects have been observed at high concentrations (1 mM), while neurotoxicity is observed at lower concentrations. It enhances agonist effectiveness at the strychnine-insensitive glycine

Condiciones de almacenamiento de almacenamiento

Store at -80°C

Enviado en

Dry ice packs + Cold packs

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

Nombres e identificadores

• Sonrisas canónicas: C(CCNCCCN)CNCCCN.Cl.Cl.Cl.Cl
• IUPAC Name: N,N'-bis(3-aminopropyl)butane-1,4-diamine;tetrahydrochloride
• InChIKey: XLDKUDAXZWHPFH-UHFFFAOYSA-N
• INCHI: 1S/C10H26N4.4ClH/c11-5-3-9-13-7-1-2-8-14-10-4-6-12;;;;/h13-14H,1-12H2;4*1H
• Isómeros SMILES: C(CCNCCCN)CNCCCN.Cl.Cl.Cl.Cl
• WGK Alemania: 3
• RTECS: EJ7230000
• CAS alternativo: 1255099-40-1
• PubChem CID: 9384
• Peso molecular: 348.18
• Reaxy-Rn: 3911771

Taxonomic Classification

Taxonomy Tree

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

• Kingdom: Organic compounds
• Superclass: Organic nitrogen compounds
• Clase: Organonitrogen compounds
• Subclass: Amines
• Intermediate Tree Nodes: Secondary amines
• Direct Parent: Dialkylamines
• Alternative Parents: Organopnictogen compounds Monoalkylamines Hydrochlorides Hydrocarbon derivatives
• Molecular Framework: Aliphatic acyclic compounds
• Substituents: Secondary aliphatic amine - Organopnictogen compound - Hydrocarbon derivative - Hydrochloride - Primary amine - Primary aliphatic amine - Aliphatic acyclic compound
• Descripción: 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

Objetivos asociados (humanos)

PMP22 Tbio Peripheral myelin protein 22 (699 Activities)

Discover Target: PMP22

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

Objetivos asociados (no humanos)

rep Replicase polyprotein 1ab (378 Activities)

Discover Target: rep

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

Mapt Microtubule-associated protein tau (6 Activities)

Discover Target: Mapt

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

nfo Endonuclease 4 (425 Activities)

Discover Target: nfo

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

Mecanismos de acción

Propiedades químicas y físicas

• Sensibilidad: Hygroscopic
• Punto de fusión (°C): 315°C
• Peso molecular: 348.200 g/mol
• Hydrogen Bond Donor Count: 8
• Hydrogen Bond Acceptor Count: 4
• Rotatable Bond Count: 11
• Exact Mass: 348.12 Da
• Monoisotopic Mass: 346.122 Da
• Topological Polar Surface Area: 76.100 Ų
• Heavy Atom Count: 18
• Formal Charge: 0
• Complexity: 86.100
• 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

XLogP3

Referencias

1. Shijin Xiong, Xiaoyan Xu, Qiaozhen Liu, Yazhou Xu, Hongbing Ren, Tao Xiong, Mingyong Xie.  (2023)  Integrated metatranscriptomics and metabolomics revealed the metabolic pathways of biogenic amines during Laotan Suancai fermentation.  Food Bioscience,      [PMID:] [10.1016/j.fbio.2023.103517]

2. Yu Wang, Xueping Kong, Fei Li, Bao Li, Lixin Wu, Kai Chen, Yuqing Wu.  (2022)  Mo154 Synergistically Enhanced Antibiofilm and Antibacterial Effects of Spermine via Coassembly.  ACS Applied Bio Materials,      [PMID:36264761] [10.1021/acsabm.2c00692]

3. Yanan Liu, Yuhao Huang, Qileng Aori, Yu Wang, Sai Zhao, Zhen-Lin Xu.  (2026)  A sustained-release antibacterial gelatin hydrogel based on metal-phenolic networks for long-term preservation of prefabricated meat.  FOOD CHEMISTRY,      [PMID:] [10.1016/j.foodchem.2026.149080]