5-hydroxydecanoic acid sodium - ≥97%(HPLC) , CAS No.71186-53-3

CAS: 71186-53-3 Cat. No.: H299595 Peso molecular: 210.25

GRADE & PURITY ≥97%(HPLC)

Synonyms

LP00628 | 5-Hydroxydecanoate (sodium) | H-135 | 5-Hydroxycapric acid sodium salt | HMS1361O06 | NCGC00016152-02 | 1-[3-(dimethylamino)propyl]-3-ethyl carbodiimide hydrochloride | 5-HD;5-hydroxydecanoate sodium salt | HY-136615 | TETRABUTYLAMMONIUM FLUORID

Storage

Store at 2-8°C

Shipped In

Wet ice

Specifications

Sinónimos

LP00628 | 5-Hydroxydecanoate (sodium) | H-135 | 5-Hydroxycapric acid sodium salt | HMS1361O06 | NCGC00016152-02 | 1-[3-(dimethylamino)propyl]-3-ethyl carbodiimide hydrochloride | 5-HD;5-hydroxydecanoate sodium salt | HY-136615 | TETRABUTYLAMMONIUM FLUORID

Especificaciones y pureza

≥97%(HPLC)

Mecanismos bioquímicos y fisiológicos

Mitochondrial K ATP channel inhibitor. Inhibits the proliferation of hypoxic human pulmonary artery smooth muscle cells (HPASMC) by blocking mitochondrial K ATP channels. Active in vivo.

Condiciones de almacenamiento de almacenamiento

Store at 2-8°C

Enviado en

Wet ice

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

Tipo de acción

INHIBITOR

Nota

Wherever possible, you should prepare and use solutions on the same day. However, if you need to make up stock solutions in advance, we recommend that you store the solution as aliquots in tightly sealed vials at -20°C. Generally, these will be useable for up to one month. Before use, and prior to opening the vial we recommend that you allow your product to equilibrate to room temperature for at least 1 hour. Need more advice on solubility, usage and handling? Please visit our frequently asked questions (FAQ) page for more details.

Pureza

≥97%(HPLC)

Nombres e identificadores

• Pubchem Sid: 504769610
• Pubchem Sid Url: https://pubchem.ncbi.nlm.nih.gov/substance/504769610
• Sonrisas canónicas: CCCCCC(CCCC(=O)[O-])O.[Na+]
• IUPAC Name: sodium;5-hydroxydecanoate
• InChIKey: YNAGNECWEKMWRM-UHFFFAOYSA-M
• INCHI: 1S/C10H20O3.Na/c1-2-3-4-6-9(11)7-5-8-10(12)13;/h9,11H,2-8H2,1H3,(H,12,13);/q;+1/p-1
• Isómeros SMILES: CCCCCC(CCCC(=O)[O-])O.[Na+]
• CAS alternativo: 624-00-0
• Peso molecular: 210.25
• Reaxy-Rn: 8171328
• Reaxys-RN_link_address: https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=8171328&ln=

Taxonomic Classification

Taxonomy Tree

• Kingdom Organic compounds
  • Superclass Lipids and lipid-like molecules
    • Clase Fatty Acyls
      • Subclass Fatty acids and conjugates

• Kingdom: Organic compounds
• Superclass: Lipids and lipid-like molecules
• Clase: Fatty Acyls
• Subclass: Fatty acids and conjugates
• Intermediate Tree Nodes: Not available
• Direct Parent: Medium-chain fatty acids
• Alternative Parents: Hydroxy fatty acids Secondary alcohols Carboxylic acid salts Monocarboxylic acids and derivatives Carboxylic acids Organic zwitterions Organic sodium salts Organic oxides Hydrocarbon derivatives Carbonyl compounds
• Molecular Framework: Aliphatic acyclic compounds
• Substituents: Medium-chain fatty acid - Hydroxy fatty acid - Carboxylic acid salt - Secondary alcohol - Monocarboxylic acid or derivatives - Carboxylic acid - Carboxylic acid derivative - Organic alkali metal salt - Organic sodium salt - Organic salt - Organic zwitterion - Organic oxide - Organooxygen compound - Organic oxygen compound - Alcohol - Carbonyl group - Hydrocarbon derivative - Aliphatic acyclic compound
• Descripción: This compound belongs to the class of organic compounds known as medium-chain fatty acids. These are fatty acids with an aliphatic tail that contains between 4 and 12 carbon atoms.
• 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)

EHMT2 Tchem Histone-lysine N-methyltransferase, H3 lysine-9 specific 3 (93046 Activities)

Discover Target: EHMT2

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

GMNN Tbio Geminin (128009 Activities)

Discover Target: GMNN

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

RAN Tchem GTP-binding nuclear protein Ran/Importin subunit beta-1/Snurportin-1 (21853 Activities)

Discover Target: RAN

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

Mecanismos de acción

Propiedades químicas y físicas

• Solubilidad: H2O: 10 mg/mL, clear
• Peso molecular: 210.250 g/mol
• Hydrogen Bond Donor Count: 1
• Hydrogen Bond Acceptor Count: 3
• Rotatable Bond Count: 8
• Exact Mass: 210.123 Da
• Monoisotopic Mass: 210.123 Da
• Topological Polar Surface Area: 60.400 Ų
• Heavy Atom Count: 14
• Formal Charge: 0
• Complexity: 139.000
• Isotope Atom Count: 0
• Defined Atom Stereocenter Count: 0
• Undefined Atom Stereocenter Count: 1
• Defined Bond Stereocenter Count: 0
• Undefined Bond Stereocenter Count: 0
• The total count of all stereochemical bonds: 0
• Covalently-Bonded Unit Count: 2

XLogP3