Dexamethason - BioReagenz, für Zellkultur, Moligand™, ≥97%, Pulver , CAS No.50-02-2

CAS: 50-02-2 Cat. No.: D754934 Summenformel: C₂₂H₂₉FO₅ Molekulargewicht: 392.46 Beilstein Registry Number: 2066651 EG-Nummer: 200-003-9

GRADE & PURITY BioReagent, Moligand™, for Cell culture, ≥97%, powder

Synonyms

Prednisolon F | 9α-Fluor-16α-methyl-11β,17α,21-trihydroxy-1,4-pregnadien-3,20-dion | (11β,16α)-9-Fluor-11,17,21-trihydroxy-16-methylpregna-1,4-dien-3,20-dion | 9α-Fluor-16α-methylprednisolon | NSC 34521 | MK 125

Storage

Lagerung bei 2-8°C, vor Licht geschützt

Shipped In

Nasses Eis

Übersicht

Dexamethason wird zur Untersuchung von Apoptose, Zellsignalwegen, Zelldifferenzierung und Genexpression verwendet.

Specifications

Synonyme

Prednisolon F | 9α-Fluor-16α-methyl-11β,17α,21-trihydroxy-1,4-pregnadien-3,20-dion | (11β,16α)-9-Fluor-11,17,21-trihydroxy-16-methylpregna-1,4-dien-3,20-dion | 9α-Fluor-16α-methylprednisolon | NSC 34521 | MK 125

Spezifikationen & Reinheit

BioReagenz, für Zellkultur, Moligand™, ≥97%, Pulver

Biochemische und physiologische Mechanismen

Dexamethason (Hexadecadrol) ist ein Glukokortikoidrezeptor-Agonist, ein Apoptose-Induktor und ein häufiger Krankheitsauslöser bei Versuchstieren, die Modelle für Muskelschwund, Bluthochdruck und Depression konstruieren. Dexamethason kann die Produktion vo

Storage

Lagerung bei 2-8°C, vor Licht geschützt

Verschickt in

Nasses Eis

Note

BioReagent, für die Zellkultur, Moligand™

Reinheit

≥97%

Produkteigenschaften

• ALogP: 1.9

Namen und Kennungen

• Pubchem Sid: 528771144
• Kanonisches Lächeln: CC1CC2C3CCC4=CC(=O)C=CC4(C3(C(CC2(C1(C(=O)CO)O)C)O)F)C
• IUPAC Name: (8S,9R,10S,11S,13S,14S,16R,17R)-9-fluoro-11,17-dihydroxy-17-(2-hydroxyacetyl)-10,13,16-trimethyl-6,7,8,11,12,14,15,16-octahydrocyclopenta[a]phenanthren-3-one
• InChIKey: UREBDLICKHMUKA-CXSFZGCWSA-N
• INCHI: 1S/C22H29FO5/c1-12-8-16-15-5-4-13-9-14(25)6-7-19(13,2)21(15,23)17(26)10-20(16,3)22(12,28)18(27)11-24/h6-7,9,12,15-17,24,26,28H,4-5,8,10-11H2,1-3H3/t12-,15+,16+,17+,19+,20+,21+,22+/m1/s1
• Isomere SMILES: C[C@@H]1C[C@H]2[C@@H]3CCC4=CC(=O)C=C[C@@]4([C@]3([C@H](C[C@@]2([C@]1(C(=O)CO)O)C)O)F)C
• WGK Deutschland: 2
• RTECS: TU3980000
• Alternative CAS-Nummer: 23495-06-9,50-02-2
• NSC-Nummer: 34521
• MeSH-Eintrag: Decaject;Decaject L.A.;Decaject-L.A.;Decameth;Decaspray;Dexamethasone;Dexasone;Dexpak;Hexadecadrol;Hexadrol;Maxidex;Methylfluorprednisolone;Millicorten;Oradexon
• Molekulargewicht: 392.46
• Beilstein: 2066651
• Reaxy-Rn: 2341697
• Reaxys-RN_link_address: https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=2341697&ln=

Taxonomic Classification

Taxonomy Tree

• Kingdom Organic compounds
  • Superclass Lipids and lipid-like molecules
    • Klasse Steroids and steroid derivatives
      • Subclass Hydroxysteroids

• Kingdom: Organic compounds
• Superclass: Lipids and lipid-like molecules
• Klasse: Steroids and steroid derivatives
• Subclass: Hydroxysteroids
• Intermediate Tree Nodes: Not available
• Direct Parent: 21-hydroxysteroids
• Alternative Parents: Gluco/mineralocorticoids, progestogins and derivatives 20-oxosteroids 11-beta-hydroxysteroids 17-hydroxysteroids 3-oxo delta-1,4-steroids Halogenated steroids Delta-1,4-steroids Tertiary alcohols Alpha-hydroxy ketones Secondary alcohols Fluorohydrins Cyclic ketones Cyclic alcohols and derivatives Alkyl fluorides Hydrocarbon derivatives Organic oxides Organofluorides Primary alcohols
• Molecular Framework: Aliphatic homopolycyclic compounds
• Substituents: Progestogin-skeleton - 21-hydroxysteroid - Pregnane-skeleton - 20-oxosteroid - 3-oxo-delta-1,4-steroid - 3-oxosteroid - 17-hydroxysteroid - 11-hydroxysteroid - 11-beta-hydroxysteroid - 9-halo-steroid - Halo-steroid - Oxosteroid - Delta-1,4-steroid - Alpha-hydroxy ketone - Cyclic alcohol - Tertiary alcohol - Ketone - Fluorohydrin - Halohydrin - Secondary alcohol - Cyclic ketone - Organooxygen compound - Alcohol - Primary alcohol - Hydrocarbon derivative - Organic oxide - Carbonyl group - Organic oxygen compound - Alkyl halide - Alkyl fluoride - Organohalogen compound - Organofluoride - Aliphatic homopolycyclic compound
• Beschreibung: This compound belongs to the class of organic compounds known as 21-hydroxysteroids. These are steroids carrying a hydroxyl group at the 21-position of the steroid backbone.
• External Descriptors: Pregnane and derivatives [Fig]

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

Chemische und physikalische Eigenschaften

• Löslichkeit: methanol: 25 mg/mL
• Empfindlichkeit: Light sensitive
• Schmelzpunkt (°C): 262-264°C
• Molekulargewicht: 392.500 g/mol
• XLogP3: 1.900
• Hydrogen Bond Donor Count: 3
• Hydrogen Bond Acceptor Count: 6
• Rotatable Bond Count: 2
• Exact Mass: 392.2 Da
• Monoisotopic Mass: 392.2 Da
• Topological Polar Surface Area: 94.800 Ų
• Heavy Atom Count: 28
• Formal Charge: 0
• Complexity: 805.000
• Isotope Atom Count: 0
• Defined Atom Stereocenter Count: 8
• 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: 1