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D1756
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Change View25 MG€37.30100 MG€87.30500 MG€267.001 G€407.005 G€1,660.00Synonym(s):(11β,16α)-9-Fluoro-11,17,21-trihydroxy-16-methylpregna-1,4-diene-3,20-dione, 9α-Fluoro-16α-methyl-11β,17α,21-trihydroxy-1,4-pregnadiene-3,20-dione, 9α-Fluoro-16α-methylprednisolone, Prednisolone FEmpirical Formula (Hill Notation):C22H29FO5CAS Number:50-02-2Molecular Weight:392.46Beilstein:2066651EC Number:200-003-9MDL number:MFCD00064136PubChem Substance ID:24893536NACRES:NA.77
≥98% (HPLC)
powder
off-white
262-264 °C (lit.)
methanol: 25 mg/mL
Merck & Co., Inc., Kenilworth, NJ, U.S.
2-8°C
C[C@@H]1C[C@H]2[C@@H]3CCC4=CC(=O)C=C[C@]4(C)[C@@]3(F)[C@@H](O)C[C@]2(C)[C@@]1(O)C(=O)CO
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
Dexamethasone has been used:
Dexamethasone is known to be effective against relapsed multiple myeloma.[4] It is found to decrease inflammation associated with cerebrospinal fluid and central nervous system (CNS) complications, such as hearing loss.[5]Glucocorticoid anti-inflammatory agent. Regulates T cell survival, growth, and differentiation. Inhibits the induction of nitric oxide synthase.
This compound is featured on the Nuclear Receptors (Steroids) page of the Handbook of Receptor Classification and Signal Transduction. To browse other handbook pages, click here.This compound was developed by Merck & Co., Inc., Kenilworth, NJ, U.S.. To browse the list of other pharma-developed compounds and Approved Drugs/Drug Candidates, click here.
Bottomless glass bottle. Contents are inside inserted fused cone.
Dilute 1 mg/ml stock solution 1:50 with sterile media and store frozen in working aliquots to avoid repeated freeze-thaw.
Danger
P201 - P202 - P280 - P308 + P313 - P405 - P501
Repr. 1B
6.1C - Combustible, acute toxic Cat.3 / toxic compounds or compounds which causing chronic effects
WGK 3
Not applicable
Not applicable
dust mask type N95 (US), Eyeshields, Gloves