CAS 4419-39-0|Beclometasone

Introduction:Basic information about CAS 4419-39-0|Beclometasone, including its chemical name, molecular formula, synonyms, physicochemical properties, and safety information, etc.
Common NameBeclometasone
CAS Number4419-39-0Molecular Weight521.042
Density1.3±0.1 g/cm3Boiling Point630.5±55.0 °C at 760 mmHg
Molecular FormulaC22H29ClO5Melting Point210ºC
MSDSChineseUSAFlash Point335.1±31.5 °C

Names

Namebeclomethasone
SynonymMore Synonyms

Beclometasone BiologicalActivity

DescriptionBeclometasone (Beclomethasone) is a prototype glucocorticoid receptor agonist.
Related CatalogSignaling Pathways >>GPCR/G Protein >>Glucocorticoid ReceptorResearch Areas >>Inflammation/Immunology
Target

Glucocorticoid Receptor[1]

In VitroAn inhibition of the normal physiological neutrophil migration and of neutrophil chemotaxis directed by wounding-induced inflammation is detected at 4 h after administration of 25 μM Beclomethasone. Tumour cell invasion and micrometastasis is also reduced in embryos incubated in 25 μM Beclomethasone 4 h before implantation. In addition, the lysyl oxidase inhibitor β-aminoproprionitrile (βAPN) largely reduces fibrillar collagen and enhances the CHT-TF transmigration of neutrophils, leading to a significant increase of tumour cell invasion and subsequent formation of micrometastases. Notably, βAPN inhibits neutrophil chemotaxis induced by inflammation, indicating that the increase of tumour cell invasion in βAPN-treated embryos is correlated with enhanced non-pathological neutrophil migration, but not with inflammation[1].
Cell AssayThe transgenic lines Tg(fli1:GFP) and Tg(mpx:GFP) are used in this study. 0.2 mM N-phenylthiourea (PTU) is applied to prevent pigment formation from 1 day post-fertilization (dpf). For Pu.1 knockdown, Pu.1 MO (1 mM for partial knockdown and 2 mM for complete knockdown is injected into the yolk at the one-cell stage. For pharmacological inhibition, the VEGFR tyrosine kinase inhibitors KRN633 (0.1-1 μM) or Sunitinib (0.1-1 μM), Beclomethasone (25 μM) and β-amino-proprionitrile (βAPN, 500 μM) are applied directly to the egg water and refreshed every 2 days. For pharmacological inhibition, Beclomethasone is applied to the embryos 4 h before implantation and KRN633, Sunitinib and βAPN are applied 4-6 h post-implantation. For each cell line or condition, data are representative of ≥ three independent experiments, with ≥30 embryos/group. Experiments are discarded when the survival rate of the control group is <90%[1].
References

[1]. He S, et al. Neutrophil-mediated experimental metastasis is enhanced by VEGFR inhibition in a zebrafish xenograft model. J Pathol. 2012 Aug;227(4):431-45.

Chemical & Physical Properties

Density1.3±0.1 g/cm3
Boiling Point630.5±55.0 °C at 760 mmHg
Melting Point210ºC
Molecular FormulaC22H29ClO5
Molecular Weight521.042
Flash Point335.1±31.5 °C
Exact Mass520.222778
PSA94.83000
LogP4.59
Vapour Pressure0.0±4.2 mmHg at 25°C
Index of Refraction1.564
InChIKeyNBMKJKDGKREAPL-DVTGEIKXSA-N
SMILESCC1CC2C3CCC4=CC(=O)C=CC4(C)C3(Cl)C(O)CC2(C)C1(O)C(=O)CO
Storage condition2-8°C

Safety Information

Personal Protective EquipmentEyeshields;Gloves;type N95 (US);type P1 (EN143) respirator filter
Hazard CodesXn
RIDADRNONH for all modes of transport
WGK Germany3

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Synonyms

Beclometasone
(8S,9R,10S,11S,13S,14S,16S,17R)-9-chloro-11,17-dihydroxy-17-(2-hydroxyacetyl)-10,13,16-trimethyl-6,7,8,11,12,14,15,16-octahydrocyclopenta[a]phenanthren-3-one
Beclomethasone
EINECS 224-585-9
MFCD00135614
Pregna-1,4-diene-3,20-dione, 9-chloro-11-hydroxy-16-methyl-17,21-bis(1-oxopropoxy)-
beclometasone 17,21-dipropionate
9-Chloro-11-hydroxy-16-methyl-3,20-dioxopregna-1,4-diene-17,21-diyl dipropanoate
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