MURISTERONE A
MURISTERONE A Basic information
- Product Name:
- MURISTERONE A
- Synonyms:
-
- 2B,3B,5A,11A,14,20,22-HEPTAHYDROXY-5B-7-CHOLESTEN-6-ONE
- 2BETA,3BETA,5ALPHA,11ALPHA,14,20,22-HEPTAHYDROXY-5BETA,7-CHOLESTEN-6-ONE
- 2BETA,3BETA,5BETA,11ALPHA,14ALPHA,20R,22R-HEPTAHYDROXYCHOLEST-7-EN-6-ONE
- 5B, 7-CHOLESTENE-2B,3B,5A,11A,14,20,22-HEPTOL-6-ONE
- 5BETA,7-CHOLESTENE-2BETA,3BETA,5ALPHA,11ALPHA,14,20,22-HEPTOL-6-ONE
- MurA, 2β,3β,5β,11α,14α,20R,22R-Heptahydroxycholest-7-en-6-one
- (22R)-2β,3β,5,11α,14,20,22-Heptahydroxy-5β-cholest-7-en-6-one
- Ecdysonic sterol
- CAS:
- 38778-30-2
- MF:
- C27H44O8
- MW:
- 496.63
- Product Categories:
-
- Miscellaneous Natural Products
- Mol File:
- 38778-30-2.mol
MURISTERONE A Chemical Properties
- Boiling point:
- 707.2±60.0 °C(Predicted)
- Density
- 1.33±0.1 g/cm3(Predicted)
- storage temp.
- −20°C
- solubility
- Soluble in DMSO
- form
- solid
- pka
- 11.78±0.70(Predicted)
- color
- white
MSDS
- Language:English Provider:SigmaAldrich
MURISTERONE A Usage And Synthesis
Description
Muristerone A is a natural analog of 20-hydroxyecdysone . It is an agonist of the ecdysteroid receptor (Kd = 1 nM), a nuclear receptor that heterodimerizes with a retinoid X receptor ortholog and regulates arthropod development. Muristerone A is used as an agonist in ecdysone-inducible gene expression systems in mammalian cells. However, it inhibits apoptosis in the human colon carcinoma cell line RKO by inducing the upregulation of Bcl-xL, suggesting limitations in its use in certain types of studies.
Uses
Muristerone A, an ecdysteroid, is widely used for the induction of ecdysteroid-dependent transcription in mammalian cells.
Biological Activity
Ecdysone analog that acts as an inducer of ecdysone-inducible gene expression systems in mammalian cells and transgenic animals. Stimulates Bcl-XL mRNA transcription and inhibits TRAIL- and hFasL-induced apoptosis in RKO cells.
storage
+4°C
References
[1] A C ZELHOF. Identification and characterization of a Drosophila nuclear receptor with the ability to inhibit the ecdysone response.[J]. Proceedings of the National Academy of Sciences of the United States of America, 1995, 92 23: 10477-10481. DOI: 10.1073/pnas.92.23.10477
[2] T M LANDON. Characterization and partial purification of the Drosophila Kc cell ecdysteroid receptor.[J]. The Journal of Biological Chemistry, 1988, 263 10: 4693-4697.
[3] MARKUS LEZZI. Ligand-induced heterodimerization between the ligand binding domains of the Drosophila ecdysteroid receptor and ultraspiracle[J]. The FEBS journal, 2009, 269 13: 3237-3245. DOI: 10.1046/j.1432-1033.2002.03001.x
[4] D NO R M E T P Yao. Ecdysone-inducible gene expression in mammalian cells and transgenic mice.[J]. Proceedings of the National Academy of Sciences of the United States of America, 1996, 93 8: 3346-3351. DOI: 10.1073/pnas.93.8.3346
[5] E SAEZ. Identification of ligands and coligands for the ecdysone-regulated gene switch.[J]. Proceedings of the National Academy of Sciences of the United States of America, 2000, 97 26: 14512-14517. DOI: 10.1073/pnas.260499497
[6] I OEHME M Z S B?sser. Agonists of an ecdysone-inducible mammalian expression system inhibit Fas Ligand- and TRAIL-induced apoptosis in the human colon carcinoma cell line RKO[J]. Cell Death and Differentiation, 2005, 13 2: 189-201. DOI: 10.1038/sj.cdd.4401730
MURISTERONE ASupplier
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- 821-50328103-801 18930552037
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- 021-51320588
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