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  • BioBioPha
  • China
  • Product Name: Batatasin III
  • Price: ¥1000.0/5mg
  • Purity: 98.0%
  • Stocking Period: 10 Day
  • Contact: Xueping-Zheng


56684-87-8

56684-87-8 structure
56684-87-8 structure
  • Name: Batatasin III
  • Chemical Name: 3-Methoxy-5-[2-(3-methoxyphenyl)ethyl]phenol
  • CAS Number: 56684-87-8
  • Molecular Formula: C16H18O3
  • Molecular Weight: 258.31200
  • Catalog: Signaling Pathways PI3K/Akt/mTOR Akt
  • Create Date: 2017-06-22 00:22:51
  • Modify Date: 2024-01-11 10:07:55
  • Batatasin III, a stilbenoid, inhibits cancer migration and invasion by suppressing epithelial to mesenchymal transition (EMT) and FAK-AKT Signals. Batatasin III has anti-cancer activities[1].

Name 3-Methoxy-5-[2-(3-methoxyphenyl)ethyl]phenol
Synonyms 3-Ethyl-1-<2-(3-indolyl)-ethyl>-piperidin
3-[2-(3-ethyl-piperidin-1-yl)-ethyl]-indole
batatatsin III
batatasin III
1-<2-(3-indolyl)ethyl>-3-ethylpiperidine
1H-Indole,3-[2-(3-ethyl-1-piperidinyl)ethyl]
3,3'-dihydroxy-5-methoxybibenzyl
3-[2-(3-hydroxyphenyl)ethyl]-5-methoxyphenol
Batatasin Ⅲ
Description Batatasin III, a stilbenoid, inhibits cancer migration and invasion by suppressing epithelial to mesenchymal transition (EMT) and FAK-AKT Signals. Batatasin III has anti-cancer activities[1].
Related Catalog
Target

Akt

In Vitro Batatasin III (25-100 μM; 48 h) exhibits anti-proliferative activity in H460 cells. Batatasin III at concentrations lower than 100 μM has no cytotoxic effects[1]. Batatasin III significantly suppresses EMT indicated by the decrease of N-cadherin and Vimentin, and up-regulation of E-cadherin[1].
References

[1]. Tatchakorn Pinkhien, et al. Batatasin III Inhibits Migration of Human Lung Cancer Cells by Suppressing Epithelial to Mesenchymal Transition and FAK-AKT Signals. Anticancer Res. 2017 Nov;37(11):6281-6289.

Density 1.126g/cm3
Boiling Point 406.1ºC at 760 mmHg
Molecular Formula C16H18O3
Molecular Weight 258.31200
Flash Point 199.4ºC
Exact Mass 258.12600
PSA 38.69000
LogP 3.19460
Index of Refraction 1.572

~%

56684-87-8 structure

56684-87-8

Literature: Hashimoto,T. et al. Phytochemistry (Elsevier), 1974 , vol. 13, p. 2849 - 2852
Precursor  2

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