Shanghai Nianxing Industrial Co., Ltd
China
Product Name: 1,3,5(10)-Estratrien-3,4,17beta-triol 4-methyl ether
Price: Check
Purity: 98.0%
Stocking Period: 10 Day
Contact: Yang
Email: sales@echemcloud.com

Dayang Chem (Hangzhou) Co., Ltd.
China
Product Name: 1,3,5(10)-Estratrien-3,4,17beta-triol 4-methyl ether
Price: $Inquiry/100g $Inquiry/1kg $Inquiry/100kg $Inquiry/1000kg
Purity: 98.0%
Stocking Period: Inquiry
Contact: Ms Wang
Email: enquiry@dycnchem.com

26788-23-8

26788-23-8 structure

26788-23-8 structure

Name: 1,3,5(10)-Estratrien-3,4,17beta-triol 4-methyl ether
Chemical Name: 4-methoxyestradiol
CAS Number: 26788-23-8
Molecular Formula: C₁₉H₂₆O₃
Molecular Weight: 302.40800
Catalog: Signaling Pathways Cell Cycle/DNA Damage DNA/RNA Synthesis
Create Date: 2018-12-18 11:13:29
Modify Date: 2025-08-29 08:53:00
4-Methoxyestradiol is methoxylestradiol that induces oxidative DNA damage in human lung epithelial cells. 4-Methoxyestradiol also elevates ROS and SOD activities in H1355 cells[1].

Name	4-methoxyestradiol
Synonyms	4-Methoxyestrone 4-Hydroxyestrone-4-methyl ether 4-methoxy-E1 4-methoxy-E2

Description	4-Methoxyestradiol is methoxylestradiol that induces oxidative DNA damage in human lung epithelial cells. 4-Methoxyestradiol also elevates ROS and SOD activities in H1355 cells[1].
Related Catalog	Research Areas >> Cancer Signaling Pathways >> Cell Cycle/DNA Damage >> DNA/RNA Synthesis
References	[1]. Yahsin Cheng, et al. 4-Methoxyestradiol-induced oxidative injuries in human lung epithelial cells. Toxicol Appl Pharmacol. 2007 May 1;220(3):271-7.

Density	1.178g/cm3
Boiling Point	472ºC at 760mmHg
Molecular Formula	C₁₉H₂₆O₃
Molecular Weight	302.40800
Flash Point	239.2ºC
Exact Mass	302.18800
PSA	49.69000
LogP	3.61780
Vapour Pressure	1.03E-09mmHg at 25°C
Index of Refraction	1.586

1630-83-7 structure

1630-83-7

124-41-4 structure

124-41-4

~81%

26788-23-8 structure

26788-23-8

Literature: Chen, Shu-hua; Luo, Guan-rong; Wu, Xu-sen; Chen, Min; Zhao, Hua-ming Steroids, 1986 , vol. 47, # 1 p. 63 - 66

61748-87-6 structure

61748-87-6

124-41-4 structure

124-41-4

~95%

26788-23-8 structure

26788-23-8

Literature: Numazawa, Mitsuteri; Ogura, Yuko; Kimura, Katsuhiko; Nagaoka, Masao Journal of Chemical Research, Miniprint, 1985 , # 11 p. 3701 - 3715

19590-55-7 structure

19590-55-7

~%

26788-23-8 structure

26788-23-8

Literature: Numazawa, Mitsuteri; Ogura, Yuko; Kimura, Katsuhiko; Nagaoka, Masao Journal of Chemical Research, Miniprint, 1985 , # 11 p. 3701 - 3715

50-28-2 structure

50-28-2

~%

26788-23-8 structure

26788-23-8

Literature: Numazawa, Mitsuteri; Ogura, Yuko; Kimura, Katsuhiko; Nagaoka, Masao Journal of Chemical Research, Miniprint, 1985 , # 11 p. 3701 - 3715

15833-07-5 structure

15833-07-5

~%

26788-23-8 structure

26788-23-8

Literature: Numazawa, Mitsuteri; Ogura, Yuko; Kimura, Katsuhiko; Nagaoka, Masao Journal of Chemical Research, Miniprint, 1985 , # 11 p. 3701 - 3715

17756-86-4 structure

17756-86-4

~%

26788-23-8 structure

26788-23-8

Literature: Numazawa, Mitsuteri; Ogura, Yuko; Kimura, Katsuhiko; Nagaoka, Masao Journal of Chemical Research, Miniprint, 1985 , # 11 p. 3701 - 3715

5976-61-4 structure

5976-61-4

14031-35-7 structure

14031-35-7

~%

26788-23-8 structure

26788-23-8

Literature: Takemura, Hitomi; Uchiyama, Harue; Ohura, Takeshi; Sakakibara, Hiroyuki; Kuruto, Ryoko; Amagai, Takashi; Shimoi, Kayoko Journal of Steroid Biochemistry and Molecular Biology, 2010 , vol. 118, # 1-2 p. 70 - 76

186581-53-3 structure

186581-53-3

5976-61-4 structure

5976-61-4

~18%

26788-23-8 structure

26788-23-8

5976-66-9 structure

5976-66-9

Detail

Literature: Teranishi; Fujii; Yamazaki; Miyabo Chemical and Pharmaceutical Bulletin, 1983 , vol. 31, # 9 p. 3309 - 3314

Precursor 8
1630-83-7 124-41-4 61748-87-6 19590-55-7
50-28-2 15833-07-5 5976-61-4 186581-53-3
DownStream 0

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