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  • DC Chemicals Limited
  • China
  • Product Name: YL-109
  • Price: $600.0/100mg $1100.0/250mg $2200.0/1g
  • Purity: 98.0%
  • Stocking Period: 3 Day
  • Contact: Tony Cao

36341-25-0

36341-25-0 structure
36341-25-0 structure
  • Name: YL-109
  • Chemical Name: 4-(3H-1,3-benzothiazol-2-ylidene)-2-methoxycyclohexa-2,5-dien-1-one
  • CAS Number: 36341-25-0
  • Molecular Formula: C14H11NO2S
  • Molecular Weight: 257.30800
  • Catalog: Research Areas Cancer
  • Create Date: 2016-12-13 20:50:05
  • Modify Date: 2024-01-05 21:52:23
  • YL-109 is a novel anticancer agent which has ability to inhibit breast cancer cell growth and invasiveness in vitro and in vivo.IC50 value: 85.7 nM(MCF-7 cells proliferation) [1]Target: AhR signaling activcatorin vitro: YL-109 strongly inhibited cell proliferation of MCF-7 cells in a dose-dependent manner (IC50= 85.8 nM). Surprisingly, YL-109 had an anti-proliferative effect in a dose-dependent manner (IC50 = 4.02 μM) on MDA-MB-231 cells. YL-109 repressed the sphere-forming ability and the expression of stem cell markers in MDA-MB-231 mammosphere cultures. YL-109 increased the expression of carboxyl terminus of Hsp70-interacting protein (CHIP), which suppresses tumorigenic and metastatic potential of breast cancer cells by inhibiting the oncogenic pathway. YL-109 induced CHIP transcription because of the recruitment of the aryl hydrocarbon receptor (AhR) to upstream of CHIP gene in MDA-MB-231 cells. Consistently, the antitumor effects of YL-109 were depressed by CHIP or AhRknockdown in MDA-MB-231 cells [1].in vivo: Mice treated with vehicle showed significantly enlarged tumors, whereas mice treated with YL-109 showed attenuated tumor growth using MCF-7 cells. Interestingly, YL-109 also suppressed tumor growth in mice injected with MDA-MB-231 cells. Compared with the vehicle control, YL-109 significantly reduced lung metastasis [1].

Name 4-(3H-1,3-benzothiazol-2-ylidene)-2-methoxycyclohexa-2,5-dien-1-one
Synonyms 2-(4-hydroxy-3-methoxyphenyl)benzo[d]thiazole
2-(3-methoxy-4-hydroxyphenyl)benzothiazole
4-(benzo[d]thiazol-2-yl)-2-methoxyphenol
4-(1,3-benzothiazol-2-yl)-2-methoxyphenol
Phenol,4-(2-benzothiazolyl)-2-methoxy
2-(4-HYDROXY-3-METHOXYPHENYL)BENZOTHIAZOLE
4-benzothiazol-2-yl-2-methoxyphenol
YL-109
Description YL-109 is a novel anticancer agent which has ability to inhibit breast cancer cell growth and invasiveness in vitro and in vivo.IC50 value: 85.7 nM(MCF-7 cells proliferation) [1]Target: AhR signaling activcatorin vitro: YL-109 strongly inhibited cell proliferation of MCF-7 cells in a dose-dependent manner (IC50= 85.8 nM). Surprisingly, YL-109 had an anti-proliferative effect in a dose-dependent manner (IC50 = 4.02 μM) on MDA-MB-231 cells. YL-109 repressed the sphere-forming ability and the expression of stem cell markers in MDA-MB-231 mammosphere cultures. YL-109 increased the expression of carboxyl terminus of Hsp70-interacting protein (CHIP), which suppresses tumorigenic and metastatic potential of breast cancer cells by inhibiting the oncogenic pathway. YL-109 induced CHIP transcription because of the recruitment of the aryl hydrocarbon receptor (AhR) to upstream of CHIP gene in MDA-MB-231 cells. Consistently, the antitumor effects of YL-109 were depressed by CHIP or AhRknockdown in MDA-MB-231 cells [1].in vivo: Mice treated with vehicle showed significantly enlarged tumors, whereas mice treated with YL-109 showed attenuated tumor growth using MCF-7 cells. Interestingly, YL-109 also suppressed tumor growth in mice injected with MDA-MB-231 cells. Compared with the vehicle control, YL-109 significantly reduced lung metastasis [1].
Related Catalog
References

[1]. Hiyoshi H, et al. 2-(4-Hydroxy-3-methoxyphenyl)-benzothiazole suppresses tumor progression and metastatic potential of breast cancer cells by inducing ubiquitin ligase CHIP. Sci Rep. 2014 Nov 18;4:7095.

Density 1.327g/cm3
Boiling Point 446.448ºC at 760 mmHg
Molecular Formula C14H11NO2S
Molecular Weight 257.30800
Flash Point 223.804ºC
Exact Mass 257.05100
PSA 70.59000
LogP 3.67750
Index of Refraction 1.685
Hazard Codes Xi
HS Code 2934200090

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36341-25-0 structure

36341-25-0

Literature: Das, Sudipto; Samanta, Suvendu; Maji, Swarup Kumar; Samanta, Partha Kumar; Dutta, Amit Kumar; Srivastava, Divesh N.; Adhikary, Bibhutosh; Biswas, Papu Tetrahedron Letters, 2013 , vol. 54, # 9 p. 1090 - 1096

~85%

36341-25-0 structure

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Literature: Ma, Dawei; Xue, Peng; Jiang, Yongwen; Xie, Siwei; Zhang, Xiaojing; Dong, Jinhua Angewandte Chemie, International Edition, 2009 , vol. 48, # 23 p. 4222 - 4225

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36341-25-0 structure

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Literature: Hyvl, Jakub; Srogl, Jiri European Journal of Organic Chemistry, 2010 , # 15 p. 2849 - 2851

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36341-25-0 structure

36341-25-0

Literature: Liu, Saiwen; Chen, Ru; Guo, Xiangyu; Yang, Huiqiong; Deng, Guojun; Li, Chao-Jun Green Chemistry, 2012 , vol. 14, # 6 p. 1577 - 1580

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36341-25-0 structure

36341-25-0

Literature: Bogert; Stull Journal of the American Chemical Society, 1925 , vol. 47, p. 3078 Journal of the Chemical Society, 1926 , vol. 48, p. 250 Full Text View citing articles Show Details Claasz Chemische Berichte, 1916 , vol. 49, p. 1145

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36341-25-0 structure

36341-25-0

Literature: Bogert; Stull Journal of the American Chemical Society, 1925 , vol. 47, p. 3078 Journal of the Chemical Society, 1926 , vol. 48, p. 250

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36341-25-0 structure

36341-25-0

Literature: Rudolph, Joachim; Chen, Libing; Majumdar, Dyuti; Bullock, William H.; Burns, Michael; Claus, Thomas; Dela Cruz, Fernando E.; Daly, Michelle; Ehrgott, Frederick J.; Johnson, Jeffrey S.; Livingston, James N.; Schoenleber, Robert W.; Shapiro, Jeffrey; Yang, Ling; Tsutsumi, Manami; Ma, Xin Journal of Medicinal Chemistry, 2007 , vol. 50, # 5 p. 984 - 1000
HS Code 2934200090
Summary 2934200090. other compounds containing in the structure a benzothiazole ring-system (whether or not hydrogenated), not further fused. VAT:17.0%. Tax rebate rate:13.0%. . MFN tariff:6.5%. General tariff:20.0%