666859-49-0

666859-49-0 structure

666859-49-0 structure

Name: Telomerase-IN-1
Chemical Name: Telomerase-IN-1
CAS Number: 666859-49-0
Molecular Formula: C₂₁H₂₃FN₂O₄
Molecular Weight: 386.417
Catalog: Signaling Pathways Cell Cycle/DNA Damage Telomerase
Create Date: 2018-03-03 22:55:07
Modify Date: 2024-01-03 18:32:55
Telomerase-IN-1 is a Telomerase inhibitor with an IC50 of 0.19 μM.

Name	Telomerase-IN-1
Synonyms	(4-Fluorophenyl){1-[2-methoxy-2-(4-nitrophenyl)ethyl]-4-piperidinyl}methanone Methanone, (4-fluorophenyl)[1-[2-methoxy-2-(4-nitrophenyl)ethyl]-4-piperidinyl]-

Description	Telomerase-IN-1 is a Telomerase inhibitor with an IC50 of 0.19 μM.
Related Catalog	Signaling Pathways >> Cell Cycle/DNA Damage >> Telomerase Research Areas >> Cancer
Target	IC50: 0.19 μM (Telomerase) [1]
In Vitro	Our in vitro studies show that title compound (Telomerase-IN-1) has high inhibitory activity against telomerase and high antiproliferative capacity on SMMC-7721 cells, and has no obvious toxic effect on human normal hepatocyte cells. Telomerase-IN-1 treatment decreases the growth of cancer cells in dose- and time-dependent manners; however, the viability of L-02 shows slight changes in the compound at 10 μM. 48 h of SMMC-7721 cell treatment with the Telomerase-IN-1 (20, 40, and 80 nM) causes increase of apoptosis. Forty-eight hours of SMMC-7721 cell treatment with the Telomerase-IN-1(20, 40, and 80 nM) causes significant accumulation of green fluorescence, indicating a decrease in MMP. At 40 nM, Telomerase-IN-1 significantly increases expressions of cyt-c and Bax, but the Bcl-2 level is decreased[1].
In Vivo	Our in vivo studies show that this compound (Telomerase-IN-1) significantly inhibits tumor growth in xenograft tumor models. Results show that endoplasmic reticulum stress (ERS) through ER over response (EOR) activates the expression of hTERT, and then induces ERS, which is believed to be intricately associated with oxidative stress and mitochondrial dysfunction, resulting in apoptotic cell death, thereby modulating the expression of downstream signaling molecules including CHOP (CAAT/enhancer-binding protein homologous protein)) and mitochondrion pathway of apoptosis, leading to inhibition of cell proliferation[1].
Cell Assay	The effect of the title compound (Telomerase-IN-1) on the viability of human hepatoma cancer cell (SMMC-7721) is examined by increasing concentrations (3.2, 16, 80, 400, and 2000 nM). A normal liver cell line (L-02) is used as control. Cell viability is measured by MTTassay at 48 h[1].
Animal Admin	To test whether the Telomerase-IN-1 shows any antitumor effect in vivo, SMMC-7721 cells are xenografted into nude mice, and then the tumor-bearing animals are treated with the Telomerase-IN-1 (25, 50, and 100 μM/daily) for 37 days by intraperitoneal injection[1].
References	[1]. Cheng X, et al. Discovery of (4-bromophenyl)(3-hydroxy-4-methoxyphenyl)methanone through upregulating hTERT induces cell apoptosis and ERS. Cell Death Dis. 2017 Aug 24;8(8):e3016.

Density	1.2±0.1 g/cm3
Boiling Point	512.7±50.0 °C at 760 mmHg
Molecular Formula	C₂₁H₂₃FN₂O₄
Molecular Weight	386.417
Flash Point	263.9±30.1 °C
Exact Mass	386.164185
LogP	3.62
Vapour Pressure	0.0±1.3 mmHg at 25°C
Index of Refraction	1.573