中文名 | 2,3,4,5-Tetra-(4-Pyridyl) Thiophene |
英文名 | 2,3,4,5-Tetra-(4-Pyridyl) Thiophene |
别名 | 2,3,4,5-四-(4-吡啶)噻吩 2,3,4,5-四(4-吡啶基)噻吩 4,44乔,4乔(2,3,4,5-Thiophentetrayl)tetrakis-pyridine 4,4?4乔,4乔?(2,3,4,5-Thiophentetrayl)tetrakis-pyridine |
英文别名 | GANT58 Nsc75503 2,3,4,5-TETRA-(4-PYRIDYL) THIOPHENE 2,3,4,5-Tetra-(4-Pyridyl) Thiophene 1,2,3,4-Tetrakis(4-pyridyl)thiophene -(2,3,4,5-Thiophentetrayl)tetrakis-pyridine Pyridine, 4,4',4'',4'''-(2,3,4,5-thiophenetetrayl)tetrakis- |
CAS | 64048-12-0 |
EINECS | 200-258-5 |
化学式 | C24H16N4S |
分子量 | 392.48 |
密度 | 1.254 |
熔点 | 252-253℃ |
沸点 | 414.1±40.0 °C(Predicted) |
溶解度 | DMSO: >10 mg/mL |
酸度系数 | 4.50±0.10(Predicted) |
存储条件 | Keep in dark place,Sealed in dry,2-8°C |
外观 | 黄色固体 |
颜色 | white to pale yellow |
体外研究 | GANT58 is a downstream inhibitor of Hh signaling. GANT58 is an indeed inhibitor of Hh signaling downstream of Smo and Sufu. GANT58 mainly acts at the nuclear level because transcription induced by GLI1 with a mutated nuclear export signal is still blocked. GANT58 efficiently inhibits in vitro tumor cell proliferation in a GLI-dependent manner and successfully blocks cell growth using human prostate cancer cells harboring downstream activation of the Hh pathway. GANT58 (NSC75503) has been shown to inhibit transcriptional activation by GLI1 (as well as by the other GLI species). GANT58 has been shown to inhibit GLI transactivation. |
体内研究 | Nude mice are injected s.c. with GLI1-positive 22Rv1 prostate cancer cells, and tumors are established (median size ≈250 mm 3 ). Nude mice are treated with daily s.c. injections at a concentration of 50 mg/kg of cyclopamine, GANT61, GANT58, or solvent only (n=4-5 for each group). However, after 3 days, cyclopamine-treated animals presented with severe ulcerations at the injection sites. Therefore, changing the treatment regimen to injections only every second day. To be able to compare all compounds, this protocol is also introduced for the GANTs, although mice treated with these compounds showed no such signs of toxicity. All injections are done 2-3 cm away from the tumors. During an 18-day treatment period, suppression of tumor cell growth is observed for all compounds. Treatment with cyclopamine or GANT58 results in the inhibition of additional xenograft growth and limited the increase in tumor size. |
WGK Germany | 3 |
上游原料 | 1,2-二(4-吡啶基)乙烯 1,2-二吡啶乙炔 4-甲基吡啶 4-吡啶甲醛 |
下游产品 | 1,2-双(4-吡啶基)乙烷 |
1mg | 5mg | 10mg | |
---|---|---|---|
1 mM | 2.548 ml | 12.74 ml | 25.479 ml |
5 mM | 0.51 ml | 2.548 ml | 5.096 ml |
10 mM | 0.255 ml | 1.274 ml | 2.548 ml |
5 mM | 0.051 ml | 0.255 ml | 0.51 ml |
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