CAS NO: | 881639-98-1 |
生物活性 | G-1 is a nonsteroidal, high-affinity and selective agonist ofGPR30with aKiof 11 nM. | ||||||||||||||||
IC50& Target | Ki: 11 nM (GPR30)[1] | ||||||||||||||||
体外研究 (In Vitro) | G-1 is a nonsteroidal, high-affinity and selective agonist of GPR30 with a Kiof 11 nM[1]. Treatment with G-1 (10 μM and 100 μM) for 48 and 72 h significantly decreases cell proliferation (P<0.001). At 72 h, the IC50value for G-1 is calculated to be 20 μM. Treatment of A549 cells with G-1 at a concentration of 20 μM reveals a significant increase in apoptosis, consistent with its antiproliferative effect (P<0.001)[2]. Cell cycle analysis of H295R cells after 24 h of G-1 treatment demonstrates a cell cycle arrest in the G2phase. The presence of G-1 increases Bax expression while decreases Bcl-2[3]. | ||||||||||||||||
体内研究 (In Vivo) | The results at 14 days post-injury show that the Basso mouse scale (BMS) scores are significantly higher in the G-1 group compared with the other groups (P<0.05). The number of caspase-3-positive cells in the cross sections is counted, and G-1 group has fewer positive cells compare with the other groups (P<0.05), and there is no difference between the two groups (P>0.05)[1]. G-1 administration produces a statistically significant decrease in tumor volume from day 14 post treatment. Grafted tumors harvested after three-week treatment with G-1 show a significant decrease in tumor weight compare to vehicle treated animals[3]. | ||||||||||||||||
分子量 | 412.28 | ||||||||||||||||
性状 | Solid | ||||||||||||||||
Formula | C21H18BrNO3 | ||||||||||||||||
CAS 号 | 881639-98-1 | ||||||||||||||||
运输条件 | Room temperature in continental US; may vary elsewhere. | ||||||||||||||||
储存方式 |
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溶解性数据 | In Vitro: DMSO : 50 mg/mL(121.28 mM;Need ultrasonic) 配制储备液
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以下溶剂前显示的百
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