化合物 T23819
中文名称 | 化合物 T23819 |
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中文同义词 | 化合物 T23819;N,N'-[9[[4-(二甲氨基)苯基]氨基]-3,6-吖啶二基]双(1-吡咯烷丙酰胺)三盐酸盐;三盐酸BRACO-19;BRACO19 3HCL |
英文名称 | N,N′-(9-(4-(Dimethylamino)phenylamino)acridine-3,6-diyl)bis(3-(pyrrolidin-1-yl)propanamide) trihydrochloride |
英文同义词 | N,N′-(9-(4-(Dimethylamino)phenylamino)acridine-3,6-diyl)bis(3-(pyrrolidin-1-yl)propanamide) trihydrochloride;BRACO19 trihydrochloride;N,N'-[9[[4-(Dimethylamino)phenyl]amino]-3,6-acridinediyl]bis-1-pyrrolidinepropanamide trihydrochloride;BRACO-19 (BRACO19);N,N-[9[[4-(Dimethylamino)phenyl]amino]-3,6-acridinediyl]bis-1-pyrrolidinepropanamide Trihydrochlori;BRACO19 HCl;BRACO19 hydrochloride |
CAS号 | 1177798-88-7 |
分子式 | C35H44ClN7O2 |
分子量 | 630.23 |
EINECS号 | |
相关类别 | |
Mol文件 | 1177798-88-7.mol |
结构式 | ![]() |
化合物 T23819 性质
储存条件 | 2-8°C |
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溶解度 | H2O:可溶5mg/mL,澄清 |
形态 | 粉末 |
颜色 | 黄色至棕色 |
IC50: telomerase
Braco-19 trihydrochloride, as a well-known GQ binding ligand, interacts specifically with the HAdV GQs and increases their stability, and blocks the HAdV multiplication.BRACO-19 trihydrochloride (1.0-10 μM; 5 day) cause zero growth inhibition is found 1 μM, the IC 50 for BRACO-19 in UXF1138L cells is 2.5 μM, the IC 100 is 5 μM.BRACO-19 trihydrochloride (1 μM; 24 hours) shows dramatically reduced nuclear hTERT expression. However, residual cytoplasmic hTERT staining is observed accompanied by the occurrence of atypical mitoses.BRACO-19 trihydrochloride (0-40 μM; 24 hours) decreases the AdV virus growth in a dose-dependent manner in eGFP-transinfected HEK 293 cells.BRACO-19 trihydrochloride (0-150 μM; 24 hours) shows a decrease in band intensity in an increasing concentration-dependent manner.
Cell Viability Assay
Cell Line: | HEK 293 cells |
Concentration: | 20 μM; 40 μM |
Incubation Time: | 24 hours |
Result: | Displayed low cytotoxicity and decreased the eGFP fluorescence. |
BRACO-19 trihydrochloride (oral administration or intraperitoneal injection; 2 or 5 mg/kg; 3 weeks) oral dosing regimen are always inactive and the animals have to be sacrificed due to high tumor burden before overall termination of the study, Chronic, i.p. BRACO-19 administration, qdx5 is efficient in inhibiting tumor growth in earlystage xenografts but not advanced-stage xenografts. BRACO-19 trihydrochloride (intraperitoneal injection; 2 mg/kg; 3 weeks; starting 6 days after transplantation of UXF1138LX fragments) inhibits tumor growth significantly and under these conditions, marked single-agent antitumor activity is observed, with some animals in the group showing complete regressions (5 of 12 tumors).
Animal Model: | Established UXF1138LX Xenografts in nude mice |
Dosage: | 2 mg/kg |
Administration: | Intraperitoneal injection; 3 weeks; starting 6 days after transplantation of UXF1138LX fragments |
Result: | Showed partial tumor regressions with an optimal T/C on day 28 of 4.1%, equal to 95.9% inhibition of tumor growth compared with control. |