614-47-1
基本信息
苯丙烯酰苯
苯基苯乙烯基甲酮
苯苏合香稀甲酮
苯乙烯基本基甲酮
苄差苯乙酮
亚苄基代苯乙酮
查尔酮
1,3-二苯-2-丙烯-1-酮
1,3-二苯基-2-丙烯-1-酮
反-查耳酮,苯乙烯基苯基酮
1,3-DIPHENYL-2-PROPEN-I-ONE
1,3-DIPHENYL-2-PROPENONE
1,3-DIPHENYL-3-PROPEN-1-ONE
1,3-DIPHENYLPROP-2-EN-1-ONE
2-BENZALACETOPHENONE
2-BENZYLIDENEACETOPHENONE
(2E)-1,3-DIPHENYLPROP-2-EN-1-ONE
3-PHENYLACRYLOPHENONE
BENZALACETOPHENONE
BENZYLIDENEACETOPHENONE
BENZYLIDINEACETOPHENONE
CHALCONE
CHALKONE
(E)-CHALCONE
PHENYL STYRYL KETONE
TRANS-BENZYLIDENEACETOPHENONE
TRANS-CHALCONE
(e)-1,3-diphenyl-2-propen-1-one
(e)-benzylideneacetophenone
物理化学性质
| 熔点 | 55-59 °C |
| 沸点 | 208 °C25 mm Hg(lit.) |
| 密度 | 1.0712 |
| 折射率 | 1.5361 (estimate) |
| 闪点 | >230 °F |
| 储存条件 | Sealed in dry,Room Temperature |
| 溶解度 | 可溶于氯仿（少许） |
| 形态 | 固体 |
| 颜色 | 淡黄色 |
| 气味 (Odor) | at 100.00 %. floral balsam herbal |
| 香型 | floral |
| 水溶解性 | Soluble in chloroform, ether, benzene, and ethanol (slightly). Insoluble in water. |
| Merck | 14,2037 |
| BRN | 509985 |
| LogP | 4.013 (est) |
| CAS 数据库 | 614-47-1(CAS DataBase Reference) |
| NIST化学物质信息 | Benzalacetophenone(614-47-1) |
安全数据
| 危险性符号(GHS) |  GHS07 |
| 警示词 | 警告 |
| 危险性描述 | H302-H319-H335 |
| 防范说明 | P261-P264-P270-P271-P301+P312-P305+P351+P338 |
| 危险品标志 | Xn,Xi |
| 危险类别码 | R22-R36/37 |
| 安全说明 | S22-S36/37/39-S45 |
| WGK Germany | 3 |
| RTECS号 | UD5576750 |
| 海关编码 | 29143990 |
常见问题列表
在氮气下，将[Ni（dmpymt）2] 6（5 mol％Ni），KOH（1.0 mmol），苯甲醇（1.5 mmol）和1-苯基乙醇（1.0 mmol）与甲苯（2.5 mL）/ t-BuOH（0.5 mL）加入50毫升Schlenk试管中，将试管置于70°C油浴中，在缓慢，稳定的氮气流中搅拌混合物36小时，将混合物冷却至室温，加水（10毫升）。 用CH2Cl2（3×10 mL）萃取水溶液，用无水Na2SO4干燥合并的萃取液，除去溶剂，在短时间快速柱色谱上纯化粗产物得到反式-查耳酮。
trans-Chalcone competitively inhibits porcine pancreatic α-amylase with a Ki of 48 μM.
trans-Chalcone (30.23-98.03 μM; 24 hours) induces cell cycle arrest and apoptosis in MCF-7 cells.
trans-Chalcone (30.23-98.03 μM; 24 hours) reduces the expression of the apoptosis-related protein Bcl-2 and induces the expression of the CIDEA gene.
trans-Chalcone (58.25 μM; 6, 24 hours) has greater inhibition of Bcl-2, induction of APAF1 and BAX, and strong induction of CIDEA in 24 hours.
trans-Chalcone (24 hours) inhibits MCF-7 cell viability (IC
20
=30.23 μM; IC
50
=58.25 μM; IC
80
=98.03 μM). trans-Chalcone (48 h) has IC
50
s of 41.53 μM and 48.41 μM for MCF-7 and 3T3 cell lines, respectively. trans-Chalcone exhibits a pronounced cytotoxicity activity.
Apoptosis Analysis
| Cell Line: | MCF-7 cell |
| Concentration: | 30.23, 58.25, 98.03 μM |
| Incubation Time: | 24 hours |
| Result: | Induced apoptosis of the breast cancer cell line. |
Cell Cycle Analysis
| Cell Line: | MCF-7 cell |
| Concentration: | 30.23, 58.25, 98.03 μM |
| Incubation Time: | 24 hours |
| Result: | Caused cell cycle arrest in G1. |
Western Blot Analysis
| Cell Line: | MCF-7 cell |
| Concentration: | 20, 40, 80 μM |
| Incubation Time: | 24, 48 hours |
| Result: |
Reduced the expression of the apoptosis-related protein Bcl-2 and induced the expression of the CIDEA gene.
There was marked degradation of cyclin D1 at 48 h. |
RT-PCR
| Cell Line: | MCF-7 cell |
| Concentration: | 58.25 μM |
| Incubation Time: | 6, 24 hours |
| Result: | Had greater inhibition of Bcl-2, induction of APAF1 and BAX, and strong induction of CIDEA in 24 hours. |