Hinokitiol
CAS No. 499-44-5
Hinokitiol ( 4-Isopropyltropolone;β-Thujaplicin )
产品货号. M14672 CAS No. 499-44-5
Hinokitiol (4-Isopropyltropolone;β-Thujaplicin) is a tropolone-related natural compound that can induces apoptosis and cell cycle arrest.
纯度: >98% (HPLC)
COA
Datasheet
HNMR
HPLC
MSDS
Handing Instructions
规格 | 价格/人民币 | 库存 | 数量 |
25MG | ¥243 | 有现货 |
|
50MG | ¥340 | 有现货 |
|
100MG | ¥599 | 有现货 |
|
200MG | ¥786 | 有现货 |
|
500MG | 获取报价 | 有现货 |
|
1G | 获取报价 | 有现货 |
|
生物学信息
-
产品名称Hinokitiol
-
注意事项本公司产品仅用于科研实验,不得用于人体或动物的临床与诊断
-
产品简述Hinokitiol (4-Isopropyltropolone;β-Thujaplicin) is a tropolone-related natural compound that can induces apoptosis and cell cycle arrest.
-
产品描述Hinokitiol (4-Isopropyltropolone;β-Thujaplicin) is a tropolone-related natural compound that can induces apoptosis and cell cycle arrest, exhibits anti-inflammatory and anti-tumor activities; inhibits the proliferation of Chlamydia trachomatis with MIC of 32 ug/mL; also can harness such gradients to restore iron transport into, within, and/or out of cells.
-
同义词4-Isopropyltropolone;β-Thujaplicin
-
通路Apoptosis
-
靶点Apoptosis
-
受体ERα
-
研究领域Neurological Disease
-
适应症——
化学信息
-
CAS Number499-44-5
-
分子量164.20
-
分子式C10H12O2
-
纯度>98% (HPLC)
-
溶解度Chloroform: Soluble DMSO: 29 mg/mL (176.6 mM) ( < 1 mg/ml refers to the product slightly soluble or insoluble )
-
SMILESCC(C)C1=CC(=O)C(=CC=C1)O
-
化学全称2-hydroxy-4-(1-methylethyl)-2,4,6-cycloheptatrien-1-one
运输与储存
-
储存条件(-20℃)
-
运输条件With Ice Pack
-
稳定性≥ 2 years
参考文献
1. Yamano H, et al. Antimicrob Agents Chemother. 2005 Jun;49(6):2519-21.
2. Seo JS, et al. BMC Cell Biol. 2017 Feb 27;18(1):14.
3. Grillo AS, et al. Science. 2017 May 12;356(6338):608-616.
2. Seo JS, et al. BMC Cell Biol. 2017 Feb 27;18(1):14.
3. Grillo AS, et al. Science. 2017 May 12;356(6338):608-616.
产品手册
关联产品
-
SCH79797 dihydrochlo...
SCH79797 dihydrochloride is an effective and selective antagonist of protease activated receptor 1 (PAR1) with an IC50 of 70 nM and a Ki of 35 nM.
-
Mepazine
Mepazine is a potent and selective inhibitor of MALT1. Mepazine inhibits GSTMALT1 full length and GSTMALT1 325-760 with IC50s of 0.83 μM and 0.42 μM.
-
Adarotene
Adarotene is an effective apoptosis inducer. It surprisingly produces DNA damage and exhibits a potent antiproliferative activity on a large panel of human tumor cells.