021-51111890
购物车（）
sales@molnova.cn
Thozalinone
CAS No. 655-05-0
Thozalinone ( —— )
产品货号. M27185 CAS No. 655-05-0
Thozalinone is a psychostimulant agent inducing the release of norepinephrine and dopamine.
纯度: >98% (HPLC)
COA
Datasheet
HNMR
HPLC
MSDS
Handing Instructions
| 规格 | 价格/人民币 | 库存 | 数量 |
| 5MG | ￥405 | 有现货 |
|
| 10MG | ￥608 | 有现货 |
|
| 25MG | ￥1037 | 有现货 |
|
| 50MG | ￥1555 | 有现货 |
|
| 100MG | ￥2325 | 有现货 |
|
| 200MG | ￥3491 | 有现货 |
|
| 500MG | ￥5775 | 有现货 |
|
| 1G | 获取报价 | 有现货 |
|
生物学信息
-
产品名称Thozalinone
-
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Thozalinone is a psychostimulant agent inducing the release of norepinephrine and dopamine.
-
产品描述Thozalinone is a psychostimulant agent inducing the release of norepinephrine and dopamine.(In Vivo):In ICR male mice, Thozalinone (100 mg/kg, ip) test (SI) appear to provide the best prediction for the PS-inducing potencies among DL-DOPA, apomorphine, and amphetamine.
-
同义词——
-
通路Others
-
靶点Other Targets
-
受体——
-
研究领域——
-
适应症——
化学信息
-
CAS Number655-05-0
-
分子量204.2
-
分子式C11H12N2O2
-
纯度>98% (HPLC)
-
溶解度——
-
SMILESCN(C)C1=NC(=O)C(O1)c1ccccc1
-
化学全称——
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.Millner OE Jr, et al. Flurofamide: a potent inhibitor of bacterial urease with potential clinical utility in the treatment of infection induced urinary stones. J Urol. 1982 Feb;127(2):346-50.
产品手册
关联产品
-
L-Asparaginase
L-Asparaginase (L-?ASNase), a hydrolase that catalyzes the conversion of L-asparagine, used in acute lymphoblastic leukemia treatment.Asparaginase is an enzyme that is used as a medication. As a medication, L-asparaginase is used to treat acute lymphoblastic leukemia (ALL), acute myeloid leukemia (AML), and non-Hodgkin's lymphoma. It is given by injection into a vein, muscle, or under the skin.
-
Methyl nomilinate
Methyl nomilinate from citrus can modulate cell cycle regulators to induce cytotoxicity in human colon cancer (SW480) cells in vitro.
-
Isonardosinone
Isonardosinone shows potential role in the treatment of neuroinflammation conditions, it inhibits NF-?oB- and MAPK-mediated inflammatory pathways.
