首页 > 产品 > 特色产品

Dasotraline(SEP-225289) free base

产品编号: DC8162 Featured
Dasotraline(SEP-225289) free base
结构式
675126-05-3
此产品仅供科研所需，我们不出售给病人
​我们将匹配市场上最好的价格给您
Email：order@dcbio.cn
免费咨询电话：4008862077
询盘
我们的合作伙伴:
  • 20
  • 19
  • 18
  • 17
  • 16
  • 15
  • 14
  • 12
  • 11
  • 10
  • 9
  • 8
  • 13
  • 6
  • 5
  • 4
  • 3
  • 2
  • 1
中国地区超过5000个高品质化合物库存
应用领域
Dasotraline 是一种三重再摄取抑制剂，阻断多巴胺 (dopamine)，去甲肾上腺素 (norepinephrine) 和 5-羟色胺 (5-HT) 转运蛋白，IC50 值分别为 4, 6 和 11 nM。
化学性质生物活性化合物的使用COA & MSDS相关产品产品说明书
Cas No.: 675126-05-3
名称: (1R,4S)-4-(3,4-dichlorophenyl)-1,2,3,4-tetrahydronaphthalen-1-amine
别名: SEP-225289
SMILES: N[C@@H]1CC[C@@H](C2=CC=C(Cl)C(Cl)=C2)C3=CC=CC=C31
分子式: C16H15Cl2N
分子量: 292.3
纯度:
保存条件: 2 years -20°C Powder, 2 weeks 4°C in DMSO, 6 months -80°C in DMSO
Description:
In Vivo:
In Vitro:
References: For the detailed information of Dasotraline(SEP-225289), the solubility of Dasotraline(SEP-225289) in water, the solubility of Dasotraline(SEP-225289) in DMSO, the solubility of Dasotraline(SEP-225289) in PBS buffer, the animal experiment (test) of Dasotraline(SEP-225289), the cell expriment (test) of Dasotraline(SEP-225289), the in vivo, in vitro and clinical trial test of Dasotraline(SEP-225289), the EC50, IC50,and affinity,of Dasotraline(SEP-225289), For the detailed information of Dasotraline(SEP-225289), the solubility of Dasotraline(SEP-225289) in water, the solubility of Dasotraline(SEP-225289) in DMSO, the solubility of Dasotraline(SEP-225289) in PBS buffer, the animal experiment (test) of Dasotraline(SEP-225289), the cell expriment (test) of Dasotraline(SEP-225289), the in vivo, in vitro and clinical trial test of Dasotraline(SEP-225289), the EC50, IC50,and affinity,of Dasotraline(SEP-225289), Please contact DC Chemicals.
Kinase Assay:
Cell Assay:
Animal Administration:
References:
MSDS
COA
LOT NO. DOWNLOAD
2018-0101
产品编号 产品名称 应用领域
DC12654 PLX8394 PLX8394 是一种有效的，选择性的 BRaf 抑制剂，抑制 BRAFV600E 活性的 IC50 值约为 5 nM。
DC9743 CB1954(Tretazicar) CB1954(Tretazicar) in stock,price: 350 USD/100mg. CB1954(Tretazicar) is a anticancer prodrug that is converted in the presence of the enzyme NQO2 and co-substrate caricotamide ( EP-0152R) (EP) into a potent cytotoxic bifunctional alkylating agent.It can
DC26175 NLX-101（F-15599） NLX-101（F-15599） is a novel compound that activates serotonin 5-HT1A receptors with exceptional selectivity, having over 1000-fold higher affinity for this target over other receptors.
DC26173 YM-53601 YM-53601 is a squalene synthase inhibitor (IC50s = 79 and 90 nM in HepG2 cells and rat liver microsomes, respectively).
DC26160 Ethosalamide Etosalamide, also known as Ethosalamide, is an antipyretic and analgesics agent.
DC26155 Sulfaphenazole Sulfaphenazole is an inhibitor of CYP2C9 (Ki = 0.3 μM) that demonstrates at least 100-fold selectivity over other CYP450 isoforms (Kis = 63 and 29 μM for CYP2C8 and CYP2C18, respectively, and no activity at CYP1A1, CYP1A2, CYP3A4, CYP2C19).
DC26151 Naloxone (hydrochloride) Naloxone is an opioid inverse agonist drug used to counter the effects of opiate overdose.
DC26139 2-(5-Chloro-1H-indol-2-yl)acetic acid 2-(5-Chloro-1H-indol-2-yl)acetic acid|CAS 720000-48-6
DC12542 GOT1 inhibitor 2c GOT1抑制剂2c是谷氨酸草酰乙酸转氨酶1（GOT1）的一流的非共价抑制剂，IC50为8.2μM。
DC12541 iGOT1-01 iGOT1-01 is a small molecule inhibitor of aspartate aminotransferase 1 (glutamate oxaloacetate transaminase 1 (GOT1)) with IC50 of 11.3 uM.
​ 免费咨询电话：4008862077
​ QQ：1026657369
​ 邮箱：order@dcbio.cn
我们所有的产品仅供研究所需，严禁用于人体和其他目的
站点地图|隐私政策Copyright © 2018-2020 All Rights Reserved. 技术支持:库价软件