Naltrexone hydrochloride
CAS No. 16676-29-2
Naltrexone hydrochloride ( NIH 8503 )
产品货号. M12543 CAS No. 16676-29-2
一种有效的竞争性 μ、κ、δ 和 σ 阿片受体拮抗剂,MOR、KOR 和 DOR 的 Ki 值分别为 0.0825 nM、0.509 nM 和 8.02 nM。
纯度: >98% (HPLC)
COA
Datasheet
HNMR
HPLC
MSDS
Handing Instructions
| 规格 | 价格/人民币 | 库存 | 数量 |
| 5MG | ¥138 | 有现货 |
|
| 10MG | ¥182 | 有现货 |
|
| 25MG | ¥272 | 有现货 |
|
| 50MG | ¥386 | 有现货 |
|
| 100MG | ¥537 | 有现货 |
|
| 500MG | ¥1305 | 有现货 |
|
| 1G | 获取报价 | 有现货 |
|
| 1 mL x 10 mM in DMSO | ¥228 | 有现货 |
|
生物学信息
-
产品名称Naltrexone hydrochloride
-
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
-
产品简述一种有效的竞争性 μ、κ、δ 和 σ 阿片受体拮抗剂,MOR、KOR 和 DOR 的 Ki 值分别为 0.0825 nM、0.509 nM 和 8.02 nM。
-
产品描述A potent, competitive antagonist for μ, κ, δ, and σ-opioid receptors with Ki of 0.0825 nM, 0.509 nM, and 8.02 nM, for MOR, KOR, and DOR, respectively; also inhibits IL-6 and TNFα production in human immune cell subsets following stimulation with ligands for intracellular TLRs; a TLR-4 antognist that inhibits LPS-induced TLR4 downstream NO production in microglia BV-2 cells (IC50=105 uM).Alcoholism Approved.
-
体外实验——
-
体内实验——
-
同义词NIH 8503
-
通路Endocrinology/Hormones
-
靶点Opioid Receptor
-
受体OpioidReceptor
-
研究领域Neurological Disease
-
适应症Alcoholism
化学信息
-
CAS Number16676-29-2
-
分子量377.8618
-
分子式C20H24ClNO4
-
纯度>98% (HPLC)
-
溶解度DMSO: ≥ 33 mg/mL
-
SMILESC1CC1CN2CC[C@]34[C@@H]5C(=O)CC[C@]3([C@H]2CC6=C4C(=C(C=C6)O)O5)O.Cl
-
化学全称Morphinan-6-one, 17-(cyclopropylmethyl)-4,5-epoxy-3,14-dihydroxy-, hydrochloride (1:1), (5α)-
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. Codd EE, et al. J Pharmacol Exp Ther. 1995 Sep;274(3):1263-70.
2. Cant R, et al. Front Immunol. 2017 Jul 11;8:809.
3. Selfridge BR, et al. J Med Chem. 2015 Jun 25;58(12):5038-52.
产品手册
关联产品
-
[Nphe1]Nociceptin(1-...
Selective and competitive nociceptin receptor antagonist, devoid of any agonist activity. Binds selectively to recombinant nociceptin receptors (pKi = 8.4), and competitively antagonizes the actions of nociceptin in vitro and in vivo.
-
Alvimopan dihydrate
一种选择性外周作用的 μ-阿片类拮抗剂,IC50 为 1.7 nM,用于治疗术后肠梗阻;防止静脉注射吗啡的胃肠道反应而不影响镇痛;口服活性。
-
Samidorphan HCl
Samidorphan HCl is an orally active and highly potent modulator of the opioid system that binds to μ‐opioid, κ‐opioid, and delta-opioid receptors. Samidorphan HCl is a novel μ-opioid receptor antagonist, a partial agonist for k-opioid and delta-opioid receptors. Samidorphan HCl can be used to prevent and treat schizophrenia.
021-51111890
购物车()
sales@molnova.cn

