首页   >  
Neuro Signaling Pathway
  • Hormone Pathay
  • GPCR/G Protein
  >  
Opioid Receptor

所有产品分类

所有产品

信号通路

研究领域

天然产物

抗体

多肽

催化剂

杂质对照品

医药中间体

基础原料

Opioid Receptor

结构式 货号 产品名称 CAS号
Nalbuphine 结构式
BCP49246 纳布啡 20594-83-6
Nalbuphine is a narcotic used as a pain medication. It appears to be an agonist at kappa opioid receptors and an antagonist or partial agonist at mu opioid receptors.
Nalbuphine hydrochloride 结构式
BCP49247 纳布啡盐酸盐 23277-43-2
Nalbuphine Hydrochloride is the hydrochloride salt form of nalbuphine, a synthetic phenanthrene opioid with opiate agonist and antagonist effects, used to treat moderate to severe pain and provide preoperative and postoperative analgesia and sedation.
Naloxone HCl 结构式
BCP06880 盐酸纳洛酮 357-08-4
Naloxone hydrochloride is a hydrochloride resulting from the formal reaction of equimolar amounts of naloxone and hydrogen chloride. A specific opioid antagonist, it is used to reverse the effects of opioids, both following their use of opioids during surgery and in cases of known or suspected opioid overdose. It has a role as an antidote to opioid poisoning, a mu-opioid receptor antagonist and a central nervous system depressant. It contains a naloxone(1+).
CTOPA 结构式
BCP24191 CTOPA 103429-31-8
CTOP is a potent and selective μ opioid receptor antagonist (Ki values are 0.96 and >10,000 nM for μ and δ receptors respectively).
Bevenopran 结构式
BCP48962 Bevenopran 676500-67-7
Bevenopran is a peripheral μ-opioid receptor antagonist.
Axelopran 结构式
BCP47463 奥泼佐米 949904-48-7
Axelopran, also known as TD-1211, is a potent, selective, and peripherally-restricted μ-, κ-, and δ-opioid receptor antagonist, with similar affinity for the μ- and κ-opioid receptors and about an order of magnitude lower affinity for the δ-opioid recept
BMS-986122 结构式
BCP46445 BMS-986122 313669-88-4
BMS-986122 is a positive allosteric modulator of the μ-Opioid Receptor.
Difelikefalin TFA 结构式
BCP44865 Difelikefalin TFA 2742623-88-5
Difelikefalin is a κ-opioid receptor (KOR) agonist. It activates KOR in HEK293 cells expressing the human receptor (EC50 = 0.16 nM in a transactivation assay) and inhibits forskolin-induced cAMP production in R1.G1 mouse thyoma cells (EC50 = 0.048 nM).
U-54494A 结构式
BCP44497 U-54494A 92953-41-8
U-54494A is a κ-opioid agonist and a potential NMDA antagonist. U-54494A hydrochloride is used as an anticonvulsant.
Difelikefalin HCl 结构式
BCP44189 Difelikefalin HCl 2413256-25-2
Difelikefalin is a novel and potent kappa opioid receptor agonist.
123下一页末页共 69 条记录 1 / 7 页 
2853530910