TRV130 (Oliceridine)

Catalog No. A14337

TRV130 (Oliceridine)引发强大的G蛋白信号传导,其功效和功效与吗啡相似,但Δε-arrestin2募集和受体内化作用远少于吗啡。
  • Marthe M Vandeputte, .et al. Characterization of recent non-fentanyl synthetic opioids via three different in vitro μ-opioid receptor activation assays, Arch Toxicol, 2022, Mar;96(3):877-897 PMID: 35072756
  • Lakshmi Vasudevan, .et al. Assessment of Structure-Activity Relationships and Biased Agonism at the Mu Opioid Receptor of Novel Synthetic Opioids Using a Novel, Stable Bio-Assay Platform, Biochem Pharmacol, 2020, Mar 14;177:113910 PMID: 32179045
  • Anna M. Gutridge, .et al. G protein-biased kratom-alkaloids and synthetic carfentanil-amide opioids as potential treatments for alcohol use disorder, Br J Pharmaco, 2019, 08 November
  • Yudin Y, .et al. The G protein?\biased agents PZM21 and TRV130 are partial agonists of μ?\opioid receptor?\mediated signaling to ion channels, Br J Pharmacol, 2019, May 9 PMID: 31074038
  • Yevgen Yudin, .et al. The G protein-biased PZM21 and TRV130 act as partial agonists of μ-opioid receptors signaling to ion channel targets, bioRxiv, 2018, 2018
  • Araldi D, .et al. Mu-Opioid Receptor (MOR) Biased Agonists Induce Biphasic Dose-dependent Hyperalgesia and Analgesia, and Hyperalgesic Priming in the Rat, Neuroscience, 2018, Dec 1; 394: 60-71 PMID: 30342200
Catalog Num A14337
M. Wt 423.01
Formula C22H31ClN2O2S
Purity >98%
Storage at -20°C 3 years Powder
CAS No. 1401028-24-7
Synonyms TRV 130, TRV-130
SMILES COC1=C(SC=C1)CNCC[C@]2(CCOC3(C2)CCCC3)C4=CC=CC=N4
TRV130 (Oliceridine)引发强大的G蛋白信号传导,其功效和功效与吗啡相似,但Δε-arrestin2募集和受体内化作用远少于吗啡。
Concentration / Solvent Volume / Mass 1 mg 5 mg 10 mg
0.1 mM 23.64 mL 118.2 mL 236.4 mL
0.5 mM 4.73 mL 23.64 mL 47.28 mL
1 mM 2.36 mL 11.82 mL 23.64 mL
5 mM 0.47 mL 2.36 mL 4.73 mL

*The above data is based on the productmolecular weight 423.01. Batch specific molecular weights may vary from batch to batch due to solvent of hydration, which will affect the solvent volumes required to prepare stock solutions.