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β-Hydroxy-acetylfentanyl is a synthetic opioid derivative, structurally related to fentanyl, a powerful and fast-acting painkiller. It is known for its high potency, being significantly more powerful than morphine, and is used in medical settings for severe pain management, particularly in cases where other opioids are not effective. However, due to its potency, it also carries a high risk of addiction, overdose, and has been associated with the illicit drug trade. The chemical structure of β-hydroxy-acetylfentanyl features a β-hydroxy group and an acetyl group attached to the fentanyl molecule, which contributes to its increased potency. It is important to note that the use of such substances is heavily regulated and should only be administered under the supervision of a medical professional due to the potential for serious health risks.

1453-59-4

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1453-59-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1453-59-4 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 1,4,5 and 3 respectively; the second part has 2 digits, 5 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 1453-59:
(6*1)+(5*4)+(4*5)+(3*3)+(2*5)+(1*9)=74
74 % 10 = 4
So 1453-59-4 is a valid CAS Registry Number.

1453-59-4Downstream Products

1453-59-4Relevant academic research and scientific papers

Metabolism of fentanyl and acetylfentanyl in human-induced pluripotent stem cell-derived hepatocytes

Kanamori, Tatsuyuki,Iwata, Yuko Togawa,Segawa, Hiroki,Yamamuro, Tadashi,Kuwayama, Kenji,Tsujikawa, Kenji,Inoue, Hiroyuki

, p. 106 - 114 (2018)

To evaluate the capability of human-induced pluripotent stem cell-derived hepatocytes (h-iPS-HEP) in drug metabolism, the profiles of the metabolites of fentanyl, a powerful synthetic opioid, and acetylfentanyl, an N-acetyl analog of fentanyl, in the cells were determined and analyzed. Commercially available h-iPSHEP were incubated with fentanyl or acetylfentanyl for 24 or 48 h. After enzymatic hydrolysis, the medium was deproteinized with acetonitrile, then analyzed by LC/MS. Desphenethylated metabolites and some hydroxylated metabolites, including 4′-hydroxy-fentanyl and β-hydroxy-fentanyl, were detected as metabolites of fentanyl and acetylfentanyl in the medium. The main metabolite of fentanyl with h-iPS-HEP was the desphenethylated metabolite, which was in agreement with in vivo results. These results suggest that h-iPSHEP may be useful as a tool for investigating drug metabolism.

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