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Azacyclonol 5-HT Receptor chemical

Azacyclonol (MER 17, MDL 4829), also known as γ-pipradol, is a drug used to diminish hallucinations in psychotic individuals.

Azacyclonol 5-HT Receptor chemical Chemical Structure

Chemical Structure

Molecular Weight: 267.37

Purity & Quality Control

Batch: S319601 DMSO]53 mg/mL]false]Ethanol]53 mg/mL]false]Water]2 mg/mL]false Purity: 99.99%
99.99

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Mechanism of Action

In vitro

In vitro The formation of Azacyclonol in human intestinal microsomes is linear with respect to time up to 60 min. The rates of formation of this compound increases linearly with microsomal protein concentration up to 2 mg/mL. The apparent Km and Vmax values of this chemical are 0.82 μM and 60 pmol/min/mg protein in microsomes from human liver. [1] The formation of this compound and terfenadine alcohol from terfenadine is confirmed to be catalyzed predominantly by CYP3A(4) isozyme, and the ratio of the rate of terfenadine alcohol formation to that of this chemical is 3:1. [2] The amount of this compound eliminated renally increases on average 2-fold after rifampin dosing. [3]

In Vivo

In vivo Azacyclonol (i.v.) impairs the response of the nictitating membrane to both post- and preganglionic stimulation. The activity of this compound in depressing transmission through the cat superior ceivical ganglion is 6.63%. [4]

References

  • https://pubmed.ncbi.nlm.nih.gov/9279883/
  • https://pubmed.ncbi.nlm.nih.gov/7587944/
  • https://pubmed.ncbi.nlm.nih.gov/11240975/
  • https://pubmed.ncbi.nlm.nih.gov/19108183/

Chemical Information

Molecular Weight 267.37 Formula

C18H21NO

CAS No. 115-46-8 SDF Download SDF
Synonyms MER 17, MDL 4829
Smiles C1CNCCC1C(C2=CC=CC=C2)(C3=CC=CC=C3)O

Storage and Stability

Storage (From the date of receipt)

In vitro
Batch:

DMSO : 53 mg/mL ( (198.22 mM) Moisture-absorbing DMSO reduces solubility. Please use fresh DMSO.)

Ethanol : 53 mg/mL

Water : 2 mg/mL


Molecular Weight Calculator

In vivo
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In vivo Formulation Calculator

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