1. Neuronal Signaling
  2. AChE
  3. Rhodiosin

Rhodiosin 

Cat. No.: HY-N2425 Purity: 99.07%
Handling Instructions

Rhodiosin, isolated from the root of Rhodiola crenulata, is a specific non-competitive cytochrome P450 2D6 inhibitor with an IC50 of 0.420 μM and a Ki of 0.535 μM. Rhodiosin exhibits potent, dose-dependent inhibitory effects on acetylcholinesterase (AChE) with IC50 ranged from 57.50 to 2.43 μg/mL. Rhodiosin exhibits potent DPPH free radical scavenging activities, with an IC50 of 27.77 μM.

For research use only. We do not sell to patients.

Rhodiosin Chemical Structure

Rhodiosin Chemical Structure

CAS No. : 86831-54-1

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10 mM * 1 mL in DMSO USD 266 In-stock
Estimated Time of Arrival: December 31
5 mg USD 198 In-stock
Estimated Time of Arrival: December 31
10 mg USD 336 In-stock
Estimated Time of Arrival: December 31
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Based on 1 publication(s) in Google Scholar

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Description

Rhodiosin, isolated from the root of Rhodiola crenulata, is a specific non-competitive cytochrome P450 2D6 inhibitor with an IC50 of 0.420 μM and a Ki of 0.535 μM[1]. Rhodiosin exhibits potent, dose-dependent inhibitory effects on acetylcholinesterase (AChE) with IC50 ranged from 57.50 to 2.43 μg/mL[2]. Rhodiosin exhibits potent DPPH free radical scavenging activities, with an IC50 of 27.77 μM[3].

IC50 & Target

IC50: 0.420 μM (cytochrome P450 2D6)[1];57.50-2.43 μg/mL (AChE)[2];27.77 μM (DPPH free radical scavenging)[3]

Molecular Weight

610.52

Formula

C₂₇H₃₀O₁₆

CAS No.

86831-54-1

SMILES
Shipping

Room temperature in continental US; may vary elsewhere.

Storage

4°C, protect from light

*In solvent : -80°C, 6 months; -20°C, 1 month (protect from light)

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Keywords:

RhodiosinAChEAcetylcholinesteraseInhibitorinhibitorinhibit

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