Cat. No.: HY-N0267

Hypaconitine

2 Cited Publications

Customer Review

Based on 2 publication(s) in Google Scholar

Hypaconitine inhibits the KCNH2 current with an IC₅₀ of 8.1 nM, and exhibits cardiotoxicity. Hypaconitine inhibits TGF-β1-induced epithelial-mesenchymal transition (EMT) in A549 cell through the inhibition of NF-κB nuclear translocation. Hypaconitine acts as the neuromuscular blocker. Hypaconitine is orally active.

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

Purity: 99.49%
CAS No.: 6900-87-4
Formula: C₃₃H₄₅NO₁₀
Molecular Weight:615.71

Storage:

Powder -20°C, 3 years , 4°C, 2 years ; In solvent -80°C, 2 years , -20°C, 1 year

Hypaconitine Chemical Structure

CAS No.: 6900-87-4

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Top Publications Citing

Use of MCE Products

Fluorescent Dye

Strong Fluorescence Signal / Multi-Disciplinary Applications / High Fluorescence Specificity

Biological Activity
- Description
- In Vitro
- In Vivo
Chemical Information
Publications (2)
Solvent & Solubility
- In Vitro
- In Vivo
Purity & Documentation
References
Help & FAQs
Classifications
Bioz

Biological Activity

Description

All NF-κB Isoforms :

All Calcium Channel Isoforms :

In Vitro

Hypaconitine (0-8 μM, 48 h) reverses TGF-β1-induced cell morphological changes (such as the disappearance of intercellular junctions and the appearance of spindle-shaped appearance), reverses the conversion of E-cadherin to N-cadherin in TGF-β1 administrated A549 cell and H1299 cell, reverses TGF-β1-induced cell migration and invasion of cell A549 and H1299^[1].
Hypaconitine (10-60 μM, 24 h) regulates the calcium influx and calcium release through store-operated Ca²⁺ channels, and exhibits cytotoxicity in HCN-2 neuronal cells^[3].
Hypaconitine (0-5 μM, 60 min) inhibits nerve-evoked twitch tension and nerve compound action potential in phrenic mouse diaphragm cells^[4].

MedChemExpress (MCE) has not independently confirmed the accuracy of these methods. They are for reference only.

Cell Viability Assay^[3]

Cell Line:

HCN-2 cell
Concentration:

10-60 μM
Incubation Time:

24 h
Result:

Inhibited the cell viability.

Cell Migration Assay ^[1]

Cell Line:

A549
Concentration:

0-8 μM
Incubation Time:

48 h
Result:

Inhibited the cell migration.

In Vivo

Hypaconitine (50-450 μg/kg, po, single dose) prolongs the QT interval in conscious beagle dog models, exhibits potential cardiotoxicity^[2].

MedChemExpress (MCE) has not independently confirmed the accuracy of these methods. They are for reference only.

Animal Model:

Beagle dog models^[2]
Dosage:

50-450 μg/kg
Administration:

po, single dose
Result:

Prolonged the QTcV interval (QT interval corrected using the Van de Water formula) with a maximum prolongation of 23%.

Chemical Information

CAS No. 6900-87-4
Appearance Solid
Molecular Weight 615.71
Formula C₃₃H₄₅NO₁₀
Color White to off-white
SMILES

CO[C@@H](CC1)C23[C@@](C[C@@]4(O)[C@@H]5OC(C6=CC=CC=C6)=O)([H])[C@@]5([H])[C@](OC(C)=O)([C@@H](O)[C@@H]4OC)C7C2N(C)C[C@@]1(COC)[C@@]3([H])[C@H]7OC
Structure Classification
- Alkaloids
- Other Alkaloids
Initial Source
Shipping

Room temperature in continental US; may vary elsewhere.

Storage

Powder	-20°C	3 years
	4°C	2 years
In solvent	-80°C	2 years
	-20°C	1 year

Publications (2)

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Journal Impact Factor

Chem Biol Interact

Circadian Cyp3a11 metabolism contributes to chronotoxicity of hypaconitine in mice. [Abstract]

2019 Aug 1:308:288-293. PMID: 31150629
Xenobiotica

Comparative HPLC-MS/MS-based pharmacokinetic studies of multiple diterpenoid alkaloids following the administration of Zhenwu Tang and Radix Aconiti Lateralis Praeparata extracts to rats. [Abstract]

2021 Mar;51(3):345-354. PMID: 33332226

Solvent & Solubility

In Vitro:

DMSO : 50 mg/mL (81.21 mM; Need ultrasonic; Hygroscopic DMSO has a significant impact on the solubility of product, please use newly opened DMSO)

View the Complete Stock Solution Preparation Table

Preparing Stock Solutions

View the Complete Stock Solution Preparation Table

Concentration Solvent Mass

1 mg

5 mg

10 mg

Concentration

Solvent

Mass

1 mM

1.6241 mL

8.1207 mL

16.2414 mL

5 mM

0.3248 mL

1.6241 mL

3.2483 mL

10 mM

0.1624 mL

0.8121 mL

1.6241 mL

Please refer to the solubility information to select the appropriate solvent. Once prepared, please aliquot and store the solution to prevent product inactivation from repeated freeze-thaw cycles.

Storage method and period of stock solution: -80°C, 2 years; -20°C, 1 year. When stored at -80°C, please use it within 2 years. When stored at -20°C, please use it within 1 year.

Molarity Calculator

Mass (g) = Concentration (mol/L) × Volume (L) × Molecular Weight (g/mol)

Mass Mass

Concentration Concentration

Volume Volume

Molecular Weight Molecular Weight

Dilution Calculator

Concentration _(start) × Volume _(start) = Concentration _(final) × Volume _(final)

Concentration _(start) Concentration _(start)

Volume _(start) Volume _(start)

Concentration _(final) Concentration _(final)

Volume _(final) Volume _(final)

In Vivo:

Select the appropriate dissolution method based on your experimental animal and administration route.

Stock Solution Working Solution

For the following dissolution methods, please ensure to first prepare a clear stock solution using an In Vitro approach and then sequentially add co-solvents:
To ensure reliable experimental results, the clarified stock solution can be appropriately stored based on storage conditions. As for the working solution for In Vivo experiments, it is recommended to prepare freshly and use it on the same day.
The percentages shown for the solvents indicate their volumetric ratio in the final prepared solution. If precipitation or phase separation occurs during preparation, heat and/or sonication can be used to aid dissolution.

Protocol 1

Add each solvent one by one: 10% DMSO 40% PEG300 5% Tween-80 45% Saline

Solubility: ≥ 2.5 mg/mL (4.06 mM); Clear solution

This protocol yields a clear solution of ≥ 2.5 mg/mL (saturation unknown).

Taking 1 mL working solution as an example, add 100 μL DMSO stock solution (25.0 mg/mL) to 400 μL PEG300, and mix evenly; then add 50 μL Tween-80 and mix evenly; then add 450 μL Saline to adjust the volume to 1 mL.

Protocol 2

Add each solvent one by one: 10% DMSO 90% Corn Oil

Solubility: ≥ 2.5 mg/mL (4.06 mM); Clear solution

This protocol yields a clear solution of ≥ 2.5 mg/mL (saturation unknown). If the continuous dosing period exceeds half a month, please choose this protocol carefully.

Taking 1 mL working solution as an example, add 100 μL DMSO stock solution (25.0 mg/mL) to 900 μL Corn oil, and mix evenly.

In Vivo Dissolution Calculator

Please enter the basic information of animal experiments:

Dosage Dosage
mg/kg
Animal Weight (Per Animal) Animal Weight (Per Animal)
g
Dosing Volume (Per Animal) Dosing Volume (Per Animal)
μL
Number of Animals Number of Animals

Recommended: Prepare an additional quantity of animals to account for potential losses during experiments.

Recommended: Prepare an additional quantity of animals to account for potential losses during experiments.

Please enter your animal formula composition:

%
DMSO +

Recommended: Keep the proportion of DMSO in working solution below 2% if your animal is weak.
%
+
+
%
Tween-80 + +
%
Saline +

The co-solvents required include: DMSO, . All of co-solvents are available by MedChemExpress (MCE). , Tween 80. All of co-solvents are available by MedChemExpress (MCE).

Working solution concentration: 0.22 mg/mL

Purity & Documentation

Select Batch:

Purity: 99.98%

Assay: 99.98%

ee.: 99.98%

Data Sheet (290 KB)
SDS (479 KB)
- English - EN (479 KB)
- Français - FR (479 KB)
- Deutsch - DE (479 KB)
- Norwegian - NO (479 KB)
- Español - ES (479 KB)
- Swedish - SV (479 KB)
- Italian - IT (479 KB)
- Korean - KR (479 KB)
- Portuguese - PT (479 KB)
COA (2659 KB)
Elemental Analysis Report (2659 KB)
HNMR (2659 KB)
CNMR (2659 KB)
RP-HPLC (2659 KB)
NP-HPLC (2659 KB)
MS (2659 KB)
LCMS (2659 KB)
IR (2659 KB)
GC (2659 KB)
OR (2659 KB)
SDS-PAGE (2659 KB)
SEC-HPLC (2659 KB)
Other Report (2659 KB)
Handling Instructions (2659 KB)

References

[1]. Feng HT, et al., Hypaconitine inhibits TGF-β1-induced epithelial-mesenchymal transition and suppresses adhesion, migration, and invasion of lung cancer A549 cells. Chin J Nat Med. 2017 Jun;15(6):427-435. [Content Brief]

[2]. Xie S, et al., Hypaconitine-induced QT prolongation mediated through inhibition of KCNH2 (hERG) potassium channels in conscious dogs. J Ethnopharmacol. 2015 May 26;166:375-9. [Content Brief]

[3]. Hsu SS, et al., Mechanism of action of a diterpene alkaloid hypaconitine on cytotoxicity and inhibitory effect of BAPTA-AM in HCN-2 neuronal cells. Clin Exp Pharmacol Physiol. 2021 May;48(5):801-810. [Content Brief]

[4]. Muroi M, et al., Blocking effects of hypaconitine and aconitine on nerve action potentials in phrenic nerve-diaphragm muscles of mice. Neuropharmacology. 1990 Jun;29(6):567-72. [Content Brief]

Help & FAQs

How should lyophilized recombinant proteins be reconstituted and stored?

1. Before opening the cap, centrifuge the vial at 13000 rpm for 20-30 seconds. This step will ensure that any lyophilized powder that may have adhered to the cap or walls is collected at the bottom of the vial, minimizing the risk of product loss.

Complete Stock Solution Preparation Table

Storage method and period of stock solution: -80°C, 2 years; -20°C, 1 year. When stored at -80°C, please use it within 2 years. When stored at -20°C, please use it within 1 year.

Optional Solvent	Concentration Solvent Mass	1 mg	5 mg	10 mg	25 mg
DMSO	1 mM	1.6241 mL	8.1207 mL	16.2414 mL	40.6035 mL
	5 mM	0.3248 mL	1.6241 mL	3.2483 mL	8.1207 mL
	10 mM	0.1624 mL	0.8121 mL	1.6241 mL	4.0604 mL
	15 mM	0.1083 mL	0.5414 mL	1.0828 mL	2.7069 mL
	20 mM	0.0812 mL	0.4060 mL	0.8121 mL	2.0302 mL
	25 mM	0.0650 mL	0.3248 mL	0.6497 mL	1.6241 mL
	30 mM	0.0541 mL	0.2707 mL	0.5414 mL	1.3535 mL
	40 mM	0.0406 mL	0.2030 mL	0.4060 mL	1.0151 mL
	50 mM	0.0325 mL	0.1624 mL	0.3248 mL	0.8121 mL
	60 mM	0.0271 mL	0.1353 mL	0.2707 mL	0.6767 mL
	80 mM	0.0203 mL	0.1015 mL	0.2030 mL	0.5075 mL

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Hypaconitine

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Publications Citing Use of MedChemExpress (MCE) Hypaconitine

All NF-κB Isoforms

All Calcium Channel Isoforms

Biological Activity

Chemical Information

Publications (2)

Solvent & Solubility

Purity & Documentation

References

Help & FAQs

Complete Stock Solution Preparation Table

Hypaconitine Related Classifications

HY-N0267 Related Classifications