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Magnocurarine chloride

Cat No.:V139289 Purity: ≥98%
Magnocurarine chloride is a neuromuscular junction blocker that inhibits muscle contraction by functionally blocking signal transmission without directly damaging nerve or muscle tissue.
Magnocurarine chloride
Magnocurarine chloride Chemical Structure CAS No.: 75413-87-5
Product category: nAChR
This product is for research use only, not for human use. We do not sell to patients.
Size Price
500mg
1g
Other Sizes
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Product Description
Magnolacrine chloride is a neuromuscular junction blocker that inhibits muscle contraction by functionally blocking signal transmission without directly damaging nerve or muscle tissue. In frog, mouse, and rabbit models, magnesium curare chloride exhibits dose-dependent paralytic effects, with symptoms progressively worsening from limb weakness and loss of righting reflex to respiratory depression and even cardiac arrest. Although high doses can lead to complete cessation of movement, magnesium curare chloride does not affect spinal multineuronal reflexes in frogs. In various animal models, the bioactivity of magnesium curare chloride is similar to that of tubocurarine (1).
Biological Activity I Assay Protocols (From Reference)
ln Vivo
Magnesium curare (0.25–1 mg/10 g; via peritoneal lymph sac injection; single dose) can induce dose-dependent neuromuscular paralysis in frogs. A dose of 0.75 mg/10 g can cause complete respiratory paralysis (lasting 165 minutes), while a dose of 1 mg/10 g has no effect on spinal multineuronal reflexes [1]. Magnesium curare (5–15.63 mg/kg; intravenous injection; single dose) can induce dose-dependent neuromuscular blockade and respiratory effects in rabbits anesthetized with ethyl carbamate. A dose of 15 mg/kg can induce complete muscle paralysis and respiratory arrest, with animals fully recovering within 25–30 minutes [1].
Animal Protocol
Animal/Disease Models:Frogs collected in autumn [1]
Doses: 0.25 mg/10g; 0.5 mg/10g; 0.75 mg/10g; 1.0 mg/10g; 1 mg/10g
Route of Administration: Ventral lymph sac; Single dose
Experimental Results: At a dose of 0.25 mg/10g, the righting reflex was weakened but not completely eliminated. At a dose of 0.5 mg/10g, the righting reflex disappeared, but the skin reflex was weakened, and respiratory movements were visible. At a dose of 0.75 mg/10g, all movements (including respiration) stopped, and paralysis lasted for 165 minutes. At a dose of 1.0 mg/10g, complete paralysis was caused, lasting for 330 minutes. Twenty-five minutes after injection of 0.75 mg/10g of the drug into the unligated lower limb, the contractile response of the gastrocnemius muscle to sciatic nerve stimulation was completely blocked, while the ligated (untreated) lower limb remained responsive. At a dose of 1 mg/10g, the drug did not inhibit spinal multineuronal reflexes because even with complete limb paralysis, the gastrocnemius muscle of the untreated (ligated) lower limb could still contract upon sciatic nerve stimulation.
Animal/Disease Models:Rabbits (2.0-2.5 kg; ethyl carbamate anesthesia) [1]
Doses: 15.63 mg/kg (head drop); 5 mg/kg; 10 mg/kg; 15 mg/kg
Route of Administration: Intravenous injection; single dose (within 5 seconds); intravenous injection; 2 mg/15 seconds infusion
Experimental Results: The 15.63 mg/kg dose (2 mg/15 seconds administration) caused head drop. The 5 mg/kg dose reduced the strength of gastrocnemius muscle contraction for 5-8 minutes, resulting in early respiratory depression, followed by respiratory stimulation lasting 8-10 minutes. The 10 mg/kg dose significantly inhibited muscle spasms and respiration more than the 5 mg/kg dose, and for a longer duration. Within 1 minute after injection, it completely inhibits gastrocnemius muscle contraction and stops respiratory movement. Muscle response and spontaneous breathing begin to recover 7-8 minutes after injection, and complete recovery occurs within 25-30 minutes at a dose of 15 mg/kg.
References

[1]. Curare-like action of magnocurarine, isolated from Magnolia obovata[J]. The Japanese Journal of Pharmacology, 1953, 2(2): 89-96.

[2]. Neuromuscular blocking action of alkaloids from a Japanese crude drug “Shin-I”(Flos Magnoliae) in frog skeletal muscle[J]. Planta medica, 1983, 48(05): 43-47.

These protocols are for reference only. InvivoChem does not independently validate these methods.
Physicochemical Properties
Molecular Formula
C19H24CLNO3
Molecular Weight
349.85
CAS #
75413-87-5
Appearance
Typically exists as solids at room temperature
SMILES
COC(C=C(CC[N+]1(C)C)C([C@H]1CC2=CC=C(C=C2)O)=C3)=C3O.[Cl-]
HS Tariff Code
2934.99.9001
Storage

Powder      -20°C    3 years

                     4°C     2 years

In solvent   -80°C    6 months

                  -20°C    1 month

Shipping Condition
Room temperature (This product is stable at ambient temperature for a few days during ordinary shipping and time spent in Customs)
Solubility Data
Solubility (In Vitro)
May dissolve in DMSO (in most cases), if not, try other solvents such as H2O, Ethanol, or DMF with a minute amount of products to avoid loss of samples
Solubility (In Vivo)
Note: Listed below are some common formulations that may be used to formulate products with low water solubility (e.g. < 1 mg/mL), you may test these formulations using a minute amount of products to avoid loss of samples.

Injection Formulations
(e.g. IP/IV/IM/SC)
Injection Formulation 1: DMSO : Tween 80: Saline = 10 : 5 : 85 (i.e. 100 μL DMSO stock solution 50 μL Tween 80 850 μL Saline)
*Preparation of saline: Dissolve 0.9 g of sodium chloride in 100 mL ddH ₂ O to obtain a clear solution.
Injection Formulation 2: DMSO : PEG300Tween 80 : Saline = 10 : 40 : 5 : 45 (i.e. 100 μL DMSO 400 μLPEG300 50 μL Tween 80 450 μL Saline)
Injection Formulation 3: DMSO : Corn oil = 10 : 90 (i.e. 100 μL DMSO 900 μL Corn oil)
Example: Take the Injection Formulation 3 (DMSO : Corn oil = 10 : 90) as an example, if 1 mL of 2.5 mg/mL working solution is to be prepared, you can take 100 μL 25 mg/mL DMSO stock solution and add to 900 μL corn oil, mix well to obtain a clear or suspension solution (2.5 mg/mL, ready for use in animals).
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Injection Formulation 4: DMSO : 20% SBE-β-CD in saline = 10 : 90 [i.e. 100 μL DMSO 900 μL (20% SBE-β-CD in saline)]
*Preparation of 20% SBE-β-CD in Saline (4°C,1 week): Dissolve 2 g SBE-β-CD in 10 mL saline to obtain a clear solution.
Injection Formulation 5: 2-Hydroxypropyl-β-cyclodextrin : Saline = 50 : 50 (i.e. 500 μL 2-Hydroxypropyl-β-cyclodextrin 500 μL Saline)
Injection Formulation 6: DMSO : PEG300 : castor oil : Saline = 5 : 10 : 20 : 65 (i.e. 50 μL DMSO 100 μLPEG300 200 μL castor oil 650 μL Saline)
Injection Formulation 7: Ethanol : Cremophor : Saline = 10: 10 : 80 (i.e. 100 μL Ethanol 100 μL Cremophor 800 μL Saline)
Injection Formulation 8: Dissolve in Cremophor/Ethanol (50 : 50), then diluted by Saline
Injection Formulation 9: EtOH : Corn oil = 10 : 90 (i.e. 100 μL EtOH 900 μL Corn oil)
Injection Formulation 10: EtOH : PEG300Tween 80 : Saline = 10 : 40 : 5 : 45 (i.e. 100 μL EtOH 400 μLPEG300 50 μL Tween 80 450 μL Saline)


Oral Formulations
Oral Formulation 1: Suspend in 0.5% CMC Na (carboxymethylcellulose sodium)
Oral Formulation 2: Suspend in 0.5% Carboxymethyl cellulose
Example: Take the Oral Formulation 1 (Suspend in 0.5% CMC Na) as an example, if 100 mL of 2.5 mg/mL working solution is to be prepared, you can first prepare 0.5% CMC Na solution by measuring 0.5 g CMC Na and dissolve it in 100 mL ddH2O to obtain a clear solution; then add 250 mg of the product to 100 mL 0.5% CMC Na solution, to make the suspension solution (2.5 mg/mL, ready for use in animals).
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Oral Formulation 3: Dissolved in PEG400
Oral Formulation 4: Suspend in 0.2% Carboxymethyl cellulose
Oral Formulation 5: Dissolve in 0.25% Tween 80 and 0.5% Carboxymethyl cellulose
Oral Formulation 6: Mixing with food powders


Note: Please be aware that the above formulations are for reference only. InvivoChem strongly recommends customers to read literature methods/protocols carefully before determining which formulation you should use for in vivo studies, as different compounds have different solubility properties and have to be formulated differently.

 (Please use freshly prepared in vivo formulations for optimal results.)
Preparing Stock Solutions 1 mg 5 mg 10 mg
1 mM 2.8584 mL 14.2918 mL 28.5837 mL
5 mM 0.5717 mL 2.8584 mL 5.7167 mL
10 mM 0.2858 mL 1.4292 mL 2.8584 mL

*Note: Please select an appropriate solvent for the preparation of stock solution based on your experiment needs. For most products, DMSO can be used for preparing stock solutions (e.g. 5 mM, 10 mM, or 20 mM concentration); some products with high aqueous solubility may be dissolved in water directly. Solubility information is available at the above Solubility Data section. Once the stock solution is prepared, aliquot it to routine usage volumes and store at -20°C or -80°C. Avoid repeated freeze and thaw cycles.

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An example of molarity calculation using the molarity calculator is shown below:
What is the mass of compound required to make a 10 mM stock solution in 5 ml of DMSO given that the molecular weight of the compound is 350.26 g/mol?
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  • The answer of 17.513 mg appears in the Mass box. In a similar way, you may calculate the volume and concentration.

Dilution Calculator allows you to calculate how to dilute a stock solution of known concentrations. For example, you may Enter C1, C2 & V2 to calculate V1, as detailed below:

What volume of a given 10 mM stock solution is required to make 25 ml of a 25 μM solution?
Using the equation C1V1 = C2V2, where C1=10 mM, C2=25 μM, V2=25 ml and V1 is the unknown:
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  • The answer of 62.5 μL (0.1 ml) appears in the Volume (Start) box
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Note: Chemical formula is case sensitive: C12H18N3O4  c12h18n3o4
Instructions to calculate molar mass (molecular weight) of a chemical compound:
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Definitions of molecular mass, molecular weight, molar mass and molar weight:
  • Molecular mass (or molecular weight) is the mass of one molecule of a substance and is expressed in the unified atomic mass units (u). (1 u is equal to 1/12 the mass of one atom of carbon-12)
  • Molar mass (molar weight) is the mass of one mole of a substance and is expressed in g/mol.
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In vivo Formulation Calculator (Clear solution)
Step 1: Enter information below (Recommended: An additional animal to make allowance for loss during the experiment)
Step 2: Enter in vivo formulation (This is only a calculator, not the exact formulation for a specific product. Please contact us first if there is no in vivo formulation in the solubility section.)
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Calculation results

Working concentration mg/mL;

Method for preparing DMSO stock solution mg drug pre-dissolved in μL DMSO (stock solution concentration mg/mL). Please contact us first if the concentration exceeds the DMSO solubility of the batch of drug.

Method for preparing in vivo formulation:Take μL DMSO stock solution, next add μL PEG300, mix and clarify, next addμL Tween 80, mix and clarify, next add μL ddH2O,mix and clarify.

(1) Please be sure that the solution is clear before the addition of next solvent. Dissolution methods like vortex, ultrasound or warming and heat may be used to aid dissolving.
             (2) Be sure to add the solvent(s) in order.

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