Corynantheidine (Synonyms: (-)-Corynantheidine, 9-demethoxy Mitragynine) |
Catalog No.GC52243 |
An alkaloid with antinociceptive activity
Products are for research use only. Not for human use. We do not sell to patients.
Cas No.: 23407-35-4
Sample solution is provided at 25 µL, 10mM.
Corynantheidine is an alkaloid that has been found in M. speciosa (Kratom in Thai) and has antinociceptive activity.1,2 It is a partial agonist of the μ-opioid receptor that lacks β-arrestin recruitment activity.1 Corynantheidine selectively binds to μ-opioid receptors over κ- and δ-opioid receptors (Kis = 57.1, 385.4, and 172 nM, respectively, for the mouse receptors) and is selective for the μ-opioid receptor (EC50 = 104.24 nM) over the κ- and δ-opioid receptors, for which it has no activity, in [35S]GTPγS assays. It also binds to α1D- and α2A-adrenergic receptors and NMDA receptors (Kis = 41, 74, and 83 nM, respectively, for the human receptors), among others.1,2 Corynantheidine (10-100 nmol, i.c.v.) increases the latency to tail withdrawal in the tail-flick test in mice.1
1.Chakraborty, S., Uprety, R., Daibani, A.E., et al.Kratom alkaloids as probes for opioid receptor function: Pharmacological characterization of minor indole and oxindole alkaloids from kratomACS Chem. Neurosci.12(14)2661-2678(2021) 2.Obeng, S., Kamble, S.H., Reeves, M.E., et al.Investigation of the adrenergic and opioid binding affinities, metabolic stability, plasma protein binding properties, and functional effects of selected indole-based kratom alkaloidsJ. Med. Chem.63(1)433-439(2020)
Cas No. | 23407-35-4 | SDF | |
Synonyms | (-)-Corynantheidine, 9-demethoxy Mitragynine | ||
Canonical SMILES | CC[C@@H]1CN2[C@@](C(NC3=CC=CC=C34)=C4CC2)([H])C[C@@H]1/C(C(OC)=O)=C\OC | ||
Formula | C22H28N2O3 | M.Wt | 368.5 |
Solubility | DMF: 1 mg/ml,DMSO: 2 mg/ml,Ethanol: insol,PBS (pH 7.2): insol | Storage | -20°C |
General tips | Please select the appropriate solvent to prepare the stock solution according to the
solubility of the product in different solvents; once the solution is prepared, please store it in
separate packages to avoid product failure caused by repeated freezing and thawing.Storage method
and period of the stock solution: When stored at -80°C, please use it within 6 months; when stored
at -20°C, please use it within 1 month. To increase solubility, heat the tube to 37°C and then oscillate in an ultrasonic bath for some time. |
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Shipping Condition | Evaluation sample solution: shipped with blue ice. All other sizes available: with RT, or with Blue Ice upon request. |
Prepare stock solution | |||
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1 mg | 5 mg | 10 mg |
1 mM | 2.7137 mL | 13.5685 mL | 27.137 mL |
5 mM | 0.5427 mL | 2.7137 mL | 5.4274 mL |
10 mM | 0.2714 mL | 1.3569 mL | 2.7137 mL |
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Working concentration: mg/ml;
Method for preparing DMSO master liquid: mg drug pre-dissolved in μL DMSO ( Master liquid 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 master liquid, next addμL PEG300, mix and clarify, next addμL Tween 80, mix and clarify, next add μL ddH2O, mix and clarify.
Method for preparing in vivo formulation: Take μL DMSO master liquid, next add μL Corn oil, mix and clarify.
Note: 1. Please make sure the liquid is clear before adding the next solvent.
2. Be sure to add the solvent(s) in order. You must ensure that the solution obtained, in the previous addition, is a clear solution before proceeding to add the next solvent. Physical methods such as vortex, ultrasound or hot water bath can be used to aid dissolving.
3. All of the above co-solvents are available for purchase on the GlpBio website.
Quality Control & SDS
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- Purity: >98.00%
- COA (Certificate Of Analysis)
- SDS (Safety Data Sheet)
- Datasheet
Average Rating: 5
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