Calebassine
Calebassine is a competitive neuromuscular blocking agent, it is also a Mdm2/MdmX inhibitor.
Inquire / Order:
manager@chemfaces.com
Technical Inquiries:
service@chemfaces.com
Tel:
+86-27-84237783
Fax:
+86-27-84254680
Address:
1 Building, No. 83, CheCheng Rd., Wuhan Economic and Technological Development Zone, Wuhan, Hubei 430056, PRC
Providing storage is as stated on the product vial and the vial is kept tightly sealed, the product can be stored for up to
24 months(2-8C).
Wherever possible, you should prepare and use solutions on the same day. However, if you need to make up stock solutions in advance, we recommend that you store the solution as aliquots in tightly sealed vials at -20C. Generally, these will be useable for up to two weeks. Before use, and prior to opening the vial we recommend that you allow your product to equilibrate to room temperature for at least 1 hour.
Need more advice on solubility, usage and handling? Please email to: service@chemfaces.com
The packaging of the product may have turned upside down during transportation, resulting in the natural compounds adhering to the neck or cap of the vial. take the vial out of its packaging and gently shake to let the compounds fall to the bottom of the vial. for liquid products, centrifuge at 200-500 RPM to gather the liquid at the bottom of the vial. try to avoid loss or contamination during handling.
Current Topics in Nutraceutical Research2021, 19(1),p90-105.
Arch Biochem Biophys.2018, 644:93-99
Data Science for Genomics2023, 107-128.
Front Microbiol.2023, 14:1232039.
Nutrients.2023, 15(6):1335.
Vojnosanit Pregl2016, 75(00):391-391
Food Science and Preservation2024, 31(3):486-498.
Phytochemistry.2017, 141:162-170
J Pharm Biomed Anal.2019, 164:119-127
STAR Protoc.2024, 5(2):102990.
Related and Featured Products
Arch Int Pharmacodyn Ther. 1975 Jun;215(2):246-58.
Chemical structure and pharmacological (curarizing) properties of various indole alkaloids extracted from an African Strychnos.[Pubmed:
126050]
The chemical separation and identification of ten alkaloids extracted from the roots of Strychnos usambarensis are described.
METHODS AND RESULTS:
The elucidation of their structure by means of elementary analysis, I. R., U.V, and mass spectrometry allows their classification into bistertiary amines, hybrid and bisquaternary ammonium derivatives. This classification is reflected in the pharmacological properties. One of the tertiary amine alkaloids (usambarensine) presents atopine-like and spasmolytic activities while the bisquaternary ammonium compounds (dihydrotoxiferine, Calebassine, C-curarine and afrocurarine) are competitive neuromuscular blocking agents.
