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Home > Natural Products > Alkaloids (Find 30 items)

Alkaloids

Corynoxine

(6877-32-3)
Corynoxine is an enantiomer of Corynoxine B; induces autophagy in different neuronal cell lines, including N2a and SHSY-5Y cells.IC50 value:Tareget: Autophagy inducerIn vivo, Cory promotes the formation of autophagosomes in the fat bodies of Drosophila. By inducing autophagy, Cory promotes the clearance of wild-type and A53T α-syn in inducible PC12 cells. Interestingly, different from its enantiomer Cory B, Cory induces autophagy through the Akt/mTOR pathway as evidenced by the reduction

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Coixol

(532-91-2)
Coixol is a natural product extracted from Coix Lachryma-Jobi var. ma-yuen.IC50 value:Target:In vitro: Confluent NCI-H292 cells were pretreated with oleic acid, linoleic acid, glyceryl trilinoleate, beta-stigmasterol or coixol for 30 min and then stimulated with PMA (phorbol 12-myristate 13-acetate), EGF (epidermal growth factor) or TNF-α (tumor necrosis factor-α) for 24 h. Coixol inhibited the expression of MUC5AC mucin gene and production of MUC5AC mucin protein, induced by EGF or TNF-

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Coclaurine

(486-39-5)
Coclaurine is a class of tetrahydroisoquinoline alkaloids isolated from Sarcopetalum harveyanum. Coclaurine is a nicotinic acetylcholine receptor (nAChRs) antagonist[1][2].

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Canadine

(5096-57-1)
(S)-(-)-Canadine is a protoberberine alkaloidwhich potently block functional KATP channels natively expressed on midbrain dopamine neurons. Canadine is used for treatment of degenerative diseases or conditions associated with KATP channel signaling. (S)-(-)-Canadine has a strong central nervous system-depressing activity and is used in the preparation of tetrahydroprotoberberine derivatives as new antipsychotic agents.

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Canthin-6-one

(479-43-6)
ChEBI: An indole alkaloid that is 6H-indolo[3,2,1-de][1,5]naphthyridine substituted by an oxo group at position 6.

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Cyclo(L-Phe-L-Pro)

(3705-26-8)
Cyclo(L-Phe-L-Pro) is a diketopiperazine formed by the fusion of phenylalanine and proline, reported as a secondary metabolite of fungi and bacteria. In Pseudomonas aeruginosa, cyclo(L-Phe-L-Pro) is capable of activating N-acylhomoserine lactones (AHLs). Cyclo(L-Phe-L-Pro) is also capable of activating or antagonizing other LuxR-based quorum-sensing systems. While the mode of action of cyclo(L-Phe-L-Pro) is not known, its activity suggests the existence of cross talk among bacterial signalling s

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Alkaloids exist in nature (mainly plants, but some also exist in animals), a type of nitrogen-containing basic organic compounds, which have alkaloid-like properties. According to the basic structure of alkaloids, it can be divided into about 60 categories. Main types: organic amines, pyrrolidines, pyridines, isoquinolines, indoles, scopolamines, imidazoles, quinazolones, purines, steroids, diterpenes, and others.

Frequently Asked Questions

What are alkaloids and why are they important in pharmaceuticals?

Alkaloids are naturally occurring organic compounds that contain basic nitrogen atoms, commonly derived from plants such as poppies, cinchona bark, and tobacco. They are vital in pharmaceuticals due to their potent biological activities—many serve as the active ingredients in medications for pain relief (e.g., morphine), malaria treatment (e.g., quinine), and cancer therapy (e.g., vinblastine). Their structural complexity and pharmacological efficacy make them indispensable in drug discovery and development.

How are alkaloids extracted and purified for commercial use?

Alkaloids are typically extracted from plant sources using solvent-based methods such as acid-base extraction, which leverages their solubility differences in acidic and alkaline conditions. After initial extraction, purification is achieved through techniques like crystallization, column chromatography, or preparative HPLC to ensure high purity levels required for pharmaceutical applications. Reputable suppliers follow Good Manufacturing Practices (GMP) and validate purity via analytical methods like HPLC, NMR, and mass spectrometry.

What are common types of alkaloids used in medicine?

Common medicinal alkaloids include morphine and codeine (analgesics from opium poppy), quinine and artemisinin (antimalarials), atropine (used in ophthalmology and as an antidote for nerve agent poisoning), vincristine and vinblastine (anticancer agents from Madagascar periwinkle), and caffeine (a central nervous system stimulant). Each alkaloid has a specific mechanism of action and therapeutic application, underscoring their diverse roles in modern medicine.

How to choose a reliable supplier of high-purity alkaloids?

When selecting a supplier for high-purity alkaloids, consider: (1) regulatory compliance—ensure they adhere to GMP, ISO, or FDA standards; (2) analytical documentation—certificates of analysis (CoA) with data from HPLC, GC, or NMR should be provided; (3) sourcing transparency—reputable suppliers disclose botanical origin and extraction methods; (4) batch consistency and scalability for research or production needs; and (5) technical support and shipping reliability. Partnering with certified chemical or pharmaceutical ingredient suppliers minimizes quality and legal risks.

Are synthetic alkaloids as effective as natural ones?

Synthetic alkaloids can be equally or even more effective than their natural counterparts, especially when structural modifications enhance bioavailability, reduce toxicity, or improve stability. For example, semi-synthetic opioids like oxycodone are derived from natural thebaine but optimized for clinical use. However, some complex alkaloids (e.g., those with multiple chiral centers) remain challenging to synthesize economically, making natural extraction preferable. The choice between natural and synthetic depends on the intended application, cost, regulatory requirements, and desired pharmacokinetic profile.

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