Date published: 2025-9-5

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Alkaloids

Santa Cruz Biotechnology now offers a broad range of alkaloids for use in various applications. Alkaloids are a diverse group of naturally occurring organic compounds that primarily contain basic nitrogen atoms. They are typically derived from plant sources, though some can be found in fungi, bacteria, and animals. Alkaloids have a wide range of chemical structures and biological activities, making them critical to numerous fields of scientific research. In organic chemistry, alkaloids are studied for their complex molecular architectures and synthetic challenges, providing insights into advanced synthetic methodologies and reaction mechanisms. Researchers investigate alkaloids to understand their biosynthesis pathways, which can lead to innovative approaches in bioengineering and the sustainable production of these compounds. In ecological and environmental studies, alkaloids are examined for their roles in plant defense mechanisms, interactions with herbivores, and their effects on ecosystems. Additionally, alkaloids have significant applications in analytical chemistry, where they are used as standards and reference materials for various analytical techniques, including chromatography and mass spectrometry. In the field of biochemistry, alkaloids are key to studying enzyme interactions, receptor binding, and signal transduction pathways. By offering a diverse selection of alkaloids, Santa Cruz Biotechnology supports a wide range of scientific endeavors, enabling researchers to select the appropriate compounds for their specific experimental needs. This extensive range of alkaloids facilitates innovation and discovery across multiple scientific disciplines, including chemistry, biology, environmental science, and materials science. View detailed information on our available alkaloids by clicking on the product name.

Items 191 to 194 of 194 total

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Product NameCAS #Catalog #QUANTITYPriceCitationsRATING

β-Nicotyrine

487-19-4sc-212391
sc-212391A
10 mg
25 mg
$342.00
$658.00
1
(3)

β-Nicotyrine, an alkaloid, showcases a distinctive nitrogen-containing heterocyclic structure that promotes unique hydrogen bonding interactions with surrounding molecules. This compound's electron-rich aromatic system enhances its reactivity, allowing for selective electrophilic substitutions. Its ability to form stable complexes with metal ions can influence catalytic pathways, while its moderate polarity aids in solubility across diverse solvents, affecting its distribution and interaction dynamics in various environments.

Dihydroergotamine Methanesulfonate Salt

6190-39-2sc-294343
sc-294343A
sc-294343B
10 mg
25 mg
100 mg
$41.00
$47.00
$91.00
1
(0)

Dihydroergotamine Methanesulfonate Salt, an alkaloid, features a complex polycyclic structure that facilitates intricate stereoelectronic interactions. Its unique nitrogen atoms contribute to diverse coordination chemistry, enabling the formation of dynamic supramolecular assemblies. The compound exhibits notable solubility characteristics, influenced by its ionic nature, which can alter its reactivity profiles in various media. Additionally, its capacity for conformational flexibility allows for distinct molecular recognition processes.

Hordenine

539-15-1sc-279195
sc-279195A
100 mg
1 g
$77.00
$561.00
(0)

Hordenine is a phenethylamine alkaloid characterized by its unique structural features that facilitate specific interactions with neurotransmitter receptors. Its hydrophilic nature allows for effective solvation in polar environments, influencing its bioavailability. The compound exhibits notable reactivity in oxidative pathways, where it can undergo enzymatic transformations, leading to the formation of various metabolites. Additionally, its ability to modulate ion channel activity highlights its role in cellular signaling processes.

(S)-Reticuline

1699-46-3sc-394153
sc-394153A
sc-394153B
1 mg
50 mg
100 mg
$450.00
$2352.00
$3000.00
1
(0)

(S)-Reticuline, an alkaloid, exhibits intriguing stereochemistry that influences its binding affinity to various biological receptors. Its unique structural conformation allows for selective interactions with neurotransmitter systems, potentially modulating synaptic activity. The presence of multiple functional groups facilitates diverse reaction pathways, including oxidation and methylation, while its solubility characteristics enable effective partitioning in biological environments, impacting its kinetic behavior in metabolic processes.