
Toxines
Les toxines sont des substances toxiques produites par des organismes vivants qui peuvent causer des dommages à d'autres organismes. La recherche sur les toxines comprend l'étude de leurs mécanismes d'action, de leurs effets sur les systèmes biologiques et de leurs utilisations potentielles en médecine et en agriculture. Ce domaine implique également le développement d'antidotes et de traitements pour l'exposition aux toxines. Chez CymitQuimica, nous fournissons des composés toxiques de haute qualité pour soutenir la recherche en toxicologie, pharmacologie et domaines connexes, garantissant une manipulation précise et sûre dans vos expériences.
Produits appartenant à la catégorie "Toxines"
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Isopimaric Acid
CAS :Formule :C20H30O2Degré de pureté :≥ 98.0%Couleur et forme :White to off-white powderMasse moléculaire :302.45orcinol
CAS :orcinol (5-Methylresorcin) is anxiolytic agent without sedative effect.Formule :C7H8O2Degré de pureté :99.86%Couleur et forme :Pink-Grey To Pink-Brown Cryst Powder Or CrystalsMasse moléculaire :124.14Lomustine
CAS :Formule :C9H16ClN3O2Degré de pureté :≥ 98.0%Couleur et forme :White to light-yellow powderMasse moléculaire :233.70Picrotoxin
CAS :Formule :C30H34O13Degré de pureté :≥ 98.0%Couleur et forme :White to off-white powderMasse moléculaire :602.58Enniatin A1
CAS :Enniatin A1 is a cyclic hexadepsipeptide, which is a secondary metabolite produced by various Fusarium species. This compound is primarily derived from Fusarium fungi and exhibits notable bioactivity due to its ionophoric properties. The mode of action involves its ability to disrupt ion gradients across cellular membranes. Enniatin A1 functions by forming complexes with cations, particularly alkali and alkaline earth metal ions, facilitating their transport across lipid membranes and ultimately perturbing cellular homeostasis. The uses and applications of Enniatin A1 are broad, particularly in mycological and pharmacological research. It is commonly studied for its antifungal properties, as it influences the bioenergetics of fungal cells, leading to their growth inhibition or death. Furthermore, its potential anticancer activity is an area of active investigation, where it is assessed for its ability to induce apoptosis in cancer cells. Enniatin A1 serves as an essential tool in studying ion transport mechanisms and as a lead compound in the development of novel antifungal and anticancer agents. Its biogenic origin and specific mode of action make it a molecule of significant interest in various scientific domains.Degré de pureté :Min. 95%Verruculogen
CAS :Formule :C27H33N3O7Degré de pureté :≥ 95.0%Couleur et forme :Off-white to brown solidMasse moléculaire :511.6Valrubicin
CAS :Formule :C34H36F3NO13Degré de pureté :95.0 - 103.0 % (dried basis)Couleur et forme :Orange to orange-red crystalline powderMasse moléculaire :723.64Topotecan
CAS :Formule :C23H23N3O5·xHCl·yH2ODegré de pureté :≥ 97%Couleur et forme :Off-white to yellow powder or solidMasse moléculaire :421.45 (anhydrous)Fumonisin B2
CAS :Fumonisin B2 is a mycotoxin, which is a naturally occurring toxin produced by certain species of fungi. Specifically, it is produced by Fusarium species, such as Fusarium verticillioides and Fusarium proliferatum, commonly found in cereal crops like corn. This mycotoxin disrupts cellular lipid metabolism, particularly the sphingolipid pathway, by inhibiting the enzyme ceramide synthase. This disruption can lead to cell dysfunction and contributes to the pathogenesis of animal diseases. The primary applications of Fumonisin B2 research are in the domains of animal health and food safety. In agricultural contexts, understanding its effects and developing methods to mitigate its impact are essential for ensuring the safety of animal feed. Additionally, due to its presence in the food chain, it is crucial to study Fumonisin B2 for its potential health risks in human consumption. Researchers focus on detection methods, toxicology studies, and management strategies to limit exposure and reduce risks associated with this mycotoxin.Degré de pureté :Min. 95%Cytarabine
CAS :Formule :C9H13N3O5Degré de pureté :98.0 - 102.0 % (dried basis)Couleur et forme :White crystalline powderMasse moléculaire :243.22Enniatin A
CAS :Enniatin A is a cyclic depsipeptide, which is a secondary metabolite produced by certain Fusarium fungi. It functions as an ionophore, facilitating the transport of ions across cellular membranes. This activity stems from its ability to form complexes with metallic cations, disrupting ion gradients and membrane potential. As a result, Enniatin A can affect various cellular processes, including signal transduction and energy metabolism. Enniatin A has garnered interest in the scientific community due to its potential applications in agriculture and medicine. In agriculture, its antifungal and antibacterial properties could be leveraged to develop natural pesticides. In medicine, its cytotoxic activity is being explored for potential anticancer therapies. However, its exact mechanism remains a subject of ongoing research, with studies focusing on its interactions at the molecular level. Enniatin A's bioactivity underlines its significance as a tool for studying ion transport and cellular homeostasis. Continued investigation into this compound could reveal further applications and enhance our understanding of cellular processes affected by ion gradients.Degré de pureté :Min. 95%MS049
CAS :MS 049 is a potent, selective, and cell-active dual inhibitor of PRMT4 and PRMT6 with IC 50 of 34 nM and 43 nM, respectively.Formule :C15H24N2ODegré de pureté :≥95%Couleur et forme :SolidMasse moléculaire :248.36Ref: TM-T4378
2mg35,00€5mg51,00€10mg85,00€25mg158,00€50mg235,00€100mg354,00€200mg520,00€1mL*10mM (DMSO)55,00€Fusarenon X
CAS :Fusarenon X is a mycotoxin, which is a secondary metabolite produced by certain species of the Fusarium fungi. This compound is primarily derived from Fusarium graminearum and Fusarium crookwellense, which are fungi commonly found in various cereal grains, particularly in temperate regions. The mode of action of Fusarenon X involves inhibition of protein synthesis by interfering with ribosomal function, a mechanism that significantly impacts rapidly dividing cells. This cytotoxic effect is primarily due to its ability to induce apoptosis through disruptions in cellular processes and pathways. In scientific research, Fusarenon X is utilized to study its toxicological impact on both human and animal cells, offering insights into mechanisms of toxicity, carcinogenic potential, and its impact on food safety. Due to its ability to affect fundamental cellular processes, it is also investigated in the context of cancer research, particularly in understanding how similar agents could be utilized or modulated for therapeutic purposes. However, the primary concern remains its presence in contaminated food supplies and the implication for human and animal health.Degré de pureté :Min. 95%