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| Product | Description | |
|---|---|---|
| Aconitine | Neurotoxin. Activates tetrodotoxin-sensitive Na+ channels, inducing presynaptic depolarization, thus blocking the nerve action potential which, in turn, blocks the release of neurotransmitters and decreases the end plate potential at the neuromuscular junction. Aconitine also blocks norepinephrine reuptake. In the heart, aconitine induces ventricular tachycardia after intracoronary injection. In cultured ventricular myocytes, aconitine increases the duration of the action potential and induces the appearance of early after depolarization. Group: Biochemicals. Alternative Names: (1α, 3α, 6α, 14α, 15α, 16 β ) -20-Ethyl-1, 6, 16-trimethoxy-4- (methoxymethyl) aconitane-3, 8, 13, 14, 15-pentol 8-Acetate 14-Benzoate. Grades: Highly Purified. CAS No. 302-27-2. Pack Sizes: 10mg. US Biological Life Sciences. |  Worldwide |
| 10-Hydroxy Aconitine | 10-Hydroxy Aconitine is a toxic constituent from aconitum plants and known for its effects against rheumatism and rheumatoid arthritis. Group: Biochemicals. Grades: Highly Purified. CAS No. 41849-35-8. Pack Sizes: 1mg, 2.5mg. Molecular Formula: C34H47NO12, Molecular Weight: 661.74. US Biological Life Sciences. | Worldwide |
| 3-Acetylaconitine | 3-Acetylaconitine. Group: Biochemicals. Alternative Names: Aconitine 3-acetate; Aconitine 3-monoacetate; Flaconitine. Grades: Plant Grade. CAS No. 77181-26-1. Pack Sizes: 20mg. Molecular Formula: C36H49NO12, Molecular Weight: 687.774. US Biological Life Sciences. | Worldwide |
| Acetylaconitine | Acetylaconitine is a diterpenoid alkaloid isolated from the roots of Aconitum kusnezoffii Reichb. It is used in analgesia in rats for the treatment of chronic pain and rheumatoid arthritis. Uses: Acetylaconitine is used in analgesia in rats for the treatment of chronic pain and rheumatoid arthritis. Synonyms: Aconitine 3-acetate; (16beta)-3,8-bis(acetyloxy)-20-ethyl-13,15-dihydroxy-1,6,16-trimethoxy-4-(methoxymethyl)aconitan-14-yl benzoate. Grades: >98%. CAS No. 77181-26-1. Molecular formula: C36H49NO12. Mole weight: 687.77. |  |
| Benzoylmesaconine-7-Palmitate | Benzoylmesaconine-7-Palmitate is an alkaloid isolated from aconitum carmichaeli Debx. Benzoylmesaconine has powerful antinociceptive, antiarrhythmic and properties due to their ability to blockade voltage-dependent sodium channels, but has less toxic monoesters than aconitine and mesaconitine. Grades: > 98%. Molecular formula: C47H73NO11. Mole weight: 828.08. | |
| Xanthotoxol | A hydroxylated psoralen that inhibits neutrophil infiltration and brain edema induced by focal cerebral ischemia-reperfusion injury in rats. A potentially useful antiarrhythmic agent. It has been shown to be effective in the prevention of ventricular fibrillation of mice induced by chloroform, of rats induced by calcium chloride, and in treatment of rat arrhythmia induced by aconitine. Recent studies show that it may also have antioxidant and anticancer activities. Group: Biochemicals. Alternative Names: 9-Hydroxy-7H-furo[3,2-g][1]benzopyran-7-one; 6,7-Dihydroxy-5-benzofuranacrylic Acid δ-Lactone; 3-(6,7-Dihydroxy-5-benzofuranyl)-2-propenoic Acid δ-Lactone; 8-Hydroxypsoralen; NSC 401269. Grades: Highly Purified. CAS No. 2009-24-7. Pack Sizes: 25mg. US Biological Life Sciences. | Worldwide |
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