CAS 302-27-2: Aconitine
Formula:C34H47NO11
InChI:InChI=1S/C34H47NO11/c1-7-35-15-31(16-41-3)20(37)13-21(42-4)33-19-14-32(40)28(45-30(39)18-11-9-8-10-12-18)22(19)34(46-17(2)36,27(38)29(32)44-6)23(26(33)35)24(43-5)25(31)33/h8-12,19-29,37-38,40H,7,13-16H2,1-6H3/t19-,20-,21+,22-,23+,24+,25-,26-,27+,28-,29+,31+,32-,33+,34-/m1/s1
InChI key:InChIKey=XFSBVAOIAHNAPC-NPVHKAFCSA-N
SMILES:O(C)[C@@H]1[C@@]23[C@]4([C@](COC)(CN(CC)[C@@]2([C@]([C@@H]4OC)([C@]5(OC(C)=O)[C@@]6([C@]3(C[C@@](O)([C@@H]6OC(=O)C7=CC=CC=C7)[C@@H](OC)[C@@H]5O)[H])[H])[H])[H])[C@H](O)C1)[H]
Synonyms:- (1Beta,3Alpha,5Xi,6Alpha,14Alpha,15Alpha,16Beta)-8-(Acetyloxy)-20-Ethyl-3,13,15-Trihydroxy-1,6,16-Trimethoxy-4-(Methoxymethyl)Aconitan-14-Yl Benzoate
- (3Alpha,6Alpha,14Alpha,15Alpha,16Beta)-8-(Acetyloxy)-20-Ethyl-3,13,15-Trihydroxy-1,6,16-Trimethoxy-4-(Methoxymethyl)Aconitan-14-Yl Benzoate
- (3Alpha,6Alpha,9Alpha,10Alpha,13Alpha,14Alpha,15Alpha,16Beta)-8-(Acetyloxy)-20-Ethyl-3,13,15-Trihydroxy-1,6,16-Trimethoxy-4-(Methoxymethyl)Aconitan-14-Yl Benzoate
- 2H-12,3,6a-Ethanylylidene-7,9-methanonaphth[2,3-b]azocine, aconitane-3,8,13,14,15-pentol deriv.
- 2H-12,3,6a-Ethanylylidene-7,9-methanonaphth[2,3-b]azocine-4,8,9,11,11a(1H,7H)-pentol, 1-ethyldecahydro-6,10,13-trimethoxy-3-(methoxymethyl)-, 11a-acetate 8-benzoate
- Acetylbenzoylaconine
- Aconitane-3,8,13,14,15-pentol, 20-ethyl-1,6,16-trimethoxy-4-(methoxymethyl)-, 8-acetate 14-benzoate, (1α,3α,6α,14α,15α,16β)-
- Aconitin
- Aconitina
- Aconitine
- MeSH ID: D000157
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Found 10 products.
Aconitine, 98%
CAS:Opens tetrodotoxin-sensitive sodium channels. Useful for creating models of cardiac arrhythmia This Thermo Scientific Chemicals brand product was originally part of the Alfa Aesar product portfolio. Some documentation and label information may refer to the legacy brand. The original Alfa Aesar product / item code or SKU reference has not changed as a part of the brand transition to Thermo Scientific Chemicals.Formula:C34H47NO11Purity:98%Color and Shape:White to off-white, PowderMolecular weight:645.75Aconitine
CAS:Natural alkaloidFormula:C34H47NO11Purity:≥ 95.0 % (HPLC)Color and Shape:PowderMolecular weight:645.75Aconitine
CAS:Controlled ProductApplications 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.Used in producing heart arrhythmia in experimental animals. Not a dangerous good if item is equal to or less than 1g/ml and there is less than 100g/ml in the package References Derbre, S., et al.: Anal. Bioanal. Chem., 398, 1747 (2010), Li, M., et al.: J. Pharm. Biomed. Anal., 53, 1063 (2010),Formula:C34H47NO11Color and Shape:NeatMolecular weight:645.74Aconitine
CAS:Aconitine, one of the major Aconitum alkaloids, is a highly toxic compound from the Aconitum species, it appears to exert a long-lasting cholinergic action in the causation of severe arrhythmias leading to death.Formula:C34H47NO11Purity:95%~99%Molecular weight:645.746Aconitine
CAS:Formula:C34H47NO11Purity:≥ 98.0%Color and Shape:White to off-wihite crystalline powderMolecular weight:645.75Aconitine
CAS:Toxin with analgesic and antipyretic activityFormula:C34H47NO11Purity:Min. 95%Color and Shape:White PowderMolecular weight:645.75 g/molAconitine 100 µg/mL in Acetonitrile
CAS:Formula:C34H47NO11Color and Shape:Single SolutionMolecular weight:645.74LC PestiMix 6 10 µg/mL in Acetonitrile
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Color and Shape:Mixture
