Product Information
Name:Aconitine
Controlled Product
Synonyms:
- 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)-
- 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 (7CI)
- Aconitine (8CI)
- 2H-12,3,6a-Ethanylylidene-7,9-methanonaphth[2,3-b]azocine
- aconitane-3,8,13,14,15-pentol deriv.
- (1α,3α,6α,14α,15α,16β)-20-Ethyl-1,6,16-trimethoxy-4-(methoxymethyl)aconitane-3,8,13,14,15-pentol 8-acetate 14-benzoate
Brand:TRC
Description:Applications 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 packageReferences Derbre, S., et al.: Anal. Bioanal. Chem., 398, 1747 (2010), Li, M., et al.: J. Pharm. Biomed. Anal., 53, 1063 (2010),
Notice:Our products are intended for lab use only. For any other use, please contact us.
Chemical properties
Molecular weight:645.74
Formula:C34H47NO11
Color/Form:Neat
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-VVRUJSPOSA-N
SMILES:CCN1C[C@]2(COC)[C@H]3[C@@H](OC)[C@H]4[C@H]1C3([C@H](OC)C[C@H]2O)[C@@H]1C[C@]2(O)[C@@H](OC)[C@H](O)[C@@]4(OC(C)=O)[C@H]1[C@H]2OC(=O)c1ccccc1
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