CAS 97792-45-5
:Lappaconitine hydrobromide
Description:
Lappaconitine hydrobromide is a chemical compound derived from the plant genus Aconitum, commonly known as monkshood. It is classified as an alkaloid, specifically a type of aconitine, which is known for its potent pharmacological effects. This compound typically appears as a white to off-white crystalline powder and is soluble in water and alcohol, making it suitable for various applications in medicinal chemistry. Lappaconitine hydrobromide exhibits analgesic and anti-inflammatory properties, which have been explored for potential therapeutic uses, particularly in pain management. However, it is important to note that compounds from the Aconitum species can be highly toxic, and their use must be approached with caution due to the risk of severe side effects, including cardiovascular and neurological complications. As with many alkaloids, the pharmacokinetics and safety profile of lappaconitine hydrobromide require thorough investigation before clinical application. Proper handling and dosage are critical to mitigate toxicity risks associated with this compound.
Formula:C32H44N2O8·BrH
InChI:InChI=1S/C32H44N2O8.BrH/c1-6-34-16-29(42-28(36)18-9-7-8-10-21(18)33-17(2)35)12-11-25(40-4)31-23(29)14-20(26(31)34)30(37)15-22(39-3)19-13-24(31)32(30,38)27(19)41-5;/h7-10,19-20,22-27,37-38H,6,11-16H2,1-5H3,(H,33,35);1H/t19-,20+,22+,23-,24+,25+,26-,27+,29-,30+,31+,32+;/m1./s1
InChI key:InChIKey=CFFYROOPXPKMEQ-IPZKEBFRSA-N
SMILES:O(C)[C@@H]1[C@@]23[C@]4([C@](OC(=O)C5=C(NC(C)=O)C=CC=C5)(CN(CC)[C@@]2([C@](C4)([C@]6(O)[C@]7(O)[C@]3(C[C@@]([C@@H]7OC)([C@@H](OC)C6)[H])[H])[H])[H])CC1)[H].Br
Synonyms:- (1a,14a,16b)-20-Ethyl-1,14,16-trimethoxyaconitane-4,8,9-triol 4-(2-(acetylamino)benzoate) hydrobromide
- 2H-12,3,6a-Ethanylylidene-7,9-methanonaphth[2,3-b]azocine, aconitane-4,8,9-triol deriv.
- Aconitane-4,8,9-triol, 20-ethyl-1,14,16-trimethoxy-, 4-[2-(acetylamino)benzoate], hydrobromide (1:1), (1α,14α,16β)-
- Aconitane-4,8,9-triol, 20-ethyl-1,14,16-trimethoxy-, 4-[2-(acetylamino)benzoate], monohydrobromide, (1α,14α,16β)-
- Allafort
- Allapinine
- Lappaconite Hydrobromide
- Lappaconitin hydrobromide
- Lappaconitine hydrobromide
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Found 6 products.
Lappaconitine Hydrobromide
CAS:Formula:C32H44N2O8·HBrPurity:>95.0%(N)Color and Shape:White to Light yellow powder to crystalMolecular weight:665.62Lappaconitine hydrobromide
CAS:<p>Lappaconitine hydrobromide (Allapinine) is a kind of alkaloid extracted from Aconitum sinomontanum Nakai. It has anti-inflammatory effects.</p>Formula:C32H44N2O8·HBrPurity:97.23%Color and Shape:White PowderMolecular weight:665.61Lappaconitine Hydrobromide
CAS:Controlled Product<p>Applications Hydrobromide salt of (+)-Lappaconitine (L175850), a potential antitumor agent agent that induces HL-60 differentiation and apoptosis with analgesic activity as well.<br> Not a dangerous good if item is equal to or less than 1g/ml and there is less than 100g/ml in the package<br>References Xu, M. et al.: Lat. Am. J. Pharm., 32, 1433 (2013); Yunusov, M.et al.: Russ. Chem. Bull., 60, 633 (2011);<br></p>Formula:C32H45BrN2O8Color and Shape:White To Off-WhiteMolecular weight:665.61Lappaconitine Hydrobromide
CAS:Controlled Product<p>Hydrobromide form of lappaconitine, lappaconitine hydrobromide is clinically used to reduce swelling and inflammation while providing a local anesthetic effect. The molecular structure of lappaconitine was first reported in 1895. Traditionally used for pain relief, lappaconitine is a plant-derived C18-diuterpenoid alkaloid. In rats, the antinociceptive action of lappaconitine has been shown to be based on the enhanced expression of dynorphin A in the spinal microglia.</p>Formula:C32H44N2O8·HBrPurity:Min. 95%Color and Shape:White PowderMolecular weight:665.61 g/mol






