CAS 32854-75-4
:Lappaconitine
Description:
Lappaconitine is a naturally occurring alkaloid derived from various species of the Aconitum plant, commonly known as monkshood or wolfsbane. It is characterized by its complex bicyclic structure, which includes a nitrogen atom in its ring system, contributing to its pharmacological properties. Lappaconitine exhibits analgesic and anti-inflammatory effects, making it of interest in medicinal chemistry. It acts primarily on the central nervous system, where it can influence pain pathways. The compound is known for its potential toxicity, as many Aconitum species contain other toxic alkaloids, necessitating careful handling and dosage considerations. Lappaconitine's solubility is generally low in water but may vary in organic solvents, which is important for its extraction and formulation in pharmaceutical applications. Additionally, its pharmacokinetics, including absorption, distribution, metabolism, and excretion, are crucial for understanding its therapeutic potential and safety profile. Overall, Lappaconitine represents a significant area of research in natural product chemistry and pharmacology, with ongoing studies exploring its mechanisms of action and potential therapeutic uses.
Formula:C32H44N2O8
InChI:InChI=1S/C32H44N2O8/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)/t19-,20+,22+,23-,24+,25+,26-,27+,29-,30+,31+,32+/m1/s1
InChI key:InChIKey=NWBWCXBPKTTZNQ-QOQRDJBUSA-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]
Synonyms:- (14Alpha,16Beta)-20-Ethyl-8,9-Dihydroxy-1,14,16-Trimethoxyaconitan-4-Yl 2-(Acetylamino)Benzoate
- (1A,14A,16B)-20-Ethyl-1,14,16-Trimethoxyaconitane-4,8,9-Triol 4-(2-Acetylamino)Benzoate)
- (1Alpha,10Alpha,13Alpha,14Alpha,16Beta,17Xi)-20-Ethyl-8,9-Dihydroxy-1,14,16-Trimethoxyaconitan-4-Yl 2-(Acetylamino)Benzoate
- 2H-12,3,6a-Ethanylylidene-7,9-methanonaphth[2,3-b]azocine, aconitane-4,8,9-triol deriv.
- Acetyl-10-deoxysepaconitine
- Aconitane-4,8,9-triol, 20-ethyl-1,14,16-trimethoxy-, 4-(2-acetylamino)benzoate), (1-alpha,14-alpha,16-beta)-
- Aconitane-4,8,9-triol, 20-ethyl-1,14,16-trimethoxy-, 4-[2-(acetylamino)benzoate], (1α,14α,16β)-
- Brn 0072755
- Lannaconitine
- Lappaconitine
- 5-21-06-00291 (Beilstein Handbook Reference)
Sort by
Purity (%)
0
100
|
0
|
50
|
90
|
95
|
100
Found 8 products.
Lappaconitine Hydrobromide
CAS:Formula:C32H44N2O8·HBrPurity:>95.0%(N)Color and Shape:White to Light yellow powder to crystalMolecular weight:665.62Lappaconitine
CAS:<p>Lappaconitine ((+)-Lappaconitine), isolated from Aconitum sinomontanum Nakai, was characterized as an analgesic.</p>Formula:C32H44N2O8Purity:99.68%Color and Shape:White PowderMolecular weight:584.7Lappaconitine
CAS:Formula:C32H44N2O8Purity:>98.0%(HPLC)Color and Shape:White to Light yellow powder to crystalMolecular weight:584.71Lappaconitine
CAS:Controlled Product<p>Traditionally used for pain relief, lappaconitine is a plant-derived C18-diterpenoid alkaloid. The molecular structure of lappaconitine was first reported in 1895. In rats, the antinociceptive action of lappaconitine has been shown to be based on the enhanced expression of dynorphin A in the spinal microglia. Lappaconitine hydrobromide is clinically used to reduce swelling and inflammation while providing a local anesthetic effect.</p>Formula:C32H44N2O8Purity:Min. 98 Area-%Color and Shape:PowderMolecular weight:584.7 g/mol(+)-Lappaconitine >90%
CAS:Controlled Product<p>Stability Hygroscopic<br>Applications (+)-Lappaconitine is 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);<br></p>Formula:C32H44N2O8Purity:>90%Color and Shape:NeatMolecular weight:584.70






