LAPPACONITINE HYDROBROMIDE

Details

Stereochemistry	ABSOLUTE
Molecular Formula	C32H44N2O8.BrH
Molecular Weight	665.612
Optical Activity	UNSPECIFIED
Defined Stereocenters	12 / 12
E/Z Centers	0
Charge	0

SHOW SMILES / InChI

Structure Search

SMILES

Br.[H][C@@]12C[C@H]3[C@H](OC)[C@]1(O)[C@](O)(C[C@@H]3OC)[C@H]4C[C@H]5[C@@]26[C@H](CC[C@]5(CN(CC)[C@]46[H])OC(=O)C7=C(NC(C)=O)C=CC=C7)OC

InChI

InChIKey=CFFYROOPXPKMEQ-IPZKEBFRSA-N

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

HIDE SMILES / InChI

Molecular Formula	C32H44N2O8
Molecular Weight	584.7004
Charge	0
Count

Stereochemistry	ABSOLUTE
Additional Stereochemistry	No
Defined Stereocenters	11 / 12
E/Z Centers	0
Optical Activity	UNSPECIFIED

Molecular Formula	BrH
Molecular Weight	80.912
Charge	0
Count

Stereochemistry	ACHIRAL
Additional Stereochemistry	No
Defined Stereocenters	0 / 0
E/Z Centers	0
Optical Activity	NONE

Description
Sources: https://www.ncbi.nlm.nih.gov/pubmed/28463565 | https://www.ncbi.nlm.nih.gov/pubmed/25796978 | https://www.ncbi.nlm.nih.gov/pubmed/3207434 | http://en.pharmacodia.com/web/drug/1_21542.htmlhttp://www.rlsnet.ru/tn_index_id_73352.htm

Lappaconitine is an alkaloid isolated from the root of Aconltitum sinomantanum Nakai. It has a strong analgesic activity that does not involve the opioid receptor. It was shown to have class-I antiarrhythmic action and irreversibly blocks cloned human heart (hH1) channels by binding to the site 2 receptor.

CNS Activity

Originator

Approval Year

Targets

Primary Target	Pharmacology	Potency
Acetylcholinesterase 207 Target ID: CHEMBL220 Sources: https://www.ncbi.nlm.nih.gov/pubmed/28463565	Inhibitor 8297	6.13 µM [IC50]
sodium channel activity 16 Target ID: GO:0005272 Sources: https://www.ncbi.nlm.nih.gov/pubmed/9459571 \| https://www.ncbi.nlm.nih.gov/pubmed/20594622	Inhibitor 8297	14.1 µM [IC50]
P2X purinoceptor 3 9 Target ID: CHEMBL4824 Sources: https://www.ncbi.nlm.nih.gov/pubmed/21272608	Antagonist 2778
Sodium channel protein type V alpha subunit 49 Target ID: CHEMBL1980 Sources: https://www.ncbi.nlm.nih.gov/pubmed/11160852	Blocker 537
Sodium channel protein type V alpha subunit 49 Target ID: CHEMBL1980 Sources: https://www.ncbi.nlm.nih.gov/pubmed/11160852	Blocker 537

Conditions

Condition	Modality	Highest Phase	Product
Pain 614 Sources: https://www.ncbi.nlm.nih.gov/pubmed/3207434 https://www.ncbi.nlm.nih.gov/pubmed/21272608	Primary	Phase I 428	Unknown Approved Use Unknown
Arrhythmia 38 Sources: http://en.pharmacodia.com/web/drug/1_21542.html http://adisinsight.springer.com/drugs/800002254	Primary	Phase II 1132	Unknown Approved Use Unknown
Postoperative pain 22 Sources: https://www.ncbi.nlm.nih.gov/pubmed/26242116	Palliative	Phase II 1132	Unknown Approved Use Unknown
Pre-excitation syndromes 3 Sources: http://www.rlsnet.ru/tn_index_id_4134.htm	Primary	Approved 8429	ALLAPININ Approved Use Excerts membrane stabilizing action, influences sodium channels, belongs to IC class of antiarrhythmic agents. Causes slowing of atrioventricular and intraventricular condution, shortens the effective and functional refractory periods in the atria and ventricles. Does does not affect the duration of the interval QT, conductivity in the AV node anterograde direction, heart rate and blood pressure, myocardial contractility (in the absence of heart failure events). Provides moderate antispasmodic, vasodilating, cholinolytic and sedative effect.
Supraventricular tachycardia 8 Sources: http://www.rlsnet.ru/tn_index_id_4134.htm	Primary	Approved 8429	ALLAPININ Approved Use Excerts membrane stabilizing action, influences sodium channels, belongs to IC class of antiarrhythmic agents. Causes slowing of atrioventricular and intraventricular condution, shortens the effective and functional refractory periods in the atria and ventricles. Does does not affect the duration of the interval QT, conductivity in the AV node anterograde direction, heart rate and blood pressure, myocardial contractility (in the absence of heart failure events). Provides moderate antispasmodic, vasodilating, cholinolytic and sedative effect.
Premature depolarization, unspecified 3 Sources: http://www.rlsnet.ru/tn_index_id_4134.htm	Primary	Approved 8429	ALLAPININ Approved Use Excerts membrane stabilizing action, influences sodium channels, belongs to IC class of antiarrhythmic agents. Causes slowing of atrioventricular and intraventricular condution, shortens the effective and functional refractory periods in the atria and ventricles. Does does not affect the duration of the interval QT, conductivity in the AV node anterograde direction, heart rate and blood pressure, myocardial contractility (in the absence of heart failure events). Provides moderate antispasmodic, vasodilating, cholinolytic and sedative effect.
Atrial fibrillation and flutter 3 Sources: http://www.rlsnet.ru/tn_index_id_4134.htm	Primary	Approved 8429	ALLAPININ Approved Use Excerts membrane stabilizing action, influences sodium channels, belongs to IC class of antiarrhythmic agents. Causes slowing of atrioventricular and intraventricular condution, shortens the effective and functional refractory periods in the atria and ventricles. Does does not affect the duration of the interval QT, conductivity in the AV node anterograde direction, heart rate and blood pressure, myocardial contractility (in the absence of heart failure events). Provides moderate antispasmodic, vasodilating, cholinolytic and sedative effect.
Ventricular tachycardia 11 Sources: http://www.rlsnet.ru/tn_index_id_4134.htm	Primary	Approved 8429	ALLAPININ Approved Use Excerts membrane stabilizing action, influences sodium channels, belongs to IC class of antiarrhythmic agents. Causes slowing of atrioventricular and intraventricular condution, shortens the effective and functional refractory periods in the atria and ventricles. Does does not affect the duration of the interval QT, conductivity in the AV node anterograde direction, heart rate and blood pressure, myocardial contractility (in the absence of heart failure events). Provides moderate antispasmodic, vasodilating, cholinolytic and sedative effect.

PubMed

Title	Date	PubMed
Pharmacological studies of lappaconitine. Analgesic activities.	1988 Jul	3207434
Irreversible block of human heart (hH1) sodium channels by the plant alkaloid lappaconitine.	2001 Feb	11160852
Comparative metabolism of Lappaconitine in rat and human liver microsomes and in vivo of rat using ultra high-performance liquid chromatography-quadrupole/time-of-flight mass spectrometry.	2015 Jun 10	25796978
Selective dual cholinesterase inhibitors from Aconitum laeve.	2018 Feb	28463565

Patents

Sample Use Guides

In Vivo Use Guide

Lappaconitine (8 mg) was intravenously dripped to patients in the lappaconitine group 30 min before ending the operation. PCIA started as soon as the end of the surgery and the total dose of lappaconitine was 36 mg.

Route of Administration: Intravenous

In Vitro Use Guide

Right isolated guinea-pig atria became bradycardic at 3 uM lappaconitine, and at 4.5 uM one of six right atria ceased contracting. Asystolia was also observed in left atria at concentrations about 600 nM, but all of the asystolic atria resumed contraction as the stimulation current was increased, indicating an elevation of the excitation threshold.

Substance Class	Chemical Created by `admin` on `Sat Dec 16 05:00:43 UTC 2023` Edited by `admin` on `Sat Dec 16 05:00:43 UTC 2023`
Record UNII	HTD60494V5
Record Status	`Validated (UNII)`
Record Version

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Name

Type

Language

LAPPACONITINE HYDROBROMIDE

Common Name

English

ALLAFORT

Common Name

English

ACONITANE-4,8,9-TRIOL, 20-ETHYL-1,14,16-TRIMETHOXY-, 4-(2-(ACETYLAMINO)BENZOATE), MONOHYDROBROMIDE, (1.ALPHA.,14.ALPHA.,16.BETA.)-

Systematic Name

English

ALLAPININE

Common Name

English

ACONITANE-4,8,9-TRIOL, 20-ETHYL-1,14,16-TRIMETHOXY-, 4-(2-(ACETYLAMINO)BENZOATE), HYDROBROMIDE (1:1), (1.ALPHA.,14.ALPHA.,16.BETA.)-

Systematic Name

English

Lappaconitine hydrobromide [WHO-DD]

Common Name

English

Code System Code Type Description

PUBCHEM

90479363