U.S. Department of Health & Human Services Divider Arrow National Institutes of Health Divider Arrow NCATS

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 of LAPPACONITINE HYDROBROMIDE

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

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

Unknown
139594
Targets

Targets

Primary TargetPharmacologyConditionPotency
Inhibitor
8297
 6.13 µM [IC50]
Inhibitor
8297
 14.1 µM [IC50]
Antagonist
2778
Blocker
537
Blocker
537
Conditions

Conditions

ConditionModalityTargetsHighest PhaseProduct
Primary
Phase I
428
Unknown

Approved Use

Unknown
Primary
Phase II
1132
Unknown

Approved Use

Unknown
Palliative
Phase II
1132
Unknown

Approved Use

Unknown
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.
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.
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.
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.
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

PubMed

TitleDatePubMed
Pharmacological studies of lappaconitine. Analgesic activities.
1988 Jul
Irreversible block of human heart (hH1) sodium channels by the plant alkaloid lappaconitine.
2001 Feb
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
Patents

Patents

RU2513580C1
3
RU2518742C2
3
US5290784
3
US5547956
3

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 GMT 2023
Edited
by admin
on Sat Dec 16 05:00:43 GMT 2023
Record UNII
HTD60494V5
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
LAPPACONITINE HYDROBROMIDE
WHO-DD  
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
Created by admin on Sat Dec 16 05:00:43 GMT 2023 , Edited by admin on Sat Dec 16 05:00:43 GMT 2023
PRIMARY
FDA UNII
HTD60494V5
Created by admin on Sat Dec 16 05:00:43 GMT 2023 , Edited by admin on Sat Dec 16 05:00:43 GMT 2023
PRIMARY
EPA CompTox
DTXSID10913652
Created by admin on Sat Dec 16 05:00:43 GMT 2023 , Edited by admin on Sat Dec 16 05:00:43 GMT 2023
PRIMARY
EVMPD
SUB32654
Created by admin on Sat Dec 16 05:00:43 GMT 2023 , Edited by admin on Sat Dec 16 05:00:43 GMT 2023
PRIMARY
SMS_ID
100000125921
Created by admin on Sat Dec 16 05:00:43 GMT 2023 , Edited by admin on Sat Dec 16 05:00:43 GMT 2023
PRIMARY
CAS
97792-45-5
Created by admin on Sat Dec 16 05:00:43 GMT 2023 , Edited by admin on Sat Dec 16 05:00:43 GMT 2023
PRIMARY
Related Record Type Details
Structure of LAPPACONITINE
PARENT -> SALT/SOLVATE
NIH
NCATS
PRIVACY ACT
ACCESSIBILITY
DISCLAIMER
HHS VULNERABILITY DISCLOSURE
For language access assistance, contact the NCATS Public Information Officer
National Center for Advancing Translational Sciences (NCATS),
6701 Democracy Boulevard, Bethesda MD 20892-4874 • 301-594-8966