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Details

Stereochemistry RACEMIC
Molecular Formula 2C10H20NO4.C10H6O6S2
Molecular Weight 722.821
Optical Activity ( + / - )
Defined Stereocenters 0 / 2
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of ACLATONIUM NAPADISILATE

SMILES

CC(OC(C)=O)C(=O)OCC[N+](C)(C)C.CC(OC(C)=O)C(=O)OCC[N+](C)(C)C.[O-]S(=O)(=O)C1=CC=CC2=C(C=CC=C12)S([O-])(=O)=O

InChI

InChIKey=HELVYVGHOJPCEV-UHFFFAOYSA-L
InChI=1S/2C10H20NO4.C10H8O6S2/c2*1-8(15-9(2)12)10(13)14-7-6-11(3,4)5;11-17(12,13)9-5-1-3-7-8(9)4-2-6-10(7)18(14,15)16/h2*8H,6-7H2,1-5H3;1-6H,(H,11,12,13)(H,14,15,16)/q2*+1;/p-2

HIDE SMILES / InChI

Molecular Formula C10H20NO4
Molecular Weight 218.2701
Charge 1
Count
Stereochemistry MIXED
Additional Stereochemistry No
Defined Stereocenters 0 / 1
E/Z Centers 0
Optical Activity ( + / - )

Molecular Formula C10H6O6S2
Molecular Weight 286.281
Charge -2
Count
Stereochemistry ACHIRAL
Additional Stereochemistry No
Defined Stereocenters 0 / 0
E/Z Centers 0
Optical Activity NONE

Aclatonium (also known as aclatonium napadisilate) is a cholinergic agonist that has been developed and used in Asia as an activator of gastrointestinal motility.

Approval Year

Conditions

Conditions

ConditionModalityTargetsHighest PhaseProduct
PubMed

PubMed

TitleDatePubMed
Patents

Patents

Sample Use Guides

In Vivo Use Guide
Aclatonium should be given at the dosage of 300 mg/day.
Route of Administration: Other
The effect of aclotonium on exocrine pancreatic secretion and insulin release was investigated in the isolated, perfused rat pancreas. The effect of the drug on insulin release was detectable at a concentration of 0.1uM, while the increase in exocrine secretion was observed at 1.0 uM.
Substance Class Chemical
Created
by admin
on Fri Dec 15 17:28:34 GMT 2023
Edited
by admin
on Fri Dec 15 17:28:34 GMT 2023
Record UNII
YX23434YHQ
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
ACLATONIUM NAPADISILATE
INN   JAN   MART.   MI   WHO-DD  
INN  
Official Name English
1,5-NAPHTHALENEDISULFONIC ACID, ION(2-), BIS(2-(2-(ACETYLOXY)-1-OXOPROPOXY)-N,N,N-TRIMETHYLETHANAMINIUM)
Common Name English
CHOLINE 1,5-NAPHTHALENEDISULPHONATE (2:1), DILACTATE, DIACETATE
Common Name English
ACLATONIUM NAPADISILATE [MI]
Common Name English
ETHANAMINIUM, 2-(2-(ACETYLOXY)-1-OXOPROPOXY)-N,N,N-TRIMETHYL-, 1,5-NAPHTHALENEDISULFONATE (2:1)
Common Name English
ETHANAMINIUM, 2-(2-(ACETYLOXY)-1-OXOPROPOXY)-N,N,N-TRIMETHYL-, 1,5-NAPHTHALENEDISULPHONATE (2:1)
Common Name English
aclatonium napadisilate [INN]
Common Name English
Aclatonium napadisilate [WHO-DD]
Common Name English
ACLATONIUM NAPADISILATE [MART.]
Common Name English
ACLATONIUM NAPADISILATE [JAN]
Common Name English
TM 723
Code English
ACLATONIUM NAPADISYLATE
Common Name English
TM-723
Code English
CHOLINE 1,5-NAPHTHALENEDISULFONATE (2:1), DILACTATE, DIACETATE
Common Name English
Classification Tree Code System Code
NCI_THESAURUS C47796
Created by admin on Fri Dec 15 17:28:34 GMT 2023 , Edited by admin on Fri Dec 15 17:28:34 GMT 2023
Code System Code Type Description
FDA UNII
YX23434YHQ
Created by admin on Fri Dec 15 17:28:34 GMT 2023 , Edited by admin on Fri Dec 15 17:28:34 GMT 2023
PRIMARY
CAS
55077-30-0
Created by admin on Fri Dec 15 17:28:34 GMT 2023 , Edited by admin on Fri Dec 15 17:28:34 GMT 2023
PRIMARY
NCI_THESAURUS
C91037
Created by admin on Fri Dec 15 17:28:34 GMT 2023 , Edited by admin on Fri Dec 15 17:28:34 GMT 2023
PRIMARY
PUBCHEM
6918580
Created by admin on Fri Dec 15 17:28:34 GMT 2023 , Edited by admin on Fri Dec 15 17:28:34 GMT 2023
PRIMARY
INN
4832
Created by admin on Fri Dec 15 17:28:34 GMT 2023 , Edited by admin on Fri Dec 15 17:28:34 GMT 2023
PRIMARY
SMS_ID
100000084606
Created by admin on Fri Dec 15 17:28:34 GMT 2023 , Edited by admin on Fri Dec 15 17:28:34 GMT 2023
PRIMARY
ChEMBL
CHEMBL2110902
Created by admin on Fri Dec 15 17:28:34 GMT 2023 , Edited by admin on Fri Dec 15 17:28:34 GMT 2023
PRIMARY
EVMPD
SUB05244MIG
Created by admin on Fri Dec 15 17:28:34 GMT 2023 , Edited by admin on Fri Dec 15 17:28:34 GMT 2023
PRIMARY
EPA CompTox
DTXSID7048665
Created by admin on Fri Dec 15 17:28:34 GMT 2023 , Edited by admin on Fri Dec 15 17:28:34 GMT 2023
PRIMARY
MERCK INDEX
m1375
Created by admin on Fri Dec 15 17:28:34 GMT 2023 , Edited by admin on Fri Dec 15 17:28:34 GMT 2023
PRIMARY Merck Index
Related Record Type Details
PARENT -> SALT/SOLVATE
Related Record Type Details
ACTIVE MOIETY