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Details

Stereochemistry ABSOLUTE
Molecular Formula C24H39N3O3
Molecular Weight 417.5848
Optical Activity UNSPECIFIED
Defined Stereocenters 1 / 1
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of IDAVERINE

SMILES

CCN(CCCC(=O)N1CCC(CC1)C(=O)N(C)C)[C@@H](C)CC2=CC=C(OC)C=C2

InChI

InChIKey=FUWZBLSXACKFQX-IBGZPJMESA-N
InChI=1S/C24H39N3O3/c1-6-26(19(2)18-20-9-11-22(30-5)12-10-20)15-7-8-23(28)27-16-13-21(14-17-27)24(29)25(3)4/h9-12,19,21H,6-8,13-18H2,1-5H3/t19-/m0/s1

HIDE SMILES / InChI

Molecular Formula C24H39N3O3
Molecular Weight 417.5848
Charge 0
Count
Stereochemistry ABSOLUTE
Additional Stereochemistry No
Defined Stereocenters 1 / 1
E/Z Centers 0
Optical Activity UNSPECIFIED

Idaverine, a muscarinic M2 receptor antagonist, that didn’t prevent motion sickness of cats. Clinical trials for human have shown that the compound was well tolerated.

Approval Year

PubMed

PubMed

TitleDatePubMed
Contraction of guinea-pig gallbladder: muscarinic M3 or M4 receptors?
1997-07-30
Involvement of muscarinic M2 and M3, but not of M1 and M4 receptors in vagally stimulated contractions of rabbit bronchus/trachea.
1994-04
Patents

Sample Use Guides

idaverine was studied in an open, cross-over, partially randomized design after single oral (2 mg) and intravenous (1 and 2 mg doses to 12 healthy male subjects.
Route of Administration: Other
Substance Class Chemical
Created
by admin
on Mon Mar 31 17:51:01 GMT 2025
Edited
by admin
on Mon Mar 31 17:51:01 GMT 2025
Record UNII
U6212R3SLC
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
(+)-1-(4-(ETHYL((S)-P-METHOXY-.ALPHA.-METHYLPHENETHYL)AMINO)BUTYRYL)-N,N-DIMETHYLISONIPECOTAMIDE
Preferred Name English
IDAVERINE
INN  
INN  
Official Name English
idaverine [INN]
Common Name English
Classification Tree Code System Code
NCI_THESAURUS C29698
Created by admin on Mon Mar 31 17:51:01 GMT 2025 , Edited by admin on Mon Mar 31 17:51:01 GMT 2025
Code System Code Type Description
EVMPD
SUB08112MIG
Created by admin on Mon Mar 31 17:51:01 GMT 2025 , Edited by admin on Mon Mar 31 17:51:01 GMT 2025
PRIMARY
PUBCHEM
10341921
Created by admin on Mon Mar 31 17:51:01 GMT 2025 , Edited by admin on Mon Mar 31 17:51:01 GMT 2025
PRIMARY
ChEMBL
CHEMBL2106340
Created by admin on Mon Mar 31 17:51:01 GMT 2025 , Edited by admin on Mon Mar 31 17:51:01 GMT 2025
PRIMARY
FDA UNII
U6212R3SLC
Created by admin on Mon Mar 31 17:51:01 GMT 2025 , Edited by admin on Mon Mar 31 17:51:01 GMT 2025
PRIMARY
MESH
C073809
Created by admin on Mon Mar 31 17:51:01 GMT 2025 , Edited by admin on Mon Mar 31 17:51:01 GMT 2025
PRIMARY
CAS
100927-13-7
Created by admin on Mon Mar 31 17:51:01 GMT 2025 , Edited by admin on Mon Mar 31 17:51:01 GMT 2025
PRIMARY
SMS_ID
100000083675
Created by admin on Mon Mar 31 17:51:01 GMT 2025 , Edited by admin on Mon Mar 31 17:51:01 GMT 2025
PRIMARY
EPA CompTox
DTXSID80881410
Created by admin on Mon Mar 31 17:51:01 GMT 2025 , Edited by admin on Mon Mar 31 17:51:01 GMT 2025
PRIMARY
INN
5956
Created by admin on Mon Mar 31 17:51:01 GMT 2025 , Edited by admin on Mon Mar 31 17:51:01 GMT 2025
PRIMARY
NCI_THESAURUS
C97988
Created by admin on Mon Mar 31 17:51:01 GMT 2025 , Edited by admin on Mon Mar 31 17:51:01 GMT 2025
PRIMARY
Related Record Type Details
ACTIVE MOIETY