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Details

Stereochemistry ABSOLUTE
Molecular Formula C26H35N3O5.2ClH
Molecular Weight 542.495
Optical Activity UNSPECIFIED
Defined Stereocenters 4 / 4
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of DIMETHYLAMINOETHYL RESERPILINATE DIHYDROCHLORIDE

SMILES

Cl.Cl.COC1=C(OC)C=C2C(NC3=C2CCN4C[C@H]5[C@H](C)OC=C([C@H]5C[C@H]34)C(=O)OCCN(C)C)=C1

InChI

InChIKey=RDKIYVYHCBJDMF-DGCKWTARSA-N
InChI=1S/C26H35N3O5.2ClH/c1-15-19-13-29-7-6-16-18-11-23(31-4)24(32-5)12-21(18)27-25(16)22(29)10-17(19)20(14-34-15)26(30)33-9-8-28(2)3;;/h11-12,14-15,17,19,22,27H,6-10,13H2,1-5H3;2*1H/t15-,17-,19-,22+;;/m0../s1

HIDE SMILES / InChI

Molecular Formula C26H35N3O5
Molecular Weight 469.5732
Charge 0
Count
Stereochemistry ABSOLUTE
Additional Stereochemistry No
Defined Stereocenters 4 / 4
E/Z Centers 0
Optical Activity UNSPECIFIED

Molecular Formula ClH
Molecular Weight 36.461
Charge 0
Count
Stereochemistry ACHIRAL
Additional Stereochemistry No
Defined Stereocenters 0 / 0
E/Z Centers 0
Optical Activity NONE

Description
Curator's Comment: description was created based on several sources, including https://www.ncbi.nlm.nih.gov/pubmed/5977060 | https://www.ncbi.nlm.nih.gov/pubmed/13959902

Dimethylaminoethyl reserpilinate is reserpilinate derivative with hypotensive activity. Given subcutaneously to rats in doses 200 mg/kg dimethylaminoethane reserpilinate increased very slightly the gastric motility but showed no ulcerogenic effect.

Originator

Sources: Bulletin de l'Academie Royale de Medecine de Belgique, Volume 25, Pages 586-601, Journal, 1960

Approval Year

Conditions

Conditions

ConditionModalityTargetsHighest PhaseProduct
PubMed

PubMed

TitleDatePubMed
[Effects of dimethylaminoethyl reserpilinate on the stomach in rats].
1966-10
Patents

Patents

Sample Use Guides

200 mg/kg
Route of Administration: Other
In Vitro Use Guide
Unknown
Substance Class Chemical
Created
by admin
on Mon Mar 31 18:18:28 GMT 2025
Edited
by admin
on Mon Mar 31 18:18:28 GMT 2025
Record UNII
D1301HM9JD
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
DIMETHYLAMINOETHYLRESERPILINATE HCL
WHO-DD  
Preferred Name English
DIMETHYLAMINOETHYL RESERPILINATE DIHYDROCHLORIDE
JAN  
Common Name English
RESERPILIC ACID DIMETHYLAMINOETHYL ESTER DIHYDROCHLORIDE [MI]
Common Name English
RESERPILIC ACID DIMETHYLAMINOETHYL ESTER DIHYDROCHLORIDE
MI  
Common Name English
PARATENSIOL
Brand Name English
RESPORISAN
Brand Name English
DIMETHYLAMINOETHYL RESERPILINATE DIHYDROCHLORIDE [JAN]
Common Name English
Dimethylaminoethylreserpilinate hcl [WHO-DD]
Common Name English
DIMETHYLAMINOETHYL 16,17-DIDEHYDRO-10,11-DIMETHOXY-19.ALPHA.-METHYL-3.BETA.,20.ALPHA.-OXAYOHIMBAN-16-CARBOXYLATE DIHYDROCHLORIDE
Common Name English
Classification Tree Code System Code
NCI_THESAURUS C270
Created by admin on Mon Mar 31 18:18:28 GMT 2025 , Edited by admin on Mon Mar 31 18:18:28 GMT 2025
Code System Code Type Description
FDA UNII
D1301HM9JD
Created by admin on Mon Mar 31 18:18:28 GMT 2025 , Edited by admin on Mon Mar 31 18:18:28 GMT 2025
PRIMARY
EVMPD
SUB13612MIG
Created by admin on Mon Mar 31 18:18:28 GMT 2025 , Edited by admin on Mon Mar 31 18:18:28 GMT 2025
PRIMARY
CAS
3735-84-0
Created by admin on Mon Mar 31 18:18:28 GMT 2025 , Edited by admin on Mon Mar 31 18:18:28 GMT 2025
PRIMARY
SMS_ID
100000079230
Created by admin on Mon Mar 31 18:18:28 GMT 2025 , Edited by admin on Mon Mar 31 18:18:28 GMT 2025
PRIMARY
EPA CompTox
DTXSID30958464
Created by admin on Mon Mar 31 18:18:28 GMT 2025 , Edited by admin on Mon Mar 31 18:18:28 GMT 2025
PRIMARY
ECHA (EC/EINECS)
223-102-9
Created by admin on Mon Mar 31 18:18:28 GMT 2025 , Edited by admin on Mon Mar 31 18:18:28 GMT 2025
PRIMARY
MERCK INDEX
m9534
Created by admin on Mon Mar 31 18:18:28 GMT 2025 , Edited by admin on Mon Mar 31 18:18:28 GMT 2025
PRIMARY Merck Index
ChEMBL
CHEMBL2106350
Created by admin on Mon Mar 31 18:18:28 GMT 2025 , Edited by admin on Mon Mar 31 18:18:28 GMT 2025
PRIMARY
NCI_THESAURUS
C83676
Created by admin on Mon Mar 31 18:18:28 GMT 2025 , Edited by admin on Mon Mar 31 18:18:28 GMT 2025
PRIMARY
PUBCHEM
71463
Created by admin on Mon Mar 31 18:18:28 GMT 2025 , Edited by admin on Mon Mar 31 18:18:28 GMT 2025
PRIMARY
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PARENT -> SALT/SOLVATE
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ACTIVE MOIETY