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

Details

Stereochemistry ABSOLUTE
Molecular Formula C24H34N2O2.2ClH
Molecular Weight 455.461
Optical Activity UNSPECIFIED
Defined Stereocenters 5 / 5
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of EUPROCIN HYDROCHLORIDE

SMILES

Cl.Cl.[H][C@]1(C[C@@H]2CC[N@]1C[C@@H]2CC)[C@H](O)C3=C4C=C(OCCC(C)C)C=CC4=NC=C3

InChI

InChIKey=SIEYZYONZYIIJH-AGSMNRHJSA-N
InChI=1S/C24H34N2O2.2ClH/c1-4-17-15-26-11-8-18(17)13-23(26)24(27)20-7-10-25-22-6-5-19(14-21(20)22)28-12-9-16(2)3;;/h5-7,10,14,16-18,23-24,27H,4,8-9,11-13,15H2,1-3H3;2*1H/t17-,18-,23-,24+;;/m0../s1

HIDE SMILES / InChI

Molecular Formula C24H34N2O2
Molecular Weight 382.539
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

EUPROCIN, a cupreine derivative, is a local anesthetic.

Approval Year

PubMed

PubMed

TitleDatePubMed
Patents

Patents

Substance Class Chemical
Created
by admin
on Fri Dec 15 15:28:54 GMT 2023
Edited
by admin
on Fri Dec 15 15:28:54 GMT 2023
Record UNII
EVA0339N2N
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
EUPROCIN HYDROCHLORIDE
USAN  
USAN  
Official Name English
O(SUP 6)'-ISOPENTYLHYDROCUPREINE DIHYDROCHLORIDE
Common Name English
EUPROCIN HCL
Common Name English
CINCHONAN-9-OL, 10,11-DIHYDRO-6'-(3-METHYLBUTOXY)-, DIHYDROCHLORIDE, (8.ALPHA.,9R)-
Common Name English
EUPROCIN HYDROCHLORIDE [USAN]
Common Name English
WL-287
Code English
WL 287
Code English
Classification Tree Code System Code
NCI_THESAURUS C245
Created by admin on Fri Dec 15 15:28:54 GMT 2023 , Edited by admin on Fri Dec 15 15:28:54 GMT 2023
Code System Code Type Description
NCI_THESAURUS
C75096
Created by admin on Fri Dec 15 15:28:54 GMT 2023 , Edited by admin on Fri Dec 15 15:28:54 GMT 2023
PRIMARY
ChEMBL
CHEMBL2110608
Created by admin on Fri Dec 15 15:28:54 GMT 2023 , Edited by admin on Fri Dec 15 15:28:54 GMT 2023
PRIMARY
PUBCHEM
68544
Created by admin on Fri Dec 15 15:28:54 GMT 2023 , Edited by admin on Fri Dec 15 15:28:54 GMT 2023
PRIMARY
CAS
18984-80-0
Created by admin on Fri Dec 15 15:28:54 GMT 2023 , Edited by admin on Fri Dec 15 15:28:54 GMT 2023
PRIMARY
FDA UNII
EVA0339N2N
Created by admin on Fri Dec 15 15:28:54 GMT 2023 , Edited by admin on Fri Dec 15 15:28:54 GMT 2023
PRIMARY
EPA CompTox
DTXSID10940509
Created by admin on Fri Dec 15 15:28:54 GMT 2023 , Edited by admin on Fri Dec 15 15:28:54 GMT 2023
PRIMARY
Related Record Type Details
PARENT -> SALT/SOLVATE
Related Record Type Details
ACTIVE MOIETY