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Details

Stereochemistry ACHIRAL
Molecular Formula C18H27NO4
Molecular Weight 321.4113
Optical Activity NONE
Defined Stereocenters 0 / 0
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of ETOXERIDINE

SMILES

CCOC(=O)C1(CCN(CCOCCO)CC1)C2=CC=CC=C2

InChI

InChIKey=KJTKYGFGPQSRRA-UHFFFAOYSA-N
InChI=1S/C18H27NO4/c1-2-23-17(21)18(16-6-4-3-5-7-16)8-10-19(11-9-18)12-14-22-15-13-20/h3-7,20H,2,8-15H2,1H3

HIDE SMILES / InChI

Molecular Formula C18H27NO4
Molecular Weight 321.4113
Charge 0
Count
Stereochemistry ACHIRAL
Additional Stereochemistry No
Defined Stereocenters 0 / 0
E/Z Centers 0
Optical Activity NONE

Etoxeridine (Carbetidine or Wy2039), a piperidine derivative, is a narcotic analgetic.

Originator

Curator's Comment: refernce retrieved from https://link.springer.com/chapter/10.1007%2F978-1-4757-2085-3_5

Approval Year

PubMed

PubMed

TitleDatePubMed
[Pharmacological study of carbetidine, a new synthetic analgesic].
1958 May 1
Studies on the respiratory and circulatory effects of carbetidine HCI used for supplementation of thiopentone sodium-nitrous oxide-oxygen anaesthesia.
1959 Aug
[Brief note on a new synthetic analgesic: carbetidine hydrochloride].
1959 Jun
Patents
Substance Class Chemical
Created
by admin
on Sat Dec 16 16:47:22 UTC 2023
Edited
by admin
on Sat Dec 16 16:47:22 UTC 2023
Record UNII
RHW35E1G7E
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
ETOXERIDINE
INN  
INN  
Official Name English
etoxeridine [INN]
Common Name English
UCB 2073
Code English
WY-2039
Code English
1-(2-(2-HYDROXYETHOXY)ETHYL)-4-PHENYLPIPERIDINE-4-CARBOXYLIC ACID ETHYL ESTER
Systematic Name English
CARBETIDINE
Common Name English
UCB-2073
Code English
IDS-NE-008
Code English
4-PIPERIDINECARBOXYLIC ACID, 1-(2-(2-HYDROXYETHOXY)ETHYL)-4-PHENYL-, ETHYL ESTER
Systematic Name English
Classification Tree Code System Code
NCI_THESAURUS C241
Created by admin on Sat Dec 16 16:47:22 UTC 2023 , Edited by admin on Sat Dec 16 16:47:22 UTC 2023
DEA NO. 9625
Created by admin on Sat Dec 16 16:47:22 UTC 2023 , Edited by admin on Sat Dec 16 16:47:22 UTC 2023
Code System Code Type Description
EPA CompTox
DTXSID30196980
Created by admin on Sat Dec 16 16:47:22 UTC 2023 , Edited by admin on Sat Dec 16 16:47:22 UTC 2023
PRIMARY
FDA UNII
RHW35E1G7E
Created by admin on Sat Dec 16 16:47:22 UTC 2023 , Edited by admin on Sat Dec 16 16:47:22 UTC 2023
PRIMARY
SMS_ID
100000082114
Created by admin on Sat Dec 16 16:47:22 UTC 2023 , Edited by admin on Sat Dec 16 16:47:22 UTC 2023
PRIMARY
INN
726
Created by admin on Sat Dec 16 16:47:22 UTC 2023 , Edited by admin on Sat Dec 16 16:47:22 UTC 2023
PRIMARY
WIKIPEDIA
ETOXERIDINE
Created by admin on Sat Dec 16 16:47:22 UTC 2023 , Edited by admin on Sat Dec 16 16:47:22 UTC 2023
PRIMARY
DRUG BANK
DB01505
Created by admin on Sat Dec 16 16:47:22 UTC 2023 , Edited by admin on Sat Dec 16 16:47:22 UTC 2023
PRIMARY
CFR
21 CFR 1308.11
Created by admin on Sat Dec 16 16:47:22 UTC 2023 , Edited by admin on Sat Dec 16 16:47:22 UTC 2023
PRIMARY (a) Schedule I shall consist of the drugs and other substances, by whatever official name, common or usual name, chemical name, or brand name designated, listed in this section. Each drug or substance has been assigned the DEA Controlled Substances Code Number set forth opposite it. (b)Opiates. Unless specifically excepted or unless listed in another schedule, any of the following opiates, including their isomers, esters, ethers, salts, and salts of isomers, esters and ethers, whenever the existence of such isomers, esters, ethers and salts is possible within the specific chemical designation (for purposes of paragraph (b)(34) only, the term isomer includes the optical and geometric isomers):
NCI_THESAURUS
C65599
Created by admin on Sat Dec 16 16:47:22 UTC 2023 , Edited by admin on Sat Dec 16 16:47:22 UTC 2023
PRIMARY
EVMPD
SUB07343MIG
Created by admin on Sat Dec 16 16:47:22 UTC 2023 , Edited by admin on Sat Dec 16 16:47:22 UTC 2023
PRIMARY
CAS
469-82-9
Created by admin on Sat Dec 16 16:47:22 UTC 2023 , Edited by admin on Sat Dec 16 16:47:22 UTC 2023
PRIMARY
ChEMBL
CHEMBL2104254
Created by admin on Sat Dec 16 16:47:22 UTC 2023 , Edited by admin on Sat Dec 16 16:47:22 UTC 2023
PRIMARY
ECHA (EC/EINECS)
207-423-1
Created by admin on Sat Dec 16 16:47:22 UTC 2023 , Edited by admin on Sat Dec 16 16:47:22 UTC 2023
PRIMARY
PUBCHEM
61122
Created by admin on Sat Dec 16 16:47:22 UTC 2023 , Edited by admin on Sat Dec 16 16:47:22 UTC 2023
PRIMARY
Related Record Type Details
PARENT -> SALT/SOLVATE
SALT/SOLVATE -> PARENT
APPROXIMATE PURE ANHYDROUS DRUG CONTENT (IN PERCENT)
Related Record Type Details
ACTIVE MOIETY