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

Details

Stereochemistry RACEMIC
Molecular Formula C22H27N3O4.ClH
Molecular Weight 433.928
Optical Activity ( + / - )
Defined Stereocenters 0 / 1
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of DIPERODON HYDROCHLORIDE

SMILES

Cl.O=C(NC1=CC=CC=C1)OCC(CN2CCCCC2)OC(=O)NC3=CC=CC=C3

InChI

InChIKey=OWULVAZDMWJBLB-UHFFFAOYSA-N
InChI=1S/C22H27N3O4.ClH/c26-21(23-18-10-4-1-5-11-18)28-17-20(16-25-14-8-3-9-15-25)29-22(27)24-19-12-6-2-7-13-19;/h1-2,4-7,10-13,20H,3,8-9,14-17H2,(H,23,26)(H,24,27);1H

HIDE SMILES / InChI

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

Molecular Formula C22H27N3O4
Molecular Weight 397.4675
Charge 0
Count
Stereochemistry RACEMIC
Additional Stereochemistry No
Defined Stereocenters 0 / 1
E/Z Centers 0
Optical Activity ( + / - )

Description
Curator's Comment: https://books.google.ru/books?id=GEXMBQAAQBAJ&pg=PA126&lpg=PA126&dq=diperodon+hemorrhoids&source=bl&ots=bCxlkt8R8h&sig=WdZ_xvaAZOgtxGZ2fAgci9gfLh0&hl=ru&sa=X&ved=0ahUKEwjT0uyqqpXMAhVHQZoKHb3YDBgQ6AEIHzAA#v=onepage&q=diperodon%20hemorrhoids&f=false https://www.ncbi.nlm.nih.gov/pubmed/12367714 https://books.google.ru/books?id=07g30rxCA0EC&pg=PA112&lpg=PA112&dq=diperodon+was+discovered&source=bl&ots=KjNHtaThll&sig=8zuZga1hLvXSs0x_oezYLJkx02M&hl=ru&sa=X&ved=0ahUKEwiOxbXetZXMAhXJDywKHeqwACAQ6AEIPjAF#v=onepage&q=diperodon%20was%20discovered&f=false

Diperodon is one of several phenylurethane derivatives of dialkyl amino alcohols which have demonstrated significant local anaesthetic activity.

Approval Year

Doses

Doses

DosePopulationAdverse events​
1 % multiple, topical
Dose: 1 %
Route: topical
Route: multiple
Dose: 1 %
Sources:
unhealthy, 30
n = 1
Health Status: unhealthy
Condition: psoriasis
Age Group: 30
Sex: M
Population Size: 1
Sources:
Other AEs: Allergy...
AEs

AEs

AESignificanceDosePopulation
Allergy
1 % multiple, topical
Dose: 1 %
Route: topical
Route: multiple
Dose: 1 %
Sources:
unhealthy, 30
n = 1
Health Status: unhealthy
Condition: psoriasis
Age Group: 30
Sex: M
Population Size: 1
Sources:
Overview

Overview

CYP3A4CYP2C9CYP2D6hERG

OverviewOther

Other InhibitorOther SubstrateOther Inducer

Drug as perpetrator​

Drug as perpetrator​

TargetModalityActivityMetaboliteClinical evidence
yes
PubMed

PubMed

TitleDatePubMed
In vitro study of enzymatic hydrolysis of diperodon enantiomers in blood serum by two-dimensional LC.
2002 Oct 15
Patents

Patents

Sample Use Guides

In Vivo Use Guide
Unknown
Route of Administration: Unknown
In Vitro Use Guide
Unknown
Substance Class Chemical
Created
by admin
on Fri Dec 15 15:02:42 GMT 2023
Edited
by admin
on Fri Dec 15 15:02:42 GMT 2023
Record UNII
5YZ5R8I73Y
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
DIPERODON HYDROCHLORIDE
GREEN BOOK   MART.   MI   VANDF   WHO-DD  
Common Name English
DIPERODON HYDROCHLORIDE [GREEN BOOK]
Common Name English
DIPERODON HYDROCHLORIDE [MART.]
Common Name English
DIPERODON HYDROCHLORIDE [VANDF]
Common Name English
DIPERODON HYDROCHLORIDE [MI]
Common Name English
DIOTHANE HYDROCHLORIDE
Brand Name English
PROCTODON
Brand Name English
NSC-76069
Code English
DIPERODON HCL
Common Name English
Diperodon hydrochloride [WHO-DD]
Common Name English
1,2-PROPANEDIOL, 3-(1-PIPERIDINYL)-, 1,2-BIS(N-PHENYLCARBAMATE), HYDROCHLORIDE (1:1)
Systematic Name English
Classification Tree Code System Code
NCI_THESAURUS C245
Created by admin on Fri Dec 15 15:02:42 GMT 2023 , Edited by admin on Fri Dec 15 15:02:42 GMT 2023
Code System Code Type Description
MERCK INDEX
m148
Created by admin on Fri Dec 15 15:02:42 GMT 2023 , Edited by admin on Fri Dec 15 15:02:42 GMT 2023
PRIMARY Merck Index
ECHA (EC/EINECS)
208-659-8
Created by admin on Fri Dec 15 15:02:42 GMT 2023 , Edited by admin on Fri Dec 15 15:02:42 GMT 2023
PRIMARY
SMS_ID
100000079254
Created by admin on Fri Dec 15 15:02:42 GMT 2023 , Edited by admin on Fri Dec 15 15:02:42 GMT 2023
PRIMARY
EVMPD
SUB13620MIG
Created by admin on Fri Dec 15 15:02:42 GMT 2023 , Edited by admin on Fri Dec 15 15:02:42 GMT 2023
PRIMARY
NCI_THESAURUS
C75091
Created by admin on Fri Dec 15 15:02:42 GMT 2023 , Edited by admin on Fri Dec 15 15:02:42 GMT 2023
PRIMARY
PUBCHEM
10830
Created by admin on Fri Dec 15 15:02:42 GMT 2023 , Edited by admin on Fri Dec 15 15:02:42 GMT 2023
PRIMARY
DRUG BANK
DBSALT001677
Created by admin on Fri Dec 15 15:02:42 GMT 2023 , Edited by admin on Fri Dec 15 15:02:42 GMT 2023
PRIMARY
ChEMBL
CHEMBL2109119
Created by admin on Fri Dec 15 15:02:42 GMT 2023 , Edited by admin on Fri Dec 15 15:02:42 GMT 2023
PRIMARY
CAS
537-12-2
Created by admin on Fri Dec 15 15:02:42 GMT 2023 , Edited by admin on Fri Dec 15 15:02:42 GMT 2023
PRIMARY
FDA UNII
5YZ5R8I73Y
Created by admin on Fri Dec 15 15:02:42 GMT 2023 , Edited by admin on Fri Dec 15 15:02:42 GMT 2023
PRIMARY
RXCUI
133043
Created by admin on Fri Dec 15 15:02:42 GMT 2023 , Edited by admin on Fri Dec 15 15:02:42 GMT 2023
PRIMARY RxNorm
EPA CompTox
DTXSID1045324
Created by admin on Fri Dec 15 15:02:42 GMT 2023 , Edited by admin on Fri Dec 15 15:02:42 GMT 2023
PRIMARY
NSC
76069
Created by admin on Fri Dec 15 15:02:42 GMT 2023 , Edited by admin on Fri Dec 15 15:02:42 GMT 2023
PRIMARY
Related Record Type Details
PARENT -> SALT/SOLVATE
ENANTIOMER -> RACEMATE
ENANTIOMER -> RACEMATE
Related Record Type Details
ACTIVE MOIETY