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Details

Stereochemistry ABSOLUTE
Molecular Formula C14H26N4O3
Molecular Weight 298.3812
Optical Activity UNSPECIFIED
Defined Stereocenters 2 / 2
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of PAREPTIDE

SMILES

CC(C)C[C@@H](N(C)C(=O)[C@@H]1CCCN1)C(=O)NCC(N)=O

InChI

InChIKey=BXCQMQVEMFYKJC-WDEREUQCSA-N
InChI=1S/C14H26N4O3/c1-9(2)7-11(13(20)17-8-12(15)19)18(3)14(21)10-5-4-6-16-10/h9-11,16H,4-8H2,1-3H3,(H2,15,19)(H,17,20)/t10-,11+/m0/s1

HIDE SMILES / InChI

Molecular Formula C14H26N4O3
Molecular Weight 298.3812
Charge 0
Count
Stereochemistry ABSOLUTE
Additional Stereochemistry No
Defined Stereocenters 2 / 2
E/Z Centers 0
Optical Activity UNSPECIFIED

Description
Sources: Elks J., The Dictionary of Drugs: Chemical Data: Chemical Data, Structures, retrieved from:

Pareptide was developed as an antiparkinsonian drug. However, information about the further development of this drug is not available.

Approval Year

PubMed

PubMed

TitleDatePubMed
Trace analysis of the MIF analogue pareptide in blood plasma by high-performance liquid chromatography and short-wavelength excitation fluorometry.
1979 Aug 21
Pharmacological activities of the MIF-1 analogues Pro-Leu-Gly, Tyr-Pro-Leu-Gly and pareptide.
1987 Nov-Dec
Substance Class Chemical
Created
by admin
on Fri Dec 15 16:08:11 GMT 2023
Edited
by admin
on Fri Dec 15 16:08:11 GMT 2023
Record UNII
4743XI19RY
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
PAREPTIDE
INN  
INN  
Official Name English
pareptide [INN]
Common Name English
N-(D-1-((CARBAMOYLMETHYL)CARBAMOYL)-3-METHYLBUTYL)-N-METHYL-L-2-PYRROLIDINECARBOXAMIDE
Common Name English
GLYCINAMIDE, L-PROLYL-N-METHYL-D-LEUCYL-
Systematic Name English
Classification Tree Code System Code
NCI_THESAURUS C38149
Created by admin on Fri Dec 15 16:08:11 GMT 2023 , Edited by admin on Fri Dec 15 16:08:11 GMT 2023
Code System Code Type Description
INN
4347
Created by admin on Fri Dec 15 16:08:11 GMT 2023 , Edited by admin on Fri Dec 15 16:08:11 GMT 2023
PRIMARY
PUBCHEM
10086055
Created by admin on Fri Dec 15 16:08:11 GMT 2023 , Edited by admin on Fri Dec 15 16:08:11 GMT 2023
PRIMARY
EVMPD
SUB09623MIG
Created by admin on Fri Dec 15 16:08:11 GMT 2023 , Edited by admin on Fri Dec 15 16:08:11 GMT 2023
PRIMARY
ChEMBL
CHEMBL2111011
Created by admin on Fri Dec 15 16:08:11 GMT 2023 , Edited by admin on Fri Dec 15 16:08:11 GMT 2023
PRIMARY
DAILYMED
4743XI19RY
Created by admin on Fri Dec 15 16:08:11 GMT 2023 , Edited by admin on Fri Dec 15 16:08:11 GMT 2023
PRIMARY
MESH
C024569
Created by admin on Fri Dec 15 16:08:11 GMT 2023 , Edited by admin on Fri Dec 15 16:08:11 GMT 2023
PRIMARY
FDA UNII
4743XI19RY
Created by admin on Fri Dec 15 16:08:11 GMT 2023 , Edited by admin on Fri Dec 15 16:08:11 GMT 2023
PRIMARY
CAS
61484-38-6
Created by admin on Fri Dec 15 16:08:11 GMT 2023 , Edited by admin on Fri Dec 15 16:08:11 GMT 2023
PRIMARY
NCI_THESAURUS
C66319
Created by admin on Fri Dec 15 16:08:11 GMT 2023 , Edited by admin on Fri Dec 15 16:08:11 GMT 2023
PRIMARY
EPA CompTox
DTXSID50210450
Created by admin on Fri Dec 15 16:08:11 GMT 2023 , Edited by admin on Fri Dec 15 16:08:11 GMT 2023
PRIMARY
RXCUI
2619909
Created by admin on Fri Dec 15 16:08:11 GMT 2023 , Edited by admin on Fri Dec 15 16:08:11 GMT 2023
PRIMARY
SMS_ID
100000082815
Created by admin on Fri Dec 15 16:08:11 GMT 2023 , Edited by admin on Fri Dec 15 16:08:11 GMT 2023
PRIMARY
Related Record Type Details
SALT/SOLVATE -> PARENT
SALT/SOLVATE -> PARENT
Related Record Type Details
ACTIVE MOIETY