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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

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
Pharmacological activities of the MIF-1 analogues Pro-Leu-Gly, Tyr-Pro-Leu-Gly and pareptide.
1987-11-01
Pro-Leu-Gly-NH2 and pareptide inhibit development of tolerance to haloperidol catalepsy in the mouse.
1984-09-01
Determination of the melanotropin-inhibiting factor analogue pareptide in urine by high-performance liquid chromatography.
1981-03-13
Trace analysis of the MIF analogue pareptide in blood plasma by high-performance liquid chromatography and short-wavelength excitation fluorometry.
1979-08-21
Name Type Language
N-(D-1-((CARBAMOYLMETHYL)CARBAMOYL)-3-METHYLBUTYL)-N-METHYL-L-2-PYRROLIDINECARBOXAMIDE
Preferred Name English
PAREPTIDE
INN  
INN  
Official Name English
pareptide [INN]
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 Mon Mar 31 18:19:58 GMT 2025 , Edited by admin on Mon Mar 31 18:19:58 GMT 2025
Code System Code Type Description
INN
4347
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PUBCHEM
10086055
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EVMPD
SUB09623MIG
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ChEMBL
CHEMBL2111011
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DAILYMED
4743XI19RY
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MESH
C024569
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FDA UNII
4743XI19RY
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CAS
61484-38-6
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NCI_THESAURUS
C66319
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EPA CompTox
DTXSID50210450
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RXCUI
2619909
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SMS_ID
100000082815
Created by admin on Mon Mar 31 18:19:58 GMT 2025 , Edited by admin on Mon Mar 31 18:19:58 GMT 2025
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