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Details

Stereochemistry ABSOLUTE
Molecular Formula C14H26N4O3.ClH
Molecular Weight 334.842
Optical Activity UNSPECIFIED
Defined Stereocenters 2 / 2
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of PAREPTIDE HYDROCHLORIDE

SMILES

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

InChI

InChIKey=GOTJGGBFFYUZOH-VZXYPILPSA-N
InChI=1S/C14H26N4O3.ClH/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);1H/t10-,11+;/m0./s1

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 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

2022
324
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
Substance Class Chemical
Created
by admin
on Mon Mar 31 21:05:05 GMT 2025
Edited
by admin
on Mon Mar 31 21:05:05 GMT 2025
Record UNII
GC65JE8O95
Record Status Validated (UNII)
Record Version
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Name Type Language
GLYCINAMIDE, L-PROLYL-N-METHYL-D-LEUCYL-, MONOHYDROCHLORIDE
Preferred Name English
PAREPTIDE HYDROCHLORIDE
Common Name English
Code System Code Type Description
FDA UNII
GC65JE8O95
Created by admin on Mon Mar 31 21:05:05 GMT 2025 , Edited by admin on Mon Mar 31 21:05:05 GMT 2025
PRIMARY
PUBCHEM
73425452
Created by admin on Mon Mar 31 21:05:05 GMT 2025 , Edited by admin on Mon Mar 31 21:05:05 GMT 2025
PRIMARY
CAS
63236-23-7
Created by admin on Mon Mar 31 21:05:05 GMT 2025 , Edited by admin on Mon Mar 31 21:05:05 GMT 2025
PRIMARY
Related Record Type Details
Structure of PAREPTIDE
PARENT -> SALT/SOLVATE
Related Record Type Details
Structure of PAREPTIDE
ACTIVE MOIETY
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