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Details

Stereochemistry ABSOLUTE
Molecular Formula 2C14H26N4O3.H2O4S
Molecular Weight 694.841
Optical Activity UNSPECIFIED
Defined Stereocenters 4 / 4
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of PAREPTIDE SULFATE

SMILES

OS(O)(=O)=O.CC(C)C[C@@H](N(C)C(=O)[C@@H]1CCCN1)C(=O)NCC(N)=O.CC(C)C[C@@H](N(C)C(=O)[C@@H]2CCCN2)C(=O)NCC(N)=O

InChI

InChIKey=DPOZYRPNCJEMMY-DDRMSGASSA-N
InChI=1S/2C14H26N4O3.H2O4S/c2*1-9(2)7-11(13(20)17-8-12(15)19)18(3)14(21)10-5-4-6-16-10;1-5(2,3)4/h2*9-11,16H,4-8H2,1-3H3,(H2,15,19)(H,17,20);(H2,1,2,3,4)/t2*10-,11+;/m00./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

Molecular Formula H2O4S
Molecular Weight 98.078
Charge 0
Count
Stereochemistry ACHIRAL
Additional Stereochemistry No
Defined Stereocenters 0 / 0
E/Z Centers 0
Optical Activity NONE

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
Substance Class Chemical
Created
by admin
on Mon Mar 31 18:26:25 GMT 2025
Edited
by admin
on Mon Mar 31 18:26:25 GMT 2025
Record UNII
1CMY36S198
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
PAREPTIDE SULFATE
USAN  
USAN  
Official Name English
AY-24,856
Preferred Name English
N-(D-1-((CARBAMOYLMETHYL)CARBAMOYL)-3-METHYLBUTYL)-N-METHYL-L-2-PYRROLIDINECARBOXAMIDE SULFATE (2:1)
Common Name English
GLYCINAMIDE, L-PROLYL-N-METHYL-D-LEUCYL-, SULFATE (2:1)
Common Name English
AY-24856
Code English
N-(D-1-((CARBAMOYLMETHYL)CARBAMOYL)-3-METHYLBUTYL)-N-METHYL-L-2-PYRROLIDINECARBOXAMIDE SULPHATE (2:1)
Common Name English
PAREPTIDE SULFATE [USAN]
Common Name English
PAREPTIDE SULPHATE
Common Name English
GLYCINAMIDE, L-PROLYL-N-METHYL-D-LEUCYL-, SULPHATE (2:1)
Common Name English
Code System Code Type Description
SMS_ID
300000055572
Created by admin on Mon Mar 31 18:26:25 GMT 2025 , Edited by admin on Mon Mar 31 18:26:25 GMT 2025
PRIMARY
FDA UNII
1CMY36S198
Created by admin on Mon Mar 31 18:26:25 GMT 2025 , Edited by admin on Mon Mar 31 18:26:25 GMT 2025
PRIMARY
PUBCHEM
20055517
Created by admin on Mon Mar 31 18:26:25 GMT 2025 , Edited by admin on Mon Mar 31 18:26:25 GMT 2025
PRIMARY
EPA CompTox
DTXSID50977051
Created by admin on Mon Mar 31 18:26:25 GMT 2025 , Edited by admin on Mon Mar 31 18:26:25 GMT 2025
PRIMARY
CAS
61484-39-7
Created by admin on Mon Mar 31 18:26:25 GMT 2025 , Edited by admin on Mon Mar 31 18:26:25 GMT 2025
PRIMARY
NCI_THESAURUS
C166488
Created by admin on Mon Mar 31 18:26:25 GMT 2025 , Edited by admin on Mon Mar 31 18:26:25 GMT 2025
PRIMARY
CAS
89026-25-5
Created by admin on Mon Mar 31 18:26:25 GMT 2025 , Edited by admin on Mon Mar 31 18:26:25 GMT 2025
NON-SPECIFIC STOICHIOMETRY
ChEMBL
CHEMBL2111011
Created by admin on Mon Mar 31 18:26:25 GMT 2025 , Edited by admin on Mon Mar 31 18:26:25 GMT 2025
PRIMARY
Related Record Type Details
PARENT -> SALT/SOLVATE
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ACTIVE MOIETY