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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
Trace analysis of the MIF analogue pareptide in blood plasma by high-performance liquid chromatography and short-wavelength excitation fluorometry.
1979 Aug 21
Determination of the melanotropin-inhibiting factor analogue pareptide in urine by high-performance liquid chromatography.
1981 Mar 13
Pro-Leu-Gly-NH2 and pareptide inhibit development of tolerance to haloperidol catalepsy in the mouse.
1984 Sep-Oct
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 16:22:35 GMT 2023
Edited
by admin
on Fri Dec 15 16:22:35 GMT 2023
Record UNII
1CMY36S198
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
PAREPTIDE SULFATE
USAN  
USAN  
Official 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
AY-24,856
Code English
GLYCINAMIDE, L-PROLYL-N-METHYL-D-LEUCYL-, SULPHATE (2:1)
Common Name English
Code System Code Type Description
FDA UNII
1CMY36S198
Created by admin on Fri Dec 15 16:22:35 GMT 2023 , Edited by admin on Fri Dec 15 16:22:35 GMT 2023
PRIMARY
PUBCHEM
20055517
Created by admin on Fri Dec 15 16:22:35 GMT 2023 , Edited by admin on Fri Dec 15 16:22:35 GMT 2023
PRIMARY
EPA CompTox
DTXSID50977051
Created by admin on Fri Dec 15 16:22:35 GMT 2023 , Edited by admin on Fri Dec 15 16:22:35 GMT 2023
PRIMARY
CAS
61484-39-7
Created by admin on Fri Dec 15 16:22:35 GMT 2023 , Edited by admin on Fri Dec 15 16:22:35 GMT 2023
PRIMARY
NCI_THESAURUS
C166488
Created by admin on Fri Dec 15 16:22:35 GMT 2023 , Edited by admin on Fri Dec 15 16:22:35 GMT 2023
PRIMARY
CAS
89026-25-5
Created by admin on Fri Dec 15 16:22:35 GMT 2023 , Edited by admin on Fri Dec 15 16:22:35 GMT 2023
NON-SPECIFIC STOICHIOMETRY
ChEMBL
CHEMBL2111011
Created by admin on Fri Dec 15 16:22:35 GMT 2023 , Edited by admin on Fri Dec 15 16:22:35 GMT 2023
PRIMARY
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ACTIVE MOIETY