U.S. Department of Health & Human Services Divider Arrow National Institutes of Health Divider Arrow NCATS
Eledoisin is an endecapeptide tachykinin receptor ligand. Originally it was isolated from salivary glands of Mediterranean octopod, Eledone moschata. Eledoisin is a powerful vasodilator and hypotensive agent in most animal species.

Approval Year

PubMed

PubMed

TitleDatePubMed
The unpredicted high affinities of a large number of naturally occurring tachykinins for chimeric NK1/NK3 receptors suggest a role for an inhibitory domain in determining receptor specificity.
1996-08-23
Molecular characterisation, expression and localisation of human neurokinin-3 receptor.
1992-03-24
Patents
Substance Class Protein
Created
by admin
on Mon Mar 31 18:14:58 GMT 2025
Edited
by admin
on Mon Mar 31 18:14:58 GMT 2025
Protein Sub Type
Sequence Type COMPLETE
Record UNII
OKY3285J18
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
ELEDOISIN
INN   MART.   MI   WHO-DD  
INN  
Official Name English
ELD 950
Preferred Name English
ELEDOISIN [MART.]
Common Name English
PGLU-PRO-SER-LYS-ASP-ALA-PHE-ILE-GLY-LEU-MET-NH2
Common Name English
5-OXO-L-PROLYL-L-PROLYL-L-SERYL-L-LYSYL-L-ASPARTYL-L-ALANYL-L-PHENYLALANYL-L-ISOLEUCYLGLYCYL-L-LEUCYL-L-METHIONINAMIDE
Common Name English
5-OXOPRO-PRO-SER-LYS-ASP-ALA-PHE-ILE-GLY-LEU-MET-NH2
Common Name English
ELD-950
Code English
Eledoisin [WHO-DD]
Common Name English
eledoisin [INN]
Common Name English
ELEDOISIN [MI]
Common Name English
Classification Tree Code System Code
NCI_THESAURUS C894
Created by admin on Mon Mar 31 18:14:58 GMT 2025 , Edited by admin on Mon Mar 31 18:14:58 GMT 2025
Code System Code Type Description
CAS
69-25-0
Created by admin on Mon Mar 31 18:14:58 GMT 2025 , Edited by admin on Mon Mar 31 18:14:58 GMT 2025
PRIMARY
MERCK INDEX
m4858
Created by admin on Mon Mar 31 18:14:58 GMT 2025 , Edited by admin on Mon Mar 31 18:14:58 GMT 2025
PRIMARY Merck Index
NCI_THESAURUS
C80866
Created by admin on Mon Mar 31 18:14:58 GMT 2025 , Edited by admin on Mon Mar 31 18:14:58 GMT 2025
PRIMARY
EPA CompTox
DTXSID1046926
Created by admin on Mon Mar 31 18:14:58 GMT 2025 , Edited by admin on Mon Mar 31 18:14:58 GMT 2025
PRIMARY
FDA UNII
OKY3285J18
Created by admin on Mon Mar 31 18:14:58 GMT 2025 , Edited by admin on Mon Mar 31 18:14:58 GMT 2025
PRIMARY
WIKIPEDIA
ELEDOISIN
Created by admin on Mon Mar 31 18:14:58 GMT 2025 , Edited by admin on Mon Mar 31 18:14:58 GMT 2025
PRIMARY
SMS_ID
100000080541
Created by admin on Mon Mar 31 18:14:58 GMT 2025 , Edited by admin on Mon Mar 31 18:14:58 GMT 2025
PRIMARY
INN
3278
Created by admin on Mon Mar 31 18:14:58 GMT 2025 , Edited by admin on Mon Mar 31 18:14:58 GMT 2025
PRIMARY
PUBCHEM
10328936
Created by admin on Mon Mar 31 18:14:58 GMT 2025 , Edited by admin on Mon Mar 31 18:14:58 GMT 2025
PRIMARY
ChEMBL
CHEMBL373569
Created by admin on Mon Mar 31 18:14:58 GMT 2025 , Edited by admin on Mon Mar 31 18:14:58 GMT 2025
PRIMARY
EVMPD
SUB06481MIG
Created by admin on Mon Mar 31 18:14:58 GMT 2025 , Edited by admin on Mon Mar 31 18:14:58 GMT 2025
PRIMARY
DRUG CENTRAL
2955
Created by admin on Mon Mar 31 18:14:58 GMT 2025 , Edited by admin on Mon Mar 31 18:14:58 GMT 2025
PRIMARY
Related Record Type Details
SALT/SOLVATE -> PARENT
INGREDIENT -> STARTING MATERIAL
INGREDIENT -> STARTING MATERIAL
Related Record Type Details
ACTIVE MOIETY

Structural Modifications

Modification Type Location Site Location Type Residue Modified Extent Fragment Name Fragment Approval
AMINO ACID SUBSTITUION [1_11] METHIONINE METHIONINAMIDE QSM06A70MD
AMINO ACID SUBSTITUION [1_1] PROLINE PIDOLIC ACID SZB83O1W42
Name Property Type Amount Referenced Substance Defining Parameters References
Molecular Formula CHEMICAL
MOL_WEIGHT:NUMBER(CALCULATED) CHEMICAL