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Details

Stereochemistry ABSOLUTE
Molecular Formula C32H49N9O5
Molecular Weight 639.7888
Optical Activity UNSPECIFIED
Defined Stereocenters 4 / 4
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of ELAMIPRETIDE

SMILES

CC1=CC(O)=CC(C)=C1C[C@H](NC(=O)[C@H](N)CCCNC(N)=N)C(=O)N[C@@H](CCCCN)C(=O)N[C@@H](CC2=CC=CC=C2)C(N)=O

InChI

InChIKey=SFVLTCAESLKEHH-WKAQUBQDSA-N
InChI=1S/C32H49N9O5/c1-19-15-22(42)16-20(2)23(19)18-27(41-29(44)24(34)11-8-14-38-32(36)37)31(46)39-25(12-6-7-13-33)30(45)40-26(28(35)43)17-21-9-4-3-5-10-21/h3-5,9-10,15-16,24-27,42H,6-8,11-14,17-18,33-34H2,1-2H3,(H2,35,43)(H,39,46)(H,40,45)(H,41,44)(H4,36,37,38)/t24-,25+,26+,27+/m1/s1

HIDE SMILES / InChI
Elamipretide or SS-31 (D-Arg-2', 6'-dimethyltyrosine-Lys-Phe-NH2) is a mitochondria-targeted antioxidant. Elamipretide, is a peptide compound that readily penetrates cell membranes, and targets the inner mitochondrial membrane where it binds reversibly to cardiolipin. In preclinical or clinical studies, elamipretide increases mitochondrial respiration, improves the electron transport chain function and ATP production and reduces formation of pathogenic ROS levels. This elamipretide-cardiolipin association has been shown to normalize the structure of the inner mitochondrial membrane, thereby improving mitochondrial function. Functional benefit is achieved through improvement of ATP production and interruption and potential reversal of damaging oxidative stress. Stealth BioTherapeutics is investigating elamipretide in late stage clinical studies in three primary mitochondrial diseases—primary mitochondrial myopathy, Barth syndrome and Leber’s hereditary optic neuropathy – as well as an earlier stage clinical study in dry age-related macular degeneration.

Approval Year

PubMed

PubMed

TitleDatePubMed

Sample Use Guides

A Study Investigating the Safety, Tolerability, and Efficacy of MTP-131 for the Treatment of Mitochondrial Myopathy (MMPOWER) was a phase I/II multicenter, randomized, double-blind, placebo-controlled trial of elamipretide in 36 participants with genetically confirmed PMM. Participants were randomized to intravenous elamipretide (0.01, 0.1, and 0.25 mg/kg/h or placebo for 2 hours in a dose-escalating sequence).
Route of Administration: Intravenous
Treatment with tert-butyl hydroperoxide (tBHP) for 24 h resulted in lipid peroxidation and significant cell death via apoptosis in both N2A and SH-SY5Y cells, with phosphatidylserine translocation, nuclear condensation and increased caspase activity. Cells treated with tBHP showed significant increase in intracellular ROS, mitochondrial depolarization and reduced mitochondrial viability. Concurrent treatment with <1 nM elamipretide significantly decreased intracellular ROS, increased mitochondrial potential, and prevented tBHP-induced apoptosis.
Name Type Language
ELAMIPRETIDE
INN   USAN   WHO-DD  
INN   USAN  
Official Name English
BENDAVIA
Brand Name English
SS-31
Code English
RX-31
Code English
SZETO-SCHILLER PEPTIDE
Common Name English
MTP131
Code English
OCUVIA
Brand Name English
D-ARGINYL-2,6-DIMETHYL-L-TYROSYL-L-LYSYL-L-PHENYLALANINAMIDE
Systematic Name English
RX31
Code English
NH2-D-ARG-DMT-LYS-PHE-NH2
Common Name English
SS31
Code English
ELAMIPRETIDE [USAN]
Common Name English
Elamipretide [WHO-DD]
Common Name English
MTP-131
Code English
elamipretide [INN]
Common Name English
L-PHENYLALANINAMIDE, D-ARGINYL-2,6-DIMETHYL-L-TYROSYL-L-LYSYL-
Systematic Name English
Classification Tree Code System Code
FDA ORPHAN DRUG 597417
Created by admin on Sat Dec 16 09:12:31 GMT 2023 , Edited by admin on Sat Dec 16 09:12:31 GMT 2023
FDA ORPHAN DRUG 609417
Created by admin on Sat Dec 16 09:12:31 GMT 2023 , Edited by admin on Sat Dec 16 09:12:31 GMT 2023
FDA ORPHAN DRUG 607817
Created by admin on Sat Dec 16 09:12:31 GMT 2023 , Edited by admin on Sat Dec 16 09:12:31 GMT 2023
FDA ORPHAN DRUG 794420
Created by admin on Sat Dec 16 09:12:31 GMT 2023 , Edited by admin on Sat Dec 16 09:12:31 GMT 2023
Code System Code Type Description
USAN
DE-80
Created by admin on Sat Dec 16 09:12:31 GMT 2023 , Edited by admin on Sat Dec 16 09:12:31 GMT 2023
PRIMARY
DRUG BANK
DB11981
Created by admin on Sat Dec 16 09:12:31 GMT 2023 , Edited by admin on Sat Dec 16 09:12:31 GMT 2023
PRIMARY
EPA CompTox
DTXSID50471988
Created by admin on Sat Dec 16 09:12:31 GMT 2023 , Edited by admin on Sat Dec 16 09:12:31 GMT 2023
PRIMARY
CAS
736992-21-5
Created by admin on Sat Dec 16 09:12:31 GMT 2023 , Edited by admin on Sat Dec 16 09:12:31 GMT 2023
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WIKIPEDIA
Elamipretide
Created by admin on Sat Dec 16 09:12:31 GMT 2023 , Edited by admin on Sat Dec 16 09:12:31 GMT 2023
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NCI_THESAURUS
C171874
Created by admin on Sat Dec 16 09:12:31 GMT 2023 , Edited by admin on Sat Dec 16 09:12:31 GMT 2023
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INN
10154
Created by admin on Sat Dec 16 09:12:31 GMT 2023 , Edited by admin on Sat Dec 16 09:12:31 GMT 2023
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FDA UNII
87GWG91S09
Created by admin on Sat Dec 16 09:12:31 GMT 2023 , Edited by admin on Sat Dec 16 09:12:31 GMT 2023
PRIMARY
PUBCHEM
11764719
Created by admin on Sat Dec 16 09:12:31 GMT 2023 , Edited by admin on Sat Dec 16 09:12:31 GMT 2023
PRIMARY