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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

Molecular Formula C32H49N9O5
Molecular Weight 639.7888
Charge 0
Count
MOL RATIO 1 MOL RATIO (average)
Stereochemistry ABSOLUTE
Additional Stereochemistry No
Defined Stereocenters 4 / 4
E/Z Centers 0
Optical Activity UNSPECIFIED

Description

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.

Originator

Approval Year

Cmax

ValueDoseCo-administeredAnalytePopulation
35.8 ng/mL
0.02 mg/kg 1 times / day steady-state, intravenous
ELAMIPRETIDE plasma
Homo sapiens
498 ng/mL
0.2 mg/kg 1 times / day steady-state, intravenous
ELAMIPRETIDE plasma
Homo sapiens
1050 ng/mL
0.5 mg/kg 1 times / day steady-state, intravenous
ELAMIPRETIDE plasma
Homo sapiens
1418 ng/mL
0.5 mg/kg 1 times / day steady-state, intravenous
ELAMIPRETIDE plasma
Homo sapiens

AUC

ValueDoseCo-administeredAnalytePopulation
140 ng × h/mL
0.02 mg/kg 1 times / day steady-state, intravenous
ELAMIPRETIDE plasma
Homo sapiens
1992 ng × h/mL
0.2 mg/kg 1 times / day steady-state, intravenous
ELAMIPRETIDE plasma
Homo sapiens
4050 ng × h/mL
0.5 mg/kg 1 times / day steady-state, intravenous
ELAMIPRETIDE plasma
Homo sapiens
5468 ng × h/mL
0.5 mg/kg 1 times / day steady-state, intravenous
ELAMIPRETIDE plasma
Homo sapiens

T1/2

ValueDoseCo-administeredAnalytePopulation
4 h
0.5 mg/kg 1 times / day steady-state, intravenous
ELAMIPRETIDE plasma
Homo sapiens

PubMed

Sample Use Guides

In Vivo Use Guide
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
In Vitro Use Guide
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.
Substance Class Chemical
Record UNII
87GWG91S09
Record Status Validated (UNII)
Record Version