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
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
Molecular Formula | C32H49N9O5 |
Molecular Weight | 639.7888 |
Charge | 0 |
Count |
|
Stereochemistry | ABSOLUTE |
Additional Stereochemistry | No |
Defined Stereocenters | 4 / 4 |
E/Z Centers | 0 |
Optical Activity | UNSPECIFIED |
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
Sample Use Guides
In Vivo Use Guide
Sources: https://www.ncbi.nlm.nih.gov/pubmed/29500292
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
Sources: https://www.ncbi.nlm.nih.gov/pubmed/16216225
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
Created
by
admin
on
Edited
Sat Dec 16 09:12:31 GMT 2023
by
admin
on
Sat Dec 16 09:12:31 GMT 2023
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Record UNII |
87GWG91S09
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Record Status |
Validated (UNII)
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Record Version |
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FDA ORPHAN DRUG |
597417
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FDA ORPHAN DRUG |
609417
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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 ORPHAN DRUG |
607817
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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 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
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DE-80
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DB11981
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DTXSID50471988
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736992-21-5
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Elamipretide
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C171874
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10154
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87GWG91S09
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11764719
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SALT/SOLVATE -> PARENT |
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TARGET->LIGAND |
Improves impaired mitochondrial
function in HF, with no effect on normal mitochondrial function in nonfailing hearts;
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ACTIVE MOIETY |
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