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Details

Stereochemistry ABSOLUTE
Molecular Formula C32H49N9O5.3ClH
Molecular Weight 749.172
Optical Activity UNSPECIFIED
Defined Stereocenters 4 / 4
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of ELAMIPRETIDE HYDROCHLORIDE

SMILES

Cl.Cl.Cl.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=NGOPFUMILSNWHH-QTSNMJAOSA-N
InChI=1S/C32H49N9O5.3ClH/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);3*1H/t24-,25+,26+,27+;;;/m1.../s1

HIDE SMILES / InChI

Molecular Formula ClH
Molecular Weight 36.461
Charge 0
Count
Stereochemistry ACHIRAL
Additional Stereochemistry No
Defined Stereocenters 0 / 0
E/Z Centers 0
Optical Activity NONE

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.

Approval Year

PubMed

PubMed

TitleDatePubMed
Mitochondrial targeting with antioxidant peptide SS-31 prevents mitochondrial depolarization, reduces islet cell apoptosis, increases islet cell yield, and improves posttransplantation function.
2007 Jan

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.
Substance Class Chemical
Created
by admin
on Sat Dec 16 14:44:34 GMT 2023
Edited
by admin
on Sat Dec 16 14:44:34 GMT 2023
Record UNII
E40WZ3BK2D
Record Status Validated (UNII)
Record Version
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Name Type Language
ELAMIPRETIDE HYDROCHLORIDE
USAN  
Official Name English
ELAMIPRETIDE TRIHYDROCHLORIDE
Common Name English
ELAMIPRETIDE HYDROCHLORIDE [USAN]
Common Name English
D-ARGINYL-2,6-DIMETHYL-L-TYROSYL-L-LYSYL-L-PHENYLALANINAMIDE, TRIHYDROCHLORIDE
Systematic Name English
L-PHENYLALANINAMIDE, O-ARGINYL-2,6-DIMETHYL-L-TYROSYL-L-LYSYL-, HYDROCHLORIDE (1:3)
Systematic Name English
Classification Tree Code System Code
FDA ORPHAN DRUG 874722
Created by admin on Sat Dec 16 14:44:34 GMT 2023 , Edited by admin on Sat Dec 16 14:44:34 GMT 2023
Code System Code Type Description
FDA UNII
E40WZ3BK2D
Created by admin on Sat Dec 16 14:44:34 GMT 2023 , Edited by admin on Sat Dec 16 14:44:34 GMT 2023
PRIMARY
NCI_THESAURUS
C171875
Created by admin on Sat Dec 16 14:44:34 GMT 2023 , Edited by admin on Sat Dec 16 14:44:34 GMT 2023
PRIMARY
CAS
2244098-12-0
Created by admin on Sat Dec 16 14:44:34 GMT 2023 , Edited by admin on Sat Dec 16 14:44:34 GMT 2023
PRIMARY
USAN
GH-61
Created by admin on Sat Dec 16 14:44:34 GMT 2023 , Edited by admin on Sat Dec 16 14:44:34 GMT 2023
PRIMARY
PUBCHEM
137528200
Created by admin on Sat Dec 16 14:44:34 GMT 2023 , Edited by admin on Sat Dec 16 14:44:34 GMT 2023
PRIMARY
SMS_ID
300000011144
Created by admin on Sat Dec 16 14:44:34 GMT 2023 , Edited by admin on Sat Dec 16 14:44:34 GMT 2023
PRIMARY
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