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Details

Stereochemistry ABSOLUTE
Molecular Formula C17H23N7O5
Molecular Weight 405.4084
Optical Activity UNSPECIFIED
Defined Stereocenters 3 / 3
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of TALTIRELIN

SMILES

CN1C(=O)C[C@H](NC1=O)C(=O)N[C@@H](CC2=CN=CN2)C(=O)N3CCC[C@H]3C(N)=O

InChI

InChIKey=LQZAIAZUDWIVPM-SRVKXCTJSA-N
InChI=1S/C17H23N7O5/c1-23-13(25)6-10(22-17(23)29)15(27)21-11(5-9-7-19-8-20-9)16(28)24-4-2-3-12(24)14(18)26/h7-8,10-12H,2-6H2,1H3,(H2,18,26)(H,19,20)(H,21,27)(H,22,29)/t10-,11-,12-/m0/s1

HIDE SMILES / InChI

Description
Curator's Comment: description was created based on several sources, including https://www.drugs.com/international/taltirelin.html | https://www.ncbi.nlm.nih.gov/pubmed/23087672 | https://www.ncbi.nlm.nih.gov/pubmed/25142535

Taltirelin (TA-0910), a synthetic thyrotropin-releasing hormone (TRH) analog, has been developed by Tanabe Seiyaku for the treatment of neurodegenerative diseases. Taltirelin mimics the physiological actions of TRH, but with a much longer half-life and duration of effects, and little development of tolerance following prolonged dosing. Taltirelin has nootropic, neuroprotective and analgesic effects. Taltirelin is primarily being researched for the treatment of spinocerebellar ataxia; limited research has also been carried out with regard to other neurodegenerative disorders, e.g., spinal muscular atrophy.

Approval Year

Targets

Targets

Primary TargetPharmacologyConditionPotency
36.0 nM [EC50]
Conditions

Conditions

ConditionModalityTargetsHighest PhaseProduct
Primary
Ceredist

Approved Use

Unknown
PubMed

PubMed

TitleDatePubMed
Neuroprotective effect and brain receptor binding of taltirelin, a novel thyrotropin-releasing hormone (TRH) analogue, in transient forebrain ischemia of C57BL/6J mice.
2002 Dec 20
Blood-brain permeability of [3H]-(3-methyl-His2)thyrotropin-releasing hormone (MeTRH) in mice: effects of TRH and its analogues.
2003
The synthetic TRH analogue taltirelin exerts modality-specific antinociceptive effects via distinct descending monoaminergic systems.
2007 Feb
Taltirelin is a superagonist at the human thyrotropin-releasing hormone receptor.
2012
Patents

Sample Use Guides

Patients took taltirelin (5 mg bid) or placebo for 28 to 52 weeks.
Route of Administration: Oral
HEK-EM 293 (human embryonic kidney) cells stably expressing TRH-R were seeded in black-walled, clear bottomed 96-well plates (Corning, NY, USA) at a density of 60,000 cells/well in DMEM with 10% fetal bovine serum and incubatedfor24hat37◦C in5%CO2. The following day, the culture media was replaced with 100 μl of Hank’s balanced salt solution with 20 mM HEPES, pH 7.5 and the cells were loaded with100 μl of calcium 4 fluorescent dye (Molecular Devices, Sunnyvale, CA, USA) for 1 h at room temperature before addition of compounds .Transient changes in intracellular [Ca++] induced by TALTIRELIN were measured using the FLIPRTETRA system (Molecular Devices, Sunnyvale, CA, USA). Changes in fluorescence were detected at the emission wavelength ranges from 515 to 575 nm. The agonistic responses of ligands were assessed immediately upon their addition in a concentration range from 0.1 nMto30 μM.
Name Type Language
TALTIRELIN
INN   MART.   MI   WHO-DD  
INN  
Official Name English
TALTIRELIN [MART.]
Common Name English
TALTIRELIN [MI]
Common Name English
TA-0910
Code English
taltirelin [INN]
Common Name English
Taltirelin [WHO-DD]
Common Name English
Classification Tree Code System Code
NCI_THESAURUS C76367
Created by admin on Sat Dec 16 16:20:17 GMT 2023 , Edited by admin on Sat Dec 16 16:20:17 GMT 2023
Code System Code Type Description
WIKIPEDIA
TALTIRELIN
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MERCK INDEX
m10447
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PRIMARY Merck Index
DRUG CENTRAL
2560
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INN
7503
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CAS
103300-74-9
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FDA UNII
DOZ62MV6A5
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NCI_THESAURUS
C77011
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PUBCHEM
114750
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SMS_ID
100000083229
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EVMPD
SUB10816MIG
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CHEBI
135653
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ChEMBL
CHEMBL2107016
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EPA CompTox
DTXSID0043763
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