L-Prolinamide, N-[[(4S)-hexahydro-1-methyl-2,6-dioxo-4-pyrimidinyl]carbonyl]-L-histidyl-, hydrate (1:4)
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L-Prolinamide, N-[[(4S)-hexahydro-1-methyl-2,6-dioxo-4-pyrimidinyl]carbonyl]-L-histidyl-, hydrate (1:4)
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CAS No:
201677-75-0
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Formula:
C17H23N7O5.4H2O
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Chemical Name:
L-Prolinamide, N-[[(4S)-hexahydro-1-methyl-2,6-dioxo-4-pyrimidinyl]carbonyl]-L-histidyl-, hydrate (1:4)
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Synonyms:
L-Prolinamide,N-[[(4S)-hexahydro-1-methyl-2,6-dioxo-4-pyrimidinyl]carbonyl]-L-histidyl-,hydrate (1:4);L-Prolinamide,N-[[(4S)-hexahydro-1-methyl-2,6-dioxo-4-pyrimidinyl]carbonyl]-L-histidyl-,tetrahydrate;Taltirelin hydrate
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CAS No:
Description
Taltirelin tetrahydrate is a hydrate that is the tetrahydrate form of taltirelin. It activates neuronal cells by promoting the release and turnover of neurotransmitters (acetylcholine, dopamine) and its nerve growth factor-like action. The drug is approved in Japan and used to treat ataxia (daily activities such as gait, eating, and conversation) in patients suffering from spinocerebellar degeneration. It has a role as a central nervous system drug. It contains a taltirelin.|Taltirelin Hydrate is the hydrate of tatirelin, a thyrotropin releasing hormone (TRH) analogue with potential neuroprotective, analgesic and central nervous system-stimulating (CNS)/analeptic activities. Taltirelin mimics the physiological actions of TRH on the CNS while exerting a minimal effect on the release of thyrotrophin (TSH) from the anterior lobe of the pituitary. Like TRH, the mechanism of action of this agent in the CNS has not been fully elucidated mechanism, but may involve various cerebral monoamine pathways. Compared to TRH, taltirelin has a much longer half-life and duration of effects.
L-Prolinamide, N-[[(4S)-hexahydro-1-methyl-2,6-dioxo-4-pyrimidinyl]carbonyl]-L-histidyl-, hydrate (1:4) Basic Attributes
477.47000
477.21832559 g/mol
525OEO6W15
DTXSID3021300
C79830
Drug Information
Drugs used to specifically facilitate learning or memory, particularly to prevent the cognitive deficits associated with dementias. These drugs act by a variety of mechanisms. (See all compounds classified as Nootropic Agents.)
(1-methyl-4,5-dihydroorotyl)-histidyl-prolinamide
Computed Properties
Molecular Weight:477.5
Hydrogen Bond Donor Count:8
Hydrogen Bond Acceptor Count:10
Rotatable Bond Count:6
Exact Mass:477.21832559
Monoisotopic Mass:477.21832559
Topological Polar Surface Area:175
Heavy Atom Count:33
Complexity:714
Defined Atom Stereocenter Count:3
Covalently-Bonded Unit Count:5
Compound Is Canonicalized:Yes
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