Structure via PubChem · Public domain (PubChem)
In the Vinony graph
Vinony's link graph records 7 inbound references to thiamine triphosphate, and connects out to Animalia, plant and mammal.
Vinony files it under Biomolecules, Pyrimidines and Thiamine.
Vinony links it to 8 Wikipedia language editions.
Chemical data
- Formula
- C12H19N4O10P3S
- Molecular weight
- 504.29 g/mol
- IUPAC name
- [[2-[3-[(4-amino-2-methylpyrimidin-5-yl)methyl]-4-methyl-1,3-thiazol-3-ium-5-yl]ethoxy-hydroxyphosphoryl]oxy-hydroxyphosphoryl] hydrogen phosphate
- SMILES
- CC1=C(SC=[N+]1CC2=CN=C(N=C2N)C)CCOP(=O)(O)OP(=O)(O)OP(=O)(O)[O-]
- InChIKey
- IWLROWZYZPNOFC-UHFFFAOYSA-N
- XLogP
- -2.3
- Polar surface area
- 247 Ų
- H-bond donors
- 4
- H-bond acceptors
- 14
- Formal charge
- 0
via PubChem
Research
548 papers- The importance of thiamine (vitamin B1) in humans.Bioscience reports · 2023
- Thiamine triphosphate: a ubiquitous molecule in search of a physiological role.Metabolic brain disease · 2014
- On the nature of thiamine triphosphate in Arabidopsis.Plant direct · 2020
- Pyrimidines maintain mitochondrial pyruvate oxidation to support de novo lipogenesis.Science (New York, N.Y.) · 2024
- Polyphosphate Kinases Phosphorylate Thiamine Phosphates.Microbial physiology · 2023
via PubMed
Wikidata facts
- Subclass of
- cation
- Mass
- 504.003474
Show 4 more facts
- chemical formula
- C₁₂H₁₉N₄O₁₀P₃S
- found in taxon
- Homo sapiens
- Commons category
- Thiamine triphosphate
- canonical SMILES
- CC1=C(SC=[N+]1CC2=CN=C(N=C2N)C)CCOP(=O)(O)OP(=O)(O)OP(=O)(O)[O-]
Sources (2)
via Wikidata · CC0
Connections
Animalia
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plant
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mammal
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fungi
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bacteria
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amino acid
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glucose
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digital object identifier
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chemical formula
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Escherichia coli
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redox
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alkali
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thiamine(1+) ion
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molar mass
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chromatography
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PubMed
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bibcode
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CAS Registry Number
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PubMed Central
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PubChem
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