MOA It is thought that the mechanism of action of thiamine on endothelial cells is related to a reduction in intracellular protein glycation by redirecting ...
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InChIKey: JZRWCGZRTZMZEH-UHFFFAOYSA-N. Instrument Type: MS Type: Ion Mode: Both, Edit / Resubmit Query. Results : 18 Hit. ( 1 - 18 Displayed ) ...
Large-scale non-redundant database of pointers between chemical structures and chemistry resources.
THIAMINE ION. UNII: 4ABT0J945J; Formula: C12H17N4OS; Preferred Substance Name: THIAMINE ION; InChIKey: JZRWCGZRTZMZEH-UHFFFAOYSA-N ...
3 InChIKey. JZRWCGZRTZMZEH-SHESLYCYSA-N. Computed by InChI 1.0.6 (PubChem release 2021.05.07). PubChem. 2.1.4 Canonical SMILES. CC1=C(SC=[N+]1CC2=CN=C(N=C2N)C) ...
Search Google for chemicals with the same backbone, JZRWCGZRTZMZEH ; Search PubMed clinical trials, thiamine ; Search PubMed titles, thiamine ; Search PubMed ...
Formula, C12H17N4OS+ ; IUPAC Name, 2-[3-[(4-amino-2-methyl-pyrimidin-5-yl)methyl]-4-methyl-thiazol-3-ium-5-yl]ethanol ; Molecular Mass, 265.355 g·mol ; Heat of ...
JZRWCGZRTZMZEH-UHFFFAOYSA-N, View other enantiomers/diastereomers of this metabolite in RefMet. Super Class, Nucleic acids. Main Class, Pyrimidines. Sub Class ...
InChIKey: JZRWCGZRTZMZEH-UHFFFAOYSA-N; SMILES: Cc1ncc(C[n+]2csc(CCO)c2C)c(N)n1; Is co-factor?: No; Is core?: Yes; Is obsolete?: No; Aliases ...
InChIKey=JZRWCGZRTZMZEH-UHFFFAOYSA-N. SureCN10075. PubChem. 4 Patents. 4.1 Depositor-Supplied Patent Identifiers. PubChem. Link to all deposited patent ...