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Oxythiamine

Names

[ CAS No. ]:
136-16-3

[ Name ]:
Oxythiamine

[Synonym ]:
Oxythiamine HCl
5-[[5-(2-Hydroxyethyl)-4-Methyl-Thiazol-3-ium-3-yl]Methyl]-2-Methyl-3H-Pyrimidin-4-One Chloride
5-[[5-(2-Hydroxyethyl)-4-Methyl-3-Thiazol-3-iumyl]Methyl]-2-Methyl-3H-Pyrimidin-4-One Chloride
3-[(3,4-Dihydro-2-Methyl-4-Oxo-5-Pyrimidinyl)Methyl]-5-(2-Hydroxyethyl)-4-Methyl-Thiazolium
5-[2-Hydroxyethyl]-3-[4-hydroxy-2-methyl-5-pyrimidinylmethyl]-4-methylthiazolium chloride hydrochloride

Biological Activity

[Description]:

Oxythiamine, an antimetabolite and a vitamin B1 antagonist, is a well-known thiamine antagonist and inhibitor of transketolase.

[Related Catalog]:

Signaling Pathways >> Others >> Others
Research Areas >> Cancer

[Target]

Vitamin B1, Thiamine, Transketolase[1].


[In Vitro]

Oxythiamine, an antimetabolite and a vitamin B1 antagonist, is a well-known thiamine antagonist and inhibitor of transketolase. Oxythiamine alters protein expression in a dose dependent manner. The level of alpha-enolase is increased by Oxythiamine treatment, while expression of 14-3-3 protein beta/alpha is suppressed by Oxythiamine at a stratified dose. Oxythiamine causes dynamic changes of total protein expression in time dependent fashion. Oxythiamine suppresses expression of cellular phosphor proteins significantly[2].

[Cell Assay]

Human pancreatic carcinoma cell line MIA PaCa-2 is used throughout the study. Experiments are set up in two groups: dose and time-dependent groups. For the dose-dependent group, the cells are stimulated with 5, 50 and 500 μM Oxythiamine (OT) for 48 hours, respectively. The unstimulated cells are considered as control. For the time-dependent group, the cells are stimulated with 50 μM Oxythiamine in MEM containing natural amino acids or 50% of 15 N algal amino acid mixture for 12 and 48 h. The unstimulated cells are considered as the zero time point. Each treatment is repeated four times with 10 mL/flask. The cell pellets are then collected for further analysis[2].

[References]

[1]. Moradi H, et al. Functional thiamine deficiency in end-stage renal disease: malnutrition despite ample nutrients. Kidney Int. 2016 Aug;90(2):252-254.

[2]. Wang J, et al. Inhibition of transketolase by oxythiamine altered dynamics of protein signals in pancreatic cancer cells. Exp Hematol Oncol. 2013 Jul 27;2:18.


[Related Small Molecules]

Captisol | Cyclosporin A | H2DCFDA | 0MPTP hydrochloride | GW4869 | Etomoxir | TD139 | Mitoquinone mesylate | GSK2795039 | JC-1 | BAPTA-AM | AP 20187 | Setanaxib (GKT137831) | D-Luciferin | Crotaline

Chemical & Physical Properties

[ Molecular Formula ]:
C12H16N3O2S

[ Molecular Weight ]:
266.34

[ PSA ]:
98.36000

[ LogP ]:
2.33510

[ Storage condition ]:
2-8℃


Related Compounds

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