IUPACName=2- [3- [(4-amino-2-methyl- pyrimidin-5-yl)methyl] - 4-methyl-thiazol-5-yl] ethanol
Section1= Chembox Identifiers
SMILES= [Cl-] .Cc1c(CCO)sc [n+] 1Cc2cncnc2N
Section2= Chembox Properties
MeltingPt=248-260 °C (hydrochloride salt)
Section3= Chembox Hazards
Autoignition= :"For the similarly spelled pyrimidine, see
Thiamin or thiamine, also known as
vitaminB1 and aneurine hydrochloride, is the term for a family of molecules sharing a common structural feature responsible for its activity as a vitamin. It is one of the B vitamins. Its most common form is a colorless chemical compound with a chemical formulaC12H17N4OS. This form of thiamin is solublein water, methanol, and glyceroland practically insoluble in acetone, ether, chloroform, and benzene. Another form of thiamin known as TTFD has different solubility properties and belongs to a family of molecules often referred to as fat-soluble thiamins. Thiamin decomposes if heated. Its chemical structure contains a pyrimidinering and a thiazolering.
Thiamin is one of only four nutrients associated with a pandemic human deficiency disease. It is essential for neural function and carbohydrate metabolism. Thiamin deficiency results in
beriberi, a disease characterized by a bewildering variety of [http://ecam.oxfordjournals.org/cgi/content/abstract/3/1/49?ijkey=UJiBzBnDXsxRKnp&keytype=ref symptoms] . Common symptoms often involve the nervous system and the heart. In less severe deficiency, nonspecific signs include malaise, weight loss, irritability and confusion. [ Combs,G. F. Jr. "The vitamins: Fundamental Aspects in Nutrition and Health". 3rd Edition. Ithaca, NY: Elsevier Academic Press; 2008; pg.266]
Thiamin was first discovered in 1910 by
Umetaro Suzukiin Japanwhen researching how rice brancured patients of beriberi. He named it aberic acid (later oryzanin). He did not determine its chemical composition, nor that it was an amine. It was first crystallized by Jansen and Donath in 1926 (they named it aneurin, for antineuritic vitamin). Its chemical composition and synthesis was finally reported by Robert R. Williamsin 1935. He also coined the current name for it, thiamin.
Thiamin is found in a wide variety of many foods at low concentrations. Yeast and liver are the most highly concentrated sources of thiamin, cereal grains, however, are the most important dietary sources of thiamin in the diet as these foods are consumed readily in most diets. Of the cereal grains, whole grains contain more thiamin than refined grains. Thiamin is found in the outer layers of the grain as well as the germ. During the refining process these segments of the grain are removed therefore decreasing the thiamin content in products such as white rice and white bread. For example, 100 g of whole wheat flour contains 0.55 mg of thiamin while 100 g of white flour only contains 0.06 mg of thiamin. In addition to cereal grains some vegetables and meats are also good sources of thiamin. Listed below are foods rich in thiamin. [Combs GF. The vitamins: fundamental aspects in nutrition and health. 3rd Ed. Elsevier: Boston, 2008.]
* Whole grain flour (
Liver(beef or pork)
Thiamin in foods can be degraded in a variety of ways. Sulfites, which are added to foods usually as a preservative, [McGuire, M. and K.A. Beerman. Nutritional Sciences: From Fundamentals to Foods. 2007. California: Thomas Wadsworth.] will attack thiamin at the methylene bridge in the structure, cleaving the pyrimidine ring from the thiazole ring. [Combs, G.F. The Vitamins: Fundamental Aspects in Nutrition and Health. 2008. San Diego: Elsevier] The rate of this reaction is increased under acidic conditions. Thiamin can also be degraded by thiaminases. Some thiaminases are produced by bacteria. Bacterial thiaminases are cell surface enzymes that must dissociate from the membrane before being activated. The dissociation can occur in ruminants under acidotic conditions. Rumen bacteria also reduce sulfate to sulfite, therefore high dietary intakes of sulfate can have thiamin-antagonistic activities.
Plant thiamin antagonists are heat stable and occur as both the ortho and para hydroxyphenols. Some examples of these antagonists are caffeic acid, chlorogenic acid and tannic acid. These compounds interact with the thiamin to oxidize the thiazole ring, thus rendering it unable to be absorbed. Two flavonoids, quercetin and rutin, have also been implicated as thiamin antagonists. [Combs, G.F. The Vitamins: Fundamental Aspects in Nutrition and Health. 2008. San Diego: Elsevier]
Thiamin is released by the action of phosphatase and pyrophosphatase in the upper small intestine. At low concentrations the process is carrier mediated and at higher concentrations, absorption occurs via passive diffusion. Active transport is greatest in the jejunum and ileum. The cells of the intestinal mucosa have thiamin pyrophosphokinase activity, but it is unclear whether the enzyme is linked to active absorption. The majority of thiamin present in the intestine is in the phosphorylated form, but when thiamin arrives on the serosal side of the intestine it is often in the free form. The uptake of thiamin by the mucosal cell is likely coupled in some way to its phosphorylation/dephosphorylation. On the serosal side of the intestine, evidence has shown that discharge of the vitamin by those cells is dependent on Na+-dependent ATPase. [ Combs,G. F. Jr. "The vitamins: Fundamental Aspects in Nutrition and Health". 3rd Edition. Ithaca, NY: Elsevier Academic Press; 2008; pg.268]
Bound to serum proteins
The majority of thiamin in
serumis bound to proteins, mainly albumin. Approximately 90% of total thiamin in blood is in erythrocytes. A specific binding protein called thiamin-binding protein (TBP) has been identified in rat serum and is believed to be a hormonally regulated carrier protein that is important for tissue distribution of thiamin. [ Combs,G. F. Jr. "The vitamins: Fundamental Aspects in Nutrition and Health". 3rd Edition. Ithaca, NY: Elsevier Academic Press; 2008]
Uptake of thiamin by cells of the blood and other tissues occurs via active transport. About 80% of intracellular thiamin is phosphorylated and most is bound to proteins. In some tissues, thiamin uptake and secretion appears to be mediated by a soluble thiamin transporter that is dependent on Na+ and a transcellular proton gradient. The highest concentration of the transporter have been found in skeletal muscle, heart, and placenta. [ Combs,G. F. Jr. "The vitamins: Fundamental Aspects in Nutrition and Health". 3rd Edition. Ithaca, NY: Elsevier Academic Press; 2008]
Human storage of thiamin is about 25 to 30 mg with the greatest concentrations in skeletal muscle, heart, brain, liver, and kidneys. Thiamin monophosphate(TMP) and free thiamin is present in plasma, milk, cerebrospinal fluid, and likely all extracellular fluids. Unlike the highly phosphorylated forms of thiamin, TMP and free thiamin are capable of crossing cell membranes. Thiamin contents in human tissues are less than those of other species. [ Combs,G. F. Jr. "The vitamins: Fundamental Aspects in Nutrition and Health". 3rd Edition. Ithaca, NY: Elsevier Academic Press; 2008]
Thiamin deficiency can lead to myriad problems including
neurodegeneration, wasting and death. A lack of thiamin can be caused by malnutrition, alcoholism, a diet high in thiaminase-rich foods (raw freshwater fish, raw shellfish, ferns) and/or foods high in anti-thiamin factors ( tea, coffee, betel nuts). [ [http://lpi.oregonstate.edu/infocenter/vitamins/thiamin/index.html "Thiamin"] , Jane Higdon, Micronutrient Information Center, Linus Pauling Institute]
Well-known syndromes caused by thiamin deficiency include
Wernicke-Korsakoff syndromeand beriberi, diseases also common with chronic alcoholism.
There is only one book in English devoted entirely to the clinical use of vitamin B1. It was written by
Derrick Lonsdale. According to the author, early signs of thiamin deficiency include anorexia, insomnia, sleep apnea, dementia, depression, impotence, and infertility. Extensive published research reviewed in the book provides statistically significant data supporting this position.
An important property of thiamin that distinguishes it from the other three vitamins associated with vitamin deficiency (vitamin C, vitamin B3, and vitamin D) is that it is extracted from food in the digestive tract in a form that requires specialized proteins for absorption into the bloodstream. Once in the bloodstream, this form of thiamin requires specialized proteins for distribution to cells throughout the body.
Because thiamin requires specialized transport proteins, malfunctions of these proteins can cause localized deficiency even when the diet contains more than twice the recommended daily allowance. A form of thiamin that does not require specialized transport proteins for absorption and distribution is produced commercially in Japan. It is known as TTFD. A google scholar search of "thiamin TTFD" results in over 1000 references to peer-reviewed research related to preventing and treating disease with TTFD.
Polioencephalomalacia (PEM), is the most common thiamin deficiency disorder in young ruminant and nonruminant animals. Symptoms of PEM include a profuse, but transient diarrhea, listlessness, circling movements, star gazing or opisthotonus (head drawn back over neck), and muscle tremors. [National Research Council. 1996. Nutrient Requirements of Beef Cattle, Seventh Revised Ed. Washington, D.C.: National Academy Press.]
It is thought that many people with
diabeteshave a deficiency of thiamin and that this may be linked to some of the complications that can occur.cite journal |author=Thornalley PJ |title=The potential role of thiamine (vitamin B(1)) in diabetic complications |journal=Curr Diabetes Rev |volume=1 |issue=3 |pages=287–98 |year=2005 |pmid=18220605 |doi=] [ [http://news.bbc.co.uk/1/hi/health/6935482.stm Diabetes problems 'vitamin link'] , BBC News, Tuesday, 7 August 2007]
Alcoholic Brain Disease [Martin, PR, Singleton, CK, Hiller-Sturmhofel, S (2003). "The role of thiamine deficiency in alcoholic brain disease" Alcohol Research and Health. 27:134-142]
Thiamin and thiamin-using enzymes are present in all cells of the body, thus, a thiamin deficiency would seem to adversely affect all of the organ systems. However, the nervous system (and heart) shows particular sensitivity to the effects of a thiamin deficiency at the cellular level.
Nerve cells and other supporting cells (such as glial cells) of the nervous system require thiamin. Examples of neurologic disorders that are linked to alcohol abuse include Wernicke’s encephalopathy (
Wernicke-Korsakoff syndrome) and Korsakoff’s psychosis (alcohol amnestic disorder) as well as varying degrees of cognitive impairment.
How does alcoholism induce thiamin deficiency? The enzymes transketolase, pyruvate dehydrogenase (PDH) and alpha-ketoglutarate dehydrogenase (α-KGDH) all require thiamin as a cofactor in order to function in carbohydrate metabolism. Therefore, a thiamin deficiency would be detrimental to the functionality of these enzymes. Transketolase is important in the pentose phosphate pathway. PDH and α-KGDH function in biochemical pathways that result in the generation of adenosine triphosphate (ATP), which is a major form of energy for the cell. PDH is also needed for the production of acetylcholine, a neurotransmitter, and for myelin synthesis. During metabolism, PDH determines whether the process is aerobic or anaerobic, and α-KGDH is responsible for determining the rate of the citric acid cycle.
What are the mechanisms of alcohol-induced thiamin deficiency? 1) Inadequate nutritional intake: Alcoholics tend to intake less than the recommended amount of thiamin, however it is also seen that others have an extremely high level of free thiamin, suggesting an inability of these individuals to convert thiamin to the biologically active, phosphorylated form. 2) Decreased uptake of thiamin from the GI tract: Active transport of thiamin into the enterocyte occurs mostly in conditions of low thiamin concentration. The absorption is disturbed during acute alcohol exposure as illustrated by less thiamin being converted into the phosphate-containing form, suggesting a dysfunction of the enzyme responsible for this transformation: thiamin diphosphokinase.3) Impaired thiamin utilization: Magnesium, which is required for the binding of thiamin to thiamin-using enzymes within the cell, is also deficient due to chronic alcohol consumption. The inefficient utilization of any thiamin that does reach the cells will further exacerbate the thiamin deficiency.
Following improved nutrition and the removal of alcohol consumption, some impairments linked with thiamin deficiency are reversed; particularly poor brain functionality.
Thiamin deficiency in poultry
As most feedstuffs used in poultry diets contain enough quantities of vitamins to meet the requirements in this species, deficiencies in this vitamin does not occur with commercial diets. This was, at least, the opinion in the
1960s. [Merck veterinary manual, ed 1967, pp 1440-1441.]
Mature chickens show signs 3 weeks after being fed a deficient diet. In young chicks, it can appear before 2 weeks of age.
Onset is sudden in young chicks. There is anorexia and an unsteady gait. Later on, there are locomotor signs, beginning with an apparent paralysis of the flexor ot the toes. The characteristic position is called "stargazing", meaning a chick "sitting on its hocks and the head in
Response to administration of the vitamin is rather quick, occurring a few hours later. [R.E. Austic and M.L. Scott, Nutritional deficiency diseases, in "Diseases of poultry, ed. by M.S. Hofstad, Iowa State University Press, Ames, Iowa, USA ISBN 0-8138-0430-2, p. 50.]
[http://www.merckvetmanual.com/mvm/index.jsp?cfile=htm/bc/206934.htm The disease is described more carefully here]
Differential diagnosis include
riboflavin deficiencyand avian encephalomyelitis. In riboflavin deficiency, the "curled toes" is a characteristic symptom. Muscle tremor is typical of avian encephalomyelitis. A therapeutic diagnosiscan be tried by supplementing Vitamin B1 only in affectd bird. If the animals do not respond in a few hours, Vitamin B1 deficiency can be excluded.
Cerebrocortical necrosis in ruminants
Cerebrocortical necrosis is a not uncommon conditions seen in
calvesand lambs, which rapidly responds to injection of thiamin. Nevertheless, it is not clear if it is a secondary Vitamin B1 deficiency or a therapeutical effect of thiamin.
A positive diagnosis test for thiamin deficiency can be ascertained by measuring the activity of the enzyme
transketolasein erythrocytes. Thiamin can also be seen directly in whole blood following the conversion of thiamin to a fluorescentthiochrome derivative. However, this test may not reveal the deficiency in diabetic patients. [ [http://www2.warwick.ac.uk/newsandevents/pressreleases/researchers_find_vitamin/ Researchers find vitamin B1 deficiency key to vascular problems for diabetic patients] , University of Warwick]
Thiamin phosphate derivatives
There are four known natural thiamin phosphate derivatives:
thiamin monophosphate(ThMP), thiamin diphosphate(ThDP) or thiamin pyrophosphate(TPP), thiamin triphosphate(ThTP), and the recently discovered adenosine thiamin triphosphate(AThTP).
Thiamin pyrophosphate(TPP), also known as "thiamin diphosphate" (ThDP), and cocarboxylaseis a coenzymefor several enzymes that catalyze the dehydrogenation( decarboxylationand subsequent conjugation to Coenzyme A) of alpha-keto acids. Examples include:
pyruvate dehydrogenaseand α-ketoglutarate dehydrogenase ( metabolismof carbohydrates)
branched-chain alpha-keto acid dehydrogenase
transketolase(functions in the pentose phosphate pathwayto synthesize NADPHand the pentose sugars deoxyriboseand ribose)
* In other species:
pyruvate decarboxylase(in yeast)
** several additional
TPP is synthesized by the enzyme
thiamin pyrophosphokinase, which requires free thiamin, magnesium, and adenosine triphosphate.
Thiamin triphosphate(ThTP) was long considered a specific neuroactive form of thiamin. However, recently it was shown that ThTP exists in bacteria, fungi, plantsand animalssuggesting a much more general cellular role. In particular in " E. coli" it seems to play a role in response to amino acid starvation.
Adenosine thiamin triphosphate
Adenosine thiamin triphosphate(AThTP) or thiaminylated adenosine triphosphate has recently been discovered in " Escherichia coli" where it accumulates as a result of carbon starvation. In "E. coli", AThTP may account for up to 20 % of total thiamin. It also exists in lesser amounts in yeast, roots of higher plants and animal tissues.
Genetic diseases of thiamin transport are rare but serious. Thiamin Responsive Megaloblastic Anemia with diabetes mellitus and sensorineural deafness (TRMA)Thiamine Responsive Megaloblastic Anemia with severe diabetes mellitus and sensorineural deafness (TRMA) PMID 249270] is an autosomal recessive disorder caused by mutations in the gene
SLC19A2,SLC19A2 PMID 603941] a high affinity thiamin transporter. TRMA patients do not show signs of systemic thiamin deficiency, suggesting redundancy in the thiamin transport system. This has led to the discovery of a second high affinity thiamin transporter, SLC19A3.SLC19A3 PMID 606152] [OMIM|249270]
The RDA in most countries is set at about 1.4 mg. However, tests on volunteers at daily doses of about 50 mg have claimed an increase in mental acuity. [ [http://www.newhope.com/nutritionsciencenews/NSN_backs/Jan_99/thiamine.cfm Thiamine's Mood-Mending Qualities] , Richard N. Podel, Nutrition Science News, January 1999.]
Thiamin as an insect repellent
Some old studies suggested that the ingestion of large doses of thiamin (25 to 50 mg three times per day) could be effective as an
oral insect repellentagainst mosquito bites. [Pediatric Clinics of North America, 16:191, 1969] Fact|date=August 2008 However, there is now conclusive evidence that thiamin has no efficacy against mosquitoe bites. [ [http://clinicalevidence.bmj.com/ceweb/conditions/ind/0903/0903_I1177594695224.jsp BMJ Clinical Evidence] ] [cite journal
author = Ives AR, Paskewitz SM
year = 2005
title = Testing vitamin B as a home remedy against mosquitoes
journal = J. Am. Mosq. Control. Assoc.
volume = 21
issue = 2
pages = 213-217
pmid = 16033124
url = http://apt.allenpress.com/perlserv/?request=get-abstract&doi=10.1043%2F8756-971X(2005)021%5B0213%3ATVBAAH%5D2.3.CO%3B2&ct=1] [cite journal
author = Khan AA, Maibach HI, Strauss WG, Fenley WR.
year = 2005
title = Vitamin B1 is not a systemic mosquito repellent in man
journal = Trans. St. Johns Hosp. Dermatol. Soc.
volume = 55
issue = 1
pages = 99-102
pmid = 4389912
url =] [cite journal
author = Strauss WG, Maibach HI, Khan AA
year = 1968
title = Drugs and disease as mosquito repellents in man
journal = Am. J. Trop. Med. Hyg.
volume = 17
issue = 3
pages = 461-464
pmid = 4385133
url = ]
A 2002 pilot study administered thiamin tetrahydrofurfuryl disulfide (TTFD) rectally to ten
autism spectrumchildren, and found beneficial clinical effect in eight. [cite journal |author=Lonsdale D, Shamberger RJ, Audhya T |title=Treatment of autism spectrum children with thiamin tetrahydrofurfuryl disulfide: a pilot study |journal=Neuro Endocrinol. Lett |volume=23 |issue=4 |pages=303–8 |year=2002 |pmid=12195231 |url=http://www.nel.edu/pdf_w/23_4/NEL230402A02_Lonsdale_rw.pdf |format=PDF |accessdate=2007-08-10] There have been no follow-up trials.
* [http://www.ncbi.nlm.nih.gov/books/bv.fcgi?rid=bnchm.section.3106 "Branched-Chain Amino Acid Metabolism"] at ncbi.nlm.nih.gov
* [http://www.merckvetmanual.com/mvm/index.jsp?cfile=htm/bc/206934.htm Thiamin deficiency in poultry]
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