Benfotiamine: Difference between revisions

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==Research==
==Research==
Benfotiamine has been studied in laboratory models of [[diabetic retinopathy]], [[neuropathy]], and [[nephropathy]].<ref name="pmid20188835">{{cite journal |vauthors=Balakumar P, Rohilla A, Krishan P, Solairaj P, Thangathirupathi A |title=The multifaceted therapeutic potential of benfotiamine |journal=Pharmacol Res |volume=61 |issue=6 |pages=482–8 |year=2010 |pmid=20188835 |doi=10.1016/j.phrs.2010.02.008}}</ref>
Benfotiamine has been studied in laboratory models of [[diabetic retinopathy]], [[neuropathy]], and [[nephropathy]].<ref name="pmid20188835">{{cite journal |vauthors=Balakumar P, Rohilla A, Krishan P, Solairaj P, Thangathirupathi A |title=The multifaceted therapeutic potential of benfotiamine |journal=Pharmacol Res |volume=61 |issue=6 |pages=482–8 |year=2010 |pmid=20188835 |doi=10.1016/j.phrs.2010.02.008}}</ref> As of 2015 there had been one clinical study of benfotiamine in [[diabetic neuropathy].<ref>{{cite journal|last1=Raval|first1=AD|last2=Thakker|first2=D|last3=Rangoonwala|first3=AN|last4=Gor|first4=D|last5=Walia|first5=R|title=Vitamin B and its derivatives for diabetic kidney disease.|journal=The Cochrane database of systematic reviews|date=12 January 2015|volume=1|pages=CD009403|doi=10.1002/14651858.CD009403.pub2|pmid=25579852}}</ref>


Administration of benfotiamine may increase intracellular levels of [[thiamine diphosphate]], a cofactor of [[transketolase]].<ref name="pmid20188835" />
Administration of benfotiamine may increase intracellular levels of [[thiamine diphosphate]], a cofactor of [[transketolase]].<ref name="pmid20188835" />

Revision as of 20:11, 14 March 2017

Benfotiamine
Clinical data
Trade namesMilgamma
Other namesS-Benzoylthiamine O-monophosphate
AHFS/Drugs.comInternational Drug Names
Routes of
administration
Oral
ATC code
Legal status
Legal status
Identifiers
  • S-[2-{[(4-Amino-2-methylpyrimidin-5-yl)methyl] (formyl)amino}-5-(phosphonooxy)pent-2-en-3-yl] benzenecarbothioate
CAS Number
PubChem CID
ChemSpider
UNII
ChEBI
ChEMBL
CompTox Dashboard (EPA)
ECHA InfoCard100.040.906 Edit this at Wikidata
Chemical and physical data
FormulaC19H23N4O6PS
Molar mass466.448 g/mol g·mol−1
3D model (JSmol)
  • O=P(O)(O)OCCC(/SC(=O)c1ccccc1)=C(/N(C=O)Cc2cnc(nc2N)C)C
  • InChI=1S/C19H23N4O6PS/c1-13(23(12-24)11-16-10-21-14(2)22-18(16)20)17(8-9-29-30(26,27)28)31-19(25)15-6-4-3-5-7-15/h3-7,10,12H,8-9,11H2,1-2H3,(H2,20,21,22)(H2,26,27,28)/b17-13- checkY
  • Key:BTNNPSLJPBRMLZ-LGMDPLHJSA-N checkY
 ☒NcheckY (what is this?)  (verify)

Benfotiamine (rINN, or S-benzoylthiamine O-monophosphate) is a synthetic S-acyl derivative of thiamine (vitamin B1).

It has been licensed for use in Germany since 1993 under the trade name Milgamma. (Combinations with pyridoxine or cyanocobalamin are also sold under this name.) It is prescribed there for treating sciatica and other painful nerve conditions.

It is marketed as a medicine and/or dietary supplement, depending on the respective Regulatory Authority.[citation needed]

Uses

Benfotiamine is primarily marketed as an antioxidant dietary supplement.

Pharmacology

After absorption, benfotiamine can be dephosphorylated by cells bearing an ecto-alkaline phosphatase to the lipid-soluble S-benzoylthiamine.[1] Benfotiamine should not be confused with allithiamine, a naturally occurring thiamine disulfide derivative with a distinct pharmacological profile.[2]

Research

Benfotiamine has been studied in laboratory models of diabetic retinopathy, neuropathy, and nephropathy.[3] As of 2015 there had been one clinical study of benfotiamine in [[diabetic neuropathy].[4]

Administration of benfotiamine may increase intracellular levels of thiamine diphosphate, a cofactor of transketolase.[3]

See also

References

  1. ^ Yamazaki, M (1968). "Studies on the absorption of S-benzoylthiamine O-monophosphate : (I) Metabolism in tissue homogenates". Vitamins. 38 (1): 12–20.
  2. ^ Volvert, M.L.; Seyen, S.; Piette, M.; Evrard, B.; Gangolf, M.; Plumier, J.C.; Bettendorff, L. (2008). "Benfotiamine, a synthetic S-acyl thiamine derivative, has different mechanisms of action and a different pharmacological profile than lipid-soluble thiamine disulfide derivatives". BMC Pharmacology. 8 (1): 10. doi:10.1186/1471-2210-8-10. PMC 2435522. PMID 18549472.{{cite journal}}: CS1 maint: unflagged free DOI (link)
  3. ^ a b Balakumar P, Rohilla A, Krishan P, Solairaj P, Thangathirupathi A (2010). "The multifaceted therapeutic potential of benfotiamine". Pharmacol Res. 61 (6): 482–8. doi:10.1016/j.phrs.2010.02.008. PMID 20188835.
  4. ^ Raval, AD; Thakker, D; Rangoonwala, AN; Gor, D; Walia, R (12 January 2015). "Vitamin B and its derivatives for diabetic kidney disease". The Cochrane database of systematic reviews. 1: CD009403. doi:10.1002/14651858.CD009403.pub2. PMID 25579852.

External links