Jump to content
 







Main menu
   


Navigation  



Main page
Contents
Current events
Random article
About Wikipedia
Contact us
Donate
 




Contribute  



Help
Learn to edit
Community portal
Recent changes
Upload file
 








Search  

































Create account

Log in
 









Create account
 Log in
 




Pages for logged out editors learn more  



Contributions
Talk
 



















Contents

   



(Top)
 


1 References  





2 External links  














4-Deoxypyridoxine






العربية
تۆرکجه
فارسی
Српски / srpski
Srpskohrvatski / српскохрватски
 

Edit links
 









Article
Talk
 

















Read
Edit
View history
 








Tools
   


Actions  



Read
Edit
View history
 




General  



What links here
Related changes
Upload file
Special pages
Permanent link
Page information
Cite this page
Get shortened URL
Download QR code
Wikidata item
 




Print/export  



Download as PDF
Printable version
 




In other projects  



Wikimedia Commons
 
















Appearance
   

 






From Wikipedia, the free encyclopedia
 


4-Deoxypyridoxine
4-Deoxypyridoxine
Names
Preferred IUPAC name

5-(Hydroxymethyl)-2,4-dimethylpyridin-3-ol

Identifiers

CAS Number

3D model (JSmol)

  • Interactive image
  • ChemSpider

    PubChem CID

    UNII

    CompTox Dashboard (EPA)

    • InChI=1S/C8H11NO2/c1-5-7(4-10)3-9-6(2)8(5)11/h3,10-11H,4H2,1-2H3 checkY

      Key: KKOWAYISKWGDBG-UHFFFAOYSA-N checkY

    • InChI=1/C8H11NO2/c1-5-7(4-10)3-9-6(2)8(5)11/h3,10-11H,4H2,1-2H3

      Key: KKOWAYISKWGDBG-UHFFFAOYAH

    • CC1=C(C(=NC=C1CO)C)O

    • Oc1c(c(cnc1C)CO)C

    Properties

    Chemical formula

    C8H11NO2
    Molar mass 153.181 g·mol−1

    Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).

    ☒N verify (what is checkY☒N ?)

    Infobox references

    4-Deoxypyridoxine is a vitamin B6 antagonist.[1] It may be toxic to developing embryos since it can have negative effects on collagen and elastin during development.[2] The presence of this compound can produce vitamin B6 deficiency, which suppresses the immune system.[3] 4-Deoxypyridoxine lowers vitamin B6 concentration by competitively inhibiting some of the enzymes necessary for the regeneration of vitamin B6.[4] The related immunosuppression can be beneficial in animal models of Trichinella spiralis infections.[5] 4-Deoxypyridoxine has also been described as an inhibitor of sphingosine-1-phosphate lyase.[6] The inhibition of sphingosine-1-phosphate lyase by 4-deoxypyridoxine has been shown to prevent cell death of ex vivo animal pancreatic islets. The use of 4-deoxypyridoxine to prevent stress-induced apoptosis is suggest that the compound, as well as other inhibitors of sphingosine-1-phosphate lyase, could be used to increase the viability of donor pancreatic tissue in the treatment of diabetes.[7]

    References

    [edit]
    1. ^ Coburn SP, Mahuren JD, Schaltenbrand WE, Wostmann BS, Madsen D (1 February 1981). "Effects of vitamin B-6 deficiency and 4'- deoxypyridoxine on pyridoxal phosphate concentrations, pyridoxine kinase and other aspects of metabolism in the rat". J. Nutr. 111 (2): 391–8. doi:10.1093/jn/111.2.391. PMID 6257871.
  • ^ Bird TA, Levene CI (1983). "The effect of a vitamin B-6 antagonist, 4-deoxypyridoxine, on the cross-linking of collagen in the developing chick embryo". Biochem. J. 210 (3): 633–8. doi:10.1042/bj2100633. PMC 1154271. PMID 6135414.
  • ^ Trakatellis A, Dimitriadou A, Exindari M, et al. (1992). "Effect of pyridoxine deficiency on immunological phenomena". Postgrad Med J. 68 (Suppl 1): S70–7. PMID 1409221.
  • ^ Sheridan, E.; Gillespie, S.; Johnson, C. R.; Lecavalier, L.; Smith, T.; Swiezy, N.; Turner, K.; Pritchett, J.; Mruzek, D. W.; Evans, A. N.; Bearss, K.; Scahill, L. (2021). "Using Parent Target Problem Narratives to Evaluate Outcomes in Children with Autism Spectrum Disorder". Research on Child and Adolescent Psychopathology. 49 (11): 1527–1535. doi:10.1007/s10802-021-00843-8. PMID 34213717. S2CID 235709478.
  • ^ Frydas S, Papaioanou N, Vlemmas I, et al. (1999). "Vitamin B6-deficient diet plus 4-deoxypyridoxine (4-DPD) reduces the inflammatory response induced by T. spiralis in diaphragm, masseter and heart muscle tissue of mice". Mol. Cell. Biochem. 197 (1–2): 79–85. doi:10.1023/A:1006958310081. PMID 10485327. S2CID 23457740.
  • ^ Weigel, Cynthia; Hüttner, Sören S.; Ludwig, Kristin; Krieg, Nadine; Hofmann, Susann; Schröder, Nathalie H.; Robbe, Linda; Kluge, Stefan; Nierhaus, Axel; Winkler, Martin S.; Rubio, Ignacio (2020-08-01). "S1P lyase inhibition protects against sepsis by promoting disease tolerance via the S1P/S1PR3 axis". eBioMedicine. 58: 102898. doi:10.1016/j.ebiom.2020.102898. ISSN 2352-3964. PMC 7381498. PMID 32711251.
  • ^ Lee, Hakmo; Seon Park, Ho; Hee Hong, Shin; Kyung Choi, Ok; Cho, Sung-Dae; Park, Jongwoo; Eun Oh, Ju; Soo Chung, Sung; Jung, Hye Seung; Park, Kyong Soo (2013). "4-deoxypyridoxine improves the viability of isolated pancreatic islets ex vivo". Islets. 5 (3): 116–121. doi:10.4161/isl.25254. PMID 23756681. S2CID 22959354.
  • [edit]
    Retrieved from "https://en.wikipedia.org/w/index.php?title=4-Deoxypyridoxine&oldid=1224816589"

    Categories: 
    Immunosuppressants
    Hydroxypyridines
    Primary alcohols
    Vitamin B6 antagonists
    Hidden categories: 
    Chemical articles with multiple compound IDs
    Multiple chemicals in an infobox that need indexing
    Articles without EBI source
    Articles without KEGG source
    Articles containing unverified chemical infoboxes
    Chembox image size set
    Articles with short description
    Short description matches Wikidata
    Commons category link from Wikidata
     



    This page was last edited on 20 May 2024, at 16:51 (UTC).

    Text is available under the Creative Commons Attribution-ShareAlike License 4.0; additional terms may apply. By using this site, you agree to the Terms of Use and Privacy Policy. Wikipedia® is a registered trademark of the Wikimedia Foundation, Inc., a non-profit organization.



    Privacy policy

    About Wikipedia

    Disclaimers

    Contact Wikipedia

    Code of Conduct

    Developers

    Statistics

    Cookie statement

    Mobile view



    Wikimedia Foundation
    Powered by MediaWiki