Adenosine thiamine diphosphate

Nowadays, Adenosine thiamine diphosphate is a topic that has gained great relevance in today's society. For several years now, Adenosine thiamine diphosphate has been a source of debate and reflection in different areas, whether in politics, culture, economics or technology. Adenosine thiamine diphosphate has sparked the interest of experts and scholars, as well as ordinary people seeking to understand more about this topic. In this article, we will explore the different aspects and perspectives related to Adenosine thiamine diphosphate, analyzing its impact and relevance today.
Adenosine thiamine diphosphate
Names
Systematic IUPAC name
(22R,23S,24R,25R)-16,134-Diamino-23,24,5,7-tetrahydroxy-114,132-dimethyl-5,7-dioxo-4,6,8-trioxa-5λ5,7λ5-diphospha-113λ5-1(9)-purina-13(5)-pyrimidina-11(5,3)-thiazola-2(2,5)-oxolanatridecaphan-113-ylium
Identifiers
3D model (JSmol)
  • InChI=1S/C22H29N9O10P2S/c1-11-15(44-10-30(11)6-13-5-25-12(2)29-19(13)23)3-4-38-42(34,35)41-43(36,37)39-7-14-17(32)18(33)22(40-14)31-9-28-16-20(24)26-8-27-21(16)31/h5,8-10,14,17-18,22,32-33H,3-4,6-7H2,1-2H3,(H5-,23,24,25,26,27,29,34,35,36,37)/p+1/t14-,17+,18+,22-/m1/s1
    Key: YLSJMTRFGUMRTH-HPXJRWHBSA-O
  • acid: CC1=C(SC=1CC2=CN=C(N=C2N)C)CCOP(=O)(O)OP(=O)(O)OC3(((O3)N4C=NC5=C(N=CN=C54)N)O)O
Properties
C22H28N9O10P2S−
Molar mass 674.50 g/mol
Except where otherwise noted, data are given for materials in their standard state (at 25 °C , 100 kPa).
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Adenosine thiamine diphosphate (AThDP), or thiaminylated adenosine diphosphate (ADP) is a naturally occurring thiamine adenine nucleotide. It was chemically synthesized and exists in small amounts in vertebrate liver. Its biological significance remains unknown.[1][2]

See also

References

  1. ^ Bettendorff L (November 2021). "Update on Thiamine Triphosphorylated Derivatives and Metabolizing Enzymatic Complexes". Biomolecules. 11 (11): 1645. doi:10.3390/biom11111645. PMC 8615392. PMID 34827643.
  2. ^ Frédérich M.; Delvaux D.; Gigliobianco T.; Gangolf M.; Dive G.; Mazzucchelli G.; Elias B.; De Pauw E.; Angenot L.; Wins P.; Bettendorff L. (2009). "Thiaminylated adenine nucleotides — chemical synthesis, structural characterization and natural occurrence FEBS J.". The FEBS Journal. 276 (12): 3256–3268. doi:10.1111/j.1742-4658.2009.07040.x. PMID 19438713. S2CID 23313946.
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