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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
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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.".
57:)-1,13-Diamino-2,2,5,7-tetrahydroxy-11,13-dimethyl-5,7-dioxo-4,6,8-trioxa-5λ,7λ-diphospha-11λ-1(9)-purina-13(5)-pyrimidina-11(5,3)-thiazola-2(2,5)-oxolanatridecaphan-11-ylium
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262:. It was chemically synthesized and exists in small amounts in vertebrate liver. Its biological significance remains unknown.
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258:(AThDP), or thiaminylated adenosine diphosphate (ADP) is a naturally occurring thiamine adenine
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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
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292:"Update on Thiamine Triphosphorylated Derivatives and Metabolizing Enzymatic Complexes"
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Except where otherwise noted, data are given for materials in their
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135:Key: YLSJMTRFGUMRTH-HPXJRWHBSA-O
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356:10.1111/j.1742-4658.2009.07040.x
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290:Bettendorff L (November 2021).
272:Adenosine thiamine triphosphate
217:(at 25 °C , 100 kPa).
17:Adenosine thiamine diphosphate
256:Adenosine thiamine diphosphate
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207:674.50 g/mol
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37:Systematic IUPAC name
309:10.3390/biom11111645
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244:Infobox references
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350:(12): 3256–3268.
252:Chemical compound
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302:(11): 1645.
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296:Biomolecules
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64:Identifiers
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411:Pyrimidines
391:Nucleotides
165:Properties
107:acid:
81:acid:
385:Categories
278:References
260:nucleotide
203:Molar mass
70:3D model (
406:Thiazoles
396:Thiamine
372:23313946
364:19438713
328:34827643
266:See also
197:S
110:53481915
401:Purines
319:8615392
237:what is
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232:verify
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149:SMILES
31:Names
368:S2CID
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193:P
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185:N
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55:R
51:R
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43:R
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