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Chemical Structure| 21138-24-9 Chemical Structure| 21138-24-9
Chemical Structure| 21138-24-9

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L-Inosine is an endogenous purine nucleoside with anti-inflammatory, immunomodulatory, and neuroprotective effects, commonly used in research on nerve injury and immune diseases.

4.5 *For Research Use Only! Not for Human Use. We Do Not Sell to Patients.

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Product Details of L-Inosine

CAS No. :21138-24-9
Formula : C10H12N4O5
M.W : 268.23
SMILES Code : O=C1NC=NC2=C1N=CN2[C@H]3O[C@@H](CO)[C@H](O)[C@@H]3O
English Name :9-((2S,3S,4R,5S)-3,4-Dihydroxy-5-(hydroxymethyl)tetrahydrofuran-2-yl)-1H-purin-6(9H)-one
MDL No. :MFCD00673221

Safety of L-Inosine

Application In Synthesis of L-Inosine

* All experimental methods are cited from the reference, please refer to the original source for details. We do not guarantee the accuracy of the content in the reference.

  • Downstream synthetic route of [ 21138-24-9 ]

[ 21138-24-9 ] Synthesis Path-Downstream   1~3

YieldReaction ConditionsOperation in experiment
47% 5 9-β-L-Ribofuranosylhypoxanthine (11) EXAMPLE 5 9-β-L-Ribofuranosylhypoxanthine (11) A mixture of 9 (1.05 g, 1.70 mmol), mercaptoethanol (0.48 ml, 6.9 mmol), and NaOMe in MeOH (100 ml) was refluxed for four hours. The reaction mixture was cooled, neutralized with glacial acetic acid and evaporated to dryness. The solid obtained was washed with CHCl3 and the residue was crystallized from EtOH to give pure 11 (6.198 g, 47%) as white crystals: m.p. 212°-213° C. (dec).
  • 2
  • [ CAS Unavailable ]
  • [ 21138-24-9 ]
  • [ CAS Unavailable ]
YieldReaction ConditionsOperation in experiment
>99 In water aq. soln. of Pt(S-Et-L-Cys)Cl2 and inosine (molar ratio 1:2) is stirredwith heating at 50-60°C overnight; soln. is evapd., excess acetone added, complex filtered and dried at room temp. and then 110°C in vac.; elem. anal.;
  • 3
  • [ 21434-64-0 ]
  • [ 21138-24-9 ]
  • [ CAS Unavailable ]
YieldReaction ConditionsOperation in experiment
>99 In water aq. soln. of Pt(S-Me-L-Cys)Cl2 and inosine (molar ratio 1:2) is stirredwith heating at 50-60°C overnight; soln. evapd., excess acetone added, complex filtered and dried at room temp. and then 110°C in vac.; elem. anal.;
 

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