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Documenti fondamentali

I4125

Sigma-Aldrich

Inosine

≥99% (HPLC)

Sinonimo/i:

(−)-Inosine, Hypoxanthine 9-β-D-ribofuranoside

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About This Item

Formula empirica (notazione di Hill):
C10H12N4O5
Numero CAS:
Peso molecolare:
268.23
Beilstein:
624896
Numero CE:
Numero MDL:
Codice UNSPSC:
41106305
ID PubChem:
NACRES:
NA.51

Livello qualitativo

Saggio

≥99% (HPLC)

Punto di fusione

222-226 °C (dec.) (lit.)

Stringa SMILE

OC[C@H]1O[C@H]([C@H](O)[C@@H]1O)n2cnc3C(=O)NC=Nc23

InChI

1S/C10H12N4O5/c15-1-4-6(16)7(17)10(19-4)14-3-13-5-8(14)11-2-12-9(5)18/h2-4,6-7,10,15-17H,1H2,(H,11,12,18)/t4-,6-,7-,10-/m1/s1
UGQMRVRMYYASKQ-KQYNXXCUSA-N

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Descrizione generale

Inosine is a non-canonical nucleotide majorly present as monophosphate. It has ability to base pair with deoxythymidine, deoxyadenosine and deoxyguanosine. Incorporation of inosine in place of guanine modulates translational events. Inosine has antioxidant, anti-inflammatory and neuroprotective functionality. Inosine is prescribed as a therapeutic supplement for nerve injury, inflammation and oxidative stress. It modulates biological processes through adenosine receptors. Its enhances neurite outgrowth in depressive disorders via adenosine receptors. Inosine is also used for treating sepsis in infections.

Applicazioni

Inosine has been used:
  • as a medium supplement in nucleotide rescue experiments in pancreatic cancer cell lines.
  • as a component in holidic (synthetic) medium and in larval two-choice preference assay.
  • as a reference standard in mass spectroscopy.

Azioni biochim/fisiol

Inosine is a potent stimulator of nerve growth factor (NGF) induced neurite outgrowth. The elevated levels of inosine in brain following injury are associated with the increased expression proteins related to axonal regeneration and growth. Mice given inosine demonstrated enhanced recovery of fine motor control following ischemic brain damage. Inosine may be used in studies of the process A-to-I RNA editing.

Codice della classe di stoccaggio

11 - Combustible Solids

Classe di pericolosità dell'acqua (WGK)

WGK 2

Punto d’infiammabilità (°F)

Not applicable

Punto d’infiammabilità (°C)

Not applicable

Dispositivi di protezione individuale

Eyeshields, Gloves, type N95 (US)


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I clienti hanno visto anche

Slide 1 of 7

1 of 7

Inosine induces context-dependent recoding and translational stalling
Licht K, et al.
Nucleic Acids Research (2018)
Oral administration of inosine produces antidepressant-like effects in mice
Muto J, et al.
Scientific Reports, 4, 4199-4199 (2014)
Inosine-a Multifunctional Treatment for Complications of Neurologic Injury
Doyle C, et al.
Cellular Physiology and Biochemistry, 49(6), 2293-2303 (2018)
Inosine in DNA and RNA
Alseth I, et al.
Current Opinion in Genetics & Development, 26, 116-123 (2014)
Inosine reduces systemic inflammation and improves survival in septic shock induced by cecal ligation and puncture
Liaudet L, et al.
American Journal of Respiratory and Critical Care Medicine, 164(7), 1213-1220 (2001)

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