Inozin pranobeks

Inozin pranobeks
IUPAC ime
Drugi nazivi	Izoprinozin; Metizoprinol
Identifikacija
CAS registarski broj	36703-88-5
PubChem	37510
ChemSpider	16736312
KEGG	D01995
ATC code	J05AX05
Jmol-3D slike	Slika 1
Svojstva
Molekulska formula	C52H78N10O17
Molarna masa	1115,23 g/mol
	; ; Ukoliko nije drugačije napomenuto, podaci se odnose na standardno stanje (25 °C, 100 kPa) materijala
	Infobox references

Inozin pranobeks (izoprinozin ili metizoprinol) je kombinacija inozina, acetamidobenzojeve kiseline, i dimetilaminoizopropanol koja se koristi kao antivirusni lek.

Kratke činjenice Identifikacija, Svojstva ...

Zatvori

Inozin pranobeks ne utiče na same viruse. On deluje kao moćni imunostimulant. On se uglavnom koristi za tretiranje retkih komplikacija morbila subakutnog skleroznog panencefalitisa zajedno sa intratekalnom interferonskom terapijom.^[5]

[1]
Li Q, Cheng T, Wang Y, Bryant SH (2010). „PubChem as a public resource for drug discovery.”. Drug Discov Today 15 (23-24): 1052-7. DOI:10.1016/j.drudis.2010.10.003. PMID 20970519. edit
[2]
Evan E. Bolton, Yanli Wang, Paul A. Thiessen, Stephen H. Bryant (2008). „Chapter 12 PubChem: Integrated Platform of Small Molecules and Biological Activities”. Annual Reports in Computational Chemistry 4: 217-241. DOI:10.1016/S1574-1400(08)00012-1.
[3]
Hettne KM, Williams AJ, van Mulligen EM, Kleinjans J, Tkachenko V, Kors JA. (2010). „Automatic vs. manual curation of a multi-source chemical dictionary: the impact on text mining”. J Cheminform 2 (1): 3. DOI:10.1186/1758-2946-2-3. PMID 20331846. edit
[4]
Joanne Wixon, Douglas Kell (2000). „Website Review: The Kyoto Encyclopedia of Genes and Genomes — KEGG”. Yeast 17 (1): 48–55. DOI:10.1002/(SICI)1097-0061(200004)17:1<48::AID-YEA2>3.0.CO;2-H.
[5]
Campoli-Richards DM, Sorkin EM, Heel RC. (Nov 1986). „Inosine pranobex. A preliminary review of its pharmacodynamic and pharmacokinetic properties, and therapeutic efficacy”. Drugs 32 (5): 383-424.

Inozin

Portal Hemija

[1] [1]
Li Q, Cheng T, Wang Y, Bryant SH (2010). „PubChem as a public resource for drug discovery.”. Drug Discov Today 15 (23-24): 1052-7. DOI:10.1016/j.drudis.2010.10.003. PMID 20970519. edit

[2] [2]
Evan E. Bolton, Yanli Wang, Paul A. Thiessen, Stephen H. Bryant (2008). „Chapter 12 PubChem: Integrated Platform of Small Molecules and Biological Activities”. Annual Reports in Computational Chemistry 4: 217-241. DOI:10.1016/S1574-1400(08)00012-1.

[3] [3]
Hettne KM, Williams AJ, van Mulligen EM, Kleinjans J, Tkachenko V, Kors JA. (2010). „Automatic vs. manual curation of a multi-source chemical dictionary: the impact on text mining”. J Cheminform 2 (1): 3. DOI:10.1186/1758-2946-2-3. PMID 20331846. edit

[4] [4]
Joanne Wixon, Douglas Kell (2000). „Website Review: The Kyoto Encyclopedia of Genes and Genomes — KEGG”. Yeast 17 (1): 48–55. DOI:10.1002/(SICI)1097-0061(200004)17:1<48::AID-YEA2>3.0.CO;2-H.

[5] [5]
Campoli-Richards DM, Sorkin EM, Heel RC. (Nov 1986). „Inosine pranobex. A preliminary review of its pharmacodynamic and pharmacokinetic properties, and therapeutic efficacy”. Drugs 32 (5): 383-424.

[1]

[2]

[3]

[4]

[5]

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Inozin pranobeks

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Reference

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