2-Amino-1-metil-6-fenilimidazo(4,5-b)piridin

2-Amino-1-metil-6-fenilimidazo(4,5-b)piridin
	2-Amino-1-metil-6-fenilimidazo(4,5-b)piridin
Drugi nazivi	PhIP
Identifikacija
CAS registarski broj	105650-23-5
PubChem	1530
ChemSpider	1476
DrugBank	DB08398
ChEMBL	CHEMBL1213271 =
Jmol-3D slike	Slika 1
SMILES
	n1cc(cc2c1nc(n2C)N)c3ccccc3
InChI
	InChI=1S/C13H12N4/c1-17-11-7-10(9-5-3-2-4-6-9)8-15-12(11)16-13(17)14/h2-8H,1H3,(H2,14,15,16) =; Kod: UQVKZNNCIHJZLS-UHFFFAOYSA-N = InChI=1/C13H12N4/c1-17-11-7-10(9-5-3-2-4-6-9)8-15-12(11)16-13(17)14/h2-8H,1H3,(H2,14,15,16); Kod: UQVKZNNCIHJZLS-UHFFFAOYAX
Svojstva
Molekulska formula	C13H12N4
Molarna masa	224.26 g mol−1
Agregatno stanje	bela čvrsta materija
Gustina	1,3 gcm−3
Tačka topljenja	300 °C, 573 K, 572 °F
Tačka ključanja	468.9 °C, 742 K, 876 °F
Rastvorljivost u vodi	407,1 mg/L
Opasnost
Opasnost u toku rada	T
	; ; Ukoliko nije drugačije napomenuto, podaci se odnose na standardno stanje (25 °C, 100 kPa) materijala
	Infobox references

PhIP (2-Amino-1-metil-6-fenilimidazo(4,5-b)piridin) jedan je od najzastupljenijih heterocikličnigh amina (HCA) u kuvanom mesu. PhIP se formira na visokim temperaturama reakcijom između kreatina ili kreatinina (prisutnog u mišićnom tkivu), aminokiselina, i šećera. PhIP formiranje se povećava sa povećanjem temperature i dužinom kuvanja, a takođe je zavisno od metoda kuvanja i tipa mesa. Smatra se da može da bude kancirogen.^[5]^[6].^[7]

Reference

↑ 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
↑ 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.
↑ 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
↑ Gaulton A, Bellis LJ, Bento AP, Chambers J, Davies M, Hersey A, Light Y, McGlinchey S, Michalovich D, Al-Lazikani B, Overington JP. (2012). „ChEMBL: a large-scale bioactivity database for drug discovery”. Nucleic Acids Res 40 (Database issue): D1100-7. DOI:10.1093/nar/gkr777. PMID 21948594. edit
↑ U.S. Department of Health and Human Services, Public Health Service, National Toxicology Program. (2011). Report on Carcinogens, 12th ed., p. 222.
↑ International Agency for Research on Cancer (IARC) (1997) PhIP (2-amino-1-methyl-6-phenylimidazo[4,5-b]pyridine)(Group 2B). Summaries & Evaluations. http://www.inchem.org/documents/iarc/vol56/08-phip.html
↑ Cross, A., & Sinha, R. (2004) Meat-Related Mutagens/Carcinogens in the Etiology of Colorectal Cancer. Environmental and Molecular Mutagenesis. 44:45-55.

[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] Gaulton A, Bellis LJ, Bento AP, Chambers J, Davies M, Hersey A, Light Y, McGlinchey S, Michalovich D, Al-Lazikani B, Overington JP. (2012). „ChEMBL: a large-scale bioactivity database for drug discovery”. Nucleic Acids Res 40 (Database issue): D1100-7. DOI:10.1093/nar/gkr777. PMID 21948594. edit

[5] U.S. Department of Health and Human Services, Public Health Service, National Toxicology Program. (2011). Report on Carcinogens, 12th ed., p. 222.

[6] International Agency for Research on Cancer (IARC) (1997) PhIP (2-amino-1-methyl-6-phenylimidazo[4,5-b]pyridine)(Group 2B). Summaries & Evaluations. http://www.inchem.org/documents/iarc/vol56/08-phip.html

[cross-7] Cross, A., & Sinha, R. (2004) Meat-Related Mutagens/Carcinogens in the Etiology of Colorectal Cancer. Environmental and Molecular Mutagenesis. 44:45-55.

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