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Synthesis and evaluation of 1-(substituted)-3-prop-2-ynylureas as antiangiogenic agents.
Bioorg Med Chem Lett. 2012 Apr 15;22(8):3001-5. doi: 10.1016/j.bmcl.2012.02.029. Epub 2012 Feb 22.
Bioorg Med Chem Lett. 2012.
PMID: 22414612
5-Substituted pyrido[2,3-d]pyrimidine, an inhibitor against three receptor tyrosine kinases.
Kammasud N, Boonyarat C, Sanphanya K, Utsintong M, Tsunoda S, Sakurai H, Saiki I, André I, Grierson DS, Vajragupta O.
Kammasud N, et al. Among authors: sanphanya k.
Bioorg Med Chem Lett. 2009 Feb 1;19(3):745-50. doi: 10.1016/j.bmcl.2008.12.023. Epub 2008 Dec 10.
Bioorg Med Chem Lett. 2009.
PMID: 19110422
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Novel VEGFR-2 kinase inhibitors identified by the back-to-front approach.
Sanphanya K, Wattanapitayakul SK, Phowichit S, Fokin VV, Vajragupta O.
Sanphanya K, et al.
Bioorg Med Chem Lett. 2013 May 15;23(10):2962-7. doi: 10.1016/j.bmcl.2013.03.042. Epub 2013 Mar 20.
Bioorg Med Chem Lett. 2013.
PMID: 23562241
Free PMC article.
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Determination of levocetirizine in human plasma by LC-MS-MS: validation and application in a pharmacokinetic study.
Wichitnithad W, Jithavech P, Sanphanya K, Vicheantawatchai P, Rojsitthisak P.
Wichitnithad W, et al. Among authors: sanphanya k.
J Chromatogr Sci. 2015 Nov-Dec;53(10):1663-72. doi: 10.1093/chromsci/bmv069. Epub 2015 Jun 17.
J Chromatogr Sci. 2015.
PMID: 26084706
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Simple HPLC determination of benzalkonium chloride in ophthalmic formulations containing antazoline and tetrahydrozoline.
Rojsitthisak P, Wichitnithad W, Pipitharome O, Sanphanya K, Thanawattanawanich P.
Rojsitthisak P, et al. Among authors: sanphanya k.
PDA J Pharm Sci Technol. 2005 Sep-Oct;59(5):332-7.
PDA J Pharm Sci Technol. 2005.
PMID: 16316068
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Antiangiogenic Effects of VH02, a Novel Urea Derivative: In Vitro and in Vivo Studies.
Phowichit S, Kobayashi M, Fujinoya Y, Sato Y, Sanphanya K, Vajragupta O, Chularojmontri L, Wattanapitayakul SK.
Phowichit S, et al. Among authors: sanphanya k.
Molecules. 2016 Sep 21;21(9):1258. doi: 10.3390/molecules21091258.
Molecules. 2016.
PMID: 27657036
Free PMC article.
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