Chemical Name: N-(1-Hydroxy-2-(hydroxymethyl)-4-(4-octylphenyl)butan-2-yl)acetamide
Smiles: OCC(NC(C)=O)(CO)CCC1=CC=C(CCCCCCCC)C=C1
Inchi: InChI=1/C21H35NO3/c1-3-5-6-7-8-9-10-18-11-13-19(14-12-18)15-16-21(22,17-23)20(24)25-4-2/h11-14,23H,3-10,15-17,22H2,1-2H3
Fingolimod promotes angiogenesis and attenuates ischemic brain damage via modulating microglial polarization
KeShanga1JiaHeb1JingZoubChuanQinaLiLincLuo-QiZhouaLin-LinYangbLong-JunWudWeiWangaKe-BinZhanbDai-ShiTiana
Brain Research Volume 1726, 1 January 2020, 146509
Rapid Determination of Fingolimod Hydrochloride‑Related Substances and Degradation Products in API and Pharmaceutical Dosage Forms by Use of a Stability‑Indicating UPLC Method
N. Rajan · K. Anver Basha
Chromatographia (2014) 77:1545–1552
Development and validation of Immunomodulating drug Fingolimod by RPHPLC method with detailed force degradation study
Ravi V Ghediya1,2, Madhavi Patel1,2,3, Darshana Pandya1,2, Anamik K Shah1,2, Ranjan C Khunt
Chemistry & Biology Interface, 2016, 6, 4, 210-223