Nome Químico: 2-Amino-2-(4-octylphenethyl)propane-1,3-diyl diacetate
Sorrisos: NC(COC(C)=O)(COC(C)=O)CCC1=CC=C(C=C1)CCCCCCCC
Inchi: InChI=1S/C45H54N4O8/c1-8-27-19-28-22-44(40(51)55-6,36-30(25-48(23-27)24-28)29-13-10-11-14-33(29)46-36)32-20-31-34(21-35(32)54-5)47(4)38-43(31)16-18-49-17-12-15-42(9-2,37(43)49)39(57-26(3)50)45(38,53)41(52)56-7/h10-15,19-21,28,37-39,46,53H,8-9,16-18,22-25H2,1-7H3/t28-,37-,38+,39+,42+,43+,44+,45-/m0/s1
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