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Fingolimod hydrochloride

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Products Intro: Product Name:Fingolimod hydrochloride
Purity:98%(Min,HPLC) Package:100g;1kg;5kg,10kg,25kg,50kg
Company Name: Henan DaKen Chemical CO.,LTD.
Tel: +86-371-55531817
Products Intro: Product Name:Fingolimod hydrochloride
Purity:99% Package:100g,500g,1kg,5kg,10kg
Company Name: Henan Tianfu Chemical Co.,Ltd.
Tel: 0371-55170693
Products Intro: CAS:162359-56-0
Purity:99% Package:500G;1KG;5KG;25KG
Tel: +86 21 5161 9050/ 5187 7795
Products Intro: Product Name:Fingolimod hydrochloride
Purity:0.99 Package:5G,10G,25G,50G,100G,250G,1KG
Company Name: Lianyungang happen teng technology co., LTD
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Products Intro: Product Name:fingolimod hydrochloride
Purity:98.00% Package:1kg,10kg,50kg,100kg

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Fingolimod hydrochloride Basic information
Oral drug for the treatment of multiple sclerosis
Product Name:Fingolimod hydrochloride
Synonyms:Fingolimod (FTY720) hydrochloride;Fin;limod hydrochloride;fingolimod hydrochloride;FTY720;2-AMINO-2-[2-(4-OCTYLPHENYL)ETHYL]-1,3-PROPANEDIOL, HYDROCHLORIDE;2-amino-2-[2-(4-octylphenyl)ethyl]propane-1,3-diol hydrochloride;Fingolimod HCl
Product Categories:Pharmaceuticals;Aromatics;Intermediates & Fine Chemicals;Metabolites & Impurities;Other APIs;API;Pharmaceutical intermediate;Inhibitors;Metabolites;All Inhibitors
Mol File:162359-56-0.mol
Fingolimod hydrochloride Structure
Fingolimod hydrochloride Chemical Properties
Melting point 102-107°C
storage temp. -20°C Freezer
solubility water: soluble10mg/mL, clear
form powder
color white to beige
Merck 14,4083
CAS DataBase Reference162359-56-0(CAS DataBase Reference)
Safety Information
Hazard Codes Xi
Risk Statements 36/37/38-52/53
Safety Statements 26-61
WGK Germany 3
RTECS TY3130000
HS Code 29221990
ToxicityLD50 orally in rats: 300-600 mg/kg (Troncoso)
MSDS Information
Fingolimod hydrochloride Usage And Synthesis
Oral drug for the treatment of multiple sclerosisFingolimod hydrochloride is the first oral drug for the treatment of multiple sclerosis. It is successfully developed by the pharmaceutical company Novartis, and it has been approved for marketing by the US Food and Drug Administration (FDA). The recommended dose is 0.5mg once a day for oral administration.
Multiple sclerosis is a debilitating neurological disease that can cause the patient to lose a sense of balance, appear muscle spasms and other movement disorders. The disease has been treated with injectable drugs. This kind of medication brought great inconvenience to patients.
Fingolimod is a sphingosine-l-phosphate (S1PR) receptor modulator. After phosphorylation, It is bound to s1P receptor that is on the surface of lymphocyte, which will change lymphocyte migration, and promote cells into the lymphatic tissue, and prevent lymphocytes from leaving the lymphoid tissue and get into the graft. Thereby, it will prevent these cells from infiltrating the central nervous system (CNS), which achieves the effect of immunosuppression. According to the drug's introduction, drugmaker Novartis said that this process of pharmacological effects is reversible. If medication is stopped, the level of lymphocytes in circulating system will return to normal.
The above information is edited by the chemicalbook of Kui Ming.
DescriptionApproved by the U.S. FDA in September 2010, fingolimod (also referred to as FTY720) is the first approved oral therapy for the relapsing-remitting form ofmultiple sclerosis (RRMS). Because of fingolimod’s structural resemblance to sphingosine, a metabolite of sphingolipids that constitutes the cell membrane of all eukaryotic cells, it was hypothesized that fingolimod may be affecting sphingolipid metabolism in cells. A series of elegant in vitro and in vivo studies confirmed that fingolimod is converted to (S)-fingolimod phosphate primarily by sphingosine kinase- 2 and that (S)-fingolimod phosphate mediates multiple biological processes by binding to novel GPCR’s referred to as sphingosine-1-phosphate (S1P) receptors. S1P receptors are divided into five subtypes, S1P1–5, which have varying tissue and cellular distribution. S1P1–3 receptors are ubiquitously expressed in the immune, cardiovascular, and central nervous systems, S1P4 is restricted to the hematopoietic system, and S1P5 is mostly localized in the white matter of CNS. S1P1–3 receptors play important roles in endothelial barrier function, maintaining vascular tone, regulating heart rate and allowing for lymphocyte egress fromsecondary lymphoid organs. The functional role of S1P4 is unknown,while the S1P5 receptor is thought to be involved in natural killer cell trafficking and oligodendrocyte function.
Chemical PropertiesWhite Solid
OriginatorYoshitomi Pharmaceutical Industries (now Mitsubishi Tanabe Pharma) (United States)
UsesA derivative of ISP-1 (myriocin), a fungal metabolite of the Chinese herb Iscaria sinclarii as well as a structural analogue of Sphingosine. It is a novel immune modulator that prolongs allograft transplant survival in numberour models by inhibitin
UsesOral medicine for the treatment of multiple sclerosis
UsesFTY720 is a derivative of ISP-1 (myriocin), a fungal metabolite of the Chinese herb Iscaria sinclarii as well as a structural analogue of Sphingosine. FTY720 is a novel immune modulator that prolong s allograft transplant survival in numberour models by inhibiting lymphocyte emigration from lymphoid organs. FTY720 us reported to be phosphorylated by sphingosine kinase to FTY720-P, which has been shown to potently stimulate GTPgS binding activity in S1P-transfected CHO cells (EC50 = 210 pM, 4.9 nM, 4.3 nM, and 1 nM for S1P1, S1P3, S1P4 and S1P5, respectively).
UsesA cell-permeable aminopropanediol immunosuppressive agent that displays lymphocyte sequestration properties.
DefinitionChEBI: The hydrochloride salt of 2-amino-2-[2-(4-octylphenyl) ethyl]-1,3-propanediol (fingolimod).
Brand nameGilenya
Fingolimod hydrochloride Preparation Products And Raw materials
Tag:Fingolimod hydrochloride(162359-56-0) Related Product Information
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