Fingolimod (FTY720) is a potent sphingosine-1-phosphate (S1P) receptors agonist with IC50 of 0.137, 10.98 nM for (S)- and (R)- FTY720-phosphate, respectively and reverses the effects of BCR-ABL kinase. It is a novel immunomodulating agent and can sequester lymphocytes in lymph nodes, preventing them from moving to the central nervous system for auto-immune responses in multiple sclerosis and was originally proposed as a anti-rejection medication indicated post-transplantation.

 June 21, 2017

prudect name : Fingolimod (FTY720) is a potent sphingosine-1-phosphate (S1P) receptors agonist with IC50 of 0.137, 10.98 nM for (S)- and (R)- FTY720-phosphate, respectively and reverses the effects of BCR-ABL…

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Tetrasodium [4-[(E)-1-Ethyl-2-(4-Phosphonatooxyphenyl)But-1-Enyl]Phenyl] Phosphate; Tetrasodium [4-[(E)-1-Ethyl-2-(4-Phosphatophenyl)But-1-Enyl]Phenyl] Phosphate; 4,4¡¯-Dihydroxy-Alpha,Alpha¡¯-Diethyl-Stilben-Diphosphate Tetrasodium

prudect name : Tetrasodium [4-[(E)-1-Ethyl-2-(4-Phosphonatooxyphenyl)But-1-Enyl]Phenyl] Phosphate; Tetrasodium [4-[(E)-1-Ethyl-2-(4-Phosphatophenyl)But-1-Enyl]Phenyl] Phosphate; 4,4¡¯-Dihydroxy-Alpha,Alpha¡¯-Diethyl-Stilben-Diphosphate TetrasodiumFOSFOMYCIN SODIUM Synonyms: Diethylstilbestrol diphosphate tetrasodiumCAS NO: 23519-26-8Molecular Formula: C18H18Na4O8P2Molecular Weight: 516.24Purity: 98% minSolubility: Storage: ACP103 References PubMed ID：:http://www.ncbi.nlm.nih.gov/pubmed/18515001

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prudect name : FasudilSynonyms: CAS NO: 103745-39-7Molecular Formula: C14H17N3O2SMolecular Weight: 291.37Purity: 99%Solubility: Storage: −20°C 2

prudect name : Fasudil Synonyms: CAS NO: 103745-39-7Molecular Formula: C14H17N3O2SMolecular Weight: 291.37Purity: 99%Solubility: Storage: −20°C 2 years GSK-2656157 References PubMed ID：:http://www.ncbi.nlm.nih.gov/pubmed/18514995

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Ciproxifan, Antagonists of H3-type histamine receptors exhibit cognitive-enhancing properties in various memory paradigms as well as evidence of antipsychotic activity in normal animals.Ciproxifan is an extremely potent histamine H3 inverse agonist/antagonist.Ciproxifan produces wakefulness and attentiveness in animal studies, and produced cognitive enhancing effects without prominent stimulant effects at relatively low levels of receptor occupancy, and pronounced wakefulness at higher doses.It has therefore been proposed as a potential treatment for sleep disorders such as narcolepsy and to improve vigilance in old age, particularly in the treatment of conditions such as Alzheimer¡¯s disease.It also potentiated the effects of antipsychotic drugs, and has been suggested as an adjuvant treatment for schizophrenia.

prudect name : Ciproxifan, Antagonists of H3-type histamine receptors exhibit cognitive-enhancing properties in various memory paradigms as well as evidence of antipsychotic activity in normal animals.Ciproxifan is an extremely potent…

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Faropenem sodium antibiotics for the carbopenems

prudect name : Faropenem sodium antibiotics for the carbopenemsFaropenem sodium hemipentahydrate Synonyms: CAS NO: 106560-14-9Molecular Formula: 2(C12H14NNaO5S).5(H20)Molecular Weight: 704.67Purity: ≥99%Solubility: Storage: −20°C 2 years CHIR99021 References PubMed ID：:http://www.ncbi.nlm.nih.gov/pubmed/18514969

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APO866 at low concentrations ranging from 0.09-27 nM induces dose-dependent cytotoxicity in 41 hematologic malignant cells including acute myeloid leukemia [AML], acute lymphoblastic leukemia [ALL], mantle cell lymphoma [MCL], chronic lymphocytic leukemia [CLL], and T-cell lymphoma. APO866 at low concentrations ranging from 0-10 nM induces cell death, this effect is independent of caspase activation but is associated with depolarization of mitochondrial membrane. APO866 at concentrations ranging from 0-10 nM dose-dependently induces depletion of intracellular NAD and ATP contents and cell death in various hematologic cancer cells.APO866 at concentration of 10 nM inhibits PBEF-induced secretion of MMP-3, CCL2, and CXCL8 in HFFF2 cells.

prudect name : APO866 at low concentrations ranging from 0.09-27 nM induces dose-dependent cytotoxicity in 41 hematologic malignant cells including acute myeloid leukemia [AML], acute lymphoblastic leukemia [ALL], mantle cell…

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Fotemustine the nitrosourea class of anti-mitotic cells inhibitor, with and carbamyl alkylation of the role of animal experiments demonstrated its broad-spectrum anti-tumor activity.

prudect name : Fotemustine the nitrosourea class of anti-mitotic cells inhibitor, with and carbamyl alkylation of the role of animal experiments demonstrated its broad-spectrum anti-tumor activity.Fotemustine Synonyms: CAS NO: 92118-27-9Molecular…

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R-Tiacumicin B; Tiacumicin B; OPT-80; PAR-101; 3-(((6-Deoxy-4-O-(3,5-dichloro-2-ethyl-4,6-dihydroxybenzoyl)-2-O-methyl-b-D-mannopyranosyl)oxy)-methyl)-12(R)-[(6-deoxy-5-C-methyl-4-O-(2-methyl-1-oxopropyl)-b-D-lyxo-hexopyranosyl)oxy]-11(S)-ethyl-8(S)-hydroxy-18(S)-(1(R)-hydroxyethyl)-9,13,15-trimethyloxacyclooctadeca-3,5,9,13,15-pentaene-2-one; Lipiarmycin

prudect name : R-Tiacumicin B; Tiacumicin B; OPT-80; PAR-101; 3-(((6-Deoxy-4-O-(3,5-dichloro-2-ethyl-4,6-dihydroxybenzoyl)-2-O-methyl-b-D-mannopyranosyl)oxy)-methyl)-12(R)-[(6-deoxy-5-C-methyl-4-O-(2-methyl-1-oxopropyl)-b-D-lyxo-hexopyranosyl)oxy]-11(S)-ethyl-8(S)-hydroxy-18(S)-(1(R)-hydroxyethyl)-9,13,15-trimethyloxacyclooctadeca-3,5,9,13,15-pentaene-2-one; LipiarmycinFidaxomicin Synonyms: CAS NO: 873857-62-6Molecular Formula: 52H74Cl2O18Molecular Weight: 1058.04Purity: 98% minSolubility: In DMSOStorage: -20°C TL32711 References PubMed ID：:http://www.ncbi.nlm.nih.gov/pubmed/18514883

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prudect name : FluoxydineSynonyms: 5-Fluoro-3H-pyrimidin-4-oneCAS NO: 671-35-2Molecular Formula: C4H3FN2OMolecular Weight: 114.08Purity: 99%Solubility: Storage: −20°C

prudect name : Fluoxydine Synonyms: 5-Fluoro-3H-pyrimidin-4-oneCAS NO: 671-35-2Molecular Formula: C4H3FN2OMolecular Weight: 114.08Purity: 99%Solubility: Storage: −20°C 2 years R115777 References PubMed ID：:http://www.ncbi.nlm.nih.gov/pubmed/18514783

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Foretinib(GSK1363089, XL880) is a novel MET and VEGFR2/KDR kinases inhibitor with an IC50 of 0.4 and 0.8 nM for MET and KDR, respectively. Foretinib(GSK1363089, XL880) inhibits HGF receptor family tyrosine kinases with an IC50 of 3 nM for Ron. Foretinib(GSK1363089, XL880) also inhibits KDR, Flt-1, and Flt-4 with IC50 of 0.9, 6.8 and 2.8 nM, respectively. In addition, EXEL-2880 inhibits members of the platelet-derived growth factor receptor family and the angiopoietin-1 receptor Tie-2. Foretinib(GSK1363089, XL880) exhibits modest activity against fibroblast growth factor receptor 1 and epidermal growth factor receptor and is inactive against 50 serine/threonine kinases, including cyclin-dependent kinases and protein kinase C isoforms. To delineate the cellular effect of Foretinib(GSK1363089, XL880), VEGF- induced extracellular signal-regulated kinase phosphorylation was used to assess the effect of the compound on phosphorylation of KDR in human umbilical vein endothelial cells that resulted in an IC50 of 16 nM. Foretinib(GSK1363089, XL880) is the 1st orally available small molecule inhibitor of Met to enter the clinic and appears to be generally well tolerated. Anti-tumor activity has been observed and Foretinib may represent an active treatment option for patients with papillary renal-cell carcinoma.

prudect name : Foretinib(GSK1363089, XL880) is a novel MET and VEGFR2/KDR kinases inhibitor with an IC50 of 0.4 and 0.8 nM for MET and KDR, respectively. Foretinib(GSK1363089, XL880) inhibits HGF…

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