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  • T10570Fostemsavir TrisFostemsavir Tris,BMS-663068 Tris,

    Fostemsavir Tris is the prodrug of BMS-626529. Fostemsavir Tris is an attachment inhibitor that targets HIV-1 gp120 and prevents its binding to CD4+ T cells.

    价 格：￥电议型 号：T10570产 地：美洲

  • T10643c-Fms-IN-1c-Fms-IN-1

    c-Fms-IN-1 is an inhibitor of FMS kinase (IC50: 0.0008 μM).

    价 格：￥电议型 号：T10643产 地：美洲

  • T10649c-Fms-IN-3c-Fms-IN-3

    c-Fms-IN-3 is a novel inhibitor of the c-Fms kinase with potential as an antirheumatic agent and anti-inflammatory agent.

    价 格：￥电议型 号：T10649产 地：美洲

  • T10656trans-C75trans-C75,(±)-C75,

    trans-C75 is an enantiomer of C75. C75 is an inhibitor of fatty acid synthase (FASN).

    价 格：￥电议型 号：T10656产 地：美洲

  • T10775c-Fms-IN-2c-Fms-IN-2

    c-Fms-IN-2 is an inhibitor of FMS kinase (IC50: 0.024 μM).

    价 格：￥电议型 号：T10775产 地：美洲

  • T10823cis-Pralsetinibcis-Pralsetinib,cis-BLU-667,

    trans-Pralsetinib (trans-BLU-667) is an inhibitor of rearranged during transfection (RET) extracted from patent US20170121312A1 (Compound Example 129).

    价 格：￥电议型 号：T10823产 地：美洲

  • T10824cis-Urocanic acidcis-Urocanic acid,(Z)-Urocanic acid,cis-UCA

    cis-Urocanic acid is a 5-HT2A receptor agonist (Kd: 4.6 nM). It is an immune modulator that induces immunosuppression by binding to the 5-HT2A receptor.

    价 格：￥电议型 号：T10824产 地：美洲

  • T1098Denatonium benzoateDenatonium benzoate,THS-839,

    Denatonium, a quaternary ammonium cation, is a compound of a salt with an inert anion like saccharide or benzoate. Its structure is involved in the local anesthetic lidocaine which difference only is the addition of a benzyl group to the amino nitrogen.

    价 格：￥电议型 号：T1098产 地：美洲

  • T11071Dofequidar fumarateDofequidar fumarate,MS-209,

    It has been reported that an orally active quinoline compound, dofenacid fumarate (MS-209 fumarate), can overcome MDR by inhibiting ABCB1/P-gp, ABCC1/MDR-related protein 1 or both. IC50 value: Target: In vitro P-gp: 3 microM MS-209 effectively overcomes d

    价 格：￥电议型 号：T11071产 地：美洲

  • T1109ZucapsaicinZucapsaicin,cis-Capsaicin,Civamide

    Zucapsaicin is a medication used to treat osteoarthritis of the knee and Others neuropathic pain.Zucapsaicin is a synthetic cis isomer of natural capsaicin that has shown therapeutic efficacy in pain accompanying osteoarthritis of the knee.

    价 格：￥电议型 号：T1109产 地：美洲

  • T11156Nazartinib S-enantiomerNazartinib S-enantiomer,EGF816 (S-enantiomer),

    Nazartinib is an EGFR inhibitor. Nazartinib S-enantiomer is the less active S-enantiomer of Nazartinib.

    价 格：￥电议型 号：T11156产 地：美洲

  • T11182EMD638683 S-FormEMD638683 S-Form

    ?EMD638683 is a highly selective SGK1 inhibitor with IC50 of 3 μM.?EMD638683 S-Form is the S-form of EMD638683.

    价 格：￥电议型 号：T11182产 地：美洲

  • T11213Epertinib hydrochlorideEpertinib hydrochloride,S-22611 hydrochloride,

    Epertinib shows potent antitumor activity.?Epertinib hydrochloride is a potent, orally active, reversible, and selective tyrosine kinase inhibitor of EGFR, HER2 and HER4, with IC50s of 1.48 nM, 7.15 nM and 2.49 nM, respectively.

    价 格：￥电议型 号：T11213产 地：美洲

  • T11213LEpertinibEpertinib,S-22611,

    Epertinib displays strong antitumor activity. Epertinib is a reversible and selective tyrosine kinase inhibitor of EGFR, HER2 and HER4 (IC50s of 1.48 nM, 7.15 nM and 2.49 nM, respectively).

    价 格：￥电议型 号：T11213L产 地：美洲

  • T1124FlumethasoneFlumethasone,Flumetasone,RS-2177

    Flumethasone is a glucocorticoid receptor agonist, with anti-inflammatory, antipruritic and vasoconstrictive properties.

    价 格：￥电议型 号：T1124产 地：美洲

  • T11266FAS-IN-1FAS-IN-1

    FAS-IN-1 is a potent inhibitor of Fatty acid synthase (FAS) wtih IC50 of 10 nM.

    价 格：￥电议型 号：T11266产 地：美洲

  • T11285FIDAS-5FIDAS-5

    ?FIDAS-5 effectively competes against S-adenosylmethionine (SAM) for MAT2A binding.?FIDAS-5 has anticancer activities.?FIDAS-5 is a potent and orally active methionine S-adenosyltransferase 2A (MAT2A) inhibitor with an IC50 of 2.1 μM.

    价 格：￥电议型 号：T11285产 地：美洲

  • T11378GDC-0834 S-enantiomerGDC-0834 S-enantiomer

    ?GDC-0834 is a potent and selective BTK inhibitor.GDC-0834 (S-enantiomer) is the S-enantiomer of GDC-0834.

    价 格：￥电议型 号：T11378产 地：美洲

  • T11413Glucagon receptor antagonists-1Glucagon receptor antagonists-1

    Glucagon receptor antagonist -1 is a highly effective glucagon receptor antagonist.

    价 格：￥电议型 号：T11413产 地：美洲

  • T11414Glucagon receptor antagonists-2Glucagon receptor antagonists-2

    Glucagon receptor antagonist -2 is a highly effective glucagon receptor antagonist.

    价 格：￥电议型 号：T11414产 地：美洲

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