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Smo | TargetMol

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Smo

Smoothened (Smo), a class Frizzled G protein-coupled receptor (class F GPCR), transduces the Hedgehog (Hh) signal across the cell membrane. The Hh signaling pathway includes both canonical and noncanonical pathways. The canonical Hh pathway functions through major Hh molecules such as Hh ligands, PTCH, Smo, and GLI, whereas the noncanonical Hh pathway involves the activation of Smo or GLI through other pathways. The Hh signaling cascade is initiated by the binding of the Hh protein ligand to its cellular membrane receptor, Patched (PTCH), which relieves PTCH-mediated repression of the seven-transmembrane (7TM) protein Smo. Activated Smo transduces the signal to the GLI family of transcription factors, which translocate to the nucleus to regulate numerous gene products involved in tissue patterning and cell differentiation.

  • Sonidegib diphosphate
    T157271218778-77-8
    Sonidegib diphosphate (LDE225 diphosphate) is an effective and selective Smo antagonist (IC50: 1.3 nM and 2.5 nM for mouse and human Smo in a binding assay, respectively).
    • ¥10,000
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  • GI-560192
    T64351301326-41-0
    GI-560192 (RL-0070933) is a potent smo cilial modulator with an EC50 value of 0.02 µM. GI-560192 modulates the translocation and/or accumulation of smoothened to the primary cilia by hedgehog signaling pathway.
    • ¥45,000
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  • 20(S)-Hydroxycholesterol
    T10085516-72-3在庫ざいこ
    20(S)-Hydroxycholesterol (20αあるふぁ-Hydroxycholesterol) is an allosteric activator of the oncoprotein smoothened (Smo).
    • ¥7,000
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  • LEQ506
    T118381204975-42-7在庫ざいこ
    • ¥22,500
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  • Purmorphamine
    T1810483367-10-8
    Purmorphamine (Shh Signaling Antagonist VI), which directly binds and activates Smoothened, blocks BODIPY-cyclopamine binding to Smo. It also is an inducer of osteoblast differentiation.
    • ¥12,000
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  • HhAntag
    T3460496794-70-8
    HhAntag is a small molecule inhibitor of GLI1-mediated transcription, an essential down-stream element of the Hedgehog (Hh) pathway with the anti-tumor activity.
    • ¥14,500
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  • Cyclopamine
    T28254449-51-8
    Cyclopamine (11-Deoxojervine), a Smoothened (Smo) antagonist (IC50: 46 nM in TM3Hh12 cells), belongs to the group of steroidal jerveratrum alkaloids.
    • ¥11,000
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  • SAG
    T1779912545-86-9
    SAG (Smoothened Agonist) is a Smo receptor agonist (EC50=3 nM) that is cell-permeable and selective. SAG regulates Smo activity by binding directly to the Smo helix and can activate the Hedgehog signaling pathway.
    • ¥11,000
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  • SANT-1
    T2450304909-07-7
    SANT-1 directly binds to Smoothened (Smo) receptor (Kd: 1.2 nM) and inhibits Smo agonist effects (IC50: 20 nM).
    • ¥7,000
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  • PF-5274857
    T54651373615-35-0
    PF-5274857 (PF-5274857 free base) is an effective and selective hedgehog signaling pathway inhibitor (IC50: 5.8 nM and a Ki: 4.6 nM). PF-5274857 is a potentially attractive clinical candidate for the treatment of tumor types including brain tumors and brain metastasis driven by an activated Hh pathway.PF-5274857 was found to effectively penetrate the blood-brain barrier and inhibit Smo activity in the brain of primary medulloblastoma mice, resulting in improved animal survival rates. PF-5274857 was orally available and metabolically stable in vivo.
    • ¥7,000
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  • MRT-14
    T95311263131-83-4
    MRT-14 is a potent Smo antagonist and can be used in several types of cancers linked to abnormal Hh signaling studies.
    • ¥8,000
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  • MRT-83
    T121091263131-92-5
    MRT-83 is a potent Smo antagonist.
    • ¥10,000
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  • AZD8542
    T267231126366-36-6
    AZD8542 is an antagonist of Smoothened (SMO) and a Hedgehog (Hh) pathway antagonist with anticancer and antiproliferative activity that inhibits the growth of tumors in living organisms, and is used in the study of prostate and colon cancer.
    • ¥76,500
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  • IHR-1
    T24159548779-60-8
    IHR-1 is a Potent Smo antagonist (IC50 = 7.6 nM). Selectively inhibits Hedgehog signaling over Wnt and Notch signaling pathways. Blocks Smo accumulation in primary cilium in vitro.
    • ¥11,000
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  • Jervine
    T3363469-59-0
    The biological activity of Jervine (Jerwiny) is mediated via its interaction with the 7 passes transmembrane protein Smoothened. Jervine binds with and inhibits smoothened, which is an integral part of the Hedgehog signaling pathways. With smoothened inhibited, the GLI1 transcription cannot be activated and Hedgehog target genes cannot be transcribed.
    • ¥15,000
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  • MK-4101
    T6891935273-79-3
    MK-4101, an effective inhibitor of the Hedgehog pathway, has anti-tumor activity through the induction of extensive apoptosis and inhibition of proliferation in tumor cells.
    • ¥9,000
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  • Taladegib
    T26661258861-20-9
    Taladegib (LY2940680) is an orally bioavailable small molecule antagonist of the Hedgehog (Hh)-ligand cell surface receptor smoothened (Smo) with potential antineoplastic activity.
    • ¥9,500
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  • Sonidegib
    T1926956697-53-3
    Sonidegib (Erismodegib), a Smoothened (Smo) antagonist, inhibits Hedgehog (Hh) signaling with IC50 of 1.3 nM (mouse) and 2.5 nM (human), respectively.
    • ¥12,500
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  • ALLO-2
    T141881357350-60-7
    ALLO-2 is a Inhibitor of Drug-Resistant Smo Mutant.It inhibits Smo agonist Hh-Ag1.5-induced luciferase expression in TM3-Gli-Luc cells with IC50 of 6 nM.
    • ¥27,000
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  • DY131
    T225095167-41-2
    DY131 (DY-131) is a novel selective agonist of ERRβべーた and ERRγがんま.
    • ¥11,000
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  • JNJ-1289
    T60738792898-18-1
    JNJ-1289 is a selective, potent, and competitive inhibitor of human spermine oxidase (hSMOX) with an IC50 value of 50 nM.JNJ-1289 has potential anticancer and anti-inflammatory activity for the study of polyamine catabolic disorders.
    • ¥45,500
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  • Glasdegib
    T65141095173-27-5
    Glasdegib (PF-04449913) (PF-04449913) is a potent, and orally bioavailable Smoothened (Smo) inhibitor with IC50 of 5 nM. Phase 2.
    • ¥8,500
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  • Halcinonide
    T01073093-35-4
    Halcinonide (Halciderm), a high-efficiency corticosteroid, is served as an anti-inflammatory agent used in topical preparations.
    • ¥9,500
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  • BMS-833923
    T22991059734-66-5
    BMS-833923 (XL-139), an orally bioavailable Smoothened antagonist, inhibits BODIPY cyclopamine binding to SMO in a dose-dependent manner (IC50: 21 nM).
    • ¥10,500
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