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Results for "

anti-osteoporosis

" in MedChemExpress (MCE) Product Catalog:

17

Inhibitors & Agonists

7

Natural
Products

Cat. No. Product Name Target Research Areas Chemical Structure
  • HY-49069

    Others Others
    Anti-osteoporosis agent-7 (Compound 133) is a potential anti-osteoporosis agent showing high inhibition of osteoclast formation.
    <em>Anti-osteoporosis</em> agent-7
  • HY-149472

    NF-κB PI3K Inflammation/Immunology
    Anti-osteoporosis agent-4 (Compound 11h) inhibits differentiation of primary osteoclasts. Anti-osteoporosis agent-4 attenuates RANKL-induced osteoclastogenesis. Anti-osteoporosis agent-4 inhibits osteoclast formation with an IC50 value of 358.29 nM. Anti-osteoporosis agent-4 inhibits PI3K/AKT and IκBα/NF-κB signaling pathway activation .
    <em>Anti-osteoporosis</em> agent-4
  • HY-N11514

    Others Inflammation/Immunology
    Anti-osteoporosis agent-2 (Compound 10) is an anti-osteoporosis agent. Anti-osteoporosis agent-2 inhibits differentiation on osteoclast induced by RANKL .
    <em>Anti-osteoporosis</em> agent-2
  • HY-149852

    Others Inflammation/Immunology
    Anti-osteoporosis agent-3 (Compound 11), a PMSA derivative, is an anti-osteoporosis agent. Anti-osteoporosis agent-3 inhibits osteoclastogenesis with an IC50 value of 322.9 nM in vitro. Anti-osteoporosis agent-3 also blocks the formation of F-action belts and bone resorption .
    <em>Anti-osteoporosis</em> agent-3
  • HY-155985

    Others Metabolic Disease
    Anti-osteoporosis agent-6 (compound 174) is an anti-osteoporosis agent. Anti-osteoporosis agent-6 has 14.11% inhibition rate against osteoclast formation at 10 μM .
    <em>Anti-osteoporosis</em> agent-6
  • HY-155977

    Others Others
    Anti-osteoporosis agent-5 (compound 189) is a potent inhibitor of the formation of osteoclasts .
    <em>Anti-osteoporosis</em> agent-5
  • HY-145896

    Apoptosis Inflammation/Immunology
    Anti-osteoporosis agent-1 (comp 4aa) is a potent replication protein A (RPA) inhibitor (IC50=18 µM) .
    <em>Anti-osteoporosis</em> agent-1
  • HY-N10370

    Others Cancer
    Morusignin L is an active compound that shows anti-osteoporosis activities .
    Morusignin L
  • HY-N0824
    Syringin
    1 Publications Verification

    Eleutheroside B

    Autophagy Cardiovascular Disease Neurological Disease Inflammation/Immunology Cancer
    Syringin (Eleutheroside B) is an active natural phenolic glycoside possessing various pharmacological activities, including anti-inflammatory, anti-irradiation, anti-osteoporosis and anticancer activities. Syringin also can be used to enhance memory, relieve fatigue, improve human cognition and protect ischemia heart against cerebrovascular damage, etc .
    Syringin
  • HY-N2290

    Others Metabolic Disease
    Baohuoside VII is a flavonoid isolated from Herba Epimedii, with anti-osteoporosis activities .
    Baohuoside VII
  • HY-N0213
    Peiminine
    3 Publications Verification

    Verticinone; Raddeanine

    Autophagy Caspase Bcl-2 Family PARP p38 MAPK ERK NF-κB Apoptosis Inflammation/Immunology Cancer
    Peiminine is a compound that can be isolated from Bolbostemma paniculatum (Maxim) Franquet (Cucurbitaceae family). Peiminine can induce apoptosis in human hepatocellular carcinoma HepG2 cells through both extrinsic and intrinsic apoptotic pathways. Peiminine has anti-inflammatory, anticancer, anti-osteoporosis, cardioprotective and other activities in many animal models .
    Peiminine
  • HY-W009208

    Endogenous Metabolite Metabolic Disease
    Calcium L-Threonate is an anti-osteoporosis agent, and widely used as a calcium supplement . Calcium L-Threonate also stimulates the uptake of ascorbic acid .
    Calcium L-Threonate
  • HY-N0705
    Curculigoside
    5 Publications Verification

    JAK STAT NF-κB Neurological Disease Inflammation/Immunology Cancer
    Curculigoside is the main saponin in C. orchioide, exerts significant antioxidant, anti-osteoporosis, antidepressant and neuroprotection effects. Curculigoside possesses significant anti-arthritic effects in vivo and in vitro via regulation of the JAK/STAT/NF-κB signaling pathway .
    Curculigoside
  • HY-155960

    Others Inflammation/Immunology
    SH491 (Compound 33) is an antiosteoporosis agent. SH491 inhibits RANKL-induced osteoclast differentiation on bone-marrow-derived monocytes (BMMs) (IC50: 11.8 nM). SH491 inhibits the expression of osteoclastogenesis-related marker genes (TRAP, CTSK, MMP-9, and ATPase v0d2) and proteins (TRAP, CTSK, MMP-9) .
    SH491
  • HY-124156

    Wnt Metabolic Disease
    KY-02327, a metabolically stabilized KY-02061 analog, is a potent Dishevelled (Dvl)-CXXC5 interaction inhibitor. KY-02327 shows an activating effect on the Wnt/β-catenin pathway, resulting in promotion of osteoblast differentiation .
    KY-02327
  • HY-124156A

    Wnt Metabolic Disease
    KY-02327 acetate, a metabolically stabilized KY-02061 analog, is a potent Dishevelled (Dvl)-CXXC5 interaction inhibitor. KY-02327 acetate shows an activating effect on the Wnt/β-catenin pathway, resulting in promotion of osteoblast differentiation .
    KY-02327 acetate
  • HY-N1940
    β-Anhydroicaritin
    1 Publications Verification

    β-Anhydroicaritin is isolated from Boswellia carterii Birdware, has important biological and pharmacological effects, such as antiosteoporosis, estrogen regulation and antitumor properties . β-Anhydroicaritin ameliorates the degradation of periodontal tissue and inhibits the synthesis and secretion of TNF-α and MMP-3 in diabetic rats . β-Anhydroicaritin decreases the overproduction of NO, IL-10, TNF-α, MCP-1 and IL-6 in inperitonitis mice. β-Anhydroicaritin inhibits the elevation of intracellular Ca 2+, and markedly decreases iNOS protein expression .
    β-Anhydroicaritin

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