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Results for "

genipin

" in TargetMol Product Catalog
  • Inhibitors & Agonists
    6
    TargetMol | All_Pathways
  • Natural Products
    4
    TargetMol | Natural_Products
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    1
    TargetMol | Standard_Products
Genipin
(+)-Genipin
T22106902-77-8
Genipin ((+)-Genipin), an active aglycone derived from an iridoid glycoside called geniposide, is found in the fruit of Gardenia jasminoides Ellis.
  • $50
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TargetMol | Citations Cited
Genipin 1-β-D-gentiobioside
genipin-1-b-D-gentiobioside, Genipin gentiobioside, Genipin 1-β-gentiobioside, Genipin 1-gentiobioside
T4S229929307-60-6
Genipin 1-β-D-gentiobioside is a natural product for research related to life sciences. The catalog number is T4S2299 and the CAS number is 29307-60-6.
  • $35
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Genipin 10-O-glucoside
T125455
Genipin 10-O-glucoside is a useful organic compound for research related to life sciences and the catalog number is T125455.
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Genipin (Standard)
TMSM-22166902-77-8
Genipin (Standard) is a reference standard for research and analysis in studies involving Genipin. Genipin ((+)-Genipin), an active aglycone derived from an iridoid glycoside called geniposide, is found in the fruit of Gardenia jasminoides Ellis.
  • $747
7-10 days
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MRC-G-001
T211674
MRC-G-001 is a Genipin derivative with an IC50 value of 117 μM against A549 cancer cells. It inhibits the phosphorylation of EGFR, JAK1, and STAT3, and modulates the expression of proteins related to epithelial-mesenchymal transition (EMT), thereby suppressing cell migration and invasion. MRC-G-001 induces cell cycle arrest and apoptosis (apoptosis) and is applicable in studies of cancers, including non-small cell lung cancer.
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Xanthine oxidase-IN-21
T214067
Xanthine oxidase-IN-21, a Genipin derivative, is an orally effective mixed competitive inhibitor of xanthine oxidase (XOD) with an IC50 of 0.68 μM. It alleviates renal fibrosis by reducing α-SMA expression and modulates the NF-κB pathway to inhibit pro-inflammatory cytokines IL-1β, IL-6, and TNF-α. Additionally, Xanthine oxidase-IN-21 suppresses the expression of URAT1 and GLUT9, promoting uric acid excretion and lowering serum uric acid levels. This compound exhibits significant hepatorenal protective effects and can be used in research on hyperuricemia.
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