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Results for "

anti-carcinogenic

" in TargetMol Product Catalog.
  • Inhibitors & Agonists
    21
    TargetMol | All_Pathways
  • Peptide Products
    1
    TargetMol | Peptide_Products
  • Natural Products
    14
    TargetMol | Natural_Products
  • Reference Standards
    4
    TargetMol | Standard_Products
  • 2,5-Dimethyl-3(2H)-furanone
    2,5-Dimethyl-2,3-dihydrofuran-3-one
    T2230914400-67-0
    2,5-Dimethyl-3(2H)-furanone (2,5-Dimethyl-2,3-dihydrofuran-3-one) is a non-genotoxic flavoring substance [1].
    • $30
    In Stock
    Size
    QTY
  • (Iso)-Flavokawain A
    Flavokavain A
    T3S07373420-72-2
    NSC-37445 has anti-tumor activity, such as inhibits growth of bladder tumor cells in a nude mice model , prevents the recurrence and progression of non-muscle-invasive urothelial cell carcinoma. NSC-37445 can significantly reduce the expression of CDK1-inhibitory kinases, Myt1 and Wee1, and cause cyclin B1 protein accumulation leading to CDK1 activation in T24 cells. 3. Flavokawain A (Flavokavain A) may exert anti-inflammatory responses by suppressing LPS-induced expression of pro-inflammatory mediators via blockage of NF-κB-AP-1-JNK/p38 MAPK signaling pathways in the murine macrophages.
    • $42
    In Stock
    Size
    QTY
    TargetMol | Citations Cited
  • D-Saccharic acid 1,4-lactone hydrate
    T4131961278-30-6
    D-Saccharic acid 1,4-lactone hydrate is a potent β-glucuronidase inhibitor (IC50=48.4 μM) that possesses anticarcinogenic, detoxifying, and antioxidant properties[1][2].
    • $31
    In Stock
    Size
    QTY
    TargetMol | Citations Cited
  • 7-Hydroxyflavanone
    T79996515-36-2
    7-Hydroxyflavanone shows antimicrobial activity against Streptococcus pneumoniae clinical isolates.
    • $40
    In Stock
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    QTY
  • Erastin
    T1765571203-78-6
    Erastin is an iron death activator that acts on the mitochondrial VDAC in a ROS- and iron-dependent manner. Erastin has anti-tumor activity and acts selectively on tumor cells with RAS-carcinogenic mutations.
    • $41
    In Stock
    Size
    QTY
    TargetMol | Inhibitor Hot
    TargetMol | Citations Cited
  • Hesperidin
    Hesperetin 7-rutinoside, Cirantin
    T1035520-26-3
    Hesperidin (Cirantin) is a flavanone glycoside found in citrus fruits with antioxidant, anti-inflammatory, anti-carcinogenic, and antihypertensive and lipid-lowering activity.
    • $50
    In Stock
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    QTY
    TargetMol | Citations Cited
  • Daidzin
    NPI-031D, Daidzoside, Daidzein 7-O-glucoside, Daidzein 7-glucoside
    T2901552-66-9
    Daidzin (Daidzoside) is an isoflavone isolated from soya bean with anti-oxidant, anti-carcinogenic, and anti-atherosclerotic activities.
    • $37
    In Stock
    Size
    QTY
    TargetMol | Citations Cited
  • Auraptene
    7-geranyloxycoumarin
    T4115495-02-3
    Auraptene is a coumarin derived from citrus plants that bears a geranyloxyl moiety at its C-7. It has anti-inflammatory, anti-carcinogenic, anti-bacterial, neuroprotective, and hepatoprotective activities. It inhibits leukocyte activation and induces phas
    • $30
    In Stock
    Size
    QTY
    TargetMol | Citations Cited
  • Achillin
    NSC-156236, NSC156236, NSC 156236
    T236145956-04-7
    Achillin is a compound isolated from herbs. It may have anti-inflammatory and anti-carcinogenic activities.
    • Inquiry Price
    3-6 months
    Size
    QTY
  • Bis(diazoacetyl)butane
    Supermutagen, DAB (mutagen), 1,4-Bis-diazoacetylbutane, 1,4-Bis(diazoacetyl)butane
    T237971448-16-4
    Bis(diazoacetyl)butane is a mutagen and traditionally related to radio-mimetic chemical mutagens due to the similarity of appearance of mutagenic action of this mutagen and physical mutagens. It also has anti-tumor and carcinogenic activity.
    • $1,520
    6-8 weeks
    Size
    QTY
  • Almurtide
    T7386261136-12-7
    Almurtide (nor-MDP), a derivative of muramyl dipeptide, exhibits anti-inflammatory and anti-tumor properties. It demonstrates protective effects in mice against infections caused by Pseudomonas aeruginosa when administered intraperitoneally and Candida albicans when administered intravenously. Furthermore, Almurtide has been shown to inhibit the carcinogenic Friend leukemia virus [1] [2] [3].
    • Inquiry Price
    Inquiry
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  • Rutin trihydrate
    T77201250249-75-3
    Rutin (Rutoside) trihydrate, a natural flavonoid glycoside, exhibits multifaceted therapeutic properties, including antioxidant, anti-inflammatory, anti-diabetic, and anti-carcinogenic activities. Additionally, it has demonstrated cardioprotective and neuroprotective effects [1] [2] [3].
    • $123
    35 days
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  • β-Boswellic acid (Standard)
    TMSM-0579631-69-6
    β-Boswellic acid (Standard) is a reference standard for research and analysis in studies involving β-Boswellic acid. β-Boswellic acid (Beta-boswellic acid) and its derivatives (the major constituents of Boswellin) have anti-carcinogenic, anti-tumor, and anti-hyperlipidemic activities.
    • $1,090
    7-10 days
    Size
    QTY
  • Auraptene (Standard)
    Aurapten (Standard)
    TMSM-1063495-02-3
    Auraptene (Standard) is a reference standard for research and analysis in studies involving Auraptene. Auraptene is a coumarin derived from citrus plants that bears a geranyloxyl moiety at its C-7. It has anti-inflammatory, anti-carcinogenic, anti-bacterial, neuroprotective, and hepatoprotective activities. It inhibits leukocyte activation and induces phase II enzymes during the initiation phase of carcinogenesis.1 When examined for its potential use in Alzheimer's disease treatment, auraptene was shown to inhibit β-secretase (BACE1) activity with an IC50 value of 345.1 μM.
    • $645
    7-10 days
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  • Daidzin (Standard)
    TMSM-1148552-66-9
    Daidzin (Standard) is a reference standard for research and analysis in studies involving Daidzin. Daidzin (Daidzoside) is an isoflavone isolated from soya bean with anti-oxidant, anti-carcinogenic, and anti-atherosclerotic activities.
    • $57
    7-10 days
    Size
    QTY
  • Rutin trihydrate (Standard)
    TMSM-2062250249-75-3
    Rutin trihydrate (Standard) is the standard substance of Rutin trihydrate, and it is applicable for quantitative analysis, quality control, and related research in biochemical experiments. Rutin (Rutoside) trihydrate, a natural flavonoid glycoside, exhibits multifaceted therapeutic properties, including antioxidant, anti-inflammatory, anti-diabetic, and anti-carcinogenic activities. Additionally, it has demonstrated cardioprotective and neuroprotective effects .
    • $36
    7-10 days
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  • β-Boswellic acid
    Beta-boswellic acid
    TN1097631-69-6
    β-Boswellic acid (Beta-boswellic acid) and its derivatives (the major constituents of Boswellin) have anti-carcinogenic, anti-tumor, and anti-hyperlipidemic activities.
    • $56
    In Stock
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    TargetMol | Citations Cited
  • 3-Epicabraleahydroxylactone
    TN292635833-72-8
    3-Epicabraleahydroxylactone has anti-tumor promoting effect, it has anti-carcinogenic activity by the inhibitory effect on the induction of Epstein-Barr virus early antigen(EBV-EA) by the tumor promoter.
    • $250
    Inquiry
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  • 4beta-Hydroxywithanolide E
    TN307054334-04-2
    4beta-Hydroxywithanolide E(4bHWE) can inhibit the growth of colon cancer monolayer and spheroid cultures, it assert its anti-tumor activity in carcinogenic progression and develop into a dietary chemopreventive agent, it affects alternative splicing by mo
    • $2,750
    35 days
    Size
    QTY
  • Odorine
    TN469572755-20-5
    Odorine has potent anti-carcinogenic effect by inhibiting both the initiation and promotion stages of two-stage skin carcinogenesis. It was found to inhibit the growth of the vinblastine-resistant KB cells by enhancing the anticancer activity of vinblastine.
    • $520
    Inquiry
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  • DPMI-ω
    TP4288
    DPMI-ω is a dual-specific D-peptide antagonist of the carcinogenic proteins MDM2 and MDMX. When loaded onto gold nanoparticles, DPMI-ω effectively penetrates tumor cells and kills them by reactivating the p53 signaling pathway. It disrupts the p53-MDM2/MDMX complex and inhibits the growth of B16 melanoma while inducing G0/G1 phase cell cycle arrest. Combined with anti-PD1 antibodies, DPMI-ω enhances immunotherapy by amplifying CD3+/CD8+ cytotoxic T cells and inhibiting CD4+/CD25+ regulatory T cells. DPMI-ω is applicable in melanoma research.
    • Inquiry Price
    Inquiry
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