1. Immunology/Inflammation NF-κB Metabolic Enzyme/Protease
  2. Toll-like Receptor (TLR) NF-κB MMP
  3. Chymotrypsin

Chymotrypsin  (Synonyms: α-キモトリプシン; EC 3.4.21.1; Chymotrypsin A)

製品番号: HY-108910
COA 取扱説明書 Technical Support

Chymotrypsin (EC 3.4.21.1; Chymotrypsin A) is an orally effective inhibitor targeting molecules such as TLR4, NF-κB, MMP-1, TNF-α, IL-1β, and IL-6. Chymotrypsin downregulates the TLR4/NF-κB signaling pathway, inhibiting the release of inflammatory factors, reducing cell infiltration and tissue damage. It also reduces the expression of tumor cell adhesion molecules (such as CD44 and CD54) and can be specifically detected by fluorescent probes (such as NBD-3). Chymotrypsin has anti-inflammatory, hepatoprotective, joint damage-reducing, liver protection against lipotoxicity, and anti-tumor metastasis functions. It can be used in research on diseases such as rheumatoid arthritis, non-alcoholic fatty liver disease, and melanoma metastasis. Chymotrypsin can be used in studies of inflammation, edema, and expectoration.

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CAS 番号 : 9004-07-3

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Based on 2 publication(s) in Google Scholar

Other Forms of Chymotrypsin:

Top Publications Citing Use of Products

    Chymotrypsin purchased from MedChemExpress. Usage Cited in: Nat Protoc. 2025 May;20(5):1158-1195.  [Abstract]

    Vibrio cholerae cytolysin (VCC) was produced as an inactive pro-toxin (80 kDa), and the mature toxin (65 kDa) was generated through proteolysis by Chymotrypsin (incubated with VCC at 1000:1 molar ratio; room temperature; 2 h). A representative gel for in-house produced His-tagged pro-VCC and its proteolysis activation was shown. Both the toxin purity (the major band was toxin, with few degradation bands) and activation efficiency were satisfactory.

    Toll-like Receptor (TLR) アイソフォーム固有の製品をすべて表示:

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    製品説明

    Chymotrypsin (EC 3.4.21.1; Chymotrypsin A) is an orally effective inhibitor targeting molecules such as TLR4, NF-κB, MMP-1, TNF-α, IL-1β, and IL-6. Chymotrypsin downregulates the TLR4/NF-κB signaling pathway, inhibiting the release of inflammatory factors, reducing cell infiltration and tissue damage. It also reduces the expression of tumor cell adhesion molecules (such as CD44 and CD54) and can be specifically detected by fluorescent probes (such as NBD-3). Chymotrypsin has anti-inflammatory, hepatoprotective, joint damage-reducing, liver protection against lipotoxicity, and anti-tumor metastasis functions. It can be used in research on diseases such as rheumatoid arthritis, non-alcoholic fatty liver disease, and melanoma metastasis. Chymotrypsin can be used in studies of inflammation, edema, and expectoration[1][2][3][4][5].

    IC50 & Target

    MMP-1

     

    TLR4

     

    体外実験

    Chymotrypsin mixed with Trypsin (HY-129047) and Papain (HY-P1645) was used as a treatment group in in vitro studies (with a Chymotrypsin content of 0.2 mg/0.1 mL), causing a decrease in CD44 expression in SMMU-2, SK-MEL 28, B16F10 melanoma cells, MOLT 4/8 leukemia cells, and breast cancer cells[3].
    Chymotrypsin selectively reduces the density of CD4, CD44, and CD80 molecules in peripheral lymphocytes[3].
    Chymotrypsin can be detected by the probe NBD-3 (2 mM), with a detection concentration of 0-6 g/mL and a reaction time of 20 minutes, producing red fluorescence at 634 nm under an excitation wavelength of 550 nm, with a detection limit of 15. ng/mL. Furthermore, its activity can be inhibited by the inhibitor phenylmethylsulfonyl fluoride (PMSF)[4];

    MedChemExpress (MCE) has not independently confirmed the accuracy of these methods. They are for reference only.

    Immunofluorescence[3]

    Cell Line: SMMU-2 melanoma cells, SK-MEL 28 melanoma cells, MOLT 4/8 leukemia cells, mammary carcinoma cells, peripheral lymphocytes, B16F10 mouse melanoma cells
    Concentration: Mixture containing chymotrypsin (0.2 mg/0.1 ml), trypsin (0.2 mg/0.1 ml), and papain (0.5 mg/0.1 ml)
    Incubation Time:
    Result: Exposure to the mixture of chymotrypsin, trypsin, and papain reduced the expression of CD44 in SMMU-2 melanoma cells, SK-MEL 28 melanoma cells, MOLT 4/8 leukemia cells, mammary carcinoma cells, and B16F10 mouse melanoma cells.
    Additionally, it selectively decreased the density of CD4, CD44, and CD80 molecules on peripheral lymphocytes in vitro.
    体内実験

    Chymotrypsin (0.53 mg/kg, 1.06 mg/kg; injected into the plantar surface of the left hind paw) reduces joint damage, inhibited paw swelling and arthritis scores, and reduces pathological changes such as synovial hyperplasia and inflammatory cell infiltration in a Sprague-Dawley rat adjuvant-induced arthritis (AIA) model. Chymotrypsin also downregulates the protein and mRNA expression of MMP-1, TNF-α, IL-1β, IL-6 in serum and TLR4, NF-κB in synovial tissue[1].
    Chymotrypsin (in combination with trypsin, 3 EAU/kg; oral gavage; once daily; 5 weeks) protectes the liver from damage in an olanzapine-induced non-alcoholic steatohepatitis (NASH) model in young adult male albino rats, significantly reducing olanzapine-induced elevated ALT, AST, ALP, total cholesterol, and LDL-C, reducing steatosis scores and hepatocyte necrosis, increasing Ki67 expression, and not affecting the memory function of the rats[2].
    Chymotrypsin (mixed with trypsin and papain, 0.2 mg/0.1 mL mixture; rectal administration; twice daily; 100 days) inhibits primary tumor growth, reduces tumor recurrence and metastasis (including lung and distant metastasis), prolongs mouse survival time, and reduced the expression of CD44 and CD54 molecules in tumor cells in a B16 melanoma metastasis model in female inbred C57Bl6 mice[3].
    The NBD-3 probe detects endogenous chymotrypsin in mouse liver[4].

    MedChemExpress (MCE) has not independently confirmed the accuracy of these methods. They are for reference only.

    Animal Model: Sprague-Dawley rats adjuvant-induced arthritis (AIA) model[1]
    Dosage: Low dose 0.53 mg/kg, high dose 1.06 mg/kg
    Administration:
    Result: Attenuated joint damage of AIA rats, suppressed paw swelling and arthritic scores, and reduced synovial hyperplasia, inflammatory cell infiltration, pannus formation, and bone destruction.
    The overproduction of MMP-1, TNF-α, IL-1β, and IL-6 in serum was remarkably attenuated, and the protein levels of TLR4 and NF-κB in synovial tissue as well as the mRNA expression of TLR4, NF-κB, TNF-α, IL-1β, and IL-6 in synovial tissue were substantially declined.
    Animal Model: Female inbred C57Bl6 mice (average body weight 18-20 g) syngeneic B16 melanoma metastatic model[3]
    Dosage: 0.2 mg chymotrypsin combined with 0.2 mg trypsin and 0.5 mg papain per 0.1 mL
    Administration:
    Result: Inhibited the growth of primary tumors, with the mean tumor size in the treated group (E1) being statistically significantly smaller (47.2 mm3) than that in all control groups.
    Reduced the number of tumor recurrences (6% in E1 and 2% in E2 vs 30% in C1 and C2) and considerably curtailed metastasis (46% pulmonary metastases in E1 and 68% in E2 vs 95% in C1 and 90% in C2).
    Extended the survival time of the mice, with the mean survival time of 72.06 days in E1 and 54.92 days in E2, compared to 27.25 days in C1 and 28.65 days in C2, and 46% of mice in E1 and 30% in E2 survived until the end of the 100-day study.
    Correlated with a decreased expression of CD44 and CD54 molecules in ascitic tumor cells.
    臨床実験
    CAS 番号
    Appearance

    Solid

    Color

    White to off-white

    SMILES

    [Chymotrypsin]

    EC Number

    3.4.21.1

    Enzyme Activity

    ≥1000 U/mg soild

    Unit Definition

    One unit is defined as the amount of enzyme that causes a decrease in the absorbance at 237 nm of 0.001 in per minute at 25°C, pH 7.0.

    輸送条件

    Room temperature in continental US; may vary elsewhere.

    保管条件

    Please store the product under the recommended conditions in the Certificate of Analysis.

    溶剤 & 溶解度
    体外: 

    H2O : ≥ 33.33 mg/mL

    *"≥" means soluble, but saturation unknown.

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    製品名:
    Chymotrypsin
    製品番号:
    HY-108910
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