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sincalide sin  (MedChemExpress)


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    MedChemExpress sincalide sin
    Fig. 3. In vitro effect of Caba-780 on RCC cells and normal human embryonic kidney cells. (A) Cytotoxicity assay using the Cell Counting <t>Kit-8</t> <t>(CCK-8)</t> method. ACHN, 786-O, and HEK293 cells were incubated with different concentrations (0–20 μM) of Caba-780, IR-780, and cabazitaxel. The IC50 values of Caba- 780 for ACHN, 786-O, and HEK293 cells were 11.5 μM and 1.9 μM, 8.7 μM respectively, and the IC50 values of IR-780 for ACHN, 786-O, and HEK293 were 31.2 μM and 10.4 μM, 5.5 μM, respectively. The IC50 of cabazitaxel could not be calculated for each group. Dose-dependent inhibition of cell growth by Caba-780 was found. The inhibitory effect of Caba-780 on tumor growth was stronger than that of other drugs, and its toxicity to normal cells was weaker than that of IR-780. (B) Plate colony-formation assay. IR-780 had little effect on the clonal growth of the two RCC cell lines (ACHN on the left and 786-O on the right), and the cabazitaxel group had some clone formation, while there was almost no colony formation in the Caba-780 group.
    Sincalide Sin, supplied by MedChemExpress, used in various techniques. Bioz Stars score: 92/100, based on 2 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/result/sincalide sin/product/MedChemExpress
    Average 92 stars, based on 2 article reviews
    sincalide sin - by Bioz Stars, 2026-02
    92/100 stars

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    1) Product Images from "Coupling the near-infrared fluorescent dye IR-780 with cabazitaxel makes renal cell carcinoma chemotherapy possible."

    Article Title: Coupling the near-infrared fluorescent dye IR-780 with cabazitaxel makes renal cell carcinoma chemotherapy possible.

    Journal: Biomedicine & pharmacotherapy = Biomedecine & pharmacotherapie

    doi: 10.1016/j.biopha.2019.109001

    Fig. 3. In vitro effect of Caba-780 on RCC cells and normal human embryonic kidney cells. (A) Cytotoxicity assay using the Cell Counting Kit-8 (CCK-8) method. ACHN, 786-O, and HEK293 cells were incubated with different concentrations (0–20 μM) of Caba-780, IR-780, and cabazitaxel. The IC50 values of Caba- 780 for ACHN, 786-O, and HEK293 cells were 11.5 μM and 1.9 μM, 8.7 μM respectively, and the IC50 values of IR-780 for ACHN, 786-O, and HEK293 were 31.2 μM and 10.4 μM, 5.5 μM, respectively. The IC50 of cabazitaxel could not be calculated for each group. Dose-dependent inhibition of cell growth by Caba-780 was found. The inhibitory effect of Caba-780 on tumor growth was stronger than that of other drugs, and its toxicity to normal cells was weaker than that of IR-780. (B) Plate colony-formation assay. IR-780 had little effect on the clonal growth of the two RCC cell lines (ACHN on the left and 786-O on the right), and the cabazitaxel group had some clone formation, while there was almost no colony formation in the Caba-780 group.
    Figure Legend Snippet: Fig. 3. In vitro effect of Caba-780 on RCC cells and normal human embryonic kidney cells. (A) Cytotoxicity assay using the Cell Counting Kit-8 (CCK-8) method. ACHN, 786-O, and HEK293 cells were incubated with different concentrations (0–20 μM) of Caba-780, IR-780, and cabazitaxel. The IC50 values of Caba- 780 for ACHN, 786-O, and HEK293 cells were 11.5 μM and 1.9 μM, 8.7 μM respectively, and the IC50 values of IR-780 for ACHN, 786-O, and HEK293 were 31.2 μM and 10.4 μM, 5.5 μM, respectively. The IC50 of cabazitaxel could not be calculated for each group. Dose-dependent inhibition of cell growth by Caba-780 was found. The inhibitory effect of Caba-780 on tumor growth was stronger than that of other drugs, and its toxicity to normal cells was weaker than that of IR-780. (B) Plate colony-formation assay. IR-780 had little effect on the clonal growth of the two RCC cell lines (ACHN on the left and 786-O on the right), and the cabazitaxel group had some clone formation, while there was almost no colony formation in the Caba-780 group.

    Techniques Used: In Vitro, Cytotoxicity Assay, Cell Counting, CCK-8 Assay, Incubation, Inhibition, Colony Assay



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    sincalide sin  (MedChemExpress)
    92
    MedChemExpress sincalide sin
    Fig. 3. In vitro effect of Caba-780 on RCC cells and normal human embryonic kidney cells. (A) Cytotoxicity assay using the Cell Counting <t>Kit-8</t> <t>(CCK-8)</t> method. ACHN, 786-O, and HEK293 cells were incubated with different concentrations (0–20 μM) of Caba-780, IR-780, and cabazitaxel. The IC50 values of Caba- 780 for ACHN, 786-O, and HEK293 cells were 11.5 μM and 1.9 μM, 8.7 μM respectively, and the IC50 values of IR-780 for ACHN, 786-O, and HEK293 were 31.2 μM and 10.4 μM, 5.5 μM, respectively. The IC50 of cabazitaxel could not be calculated for each group. Dose-dependent inhibition of cell growth by Caba-780 was found. The inhibitory effect of Caba-780 on tumor growth was stronger than that of other drugs, and its toxicity to normal cells was weaker than that of IR-780. (B) Plate colony-formation assay. IR-780 had little effect on the clonal growth of the two RCC cell lines (ACHN on the left and 786-O on the right), and the cabazitaxel group had some clone formation, while there was almost no colony formation in the Caba-780 group.
    Sincalide Sin, supplied by MedChemExpress, used in various techniques. Bioz Stars score: 92/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/result/sincalide sin/product/MedChemExpress
    Average 92 stars, based on 1 article reviews
    sincalide sin - by Bioz Stars, 2026-02
    92/100 stars
    		  Buy from Supplier

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    Fig. 3. In vitro effect of Caba-780 on RCC cells and normal human embryonic kidney cells. (A) Cytotoxicity assay using the Cell Counting Kit-8 (CCK-8) method. ACHN, 786-O, and HEK293 cells were incubated with different concentrations (0–20 μM) of Caba-780, IR-780, and cabazitaxel. The IC50 values of Caba- 780 for ACHN, 786-O, and HEK293 cells were 11.5 μM and 1.9 μM, 8.7 μM respectively, and the IC50 values of IR-780 for ACHN, 786-O, and HEK293 were 31.2 μM and 10.4 μM, 5.5 μM, respectively. The IC50 of cabazitaxel could not be calculated for each group. Dose-dependent inhibition of cell growth by Caba-780 was found. The inhibitory effect of Caba-780 on tumor growth was stronger than that of other drugs, and its toxicity to normal cells was weaker than that of IR-780. (B) Plate colony-formation assay. IR-780 had little effect on the clonal growth of the two RCC cell lines (ACHN on the left and 786-O on the right), and the cabazitaxel group had some clone formation, while there was almost no colony formation in the Caba-780 group.

    Journal: Biomedicine & pharmacotherapy = Biomedecine & pharmacotherapie

    Article Title: Coupling the near-infrared fluorescent dye IR-780 with cabazitaxel makes renal cell carcinoma chemotherapy possible.

    doi: 10.1016/j.biopha.2019.109001

    Figure Lengend Snippet: Fig. 3. In vitro effect of Caba-780 on RCC cells and normal human embryonic kidney cells. (A) Cytotoxicity assay using the Cell Counting Kit-8 (CCK-8) method. ACHN, 786-O, and HEK293 cells were incubated with different concentrations (0–20 μM) of Caba-780, IR-780, and cabazitaxel. The IC50 values of Caba- 780 for ACHN, 786-O, and HEK293 cells were 11.5 μM and 1.9 μM, 8.7 μM respectively, and the IC50 values of IR-780 for ACHN, 786-O, and HEK293 were 31.2 μM and 10.4 μM, 5.5 μM, respectively. The IC50 of cabazitaxel could not be calculated for each group. Dose-dependent inhibition of cell growth by Caba-780 was found. The inhibitory effect of Caba-780 on tumor growth was stronger than that of other drugs, and its toxicity to normal cells was weaker than that of IR-780. (B) Plate colony-formation assay. IR-780 had little effect on the clonal growth of the two RCC cell lines (ACHN on the left and 786-O on the right), and the cabazitaxel group had some clone formation, while there was almost no colony formation in the Caba-780 group.

    Article Snippet: IR-780 was purchased from Heowns Biological Technology Co., Ltd. (Tianjin, China), cabazitaxel was purchased from Dalian Meilun Biological Technology Co., Ltd. (Dalian, China), sulfobromophthalein sodium (BSP) was purchased from Alfa Aesar Chemical Co., Ltd. (Tianjin, China), rifampin (RIF) was purchased from TCI Development Co., Ltd. (Shanghai, China), sincalide (SIN) and estradiol (EST) were from Medchem Express (MCE, USA), MitoSPy Orange CMTMRos, Lyso Tracker Green DND‐26 and 4′,6-diamidino-2-phenyindole (DAPI) were from Cell Signaling Technology (CST, USA), Cell Counting Kit-8 (CCK8) was from Dojindo Molecular Technologies, Inc. (Tokyo, Japan), RPMI-1640, DMEM, and Fetal bovine serum (FBS) were from Gibco (Gaithersburg, MD, USA), crystal violet, trypsin, dimethyl sulfoxide (DMSO) and paraformaldehyde were from Thermo-Fisher Scientific (Waltham, MA, USA).

    Techniques: In Vitro, Cytotoxicity Assay, Cell Counting, CCK-8 Assay, Incubation, Inhibition, Colony Assay