14 Results for "

vinblastine

" in MedChemExpress (MCE) Product Catalog:
Products (14)

14 Results for "vinblastine" in MCE Product Catalog:

23
23 Publications Verification
Cat. No.: HY-13780
CAS No.: 143-67-9
Purity:  99.86%
Synonyms: Vincaleukoblastine sulfate salt
Vinblastine sulfate is a cytotoxic alkaloid used against various cancer types. Vinblastine sulfate inhibits the formation of microtubule and suppresses nAChR with an IC50 of 8.9 μM.
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2
2 Cited Publications
Cat. No.: HY-14949
CAS No.: 849550-05-6
Purity:  99.86%
Synonyms: TTI-237
Target:  

Microtubule/Tubulin

Research Areas:  

Cancer

Cevipabulin (TTI-237) is an oral, microtubule-active antitumor compound and inhibits the binding of [ 3H] vinblastine to tubulin, with an IC50 of 18-40 nM for cytotoxicity in human tumor cell line .
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1
1 Cited Publications
Cat. No.: HY-128902
CAS No.: 2055896-92-7
Purity:  92.87%
Research Areas:  

Cancer

MC-Val-Cit-PAB-vinblastine is a agent-linker conjugate for ADC with potent antitumor activity by using vinblastine (an microtubule protein inhibitor), linked via the ADC linker MC-Val-Cit-PAB.
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Cat. No.: HY-112749
CAS No.: 1374524-68-1
ME-344 is an Isoflavone. ME-344 increases mitochondrial ROS generation. ME-344 inhibits tubulin polymerization. ME-344 inhibits HO-1 and impacts its mitochondrial translocation. ME-344 induces Apoptosis through Caspase 3 activation. ME-344 synergizes with Vinblastine in leukemia cells. ME-344 displays anti-tumor activity against leukemia and lung tumor. ME-344 can be used in the research of lung cancer, acute myeloid leukemia, and HER2-negative breast cancer .
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Cat. No.: HY-13780R
CAS No.: 143-67-9
Synonyms: Vincaleukoblastine sulfate salt (Standard)
Vinblastine (sulfate) (Standard) is the analytical standard of Vinblastine (sulfate). This product is intended for research and analytical applications. Vinblastine sulfate is a cytotoxic alkaloid used against various cancer types. Vinblastine sulfate inhibits the formation of microtubule and suppresses nAChR with an IC50 of 8.9 μM.
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Cat. No.: HY-16514
CAS No.: 53643-48-4
Research Areas:  

Cancer

Vindesine is a derivative of Vinblastine (HY-13780). Vindesine binds to and stabilizes tubulin . Vindesine inhibits mitosis in cancer cells and prevents the invasion of normal tissues by malignant cells. Vindesine can be used in cancer research .
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Cat. No.: HY-177021
CAS No.: 849550-36-3
Research Areas:  

Cancer

Tubulin-IN-51 is an orally available, potent tubulin inhibitor (IC50 = 31 nM). Tubulin-IN-51 promotes tubulin polymerization in vitro and does not compete with Paclitaxel (HY-B0015) for binding. Tubulin-IN-51 inhibits the binding of Vinblastine (HY-13780) to tubulin. Tubulin-IN-51 downregulates the proportion of cells in the G1 phase and induces apoptosis. Tubulin-IN-51 inhibits tumor growth in multiple nude mouse xenograft models .
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Cat. No.: HY-N15081
CAS No.: 148441-26-3
Target:  

Others

5-N-Acetylardeemin potentiated the cytotoxicity of the anticancer agent Vinblastine (HY-13780) in multidrug resistant human tumor cells .
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Cat. No.: HY-128941
CAS No.: 1452145-13-9
Research Areas:  

Cancer

CCK2R Ligand-Linker Conjugates 1 is a ligand-linker conjugate, which conjugates to the cytotoxic antimicrotubule agents Desacetyl Vinblastine Hydrazide (DAVBH) and Tubulysin B Hydrazide (TubBH) via a hydrophilic peptide linker .
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Cat. No.: HY-W740505
Anhydro Vinblastine Disulfate-d3 is the deuterium labeled Anhydro Vinblastine Disulfate.
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Cat. No.: HY-P10589
CAS No.: 89085-54-1
Target:  

Microtubule/Tubulin

Research Areas:  

Cancer

Phomopsinamine A is a derivative of Phomopsin A (HY-N6793). Phomopsinamine A is an inhibitor for tubulin polymerization with IC50 of 0.53 μM. Phomopsinamine A inhibits the binding of Vinblastine (HY-13780) to tubulin (IC50 =0.56 μM), promotes the the binding of Colchicine (HY-16569) to tubulin (IC50 =0.32 μM) .
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Cat. No.: HY-157876
Target:  

P-glycoprotein BCRP

Research Areas:  

Cancer

Anticancer agent 191 (Compound 2) is a derivative of probenecid (HY-B0545). As a cancer cell efflux inhibitor, Anticancer agent 191 is designed to inhibit P-glycoprotein (P-gp), breast cancer resistance protein (BCRP), and/or multiple multidrug resistance proteins (MRPs). Anticancer agent 191 increases the accumulation of vinblastine in cancer cells, which is used for cancer research .
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Cat. No.: HY-N15297
CAS No.: 10092-04-3
Isotenulin inhibits the efflux function of P-glycoprotein by stimulation of P-glycoprotein ATPase, thereby overcoming the multidrug resistance (MDR) of cancer cells. Isotenulin exhibits cytotoxicity in multidrug-resistant cancer cell KB-vin and sensitive cancer cell HeLaS3. Isotenulin exhibits synergistic effect with Paclitaxel (HY-B0015), Vinblastine (HY-13780) and Doxorubicin (HY-15142) .
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Cat. No.: HY-133005
CAS No.: 3352-69-0
Synonyms: 4-Desacetylvinblastine; Desacetylvincaleukoblastine
Target:  

Drug Metabolite

Research Areas:  

Cancer

Desacetylvinblastine (4-Desacetylvinblastine) is the major metabolite of Vinblastine (HY-13780) and a cytotoxic agent. When used alone, desacetylvinblastine has poor anti-tumor effects, but it can exert significant anti-tumor activity when in the presence of specific conjugates .
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