The protein ovary testis transcribed olfactory receptor family 52 subfamily E member 19 plays a significant role in certain cancer cells, influencing their proliferation and survival. The inhibition of this protein can be achieved through a targeted approach involving various kinase inhibitors, each disrupting specific signaling pathways crucial for the survival and growth of cancer cells expressing this protein. Sorafenib and Sunitinib, as multi-targeted receptor tyrosine kinase inhibitors, specifically target VEGFR and PDGFR, which are involved in angiogenesis and cell proliferation. By inhibiting these kinases, they disrupt the signaling pathways crucial for tumor cell proliferation and angiogenesis, thereby exerting an inhibitory effect on cells expressing the ovary testis transcribed protein. Similarly, Dasatinib's inhibition of Src family kinases affects cellular processes like cell growth and survival, which are vital for the function of this protein in cancer cells. Erlotinib and Lapatinib, by targeting EGFR and HER2/neu respectively, disrupt important signaling pathways contributing to the proliferation and survival of cells where this protein is expressed.
Furthermore, Imatinib's selective inhibition of BCR-ABL, c-Kit, and PDGF receptors blocks kinase activity, thus inhibiting signaling pathways critical for cancer cell growth and survival where the ovary testis transcribed protein is involved. Nilotinib, as a selective BCR-ABL tyrosine kinase inhibitor, functions in a similar manner. Pazopanib and Vandetanib, by inhibiting multiple receptors, including VEGFR, EGFR, and RET-tyrosine kinases, interfere with crucial signaling pathways, leading to the inhibition of cancer cells expressing this protein. Axitinib's potent inhibition of VEGFR1, 2, and 3 impedes angiogenesis and tumor growth, affecting cells where the ovary testis transcribed protein is active. Afatinib, through its irreversible inhibition of EGFR and HER2, disrupts key signaling pathways, crucial for the survival and proliferation of cells expressing this protein. Lastly, Crizotinib targets ALK, ROS1, and MET tyrosine kinase, affecting cell survival and proliferation pathways, thereby inhibiting the function of cells expressing the ovary testis transcribed protein. These inhibitors collectively demonstrate the potential of targeted inhibition of specific signaling pathways in affecting the function of ovary testis transcribed olfactory receptor family 52 subfamily E member 19 in cancer cells.
SEE ALSO...
| Product Name | CAS # | Catalog # | QUANTITY | Price | Citations | RATING |
|---|---|---|---|---|---|---|
Sorafenib | 284461-73-0 | sc-220125 sc-220125A sc-220125B | 5 mg 50 mg 500 mg | $56.00 $260.00 $416.00 | 129 | |
Sorafenib, a kinase inhibitor, targets multiple kinases like VEGFR and PDGFR which are involved in angiogenesis and cell proliferation. By inhibiting these kinases, Sorafenib disrupts the signaling pathways crucial for tumor cell proliferation and angiogenesis, thereby inhibiting the growth of cancer cells expressing ovary testis transcribed olfactory receptor family 52 subfamily E member 19. | ||||||
Dasatinib | 302962-49-8 | sc-358114 sc-358114A | 25 mg 1 g | $47.00 $145.00 | 51 | |
Dasatinib is a potent inhibitor of multiple tyrosine kinases including BCR-ABL and Src family kinases. By inhibiting Src kinases, Dasatinib affects cellular processes like cell growth and survival that are vital for the function of ovary testis transcribed olfactory receptor family 52 subfamily E member 19 in cancer cells, leading to their inhibition. | ||||||
Erlotinib, Free Base | 183321-74-6 | sc-396113 sc-396113A sc-396113B sc-396113C sc-396113D | 500 mg 1 g 5 g 10 g 100 g | $85.00 $132.00 $287.00 $495.00 $3752.00 | 42 | |
Erlotinib is an EGFR inhibitor, specifically targeting the epidermal growth factor receptor tyrosine kinase. By blocking EGFR, Erlotinib disrupts important signaling pathways that contribute to the proliferation and survival of cells expressing ovary testis transcribed olfactory receptor family 52 subfamily E member 19, thereby inhibiting these cells. | ||||||
Imatinib | 152459-95-5 | sc-267106 sc-267106A sc-267106B | 10 mg 100 mg 1 g | $25.00 $117.00 $209.00 | 27 | |
Imatinib is a selective tyrosine kinase inhibitor, particularly targeting BCR-ABL, c-Kit, and PDGF receptors. It blocks the kinase activity of these proteins, thus inhibiting signaling pathways critical for cancer cell growth and survival where ovary testis transcribed olfactory receptor family 52 subfamily E member 19 is expressed. | ||||||
Sunitinib, Free Base | 557795-19-4 | sc-396319 sc-396319A | 500 mg 5 g | $150.00 $920.00 | 5 | |
Sunitinib is a multi-targeted receptor tyrosine kinase inhibitor, affecting receptors like VEGFR and PDGFR. It impedes angiogenesis and cell proliferation pathways, leading to the inhibition of cells expressing ovary testis transcribed olfactory receptor family 52 subfamily E member 19. | ||||||
Lapatinib | 231277-92-2 | sc-353658 | 100 mg | $412.00 | 32 | |
Lapatinib, a dual tyrosine kinase inhibitor, targets both EGFR and HER2/neu. Inhibition of these receptors interrupts signaling pathways essential for the survival and proliferation of cells expressing ovary testis transcribed olfactory receptor family 52 subfamily E member 19. | ||||||
Nilotinib | 641571-10-0 | sc-202245 sc-202245A | 10 mg 25 mg | $205.00 $405.00 | 9 | |
Nilotinib is a selective BCR-ABL tyrosine kinase inhibitor. It blocks this kinase, thereby disrupting downstream signaling pathways involved in the proliferation and survival of cancer cells where ovary testis transcribed olfactory receptor family 52 subfamily E member 19 is expressed. | ||||||
Pazopanib | 444731-52-6 | sc-396318 sc-396318A | 25 mg 50 mg | $127.00 $178.00 | 2 | |
Pazopanib is a multi-targeted receptor tyrosine kinase inhibitor, affecting VEGFR, PDGFR, and c-Kit. By inhibiting these kinases, Pazopanib disrupts angiogenesis and cell proliferation, thus hindering the function of cells expressing ovary testis transcribed olfactory receptor family 52 subfamily E member 19. | ||||||
Vandetanib | 443913-73-3 | sc-220364 sc-220364A | 5 mg 50 mg | $167.00 $1353.00 | ||
Vandetanib selectively inhibits VEGFR, EGFR, and RET-tyrosine kinases. By blocking these kinases, Vandetanib interferes with crucial signaling pathways, leading to the inhibition of cancer cells expressing ovary testis transcribed olfactory receptor family 52 subfamily E member 19. | ||||||
Afatinib-d4 | 850140-72-6 (unlabeled) | sc-481821 | 10 mg | $4665.00 | ||
Afatinib-d4 is an irreversible inhibitor of EGFR and HER2. By covalently binding to these receptors, Afatinib disrupts key signaling pathways, leading to the inhibition of cells expressing ovary testis transcribed olfactory receptor family 52 subfamily E member 19. | ||||||