Design and Synthesis of New Thiazole Derivatives as Anticancer Agents: p56 Lck Inhibitors
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Design and Synthesis of New Thiazole Derivatives as Anticancer Agents
~EN PB NWISBN: 9783659571763 bzw. 3659571768, vermutlich in Englisch, LAP Lambert Academic Publishing, Taschenbuch, neu.
Lieferung aus: Deutschland, Versandkostenfrei.
Von Händler/Antiquariat, BuchWeltWeit Inh. Ludwig Meier e.K. [57449362], Bergisch Gladbach, Germany.
Neuware - Thiazole is an important scaffold due to variety of pharmacological properties associated with the derivatives bearing this heterocyclic. Especially their importance in the cancer chemotherapy is unparallel. In our efforts to discover new chemical pharmacophore which may lead to formation of new anticancer agent. In the present study we have reported the synthesis of some new heterocyclic derivatives comprising substituted benzothiazole and 1,3,4-thiadiazole that linked by thiazole moiety. 2-Amino thiazoles are of interest because of their diverse biological activities and clinical applications. We have reported the new series of 2-Amino Thiazole analogues to target p56 lck(lymphocyte specific tyrosine kinase) inhibitors. Synthesized compounds were characterized and confirmed by IR, 1H-NMR and Mass spectral (MS) studies. For anticancer activity, all the selected compounds submitted to National Cancer Institute (NCI) for in vitro anticancer in which Compound 8(a) shown better anticancer activity. The MTT assay was carried out which showed compound 8(a) better anticancer agent than other summarized. 132 pp. Englisch.
Von Händler/Antiquariat, BuchWeltWeit Inh. Ludwig Meier e.K. [57449362], Bergisch Gladbach, Germany.
Neuware - Thiazole is an important scaffold due to variety of pharmacological properties associated with the derivatives bearing this heterocyclic. Especially their importance in the cancer chemotherapy is unparallel. In our efforts to discover new chemical pharmacophore which may lead to formation of new anticancer agent. In the present study we have reported the synthesis of some new heterocyclic derivatives comprising substituted benzothiazole and 1,3,4-thiadiazole that linked by thiazole moiety. 2-Amino thiazoles are of interest because of their diverse biological activities and clinical applications. We have reported the new series of 2-Amino Thiazole analogues to target p56 lck(lymphocyte specific tyrosine kinase) inhibitors. Synthesized compounds were characterized and confirmed by IR, 1H-NMR and Mass spectral (MS) studies. For anticancer activity, all the selected compounds submitted to National Cancer Institute (NCI) for in vitro anticancer in which Compound 8(a) shown better anticancer activity. The MTT assay was carried out which showed compound 8(a) better anticancer agent than other summarized. 132 pp. Englisch.
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Design and Synthesis of New Thiazole Derivatives as Anticancer Agents - p56 Lck Inhibitors (2019)
~EN PB NWISBN: 9783659571763 bzw. 3659571768, vermutlich in Englisch, 132 Seiten, LAP Lambert Academic Publishing, Taschenbuch, neu.
Lieferung aus: Deutschland, Versandkosten nach: Deutschland, Versandkostenfrei.
Von Händler/Antiquariat, Syndikat Buchdienst, [4235284].
Thiazole is an important scaffold due to variety of pharmacological properties associated with the derivatives bearing this heterocyclic. Especially their importance in the cancer chemotherapy is unparallel. In our efforts to discover new chemical pharmacophore which may lead to formation of new anticancer agent. In the present study we have reported the synthesis of some new heterocyclic derivatives comprising substituted benzothiazole and 1,3,4-thiadiazole that linked by thiazole moiety. 2-Amino thiazoles are of interest because of their diverse biological activities and clinical applications. We have reported the new series of 2-Amino Thiazole analogues to target p56 lck(lymphocyte specific tyrosine kinase) inhibitors. Synthesized compounds were characterized and confirmed by IR, 1H-NMR and Mass spectral (MS) studies. For anticancer activity, all the selected compounds submitted to National Cancer Institute (NCI) for in vitro anticancer in which Compound 8(a) shown better anticancer activity. The MTT assay was carried out which showed compound 8(a) better anticancer agent than other summarized. 2019, Taschenbuch / Paperback, Neuware, H: 220mm, B: 150mm, 132, Internationaler Versand, Selbstabholung und Barzahlung, PayPal, offene Rechnung, Banküberweisung.
Von Händler/Antiquariat, Syndikat Buchdienst, [4235284].
Thiazole is an important scaffold due to variety of pharmacological properties associated with the derivatives bearing this heterocyclic. Especially their importance in the cancer chemotherapy is unparallel. In our efforts to discover new chemical pharmacophore which may lead to formation of new anticancer agent. In the present study we have reported the synthesis of some new heterocyclic derivatives comprising substituted benzothiazole and 1,3,4-thiadiazole that linked by thiazole moiety. 2-Amino thiazoles are of interest because of their diverse biological activities and clinical applications. We have reported the new series of 2-Amino Thiazole analogues to target p56 lck(lymphocyte specific tyrosine kinase) inhibitors. Synthesized compounds were characterized and confirmed by IR, 1H-NMR and Mass spectral (MS) studies. For anticancer activity, all the selected compounds submitted to National Cancer Institute (NCI) for in vitro anticancer in which Compound 8(a) shown better anticancer activity. The MTT assay was carried out which showed compound 8(a) better anticancer agent than other summarized. 2019, Taschenbuch / Paperback, Neuware, H: 220mm, B: 150mm, 132, Internationaler Versand, Selbstabholung und Barzahlung, PayPal, offene Rechnung, Banküberweisung.
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Design and Synthesis of New Thiazole Derivatives as Anticancer Agents - p56 Lck Inhibitors
~EN PB NWISBN: 9783659571763 bzw. 3659571768, vermutlich in Englisch, LAP Lambert Academic Publishing, Taschenbuch, neu.
Lieferung aus: Deutschland, Versandkostenfrei.
Design and Synthesis of New Thiazole Derivatives as Anticancer Agents: Thiazole is an important scaffold due to variety of pharmacological properties associated with the derivatives bearing this heterocyclic. Especially their importance in the cancer chemotherapy is unparallel. In our efforts to discover new chemical pharmacophore which may lead to formation of new anticancer agent. In the present study we have reported the synthesis of some new heterocyclic derivatives comprising substituted benzothiazole and 1,3,4-thiadiazole that linked by thiazole moiety. 2-Amino thiazoles are of interest because of their diverse biological activities and clinical applications. We have reported the new series of 2-Amino Thiazole analogues to target p56 lck(lymphocyte specific tyrosine kinase) inhibitors. Synthesized compounds were characterized and confirmed by IR, 1H-NMR and Mass spectral (MS) studies. For anticancer activity, all the selected compounds submitted to National Cancer Institute (NCI) for in vitro anticancer in which Compound 8(a) shown better anticancer activity. The MTT assay was carried out which showed compound 8(a) better anticancer agent than other summarized. Englisch, Taschenbuch.
Design and Synthesis of New Thiazole Derivatives as Anticancer Agents: Thiazole is an important scaffold due to variety of pharmacological properties associated with the derivatives bearing this heterocyclic. Especially their importance in the cancer chemotherapy is unparallel. In our efforts to discover new chemical pharmacophore which may lead to formation of new anticancer agent. In the present study we have reported the synthesis of some new heterocyclic derivatives comprising substituted benzothiazole and 1,3,4-thiadiazole that linked by thiazole moiety. 2-Amino thiazoles are of interest because of their diverse biological activities and clinical applications. We have reported the new series of 2-Amino Thiazole analogues to target p56 lck(lymphocyte specific tyrosine kinase) inhibitors. Synthesized compounds were characterized and confirmed by IR, 1H-NMR and Mass spectral (MS) studies. For anticancer activity, all the selected compounds submitted to National Cancer Institute (NCI) for in vitro anticancer in which Compound 8(a) shown better anticancer activity. The MTT assay was carried out which showed compound 8(a) better anticancer agent than other summarized. Englisch, Taschenbuch.
5
Design and Synthesis of New Thiazole Derivatives as Anticancer Agents: p56 Lck Inhibitors (2019)
EN PB NWISBN: 9783659571763 bzw. 3659571768, in Englisch, 132 Seiten, LAP LAMBERT Academic Publishing, Taschenbuch, neu.
Lieferung aus: Deutschland, Gewöhnlich versandfertig in 24 Stunden, Versandkostenfrei. Tatsächliche Versandkosten können abweichen.
Von Händler/Antiquariat, averdo24.
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Von Händler/Antiquariat, averdo24.
Die Beschreibung dieses Angebotes ist von geringer Qualität oder in einer Fremdsprache. Trotzdem anzeigen
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