6,7-Dihydrobenzo[f]benzo[4,5]imidazo[1,2-d][1,4]oxazepine derivatives as selective inhibitors of PI3Kα
Twenty eight new 6,7-dihydrobenzo[f]benzo[4,5]imidazo[1,2-d][1,4]oxazepine derivatives have been synthesized and evaluated for biological activities as PI3Kα inhibitors. Compound 25 showed the most potent inhibitory activity.
Gespeichert in:
| Autor*in: |
Yin, Yong [verfasserIn] |
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| Format: |
E-Artikel |
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| Sprache: |
Englisch |
| Erschienen: |
2015 |
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| Schlagwörter: |
6,7-Dihydrobenzo[f]benzo[4,5]imidazo[1,2-d][1,4]oxazepine derivatives |
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| Umfang: |
10 |
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| Übergeordnetes Werk: |
Enthalten in: A theoretical model of cyberchondria development: Antecedents and intermediate processes - Zheng, Han ELSEVIER, 2021, a Tetrahedron publication for the rapid dissemination of full original research papers and critical reviews on bioorganic chemistry, medicinal chemistry, bioinorganic chemistry and related disciplines, Amsterdam [u.a.] |
|---|---|
| Übergeordnetes Werk: |
volume:23 ; year:2015 ; number:6 ; day:15 ; month:03 ; pages:1231-1240 ; extent:10 |
| Links: |
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| DOI / URN: |
10.1016/j.bmc.2015.01.052 |
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ELV02382722X |
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| 520 | |a Twenty eight new 6,7-dihydrobenzo[f]benzo[4,5]imidazo[1,2-d][1,4]oxazepine derivatives have been synthesized and evaluated for biological activities as PI3Kα inhibitors. Compound 25 showed the most potent inhibitory activity. | ||
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| 700 | 1 | |a Qiao, Fang |4 oth | |
| 700 | 1 | |a Lu, Ai-Min |4 oth | |
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10.1016/j.bmc.2015.01.052 doi GBVA2015016000012.pica (DE-627)ELV02382722X (ELSEVIER)S0968-0896(15)00076-0 DE-627 ger DE-627 rakwb eng 540 610 540 DE-600 610 DE-600 004 VZ 53.70 bkl 05.42 bkl 53.76 bkl 54.00 bkl Yin, Yong verfasserin aut 6,7-Dihydrobenzo[f]benzo[4,5]imidazo[1,2-d][1,4]oxazepine derivatives as selective inhibitors of PI3Kα 2015 10 nicht spezifiziert zzz rdacontent nicht spezifiziert z rdamedia nicht spezifiziert zu rdacarrier Twenty eight new 6,7-dihydrobenzo[f]benzo[4,5]imidazo[1,2-d][1,4]oxazepine derivatives have been synthesized and evaluated for biological activities as PI3Kα inhibitors. Compound 25 showed the most potent inhibitory activity. 6,7-Dihydrobenzo[f]benzo[4,5]imidazo[1,2-d][1,4]oxazepine derivatives Elsevier Antitumor Elsevier PI3Kα Elsevier Zhang, Yan-Qing oth Jin, Biao oth Sha, Shao oth Wu, Xun oth Sangani, Chetan B. oth Wang, She-Feng oth Qiao, Fang oth Lu, Ai-Min oth Lv, Peng-Cheng oth Zhu, Hai-Liang oth Enthalten in Elsevier Zheng, Han ELSEVIER A theoretical model of cyberchondria development: Antecedents and intermediate processes 2021 a Tetrahedron publication for the rapid dissemination of full original research papers and critical reviews on bioorganic chemistry, medicinal chemistry, bioinorganic chemistry and related disciplines Amsterdam [u.a.] (DE-627)ELV006510728 volume:23 year:2015 number:6 day:15 month:03 pages:1231-1240 extent:10 https://doi.org/10.1016/j.bmc.2015.01.052 Volltext GBV_USEFLAG_U GBV_ELV SYSFLAG_U 53.70 Nachrichtentechnik Kommunikationstechnik: Allgemeines VZ 05.42 Telekommunikation VZ 53.76 Kommunikationsdienste Fernmeldetechnik VZ 54.00 Informatik: Allgemeines VZ AR 23 2015 6 15 0315 1231-1240 10 045F 540 |
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10.1016/j.bmc.2015.01.052 doi GBVA2015016000012.pica (DE-627)ELV02382722X (ELSEVIER)S0968-0896(15)00076-0 DE-627 ger DE-627 rakwb eng 540 610 540 DE-600 610 DE-600 004 VZ 53.70 bkl 05.42 bkl 53.76 bkl 54.00 bkl Yin, Yong verfasserin aut 6,7-Dihydrobenzo[f]benzo[4,5]imidazo[1,2-d][1,4]oxazepine derivatives as selective inhibitors of PI3Kα 2015 10 nicht spezifiziert zzz rdacontent nicht spezifiziert z rdamedia nicht spezifiziert zu rdacarrier Twenty eight new 6,7-dihydrobenzo[f]benzo[4,5]imidazo[1,2-d][1,4]oxazepine derivatives have been synthesized and evaluated for biological activities as PI3Kα inhibitors. Compound 25 showed the most potent inhibitory activity. 6,7-Dihydrobenzo[f]benzo[4,5]imidazo[1,2-d][1,4]oxazepine derivatives Elsevier Antitumor Elsevier PI3Kα Elsevier Zhang, Yan-Qing oth Jin, Biao oth Sha, Shao oth Wu, Xun oth Sangani, Chetan B. oth Wang, She-Feng oth Qiao, Fang oth Lu, Ai-Min oth Lv, Peng-Cheng oth Zhu, Hai-Liang oth Enthalten in Elsevier Zheng, Han ELSEVIER A theoretical model of cyberchondria development: Antecedents and intermediate processes 2021 a Tetrahedron publication for the rapid dissemination of full original research papers and critical reviews on bioorganic chemistry, medicinal chemistry, bioinorganic chemistry and related disciplines Amsterdam [u.a.] (DE-627)ELV006510728 volume:23 year:2015 number:6 day:15 month:03 pages:1231-1240 extent:10 https://doi.org/10.1016/j.bmc.2015.01.052 Volltext GBV_USEFLAG_U GBV_ELV SYSFLAG_U 53.70 Nachrichtentechnik Kommunikationstechnik: Allgemeines VZ 05.42 Telekommunikation VZ 53.76 Kommunikationsdienste Fernmeldetechnik VZ 54.00 Informatik: Allgemeines VZ AR 23 2015 6 15 0315 1231-1240 10 045F 540 |
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10.1016/j.bmc.2015.01.052 doi GBVA2015016000012.pica (DE-627)ELV02382722X (ELSEVIER)S0968-0896(15)00076-0 DE-627 ger DE-627 rakwb eng 540 610 540 DE-600 610 DE-600 004 VZ 53.70 bkl 05.42 bkl 53.76 bkl 54.00 bkl Yin, Yong verfasserin aut 6,7-Dihydrobenzo[f]benzo[4,5]imidazo[1,2-d][1,4]oxazepine derivatives as selective inhibitors of PI3Kα 2015 10 nicht spezifiziert zzz rdacontent nicht spezifiziert z rdamedia nicht spezifiziert zu rdacarrier Twenty eight new 6,7-dihydrobenzo[f]benzo[4,5]imidazo[1,2-d][1,4]oxazepine derivatives have been synthesized and evaluated for biological activities as PI3Kα inhibitors. Compound 25 showed the most potent inhibitory activity. 6,7-Dihydrobenzo[f]benzo[4,5]imidazo[1,2-d][1,4]oxazepine derivatives Elsevier Antitumor Elsevier PI3Kα Elsevier Zhang, Yan-Qing oth Jin, Biao oth Sha, Shao oth Wu, Xun oth Sangani, Chetan B. oth Wang, She-Feng oth Qiao, Fang oth Lu, Ai-Min oth Lv, Peng-Cheng oth Zhu, Hai-Liang oth Enthalten in Elsevier Zheng, Han ELSEVIER A theoretical model of cyberchondria development: Antecedents and intermediate processes 2021 a Tetrahedron publication for the rapid dissemination of full original research papers and critical reviews on bioorganic chemistry, medicinal chemistry, bioinorganic chemistry and related disciplines Amsterdam [u.a.] (DE-627)ELV006510728 volume:23 year:2015 number:6 day:15 month:03 pages:1231-1240 extent:10 https://doi.org/10.1016/j.bmc.2015.01.052 Volltext GBV_USEFLAG_U GBV_ELV SYSFLAG_U 53.70 Nachrichtentechnik Kommunikationstechnik: Allgemeines VZ 05.42 Telekommunikation VZ 53.76 Kommunikationsdienste Fernmeldetechnik VZ 54.00 Informatik: Allgemeines VZ AR 23 2015 6 15 0315 1231-1240 10 045F 540 |
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10.1016/j.bmc.2015.01.052 doi GBVA2015016000012.pica (DE-627)ELV02382722X (ELSEVIER)S0968-0896(15)00076-0 DE-627 ger DE-627 rakwb eng 540 610 540 DE-600 610 DE-600 004 VZ 53.70 bkl 05.42 bkl 53.76 bkl 54.00 bkl Yin, Yong verfasserin aut 6,7-Dihydrobenzo[f]benzo[4,5]imidazo[1,2-d][1,4]oxazepine derivatives as selective inhibitors of PI3Kα 2015 10 nicht spezifiziert zzz rdacontent nicht spezifiziert z rdamedia nicht spezifiziert zu rdacarrier Twenty eight new 6,7-dihydrobenzo[f]benzo[4,5]imidazo[1,2-d][1,4]oxazepine derivatives have been synthesized and evaluated for biological activities as PI3Kα inhibitors. Compound 25 showed the most potent inhibitory activity. 6,7-Dihydrobenzo[f]benzo[4,5]imidazo[1,2-d][1,4]oxazepine derivatives Elsevier Antitumor Elsevier PI3Kα Elsevier Zhang, Yan-Qing oth Jin, Biao oth Sha, Shao oth Wu, Xun oth Sangani, Chetan B. oth Wang, She-Feng oth Qiao, Fang oth Lu, Ai-Min oth Lv, Peng-Cheng oth Zhu, Hai-Liang oth Enthalten in Elsevier Zheng, Han ELSEVIER A theoretical model of cyberchondria development: Antecedents and intermediate processes 2021 a Tetrahedron publication for the rapid dissemination of full original research papers and critical reviews on bioorganic chemistry, medicinal chemistry, bioinorganic chemistry and related disciplines Amsterdam [u.a.] (DE-627)ELV006510728 volume:23 year:2015 number:6 day:15 month:03 pages:1231-1240 extent:10 https://doi.org/10.1016/j.bmc.2015.01.052 Volltext GBV_USEFLAG_U GBV_ELV SYSFLAG_U 53.70 Nachrichtentechnik Kommunikationstechnik: Allgemeines VZ 05.42 Telekommunikation VZ 53.76 Kommunikationsdienste Fernmeldetechnik VZ 54.00 Informatik: Allgemeines VZ AR 23 2015 6 15 0315 1231-1240 10 045F 540 |
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English |
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Enthalten in A theoretical model of cyberchondria development: Antecedents and intermediate processes Amsterdam [u.a.] volume:23 year:2015 number:6 day:15 month:03 pages:1231-1240 extent:10 |
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Enthalten in A theoretical model of cyberchondria development: Antecedents and intermediate processes Amsterdam [u.a.] volume:23 year:2015 number:6 day:15 month:03 pages:1231-1240 extent:10 |
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6,7-Dihydrobenzo[f]benzo[4,5]imidazo[1,2-d][1,4]oxazepine derivatives Antitumor PI3Kα |
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A theoretical model of cyberchondria development: Antecedents and intermediate processes |
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Yin, Yong @@aut@@ Zhang, Yan-Qing @@oth@@ Jin, Biao @@oth@@ Sha, Shao @@oth@@ Wu, Xun @@oth@@ Sangani, Chetan B. @@oth@@ Wang, She-Feng @@oth@@ Qiao, Fang @@oth@@ Lu, Ai-Min @@oth@@ Lv, Peng-Cheng @@oth@@ Zhu, Hai-Liang @@oth@@ |
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6,7-dihydrobenzo[f]benzo[4,5]imidazo[1,2-d][1,4]oxazepine derivatives as selective inhibitors of pi3kα |
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6,7-Dihydrobenzo[f]benzo[4,5]imidazo[1,2-d][1,4]oxazepine derivatives as selective inhibitors of PI3Kα |
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Twenty eight new 6,7-dihydrobenzo[f]benzo[4,5]imidazo[1,2-d][1,4]oxazepine derivatives have been synthesized and evaluated for biological activities as PI3Kα inhibitors. Compound 25 showed the most potent inhibitory activity. |
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Twenty eight new 6,7-dihydrobenzo[f]benzo[4,5]imidazo[1,2-d][1,4]oxazepine derivatives have been synthesized and evaluated for biological activities as PI3Kα inhibitors. Compound 25 showed the most potent inhibitory activity. |
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Twenty eight new 6,7-dihydrobenzo[f]benzo[4,5]imidazo[1,2-d][1,4]oxazepine derivatives have been synthesized and evaluated for biological activities as PI3Kα inhibitors. Compound 25 showed the most potent inhibitory activity. |
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6,7-Dihydrobenzo[f]benzo[4,5]imidazo[1,2-d][1,4]oxazepine derivatives as selective inhibitors of PI3Kα |
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