Bis(1H-indol-2yl)methanones Are Effective Inhibitors of Mutated FLT3 Tyrosine Kinase, Overcome Resistance to PKC412A In Vitro and Show Synergy with Chemotherapy.
Fischer, Thomas, Bohmer, Frank D., Huber, Christoph, Dove, Stefan, Breitenbucher, Frank, Mirea, Fian K. and Heidel, Florian (2006) Bis(1H-indol-2yl)methanones Are Effective Inhibitors of Mutated FLT3 Tyrosine Kinase, Overcome Resistance to PKC412A In Vitro and Show Synergy with Chemotherapy. Blood 108 (11), p. 1369.Date of publication of this fulltext: 19 Dec 2024 14:30
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| Item type | Article | ||||
| Journal or Publication Title | Blood | ||||
| Publisher: | AMER SOC HEMATOLOGY | ||||
|---|---|---|---|---|---|
| Place of Publication: | WASHINGTON | ||||
| Volume: | 108 | ||||
| Number of Issue or Book Chapter: | 11 | ||||
| Page Range: | p. 1369 | ||||
| Date | 2006 | ||||
| Institutions | Chemistry and Pharmacy > Institute of Pharmacy | ||||
| Identification Number |
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| Dewey Decimal Classification | 600 Technology > 610 Medical sciences Medicine 600 Technology > 615 Pharmacy | ||||
| Status | Published | ||||
| Refereed | Yes, this version has been refereed | ||||
| Created at the University of Regensburg | Yes | ||||
| Item ID | 69665 |
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