Structure of Dabrafenib
CAS No.: 1195765-45-7
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The BI-3802 was designed by Boehringer Ingelheim and could be obtained free of charge through the Boehringer Ingelheim open innovation portal opnMe.com, associated with its negative control.
Dabrafenib (GSK2118436A) is an ATP-competitive inhibitor of Raf with IC50 values of 5 nM for C-Raf and 0.6 nM for B-RafV600E.
Synonyms: GSK2118436A; GSK2118436
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Search for reports by entering the product batch number.
Batch number can be found on the product's label following the word 'Batch'.
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CAS No. : | 1195765-45-7 |
Formula : | C23H20F3N5O2S2 |
M.W : | 519.56 |
SMILES Code : | O=S(C1=C(F)C=CC=C1F)(NC2=CC=CC(C3=C(C4=NC(N)=NC=C4)SC(C(C)(C)C)=N3)=C2F)=O |
Synonyms : |
GSK2118436A; GSK2118436
|
MDL No. : | MFCD17215684 |
InChI Key : | BFSMGDJOXZAERB-UHFFFAOYSA-N |
Pubchem ID : | 44462760 |
GHS Pictogram: |
![]() |
Signal Word: | Warning |
Hazard Statements: | H302-H315-H319-H335 |
Precautionary Statements: | P261-P305+P351+P338 |
Target |
|
In Vitro:
Cell Line
|
Concentration | Treated Time | Description | References |
Primary murine melanoma cells from TBP mice | 500 nM | 10 days | To evaluate the inhibitory effect of Dabrafenib on melanoma spheroids, results showed that Dabrafenib significantly reduced the volume of spheroids. | PMC10478295 |
BGC823 cells | 10μM | 48 h | Dabrafenib significantly reduced the number of invaded BGC823 cells, indicating inhibition of cell invasion | PMC8116207 |
MKN74 cells | 10μM | 72 h | Dabrafenib significantly reduced the number of invaded MKN74 cells, indicating inhibition of cell invasion | PMC8116207 |
BGC823 cells | 10μM | 24 h | Dabrafenib significantly reduced the number of migrated BGC823 cells, indicating inhibition of cell migration | PMC8116207 |
MKN74 cells | 10μM | 48 h | Dabrafenib significantly reduced the number of migrated MKN74 cells, indicating inhibition of cell migration | PMC8116207 |
BGC823 cells | 10μM | 72 h | Dabrafenib significantly delayed wound closure in BGC823 cells, indicating inhibition of cell migration | PMC8116207 |
MKN74 cells | 10μM | 72 h | Dabrafenib significantly delayed wound closure in MKN74 cells, indicating inhibition of cell migration | PMC8116207 |
BGC823 cells | 10μM | 48 h | Dabrafenib significantly inhibited invasion ability of BGC823 cells | PMC8116207 |
MKN74 cells | 10μM | 72 h | Dabrafenib significantly inhibited invasion ability of MKN74 cells | PMC8116207 |
BGC823 cells | 10μM | 24 h | Dabrafenib significantly inhibited migration ability of BGC823 cells | PMC8116207 |
MKN74 cells | 10μM | 48 h | Dabrafenib significantly inhibited migration ability of MKN74 cells | PMC8116207 |
BGC823 cells | 10μM | 72 h | Dabrafenib significantly inhibited wound healing and migration ability of BGC823 cells | PMC8116207 |
MKN74 cells | 10μM | 72 h | Dabrafenib significantly inhibited wound healing and migration ability of MKN74 cells | PMC8116207 |
Inner ear cell line | 30 nM | Dabrafenib at a concentration of 30 nM protected neonatal mouse cochlear outer hair cells from cisplatin-induced cell death with a therapeutic index greater than 2000. | PMC10807719 | |
A375 melanoma cells | 1 μM | 9 days or more | To investigate the effect of Dabrafenib on A375 melanoma cells, results showed that these cells developed resistance to Dabrafenib treatment, but the resistance was reversible. | PMC5933935 |
MM200 cells | 100 nM | 24 h | To assess the contribution of PI3K/AKT signaling in BRAF/MEK inhibitor resistance, results showed that PI3K/AKT activation promoted cell survival but did not restore MAPK signaling. | PMC6148266 |
SKMel28 cells | 100 nM | 24 h | To assess the contribution of PI3K/AKT signaling in BRAF/MEK inhibitor resistance, results showed that PI3K/AKT activation promoted cell survival but did not restore MAPK signaling. | PMC6148266 |
WM164 cells | 160 nM | 72 h | To assess the heterogeneity of MITF expression during BRAF inhibitor treatment, the results showed that MITF expression remained heterogeneous during treatment. | PMC5538298 |
In Vivo:
Species
|
Animal Model
|
Administration | Dosage | Frequency | Description | References |
Mice | TBP mouse melanoma model | Oral | 30 mg/kg | Once daily for 5 weeks | To evaluate the therapeutic effect of Dabrafenib on melanoma, results showed that Dabrafenib significantly reduced tumor volume, but eventually all tumors developed resistance. | PMC10478295 |
Nude mice | Peritoneal metastasis model | Intraperitoneal injection | 5 mg/kg | Every 3 days for 28 days | Dabrafenib significantly reduced the number of peritoneal metastases, indicating inhibition of peritoneal metastasis | PMC8116207 |
Nude mice | Peritoneal metastasis model | Intraperitoneal injection | 5 mg/kg | Every 3 days for 28 days | Dabrafenib significantly inhibited peritoneal metastasis of MKN74 cells in nude mice | PMC8116207 |
Mice | Multidose cisplatin mouse model | Oral | 3 mg/kg | Twice daily for 42 days | Dabrafenib at a dose of 3 mg/kg BW, administered twice daily, significantly protected mice from cisplatin-induced hearing loss, and the protective effect persisted for 4 months after the completion of treatment. | PMC10807719 |
Nude mice | A375 melanoma xenograft model | Oral gavage | 100 mg/kg | Twice daily, until tumour relapse | To investigate the effect of Dabrafenib on the A375 melanoma xenograft model, results showed that GPX4 KO tumours did not relapse after Dabrafenib treatment, while GPX4 WT tumours relapsed. | PMC5933935 |
Mice | A375 tumor model | Oral | 25 mg/kg | Once daily for 20 days | To evaluate the effect of Dabrafenib combined with EDNR inhibitors on tumor growth, the results showed that combination therapy significantly inhibited tumor growth and reduced the number of AXL-high expressing cells. | PMC5538298 |
Clinical Trial:
NCT Number | Conditions | Phases | Recruitment | Completion Date | Locations |
NCT01682213 | Melanoma | PHASE2 | COMPLETED | 2025-05-19 | Memorial Sloan Kettering Cance... More >>r Center, New York, New York, 10065, United States Less << |
NCT01262963 | Cancer | PHASE1 | COMPLETED | 2011-04-08 | GSK Investigational Site, Taco... More >>ma, Washington, 98418, United States Less << |
NCT01534897 | Papillary Thyroid Carcinoma | COMPLETED | 2025-03-14 | Massachusetts General Hospital... More >>, Boston, Massachusetts, 02215, United States Less << | |
NCT06264778 | Ameloblastoma | PHASE3 | NOT_YET_RECRUITING | 2025-12-31 | - |
NCT01582997 | Cancer | PHASE1 | COMPLETED | 2015-04-16 | GSK Investigational Site, Shiz... More >>uoka, 411-8777, Japan|GSK Investigational Site, Tokyo, 104-0045, Japan Less << |
NCT01266967 | Melanoma and Brain Metastases | PHASE2 | COMPLETED | 2025-11-12 | GSK Investigational Site, Los ... More >>Angeles, California, 90095, United States|GSK Investigational Site, San Francisco, California, 94115, United States|GSK Investigational Site, San Francisco, California, 94143, United States|GSK Investigational Site, Ann Arbor, Michigan, 48019, United States|GSK Investigational Site, New York, New York, 10065, United States|GSK Investigational Site, Pittsburgh, Pennsylvania, 15232, United States|GSK Investigational Site, Nashville, Tennessee, 37232, United States|GSK Investigational Site, Houston, Texas, 77030, United States|GSK Investigational Site, Seattle, Washington, 98109, United States|GSK Investigational Site, Waratah, New South Wales, 2300, Australia|GSK Investigational Site, Westmead, New South Wales, 2145, Australia|GSK Investigational Site, Nedlands, Western Australia, 6009, Australia|GSK Investigational Site, Edmonton, Alberta, T6G 1Z2, Canada|GSK Investigational Site, Toronto, Ontario, M5G 2M9, Canada|GSK Investigational Site, Montreal, Quebec, H3T 1E2, Canada|GSK Investigational Site, Boulogne-Billancourt, 92100, France|GSK Investigational Site, Lille, 59037, France|GSK Investigational Site, Marseille Cedex 5, 13385, France|GSK Investigational Site, Villejuif, 94805, France|GSK Investigational Site, Essen, Nordrhein-Westfalen, 45122, Germany|GSK Investigational Site, Kiel, Schleswig-Holstein, 24105, Germany|GSK Investigational Site, Berlin, 10117, Germany|GSK Investigational Site, Napoli, Campania, 80131, Italy|GSK Investigational Site, Padova, Veneto, 35128, Italy Less << |
NCT01153763 | Melanoma | PHASE2 | COMPLETED | 2016-06-01 | GSK Investigational Site, Los ... More >>Angeles, California, 90025, United States|GSK Investigational Site, Los Angeles, California, 90095, United States|GSK Investigational Site, San Francisco, California, 94115, United States|GSK Investigational Site, Philadelphia, Pennsylvania, 19104, United States|GSK Investigational Site, Nashville, Tennessee, 37232, United States|GSK Investigational Site, Houston, Texas, 77030-4009, United States|GSK Investigational Site, Newcastle, New South Wales, 2300, Australia|GSK Investigational Site, Westmead, New South Wales, 2145, Australia|GSK Investigational Site, Nedlands, Western Australia, 6009, Australia|GSK Investigational Site, Bordeaux, 33075, France|GSK Investigational Site, Boulogne-Billancourt, 92100, France|GSK Investigational Site, Lille, 59037, France|GSK Investigational Site, Marseille Cedex 5, 13385, France|GSK Investigational Site, Montpellier, 34295, France|GSK Investigational Site, Paris Cedex 10, 75475, France|GSK Investigational Site, Villejuif, 94805, France|GSK Investigational Site, Essen, Nordrhein-Westfalen, 45122, Germany|GSK Investigational Site, Kiel, Schleswig-Holstein, 24105, Germany|GSK Investigational Site, Luebeck, Schleswig-Holstein, 23538, Germany|GSK Investigational Site, Berlin, 10117, Germany|GSK Investigational Site, Napoli, Campania, 80131, Italy|GSK Investigational Site, Genova, Liguria, 16132, Italy|GSK Investigational Site, Padova, Veneto, 35128, Italy Less << |
NCT01677741 | Neoplasms, Brain | PHASE1|PHASE2 | COMPLETED | 2020-12-04 | Novartis Investigative Site, P... More >>hoenix, Arizona, 85016-7710, United States|Novartis Investigative Site, Orange, California, 92868, United States|Novartis Investigative Site, Baltimore, Maryland, 21287, United States|Novartis Investigative Site, Boston, Massachusetts, 02215, United States|Novartis Investigative Site, New York, New York, 10065, United States|Novartis Investigative Site, Cincinnati, Ohio, 45229, United States|Novartis Investigative Site, Memphis, Tennessee, 38105-3678, United States|Novartis Investigative Site, Seattle, Washington, 98105, United States|Novartis Investigative Site, Parkville, Victoria, 3052, Australia|Novartis Investigative Site, Toronto, Ontario, M5G 1X8, Canada|Novartis Investigative Site, Copenhagen, DK-2100, Denmark|Novartis Investigative Site, Marseille Cedex 5, 13385, France|Novartis Investigative Site, Paris cedex 05, 75248, France|Novartis Investigative Site, Paris cedex 12, 75571, France|Novartis Investigative Site, Toulouse cedex 9, 31059, France|Novartis Investigative Site, Villejuif Cedex, 94805, France|Novartis Investigative Site, Heidelberg, Baden-Wuerttemberg, 69120, Germany|Novartis Investigative Site, Regensburg, Bayern, 93053, Germany|Novartis Investigative Site, Berlin, 13353, Germany|Novartis Investigative Site, Jerusalem, 91120, Israel|Novartis Investigative Site, Ramat-Gan, 52621, Israel|Novartis Investigative Site, Milan, 20133, Italy|Novartis Investigative Site, Esplugues De Llobregat. Barcelona, 08950, Spain|Novartis Investigative Site, Madrid, 28009, Spain|Novartis Investigative Site, Sutton, Surrey, SM2 5PT, United Kingdom|Novartis Investigative Site, London, WC1N 3JH, United Kingdom Less << |
NCT01340833 | Cancer | PHASE1 | COMPLETED | 2011-09-12 | GSK Investigational Site, Taco... More >>ma, Washington, 98418, United States Less << |
Bio Calculators | ||||
Preparing Stock Solutions | ![]() |
1mg | 5mg | 10mg |
1 mM 5 mM 10 mM |
1.92mL 0.38mL 0.19mL |
9.62mL 1.92mL 0.96mL |
19.25mL 3.85mL 1.92mL |
Tags: Dabrafenib | GSK2118436A | GSK2118436 | GSK2118436 | GSK 2118436 | GSK-2118436 | Raf | Raf kinases | BRAF V600E inhibitor | melanoma | MAPK pathway | ATP-competitive | oral bioavailability | IC50 | kinase inhibitor | 1195765-45-7
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