Structure of Foretinib
CAS No.: 849217-64-7
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Foretinib is an ATP-competitive inhibitor of HGFR and VEGFR, mostly for Met and KDR with IC50 of 0.4 nM and 0.9 nM in cell-free assays. Foretinib is less potent against Ron, Flt-1/3/4, Kit, PDGFRα/β and Tie-2, and with little activity to FGFR1 and EGFR.
Synonyms: XL880; GSK1363089; EXEL-2880
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Batch number can be found on the product's label following the word 'Batch'.
Search for reports by entering the product batch number.
Batch number can be found on the product's label following the word 'Batch'.
Search for reports by entering the product batch number.
Batch number can be found on the product's label following the word 'Batch'.
Search for reports by entering the product batch number.
Batch number can be found on the product's label following the word 'Batch'.
Search for reports by entering the product batch number.
Batch number can be found on the product's label following the word 'Batch'.
CAS No. : | 849217-64-7 |
Formula : | C34H34F2N4O6 |
M.W : | 632.65 |
SMILES Code : | O=C(NC1=CC=C(F)C=C1)C2(C(=O)NC3=CC=C(OC=4C=CN=C5C=C(OCCCN6CCOCC6)C(OC)=CC54)C(F)=C3)CC2 |
Synonyms : |
XL880; GSK1363089; EXEL-2880
|
MDL No. : | MFCD16038048 |
InChI Key : | CXQHYVUVSFXTMY-UHFFFAOYSA-N |
Pubchem ID : | 42642645 |
GHS Pictogram: | ![]() |
Signal Word: | Warning |
Hazard Statements: | H302 |
Precautionary Statements: | P280-P305+P351+P338 |
Target |
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In Vitro:
Cell Line
| Concentration | Treated Time | Description | References |
ccRCC organoids | 10 μM | 72 h | To evaluate the effect of Foretinib on ccRCC organoids, results showed that Foretinib consistently induced Cleaved-Caspase 3 activation, indicating apoptosis induction | PMC6393468 |
MDA-MB-231 cells | 1 μM | 18 h | To evaluate the effect of Foretinib in combination with PARP inhibitors on DNA damage in MDA-MB-231 cells, showing that the combination significantly increased γ-H2AX foci formation. | PMC4754671 |
MCF7A02 | 1 μM | 6 days | To validate the synthetic lethality of Foretinib in E-cadherin defective cells, results showed that E-cadherin defective cells were more sensitive to Foretinib. | PMC6296442 |
MCF10A CDH1-/- | 1 μM | 6 days | To validate the synthetic lethality of Foretinib in E-cadherin defective cells, results showed that E-cadherin defective cells were more sensitive to Foretinib. | PMC6296442 |
MV4-11 | 0.16 nM | 48 h | Inhibited the growth of FLT3-ITD mutant cells | PMC10940854 |
MOLM13 | 0.89 nM | 48 h | Inhibited the growth of FLT3-ITD mutant cells | PMC10940854 |
HCC1937 | 1 μM | 5 days | To test the effect of Foretinib in combination with afatinib, results showed that the combination treatment significantly inhibited cell growth. | PMC6987485 |
HDQP1 | 1 μM | 5 days | To test the effect of Foretinib in combination with afatinib, results showed that the combination treatment significantly inhibited cell growth. | PMC6987485 |
ES2 OVCA cells | 100 nM | 72 h | To evaluate the effect of M2-M conditioned medium on trametinib cytotoxicity, results showed that M2-M conditioned medium significantly increased the half-lethal concentration of trametinib | PMC7244320 |
CT26 cells | 100 nM | 72 h | To evaluate the effect of M2-M conditioned medium on trametinib cytotoxicity, results showed that M2-M conditioned medium significantly increased the half-lethal concentration of trametinib | PMC7244320 |
MKN-45 | 10 nM, 100 nM, 1 μM | 72 h | Evaluate the effect of Foretinib on the viability of MKN-45 cells, showing reductions in cell viability of 5.4%, 73.7%, and 85.3% at concentrations of 10 nM, 100 nM, and 1 μM, respectively. | PMC8178268 |
KATO-III | 10 nM, 100 nM, 1 μM | 72 h | Evaluate the effect of Foretinib on the viability of KATO-III cells, showing reductions in cell viability of 1.2%, 51%, and 78.5% at concentrations of 10 nM, 100 nM, and 1 μM, respectively. | PMC8178268 |
SNU-1 | 1 nM, 10 nM, 100 nM, 1 μM | 72 h | Evaluate the effect of Foretinib on the viability of SNU-1 cells, showing no significant inhibitory effect at 1 nM, 10 nM, or 100 nM, but a 68.1% reduction in cell viability at 1 μM concentration. | PMC8178268 |
sympathetic neurons | 500 nM | 16 h | Foretinib almost completely rescued neurons from degeneration | PMC5674898 |
sensory neurons | 500 nM | 48 h | Foretinib rescued sensory neurons from degeneration | PMC5674898 |
motor neurons | 500 nM | 9 days | Foretinib significantly promoted the survival of motor neurons | PMC5674898 |
In Vivo:
Species
| Animal Model
| Administration | Dosage | Frequency | Description | References |
Nude mice | MDA-MB-231 xenograft model | Oral | 5 mg/kg | 5 times per week for 26 days | To evaluate the effect of Foretinib in combination with PARP inhibitors on tumor growth in MDA-MB-231 xenograft models, showing that the combination significantly inhibited tumor growth. | PMC4754671 |
mice | K14cre;Cdh1F/F;Trp53F/F (KEP) model | oral | 25 mg/kg or 50 mg/kg | every other day for 28 days | To evaluate the anti-tumour effects of Foretinib in E-cadherin defective tumours, results showed that Foretinib significantly inhibited tumour growth and extended mouse survival. | PMC6296442 |
Mice | FLT3-ITD AML mouse model | Oral | 15 mg/kg | Once daily for 14 days | Foretinib significantly extended the survival of FLT3-ITD AML mice | PMC10940854 |
nu/nu mice | ES2 xenograft model | tail vein injection | 10 mg/kg | every 4 days, until the experimental end point | To evaluate the effect of NanoFore combined with trametinib on tumor progression, results showed that the combination therapy significantly extended the survival of mice | PMC7244320 |
Mouse | Medulloblastoma model | Continuous osmotic pump infusion into the cerebrospinal fluid | 6 mg/kg | 28 days, 0.25 μl per hour | To study the anti-tumor effects and resistance mechanisms of Foretinib in a medulloblastoma model | PMC6307130 |
NOD/SCID mice | subcutaneous and peritoneal dissemination xenograft models | intraperitoneal injection | 30 mg/kg | 3 times per week for 2 weeks | Evaluate the antitumor effects of Foretinib in gastric cancer models, showing that Foretinib monotherapy significantly inhibited tumor growth and exhibited additive effects when combined with nanoparticle paclitaxel. | PMC8178268 |
mice | sciatic nerve crush model | oral | 100 mg/kg | 4 times over 4 days | Foretinib delayed Wallerian degeneration after sciatic nerve crush | PMC5674898 |
Clinical Trial:
NCT Number | Conditions | Phases | Recruitment | Completion Date | Locations |
NCT01068587 | Lung Cancer | Phase 1 Phase 2 | Completed | - | Canada, British Columbia ... More >> BCCA - Vancouver Cancer Centre Vancouver, British Columbia, Canada, V5Z 4E6 Canada, Ontario Juravinski Cancer Centre at Hamilton Health Sciences Hamilton, Ontario, Canada, L8V 5C2 Ottawa Health Research Institute - General Division Ottawa, Ontario, Canada, K1H 8L6 Univ. Health Network-Princess Margaret Hospital Toronto, Ontario, Canada, M5G 2M9 Less << |
NCT00725712 | Neoplasms, Gastrointestinal Tr... More >>act Less << | Phase 2 | Completed | - | United States, Alabama ... More >> GSK Investigational Site Birmingham, Alabama, United States, 35294 United States, Arizona GSK Investigational Site Scottsdale, Arizona, United States, 85258 United States, California GSK Investigational Site Los Angeles, California, United States, 90024 GSK Investigational Site Stanford, California, United States, 94305 United States, District of Columbia GSK Investigational Site Washington, D.C., District of Columbia, United States, 20007 United States, Georgia GSK Investigational Site Atlanta, Georgia, United States, 30309 United States, Illinois GSK Investigational Site Chicago, Illinois, United States, 60637 United States, Massachusetts GSK Investigational Site Boston, Massachusetts, United States, 02114 United States, Michigan GSK Investigational Site Detroit, Michigan, United States, 48201 United States, Montana GSK Investigational Site Billings, Montana, United States, 59101 United States, New Mexico GSK Investigational Site Albuquerque, New Mexico, United States, 87131 United States, New York GSK Investigational Site New York, New York, United States, 10016 GSK Investigational Site New York, New York, United States, 10021 United States, North Carolina GSK Investigational Site Durham, North Carolina, United States, 27710 United States, Oregon GSK Investigational Site Portland, Oregon, United States, 97239 United States, Texas GSK Investigational Site Austin, Texas, United States, 78705 United States, Wisconsin GSK Investigational Site Madison, Wisconsin, United States, 53792 Less << |
NCT00725712 | - | Completed | - | - | |
NCT00726323 | Carcinoma, Renal Cell | Phase 2 | Completed | - | United States, California ... More >> GSK Investigational Site Greenbrae, California, United States, 94904-2007 GSK Investigational Site San Francisco, California, United States, 94115 GSK Investigational Site Stanford, California, United States, 94305 United States, Indiana GSK Investigational Site Indianapolis, Indiana, United States, 46202 United States, Maryland GSK Investigational Site Bethesda, Maryland, United States, 20892 United States, Massachusetts GSK Investigational Site Boston, Massachusetts, United States, 02115 United States, Michigan GSK Investigational Site Detroit, Michigan, United States, 48201 United States, New Jersey GSK Investigational Site New Brunswick, New Jersey, United States, 08901 United States, Ohio GSK Investigational Site Cleveland, Ohio, United States, 44195 United States, Pennsylvania GSK Investigational Site Philadelphia, Pennsylvania, United States, 19104 United States, Tennessee GSK Investigational Site Nashville, Tennessee, United States, 37232 United States, Texas GSK Investigational Site San Antonio, Texas, United States, 78229 Less << |
NCT00725764 | Neoplasms, Head and Neck | Phase 2 | Completed | - | United States, Georgia ... More >> GSK Investigational Site Atlanta, Georgia, United States, 30309 United States, Illinois GSK Investigational Site Chicago, Illinois, United States, 60637 United States, Indiana GSK Investigational Site Indianapolis, Indiana, United States, 46254 United States, Minnesota GSK Investigational Site Minneapolis, Minnesota, United States, 55407-3799 United States, Missouri GSK Investigational Site Saint Louis, Missouri, United States, 63110 United States, New Hampshire GSK Investigational Site Lebanon, New Hampshire, United States, 03756 United States, South Carolina GSK Investigational Site Charleston, South Carolina, United States, 29403 United States, Tennessee GSK Investigational Site Nashville, Tennessee, United States, 37203 United States, Texas GSK Investigational Site Houston, Texas, United States, 77030 GSK Investigational Site San Antonio, Texas, United States, 78229 United States, West Virginia GSK Investigational Site Morgantown, West Virginia, United States, 28506 Less << |
NCT00743067 | Solid Tumours | Phase 1 | Completed | - | - |
NCT00742131 | Solid Tumours | PHASE1 | COMPLETED | 2011-08-29 | - |
NCT02034097 | Cancer | Phase 2 | Withdrawn(GSK has decided to t... More >>erminate the Product Development of foretinib and conclude our Development Agreement with Exelixis) Less << | December 2016 | - |
NCT01147484 | Recurrent Breast Cancer | PHASE2 | COMPLETED | 2015-02-13 | Tom Baker Cancer Centre, Calga... More >>ry, Alberta, T2N 4N2, Canada|BCCA - Cancer Centre for the Southern Interior, Kelowna, British Columbia, V1Y 5L3, Canada|BCCA - Vancouver Cancer Centre, Vancouver, British Columbia, V5Z 4E6, Canada|QEII Health Sciences Centre, Halifax, Nova Scotia, B3H 1V7, Canada|Juravinski Cancer Centre at Hamilton Health Sciences, Hamilton, Ontario, L8V 5C2, Canada|London Regional Cancer Program, London, Ontario, N6A 4L6, Canada|Ottawa Health Research Institute - General Division, Ottawa, Ontario, K1H 8L6, Canada|Hopital Charles LeMoyne, Greenfield Park, Quebec, J4V 2H1, Canada|Allan Blair Cancer Centre, Regina, Saskatchewan, S4T 7T1, Canada Less << |
NCT01138384 | Breast Cancer | Phase 1 Phase 2 | Completed | - | Canada, British Columbia ... More >> BCCA - Cancer Centre for the Southern Interior Kelowna, British Columbia, Canada, V1Y 5L3 BCCA - Vancouver Cancer Centre Vancouver, British Columbia, Canada, V5Z 4E6 Canada, Ontario Cancer Centre of Southeastern Ontario at Kingston Kingston, Ontario, Canada, K7L 5P9 London Regional Cancer Program London, Ontario, Canada, N6A 4L6 Canada, Quebec McGill University - Dept. Oncology Montreal, Quebec, Canada, H2W 1S6 Less << |
NCT00726323 | - | Completed | - | - | |
NCT00725764 | - | Completed | - | - | |
NCT00920192 | Carcinoma, Hepatocellular | PHASE1 | COMPLETED | 2015-03-24 | GSK Investigational Site, Hong... More >> Kong, Hong Kong|GSK Investigational Site, Tainan, 70428, Taiwan|GSK Investigational Site, Taipei, 110, Taiwan|GSK Investigational Site, Taipei, 112, Taiwan|GSK Investigational Site, Bangkok, 10400, Thailand|GSK Investigational Site, Bangkok, 10700, Thailand|GSK Investigational Site, Khon Kaen, 40002, Thailand Less << |
NCT00742261 | Solid Tumours | PHASE1 | COMPLETED | 2009-06-24 | GSK Investigational Site, Detr... More >>oit, Michigan, 48201, United States|GSK Investigational Site, Houston, Texas, 77030-4009, United States Less << |
Tags: Foretinib | XL880 | GSK1363089 | GSK089 | EXEL-2880 | XL 880 | XL-880 | GSK1363089 | GSK 1363089 | GSK-1363089 | GSK089 | GSK 089 | GSK-089 | EXEL2880 | EXEL 2880 | EXEL-2880 | VEGFR | c-Met | HGFR | Vascular endothelial growth factor receptor | MET | VEGFR2 | KDR | AXL | 849217-64-7
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H420 | Harms public health and the environment by destroying ozone in the upper atmosphere |
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