Home Cart Sign in  
Chemical Structure| 849217-64-7 Chemical Structure| 849217-64-7

Structure of Foretinib
CAS No.: 849217-64-7

Chemical Structure| 849217-64-7

Foretinib

CAS No.: 849217-64-7

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

4.5 *For Research Use Only !

Cat. No.: A169062 Purity: 98%

Change View

Size Price

US Stock

Global Stock

In Stock
1mg łÇͶÊÊ Inquiry Inquiry
5mg łËď¶ÊÊ Inquiry Inquiry
100mg łÇď§¶ÊÊ Inquiry Inquiry
250mg łËîͶÊÊ Inquiry Inquiry
1g łóďǶÊÊ Inquiry Inquiry

US Stock: ship in 0-1 business day
Global Stock: ship in 5-7 days

  • 1mg

    łÇͶÊÊ

  • 5mg

    łËď¶ÊÊ

  • 100mg

    łÇď§¶ÊÊ

  • 250mg

    łËîͶÊÊ

  • 1g

    łóďǶÊÊ

In Stock

- +

US Stock: ship in 0-1 business day
Global Stock: ship in 2 weeks

  • 1-2 Day Shipping
  • High Quality
  • Technical Support
Product Citations

Alternative Products

Product Details of Foretinib

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

Safety of Foretinib

GHS Pictogram:
Signal Word:Warning
Hazard Statements:H302
Precautionary Statements:P280-P305+P351+P338

Related Pathways of Foretinib

RTK

Isoform Comparison

Biological Activity

Target
  • VEGFR1

    VEGFR1/FLT1, IC50:6.8 nM

  • VEGFR3

    VEGFR3/FLT4, IC50:2.8 nM

  • VEGFR2

    KDR, IC50:0.86 nM

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 <<

Protocol

Bio Calculators
Preparing Stock Solutions 1mg 5mg 10mg

1 mM

5 mM

10 mM

1.58mL

0.32mL

0.16mL

7.90mL

1.58mL

0.79mL

15.81mL

3.16mL

1.58mL

Dissolving Methods
Please choose the appropriate dissolution scheme according to your animal administration guide.For the following dissolution schemes, clear stock solution should be prepared according to in vitro experiments, and then cosolvent should be added in turn:

in order to ensure the reliability of the experimental results, the clarified stock solution can be properly preserved according to the storage conditions; The working fluid for in vivo experiment is recommended to be prepared now and used on the same day;

The percentage shown in front of the following solvent refers to the volume ratio of the solvent in the final solution; If precipitation or precipitation occurs in the preparation process, it can be assisted by heating and/or ultrasound.
Protocol 1
Protocol 2

References

 

Historical Records

Categories