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ChemicalBook >> CAS DataBase List >>Foretinib (GSK1363089)

Foretinib (GSK1363089)

CAS No.
849217-64-7
Chemical Name:
Foretinib (GSK1363089)
Synonyms
Foretinib;XL880;EXEL-2880;GSK089;GSK 1363089;XL-880,Foretinib;EXEL-2880/XL-880;Foretinib, >=98%;XL880(GSK1363089);Foretinib (XL-880)
CBNumber:
CB02490083
Molecular Formula:
C34H34F2N4O6
Molecular Weight:
632.65
MDL Number:
MFCD22379992
MOL File:
849217-64-7.mol
MSDS File:
SDS
TDS File:
TDS
Last updated:2026-07-17 09:03:53
Product description Number Pack Size Price
Foretinib ≥98% 16249 1mg $36
Foretinib ≥98% 16249 5mg $95
Foretinib ≥98% 16249 10mg $120
Foretinib ≥98% 16249 25mg $253
Foretinib ≥98% 16249 1mg $32
More product size

Foretinib (GSK1363089) Properties

Melting point >98°C (dec.)
Boiling point 828.5±65.0 °C(Predicted)
Density 1.372
storage temp. Sealed in dry,Store in freezer, under -20°C
solubility DMSO (Slightly), Ethanol (Slightly)
form Yellow powder.
pka 13.14±0.70(Predicted)
color Pale Yellow to Yellow
CAS DataBase Reference 849217-64-7
NCI Dictionary of Cancer Terms foretinib; XL880
FDA UNII 81FH7VK1C4
NCI Drug Dictionary foretinib

SAFETY

Risk and Safety Statements

Symbol(GHS)  Health Hazard (GHS08)Exclamation Mark (GHS07)
GHS08,GHS07
Signal word  Warning
Hazard statements  H373-H302
Precautionary statements  P260-P314-P501-P264-P270-P301+P312-P330-P501
NFPA 704
0
2 0

Foretinib (GSK1363089) price More Price(82)

Manufacturer Product number Product description CAS number Packaging Price Updated Buy
Cayman Chemical 16249 Foretinib ≥98% 849217-64-7 1mg $36 2026-04-30 Buy
Cayman Chemical 16249 Foretinib ≥98% 849217-64-7 5mg $95 2026-04-30 Buy
Cayman Chemical 16249 Foretinib ≥98% 849217-64-7 10mg $120 2026-04-30 Buy
Cayman Chemical 16249 Foretinib ≥98% 849217-64-7 25mg $253 2026-04-30 Buy
Cayman Chemical 16249 Foretinib ≥98% 849217-64-7 1mg $32 2024-03-01 Buy
Product number Packaging Price Buy
16249 1mg $36 Buy
16249 5mg $95 Buy
16249 10mg $120 Buy
16249 25mg $253 Buy
16249 1mg $32 Buy

Foretinib (GSK1363089) Chemical Properties,Uses,Production

Description

Foretinib (GSK1363089) 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. Less potent against Ron, Flt-1/3/4, Kit, PDGFRα/β and Tie-2, and little activity to FGFR1 and EGFR. Phase 2.

Description

Foretinib is a multikinase inhibitor that targets MET and VEGFR2 and also exhibits an inhibitory effect against KIT, Flt-3, PDGFRb, and Tie-2.

Uses

XL880 (GSK1363089, EXEL-2880) is an ATP-competitive inhibitor of MET and KDR with IC50 of 0.4 nM and 0.9 nM, respectively.

Uses

Foretinib (GSK1363089) is an ATP-competitive inhibitor of hepatocyte growth factor (HGF) and Vascular endothelial growth factor (VEGF) Receptor Tyrosine Kinases.

Definition

ChEBI: N1'-[3-fluoro-4-[[6-methoxy-7-[3-(4-morpholinyl)propoxy]-4-quinolinyl]oxy]phenyl]-N1-(4-fluorophenyl)cyclopropane-1,1-dicarboxamide is an aromatic ether.

Clinical Use

Foretinib has also shown to be effective against ROS1 mutations especially when acquired with crizotinib resistance. A clinical trial investigating the dosing and safety profile of combining foretinib and erlotinib was designed for advanced pretreated NSCLC patients.

Synthesis

3-fluoro-{4-[(6-(Methyloxy)-7-{[3-(4-Morpholinyl)propyl]oxy}-4-quinolinyl)oxy]phenyl}aMine

479690-10-3

1-((4-Fluorophenyl)carbamoyl)cyclopropanecarboxylic acid

849217-48-7

Foretinib (GSK1363089)

849217-64-7

Example 3: Preparation of N-[3-fluoro-4-({6-(methoxy)-7-[(3-morpholin-4-ylpropyl)oxy]quinolin-4-yl}oxy)phenyl]-N'-(4-fluorophenyl)cyclopropane-1,1 -dicarboxamide (Compound I, Form B). 3.1: Preparation of compound (I), crystalline form B. [0079] To a dry reactor (Reactor 1) was added 1-(4-fluorophenylcarbamoyl)cyclopropanecarboxylic acid (21.5 kg), THF (76 kg), and N,N-dimethylformamide (DMF, 0.09 kg), and stirred at 20 °C until completely dissolved. The reactor was cooled to about 15 °C and oxalyl chloride (12.7 kg) was slowly added over 38 min while controlling the internal temperature of the reactor below 20 °C. After the addition was complete, the transfer line was flushed with THF (3 kg). After 1 hour of reaction at about 20°C, oxalyl chloride (0.6 kg) and THF (2 kg) were added again to the reactor and the process was repeated once. Subsequently, smaller amounts of oxalyl chloride (0.13 kg) and THF (2 kg) were added a third time. To another dry reactor (reactor 2) was added water (60 L), K2CO3 (11.1 kg), 3-fluoro-4-[(6-methoxy-7-{[3-(4-morpholinyl)propyl]oxy}-4-quinolinyl)oxy]aniline (32.5 kg, see CAS Reg. No. 479690-10-3 and US2004/0242603 ) and THF (177 kg), and the temperature of the reactor contents was adjusted to about 15 °C. The contents of Reactor 1 were slowly added to Reactor 2 while keeping the temperature of Reactor 2 below 20°C. Rinse Reactor 1 with THF (5 kg) and transfer the rinse solution to Reactor 2. The temperature of the contents of Reactor 2 was adjusted to about 20 °C and the reaction was carried out for about 3 hours. Subsequently, 0.8M K2CO3 aqueous solution (171 kg) and isopropyl acetate (119 kg) were added, stirred for 10 minutes, left to stratify, and the lower aqueous phase was discarded. Repeatedly added 0.8M K2CO3 aqueous solution (171kg), mixed and left to stratify, again discarded the aqueous phase. Water (137 kg) was added, mixed and allowed to partition, and the aqueous phase was discarded. Steam-activated powdered activated carbon (Darco G-60, Norit Americas, Inc., 3.4 kg) and isopropyl acetate (3 kg) were added, stirred for about 2.5 hours, and then filtered through a filter containing diatomaceous earth into another reactor (Reactor 3). The reactor 2 was rinsed twice with isopropyl acetate (33 kg each time) and the rinsate was combined with the material in reactor 3 through the above mentioned filter. The material in Reactor 3 was concentrated to about 104 L under vacuum, keeping the temperature below 50°C. Isopropanol (161 kg) was added and again concentrated under vacuum to about 104 L, keeping the temperature below 50°C. Repeatedly added isopropanol (161 kg) and concentrated to about 100 L. Heated the material in Reactor 3 to about 75°C, held for 80 minutes, and then cooled to about 55°C. Heptane (1 kg) containing about 1% isopropanol was added and held at about 55°C for 70 minutes until crystallization was observed. Subsequently, heptane (46 kg) containing about 1% isopropanol was added and the reactor contents were kept at about 55°C for 75 minutes. The reactor contents were cooled to about 20°C over a period of about 5 hours and held at that temperature for about 12 hours. Further cooling to about 5°C and holding for 1 hour. The material in reactor 3 was transferred to a filter drier and rinsed with a mixture of isopropanol (18 kg) and heptane (8 kg). Drying at about 50°C for about 56 hours gave 42.8 kg (89% yield) of compound (I) crystalline form B as an off-white powder.

in vitro

In vitro, foretinib blocks activation of MET and VEGFR2-induced signaling pathways. In vivo experiments show a dose-dependent decrease in tumor burden in a lung metastasis experimental model.

target

Met

References

[1] qian f1, engst s, yamaguchi k, yu p, won ka, mock l, lou t, tan j, li c, tam d, lougheed j, yakes fm, bentzien f, xu w, zaks t, wooster r,greshock j, joly ah. inhibition of tumor cell growth, invasion, and metastasis by exel-2880 (xl880, gsk1363089), a novel inhibitor of hgf and vegf receptor tyrosine kinases. cancer res. 2009 oct 15;69(20):8009-16. doi: 10.1158/0008-5472.can-08-4889.

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View Lastest Price from Foretinib (GSK1363089) manufacturers

Image Update time Product Price Min. Order Purity Supply Ability Manufacturer
Foretinib pictures 2026-07-17 Foretinib
849217-64-7
$33.00-72.00 99.70% 10g TargetMol Chemicals Inc.
Foretinib (GSK1363089) pictures 2025-04-04 Foretinib (GSK1363089)
849217-64-7
1KG 98% 1Ton Henan Aochuang Chemical Co.,Ltd.
Foretinib (GSK1363089) pictures 2019-07-06 Foretinib (GSK1363089)
849217-64-7
$2.00 1 kg 99% 100kg Career Henan Chemical Co
  • Foretinib pictures
  • Foretinib
    849217-64-7
  • $33.00-72.00
  • 99.70%
  • TargetMol Chemicals Inc.

Foretinib (GSK1363089) Spectrum

849217-64-7(Foretinib (GSK1363089))Related Search:

GSK 1363089 N-[3-Fluoro-4-[[6-(methyloxy)-7-[[3-(morpholin-4-yl)propyl]oxy]quinolin-4-yl]oxy]phenyl]-N'-(4-fluorophenyl)cyclopropane-1,1-dicarboxamide N-[3-Fluoro-4-[[6-methoxy-7-[3-(4-morpholinyl)propoxy]-4-quinolinyl]oxy]phenyl]-N'-(4-fluorophenyl)-1,1-cyclopropanedicarboxamide XL-880,Foretinib XL880(GSK1363089) FORETINIB GLAXOSMITHKLINE PAPILLARY RENAL CELL CARCINOMA PHASE IIRSCH. TRIANGLE PARK, NC (SEE ALSO HEAD/NECK) (888) 825-5249 foretinib N1-{3-fluoro-4-[(6-(Methyloxy)-7-{[3-(4-Morpholinyl)propyl]oxy}-4-quinolinyl)oxy]phenyl}-N1'-(4-fluorophenyl)-1,1-cyclopropanedicarboxaMide Foretinib (GSK1363089, XL880) GSK089 GSK1363089; FORETINIB; EXEL-2880 Foretinib, Free Base EXEL-2880/XL-880 N-(3-fluoro-4-(6-Methoxy-7-(3-Morpholinopropoxy)quinolin-4-yloxy)phenyl)-N-(4-fluorophenyl)cyclopropane-1,1-dicarboxaMide N1'-[3-fluoro-4-[[6-Methoxy-7-(3-Morpholinopropoxy)-4-quinolyl]oxy]phenyl]-N1-(4-fluorophenyl)cyclopropane-1,1-dicarboxaMide GSK1363089/foretinib N-(3-Fluoro-4-((6-methoxy-7-(3-morpholinopropoxy)quinolin-4-yl)-oxy)phenyl)-N-(4-fluorophenyl)cyc Foretinib (GSK1363089) N-[3-Fluoro-4-[[6-(methyloxy)-7-[[3-(morpholin-4-yl)propyl]oxy]quinolin-4-yl]oxy]phenyl]-N'-(4-fluorophenyl)cyclopropane-1,1 Foretinib, >=98% Foretinib (XL-880) N-(3-Fluoro-4-((6-methoxy-7-(3-morpholinopropoxy)quinolin-4-yl)-oxy)phenyl)-N-(4-fluorophenyl) 1-N'-[3-FLUORO-4-({6-METHOXY-7-[3-(MORPHOLIN-4-YL)PROPOXY]QUINOLIN-4-YL}OXY)PHENYL]-1-N-(4-FLUOROPHENYL)CYCLOPROPANE-1,1-DICARBOXAMIDE Foretinib (XL880,EXEL-2880) XL880 (GSK1363089, Foretinib, EXEL-2880) XL-880;EXEL-2880;XL 880 XL-880;GSK089;EXEL-2880;XL 880;GSK-089; GSK 1363089; GSK-1363089 XL880; XL 880; XL-880; GSK1363089; GSK 1363089; GSK-1363089; GSK089; EXEL2880; FORETINIB. 1,1-Cyclopropanedicarboxamide, N-[3-fluoro-4-[[6-methoxy-7-[3-(4-morpholinyl)propoxy]-4-quinolinyl]oxy]phenyl]-N'-(4-fluorophenyl)- Foretinib (GSK1363089) USP/EP/BP N1'-[3-fluoro-4-[[6-methoxy-7-(3-morpholinopropoxy)-4-quinol... EXEL-2880 XL880 Foretinib, 10 mM in DMSO Foretinib 849217-64-7 C34H34F2N4O6 Inhibitors
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