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Gilteritinib

Gilteritinib Suppliers list
Company Name: Xi'an Yutbon Pharmaceutical Technology Co., Ltd
Tel: 029-81140587 +8618717328141
Email: sales@yutbon.com
Products Intro: Product Name:Gilteritinib
CAS:1254053-43-4
Purity:99% Package:500g,1kg,10kg,100kg Remarks:Factory stock, quality assurance, price concessions
Company Name: shandong perfect biotechnology co.ltd
Tel: +86-53169958659; +8618596095638
Email: sales@sdperfect.com
Products Intro: Product Name:Gilteritinib
CAS:1254053-43-4
Purity:98% HPLC Package:1g
Company Name: Hangzhou FandaChem Co.,Ltd.
Tel: 008657128800458; +8615858145714
Email: fandachem@gmail.com
Products Intro: Product Name:Gilteritinib
CAS:1254053-43-4
Purity:As coa Package:As request Remarks:1254053-43-4
Company Name: ATK CHEMICAL COMPANY LIMITED
Tel: +undefined-21-51877795
Email: ivan@atkchemical.com
Products Intro: Product Name:ASP-2215
CAS:1254053-43-4
Purity:98% Package:10MG;50MG;100MG,1G,5G,10G.100G
Company Name: BOC Sciences
Tel: +1-631-485-4226
Email: inquiry@bocsci.com
Products Intro: Product Name:Gilteritinib
CAS:1254053-43-4
Package:100mg Remarks:BOC Sciences also provides custom synthesis services for Gilteritinib.

Gilteritinib manufacturers

  • Gilteritinib
  • Gilteritinib pictures
  • $0.00 / 1g
  • 2024-03-12
  • CAS:1254053-43-4
  • Min. Order: 1g
  • Purity: 98% HPLC
  • Supply Ability: 1kg
  • Gilteritinib
  • Gilteritinib pictures
  • $0.00/ kg
  • 2023-12-12
  • CAS:1254053-43-4
  • Min. Order: 0.1kg
  • Purity: 99%(HPLC)
  • Supply Ability: 100kg
  • ASP-2215
  • ASP-2215 pictures
  • $0.00 / 1KG
  • 2022-09-23
  • CAS:1254053-43-4
  • Min. Order: 1KG
  • Purity: 98%
  • Supply Ability: 1ton

Related articles

Gilteritinib Basic information
Physical Form in vivo
Product Name:Gilteritinib
Synonyms:ASP-2215;2-Pyrazinecarboxamide, 6-ethyl-3-[[3-methoxy-4-[4-(4-methyl-1-piperazinyl)-1-piperidinyl]phenyl]amino]-5-[(tetrahydro-2H-pyran-4-yl)amino]-;6-Ethyl-3-[[3-methoxy-4-[4-(4-methyl-1-piperazinyl)-1-piperidinyl]phenyl]amino]-5-[(tetrahydro-2H-pyran-4-yl)amino]-2-pyrazinecarboxamide;6-ethyl-3-((3-methoxy-4-(4-(4-methylpiperazin-1-yl)piperidin-1-yl)phenyl)amino)-5-((tetrahydro-2H-pyran-4-yl)amino)pyrazine-2-carboxamide;Gilteritinib (ASP2215);6-Ethyl-3-((3-methoxy-4-(4-(4-methylpiperazin-1-yl)piperidin-1-yl)phenyl)-amino)-5-((tetrahydr;ASP2215(Gilteritinib);Gilteritinib(free base)
CAS:1254053-43-4
MF:C29H44N8O3
MW:552.71
EINECS:
Product Categories:API
Mol File:1254053-43-4.mol
Gilteritinib Structure
Gilteritinib Chemical Properties
Melting point >157°C (dec.)
Boiling point 696.9±55.0 °C(Predicted)
density 1.242±0.06 g/cm3(Predicted)
storage temp. -20°C
solubility Soluble in DMSO (25 mg/ml)
form solid
pka14.39±0.50(Predicted)
color Off-white to pale pink
Stability:Stable for 1 year as supplied. Solutions in DMSO may be stored at -20°C for up to 3 months.
Safety Information
MSDS Information
Gilteritinib Usage And Synthesis
Physical FormPale-yellow to Yellow-brown Solid
in vivoIn vivo, gilteritinib is distributed at high levels in xenografted tumors after oral administration. The decreased FLT3 activity and high intratumor distribution of gilteritinib translates to tumor regression and improved survival in xenograft and intra-bone marrow transplantation models of FLT3-driven AML. This antitumor activity is associated with a durable inhibition of phospho-FLT3 and phospho-STAT5. Furthermore, treatment with gilteritinib decreases the leukemic burden and prolongs survival in a mouse IBMT model. No overt toxicity is seen in mouse models treated with gilteritinib
DescriptionGilteritinib is an inhibitor of FMS-related tyrosine kinase 3 (FLT3; IC50 = 5 nM for the wild-type enzyme). It inhibits mutant forms of FLT3, including FLT3 with the internal tandem duplication mutation (FLT3-ITD), FLT3-ITD expressing the F691L mutation, and FLT3 with various tyrosine kinase domain mutations (FLT3-TKD; IC50s =1.4-1.8, 12.2, and 0.7-2 nM, respectively). Gilteritinib also inhibits Axl and c-Kit with IC50 values of 41 and 102 nM, respectively. It decreases the viability of blast cells isolated from patients with relapsed acute myeloid leukemia (AML) in a concentration-dependent manner. Formulations containing gilteritinib have been used in the treatment of AML.
UsesGilteritinib is an AXL inhibitor in cancer.
DefinitionChEBI: Gilteritinib is a member of the class of pyrazines that is pyrazine-2-carboxamide which is substituted by {3-methoxy-4-[4-(4-methylpiperazin-1-yl)piperidin-1-yl]phenyl}nitrilo, (oxan-4-yl)nitrilo and ethyl groups at positions 3,5 and 6, respectively. It is a potent inhibitor of FLT3 and AXL tyrosine kinase receptors (IC50 = 0.29 nM and 0.73 nM, respectively). Approved by the FDA for the treatment of acute myeloid leukemia in patients who have a FLT3 gene mutation. It has a role as an apoptosis inducer, an EC 2.7.10.1 (receptor protein-tyrosine kinase) inhibitor and an antineoplastic agent. It is a N-methylpiperazine, a member of piperidines, a secondary amino compound, a monomethoxybenzene, a member of pyrazines, a primary carboxamide, an aromatic amine and a member of oxanes.
ReferencesLee et al. (2017) Preclinical studies of gilteritinib, a next-generation FLT3 inhibitor; Blood?129 257 Thomas et al. (2021) Gilteritinib Inhibits Glutamine Uptake and Utilization in FLT-3-ITD-Positive AML; Cancer Ther.?20 2207
Gilteritinib Preparation Products And Raw materials
Raw materials4-Aminotetrahydropyran hydrochloride
Tag:Gilteritinib(1254053-43-4) Related Product Information
9-Cyclopentyl-2-[[2-methoxy-4-[(1-methylpiperidin-4-yl)oxy]-phenyl]amino]-7-methyl-7,9-dihydro-8H-purin-8-one Dequalinium chloride Volasertib (BI 6727) NORFLUOXETINE HYDROCHLORIDE SGI 7079 N-(1,1-Dimethylethyl)-3-[[5-methyl-2-[[4-(4-methyl-1-piperazinyl)phenyl]amino]-4-pyrimidinyl]amino]benzenesulfonamide ABX-1431 N2-[2-Methoxy-4-[4-(4-methyl-1-piperazinyl)-1-piperidinyl]phenyl]-N4-[2-[(1-methylethyl)sulfonyl]phenyl]-1,3,5-triazine-2,4-diamine UNC2541