7 Results for "

ASP2215

" in MedChemExpress (MCE) Product Catalog:
Products (7)

7 Results for "ASP2215" in MCE Product Catalog:

44
44 Publications Verification
Cat. No.: HY-12432
CAS No.: 1254053-43-4
Purity:  99.84%
Synonyms: ASP2215
Target:  

FLT3 TAM Receptor

Research Areas:  

Cancer

Gilteritinib (ASP2215) is a potent and ATP-competitive FLT3/AXL inhibitor with IC50s of 0.29 nM/0.73 nM, respectively.
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44
44 Publications Verification
Cat. No.: HY-12432A
CAS No.: 1254053-84-3
Purity:  99.75%
Synonyms: ASP2215 hemifumarate
Target:  

FLT3 TAM Receptor

Research Areas:  

Cancer

Gilteritinib (ASP2215) hemifumarate is a potent and ATP-competitive FLT3/AXL inhibitor with IC50 of 0.29 nM/0.73 nM, respectively.
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3
3 Cited Publications
Cat. No.: HY-P0227
CAS No.: 168482-23-3
Target:  

Melanocortin Receptor

Research Areas:  

Metabolic Disease

SHU 9119 is a potent human melanocortin 3 and 4 receptors (MC3/4R) antagonist and a partial MC5R agonist; with IC50 values of 0.23, 0.06, and 0.09 nM for human MC3R, MC4R and MC5R, respectively.
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Cat. No.: HY-12432R
CAS No.: 1254053-43-4
Synonyms: ASP2215 (Standard)
Research Areas:  

Cancer

Gilteritinib (Standard) is the analytical standard of Gilteritinib. This product is intended for research and analytical applications. Gilteritinib (ASP2215) is a potent and ATP-competitive FLT3/AXL inhibitor with IC50s of 0.29 nM/0.73 nM, respectively.
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Cat. No.: HY-12432S1
CAS No.: 2377109-74-3
Purity:  ≥98.0%
Synonyms: ASP2215-d8
Gilteritinib-d8 is deuterium labeled Gilteritinib. Gilteritinib (ASP2215) is a potent and ATP-competitive FLT3/AXL inhibitor with IC50s of 0.29 nM/0.73 nM, respectively.
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Cat. No.: HY-12432AR
CAS No.: 1254053-84-3
Synonyms: ASP2215 hemifumarate (Standard)
Research Areas:  

Cancer

Gilteritinib hemifumarate (Standard) is the analytical standard of Gilteritinib hemifumarate. This product is intended for research and analytical applications. Gilteritinib (ASP2215) hemifumarate is a potent and ATP-competitive FLT3/AXL inhibitor with IC50 of 0.29 nM/0.73 nM, respectively.
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Cat. No.: HY-P1208
CAS No.: 667430-81-1
Target:  

Melanocortin Receptor

Research Areas:  

Inflammation/Immunology

PG-931, an analog of SHU 9119 (HY-P0227), is a potent melanocortin 4 (MC4) receptor (IC50=0.58 nM) agonist and is more selective than for the hMC3R (IC50=55 nM) or the hMC5R (IC50=2.4 nM). PG-931 can reverse haemorrhagic shock and prevent multiple organ damage in vivo .
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