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ARQ 621

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Company Name: Hubei Jusheng Technology Co.,Ltd.
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Products Intro: Product Name:ARQ 621
CAS:1095253-39-6
Purity:0.99 Package:5KG;1KG
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Products Intro: Product Name:ARQ 621
CAS:1095253-39-6
Purity:99.9% Package:25kgs/Drum;200kgs/Drum Remarks:FDA GMP CEP Approved Manufacturer
Company Name: InvivoChem
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Products Intro: Product Name:ARQ 621
CAS:1095253-39-6
Purity:98% Package:2mg Remarks:V1631
Company Name: LEAP CHEM CO., LTD.
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Products Intro: Product Name:ARQ 621
CAS:1095253-39-6
Package:1g; 5g; 25g; 1kg; 5kg; 25kg
Company Name: Nantong HI-FUTURE Biology Co., Ltd.
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Products Intro: Product Name:ARQ621
CAS:1095253-39-6
Purity:0.98 Package:5mg,10mg,100mg,500mg,1g,5g,10g,more
ARQ 621 Basic information
Product Name:ARQ 621
Synonyms:ARQ 621;N-(3-aminopropyl)-3-chloro-N-[(1R)-1-[7-chloro-3,4-dihydro-4-oxo-3-(phenylamino)-2-quinazolinyl]-3-butyn-1-yl]-2-fluoro-benzamide;ARQ-621;ARQ621;Benzamide, N-(3-aminopropyl)-3-chloro-N-[(1R)-1-[7-chloro-3,4-dihydro-4-oxo-3-(phenylamino)-2-quinazolinyl]-3-butyn-1-yl]-2-fluoro-;ARQ 621 USP/EP/BP;motor,inhibit,cell,ARQ 621,division,protein,Inhibitor,microtubule,ARQ621,Kinesin,Anti-tumor,Eg5,ARQ-621;(R)-N-(3-Aminopropyl)-3-chloro-N-(1-(7-chloro-4-oxo-3-(phenylamino)-3,4-dihydroquinazolin-2-yl)but-3-yn-1-yl)-2-fluorobenzamide
CAS:1095253-39-6
MF:C28H24Cl2FN5O2
MW:552.43
EINECS:
Product Categories:Inhibitors
Mol File:1095253-39-6.mol
ARQ 621 Structure
ARQ 621 Chemical Properties
Boiling point 730.6±70.0 °C(Predicted)
density 1.34±0.1 g/cm3(Predicted)
storage temp. Store at -20°C
solubility Soluble in DMSO
form Powder
pka9.40±0.10(Predicted)
Safety Information
MSDS Information
ARQ 621 Usage And Synthesis
Biological Activityarq 621 is a novel, allosteric,potent and selective inhibitor of eg5. eg5 is a member of the mitotickinesin superfamily which plays a key role in mitosis. eg5 is essential for the dynamic organization of the mitotic spindle. over-expression of eg5 leads to genomic instability and tumor formation [1].
in vitroin human liver microsomes, t1/2 of arq 621 was 53 min. the t1/2value of arq 621 in male and female mouse, rat, dog and monkey liver microsomes was 43, 53, 56, 53, 47, 44, 36, and 32 minutes, respectively [1]. ic50value of arq 621 for cyp 1a2, 2c9, 2d6, 3a4, 2c19, and 2c8 was>20, >20, >20, 4.1, 4.0, and 15 μm, respectively. arq 621 showed anti-tumor activity with potencies in the low nanomolar range across a range of human solid and hematological malignanciescancer cell types such as colon, nsclc, gastric, and hematologic cancer cell lines [1].
in vivooral administration of arq 621 showed that the bioavailability of arq 621 was approximately 9% [1].
referencessavage r e, zhong c, hall t, et al. in vitro adme properties of arq 621: a specific eg5 inhibitor[j]. cancer research, 2010, 70(8 supplement): 5783-5783.rosen l, chen l c, iyengar t, et al. arq 621, a novel potent and selective inhibitor of eg5: preclinical data and early results from a clinical phase 1 study[j]. cancer research, 2010, 70(8 supplement): 2750-2750.chen l c, rosen l s, iyengar t, et al. first-in-human study with arq 621, a novel inhibitor of eg5: final results from the solid tumors cohort[c]//asco annual meeting proceedings. 2011, 29(15_suppl): 3076.
ARQ 621 Preparation Products And Raw materials
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