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ARQ 621

Basic information Safety Supplier Related

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
Product Categories:
  • Inhibitors
Mol File:
1095253-39-6.mol
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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
pka
9.40±0.10(Predicted)
color 
White to off-white
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ARQ 621 Usage And Synthesis

Biological Activity

arq 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 vitro

in 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 vivo

oral administration of arq 621 showed that the bioavailability of arq 621 was approximately 9% [1].

References

savage 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 621Supplier

Shanghai Boyle Chemical Co., Ltd.
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Email
sales@boylechem.com
Dalian Meilun Biotech Co., Ltd.
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0411-62910999 13889544652
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meilunui@163.com
NCE Biomedical Co.,Ltd.
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4000-027-021 |24 +86-13986109188 | +86-15623472865 | +81-08033611988
AdooQ BioScience, LLC
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+1 (866) 930-6790
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info@adooq.com
DKMbiochem.Co. Ltd
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15901859516
Email
sales@DKMbiochem.com
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