Details
Stereochemistry | ABSOLUTE |
Molecular Formula | C28H24Cl2FN5O2 |
Molecular Weight | 552.427 |
Optical Activity | UNSPECIFIED |
Defined Stereocenters | 1 / 1 |
E/Z Centers | 0 |
Charge | 0 |
SHOW SMILES / InChI
SMILES
NCCCN([C@H](CC#C)C1=NC2=C(C=CC(Cl)=C2)C(=O)N1NC3=CC=CC=C3)C(=O)C4=CC=CC(Cl)=C4F
InChI
InChIKey=UPJSUQWHUVLLNW-XMMPIXPASA-N
InChI=1S/C28H24Cl2FN5O2/c1-2-8-24(35(16-7-15-32)27(37)21-11-6-12-22(30)25(21)31)26-33-23-17-18(29)13-14-20(23)28(38)36(26)34-19-9-4-3-5-10-19/h1,3-6,9-14,17,24,34H,7-8,15-16,32H2/t24-/m1/s1
Molecular Formula | C28H24Cl2FN5O2 |
Molecular Weight | 552.427 |
Charge | 0 |
Count |
|
Stereochemistry | ABSOLUTE |
Additional Stereochemistry | No |
Defined Stereocenters | 1 / 1 |
E/Z Centers | 0 |
Optical Activity | UNSPECIFIED |
DescriptionCurator's Comment: Description was created based on several sources, including http://cancerres.aacrjournals.org/content/68/9_Supplement/656
http://en.pharmacodia.com/web/drug/1_2210.html
Curator's Comment: Description was created based on several sources, including http://cancerres.aacrjournals.org/content/68/9_Supplement/656
http://en.pharmacodia.com/web/drug/1_2210.html
ARQ-621 is a small-molecule inhibitor of the kinesin-related motor protein Eg5 with potential antineoplastic activity. Eg5 kinesin-related motor protein inhibitor ARQ 621 selectively inhibits the activity of Eg5, which may result in mitotic disruption, apoptosis and cell death. The ATP-dependent Eg5 kinesin-related motor protein (also known as KIF11 or kinesin spindle protein-5) is a plus-end directed kinesin motor protein involved in the regulation of spindle dynamics, including assembly and maintenance, during mitosis. In proliferation assays, ARQ-621 showed broad spectrum cytotoxicity against a panel of human cancer cell lines, with cell cycle analysis confirming a G2/M arrest followed by apoptosis. When administered intraperitoneally to nude mice bearing human pancreatic tumors (MIA PaCa-2), complete tumor stasis was achieved with a 6.25 mg/kg dose 3 times weekly for 4 weeks. At the completion of ARQ-621 dosing, the mice showed hematology profiles indistinguishable from untreated controls with no evidence of bone marrow toxicity. A phase I trial has been completed, however research has being discontinued.
Originator
Approval Year
Sample Use Guides
In Vivo Use Guide
Sources: https://clinicaltrials.gov/ct2/show/NCT00825487
Treatment will be initiated at a dose level of 10 mg/m^2 IV infusion for an hour once weekly in 4-week (28 day) consecutive and continuous cycles. ARQ-621 should be infused IV over two hours at doses 200 mg/m^2 and higher (cohort 8 and above).
Route of Administration:
Intravenous
Substance Class |
Chemical
Created
by
admin
on
Edited
Sat Dec 16 02:15:32 GMT 2023
by
admin
on
Sat Dec 16 02:15:32 GMT 2023
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Record UNII |
UU55190C8S
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Record Status |
Validated (UNII)
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Record Version |
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1095253-39-6
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C82694
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25110841
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UU55190C8S
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DTXSID80148974
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admin on Sat Dec 16 02:15:32 GMT 2023 , Edited by admin on Sat Dec 16 02:15:32 GMT 2023
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TARGET -> INHIBITOR |
IC50
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