Details
| Stereochemistry | ABSOLUTE |
| Molecular Formula | C18H19N7O2.C3H6O3.H2O |
| Molecular Weight | 473.4824 |
| Optical Activity | UNSPECIFIED |
| Defined Stereocenters | 1 / 1 |
| E/Z Centers | 0 |
| Charge | 0 |
SHOW SMILES / InChI
SMILES
O.C[C@H](O)C(O)=O.COC1=CC=CC(OCCCN)=C1C2=CC(NC3=CN=C(C=N3)C#N)=NN2
InChI
InChIKey=SQQVRJAAUOKBIG-TYOUJGAFSA-N
InChI=1S/C18H19N7O2.C3H6O3.H2O/c1-26-14-4-2-5-15(27-7-3-6-19)18(14)13-8-16(25-24-13)23-17-11-21-12(9-20)10-22-17;1-2(4)3(5)6;/h2,4-5,8,10-11H,3,6-7,19H2,1H3,(H2,22,23,24,25);2,4H,1H3,(H,5,6);1H2/t;2-;/m.0./s1
| Molecular Formula | C3H6O3 |
| Molecular Weight | 90.0779 |
| Charge | 0 |
| Count |
|
| Stereochemistry | ABSOLUTE |
| Additional Stereochemistry | No |
| Defined Stereocenters | 1 / 1 |
| E/Z Centers | 0 |
| Optical Activity | ( + ) |
| Molecular Formula | H2O |
| Molecular Weight | 18.0153 |
| Charge | 0 |
| Count |
|
| Stereochemistry | ACHIRAL |
| Additional Stereochemistry | No |
| Defined Stereocenters | 0 / 0 |
| E/Z Centers | 0 |
| Optical Activity | NONE |
| Molecular Formula | C18H19N7O2 |
| Molecular Weight | 365.3892 |
| Charge | 0 |
| Count |
|
| Stereochemistry | ACHIRAL |
| Additional Stereochemistry | No |
| Defined Stereocenters | 0 / 0 |
| E/Z Centers | 0 |
| Optical Activity | NONE |
LY2606368 (Prexasertib) is a small-molecule Chk-1 inhibitors invented by Array and being developed by Eli Lilly and Company. Lilly is responsible for all clinical development and commercialization activities. LY2606368 is advancing in Phase 2 clinical trials for cancer. Prexasertib preferentially binds to and inhibits CHK1 and, to a lesser extent, inhibits CHK2. Chk-1 is a protein kinase that regulates the tumor cell's response to DNA damage often caused by treatment with chemotherapy. In response to DNA damage, Chk-1 blocks cell cycle progression in order to allow for repair of damaged DNA, thereby limiting the efficacy of chemotherapeutic agents. Inhibiting Chk-1 in combination with chemotherapy can enhance tumor cell death by preventing these cells from recovering from DNA damage.
Approval Year
Targets
| Primary Target | Pharmacology | Condition | Potency |
|---|---|---|---|
Target ID: CHEMBL4630 |
0.9 nM [Ki] | ||
Target ID: CHEMBL2527 |
Conditions
| Condition | Modality | Targets | Highest Phase | Product |
|---|---|---|---|---|
| Primary | Unknown Approved UseUnknown |
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| Primary | Unknown Approved UseUnknown |
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| Primary | Unknown Approved UseUnknown |
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| Primary | Unknown Approved UseUnknown |
Sample Use Guides
105 mg/m2 IV once every 14 days of a 28 day cycle
Route of Administration:
Intravenous
In a functional assay, LY2606368 (PREXASERTIB) potently abrogated the G2–M checkpoint activated by doxorubicin in p53-deficient HeLa cells with an EC50 of 9 nmol/L. LY2606368 did inhibit DNA damage-induced CHK2 autophosphorylation with an IC50 of less than 31 nmol/L. 100 nmol/L LY2606368 did not inhibit PMA-stimulated RSK but instead weakly stimulated phosphorylation of S6 on serines 235/236. LY2606368 was broadly antiproliferative with IC50 values typically <50 nmol/L in the most sensitive cell lines with a minority of cell lines showing considerable resistance with IC50's >1,000 nmol/L
| Substance Class |
Chemical
Created
by
admin
on
Edited
Sat Dec 16 18:45:25 UTC 2023
by
admin
on
Sat Dec 16 18:45:25 UTC 2023
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| Record UNII |
E4FZV27T6Z
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| Record Status |
Validated (UNII)
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| Record Version |
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157433374
Created by
admin on Sat Dec 16 18:45:25 UTC 2023 , Edited by admin on Sat Dec 16 18:45:25 UTC 2023
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E4FZV27T6Z
Created by
admin on Sat Dec 16 18:45:25 UTC 2023 , Edited by admin on Sat Dec 16 18:45:25 UTC 2023
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2100300-72-7
Created by
admin on Sat Dec 16 18:45:25 UTC 2023 , Edited by admin on Sat Dec 16 18:45:25 UTC 2023
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PARENT -> SALT/SOLVATE |
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ANHYDROUS->SOLVATE |
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ACTIVE MOIETY |
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