Details
| Stereochemistry | ACHIRAL |
| Molecular Formula | C29H40N8O3S |
| Molecular Weight | 580.745 |
| Optical Activity | NONE |
| Defined Stereocenters | 0 / 0 |
| E/Z Centers | 0 |
| Charge | 0 |
SHOW SMILES / InChI
SMILES
COC1=CC(=CC=C1NC2=NC(NC3=CC=CC=C3S(=O)(=O)C(C)C)=NC=N2)N4CCC(CC4)N5CCN(C)CC5
InChI
InChIKey=MGGBYMDAPCCKCT-UHFFFAOYSA-N
InChI=1S/C29H40N8O3S/c1-21(2)41(38,39)27-8-6-5-7-25(27)33-29-31-20-30-28(34-29)32-24-10-9-23(19-26(24)40-4)36-13-11-22(12-14-36)37-17-15-35(3)16-18-37/h5-10,19-22H,11-18H2,1-4H3,(H2,30,31,32,33,34)
| Molecular Formula | C29H40N8O3S |
| Molecular Weight | 580.745 |
| Charge | 0 |
| Count |
|
| Stereochemistry | ACHIRAL |
| Additional Stereochemistry | No |
| Defined Stereocenters | 0 / 0 |
| E/Z Centers | 0 |
| Optical Activity | NONE |
ASP-3026 is a ALK tyrosine kinase receptor inhibitor which was developed by Astellas Pharma for the treatment of cancer conditions. The drug is being tested in phase I of clinical trials in patients with solid tumors, B-cell lymphoma and non-small cell lung carcinoma. The drug was discontinued for strategic reasons.
Originator
Approval Year
Targets
| Primary Target | Pharmacology | Condition | Potency |
|---|---|---|---|
Target ID: CHEMBL4247 Sources: https://www.ncbi.nlm.nih.gov/pubmed/24419060 |
3.5 nM [IC50] |
Conditions
| Condition | Modality | Targets | Highest Phase | Product |
|---|---|---|---|---|
| Primary | Unknown Approved UseUnknown |
|||
| Primary | Unknown Approved UseUnknown |
|||
| Primary | Unknown Approved UseUnknown |
Cmax
| Value | Dose | Co-administered | Analyte | Population |
|---|---|---|---|---|
961 ng/mL EXPERIMENT https://pubmed.ncbi.nlm.nih.gov/26966027 |
525 mg single, oral dose: 525 mg route of administration: Oral experiment type: SINGLE co-administered: |
ASP-3026 plasma | Homo sapiens population: UNHEALTHY age: ADULT sex: FEMALE / MALE food status: UNKNOWN |
|
1331 ng/mL EXPERIMENT https://pubmed.ncbi.nlm.nih.gov/26966027 |
525 mg 1 times / day multiple, oral dose: 525 mg route of administration: Oral experiment type: MULTIPLE co-administered: |
ASP-3026 plasma | Homo sapiens population: UNHEALTHY age: ADULT sex: FEMALE / MALE food status: UNKNOWN |
|
1633 ng/mL EXPERIMENT https://pubmed.ncbi.nlm.nih.gov/26966027 |
800 mg single, oral dose: 800 mg route of administration: Oral experiment type: SINGLE co-administered: |
ASP-3026 plasma | Homo sapiens population: UNHEALTHY age: ADULT sex: FEMALE / MALE food status: UNKNOWN |
|
4854 ng/mL EXPERIMENT https://pubmed.ncbi.nlm.nih.gov/26966027 |
800 mg 1 times / day multiple, oral dose: 800 mg route of administration: Oral experiment type: MULTIPLE co-administered: |
ASP-3026 plasma | Homo sapiens population: UNHEALTHY age: ADULT sex: FEMALE / MALE food status: UNKNOWN |
AUC
| Value | Dose | Co-administered | Analyte | Population |
|---|---|---|---|---|
11746 ng × h/mL EXPERIMENT https://pubmed.ncbi.nlm.nih.gov/26966027 |
525 mg single, oral dose: 525 mg route of administration: Oral experiment type: SINGLE co-administered: |
ASP-3026 plasma | Homo sapiens population: UNHEALTHY age: ADULT sex: FEMALE / MALE food status: UNKNOWN |
|
19993 ng × h/mL EXPERIMENT https://pubmed.ncbi.nlm.nih.gov/26966027 |
525 mg 1 times / day multiple, oral dose: 525 mg route of administration: Oral experiment type: MULTIPLE co-administered: |
ASP-3026 plasma | Homo sapiens population: UNHEALTHY age: ADULT sex: FEMALE / MALE food status: UNKNOWN |
|
21796 ng × h/mL EXPERIMENT https://pubmed.ncbi.nlm.nih.gov/26966027 |
800 mg single, oral dose: 800 mg route of administration: Oral experiment type: SINGLE co-administered: |
ASP-3026 plasma | Homo sapiens population: UNHEALTHY age: ADULT sex: FEMALE / MALE food status: UNKNOWN |
|
78081 ng × h/mL EXPERIMENT https://pubmed.ncbi.nlm.nih.gov/26966027 |
800 mg 1 times / day multiple, oral dose: 800 mg route of administration: Oral experiment type: MULTIPLE co-administered: |
ASP-3026 plasma | Homo sapiens population: UNHEALTHY age: ADULT sex: FEMALE / MALE food status: UNKNOWN |
T1/2
| Value | Dose | Co-administered | Analyte | Population |
|---|---|---|---|---|
24.9 h EXPERIMENT https://pubmed.ncbi.nlm.nih.gov/26966027 |
525 mg 1 times / day multiple, oral dose: 525 mg route of administration: Oral experiment type: MULTIPLE co-administered: |
ASP-3026 plasma | Homo sapiens population: UNHEALTHY age: ADULT sex: FEMALE / MALE food status: UNKNOWN |
|
37.9 h EXPERIMENT https://pubmed.ncbi.nlm.nih.gov/26966027 |
800 mg 1 times / day multiple, oral dose: 800 mg route of administration: Oral experiment type: MULTIPLE co-administered: |
ASP-3026 plasma | Homo sapiens population: UNHEALTHY age: ADULT sex: FEMALE / MALE food status: UNKNOWN |
PubMed
| Title | Date | PubMed |
|---|---|---|
| The ALK inhibitor ASP3026 eradicates NPM-ALK⁺ T-cell anaplastic large-cell lymphoma in vitro and in a systemic xenograft lymphoma model. | 2014-07-30 |
|
| The selective anaplastic lymphoma receptor tyrosine kinase inhibitor ASP3026 induces tumor regression and prolongs survival in non-small cell lung cancer model mice. | 2014-02 |
Patents
Sample Use Guides
In Vivo Use Guide
Sources: https://www.ncbi.nlm.nih.gov/pubmed/26966027
ASP-3026 should be taken at a dose 25-800 mg once daily in 28-day cycles.
Route of Administration:
Oral
In Vitro Use Guide
Sources: https://www.ncbi.nlm.nih.gov/pubmed/25026277
Karpas 299, SR-786, and SU-DHL-1 cells were treated with ASP-3026 (0.5, 1.5, and 2.5 uM) for 48 h and the drug was shown to induce significant apoptosis in the cell lines.
| Substance Class |
Chemical
Created
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admin
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Edited
Mon Mar 31 21:24:22 GMT 2025
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on
Mon Mar 31 21:24:22 GMT 2025
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| Record UNII |
HP4L6MXF10
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Validated (UNII)
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TARGET -> INHIBITOR |
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ACTIVE MOIETY |