Details
| Stereochemistry | ABSOLUTE |
| Molecular Formula | C17H16ClN3O |
| Molecular Weight | 313.781 |
| Optical Activity | UNSPECIFIED |
| Defined Stereocenters | 1 / 1 |
| E/Z Centers | 0 |
| Charge | 0 |
SHOW SMILES / InChI
SMILES
NC[C@@](O)(C1=CC=C(Cl)C=C1)C2=CC=C(C=C2)C3=CNN=C3
InChI
InChIKey=IIRWNGPLJQXWFJ-KRWDZBQOSA-N
InChI=1S/C17H16ClN3O/c18-16-7-5-15(6-8-16)17(22,11-19)14-3-1-12(2-4-14)13-9-20-21-10-13/h1-10,22H,11,19H2,(H,20,21)/t17-/m0/s1
| Molecular Formula | C17H16ClN3O |
| Molecular Weight | 313.781 |
| 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
https://www.ncbi.nlm.nih.gov/pubmed/22781553
Curator's Comment: Description was created based on several sources, including
https://www.ncbi.nlm.nih.gov/pubmed/22781553
AT13148, being developed by Astex Pharmaceuticals and its collaborators, is an orally active small molecule inhibitor of Rho activated kinases (ROCK) 1 and 2 and of protein kinase (PK) A and is currently in phase 1 clinical studies under Cancer Research UK’s Clinical Development Program (CDP). AT13148 is currently being tested in a phase 1 clinical trial in patients with advanced solid tumors.
Approval Year
Targets
| Primary Target | Pharmacology | Condition | Potency |
|---|---|---|---|
| 3.0 nM [IC50] | |||
| 4.0 nM [IC50] | |||
Target ID: CHEMBL3231 Sources: https://www.ncbi.nlm.nih.gov/pubmed/22781553 |
6.0 nM [IC50] | ||
| 8.0 nM [IC50] |
Conditions
| Condition | Modality | Targets | Highest Phase | Product |
|---|---|---|---|---|
| Primary | Unknown Approved UseUnknown |
Cmax
| Value | Dose | Co-administered | Analyte | Population |
|---|---|---|---|---|
50 nM |
20 mg 1 times / day multiple, oral dose: 20 mg route of administration: Oral experiment type: MULTIPLE co-administered: |
AT-13148 plasma | Homo sapiens population: UNHEALTHY age: ADULT sex: UNKNOWN food status: UNKNOWN |
|
50 nM |
20 mg 1 times / day multiple, oral dose: 20 mg route of administration: Oral experiment type: MULTIPLE co-administered: |
AT-13148 plasma | Homo sapiens population: UNHEALTHY age: ADULT sex: UNKNOWN food status: UNKNOWN |
|
400 nM EXPERIMENT https://pubmed.ncbi.nlm.nih.gov/32616501 |
180 mg single, oral dose: 180 mg route of administration: Oral experiment type: SINGLE co-administered: |
AT-13148 plasma | Homo sapiens population: UNHEALTHY age: ADULT sex: FEMALE / MALE food status: UNKNOWN |
|
400 nM EXPERIMENT https://pubmed.ncbi.nlm.nih.gov/32616501 |
160 mg single, oral dose: 160 mg route of administration: Oral experiment type: SINGLE co-administered: |
AT-13148 plasma | Homo sapiens population: UNHEALTHY age: ADULT sex: UNKNOWN food status: UNKNOWN |
|
20 nM EXPERIMENT https://pubmed.ncbi.nlm.nih.gov/32616501 |
5 mg single, oral dose: 5 mg route of administration: Oral experiment type: SINGLE co-administered: |
AT-13148 plasma | Homo sapiens population: UNHEALTHY age: ADULT sex: FEMALE / MALE food status: UNKNOWN |
|
120 nM EXPERIMENT https://pubmed.ncbi.nlm.nih.gov/32616501 |
40 mg single, oral dose: 40 mg route of administration: Oral experiment type: SINGLE co-administered: |
AT-13148 plasma | Homo sapiens population: UNHEALTHY age: ADULT sex: FEMALE / MALE food status: UNKNOWN |
|
700 nM EXPERIMENT https://pubmed.ncbi.nlm.nih.gov/32616501 |
300 mg single, oral dose: 300 mg route of administration: Oral experiment type: SINGLE co-administered: |
AT-13148 plasma | Homo sapiens population: UNHEALTHY age: ADULT sex: FEMALE / MALE food status: UNKNOWN |
AUC
| Value | Dose | Co-administered | Analyte | Population |
|---|---|---|---|---|
20000 nM × h EXPERIMENT https://pubmed.ncbi.nlm.nih.gov/32616501 |
180 mg single, oral dose: 180 mg route of administration: Oral experiment type: SINGLE co-administered: |
AT-13148 plasma | Homo sapiens population: UNHEALTHY age: ADULT sex: FEMALE / MALE food status: UNKNOWN |
|
20000 nM × h EXPERIMENT https://pubmed.ncbi.nlm.nih.gov/32616501 |
160 mg single, oral dose: 160 mg route of administration: Oral experiment type: SINGLE co-administered: |
AT-13148 plasma | Homo sapiens population: UNHEALTHY age: ADULT sex: UNKNOWN food status: UNKNOWN |
|
900 nM × h EXPERIMENT https://pubmed.ncbi.nlm.nih.gov/32616501 |
5 mg single, oral dose: 5 mg route of administration: Oral experiment type: SINGLE co-administered: |
AT-13148 plasma | Homo sapiens population: UNHEALTHY age: ADULT sex: FEMALE / MALE food status: UNKNOWN |
|
2100 nM × h EXPERIMENT https://pubmed.ncbi.nlm.nih.gov/32616501 |
40 mg single, oral dose: 40 mg route of administration: Oral experiment type: SINGLE co-administered: |
AT-13148 plasma | Homo sapiens population: UNHEALTHY age: ADULT sex: FEMALE / MALE food status: UNKNOWN |
|
40000 nM × h EXPERIMENT https://pubmed.ncbi.nlm.nih.gov/32616501 |
300 mg single, oral dose: 300 mg route of administration: Oral experiment type: SINGLE co-administered: |
AT-13148 plasma | Homo sapiens population: UNHEALTHY age: ADULT sex: FEMALE / MALE food status: UNKNOWN |
T1/2
| Value | Dose | Co-administered | Analyte | Population |
|---|---|---|---|---|
24 h |
20 mg 1 times / day multiple, oral dose: 20 mg route of administration: Oral experiment type: MULTIPLE co-administered: |
AT-13148 plasma | Homo sapiens population: UNHEALTHY age: ADULT sex: UNKNOWN food status: UNKNOWN |
|
24 h |
20 mg 1 times / day multiple, oral dose: 20 mg route of administration: Oral experiment type: MULTIPLE co-administered: |
AT-13148 plasma | Homo sapiens population: UNHEALTHY age: ADULT sex: UNKNOWN food status: UNKNOWN |
|
40 h EXPERIMENT https://pubmed.ncbi.nlm.nih.gov/32616501 |
180 mg single, oral dose: 180 mg route of administration: Oral experiment type: SINGLE co-administered: |
AT-13148 plasma | Homo sapiens population: UNHEALTHY age: ADULT sex: FEMALE / MALE food status: UNKNOWN |
|
40 h EXPERIMENT https://pubmed.ncbi.nlm.nih.gov/32616501 |
160 mg single, oral dose: 160 mg route of administration: Oral experiment type: SINGLE co-administered: |
AT-13148 plasma | Homo sapiens population: UNHEALTHY age: ADULT sex: UNKNOWN food status: UNKNOWN |
|
60 h EXPERIMENT https://pubmed.ncbi.nlm.nih.gov/32616501 |
5 mg single, oral dose: 5 mg route of administration: Oral experiment type: SINGLE co-administered: |
AT-13148 plasma | Homo sapiens population: UNHEALTHY age: ADULT sex: FEMALE / MALE food status: UNKNOWN |
|
15 h EXPERIMENT https://pubmed.ncbi.nlm.nih.gov/32616501 |
40 mg single, oral dose: 40 mg route of administration: Oral experiment type: SINGLE co-administered: |
AT-13148 plasma | Homo sapiens population: UNHEALTHY age: ADULT sex: FEMALE / MALE food status: UNKNOWN |
|
60 h EXPERIMENT https://pubmed.ncbi.nlm.nih.gov/32616501 |
300 mg single, oral dose: 300 mg route of administration: Oral experiment type: SINGLE co-administered: |
AT-13148 plasma | Homo sapiens population: UNHEALTHY age: ADULT sex: FEMALE / MALE food status: UNKNOWN |
Doses
| Dose | Population | Adverse events |
|---|---|---|
240 mg 3 times / week multiple, oral Highest studied dose Dose: 240 mg, 3 times / week Route: oral Route: multiple Dose: 240 mg, 3 times / week Sources: |
unhealthy, 34–76 |
DLT: Elevated liver enzymes... Dose limiting toxicities: Elevated liver enzymes (16.7%) Sources: |
240 mg 3 times / week multiple, oral Highest studied dose Dose: 240 mg, 3 times / week Route: oral Route: multiple Dose: 240 mg, 3 times / week Sources: |
unhealthy, 34–76 |
DLT: Pneumonitis... Dose limiting toxicities: Pneumonitis (grade 3, 14.3%) Sources: |
300 mg 3 times / week multiple, oral Highest studied dose Dose: 300 mg, 3 times / week Route: oral Route: multiple Dose: 300 mg, 3 times / week Sources: |
unhealthy, 34–76 |
DLT: Hypotension, Hypotension... Other AEs: Hypotension... Dose limiting toxicities: Hypotension (grade 3, 20%) Other AEs:Hypotension (grade 4, 20%) Hypotension (grade 2, 40%) Sources: |
180 mg 3 times / week multiple, oral MTD Dose: 180 mg, 3 times / week Route: oral Route: multiple Dose: 180 mg, 3 times / week Sources: |
unhealthy, 34–76 |
DLT: Maculopapular rash... Dose limiting toxicities: Maculopapular rash (grade 3, 14.3%) Sources: |
AEs
| AE | Significance | Dose | Population |
|---|---|---|---|
| Elevated liver enzymes | 16.7% DLT |
240 mg 3 times / week multiple, oral Highest studied dose Dose: 240 mg, 3 times / week Route: oral Route: multiple Dose: 240 mg, 3 times / week Sources: |
unhealthy, 34–76 |
| Pneumonitis | grade 3, 14.3% DLT |
240 mg 3 times / week multiple, oral Highest studied dose Dose: 240 mg, 3 times / week Route: oral Route: multiple Dose: 240 mg, 3 times / week Sources: |
unhealthy, 34–76 |
| Hypotension | grade 2, 40% | 300 mg 3 times / week multiple, oral Highest studied dose Dose: 300 mg, 3 times / week Route: oral Route: multiple Dose: 300 mg, 3 times / week Sources: |
unhealthy, 34–76 |
| Hypotension | grade 3, 20% DLT |
300 mg 3 times / week multiple, oral Highest studied dose Dose: 300 mg, 3 times / week Route: oral Route: multiple Dose: 300 mg, 3 times / week Sources: |
unhealthy, 34–76 |
| Hypotension | grade 4, 20% DLT |
300 mg 3 times / week multiple, oral Highest studied dose Dose: 300 mg, 3 times / week Route: oral Route: multiple Dose: 300 mg, 3 times / week Sources: |
unhealthy, 34–76 |
| Maculopapular rash | grade 3, 14.3% DLT |
180 mg 3 times / week multiple, oral MTD Dose: 180 mg, 3 times / week Route: oral Route: multiple Dose: 180 mg, 3 times / week Sources: |
unhealthy, 34–76 |
Sample Use Guides
In Vivo Use Guide
Sources: https://www.ncbi.nlm.nih.gov/pubmed/22781553
Mice: 50 mg/kg p.o.
Route of Administration:
Oral
In Vitro Use Guide
Sources: https://www.ncbi.nlm.nih.gov/pubmed/22781553
Screening of AT-13148 against a panel of kinases at 10
umol/L revealed >80% inhibition of the structurally related
AGC kinases AKT, PKA, ROCK2, p70S6K, MSK, RSK1/2, and
SGK
| Substance Class |
Chemical
Created
by
admin
on
Edited
Mon Mar 31 22:12:39 GMT 2025
by
admin
on
Mon Mar 31 22:12:39 GMT 2025
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| Record UNII |
A49037RP1E
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| Record Status |
Validated (UNII)
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| Record Version |
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| Code System | Code | Type | Description | ||
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C101786
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24905401
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100000166972
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SUB181270
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CHEMBL3544960
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1056901-62-2
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A49037RP1E
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| Related Record | Type | Details | ||
|---|---|---|---|---|
|
TARGET -> INHIBITOR |
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IC50
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COMPETITIVE INHIBITOR
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ACTIVE MOIETY |