Details
| Stereochemistry | ABSOLUTE |
| Molecular Formula | C17H13ClN2O4 |
| Molecular Weight | 344.749 |
| Optical Activity | UNSPECIFIED |
| Defined Stereocenters | 1 / 1 |
| E/Z Centers | 0 |
| Charge | 0 |
SHOW SMILES / InChI
SMILES
C[C@@H](OC1=CC=C(OC2=NC3=CC(Cl)=CC=C3N=C2)C=C1)C(O)=O
InChI
InChIKey=NUQZXROIVGBRGR-SNVBAGLBSA-N
InChI=1S/C17H13ClN2O4/c1-10(17(21)22)23-12-3-5-13(6-4-12)24-16-9-19-14-7-2-11(18)8-15(14)20-16/h2-10H,1H3,(H,21,22)/t10-/m1/s1
| Molecular Formula | C17H13ClN2O4 |
| Molecular Weight | 344.749 |
| Charge | 0 |
| Count |
|
| Stereochemistry | ABSOLUTE |
| Additional Stereochemistry | No |
| Defined Stereocenters | 1 / 1 |
| E/Z Centers | 0 |
| Optical Activity | UNSPECIFIED |
XK-469 (2-[4-(7-chloro-2-quinoxalinyloxy)phenoxy]-propionic acid) is a novel synthetic quinoxaline phenoxypropionic acid derivative. The R-isomer of XK-469 was approximately twice as effective as the S-isomer of XK-469R. R( )-isomers induce reversible protein DNA crosslinks in mammalian cells. It acts as a selective topoisomerase IIβ inhibitor. A phase I study was performed to determine the safety and pharmacokinetics of XK-469, (R)- in patients with various neoplasms.
Originator
Approval Year
Targets
| Primary Target | Pharmacology | Condition | Potency |
|---|---|---|---|
Target ID: CHEMBL3396 |
|||
Target ID: CHEMBL2149 Sources: https://www.ncbi.nlm.nih.gov/pubmed/11403918 |
0.35 µM [Kd] |
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 |
|---|---|---|---|---|
292.3 μg/mL EXPERIMENT https://pubmed.ncbi.nlm.nih.gov/18650079 |
3200 mg single, intravenous dose: 3200 mg route of administration: Intravenous experiment type: SINGLE co-administered: |
XK-469, (R)- plasma | Homo sapiens population: UNHEALTHY age: ADULT sex: FEMALE / MALE food status: UNKNOWN |
|
146.3 μg/mL EXPERIMENT https://pubmed.ncbi.nlm.nih.gov/18650079 |
1100 mg single, intravenous dose: 1100 mg route of administration: Intravenous experiment type: SINGLE co-administered: |
XK-469, (R)- plasma | Homo sapiens population: UNHEALTHY age: ADULT sex: FEMALE / MALE food status: UNKNOWN |
|
27.9 μg/mL EXPERIMENT https://pubmed.ncbi.nlm.nih.gov/18650079 |
240 mg single, intravenous dose: 240 mg route of administration: Intravenous experiment type: SINGLE co-administered: |
XK-469, (R)- plasma | Homo sapiens population: UNHEALTHY age: ADULT sex: FEMALE / MALE food status: UNKNOWN |
|
4.1 μg/mL EXPERIMENT https://pubmed.ncbi.nlm.nih.gov/18650079 |
30 mg single, intravenous dose: 30 mg route of administration: Intravenous experiment type: SINGLE co-administered: |
XK-469, (R)- plasma | Homo sapiens population: UNHEALTHY age: ADULT sex: FEMALE / MALE food status: UNKNOWN |
|
14.3 μg/mL EXPERIMENT https://pubmed.ncbi.nlm.nih.gov/18650079 |
120 mg single, intravenous dose: 120 mg route of administration: Intravenous experiment type: SINGLE co-administered: |
XK-469, (R)- plasma | Homo sapiens population: UNHEALTHY age: ADULT sex: FEMALE / MALE food status: UNKNOWN |
|
105.1 μg/mL EXPERIMENT https://pubmed.ncbi.nlm.nih.gov/18650079 |
850 mg single, intravenous dose: 850 mg route of administration: Intravenous experiment type: SINGLE co-administered: |
XK-469, (R)- plasma | Homo sapiens population: UNHEALTHY age: ADULT sex: FEMALE / MALE food status: UNKNOWN |
|
173.1 μg/mL EXPERIMENT https://pubmed.ncbi.nlm.nih.gov/18650079 |
1400 mg single, intravenous dose: 1400 mg route of administration: Intravenous experiment type: SINGLE co-administered: |
XK-469, (R)- plasma | Homo sapiens population: UNHEALTHY age: ADULT sex: FEMALE / MALE food status: UNKNOWN |
|
247.6 μg/mL EXPERIMENT https://pubmed.ncbi.nlm.nih.gov/18650079 |
2000 mg single, intravenous dose: 2000 mg route of administration: Intravenous experiment type: SINGLE co-administered: |
XK-469, (R)- plasma | Homo sapiens population: UNHEALTHY age: ADULT sex: FEMALE / MALE food status: UNKNOWN |
|
293.9 μg/mL EXPERIMENT https://pubmed.ncbi.nlm.nih.gov/18650079 |
2500 mg single, intravenous dose: 2500 mg route of administration: Intravenous experiment type: SINGLE co-administered: |
XK-469, (R)- plasma | Homo sapiens population: UNHEALTHY age: ADULT sex: FEMALE / MALE food status: UNKNOWN |
AUC
| Value | Dose | Co-administered | Analyte | Population |
|---|---|---|---|---|
16.445 μg × h/mL EXPERIMENT https://pubmed.ncbi.nlm.nih.gov/18650079 |
3200 mg single, intravenous dose: 3200 mg route of administration: Intravenous experiment type: SINGLE co-administered: |
XK-469, (R)- plasma | Homo sapiens population: UNHEALTHY age: ADULT sex: FEMALE / MALE food status: UNKNOWN |
|
7.903 μg × h/mL EXPERIMENT https://pubmed.ncbi.nlm.nih.gov/18650079 |
1100 mg single, intravenous dose: 1100 mg route of administration: Intravenous experiment type: SINGLE co-administered: |
XK-469, (R)- plasma | Homo sapiens population: UNHEALTHY age: ADULT sex: FEMALE / MALE food status: UNKNOWN |
|
1.285 μg × h/mL EXPERIMENT https://pubmed.ncbi.nlm.nih.gov/18650079 |
240 mg single, intravenous dose: 240 mg route of administration: Intravenous experiment type: SINGLE co-administered: |
XK-469, (R)- plasma | Homo sapiens population: UNHEALTHY age: ADULT sex: FEMALE / MALE food status: UNKNOWN |
|
162 μg × h/mL EXPERIMENT https://pubmed.ncbi.nlm.nih.gov/18650079 |
30 mg single, intravenous dose: 30 mg route of administration: Intravenous experiment type: SINGLE co-administered: |
XK-469, (R)- plasma | Homo sapiens population: UNHEALTHY age: ADULT sex: FEMALE / MALE food status: UNKNOWN |
|
347 μg × h/mL EXPERIMENT https://pubmed.ncbi.nlm.nih.gov/18650079 |
120 mg single, intravenous dose: 120 mg route of administration: Intravenous experiment type: SINGLE co-administered: |
XK-469, (R)- plasma | Homo sapiens population: UNHEALTHY age: ADULT sex: FEMALE / MALE food status: UNKNOWN |
|
5.161 μg × h/mL EXPERIMENT https://pubmed.ncbi.nlm.nih.gov/18650079 |
850 mg single, intravenous dose: 850 mg route of administration: Intravenous experiment type: SINGLE co-administered: |
XK-469, (R)- plasma | Homo sapiens population: UNHEALTHY age: ADULT sex: FEMALE / MALE food status: UNKNOWN |
|
16.473 μg × h/mL EXPERIMENT https://pubmed.ncbi.nlm.nih.gov/18650079 |
1400 mg single, intravenous dose: 1400 mg route of administration: Intravenous experiment type: SINGLE co-administered: |
XK-469, (R)- plasma | Homo sapiens population: UNHEALTHY age: ADULT sex: FEMALE / MALE food status: UNKNOWN |
|
11.204 μg × h/mL EXPERIMENT https://pubmed.ncbi.nlm.nih.gov/18650079 |
2000 mg single, intravenous dose: 2000 mg route of administration: Intravenous experiment type: SINGLE co-administered: |
XK-469, (R)- plasma | Homo sapiens population: UNHEALTHY age: ADULT sex: FEMALE / MALE food status: UNKNOWN |
|
13.905 μg × h/mL EXPERIMENT https://pubmed.ncbi.nlm.nih.gov/18650079 |
2500 mg single, intravenous dose: 2500 mg route of administration: Intravenous experiment type: SINGLE co-administered: |
XK-469, (R)- plasma | Homo sapiens population: UNHEALTHY age: ADULT sex: FEMALE / MALE food status: UNKNOWN |
T1/2
| Value | Dose | Co-administered | Analyte | Population |
|---|---|---|---|---|
49 h EXPERIMENT https://pubmed.ncbi.nlm.nih.gov/18650079 |
3200 mg single, intravenous dose: 3200 mg route of administration: Intravenous experiment type: SINGLE co-administered: |
XK-469, (R)- plasma | Homo sapiens population: UNHEALTHY age: ADULT sex: FEMALE / MALE food status: UNKNOWN |
|
55 h EXPERIMENT https://pubmed.ncbi.nlm.nih.gov/18650079 |
1100 mg single, intravenous dose: 1100 mg route of administration: Intravenous experiment type: SINGLE co-administered: |
XK-469, (R)- plasma | Homo sapiens population: UNHEALTHY age: ADULT sex: FEMALE / MALE food status: UNKNOWN |
|
56 h EXPERIMENT https://pubmed.ncbi.nlm.nih.gov/18650079 |
240 mg single, intravenous dose: 240 mg route of administration: Intravenous experiment type: SINGLE co-administered: |
XK-469, (R)- plasma | Homo sapiens population: UNHEALTHY age: ADULT sex: FEMALE / MALE food status: UNKNOWN |
|
57 h EXPERIMENT https://pubmed.ncbi.nlm.nih.gov/18650079 |
30 mg single, intravenous dose: 30 mg route of administration: Intravenous experiment type: SINGLE co-administered: |
XK-469, (R)- plasma | Homo sapiens population: UNHEALTHY age: ADULT sex: FEMALE / MALE food status: UNKNOWN |
|
30 h EXPERIMENT https://pubmed.ncbi.nlm.nih.gov/18650079 |
120 mg single, intravenous dose: 120 mg route of administration: Intravenous experiment type: SINGLE co-administered: |
XK-469, (R)- plasma | Homo sapiens population: UNHEALTHY age: ADULT sex: FEMALE / MALE food status: UNKNOWN |
|
43 h EXPERIMENT https://pubmed.ncbi.nlm.nih.gov/18650079 |
850 mg single, intravenous dose: 850 mg route of administration: Intravenous experiment type: SINGLE co-administered: |
XK-469, (R)- plasma | Homo sapiens population: UNHEALTHY age: ADULT sex: FEMALE / MALE food status: UNKNOWN |
|
107 h EXPERIMENT https://pubmed.ncbi.nlm.nih.gov/18650079 |
1400 mg single, intravenous dose: 1400 mg route of administration: Intravenous experiment type: SINGLE co-administered: |
XK-469, (R)- plasma | Homo sapiens population: UNHEALTHY age: ADULT sex: FEMALE / MALE food status: UNKNOWN |
|
47 h EXPERIMENT https://pubmed.ncbi.nlm.nih.gov/18650079 |
2000 mg single, intravenous dose: 2000 mg route of administration: Intravenous experiment type: SINGLE co-administered: |
XK-469, (R)- plasma | Homo sapiens population: UNHEALTHY age: ADULT sex: FEMALE / MALE food status: UNKNOWN |
|
42 h EXPERIMENT https://pubmed.ncbi.nlm.nih.gov/18650079 |
2500 mg single, intravenous dose: 2500 mg route of administration: Intravenous experiment type: SINGLE co-administered: |
XK-469, (R)- plasma | Homo sapiens population: UNHEALTHY age: ADULT sex: FEMALE / MALE food status: UNKNOWN |
PubMed
| Title | Date | PubMed |
|---|---|---|
| In vitro-in vivo correlation for intrinsic clearance for drugs metabolized by human aldehyde oxidase. | 2010-08 |
|
| A phase I and pharmacokinetic study of the quinoxaline antitumour Agent R(+)XK469 in patients with advanced solid tumours. | 2008-08 |
|
| A phase I and pharmacokinetic study of XK469R (NSC 698215), a quinoxaline phenoxypropionic acid derivative, in patients with refractory acute leukemia. | 2008-08 |
|
| Mitotic arrest induced by XK469, a novel antitumor agent, is correlated with the inhibition of cyclin B1 ubiquitination. | 2002-01-01 |
Patents
Sample Use Guides
In Vivo Use Guide
Sources: https://www.ncbi.nlm.nih.gov/pubmed/18650079
850-1100 mg/d on days 1, 3 and 5 of a 21-d cycle and 2500 mg on day 1 of a 21-d cycle.
Route of Administration:
Intravenous
In Vitro Use Guide
Sources: https://www.ncbi.nlm.nih.gov/pubmed/11403918
Exposure of L1210 cells to a 7 uM concentration of the R (+) form of XK469 for 4 h led to a 50% loss of viability.
| Substance Class |
Chemical
Created
by
admin
on
Edited
Mon Mar 31 22:38:39 GMT 2025
by
admin
on
Mon Mar 31 22:38:39 GMT 2025
|
| Record UNII |
8VSJ573G09
|
| Record Status |
Validated (UNII)
|
| Record Version |
|
-
Download
| Name | Type | Language | ||
|---|---|---|---|---|
|
Common Name | English | ||
|
Preferred Name | English | ||
|
Systematic Name | English |
| Code System | Code | Type | Description | ||
|---|---|---|---|---|---|
|
8VSJ573G09
Created by
admin on Mon Mar 31 22:38:39 GMT 2025 , Edited by admin on Mon Mar 31 22:38:39 GMT 2025
|
PRIMARY | |||
|
DTXSID80166279
Created by
admin on Mon Mar 31 22:38:39 GMT 2025 , Edited by admin on Mon Mar 31 22:38:39 GMT 2025
|
PRIMARY | |||
|
157542-91-1
Created by
admin on Mon Mar 31 22:38:39 GMT 2025 , Edited by admin on Mon Mar 31 22:38:39 GMT 2025
|
PRIMARY | |||
|
3246729
Created by
admin on Mon Mar 31 22:38:39 GMT 2025 , Edited by admin on Mon Mar 31 22:38:39 GMT 2025
|
PRIMARY | |||
|
698215
Created by
admin on Mon Mar 31 22:38:39 GMT 2025 , Edited by admin on Mon Mar 31 22:38:39 GMT 2025
|
PRIMARY |
| Related Record | Type | Details | ||
|---|---|---|---|---|
|
|
ACTIVE MOIETY |