U.S. Department of Health & Human Services Divider Arrow National Institutes of Health Divider Arrow NCATS

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
Structure of XK-469 FREE ACID, (R)-

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

HIDE SMILES / InChI

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.

Approval Year

TargetsConditions

Conditions

ConditionModalityTargetsHighest PhaseProduct
Primary
Unknown

Approved Use

Unknown
Primary
Unknown

Approved Use

Unknown
Primary
Unknown

Approved Use

Unknown
Cmax

Cmax

ValueDoseCo-administeredAnalytePopulation
27.9 μg/mL
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
247.6 μg/mL
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
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
292.3 μg/mL
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
173.1 μg/mL
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
4.1 μg/mL
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
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
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
146.3 μg/mL
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
AUC

AUC

ValueDoseCo-administeredAnalytePopulation
1.285 μg × h/mL
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
11.204 μg × h/mL
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
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
16.445 μg × h/mL
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
16.473 μg × h/mL
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
162 μg × h/mL
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
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
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
7.903 μg × h/mL
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
T1/2

T1/2

ValueDoseCo-administeredAnalytePopulation
56 h
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
47 h
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
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
49 h
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
107 h
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
57 h
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
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
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
55 h
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
PubMed

PubMed

TitleDatePubMed
Mitotic arrest induced by XK469, a novel antitumor agent, is correlated with the inhibition of cyclin B1 ubiquitination.
2002 Jan 1
A phase I and pharmacokinetic study of the quinoxaline antitumour Agent R(+)XK469 in patients with advanced solid tumours.
2008 Aug
In vitro-in vivo correlation for intrinsic clearance for drugs metabolized by human aldehyde oxidase.
2010 Aug
Patents

Patents

Sample Use Guides

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
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 Sat Dec 16 09:23:38 GMT 2023
Edited
by admin
on Sat Dec 16 09:23:38 GMT 2023
Record UNII
8VSJ573G09
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
XK-469 FREE ACID, (R)-
Common Name English
PROPANOIC ACID, 2-(4-((7-CHLORO-2-QUINOXALINYL)OXY)PHENOXY)-, (2R)-
Systematic Name English
NSC-698215
Code English
Code System Code Type Description
FDA UNII
8VSJ573G09
Created by admin on Sat Dec 16 09:23:39 GMT 2023 , Edited by admin on Sat Dec 16 09:23:39 GMT 2023
PRIMARY
EPA CompTox
DTXSID80166279
Created by admin on Sat Dec 16 09:23:39 GMT 2023 , Edited by admin on Sat Dec 16 09:23:39 GMT 2023
PRIMARY
CAS
157542-91-1
Created by admin on Sat Dec 16 09:23:39 GMT 2023 , Edited by admin on Sat Dec 16 09:23:39 GMT 2023
PRIMARY
PUBCHEM
3246729
Created by admin on Sat Dec 16 09:23:39 GMT 2023 , Edited by admin on Sat Dec 16 09:23:39 GMT 2023
PRIMARY
NSC
698215
Created by admin on Sat Dec 16 09:23:39 GMT 2023 , Edited by admin on Sat Dec 16 09:23:39 GMT 2023
PRIMARY
Related Record Type Details
ACTIVE MOIETY