Details
Stereochemistry | ACHIRAL |
Molecular Formula | C20H21ClN4O4 |
Molecular Weight | 416.858 |
Optical Activity | NONE |
Defined Stereocenters | 0 / 0 |
E/Z Centers | 0 |
Charge | 0 |
SHOW SMILES / InChI
SMILES
CCCNC(=O)NC1=CC=C(OC2=C3C=C(OC)C(OC)=CC3=NC=N2)C=C1Cl
InChI
InChIKey=VPBYZLCHOKSGRX-UHFFFAOYSA-N
InChI=1S/C20H21ClN4O4/c1-4-7-22-20(26)25-15-6-5-12(8-14(15)21)29-19-13-9-17(27-2)18(28-3)10-16(13)23-11-24-19/h5-6,8-11H,4,7H2,1-3H3,(H2,22,25,26)
DescriptionSources: https://www.ncbi.nlm.nih.gov/pubmed/15634658Curator's Comment: Description was created based on several sources, including
http://adisinsight.springer.com/drugs/800017407
Sources: https://www.ncbi.nlm.nih.gov/pubmed/15634658
Curator's Comment: Description was created based on several sources, including
http://adisinsight.springer.com/drugs/800017407
KRN633 is a selective inhibitor of Vascular endothelial growth factor receptors VEGFR-1, -2, and -3. KRN633 also blocked the activation of mitogen-activated protein kinases by VEGF, along with human umbilical vein endothelial cell proliferation and tube formation. KRN633 inhibited tumor growth in several in vivo tumor xenograft models with diverse tissue origins, including lung, colon, and prostate, in athymic mice and rats. Kirin Brewery developed angiogenesis inhibitor KRN 633 as a treatment for solid tumours. It is in phase I clinical trials.
Originator
Approval Year
Targets
Primary Target | Pharmacology | Condition | Potency |
---|---|---|---|
Target ID: CHEMBL1868 Sources: https://www.ncbi.nlm.nih.gov/pubmed/15634658 |
170.0 nM [IC50] | ||
Target ID: CHEMBL279 Sources: https://www.ncbi.nlm.nih.gov/pubmed/15634658 |
160.0 nM [IC50] | ||
Target ID: CHEMBL1955 Sources: https://www.ncbi.nlm.nih.gov/pubmed/15634658 |
125.0 nM [IC50] |
Conditions
Condition | Modality | Targets | Highest Phase | Product |
---|---|---|---|---|
Primary | Unknown Approved UseUnknown |
Cmax
Value | Dose | Co-administered | Analyte | Population |
---|---|---|---|---|
2.29 μg/mL/(mg dose/kg) EXPERIMENT https://pubmed.ncbi.nlm.nih.gov/16432165 |
3 mg/kg single, oral dose: 3 mg/kg route of administration: Oral experiment type: SINGLE co-administered: |
KRN-633 plasma | Rattus norvegicus population: HEALTHY age: ADULT sex: MALE food status: UNKNOWN |
|
899 ng/mL EXPERIMENT https://pubmed.ncbi.nlm.nih.gov/15634658 |
20 mg/kg single, oral dose: 20 mg/kg route of administration: Oral experiment type: SINGLE co-administered: |
KRN-633 plasma | Mus musculus population: UNKNOWN age: ADULT sex: UNKNOWN food status: UNKNOWN |
AUC
Value | Dose | Co-administered | Analyte | Population |
---|---|---|---|---|
25.4 μg × h/mL/(mg dose/kg) EXPERIMENT https://pubmed.ncbi.nlm.nih.gov/16432165 |
3 mg/kg single, oral dose: 3 mg/kg route of administration: Oral experiment type: SINGLE co-administered: |
KRN-633 plasma | Rattus norvegicus population: HEALTHY age: ADULT sex: MALE food status: UNKNOWN |
|
7800 ng × h/mL EXPERIMENT https://pubmed.ncbi.nlm.nih.gov/15634658 |
20 mg/kg single, oral dose: 20 mg/kg route of administration: Oral experiment type: SINGLE co-administered: |
KRN-633 plasma | Mus musculus population: UNKNOWN age: ADULT sex: UNKNOWN food status: UNKNOWN |
T1/2
Value | Dose | Co-administered | Analyte | Population |
---|---|---|---|---|
7.93 h EXPERIMENT https://pubmed.ncbi.nlm.nih.gov/16432165 |
3 mg/kg single, oral dose: 3 mg/kg route of administration: Oral experiment type: SINGLE co-administered: |
KRN-633 plasma | Rattus norvegicus population: HEALTHY age: ADULT sex: MALE food status: UNKNOWN |
|
2.24 h EXPERIMENT https://pubmed.ncbi.nlm.nih.gov/15634658 |
20 mg/kg single, oral dose: 20 mg/kg route of administration: Oral experiment type: SINGLE co-administered: |
KRN-633 plasma | Mus musculus population: UNKNOWN age: ADULT sex: UNKNOWN food status: UNKNOWN |
Sample Use Guides
In Vivo Use Guide
Sources: https://www.ncbi.nlm.nih.gov/pubmed/15634658
In standard xenograft models, once-daily administration of KRN633 produced >50% tumor growth inhibition in LC-6-LCK, HT29, Ls174T, and LNCap cells, and slight regression of A549 tumors at 100 mg/kg/d
Route of Administration:
Oral
In Vitro Use Guide
Sources: https://www.ncbi.nlm.nih.gov/pubmed/15634658
30-100 nM KRN633 can block survival signaling by VEGF and trigger the apoptosis of HUVECs
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286370-15-8
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CHEMBL406381
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9549295
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DTXSID60429551
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E1V875I8DX
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admin on Sat Dec 16 09:27:42 GMT 2023 , Edited by admin on Sat Dec 16 09:27:42 GMT 2023
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ACTIVE MOIETY