Drug Information
Drug General Information | Top | |||
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Drug ID |
D01TDV
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Former ID |
DIB019176
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Drug Name |
PMID21742770C1
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Synonyms |
GTPL8190; BDBM50400690
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Drug Type |
Small molecular drug
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Indication | Discovery agent [ICD-11: N.A.] | Investigative | [1], [2] | |
Structure |
Download2D MOL
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Formula |
C25H28N6O2
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Canonical SMILES |
CN1CCN(CC1)C2=C(C=C(C=C2)NC3=NC4=C(C=C3)C=NN4C5=CC=C(C=C5)OC)OC
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InChI |
1S/C25H28N6O2/c1-29-12-14-30(15-13-29)22-10-5-19(16-23(22)33-3)27-24-11-4-18-17-26-31(25(18)28-24)20-6-8-21(32-2)9-7-20/h4-11,16-17H,12-15H2,1-3H3,(H,27,28)
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InChIKey |
LZQFMCFJCXQTTG-UHFFFAOYSA-N
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PubChem Compound ID | ||||
PubChem Substance ID |
Target and Pathway | Top | |||
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Target(s) | Aurora B messenger RNA (AURKB mRNA) | Target Info | Inhibitor | [2] |
Fungal Protein kinase A (Fung ypkA) | Target Info | Inhibitor | [2] | |
Serine/threonine-protein kinase 33 (STK33) | Target Info | Inhibitor | [1] | |
Pathway Interaction Database | Aurora B signaling | |||
Signaling by Aurora kinases | ||||
Aurora C signaling | ||||
FOXM1 transcription factor network | ||||
Aurora A signaling | ||||
Reactome | APC/C:Cdh1 mediated degradation of Cdc20 and other APC/C:Cdh1 targeted proteins in late mitosis/early G1 | |||
Separation of Sister Chromatids | ||||
Resolution of Sister Chromatid Cohesion | ||||
RHO GTPases Activate Formins | ||||
Mitotic Prometaphase | ||||
WikiPathways | Mitotic Metaphase and Anaphase | |||
Mitotic Prometaphase | ||||
Regulation of Microtubule Cytoskeleton | ||||
miR-targeted genes in lymphocytes - TarBase | ||||
miR-targeted genes in epithelium - TarBase | ||||
APC/C-mediated degradation of cell cycle proteins |
References | Top | |||
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REF 1 | STK33 kinase activity is nonessential in KRAS-dependent cancer cells. Cancer Res. 2011 Sep 1;71(17):5818-26. | |||
REF 2 | A Potent and Selective Quinoxalinone-Based STK33 Inhibitor Does Not Show Synthetic Lethality in KRAS-Dependent Cells. ACS Med Chem Lett. 2012 Dec 13;3(12):1034-1038. |
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