Drug Information
Drug General Information | Top | |||
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Drug ID |
D06LJL
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Former ID |
DIB019503
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Drug Name |
PMID16451062C46
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Synonyms |
GTPL8355; GSK-623906A; BDBM50181532
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Drug Type |
Small molecular drug
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Indication | Discovery agent [ICD-11: N.A.] | Investigative | [1] | |
Structure |
Download2D MOL
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Formula |
C29H33FN6O4S
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Canonical SMILES |
COC1=C(C=C2C(=C1)C(=NC=N2)NC3=NC=C(S3)CC(=O)NC4=CC(=CC=C4)F)OCCCN5CCC(CC5)CO
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InChI |
1S/C29H33FN6O4S/c1-39-25-14-23-24(15-26(25)40-11-3-8-36-9-6-19(17-37)7-10-36)32-18-33-28(23)35-29-31-16-22(41-29)13-27(38)34-21-5-2-4-20(30)12-21/h2,4-5,12,14-16,18-19,37H,3,6-11,13,17H2,1H3,(H,34,38)(H,31,32,33,35)
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InChIKey |
QNJAKUMXJFWQOG-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 | [1] |
Aurora kinase C (AURKC) | Target Info | Inhibitor | [1] | |
KEGG Pathway | Oocyte meiosis | |||
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 | ||||
EGF/EGFR Signaling Pathway | ||||
JAK/STAT | ||||
Gastric Cancer Network 1 | ||||
Integrated Breast Cancer Pathway |
References | Top | |||
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REF 1 | Discovery of novel and potent thiazoloquinazolines as selective Aurora A and B kinase inhibitors. J Med Chem. 2006 Feb 9;49(3):955-70. |
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