所有产品分类
所有产品
信号通路
- Angiogenesis/Protein Tyrosine Kinase
- Apoptosis Pathway
- Cell Cycle/DNA Damage
- Epigenetics
-
GPCR/G Protein
- Urotensin Receptor
- Melatonin Receptor
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Neuro Signaling Pathway
- Imidazoline Receptor
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Protease/Metabolic Enzyme
- COMT
- 11β HSD
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- Pyruvate Kinase
- Mitochondrial Metabolism
- ALDH
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- Serine Protease
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- E1 E2 E3 Enzyme
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研究领域
- Metabolic Disease
- Neurological Disease
- Endocrinology
- Diabetes
- Cardiovascular Disease
- Immunology
- Allergy
- Inflammation
- Infection
- Cancer
天然产物
抗体
多肽
催化剂
杂质对照品
医药中间体
基础原料
Aurora
结构式 | 货号 | 产品名称 | CAS号 |
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BCP49223 | Tinengotinib 新 | 2230490-29-4 | |
Tinengotinib is an antineoplastic tyrosine kinase inhibitor.Tinengotinib is the modulator of one or more protein kinases such as Aurora kinase and VEGFR kinase.
|
BCP48936 | Aurora Kinase Inhibitor II 新 | 331770-21-9 | |
Aurora Kinase Inhibitor II is a selective and ATP-competitive Aurora kinase inhibitor with IC50s of 310 nM and 240 nM for Aurora A and Aurora B, respectively.
|
BCP48903 | SP-146 新 | 2682114-54-9 | |
SP-146 is a potent, selective and non-ATP-competitive inhibitor of Aurora B with IC50 of 0.316 nM. SP-146 can be used for the research of triple negative breast cancer (TNBC).
|
BCP42843 | Aurora B抑制剂1 新 | 937276-52-3 | |
Aurora B inhibitor 1 is an Aurora B (Aurora-1) inhibitor extracted from patent WO2007059299A1, compound 1-3, has a Ki value of <0.010 uM.
|
BCP35921 | SP-146 新 | SP-146 | |
SP-146 is a potent, selective and non-ATP-competitive inhibitor of Aurora B with IC50 of 0.316 nM.
|
BCP33311 | Phthalazinone pyrazole 新 | 880487-62-7 | |
Phthalazinone pyrazole is a potent, selective and orally bioavailable inhibitor of Aurora-A kinase.
|
BCP30248 | Aurora Kinase Inhibitor III 新 | 879127-16-9 | |
Aurora kinase inhibitor III is a potent inhibitor of Aurora A kinase (IC50 = 42 nM).
|
BCP28083 | Cenisertib 新 | 871357-89-0 | |
Cenisertib selectively binds to and inhibits aurora kinases (AKs), a family of serine-threonine kinases which are important regulators of cell division and proliferation, and which are overexpressed in certain types of cancer.
|
BCP29563 | CCT241736 | 1402709-93-6 | |
CCT241736 is a novel, orally bioavailable, imidazo[4,5-b]pyridine derivative discovered at our Institute, highly selective for FLT3 and Aurora kinases with an S(10) selectivity score using KINOMEscan™ technology of 0.057 (fraction of 386 non-mutant kinases inhibited >90% when screened at 1 uM of CCT241736; San Diego, CA).
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