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
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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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- E1 E2 E3 Enzyme
- Elastase
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- Integrase
- Phosphodiesterase/PDE
- Phospholipase
- LXR
- Proteasome
- Cytochrome P450
- TGF beta/Smad
- Wnt/Stem Cell
- Others Pathway
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
PKD
结构式 | 货号 | 产品名称 | CAS号 |
---|
BCP37818 | CRT5 新 | 1034297-58-9 | |
CRT5 is a pyrazine benzamide that prevents activation of all three isoforms of PKD in endothelial cells treated with VEGF (IC50s = 1, 2, and 1.5 nM for PKD1, PKD2, and PKD3, respectively).
|
BCP09714 | CID797718 | 370586-05-3 | |
CID 797718 is a potential PKD binding agent.
|
BCP09959 | kb-NB77-78 | 1350622-33-1 | |
kb-NB77-78 is an analog of CID797718, which is a by-product of the synthesis of the parental compound, CID755673(PKD1 inhibitor).
|
BCP19777 | CRT0066101 dihydrochloride 新 | 1883545-60-5 | |
CRT0066101 dihydrochloride is a potent and specific PKD inhibitor with IC50 values of 1, 2.5 and 2 nM for PKD1, 2, and 3 respectively.
|
BCP06823 | CID-2011756 | 638156-11-3 | |
CID-2011756 is a cell-active ATP competitive and specific PKD1 inhibitor that inhibits phorbol ester-induced endogenous PKD1 activation in LNCaP prostate cancer cells.
|
BCP09660 | CID 755673 | 521937-07-5 | |
CID 755673 is a selective and potent protein kinase D1-D3, PKC, CAK, PLK1 and CAMKIIα inhibitor.
|
BCP06729 | kb NB 142-70 | 1233533-04-4 | |
kb NB 142-70 is a selective protein kinase D (PKD) inhibitor (IC50 values are 28.3, 58.7 and 53.2 nM for PKD1, 2 and 3 respectively).
|