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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- nAChR
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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
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- Phosphatase
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- HCV Protease
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- Factor Xa
- DPP
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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
CaMK
结构式 | 货号 | 产品名称 | CAS号 |
---|
BCP46455 | 钙调蛋白抑制剂 新 | 57265-65-3 | |
Calmidazolium chloride is a calmodulin (CaMK) antagonist, antagonizing CaM-dependent phosphodiesterase and calmodulin-induced activation of erythrocyte Ca2+-transporting ATPase with IC50s of 0.15 and 0.35 μM, respectively. Also in anti-cancer research. Calmidazolium binds to CaMK with a Kd of 3 nM.
|
BCP37347 | 赤霉酸盐酸盐 新 | 78957-85-4 | |
A-3 hydrochloride is an inhibitor of PKA, PKC, and casein kinase I and II, and MLCK.
|
BCP35203 | KN92 新 | 176708-42-2 | |
KN-92 is an inactive derivative of KN-93.
|
BCP28798 | A 484954 新 | 142557-61-7 | |
A 484954 is a selective inhibitor of eEF2K with IC50 value of 0.28 μM.
|
BCP29662 | NH125 | 278603-08-0 | |
NH125 is a selective eEF-2 kinase inhibitor with IC50 of 60 nM, >125-fold selectivity over PKC, PKA, and CaMKII, and also a potent histidine kinase inhibitor.
|
BCP07924 | 头孢曲嗪 | 51627-14-6 | |
Cefatrizine, also known as BL-S-640 and S-640P, is a eukaryotic elongation factor-2 kinase inhibitor with an anti-proliferative activity toward breast cancer cells.
|
BCP19054 | CaMKII-IN-1 | 1208123-85-6 | |
CaMKII-IN-1 is a potent and highly selective CaMKII inhibitor with IC50 of 63 nM; significantly high selectivity against CaMKIV, MLCK, p38a, Akt1, and PKC.
|
BCP02708 | KN62 | 127191-97-3 | |
KN-62 is selective, cell-permeable inhibitor of CaM kinase II (IC50 = 0.9 μM).
|
BCP19299 | STO-609 acetate | 1173022-21-3 | |
STO-609 is a cell-permeable inhibitor of calcium/calmodulin-dependent kinase kinases (CaMKK) isoforms CaMKKα and CaMKKβ (Ki = 80 and 15 ng/ml, respectively).
|
BCP25514 | STO-609 | 52029-86-4 | |
STO-609 is a selective and cell-permeable inhibitor of the Ca2+/calmodulin-dependent protein kinase kinase (CaM-KK), with Ki values of 80 and 15 ng/mL for recombinant CaM-KKα and CaM-KKβ, respectively.
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