76 Results for "

Ca2 /calmodulin

" in MedChemExpress (MCE) Product Catalog:
Products (76)

76 Results for "Ca2 /calmodulin" in MCE Product Catalog:

Cat. No.: HY-P85537
Synonyms: Brain Ca; 2; Calmodulin dependent protein kinase type 4; Brain Ca; 2; Calmodulin dependent protein kinase type IV; Brain Ca -Calmodulin dependent protein kinase type IV; Calcium / Calmodulin dependent protein kinase type 4 Catalytic chain; Calcium / Calmodulin dependent protein kinase type IV Catalytic chain; Calcium/Calmodulin dependent protein kinase IV; Calcium/Calmodulin dependent protein kinase type IV; Calcium/Calmodulin-dependent protein kinase type IV; CaM kinase 4; CaM kinase GR; CaM kinase IV; CaM kinase-GR; CaMK 4; CaMK GR; CaMK IV; CaMK4; CaMKGR; IV; KCC4_HUMAN; MGC36771.

Host:  

Mouse

Application:  

WB

Reactivity:  

Human

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Cat. No.: HY-P2209
CAS No.: 53947-96-9
Synonyms: Daechuine S27; N-Demethylamphibine H
Nummularine B (Daechuine S27; N-Demethylamphibine H) is an anti-parasite agent. Nummularine B inhibits calmodulin-dependent phosphodiesterase activity with an IC50 of 16.8 μM. Nummularine B inhibits the growth of Plasmodium and Leishmania donovani in vitro. Nummularine B inhibits the calmodulin-dependent activity of actomyosin Ca 2+-ATPase. Nummularine B is applicable to research related to malaria and visceral leishmaniasis .
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Cat. No.: HY-P700579
Purity:  ≥ 90%, as determined by reducing SDS-PAGE.
Synonyms: CaMK4; CaM Kinase IV; Calcium/Calmodulin Dependent Protein Kinase IV; CaMK IV; CaMK-GR; Brain Ca(2+)-Calmodulin-Dependent Protein Kinase Type IV; CaMKIV; CaM Kinase-GR; Calcium/Calmodulin-Dependent Protein Kinase Type IV Catalytic Chain; CaMK-GR; Brain Ca
Species:  
Rat
Source:  
E. coli
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Cat. No.: HY-P75457
Purity:  ≥ 95%, as determined by reducing SDS-PAGE.
Synonyms: CaMK4; CaM Kinase IV; Calcium/Calmodulin Dependent Protein Kinase IV; CaMK IV; CaMK-GR; Brain Ca(2+)-Calmodulin-Dependent Protein Kinase Type IV; CaMKIV; CaM Kinase-GR; Calcium/Calmodulin-Dependent Protein Kinase Type IV Catalytic Chain; CaMK-GR; Brain Ca
Species:  
Mouse
Source:  
Sf9 insect cells
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Cat. No.: HY-N18431
CAS No.: 129744-24-7
Synonyms: ST-A TFA
Stellettamide A TFA is a marine toxin found in a marine sponge. Stellettamide A TFA is a calmodulin inhibitor. Stellettamide A TFA can inhibit Ca 2+/Mg 2+ ATPase, phosphodiesterase, myosin light chain , and Mg 2+-ATPase. Stellettamide A TFA inhibits high K +- and Ca 2+-induced contraction in permeabilized smooth muscle. Stellettamide A TFA exhibits antifungal activity against Mortierella remannianus. Stellettamide A TFA can be used for the research of fungal infection .
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Cat. No.: HY-P76761
Purity:  ≥ 85%, as determined by reducing SDS-PAGE.
Synonyms: CaMK2A; CaM-Kinase II Alpha Chain; Prev. CaMKA; CaMK-II Subunit Alpha; CaMKIINalpha; Ca2+/Calmodulin-Dependent Protein Kinase II Alpha Subunit; KIAA0968; Calcium/Calmodulin-Dependent Protein Kinase; Calcium/Calmodulin-Dependent Protein Kinase (CaM Kinase)
Species:  
Human
Source:  
Sf9 insect cells
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Cat. No.: HY-P702652
Purity:  ≥ 80%, as determined by reducing SDS-PAGE.
Synonyms: CaMK4; CaM Kinase IV; Calcium/Calmodulin Dependent Protein Kinase IV; CaMK IV; CaMK-GR; Brain Ca(2+)-Calmodulin-Dependent Protein Kinase Type IV; CaMKIV; CaM Kinase-GR; Calcium/Calmodulin-Dependent Protein Kinase Type IV Catalytic Chain; CaMK-GR; Brain Ca
Species:  
Human
Source:  
Sf9 insect cells
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Cat. No.: HY-N18114
CAS No.: 162426-22-4
rel-(E)-6,7-Transdihydroxyligustilide is a compound found in the dried tuberous roots of Polygonum multiflorum. rel-(E)-6,7-Transdihydroxyligustilide inhibits Ca 2+‑ATPase in calmodulin-deficient human erythrocyte membranes. rel-(E)-6,7-Transdihydroxyligustilide is used for the research of hyperlipidemia .
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Cat. No.: HY-119884
CAS No.: 1261080-40-3
Research Areas:  

Cancer

DC-120 is an ATP-competitive AKT inhibitor, with particular activity against AKT1 (an IC50 of 0.153 μM). DC-120 functionally blocks AKT kinase activity and reduces the phosphorylation levels of FOXO3a and GSK-3β. DC-120 induces cancer cell apoptosis (apoptosis) and inhibits cancer cell proliferation. DC-120 activates the mTORC1 pathway via the Ca 2+/calmodulin (calmodulin)/hVps34 signaling pathway. DC-120 abrogates AKT-mediated inhibition of CRAF, thereby activating the MEK/ERK MAPK pathway. DC-120 exerts anti-tumor activity in a nude mouse hepatocellular carcinoma xenograft model. DC-120 can be used for hepatocellular carcinoma-related research .
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Cat. No.: HY-P810844
Synonyms: Adenylate cyclase type 1, ATP pyrophosphate-lyase 1, Adenylate cyclase type I, Adenylyl cyclase 1, Ca(2+)/Calmodulin-activated adenylyl cyclase, ADCY1

Host:  

Rabbit

Application:  

WB, IHC-P, ICC/IF

Reactivity:  

Human, Mouse, Rat

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Cat. No.: HY-P811357
Synonyms: KIAA0015, POPX2, PPM1F, Protein phosphatase 1F, Ca(2+)/Calmodulin-dependent protein kinase phosphatase, Partner of PIX 2, Protein fem-2 homolog, CaM-kinase phosphatase, CaMKPase, hFem-2

Host:  

Rabbit

Application:  

WB, IHC-P

Reactivity:  

Human, Mouse

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Cat. No.: HY-P87013
Synonyms: Ca(2+)/Calmodulin-dependent protein kinase phosphatase N antibody; CaMKN antibody; CaMKP-N antibody; CaMKP-nucleus antibody; KIAA1072 antibody; Nuclear Calmodulin dependent protein kinase phosphatase antibody; Partner of PIX 1 antibody; Partner of PIX-alpha antibody; Partner of PIXA antibody; POPX1 antibody; Ca(2+)/Calmodulin-dependent protein kinase phosphatase N antibody; CaMKN antibody; CaMKP-N antibody; CaMKP-nucleus antibody; KIAA1072 antibody; Nuclear Calmodulin dependent protein kinase phosphatase antibody; Partner of PIX 1 antibody; Partner of PIX-alpha antibody; Partner of PIXA antibody; POPX1 antibody; PP2CH antibody; Ppm1e antibody; PPM1E_HUMAN antibody; Protein phosphatase 1E antibody; Protein phosphatase Mg2+/Mn2+ dependent 1E antibody;

Host:  

Rabbit

Application:  

WB

Reactivity:  

Human

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Cat. No.: HY-19805R
CAS No.: 52029-86-4
STO-609 (Standard) is the analytical standard of STO-609 (HY-19805). This product is intended for research and analytical applications. STO-609 is a selective and cell-permeable inhibitor of the Ca 2+/calmodulin-dependent protein Kinase Kinase (CaM-KK), with Ki values of 80 and 15 ng/mL for recombinant CaM-KKα and CaM-KKβ, respectively. STO-609 inhibits AMP-activated protein Kinase Kinase (AMPKK) activity in HeLa cell lysates with an IC50 ~0.02 g/ml.
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Cat. No.: HY-P703005
Purity:  ≥ 80%, as determined by reducing SDS-PAGE.
Synonyms: PPM1F; Protein Phosphatase 1F (PP2C Domain Containing); Protein Phosphatase, Mg2+/Mn2+ Dependent 1F; CaM-Kinase Phosphatase; Ca(2+)/Calmodulin-Dependent Protein Kinase Phosphatase; Protein Fem-2 Homolog; CaMKPase; Protein Phosphatase 1F (PP2C Domain Conta
Species:  
Human
Source:  
E. coli
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Cat. No.: HY-N2595
CAS No.: 5574-24-3
Synonyms: O-Methylatheroline
Oxoglaucine (O-Methylatheroline) is a natural product with multiple activities including autophagy activation, anti-inflammation, antibacterial activity, and immunoregulation. Oxoglaucine inhibits the TRPV5/calmodulin/CAMK-II pathway, suppresses TGFβ-induced Smad2 phosphorylation by upregulating Smad7, blocks Ca 2+ influx, activates autophagy, alleviates apoptosis and inflammation, inhibits ROS production and the expression of fibrosis markers in hepatocytes, and regulates immune cell populations and responses. Oxoglaucine protects against infections caused by Candida albicans and Klebsiella pneumoniae, and exerts effects on adjuvant-induced arthritis. Oxoglaucine can be used in studies related to arthritis, liver fibrosis, bacterial infections, and fungal infections .
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Cat. No.: HY-W751362
CAS No.: 14176-10-4
Cetiedil is a vasodilator and potassium channel blocker with anti-sickle cell and analgesic activities. Cetiedil increases cyclic adenosine monophosphate levels, relaxes vascular smooth muscle, and blocks the action of Bradykinin (HY-P0206). Cetiedil inhibits platelet aggregation, reduces plasma fibrinogen concentration and blood viscosity, suppresses sickling of sickle red blood cells and improves their filterability, and decreases irreversible sickle cells. Cetiedil binds to calmodulin, inhibits Ca 2+-dependent potassium permeability of erythrocyte membranes, increases sodium permeability of erythrocytes, and regulates polymorphonuclear leukocyte function. Cetiedil can be used in research related to intermittent claudication, arteriosclerosis obliterans, diabetic arteriosclerosis, Raynaud's disease, angina pectoris, and sickle cell anemia .
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