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Targeted therapy! The Capetin Prize winning "Click Chemistry" can be used like this!Targeted therapy! The Nobel Prize winning "Click Chemistry" can be used like this!2025-02-06
19 Results for "
CaMKI
" in MedChemExpress (MCE) Product Catalog:
Products (19)
19 Results for "CaMKI" in MCE Product Catalog:
Target:
Research Areas:
CS640 (Compound 19) is a chemical probe and a calmodulin-dependent kinase inhibitor. CS640 inhibits CaMK1D, CaMK1B, CaMK1A, CaMK1G, MEK5, RIPK4, mLK3 and PIP5K1, with IC50 values of 8, 3, 1, 1, 25 nM, 5.69, 2.75 and 11.2 μM, respectively. CS640 blocks Aβ-induced hyperphosphorylation of tau protein at the Thr181 site, but fails to protect primary mouse cortical neurons from Aβ-induced toxic damage. CS640 is applicable to research related to Alzheimer's disease .
Cat. No.: HY-P10316
CAS No.: 205598-38-5
Synonyms: Calmodulin-Dependent Protein Kinase I (299-320) Binding Domain
Cat. No.: HY-RS01851
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CAMK1 Human Pre-designed siRNA Set A contains three designed siRNAs for CAMK1 gene (Human), as well as a negative control, a positive control, and a FAM-labeled negative control.
Cat. No.: HY-RS11915
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Research Areas:
Rgs19 Rat Pre-designed siRNA Set A contains three designed siRNAs for Rgs19 gene (Rat), as well as a negative control, a positive control, and a FAM-labeled negative control.
Cat. No.: HY-RS24641
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Research Areas:
Camk1 Rat Pre-designed siRNA Set A contains three designed siRNAs for Camk1 gene (Rat), as well as a negative control, a positive control, and a FAM-labeled negative control.
Target:
Research Areas:
CaMKP inhibitor sodium (compound 5) is an inhibitor of Ca 2+/neutral protein-dependent protein concentration (CaMKP) and its nuclear type (CaMKP-N) (IC50: 6.4 μM, CaMKP; 6.6 μM, CaMKP-N). CaMKP is one type of Ser/Thr protein, which can be passed through to remove the oxidized oxidized protein (CaMK). CaMKP inhibitor sodium inhibits CaMKP mediated phospho-CaMKI hydrolysis, unaffectes protein phosphoric acid 2C (PP2C) and calcineurin (CaN) .
Cat. No.: HY-P702654
Purity: ≥ 80%, as determined by reducing SDS-PAGE.
Synonyms: CAMK1; calcium/calmodulin-dependent protein kinase I; calcium/calmodulin-dependent protein kinase type 1; CaMKI; caM-KI; CaMKI-alpha; caM kinase I alpha; CaMKI; MGC120317; MGC120318;
Species:
Source:
Cat. No.: HY-P705662
Purity: ≥ 85%, as determined by reducing SDS-PAGE.
Synonyms: rHuCAMK1, His; Calcium/Calmodulin-Dependent Protein Kinase Type 1; CaM Kinase I; CaMKI-Alpha; CAMK1
Cat. No.: HY-P76191
Purity: ≥ 85%, as determined by reducing SDS-PAGE.
Synonyms: Calcium/calmodulin-dependent protein kinase type 1G; CaMKI gamma; CLICK III; CLICK3; VWS1
Species:
Source:
Cat. No.: HY-P82592A
Synonyms: CAM kinase 2 delta; CAM kinase II delta; CaM kinase II delta subunit; CaM kinase II subunit delta; CAMK 2d; CaMK-II delta subunit; CAMK2D; CaMKI
Cat. No.: HY-P702653
Purity: ≥ 80%, as determined by reducing SDS-PAGE.
Synonyms: Calcium/calmodulin-dependent protein kinase type 1D; CaM kinase I delta; CaM kinase ID; CaM-KI delta; CaMKI delta; CaMKID
Species:
Source:
Cat. No.: HY-P701757
Purity: ≥ 90%, as determined by reducing SDS-PAGE.
Synonyms: PNCK; Calcium/calmodulin-dependent protein kinase type 1B; CaM kinase I beta; CaM kinase IB; CaM-KI beta; CaMKI-beta; Pregnancy up-regulated non-ubiquitously-expressed CaM kinase
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Source:
Cat. No.: HY-184599
Research Areas:
OICR-403184 is a selective RNA-dependent protein kinase (PKR) inhibitor with limited brain penetration, with an IC50 of 263 nM. OICR-403184 blocks the phosphorylation of eIF2α downstream of PKR. OICR-403184 is applicable to the research of inflammatory bowel disease .
Cat. No.: HY-P80580A
Synonyms: CaM K1; CaM KI; CaMK 1; CAMK I; CaMK1 alpha; CAMK1 PEN; CaMKI alpha
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Protocols
Targeted therapy! The Capetin Prize winning "Click Chemistry" can be used like this!Targeted therapy! The Nobel Prize winning "Click Chemistry" can be used like this!A suitable model is crucial in drug screening experiments. Organs can mimic the three-dimensional functional structure of internal organs, have similar spatial organization to corresponding organs, maintain some key characteristics, and reproduce some physiological functions. They are widely used for modeling and personalized drug screening physiological functions.2025-02-06
