26 Results for "

SK2

" in MedChemExpress (MCE) Product Catalog:
Products (26)

26 Results for "SK2" in MCE Product Catalog:

7
7 Cited Publications
Cat. No.: HY-16015
CAS No.: 915385-81-8
Synonyms: ABC294640
Target:  

SphK

Research Areas:  

Cancer

Opaganib (ABC294640) is a selective, competitive sphingosine kinase 2 (SK2) inhibitor with Ki of 9.8 μM.
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Cat. No.: HY-102070
CAS No.: 1063331-94-1
Purity:  99.62%
Target:  

Potassium Channel

Research Areas:  

Neurological Disease

NS13001 is a potent, selective, orally active allosteric positive modulator of SK channels (small conductance calcium-activated potassium channels). The EC50s are 1.8 and 0.14 μM for SK2 and SK3, respectively. NS13001 holds promise as a potential therapeutic agent for treatment of spinocerebellar ataxia type 2 (SCA2) and possibly other cerebellar ataxias .
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Cat. No.: HY-P991600

Target:  

Interleukin Related

Research Areas:  

Inflammation/Immunology Cancer

Anti-IL-6 Antibody (Chugai SK2) is a murine monoclonal antibody, targeting IL-6. Anti-IL-6 Antibody (Chugai SK2) can be used for inflammatory diseases and cancers research, such as rheumatoid arthritis (RA), crohn's disease (CD) and pancreatic, lung and colon cancer .
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Cat. No.: HY-12550
CAS No.: 660846-41-3
Purity:  98.79%
Target:  

Potassium Channel

Research Areas:  

Neurological Disease

GW542573X is a potent and selective Ca 2+-activated K + 2 (SK2) channels activator. GW542573X induces the Ca 2+-response curve of hSK1 that left-shifted from an EC50 (Ca 2+) value of 410 nM to 240 nM .
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Cat. No.: HY-12005R
CAS No.: 162359-56-0
Synonyms: FTY720 (Standard)
Fingolimod (hydrochloride) (Standard) is the analytical standard of Fingolimod (hydrochloride). This product is intended for research and analytical applications. Fingolimod hydrochloride (FTY720), an analog of sphingosine, is a potent sphingosine 1-phosphate (S1P) receptors modulator. Fingolimod hydrochloride is phosphorylated by sphingosine kinases, particularly by SK2, and then binds S1PR1, 3, 4, and 5. Fingolimod hydrochloride induces the internalization of S1P1, and consequently, inhibits S1P activity. Fingolimod hydrochloride also is a pak1 activator .
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Cat. No.: HY-16015A
CAS No.: 1185157-59-8
Synonyms: ABC294640 hydrochloride
Target:  

SphK

Research Areas:  

Cancer

Opaganib (ABC294640) hydrochloride is a selective, competitive sphingosine kinase 2 (SK2) inhibitor with Ki of 9.8 μM.
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Cat. No.: HY-12900
CAS No.: 1425049-20-2
Target:  

SphK

Research Areas:  

Inflammation/Immunology Cancer

RB-005 is a selective inhibitor of sphingosine kinase 1 (SK1) (IC50=3.6 µM), with weaker inhibition of another isoenzyme, SK2. The selective inhibition of RB-005 helps to distinguish the biological functions and roles of SK1 and SK2, which can be used in the study of inflammatory diseases and cancer .
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Cat. No.: HY-16015R
CAS No.: 915385-81-8
Synonyms: ABC294640 (Standard)
Research Areas:  

Cancer

Opaganib (Standard) is the analytical standard of Opaganib. This product is intended for research and analytical applications. Opaganib (ABC294640) is a selective, competitive sphingosine kinase 2 (SK2) inhibitor with Ki of 9.8 μM.
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Cat. No.: HY-RS13667
Research Areas:  

Others

SPHK2 Human Pre-designed siRNA Set A contains three designed siRNAs for SPHK2 gene (Human), as well as a negative control, a positive control, and a FAM-labeled negative control.

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Cat. No.: HY-P1424
CAS No.: 1061556-49-7
Target:  

Potassium Channel

Research Areas:  

Neurological Disease

Lei-Dab7 is a potent and selective SK2 (KCa2.2) channels blocker with a Kd of 3.8 nM. Lei-Dab7 shows low or no activity on KCa1, KCa3, Kv and Kir2.1 channels [2].
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Cat. No.: HY-P702913
Purity:  ≥ 90%, as determined by reducing SDS-PAGE.
Synonyms: SPHK2; Sphingosine Kinase; Sphingosine Kinase 2; SPK-2; SPK 2; SK-2; SK 2; SK2
Species:  
Human
Source:  
Sf9 insect cells
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Cat. No.: HY-P5154
Target:  

Potassium Channel

Research Areas:  

Neurological Disease

Tamapin is a venom peptide, targeting to small conductance Ca(2+)-activated K(+) (SK) channels. Tamapin is a selctive blocker of SK2 (Potassium Channel). Tamapin inhibits SK channel-mediated currents in pyramidal neurons of the hippocampus. Tamapin can be isolated from the Indian red scorpion (Mesobuthus tamulus) .
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Cat. No.: HY-P5154A
Target:  

Potassium Channel

Research Areas:  

Neurological Disease

Tamapin TFA is a venom peptide, targeting to small conductance Ca(2+)-activated K(+) (SK) channels. Tamapin TFA is a selctive blocker of SK2 (Potassium Channel). Tamapin TFA inhibits SK channel-mediated currents in pyramidal neurons of the hippocampus. Tamapin TFA can be isolated from the Indian red scorpion (Mesobuthus tamulus) .
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Cat. No.: HY-120355A
CAS No.: 2387505-59-9
Purity:  98.3%
Target:  

Potassium Channel

Research Areas:  

Cardiovascular Disease

AP14145 hydrochloride is a potent KCa2 (SK) channel negative allosteric modulator with an IC50 of 1.1 μM for KCa2.2 (SK2) and KCa2.3 (SK3) channels. AP14145 hydrochloride inhibition strongly depends on two amino acids, S508 and A533 in the channel. AP14145 hydrochloride prolonged atrial effective refractory period (AERP) in rats and demonstrates antiarrhythmic effects in a Vernakalant-resistant porcine model of atrial fibrillation (AF) [2].
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Cat. No.: HY-P1424A
Target:  

Potassium Channel

Research Areas:  

Neurological Disease

Lei-Dab7 TFA is a high affinity, selective KCa2.2 (SK2) channel blocker (Kd=3.8 nM). Lei-Dab7 TFA exhibits >200-fold selectivity for KCa2.2 over KCa2.1, KCa2.3, KCa3.1, Kv and Kir2.1. Lei-Dab7 TFA increases theta-burst responses and increases LTP in rat hippocampal slices in vitro.
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Cat. No.: HY-P89037
Synonyms: ATPSK2; BCYM4; SK2

Host:  

Mouse

Application:  

WB, IHC-P

Reactivity:  

Human, Mouse, Rat

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Cat. No.: HY-P89037A
Synonyms: ATPSK2; BCYM4; SK2

Host:  

Mouse

Application:  

WB, IHC-P

Reactivity:  

Human, Mouse, Rat

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Cat. No.: HY-124368
CAS No.: 1491909-40-0
Target:  

SphK

Research Areas:  

Inflammation/Immunology

RB-042 is a SK1 and SK2 inhibitor with IC50 values of 5.3 μM and 5.0 μM, respectively. RB-042 is applicable to the research of inflammatory diseases [2].
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Cat. No.: HY-P85786
Synonyms: Sphingosine kinase 2; SK 2; SPK 2;

Host:  

Mouse

Application:  

WB, IHC-P

Reactivity:  

Human, Mouse, Rat

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Cat. No.: HY-112385
CAS No.: 917236-13-6
Target:  

SphK PERK

Research Areas:  

Cancer

ABC294735 is an orally active SK1/SK2 inhibitor. Combination of ABC294735 with Sorafenib (HY-10201) reduces pERK. ABC294735 exhibits anticancer activity against pancreatic adenocarcinoma and renal cell carcinoma. ABC294735 can be used in research related to pancreatic adenocarcinoma and renal cell carcinoma .
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