29 Results for "

SK1

" in MedChemExpress (MCE) Product Catalog:
Products (29)

29 Results for "SK1" in MCE Product Catalog:

2
2 Cited Publications
Cat. No.: HY-110105
CAS No.: 875755-24-1
Purity:  99.76%
Target:  

Potassium Channel

Research Areas:  

Neurological Disease

NS8593 hydrochloride is a potent and selective small conductance Ca 2+-activated K + channels (SK channels) inhibitor. NS8593 hydrochloride reversibly inhibits SK3-mediated currents with a Kd value of 77 nM. NS8593 hydrochloride inhibits all the SK1-3 subtypes Ca 2+-dependently (Kds of 0.42, 0.60, and 0.73 μM, respectively, at 0.5 μM Ca 2+), and does not affect the Ca 2+-activated K + channels of intermediate and large conductance (hIK and hBK channels, respectively) [1] .
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2
2 Cited Publications
Cat. No.: HY-101805
CAS No.: 1218816-71-7
Purity:  98.72%
Target:  

SphK

Research Areas:  

Inflammation/Immunology Cancer

SK1-IN-1 is a potent sphingosine kinase 1 (SPHK1) inhibitor with an IC50 of 58 nM.
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1
1 Cited Publications
Cat. No.: HY-119016
CAS No.: 1072443-89-0
Purity:  98.47%
Synonyms: BML-258
Target:  

SphK CaMK

Research Areas:  

Cancer

SK1-I (BML-258), an analog of sphingosine, is an isozyme-specific competitive SPHK1 inhibitor with a Ki value of 10 μM [1]. SK1-I shows no activity at SPHK1 PKCα, PKCδ, PKA, AKT1, ERK1, EGFR, CDK2, IKKβ or CamK2β. SK1-I enhances autophagy and has antitumor activity .
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Cat. No.: HY-137952
CAS No.: 875755-39-8
Research Areas:  

Neurological Disease

NS8593 is an SK channel (small conductance Ca 2+-activated K+ channels) inhibitor. NS8593 reversibly inhibited recombinant SK3-mediated currents (human SK3 and rat SK3). NS8593 inhibits all the SK1-3 subtypes Ca 2+-dependently (Kd = 0.42, 0.60, and 0.73 μM, respectively, at 0.5 μM Ca 2+). NS8593 does not affect the Ca 2+-activated K channels of intermediate and large conductance (hlk and hBK channels, respectively). NS8593 can also inhibit TRPM7 (melastatin-related TRP cation channel 7) (IC50 = 1.6 mM). NS8593 can be used for the study of central nervous system (CNS) related diseases [1] .
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Cat. No.: HY-112485
CAS No.: 1142015-25-5
Target:  

SphK Drug Derivative

Research Areas:  

Cancer

(R)-FTY720-vinylphosphonate is a sphingosine kinase 1 (SK1) inhibitor. (R)-FTY720-ene-phosphonate is also an FTY720 analogue. (R)-FTY720-vinylphosphonate is promising for research of solid tumors like breast cancer [1].
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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 [1].
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Cat. No.: HY-101805R
CAS No.: 1218816-71-7
Research Areas:  

Inflammation/Immunology Cancer

SK1-IN-1 (Standard) is the analytical standard of SK1-IN-1 (HY-101805). This product is intended for research and analytical applications. SK1-IN-1 is a potent sphingosine kinase 1 (SPHK1) inhibitor with an IC50 of 58 nM.
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Cat. No.: HY-P702765
Purity:  ≥ 90%, as determined by reducing SDS-PAGE.
Synonyms: SPHK1; SK 1; Sphingosine Kinase 1; Sphingosine Kinase; SPHK; SPHK1 Protein; Acetyltransferase SPHK1; SK1; SPK 1; SPK
Species:  
Human
Source:  
Sf9 insect cells
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Cat. No.: HY-P73631
Purity:  ≥ 95%, as determined by reducing SDS-PAGE.
Synonyms: SPHK1; SK 1; Sphingosine Kinase 1; Sphingosine Kinase; SPHK; SPHK1 Protein; Acetyltransferase SPHK1; SK1; SPK 1; SPK
Species:  
Human
Source:  
Sf9 insect cells
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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 [1] .
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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 [1].
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Cat. No.: HY-RS10030
Research Areas:  

Others

PAPSS1 Human Pre-designed siRNA Set A contains three designed siRNAs for PAPSS1 gene (Human), as well as a negative control, a positive control, and a FAM-labeled negative control.

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Cat. No.: HY-RS13665
Research Areas:  

Others

Sphk1 Mouse Pre-designed siRNA Set A contains three designed siRNAs for Sphk1 gene (Mouse), as well as a negative control, a positive control, and a FAM-labeled negative control.

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Cat. No.: HY-RS07169
Research Areas:  

Others

KCNN1 Human Pre-designed siRNA Set A contains three designed siRNAs for KCNN1 gene (Human), as well as a negative control, a positive control, and a FAM-labeled negative control.

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Cat. No.: HY-P8F004A
Synonyms: CD8,CD8-FITC,SK1

Host:  

Mouse

Application:  

FC

Reactivity:  

Human

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Cat. No.: HY-P8F004C
Synonyms: CD8,CD8-PE,SK1

Host:  

Mouse

Application:  

FC

Reactivity:  

Human

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Cat. No.: HY-P8F004F
Synonyms: CD8,CD8-PerCP,SK1

Host:  

Mouse

Application:  

FC

Reactivity:  

Human

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Cat. No.: HY-P8F004I
Synonyms: CD8,CD8-APC,SK1

Host:  

Mouse

Application:  

FC

Reactivity:  

Human

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Cat. No.: HY-P80337
Synonyms: SK1, SPHK, SPK, SPHK1, Sphingosine kinase 1, SK 1, SPK 1, Acetyltransferase SPHK1

Host:  

Rabbit

Application:  

WB, IHC-P, FC

Reactivity:  

Human

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Cat. No.: HY-P89415
Synonyms: SK1, SPHK, SPK, SPHK1, Sphingosine kinase 1, SK 1, SPK 1, Acetyltransferase SPHK1

Host:  

Rabbit

Application:  

WB, FC

Reactivity:  

Human, Mouse, Rat

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