255 Results for "

SK

" in MedChemExpress (MCE) Product Catalog:
Products (255)

255 Results for "SK" in MCE Product Catalog:

41
41 Publications Verification
Cat. No.: HY-N0219
CAS No.: 485-49-4
Synonyms: (+)-Bicuculline
Bicuculline ((+)-Bicuculline) is A competing neurotransmitter GABAA receptor antagonist (IC50=2 μM). Bicuculline also blocks Ca 2+ activating potassium (SK) channels and subsequently blocks slow post-hyperpolarization (slow AHP). Bicuculline has anticonvulsant activity. Bicuculline can be used to induce seizures in mice .
loading...
    loading...
17
17 Cited Publications
Cat. No.: HY-126823
CAS No.: 234075-45-7
Purity:  95.33%
Synonyms: PGSK diacetate (5/6-mixture)
Target:  

Fluorescent Dye

Research Areas:  

Others

Phen green SK (PGSK) diacetate (PGSK diacetate (5/6-mixture)) is a metal ion-sensitive fluorescent probe that can penetrate cell membranes. Phen green SK (PGSK) diacetate can react with a variety of metal ions, including Fe 2+, Cd 2+, Co 2+, Ni 2+, Zn 2+, etc. Phen green SK (PGSK) diacetate chelates Fe 2+, resulting in fluorescence quenching, which can be restored when a membrane-permeable chelator is added, thereby reflecting the changes in the intracellular chelatable iron pool. The excitation/emission maxima of Phen green SK diacetate are 507/532 nm, respectively .
loading...
    loading...
15
15 Cited Publications
Cat. No.: HY-15894A
CAS No.: 173326-37-9
Purity:  98.66%
BQ-788 is a potent, selective ETB receptor antagonist with IC50 of 1.2 nM for inhibition of ET-1 binding to human Girardi heart cells, poorly inhibiting the binding to ETA receptors in human neuroblastoma cell line SK-N-MC cells with IC50 of 1300 nM .
loading...
    loading...
13
13 Cited Publications
Cat. No.: HY-P0256
CAS No.: 24345-16-2
Synonyms: Apamine
Apamin (Apamine) is an 18 amino acid peptide neurotoxin found in apitoxin (bee venom), is known as a specifically selective blocker of Ca 2+-activated K + (SK) channels and exhibits anti-inflammatory and anti-fibrotic activity .
loading...
    loading...
13
13 Cited Publications
Cat. No.: HY-P0256A
Synonyms: Apamine TFA
Apamin TFA (Apamine TFA) is an 18 amino acid peptide neurotoxin found in apitoxin (bee venom), is known as a specifically selective blocker of Ca 2+-activated K + (SK) channels and exhibits anti-inflammatory and anti-fibrotic activity .
loading...
    loading...
11
11 Cited Publications
Cat. No.: HY-P7155A
Purity:  ≥ 95%, as determined by reducing SDS-PAGE.
Synonyms: rHuDKK-1; hDkk-1; SK
Species:  
Source:  
loading...
    loading...
8
8 Cited Publications
Cat. No.: HY-13822
CAS No.: 312636-16-1
Purity:  99.25%
Target:  

SphK Wnt Apoptosis

Research Areas:  

Cancer

SKI-II is an oral active and synthetic inhibitor of sphingosine kinase (SK) activity, with IC50 values of 78 μM and 45 μM for SK1 and for SK2, respectively. SKI II causes an irreversible inhibition of SK1 by inducing its lysosomal and/or proteasomal degradation .
loading...
    loading...
6
6 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.
loading...
    loading...
6
6 Cited Publications
Cat. No.: HY-P7154
Purity:  ≥ 95%, as determined by reducing SDS-PAGE.
Synonyms: rMuDKK-1; mDkk-1; Dickkopf-1
Species:  
Source:  
CHO
loading...
    loading...
6
6 Cited Publications
Cat. No.: HY-129029
CAS No.: 66722-44-9
Purity:  99.78%
Bisoprolol is a potent, selective and orally active β1-adrenergic receptor blocker with little activity on β2-receptor. Bisoprolol has the potential for hypertension, coronary artery disease and stable ventricular dysfunction research .
loading...
    loading...
6
6 Cited Publications
Cat. No.: HY-B0076
CAS No.: 104344-23-2
Bisoprolol hemifumarate is a potent, selective and orally active β1-adrenergic receptor blocker with little activity on β2-receptor. Bisoprolol hemifumarate has the potential for hypertension, coronary artery disease and stable ventricular dysfunction research .
loading...
    loading...
5
5 Cited Publications
Cat. No.: HY-139156
CAS No.: 2523016-96-6
Purity:  99.86%
Target:  

PROTACs PARP

Research Areas:  

Cancer

SK-575 is a highly potent and specific proteolysis-targeting chimera (PROTAC) degrader of PARP1, with an IC50 of 2.30 nM. SK-575 potently inhibits the growth of cancer cells bearing BRCA1/2 mutations .
loading...
    loading...
5
5 Cited Publications
Cat. No.: HY-P72968
Purity:  ≥ 95%, as determined by reducing SDS-PAGE.
Synonyms: Dickkopf-related protein 1; Dickkopf-1; Dkk-1; SK; DKK1
Species:  
Source:  
loading...
    loading...
3
3 Cited Publications
Cat. No.: HY-14877
CAS No.: 739366-20-2
Purity:  99.91%
Synonyms: SK-0403
Anagliptin (SK-0403) is a highly selective, potent, orally active inhibitor of dipeptidyl peptidase 4 (DPP-4), with an IC50 of 3.8 nM, and less selective at DPP-8 and DDP-9 with IC50s of 68 nM and 60 nM, respectively .
loading...
    loading...
3
3 Cited Publications
Cat. No.: HY-B1462
CAS No.: 95-25-0
Chlorzoxazone is a SK-type potassium channel activator. Chlorzoxazone modulates FOXO3 phosphorylation and . Chlorzoxazone enhances immunosuppression, attenuates vasoconstriction, attenuates cognitive deficits, and improves experimental autoimmune encephalomyelitis .
loading...
    loading...
2
2 Cited Publications
Cat. No.: HY-109160
CAS No.: 2167246-24-2
Purity:  99.27%
Synonyms: CAD-1883
Target:  

Potassium Channel

Research Areas:  

Neurological Disease

Rimtuzalcap (CAD-1883) is a first-in-class selective positive allosteric modulator of small-conductance calcium-activated potassium channels (SK channels). Rimtuzalcap can be used for the research of movement disorders including essential tremor (ET) and spinocerebellar ataxia (SCA) .
loading...
    loading...
2
2 Cited Publications
Cat. No.: HY-12895
CAS No.: 24418-86-8
Purity:  98.95%
Target:  

SphK PI3K Apoptosis

Research Areas:  

Cancer

SKI V is a noncompetitive and potent non-lipid sphingosine kinase (SPHK; SK) inhibitor with an IC50 of 2 μM for GST-hSK. SKI V potently inhibits PI3K with an IC50 of 6 μM for hPI3k. SKI V decreases formation of the mitogenic second messenger sphingosine-1-phosphate (S1P). SKI V induces apoptosis and has antitumor activity .
loading...
    loading...
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.
loading...
    loading...
2
2 Cited Publications
Cat. No.: HY-148266
CAS No.: 1831169-11-9
Purity:  ≥98.0%
Target:  

E1/E2/E3 Enzyme

Research Areas:  

Cancer

UBA5-IN-1 (compound 8.5) is a selective UBA5 inhibitor with an IC50 value of 4.0 μM. UBA5-IN-1 inhibits cell proliferation of Sk-Luci6 cancer cells with high expression levels of UBA5 .
loading...
    loading...
2
2 Cited Publications
Cat. No.: HY-P72969
Purity:  ≥ 95%, as determined by reducing SDS-PAGE.
Synonyms: Dickkopf-related protein 1; Dickkopf-1; Dkk-1; SK; DKK1
Species:  
Source:  
loading...
    loading...