10081 Results for "

SET

" in MedChemExpress (MCE) Product Catalog:
Products (10081)

10081 Results for "SET" in MCE Product Catalog:

14
14 Publications Verification
Cat. No.: HY-18627A
CAS No.: 1627607-87-7
Synonyms: (R)-PFI-2 hydrochloride
PFI-2 ((R)-PFI-2 hydrochloride) hydrochloride is a potent and selective SET domain containing lysine methyltransferase 7 (SETD7) inhibitor. (R)-PFI-2 shows high inhibiting activity with IC50 value of 2.0  nM and (S)-PFI-2 shows inhibiting activity with IC50  value of 1.0  μM. PFI-2 hydrochloride can be used for the research of chronic kidney disease and inflammation response in the development of renal fibrosis .
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14
14 Publications Verification
Cat. No.: HY-18627
CAS No.: 1627676-59-8
Synonyms: (R)-PFI-2
PFI-2 ((R)-PFI-2 hydrochloride) hydrochloride, a chemical probe, is a potent and selective SET domain containing lysine methyltransferase 7 (SETD7) inhibitor. (R)-PFI-2 shows high inhibiting activity with IC50 value of 2.0 nM and (S)-PFI-2 shows inhibiting activity with IC50 value of 1.0 μM. PFI-2 hydrochloride can be used for the research of chronic kidney disease and inflammation response in the development of renal fibrosis .
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6
6 Cited Publications
Cat. No.: HY-141539A
Purity:  99.77%
Research Areas:  

Cancer

SETDB1-TTD-IN-1 TFA is a potent, selective and endogenous binder competitive ligand of SET domain bifurcated protein 1 tandem tudor domain (SETDB1-TTD) that binds to TTD, with a Kd of 88 nM. SETDB1-TTD-IN-1 TFA increases SETDB1 methyltransferase activity. SETDB1-TTD-IN-1 TFA can be used for the research of biological functions and disease associations of SETDB1-TTD .
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2
2 Cited Publications
Cat. No.: HY-132222
CAS No.: 2313525-20-9
Purity:  99.78%
Target:  

TRP Channel

Research Areas:  

Cancer

SET2 is a selective TRPV2 antagonist (IC50=0.46 μM). SET2 blocks the TRP channel and suppresses prostate cancer cells migration. SET2 reduces the lysophosphatidic acid (LPA, a TRPV2 activator)-induced cytoplasmic calcium increases .
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2
2 Cited Publications
Cat. No.: HY-P74394
Purity:  ≥ 95%, as determined by reducing SDS-PAGE.
Synonyms: V-SET domain containing T-cell activation inhibitor 1; VTCN1; Protein B7S1; B7-H4
Species:  
Source:  
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1
1 Cited Publications
Cat. No.: HY-154812
CAS No.: 2604513-16-6
Purity:  99.81%
Synonyms: KTX-1001
Research Areas:  

Cancer

Gintemetostat (KTX-1001) is an orally active, highly specific NSD2/MMSET histone methyltransferase inhibitor with human NSD2 IC50 values ranging 0.460-2.17 nM and NSD2 SET domain IC50 of 2.32 nM and Kd values ranging 6.3-70.4 nM .Gintemetostat reduces H3K36me2 levels, impairs multiple myeloma cell adhesion and colony formation, enhances cytotoxicity, boosts T-cell activation, and sensitizes resistant multiple myeloma cells to other agents .Gintemetostat can be used for the research of multiple myeloma and relapsed and refractory multiple myeloma .
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1
1 Cited Publications
Cat. No.: HY-138283
CAS No.: 1210906-48-1
Purity:  99.82%
Research Areas:  

Cancer

MR837 is an inhibitor of NSD2-PWWP1. MR837 can bind with human nuclear receptor binding SET domain protein 2 (PWWP domain) .
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1
1 Cited Publications
Cat. No.: HY-P74395
Purity:  ≥ 95%, as determined by reducing SDS-PAGE.
Synonyms: V-SET domain containing T-cell activation inhibitor 1; VTCN1; Protein B7S1; B7-H4
Species:  
Source:  
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Cat. No.: HY-147914
CAS No.: 2797183-37-8
Purity:  98.72%
Target:  

Apoptosis

Research Areas:  

Cancer

NSD2-IN-1 (compound 38) is a potent and high selective NSD2-PWWP1 (nuclear receptor-binding SET domain 2-PWWP1) inhibitor, with an IC50 of 0.11 μM. NSD2-IN-1 can bind to NSD2-PWWP1 and then affect the expression of genes regulated by NSD2. NSD2-IN-1 induces apoptosis and cell cycle arrest .
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Cat. No.: HY-134338
CAS No.: 1314008-27-9
Purity:  99.86%
Research Areas:  

Others

Ipflufenoquin is an insecticide with the potential to control primary infection with apple scab. Ipflufenoquin should be applied between half an inch of green and fruit set .
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Cat. No.: HY-177605
Target:  

DNA/RNA Synthesis

Research Areas:  

Others

ddNTP Set trisodium contains ddATP (HY-128036B), ddCTP (HY-137697D), ddGTP (HY-134103A), and ddTTP (HY-137694B).
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Cat. No.: HY-RS00166
Research Areas:  

Others

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

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Cat. No.: HY-RS29482
Research Areas:  

Others

CERS6 Cattle Pre-designed siRNA Set A is a siRNA containing three designed siRNAs for CERS6 gene (Cattle).
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Cat. No.: HY-RS00035
Research Areas:  

Others

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

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Cat. No.: HY-RS00122
Research Areas:  

Others

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

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Cat. No.: HY-RS00130
Research Areas:  

Others

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

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Cat. No.: HY-178321
Research Areas:  

Cancer

UNC10088 is a molecular glue targeting NSD2. UNC10088 mediates the formation of a stable ternary complex between SCFFBXO22 and the NSD2 PWWP1 domain. UNC10088 promotes ubiquitination of the SCFFBXO22-dependent NSD2 PWWP1 domain through reversible covalent bonding with the C326 region of FBXO22. UNC10088 could be used in cancer research .
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Cat. No.: HY-19546A
CAS No.: 1906920-28-2
Research Areas:  

Cancer

(R)-BAY-598 ((R)-4) is a potent inhibitor of protein-lysine methyltransferase SMYD2, with the IC50 of 1.7 μM .
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Cat. No.: HY-134338R
CAS No.: 1314008-27-9
Research Areas:  

Others

(R)-Omeprazole (sodium) (Standard) is the analytical standard of (R)-Omeprazole (sodium). This product is intended for research and analytical applications. (R)-Omeprazole sodium is a gastric acid resistant compound with activity to inhibit gastric acid secretion. (R)-Omeprazole sodium is metabolized in vivo, and its metabolism is primarily affected by cytochrome P450 enzymes. The interaction between (R)-Omeprazole sodium and mannitol may affect its bioavailability in formulations. (R)-Omeprazole sodium exhibits reversible direct and metabolism-dependent inhibition of CYP2C19 .
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Cat. No.: HY-RS12738
Research Areas:  

Others

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

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