51 Results for "

Fto

" in MedChemExpress (MCE) Product Catalog:
Products (51)

51 Results for "Fto" in MCE Product Catalog:

Cat. No.: HY-175885
PROTAC FTO degrader 1 is a Fat Mass and Obesity-associated Protein (FTO) PROTAC degrader. PROTAC FTO degrader 1 selectively degrades FTO depending on VHL E3 ligase and ubiquitin-proteasome system. PROTAC FTO degrader 1 can increase m6A modifications on mRNAs associated with ribosome biogenesis and promote their YTHDF2-mediated decay. PROTAC FTO degrader 1 can inhibit cancer cells proliferation and induce apoptosis. PROTAC FTO degrader 1 can be used for the research of cancer, such as acute myeloid leukemia (AML) .
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Cat. No.: HY-RS05136
Research Areas:  

Others

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

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Cat. No.: HY-139821
CAS No.: 2763577-75-7
Research Areas:  

Cancer

FTO-IN-5 is a potent and selective FTO inhibitor, with an IC50 of 0.087 μM for FTO demethylase activity and a Kd of 28.0 nM for direct binding to FTO. The IC50 of FTO-IN-5 for ALKBH5 is 8.98 μM. FTO-IN-5 can be used in studies related to FTO demethylase activity and cancer .
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Cat. No.: HY-179267
FTO-IN-16 (Compound 8a-1), a FTO-IN-15 (HY-179266) prodrug, is a potent FTO inhibitor. FTO-IN-16 suppresses acute myeloid leukemia (AML) cell viability, increases m 6A levels, downregulates c-Myc and CEBPA, and upregulates ASB2 and RARA. FTO-IN-16 induces apoptosis. FTO-IN-16 demonstrates strong in vivo efficacy in AML mouse xenografts. FTO-IN-16 can be used for the research of AML .
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Cat. No.: HY-132865
CAS No.: 2585198-87-2
Purity:  99.79%
Research Areas:  

Cancer

FTO-IN-3 is a FTO inhibitor that impair self-renewal in glioblastoma stem cells.
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Cat. No.: HY-145238
CAS No.: 2968347-63-7
Purity:  98.94%
Research Areas:  

Others

FTO-IN-6 is a selective fat mass and obesity associated protein (FTO) inhibitor.
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Cat. No.: HY-14280R
CAS No.: 130929-57-6
Research Areas:  

Neurological Disease Cancer

Entacapone (Standard) is the analytical standard of Entacapone. This product is intended for research and analytical applications. Entacapone is a potent, reversible, peripherally acting and orally active catechol-O-methyltransferase (COMT) inhibitor. Entacapone inhibits COMT from rat brain, erythrocytes and liver with IC50 values of 10 nM, 20 nM, and 160 nM, respectively. Entacapone is selective for COMT over other catecholamine metabolizing enzymes, including MAO-A, MAO-B, phenolsulphotransferase M (PST-M) and PST-P (IC50s>50 µM). Entacapone can be used for the research of Parkinson's disease . Entacapone serves as a inhibitor of FTO demethylation with an IC50 of 3.5 μM, can be used for the research of metabolic disorders .
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Cat. No.: HY-117426
CAS No.: 1585219-04-0
Purity:  99.10%
Research Areas:  

Cancer

MO-I-500 is a pharmacological of FTO inhibitor with an IC50 of 8.7 μM for the inhibition of purified FTO demethylase catalyzing demethylation of an artificial small methylated substrate. MO-I-500 can be used for the research of rare panresistant triple-negative inflammatory breast cancer .
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Cat. No.: HY-131871
CAS No.: 1808089-27-1
Purity:  99.25%
Research Areas:  

Cancer

Ethyl LipotF is a selective FTO inhibitor that significant increases modified N6-methyladenosine (m6A) levels in HeLa cells in a concentration-dependent manner .
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Cat. No.: HY-168483
CAS No.: 687600-25-5
FTO-IN-13 (compound 8t) is a potent FTO inhibitor. FTO-IN-13 shows antiproliferative activity. FTO-IN-13 induces apoptosis. FTO-IN-13 decreases the protein expression of Bcl-2 and Caspase 3 active. FTO-IN-13 decreases MYC and CEBPA gene expression. FTO-IN-13 shows anticancer activity .
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Cat. No.: HY-W026109
CAS No.: 955328-22-0
FTO-IN-12 (Compound 2) is an inhibitor of fat mass and obesity-related protein (FTO). Kd and IC50 values are 185 nM and 1.46 μM, respectively. FTO-IN-12 can be used in the study of neurodegenerative diseases .
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Cat. No.: HY-RS05138
Research Areas:  

Others

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

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Cat. No.: HY-W588293
CAS No.: 958-74-7
Research Areas:  

Others

3-Methylthymidine can be used to detect fat mass and obesity-associated protein (FTO) activity .
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Cat. No.: HY-N10340
CAS No.: 182261-83-2
Synonyms: Clauszoline I
Clausine E, is a alkaloid which can be isolated from Clausena excavata, is a inhibitor of fat mass and obesity-associated protein (FTO) demethylase. Clausine E shows inhibitory activities against proliferation of synoviocytes and cancer cells.
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Cat. No.: HY-175886
FTO ligand-1 is a FTO ligand for FTO PROTAC degrader FP54 (HY-175885). FTO ligand-1 can inhibit cell proliferation and block the FP54-induced FTO degradation. FTO ligand-1 can be used for research of cancer, such as acute myeloid leukemia (AML) .
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Cat. No.: HY-156405
FTO-IN-10 (compound 7) is a potent human demethylase FTO (the fat mass and obesity-associated protein) inhibitor with an IC50 of 4.5 μM. FTO-IN-10 enters the FTO’s structural domain II binding pocket through hydrophobic and hydrogen bonding interactions. FTO-IN-10 induces DNA damage and autophagic cell death in A549 cells .
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Cat. No.: HY-14280A
CAS No.: 1047659-02-8
Target:  

COMT

Research Areas:  

Neurological Disease Cancer

Entacapone sodium salt is a potent, reversible, peripherally acting and orally active catechol-O-methyltransferase (COMT) inhibitor. Entacapone sodium salt inhibits COMT from rat brain, erythrocytes and liver with IC50 values of 10 nM, 20 nM, and 160 nM, respectively. Entacapone sodium salt is selective for COMT over other catecholamine metabolizing enzymes, including MAO-A, MAO-B, phenolsulphotransferase M (PST-M) and PST-P (IC50s>50 µM). Entacapone sodium salt can be used for the research of Parkinson's disease . Entacapone sodium salt serves as as a inhibit of FTO demethylation with an IC50 of 3.5 μM, can be used for the research of metabolic disorders .
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Cat. No.: HY-132863
CAS No.: 2585198-85-0
Research Areas:  

Cancer

FTO-IN-2 is a FTO inhibitor that impairs self-renewal in glioblastoma stem cells.
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Cat. No.: HY-179266
Research Areas:  

Cancer

FTO-IN-15 (Compound 8a) is a potent and selective dual-competitive FTO inhibitor with an IC50 of 43.7 nM, showing high selectivity over ALKBH3 and ALKBH5. FTO-IN-15 substantially inhibits FTO demethylation by simultaneously occupying the substrate and 2-oxoglutarate (2-OG) pockets. FTO-IN-15 can be used for the research of acute myeloid leukemia (AML) .
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Cat. No.: HY-139820
CAS No.: 2763577-74-6
FTO-IN-4 is a potent and selective inhibitor of fat mass obesity-associated protein (FTO).
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