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Results for "

ets

" in TargetMol Product Catalog
  • Inhibitors & Agonists
    14
    TargetMol | Inhibitors_Agonists
  • Compound Libraries
    2
    TargetMol | Compound_Libraries
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    1
    TargetMol | Dye_Reagents
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    TargetMol | Natural_Products
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    TargetMol | Antibody_Products
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    TargetMol | Inhibitors_Agonists
VPC-18005
T600512242480-48-2
VPC-18005 is a luciferase inhibitor. VPC-18005 inhibits ERG-induced transcription and interacts directly with the ERG-ETS domain thereby disrupting the ERG binding to DNA.
  • $41
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Flumetsulam
XRD-498, XRD498, XRD 498
T1995498967-40-9
Flumetsulam (XRD 498) is a triazolopyrimidine herbicide.
  • $50
In Stock
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TargetMol | Inhibitor Sale
Chikusetsusaponin IVa
Calenduloside F
T386351415-02-2
Chikusetsusaponin IVa (Calenduloside F) is a novel AMPK activator, can induce insulin secretion from βTC3 cells via GPR4 mediated calcium and PKC pathways, may be developed into a new potential for therapeutic agent used in T2DM patients.
  • $41
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TargetMol | Citations Cited
Sotetsuflavone
TN22222608-21-1
Sotetsuflavone, with an IC50 of 0.16 μM, stands as the most active compound in its series, acting as a potent inhibitor of DENV-NS5 RdRp (Dengue virus NS5 RNA-dependent RNA polymerase).
  • $1,320
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TargetMol | Citations Cited
Chikusetsusaponin V methyl ester
T125004
Chikusetsusaponin V methyl ester is a useful organic compound for research related to life sciences and the catalog number is T125004.
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Metsulfuron-methyl
T2124674223-64-6
Metsulfuron-methyl is a systemic selective wheat field high-efficiency sulfonylurea herbicide, which mainly controls most broadleaf weeds and grass weeds in wheat fields.
  • $38
In Stock
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Metsulfuron-d6
TMIR-0021
Metsulfuron-d6 is a deuterated compound of Metsulfuron. Metsulfuron has a CAS number of 74223-64-6. Metsulfuron-methyl is a systemic selective wheat field high-efficiency sulfonylurea herbicide, which mainly controls most broadleaf weeds and grass weeds in wheat fields.
  • Inquiry Price
7-10 days
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Flumetsulam (Standard)
TMSM-120998967-40-9
Flumetsulam (Standard) is the standard substance of Flumetsulam, and it is applicable for quantitative analysis, quality control, and related research in biochemical experiments. Flumetsulam (XRD 498) is a triazolopyrimidine herbicide.
  • Inquiry Price
7-10 days
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Rhetsinine
TN10048526-43-2
Rhetsinine is an aldose reductase inhibitor identified in Evodia rutaecarpa, with an IC50 value of 24.1 μM. At a concentration of 100 μM, Rhetsinine significantly reduces sorbitol accumulation, achieving an inhibition rate of 79.3%. This compound is applicable in research concerning diabetic complications, such as diabetic neuropathy and retinopathy.
  • Inquiry Price
10-14 weeks
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Chikusetsusaponin Ib
Chikusetsu saponin Ib
TN244359252-87-8
Chikusetsusaponin Ib (Chikusetsu saponin Ib) is an inhibitor of AChE and can be used in studies about anti-Alzheimer's diseases.
  • $117
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Chikusetsusaponin-IVa methyl ester
TN871958546-61-5
Chikusetsusaponin-IVa methyl ester is a natural product that can be used in related research in the field of life sciences. Its product number is TN8719.
  • Inquiry Price
7-10 days
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Potassium chloride, meets analytical specification of Ph. Eur., BP, USP, FCC, E508, ≤0.0001% Al
7447-40-7
TSH-00496
Potassium chloride is an inorganic salt that meets the analytical specifications of Ph. Eur., BP, USP, FCC, and E508, with an aluminum content of ≤0.0001%. It is suitable for use in buffer solution preparation.
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TK216
T131661903783-48-1
TK216 is a potent inhibitor of E26 transformation-specific (ETS) with anticancer activity.
  • $37
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Mivebresib
ABBV-075
T37121445993-26-9
Mivebresib (ABBV-075), also known as ABBV-075, is a potent BET inhibitor (bromodomain (BRD)-containing protein) with potential antineoplastic activity. Upon administration, the bromodomain inhibitor ABBV-075 binds to the acetyl-lysine binding site in the BRD of certain BRD-containing protein(s), thereby preventing the interaction between those proteins and acetylated histones. This disrupts chromatin remodeling, prevents the expression of certain growth-promoting genes, and leads to an inhibition of cell growth in susceptible tumors. Also a potent inhibitor of MYC and the TMPRSS2-ETS fusion proteins.
  • $53
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