Products from TargetMol
TargetMol, based in Boston, Massachusetts, was founded in 2015 and is a drug screening expert in the life science community. The company offers diverse compound libraries, including FDA-approved libraries, and covers a broad spectrum of small molecule compounds such as inhibitors and agonists as well as recombinant proteins and natural products. TargetMol's products are used by researchers worldwide in areas such as cancer research, neurobiology, inflammation, immunology and metabolism.
More information at: www.targetmol.com
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FITC-PEG-NHS (MW 1000)
Item number: TGM-T207017-10mg
Description: FITC-PEG-NHS (MW 1000) is a fluorescent dye composed of polyethylene glycol (PEG), fluorescein isothiocyanate (FITC), and N-hydroxysuccinimide (NHS) groups. The NHS group can react with amine-containing groups. FITC-PEG-NHS (MW 1000) is utilized for fluorescence labeling and imaging.
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CDC20-IN-2
Item number: TGM-T207018-10mg
Description: CDC20-IN-2 (14c) is an inhibitor of Cdc20 with a KD of 7.65 µM, inducing G2/M phase arrest, promoting DNA damage accumulation, and stabilizing key substrates such as Cyclin B1 and Bim. This leads to enhanced apoptosis, as well as inhibition of tumor cell proliferation and migration. Target: Apoptosis,...
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CypB-IN-1
Item number: TGM-T207041-10mg
Description: CypB-IN-1 (Compound 11) is an inhibitor of cyclophilin B (CypB) with a dissociation constant (Kd) of 12 nM. It is used in research related to metabolic dysfunction-associated steatohepatitis (MASH) and the liver fibrosis diseases it induces. Target: Others
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m-PEG2000-PEI-Cy5
Item number: TGM-T207042-10mg
Description: mPEG-PEI-Cy5 (MW 2000) is a fluorescent dye composed of methoxy polyethylene glycol (mPEG), Cy5, and polyethyleneimine (PEI). This compound is suitable for applications in fluorescence labeling and imaging.
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Picene
Item number: TGM-T207079-10mg
Target: Others. Smiles: c1ccc2c(c1)ccc1c2ccc2c3ccccc3ccc12
| MW: | 278.35 D |
From 183.00€
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Carbonic anhydrase inhibitor 31
Item number: TGM-T207175-10mg
Description: Carbonic anhydrase inhibitor31 is an mtCA2 inhibitor (Ki: 5.2 nM) that can be used in antituberculosis research. Target: Carbonic Anhydrase
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Hodgkinsine trimethyl iodide
Item number: TGM-T207177-10mg
Description: Hodgkinsinetrimethyl (iodide) is the trimethyl iodide derivative of Hodgkinsine. Hodgkinsine functions as an opioid receptor agonist and NMDA receptor antagonist, offering analgesic and antihyperalgesic effects. Additionally, Hodgkinsine exhibits antiviral, antibacterial, and antifungal activities....
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Antifibrotic agent 1
Item number: TGM-T207178-10mg
Description: Antifibrotic agent 1 is an orally active medication designed to treat idiopathic pulmonary fibrosis (IPF). It effectively mitigates IPF-related processes, including TGF-beta-induced epithelial-mesenchymal transition (EMT) and fibroblast-to-myofibroblast transition (FMT), as well as profibrotic M2...
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Cy5 HA MA (MW 3000)
Item number: TGM-T207201-10mg
Description: Cy5 HA MA (MW 3000) is a methacrylate derivative of hyaluronic acid labeled with CY5, extensively utilized in the fields of biomarking and imaging, drug delivery, and tissue engineering and regenerative medicine (Ex/Em = 633/670 nm). Target: Others
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Insecticidal agent 24
Item number: TGM-T207207-10mg
Description: Insecticidal agent 24 is an orally active pyridinyl spiroindoline lead compound. It demonstrates antimalarial activity with Pf NF54IC50 of 0.08 µM. Insecticidal agent 24 also inhibits hERG activity with an IC50 of 6.5 µM. In a humanized immunodeficient NSG mouse model of malaria infection, it...
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AMTG-DA1
Item number: TGM-T207222-10mg
Description: AMTG-DA1 is a ligand for the gastrin-releasing peptide receptor (GRPR), and it can be utilized in cancer research. Target: Bombesin Receptor
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CHK1-IN-12
Item number: TGM-T207228-10mg
Description: CHK1-IN-12 (Compound example 1-5) is a highly selective and orally active checkpoint kinase 1 (CHK1) inhibitor, demonstrating an in vitro enzyme IC50 of â%¤10 nM and a cellular IC50 of â%¤50 nM. This compound suppresses the phosphorylation activity of CHK1 kinase, disrupts DNA damage response pathways,...
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