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meh

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  • Inhibitors & Agonists
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    TargetMol | Inhibitors_Agonists
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    TargetMol | Peptide_Products
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mEH-IN-1
T616902418576-06-2
mEH-IN-1 (Compound 62) is a potent inhibitor of microsomal epoxide hydrolase (mEH), with an IC50 value of 2.2 nM. This α β-fold hydrolase enzyme is widely expressed in mammalian tissues and primarily localized in the endoplasmic reticulum (ER) of eukaryotic cells, responsible for hydrolyzing various epoxide-containing molecules. Research on mEH-IN-1 can enhance the understanding of preeclampsia, hypercholanemia, and cancer [1].
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6-8 weeks
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Emeheterone
TN3928117333-12-7
Emeheterone is a natural product from the fresh fruiting bodies of the basidiomycetes Albatrellus confluens.
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SYSMEHFRWGKPS
TP1748
SYSMEHFRWGKPS, a 13-amino acid peptide, is characterized by its specific arrangement of amino acids (SYSMEHFRWGKPS) in a sequential manner.
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4-Chloro-2,6-dimehtylpyridine
TNU07243512-75-2
4-Chloro-2,6-dimehtylpyridine belongs to Heterocyclic Compounds - Pyridines; Intermediates and Building Blocks - Electrophile.
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7-10 days
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Elaidamide
T381434303-70-2
Elaidamide is a fatty acid amide that has been found in the cerebrospinal fluid of sleep-deprived cats.1 It inhibits rat microsomal epoxide hydrolase (mEH; Ki = 70 nM).2 Elaidamide also inhibits porcine pancreatic and human synovial phospholipase A2 (PLA2).3 In vivo, elaidamide (10 mg/animal) induces physiological sleep in rats.1References1. Cravatt, B.F., Prospero-Garcia, O., Siuzdak, G., et al. Chemical characterization of a family of brain lipids that induce sleep. Science 268(5216), 1506-1509 (1995).2. Morisseau, C., Newman, J.W., Dowdy, D.L., et al. Inhibition of microsomal epoxide hydrolases by ureas, amides, and amines. Chem. Res. Toxicol. 14(4), 409-415 (2001).3. Jain, M.K., Ghomashchi, F., Yu, B.Z., et al. Fatty acid amides: scooting mode-based discovery of tight-binding competitive inhibitors of secreted phospholipases A2. J. Med. Chem. 35(19), 3584-3586 (1992). Elaidamide is a fatty acid amide that has been found in the cerebrospinal fluid of sleep-deprived cats.1 It inhibits rat microsomal epoxide hydrolase (mEH; Ki = 70 nM).2 Elaidamide also inhibits porcine pancreatic and human synovial phospholipase A2 (PLA2).3 In vivo, elaidamide (10 mg/animal) induces physiological sleep in rats.1 References1. Cravatt, B.F., Prospero-Garcia, O., Siuzdak, G., et al. Chemical characterization of a family of brain lipids that induce sleep. Science 268(5216), 1506-1509 (1995).2. Morisseau, C., Newman, J.W., Dowdy, D.L., et al. Inhibition of microsomal epoxide hydrolases by ureas, amides, and amines. Chem. Res. Toxicol. 14(4), 409-415 (2001).3. Jain, M.K., Ghomashchi, F., Yu, B.Z., et al. Fatty acid amides: scooting mode-based discovery of tight-binding competitive inhibitors of secreted phospholipases A2. J. Med. Chem. 35(19), 3584-3586 (1992).
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6-8 weeks
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