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Organic compounds that are derived from or have a benzene group in their molecular structure. Benzene is an aromatic organic molecule composed of 6 carbon atoms and 6 hydrogen atoms that form a ring. Includes derivatives and substituted molecules.
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Medchemexpress, HY-103000 10mg HSF1A CAS:1196723-93-9 HSF1A is a cell-permeable activator of heat shock transcription factor 1 (HSF1). Purity:>98% Medchemexpress has over 10000 novel life-science reagents, reference compounds, APIs and natural compounds for laboratory and scientific use. Other quantity can also be offered.
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Medchemexpress, HY-103022 10mg Repotrectinib CAS:1802220-02-5 Repotrectinib (TPX-0005) is a potent ROS1 (IC50=0.07 nM) and TRK (IC50=0.83/0.05/0.1 nM for TRKA/B/C) inhibitor. Repotrectinib potently inhibits WT ALK (IC50=1.01 nM). Repotrectinib has anti-cancer activity[2]. Purity:>98% Medchemexpress has over 10000 novel life-science reagents, reference compounds, APIs and natural compounds for laboratory and scientific use. Other quantity can also be offered.
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3-Hydroxybenzoic acid is an orally active endogenous metabolite that functions as an agonist for GPR81 and GPR109A. It acts as a stress response desensitizer and can be utilized for anti-inflammatory and analgesic research.
Orally active endogenous metabolite
Agonist for GPR81 and GPR109A
Acts as a stress response desensitizer
Suitable for anti-inflammatory studies
Suitable for analgesic studies
Protects against stress-triggered alterations in body weights and core temperatures
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Linoleyl alcohol is a fatty alcohol and a structural analog of Linoleic acid, lacking an α-carboxyl group. This product is intended for research use only and is not sold to patients.
Provided as a colorless to light yellow liquid
Molecular weight of 266.46
Purity of 99.8%
Soluble in DMSO (100 mg/mL)
Supports research on weight-loss and metabolic syndrome management
Store pure form at -20°C for up to 3 years
Store in solvent at -80°C for 6 months or -20°C for 1 month
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TK-112690 is an inhibitor of UPP1 (uridine phosphorylase). It inhibits both murine and human small intestinal uridine phosphorylase. This compound increases plasma uridine concentration in mice and is valuable for research into cancer and pulmonary fibrosis, demonstrating potential in mitigating chemotherapy-induced side effects.
Inhibits UPP1 (uridine phosphorylase)
Effective against murine and human small intestinal uridine phosphorylase
Increases plasma uridine concentration in mice
Applicable in cancer research
Applicable in pulmonary fibrosis research
Mitigates methotrexate-induced weight loss
Reduces methotrexate-induced mucosal permeability loss
Reduces pulmonary fibrosis
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