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Vanillin acetate is a phenol ester synthesized from vanillin through treatment with acetic anhydride. It features a benzene ring substituted by a hydroxyl group and an ester group. Its initial source is microorganisms.
Nature: A phenol ester.
Synthesis: Can be synthesized from vanillin by treatment with acetic anhydride.
Structure: Contains a benzene ring substituted by a hydroxyl group and an ester group.
Purity: Available with a purity of 99.91% and 99.94% (Select Batch).
Physical form: Appears as a solid.
Color: Ranges from white to light yellow.
Applications: Intended for research use only.
Solubility (in vitro): Soluble in DMSO at concentrations of 100 mg/mL (514.97 mM) or greater.
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Cyproterone acetate is an androgen receptor (AR) antagonist with IC50 of 7 1 nM as well as a weak progesterone receptor agonist with weak pro-gestational and glucocorticoid activity
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Fludrocortisone (9 -fluorocortisol) is a synthetic pregnane steroid and a halogenated derivative of cortisol It is used to treat adrenogenital syndrome postural hypotension and adrenal insufficiency
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A potent arginase inhibitor (Ki = 0.5 µM for the rat liver enzyme); ~40-fold more potent than NOHA as an inhibitor of arginase from mouse macrophages (IC50 = 10-12 µM); not a substrate for any of the 3 NOS isoforms; does not inhibit nNOS or iNOS
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Ammonium acetate is a colorless hygroscopic solid. It can be prepared by reacting glacial acetic acid with ammonia or ammonium carbonate. It has been reported as potential inhibitor of Pd/C mediated hydrogenolysis of benzyl ether.
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Alpha-Terpinyl acetate is a monoterpene ester derived from Laurus nobilis L. essential oil. It acts as a competitive P450 2B6 substrate, binding to the active site with a Kd value of 5.4 μM. It also inhibits bupropion hydroxylation activity of P450 2B6 with an IC50 value of 10.4 μM.
Purity: 93.88%
Appearance: liquid, colorless to light yellow
Molecular weight: 196.29
Formula: C12H20O2
Classified as: terpenoids, other monoterpenes
Derived from: Laurus nobilis L. plants
Storage (pure): -20°C for 3 years; 4°C for 2 years
Storage (in solvent): -80°C for 6 months; -20°C for 1 month
Solubility: DMSO: 100 mg/mL
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Roxatidine Acetate Hydrochloride is a potent, selective, competitive, and orally active histamine H2-receptor antagonist. It demonstrates antisecretory potency against gastric acid secretion and can suppress inflammatory responses. It is used for gastric and duodenal ulcers research and also exhibits antitumor activity.
Potent, selective, competitive, and orally active histamine H2-receptor antagonist
Demonstrates antisecretory potency against gastric acid secretion
Suppresses inflammatory responses by inhibiting NF-κB and p38 MAPK activation
Used for gastric and duodenal ulcers research
Exhibits antitumor activity
Suppresses growth of colon 38 tumor implants in mice
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