25s

3-Methyluridine is a modified nucleoside of cellular RNA.

(25S)-12β-Hydroxyspirost-4-en-3-one, a natural compound isolated from Dioscorea chiupasensis [1].

(25S)-3Alpha,7alpha,12alpha-trihydroxy-5beta-cholestan-26-oyl-CoA is a nucleoside metabolite.

Antcin-B exhibits a high-affinity inhibition of 3CLPro, which is potentially significant in SARS-CoV-2 research [1].

(25S)-delta7-Dafachronic acid, an orphan nuclear receptor DAF-12 ligand, inhibits the dauer-promoting activity of DAF-12.

25S-Inokosterone is a plant ecdysosteroid isolated from the roots of Achyranthes bidentata. 25S-Inokosterone shows potential for use in studies of LPS-induced acute kidney injury.

[(1S,3R,13S,14S,17S,18R,19R,20S,21S,23R,24R,25S)-18,19,21,24-tetrakis(acetyloxy)-25-hydroxy-3,13,14,25-tetramethyl-6,15,22-trioxo-2,5,16-trioxa-11-azapentacyclo[15.7.1.0^{1,20}.0^{3,23}.0^{7,12}]pentacosa-7(12),8,10-trien-20-yl]methyl acetate is a high-purity biochemical reagent suitable for biochemical experiments and drug synthesis research.

(1beta,3beta,25S)-3-Hydroxyspirost-5-en-1-yl 2-O-(6-deoxy-alpha-L-mannopyranosyl)-beta-D-xylopyranoside is a natural product

Seladelpar sodium salt (MBX-8025) is an orally active and specific PPARδ agonist with an EC50 of 2 nM, demonstrating over 750-fold and 2500-fold selectivity compared to the PPARα and PPARγ receptors, respectively.

CP-74725, sodium salt is a bio-active chemical.

MBX-8025 is an agonist of peroxisome proliferator-activated receptor δ (PPARδ).1 It is greater than 750- and 2,500-fold selective for PPARδ over PPARα and PPARγ. MBX-8025 (10 mg/kg per day for eight weeks) reduces increases in fasting blood glucose and serum insulin levels, and decreases insulin resistance in Alms1 mutant (foz/foz) mice fed an atherogenic diet as a model of diet-induced obesity, type 2 diabetes, and non-alcoholic steatohepatitis (NASH).2 It also decreases serum alanine transaminase (ALT), as well as serum and hepatic cholesterol and triglyceride, levels and reduces markers of NASH in the same model. |1. Bays, H.E., Schwartz, S., Littlejohn, T., 3rd, et al. MBX-8025, a novel peroxisome proliferator receptor-δ agonist: Lipid and other metabolic effects in dyslipidemic overweight patients treated with and without atorvastatin. J. Clin. Endocrinol. Metab. 96(9), 2889-2897 (2011).|2. Haczeyni, F., Wang, H., Barn, V., et al. The selective peroxisome proliferator-activated receptor-delta agonist seladelpar reverses nonalcoholic steatohepatitis pathology by abrogating lipotoxicity in diabetic obese mice. Hepatol. Commun. 1(7), 663-674 (2017).

Labeled Amino Acid And Carnitine Mix25 Set I (Standard) is a reference standard of Labeled Amino Acid And Carnitine Mix25 Set I intended for quantitative analysis, quality control, and related biochemical research applications.

Labeled Amino Acid And Carnitine Mix25 Set I-A (Standard) is a reference standard of Labeled Amino Acid And Carnitine Mix25 Set I-A intended for quantitative analysis, quality control, and related biochemical research applications.

Labeled Amino Acid And Carnitine Mix25 Set I-B (Standard) is a reference standard of Labeled Amino Acid And Carnitine Mix25 Set I-B intended for quantitative analysis, quality control, and related biochemical research applications.

7,22,25-Stigmastatrienol is a natural product

25(S)-Hydroxyprotopanaxatriol is a natural product for research related to life sciences. The catalog number is TN2827 and the CAS number is 113539-03-0.

25(S)Ruscogenin 3-O-α-L-rhamnopyranoside, derived from the fibrous roots of Ophiopogon japonicus and Liriope spicata var. prolifera, demonstrates anti-inflammatory properties. It effectively inhibits neutrophil responses to PMA, achieving an IC 50 of 1.13 μM.

1. Gitogenin, tigogenin, and solasodine are novel selective inhibitors of UGT1A4, and do not inhibit the activities of major human CYP isoforms. 2. Gitogenin and (25S)-5α-furastan-3β, 22, 26-triol are the inhibitors of enzyme α-glucosidase with IC50 value

Gitogenin (Standard) is a reference standard for research and analysis in studies involving Gitogenin. 1. Gitogenin, tigogenin, and solasodine are novel selective inhibitors of UGT1A4, and do not inhibit the activities of major human CYP isoforms. 2. Gitogenin and (25S)-5α-furastan-3β, 22, 26-triol are the inhibitors of enzyme α-glucosidase with IC50 values of 37.2±0.18 and 33.5±0.22 uM, respectively.3. Gitogenin shows moderate stimulation of release activity on growth hormone from rat pituitary cells.