Ocedurenone, a corticosteroid receptor antagonist, is a compound utilized in the investigation of kidney disease (WO2018054357, compound I).

AZD2906, a selective glucocorticoid receptor (GR) agonist, demonstrates inhibitory concentrations (IC50s) of 2.2 nM in human GR, 0.3 nM in rat peripheral blood mononuclear cells (PBMC), 41.6 nM in human whole blood, and 7.5 nM in rat whole blood, respectively[1]. Additionally, it induces an increase in micronucleated immature erythrocytes within rat bone marrow.

(S)-Baxdrostat is an S-enantiomer of Baxdrostat, which functions as an inhibitor of aldosterone synthase [1].

ZK 216348是一种非甾体选择性糖皮质激素受体 (glucocorticoid receptor) 激动剂，其IC50为20.3 nM。ZK 216348还能够与孕激素受体和盐皮质激素受体结合，IC50分别为20.4 nM和79.9 nM，可用于研究炎症性肠病（IBD）。

18-Oxocortisol is a cortisol derivative generated by aldosterone synthase (CYP11B2). It acts as a naturally occurring mineralocorticoid agonist and serves as a biomarker in adrenal vein sampling.

Triamcinolone acetonide-d6 是 Triamcinolone acetonide 的氘代化合物。Triamcinolone acetonide 的 CAS 号为 76-25-5。Triamcinolone acetonide 是皮质类固醇。 它是皮质类固醇激素受体激动剂。 它是抗炎糖皮质激素，局部用于治疗各种皮肤疾病。它的有效性是 prednisone 的八倍。

Hydrocortisone-d3是一种氘代标记的Hydrocortisone。Hydrocortisone (Cortisol) 属于肾上腺皮质分泌的类固醇激素或糖皮质激素。

Loteprednol 是一种合成皮质类固醇，归属于糖皮质激素类别，具有抗炎、抗过敏和免疫抑制活性。Loteprednol 可用于眼部炎症的研究。

α-Cortolone, a metabolite of the glucocorticoid cortisol (hydrocortisone), is produced through the action of 20α-hydroxysteroid dehydrogenase (20α-HSD) via a tetrahydrocortisone (THE) intermediate. Studies indicate that urinary levels of α-cortolone are reduced in patients experiencing severe anorexia nervosa and postmenopausal women diagnosed with endometrial adenocarcinoma, in comparison to postmenopausal women without the condition.