ADL-5747 (ADL-5747 (free base)) (free base)是一种δ opioid 受体激动剂，可用于治疗神经系统疾病、皮肤和肌肉骨骼疾病，可用于研究疱疹后神经痛、膝关节炎和疼痛。

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.

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。

Fosdagrocorat is an agonist of the dissociated glucocorticoid receptor.

Dagrocorat is a novel and dissociated agonist of glucocorticoid receptor.

RU 26752 是盐皮质激素受体的拮抗剂。在大鼠试验中，该化合物有效阻止了醛固酮诱导的高血压。

SRC-1 (686-700) 是一种含有第二个 LXXLL 基序的生物活性肽，构成自类固醇受体共激活剂 (SRC1) NR 盒 II 的氨基酸 686 至 700 片段。这种共激活蛋白能够以配体依赖的方式与核受体发生相互作用，并增强转录活性。

C108297 is a glucocorticoid receptor modulator. C108297 prevents both diet-induced obesity and inflammation. C108297 decreased food and fructose intake and increased lipolysis in white adipose tissue (WAT) and free fatty acid levels in plasma, resulting i

Gypenoside LXXV是一种发现于Panax ginseng的天然皂苷，能够和Glucocorticoid receptor结合并转移到细胞核内，从而促进伤口愈合和上调CTGF。