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GPCR/G Protein
Glucocorticoid Receptor

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Glucocorticoid Receptor

Chemical Structure Cat. No. Product Name CAS No.
Vamorolone Chemical Structure
BCP47443 Vamorolone 13209-41-1
Vamorolone (VBP15) is a first-in-class, orally active dissociative steroidal anti-inflammatory drug and membrane-stabilizer. Vamorolone improves muscular dystrophy without side effects. Vamorolone shows potent NF-κB inhibition and substantially reduces hormonal effects.
Amcinonide Chemical Structure
BCP47048 Amcinonide 51022-69-6
Amcinonide is an inhibitor of nitric oxide (NO) release from activated microglia with IC50 of 3.38 nM.
Mometasone Chemical Structure
BCP45832 Mometasone 105102-22-5
Mometasone is a synthetic topical glucocorticoid receptor (GR) agonist with anti-inflammatory, anti-pruritic and vasoconstrictive properties.
Beclometasone Chemical Structure
BCP45831 Beclometasone 4419-39-0
Beclomethasone is a glucocorticoid which is used in chronic asthma and allergic rhinitis. It acts as an antiallergic, antiasthmatic (inhalant) and topical anti-inflammatory.
Glucocorticoid receptor modulator-1 Chemical Structure
BCP43161 Glucocorticoid receptor modulator-1 2452396-89-1
Glucocorticoid receptor modulator-1 is a novel Glucocorticoid receptor modulator.
Dexamethasone palmitate Chemical Structure
BCP44268 Dexamethasone palmitate 14899-36-6
Dexamethasone palmitate is a liposteroid for treatment of hemophagocytic lymphohistiocytosis.
Fludrocortisone acetate Chemical Structure
BCP38927 Fludrocortisone acetate 514-36-3
Fludrocortisone acetate is a synthetic corticosteroid with more mineralocorticoid than glucocorticoid activity.
Hydrocortisone sodium phosphate Chemical Structure
BCP38924 Hydrocortisone sodium phosphate 6000-74-4
Hydrocortisone sodium succinate Chemical Structure
BCP38923 Hydrocortisone sodium succinate 125-04-2
Hydrocortisone sodium succinate is a glucocorticoid which is used to alleviate allergic reactions, particularly those of the skin and gums.
Exicorilant Chemical Structure
BCP36976 Exicorilant 1781244-77-6
Exicorilant is a potent, selective glucocorticoid receptor (GR) antagonist, exhibits no cross-reactivity for the PR and AR receptors.
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