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Cat. No. | Product Name | Target | Signaling Pathways |
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T11417 |
Glucocorticoid receptor agonist
|
Others | Others |
Glucocorticoid receptor agonist is an effective glucocorticoid receptor agonist. | |||
T37908 |
Glucocorticoid receptor agonist-1
|
Glucocorticoid Receptor | Endocrinology/Hormones |
Glucocorticoid receptor agonist-1是一种强效糖皮质激素受体激动剂,其 IC50 值为 2.8 nM。 | |||
T74697 | Glucocorticoid receptor agonist-2 | ||
Glucocorticoid receptoragonist-2 (compound 21) 作为一种糖皮质激素受体激动剂,具有 6.6 nM 的 IC50 值,主要用于抗炎 ADC 分子的合成。同时,它也是 ABBV-3373 的活性对照物。 | |||
T74116 | Glucocorticoid receptor agonist-1 Ala-Ala-Mal | ||
Glucocorticoid receptoragonist-1 Ala-Ala-Mal (化合物 88) 是一种糖皮质激素,是糖皮质激素受体激动剂。Glucocorticoid receptoragonist-1 Ala-Ala-Mal 可与Adalimumab 偶联制备ADC。 | |||
T77869 |
Glucocorticoid receptor agonist-2 Ala-Ala-Mal
|
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Glucocorticoid receptor agonist-2 Ala-Ala-Mal(化合物79)是ABBV-3373的活性对照,可用于合成抗炎ADC分子。 | |||
T77835 |
Glucocorticoid receptor agonist-1 phosphate Gly-Glu-Br
|
||
Glucocorticoid receptor agonist-1 phosphate Gly-Glu-Br 为ADC linker,适用于ABBV-154、ABBV-927及ABBV-368或相似化合物的合成。 | |||
T82303 |
Glucocorticoid receptor agonist-1 phosphate Gly-Glu TFA
|
||
Glucocorticoid receptor agonist-1 phosphate Gly-Glu (TFA) 是用于抗体-药物偶联物 (Antibody-Drug Conjugates (ADCs)) 合成的可降解 Linker。 | |||
T75130 | Glucocorticoid receptor agonist-1 phosphate Ala-Ala-Br | ||
Glucocorticoid receptor agonist-1 phosphate Ala-Ala-Br 作为一种Drug-linker conjugates for ADC,主要用于抗CD40抗体活性分子偶联物 (ADCs) 的合成, 充当反应试剂。 | |||
T75016 | Glucocorticoid receptor agonist-1 phosphate Ala-Ala-Mal | ||
Glucocorticoid receptoragonist-1 phosphate Ala-Ala-Mal 是一种糖皮质激素受体激动剂。Glucocorticoid receptoragonist-1 phosphate Ala-Ala-Mal 可用于抗 CD40抗体偶联活性分子(ADC)。Glucocorticoid receptoragonist-1 phosphate Ala-Ala-Mal 可用于炎症和免疫调节的研究。 | |||
T15102 |
Dexamethasone palmitate
地塞米松棕榈酸酯,DXP |
Glucocorticoid Receptor | Endocrinology/Hormones |
Dexamethasone palmitate (DXP) (DXP) 是 Dexamethasone 的前药。Dexamethasone 是糖皮质激素受体激动剂。与Dexamethasone 相比, DXP 对糖皮质激素受体的亲和力低 47 倍。DXP 显示出抗炎活性。 | |||
T0270 |
Hydrocortisone 17-butyrate
丁酸氢化可的松,Cortisol 17-butyrate,Hydrocortisone butyrate |
Glucocorticoid Receptor; Annexin A; Adrenergic Receptor | Endocrinology/Hormones; GPCR/G Protein; Neuroscience |
Hydrocortisone 17-butyrate (Cortisol 17-butyrate) 是一种肾上腺皮质激素类药物。 | |||
T22818 |
GSK9027
GR agonist 23a,GSK 9027,GSK-9027 |
Glucocorticoid Receptor | Endocrinology/Hormones |
GSK9027 (GR agonist 23a) 是一种非甾体糖皮质激素受体 (GR) 激动剂。GSK9027 (GR agonist 23a) 在2×GRE报告基因上对比地塞米松的活性属于部分激动剂,活性较地塞米松活性较弱。 | |||
T8396 |
Prednisone acetate
Prednisone 21-acetate,醋酸泼尼松 |
Glucocorticoid Receptor | Endocrinology/Hormones |
Prednisone acetate (Prednisone 21-acetate) 是泼尼松的醋酸盐形式,它是一种糖皮质激素受体激动剂,具有抗炎和免疫调节作用。 | |||
T1124 |
Flumethasone
氟米松,Flumetasone,RS-2177,NSC-54702 |
Glucocorticoid Receptor | Endocrinology/Hormones |
Flumethasone (RS-2177) 是皮质类固醇,可局部用药。它可与 Clioquinol 联合使用,研究外耳炎和耳真菌病。它作用于动物模型时,抗炎活性比 Cortisone 高 420 倍。 | |||
T15451 |
GW-870086
|
Glucocorticoid Receptor | Endocrinology/Hormones |
GW-870086 是抗炎剂,是糖皮质激素受体激动剂,在 A549 细胞中,能够降低 NFκB 报告基因活性(pIC50: 10.1)。 | |||
T0188 |
Fluticasone (propionate)
丙酸氟替卡松,CCI-187881,氟替卡松丙酸酯,Fluticasone propionate |
Glucocorticoid Receptor; Virus Protease; Estrogen/progestogen Receptor; Phospholipase; Endogenous Metabolite | Endocrinology/Hormones; Metabolism; Microbiology/Virology |
Fluticasone propionate (CCI-187881) 是一种选择性糖皮质激素受体激动剂,是一种局部抗炎激素,亲和力KD 为 0.5 nM。具有抗病毒活性。 | |||
T1076 |
Dexamethasone
MK 125,Prednisolone F,NSC 34521,Hexadecadrol,地塞米松 |
Glucocorticoid Receptor; Mitophagy; IL Receptor; SARS-CoV; Antibacterial; Antibiotic; Autophagy; Complement System | Autophagy; Endocrinology/Hormones; Immunology/Inflammation; Microbiology/Virology |
Dexamethasone (Hexadecadrol) 是一种糖皮质激素受体激动剂和一种 IL 受体调节剂。Dexamethasone 具有抗炎和免疫抑制活性,可诱导自噬。Dexamethasone 抑制 LPS 诱导的巨噬细胞炎症反应。 | |||
T1666 |
Fludrocortisone acetate
9α-Fluorcortisol acetate,9α-Fludrocortisone acetate,醋酸氟氢可的松,9α-fluorocortisol acetate |
Glucocorticoid Receptor; Autophagy | Autophagy; Endocrinology/Hormones |
Fludrocortisone acetate (9α-Fludrocortisone acetate) 是一种合成的盐皮质激素,可减少尿液中钠丢失量,也用于增加血压,有用于阿狄森氏病的研究潜力。 | |||
T0820 |
Triamcinolone acetonide
曲安奈德,Aristogel,Azmacort,Aristoderm |
Glucocorticoid Receptor | Endocrinology/Hormones |
Triamcinolone acetonide (Azmacort) 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。 | |||
T28623 |
RU28362
RU-28362,RU 28362 |
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RU28362 is an agonist of glucocorticoid receptor. | |||
T15340 |
Fosdagrocorat
PF-04171327 |
Others | Others |
Fosdagrocorat is an agonist of the dissociated glucocorticoid receptor. | |||
T15048 |
Dagrocorat
PF-00251802 |
Others | Others |
Dagrocorat is a novel and dissociated agonist of glucocorticoid receptor. | |||
T68224 |
GSK866
|
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GSK866 is a selective glucocorticoid receptor agonist (SEGRA). | |||
T13451L |
Mapracorat
BOL-303242X,ZK-245186 |
Others | Others |
Mapracorat is a novel non-steroidal selective agonist of glucocorticoid receptor. | |||
T13451 |
(S)-Mapracorat
(S)-ZK-245186,(S)-BOL-303242X |
Others | Others |
(S)-Mapracorat is a selective and less active agonist of glucocorticoid receptor. | |||
T38540 |
BAY 1003803
|
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BAY 1003803 is a glucocorticoid receptor agonist for the topical treatment of psoriasis or severe atopic dermatitis. | |||
T40697 |
Glucocorticoids receptor agonist 2
|
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Glucocorticoid receptor agonist 2 is a highly effective anti-inflammatory compound, derived from arylpyrazole, that actively binds to and activates the glucocorticoid receptor. This compound exhibits potent anti-inflammatory properties without disrupting insulin secretion. | |||
T71346 |
MS4
|
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MS4 is a novel glucocorticoid receptor (GR) agonist with anti-inflammatory activity and displaying reduced impact on islets. | |||
T40808 |
Glucocorticoids receptor agonist 1
|
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Glucocorticoids receptor agonist 1 (GRA-1) is a highly effective arylpyrazole-based compound that acts as an agonist for the glucocorticoid receptor. GRA-1 exhibits strong anti-inflammatory properties while maintaining insulin secretion function. | |||
T17291 |
ZK 216348
(+)-ZK 216348 |
Others | Others |
ZK 216348 also binds to Progesterone and mineralocorticoid receptors (IC50s: 20.4 nM and 79.9 nM, respectively). ZK 216348 is a nonsteroidal selective glucocorticoid receptor agonist (IC50: 20.3 nM). ZK 216348 has an anti-inflammatory activity similar to | |||
T39088 |
Mc-Dexamethasone
|
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Mc-Dexamethasone is a drug-linker conjugate for ADC . Mc-Dexamethasone is made toxin Dexamethasone conjugated to the non-cleavable MC linker. Dexamethasone is a glucocorticoid receptor agonist. | |||
T63801 |
Beclometasone dipropionate monohydrate
|
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Beclometasone dipropionate monohydrate 是一种 Beclometasone 的前体药物,是一种口服具有活力的糖皮质激素受体激动剂,能够激动糖皮质激素受体,抑制炎症和过度增殖。Beclometasone dipropionate monohydrate 能够用于研究哮喘。 | |||
T10494 |
Beclomethasone 17-propionate
Beclomethasone-17-monopropionate,17-BMP |
Others | Others |
Beclomethasone 17-propionate is an active metabolite of Beclomethasone dipropionate and an agonist of the glucocorticoid receptor (GR). It exhibits greater affinity for GR than Beclomethasone dipropionate. Beclomethasone 17-propionate effectively suppress | |||
T14374 |
AZD2906
|
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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. | |||
T75009 | PPARγ/GR modulator 1 | ||
PPARγ/GR modulator 1 是一种口服活性的 PPARγ和糖皮质激素受体 (GR) 的双动激动剂,Ki 值分别为 3.3 和 33.6 μM。PPARγ/GR modulator 1 可用于研究代谢疾病,例如糖尿病。 | |||
T69930 |
LEO 134310
|
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LEO 134310 是一种选择性非甾体糖皮质激素受体 (GR) 激动剂,优化用于局部治疗。LEO 134310 在 GR 结合试验中显示出高亲和力(EC50为 14 nM)。LEO 134310 可用于皮肤病。 |
Cat. No. | Product Name | Target | Signaling Pathways |
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T1683 |
Actriol
异雌三醇,Epiestriol |
Glucocorticoid Receptor | Endocrinology/Hormones |
Actriol (Epiestriol) 是内源性雌激素雌酮的代谢物,拥有抗炎及抗菌活性。 |