99
15
Cat. No. | Product Name | Target | Signaling Pathways |
---|---|---|---|
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。 | |||
T11417 |
Glucocorticoid receptor agonist
|
Others | Others |
Glucocorticoid receptor agonist is an effective glucocorticoid receptor agonist. | |||
T67742 |
EX-A5386
Glucocorticoid receptor modulator-1 |
Glucocorticoid Receptor | Endocrinology/Hormones |
EX-A5386 (Glucocorticoid receptor modulator-1)是一种有效的糖皮质激素受体调节剂,IC50/EC50<100nM。 | |||
T14377 |
AZD5423
|
Glucocorticoid Receptor | Endocrinology/Hormones |
AZD5423 是可吸入的非甾体糖皮质激素受体选择性调节剂,能够有效降改善轻度过敏性哮喘患者的过敏原诱导反应。 | |||
T8777 |
Beclometasone
倍氯米松,BecloMethasone |
Glucocorticoid Receptor | Endocrinology/Hormones |
Beclometasone 是糖皮质激素受体激动剂。 | |||
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)。 | |||
T14981 |
Clobetasone butyrate
|
Glucocorticoid Receptor | Endocrinology/Hormones |
Clobetasone butyrate 是糖皮质类固醇,特别是在皮肤上,具有局部抗炎活性。它可用于改善皮质类固醇反应性症状,如特应性皮炎、牛皮癣。 | |||
T17217 |
Vamorolone
地塞米松EP杂质E,VBP15 |
Glucocorticoid Receptor; NF-κB | Endocrinology/Hormones; NF-κB |
Vamorolone (VBP15) 是一种首创的,具有口服活性的解离性类固醇 (dissociative steroidal) 抗炎药和膜稳定剂。它抑制 (NF-κB) 抑制作用,并降低了激素的影响。它改善肌营养不良,无副作用。 | |||
T63539 | Glucocorticoid receptor-IN-2 | ||
Glucocorticoid receptor-IN-2 是糖皮质激素受体 (glucocorticoid receptor (GR)) 的选择性调节剂,表现出抗炎活性。Glucocorticoid receptor-IN-2 具有良好的转录抑制作用,能够作用于 hMMP1 (IC50: 0.171 nM),也具有一定的转录激活作用,能够作用于 MMTV (EC50: 0.94 nM)。 | |||
T3316 |
Fluorometholone
氟米龙,Fluoromethalone,Cortilet,Oxylone,Delmeson |
Glucocorticoid Receptor | Endocrinology/Hormones |
Fluorometholone (Fluoromethalone) 是合成糖皮质激素,具有抗炎和抗过敏作用。它可用作糖皮质激素受体激动剂,能够用于干眼症的研究。 | |||
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。 | |||
T1163 |
Betamethasone valerate
Betnovate,倍他米松戊酸酯,Betaderm,Betamethasone 17-valerate,Luxiq |
Glucocorticoid Receptor | Endocrinology/Hormones |
Betamethasone valerate (Luxiq) 的 17 戊酸酯,是一种具有抗炎活性的局部皮质类固醇。它能够抑制放射标记的糖皮质激素地塞米松与人表皮(IC50:5 nM)及小鼠皮肤(IC50:6 nM)的结合。它可用于研究复发性口疮。 | |||
T63551 |
Glucocorticoid receptor-IN-1
|
||
Glucocorticoid receptor-IN-1 是糖皮质激素受体 (glucocorticoid receptor (GR)) 对选择性调节剂,表现出抗炎活性。Glucocorticoid receptor-IN-1 具有良好的转录抑制作用,能够作用于 hMMP1 (IC50: 2.11 nM),也具有转录激活效果,能够作用于 MMTV (EC50: 5.59 nM)。 | |||
T72102 | Glucocorticoid receptor modulator 1 | ||
Glucocorticoid receptor modulator1 是一种高效且具有口服活性的 NF-κB 和 AP-1抑制剂,IC50分别为 9 nM 和 130 nM。Glucocorticoid receptor modulator1 可有效降低炎症因子 IL-6、IL-1β、TNF-α 的表达,可缓解小鼠皮炎。 | |||
T0261 |
Amcinonide
安西奈德,CL-34699 |
Glucocorticoid Receptor; Annexin A | Endocrinology/Hormones; GPCR/G Protein |
Amcinonide (CL-34699) 是皮质类固醇。它能够抑制NO 从活化的小胶质细胞释放(IC50:3.38 nM),具有糖皮质激素受体亲和力。 它是皮质类固醇激素受体激动剂。 | |||
T6502 |
Fluocinonide
醋酸氟轻松,Lidex,Metosyn,氟轻松,Topsyn |
Glucocorticoid Receptor | Endocrinology/Hormones |
Fluocinonide (Topsyn) 是一种糖皮质激素类固醇,具有抗炎作用,可作用于皮肤疾病的研究。 | |||
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。 | |||
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。 | |||
T0181 |
Loteprednol etabonate
Lotemax,Alrex,氯替泼诺 |
Glucocorticoid Receptor; Antibacterial; Antibiotic | Endocrinology/Hormones; Microbiology/Virology |
Loteprednol etabonate (Lotemax) 是具有抗炎活性的皮质类固醇,用于眼科。 | |||
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。 | |||
T1749 |
AL 082D06
D-06,AL082D06 |
Glucocorticoid Receptor | Endocrinology/Hormones |
AL 082D06 (D-06) 是非甾体类糖皮质激素受体 (GR) 选择性拮抗剂(Ki:210 nM)。 | |||
T2526 |
Ciclesonide
Zetonna,环索奈德,RPR251526,Omnaris,Alvesco |
Glucocorticoid Receptor | Endocrinology/Hormones |
Ciclesonide (Alvesco) 是一种糖皮质激素,具有强效抗炎活性,可用于研究哮喘。 | |||
T0367 |
Fluocinolone (Acetonide)
Fluocinolone acetonide,醋酸肤轻松,Flucort-N |
Glucocorticoid Receptor | Endocrinology/Hormones |
Fluocinolone Acetonide (Flucort-N) 是一种糖皮质激素衍生物,能够作用于各种皮肤病的研究。 | |||
TQ0225 |
Velsecorat
AZD7594,AZ13189620 |
Glucocorticoid Receptor | Endocrinology/Hormones |
Velsecorat (AZD7594) 是非甾体类糖皮质激素受体的选择性调节剂(IC50:0.9 nM)。 | |||
T6713 |
Ulipristal
|
Estrogen/progestogen Receptor; Progesterone Receptor | Endocrinology/Hormones; Others |
Ulipristal 是性孕酮受体 (progesterone receptor) 的选择性调节剂。它能够与孕激素受体结合,抑制 PR 介导的基因表达,降低生殖系统中孕激素的活性。 | |||
T0094 |
Budesonide
Entocort,Pulmicort,布地奈德,Rhinocort |
Glucocorticoid Receptor | Endocrinology/Hormones |
Budesonide (Pulmicort) 是吸入型糖皮质类固醇,是一种口服具有活性的糖皮质激素受体激动剂。它能够减小肺部肿瘤的体积,逆转 DNA 低度甲基化,调节基因的 mRNA 表达。它是能够用于哮喘的抗炎药。 | |||
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。 | |||
T1531 |
Mometasone furoate
糠酸莫美他松,糠酸莫米松,Sch32088 |
Glucocorticoid Receptor | Endocrinology/Hormones |
Mometasone furoate (Sch32088) 是糖皮质激素受体激动剂,具有抗炎和抗过敏作用。它是皮质固醇类试剂,动物模型中,可局部应用于气道炎症、慢性皮肤湿疹、哮喘。 | |||
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。 | |||
T77869 |
Glucocorticoid receptor agonist-2 Ala-Ala-Mal
|
||
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。 | |||
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。 | |||
T6580 |
Meprednisone
SCH 4358,Methylprednisone,NSC 527579,Betanisona,Betapar,泼尼松 |
Glucocorticoid Receptor; Autophagy | Autophagy; Endocrinology/Hormones |
Meprednisone (Betapar) 是糖皮质激素,用于糖皮质激素受体,是泼尼松的甲基化衍生物。 | |||
T22367 |
Methylprednisolone succinate
Methylprednisolone hemisuccinate,Methylprednisolone hydrogen succinate,甲基泼尼松龙琥珀酸酯 |
Glucocorticoid Receptor | Endocrinology/Hormones |
Methylprednisolone succinate (Methylprednisolone hemisuccinate) 是合成的糖皮质激素,常用作抗炎剂。 | |||
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。 | |||
T21404 |
Fluticasone furoate
Veramyst,Allermist,Avamys,糠酸氟替卡松,Fluticasone furoate |
Glucocorticoid Receptor | Endocrinology/Hormones |
Fluticasone furoate (Avamys) 是一种合成的三氟化皮质类固醇,衍生自氟替卡松,Kd 为 0.3 nM。Fluticasone furoate 具有有效的抗炎、抗哮喘活性和低全身暴露。Fluticasone furoate 可用作过敏性鼻炎治疗研究的鼻喷雾剂。 | |||
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。 | |||
T2527 |
Ulipristal acetate
Ulipristal,醋酸乌利司他,CDB-2914 |
Estrogen/progestogen Receptor; Progesterone Receptor; Autophagy | Autophagy; Endocrinology/Hormones; Others |
Ulipristal acetate (CDB-2914) 是一种具有抗孕酮活性的选择性孕酮受体调节剂。它可抑制子宫平滑肌瘤病的生长。它通过抑制或延迟排卵和影响子宫内膜组织,可用作紧急避孕药。 | |||
T1102 |
Mifepristone
C-1073,RU486,RU 38486,米非司酮 |
Glucocorticoid Receptor; Estrogen/progestogen Receptor; Progesterone Receptor; NO Synthase; Autophagy | Autophagy; Endocrinology/Hormones; Immunology/Inflammation; Others |
Mifepristone (C-1073) 是一种黄体酮受体和糖皮质激素受体拮抗剂,在体外实验中的 IC50值分别为 0.2 nM 和 2.6 nM。 | |||
T16079 |
Mirodenafil
米罗那非,SK3530 |
PDE | Metabolism |
Mirodenafil 是一种磷酸二酯酶5(PDE-5)抑制剂,可用于勃起功能紊乱的研究。 | |||
T1127 |
Beclometasone dipropionate
Beclovent,Beclomethasone dipropionate,二丙酸倍氯米松,丙酸倍氯米松,Beconase,Vancenase |
Glucocorticoid Receptor | Endocrinology/Hormones |
Beclometasone dipropionate (Vancenase) 是具有口服活性的糖皮质激素,具有抗炎和免疫抑制作用。它是Betamethasone 的前体药物,Betamethasone 是 LPS 诱导的炎症及 MMP 释放的抑制剂。 | |||
T0947L |
Dexamethasone Phosphate disodium
地塞米松磷酸二钠,EGP-437,EGP437. Dex-Phos,EGP 437 |
Glucocorticoid Receptor | Endocrinology/Hormones |
Dexamethasone Phosphate disodium (EGP437. Dex-Phos) 是糖皮质激素受体激动剂。 | |||
T0208 |
Prednisolone disodium phosphate
泼尼松龙21-磷酸二钠,Prednisolone phosphate sodium,Prednisolone 21-phosphate disodium,泼尼松龙磷酸钠 |
Glucocorticoid Receptor | Endocrinology/Hormones |
Prednisolone disodium phosphate是一种合成的糖皮质素,具有抗炎和免疫调节作用。 | |||
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。 | |||
T1559 |
Betamethasone dipropionate
Diprolene AF,SCH 11460,二丙酸倍他米松,Betamethasone 17,21-dipropionate,Diprolene,倍他米松二丙酸酯,Diprosone |
Glucocorticoid Receptor | Endocrinology/Hormones |
Betamethasone dipropionate (SCH 11460) 是糖皮质激素类固醇,具有免疫抑制、抗炎作用。 | |||
T0947 |
Dexamethasone acetate
Dexamethasone 21-acetate,醋酸地塞米松,Dexamethason acetate,NSC 39471 |
Glucocorticoid Receptor; Mitophagy; IL Receptor; Annexin A; NOS; Antibacterial; Autophagy | Autophagy; Endocrinology/Hormones; GPCR/G Protein; Immunology/Inflammation; Microbiology/Virology |
Dexamethasone acetate (NSC 39471) 是一种糖皮质素类甾体,有抗炎和免疫抑制活性。它可研究眼部感染。 | |||
TQ0126 |
Mirodenafil dihydrochloride
SK-3530 dihydrochloride,米罗那非二盐酸盐 |
PDE | Metabolism |
Mirodenafil dihydrochloride 是一种磷酸二酯酶5(PDE-5)抑制剂,可作用于勃起功能紊乱的研究。 | |||
T4602 |
Hydrocortisone hemisuccinate
Hydrocortisone 21-he,氢化可的松琥珀酸酯,hydrocortisone 21-hemisuccinate*free acid,Hydrocortisone 21-hemisuccinate |
Glucocorticoid Receptor; Others; Interleukin | Endocrinology/Hormones; Immunology/Inflammation; Others |
Hydrocortisone hemisuccinate (hydrocortisone 21-hemisuccinate*free acid) 是糖皮质激素, 是口服有活性的甾体抗炎剂。它能够降低IL-6(IC50:6.7 μM)、IL-3(IC50:21.4 μM)的生物活性,可用于研究溃疡性结肠炎。 | |||
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。 | |||
T34383 |
Rofleponide
|
Glucocorticoid Receptor | Endocrinology/Hormones |
Rofleponide 是一种人工合成的糖皮质激素,与大鼠胸腺糖皮质激素受体有很高的亲和力。 | |||
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。 |
Cat. No. | Product Name | Target | Signaling Pathways |
---|---|---|---|
T1614 |
Hydrocortisone
氢化可的松,Cortisol |
Glucocorticoid Receptor; Endogenous Metabolite | Endocrinology/Hormones; Metabolism |
Hydrocortisone (Cortisol) 是一种糖皮质激素,由肾上腺素皮质分泌。Hydrocortisone 激动糖皮质激素受体,可促进蛋白质分解代谢、糖异生、毛细血管壁稳定性、肾脏钙排泄,并抑制免疫和炎症反应。 | |||
T1560 |
Prednisolone
氢化泼尼松,Predonine,Hydroretrocortine,泼尼松龙,Metacortandralone |
Glucocorticoid Receptor; Endogenous Metabolite | Endocrinology/Hormones; Metabolism |
Prednisolone (Hydroretrocortine) 是有口服活性的皮质类固醇和糖皮质激素。它的抗炎特性约为氢化可的松的四倍,同时减少了水和盐的保留。它能够用于眼部抗炎研究。 | |||
T1168 |
Desonide
Tridesilon,地索奈德,Locapred,Prednacinolone |
Glucocorticoid Receptor | Endocrinology/Hormones |
Desonide (Prednacinolone) 是一种非氟化皮质类固醇抗炎剂,能够作用于糖皮质激素受体。 | |||
T0798 |
Triamcinolone
Fluoxyprednisolone,曲安西龙,Aristocort,Rodinolone |
Glucocorticoid Receptor; COX | Endocrinology/Hormones; Immunology/Inflammation; Neuroscience |
Triamcinolone (Aristocort) 是一种皮质类固醇激素受体激动剂,也是一种合成的长效糖皮质激素,具有抗炎活性。 | |||
T2810 |
(20S)-Protopanaxatriol
原人参三醇,20(S)-APPT,20 (S)-原人参三醇,g-PPT |
Apoptosis; Estrogen Receptor/ERR; Glucocorticoid Receptor; Estrogen/progestogen Receptor; Liver X Receptor | Apoptosis; Endocrinology/Hormones; Metabolism |
(20S)-Protopanaxatriol (g-PPT) 是人参皂苷的代谢物,通过糖皮质激素受体和雌激素受体起作用,同时为LXRα的抑制剂,具有广泛的抗癌活性。 | |||
T2884 |
Cortisone
Kendall's compound E,17-Hydroxy-11-dehydrocorticosterone,可的松 |
Glucocorticoid Receptor; Endogenous Metabolite | Endocrinology/Hormones; Metabolism |
Cortisone (17-Hydroxy-11-dehydrocorticosterone) 是 Cortisol(一种糖皮质激素)的氧化代谢产物。Cortisone 具有消炎和免疫抑制的作用。Cortisone 在高浓度下对 Glucocorticoid 与Glucocorticoid-receptor 的结合具有部分干预作用。 | |||
T1243 |
Hydrocortisone acetate
Cortisol 21-acetate,Hydrocortisone 21-acetate,醋酸氢化可的松 |
Glucocorticoid Receptor; Annexin A; Endogenous Metabolite | Endocrinology/Hormones; GPCR/G Protein; Metabolism |
Hydrocortisone acetate (Cortisol 21-acetate) 是皮质类固醇,能够减少轻微皮肤刺激或痔疮引起的肿胀、搔痒和疼痛。 | |||
T1261 |
Medroxyprogesterone Acetate
Medroxyprogesterone 17-acetate,Provera,Metigestrona,NSC-26386,醋酸甲羟孕酮,Farlutin,安宫黄体酮,Medroxyprogesterone (acetate) |
Glucocorticoid Receptor; Estrogen/progestogen Receptor; Progesterone Receptor; Androgen Receptor; Endogenous Metabolite | Endocrinology/Hormones; Metabolism; Others |
Medroxyprogesterone Acetate (Farlutin) 是广泛使用的合成类固醇,与雄激素,孕酮及糖皮质激素受体均有作用。 | |||
T0034 |
Cortisone acetate
醋酸可的松,Cortisone 21-acetate,NSC 49420 |
Glucocorticoid Receptor; Endogenous Metabolite | Endocrinology/Hormones; Metabolism |
Cortisone acetate (NSC-49420) 是 Cortisol(一种糖皮质激素)的氧化代谢产物。它在高浓度下能够部分干预 Glucocorticoid 与Glucocorticoid-receptor 的结合。它具有免疫抑制和消炎的作用。 | |||
T2748 |
Cortodoxone
可托多松,11-Deoxycortisol,cortexolone,17α,21-dihydroxyprogesterone,Reichstein's substance S,11-Desoxycortisol |
Glucocorticoid Receptor; Endogenous Metabolite | Endocrinology/Hormones; Metabolism |
Cortodoxone (11-Desoxycortisol) 是糖皮质类固醇激素,能够氧化为皮质醇。 | |||
T0948L |
Corticosterone
皮质酮,17-Deoxycortisol,11β,21-Dihydroxyprogesterone,Kendall's compound B,肾上腺酮,Corticosterone (From plants) |
Glucocorticoid Receptor; Endogenous Metabolite | Endocrinology/Hormones; Metabolism |
Corticosterone (Kendall's compound B) 是一种肾上腺皮质类固醇,有盐皮质激素和糖皮质激素的活性,具有口服活性。Corticosterone 参与体内能量、免疫反应和应激反应的调节。 | |||
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。 | |||
T6343 |
Geldanamycin
格尔德霉素,NSC 122750 |
HSP; Influenza Virus; Tyrosine Kinases; Antibacterial; Antibiotic | Cytoskeletal Signaling; Metabolism; Microbiology/Virology; Tyrosine Kinase/Adaptors |
Geldanamycin 是一种 HSP90 抑制剂(Kd:1.2 μM),可特异性破坏糖皮质激素受体 (GR)/HSP 的结合。 | |||
T1429 |
17α-Hydroxyprogesterone
Hydroxyprogesterone,17-OHP,羟孕酮,17-Hydroxyprogesterone,17α-羟孕酮 |
Estrogen/progestogen Receptor; Progesterone Receptor; Endogenous Metabolite | Endocrinology/Hormones; Metabolism; Others |
17α-Hydroxyprogesterone (17-OHP) 是一种内源性孕激素,其他类固醇激素(包括糖皮质激素,雌激素,和雄激素)生物合成的化学中间体。 | |||
TN3537 |
Braylin
|
IL Receptor; TNF; NF-κB | Apoptosis; Immunology/Inflammation; NF-κB |
Braylin has anti-inflammatory, antinociceptive and immunomodulatory effects, which possibly act through the glucocorticoid receptor activation and by inhibition of the transcriptional activity of NF-κB. Braylin is also a phosphodiesterase-4 inhibitor, it could represent an ideal prototype of glucocorticoid receptor ligand, able to induce synergic immunomodulatory effects. |