152
19
18
17
Cat. No. | Product Name | Target | Signaling Pathways |
---|---|---|---|
T37908 |
Glucocorticoid receptor agonist-1
|
Glucocorticoid Receptor; ADC Cytotoxin | Antibody-drug Conjugate/ADC Related; 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。 | |||
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。 | |||
T11417 |
Glucocorticoid receptor agonist
|
Others | Others |
Glucocorticoid receptor agonist is an effective glucocorticoid receptor agonist. | |||
T63539 |
Glucocorticoid receptor-IN-2
|
Others | Others |
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)。 | |||
T63551 |
Glucocorticoid receptor-IN-1
|
Others | Others |
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
|
Others | Others |
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。 | |||
T9977 |
SGK1-IN-4
|
SGK | Metabolism |
SGK1-IN-4 是 SGK1 的特异性抑制剂,可用于骨关节炎研究。 | |||
T74697 |
Glucocorticoid receptor agonist-2
|
Others; ADC Cytotoxin | Antibody-drug Conjugate/ADC Related; Others |
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。 | |||
T6635 |
EMD638683
|
SGK | Metabolism |
EMD638683 是一种具有抗高血压效力的新型 SGK 抑制剂,IC50=3 μM。 | |||
T2622 |
GSK 650394
GSK650394 |
SGK; Influenza Virus | Metabolism; Microbiology/Virology |
GSK 650394 是一种新颖的 SGK 抑制剂,可抑制流感病毒复制。它还是一种血清和糖皮质激素调节的激酶 1 抑制剂。 | |||
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)。 | |||
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。 | |||
T77869 |
Glucocorticoid receptor agonist-2 Ala-Ala-Mal
|
Others; Drug-Linker Conjugates for ADC | Antibody-drug Conjugate/ADC Related; Others |
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。 | |||
T82303 |
Glucocorticoid receptor agonist-1 phosphate Gly-Glu TFA
|
Others; ADC Linker | Antibody-drug Conjugate/ADC Related; Others |
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。 | |||
T77835 |
Glucocorticoid receptor agonist-1 phosphate Gly-Glu-Br
|
Others; ADC Linker | Antibody-drug Conjugate/ADC Related; Others |
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。 | |||
T74116 |
Glucocorticoid receptor agonist-1 Ala-Ala-Mal
|
Others; Drug-Linker Conjugates for ADC | Antibody-drug Conjugate/ADC Related; Others |
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。 | |||
T75130 |
Glucocorticoid receptor agonist-1 phosphate Ala-Ala-Br
|
Others; Drug-Linker Conjugates for ADC | Antibody-drug Conjugate/ADC Related; Others |
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。 | |||
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。 | |||
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。 | |||
T75016 |
Glucocorticoid receptor agonist-1 phosphate Ala-Ala-Mal
|
Others; Drug-Linker Conjugates for ADC | Antibody-drug Conjugate/ADC Related; Others |
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。 | |||
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。 | |||
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。 | |||
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。 | |||
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。 | |||
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。 | |||
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)。 | |||
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; ADC Cytotoxin | Antibody-drug Conjugate/ADC Related; 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。 | |||
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。 | |||
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。 | |||
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。 | |||
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。 | |||
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。 | |||
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。 | |||
T6503 |
Fluorometholone Acetate
NSC 47438,Flarex,Eflone,氟米龙醋酸酯,Oxylone acetate |
Glucocorticoid Receptor; Carbonic Anhydrase | Endocrinology/Hormones; Metabolism |
Fluorometholone Acetate (Oxylone acetate) 是合成的糖皮质激素皮质类固醇及皮质类固醇酯。它有效抑制碳酸酐酶 (CA) 对 hCA-I(IC50:2.18 μM)和 hCA-II(IC50:17.5 μM)。它具有抗炎活性,可用于研究外部眼部炎症。 | |||
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; ADC Cytotoxin | Antibody-drug Conjugate/ADC Related; 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。 | |||
T19913 |
CKI-7
CKI 7 2HCl,CKI-7 dihydrochloride,N-(2-氨基乙基)-5-氯异喹啉-8-磺酰胺二盐酸盐,CKI7 2HCl,CKI 7 dihydrochloride,CKI7 dihydrochloride,CKI-7 2HCl |
ROCK; SGK; Casein Kinase; CDK; S6 Kinase | Cell Cycle/Checkpoint; Cytoskeletal Signaling; MAPK; Metabolism; PI3K/Akt/mTOR signaling; Stem Cells |
CKI-7 是一种有效且 ATP 竞争性的酪蛋白激酶 1 抑制剂,IC50为 6 μM,Ki 为 8.5 μM。它选择性抑制 Cdc7激酶,还抑制 SGK,S6K1以及 MSK1。 | |||
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。 | |||
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。 | |||
T1018 |
Prednisone
泼尼松,强的松,Dehydrocortisone |
Apoptosis; Glucocorticoid Receptor; MRP | Apoptosis; Endocrinology/Hormones; Immunology/Inflammation |
Prednisone (Dehydrocortisone) 是一种皮质类固醇试剂,有免疫抑制作用。 | |||
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; ADC Cytotoxin | Antibody-drug Conjugate/ADC Related; 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。 | |||
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。 |
Cat. No. | Product Name | Target | Signaling Pathways |
---|---|---|---|
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。 | |||
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。 | |||
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。 | |||
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。 | |||
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。 | |||
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。 | |||
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。 | |||
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。 | |||
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。 | |||
T0269 |
Dichlorisone Acetate
糊状叶绿素,Diloderm,醋酸二氯松 |
Endogenous Metabolite; AChE | Metabolism; Neuroscience |
Dichlorisone Acetate (Diloderm) 一种是合成的糖皮质激素皮质类固醇,具有抗炎特性。 | |||
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。 | |||
T2S2043 |
Dracorhodin perchlorate
Dracorhodin perochlorate,血竭素高氯酸盐,Dracohodin perochlorate |
Apoptosis; Others | Apoptosis; Others |
Dracorhodin perchlorate 是来源于中药血竭的一种天然产物。它抑制细胞生长,并以剂量和时间依赖性方式诱导成纤维细胞凋亡,将细胞周期阻滞在 G1 期,可作为抗乳腺癌的候选药物。 | |||
T5S2343 |
Acetylshikonin
乙酰紫草素,Acetyl shikonin |
Others; P450; AChE | Metabolism; Neuroscience; Others |
Acetylshikonin 来源于紫草根,具有抗癌、抗炎作用。它是一种 AChE 抑制剂,具有很强的抗凋亡活性。它是一种非选择性的细胞色素 P450抑制剂,对所有 P450 亚型抑制的 IC50值范围为 1.4-4.0 μM。 | |||
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. | |||
T13517 |
Allotetrahydrocortisol
5a-Tetrahydrocortisol |
Others | Others |
Allotetrahydrocortisol (5a-Tetrahydrocortisol) is a metabolite of Cortisol. Cortisol is the main glucocorticoid in human. |
Cat. No. | Product Name | Species | Expression System |
---|---|---|---|
TMPH-02792 |
Myocilin Protein, Mouse, Recombinant (His)
Myoc,Myocilin,Trabecular meshwork-induced glucocorticoid... |
Mouse | E. coli |
Myocilin Protein, Mouse, Recombinant (His) is expressed in E. coli expression system with N-6xHis tag. The predicted molecular weight is 35.4 kDa and the accession number is O70624. | |||
TMPH-02793 |
Myocilin Protein, Mouse, Recombinant (His & Myc)
Trabecular meshwork-induced glucocorticoid response... |
Mouse | Baculovirus Insect Cells |
Myocilin Protein, Mouse, Recombinant (His & Myc) is expressed in Baculovirus insect cells with N-10xHis and C-Myc tag. The predicted molecular weight is 35.2 kDa and the accession number is O70624. | |||
TMPY-04561 |
SGK3 Protein, Human, Recombinant (His & GST)
serum/glucocorticoid regulated kinase family, membe... |
Human | Baculovirus Insect Cells |
Serine / threonine-protein kinase Sgk3, also known as Serum / glucocorticoid-regulated kinase 3, Serum / glucocorticoid-regulated kinase-like and SGK3, is a cytoplasmic vesicle protein that belongs to the protein kinase superfamily and AGC Ser/Thr protein kinase family. SGK3 contains one AGC-kinase C-terminal domain, one protein kinase domain and one PX (phox homology) domain. Two specific sites of SGK3, one in the kinase domain (Thr-32) and the other in the C-terminal regulatory region (Ser-486... | |||
TMPY-06836 |
NR3C1 Protein, Human, Recombinant (His)
GCCR,GRL,GR,nuclear receptor subfamily 3, group C, member 1 ... |
Human | E. coli |
NR3C1 (Nuclear Receptor Subfamily 3 Group C Member 1) is a Protein Coding gene. This gene encodes glucocorticoid receptor, which can function both as a transcription factor that binds to glucocorticoid response elements in the promoters of glucocorticoid responsive genes to activate their transcription, and as a regulator of other transcription factors. NR3C1 is a transcriptional regulator of many drug-metabolizing enzymes and anti-inflammatory molecules. NR3C1 polymorphisms associate with obesi... | |||
TMPY-02248 |
Myocilin Protein, Human, Recombinant (His)
myocilin, trabecular meshwork inducible glucocorticoid |
Human | HEK293 Cells |
Myocilin, also known as Trabecular meshwork-induced glucocorticoid response protein, MYOC, and GLC1A, is a protein that contains one olfactomedin-like domain. Myocilin / MYOC may participate in the obstruction of fluid outflow in the trabecular meshwork. Myocilin / MYOC is expressed in large amounts in various types of muscle, ciliary body, papillary sphincter, skeletal muscle, heart, and other tissues. Myocilin / MYOC is expressed predominantly in the retina. In normal eyes, it is found in the ... | |||
TMPJ-00110 |
GITR/TNFRSF18 Protein, Mouse, Recombinant (hFc & His)
Tnfrsf18,GITR-D,CD357,AITR,Tumor necrosis factor receptor su... |
Mouse | HEK293 Cells |
Tumor necrosis factor receptor superfamily member 18(Gitr) contains 3 TNFR-Cys repeats and it have four isforms.IsformA、isformB and isformC is single-pass type I membrane protein and isformD is a secreted protein. The protein is the receptor for TNFSF18.It seems to be involved in interactions between activated T-lymphocytes and endothelial cells and in the regulation of T-cell receptor-mediated cell death. It mediated NF-kappa-B activation via the TRAF2/NIK pathway.It binds to TRAF1, TRAF2, and... | |||
TMPJ-00432 |
GITR Ligand/TNFSF18 Protein, Cynomolgus, Recombinant (His)
GITRL,TNFSF18,Activation-inducible TNF-related ligand,AITRL,... |
Cynomolgus | HEK293 Cells |
TNFSF18 is a single-pass type II membrane protein. It is expressed at high levels in the small intestine, ovary, testis, kidney and endothelial cells. TNFSF18 cytokine binds to TNFRSF18/AITR/GITR. It regulates T-cell responses, and functions as costimulator and lower the threshold for T-cell activation and T-cell proliferation. It is Important for interactions between activated T-lymphocytes and endothelial cells and Promotes leukocyte adhesion to endothelial cells. TNFSF18 mediates activation ... | |||
TMPJ-01319 |
TINAGL1 Protein, Human, Recombinant (His)
LCN7,Tubulointerstitial nephritis antigen-like (TINAGL1),Oxi... |
Human | HEK293 Cells |
TINAGL1 is a secreted protein and contains one SMB (somatomedin-B) domain. TINAGL1 is expressed in aorta, lymph nodes, heart, bone marrow, placenta, lung, kidney, skeletal muscle, pancreas, thyroid, adrenal gland and so on. TINAGL1 may be implicated in the adrenocortical zonation and in mechanisms for repressing the CYP11B1 gene expression in adrenocortical cells. | |||
TMPY-01117 |
MRAP Protein, Human, Recombinant (hFc)
FALP,FGD2,melanocortin 2 receptor accessory protein,GCCD2,B2... |
Human | HEK293 Cells |
MRAP (Melanocortin 2 Receptor Accessory Protein) is a Protein Coding gene. This gene encodes a melanocortin receptor-interacting protein. It belongs to the MRAP family. MRAP, which contains a single transmembrane domain, has a unique structure, an antiparallel homodimer. MRAP is a single transmembrane domain accessory protein and a critical component of the hypothamo pituitary-adrenal axis. MRAP is highly expressed in the adrenal gland and is essential for adrenocorticotropin hormone (ACTH) rece... | |||
TMPH-00844 |
HSD11B2 Protein, Human, Recombinant (His)
HSD11B2,11-beta-hydroxysteroid dehydrogenase type 2,Short ch... |
Human | P. pastoris (Yeast) |
Catalyzes the conversion of cortisol to the inactive metabolite cortisone. Modulates intracellular glucocorticoid levels, thus protecting the nonselective mineralocorticoid receptor from occupation by glucocorticoids. HSD11B2 Protein, Human, Recombinant (His) is expressed in yeast with N-6xHis tag. The predicted molecular weight is 46.1 kDa and the accession number is P80365. | |||
TMPK-00053 |
GITR Ligand/TNFSF18 Protein, Human, Recombinant (His & Flag)
AITRL,TNFSF18,TL6,GITR Ligand,GITRL |
Human | HEK293 Cells |
Glucocorticoid-induced TNFR-related protein (TNFRSF18, GITR, CD357), expressed by T cells, and its ligand (TNFSF18, GITRL), expressed by myeloid populations, provide co-stimulatory signals that boost T cell activity. Due to the important role that GITR plays in regulating immune functions, agonistic stimulation of GITR is a promising therapeutic concept. GITR Ligand/TNFSF18 Protein, Human, Recombinant (His & Flag) is expressed in HEK293 mammalian cells with N-His-Flag tag. The predicted molecula... | |||
TMPK-01064 |
GITR Ligand/TNFSF18 Protein, Mouse, Recombinant (hFc)
GITRL,GITR Ligand,TL6,TNFSF18,AITRL |
Mouse | HEK293 Cells |
Glucocorticoid-induced TNFR-related protein (TNFRSF18, GITR, CD357), expressed by T cells, and its ligand (TNFSF18, GITRL), expressed by myeloid populations, provide co-stimulatory signals that boost T cell activity. Due to the important role that GITR plays in regulating immune functions, agonistic stimulation of GITR is a promising therapeutic concept. GITR Ligand/TNFSF18 Protein, Mouse, Recombinant (hFc) is expressed in HEK293 mammalian cells with N-hFc tag. The predicted molecular weight is ... | |||
TMPK-00054 |
GITR Ligand/TNFSF18 Protein (Primary Amine Labeling), Human, Recombinant (His & Flag), Biotinylated
TL6,GITR Ligand,TNFSF18,AITRL,GITRL |
Human | HEK293 Cells |
Glucocorticoid-induced TNFR-related protein (TNFRSF18, GITR, CD357), expressed by T cells, and its ligand (TNFSF18, GITRL), expressed by myeloid populations, provide co-stimulatory signals that boost T cell activity. Due to the important role that GITR plays in regulating immune functions, agonistic stimulation of GITR is a promising therapeutic concept. GITR Ligand/TNFSF18 Protein (Primary Amine Labeling), Human, Recombinant (His & Flag), Biotinylated is expressed in HEK293 mammalian cells with... | |||
TMPK-00133 |
GITR/TNFRSF18 Protein, Human, Recombinant (aa 26-161, His)
GITR-D,AITR,GITR,CD357,TNFRSF18 |
Human | HEK293 Cells |
GITR (glucocorticoid-induced tumor necrosis factor receptor), also known as AITR and TNFRSF18, is a 40 kDa transmembrane glycoprotein that functions in immune regulation.GIRT is a receptor for TNFSF18. Seems to be involved in interactions between activated T-lymphocytes and endothelial cells and in the regulation of T-cell receptor-mediated cell death. Mediated NF-kappa-B activation via the TRAF2/NIK pathway. GITR/TNFRSF18 Protein, Human, Recombinant (aa 26-161, His) is expressed in HEK293 mamma... | |||
TMPK-01086 |
GITR/TNFRSF18 Protein, Mouse, Recombinant (aa 22-153, His)
TNFRSF18,AITR,GITR-D,CD357,GITR |
Mouse | HEK293 Cells |
GITR (glucocorticoid-induced tumor necrosis factor receptor), also known as AITR and TNFRSF18, is a 40 kDa transmembrane glycoprotein that functions in immune regulation.GIRT is a receptor for TNFSF18. Seems to be involved in interactions between activated T-lymphocytes and endothelial cells and in the regulation of T-cell receptor-mediated cell death. Mediated NF-kappa-B activation via the TRAF2/NIK pathway. GITR/TNFRSF18 Protein, Mouse, Recombinant (aa 22-153, His) is expressed in HEK293 mamma... | |||
TMPK-00132 |
GITR/TNFRSF18 Protein, Human, Recombinant (aa 26-161, His & Avi), Biotinylated
GITR-D,CD357,AITR,GITR,TNFRSF18 |
Human | HEK293 Cells |
GITR (glucocorticoid-induced tumor necrosis factor receptor), also known as AITR and TNFRSF18, is a 40 kDa transmembrane glycoprotein that functions in immune regulation.GIRT is a receptor for TNFSF18. Seems to be involved in interactions between activated T-lymphocytes and endothelial cells and in the regulation of T-cell receptor-mediated cell death. Mediated NF-kappa-B activation via the TRAF2/NIK pathway. GITR/TNFRSF18 Protein, Human, Recombinant (aa 26-161, His & Avi), Biotinylated is expre... | |||
TMPK-01260 |
GITR/TNFRSF18 Protein, Cynomolgus, Recombinant (aa 20-156, His)
TNFRSF18,GITR-D,AITR,CD357,GITR |
Cynomolgus | HEK293 Cells |
GITR (glucocorticoid-induced tumor necrosis factor receptor), also known as AITR and TNFRSF18, is a 40 kDa transmembrane glycoprotein that functions in immune regulation.GIRT is a receptor for TNFSF18. Seems to be involved in interactions between activated T-lymphocytes and endothelial cells and in the regulation of T-cell receptor-mediated cell death. Mediated NF-kappa-B activation via the TRAF2/NIK pathway. GITR/TNFRSF18 Protein, Cynomolgus, Recombinant (aa 20-156, His) is expressed in HEK293 ... | |||
TMPY-01383 |
PRMT6 Protein, Human, Recombinant (His & Flag)
protein arginine methyltransferase 6,HRMT1L6 |
Human | HEK293 Cells |
Protein arginine N-methyltransferase 6, also known as Histone-arginine N-methyltransferase PRMT6, PRMT6, and HRMT1L6, is a member of the protein arginine N-methyltransferase family and PRMT6 subfamily. PRMT6 is highly expressed in kidney and testes. PRMT6 is known to catalyze the generation of asymmetric dimethylarginine in polypeptides. It has been implicated in human immunodeficiency virus pathogenesis, DNA repair, and transcriptional regulation. PRMT6 is known to methylate histone H3 Arg-2 (H... |
Cat. No. | Product Name | Target | Signaling Pathways |
---|---|---|---|
TMID-0130 |
CORTISONE(2,2,4,6,6,9,12,12-d8)
|
||
CORTISONE(2,2,4,6,6,9,12,12-d8) 是 CORTISONE 的氘代化合物。CORTISONE 的 CAS 号为 53-06-5。Cortisone 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。 | |||
T19416 |
Medroxyprogesterone acetate D3
MPA D3,Medroxyprogesterone 17-acetate D3 |
Others | Others |
Medroxyprogesterone acetate D3 is deuterium labeled Medroxyprogesterone acetate. Medroxyprogesterone acetate is a widely used synthetic steroid by its interaction with progesterone, androgen and glucocorticoid receptors. | |||
TMIJ-0193 |
Hydrocortisone-d4
|
||
Hydrocortisone-d4 是 Hydrocortisone 的氘代化合物。Hydrocortisone 的 CAS 号为 50-23-7。Hydrocortisone 是肾上腺皮质分泌的糖皮质激素。 | |||
TMID-0229 |
Cortisol-1,2-d2
|
||
Cortisol-1,2-d2 是 Cortisol 的氘代化合物。Cortisol 的 CAS 号为 50-23-7。Hydrocortisone 是肾上腺皮质分泌的糖皮质激素。 | |||
TMIJ-0204 |
Betamethasone-d10 Dipropionate
|
||
Betamethasone-d10 Dipropionate 是 Betamethasone Dipropionate 的氘代化合物。Betamethasone Dipropionate 的 CAS 号为 5593-20-4。Betamethasone dipropionate 是糖皮质激素类固醇,具有免疫抑制、抗炎作用。 | |||
TMID-0144 |
Prednisolone-d8
|
||
Prednisolone-d8 是 Prednisolone 的氘代化合物。Prednisolone 的 CAS 号为 50-24-8。Prednisolone 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。 | |||
TMID-0111 |
11-Deoxycortisol-2,2,4,6,6-d5
|
||
11-Deoxycortisol-2,2,4,6,6-d5 是 11-Deoxycortisol 的氘代化合物。11-Deoxycortisol 的 CAS 号为 152-58-9。Cortodoxone是糖皮质类固醇激素,能够氧化为皮质醇。 | |||
TMID-0143 |
Prednisolone-d4
|
||
Prednisolone-d4 是 Prednisolone 的氘代化合物。Prednisolone 的 CAS 号为 50-24-8。Prednisolone 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。 | |||
TMIJ-0209 |
Beclomethasone-17-Monopropionate-d3
|
||
Beclomethasone-17-Monopropionate-d3 是 Beclomethasone-17-Monopropionate 的氘代化合物。Beclomethasone-17-Monopropionate 的 CAS 号为 5534-18-9。 | |||
TMIJ-0498 |
Fluticasone Propionate-d5
|
||
Fluticasone Propionate-d5 是 Fluticasone Propionate 的氘代化合物。Fluticasone Propionate 的 CAS 号为 80474-14-2。Fluticasone propionate 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,绝对亲和力KD为 0.5 nM。具有抗病毒活性。 | |||
TMIJ-0162 |
Dexamethasone-d4
|
||
Dexamethasone-d4 是 Dexamethasone 的氘代化合物。Dexamethasone 的 CAS 号为 50-02-2。Dexamethasone是一种糖皮质激素受体激动剂和一种 IL 受体调节剂。在脂多糖诱导的巨噬细胞炎症反应中,它抑制含有炎性 microRNA-155 的外泌体的产生。 | |||
T71893 |
Clobetasol Propionate-d5
|
||
Clobetasol propionate-d5 is intended for use as an internal standard for the quantification of clobetasol propionate by GC- or LC-MS. Clobetasol propionate is a corticosteroid. It binds to glucocorticoid receptors in a cell-free assay and inhibits proliferation of primary human skin fibroblasts when used at a concentration of 5 µg/ml. Topical administration of clobetasol propionate reduces croton oil-induced ear edema in mice. Formulations containing clobetasol propionate have been used in the t... | |||
TMIJ-0208 |
Beclomethasone Dipropionate-d6
|
||
Beclomethasone Dipropionate-d6 是 Beclomethasone Dipropionate 的氘代化合物。Beclomethasone Dipropionate 的 CAS 号为 5534-09-8。Betamethasone dipropionate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。 | |||
TMID-0248 |
Triamcinolone acetonide-d6
|
||
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。 | |||
TMID-0006 |
Budesonide-d8
mixture of diastereomers-d8 |
||
Budesonide-d8 是 Budesonide 的氘代化合物。Budesonide 的 CAS 号为 51333-22-3。Budesonide 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。 | |||
TMIH-0235 |
Finerenone-d5
|
||
Finerenone-d5 是 Finerenone 的氘代化合物。Finerenone 的 CAS 号为 1050477-31-0。Finerenone 是一种选择性、具有口服活性的、非甾体类盐皮质激素受体拮抗剂 (IC50=18 nM)。与糖皮质激素受体、雄激素受体和孕酮受体相比,它表现出良好的选择性 (>500-fold)。它在心肾疾病研究中具有潜在的应用前景,如 2 型糖尿病和慢性肾脏疾病。 | |||
TMID-0115 |
Dehydroepiandrosterone-2,2,3,4,4,6-d6
DHEA-d6 |
||
Dehydroepiandrosterone-2,2,3,4,4,6-d6 是 Dehydroepiandrosterone 的氘代化合物。Dehydroepiandrosterone 的 CAS 号为 53-43-0。Dehydroepiandrosterone 是一种类固醇激素。它通过多种信号传导途径介导其作用,并通过转化成雄激素和雌激素衍生物(例如,雄激素,雌激素,7α和7β DHEA (Prasterone),以及7α和7β表雄甾酮衍生物)在特异性受体上起作用。 |