Cat. No. | Product Name | Target | Signaling Pathways |
---|---|---|---|
T1831 |
StemRegenin 1
SR1 |
AhR; Aryl Hydrocarbon Receptor | Immunology/Inflammation; Metabolism |
StemRegenin 1 (SR1) 是一种芳香烃受体拮抗剂,IC50为 127 nM。 | |||
T60037 |
SR15006
|
DNA/RNA Synthesis | Cell Cycle/Checkpoint; DNA Damage/DNA Repair |
SR15006 是 Krüppel 样因子 5 (KLF5) 抑制剂 (IC50 = 41.6 nM)。 | |||
T6082 |
SSR128129E
SSR |
FGFR | Angiogenesis; Tyrosine Kinase/Adaptors |
SSR128129E (SSR) 是一种变构和口服活性 FGFR1 抑制剂 (IC50:1.9 μM),但不影响其他相关的 RTK。 | |||
T22429 |
SR18662
|
DNA/RNA Synthesis | Cell Cycle/Checkpoint; DNA Damage/DNA Repair |
SR18662 是 ML264 类似物,可抑制 Krüppel 样因子 5 (KLF5),IC50 为 4.4 nM,降低多种结直肠癌细胞系的活力并诱导细胞凋亡。 | |||
T12998 |
SR10067
|
Others; Autophagy | Autophagy; Others |
SR10067 是选择性的Rev-Erbα/β的激动剂,其对Rev-Erbβ 和Rev-Erbα 的IC50分别为 160 nM 和 170 nM。SR10067可以透过大脑的。SR10067具有抗焦虑活性。 | |||
T23383 |
SR11237
SR 11237 |
Others; RAR/RXR | Metabolism; Others |
SR11237 是一种泛视黄醇 X 受体 (RXR) 激动剂。 SR11237 导致 RXR/RXR 同源二聚体形成并反式激活包含 RXR 反应元件的报告基因。 | |||
T16928 |
SR144528
|
Cannabinoid Receptor | GPCR/G Protein |
SR144528 是 CB2 受体的拮抗剂 (Ki = 0.6 nM) 并抑制微粒体 ACAT 活性 (IC50 = 3.6 μM)。 | |||
T6994 |
SR12813
SR-12813,SR 12813,GW 485801 |
HMG-CoA Reductase; Autophagy | Autophagy; Metabolism |
SR12813 (GW 485801) 是一种人孕烷X 受体激动剂,还是一种 3-羟基-3-甲基-戊二酰辅酶 A 还原酶抑制剂,IC50值为 0.85 μM。 | |||
T4594 |
SR1078
SR 1078 |
ROR | Metabolism |
SR1078 是视黄酸受体相关孤儿受体 (RORα/RORγ) 激动剂。它能够与 RORα 和 RORγ 的配体结合区直接结合,增强该受体的转录活性,促使 RORα/γ 靶基因的转录。 | |||
T5163 |
SR1001
|
ROR | Metabolism |
SR1001 是选择性RORα及RORγt 的反向激动剂,其Ki 分别为 172 和 111 nM。 | |||
T28856 |
SSR180711 hydrochloride
SSR-180711A HCl,SSR-180711C HCl,SR-180711 HCl |
AChR | Neuroscience |
SSR180711 hydrochloride (SSR-180711A HCl) 是一种具有选择性的 Alpha7 尼古丁乙酰胆碱部分激动剂,可用于研究神经分裂和认知障碍。 | |||
T4407 |
SR17018
|
Opioid Receptor | Endocrinology/Hormones; GPCR/G Protein; Neuroscience |
SR17018 是一种 μ-阿片受体 (MOR) 激动剂,与 GTPγS 结合,EC50 为 97 nM。 | |||
T23389 |
SR1664
SR 1664 |
PPAR | DNA Damage/DNA Repair; Metabolism |
SR1664 是一种PPARγ拮抗剂,与结合PPARγ,可有效抑制 Cdk5 介导的PPARγ磷酸化,IC50为80 nM,Ki 为 28.67 nM。 | |||
T28855 |
SSR126768A
SSR-126768A,SSR 126768A |
Oxytocin Receptor | Endocrinology/Hormones; GPCR/G Protein |
SSR126768A 是一种新型且具有选择性、口服活性和有效性的催产素(OT)受体拮抗剂,对子宫收缩有抑制作用,可用于预防早产。 | |||
T28845 |
SR142948A HCl
SR142948A,SR 142948A,SR-142948A,SR142948A hydrochloride |
||
SR 142948A is a non-peptide antagonist of neurotensin receptor. SR 142948A affects the expression of c-Fos and has properties of antipsychotic agent. SR 142948A blocks hypothermia and analgesia induced by neurotensin. It blocks the increase in the concent | |||
T63206 | SR12418 | ||
SR12418 是一种特异性的 REV-ERB 合成配体,能够作用于 REV-ERBα (IC50: 68 nM) 和 REV-ERBβ (IC50: 119 nM),可用于研究实验性自身免疫性脑脊髓炎 (EAE) 和结肠炎。 | |||
T28846 |
SR16835
AT-202,AT202,SR 16835,SR-16835 |
||
SR16835 is a NOP receptor agonist, with low-affinity bifunctional activity at the μ opioid receptor. | |||
T24828 |
SR14150
SR-14150,SR 14150 |
||
SR14150 is a partial agonist of high-affinity NOP receptor. | |||
T69671 | SR1903 TFA | ||
SR-1903 is a modulator of retinoic acid receptor-related orphan receptor γ (RORγ) and liver X receptor (LXR). It is an inverse agonist of RORγ and an agonist of LXR. It also binds to peroxisome proliferator-activated receptor γ (PPAR) but does not activate it. SR-1903 inhibits LPS-induced expression of triggering receptor expressed on myeloid cells 1 (TREM-1). It also inhibits LPS-induced expression of the LXR target genes IL-6 and IL-33 and increases expression of ABCG1, FASN, and SCD-1. SR-190... | |||
T13003 |
SSR128129E free acid
SSR free acid |
FGFR | Angiogenesis; Tyrosine Kinase/Adaptors |
SSR128129E free acid is an orally available and allosteric inhibitor of FGFR(IC50 of 1.9 μM for FGFR1). | |||
T12999 | SR121566A | Others | Others |
SR121566A is a novel non-peptide antagonist of Glycoprotein IIb/IIIa (GP IIb-IIIa). | |||
T26223 |
SR1555 HCl
SR-1555,SR1555,SR 1555 |
||
SR1555 is a selective RORγ inverse agonist that inhibits the development and function of TH17 cells, a subset of T cells that have been involved in the pathology of several autoimmune diseases such as rheumatoid arthritis and multiple sclerosis. | |||
T62239 |
HSR1304
|
||
HSR1304 (Compound 5d) 是一种 NFκB 的有效抑制剂。其中多功能转录因子核因子-κB (NF-κB) 广泛的参与多种人类疾病(如癌症、慢性炎症)。HSR1304 具有潜力进行癌症疾病的研究。 |