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。 | |||
T23384 |
SR 11302
|
DNA/RNA Synthesis | Cell Cycle/Checkpoint; DNA Damage/DNA Repair |
SR 11302 是一种类视黄醇,是一种激活蛋白-1 转录因子抑制剂,能够特异性抑制 AP-1 活性,而不会激活视黄酸反应元件 (RARE) 的转录。 | |||
T12075 |
ML-180
SR1848 |
Others | Others |
ML-180 (SR1848) 是孤儿核受体肝受体同源物 1 (LRH-1;NR5A2) 的反向激动剂(IC50:3.7 µM)。它不抑制类固醇生成因子 1 (SF-1;NR5A1; IC50>10 µM)。 它具有潜在的抗依赖 LRH-1 癌症作用。 | |||
T1615 |
Irbesartan
厄贝沙坦,SR-47436,BMS-186295 |
Apoptosis; RAAS | Apoptosis; Endocrinology/Hormones |
Irbesartan (SR-47436) 是一种 1 型血管紧张素 II 受体拮抗剂,IC50为1.3 nM。 | |||
T14667 |
BLT-1
|
Others; HCV Protease | Microbiology/Virology; Others; Proteases/Proteasome |
BLT-1 是一种氨基硫脲铜螯合剂,是一种选择性清除受体 B1 型 (SR-BI) 抑制剂,抑制高密度脂蛋白 (HDL) 和 SR-BI 介导的细胞之间的脂质转移。 | |||
T26221 |
MCT1-IN-2
SR13800,SR-13800,SR 13800 |
||
SR13800 is a monocarboxylate transporter 1 (MCT1) inhibitor with cell-permeable. | |||
T28041 |
Mimopezil
ZT-1 LA,Debio-9902-SR,Debio-9902,ZT-1 |
||
Mimopezil is an acetylcholinesterase (AChE) inhibitor. | |||
T16074 |
Mifobate
SR-202,米福贝特 |
PPAR | DNA Damage/DNA Repair; Metabolism |
Mifobate (SR-202) 是一种有效且特异性的 PPARγ拮抗剂,可选择性抑制噻唑烷二酮 (TZD) 诱导的 PPARγ 转录活性,IC50为140 μM,具有抗肥胖和抗糖尿病作用。 | |||
T1519 |
Rimonabant hydrochloride
盐酸利莫那班,SR 151716A,SR 141716A |
Cannabinoid Receptor; Antibacterial | GPCR/G Protein; Microbiology/Virology |
Rimonabant hydrochloride (SR 141716A) 是中心大麻素受体 1 的高效选择性反向激动剂, Ki 值为1.8 nM。它也能够抑制分枝杆菌膜蛋白3。 | |||
T28847 | SR-17398 | ||
SR-17398 is an inhibitor of Unc-51-Like Kinase 1 (ULK1) (IC50 = 22.4 uM). | |||
T81107 | SR-29065 | ||
SR-29065是选择性REV-ERBα激动剂,适用于研究自身免疫性疾病。 | |||
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... | |||
T80770 |
wt hMLN TFA
|
||
wt hMLN (TFA) 是一种微量蛋白,能够抑制SR Ca2+泵 (SERCA);在骨骼肌的钙稳态调节中具有重要功能。 | |||
T35638 |
SR 1903
|
||
SR 1903 is a modulator of retinoic acid receptor-related orphan receptor γ (RORγ) and liver X receptor (LXR).1 It is an inverse agonist of RORγ (IC50 = ~100 nM in a cell-based reporter assay) and an agonist of LXR. It also binds to peroxisome proliferator-activated receptor γ (PPARγ; IC50 = 209 nM) but does not activate it. SR 1903 (10 μM) inhibits LPS-induced expression of triggering receptor expressed on myeloid cells 1 (TREM-1) in RAW 264.7 cells. It also inhibits LPS-induced expression of th... | |||
T76872 | Neihulizumab | ||
Neihulizumab (ALTB-168) 是一种免疫检查点激动性抗体,可与人 CD162 (PSGL-1)结合,导致活化的 T 细胞下调。Neihulizumab 可用于类固醇难治性急性移植物抗宿主病 (SR-aGVHD)、银屑病、银屑病关节炎和溃疡性结肠炎的研究。 | |||
T74489 |
SIAIS117
|
||
SIAIS117 是一种有效的 Brigatinib-PROTAC 降解剂。SIAIS117 是一种基于 Brigatinib 和 VHL-1 结合的ALKPROTAC。SIAIS117 能有效降解ALK G1202R 点突变SIAIS117可阻断 SR 和 H2228 癌细胞株的生长。SIAIS117 具有潜在的小细胞肺癌的抗增殖能力。 | |||
T81108 |
SR-1114
|
PROTACs | PROTAC |
SR-1114 是一种创新的PROTACENL降解剂,能够在MV4;11、MOLM-13和OCI/AML-2细胞中迅速降解ENL,其DC50值分别为150 nM 、311 nM 和1.65 μM。 | |||
T71009 |
Dolutegravir SR Isomer
|
||
Dolutegravir SR Isomer is an isomeric derivative of Dolutegravir -- a second generation HIV-1 integrase strand transfer inhibitor. Dolutegravir has been shown to potently inhibit HIV replication in cells such as peripheral blood mononuclear cells (PBMCs), MT-4 cells and CIP4 cells infected with a self-inactivating PHIV lentiviral vector. | |||
T37449 |
SR 12460
|
||
SR 12460 is a mimetic of the IκB kinase β (IKKβ) NEMO/IKKγ-binding domain (NBD) that inhibits the protein-protein interaction between the IKK complex subunits NF-κB essential modulator (NEMO/IKKγ) and IKKβ.1It inhibits TNF-α-induced NF-κB activation in a reporter assay when used at concentrations ranging from 25 to 150 μM. It reduces LPS-induced production of IL-6 in RAW 264.7 cells. SR 12460 (30 mg/kg) improves grip strength in themdxmouse model of Duchenne muscular dystrophy. 1.Zhao, J., Zhang... | |||
T83422 |
1-Palmitoyl-2-succinyl-sn-glycerophosphorylcholine
|
||
1-Palmitoyl-2-succinyl-sn-glycerophosphorylcholine 是一种由磷酸甘油、胆碱和棕榈酸构成的甘油磷酸胆碱类化合物,通常在体内氧化应激位点累积。该化合物是 B 类清道夫受体 (CD36和SR-BI) 的有效配体,特别是氧化磷脂 oxPC(CD36)。此外,氧化磷脂 (oxPLs) 在肿瘤细胞凋亡中扮演关键角色,并且在恶性胆管狭窄疾病中可能会有所增加。 | |||
T73677 | SR 142948 dihydrochloride | ||
SR 142948 dihydrochloride是一种口服活性高、选择性强的非肽类神经降压素受体(NT)拮抗剂,其在h-NTR1-CHO细胞、HT-29细胞和成年大鼠脑中IC50分别为1.19 nM、0.32 nM、3.96 nM。在HT-29细胞中,该化合物能够有效拮抗NT诱导的肌醇单磷酸盐形成,IC50为3.9 nM。此外,SR 142948 dihydrochloride在体内能够阻断NT诱导的体温下降、镇痛和转向行为,且具有良好的血脑屏障通透性,适用于精神疾病研究。 | |||
T80556 |
wt hMLN
|
Calcium Channel | Membrane transporter/Ion channel; Metabolism |
wt hMLN为抑制SR Ca2+泵(SERCA)的微量蛋白,对骨骼肌钙稳态具有关键作用。 | |||
T37127 |
L-AP4 monohydrate
L-AP4 monohydrate |
||
L-AP4 (L-APB) monohydrate is a potent and specific agonist for the group III mGluRs, with EC50s of 0.13, 0.29, 1.0, 249 μM for mGlu4, mGlu8, mGlu6 and mGlu7 receptors, respectively[1][2]. L-AP4 (5-30 μg, intrathecal inhection 4-5 days) significantly increases the paw withdrawal threshold in response to application of von Frey filaments in eight nerve-ligated rats in a dose-dependent manner. Intrathecal administration of different doses of L-AP4 is not associated with any evident motor dysfunctio... | |||
T36618 |
Rupatadine
|
||
Rupatadine (UR-12592) is a potent dual PAF/H1 antagonist with Ki of 0.55/0.1 uM(rabbit platelet membranes/guinea pig cerebellum membranes).IC50 value:Target: PAF/H1 antagonistin vitro: Rupatadine competitively inhibited histamine-induced guinea pig ileum contraction (pA2 = 9.29 +/- 0.06) without affecting contraction induced by ACh, serotonin or leukotriene D4 (LTD4). It also competitively inhibited PAF-induced platelet aggregation in washed rabbit platelets (WRP) (pA2 = 6.68 +/- 0.08) and in hu... |