38
11
Cat. No. | Product Name | Target | Signaling Pathways |
---|---|---|---|
T13613 |
ChX710
|
STING | Immunology/Inflammation |
ChX710可以引发 I 型干扰素对细胞溶质 DNA 的反应,其特异性细胞干扰素刺激基因 (ISG) 诱导 ISRE 启动子序列和干扰素调节因子 (IRF) 3 的磷酸化。 | |||
T7329 |
C-178
|
STING | Immunology/Inflammation |
C-178 是 STING 选择性共价抑制剂,与 Cys91 结合抑制小鼠中由不同的激活剂引起的 STING 反应。 | |||
T13015 |
STING agonist-4
|
STING | Immunology/Inflammation |
STING agonist-4 是 是干扰素基因 (STING) 受体刺激剂的激动剂,IC50为 20 nM。 | |||
T9853 |
STING activator Compound 53
|
STING | Immunology/Inflammation |
基于 oxindole 核心结构的 STING activator Compound 53 在永生化细胞和原代细胞中表现出强大的 STING(人 EC50 185 nM)的靶向功能激活以及与 STING 激活一致的细胞因子诱导指纹。 | |||
T9554 |
SN-008
|
STING | Immunology/Inflammation |
SN-008 是 SN-011 的低活性类似物,可作为阴性对照。 | |||
T5674 |
H-151
|
STING | Immunology/Inflammation |
H-151 是一种 STING 拮抗剂,具有高效性和选择性。H-151 与 STING 的 Cys91 共价结合,抑制 Cys91 的棕榈酰化,从而抑制 STING 的活性。H-151 可用于体内外自身炎症性疾病的研究。 | |||
T5516 |
diABZI STING agonist-1 trihydrochloride
|
STING | Immunology/Inflammation |
diABZI STING agonist-1 trihydrochloride 是选择性的干扰素基因刺激受体(STING)激动剂,在人和小鼠中的 EC50值分别为 130 和 186 nM。 | |||
T8798 |
MSA-2
|
STING | Immunology/Inflammation |
MSA-2 是可口服的非核苷酸 STING 激动剂,以具有纳摩尔亲和力的非共价二聚体形式与 STING 结合。它在同基因小鼠肿瘤模型中显示抗肿瘤活性,与抗 PD-1 协同作用,可刺激肿瘤分泌干扰素-β,诱导肿瘤消退,具有持久的抗肿瘤免疫。 | |||
T6919 |
Omaveloxolone
RTA-408 |
Apoptosis; Others; Nrf2; STING | Apoptosis; Immunology/Inflammation; Others |
Omaveloxolone (RTA-408) 是一种抗氧化炎症调节剂,可激活Nrf2并抑制一氧化氮。它通过抑制 STING 依赖的 NF-κb 信号通路,来抑制破骨细胞的生成。 | |||
T5154 |
C-176
C176,STING inhibitor 1 |
STING | Immunology/Inflammation |
C-176 (STING inhibitor 1) 是干扰素基因刺激受体的一种强效共价抑制剂。 | |||
T8655 |
SR-717
|
STING | Immunology/Inflammation |
SR-717 是一种 cGAMP 的类似物,一种非核苷类 STING 激动剂,可以诱导 STING 形成“封闭”的激活构象。SR-717 具有抗肿瘤活性,可以促进免疫细胞的激活以及抗原的交叉提呈。 | |||
T9029 |
STING-IN-3
C-171 |
STING | Immunology/Inflammation |
STING-IN-3 (C-171) 是干扰素基因刺激物 (STING) 的抑制剂。 它与 STING 结合,抑制其棕榈酰化,并阻止 TBK1 的募集和磷酸化。 | |||
T9028 |
STING-IN-2
C-170 |
STING | Immunology/Inflammation |
STING-IN-2 (C-170) 是一种 STING 共价抑制剂,可抑制小鼠 STING (mmSTING) 和人类 STING (hsSTING),可用于自身炎症性疾病的研究。 | |||
T8328 |
STING agonist-1
G10 |
Virus Protease; STING | Immunology/Inflammation; Microbiology/Virology |
STING agonist-1 (G10)是一种人类特异性 STING 激动剂,可引发针对新兴甲病毒的抗病毒活性。它抑制甲病毒属 VEEV 复制,IC90值为 24.57 μM。 | |||
T10252L2 |
ADU-S100 ammonium salt
ML RR-S2 CDA ammonium salt,MIW815 ammonium salt |
STING | Immunology/Inflammation |
ADU-S100 ammonium salt (ML RR-S2 CDA ammonium salt) 是干扰素基因刺激物的激活剂。 ADU-S100 ammonium salt 可导致有效的全身性肿瘤消退和免疫。 | |||
T9137 |
SN-011
[1,1'-Biphenyl]-4-carboxamide, N-[3-[[(4-fluorophenyl)sulfonyl]amino]-4-hydroxyphenyl]-,GUN35901 |
STING | Immunology/Inflammation |
SN-011 (GUN35901) 是选择性 STING 抑制剂,可与环状二核苷酸 (CDN) 竞争 STING 二聚体的结合口袋,从而阻断 CDN 结合和 STING 激活。它用于 STING 驱动的自身免疫和炎症性疾病的研究,抑制 STING 信号传导的 IC50值为 76 nM。 | |||
T7081 |
CCCP
Carbonyl Cyanide m-Chlorophenylhydrazone,Carbonyl cyanide 3-chlorophenylhydrazone,羰基氰化氯苯腙 |
Apoptosis; IκB/IKK; COX; Mitochondrial Metabolism; STING; IFNAR; Antibacterial | Apoptosis; Immunology/Inflammation; Metabolism; Microbiology/Virology; Neuroscience; NF-κB |
CCCP (Carbonyl Cyanide m-Chlorophenylhydrazone) 是一种氧化磷酸化 (OXPHOS) 抑制剂,线粒体质子载体解偶联剂。CCCP 抑制 STING 及其下游信号分子 TBK1 和 IRF3 的激活。 | |||
T6273 |
Vadimezan
DMXAA,伐地美生,5,6-Dimethylxanthenone-4-acetic Acid,NSC 640488,ASA-404 |
Influenza Virus; VDA; STING; IFNAR | Angiogenesis; Immunology/Inflammation; Microbiology/Virology |
Vadimezan (DMXAA) 是一种血管破坏剂,一种鼠 STING 激动剂,也是一种细胞因子如 I 型 IFN 的诱导剂。Vadimezan 具有抗肿瘤活性,可以诱导肿瘤中的血流快速停止,但不影响正常组织中的血流。 | |||
T28159 |
Nerisopam
EGIS-6775,GYKI 52322,GYKI52322,EGIS6775,GYKI-52322 |
GABA Receptor | Membrane transporter/Ion channel; Neuroscience |
Nerisopam 是一种γ-氨基丁酸(GABA)受体激动剂。 | |||
T8441 |
Lerisetron
|
5-HT Receptor | GPCR/G Protein; Neuroscience |
Lerisetron 是5-HT3拮抗剂,与 5-HT3受体具有高亲和力(pKi:9.2)。它对尿烷麻醉大鼠的 5-HT 引发的反射性心率过缓具有抑制作用。 | |||
T0511 |
Tolperisone hydrochloride
盐酸托哌酮,Muscalm,Midocalm,托哌酮盐酸盐,Tolperisone HCl |
Sodium Channel | Membrane transporter/Ion channel |
Tolperisone hydrochloride (Muscalm) 是中枢作用肌肉松弛剂,可用于研究神经疾病引起的病理性横纹肌硬化(锥体束损伤、脊髓病、多发性硬化症、脑脊髓炎)、痉挛性麻痹及其他肌肉张力障碍相关的脑病。 | |||
T68087 |
Inaperisone
|
Others | Others |
Inaperisone 是一种新型的中枢作用的肌肉松弛剂,对排尿反射有抑制作用。Inaperisone 可能通过间接作用于脑干的GABAB 受体来抑制排尿反射。 | |||
T70489 |
Enerisant HCl
|
P450; Histamine Receptor | GPCR/G Protein; Immunology/Inflammation; Metabolism; Neuroscience |
Enerisant HCl是一种新型强效选择性组胺H3受体拮抗剂,是P-gp的底物,由细胞色素P450(CYP)和转运蛋白介导。 | |||
T28778 |
Silperisone HCl
RGH5002,SILA336,RGH-5002,Silperisone hydrochloride,SILA-336 |
||
Silperisone HCl (RGH-5002) 阻断细胞中的钠和钙通道,使肌肉细胞的兴奋度和收缩度降低,降低外周张力,充当肌肉松弛剂和外周血管扩张剂。 Silperisone HCl 可用于治疗脊髓损伤引起的复发性疼痛性肌阵挛、脑血管病引起的异常高肌张力、肌张力症状、锥体紧张综合征、多发性硬化症肌痉挛和脊髓炎。Silperisone 是钠通道蛋白2型α通道阻滞剂。Silperisone 是一种类似于tolperisone 的有机硅化合物,具有中枢作用的肌肉松弛剂特性。 | |||
T11035 |
diABZI STING agonist-1 (Tautomerism)
diABZI STING agonist (Compound 3) |
STING | Immunology/Inflammation |
diABZI STING agonist-1 (Tautomerism) (diABZI STING agonist (Compound 3)) 是一个选择性的干扰素基因刺激受体 (STING) 的激动剂,其在人和小鼠中的 EC50 值分别为 130 nM 和 186 nM。。 | |||
T5005 |
Eperisone hydrochloride
|
Others | Others |
Eperisone Hydrochloride 是一种抗痉挛试剂,用于肌肉僵硬和疼痛为特征的疾病的相关研究。它是一种中枢作用的肌肉松弛剂,抑制疼痛反射通路,具有血管扩张作用。它通过放松骨骼肌和血管平滑肌来起作用,例如减少肌张力,改善循环和抑制疼痛反射。 | |||
T67828 |
Enerisant
|
||
Enerisant 是一种组胺H3受体拮抗剂/逆激动剂。体外研究表明,Enerisant 是一种有效的、高选择性的、竞争性的组胺H3受体拮抗剂,其选择性比其他组胺受体亚型高3000倍以上。 | |||
T124126 |
Asteriscunolide A
|
||
Asteriscunolide A 是一种有用的有机化合物,可用于生命科学领域的相关研究,其产品编号为 T124126。 | |||
T125924 |
Pterisolic acid B
|
||
Pterisolic acid B 是一种有用的有机化合物,可用于生命科学领域的相关研究,其产品编号为 T125924。 | |||
T32561 |
Lanperisone
|
||
Lanperisone is a muscle relaxant. | |||
T125921 |
Monnieriside A
|
||
Monnieriside A 是一种有用的有机化合物,可用于生命科学领域的相关研究,其产品编号为 T125921。 | |||
T28160 |
Nerispirdine HCl
HP-184,HP 184,Nerispirdine hydrochloride,HP184 |
||
Nerispirdine is a acetylcholine release enhancer, sodium channel blocker and K(V) 2.1 channel blocker. Nerispirdine inhibits voltage-dependent Na(+) channel currents recorded from human SH-SY5Y cells with an IC(50) of 11.9 micromol/L when measured from a | |||
T125082 |
Pierisformoside B
|
||
Pierisformoside B 是一种有用的有机化合物,可用于生命科学领域的相关研究。其产品编号为 T125082,CAS号为 308335-44-6。 | |||
T71356 | Lanperisone HCl | ||
Lanperisone, also known as NK433, is a muscle relaxant. NK433 inhibited the facilitation of the flexor reflex mediated by group II afferent fibers that was induced by intrathecal administration of noradrenaline-HCl. NK433 had effects more than three times stronger and tending to be longer-lasting than those of eperisone-HCl. These results suggest that NK433 exerts a non-selective inhibition on spinal reflexes and that inhibition of the descending noradrenergic tonic facilitation within the spina... | |||
T81509 |
Perisulfakinin
|
||
Perisulfakinin为一神经肽,能传递饱腹信号并抑制促进常规活动的中枢神经元活动。 | |||
T40744 |
Eperisone
|
||
Eperisone is a centrally acting muscle relaxant and antispastic agent utilized in the treatment of conditions distinguished by muscle stiffness and pain. Its mechanism of action involves the relaxation of skeletal muscles and vascular smooth muscles, resulting in a range of beneficial effects including reduction of myotonia, enhancement of circulation, and suppression of the pain reflex. Additionally, Eperisone exhibits inhibitory properties on the pain reflex pathway and exerts a vasodilator ef... | |||
T71281 |
Nerispirdine
|
||
Nerispirdine is a biochemical that inhibits batrachotoxin binding to voltage-dependent sodium channels. | |||
T21077 |
Tolperisone free base
Mydeton,Atmosgen free base,Mideton,Menopatol,Besnoline free base,Mydocalm |
||
Tolperisone free base, a centrally acting muscle relaxant, has been used for the symptomatic treatment of spasticity and muscle spasm. |
Cat. No. | Product Name | Target | Signaling Pathways |
---|---|---|---|
TN5576 | Pterisolic acid E | ||
Pterisolic acid E is a natural product from Pteris semipinnata. | |||
TN4845 |
Pterisolic acid D
|
Others | Others |
Pterisolic acid D 是一种天然产物,可用于生命科学领域的相关研究。其产品编号为 TN4845,CAS号为 1401419-88-2。 | |||
T83260 |
6β,7β-Epoxyasteriscunolide A
|
||
6β,7β-Epoxyasteriscunolide A 是一种具有细胞毒性的倍半萜类化合物,其对 HL-60 和 MOLT-3 白血病细胞系展现出的 IC50 值介于 4.1-5.4 μM 之间。 | |||
TN1948 | Monnieriside G | Others | Others |
Monnieriside G is a natural product from Cnidium monnieri. | |||
TN1356 |
Acetyl Perisesaccharide C
乙酰杠柳寡糖 C,乙酰杠柳寡糖C |
Others | Others |
Acetyl Perisesaccharide C is a natural product | |||
T81766 | Monnierisides A | ||
Monnierisides A为来源于Cnidium Monnieri的色酮苷,通过分离工艺得到。 | |||
TN2056 |
Perisesaccharide B
|
Others | Others |
Perisesaccharide B is a natural product | |||
TN2057 |
Perisesaccharide C
|
Others | Others |
Perisesaccharide C is a natural product | |||
TN4843 | Pterisolic acid A | Others | Others |
Pterisolic acid A shows moderate activity against HCT-116,Hep G2 and BGC-823 cell lines. | |||
TN4844 |
Pterisolic acid C
|
Others | Others |
Pterisolic acid C is a natural product from Pteris semipinnata. | |||
TN4846 |
Pterisolic acid F
|
Others | Others |
Pterisolic acid F is a natural product from Pteris semipinnata. |