17
2
Cat. No. | Product Name | Target | Signaling Pathways |
---|---|---|---|
T3595 |
Resmetirom
VIA-3196,MGL3196 |
Thyroid hormone receptor(THR) | Endocrinology/Hormones |
Resmetirom (VIA-3196) 是一种高度选择性的THR-β激动剂(EC50:0.21 μM)。 | |||
T7688 |
4-Nonylphenylboronic acid
|
FAAH | Metabolism; Neuroscience |
4-Nonylphenylboronic acid 是 FAAH 的抑制剂。 | |||
T12717 |
Basimglurant
CTEP Derivative,RG7090 |
GluR | Neuroscience |
Basimglurant (CTEP Derivative) 是一种高效,选择性,可口服的 mGlu5负变构调节剂,Kd 值为1.1 nM。 | |||
T9970 |
mGluR3 modulator-1
1-ethyl-3-(morpholin-4-yl)-5,6,7,8-tetrahydroisoquinoline-4-carbonitrile,1-乙基-3-(1,4-氧杂氮杂环己-4-基)-5,6,7,8-四氢异喹啉-4-甲腈 |
GluR | Neuroscience |
mGluR3 modulator-1 (1-ethyl-3-(morpholin-4-yl)-5,6,7,8-tetrahydroisoquinoline-4-carbonitrile) 是 mGluR3 的正变构调节剂,可用于治疗帕金森病的研究。 | |||
T74287 |
MGlc-DAG
|
||
MGlc-DAG 是一种糖脂甘油酯,可用于合成药物递送化合物。 | |||
T61775 |
mGlu4 receptor agonist 1
|
||
mGlu4 receptor agonist 1 (compound 62) is a highly effective positive allosteric modulator of mGlu4 receptors, displaying an EC 50 of 308 nM. Additionally, it exhibits noteworthy anxiolytic and antipsychotic properties [1]. | |||
T61277 | mGluR2 modulator 4 | ||
mGluR2 modulator 4 (compound 47) is a highly potent positive allosteric modulator of mGluR2, exhibiting an EC 50 value of 0.8 μM. It holds the potential for investigating antipsychotic properties [1]. | |||
T81801 |
mGluR5 antagonist-1
|
||
mGluR5 antagonist-1,一种高亲和力的mGluR5拮抗剂,其IC50为11.5 nM,表现出抗抑郁活性。 | |||
T38910 |
mGluR2 antagonist 1
|
||
mGluR2 antagonist 1 is a potent and selective class of negative allosteric modulator targeting the metabotropic glutamate receptor 2 (mGluR2) with high oral bioavailability. It displays a remarkable affinity for mGluR2, with an IC50 value of 9 nM. Furthermore, it exhibits excellent permeability across the blood-brain barrier, making it a promising candidate for central nervous system-related studies or therapies. | |||
T60882 | mGluR2 modulator 2 | ||
mGluR2 modulator 2 (compound 2) 可用于抗精神病药物研究。mGluR2 modulator 2 是一种有效的、选择性和口服生物可利用的mGluR2正变构调节剂,EC50值为 0.13 μM。 | |||
T62202 |
mGluR2 modulator 1
|
||
mGluR2 modulator 1 (compound 95) 是一种有效的、具有血脑屏障通透性的 mGluR2 (代谢型谷氨酸受体-2)正向变构调节剂 (EC50: 0.03 μM)。mGluR2 modulator 1 能够用于研究精神病。 | |||
T38659 |
mGluR5 modulator 1
|
||
mGluR5 modulator 1 is a compound that acts as a positive allosteric modulator of the metabotropic glutamate receptor subtype 5 (mGluR5). Its primary application lies in the field of schizophrenia and cognitive impairment research. | |||
T3591 |
URB602
|
Lipase; Antibacterial | Metabolism; Microbiology/Virology |
URB602 是选择性单酰基甘油脂肪酶 (MGL) 抑制剂,非竞争性抑制大鼠脑 MGL,IC50为 28±4 μM。 | |||
T28165 |
NF-1819
NF 1819,NF1819 |
Lipase | Metabolism |
NF-1819 是一种高效、选择性的不可逆 MGL (β-内酰胺基单酰甘油脂肪酶)抑制剂。NF-1819 在体内多发性硬化症模型中缓解疾病症状,在体内急性炎性疼痛模型中表现出镇痛作用。NF-1819 具有较高的膜通透性和血脑屏障通透性。 | |||
T34521 |
SAR629
SAR 629,SAR-629 |
||
SAR-629 is an MGL inhibitor or 2-AG degradation inhibitor. | |||
T71493 |
AM6580
|
||
AM6580 is an irreversible monoacylglycerol lipase (MGL) inhibitor. | |||
T61294 |
Monoacylglycerol lipase inhibitor 1
|
||
Monoacylglycerol lipase inhibitor 1 是一种有效的单酰基甘油脂肪酶 (MGL) 抑制剂 (化合物 13)。 |
Cat. No. | Product Name | Target | Signaling Pathways |
---|---|---|---|
T5737 |
euphol
|
Others; Lipase; Endogenous Metabolite | Metabolism; Others |
Euphol 是从Euphorbia tirucalli 的汁液中分离出来的四环三萜醇,具有抗炎和免疫调节作用,口服具有活力。 它通过能够逆机制抑制单酰基甘油脂肪酶 (MGL) 的特性,IC50=315 nM。 外周 MGL 抑制能够调节内源性大麻素系统从而阻止炎症性疼痛的发展。 | |||
T4S1050 |
Pristimerin
扁塑藤素,Celastrol methyl ester |
NF-κB; Antibacterial | Microbiology/Virology; NF-κB |
Pristimerin (Celastrol methyl ester) 是一种可逆的单酰基甘油脂肪酶高效抑制剂,IC50值为93 nM。 |