Cat. No. | Product Name | Target | Signaling Pathways |
---|---|---|---|
T6009 |
TAPI1
TAPI 1,TAPI,TAPI-1 |
MMP | Proteases/Proteasome |
TAPI1 (TAPI) 是一种 ADAM17/TACE 抑制剂,可抑制细胞因子受体的脱落。 | |||
TQ0129 |
TNF Protease Inhibitor 2
TAPI-2 |
MMP | Proteases/Proteasome |
TAPI-2 is a broad-spectrum inhibitor of MMP (IC50: 20 μM), tumour necrosis factorα-converting enzyme (TACE) and a disintegrin and metalloproteinase (ADAM). | |||
TP2107 |
TAPI 0
|
||
ADAM-17 (TACE) and MMP inhibitor; attenuates TNF-α processing. Acts in concert with GM6001 to inhibit Chlamydia trachomatis growth. | |||
TP2108 |
TAPI 2
|
||
ADAM-17 (TACE) and MMP inhibitor (Ki = 120 nM at ADAM-17). Sensitizes cancer stem cells to the lethal effects of 5-FU in vitro. Blocks shedding of TNF-α from cell membranes. | |||
T4122 |
TAPI-1 trifluoroacetate (163847-77-6(free base))
|
MMP | Proteases/Proteasome |
TAPI-1 trifluoroacetate 是一种 ADAM17/TACE 抑制剂,可阻断细胞因子受体的脱落。 | |||
T70664 |
TAPI-0
|
||
TAPI-0 is a matrix metalloprotease (MMP) and TACE inhibitor. | |||
T63390 |
(S,S)-TAPI-1
|
||
(S,S)-TAPI-1 是一种 TAPI-1 的异构体。其中 TAPI-1是金属蛋白酶 (MMP) 抑制剂,也是 TACE(ADAM17) 抑制剂,对多种细胞表面蛋白脱落表现出有效的抑制作用。 | |||
T31992 |
Granotapide
|
CETP | Metabolism |
Granotapide 是一种微粒体甘油三酯转移蛋白(MTP)抑制剂,治疗和而预防动脉硬化,冠状动脉疾病,代谢综合征,肥胖,糖尿病,糖尿病前期和高血压。 | |||
T35316 |
Zometapine
CI 716,Zolazepamum,CI-716,CI716,Flupyrazapon |
Others | Others |
Zometapine (CI 716) 是一种抗抑郁化合物,是吡唑和二氮卓的衍生物。 | |||
T4223 |
Mitapivat
PKR-IN-1 |
PKM | Metabolism |
Mitapivat (PKR-IN-1) 是口服具有活性的变构丙酮酸激酶 (pyruvate kinase) 激活剂,其AC50=20 nM。它在广泛的 PKLR 基因型中增加酶活性、蛋白质稳定性和 ATP 水平。它有潜在的恢复 PK 缺乏的糖酵解途径活性的作用。 | |||
T4644 |
Tapinarof
GSK2894512,Benvitimod,苯烯莫德,WBI 1001 |
AhR; Aryl Hydrocarbon Receptor | Immunology/Inflammation; Metabolism |
Tapinarof (Benvitimod) 是一种从发光杆菌中提取的天然产物,可消除炎症。它是芳烃受体 (AhR) 激动剂,EC50为 13 nM。 | |||
T2545 |
Lomitapide Mesylate
甲磺酸洛美他派,BMS-201038 mesylate,AEGR-733 mesylate |
CETP | Metabolism |
Lomitapide Mesylate (BMS-201038 mesylate) 是一种高效MTP 蛋白抑制剂,其体外IC50值为8 nM。 | |||
T6267 |
Lomitapide
AEGR-733,洛美他派,BMS-201038 |
CETP | Metabolism |
Lomitapide (AEGR-733) 是一种高效的微粒体甘油三酯转移蛋白(MTP)抑制剂,体内试验的IC50值为8 nM。 | |||
T15006 |
Dirlotapide
CP742033,Slentrol |
Others; CETP | Metabolism; Others |
Dirlotapide (CP742033) 是一种肠道选择性微粒体甘油三酯转移蛋白(MTP)抑制剂。它可以减轻糖尿病狗的体重。Dirlotapide 以剂量依赖性方式减少食物摄入量,可能是通过增加 肽YY 释放到循环中。 | |||
T3179 |
Eptapirone
F 11440 |
5-HT Receptor | GPCR/G Protein; Neuroscience |
Eptapirone (F 11440) 是一种高效且选择性的 5-HT1A 受体激动剂,具有显着的抗抑郁和抗焦虑潜力。 | |||
T35005 |
Usistapide
R-256918,JNJ-16269110,JNJ16269110,R256918,JNJ 16269110,R 256918 |
||
UsISpide(JNJ-16269110 R256918) is an inhibitor of microsomal triglyceride transfer protein (MTTP) under development for the treatment of obesity and type 2 diabetes. | |||
T15570 |
Implitapide
英普他派,AEGR 427 |
CETP | Metabolism |
Implitapide is an inhibitor of microsomal triglyceride transfer protein (MTP). | |||
T10504 | Implitapide Racemate | Others | Others |
Implitapide Racemate is the racemate of Implitapide. Implitapide is an inhibitor of microsomal triglyceride transfer protein (MTP). | |||
T69865 |
Mitapivat sulfate
|
||
Mitapivat sulfate, also known as AG-348 sulfate hydrate, is an allosteric activator of Pyruvate Kinase (PK) that may be useful in the treatment of Pyruvate Kinase Deficiency. | |||
T7459 |
Abametapir
5 5'-二甲基-2,2-联吡啶,HA-44,BRN 0123183 |
MMP; Others; Parasite | Microbiology/Virology; Others; Proteases/Proteasome |
Abametapir (BRN 0123183) 是一种金属蛋白酶抑制剂,能够靶向对卵孵化和虱子发育至关重要的金属蛋白酶。 | |||
T69677 | Mitapivat sulfate anhydrous | ||
Mitapivat sulfate anhydrous is an allosteric activator of Pyruvate Kinase (PK) that may be useful in the treatment of Pyruvate Kinase Deficiency. | |||
T73667 | Motapizone | ||
Motapizone (NAT 05-239) 是一种选择性 PDE3抑制剂。Motapizone 适度抑制脂多糖 (LPS) 诱导的肺泡巨噬细胞中细胞因子的释放。Motapizone 还通过增加细胞内 cAMP 来抑制人血小板聚集。 | |||
T124572 |
Desacetylcentapicrin
|
||
Desacetylcentapicrin 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 T124572,CAS号为 60197-56-0。 | |||
T31801 |
Florbetapir F-18
|
||
Florbetapir F-18 is a PET agent for Abeta plaques. | |||
T70183 |
Eptapirone fumarate
|
||
Eptapirone, also known as F11440, is a potent 5HT(1A) receptor agonist with marked anxiolytic and antidepressant potential. The affinity of F 11440 for 5-HT1A binding sites (pKi, 8.33) was higher than that of buspirone (pKi, 7.50), and somewhat lower than that of flesinoxan (pKi, 8.91). In vivo, F 11440 was 4- to 20-fold more potent than flesinoxan, and 30- to 60-fold more potent than buspirone, in exerting 5-HT1A agonist activity at pre- and postsynaptic receptors in rats (measured by, for exam... | |||
T41082 |
Flobetapir
AV-45,Flobetapir |
||
Flobetapir (AV-45) is a well-tolerated imaging compound used in PET scanning. It is synthesized to create Florbetapir (18F), which is a radiopharmaceutical compound containing fluorine-18 radionuclide. |