Cat. No. | Product Name | Target | Signaling Pathways |
---|---|---|---|
T6177 |
PF-562271 besylate
PF-00562271 Besylate |
FAK; PYK2; CDK | Angiogenesis; Cell Cycle/Checkpoint; Cytoskeletal Signaling; Tyrosine Kinase/Adaptors |
PF-562271 besylate (PF-00562271 Besylate) 是一种可逆的,有效的,ATP 竞争性的 FAK(IC50:1.5 nM)和 Pyk2 (IC50:13 nM)激酶抑制剂。 | |||
T4284 |
Levamlodipine besylate
左旋氨氯地平,(S)-Amlodipine Besylate (103129-82-4(free base)) |
Calcium Channel | Membrane transporter/Ion channel; Metabolism |
Levamlodipine besylate ((S)-Amlodipine Besylate(103129-82-4(free base))) 是一种二氢吡啶钙通道阻滞剂,具有舒张血管的作用,可用于高血压和心绞痛的研究。 | |||
T6397 |
Atracurium besylate
Tracrium,51W89,BW-33A,苯磺酸阿曲库铵 |
AChR | Neuroscience |
Atracurium besylate (51W89) 是一种神经肌肉阻断剂,ED95为0.2 mg/kg。 | |||
T1459 |
Cisatracurium besylate
顺苯磺酸阿曲库铵,顺苯磺阿曲库铵,51W89 |
Adrenergic Receptor; AChR; Autophagy | Autophagy; GPCR/G Protein; Neuroscience |
Cisatracurium besylate (51W89) 是一种用于静脉内给药的非去极化骨骼肌松弛剂。 | |||
T0231 |
Amlodipine Besylate
Amlodipine benzenesulfonate,苯磺酸氨氯地平 |
Calcium Channel | Membrane transporter/Ion channel; Metabolism |
Amlodipine Besylate (Amlodipine benzenesulfonate) 是可口服的二氢吡啶钙通道阻滞剂,有抗心绞痛作用。它通过阻断电压依赖性的 L 型钙通道,从而抑制钙离子内流,用于高血压和癌症的研究。 | |||
T3086 |
Mesoridazine Besylate
Mesoridazine benzenesulfonate,Serentil,苯磺酸美索达嗪 |
Dopamine Receptor; 5-HT Receptor | GPCR/G Protein; Neuroscience |
Mesoridazine Besylate (Serentil) 是一种哌啶类精神安定药,属于称为吩噻嗪类的药物,用于治疗精神分裂症。它是硫利达嗪的代谢物。 | |||
T6174 |
R406
R-406 besylate |
Apoptosis; FLT; Syk | Angiogenesis; Apoptosis; Tyrosine Kinase/Adaptors |
R406 (R-406 besylate) 是一种具有口服活性的 ATP 竞争性 Syk/FLT3抑制剂,Ki 为 30 nM。它有效抑制 Syk 激酶活性,IC50为 41 nM。它还抑制 Lyn 和 Lck,IC50值分别为 63 nM 和 37 nM。它可减轻免疫复合物介导的炎症。 | |||
T11472L |
Molibresib besylate
I-BET 762 besylate,GSK 525762C |
CCR | Immunology/Inflammation; Microbiology/Virology |
Molibresib besylate is an inhibitor of BET bromodomain (IC50: 32.5-42.5 nM). | |||
T14357 |
Spebrutinib besylate
CC-292 (besylate),AVL-292 (benzenesulfonate) |
BTK | Angiogenesis; Tyrosine Kinase/Adaptors |
Spebrutinib besylate (AVL-292 benzenesulfonate; CC-292 besylate) is a Btk kinase activity inhibitor (IC50<0.5 nM, Kinact/Ki=7.69×104 M-1s-1s). | |||
T68567 |
AMG-131 besylate
|
||
AMG-131 besylate is a hypoglycemic agent. It is a potent PPARγ partial agonist that displays robust glucose-lowering activity in rodent models of diabetes while exhibiting a reduced side-effects profile compared to marketed TZDs. | |||
T70158 |
Quilseconazole besylate
|
||
Quilseconazole besylate, also known as VT-1129 besylate, is a potent, orally active fungal Cyp51 (lanosterol 14-α-demethylase) inhibitor. | |||
T31647 |
Epelsiban besylate
GSK-557296B,GSK557296B |
||
Epelsiban Besylate is an oral drug that is a highly selective anamol oxytocin receptor antagonist. | |||
T11400 |
Gisadenafil besylate
UK 369003-26 |
Others | Others |
Gisadenafil besylate (UK 369003-26) is a specific, orally active phosphodiesterase 5 (PDE5) inhibitor ,prevents degradation of cyclic guanosine monophosphate (cGMP), with an IC50 of 3.6 nM . | |||
T69399 | MK-0359 besylate | ||
MK-0359 besylate is a Phosphodiesterase-4 (PDE4) inhibitor. | |||
T10589 |
BPN-15606 besylate (1914989-49-3 free base)
BPN-15606 besylate |
Others | Others |
BPN-15606 besylate is a highly potent, orally active γ-secretase modulator, attenuates the production of Aβ40 and Aβ42 by SHSY5Y neuroblastoma cells (IC50s: 7 nM and 17nM). | |||
T0231L3 |
Amlodipine besylate monohydrate
|
||
Amlodipine besylate monohydrate is a medication used to lower blood pressure and prevent chest pain. | |||
T78217 |
(R)-Azasetron besylate
SENS-401 |
Phosphatase | Metabolism |
(R)-Azasetron besylate (SENS-401)是一种口服活性的钙调神经磷酸酶抑制剂,能够减轻Cisplatin引发的听力损失和耳蜗损害。 | |||
T30001 |
Amlodipine besylate, (R)-
|
||
Amlodipine besylate, (R)- is a medication used to lower blood pressure and prevent chest pain. | |||
T64425 | Crenolanib besylate | ||
Crenolanib besylate 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 T64425。 | |||
T61434 |
Mirogabalin besylate
|
||
Mirogabalin besylate is a potent and orally active ligand that selectively targets the α2δ subunit of voltage-gated calcium channels. It displays high affinity (K d ) values, namely 13.5 nM, 22.7 nM, 27 nM, and 47.6 nM, for human α2δ-1, human α2δ-2, rat α2δ-1, and rat α2δ-2, respectively. | |||
T68451 |
AG-28262 besylate
|
||
AG-28262 besylate is a VEGFR-2 Inhibitorwhich may affect alanine aminotransferase gene expression and enzymatic activity in the liver. | |||
T64081 | BPN-15606 besylate | ||
BPN-15606 besylate 是一种高效的、口服具有活力的 γ-secretase 调节剂 (GSM),能够减少 SHSY5Y 神经母细胞瘤细胞产生 Aβ42 (IC50: 7 nM) 和 Aβ40 (IC50: 17 nM) 的作用。BPN-15606 besylate 能够减少大鼠和小鼠中枢神经系统中的 Aβ42 和 Aβ40 水平。BPN-15606 besylate 表现出良好的 PK/PD 特性(包括生物利用度,半衰期和清除率)。 | |||
T29706 |
AG28262 free base
AG28262,AG-28262,AG 28262,AG-28262 besylate |
||
AG28262 is a VEFG-2 inhibitor that increases serum ALT, due in part to both gene up-regulation. | |||
T70157 |
GGTI-297
|
||
GGTI-297 is a potent, cell-permeable, and selective peptidomimetic inhibitor of GGTase I compared to Farnesyl Transferase (FTase). | |||
T69432 |
Avanafil dibesylate
|
||
Avanafil dibesylate is a PDE5 inhibitor. | |||
T36006 |
Olmesartan medoxomil impurity C
|
||
Olmesartan medoxomil impurity C is an Olmesartan medoxomil impurity. Olmesartan medoxomil is a potent and selective angiotensin AT1 receptor inhibitor with IC50 of 66.2 μM. [1]. Senda A, et al. Effects of Angiotensin II Receptor Blockers on Metabolism of Arachidonic Acid via CYP2C8. Biol Pharm Bull. 2015;38(12):1975-9. [2]. Shah S, et al. Simultaneous Quantitative Analysis of Olmesartan Medoxomil and Amlodipine Besylate in Plasma by High-performance Liquid Chromatography Technique. J Young Phar... |