目录号 | 产品详情 | 靶点 | |
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T12361 | Others | ||
Parcetasal (MR-897) 是一种非甾类体抗炎剂,在缓解疼痛方面具有研究价值。 | |||
T4542 | Others | ||
Clonixin (Clonixic acid) 是一种非甾体抗炎药,具有口服活性。 | |||
T0319 | COX | ||
Suxibuzone (Suxibuzona) 是非甾体类抗炎药 Phenylbutazone 的前药,可用于关节和肌肉疼痛研究。 | |||
T7207 | COX | ||
FK 3311 (COX-2 Inhibitor V) 是一种细胞渗透性和口服磺胺类药物,可作为 COX-2 抑制剂和非甾体抗炎药。 | |||
T0463 | COX | ||
Loxoprofen (Koloxo) 是一种非甾体类抗炎药,具有解热作用,可用于缓解疼痛的研究。它是非选择性COX 抑制剂,对 COX-1 和 COX-2 的IC50分别为 6.5 和 13.5 μM。 | |||
T0888 | COX | ||
Felbinac (Dapson) 是非甾体抗炎药,可用于肌肉炎症和关节炎的研究。 | |||
TN2282 | Others | ||
trans-Stilbene (1,2-Diphenylethylene (trans)) 可用于制备荧光增白剂、染料激光器、非甾体合成雌激素。 | |||
T0159 | Apoptosis COX PGE Synthase Prostaglandin Receptor | ||
Pranoprofen (Pyranoprofen) 可抑制COX1/2酶,阻断花生四烯酸转化为二十烷醇,减少前列腺素的合成。它是一种用于眼科的非甾体抗炎试剂。 | |||
T1582 | COX Autophagy | ||
Naproxen ((S)-Naproxen) 是COX-1和COX-2的抑制剂,在细胞试验中IC50值分别为8.72 和5.15 μM。它是丙酸衍生物和非甾体抗炎药,具有抗炎、解热和镇痛活性。 | |||
T12481 | AChR | ||
Pipecuronium bromide (RGH-1106)是一种具有选择性和有效性的 nAChR 拮抗剂,也可当作一种非去极化甾体神经肌肉阻滞剂,可使肌肉松弛,常与抗生素一起使用。 |
目录号 | 产品名/同用名 | 种属 | 表达系统 | ||
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TMPH-01640 | MRGPRX2 Protein, Human, Recombinant (His) | Human | in vitro E. coli expression system | ||
Mast cell-specific receptor for basic secretagogues, i.e. cationic amphiphilic drugs, as well as endo- or exogenous peptides, consisting of a basic head group and a hydrophobic core. Recognizes and binds small molecules containing a cyclized tetrahydroisoquinoline (THIQ), such as non-steroidal neuromuscular blocking drugs (NMBDs), including tubocurarine and atracurium. In response to these compounds, mediates pseudo-allergic reactions characterized by histamine release, inflammation and airway contraction. Acts as a receptor for a number of other ligands, including peptides and alkaloids, such as cortistatin-14, proadrenomedullin N-terminal peptides PAMP-12 and, at lower extent, PAMP-20, antibacterial protein LL-37, PMX-53 peptide, beta-defensins, and complanadine A.
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