目录号 | 产品详情 | 靶点 | |
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T25411 | |||
Fenclofenac is a non-steroidal anti-inflammatory agent that competitively supresses the binding of thyroxine(T4) and triiodothyronine (T3) by thyroxine-binding globulin(TBG). | |||
T11294 | Others | ||
Flavanone hydrazine is a potent non-steroidal anti-inflammatory agent that effectively inhibits lens protein-induced ocular inflammation. | |||
T31456 | |||
Difenpiramide 是一种非甾体抗炎剂,具有抗炎、镇痛、解热和排尿酸活性。 | |||
T30837 | |||
CGP 47645 (Leflurozole) is an oral active non-steroidal aromatase inhibitor and antitumor agent with anti-tumor and endocrine effects. | |||
T30834 | |||
CGP 45688 is an oral active non-steroidal aromatase inhibitor with anti-tumor and endocrine effects on rat breast tumors. | |||
T39499 | |||
Rintodestrant (G1T48) is an orally active, non-steroidal, selective estrogen receptor degrader (SERD) that also functions as a CDK4/6 inhibitor. | |||
T39627 | |||
Ocarocoxib, a potent COX- 2 (cyclooxygenase- 2) inhibitor, is a non-steroidal anti-inflammatory for veterinary use. | |||
T0260L | |||
Meclofenamate sodium is a potent non-steroidal anti-inflammatory agent, which can specifically inhibit chemokine-induced human polymorphonuclear leukocyte function: chemotaxis, degranulation, and superoxide anion free radical production. | |||
T33395 | |||
Miprofen is an analgesic and non-steroidal anti-inflammatory, which means it has anti-inflammatory, antipyretic, and anti-platelet aggregation activities. | |||
T20458 | |||
Aspirin DL-lysine is a non-steroidal anti-inflammatory drug. It also may inhibit cancer growth. Aspirin DL-lysine is a water-soluble, injectable aspirin derivative. |
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 | E. coli | ||
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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