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T9622MF-766EP4,arthritis,inflammation disease,AIA,inhibit,anti-tumor,MF766,MF 766,MF-766,Prostaglandin Re
MF-766 is a highly potent, selective and orally active EP4 antagonist with a Ki of 0.23 nM. It behaves as a full antagonist with an IC50 of 1.4 nM (shifted to 1.8 nM in the presence of 10% HS) in the functional assay. It can be used for cancer and inflammation diseases research[1][2].
价 格：￥电议型 号：T9622产 地：中国大陆
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T4426CEP-40783CEP 40783；CEP40783；RXDX-106
CEP-40783 is an effective, specific and orally active AXL/c-Met inhibitor (IC50: 7/12 nM). It also inhibits MER and TYRO3 (IC50: 29/19 nM).
价 格：￥电议型 号：T4426产 地：中国大陆
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T11211EP4 receptor antagonist 1
EP4 receptor antagonist 1 inhibits human and mouse EP4 receptor with IC50s of 6.1 nM and 16.2 nM, respectively. IC50s >10 μM for human EP1, EP2,and EP3 receptors.EP4 receptor antagonist 1 is a highly potent and selective competitive prostanoid EP4 recepto
价 格：￥电议型 号：T11211产 地：中国大陆
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T83779EP4 Antagonist 14；化合物 EP4 Antagonist 14Prostaglandin E2 Receptor 4 Antagonist 14|||PGE2 Receptor 4 A
EP4 antagonist 14 is a prostaglandin E2 receptor subtype EP4 antagonist, demonstrating an IC50 of 1.1 nM in a HEK293 human receptor reporter assay and blocking β-arrestin recruitment due to PGE2 with an IC50 of 0.9 nM. At 10 ?M, it reduces PGE2-stimulated mRNA levels of Il-4, macrophage mannose receptor 1 (Mrc1), chitinase-like protein 3 (Chil3), chemokine (C-X-C) motif ligand 1 (Cxcl1), triggering receptor expressed on myeloid cells 2 (Trem2), and arginase-1 (Arg1) in RAW 264.7 macrophages. Whe
价 格：￥电议型 号：T83779产 地：中国大陆
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T77699EP4-IN-1；EP4抑制剂1EP4-IN-1
EP4-IN-1 is a potent prostaglandin EP4 receptor inhibitor with potential anti-tumor, anti-inflammatory and analgesic activities for the study of immune and tumor diseases.
价 格：￥电议型 号：T77699产 地：中国大陆
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T63100EP4 receptor antagonist 2；化合物 EP4 receptor antagonist 2EP4 receptor antagonist 2
EP4 receptor antagonist 2 (compound 2-13) is a potent agonist of the EP4 receptor (IC50: 7.8 nM) and has antitumour effects.
价 格：￥电议型 号：T63100产 地：中国大陆
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T60840EP4 receptor antagonist 4；化合物 EP4 receptor antagonist 4EP4 receptor antagonist 4
EP4 receptor antagonist 4 is an agonist of EP4 receptor (human pEC 50 = 6.3) [1].
价 格：￥电议型 号：T60840产 地：中国大陆
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T4426CEP-40783；化合物CEP40783CEP 40783|||RXDX-106；CEP 40783|||RXDX-106
CEP-40783 (RXDX-106) is an effective, specific and orally active AXL/c-Met inhibitor (IC50: 7/12 nM). It also inhibits MER and TYRO3 (IC50: 29/19 nM).
价 格：￥电议型 号：T4426产 地：中国大陆
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T38595EP4 receptor antagonist 3EP4 receptor antagonist 3EP4 receptor antagonist 3
EP4 receptor antagonist 3 is a highly potent and specific inhibitor of the EP4 receptor. It is intended for research purposes in studying EP4 receptor-mediated diseases such as acute and chronic pain, osteoarthritis, rheumatoid arthritis, and cancer.
价 格：￥电议型 号：T38595产 地：中国大陆
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T37701pep4c；pep4cpep4c；pep4c
pep4c can be used for related research in the field of life sciences. Its product number is T37701 and CAS number is 243843-43-8.
价 格：￥电议型 号：T37701产 地：中国大陆
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T20871Desmedipham；化合物 T20871SN-38107|||Bentanex|||Desmediphame|||EP 475|||EP-475|||EP475；SN-38107|||Bentan
Desmedipham is a carbamate herbicide.
价 格：￥电议型 号：T20871产 地：中国大陆
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T11211EP4 receptor antagonist 1；化合物EP4 receptor antagonist 1EP4 receptor antagonist 1
EP4 Receptor Antagonist 1 is a highly potent and selective competitive prostanoid EP4 receptor antagonist, effective for cancer immunotherapy. It inhibits both human and mouse EP4 receptors with IC50 values of 6.1 nM and 16.2 nM, respectively, while displaying minimal activity (IC50s >10 μM) against human EP1, EP2, and EP3 receptors.
价 格：￥电议型 号：T11211产 地：中国大陆
