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T8507MAC-545496Bacterial,S. aureus,Antivirulence,Inhibitor,MAC545496,mprF,nanomolar,GraR,MAC-545496,MRSA,
MAC-545496 is a glycopeptide-resistance-associated protein R (GraR) inhibitor, is an antivirulence agent.
价 格：￥电议型 号：T8507产 地：中国大陆
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T6482Efaproxiral SodiumRSR-13,RSR13,Reactive Oxygen Species,RSR 13,Efaproxiral Sodium,Inhibitor,inhibit,E
Efaproxiral Sodium , a synthetic allosteric modifier of hemoglobin, is utilized for brain metastases originating from breast cancer.
价 格：￥电议型 号：T6482产 地：中国大陆
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TN4943SanguisorbigeninPBP2a,mecA,Bacterial,Sanguisorbigenin,MRSA,inhibit,Inhibitor,antibacterial
Sanguisorbigenin is a natural antimicrobial agent that inhibits methicillin-resistant Staphylococcus aureus (MRSA).
价 格：￥电议型 号：TN4943产 地：中国大陆
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T7897PK150Bacterial,MRSA,MSSA,Gram-positive,PK-150,antibacterial,PK 150,PK150,Inhibitor,VISA,inhibit
PK150 shows oral bioavailability and antibacterial activity against several pathogenic strains at submicromolar concentrations.
价 格：￥电议型 号：T7897产 地：中国大陆
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T23016MRS1220
MRS1220, a highly potent and selective human A3 adenosine receptor (hA3AR) antagonist with a Ki of 0.59 nM, has therapeutic potential for the research of diseases of the central nervous system. MRS1220 reduces glioblastoma tumor size and blood vessel formation in vivo.
价 格：￥电议型 号：T23016产 地：中国大陆
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T7387Ceftaroline fosamilN-phosphono,PPI 0903,inhibit,TAK599,MRSA,TAK 599,PPI-0903,T-91825,Bacterial,Inhib
Ceftaroline fosamil is a cephalosporin, with activity against Gram-positive pathogens.
价 格：￥电议型 号：T7387产 地：中国大陆
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T6172MRS 2578
MRS2578, an effective P2Y6 receptor antagonist with IC50 of 37 nM, shows insignificant inhibition at P2Y1, P2Y2, P2Y4, and P2Y11 receptors.
价 格：￥电议型 号：T6172产 地：中国大陆
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T33508MRS928MRS 928；3,5,7-Trimethoxyflavone；MRS-928
MRS928 is a bioactive chemical. It has a role as a plant metabolite. It derives from a galangin.
价 格：￥电议型 号：T33508产 地：中国大陆
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T16140MRS 1754
MRS 1754 is a selective antagonist radioligand for the A2B adenosine receptor. It has a very low affinity for A1 and A3 receptors of both humans and rats.
价 格：￥电议型 号：T16140产 地：中国大陆
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T16136MRS-1706
MRS-1706 has Ki values of 1.39, 112, 157, and 230 nM for human A2B, A2A, A1, and A3 receptors respectively. MRS-1706 is an effective and selective adenosine A2B receptor inverse agonist.
价 格：￥电议型 号：T16136产 地：中国大陆
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T16140MRS 1754MRS 1754
MRS 1754 is a selective antagonist radioligand for the A2B adenosine receptor. It has a very low affinity for A1 and A3 receptors of both humans and rats.
价 格：￥电议型 号：T16140产 地：美洲
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T6172MRS 2578MRS 2578
MRS2578, an effective P2Y6 receptor antagonist with IC50 of 37 nM, shows insignificant inhibition at P2Y1, P2Y2, P2Y4, and P2Y11 receptors.
价 格：￥电议型 号：T6172产 地：美洲
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T79778Anti-MRSA agent 8；化合物 Anti-MRSA agent 8Anti-MRSA agent 8
Anti-MRSA Agent 8 (Compound 7g), a derivative of DAPG, exhibits potent antibacterial properties by interacting with bacterial cell membranes and is useful for studying methicillin-resistant Staphylococcus aureus (MRSA) [1].
价 格：￥电议型 号：T79778产 地：中国大陆
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T79326MRS7925；化合物 MRS7925MRS7925
MRS7925 (Compound 43) serves as a potent antagonist of the 5-HT2B receptor, with an inhibition constant (Ki) of 17 nM, and is utilized in the study of fibrosis [1].
价 格：￥电议型 号：T79326产 地：中国大陆
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T74810Anti-MRSA agent 7；化合物 Anti-MRSA agent 7Anti-MRSA agent 7
Anti-MRSA agent 7 (Compound 12) serves as a potent antibacterial compound effectively inhibiting both S. aureus and E. coli DNA gyrases, as well as topo IV enzymes from the same organisms, with IC50 values of 0.185 μM, 0.365 μM, 0.341 μM, and 0.059 μM, respectively [1].
价 格：￥电议型 号：T74810产 地：中国大陆
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T74527Anti-MRSA agent 4；化合物 Anti-MRSA agent 4Anti-MRSA agent 4
Anti-MRSA agent 4 (compound 7a), a selective and potent inhibitor of Gram-positive Methicillin-resistant Staphylococcus aureus (MRSA) growth, demonstrates a minimum inhibitory concentration (MIC) of ≤ 0.26 ?M. It exhibits neither cytotoxic nor hemolytic activity in HEK293 cells [1].
价 格：￥电议型 号：T74527产 地：中国大陆
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T73453MRS4719；化合物 MRS4719MRS4719
MRS4719, a potent P2X4 receptor antagonist, exhibits a half-maximal inhibitory concentration (IC50) of 0.503 μM for the human P2X4 receptor. Demonstrating both neuroprotective and neuro-rehabilitative effects, it can decrease infarct volume and brain atrophy in an ischemic stroke model. Additionally, MRS4719 mitigates ATP-induced calcium influx in primary human monocyte-derived macrophages, making it a valuable tool for researching ischemic stroke.
价 格：￥电议型 号：T73453产 地：中国大陆
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T73452MRS4596；化合物 MRS4596MRS4596
MRS4596, a potent and selective antagonist of the P2X4 receptor, exhibits an IC50 of 1.38 μM for the human P2X4 receptor. This compound demonstrates both neuroprotective and neuro-rehabilitative effects in ischemic stroke models, making it valuable for research purposes in the context of ischemic stroke.
价 格：￥电议型 号：T73452产 地：中国大陆
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T72514MRS2279 diammonium；化合物 MRS2279 diammoniumMRS2279 diammonium
MRS2279 diammonium, a selective and high-affinity P2Y1 receptor antagonist, exhibits a Ki value of 2.5 nM and an IC50 value of 51.6 nM. It competitively inhibits ADP-promoted platelet aggregation, demonstrating a pKb value of 8.05.
价 格：￥电议型 号：T72514产 地：中国大陆
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T72248MRS2768 tetrasodium salt；化合物 MRS2768 tetrasodium saltMRS2768 tetrasodium salt
MRS2768 tetrasodium salt, a moderately potent and selective agonist of the P2Y2 receptor, exhibits a protective effect against ischemic damage in cardiomyocytes both in vivo and in vitro.
价 格：￥电议型 号：T72248产 地：中国大陆
