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5
Cat. No. | Product Name | Target | Signaling Pathways |
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T38206 |
3-Cysteinylacetaminophen (trifluoroacetate salt)
APAP-Cys,3-(cysteine-S-yl)acetaminophen,3-Cysteinylacetaminophen (trifluoroacetate salt) |
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3-Cysteinylacetaminophen is an acetaminophen-protein adduct formed during the metabolism of acetaminophen.[1],[2] 3-Cysteinylacetaminophen has been found in isolated human serum following therapeutic and supratherapeutic doses of acetaminophen and in the presence and absence of hepatotoxicity.[3],[4] In mice, 3-cysteinylacetaminophen decreases renal glutathione (GSH) levels, an effect that can be blocked by the γ-glutamyl inhibitor acivicin. | |||
T34785 |
TAPAP
3-Tapap |
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TAPAP binds to thrombin and trypsin. | |||
T83051 | Anti-inflammatory agent 61 | ||
Anti-inflammatory agent 61 (Compound 5b)为一种高效抗炎化合物,能够降低LPS诱导的RAW 264.7细胞中的TNF-α表达,并可缓解APAP引起的HepG2细胞炎症。 | |||
T69218 | PUMAi HCl | ||
PUMAi is an inhibitor of p53 up-regulated modulator of apoptosis (PUMA), a BH3-only Bcl-2 family member, mitigating acetaminophen (APAP)-induced hepatocyte necrosis and liver injury. |
Cat. No. | Product Name | Target | Signaling Pathways |
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T0065 |
Acetaminophen
对乙酰氨基酚,醋氨酚,4-Acetamidophenol,4'-Hydroxyacetanilide,APAP,Paracetamol |
COX; Endogenous Metabolite; Histone Acetyltransferase | Chromatin/Epigenetic; Immunology/Inflammation; Metabolism; Neuroscience |
Acetaminophen (APAP) 是一种 COX 抑制剂,抑制 COX-1 和 COX-2 (IC50=113.7/25.8 μM)。Acetaminophen 具有解热镇痛活性,以及较弱的抗炎活性。 | |||
T7036 |
2,4'-Dihydroxybenzophenone
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Antioxidant | oxidation-reduction |
2,4'-Dihydroxybenzophenone 可有效保护 C57BL/6J 小鼠免受 APAP 诱导的肝毒性。它对可卡因诱导的小鼠急性肝毒性和神经毒性具有保护作用。其机制可能与其抗氧化活性有关。 | |||
TWS1977 |
Kamebakaurin
尾叶香茶菜丙素,Kamebakaurine |
NF-κB | NF-κB |
Kamebakaurin (Kamebakaurine) 是一种提取自Isodon japonicus 中的天然产物,是一种NF-κB 的抑制剂,能够抑制 p50 的 DNA 结合活性。 | |||
T82219 | Heilaohuguosu F | ||
Heilaohuguosu F (compound 6)为一类四氢呋喃木脂素,表现出轻度肝脏保护效果。该化合物对于APAP诱导的HepG2细胞所呈现的肝毒性具有微弱的防护作用。 | |||
T82748 |
Celosin L
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Celosin L,一种三萜皂苷,具备保肝活性。该化合物能够保护HepG2 细胞免受 APAP 诱导的肝毒性伤害。 |