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Cat. No. | Product Name | Target | Signaling Pathways |
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T76099 |
Alcohol dehydrogenase
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Alcohol dehydrogenase 是细胞内的一种二聚蛋白。Alcohol dehydrogenase 是体内消耗酒精的关键酶,在肝脏中表达高,参与环境酒精的解毒机制。 | |||
T0765 |
Fomepizole
Antizol-Vet,4-甲基吡唑,甲吡唑,4-Methylpyrazole,Antizol |
P450; CAT; AChR | Metabolism; Neuroscience; oxidation-reduction |
Fomepizole (4-Methylpyrazole) 是细胞色素 P450 (CYP2E1) 抑制剂。它是乙醇脱氢酶 (alcohol dehydrogenase) 竞争性抑制剂。它能够阻断甲醇和乙二醇进一步转化为有毒代谢产物。它具有成为乙二醇或甲醇中毒的解毒剂的潜力。 | |||
T15022 |
CVT-10216
3-[[[3-[4-[(甲基磺酰基)氨基]苯基]-4-氧代-4H-苯并吡喃-7-基]氧基]甲基]苯甲酸 |
Dehydrogenase | Metabolism |
CVT-10216 是可逆的、选择性的醛脱氢酶 2(ALDH-2)抑制剂,IC50为 29 nM。对 ALDH-1的抑制作用较弱,IC50为 1.3 μM。 它可以减少偏爱酒精的大鼠过量饮酒,并表现出抗焦虑作用。 | |||
T67832 |
ALDH2 modulator 1
|
Dehydrogenase | Metabolism |
ALDH2 modulator 1 是一种有效的且具有口服活性的乙醛脱氢酶-2 (ALDH2)调节剂。ALDH2 modulator 1 可使小鼠血液中的酒精含量降低。 | |||
T73446 |
BI‑3231
|
Dehydrogenase | Metabolism |
BI‑3231 是一种具有选择性和高效性的羟基类固醇 17ß-脱氢酶 13 HSD17B13 抑制剂,抑制 hHSD17B13 和 mHSD17B13。BI‑3231 可用于研究酒精相关肝损伤、纤维化和肝硬化。 | |||
T0054 |
Disulfiram
双硫伦,Tetraethylthiuram disulfide,双硫仑,NSC 190940,TETD |
Dehydrogenase; Interleukin; Pyroptosis | Apoptosis; Immunology/Inflammation; Metabolism |
Disulfiram (TETD) 是一种乙醛脱氢酶 ALDH 的抑制剂,抑制 hALDH1 和 hALDH2 (IC50=0.15/1.45 μM),具有特异性。Disulfiram 对酒精产生急性敏感性,还可以抑制 GSDMD 孔形成。 | |||
T19930 |
Nitrosoglutathione
S-Nitrosoglutathione,S-亚硝基谷胱甘肽,SNOG,Glutathione thionitrite,GSNO |
RAAS; NO Synthase | Endocrinology/Hormones; Immunology/Inflammation |
Nitrosoglutathione (GSNO) 是一种外源性的 NO 供体,是大鼠酒精脱氢酶III 类同工酶的底物,能够减少脑血管紧张素II 依赖性及非依赖型的 AT1 受体反应。 | |||
T40793 |
2-Bromoacetamide
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2-Bromoacetamide can inactivate alcohol dehydrogenase. | |||
T20256 |
Sorbitol, L-
L-Glucitol |
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Sorbitol, L- is a sugar alcohol. It can be obtained by the reduction of glucose, which changes the aldehyde group to a hydroxyl group. It is converted to fructose by sorbitol-6-phosphate 2-dehydrogenase. Sorbitol is an isomer of mannitol, another sugar al | |||
T60363 |
Nitrefazole
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Nitrefazole 是一种4-nitroimidazole 衍生物,对醛脱氢酶(ALDH)具有强烈而持久的抑制作用,醛脱氢酶是一种参与酒精代谢的酶。 | |||
T72245 |
Fomepizole hydrochloride
4-Methylpyrazole hydrochloride |
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Fomepizole hydrochloride(4-Methylpyrazole)是一种高效、具口服活性的细胞色素P450(CYP2E1)和竞争性乙醇脱氢酶(alcohol dehydrogenase)抑制剂,阻止甲醇和乙二醇转化为有毒代谢产物,具有用于乙二醇或甲醇中毒解毒的潜力。 | |||
T70859 |
ent-Abacavir
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ent-Abacavir is an enatiomer of Abacavir. Abacavir is a carbocyclic 2'-deoxyguanosine nucleoside reverse transcriptase inhibitor and an anti-HIV drug used to treat HIV infection. Intracellular enzymes convert Abacavir to its active form, carbovir-triphosphate (CBV-TP), which then selectively inhibits HIV reverse transcriptase by incorporating into viral DNA. Abacavir is metabolized in the liver by uridine diphosphate glucuronyltransferase and alcohol dehydrogenase resulting in inactive glucuroni... |
Cat. No. | Product Name | Target | Signaling Pathways |
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TJS1382 |
Taraxerone
蒲公英赛酮 |
Dehydrogenase | Metabolism |
Taraxerone 是分离自景天的天然产物。它可以增强乙醇脱氢酶和乙醛脱氢酶活性,EC50分别为 512.42 μM 和 500.16 μM。 | |||
TN1537 |
Curcumenone
|
Others | Others |
Curcumenone may have protective effect on drunkenness, through increasing liver alcohol dehydrogenase activity. |