52
30
Cat. No. | Product Name | Target | Signaling Pathways |
---|---|---|---|
T76104 |
Xanthine oxidase
黄嘌呤氧化酶 |
||
Xanthine oxidase 是一种黄嘌呤氧化还原酶,可产生活性氧 (ROS),催化次黄嘌呤氧化为黄嘌呤,进一步催化黄嘌呤氧化为尿酸。 | |||
T10509 |
Xanthine oxidase-IN-1
4-(3-Cyano-5,6-difluoroindol-1-yl)-2-hydroxybenzoic acid |
Xanthine Oxidase | Metabolism |
Xanthine oxidase-IN-1是一种有效的黄嘌呤氧化酶抑制剂(IC50值:6.5 nM),是一种利用核酸和核苷酸介质降解产生的生物活性核苷酸在嘌呤分解代谢中起核心作用的化合物, | |||
T78984 |
Xanthine oxidase-IN-10
XO8 analog |
ROS | Immunology/Inflammation |
Xanthine oxidase-IN-10 (XO8 analog) 是一种黄嘌呤氧化酶 (XO) 抑制剂,可用于研究痛风。 | |||
T8337 |
Nequinate
|
Xanthine Oxidase; Parasite | Metabolism; Microbiology/Virology |
Nequinate 是一种喹啉化合物,是一种抗球虫剂,可预防球虫病。它抑制黄嘌呤氧化还原酶活性。 | |||
T1274 |
Benzbromarone
Desuric,Normurat,苯溴马隆,Urinorm |
Apoptosis; P450; Xanthine Oxidase | Apoptosis; Metabolism |
Benzbromarone (Desuric) 是一种高效的,耐受性良好的非竞争性黄嘌呤氧化酶抑制剂,用作排尿酸剂,研究痛风。 | |||
T22304 |
Desciclovir
BW A515U,地昔洛韦,6-Deoxyacyclovir,DCV |
Antifection | Microbiology/Virology |
Desciclovir (DCV) 是抗疱疹药物阿昔洛韦的前药,口服有活性,在体内被黄嘌呤氧化酶转化成为阿昔洛韦。 | |||
T2397 |
Topiroxostat
托匹司他,FYX-051 |
P450; ROS; Xanthine Oxidase | Immunology/Inflammation; Metabolism |
Topiroxostat (FYX-051) 是一种有效的口服黄嘌呤氧化还原酶 (XOR) 抑制剂,IC50=5.3 nM,Ki=5.7 nM。它还表现出弱的CYP3A4抑制活性 (18.6%)。它有用于高尿酸血症的研究潜力。 | |||
T72409 |
Xanthine oxidase-IN-6
|
||
Xanthine oxidase-IN-6 是一种强效的、具有口服活性的黄嘌呤氧化酶 (XOD) 混合型抑制剂,其IC50值为1.37 µM。Xanthine oxidase-IN-6 具有很强的抗高尿酸血症 (anti-hyperuricemia) 和肾保护活性。 | |||
T60626 | Xanthine oxidase-IN-7 | ||
Xanthine oxidase-IN-7 (compound1h) 是一种口服的黄嘌呤氧化酶(XO)抑制剂 (IC50 = 0.36 μM)。Xanthine oxidase-IN-7 可有效降低血清尿酸水平,在高尿酸血症和痛风的研究中具有潜力。 | |||
T61092 |
Xanthine oxidase-IN-5
|
||
Xanthine oxidase-IN-5, a powerful and orally active inhibitor of xanthine oxidase (XO), exhibits an IC50 value of 0.70 μM. It possesses favorable drug-like characteristics, with ligand efficiency (LE) and lipophilic ligand efficiency (LLE) values of 0.33 and 3.41, respectively. Moreover, Xanthine oxidase-IN-5 showcases significant hypouricemic effects in a hyperuricemic rat model [1]. | |||
T80767 | Xanthine oxidase-IN-12 | Xanthine Oxidase | Metabolism |
Xanthine oxidase-IN-12 (Compound 11), 作为一种高效的黄嘌呤氧化酶 (XO) 抑制剂,其IC50值达到91 nM。此外,Xanthine oxidase-IN-12 亦展现出抗氧化活性,能降低细胞内活性氧种 (ROS) 的水平。 | |||
T78985 |
Xanthine oxidase-IN-11
|
Xanthine Oxidase | Metabolism |
Xanthine oxidase-IN-11 (XO8 analog) 是一种有效的黄嘌呤氧化酶 (XO) 抑制剂。 | |||
T60632 | Xanthine oxidase-IN-4 | ||
Xanthine oxidase-IN-4 (化合物 19a) 是一种具有口服活性的有效黄嘌呤氧化酶 (XO) 抑制剂,IC50值为0.039 μM,可用于高尿酸血症和痛风的研究。Xanthine oxidase-IN-4 在氧嗪酸钾诱导的高尿酸血症大鼠中表现出降尿酸能力。 | |||
T0692 |
Allopurinol
Zyloric,别嘌醇,Zyloprim,Lopurin,别嘌呤醇 |
ROS; Xanthine Oxidase | Immunology/Inflammation; Metabolism |
Allopurinol (Zyloric) 是一种黄嘌呤氧化酶(XO)抑制剂,IC50=7.82±0.12 μM。 | |||
T0773 |
Febuxostat
非布索坦,TMX 67,非布司他,TEI 6720 |
ROS; Xanthine Oxidase | Immunology/Inflammation; Metabolism |
Febuxostat (TEI 6720) 是一种选择性黄嘌呤氧化酶(XO)抑制剂,Ki=0.6 nM。 | |||
T6376 |
Allopurinol Sodium
1H-吡唑并[3,4-D]嘧啶-4-醇单钠盐,Allopurinol sodium salt,Sodium allopurinol |
ROS | Immunology/Inflammation |
Allopurinol Sodium 是黄嘌呤氧化酶抑制剂,其IC50= 0.2~50 μM。它能够抗利什曼原虫,也可用于研究痛风以及高尿酸血症。 | |||
T33676 |
Niraxostat
Y 700,Y700,Y-700 |
Xanthine Oxidase | Metabolism |
Niraxostat (Y-700) 是作为黄嘌呤氧化酶抑制剂的异胞嘧啶衍生物之一。 | |||
T9366 |
Pyrazoloadenine
4-Aminopyrazolo[3,4-d]pyrimidine |
ROS | Immunology/Inflammation |
Pyrazoloadenine (4-Aminopyrazolo[3,4-d]pyrimidine) 是人黄嘌呤氧化酶的抑制剂。 | |||
T8567 |
amflutizole
|
Xanthine Oxidase | Metabolism |
amflutizole 用于治疗痛风,是一种黄嘌呤氧化酶抑制剂。 | |||
T20042 |
8-Azaadenine
NSC 32797,NSC32797,NSC-32797 |
Xanthine Oxidase | Metabolism |
8-Azaadenine (NSC-32797) 是一种黄嘌呤氧化酶抑制剂,IC50 为 0.54 μM,Ki 为 0.66 μM。 | |||
T20347 |
Deoxybenzoin
二苯基乙酮,2-Phenylacetophenone,Benzyl phenyl ketone,NSC-131456,NSC131456,NSC 131456 |
Others | Others |
Deoxybenzoin (2-Phenylacetophenone) 用于靶向免疫传感器和黄嘌呤氧化酶。它用于治疗痛风。 | |||
T60625 |
Tigulixostat
|
||
Tigulixostat 是吲哚基杂芳羧酸的新型衍生物。Tigulixostat 是一种非嘌呤选择性的黄嘌呤氧化酶抑制剂,可降低尿酸的生成。 | |||
TP1886L1 |
NoxA1ds acetate(1435893-78-9 free base)
|
NADPH-oxidase | Immunology/Inflammation |
NoxA1ds acetate(1435893-78-9 free base) 是一种有效的选择性 NADPH 氧化酶 1 (NOX1) 抑制剂 (IC50 : 20 nM)。对 NOX1 的选择性优于对 NOX2、NOX4、NOX5 和黄嘌呤氧化酶的选择性。它抑制 HT-29 人结肠癌细胞中 NOX1 衍生的 O2 产生。在体外缺氧条件下减弱 VEGF 诱导的人肺动脉内皮细胞迁移。 | |||
T50059 |
6-ethenylquinoline
|
Others | Others |
6-ethenylquinoline 是一种结构独特的芳香杂环化合物,是生产其他芳香族化合物的重要中间体,并被用作合成各种药物的起始材料,包括抗真菌剂、抗寄生虫剂和抗病毒剂。它已被证明是多种参与药物代谢的酶的抑制剂,包括细胞色素P450、醛氧化酶和黄嘌呤氧化酶等。 | |||
T69247 | Febuxostat hemihydrate | ||
Febuxostat hemihydrate is a xanthine oxidase inhibitor used to treat hyperuricemia and chronic gout. | |||
T26058 |
Renierol
|
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Renierol is a natural xanthine oxidase inhibitor with hypouricemic effects isolated from marine sponge Halicdona.SP. | |||
T39012 |
O-Desisobutyl-O-n-propyl Febuxostat
|
||
O-Desisobutyl-O-n-propyl Febuxostat, an xanthine oxidase inhibitor. | |||
T32905 |
LSPN451
LSPN 451,LSPN-451 |
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LSPN451 is an effective xanthine oxidase inhibitor and may be used to treat hyperuricemia and gout. | |||
T68437 | Febuxostat 67M-1 | ||
Febuxostat 67M-1 is an inhibitor of xanthine oxidase. It reduces uric acid production in the body and reduces the risk of gout or kidney stone formation. | |||
T11270 |
Febuxostat D9
非布司他D9 |
Others | Others |
Febuxostat D9 is deuterium labeled Febuxostat, which is a selective xanthine oxidase inhibitor with Ki of 0.6 nM. | |||
T73969 | Febuxostat impurity 6 | ||
Febuxostat impurity 6 是 Febuxostat 一种杂质。Febuxostat 是选择性黄嘌呤氧化酶 (XO) 抑制剂,Ki 为 0.6 nM。 | |||
T69282 |
Febuxostat 67M-2
|
||
Febuxostat 67M-2 is a derivative compound of Febuxostat 67M-1 which is an inhibitor of xanthine oxidase. It reduces uric acid production in the body and also used to reduce the risk of gout or kidney stone formation. | |||
T75949 |
NoxA1ds TFA
|
||
NoxA1ds TFA is a potent and selective inhibitor of NADPH oxidase 1 (NOX1), with an inhibition concentration (IC50) of 20 nM, demonstrating selectivity over NOX2, NOX4, NOX5, and xanthine oxidase. It effectively inhibits NOX1-derived O2- production in HT-29 human colon cancer cells and attenuates VEGF-induced migration of human pulmonary artery endothelial cells under hypoxic conditions in vitro. | |||
T73965 | Febuxostat n-butyl isomer | ||
Febuxostat n-butyl isomer 是 Febuxostat 一种杂质。Febuxostat 是选择性黄嘌呤氧化酶 (XO) 抑制剂,Ki 为 0.6 nM。 | |||
T73970 |
Febuxostat dicarboxylic acid impurity
|
||
Febuxostat dicarboxylic acid impurity 是 Febuxostat 一种杂质。Febuxostat 是选择性黄嘌呤氧化酶 (XO) 抑制剂,Ki 为 0.6 nM。 | |||
T73967 |
Febuxostat impurity 7
|
||
Febuxostat impurity 7 是 Febuxostat 一种杂质。Febuxostat 是选择性黄嘌呤氧化酶 (XO) 抑制剂,Ki 为 0.6 nM。 | |||
T73971 |
Febuxostat amide impurity
|
||
Febuxostat amide impurity 是 Febuxostat 一种杂质。Febuxostat 是选择性黄嘌呤氧化酶 (XO) 抑制剂,Ki 为 0.6 nM。 | |||
T73960 |
Febuxostat isopropyl isomer
|
||
Febuxostat isopropyl isomer 是 Febuxostat 一种杂质。Febuxostat 是选择性黄嘌呤氧化酶 (XO) 抑制剂,Ki 为 0.6 nM。 | |||
T73968 |
Febuxostat impurity 8
|
||
Febuxostat impurity 8 是 Febuxostat 一种杂质。Febuxostat 是选择性黄嘌呤氧化酶 (XO) 抑制剂,Ki 为 0.6 nM。 | |||
T69281 |
Febuxostat 67M-4
|
||
Febuxostat 67M-4 is a derivative compound of Febuxostat 67M-1 which is an inhibitor of xanthine oxidase. It reduces uric acid production in the body and reduces the risk of gout or kidney stone formation. | |||
TP1886 |
NoxA1ds
|
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Potent and selective NADPH oxidase 1 (NOX1) inhibitor (IC50 = 20 nM). Exhibits selectivity for NOX1 over NOX2, NOX4, NOX5 and xanthine oxidase. Inhibits NOX1-derived O2- production in HT-29 human colon cancer cells. Attenuates VEGF-induced human pulmonary | |||
T73966 |
Febuxostat sec-butoxy acid
|
||
Febuxostat sec-butoxy acid 是 Febuxostat 一种杂质。Febuxostat 是选择性黄嘌呤氧化酶 (XO) 抑制剂,Ki 为 0.6 nM。 | |||
T61060 |
Febuxostat sodium
|
||
Febuxostat (TEI 6720) sodium 在痛风和高尿酸血症研究中具有潜力,它是一种有效的、选择性的、非嘌呤的黄嘌呤氧化酶 (XO)抑制剂,Ki 值为 0.6 nM。 | |||
T79177 | URAT1&XO inhibitor 2 | Xanthine Oxidase | Metabolism |
URAT1&XO inhibitor 2 (Compound BDEO)是一种针对xanthine oxidase (黄嘌呤氧化酶) 及URAT1的双重抑制剂,对xanthine oxidase展现出优异的抑制效果,IC50值为3.3 μM。该化合物在表达URAT1的HEK293细胞中显著抑制尿酸的摄取,其Ki值达到0.145 μM。在动物模型中,URAT1&XO inhibitor 2有效降低高尿酸血症小鼠的血清尿酸水平,并增加尿酸的排泄。该化合物主要用于高尿酸血症的研究。 | |||
T35976 | 6-Formylpterin | ||
Xanthine oxidase (XO) generates reactive oxygen species, including hydrogen peroxide (H2O2), as it oxidizes specific substrates in the presence of water and oxygen. 6-Formylpterin is an oxidized pterin produced by photolytic breakdown of folic acid. It binds to one of two active sites on XO nearly quantitatively and irreversibly and prevents the metabolism of other substrates at the second site, resulting in hetero-substrate" inhibition at nanomolar concentrations. However | |||
T62350 | XO/COX/LOX-IN-1 | ||
XO/COX/LOX-IN-1 是一种黄嘌呤氧化酶/环氧酶/脂氧合酶 XO/COX/LOX 的有效抑制剂。XO/COX/LOX-IN-1 能够用于研究炎症、癌症以及代谢性疾病。 | |||
T75501 | Morin 3-O-β-D-glucopyranoside | ||
Morin 3-O-β-D-glucopyranoside 是一种天然类黄酮,具有抗真菌、抗癌和抗氧化活性。Morin 3-O-β-D-glucopyranoside 抑制逆转录酶、蛋白酪氨酸激酶和黄嘌呤氧化酶,还具有抗 HIV、抗动脉硬化和超氧化物清除活性。 | |||
T79331 |
Antioxidant agent-13
|
Xanthine Oxidase | Metabolism |
Antioxidant agent-13(Compound 5f)为一种效能显著的抗氧化剂,其抑制DPPH和FRAP的IC50值分别为80.33 μM和85.69 μM;同时,Antioxidant agent-13对LOX和XO酶的抑制作用亦强,对应IC50值为16.85 μM及23.01 μM。 | |||
T36501 |
CYPMPO
RR 071 |
||
CYPMPO is a free radical spin trap with excellent trapping capabilities toward hydroxyl and superoxide radicals in biological and chemical systems. Decay of the superoxide adduct of CYPMPO proceeds in an apparent first order fashion with half-lives of 15 and 51 minutes in a UV-illuminated hydrogen peroxide solution and a hypoxanthine/xanthine oxidase system, respectively. CYPMPO traps superoxide radicals generated by bovine neutrophils as effectively as DEPMPO.[1] The high melting point (126°C),... | |||
T79175 | URAT1&XO inhibitor 1 | Xanthine Oxidase | Metabolism |
URAT1&XO inhibitor 1(化合物29)是一种对URAT1(IC50≈10μM)和黄嘌呤氧化酶(IC50=1.01μM)具有双重抑制作用的抑制剂。该化合物能够在氧酸钾引起的高尿酸血症大鼠模型中降低血尿酸水平,已广泛应用于高尿酸血症的研究。 |
Cat. No. | Product Name | Target | Signaling Pathways |
---|---|---|---|
T16685 |
Purpurogallin
红倍酚,红陪酚 |
Xanthine Oxidase | Metabolism |
Purpurogallin 是一种从栎属植物中提取的天然酚,具有显著的黄嘌呤氧化酶抑制作用,其IC50=0.2 µM,具有抗氧化和抗炎作用。 | |||
T1694 |
Oxypurinol
Oxipurinol,羟基嘌呤 |
ROS; Xanthine Oxidase; Endogenous Metabolite | Immunology/Inflammation; Metabolism |
Oxypurinol 是一种黄嘌呤氧化酶 (xanthine oxidase) 抑制剂,是 Allopurinol 的主要特性代谢产物。它能够用于调节血尿酸水平,有潜力用于痛风的研究。 | |||
TMA0958 |
Forsythoside F
连翘酯苷F,Arenarioside,三糖苯丙素苷 |
Xanthine Oxidase | Metabolism |
Forsythoside F (Arenarioside) 是一种黄嘌呤氧化酶 (xanthine oxidase) 抑制剂,具有抗高尿酸活性。 | |||
T2858 |
Baicalein
5,6,7-Trihydroxyflavone,黄芩素,黄芩黄素 |
Ferroptosis; Influenza Virus; ROS; Xanthine Oxidase | Apoptosis; Immunology/Inflammation; Metabolism; Microbiology/Virology |
Baicalein (5,6,7-Trihydroxyflavone) 是一种黄嘌呤氧化酶抑制剂,其IC50值为 3.12 μM。 | |||
T2971 |
Phytic acid
Inositol hexaphosphate,inositol hexakisphosphate,inositol polyphosphate,myo-Inositol, hexakis(dihydrogen phosphate),植酸,Fytic Acid |
Xanthine Oxidase; Endogenous Metabolite | Metabolism |
Phytic acid (Fytic Acid) 是种子和谷粒的磷储存化合物。它被称为食品抑制剂,具有很强的螯合多价金属离子的能力,特别是钙,铁,锌和蛋白质残留物。它抑制超氧化物来源黄嘌呤氧化酶并具有抗氧化,抗炎以及神经保护作用。 | |||
T12564 |
Prudomestin
3,5,7-Trihydroxy-4',8-dimethoxyflavone,3,5,7-三羟基-8,4'-二甲氧基黄酮 |
Xanthine Oxidase | Metabolism |
Prudomestin (3,5,7-Trihydroxy-4',8-dimethoxyflavone) 是一种分离自 Prunus domestica 心材中,具有很强的黄嘌呤氧化酶(XO)抑制活性(IC50≈6 µM)。 | |||
T75504 | Xanthine oxidase-IN-8 | ||
Xanthine oxidase-IN-8 (Icarisids J) (Compound 7) 是一种 XOD 抑制剂,IC50值为 29.71 μM。 | |||
T75505 | Xanthine oxidase-IN-9 | ||
Xanthine oxidase-IN-9 (Icarisids E) (Compound 2),一种黄嘌呤氧化酶 (XOD) 高效抑制剂,具有31.81 μM 的 IC50 值。 | |||
T16527 |
Phytic acid dodecasodium salt hydrate
植酸十二钠盐,myo-Inositol, hexakis(dihydrogen phosphate) dodecasodium salt hydrate,Inositol hexaphosphate dodecasodium salt hydrate |
Others; Xanthine Oxidase; Endogenous Metabolite | Metabolism; Others |
Phytic acid dodecasodium salt hydrate (myo-Inositol, hexakis(dihydrogen phosphate) dodecasodium salt hydrate) 是种子和谷物的磷储存化合物。 Phytic acid dodecasodium salt hydrate 抑制酶促超氧化物源黄嘌呤氧化酶,IC50 为 6 mM,并具有抗氧化、神经保护和抗炎作用。 | |||
T1363 |
N-Demethylricinine
4-Methoxy-2-oxo-1,2-dihydro-pyridine-3-carbonitrile,吉莫斯特中间体二 |
ROS | Immunology/Inflammation |
N-Demethylricinine (4-Methoxy-2-oxo-1,2-dihydro-pyridine-3-carbonitrile) 被报道为 xanthine oxidase 抑制剂。 | |||
TN1002 |
Blumeatin
|
ROS | Immunology/Inflammation |
Blumeatin 是从Blumea balsamiferaDC 中分离得到,对 CCl4 和硫代乙酰胺 (TAA) 所致的肝损伤表现出保护活性。 | |||
T3750 |
4-Hydroxyacetophenone
对羟基苯乙酮,4-Acetylphenol,Piceol,p-Acetylphenol,4'-Hydroxyacetophenone |
HBV; Xanthine Oxidase | Metabolism; Microbiology/Virology |
4-Hydroxyacetophenone (4-Acetylphenol) 是蒿属植物和木香属植物中的一种黄嘌呤氧化酶抑制剂,具有保肝促胆、抗乙型肝炎病毒和抗炎作用。 | |||
T0665 |
Xanthine
2,6-Dihydroxypurine,海生丁(黄嘌呤),黄嘌呤,Isoxanthine |
Endogenous Metabolite; Adenosine Receptor | GPCR/G Protein; Metabolism; Neuroscience |
Xanthine (Isoxanthine) 是一种植物生物碱,存在于茶、咖啡和可可中。Xanthine 是温和的中枢神经系统激活剂,也是嘌呤降解途径的中间产物。 | |||
T5S0281 |
Tubuloside A
|
NOS | Immunology/Inflammation |
Tubuloside A 是一种苯乙醇苷,具有抗氧化活性和保肝活性。 | |||
TN1962 |
Myricetin 3-O-galactoside
Myricetin 3-O-beta-D-galactopyranoside |
NOS; Xanthine Oxidase | Immunology/Inflammation; Metabolism |
Myricetin 3-O-galactoside (Myricetin 3-O-beta-D-galactopyranoside) 可抑制黄嘌呤氧化酶 (xanthine oxidase; XO) 活性,脂质过氧化并清除自由基。杨梅素3- o -半乳糖苷具有很多作用包括细胞毒性、抗氧化、抗基因毒性、抗感染性、抗炎作用和抗氧化活性,其主要作用是抑制诱导型一氧化氮合酶(iNOS)的合成。Myricetin 3-O-galactoside 抑制脂质过氧化的 IC50 为 160 μg/mL。 | |||
T0617 |
Nicotinamide N-oxide
Nicotinamide-N-oxide,Nicotinamide 1-oxide,N-氧代烟酰胺,烟酰胺-N-氧化物,1-oxynicotinamide |
c-Myc; Endogenous Metabolite; CXCR; Drug Metabolite | Autophagy; Cell Cycle/Checkpoint; GPCR/G Protein; Immunology/Inflammation; Metabolism |
Nicotinamide N-oxide (Nicotinamide 1-oxide) 是生物体内烟酰胺分解代谢物,是高效选择性CXCR2受体拮抗剂。 | |||
T0626 |
Uric Acid
尿酸,2,6,8-Trioxopurine,2,6,8-Trioxypurine,2,6,8-Trihydroxypurine,Lithic acid,Urate |
Reactive Oxygen Species; Endogenous Metabolite; Phosphorylase | Immunology/Inflammation; Metabolism; NF-κB |
Uric Acid (Lithic acid) 是一种重要的抗氧化剂。Uric acid 能清除活性氧(ROS) ,如单线态氧和过氧亚硝酸盐,抑制脂质过氧化。Uric acid 有助于维持血压的稳定和抗氧化应激。 | |||
T1362 |
Hypoxanthine
次黄嘌呤,6-羟基嘌呤,6-Hydroxypurine,Purin-6-ol,Sarcine,Sarkin |
Others; Endogenous Metabolite | Metabolism; Others |
Hypoxanthine (Purin-6-ol),也被称为 purine-6-ol 或 Hyp,是一种天然存在的嘌呤衍生物,是腺苷代谢和核苷酸补救途径形成核酸的反应中间体。在正常情况下,Hypoxanthine 很容易转化为尿酸。Hypoxanthine 首先被氧化为黄嘌呤,黄嘌呤再被黄嘌呤氧化酶氧化为尿酸。 | |||
T4746 |
Purine
7H-Imidazo(4,5-d)pyrimidine,嘌呤 |
Others; Endogenous Metabolite | Metabolism; Others |
Purine (7H-Imidazo(4,5-d)pyrimidine) 是内源性代谢产物的一种。 | |||
TN5670 | Protosappanin A dimethyl acetal | ||
Protosappanin A dimethyl acetal shows significant xanthine oxidase inhibitory activity in a concentration-dependent manner. | |||
TN2180 |
Sappanchalcone
苏木查耳酮 |
IL Receptor; BCL; TNF | Apoptosis; Immunology/Inflammation |
Sappanchalcone shows xanthine oxidase inhibitory activity, is a xanthine oxidase inhibitor. | |||
TN4080 |
Fraxamoside
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Xanthine Oxidase | Metabolism |
Fraxamoside is a xanthine oxidase inhibitor (XOI) comparable in potency in vitro to the standard antigout drug allopurinol. It shows significant free radical scavenging effect against DPPH(EC50=62.6 uM). | |||
TN3208 | 7,3',4'-Trihydroxy-3-benzyl-2H-chromene | ROS | Immunology/Inflammation |
7,3',4'-Trihydroxy-3-benzyl-2H-chromene is a potential xanthine oxidase inhibitor. | |||
T38777 | Ilexoside O | ||
Ilexoside O, a triterpene saponin derived from Ilex pubescens roots, demonstrates modest inhibition of xanthine oxidase (XOD) activity with an IC50 value of 53.05 μM. | |||
T75546 | Ellagic acid 4-O-β-D-xylopyranoside | ||
Ellagic acid 4-O-β-D-xylopyranoside,天然鞣花单宁,展现抗菌活性。同时,作为黄嘌呤氧化酶 (xanthine oxidase) 抑制剂,其50为 2.1 μg/mL。 | |||
TN1503 |
Cistanoside F
肉苁蓉苷F,肉苁蓉苷 F |
NADPH-oxidase | Immunology/Inflammation |
Cistanoside F shows vasorelaxant, and antioxidative effects, it shows a strong free radical scavenging activity on 1,1-diphenyl-2-picrylhydrazyl (DPPH) radical and xanthine/xanthine oxidase (XOD) generated superoxide anion radical (O2-.). | |||
TN4433 |
Licoarylcoumarin
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cAMP; HIV Protease; Antifection | GPCR/G Protein; Microbiology/Virology; Proteases/Proteasome |
Licoarylcoumarin is a strong inhibitor of adenosine 3',5'-cyclic monophosphate (cAMP) phosphodiesterase. Licoarylcoumarin has antibacterial effects on the VRE strains; it has anti-HIV activity, and it has inhibitory effects on xanthine oxidase. | |||
TN3473 |
Axillarin
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Axillarin has antioxidant activity, it shows xanthine oxidase inhibitory activity ( IC(50) :36.0 uM). Axillarin can strongly protect primary cultured neurons against glutamate-induced oxidative stress. | |||
T82649 | Cyanidin | ||
Cyanidin,作为一种抗氧化剂,能够保护 DNA 免受裂解,有效清除自由基,并显著抑制 XO 活性。 | |||
T72594 |
Broussochalcone A
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Broussochalcone A 是一种具有抗氧化和抑制黄嘌呤氧化酶(IC50=2.21 μM)功能的化合物,能清除自由基,抑制铁诱导的脂质过氧化和脂多糖(LPS)激活的巨噬细胞中一氧化氮(NO)的合成。此外,Broussochalcone A 通过增加ROS水平和激活FOXO3信号通路,诱导人肾癌细胞的凋亡(Apoptosis)。 |