87
40
Cat. No. | Product Name | Target | Signaling Pathways |
---|---|---|---|
T23535L |
Xanthine amine congener trihydrochloride
Xanthine amine congener trihydrochloride (96865-92-8 Free base) |
Adenosine Receptor | GPCR/G Protein; Neuroscience |
Xanthine amine congener trihydrochloride 是一种有效的腺苷拮抗剂,可逆转由腺苷激动剂 N6-环己基腺苷产生的尿流量、钠排泄和心率的减少。 | |||
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。 | |||
T39387 |
Xanthine amine congener dihydrochloride
XAC dihydrochloride,Xanthine amine congener dihydrochloride |
||
Xanthine amine congener dihydrochloride (XAC dihydrochloride), a potent antagonist for both Adenosine A1 and A2 receptors, exhibits IC50 values of 1.8 nM for A1 and 114 nM for A2 receptors. Additionally, it functions as a convulsant agent in mouse models. | |||
T72078 |
Xanthine oxidoreductase-IN-4
|
Xanthine Oxidase | Metabolism |
Xanthine oxidoreductase-IN-4 是一种具有有口服活性黄嘌呤氧化还原酶 (XOR) 抑制剂,对 XOR 具有抑制作用,IC50 值为 29.3 nM。Xanthine oxidoreductase-IN-4 可用于研究高尿酸血症。 | |||
T23535 |
Xanthine amine congener
|
Adenosine Receptor | GPCR/G Protein; Neuroscience |
Xanthine amine congener 是非选择性的腺苷受体拮抗剂,在小鼠中具有诱发惊厥的作用。 | |||
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。 | |||
T72165 |
Xanthine oxidoreductase-IN-3
|
Xanthine Oxidase | Metabolism |
Xanthine oxidoreductase-IN-3 是一种具有口服活性的黄氨酸氧化还原酶 (XOR) 抑制剂(IC50 : 26.3 nM)。Xanthine oxidoreductase-IN-3 可用急性高尿酸血症的研究。 | |||
T72166 |
Xanthine oxidoreductase-IN-5
|
Xanthine Oxidase | Metabolism |
Xanthine oxidoreductase-IN-5 是一种具有口服活性的黄氨酸氧化还原酶 (XOR) 抑制剂(IC50 : 55 nM)。Xanthine oxidoreductase-IN-5 可用于急性高尿酸血症的研究。 | |||
T35156 |
Xanthine, 3-(3-methoxypropyl)-1-methyl-
|
||
Xanthine, 3-(3-methoxypropyl)-1-methyl- is a bioactive chemical. | |||
T131587 |
8-methyl-xanthine
|
||
8-methyl-xanthine 是一种有用的有机化合物,可用于生命科学领域的相关研究,其产品编号为 T131587。 | |||
T60890 |
Xanthine oxidoreductase-IN-1
|
||
Xanthine oxidoreductase-IN-1 是黄嘌呤氧化还原酶(XOR)的抑制剂,IC50值为7.0 nM。 | |||
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。 | |||
T62963 | Xanthine amine congener hydrochloride | ||
Xanthine amine congener (XAC) hydrochloride 是一种非选择性腺苷受体拮抗剂,在小鼠中能够诱发惊厥。 | |||
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。 | |||
T61162 |
Xanthine oxidoreductase-IN-2
|
||
Xanthine oxidoreductase-IN-2 (Compound IVa) is a potent inhibitor of xanthine oxidoreductase (XOR) with an IC50 value of 7.2 nM. Notably, Xanthine oxidoreductase-IN-2 demonstrates hypouricemic effects in mice, as evidenced by [1]. | |||
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。 | |||
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。 | |||
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。 | |||
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。 | |||
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。 | |||
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。 | |||
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。 | |||
T20102 |
8-Azahypoxanthine
NSC 22709,NSC-22709,阿扎次黄嘌呤,NSC22709 |
Nucleoside Antimetabolite/Analog | Cell Cycle/Checkpoint; DNA Damage/DNA Repair |
8-Azahypoxanthine (NSC-22709) 抑制次黄嘌呤-鸟嘌呤-黄嘌呤磷酸核糖基转移酶并具有抗疟特性。 | |||
T27076 |
8-Cyclopentyl-1,3-dimethylxanthine
CPT,A1受体拮抗剂,CPT |
Adenosine Receptor | GPCR/G Protein; Neuroscience |
8-Cyclopentyl-1,3-dimethylxanthine (CPT) 是一种选择性的腺苷A1受体拮抗剂,对 A1 受体和 A2 受体的Ki 值分别为 10.9 和 1440 nM。 | |||
T71327 |
Paraxanthine-d6
|
||
Paraxanthine-d6 is intended for use as an internal standard for the quantification of paraxanthine by GC- or LC-MS. Paraxanthine is an active metabolite of caffeine. It is formed via N3-demethylation of caffeine by the cytochrome P450 (CYP) isoform CYP1A2. Paraxanthine is an adenosine A1 and A2 receptor antagonist. In vivo, paraxanthine increases striatal cGMP and extracellular striatal dopamine levels and locomotor activity, as well as inhibits motor depression induced by the adenosine A1 agoni... | |||
T35739 |
Evoxanthine
|
||
Evoxanthine is an alkaloid that has been found in O. renieri and has antimalarial and anticancer activities.1,2 It is active against P. falciparum with an IC50 value of 67.6 μg/ml.1 Evoxanthine decreases proliferation of nine sensitive and drug-resistant cancer cell lines (IC50s = 6.11-80.99 μM).2 |1. Khalid, S.A., Farouk, A., Geary, T.G., et al. Potential antimalarial candidates from African plants: And in vitro approach using Plasmodium falciparum. J. Ethnopharmacol. 15(2), 201-209 (1986).|2. ... | |||
TNU1625 |
Arabinosylhypoxanthine
|
||
Arabinosylhypoxanthine 是一种有用的有机化合物,可用于生命科学领域的相关研究。其产品编号为 TNU1625,CAS号为 7013-16-3。 | |||
TNU1134 |
7-benzyl-3-methylxanthine
|
||
7-benzyl-3-methylxanthine belongs to Heterocyclic Compounds - Purines. | |||
T30905 |
Choline, compd. with 3-butyl-1-ethyl-6-thioxanthine
|
||
Choline, compd. with 3-butyl-1-ethyl-6-thioxanthine is a bioactive chemical. | |||
TNU1133 |
1,7-Dibenzyl-3-methylxanthine
|
||
1,7-Dibenzyl-3-methylxanthine belongs to Heterocyclic Compounds - Purines. | |||
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。 | |||
T27323 |
FK-453
FK453,FK 453 |
Adenosine Receptor | GPCR/G Protein; Neuroscience |
FK-453 是一种有效的非黄嘌呤腺苷 A1 受体拮抗剂,具有利尿和肾血管扩张活性。 | |||
T8567 |
amflutizole
|
Xanthine Oxidase | Metabolism |
amflutizole 用于治疗痛风,是一种黄嘌呤氧化酶抑制剂。 | |||
T68145 |
Stacofylline
|
||
Stacofylline 是一种黄嘌呤衍生物,可用于治疗偏头疼。 | |||
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。 | |||
T60625 |
Tigulixostat
LR-19074,IBI-350,LC350189 |
Xanthine Oxidase | Metabolism |
Tigulixostat (LC350189) 是一种新型黄嘌呤氧化酶抑制剂(XOI),可降低尿酸生成,可用于研究痛风相关的疾病。 | |||
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。 | |||
T14944 |
CGS 15943
|
PI3K; Adenosine Receptor | GPCR/G Protein; Neuroscience; PI3K/Akt/mTOR signaling |
CGS 15943 是一种可口服的非黄嘌呤腺苷受体拮抗剂。在转染的 CHO 细胞中,其对人 A1、A2A、A2B 和 A3 腺苷受体的 Ki 分别为 3.5、4.2、16 和 50 nM。 | |||
T68090 |
Laprafylline
|
Others | Others |
Laprafylline 是一种黄嘌呤化合物,对体内支气管收缩有抑制作用,且具有抗肿瘤活性。Laprafylline在低浓度时可充当竞争性血清素能拮抗剂,在高难度时抑制由hist引起的收缩。 | |||
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。 | |||
T67965 |
Torbafylline
|
cAMP; PI3K; PDE | GPCR/G Protein; Metabolism; PI3K/Akt/mTOR signaling |
Torbafylline 是黄嘌呤衍生物,是 磷酸二酯酶 (PDE) 抑制剂,通过 激活 PDE4/cAMP/EPAC/PI3K/Akt 途径减弱烧伤诱导的大鼠骨骼肌蛋白水解,抑制癌症和败血症大鼠增强的骨骼肌泛素 - 蛋白酶体依赖性蛋白水解。 | |||
T3097 |
Mycophenolic Acid Impurity
马替麦考酚酸杂质,5,7-dihydroxy-4-methylphthalide |
Others | Others |
Mycophenolic Acid Impurity (5,7-dihydroxy-4-methylphthalide) 是一种免疫抑制药物和有效的抗增殖剂,可用于代替旧的抗增殖剂 azathioprine。它通常用作三联疗法的一部分,包括钙调神经磷酸酶抑制剂(ciclosporin 或 tacrolimus)和prednisolone。它还可用于研究选择表达编码 XGPRT(黄嘌呤鸟嘌呤磷酸核糖基转移酶)的大肠杆菌基因的动物细胞。 | |||
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。 | |||
T1083L |
Theophylline monohydrate
Quibron,茶碱一水合物 |
HDAC; PDE; Adenosine Receptor | Chromatin/Epigenetic; DNA Damage/DNA Repair; GPCR/G Protein; Metabolism; Neuroscience |
Theophylline monohydrate (Quibron) 似乎抑制磷酸二酯酶和前列腺素的产生,调节钙通量和细胞内钙分布,并拮抗腺苷。茶碱是黄嘌呤的天然生物碱衍生物,从植物山茶花和小粒咖啡中分离出来。在生理上,该药剂可放松支气管平滑肌,产生血管舒张(脑血管除外),刺激中枢神经系统,刺激心肌,利尿,增加胃酸分泌;它还可以抑制炎症并改善横膈膜的收缩性。 |
Cat. No. | Product Name | Target | Signaling Pathways |
---|---|---|---|
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。 | |||
TMO2681 |
Xanthosine
9-Beta-D-Ribofuranosylxanthine,黄嘌呤核苷,Xanthine riboside |
Others; Endogenous Metabolite | Metabolism; Others |
Xanthosine (9-Beta-D-Ribofuranosylxanthine) 是黄嘌呤核苷,它能够提高山羊和牛的乳腺干细胞数量和产奶量。 | |||
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。 | |||
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。 | |||
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。 | |||
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)。 | |||
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。 | |||
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。 | |||
T0070 |
Pentoxifylline
Oxpentifylline,PTX,己酮可可碱,BL-191 |
HIV Protease; PDE; Adenosine Receptor; Autophagy | Autophagy; GPCR/G Protein; Metabolism; Microbiology/Virology; Neuroscience; Proteases/Proteasome |
Pentoxifylline (PTX) 是一种具有口服活性的磷酸二酯酶非选择性抑制剂,具有免疫调节、抗炎、抗纤溶、抗增殖和血液流变学改善作用。它可研究周围血管疾病、脑血管疾病和其他一些涉及局部微循环缺陷的疾病。 | |||
PDK0014 |
3-Methylxanthine
|
Endogenous Metabolite | Metabolism |
3-Methylxanthine 是一种黄嘌呤衍生物和环磷酸鸟苷(GMP)抑制剂,在豚鼠分离的气管肌肉中测得其IC50值为 920 μM。 | |||
T0543 |
7-Methylxanthine
Heteroxanthine,Heteroxanthin,7-甲基黄嘌呤 |
Nucleoside Antimetabolite/Analog; Endogenous Metabolite | Cell Cycle/Checkpoint; DNA Damage/DNA Repair; Metabolism |
7-Methylxanthine (Heteroxanthine) 是一种黄嘌呤的甲基衍生物,是人尿结石的嘌呤成分。 | |||
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。 | |||
T10021 |
1-Methylxanthine
|
Endogenous Metabolite | Metabolism |
1-Methylxanthine 是咖啡因衍生物,是咖啡因和茶碱 (1,3-二甲基黄嘌呤,TP) 在人体尿代谢产物,能够提高肿瘤细胞的放射敏感性。 | |||
T4973 |
Paraxanthine
1,7-二甲基黄嘌呤,1,7-DIMETHYLXANTHINE |
Endogenous Metabolite | Metabolism |
Paraxanthine (1,7-dimethylxanthine) 是一种 caffeine 的代谢物,能够刺激Ryanodine 受体通道来抑制多巴胺能细胞的死亡。 | |||
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。 | |||
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。 | |||
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。 | |||
T0625 |
Theobromine
3, 7-Dimethylxanthine,可可碱,3,7-Dimethylxanthine |
Endogenous Metabolite; PDE; Adenosine Receptor | GPCR/G Protein; Metabolism; Neuroscience |
Theobromine (3,7-Dimethylxanthine) 是在可可豆中发现的一种甲基黄嘌呤,抑制腺苷受体 A1 信号传导,用作支气管扩张剂和血管扩张剂。 | |||
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。 | |||
T2205 |
Acefylline
Theophylline-7-acetic acid,茶碱乙酸,Carboxymethyltheophylline,acetyloxytheophylline,Theophyllineacetic acid |
TNF; PAD; PKA; HDAC; PDE; Adenosine Receptor | Apoptosis; Chromatin/Epigenetic; DNA Damage/DNA Repair; GPCR/G Protein; Metabolism; Neuroscience; Tyrosine Kinase/Adaptors |
Acefylline (Theophylline-7-acetic acid) 是黄嘌呤衍生物,是一种腺苷受体拮抗剂。它是蛋白质精氨酸脱亚氨酶 (PAD) 激活剂,也是一种支气管扩张剂,可抑制大鼠肺 cAMP 磷酸二酯酶同工酶。 | |||
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。 | |||
T1083 |
Theophylline
Theo-24,1,3-Dimethylxanthine,茶碱 |
Endogenous Metabolite; HDAC; PDE; Adenosine Receptor; Autophagy | Autophagy; Chromatin/Epigenetic; DNA Damage/DNA Repair; GPCR/G Protein; Metabolism; Neuroscience |
Theophylline (1,3-Dimethylxanthine) 是茶中的甲基黄嘌呤衍生物,具有利尿、平滑肌松弛、支气管扩张、心脏和中枢神经系统兴奋作用。 | |||
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。 | |||
T0892 |
Diphylline
二羟丙茶碱,Dyphylline,Diprophylline |
PDE; Adenosine Receptor | GPCR/G Protein; Metabolism; Neuroscience |
Diphylline (Diprophylline) 是一种A1/A2腺苷受体拮抗剂,也是环状核苷酸磷酸二酯酶抑制剂。它是一种黄嘌呤衍生物,具有支气管扩张和血管扩张作用,有用于治疗慢性支气管炎和肺气肿的潜力。 | |||
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. | |||
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. | |||
TN4080 |
Fraxamoside
|
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). | |||
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. | |||
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-.). | |||
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。 | |||
TN4433 |
Licoarylcoumarin
|
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
|
||
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
|
||
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)。 |