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Cat. No. | Product Name | Target | Signaling Pathways |
---|---|---|---|
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。 | |||
TP2215 |
Agouti-related Protein (AGRP) (25-82), human
|
Others | Others |
Agouti-related peptide (AgRP) is a neuropeptide produced in the brain by the AgRP/NPY neuron. It is only synthesized in NPY containing cell bodies located in the ventromedial part of the arcuate nucleus in the hypothalamus. The appetite-stimulating effect | |||
T76301 |
Agouti-related Protein (AGRP) (83-132) Amide (human)
|
||
Agouti-related Protein (AGRP) (83-132) Amide (human),一种AGRP的片段,主要在下丘脑弓状核中表达。该化合物主要通过作为黑皮质素-4受体(MC4R)的反向激动剂来增加食物摄入。 | |||
T79854 |
Lingdolinurad
|
OAT | Membrane transporter/Ion channel |
Lingdolinurad 是一种靶向 hURAT1的尿酸转运蛋白抑制剂,可用于研究高尿酸血症或痛风。 | |||
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。 | |||
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。 | |||
T8567 |
amflutizole
|
Xanthine Oxidase | Metabolism |
amflutizole 用于治疗痛风,是一种黄嘌呤氧化酶抑制剂。 | |||
T0456 |
Cinchophen
2-苯基-4-喹啉羧酸,辛可芬,Cinconal |
COX | Immunology/Inflammation; Neuroscience |
Cinchophen (Cinconal) 是口服具有活性的非甾体抗炎试剂,具有抗菌活性。它可用于研究关节炎和某些肝脏疾病。 | |||
T3994 |
Verinurad
RDEA3170,维立诺雷 |
OAT | Membrane transporter/Ion channel |
Verinurad (RDEA3170) 是一种有效的、特异性的URAT1抑制剂,IC50为 25 nM。 | |||
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。 | |||
T0855 |
(R)-Naproxen
|
COX | Immunology/Inflammation; Neuroscience |
(R)-Naproxen 是一种抗炎剂,具有解热和镇痛作用。酸及其钠盐都用于治疗急性痛风或痛经、肌肉骨骼疾病、类风湿性关节炎和其他风湿病。 | |||
T32194 |
Irtemazole
R60844,R-60844,R 60844 |
Others | Others |
Irtemazole (R 60844) 是一种新型排尿酸物质,在治疗高尿酸血症和痛风方面很有价值。 | |||
T61048 |
Puliginurad
YL-90148 |
OAT | Membrane transporter/Ion channel |
Puliginurad (YL-90148) 是一种具有有效性和选择性的尿酸盐转运蛋白 (URAT) 抑制剂,对尿酸的重吸收有抑制作用。Puliginurad 可用于预防和治疗高尿酸血症和痛风。 | |||
T0435 |
Sulfinpyrazone
(+/-)-Sulfinpyrazone,G-28315,苯磺保泰松,NSC 75925 |
COX | Immunology/Inflammation; Neuroscience |
Sulfinpyrazone (NSC-75925) 是一种口服有效的尿酸剂,具有抗血栓和血小板抑制作用。它可作用于慢性和间歇性痛风性关节炎。 | |||
T6875 |
Lesinurad
RDEA594,雷西那德,来司诺雷 |
OAT | Membrane transporter/Ion channel |
Lesinurad (RDEA594) 是URAT1和OAT 抑制剂。Lesinurad 用作肾转运蛋白OAT1 和OAT3 的底物,Km 分别为 0.85 和 2 μM。 | |||
T77517 |
URAT1 inhibitor 7
|
OAT | Membrane transporter/Ion channel |
URAT1 inhibitor 7 是一种新型高效的人尿酸转运蛋白 URAT1 抑制剂 (IC50:12 nM)。URAT1 inhibitor 7 对 CYP2C9 具有抑制作用,IC50为4.2 μM。URAT1 inhibitor 7 可用于研究高尿酸血症和痛风。 | |||
T21302 |
UNC569
UNC 569 |
TAM Receptor | Tyrosine Kinase/Adaptors |
UNC569 (UNC 569) 是一种ATP 竞争性的、可逆、具有口服活性的Mer 激酶抑制剂,其IC50=2.9 nM,Ki=4.3 nM。它还抑制Axl 和Tyro3,IC50分别为 37 nM 和 48 nM。它可用于研究急性淋巴细胞白血病和非典型畸胎瘤/横纹肌瘤。 | |||
T73695 |
Canakinumab
ACZ 885,Ilaris |
IL Receptor | Immunology/Inflammation |
Canakinumab (ACZ885) 是一种重组人靶向 IL-1β 单克隆抗体。Canakinumab 显示出对人类和绒猴 IL-1β 具有抑制作用, IC50 值为分别为 43.6 和 40.8 pM。Canakinumab 具有抗炎活性,通过中和 IL-1β 信号来抑制与自身免疫性疾病相关的炎症。Canakinumab 可用于治疗痛风和冠状动脉疾病。 | |||
T32905 |
LSPN451
LSPN 451,LSPN-451 |
||
LSPN451 is an effective xanthine oxidase inhibitor and may be used to treat hyperuricemia and gout. | |||
T71808 |
Tisopurine
|
||
Tisopurine is a drug used in the treatment of gout in some countries. It reduces uric acid production through inhibiting an early stage in its production. | |||
T69247 | Febuxostat hemihydrate | ||
Febuxostat hemihydrate is a xanthine oxidase inhibitor used to treat hyperuricemia and chronic gout. | |||
T28279 |
Oxeglitazar
LM-4156,LM 4156,EMD-336340,EMD336340,EMD 336340 |
||
Oxeglitazar, a peroxisome proliferator-activated receptor (PPAR) agonist, is used potentially for the treatment of gout and type two diabetes. | |||
T78195 |
URAT1 inhibitor 8
|
||
URAT1 inhibitor8(示例247),作为一种URAT1抑制剂,具有0.001 μM的半抑制浓度(IC50),可用于痛风研究。 | |||
T13259 | URAT1 inhibitor 1 | OAT | Membrane transporter/Ion channel |
URAT1 inhibitor 1 (1g) is an inhibitor of uric acid transporter 1 (URAT1) (IC50: 32 nM), has the potential to treat hyperuricemia associated with gout. | |||
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. | |||
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. | |||
T60724 | URAT1 inhibitor 3 | ||
URAT1 inhibitor 3 是具有口服活性的URAT1的选择性抑制剂(IC 50 = 0.8 nM)。URAT1 inhibitor 3 显示出降低尿酸的功效,可用于研究痛风和高尿酸血症。 | |||
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。 | |||
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. | |||
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。 | |||
T62825 | URAT1 inhibitor 2 | ||
URAT1 inhibitor 2 是一种口服具有活力的 URAT1 和 CYP isozyme 抑制剂,对 URAT1 介导的 14C-UA 吸收、CYP1A2、CYP2C9 的 IC50 值分别为 1.36 μM、16.97 μM、5.22 μM。URAT1 inhibitor 2 是一种有前途的、能够用于研究高尿酸血症和痛风的候选药物。 | |||
T27275 | Epaminurad | ||
Epaminurad (UR-1102) 是一种口服有效的和选择性的URAT1(尿酸转运体 1) 抑制剂,其Ki 为 0.057 μM。Epaminurad 适度地抑制OAT1和OAT3(有机阴离子转运体)。Epaminurad 是一种促尿酸排泄剂。Epaminurad 可用于痛风和高尿酸血症的研究。 | |||
T11887 | LT052 | Epigenetic Reader Domain | Chromatin/Epigenetic |
LT052 是一种高活性和选择性BET BD1抑制剂,其IC50为 87.7 nM。LT052 表现出纳摩尔级别的 BRD4 BD1 的抑制活性,选择性是 BRD4 BD2 的 138 倍 (IC50=12.130 μM)。LT052 具有抗炎活性,可用于治疗急性痛风性关节炎。 | |||
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。 |
Cat. No. | Product Name | Target | Signaling Pathways |
---|---|---|---|
T3328 |
Angelic Acid
2-Methylisocrotonic acid,(Z)-2-Methylbut-2-enoic acid,当归酸,cis-2-Methyl-2-butenoic acid |
Others | Others |
Angelic Acid ((Z)-2-Methylbut-2-enoic acid) 是一种存在于Anthemis nobilis 精油中的酯,能够促进伤口愈合,具有促进安定和精神药物的作用。 | |||
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。 | |||
T41242 |
Uric acid sodium
|
Reactive Oxygen Species | Immunology/Inflammation; Metabolism; NF-κB |
Uric acid sodium 是氧自由基 (oxygen radical) 的清除剂,是一种有效的、常见的抗氧化剂,有助于维持机体血压稳定和抗氧化应激。Uric acid sodium 能清除活性氧 (ROS),如单线态氧和过氧亚硝酸盐,对脂质过氧化有抑制作用,与痛风性关节病的发病机理和草酸钙结石的形成有关。 | |||
T0256 |
Citric acid trilithium salt tetrahydrate
Lithium citrate tribasic tetrahydrate,柠檬酸三锂盐四水合物,Trilithium citrate tetrahydrate |
Dehydrogenase; GSK-3; HIF/HIF Prolyl-Hydroxylase; Antibacterial; GluR | Chromatin/Epigenetic; Metabolism; Microbiology/Virology; Neuroscience; PI3K/Akt/mTOR signaling; Stem Cells |
Citric acid trilithium salt tetrahydrate (Lithium citrate tribasic tetrahydrate) 是一种用于治疗精神疾病的药物。它也是一种医药和建筑材料, 可用于氨基酸定量分析时的梯度洗脱。 | |||
TN1713 |
Graveobioside A
木犀草素 7-芹糖(1-2)-葡萄糖苷,木犀草素7-芹糖(1-2)-葡萄糖苷 |
Others | Others |
Graveobioside A can be used in hyperuricemia and gout-resistant drugs or health foods. | |||
TWS1613 |
Erioside
桑皮苷B,mulberroside B |
Others | Others |
Erioside (mulberroside B) 存在于Lasiosiphon eriocephalus 中,有镇咳、平喘、降血糖、抗肿瘤、治疗痛风的功效。 | |||
TN5130 |
Tetrahydroamentoflavone
|
COX; Xanthine Oxidase | Immunology/Inflammation; Metabolism; Neuroscience |
Tetrahydroamentoflavone 是一种有效的 XO 抑制剂(IC50 = 92 nM,Ki = 982 nM),具有抗炎作用。Tetrahydroamentoflavone 可用于炎症和痛风的研究。 | |||
T7980 |
Hesperidin methylchalcone
|
NF-κB | NF-κB |
Hesperidin methylchalcone 抑制氧化应激,细胞因子产生和NF-κB 活化。它能够抑制炎症和疼痛,具有血管保护作用。 |