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36

抑制剂 & 化合物

8

天然产物

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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。

化合物

Allopurinol
Cat.No: T0692
Synonym: Zyloric,别嘌醇,Zyloprim,Lopurin,别嘌呤醇
Target: ROS, Xanthine Oxidase
Allopurinol Sodium
Cat.No: T6376
Synonym: 1H-吡唑并[3,4-D]嘧啶-4-醇单钠盐,Allopurinol sodium salt,Sodium allopurinol
Target: ROS
Febuxostat
Cat.No: T0773
Synonym: 非布索坦,TMX 67,非布司他,TEI 6720
Target: ROS, Xanthine Oxidase
Agouti-related Protein (AGRP) (25-82), human
Cat.No: TP2215
Synonym:
Target: Others
Agouti-related Protein (AGRP) (83-132) Amide (human)
Cat.No: T76301
Synonym:
Target:
Lingdolinurad
Cat.No: T79854
Synonym:
Target: OAT
Deoxybenzoin
Cat.No: T20347
Synonym: 二苯基乙酮,2-Phenylacetophenone,Benzyl phenyl ketone,NSC-131456,NSC131456,NSC 131456
Target: Others
Topiroxostat
Cat.No: T2397
Synonym: 托匹司他,FYX-051
Target: P450, ROS, Xanthine Oxidase
amflutizole
Cat.No: T8567
Synonym:
Target: Xanthine Oxidase
Cinchophen
Cat.No: T0456
Synonym: 2-苯基-4-喹啉羧酸,辛可芬,Cinconal
Target: COX
Verinurad
Cat.No: T3994
Synonym: RDEA3170,维立诺雷
Target: OAT
Xanthine oxidase-IN-10
Cat.No: T78984
Synonym: XO8 analog
Target: ROS
(R)-Naproxen
Cat.No: T0855
Synonym:
Target: COX
Irtemazole
Cat.No: T32194
Synonym: R60844,R-60844,R 60844
Target: Others
Puliginurad
Cat.No: T61048
Synonym: YL-90148
Target: OAT
Sulfinpyrazone
Cat.No: T0435
Synonym: (+/-)-Sulfinpyrazone,G-28315,苯磺保泰松,NSC 75925
Target: COX
Lesinurad
Cat.No: T6875
Synonym: RDEA594,雷西那德,来司诺雷
Target: OAT
URAT1 inhibitor 7
Cat.No: T77517
Synonym:
Target: OAT
UNC569
Cat.No: T21302
Synonym: UNC 569
Target: TAM Receptor
Canakinumab
Cat.No: T73695
Synonym: ACZ 885,Ilaris
Target: IL Receptor
LSPN451
Cat.No: T32905
Synonym: LSPN 451,LSPN-451
Target:
Tisopurine
Cat.No: T71808
Synonym:
Target:
Febuxostat hemihydrate
Cat.No: T69247
Synonym:
Target:
Oxeglitazar
Cat.No: T28279
Synonym: LM-4156,LM 4156,EMD-336340,EMD336340,EMD 336340
Target:
URAT1 inhibitor 8
Cat.No: T78195
Synonym:
Target:
URAT1 inhibitor 1
Cat.No: T13259
Synonym:
Target: OAT
Febuxostat 67M-4
Cat.No: T69281
Synonym:
Target:
Febuxostat 67M-1
Cat.No: T68437
Synonym:
Target:
URAT1 inhibitor 3
Cat.No: T60724
Synonym:
Target:
Febuxostat sodium
Cat.No: T61060
Synonym:
Target:
Febuxostat 67M-2
Cat.No: T69282
Synonym:
Target:
Xanthine oxidase-IN-7
Cat.No: T60626
Synonym:
Target:
URAT1 inhibitor 2
Cat.No: T62825
Synonym:
Target:
Epaminurad
Cat.No: T27275
Synonym:
Target:
LT052
Cat.No: T11887
Synonym:
Target: Epigenetic Reader Domain
Xanthine oxidase-IN-4
Cat.No: T60632
Synonym:
Target:
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。

天然产物

Angelic Acid
Cat.No: T3328
Synonym: 2-Methylisocrotonic acid,(Z)-2-Methylbut-2-enoic acid,当归酸,cis-2-Methyl-2-butenoic acid
Target: Others
Purine
Cat.No: T4746
Synonym: 7H-Imidazo(4,5-d)pyrimidine,嘌呤
Target: Others, Endogenous Metabolite
Uric acid sodium
Cat.No: T41242
Synonym:
Target: Reactive Oxygen Species
Citric acid trilithium salt tetrahydrate
Cat.No: T0256
Synonym: Lithium citrate tribasic tetrahydrate,柠檬酸三锂盐四水合物,Trilithium citrate tetrahydrate
Target: Dehydrogenase, GSK-3, HIF/HIF Prolyl-Hydroxylase, Antibacterial, GluR
Graveobioside A
Cat.No: TN1713
Synonym: 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
Target: Others
Erioside
Cat.No: TWS1613
Synonym: 桑皮苷B,mulberroside B
Target: Others
Tetrahydroamentoflavone
Cat.No: TN5130
Synonym:
Target: COX, Xanthine Oxidase
Hesperidin methylchalcone
Cat.No: T7980
Synonym:
Target: NF-κB
TargetMol Loading
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