263
59
Cat. No. | Product Name | Target | Signaling Pathways |
---|---|---|---|
T22605 |
Bifemelane hydrochloride
|
MAO; Monoamine Oxidase | Metabolism; Neuroscience |
Bifemelane hydrochloride 是一种选择性的,有效的,和竞争性的单胺氧化酶A (MAO-A)抑制剂,Ki=4.20 μM,它也非竞争性地抑制MAO-B,Ki=46.0 μM。它具有显著的抗抑郁作用,可用于研究与脑血管疾病有关的认知和情绪障碍。 | |||
T0084 |
Moclobemide
吗氯贝胺,Ro111163 |
MAO; Monoamine Oxidase | Metabolism; Neuroscience |
Moclobemide (Ro111163) 是可逆的、可透过血脑屏障的单胺氧化酶 (MAO-A) 抑制剂,能够抑制 hMAO-A (IC50=6.061 μM)。它上调慢性应激小鼠海马祖细胞的增殖。 | |||
T7048 |
1,4-Naphthoquinone
α-Naphthoquinone,Naphthalene-1,4-Dione,P-Naphthoquinone,1,4-萘醌,para-naphthoquinone |
Others; MAO; Topoisomerase | DNA Damage/DNA Repair; Metabolism; Neuroscience; Others |
1,4-Naphthoquinone (P-Naphthoquinone) 被用作单胺氧化酶和 DNA 拓扑异构酶活性的潜在抑制剂,还用于抑制乙酰转移酶活性。 | |||
T6073 |
OG-L002
|
Histone Demethylase; Monoamine Oxidase; HSV | Chromatin/Epigenetic; Microbiology/Virology; Neuroscience |
OG-L002 是一种高度选择性的 LSD1有效抑制剂,IC50为 0.02 μM。它抑制HSV IE 基因的表达,还是单胺氧化酶抑制剂,对 MAO-A 和 MAO-B 的IC50分别为 1.38 μM 和 0.72 μM。 | |||
T0006 |
Methylene Blue trihydrate
碱性亚甲蓝三水合物,Methylthionine chloride,Basic blue 9,亚甲蓝三水合物,Methylene Blue |
Guanylate cyclase; Microtubule Associated; NO Synthase; Parasite; Monoamine Oxidase | Cytoskeletal Signaling; GPCR/G Protein; Immunology/Inflammation; Microbiology/Virology; Neuroscience |
Methylene Blue trihydrate (Basic blue 9) 是鸟苷酸环化酶,单胺氧化酶 A 和 NO 合酶抑制剂。它是血管加压药,在医疗中通常用作染料。它具有抗伤害感受,抗疟疾,抗抑郁和抗焦虑作用,可用于高铁血红蛋白血症,神经退行性疾病和异环磷酰胺引起的脑病的研究。 | |||
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。 | |||
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。 | |||
T67850 |
FCE 28073
|
MAO | Metabolism; Neuroscience |
FCE 28073是一种 Monoamine oxidase B 抑制剂,IC50=0.45 μM。 | |||
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, | |||
T20719 |
Oxadiargyl
RP 020630,RP-020630,RP020630,丙炔恶草酮,Topstar |
Others | Others |
Oxadiargyl (RP020630) 是原卟啉原氧化酶抑制剂,在我国被用作除草剂。 | |||
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。 | |||
T67789 |
Bazinaprine
|
MAO | Metabolism; Neuroscience |
Bazinaprine 是一种选择性的、可逆的单胺氧化酶抑制剂(MAOI),是治疗抑郁症的候选化合物。Bazinaprine 对A 型单胺氧化酶显示出较强的抑制作用,对b 型单胺氧化酶只显示出较弱的抑制作用。Bazinaprine 在体内可逆,但在体外不可逆。 | |||
T38863 |
Luvadaxistat
TAK-831,Luvadaxistat |
||
TAK-831 is a potent and highly selective inhibitor of D-amino acid oxidase (DAAO), offering great potential for utilization in schizophrenia research. | |||
T20622 |
Fomesafen
氟磺胺草醚,PP021,PP-021,PP 021 |
Others | Others |
Fomesafen (PP-021) 是原卟啉原 IX 氧化酶的选择性抑制剂。Fomesafen (PP-021) 用作除草剂,具有低毒性和高选择性的优点。 | |||
T10079 |
MAO-IN-1
|
MAO | Metabolism; Neuroscience |
MAO-IN-1是一种高效的单胺氧化酶B (MAO B)抑制剂(IC50:20 nM),可用于研究神经系统相关疾病。 | |||
T38655 |
Trifludimoxazin
|
Others | Others |
Trifludimoxazin 可用作除草剂,是一种原卟啉原氧化酶的抑制剂。 | |||
T8567 |
amflutizole
|
Xanthine Oxidase | Metabolism |
amflutizole 用于治疗痛风,是一种黄嘌呤氧化酶抑制剂。 | |||
T5206 |
DAAO inhibitor-1
|
Others | Others |
DAAO inhibitor-1是 D-氨基酸氧化酶抑制剂(IC50:0.12 μM)。 | |||
T0821 |
Iproniazid Phosphate
磷酸异丙烟肼,Isoproniazid phosphate |
MAO; Monoamine Oxidase | Metabolism; Neuroscience |
Iproniazid Phosphate 是一种非选择性的,不可逆的单胺氧化酶抑制剂,具有抗抑郁作用。 | |||
T5053 |
Eprobemide
LIS 630,依普贝胺 |
MAO; Monoamine Oxidase | Metabolism; Neuroscience |
Eprobemide (LIS 630) 是一种非竞争性的、可逆的单胺氧化酶 A 抑制剂。 | |||
T0300 |
Pargyline
Pargylamine,Paragyline,优降宁 |
MAO; Monoamine Oxidase | Metabolism; Neuroscience |
Pargyline (Pargylamine) 是不可逆的单胺氧化酶抑制剂,对MAO-A 和MAO-B 的Ki 分别为 13 μM 和 0.5 μM,具有降压和抗癌作用。 | |||
T5323 |
Toloxatone
托洛沙酮,MD 69276 |
MAO; Monoamine Oxidase | Metabolism; Neuroscience |
Toloxatone (MD 69276) 是可逆的单胺氧化酶 A (MAOA) 抑制剂,是一种抗抑郁剂。 | |||
T39280 |
Nitrofen
|
Others | Others |
Nitrofen 是选择性接触除草剂,也是视原卟啉原氧化酶和网膜脱氢酶抑制剂。 | |||
T6099 |
Setanaxib
GKT137831 |
NADPH-oxidase; Ferroptosis; NADPH | Apoptosis; Immunology/Inflammation; Metabolism |
Setanaxib (GKT137831) 是一种有效的特异性双重 NADPH 氧化酶 (NOX1/4) 抑制剂,Ki 分别为140和110nM。 | |||
T1117 |
Clorgyline hydrochloride
盐酸氯吉林,Clorgiline hydrochloride,N-[3-(2,4-二氯苯氧基)丙基]-N-甲基-2-丙炔胺盐酸盐 |
MAO; Monoamine Oxidase | Metabolism; Neuroscience |
Clorgyline hydrochloride (Clorgiline hydrochloride) 是一种选择性、不可逆的单胺氧化酶A 抑制剂,结构上与Pargyline 相关。 | |||
T15023 |
CX-157
KP 157 |
MAO | Metabolism; Neuroscience |
CX-157 (KP 157) 是一种新型单胺氧化酶-A(MAO-A)抑制剂,可用于研究抑郁症类的神经系统疾病和癌症。 | |||
T77564 |
Coumarin102
Exciton 480 |
||
Coumarin102 (Exciton 480)是一种荧光染料。Coumarin102对Monoamine oxidase B、MAO-B和MAO-A具有较弱的抑制活性,可用来研究神经系统疾病。 | |||
T16803 |
RS 8359
|
MAO | Metabolism; Neuroscience |
RS 8359 是单胺氧化酶 A (MAO-A) 的可逆抑制剂,对 A:B 酶类型的特异性比约为 2200。 RS 8359 具有抗抑郁活性。 | |||
T0358 |
Aminoguanidine hydrochloride
Imino semicarbazide,Pimagedine hydrochloride,CP-12009-18 tartrate,Hydrazinecarboximidamide,肼甲酰亚胺酰胺一氯化氢(氨基胍盐酸盐),氨基胍盐酸盐,Guanyl hydrazine,Pimagedine |
NOS; NO Synthase | Immunology/Inflammation |
Aminoguanidine hydrochloride (Hydrazinecarboximidamide) 是二胺氧化酶抑制剂,也是一氧化氮合酶抑制剂,可用于糖尿病肾病的研究。 | |||
T24444 |
Medifoxamine
LG 152,Medifoxamina,LG-152,LG152 |
Dopamine Receptor; Monoamine Oxidase | GPCR/G Protein; Neuroscience |
Medifoxamine (LG 152) 是一种选择性非单胺氧化酶抑制剂,通过对5 HT 再摄取的抑制展现其抗抑郁活性。Medifoxamine 优先抑制多巴胺再摄取 (dopamine reuptake)。 | |||
T24680 |
PSB-1491
|
MAO | Metabolism; Neuroscience |
PSB-1491 是一种选择性和竞争性的单胺氧化酶 B 抑制剂,IC50 为 0.386 nM,是 MAO-A 的 25000 倍以上。 | |||
T4559 |
Isocarboxazid
|
Monoamine Oxidase | Neuroscience |
Isocarboxazid 是不可逆的、非选择性的单胺氧化酶 monoamine oxidase 抑制剂,其在大鼠大脑中测得的 IC50值为4.8 μM。 | |||
T22965 |
MDL 72527
N1,N4-Di(buta-2,3-dien-1-yl)butane-1,4-diamine dihydrochloride |
Others | Others |
MDL 72527 (N1,N4-Di(buta-2,3-dien-1-yl)butane-1,4-diamine dihydrochloride) 是一种多胺氧化酶 (POA) 抑制剂 | |||
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。 | |||
T12441 |
Phenelzine sulfate
硫酸苯乙肼,苯肼,硫酸盐 |
Monoamine Oxidase | Neuroscience |
Phenelzine sulfate 是一种非选择性的、不可逆的单胺氧化酶抑制剂 (MAOI),可用作抗抑郁药和抗焦虑药。 | |||
T8124 |
Sodium benzoate
Benzoic acid sodium salt,苯甲酸钠 |
Others | Others |
Sodium benzoate (Benzoic acid sodium salt) 是一种 D-氨基酸氧化酶抑制剂。它是一种食品防腐剂。 | |||
T24679 |
PSB-1434
PSB 1434,PSB1434 |
MAO | Metabolism; Neuroscience |
PSB-1434 是一种选择性和竞争性的单胺氧化酶 B 抑制剂,IC50 为 1.59 nM,相对于 MAO-A 的选择性>6000 倍。 | |||
T1025 |
Tranylcypromine (2-PCPA) hydrochloride
反苯环丙胺盐酸盐,Tranylcypromine (2-PCPA) HCl,SKF-385 HCl |
Histone Demethylase; MAO | Chromatin/Epigenetic; Metabolism; Neuroscience |
Tranylcypromine (2-PCPA) hydrochloride (SKF-385 HCl) 是一种单胺氧化酶抑制剂,对治疗重度抑郁症、心境恶劣障碍和非典型抑郁症有效。 | |||
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。 | |||
T0948 |
Adrenalone hydrochloride
Adrenalone HCl,肾上腺酮盐酸盐,盐酸肾上腺酮 |
Adrenergic Receptor | GPCR/G Protein; Neuroscience |
Adrenalone hydrochloride (Adrenalone HCl) 是一种多巴胺β氧化酶 (dopamine β oxidase) 抑制剂,结构与去甲肾上腺素转运蛋白 (NET) 配体相似,IC50=36.9 μM。它是一种肾上腺素能 (adrenergic) 激动剂,用作局部血管收缩剂和止血剂。 | |||
T1578 |
Pargyline hydrochloride
优降宁盐酸盐,Pargylamine hydrochloride |
MAO; Monoamine Oxidase | Metabolism; Neuroscience |
Pargyline hydrochloride (Pargylamine hydrochloride) 是不可逆的单胺氧化酶抑制剂,可作用于 MAO-A (Ki=13 μM) 和 MAO-B (Ki=0.5 μM) ,具有降压和抗癌作用。 | |||
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。 | |||
T83625 |
iNOS-IN-14
3-bromo-1H-indazole-7-carbonitrile |
NOS | Immunology/Inflammation |
iNOS-IN-14 (3-bromo-1H-indazole-7-carbonitrile) 是一种有效的一氧化氮合酶(NOS)抑制剂,抑制nNOS的NADPH氧化酶活性。 | |||
T77615 |
ND-011992
ND011992 |
Mitochondrial Metabolism; Antibacterial | Metabolism; Microbiology/Virology |
ND-011992 是一种靶向醌还原酶 (quinone reductases) 和醌氧化酶 (quinol oxidases)的喹唑啉类抑制剂,具有可逆性和选择性。ND-011992 对大肠杆菌 BL21*Δcyo 呼吸复合体I (respiratory complex I) 、 bo3 氧化酶(bo3 oxidase)、 bd-I 氧化酶 (bd-I oxidases) 和 bd-II 氧化酶 (bd-II oxidases)具有抑制作用,IC50 分别为 0.12、2.47、0.63 和 1.3 μM。ND-011992 可以用于研究肺结核。 | |||
T29097 |
VAS 3947
VA-S3947,VA S3947,VAS3947 |
Apoptosis; NADPH-oxidase | Apoptosis; Immunology/Inflammation |
VAS 3947 是一种特异的 NADPH 氧化酶 (NOX) 抑制剂。VAS 3947具有强大的抗血小板作用, 通过 UPR 激活,主要由于蛋白质聚集和错误折叠,独立于抗 NOX 活性诱导细胞凋亡。 | |||
T0235 |
Modaline sulfate
|
MAO; Monoamine Oxidase | Metabolism; Neuroscience |
Modaline sulfate 是一种 MAO 抑制剂,用于研究抑郁症。 | |||
T7942 |
Tranylcypromine hemisulfate
Tranylcypromine Sulfate,Tranylcypromine (hemisulfate),反苯环丙胺半硫酸盐 |
Histone Demethylase; MAO; Monoamine Oxidase | Chromatin/Epigenetic; Metabolism; Neuroscience |
Tranylcypromine hemisulfate (Tranylcypromine Sulfate) 是单胺氧化酶(MAO) 和赖氨酸特异性去甲基化酶 1 (LSD1) 的抑制剂,可用于研究抑郁症和子宫内膜异位症。 | |||
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。 | |||
T19533 |
Pyraclonil
|
Others | Others |
Pyraclonil 作为一种除草剂,有效地控制了敏感型(S)和多重抗药性(MHR)E. indica群体。Pyraclonil 作为丙啶类光 敏色素原氧化酶(PPO)抑制剂发挥作用。 |
Cat. No. | Product Name | Target | Signaling Pathways |
---|---|---|---|
TN2004 |
Obtusin
1,7-二羟基-2,3,8-三甲氧基-6-甲基蒽-9,10-二酮,决明素 |
MAO; Monoamine Oxidase | Metabolism; Neuroscience |
Obtusin 是来自决明子种子,是一种高度选择性和竞争性的人单胺氧化酶-A 抑制剂,IC50=11.12 μM,Ki=6.15 μM。它在神经退行性疾病,尤其是焦虑和抑郁中起预防作用。 | |||
T3885 |
ROSIRIDIN
6'-O-Deacetylrosiridoside C,络塞定,(-)-Rosiridin |
Others; Monoamine Oxidase | Neuroscience; Others |
Rosiridin (6'-O-Deacetylrosiridoside C) 能够抑制 MAO A 和 MAO B,有潜在的抑郁症和老年性痴呆作用。它在 10 μM 时对 MAO B 的抑制率为 83.8% (pIC50=5.38)。 | |||
TN7211 |
Tetrahydroharmine
Leptaflorine |
MAO | Metabolism; Neuroscience |
Tetrahydroharmine (Leptaflorine) 是一种天然产物,存在于植物Banisteriopsis caapi cultivar Da Vine 的茎和枝中。四氢骆驼蓬碱是一种Monoamine oxidase A 抑制剂。 | |||
Fr12415 |
Ethyl 4-hydroxyphenylacetate
|
Others | Others |
Ethyl 4-hydroxyphenylacetate 是单胺氧化酶 A 的选择性抑制剂。 | |||
T13475 |
β-Aminopropionitrile
3-氨基丙腈,3-Aminopropionitrile,BAPN |
Others; Endogenous Metabolite | Metabolism; Others |
β-Aminopropionitrile (3-Aminopropionitrile) 是赖氨酰氧化酶的特异性抑制剂。 | |||
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。 | |||
T6391 |
Apocynin
香草乙酮,Acetovanillone,Acetoguaiacone,NSC 2146,罗布麻宁 |
Apoptosis; NADPH; Autophagy | Apoptosis; Autophagy; Metabolism |
Apocynin (NSC 2146) 是一种选择性NADPH-氧化酶抑制剂,IC50为10 μM。 | |||
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。 | |||
TN1705 |
Glycyrrhisoflavone
|
MAO; Tyrosinase; NO Synthase; Immunology/Inflammation related | Immunology/Inflammation; Metabolism; Neuroscience; Proteases/Proteasome |
Glycyrrhisoflavone 是一种具有抗炎作用的酪氨酸酶抑制剂。 Glycyrrhisoflavone 抑制 α-葡萄糖苷酶和单胺氧化酶。 | |||
TQ0188 |
Miquelianin
槲皮素-3-O-葡萄糖醛酸苷,Quercetin 3-glucuronide,Quercetin 3-O-glucuronide |
stilbene oxidase; Endogenous Metabolite | Metabolism |
Miquelianin (Quercetin 3-glucuronide) 是槲皮素的代谢产物,属于类黄酮化合物。 | |||
T4716 |
Pyrrole-2-carboxylic acid
吡咯-2-羧酸,2-Pyrrolecarboxylic acid,Minaline |
Endogenous Metabolite | Metabolism |
Pyrrole-2-carboxylic acid (Minaline) 是一种天然生物碱类,从海洋细菌Pelomonas puraquaesp. Nov 中分离得到。 | |||
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。 | |||
T3740 |
Isovanillin
3-羟基-4-甲氧基苯甲醛,3-Hydroxy-p-anisaldehyde,3-Hydroxy-4-methoxybenzaldehyde,5-Formylguaiacol |
Others | Others |
Isovanillin (5-Formylguaiacol) 是一种醛氧化酶抑制剂,具有解痉挛和止泻活性。 | |||
T21164 |
Sulfentrazone
甲磺草胺,FP-846 |
Others | Others |
Sulfentrazone (FP-846) 是苯基三唑啉酮除草剂,能够抑制原卟啉原氧化酶,导致脂质细胞膜破裂,可用于控制某些阔叶和禾本科杂草。 | |||
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)。 | |||
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。 | |||
T3158 |
Harmane
Loturine,Harman,Aribine,哈尔满碱 |
Adrenergic Receptor; Monoamine Oxidase; Imidazoline Receptor | GPCR/G Protein; Neuroscience |
Harmane (Loturine) 是一种在咖啡和烟草烟雾中发现的 β-咔啉生物碱,是有效的神经毒素,可引起严重的动作震颤和精神病学表现。它还是选择性的单胺氧化酶抑制剂,具有致突变作用,对 MAO A/B 的 IC50值分别为 0.5 和 5 μM。 | |||
T4455 |
DL-3-Phenyllactic acid
DL-3-苯乳酸,3-Phenyllactic acid,2-Hydroxy-3-phenylpropanoic acid |
Others; Endogenous Metabolite; Antibacterial | Metabolism; Microbiology/Virology; Others |
DL-3-Phenyllactic acid (3-Phenyllactic acid) 是广谱抗菌化合物,对细菌和真菌具有活性。 | |||
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。 | |||
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。 | |||
T10938 |
D-Kynurenine
D-尿嘧啶,(R)-2-Amino-4-(2-aminophenyl)-4-oxobutanoic acid,ZINC901103 |
GPR; AhR; Endogenous Metabolite | Endocrinology/Hormones; GPCR/G Protein; Immunology/Inflammation; Metabolism |
D-Kynurenine (ZINC901103) 是 D-色氨酸的代谢物和 GPR109B 的激动剂。 D-Kynurenine 激活 AhR 并促进上皮细胞向间充质的转化。 D-Kynurenine 在 D-氨基酸氧化酶的荧光分析中用作底物。 | |||
TN1120 |
Osthenol
|
MAO; Monoamine Oxidase | Metabolism; Neuroscience |
Osthenol 是一种前酰化香豆素,从独活干根中分离得到。它对重组 hMAO-A 具有潜在的选择性抑制作用,IC50=0.74 µM,对 hMAO-A 和 hMAO-B 表现出较高的选择性指数。它是一种可逆的,选择性的竞争性人单胺氧化酶-A(hMAO-A)抑制剂 (Ki=0.26 µM)。 | |||
T3095 |
Tyramine
4-hydroxyphenethylamine,酪胺,para-tyramine,p-Tyramine,mydrial,Tocosine,Uteramine |
MAO; Endogenous Metabolite | Metabolism; Neuroscience |
Tyramine (Uteramine) 是天然存在于体内或某些食物中的氨基酸。Tyramine 有助于调节血压。 | |||
T3933 |
Jatrorrhizine
Yatrorizine,neprotin,药根碱 |
MAO; 5-HT Receptor; Antibacterial; AChE | GPCR/G Protein; Metabolism; Microbiology/Virology; Neuroscience |
Jatrorrhizine (neprotin) 是一种从黄连中分离得到的生物碱,具有抗菌、抗氧化、抗疟原虫和神经保护活性。它通过抑制 uptake-2 transporter 的活性减少血清素和去甲肾上腺素的摄取。它是一种有口服活性的乙酰胆碱酯酶制剂。 | |||
TN1470 |
Cassiaside B2
决明子苷B2 |
Phosphatase; MAO; 5-HT Receptor | GPCR/G Protein; Metabolism; Neuroscience |
Cassiaside B2 是蛋白酪氨酸磷酸酶1B (PTP1B) 和人单胺氧化酶A (hMAO-A) 的抑制剂。Cassiaside B2是 5-HT2C 受体的激动剂, 具有抗过敏活性。Cassiaside B2 是萘吡喃酮参比提取物(NRE)的有效成分之一。 | |||
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。 | |||
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。 | |||
T10933 |
D-Cysteine
|
Endogenous Metabolite; Antibacterial | Metabolism; Microbiology/Virology |
D-Cysteine 是一种大肠杆菌生长的有力抑制剂,是半胱氨酸的 D 型异构体。它由 D-氨基酸氧化酶介导产生 H2S,是一种对抗小脑共济失调的神经保护剂。 D-半胱氨酸可以抑制由变形链球菌和链球菌血红蛋白形成的两种生物膜的生长和致龋性。 | |||
T5S2343 |
Acetylshikonin
乙酰紫草素,Acetyl shikonin |
Others; P450; AChE | Metabolism; Neuroscience; Others |
Acetylshikonin 来源于紫草根,具有抗癌、抗炎作用。它是一种 AChE 抑制剂,具有很强的抗凋亡活性。它是一种非选择性的细胞色素 P450抑制剂,对所有 P450 亚型抑制的 IC50值范围为 1.4-4.0 μM。 | |||
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。 | |||
T19117 |
3-Deoxyglucosone
3-Deoxy-D-glucosone,2-keto-3-Deoxyglucose |
GPX; Glucagon Receptor | GPCR/G Protein; oxidation-reduction |
3-Deoxyglucosone(3-Deoxy-D-glucosone) 是美拉德反应和多元醇反应的中间体途径合成。3-Deoxyglucosone 与蛋白质氨基快速反应形成晚期糖基化末端蛋白 (AGEs)。3-Deoxyglucosone 可使谷胱甘肽过氧化物酶失活,可与低葡萄糖协同作用以增强 GLP-1 分泌,可以作为糖尿病生物学检测的标志物。 | |||
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。 | |||
T4848 |
Mandelic acid
acidomandelico,DL-Mandelic acid,扁桃酸 |
Others; Endogenous Metabolite; Antibacterial | Metabolism; Microbiology/Virology; Others |
DL-Mandelic acid (acidomandelico) 是一种 α-羟基羧酸,有抗菌活性,广泛用作医药和精细化学品的中间体,已用于研究尿路感染和阴道滴虫病,还具有较高的精子固定活性和较低的阴道刺激性。 | |||
T1311 |
4-aminobenzoic acid
PABA,Vitamin H1,Vitamin Bx,para-Aminobenzoic acid,对氨基苯甲酸 |
Endogenous Metabolite | Metabolism |
4-aminobenzoic acid (para-Aminobenzoic acid) 是一种具有紫外线吸收和抗纤维化特性的有机酸。当暴露在光线下时,4-aminobenzoic acid 吸收紫外线并通过光化学反应释放多余的能量,这可能会对DNA造成损害。4-aminobenzoic acid 还可以增加组织水平的摄氧量,并可能增强单胺氧化酶(MAO)活性以促进血清素的降解,过量可能导致纤维化变化。 | |||
T4827 |
Trimethylammonium chloride
三甲胺盐酸盐,Trimethylamine hydrochloride |
Others; Endogenous Metabolite | Metabolism; Others |
Trimethylammonium chloride (Trimethylamine hydrochloride) 是动植物分解的产物。它是造成鱼腥味的主要物质,通常与脏鱼、细菌性阴道感染和口臭有关。它也与服用大剂量胆碱有关。三甲胺尿是一种遗传性疾病,身体无法从食物中代谢三甲胺。食用富含胆碱的食物后,患者的汗液、尿液和呼吸中会出现特有的鱼腥味。三甲胺尿症是一种常染色体隐性遗传病,涉及三甲胺氧化酶缺乏症。三甲氨基尿症在罗德岛红鸡中也有发现,这种鸡产的蛋有腥味。尿液中的 Trimethylammonium chloride 是食用豆类的生物标志物。 | |||
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. | |||
TN5670 | Protosappanin A dimethyl acetal | ||
Protosappanin A dimethyl acetal shows significant xanthine oxidase inhibitory activity in a concentration-dependent manner. | |||
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. | |||
T36950 |
Rubrofusarin triglucoside
|
||
Rubrofusarin triglucoside is a glycoside compound isolated from Cassia obtusifolia Linn seeds. Rubrofusarin triglucoside inhibits human monoamine oxidase A (hMAO-A) with an IC50 of 85.5 μM[1]. [1]. Pradeep Paudel, et al. Rubrofusarin as a Dual Protein Tyrosine Phosphate 1B and Human Monoamine Oxidase-A Inhibitor: An in Vitro and in Silico Study. ACS Omega. 2019 Jul 3;4(7):11621-11630. | |||
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. | |||
T40244 |
Methyl citrate
|
||
Methyl citrate, obtained from Opuntia ficus-indica var. saboten Makino fruits, serves as a potent Monoamine oxidase B (MAO-B) inhibitor with an IC50 value of 0.23 mM. | |||
TN2790 |
2'-O-Methylperlatolic acid
|
MAO | Metabolism; Neuroscience |
2'-O-Methylperlatolic acid and confluentic acid are monoamine oxidase B inhibitors in a Brazilian plant, Himatanthus sucuuba. | |||
TN4137 | Glicoricone | MAO | Metabolism; Neuroscience |
Glicoricone acts as a partial estrogen antagonist. Glicoricone inhibited the monoamine oxidase with the IC50 values of 6.0 x 10(-5)-1.4 x 10(-4) M. | |||
T32208 |
Isogentisin
BRN 0258402,BRN-0258402,BRN0258402 |
MAO | Metabolism; Neuroscience |
Isogentisin (BRN 0258402) 是一种从龙胆科植物中分离出来的化合物,是一种用于预防吸烟引起的内皮损伤的新型化合物。Isogentisin 对单胺氧化酶具有抑制作用。 | |||
TN3116 |
5-Hydroxy-1-methoxyxanthone
|
MAO; Antifection | Metabolism; Microbiology/Virology; Neuroscience |
5-Hydroxy-1-methoxyxanthone, 1,5-dihydroxyxanthone and 6-deoxyjacareubin are all antifungal against Cladosporium cucumerinum, while they show differing degrees of inhibition of monoamine oxidase A and B. | |||
T40576 |
(S)-Salsolidine
|
||
(S)-Salsolidine, a chemical compound, functions as a weak inhibitor of monoamine oxidase (MAO), exhibiting an inhibition constant (K i ) of 63 μM. R enantiomer demonstrating a greater efficacy than (S)-Salsolidine, boasting a K i value of 26 μM compared to the S form. | |||
TN3726 | Cudraflavone B | IκB/IKK; MAO; ROS; Akt; COX; PI3K; Nrf2; Autophagy | Autophagy; Cytoskeletal Signaling; Immunology/Inflammation; Metabolism; Neuroscience; NF-κB; PI3K/Akt/mTOR signaling |
Cudraflavone B has anti-proliferative activity, mouse brain monoamine oxidase (MAO) inhibitory effects, apoptotic actions in human gastric carcinoma cells and mouse melanoma cells, and hepatoprotective activity. It may be a lead for the development of a potential candidate for human oral squamous cell carcinoma cells. | |||
TN2039 | Panaxydol | cAMP; p38 MAPK; JNK | GPCR/G Protein; MAPK |
Panaxydol has anti-cancer activity, can inhibit the growth and apoptosis of cancer cells, the signaling mechanisms involve a [Ca(2+)](i) increase, JNK and p38 MAPK activation, cAMP, MAP kinase and ROS generation through NADPH oxidase and mitochondria. | |||
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. | |||
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