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39

抑制剂 & 化合物

21

天然产物

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Cat. No. Product Name Target Signaling Pathways
T78887 ROS-IN-2

Reactive Oxygen Species Immunology/Inflammation; Metabolism; NF-κB
ROS-IN-2 (compound 85) 为次狼烷三萜衍生物,具有抑制细胞内过量ROS及其他氧化应激源生成的作用,从而保护线粒体避免受损。该化合物在心肌缺血/再灌注(MI/R)损伤研究中具有潜在应用价值。
T74671 ROS kinases-IN-2

ROS Kinase Tyrosine Kinase/Adaptors
ROS kinases-IN-2 是一种有效的 ROS kinase 抑制剂,在 10 μM 时测得抑制率为 21.53%。ROS kinases-IN-2 具有潜在的抗癌活性,可用于研究异常细胞生长。
T9560 MAO-B-IN-2

MAO-B-IN-2 是一种选择性和竞争性的MAO-B 和 BChE 抑制剂,其IC50值分别为 0.51 和 7.00 μM。MAO-B-IN-2 通过良好的 ROS 清除特性减轻 H2O2 诱导的细胞损伤。
T38404 MJ33 lithium salt

ROS Immunology/Inflammation
MJ33 lithium salt 是 NADPH 氧化酶 2 型介导的 ROS 生成抑制剂,是一种氟化磷脂类似物,可抑制过氧化物还蛋白 6 (Prdx6) 的磷脂酶 A2 (PLA2) 活性,可用于研究急性肺损伤。
T15433 GSK2795039

Apoptosis; Reactive Oxygen Species; ROS; NADPH Apoptosis; Immunology/Inflammation; Metabolism; NF-κB
GSK2795039 是一种 NADPH 氧化酶 2 抑制剂,可抑制活性氧产生和 NADPH 消耗,同时可减少细胞凋亡。
T14021 20-HETE

20-hydroxy Arachidonic Acid

Others Others
20-HETE (20-hydroxy Arachidonic Acid) is a CYP450 metabolite and a potent vasoconstrictor and it is an endogenous inhibitor of the large-conductance Ca2+-activated K+ channel in renal arterioles. 20-HETE increases NADPH oxidase, ROS, and NF-κB activity, a
T77579 JC2-11

IL Receptor; Dehydrogenase; ROS; Caspase; NOD-like Receptor (NLR); AIM2 Apoptosis; Immunology/Inflammation; Metabolism; Proteases/Proteasome
JC2-11 是一种对炎症有抑制作用的化合物。JC2-11 对含有募集结构域的蛋白质 NLRC 4、黑色素瘤 2 中缺失 (AIM 2) 和非典型 (NC) 炎症小体有抑制作用,通过破坏活性氧的产生和 caspase-1 的活性来抑制炎症小体的活化。JC2-11 减少了炎症小体中 caspase-1 (p20) 的分泌、gasdermin D (GSDMD) 的裂解、IL-1β 和乳酸脱氢酶 (LDH) 的释放。
T40723 Bromoiodoacetamide

Bromoiodoacetamide, an iodinated haloacetamide (I-HAcAm) compound, exhibits cytotoxic properties. Its mechanism of action involves the accumulation of reactive oxygen species (ROS) and induction of apoptosis in HepG-2 cells.
T60340 ROS 234

ROS 234 is a highly effective H3 antagonist, demonstrating a strong binding affinity (pK B) of 9.46 for the Guinea-pig ileum H3 receptor and a pKi of 8.90 for the Rat cerebral cortex H3 receptor. Additionally, it exhibits an ex vivo ED50 of 19.12 mg/kg (ip) in the Rat cerebral cortex. It should be noted that ROS 234 demonstrates limited central access, as reported in [1] and [2].
T79584 AChE-IN-37

AChE-IN-37,一种乙酰胆碱酯酶抑制剂,具有0.23 μM的IC50值,调节ROS水平及NRF2基因表达。
T36514 QD-394

QD-394 is an inducer of reactive oxygen species (ROS) production.1It induces lipid peroxidation, increases in intracellular accumulation of reactive oxygen species (ROS), and decreases in the reduced glutathione (GSH) to oxidized GSH (GSSG) ratio in MIA PaCa-2 pancreatic cancer cells when used at concentrations ranging from 0.5 to 10 μM. QD-394 is cytotoxic to MIA PaCa-2, PANC-1, and BxPC-3 cancer cells (IC50s = 0.64, 0.34, and 0.9 μM, respectively). QD-394 acts synergistically with napabucasin ...
T79517 ROS inducer 2

Reactive Oxygen Species Immunology/Inflammation; Metabolism; NF-κB
ROS inducer 2 (Compound I16) 是一种经体外测试显示具有良好活性的活性氧诱导剂,其EC50值为3.43 μg/mL。在体内实验中,该化合物对Xanthomonas axonopodis pv. citri表现出优异的生物活性,可以作为研究难治性植物细菌性疾病的杀菌剂。
T39754 HKPerox-2

HKPerox-2 is an excellently selective and sensitive green fluorescent probe toward H 2 O 2 over 30-fold other tested ROS/RNS in chemical and biological systems. HKPerox-2 is a O-methyl rhodol derivative and specifically recognize H 2 O 2 based on a tandem payne/dakin reaction.
T78892 Glutaminase C-IN-2

Glutaminase Proteases/Proteasome
GlutaminaseC-IN-2(compound 11)为GAC变构抑制剂,IC50值为10.64 nM。该化合物通过干扰谷氨酰胺代谢,调控细胞代谢产物,进而提高ROS水平,并展现出抗癌活性。
T79362 COX-2/15-LOX-IN-4

Lipoxygenase Metabolism
COX-2/15-LOX-IN-4(compound 5i)是一种针对COX-2和15-LOX的双重抑制剂,其IC50值分别为0.075 μM和1.97 μM。该化合物能有效地阻止LPS诱发的细胞内促炎细胞因子(IL-6, ROS)的产生,表现出明确的抗炎活性。
T60517 CL097 hydrochloride

CL097 hydrochloride 是一种有效的 TLR7和 TLR8激动剂。CL097 hydrochloride 可在巨噬细胞中诱导促炎细胞因子和 NADPH 氧化酶启动活性,从而增加 fMLF 刺激的ROS 产生。
T81647 NOX2-IN-2

NOX2-IN-2(化合物33)作为一种高效的NOX2抑制剂,其作用机制是针对p47phox-p22phox的蛋白-蛋白相互作用,具有0.24 μM的Ki值。该化合物能够抑制NOX2在细胞内产生的ROS
T79251 AChE-IN-30

AChE-IN-30,一种AChE抑制剂,其IC50为4.4 μM。该化合物显示出神经保护活性,能抑制H2O2诱导的细胞凋亡(apoptosis),其机制是通过阻止细胞内ROS的积累。AChE-IN-30适用于阿尔茨海默病的相关研究。
T79260 MCI

Reactive Oxygen Species Immunology/Inflammation; Metabolism; NF-κB
MCI具有针对性地清除活性氧(ROS)并降低环氧合酶-2(COX-2)表达的功能,COX-2的IC50值为1.23μM。在胶原诱导的关节炎(CIA)模型中展现出的抗炎效果明显,适用于类风湿性关节炎(RA)的研究。
T63995 BuChE-IN-2

BuChE-IN-2 是一种优良的丁基胆碱酯酶(BuChE) 抑制剂,能够作用于 BuChE (IC50: 1.28 μM) 和 NO (IC50: 0.67 μM)。BuChE-IN-2 能够抑制 Aβ 的聚集、ROS 的形成和螯合 Cu2+,表现出适当的血脑屏障 (BBB) 穿透性,能够用于阿尔茨海默病的研究。
T79179 GLX481304

GLX481304是一种针对Nox-2和-4的特异性抑制剂,具有1.25 μM的半抑制浓度(IC50)。它能减少离体小鼠心肌细胞中活性氧(ROS)的生成,并增强心肌收缩功能。此化合物适用于心脏缺血性损伤研究。
T79361 COX-2/15-LOX-IN-3

Lipoxygenase Metabolism
COX-2/15-LOX-IN-3 (compound 5k) 为COX-2/15-LOX的一种双重抑制剂,具有分别为0.075 μM和1.97 μM的IC50值。该化合物能显著抑制LPS诱导的细胞产生促炎细胞因子(IL-6, ROS和NO),表明其具备显著的抗炎活性。
T79146 MSU38225

MSU38225作为一种Nrf-2抑制剂,其作用机制包括提升活性氧(ROS)水平,能够有效抑制人肺癌细胞增殖,并提高其对化疗药物的敏感性,因此,在癌症研究中具有应用潜力。
T79287 SB-1295

Reactive Oxygen Species Immunology/Inflammation; Metabolism; NF-κB
SB-1295是一种口服活性CDK9/T1抑制剂,其IC50为0.17 μM。在HCT 116和MIA PaCa-2细胞中表现出抗增殖效应,并能诱导MIA PaCa-2细胞死亡,机制包括ROS生成增加、线粒体膜电位下降及细胞凋亡启动。SB-1295具备作为癌症研究工具的潜力。
T79739 CYP51/PD-L1-IN-2

CYP51/PD-L1-IN-2(compound L20)是一种具有抗真菌活性的喹唑啉化合物。它作为CYP51(IC50:0.263 μM)和PD-L1(IC50:0.017 μM)的双重抑制剂,能够在细胞周期的早期引发真菌细胞凋亡。CYP51/PD-L1-IN-2进一步显著降低IL-2、NLRP3、NF-κBp65等蛋白水平,触发线粒体损伤及ROS积累,终致真菌细胞裂解和死亡。
T72188 Nicotinamide Hydrochloride

Niacinamide Hydrochloride,Nicotinic acid amide Hydrochloride,Niacinamide Hydrochloride ; Nicotinic acid amide Hydrochloride

Nicotinamide Hydrochloride 是维生素 B3 或烟酸的一种形式,可抑制SIRT2的体外活性,其EC50值为 2 μM。 Nicotinamide Hydrochloride 可抑制 90% 的黑色素瘤细胞数量,并增加细胞内 NAD+、ATP、ROS 水平。Nicotinamide Hydrochloride 抑制黑色素瘤小鼠的肿瘤生长并提高生存率,可用于黑色素瘤等皮肤癌相关的研究。
T75833 HNGF6A TFA

HNGF6A TFA 是一种人类素类似物。HNGF6A TFA 可以增加葡萄糖刺激的胰岛素分泌和葡萄糖代谢,并可用于糖尿病的研究。HNGF6A TFA 在氧化应激期间抑制ROS 的产生。HNGF6A TFA 可以在体内预防内皮功能障碍和动脉粥样硬化。
T74629 Benz-AP

Benz-AP 是一种高效光敏剂,能产生单线态氧并与 hCES2 活性呈负相关。在 hCES2 低表达的癌细胞中,Benz-AP 表现出较高的光毒性。采用双光子激发(TPE)技术,Benz-AP 能够生成 ROS,有效杀死癌细胞和肿瘤球体。
T79738 CYP51/PD-L1-IN-1

CYP51/PD-L1-IN-1(compound L11)是一种具有抗真菌活性的喹唑啉化合物,作为CYP51(IC50: 0.884 μM)和PD-L1(IC50: 0.083 μM)的双重抑制剂,能够在细胞周期早期引发真菌细胞的凋亡。该化合物还能有效减少IL-2、NLRP3、NF-κBp65等蛋白的细胞内水平,诱导线粒体损伤及ROS积聚,进而导致真菌细胞的破裂和死亡。
T79740 CYP51/PD-L1-IN-3

CYP51/PD-L1-IN-3(compound L21)是一种具有抗真菌活性的喹唑啉化合物。作为CYP51(IC50: 0.205 μM) 和PD-L1(IC50: 0.039 μM) 的双重抑制剂,它能够引发真菌细胞在细胞周期早期的凋亡。此外,CYP51/PD-L1-IN-3 还能显著降低IL-2、NLRP3、NF-κBp65 蛋白的细胞内水平,并诱导线粒体损害及ROS 聚集,进而导致真菌细胞的裂解与死亡。
T81485 Phoenixin-14 TFA

PNX-14 TFA

Phoenixin-14 (PNX-14) TFA 是具抗焦虑、心脏保护及神经保护效果的穿透大脑屏障神经肽。它通过上调GnRH受体mRNA调控垂体促性腺激素分泌,并促进胰岛素释放。此外,Phoenixin-14 TFA保护小鼠免受缺血/再灌注(IR)伤害,通过降低ROS、提高GSH减缓氧化应激。
T74844 Antiproliferative agent-23

Antiproliferative agent-23,一种微管去稳定剂(MDA),通过扰乱微管蛋白-微管系统来发挥作用。该化合物通过降低Bcl-2蛋白水平、提高Bax和Cyt c蛋白水平以及激活半胱天冬酶级联反应和线粒体依赖途径来诱导细胞凋亡。此外,Antiproliferative agent-23还能在A549/CDDP细胞(顺铂耐药癌细胞系)中通过PERK/ATF4/CHOP信号通路激活ROS介导的内质网应激,展现出抗肿瘤活性。
T36004 1-O-Hexadecyl-sn-glycerol

1-O-Hexadecyl-sn-glycerol,(S)-(+)-Chimyl Alcohol,α-Chimyl Alcohol

1-O-Hexadecyl-sn-glycerol is a bioactive alkyl glyceryl ether. It reduces UVB-induced cell death and production of reactive oxygen species (ROS) and prostaglandin E2 in normal human epidermal keratinocytes (NHEKs). 1-O-Hexadecyl-sn-glycerol (50 μM) increases coronary flow and left ventricular developed pressure and reduces malondialdehyde (MDA) formation ex vivo in a rat heart model of ischemia/reperfusion injury. [2].Maulik, N., Tosaki, A., Engelman, R.M., et al. Myocardial salvage by chimyl al...
T36882 CAY10773

CAY10773 is a derivative of the ferroptosis inducer sorafenib .1It selectively inhibits proliferation of BEL-7402, MGC803, and T24 bladder cancer cells (IC50s = 5.77, 5.21 and 3.97 μM, respectively) over non-cancerous HCV-29 cells (IC50= 23.19 μM). CAY10773 induces apoptosis in T24 cells when used at concentrations ranging from 2 to 6 μM but induces ferroptosis at concentrations greater than or equal to 6 μM with 10 hour or longer incubation times. It increases the production of reactive oxygen ...
T72763 AChE/BuChE-IN-1

AChE/BuChE-IN-1,一种白杨素衍生物,具备对丁酰胆碱酯酶(BuChE)的选择性抑制作用,其IC50值为0.48μM。对乙酰胆碱酯酶(AChE)的抑制IC50值为7.16μM。该化合物强效清除·OH,IC50仅为0.1674μM,能够抑制活性氧(ROS)、阻止Aβ1-42的聚集(自发、Cu2+诱导及AChE诱导)。AChE/BuChE-IN-1展现出高血脑屏障(BBB)渗透性、优良的生物利用度和低细胞毒性,是阿尔茨海默病(AD)研究领域的有力候选。
T36241 Arecaidine propargyl ester (hydrobromide)

Arecaidine propargyl ester is an agonist of M2muscarinic acetylcholine receptors (mAChRs).1It selectively binds to M2over M1, M3, M4, and M5mAChRs in CHO cells expressing the human receptors (Kis = 0.0871, 1.23, 0.851, 0.977, and 0.933 μM, respectively). Arecaidine propargyl ester induces contractions in isolated guinea pig atrium (pD2= 8.67). It induces apoptosis and the production of reactive oxygen species (ROS) in U87 and U251 glioblastoma cells when used at a concentration of 100 μM.2Arecai...
T37469 Sitamaquine tosylate

Sitamaquine is an antileishmanial agent.1It is active againstL. donovani,L. infantum,L. mexicana,L. braziliensis, andL. tropica(EC50s = 9.5-19.8 μM). It inhibits mitochondrial complex II, also known as succinate dehydrogenase (SDH), in a cell-free assay when used at concentrations ranging from 10 to 200 μM.2Sitamaquine (100 μM) increases intracellular levels of reactive oxygen species (ROS) and decreases intracellular ATP levels, as well as induces phosphatidylserine externalization, chromatin f...
T21693 PPM-18

PPM-18 (NSC 73233) 是一种有效的抗炎剂,可抑制一氧化氮合酶的表达。PPM-18 是有效的 iNOS 表达抑制剂,可阻断 NF-κB 与启动子的结合。PPM-18 是维生素 K 的类似物,通过 ROS 和 AMPK 信号通路诱导膀胱癌细胞自噬和凋亡。
T36490 AZT triphosphate TEA

AZT triphosphate TFA (3'-Azido-3'-deoxythymidine-5'-triphosphate TFA) is a active triphosphate metabolite of Zidovudine (AZT). AZT triphosphate TFA exhibits antiretroviral activity and inhibits replication of HIV. AZT triphosphate TFA also inhibits the DNA polymerase of HBV. AZT triphosphate TFA activates the mitochondria-mediated apoptosis pathway[1][2][3]. Treatment with 100 μM Zidovudine (AZT) for 48h disrupts the mitochondrial tubular network via accumulation of AZT triphosphate (AZT-TP) in ...

化合物

ROS-IN-2
Cat.No: T78887
Synonym:
Target: Reactive Oxygen Species
ROS kinases-IN-2
Cat.No: T74671
Synonym:
Target: ROS Kinase
MAO-B-IN-2
Cat.No: T9560
Synonym:
Target:
MJ33 lithium salt
Cat.No: T38404
Synonym:
Target: ROS
GSK2795039
Cat.No: T15433
Synonym:
Target: Apoptosis, Reactive Oxygen Species, ROS, NADPH
20-HETE
Cat.No: T14021
Synonym: 20-hydroxy Arachidonic Acid
Target: Others
JC2-11
Cat.No: T77579
Synonym:
Target: IL Receptor, Dehydrogenase, ROS, Caspase, NOD-like Receptor (NLR), AIM2
Bromoiodoacetamide
Cat.No: T40723
Synonym:
Target:
ROS 234
Cat.No: T60340
Synonym:
Target:
AChE-IN-37
Cat.No: T79584
Synonym:
Target:
QD-394
Cat.No: T36514
Synonym:
Target:
ROS inducer 2
Cat.No: T79517
Synonym:
Target: Reactive Oxygen Species
HKPerox-2
Cat.No: T39754
Synonym:
Target:
Glutaminase C-IN-2
Cat.No: T78892
Synonym:
Target: Glutaminase
COX-2/15-LOX-IN-4
Cat.No: T79362
Synonym:
Target: Lipoxygenase
CL097 hydrochloride
Cat.No: T60517
Synonym:
Target:
NOX2-IN-2
Cat.No: T81647
Synonym:
Target:
AChE-IN-30
Cat.No: T79251
Synonym:
Target:
MCI
Cat.No: T79260
Synonym:
Target: Reactive Oxygen Species
BuChE-IN-2
Cat.No: T63995
Synonym:
Target:
GLX481304
Cat.No: T79179
Synonym:
Target:
COX-2/15-LOX-IN-3
Cat.No: T79361
Synonym:
Target: Lipoxygenase
MSU38225
Cat.No: T79146
Synonym:
Target:
SB-1295
Cat.No: T79287
Synonym:
Target: Reactive Oxygen Species
CYP51/PD-L1-IN-2
Cat.No: T79739
Synonym:
Target:
Nicotinamide Hydrochloride
Cat.No: T72188
Synonym: Niacinamide Hydrochloride,Nicotinic acid amide Hydrochloride,Niacinamide Hydrochloride ; Nicotinic acid amide Hydrochloride
Target:
HNGF6A TFA
Cat.No: T75833
Synonym:
Target:
Benz-AP
Cat.No: T74629
Synonym:
Target:
CYP51/PD-L1-IN-1
Cat.No: T79738
Synonym:
Target:
CYP51/PD-L1-IN-3
Cat.No: T79740
Synonym:
Target:
Phoenixin-14 TFA
Cat.No: T81485
Synonym: PNX-14 TFA
Target:
Antiproliferative agent-23
Cat.No: T74844
Synonym:
Target:
1-O-Hexadecyl-sn-glycerol
Cat.No: T36004
Synonym: 1-O-Hexadecyl-sn-glycerol,(S)-(+)-Chimyl Alcohol,α-Chimyl Alcohol
Target:
CAY10773
Cat.No: T36882
Synonym:
Target:
AChE/BuChE-IN-1
Cat.No: T72763
Synonym:
Target:
Arecaidine propargyl ester (hydrobromide)
Cat.No: T36241
Synonym:
Target:
Sitamaquine tosylate
Cat.No: T37469
Synonym:
Target:
PPM-18
Cat.No: T21693
Synonym:
Target:
AZT triphosphate TEA
Cat.No: T36490
Synonym:
Target:
Cat. No. Product Name Target Signaling Pathways
T6S1373 Casticin

Quercetagetin 3,6,7,4'-Tetramethyl Ether,Vitexicarpin,蔓荆子黄素

STAT JAK/STAT signaling; Stem Cells
Casticin (Vitexicarpin) 是从蔓荆子中得到的一种甲氧基黄酮,可抑制STAT3的活化,具有抗有丝分裂和抗炎活性。
T3008 Lawsone methyl ether

2-Methoxy-1,4-naphthoquinone,2-Methoxy-p-naphthoquinone,2-Methoxynaphthoquinone,2-甲氧基-1,4-萘并醌

Apoptosis; Antibacterial; Antifungal Apoptosis; Microbiology/Virology
Lawsone methyl ether (2-Methoxy-1,4-naphthoquinone) 是从凤仙花和Swertia calycina 中分离出的,有抗真菌和抗菌活性。
T2915 Bardoxolone

RTA 401,齐墩果烷三萜化合物,CDDO

Others; Nrf2 Immunology/Inflammation; Others
Bardoxolone (CDDO) 是新型核调节因子激活剂。
T5S1331 Herbacetin

c-Met/HGFR; Akt Cytoskeletal Signaling; PI3K/Akt/mTOR signaling; Tyrosine Kinase/Adaptors
Herbacetin 是一种亚麻籽中的天然类黄酮,具有多种药理活性,如抗氧化、抗炎、抗癌作用。 它是鸟氨酸脱羧酶Ornithine decarboxylase (ODC)变构抑制剂,能够直接与 ODC 上的 Asp44,Asp243 和 Glu384 结合。其中鸟氨酸脱羧酶是多胺生物合成中的限速酶。
T5S2283 Sesamolin

p38 MAPK; Caspase; JNK Apoptosis; MAPK; Proteases/Proteasome
Sesaminol 是从Justicia orbiculata 中分离得到的一种天然产物,抑制脂质过氧化,具有神经保护作用和抗氧化活性。它通过抑制JNK、p38 MAPKs 和caspase-3磷酸化,抑制MAPK 的级联反应。
T4S1050 Pristimerin

扁塑藤素,Celastrol methyl ester

NF-κB; Antibacterial Microbiology/Virology; NF-κB
Pristimerin (Celastrol methyl ester) 是一种可逆的单酰基甘油脂肪酶高效抑制剂,IC50值为93 nM。
T5S0045 Isofraxidin

6,8-Dimethoxyumbelliferone,异秦皮啶,Phytodolor,异嗪皮啶

MMP; ERK; p38 MAPK; TLR; COX Immunology/Inflammation; MAPK; Neuroscience; Proteases/Proteasome
Isofraxidin (Phytodolor) 是来自刺五加的香豆素成分,抑制MMP-7表达和人肝癌细胞侵袭。它作用于肝癌细胞,抑制ERK1/2磷酸化。它减弱iNOS 和COX-2表达,还抑制TLR4/髓样分化蛋白 2 复合物的形成。
T2860 Vanillyl Alcohol

4-Hydroxy-3-methoxybenzenemethanol,3-Methoxy-4-hydroxybenzyl alcohol,4-Hydroxy-3-methoxybenzyl alcohol,香兰醇,Vanillin alcohol,Vanillic alcohol

Apoptosis; Others Apoptosis; Others
Vanillyl Alcohol (3-Methoxy-4-hydroxybenzyl alcohol) 是一种酚类醇,具有抗血管生成、抗惊厥、抗炎、抗氧化、神经保护和抗伤害活性。它由香兰素衍生而来,在食品和饮料中用作调味剂。
T2S0618 β-Elemonic Acid

3-oxo Tirucallic Acid,β-岚香酮酸,Beta-Elemonic acid,3-Oxotirucallenoic Acid,β-榄香酮酸,Elemadienonic Acid

Apoptosis; Reactive Oxygen Species; COX Apoptosis; Immunology/Inflammation; Metabolism; Neuroscience; NF-κB
β-Elemonic Acid (3-Oxotirucallenoic Acid) 是从乳香树中分离得到的一种三萜,具有抗癌和抗炎作用。它抑制脯氨酰内肽酶,诱导细胞凋亡,活性氧和COX-2表达。
T2563 Acetyl-L-carnitine hydrochloride

Acetyl L-carnitine hydrochloride,O-Acetylcarnitine,乙酰-L-肉(毒)碱盐酸盐,O-acetyl-L-carnitine,O-Acetyl-L-carnitine hydrochloride

Others; Endogenous Metabolite Metabolism; Others
Acetyl-L-carnitine hydrochloride (Acetyl L-carnitine hydrochloride) 是一种由内源性左旋肉碱的乙酰化形式的盐酸盐组成的营养补充剂,具有潜在的神经保护、认知增强、抗抑郁和免疫调节活性。还可缓解化疗、糖尿病或其他疾病引起的周围神经病变。此外,乙酰左旋肉碱可能通过增加T淋巴细胞成熟来调节免疫反应,并可能下调促炎细胞因子对病毒(如SARS-CoV-2)的反应。它还可能破坏ACE2信号通路并抑制活性氧(ROS)的产生。
T6S1699 Shogaol

[6]-Shogaol,姜烯酚,6-姜烯酚,6-Shogaol

Lipoxygenase; Autophagy Autophagy; Metabolism
6-Shogaol (6-Shogaol) 是从生姜中分离的一种天然产物,具有抗癌、抗炎和抗氧化的多种生物活性。
T6S0139 Neobavaisoflavone

Apoptosis; DNA/RNA Synthesis Apoptosis; Cell Cycle/Checkpoint; DNA Damage/DNA Repair
Neobavaisoflavone 是一种从Psoralea corylifolia 的种子中分离出来的类黄酮。它具有抗炎,抗癌和抗氧化的作用。它在中至高浓度下可抑制 DNA 聚合酶,也可抑制血小板聚集。
T6S0735 Flavokawain B

黄卡瓦胡椒素B,Flavokavain B,Flavokawin B,2'-Hydroxy-4',6'-Dimethoxychalcone

Apoptosis; Others Apoptosis; Others
Flavokawain B (Flavokavain B) 是从卡瓦醉椒的根提取物中,分离出的查尔酮。它是一种凋亡诱导剂,可抑制各种癌细胞株生长。它以极低的无毒浓度抑制人脑内皮细胞的迁移和血管形成,具有抗血管生成活性。
T5S1097 Neferine

(R)-1,2-Dimethoxyaporphine,(-)-Neferine,甲基莲心碱

Apoptosis; NF-κB; Autophagy Apoptosis; Autophagy; NF-κB
Neferine ((-)-Neferine) 是一种双苄基异喹啉类生物碱,可强效抑制NF-κB 激活,具有抗肿瘤活性。
T2S0843 Negletein

黄芩素-7-甲醚,7-O-Methylbaicalein,Baicalein-7-methylether

IL Receptor; TNF; NOS; Interleukin Apoptosis; Immunology/Inflammation
Negletein (7-O-Methylbaicalein) 一种神经保护剂,可增强神经生长因子的作用并诱导 PC12 细胞中的神经突生长。它通过抑制TNF-α和IL-1β表现出抗炎活性,其 IC50值分别为 16.4 和 10.8 μM。它还具有抗菌、抗缺氧和抗阿尔茨海默病活性。
T6S1141 Ganoderic acid A

灵芝酸 A,灵芝酸A

Apoptosis; NF-κB; Endogenous Metabolite; Autophagy Apoptosis; Autophagy; Metabolism; NF-κB
Ganoderic acid A 能够抑制 JAK-STAT3信号通路,也能抑制细胞增殖,存活率和 ROS。 它对人骨肉瘤 HOS 和MG-63细胞具有增殖抑制、凋亡和侵袭抑制作用。
TN3653 Cimidahurinine

BCL; ROS Apoptosis; Immunology/Inflammation
Cimidahurinine can attenuate Doxorubicin (DOX)-induced cardiotoxicity in a dose-dependent manner with EC50 values of 45.79 uM; it protects against cardiotoxicity by decreasing reactive oxygen species (ROS) accumulation and downregulating apoptosis-related Bax/Bcl-2 proteins.
TN2243 Sugiol

10-Deoxoxanthoperol

IL Receptor; TNF; ROS Apoptosis; Immunology/Inflammation
Sugiol (10-Deoxoxanthoperol) 是一种枞烷二萜,可从台湾板栗树 (Calocedrus formosana) 的树皮中分离出来。Sugiol 具有抗炎活性,可有效减少脂多糖 (LPS) 刺激巨噬细胞后的活性氧 (ROS) 产生。
T79970 Taxamairin B

Taxamairin B是有效的抗炎化合物,能显著抑制LPS诱导的RAW264.7细胞中促炎因子(TNF-α, IL-1β和IL-6)表达及NO、ROS生成,并对LPS引起的急性肺损伤模型小鼠具有保护效果。
TN5463 Leachianone G

Leachianone G exhibits significant antioxidant potentials in the ABTS, ONOO(-), and total ROS assays, it also shows inhibitory activities against pancreatic lipase, it may be used as drug candidate to control obesity. Leachianone G shows potent antiviral
T78490 Polygalacturonic acid

Galacturonic acid polymer

Polygalacturonic acid(Galacturonic acid polymer)为透明胶状物,构成细胞壁关键组分。该酸应用于制备银纳米颗粒(AgNPs),充当抗氧化剂与抗炎剂,防护细胞遭受ROS增高引起的损伤,并促进伤口愈合。Polygalacturonic acid纳米颗粒亦显示抗菌性能。

天然产物

Casticin
Cat.No: T6S1373
Synonym: Quercetagetin 3,6,7,4'-Tetramethyl Ether,Vitexicarpin,蔓荆子黄素
Target: STAT
Lawsone methyl ether
Cat.No: T3008
Synonym: 2-Methoxy-1,4-naphthoquinone,2-Methoxy-p-naphthoquinone,2-Methoxynaphthoquinone,2-甲氧基-1,4-萘并醌
Target: Apoptosis, Antibacterial, Antifungal
Bardoxolone
Cat.No: T2915
Synonym: RTA 401,齐墩果烷三萜化合物,CDDO
Target: Others, Nrf2
Herbacetin
Cat.No: T5S1331
Synonym:
Target: c-Met/HGFR, Akt
Sesamolin
Cat.No: T5S2283
Synonym:
Target: p38 MAPK, Caspase, JNK
Pristimerin
Cat.No: T4S1050
Synonym: 扁塑藤素,Celastrol methyl ester
Target: NF-κB, Antibacterial
Isofraxidin
Cat.No: T5S0045
Synonym: 6,8-Dimethoxyumbelliferone,异秦皮啶,Phytodolor,异嗪皮啶
Target: MMP, ERK, p38 MAPK, TLR, COX
Vanillyl Alcohol
Cat.No: T2860
Synonym: 4-Hydroxy-3-methoxybenzenemethanol,3-Methoxy-4-hydroxybenzyl alcohol,4-Hydroxy-3-methoxybenzyl alcohol,香兰醇,Vanillin alcohol,Vanillic alcohol
Target: Apoptosis, Others
β-Elemonic Acid
Cat.No: T2S0618
Synonym: 3-oxo Tirucallic Acid,β-岚香酮酸,Beta-Elemonic acid,3-Oxotirucallenoic Acid,β-榄香酮酸,Elemadienonic Acid
Target: Apoptosis, Reactive Oxygen Species, COX
Acetyl-L-carnitine hydrochloride
Cat.No: T2563
Synonym: Acetyl L-carnitine hydrochloride,O-Acetylcarnitine,乙酰-L-肉(毒)碱盐酸盐,O-acetyl-L-carnitine,O-Acetyl-L-carnitine hydrochloride
Target: Others, Endogenous Metabolite
Shogaol
Cat.No: T6S1699
Synonym: [6]-Shogaol,姜烯酚,6-姜烯酚,6-Shogaol
Target: Lipoxygenase, Autophagy
Neobavaisoflavone
Cat.No: T6S0139
Synonym:
Target: Apoptosis, DNA/RNA Synthesis
Flavokawain B
Cat.No: T6S0735
Synonym: 黄卡瓦胡椒素B,Flavokavain B,Flavokawin B,2'-Hydroxy-4',6'-Dimethoxychalcone
Target: Apoptosis, Others
Neferine
Cat.No: T5S1097
Synonym: (R)-1,2-Dimethoxyaporphine,(-)-Neferine,甲基莲心碱
Target: Apoptosis, NF-κB, Autophagy
Negletein
Cat.No: T2S0843
Synonym: 黄芩素-7-甲醚,7-O-Methylbaicalein,Baicalein-7-methylether
Target: IL Receptor, TNF, NOS, Interleukin
Ganoderic acid A
Cat.No: T6S1141
Synonym: 灵芝酸 A,灵芝酸A
Target: Apoptosis, NF-κB, Endogenous Metabolite, Autophagy
Cimidahurinine
Cat.No: TN3653
Synonym:
Target: BCL, ROS
Sugiol
Cat.No: TN2243
Synonym: 10-Deoxoxanthoperol
Target: IL Receptor, TNF, ROS
Taxamairin B
Cat.No: T79970
Synonym:
Target:
Leachianone G
Cat.No: TN5463
Synonym:
Target:
Polygalacturonic acid
Cat.No: T78490
Synonym: Galacturonic acid polymer
Target:
TargetMol Loading
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