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36

抑制剂 & 化合物

32

天然产物

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Cat. No.	Product Name	Target	Signaling Pathways
T5460	Mofezolac 莫苯唑酸,莫非佐酸	COX	Immunology/Inflammation; Neuroscience
	Mofezolac 是一种非甾体类抗炎药，可缓解疼痛并具有抗炎活性，抑制 COX-1和COX-2的IC50为 1.44 和 447 nM。
T8719	SC99	Apoptosis; JAK; STAT	Angiogenesis; Apoptosis; Chromatin/Epigenetic; JAK/STAT signaling; Stem Cells
	SC99 是一种口服有效选择性STAT3抑制剂，靶向 JAK2-STAT3 途径，抑制血小板活化和聚集，有抗骨髓瘤和抗血栓活性。它结合在 JAK2 的 ATP 结合袋中，抑制 JAK2 和 STAT3 的磷酸化。
T3608	Carbasalate calcium Rheomin,Omegin,Alcacyl,Iromin,卡巴匹林钙,Solupsan,Carbasalate Calcium	Platelet aggregation	Others
	Carbasalate calcium (Rheomin) 是抗炎和解热剂，可用于研究疼痛的缓解。
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。
T62899	Tau-aggregation and neuroinflammation-IN-1	Microtubule Associated; NO Synthase	Cytoskeletal Signaling; Immunology/Inflammation
	Tau-aggregation and neuroinflammation-IN-1 是一种有效的 Tau 蛋白聚集体抑制剂，对 AcPHF6 和全长 tau 蛋白聚集体显示出显著的抑制活性。Tau-aggregation and neuroinflammation-IN-1具有抗炎活性且可减少 NO 释放。Tau-aggregation and neuroinflammation-IN-1 对 LSP 刺激的 BV2 细胞具有低细胞毒性。Tau-aggregation and neuroinflammation-IN-1 可逆转冈田酸诱导的大鼠记忆障碍。
T77442	Glenzocimab ACT017	Others	Others
	Glenzocimab (ACT017) 是人源化抗 GPVI 单克隆抗体的 Fab 片段。Glenzocimab 在缺血性卒中模型对胶原诱导的血小板聚集显示出抑制作用。Glenzocimab 具有研究急性缺血性脑卒中和脑血栓。
T1002	Etodolac Ultradol,AY-24236,依托度酸,Etodolic acid,Lodine	Retinoid Receptor; COX	Immunology/Inflammation; Metabolism; Neuroscience
	Etodolac (AY-24236) 是一种吡喃羧酸和非甾体抗炎药，具有解热和镇痛活性，对 COX 的 IC50为53.5 nM。
T76844	Abciximab C7E3	Integrin	Cytoskeletal Signaling
	Abciximab (C7E3) 是一种小鼠/人嵌合单克隆抗体，是一种有效的糖蛋白 IIb/IIIa (glycoprotein IIb/IIIa) 抑制剂。 Abciximab 具有抗血小板聚集和白细胞粘附的作用，通过与糖蛋白 IIb/IIIa、vitronectin 和 Mac-1 受体结合发挥作用。
T0839	Ketoprofen 酮基布洛芬,RP-19583,酮洛芬	Apoptosis; COX; MRP	Apoptosis; Immunology/Inflammation; Neuroscience
	Ketoprofen (RP-19583) 是一种非甾体抗炎剂，能够有效地抑制COX 的活性，在人血单核细胞中，对 COX-1 和 COX-2 的IC50值分别为 2 nM 和 26 nM。
T60671	MAO-B-IN-9	Beta Amyloid; Serotonin Transporter; Monoamine Oxidase	Neuroscience
	MAO-B-IN-9是一种可穿过血脑屏障的单胺氧化酶B MAO-B 抑制剂（IC50：0.18μM），具有有效性、选择性和时间依赖性。MAO-B-IN-9具有神经保护作用，可以防止Aβ1-42诱导的神经元细胞死亡，这可能与Aβ1-42的抗聚集作用有关。
T14199	ALZ-801 Valiltramiprosate	Beta Amyloid	Neuroscience
	ALZ-801 是一种可口服的小分子 β-淀粉样蛋白抗寡聚体和聚集抑制剂，是曲米酸的缬氨酸偶联前药，与母体化合物相比，具有显著改善的 PK 特性和胃肠道耐受性。它是治疗阿尔茨海默病的先进且显著改善的候选药物。
T68025	Zoliprofen	Others	Others
	Zoliprofen 是一种一种高效的且可口服的非甾体抗炎剂，具有抗炎、解热和镇痛活性，对角叉菜素、制霉菌素、刀豆球蛋白A 诱导的大鼠爪水肿，以及抗大鼠兔血清诱导的骨折或背皮水肿具有抑制作用。Zoliprofen 在大鼠和兔子中对胶原蛋白或花生四烯酸引起的血小板聚集方面比布洛芬和非诺洛芬有效20倍。Zoliprofen 对小鼠内毒素诱导的腹泻和花生四烯酸诱导的兔急性死亡抑制作用显著。
T33395	Miroprofen Miroprofene,Antopen,Y 9213,Y-9213,Miroprofeno,Miroprofenum
	Miprofen is an analgesic and non-steroidal anti-inflammatory, which means it has anti-inflammatory, antipyretic, and anti-platelet aggregation activities.
T16353	Meseclazone 美西拉宗,W2395,NSC297623	AChR	Neuroscience
	Meseclazone has anti-inflammatory, analgesic, and antipyretic activity. Meseclazone shows inhibitory potency of secondary phase ADP aggregation.
T17101	Tiopinac 硫平酸,RS 40974	Others	Others
	Tiopinac 是一种三环化合物，对动物具有高效的抗炎、镇痛和解热作用，能够抑制前列腺素合成，对人类具有适度的抗血小板聚集特性。
T78173	Aβ/tau aggregation-IN-3
	Aβ/tau aggregation-IN-3为一种高效的抗Aβ聚集剂，经Aβ-硫黄素T (Aβ-ThT) 聚集测定显示，其半抑制浓度(IC50)为0.85 μM，表现出显著的抗淀粉样蛋白活性。
T78531	Anti-amyloid agent-1
	Anti-amyloid agent-1是一种有效抗淀粉样蛋白化合物，能抑制淀粉样蛋白聚集，并为淀粉样变性治疗研究提供了有用的方法。
T27638	Israpafant Y-24180,Y 24180,Y24180
	Israpafant is a selective antagonist for the platelet-activating factor receptor ( IC50 = 0.84nM). Israpafant inhibits PAF-induced human platelet aggregation. Israpafant inhibits the activation of eosinophil cells and consequently delays the development o
T75689	Mumefural
	Mumefural，Prunus mumeSieb 加工果实中的一种生物活性成分，具有抑制血小板聚集、显示抗血栓作用及改善认知障碍的功能。
T22118	NQTrp	Microtubule Associated	Cytoskeletal Signaling
	NQTrp 是芳香萘醌-色氨酸杂交分子，可以抑制 tau 蛋白的聚集，具有抗淀粉样蛋白活性。NQTrp 对六肽 (41GCWMLY46，γD-crystallin 的 N 端)和全长 γD-crystallin 的体外聚集有抑制作用。
T68847	Aspirin calcium
	Aspirin calcium is the prototypical analgesic used in the treatment of mild to moderate pain. It has anti-inflammatory and antipyretic properties and acts as an inhibitor of cyclooxygenase which results in the inhibition of the biosynthesis of prostaglandins. Aspirin also inhibits platelet aggregation and is used in the prevention of arterial and venous thrombosis. (From Martindale, The Extra Pharmacopoeia, 30th ed, p5)
T63513	Antitumor agent-71
	Antitumor Agent-71 是一种抗肿瘤化合物，对微管蛋白 (tubulin) 的聚集表现出抑制作用。Antitumor Agent-71 拥有抗增殖作用，对肿瘤细胞系的 IC50值范围为3.98-15.70 μM。
T60940	ChE/Aβ1-42-IN-1
	ChE/Aβ1-42-IN-1 (compound 28) 是一种有效的ChE 和Aβ1-42聚集抑制剂，具有良好的血脑屏障通透性。ChE/Aβ1-42-IN-1 对 AChE、BuChE 和 Aβ1-42聚集的IC50值分别为 0.062、0.767和1.227 μM。ChE/Aβ1-42-IN-1 是一种有效的多靶点抗阿尔茨海默病剂。
T75517	Colletofragarone A2
	Colletofragarone A2，一种从真菌Colletotrichum sp. (13S020) 中分离得到的化合物，抑制p53突变蛋白和HSP90，因而具备抗癌活性。它促进p53突变蛋白的降解与聚合作用，并有能力抑制肿瘤在体内的生长。
T62602	Anticancer agent 49
	Anticancer agent 49 (compound 69) 是一种广谱抗癌剂，其表现出抗增殖活性。Anticancer agent 49 对微管蛋白聚合具有抑制作用。Anticancer agent 49 在体内显示抗肿瘤活性。Anticancer agent 49 具有潜力进行实体瘤和血液肿瘤的研究。
T35431	(±)-Clopidogrel (hydrochloride)
	Clopidogrel is an antithrombic compound whose active metabolite is a selective, irreversible antagonist of the platelet purinergic P2Y12 receptor (IC50 = 100 nM). Clopidogrel inhibits ADP-induced platelet aggregation ex vivo and functions as a prodrug whereupon biotransformation to its active metabolite via CYP2C19 in the liver enables its anti-aggregating activity. Marketed under the name Plavix , clopidogrel in combination with aspirin has been shown to be beneficial in the prevention of vascu...
T72506	Antioxidant agent-8
	Antioxidant agent-8是一种口服活性的Aβ1-42沉积抑制剂。其抑制原纤维聚集的IC50值为11.15 µM，促进原纤维分解的IC50值为6.87 µM。此外，Antioxidant agent-8对Cu2+诱导的Aβ1-42原纤维聚集有抑制作用（IC50=3.69 µM），并能促进Cu2+诱导的Aβ1-42原纤维分解（IC50=3.35 µM）。该化合物具备抗氧化活性、抗炎活性、生物安全性、血脑屏障通透性和神经保护作用。
T35600	NO-Losartan A
	Angiotensin II is a hormone that plays an important role in regulating blood pressure. Elevated levels of angiotensin II are implicated in inducing and maintaining hypertension, and also in the development of atherosclerosis. Both of these effects are mediated by the angiotensin II type 1 (AT1) receptor. Losartan is a mammalian AT1 receptor antagonist with a Ki value of 5-20 nM. In humans, losartan effectively controls hypertension while protecting renal function. Nitric oxide (NO) causes vasodi...
T36112	Clopidogrel Carboxylic Acid (hydrochloride)
	Clopidogrel is an antithrombic compound whose active metabolite is a selective, irreversible antagonist of the platelet purinergic P2Y12 receptor (IC50 = 100 nM). Clopidogrel inhibits ADP-induced platelet aggregation ex vivo and functions as a prodrug whereupon biotransformation to its active thiol metabolite via CYP2C19 in the liver enables its anti-aggregating activity. An estimated 15% of administered clopidogrel is metabolized by CYP2C19 to the thiol metabolite. Clopidogrel carboxylic acid i...
T62847	AMXI-5001
	AMXI-5001 是一种有效的、口服具有活力的 parp1/2 和微管聚合抑制剂。MXI-5001 对多种人类癌细胞显示出选择性抗肿瘤细胞毒性，其 IC50s 远低于现有的临床 PARP1/2 抑制剂。AMXI-5001 能够诱导已建立的肿瘤（包括很大的肿瘤）完全消退。
T74860	MAO-B-IN-21	Monoamine Oxidase	Neuroscience
	MAO-B-IN-21是一种有效的MAO-B抑制剂，该化合物表现出抗氧化和抗Aβ聚集的活性。该化合物还可螯合金属离子，抗神经炎症（如NO、TNF-α），具有神经保护作用，并可穿透BBB。在Aβ1-42诱导的阿尔茨海默病小鼠模型中，MAO-B-IN-21显著改善了记忆与认知功能。
T62262	Neuroinflammatory-IN-2
	Neuroinflammatory-IN-2 (compound 7i) 是一种有效的抗神经炎症剂，能够作用于 MAO-B (IC50: 10.30 μM)。Neuroinflammatory-IN-2 具有抗神经炎症活性、抗氧化活性、生物金属螯合能力和适当的血脑屏障通透性 (BBB)。Neuroinflammatory-IN-2 在 25 μM 的浓度下可以抑制 96.33% 的 Aβ1-42 聚集。Neuroinflammatory-IN-2 在 H2O2 诱导的 PC-12 细胞损伤中表现出神经保护活性。Neuroinflammatory-IN-2 能够用于研究阿尔兹海默症。
T63307	AChE-IN-6
	AChE-IN-6 是一种多功能配体，可显着抑制 AChE 的活性，对 EeAChE 和 HuAChE 的 IC50 值分别为 0.20 μM 和 37.02 nM，并具有抗 Aβ 活性 (IC50= 1.92 μM，用于自诱导 Aβ1-42 聚集；IC50= 1.80 μM，用于分解 Aβ1-42 原纤维；IC50= 2.18 μM，用于 Cu2+ 诱导的 Aβ1- 42 聚集；IC50= 1.17 μM，用于解聚 Cu2+ 诱导的 Aβ1-42 原纤维)。AChE-IN-6 对阿尔茨海默病表现出研究潜力。
T83122	Amyloid-Forming peptide GNNQQNY
	Amyloid-Forming peptide GNNQQNY是由酵母蛋白Sup35的N-末端朊病毒决定结构域中得来的七肽段，具有生物活性，并能形成淀粉样纤维。它的详细原子低聚结构之研究，使其成为揭示早期聚集阶段的理想模型。GNNQQNY二聚体以三种稳定构形存在：寄存器内并排、寄存器外并排和反向并排。对准的平行二聚体其β-pleated sheet结构中肽链间氢键较少，强调了疏水作用的重要性，相较于反向并排结构有更高的构象熵。
T82243	hAChE-IN-5	GSK-3	PI3K/Akt/mTOR signaling; Stem Cells
	hAChE-IN-5（化合物49）是一种同时针对hAChE和hBuChE的有效抑制剂，其IC50值均为0.17 μM。此外，hAChE-IN-5对GSK3β同样展现出良好的抑制活性，IC50值为0.21 μM。作为tau蛋白聚集和Aβ1-42自聚集的抑制剂，hAChE-IN-5能够结合PAS，进而阻止Aβ依赖的神经毒性。其能穿透血脑屏障（BBB），显示出成为多靶点抗阿尔茨海默病药物研究的潜力。
T36618	Rupatadine
	Rupatadine (UR-12592) is a potent dual PAF/H1 antagonist with Ki of 0.55/0.1 uM(rabbit platelet membranes/guinea pig cerebellum membranes).IC50 value:Target: PAF/H1 antagonistin vitro: Rupatadine competitively inhibited histamine-induced guinea pig ileum contraction (pA2 = 9.29 +/- 0.06) without affecting contraction induced by ACh, serotonin or leukotriene D4 (LTD4). It also competitively inhibited PAF-induced platelet aggregation in washed rabbit platelets (WRP) (pA2 = 6.68 +/- 0.08) and in hu...

化合物

Cat.No: T5460

Synonym: 莫苯唑酸,莫非佐酸

Target: COX

Cat.No: T8719

Target: Apoptosis, JAK, STAT

Carbasalate calcium

Cat.No: T3608

Synonym: Rheomin,Omegin,Alcacyl,Iromin,卡巴匹林钙,Solupsan,Carbasalate Calcium

Target: Platelet aggregation

Cat.No: T29097

Synonym: VA-S3947,VA S3947,VAS3947

Target: Apoptosis, NADPH-oxidase

Tau-aggregation and neuroinflammation-IN-1

Cat.No: T62899

Target: Microtubule Associated, NO Synthase

Cat.No: T77442

Synonym: ACT017

Target: Others

Cat.No: T1002

Synonym: Ultradol,AY-24236,依托度酸,Etodolic acid,Lodine

Target: Retinoid Receptor, COX

Cat.No: T76844

Synonym: C7E3

Target: Integrin

Cat.No: T0839

Synonym: 酮基布洛芬,RP-19583,酮洛芬

Target: Apoptosis, COX, MRP

Cat.No: T60671

Target: Beta Amyloid, Serotonin Transporter, Monoamine Oxidase

Cat.No: T14199

Synonym: Valiltramiprosate

Target: Beta Amyloid

Cat.No: T68025

Target: Others

Cat.No: T33395

Synonym: Miroprofene,Antopen,Y 9213,Y-9213,Miroprofeno,Miroprofenum

Cat.No: T16353

Synonym: 美西拉宗,W2395,NSC297623

Target: AChR

Cat.No: T17101

Synonym: 硫平酸,RS 40974

Target: Others

Aβ/tau aggregation-IN-3

Cat.No: T78173

Anti-amyloid agent-1

Cat.No: T78531

Cat.No: T27638

Synonym: Y-24180,Y 24180,Y24180

Cat.No: T75689

Cat.No: T22118

Target: Microtubule Associated

Aspirin calcium

Cat.No: T68847

Antitumor agent-71

Cat.No: T63513

ChE/Aβ1-42-IN-1

Cat.No: T60940

Colletofragarone A2

Cat.No: T75517

Anticancer agent 49

Cat.No: T62602

(±)-Clopidogrel (hydrochloride)

Cat.No: T35431

Antioxidant agent-8

Cat.No: T72506

Cat.No: T35600

Clopidogrel Carboxylic Acid (hydrochloride)

Cat.No: T36112

Cat.No: T62847

Cat.No: T74860

Target: Monoamine Oxidase

Neuroinflammatory-IN-2

Cat.No: T62262

Cat.No: T63307

Amyloid-Forming peptide GNNQQNY

Cat.No: T83122

Cat.No: T82243

Target: GSK-3

Cat.No: T36618

Cat. No.	Product Name	Target	Signaling Pathways
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。
T2230	Paeoniflorin 芍药苷,Peoniflorin	HSP; COX	Cytoskeletal Signaling; Immunology/Inflammation; Metabolism; Neuroscience
	Paeoniflorin (Peoniflorin) 是从芍药根中提取的一种蒎烷单萜糖苷，具有抗癌作用、抗氧化应激、抗血小板聚集、血管扩张、降低血液粘度和抗炎活性等多种生物活性。它是一种热休克蛋白诱导剂，通过自噬途径保护 PC12 细胞免受 MPP+和酸性损伤。
T5548	Verbenone 2-Pinen-4-one,马鞭草烯醇,(-)-Verbenone,马鞭草酮	Others	Others
	(-)-Verbenone ((-)-Verbenone) 是一种存在于 Suregada zanzibariensisVerdc 的树叶中的天然的萜烯。Verbenone 具有抗聚集信息素作用，可中断树皮甲虫对其聚集信息素的吸引。
TN6924	Anhydrosafflor yellow B (2S,3S)-6,7-dihydroxy-5-[(2E)-3-(4-hydroxyphenyl)prop-2-enoyl]-2-[(1S,2R,3R)-1,2,3,4-tetrahydroxybutyl]-3-{2,3,4-trihydroxy-5-[(2E)-3-(4-hydroxyphenyl)prop-2-enoyl]-6-oxo-3-[(2R,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]cyclohexa-1,4-dien-1,脱水红花黄色素B,AHSYB	Others	Others
	Anhydrosafflor yellow B ((2S,3S)-6,7-dihydroxy-5-[(2E)-3-(4-hydroxyphenyl)prop-2-enoyl]-2-[(1S,2R,3R)-1,2,3,4-tetrahydroxybutyl]-3-{2,3,4-trihydroxy-5-[(2E)-3-(4-hydroxyphenyl)prop-2-enoyl]-6-oxo-3-[(2R,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]cyclohexa-1,4-dien-1) 是从红花中分离出来的，可抑制 ADP 诱导的血小板聚集，在体外表现出显着的抗氧化作用，并对 H2O2 诱导的细胞毒性具有一定的活性。
T2898	Andrographolide Andrographis,穿心莲内酯	SARS-CoV; Influenza Virus; NF-κB; Autophagy	Autophagy; Microbiology/Virology; NF-κB
	Andrographolide (Andrographis) 是 NF-κB 的不可逆拮抗剂，具有抗病毒、抗炎和抗血小板聚集活性和潜在的抗肿瘤作用。
T28551	Ro 09-0680 Ro-09-0680,Ro 09 0680
	Ro 09-0680 是从丹参中提取的化合物，是一种由胶原蛋白诱导的兔血小板聚集的有效抑制剂，具有潜在的抗炎活性，可用于研究心血管疾病。
T2745	18α-Glycyrrhetinic acid 18-α-甘草次酸,甘草次酸,Enoxolone,Glycyrrhetinic acid	Apoptosis; NF-κB; Proteasome	Apoptosis; NF-κB; Proteases/Proteasome; Ubiquitination
	18α-Glycyrrhetinic acid (Enoxolone) 是 NF-kB 的抑制剂和蛋白酶体的激活剂，在多细胞生物中起到促进长寿和抗聚集因子的作用。它诱导细胞凋亡。
TN1622	Ermanin 堪非醇3,4'-二-O-甲醚	NOS; Influenza Virus; COX; HIV Protease; Antibacterial; Antibiotic	Immunology/Inflammation; Microbiology/Virology; Neuroscience; Proteases/Proteasome
	Ermanin 是一种从 Tanacetum microphyllum 中分离出来的类黄酮。Ermanin抑制血小板聚集，具有抗结核和抗病毒/细菌特性。Ermanin 可抑制 iNOS 和 COX-2 的表达，从而具有抗炎活性。Ermanin 可能具有抗 HIV-1 活性。Ermanin 在较低浓度下可有效地抑制 Dione juno 幼虫。
T2S1749	Protogracillin 原纤细薯蓣皂甙	Others	Others
	Protogracillin 是一种甾体皂苷，分离自Dioscorea zingiberensisWright (DZW) 中。从 DZW 根状茎中获得的甾体皂苷具有抗血栓作用，同时由降低心血管疾病风险的潜力。
T7030	anemarsaponin B 知母皂苷B,知母皂苷 B	p38 MAPK; NF-κB; MEK; COX; NO Synthase	Immunology/Inflammation; MAPK; Neuroscience; NF-κB
	Anemarsaponin B 是一种甾体皂苷，可降低iNOS 和COX-2的蛋白和 mRNA 水平，减少促炎细胞因子的表达和产生。它通过阻断 IκBα 的磷酸化来抑制NF-κB 的 p65 亚基的核转位，还抑制 MAP 激酶激酶 3/6 (MKK3/6) 和混合谱系激酶 3 的磷酸化。
TN1564	Delphinidin 3-glucoside chloride Delphinidin-3-O-glucoside chloride	Apoptosis; EGFR	Angiogenesis; Apoptosis; JAK/STAT signaling; Tyrosine Kinase/Adaptors
	Delphinidin 3-glucoside chloride (Delphinidin-3-O-glucoside chloride) 是从 Hibiscus sabdariffa 提取物中发现的膳食酚类物质。Delphinidin 3-glucoside chloride 具有抗氧化活性，可诱导 B 细胞慢性淋巴细胞性白血病 (B CLL) 的促凋亡作用，抑制 EGFR，抑制血小板聚集。Delphinidin 3-glucoside chloride 具有抗肿瘤活性，通过调节 pAKT/IRF1/HOTAIR 通路发挥作用。
T5S0896	Loureirin A 龙血素 A,龙血素A	Akt; PI3K	Cytoskeletal Signaling; PI3K/Akt/mTOR signaling
	Loureirin A 是一种黄酮类物质，从龙血树中分离得到，能够降低Akt 的磷酸化，具有抗血小板聚集作用。
T5S2358	Dehydrocorydaline Dehydrocorydalin,脱氢紫堇碱,13-Methylpalmatine	BCL; PARP; p38 MAPK; Caspase; Parasite; Autophagy	Apoptosis; Autophagy; Chromatin/Epigenetic; DNA Damage/DNA Repair; MAPK; Microbiology/Virology; Proteases/Proteasome
	Dehydrocorydaline (13-Methylpalmatine) 是一种生物碱。它调节Bax，Bcl-2蛋白表达，激活caspase-7，caspase-8，并使PARP 失活。它能增强p38 MAPK 活化，具有抗炎、抗癌等功效。它具有强大的抗疟疾作用，并具低细胞毒性。
T5S2357	Acetylcorynoline (+)-Corynoline Acetate,O-Acetylcorynoline,乙酰紫堇灵	Antifungal	Microbiology/Virology
	Acetylcorynoline (O-Acetylcorynoline) 是提取自 Corydalis bungeana 中的一种主要生物碱成分，具有抗炎活性。
TN3964	Epiaschantin	Others	Others
	(+)-Epiaschantin shows marginal cancer cell line inhibitory activities. It also has anti-platelet aggregation activity.
TN1095	Ginsenoside Rk2 人参皂苷RK2	VEGFR	Angiogenesis; Tyrosine Kinase/Adaptors
	Ginsenoside Rk1 has anti-tumor, and anti-platelet aggregation activities.
TN6472	Columbianetin beta-D-glucopyranoside
	Columbianetin-beta-D-glucopyranoside exhibits anti-inflammatory and analgesic properties, it also shows strong inhibiting activity against platelet aggregation.
TN1044	Quercetin 3-O-neohesperidoside	Others	Others
	Quercetin 3-O-neohesperidoside shows anti-atherosclerosis, and antiplatelet aggregation activities.
TL0017	Aristolactam AIIIa	MAPK; CDK	Cell Cycle/Checkpoint; MAPK
	Aristolactam AIIIa is a new type of Plk1 inhibitors, targeting the Polo Box domain (PBD), it has anti-tumor activity. Aristolactam IIIa shows inhibition of platelet aggregation induced by collagen or arachidonic acid.
TN3153	6-Acetyl-2,2-dimethylchroman-4-one	PAFR	GPCR/G Protein
	6-Acetyl-2,2-dimethylchroman-4-one and vanillin show anti-platelet aggregation activity induced by arachidonic acid in vitro.
TN4797	Piperolactam C	PAFR; Antifection	GPCR/G Protein; Microbiology/Virology
	Piperolactam C possesses anti-platelet aggregation activity in vitro. It can inhibit the growth of the fungi Cladosporium sphaerospermum and C. cladosporioides.
TN3445	Aristolactam BIII	PAFR	GPCR/G Protein
	Aristolactam BIII possesses anti-platelet aggregation activity in vitro, it also shows significant cytotoxic activity (IC50 values < 4 microg/mL) against P-388, HT-29 and A549 cell lines in vitro.
T40641	Crocin-4
	Crocin-4, a carotenoid compound found in saffron, possesses potent antioxidant properties and can penetrate the brain. It effectively inhibits the aggregation and deposition of Aβ fibrils, making it useful for Alzheimer's Disease research. Additionally, Crocin-4 demonstrates antitumor and anti-inflammatory activities.
T3734	3',4'-Dihydroxyacetophenone 二羟基苯乙酮,Qingxintong,4-Acetylpyrocatechol	Tyrosinase; Platelet aggregation	Others; Proteases/Proteasome
	3',4'-Dihydroxyacetophenone (Qingxintong) 是一种血管活性物质和抗氧化剂，可从Picea Schrenkiana 中分离得到，能抑制酪氨酸酶，其IC50=10 μM。
TN2106	Protodeltonin 原三角叶皂苷	BCL; PARP; Caspase	Apoptosis; Chromatin/Epigenetic; DNA Damage/DNA Repair; Proteases/Proteasome
	Protodeltonin may have anti-thrombotic activity by both improving the anticoagulation activity and inhibiting platelet aggregation action. Protodeltonin can inhibit the proliferation of a panel of established human and murine cancer cell lines in vitro.
TN6056	Zanthobungeanine 8-Methoxy-N-methylflindersine
	Zanthobungeanine has anti-inflammatory activity, it shows moderate NO production inhibitory activity with an IC50 value of 37.26 mg /L.It shows obviously inhibitoryactivity to platelet aggregation caused by platelet-activating factor (PAF). Zanthobungeani
T80656	Cannflavin A
	Cannflavin A，源自大麻(Cannabis sativa L)，具备抗癌、神经保护及抗炎活性。该化合物有效抑制Aβ1-42的聚集，并阻断犬尿氨酸-3-单加氧酶(KMO)的活性，进而通过caspase-3裂解途径激活细胞凋亡(apoptosis)。
TN3979	Epiyangambin	PAFR	GPCR/G Protein
	Epiyangambin is a phytotoxic lignan, it shows inhibition of seed germination of Agrostis stolonifera cv. penncross (Poaceae) and inhibition of development of Lactuca sativa L. (Asteraceae) seedlings in a microassay using 24-well plates. Epiyangambin exhibits significant inhibition of the transformation of murine epidermal JB6 cells, with the IC50 value of 0.15 microg/mL. (+)-Epiyangambin also has anti-platelet aggregation activity.
TN4382	Kazinol A	AMPK; mTOR	Chromatin/Epigenetic; PI3K/Akt/mTOR signaling
	Kazinol A shows strong inhibition of arachidonic acid (AA)-induced platelet aggregation. It also exhibits potent inhibition with IC50 values ranging 0.6-164 M against XOD. Kazinol A may be a candidate for the development of effective anti-cancer drug on h
T79948	Kadsurenin B
	Kadsurenin B为PAF（platelet-activating factor）拮抗剂，展现出神经保护作用。该化合物在药理学领域显示出广泛的研究潜力，包括抗菌、抗炎、神经保护、抗氧化、抗血小板聚集、细胞毒性和抗寄生虫等效能。
TN5221	(-)-Variabilin
	Variabilin, a novel inhibitor of human platelet aggregation, it is a potent RGD (Arg-Gly-Asp)-containing antagonist of the fibrinogen receptor glycoprotein IIb-IIIa (GPIIb-IIIa; αIIbβ3) and the vitronectin receptor αvβ3.Variabilin is also an antimicrobial furanosesterterpene. Variabilin is an inhibitor of human secretory and cytosolic phospholipase A2 (PLA2) activities that controls eicosanoid production in vitro and in vivo, inhibits neutrophil degranulation and superoxide generation in vitro a...
T38330	Collinin
	Collinin is a coumarin that has been found in Z. schinifolium and has diverse biological activities.1,2,3,4 It is active against drug-susceptible and -resistant strains of M. tuberculosis (MIC50s = 3.13-6.25 μg/ml).1 Collinin inhibits LPS-induced nitric oxide (NO) production (IC50 = 5.9 μM) and reduces COX-2 protein levels in RAW 264.7 cells.2 It completely inhibits aggregation of isolated rabbit platelets induced by arachidonic acid , collagen, or platelet activating factor (PAF) when used at a...

天然产物

Neobavaisoflavone

Cat.No: T6S0139

Target: Apoptosis, DNA/RNA Synthesis

Cat.No: T2230

Synonym: 芍药苷,Peoniflorin

Target: HSP, COX

Cat.No: T5548

Synonym: 2-Pinen-4-one,马鞭草烯醇,(-)-Verbenone,马鞭草酮

Target: Others

Anhydrosafflor yellow B

Cat.No: TN6924

Synonym: (2S,3S)-6,7-dihydroxy-5-[(2E)-3-(4-hydroxyphenyl)prop-2-enoyl]-2-[(1S,2R,3R)-1,2,3,4-tetrahydroxybutyl]-3-{2,3,4-trihydroxy-5-[(2E)-3-(4-hydroxyphenyl)prop-2-enoyl]-6-oxo-3-[(2R,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]cyclohexa-1,4-dien-1,脱水红花黄色素B,AHSYB

Target: Others

Andrographolide

Cat.No: T2898

Synonym: Andrographis,穿心莲内酯

Target: SARS-CoV, Influenza Virus, NF-κB, Autophagy

Cat.No: T28551

Synonym: Ro-09-0680,Ro 09 0680

18α-Glycyrrhetinic acid

Cat.No: T2745

Synonym: 18-α-甘草次酸,甘草次酸,Enoxolone,Glycyrrhetinic acid

Target: Apoptosis, NF-κB, Proteasome

Cat.No: TN1622

Synonym: 堪非醇3,4'-二-O-甲醚

Target: NOS, Influenza Virus, COX, HIV Protease, Antibacterial, Antibiotic

Cat.No: T2S1749

Synonym: 原纤细薯蓣皂甙

Target: Others

anemarsaponin B

Cat.No: T7030

Synonym: 知母皂苷B,知母皂苷 B

Target: p38 MAPK, NF-κB, MEK, COX, NO Synthase

Delphinidin 3-glucoside chloride

Cat.No: TN1564

Synonym: Delphinidin-3-O-glucoside chloride

Target: Apoptosis, EGFR

Cat.No: T5S0896

Synonym: 龙血素 A,龙血素A

Target: Akt, PI3K

Dehydrocorydaline

Cat.No: T5S2358

Synonym: Dehydrocorydalin,脱氢紫堇碱,13-Methylpalmatine

Target: BCL, PARP, p38 MAPK, Caspase, Parasite, Autophagy

Acetylcorynoline

Cat.No: T5S2357

Synonym: (+)-Corynoline Acetate,O-Acetylcorynoline,乙酰紫堇灵

Target: Antifungal

Cat.No: TN3964

Target: Others

Ginsenoside Rk2

Cat.No: TN1095

Synonym: 人参皂苷RK2

Target: VEGFR

Columbianetin beta-D-glucopyranoside

Cat.No: TN6472

Quercetin 3-O-neohesperidoside

Cat.No: TN1044

Target: Others

Aristolactam AIIIa

Cat.No: TL0017

Target: MAPK, CDK

6-Acetyl-2,2-dimethylchroman-4-one

Cat.No: TN3153

Target: PAFR

Cat.No: TN4797

Target: PAFR, Antifection

Aristolactam BIII

Cat.No: TN3445

Target: PAFR

Cat.No: T40641

3',4'-Dihydroxyacetophenone

Cat.No: T3734

Synonym: 二羟基苯乙酮,Qingxintong,4-Acetylpyrocatechol

Target: Tyrosinase, Platelet aggregation

Cat.No: TN2106

Synonym: 原三角叶皂苷

Target: BCL, PARP, Caspase

Zanthobungeanine

Cat.No: TN6056

Synonym: 8-Methoxy-N-methylflindersine

Cat.No: T80656

Cat.No: TN3979

Target: PAFR

Cat.No: TN4382

Target: AMPK, mTOR

Cat.No: T79948

Cat.No: TN5221

Cat.No: T38330

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