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Targets Recommended: Histone Methyltransferase DNA Methyltransferase Histone Acetyltransferase Methionine Adenosyltransferase (MAT) Neurotensin Receptor Monoamine Transporter Na-K-Cl cotransporter Monocarboxylate transporter Acyltransferase Transferase N-Acetylglucosaminyltransferase Angiotensin-converting Enzyme (ACE) Transaminase transporter Reverse Transcriptase Serotonin Transporter Calcium Channel

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抑制剂 & 化合物

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天然产物

化合物库

TargetMol 试剂盒

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重组蛋白

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Cat. No.	Product Name
L5900	血脑屏障通透化合物库	509 compounds
	509 个 CNS-Penetrant 生物活性小分子化合物的特有集合，用于高通量、高内涵筛选；
L7110	抗高血压化合物库	678 compounds
	678 种高血压相关的小分子，用于高通量和高内涵筛选；
L4020	NO PAINS 化合物库	9384 compounds
	TargetMol NO PAINS 化合物库包含 9384 个剔除了PAINS 的小分子活性化合物，可用于新药研发，信号通路研究，老药新用等研究。
L1380	转录因子库	695 compounds
	695 种转录因子靶向、结构新颖的化合物；
L2610	神经递质受体化合物库	1513 compounds
	1513 种与神经递质受体相关的化合物，用于高通量、高内涵筛选；
L4710	非甾体类抗炎化合物库	521 compounds
	521 种非甾体类的抗炎相关化合物，可用于高通量和高内涵筛选；
L9830	抗帕金森病化合物库	857 compounds
	857 种帕金森病相关的化合物集合，可用于高通量和高内涵筛选；

Cat. No.	Product Name	Form	Specificity Of Inhibition
CL0061	Histone Methyltransferase inhibitor kit Histone Methyltransferase inhibitor kit
C0084	Magrose Beads NH2 (10-30 μm, Ultra-suspension) 琼脂糖氨基磁珠 (10-30 μm)
C0111	Magrose Beads NTA-Nickel (Ultra-suspension) His-tag 蛋白纯化磁珠 NTA-Ni
CL0088	Angiotensin Receptor inhibitor kit Angiotensin Receptor inhibitor kit
C0086	Magrose Beads COOH (10-30 μm, Ultra-suspension) 琼脂糖羧基磁珠 (10-30 μm)
CL0150	DNA Methyltransferase/Demethylase inhibitor kit DNA Methyltransferase/Demethylase inhibitor kit
CL0077	Reverse Transcriptase inhibitor kit Reverse Transcriptase inhibitor kit
C0079	Magrose Beads OH (10-30 μm, Ultra-suspension) 琼脂糖羟基磁珠 (10-30 μm)
C0095	Magrose Beads Streptavidin (Ultra-suspension) 琼脂糖链霉亲和素磁珠

Cat. No.	Product Name	Target	Signaling Pathways
T3543	NS-638 NS 638	Calcium Channel	Membrane transporter/Ion channel; Metabolism
	NS-638 是一种 Ca2+ 通道阻滞剂，可阻断 K+ 刺激的细胞内 Ca2+ 升高，IC50值为3.4 μM。
T28197	NS-2710 NS2710,NS 2710
	NS-2710, a GABA receptor agonist, is used potentially for the treatment of anxiety.
T8494	NS-3-008 hydrochloride NS-3-008 HCl	Others	Others
	NS-3-008 hydrochloride (NS-3-008 HCl) 是一种口服具有活性的G0s2转录抑制剂(IC50:2.25 μM)。它可用于慢性肾脏疾病的研究。
T16344	NS-2028	Others; Guanylate cyclase	GPCR/G Protein; Others
	NS-2028 是一种高度选择性的可溶性鸟苷酸环化酶抑制剂。它抑制 3-吗啉代-sydnonimine 在人培养的脐静脉内皮细胞中形成环状 GMP，IC50为30mM。它抑制小鼠小脑匀浆和神经元 NO 合酶中的可溶性鸟苷酸环化酶活性，IC50分别为 17 和 20 mM。它可降低血管内皮生长因子诱导的血管生成和通透性。
T4294	NS 11021 NS11021	Potassium Channel	Membrane transporter/Ion channel
	NS 11021 (NS11021) 是特异性 Ca2+激活的大电导 K+(KCa1.1)通道激活剂。当浓度高于0.3 μM 时，它通过平行移动通道激活曲线产生更多负电位，以浓度依赖的方式激活 KCa1.1。
T3102	NS-1619	Apoptosis; Potassium Channel	Apoptosis; Membrane transporter/Ion channel
	NS 1619 是 Ca2+激活的 K+(BK) 通道的激活剂，是一种高效的松弛剂，在血管和其他组织的几个平滑肌中的 EC50约为 10 – 30 μM。它抑制A2780卵巢癌细胞增殖并诱导细胞凋亡。
T7884	NS 1738 NSC 213859	AChR	Neuroscience
	NS 1738 (NSC-213859) 是含有 α7 的神经元烟碱乙酰胆碱受体 (nAChRs) 的正变构调节剂。在卵母细胞实验中，正调节 α7nAChR，EC50为 3.4 μM。
T3214	NS-398 N-(2-cyclohexyloxy-4-nitrophenyl)methane sulfonamide,NS398	COX	Immunology/Inflammation; Neuroscience
	NS-398 (N-(2-cyclohexyloxy-4-nitrophenyl)methane sulfonamide) 是一种非甾体类抗炎剂，具有解热作用，可用于缓解疼痛的研究。它选择性抑制 COX-2的活性，IC50值为 3.8 μM。
T2067	NS11394 NS 11394	GABA Receptor	Membrane transporter/Ion channel; Neuroscience
	NS11394 是可口服GABAA 的阳性变构调节剂 (PAM)，Ki 值为 0.5 nM。它对GABAA 的选择性依次为 α5、α3、α2 和α1 受体，具有抗炎和抗焦虑活性。
T28199	NS9283 NS 9283,NS-9283	AChR	Neuroscience
	NS9283 是有效的(α4)3(β2)2烟碱型ACh 受体的正向变构调节剂。NS9283在一系列神经系统疾病中有研究价值，如注意力缺陷多动障碍、精神分裂症、帕金森病和阿尔茨海默病。
T16348	NS5806 NS-5806	Potassium Channel	Membrane transporter/Ion channel
	NS5806 是钾电流的激活剂，可增加 KV4.3/KChIP2峰值电流幅度，EC50值为 5.3 μM。它会在包含 KChIP2 的通道复合体中降低 KV4.2 和 KV4.3 电流衰减。
T16346	NS1652	Chloride channel	Membrane transporter/Ion channel
	NS1652 是可逆阴离子电导抑制剂，在人和小鼠的红细胞中，可以抑制氯离子通道，IC50值为 1.6 μM。
T3192	NS1643	Potassium Channel; HER; Autophagy	Angiogenesis; Autophagy; JAK/STAT signaling; Membrane transporter/Ion channel; Tyrosine Kinase/Adaptors
	NS1643 是一种有效的人类 ether-a-go-go 相关基因 (hERG) KV11.1 通道激活剂，EC50 为 10.5 μM。它增加了复极保留，展示出新型抗心律失常的方法。它通过减少通道失活，在高浓度下，对 erg2 (Kv11.2) 电流有明显影响。
T12266L2	Ilginatinib hydrochloride NS-018 hydrochloride	Tyrosine Kinases; JAK	Angiogenesis; Chromatin/Epigenetic; JAK/STAT signaling; Stem Cells; Tyrosine Kinase/Adaptors
	Ilginatinib hydrochloride (NS-018 hydrochloride) 是一种可口服的 JAK2强效抑制剂，IC50值为 0.72 nM，对其选择性是对 JAK1、JAK3和 Tyk2 的 46、54 和 22 倍，IC50分别为 33、39 和 22 nM。
T12255	NS19504	Potassium Channel	Membrane transporter/Ion channel
	NS19504 是 Ca2+激活的 K+通道激活剂 (EC50=11.0 µM)，对膀胱平滑肌自发性相位收缩具有松弛作用。
T28196	NS-220 LS-191458,NS 220
	NS-220, a selective agonist of peroxisome proliferator-activated receptor alpha, potently decreases plasma triglyceride and glucose levels and modifies lipoprotein profiles in KK-Ay mice.
T33734	NS 11 NS-11,NS11
	NS 11 is an RGD-nonpeptidic mimetic.
T9542	NS3861	AChR	Neuroscience
	NS3861 是烟碱型乙酰胆碱受体的激动剂，对α3β4 nAChR 具有高亲和力。能够分别与α3β4 (Ki:0.62 nM)、α3β2 (Ki:25 nM)、α4β4 (Ki:7.8 nM)、α4β2 (Ki:55 nM) 结合。
T4612	NS309	EGFR; Potassium Channel; HER	Angiogenesis; JAK/STAT signaling; Membrane transporter/Ion channel; Tyrosine Kinase/Adaptors
	NS309 是选择性钙依赖性钾离子通道 SK/IK 的激活剂，在 BK 通道上没有激活作用。
T22119	NS3694	Apoptosis	Apoptosis
	NS3694 是一种凋亡抑制剂，可抑制凋亡小体形成和半胱天冬酶活化。
T69550	NS-3736
	NS-3736 is a chloride channel inhibitor that has been shown to prevent osteoclastic acidification and resorption.
T16347	NS3623	Potassium Channel	Membrane transporter/Ion channel
	NS3623 是 hERG1 (KV11.1)钾通道激活剂，激活IKr 和Ito 电流，具有抗心律失常作用。NS3623也是 hERG1 通道抑制剂。
T12266L	Ilginatinib maleate NS-018 maleate	Tyrosine Kinases; JAK	Angiogenesis; Chromatin/Epigenetic; JAK/STAT signaling; Stem Cells; Tyrosine Kinase/Adaptors
	Ilginatinib maleate (NS-018 maleate) 是一种可口服的 JAK2强效抑制剂，IC50值为 0.72 nM，对其选择性是对 JAK1、JAK3和 Tyk2 的 46、54 和 22 倍，IC50分别为 33、39 和 22 nM。
T12266	Ilginatinib NS-018	Tyrosine Kinases; JAK	Angiogenesis; Chromatin/Epigenetic; JAK/STAT signaling; Stem Cells; Tyrosine Kinase/Adaptors
	Ilginatinib (NS-018) 是一种可口服的JAK2强效抑制剂，IC50值为 0.72 nM，对其选择性是对 JAK1、JAK3和 Tyk2 的 46、54 和 22 倍，IC50分别为 33、39 和 22 nM。
T1752	NS6180	Potassium Channel	Membrane transporter/Ion channel
	NS6180是一种高效的KCa3.1离子通道选择性抑制剂，IC50值9nM。NS6180阻止T 细胞活化和炎症反应。
T12256	NS8593 hydrochloride NS8593 HCl	Potassium Channel	Membrane transporter/Ion channel
	NS8593 hydrochloride (NS8593 HCl) 是选择性的 SK 通道抑制剂。它可逆抑制 SK3介导的电流，Kd 值为 77 nM。它抑制所有 SK1-3亚型的 Ca2+依赖性 (在 0.5 μM Ca2+时，Kd 分别为 0.42、0.60 和 0.73 μM)，并且不影响中间电导和大电导的钙激活钾通道。
T26364	NS-2359 citrate GSK-372475,GSK 372475 citrate,NS2359,GSK 372475,NS 2359,GSK372475,NS-2359
	NS-2359 is a serotonin-norepinephrine-dopamine reuptake inhibitor.
T37390	NS 6740
	High affinity α7 nAChR partial agonist (Ki = 1.1 nM in rat; Emax < 10% of the response to ACh in rat and human). Inhibits ACh (IC50 = 2.7 nM) at α7 nAChR. Reduces LPS-induced TNF-α release from microglia enriched cultures. Anti-inflammatory. Briggs et al (2009) Role of channel activation in cognitive enhancement mediated by α7 nicotinic acetylcholine receptors. Br.J.Pharmacol. 158 1486 PMID:19845675 \|Thomsen et al (2012) The α7 nicotinic acetylcholine receptor ligands methyllycaconitine, NS674...
T37389	NS 383
	ASIC blocker (IC50 values are 0.44, 2.1 μM and no effect at rat ASIC1a, ASIC3 and ASIC2a, respectively: IC50 value = 0.12 μM at human ASIC1a with no effect at ASIC2a or ASIC3). Inhibition was also observed at heteromeric ASIC channels (IC50 values are 0.79, 0.87 and 4.5 uM at rat ASIC1a+3, ASIC1a+2a and ASIC2a+3; IC5O values are 0.33 and 0.69 uM at human ASIC1a+2a and ASIC1a+3, with no effect at ASIC2a+3). Attenuates pathophysiological nociceptive behaviors in CFA-inflamed and CCI rats.
T38779	NS-102
	NS-102 is a powerful and selective antagonist of the kainate receptor (GluK2), as well as a potent antagonist of the GluR6/7 receptor.
T16732	Reproxalap NS-2,ADX-102	Others	Others
	Reproxalap (NS-2) 是一种活性醛类隔离剂，可用于干眼症的研究。它能够与醛 (包括丙二醛和 4-羟基壬醛) 共价结合。
T29687	Afacifenacin Afacifenacin fumarate,SMP-986,NS 986,NS-986,SMP 986,NS986,SMP986	AChR	Neuroscience
	Afacifenacin (SMP-986) fumarate 是一种 M3 毒蕈碱受体选择性拮抗剂，可用于研究缺血性心脏病，尿失禁和膀胱炎和其他疾病。
T23088	NS 3763	Others	Others
	NS 3763 is a kainate receptor antagonist.
T4009	NS 1209 SPD 502	GluR	Neuroscience
	NS 1209 (SPD 502) 是一种 AMPA 受体拮抗剂。
T3216	Selexipag NS-304,ACT-293987,赛乐西帕,Uptravi	Others; Prostaglandin Receptor	GPCR/G Protein; Immunology/Inflammation; Others
	Selexipag (ACT-293987) 是前列环素受体激动剂，可引起肺血管舒张，用于治疗肺动脉高压。
T16345	NS13001 N-(4-chlorophenyl)-2-(3,5-dimethylpyrazol-1-yl)-9-methylpurin-6-amine,N-(4-Chlorophenyl)-2-(3,5-dimethyl-1H-pyrazol-1-yl)-9-methyl-9H-purin-6-amine	Potassium Channel	Membrane transporter/Ion channel
	NS13001 (N-(4-Chlorophenyl)-2-(3,5-dimethyl-1H-pyrazol-1-yl)-9-methyl-9H-purin-6-amine) 是口服有效的 SK 通道选择性正向变构调节剂。NS13001 对 SK2 和 SK3 通道的 EC50分别为 1.8 μM 和 0.14 μM。NS13001 在脊髓小脑共济失调 2 型和其他小脑共济失调方面具有研究价值。
T6311	Bafetinib NS-187,巴氟替尼,INNO-406	Bcr-Abl; Src; Autophagy	Angiogenesis; Autophagy; Cytoskeletal Signaling; Tyrosine Kinase/Adaptors
	Bafetinib (INNO-406) 是一种特异性双重 Bcr-Abl/Lyn 抑制剂，IC50值为5.8和19 nM。
T33735	NS-1231
	NS-1231 exhibits neurotrophic-like effects in vitro and in vivo.
T69747	NS-3956 free base
	NS-3956 free base is a partial nAChR α4β2 LS and HS agonist with analgesic properties.
T5520L	Cetrorelix diacetate NS-75A,醋酸西曲瑞克,SB-075 acetate,SB-075 diacetate,Cetrorelix acetate,NS-75A diacetate	GNRH Receptor	GPCR/G Protein
	Cetrorelix diacetate (NS-75A) 是GnRH 受体的强效拮抗剂(IC50:1.21 nM)。
T69746	NS-3956 fumaric acid salt
	NS-3956 fumaric acid salt is a partial nAChR α4β2 LS and HS agonist with analgesic properties.
T6481	Droxinostat NS 41080,4-(4-氯-2-甲基苯氧基)-N-羟基丁酰胺	Apoptosis; HDAC	Apoptosis; Chromatin/Epigenetic; DNA Damage/DNA Repair
	Droxinostat (NS 41080) 是HDAC3、HDAC6和HDAC8抑制剂，IC50分别为16.9、2.47和1.46 μM。
T71486	NS-0011
	NS-0011 is an inhibitor of CDK5 translocation which increases CDK5 accumulation in the nucleus, suppressing both cancer cell proliferation and xenograft tumorigenesis.
T73572	NS-8
	NS-8，一种吡咯衍生物，能够激活Ca2+-敏感的K+通道。通过降低盆腔传入神经活动，NS-8有助于抑制排尿反射，适用于尿频与尿失禁的研究。
T28198	NS5818 NS-5818,NS 5818
	NS5818 inhibits ClC.
T28195	NS004 NS 004,NS-004
	NS004 is a large-conductance K+ channel opener, it inhibits mitochondrial function in glioma cells.
T24547	NS4591 NS 4591,NS-4591
	NS4591 is a modulator of SK-IK channels.
T28951	Tesofensine NS 2330,NS2330,NS-2330
	Tesofensine, a serotonin–noradrenaline–dopamine reuptake inhibitor, is used potentially for the treatment of obesity.
T15233	Endovion NS3728	Chloride channel	Membrane transporter/Ion channel
	Endovion (NS3728) 是阴离子通道抑制剂和 Anoctamin-1 (ANO 1) 通道抑制剂，也是特异性的 VRAC/VSOAC 阻断剂。
T26361	Brasofensine sulfate NS 2214,BMS 204756,NS2214,NS-2214,BMS-204756
	Brasofensine sulfate is a dopamine reuptake inhibitor.

Cat. No.	Product Name	Target	Signaling Pathways
T13626	Cottonseed oil	Others	Others
	Cottonseed oil 是一种提取自棉花种子中的食用油，是一种植物油中杀虫能力极强的油。
TN2282	trans-Stilbene 反式-1,2二苯乙烯,1,2-Diphenylethylene (trans),(E)-Stilbene	Others	Others
	trans-Stilbene (1,2-Diphenylethylene (trans)) 可用于制备荧光增白剂、染料激光器、非甾体合成雌激素。
T5256	All-trans-retinal 视黄醛,All trans-Retinal,Retinaldehyde,Vitamin A aldehyde	Others; Endogenous Metabolite	Metabolism; Others
	All-trans-retinal (Vitamin A aldehyde) 是视网膜中维生素A 代谢物之一。生理条件下，它再生为视觉发色团，11-顺式-视黄醛。
TCS1554	trans-Benzylideneacetone 反式苯亚甲基丙酮,Acetocinnamone,亚苄基丙酮	Phospholipase	Metabolism
	trans-Benzylideneacetone (Acetocinnamone) 是一种革兰氏阴性致病性线虫细菌嗜线虫(Xenorhabdus nematophila) 的代谢产物，是一种针对磷脂酶 A2 (PLA2) 的酶抑制剂，也是一种免疫抑制剂。
TN6930	5-Desmethylsinensetin	Others	Others
	5-desmethylsinensetin 是分离自Stevia satureiifoliavar.satureiifolia 的天然产物，显示出抗原生动物的活性，抑制T. cruzi epimastigotes 和trypomastigotes 的IC50分别为 0.4 μg/mL 和75.1 μg/mL。
T3812	(20R)-Ginsenoside Rg3 人参皂甙 RG3,(20R)-人参皂苷Rg3,20(R)-Ginsenoside Rg3,(20R)Ginsenoside Rg3,20(R)-Propanaxadiol	Others	Others
	(20R)-Ginsenoside Rg3 (20(R)-Propanaxadiol) 是一种人参根中的化合物，具有抑制血管内皮细胞增生（IC50= 10 nM）和抗肿瘤作用。
T36473	trans-Nerolidol
	trans-Nerolidol is a sesquiterpene that has been found in various plants, includingC. sativa, and has diverse biological activities, including antimicrobial, antioxidant, anticancer, and insecticidal properties.1,2,3,4In a disc assay,trans-nerolidol inhibits the growth ofS. aureus,B. subtilis,E. coli, andS. cerevisiaewith zones of inhibition measuring 10, 9, 10, and 4 mm, respectively.2It reduces viability of CaCo-2 adenocarcinoma cells with an IC50value of 28.7 mg/L and reduces production of re...
T22262	Ansamitocin p-3 Maytansinol isobutyrate,Antibiotic C 15003P3,NSC292222	Microtubule Associated	Cytoskeletal Signaling
	Ansamitocin p-3 (Maytansinol isobutyrate) 是一种微管抑制剂，对微管蛋白聚合的 IC50 为 3.4 μM。
TN1117	Veraguensin	p38 MAPK; NF-κB; Antibiotic; Parasite; Antifection	MAPK; Microbiology/Virology; NF-κB
	Veraguensin 来源于 Magnolia sp.。 Veraguensin 抑制骨吸收并显示出高抗寄生虫活性。
T7408	all-trans-4-Oxoretinoic acid 4-KETO全反式维甲酸,all-trans 4-Keto Retinoic Acid	Endogenous Metabolite	Metabolism
	all-trans-4-Oxoretinoic acid (all-trans 4-Keto Retinoic Acid) 是一种维生素A 的特性代谢物，能够通过作用核维甲酸受体(RARs) 来诱导基因转录。
T3920	Pseudoginsenoside F11 Ginsenoside A1,拟人参皂苷 F11,拟人参皂苷F11	Others; Endogenous Metabolite	Metabolism; Others
	Pseudoginsenoside F11 (Ginsenoside A1) 从人参根和叶中分离得到。PF11在一系列心血管和中枢神经系统疾病中具有广泛的保护作用。
TN2100	Pratensein 红车轴草素,三叶草	Others; NF-κB	NF-κB; Others
	Pratensein 是黄酮类化合物，能够减少氧化损伤和恢复突触和 BDNF 水平，改善 β-淀粉样蛋白诱导的大鼠认知障碍。
T6S1587	Notoginsenoside R2 三七皂苷R2,20(S)-Notoginsenoside R2,Ginsenoside Ng-R2	Others; Nrf2	Immunology/Inflammation; Others
	Notoginsenoside R2 (20(S)-Notoginsenoside R2) 是一种新分离三七皂苷，表现出对6-OHDA 诱导的氧化应激及细胞凋亡的保护作用。
TN4618	N-trans-Sinapoyltyramine	Others	Others
	N-trans-Sinapoyltyramine 对 HeLa 人癌细胞系表现出强烈的选择性细胞毒性，IC50 值为 9.77 ± 1.25 μm。
T3S1589	Notoginsenoside Fa	Others	Others
	Notoginsenoside Fa 是一种原人参二醇型皂苷，从P. notoginseng 提取出来得到，有激活和恢复退化脑功能的潜能。
TN6733	Kansuiphorin C KPC,甘遂大戟萜酯C	Others	Others
	Kansuiphorin C (KPC) 是一种具有多种生物活性的天然产物。它能够调节肠道菌群及相关代谢功能，并可以改善恶性腹水。
T38141	Glycerophospholipids, cephalins Phosphatidylethanolamines (egg)
	Glycerophospholipids, cephalins (Phosphatidylethanolamines (egg)) 是一种从鸡蛋中分离出来的磷脂酰乙醇胺的混合物，在 sn-1和 sn-2位置有各种脂肪酰基。Glycerophospholipids, cephalins 完全水解可得到1mol 的甘油、磷酸、乙醇胺和2mol 的脂肪酸。Phosphatidylethanolamines 在膜融合和细胞分裂过程中收缩环的拆卸中起作用，可调节膜的弯曲度。Phosphatidylethanolamines 能够在没有任何蛋白质或核酸的帮助下传播传染性朊病毒。Phosphatidylethanolamines 在细菌膜中的主要作用之一是分散由阴离子膜磷脂引起的负电荷。
T6S1495	Ginsenoside Rk3 人参皂苷Rk3,人参皂甙 Rk3	Others; NF-κB	NF-κB; Others
	Ginsenoside Rk3 是存在于 Panax notoginseng 的根中。它能够抑制 HepG2 细胞中 TNF-α 诱导的 NF-κB 转录活性，IC50=14.24±1.30 μM。
T8626	Transtorine 1,4-DIHYDRO-4-OXOQUINOLINE-2-CARBOXYLIC ACID,1,4-二氢-4-氧代喹啉-2-羧酸	GluR; NMDAR	Neuroscience
	Transtorine (1,4-DIHYDRO-4-OXOQUINOLINE-2-CARBOXYLIC ACID) 是一种 GluR 和 NMDA 抑制剂。
T3227	Danshensu Salvianic acid A,Dan shen suan A,丹参素	Apoptosis; Nrf2; Autophagy	Apoptosis; Autophagy; Immunology/Inflammation
	Danshensu (Dan shen suan A) 是丹参的有效成分，能够激活 Nrf2信号通路，具有保护心血管作用。
T3915	Ginsenoside Ro 人参皂苷Ro,Chikusetsusaponin 5,Polysciasaponin P3,人参皂苷 Ro,Chikusetsusaponin V	Calcium Channel; Reductase; Prostaglandin Receptor	Endocrinology/Hormones; GPCR/G Protein; Immunology/Inflammation; Membrane transporter/Ion channel; Metabolism
	Ginsenoside Ro (Chikusetsusaponin V) 能降低 TXA2产量，较弱降低 COX-1 和 TXAS 活性，具有 Ca2+拮抗剂的抗血小板作用，IC50为 155 μM。
T3S0013	Ethyl trans-caffeate 咖啡酸乙酯,Ethyl caffeate,Caffeic Acid Ethyl Ester	Others	Others
	Ethyl trans-caffeate (Caffeic Acid Ethyl Ester) 具有抗炎作用。它是一种有前途的天然化合物，未来在慢性肝病中的应用。它是一种有效的化学预防化合物，可防止因太阳紫外线照射引起的皮肤癌变。它是与人胰腺α-淀粉酶复合的代表性抑制剂的高分辨率结构。它强烈抑制 JB6 Cl41细胞的肿瘤转化，无毒性。 PI3K、ERK1/2 和 p38 激酶活性在体外通过与 HOEC 直接结合而受到抑制。
T2961	Notoginsenoside R1 Sanqi glucoside R1,Sanchinoside R1,三七皂苷R1	Apoptosis; ERK; Beta Amyloid	Apoptosis; MAPK; Neuroscience
	Notoginsenoside R1 (Sanchinoside R1) 是一种从三七中分离出来的皂苷，具有抗氧化、抗炎、抗血管生成和抗凋亡的活性。它有神经保护和抗缺血/再灌注损伤的心脏保护作用。
T4704	L-Anserine nitrate L-鹅肌肽硝酸盐,L-Anserine nitrate salt	Others; Endogenous Metabolite	Metabolism; Others
	L-Anserine nitrate (L-Anserine nitrate salt) 是一种存在于大多数动物组织中的二肽。在模型系统中，它是一种有效的抗氧化剂和羟基自由基清除剂。该化合物抑制醛糖和酮糖还原糖诱导的非酶蛋白糖基化。
T3813	20(R)-Ginsenoside Rh2 20(R)-人参皂苷 RH2,(20R)Ginsenoside Rh2,Ginsenoside Rh2,20(R)-人参皂苷Rh2	Apoptosis; MMP; HSV	Apoptosis; Microbiology/Virology; Proteases/Proteasome
	20(R)-Ginsenoside Rh2 (Ginsenoside Rh2) 是人参皂苷 Rh2 的次要立体异构体，具有基质金属蛋白酶抑制作用。它有抗癌、抗炎和抗氧化活性。
T4S0227	Sinensetin Pedalitin permethyl ether,甜橙素	TNF; PGE Synthase	Apoptosis; Immunology/Inflammation
	Sinensetin (Pedalitin permethyl ether) 是从水果中发现的一种甲基化黄酮，有很强的抗血管和抗炎症的能力。
T7154	trans-trans-Muconic acid	Endogenous Metabolite	Metabolism
	trans-trans-Muconic acid 是苯的尿代谢物，能够被用作人体暴露于苯的生物标志物。
T3402	20(S)-Ginsenoside Rg3 20(S)-人参皂苷 Rg3,人参皂苷 Rg3,20(S)-Ginsenoside-Rg3,Rg3,20S-Ginsenoside Rg3,Ginsenoside Rg3,S-Ginsenoside Rg3	EGFR; Beta Amyloid; Potassium Channel; NF-κB; COX; Sodium Channel; Endogenous Metabolite	Angiogenesis; Immunology/Inflammation; JAK/STAT signaling; Membrane transporter/Ion channel; Metabolism; Neuroscience; NF-κB; Tyrosine Kinase/Adaptors
	20(S)-Ginsenoside Rg3 (Rg3) 是红参的主要成分，通过抑制肿瘤细胞的粘附和侵袭来抑制肿瘤细胞肺转移。它抑制Na+和hKv1.4通道，IC50分别为 32.2±4.5 和 32.6±2.2 μM。它还抑制Aβ，NF-κB 活性和COX-2表达，抑制人脐静脉内皮细胞的增殖并具有抗血管生成活性。
T0783	Mianserin hydrochloride Mianserin HCl,Org GB 94,盐酸米安色林,ORG GB-94 HCl	Dopamine Receptor; 5-HT Receptor; Opioid Receptor; Adrenergic Receptor; Histamine Receptor	Endocrinology/Hormones; GPCR/G Protein; Immunology/Inflammation; Neuroscience
	Mianserin hydrochloride (Org GB 94) 是一种有抗抑郁活性的 H1 受体反向激动剂。
TMS2181	trans-Zeatin (E)-Zeatin,玉米素	ERK; MEK; Endogenous Metabolite	MAPK; Metabolism
	trans-Zeatin ((E)-Zeatin) 是植物细胞分裂素，可抑制紫外线诱导的MEK/ERK 的活化，在细胞生长、分化和分裂中起着重要的作用。
T3330	trans-Trimethoxyresveratrol trans-trismethoxy Resveratrol,E-Resveratrol Trimethyl Ether,MR-3,Tri-O-methylresveratrol,白藜芦醇三甲醚,3,4',5-Trimethoxy-trans-stilbene,Trimethoxystilbene	Reactive Oxygen Species	Immunology/Inflammation; Metabolism; NF-κB
	trans-Trimethoxyresveratrol (MR-3) 是一种 Resveratrol(RSV) 的衍生物，与Resveratrol(RSV)相比，它可能是一个更有效的抗炎、抗血管新生的化合物。
TN2245	Sunset Yellow FCF Food Yellow 3,Orange Yellow S,Sunset yellow,CI 15985	Androgen Receptor	Endocrinology/Hormones
	Sunset Yellow FCF (Sunset yellow) 是一种橙色偶氮染料，吸光度具有pH 依赖性。Sunset Yellow FCF 可在食品，化妆品和药品中使用，在许多食品中用作着色剂食品添加剂，它们可能具有细胞毒性和遗传毒性，因此在使用这些材料作为食品添加剂时必须小心。
TN1970	N-trans-p-coumaroyloctopamine N-p-Coumaroyloctopamine,N-对香豆酰真蛸胺,p-coumaroylnoradrenaline	Others	Others
	N-trans-p-coumaroyloctopamine (p-coumaroylnoradrenaline) 来源于马铃薯的块茎组织。
T3829	Ginsenoside F3 人参皂苷F3	Others; IFNAR; Interleukin	Immunology/Inflammation; Others
	Ginsenoside F3 是一种皂苷，提取自Panax ginseng 叶片。它能够调节1 型 (IL-2, IFN-γ) 及 2 型细胞因子(IL-4 and IL-10) 的产生和表达，有免疫增强的作用。
T64744	Ovalbumins	Endogenous Metabolite	Metabolism
	Ovalbumins 是蛋清中的主要蛋白质。Ovalbumins 具有多种生物活性，如降压、抗菌、抗癌、抗氧化和免疫调节活性。Ovalbumins 是雌激素或孕酮处理的输卵管中合成的丰富的蛋白质。Ovalbumins 通常用作研究激素控制该组织中基因表达的标志物。
T2814	Cryptotanshinone 隐丹参酮,Cryptotanshinon,Tanshinone c,隐丹参醌	STAT; Autophagy	Autophagy; JAK/STAT signaling; Stem Cells
	Cryptotanshinone (Cryptotanshinon) 是从丹参的根中提取的一种天然产物，抑制STAT3的IC50为4.6 μM，具有抗肿瘤活性。
T16016	Maytansinol 美登醇,Ansamitocin P-0	Apoptosis; Microtubule Associated	Apoptosis; Cytoskeletal Signaling
	Maytansinol (Ansamitocin P-0) 在体外抑制微管组装并导致微管分解。它与辐射联用，用于果蝇和人类癌细胞。
T11398	Ginsenoside Ra3 人参皂苷 RA3,人参皂苷RA3	Others	Others
	Ginsenoside Ra3 是分离自人参中，具有抗癌作用。
T4987	NSC 42196 Calcium α-D-heptagluconate hydrate,葡庚糖酸钙水合物,Calcium glucoheptonate	Others; Endogenous Metabolite	Metabolism; Others
	NSC 42196 (Calcium glucoheptonate) 是内源性代谢产物的一种。
T3918	Ginsenoside Rb3 人参皂苷 Rb3,Gypenoside IV,人参皂苷Rb3	NF-κB; COX; NO Synthase	Immunology/Inflammation; Neuroscience; NF-κB
	Ginsenoside Rb3 (Gypenoside IV) 是从三七中提取的一种天然产物。它在 293T 细胞系中抑制 TNFα 诱导的NF-κB 转录活性，IC50为 8.2 μM。它还抑制COX-2和iNOSmRNA 的诱导。
T3830	20(R)-Ginsenoside Rg2 20R-Ginsenoside Rg2,20R-人参皂苷Rg2,20(R)-人参皂苷 Rg2	IL Receptor	Immunology/Inflammation
	20(R)-Ginsenoside Rg2 (20R-Ginsenoside Rg2) 是一种人参皂苷。它能够抑制肺癌 NCI-H1650 细胞，具有抗癌作用。
T2873	Ginsenoside Rg2 Chikusetsusaponin I,Panaxoside Rg2,人参皂苷Rg2,Prosapogenin C2,(20S)Ginsenoside Rg2,人参皂苷 Rg2	Beta Amyloid; GSK-3; NF-κB	Neuroscience; NF-κB; PI3K/Akt/mTOR signaling; Stem Cells
	Ginsenoside Rg2 (Chikusetsusaponin I) 是一种人参的主要活性成分。它能够降低Aβ1-42积聚，抑制脂多糖介导的VCAM-1和ICAM-1表达的增加。
T2822	Ginsenoside Rb1 Gypenoside Ⅲ,人参皂苷Rb1,人参皂苷 Rb1,Gypenoside III	ATPase; Mitophagy; IRAK; NF-κB; Autophagy; HSV	Autophagy; Immunology/Inflammation; Membrane transporter/Ion channel; Microbiology/Virology; NF-κB
	Ginsenoside Rb1 (Gypenoside Ⅲ) 是中药人参的成分，可能具有抑制或阻止肿瘤生长的特性。
T0762	Trans-Anethole 茴香烯,(E)-Anethole,4-Propenylanisole	Others; Endogenous Metabolite	Metabolism; Others
	Trans-Anethole ((E)-Anethole) 是一种从Pimpinella 分离得到的苯丙烯衍生物，是茴香、桃金娘、甘草、樟脑等植物中重要气味的组成部分。它在肿瘤细胞系中，低浓度下有雌激素特性，而在高浓度下具有细胞毒性。
T2959	Ginsenoside Rh2 20(S)-Rh2,20S-Ginsenoside Rh2,人参皂苷Rh2,20(S)-Ginsenoside Rh2,人参皂苷 Rh2	Apoptosis; EGFR; Caspase; Endogenous Metabolite	Angiogenesis; Apoptosis; JAK/STAT signaling; Metabolism; Proteases/Proteasome; Tyrosine Kinase/Adaptors
	Ginsenoside Rh2 (20(S)-Ginsenoside Rh2) 诱导caspase-8和caspase-9活化。它以多途径方式诱导癌细胞凋亡。
T5S1103	Isoliensinine 异莲心碱,Isoliensinin	Apoptosis; Antioxidant	Apoptosis; oxidation-reduction
	Isoliensinine (Isoliensinin) 是从水芙蓉种子胚中提取的一种双苄基异喹啉生物碱，能诱导三阴性乳腺癌细胞凋亡，具有抗氧化、抗炎、抗癌活性。
T6S1485	Ginsenoside Rh4 人参皂苷Rh4	Others	Others
	Ginsenoside Rh4 可以安全地用作佐剂，具有低溶血作用或无溶血作用。它具有细胞毒活性，其苷元对癌细胞系具有杀伤作用。
T21651	Lansoprazole sodium 兰索拉唑钠,Lansoprazole (sodium), AG-1749 sodium	Proton pump; Phospholipase; Antibacterial	Membrane transporter/Ion channel; Metabolism; Microbiology/Virology
	Lansoprazole sodium (Lansoprazole (sodium)) 是一种质子泵抑制剂，是中性鞘磷脂酶的外泌体抑制剂，能抑制胃酸生成。
TN5028	Sinensin ZINC38908691	Others	Others
	Sinensin 是一种来自 Cudrania cochinchinensis 的草本植物中的类黄酮。
T7883	Proanthocyanidins Procyanidin	Antibacterial; Antifungal	Microbiology/Virology
	Proanthocyanidins 是一类在高等植物中广泛分布的多酚化合物，用作抗氧化剂和抗癌剂。它可研究慢性静脉功能不全、毛细血管脆弱、晒伤和视网膜病变，有抗炎、抗菌、抗真菌和保护心脏的特性。
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Cat. No.	Product Name	Species	Expression System
TMPH-03487	DNA-binding protein H-NS Protein, SerRatia marcescens, Recombinant (His) hnsA,hns,Histone-like protein HLP-II,DNA-b...	Serratia marcescens	E. coli
	A DNA-binding protein implicated in transcriptional repression and chromosome organization and compaction. Binds nucleation sites in AT-rich DNA and bridges them, forming higher-order nucleoprotein complexes and condensing the chromosome. As many horizontally transferred genes are AT-rich, it plays a central role in silencing foreign genes. A subset of genes are repressed by H-NS in association with other proteins. DNA-binding protein H-NS Protein, SerRatia marcescens, Recombinant (His) is expre...
TMPH-00616	DNA-binding protein H-NS Protein, E. coli, Recombinant (His) hns,DNA-binding protein H-NS,Protein B1,Pr...	E. coli	E. coli
	A DNA-binding protein implicated in transcriptional repression (silencing). Also involved in bacterial chromosome organization and compaction. H-NS binds tightly to AT-rich dsDNA and inhibits transcription. Binds upstream and downstream of initiating RNA polymerase, trapping it in a loop and preventing transcription. Binds to hundreds of sites, approximately half its binding sites are in non-coding DNA, which only accounts for about 10% of the genome. Many of these loci were horizontally transfe...
TMPY-01888	KRAS Protein,Human, Recombinant (Q61H, His) KRAS2,C-K-RAS,Kirsten rat sarcoma viral oncogene homolog,K-R...	Human	E. coli
	KRAS Protein,Human, Recombinant (Q61H, His) is expressed in E. coli expression system with His tag. The predicted molecular weight is 22.5 kDa and the accession number is P01116-2.
TMPY-04116	KRAS Protein,Human,Recombinant(G12C & Q61H, His) NS,CFC2,K-RAS4B,C-K-RAS,KRAS2,K-RAS2B,K-RAS,Kirsten...	Human	E. coli
	KRAS Protein,Human,Recombinant(G12C & Q61H, His) is expressed in E. coli expression system with His tag. The predicted molecular weight is 23.3 kDa and the accession number is P01116-2.
TMPY-06056	KRAS Protein, Human, Recombinant (G12D, His) KRAS1,K-RAS4B,Kirsten rat sarcoma viral oncogene homolog,RAL...	Human	E. coli
	KRAS Protein, Human, Recombinant (G12D, His) is expressed in E. coli expression system with His tag. The predicted molecular weight is 22 kDa and the accession number is P01116-2.
TMPY-04113	KRAS Protein,Human,Recombinant(G12D & Q61H, His) Kirsten rat sarcoma viral oncogene homolog,KRAS2,KI-RAS,RASK...	Human	E. coli
	KRAS Protein,Human,Recombinant(G12D & Q61H, His) is expressed in E. coli expression system with His tag. The predicted molecular weight is 23.3 kDa and the accession number is P01116-2.
TMPY-00323	Hepatitis C virus (HCV-1a) NS3 protease/helicase immunodominant region Protein (aa 1356-1459, GST) NS3	HCV	E. coli
	HCV NS3 displays three enzymatic activities: serine protease, NTPase, and RNA helicase. HCV NS3 serine protease, in association with NS4A, is responsible for the cleavages of NS3-NS4A, NS4A-NS4B, NS4B-NS5A, and NS5A-NS5B. HCV NS3 RNA helicase binds to RNA and unwinds dsRNA in the 3' to 5' direction, and likely RNA stable secondary structure in the template strand (By similarity). Cleaves and inhibits the host antiviral protein MAVS. NS3/NS4A complex also prevents phosphorylation of human IRF3, t...
TMPY-02628	Neuroserpin Protein, Mouse, Recombinant (His) PI12,serpin peptidase inhibitor, clade I (neuroserpin), memb...	Mouse	HEK293 Cells
	Neuroserpin Protein, Mouse, Recombinant (His) is expressed in HEK293 mammalian cells with His tag. The predicted molecular weight is 46 kDa and the accession number is O35684.
TMPY-04870	Zika virus (ZIKV) (strain Zika SPH2015) ZIKV-NS1 protein (His)	ZIKV	HEK293 Cells
	Zika virus NS1 antigen is one of seven non-structural proteins. NS1 is involved in RNA replication. The possible effects of NS1 on hosts include: localizes to host cell surface and secreted extracellularly, modulates signalling of the innate immune system, has possible damages to platelets and endothelial cells through anti-NS1 antibodies.
TMPY-00052	Dengue virus (DENV) (type 2, strain New Guinea C) NS1 Protein (His) DENV-NS1	DENV	HEK293 Cells
	Dengue virus (DENV) (type 2, strain New Guinea C) NS1 Protein (His) is expressed in HEK293 mammalian cells with His tag. The predicted molecular weight is 42.3 kDa and the accession number is AAC59275.1.
TMPY-06345	KRAS Protein, Human, Recombinant (His & Avi), Biotinylated RASK2,K-RAS2A,RALD,C-K-RAS,NS3,Kirsten rat sarcoma ...	Human	E. coli
	KRAS Protein, Human, Recombinant (His & Avi), Biotinylated is expressed in E. coli expression system with His and Avi tag. The predicted molecular weight is 23.78 kDa and the accession number is P01116-2.
TMPY-06138	KRAS Protein, Human, Recombinant (61Q, His) Kirsten rat sarcoma viral oncogene homolog,K-RAS2B,NS	Human	E. coli
	KRAS Protein, Human, Recombinant (61Q, His) is expressed in E. coli expression system with His tag. The predicted molecular weight is 21.9 kDa and the accession number is P01116-2.
TMPY-04903	Dengue virus (DENV) (type 3, strain Philippines/H87/1956) NS1 Protein (His) DENV-NS1	DENV	HEK293 Cells
	Dengue virus (DENV) (type 3, strain Philippines/H87/1956) NS1 Protein (His) is expressed in HEK293 mammalian cells with His tag. The predicted molecular weight is 42.1 kDa and the accession number is AAA99437.1.
TMPH-01849	Human parvovirus B19 (isolate AU) Non-capsid protein NS-1 (His & SUMO)	HPV B19	E. coli
	Human parvovirus B19 (isolate AU) Non-capsid protein NS-1 (His & SUMO) is expressed in E. coli expression system with N-6xHis-SUMO tag. The predicted molecular weight is 44.6 kDa and the accession number is P07298.
TMPU-00001	KRAS Protein, Human, Recombinant (G12S, GST) NS,C-K-RAS,K-RAS2A,KRAS1,K-RAS2B,KRAS2,K-RAS4A,CFC2...	Human	E. coli
	KRAS Protein, Human, Recombinant (G12S, GST) is expressed in E. coli expression system with GST tag. The accession number is P01116.
TMPY-02219	Influenza A H1N1 (A/Puerto Rico/8/34/Mount Sinai) Non-structural/NS1 Protein (His) NS1 Protein	H1N1	E. coli
	The NS1 Influenza protein is created by the internal protein-encoding, linear negative-sense, single-stranded RNA, NS gene segment and which also codes for the nuclear export protein or NEP, formerly referred to as the NS2 protein, which mediates the export of vRNPs. The non-structural (NS1) protein is found in Influenzavirus A, Influenzavirus B, and Influenzavirus C. The non-structural (NS1) protein of the highly pathogenic avian H5N1 viruses circulating in poultry and waterfowl in Southeast As...
TMPK-01405	HLA-A*11:01&B2M&KRAS G12V (VVVGAVGVGK) Monomer Protein, Human, MHC (E. coli, His & Avi) KI-RAS,RASK2,K-Ras 2,MHC,KRAS,KRAS1,NS3,K-RAS2A,K-R...	Human	E. coli
	Kirsten rat sarcoma 2 viral oncogene homolog (KRAS) is the most commonly mutated oncogene in human cancer. The developments of many cancers depend on sustained expression and signaling of KRAS, which makes KRAS a high-priority therapeutic target. The virtual screening approach to discover novel KRAS inhibitors and synthetic lethality interactors of KRAS are discussed in detail.
TMPK-01428	HLA-A*11:01&B2M&KRAS G12D (VVGADGVGK) Monomer Protein, Human, MHC (His & Avi) CFC2,K-RAS4B,K-Ras 2,C-K-RAS,RASK2,NS3,RALD,KI-RAS,...	Human	E. coli
	Kirsten rat sarcoma 2 viral oncogene homolog (KRAS) is the most commonly mutated oncogene in human cancer. The developments of many cancers depend on sustained expression and signaling of KRAS, which makes KRAS a high-priority therapeutic target. The virtual screening approach to discover novel KRAS inhibitors and synthetic lethality interactors of KRAS are discussed in detail.
TMPK-01443	HLA-A*11:01&B2M&KRAS G12V (VVVGAVGVGK) Monomer Protein, Human, MHC (His & Avi), FITC-Labeled KRAS1,C-K-RAS,K-RAS4B,RALD,K-Ras 2,K-RAS2A,K-RAS2B,KRAS2,	Human	HEK293 Cells
	Kirsten rat sarcoma 2 viral oncogene homolog (KRAS) is the most commonly mutated oncogene in human cancer. The developments of many cancers depend on sustained expression and signaling of KRAS, which makes KRAS a high-priority therapeutic target. The virtual screening approach to discover novel KRAS inhibitors and synthetic lethality interactors of KRAS are discussed in detail.
TMPK-01450	HLA-C*03:04&B2M&KRAS G12D (GADGVGKSAL) Monomer Protein, Human, MHC (His & Avi), Biotinylated KRAS1,MHC,K-RAS4B,KRAS,CFC2,K-RAS2B,K-Ras 2,C-K-RAS,RASK2,K-...	Human	HEK293 Cells
	Kirsten rat sarcoma 2 viral oncogene homolog (KRAS) is the most commonly mutated oncogene in human cancer. The developments of many cancers depend on sustained expression and signaling of KRAS, which makes KRAS a high-priority therapeutic target. The virtual screening approach to discover novel KRAS inhibitors and synthetic lethality interactors of KRAS are discussed in detail.

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