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Search Results for " hepatocellular carcinoma "

92

抑制剂 & 化合物

38

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Cat. No.	Product Name	Target	Signaling Pathways
T22661	CHM-1	Apoptosis; Others; Microtubule Associated	Apoptosis; Cytoskeletal Signaling; Others
	CHM-1 是细胞凋亡的诱导剂，通过激活 Cdc2 激酶活性在人肝细胞癌中显示出有效的抗肿瘤能力。 CHM-1 在体外和体内抑制微管蛋白聚合。
T22830	GYY4137 GYY 4137 morpholine salt	Others	Others
	GYY4137 (GYY 4137 morpholine salt) 是一种缓释H2S 供体，具有抗炎和抗癌作用，也具有血管扩张和抗高血压活性。
T7008	Vacquinol-1 Vacquinol 1	JNK	MAPK
	Vacquinol-1 能够激活 MAPK 通路，是MKK4特异性激活剂。它可以诱导肝细胞癌细胞凋亡，在多形性胶质母细胞瘤小鼠模型中特异性诱导人胶质母细胞瘤细胞死亡、减缓肿瘤进展并延长生存期。
T1785	Palbociclib PD 0332991,帕博西尼,帕布昔利布	CDK	Cell Cycle/Checkpoint
	Palbociclib (PD 0332991) 是一种 CDK 抑制剂，抑制 CDK4 和 CDK6 (IC50=11/16 nM)，具有口服活性。Palbociclib 具有抗肿瘤活性，有用于 ER 阳性和 HER2 阴性乳腺癌的研究潜力。
T0334	Rosiglitazone BRL49653,罗格列酮	Ferroptosis; TRP/TRPV Channel; PPAR; Autophagy	Apoptosis; Autophagy; DNA Damage/DNA Repair; Membrane transporter/Ion channel; Metabolism
	Rosiglitazone (BRL49653) 是一种 PPARγ 激动剂、TRPC5 激活剂和 TRPM3 抑制剂，具有口服活性。Rosiglitazone 也是一种降糖剂，是噻唑烷二酮类胰岛素增敏剂。
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。
T22443	Triglycidyl isocyanurate Tris(2,3-epoxypropyl) Isocyanurate,Teroxirone,TGIC,1,3,5-三缩水甘油-S-三嗪三酮,TGI	Apoptosis	Apoptosis
	Triglycidyl isocyanurate (Teroxirone) 是一种三氮烯三环氧化合物，可通过 p53的激活抑制非小细胞肺癌细胞的生长。它诱导细胞凋亡，具有抗血管生成和抗肿瘤活性，用于癌症研究。
T9945	MNK8 3-methyl-6-(naphthalen-1-yl)pyrimidine-2,4(1H,3H)-dione	STAT	JAK/STAT signaling; Stem Cells
	MNK8 (3-methyl-6-(naphthalen-1-yl)pyrimidine-2,4(1H,3H)-dione) 是一种有效的STAT3抑制剂，降低STAT3与DNA 结合的能力，对肝癌细胞也有良好的生长抑制作用。
T6646	Rosiglitazone hydrochloride 盐酸罗格列酮,BRL-49653 HCl,Rosiglitazone HCl	Ferroptosis; TRP/TRPV Channel; PPAR; Autophagy	Apoptosis; Autophagy; DNA Damage/DNA Repair; Membrane transporter/Ion channel; Metabolism
	Rosiglitazone hydrochloride (BRL-49653 HCl) 是一种降血糖药物，通过与脂肪细胞中的 PPAR 受体结合来刺激胰岛素分泌。它对 PPARγ1、PPARγ2 和 PPARγ 的EC50值分别为 30 nM、100 nM 和 60 nM。它也是TRPC5的激活剂和TRPM3的抑制剂。
T6239	Palbociclib monohydrochloride PD 0332991 hydrochloride,Palbociclib hydrochloride,帕布昔利布盐酸盐,Palbociclib (PD-0332991) HCl	CDK	Cell Cycle/Checkpoint
	Palbociclib monohydrochloride (PD 0332991 hydrochloride) 是一种口服的细胞周期蛋白依赖性激酶 (CDK) 抑制剂，具有潜在的抗肿瘤活性。它抑制 CDK4和 CDK6，IC50分别为11 nM，16 nM。它有用于 ER 阳性和 HER2 阴性乳腺癌的研究潜力。
T6240	Palbociclib Isethionate Palbociclib (PD0332991) Isethionate,帕博西尼羟乙基磺酸盐,PD 0332991 isethionate,帕布昔利布羟乙基磺酸盐	CDK	Cell Cycle/Checkpoint
	Palbociclib Isethionate (PD 0332991 isethionate) 是一种高选择性的CDK4/6抑制剂，IC50为11 nM 和16 nM。它对一组 36 种额外的蛋白激酶没有抑制作用。
T77440	Codrituzumab RG-7686,RO5137382,GC33
	Codrituzumab (GC3）是一种人源化针对 glypican-3 肝癌蛋白的抗体，可与索拉非尼联合使用来研究不可治愈的晚期肝细胞癌 (HCC）。
TQ0090	Nesbuvir HCV-796	HCV Protease	Microbiology/Virology; Proteases/Proteasome
	Nesbuvir 是一种选择性丙型肝炎病毒（HCV）非结构蛋白5B（NS5B）RNA 依赖性聚合酶抑制剂。Nesbuvir 对含1b HCV 复制子的肝癌细胞的 IC50为9nM。
T7738	H3B-6527	FGFR	Angiogenesis; Tyrosine Kinase/Adaptors
	H3B-6527 是一种在 FGF19 驱动的肝细胞癌中有效且选择性的 FGFR4 抑制剂，具有抗肿瘤活性。
T4368	Miriplatin 米铂,SM-11355	DNA Alkylator/Crosslinker	DNA Damage/DNA Repair
	Miriplatin (SM-11355) 是一种烷化剂，是一种用于 TACE 的铂络合物，有望用于治疗肝细胞癌。
T22289	CFI-402257	Kinesin	Cytoskeletal Signaling
	CFI-402257 是 Mps1/TTK 激酶的选择性抑制剂（Mps1 Ki = 0.09 nM；EC50 = 6.5 nM），可用于肝细胞癌疾病的研究。
T64529	MDL-800 MDL 800,MDL800	Sirtuin	Chromatin/Epigenetic; DNA Damage/DNA Repair
	SIRT6, responsible for deacetylation of histone H3 Nε-acetyl-lysines 9 (H3K9ac) and 56 (H3K56ac), is a tumor suppressor which has frequently been found to have low expression in various cancers. MDL-800 is a selective SIRT6 activator. It increased the deacetylase activity of SIRT6 by up to 22-fold and led to a global decrease in H3K9ac and H3K56ac levels in human hepatocellular carcinoma (HCC) cells. Also, it inhibited the proliferation of HCC cells via SIRT6-driven cell-cycle arrest and was eff...
T11421	Glutaminase-IN-1 CB839 derivative	transporter	Metabolism
	Glutaminase-IN-1 (CB839 derivative)，是一种新型 1,3,4-硒二氮基肾型谷氨酰胺酶(KGA) 的变构抑制剂，在侵袭性 H22 肝癌异种移植模型中显示出抗肿瘤活性。
TP1472	Tyroserleutide	Others	Others
	Tyroserleutide 是一种可从猪脾脏的降解产物中分离得到的小分子三肽，在体内外均对肿瘤生长具有抑制作用。
T77466	Tremelimumab Ticilimumab,CP-675206	Others	Others
	Tremelimumab 是一种细胞毒性T淋巴细胞相关抗原-4（CTLA-4）阻断抗体.Tremelimumab 常与 Durvalumab 联合使用来治疗肝癌、肺癌等实体癌。
T22424	1-(4-Chloro-3-(trifluoromethyl)phenyl)-3-(4-(4-cyanophenoxy)phenyl)urea	Apoptosis; STAT	Apoptosis; JAK/STAT signaling; Stem Cells
	SC-1 是一种 Sorafenib 的衍生物，可抑制 STAT3磷酸化，通过依赖 SHP-1 的 STAT3失活诱导细胞凋亡，具有抗癌作用。
T38846	Vevorisertib trihydrochloride ARQ 751 trihydrochloride	Akt	Cytoskeletal Signaling; PI3K/Akt/mTOR signaling
	Vevorisertib trihydrochloride(ARQ 751 trihydrochloride) 是一种具有选择性和有效性的 pan-AKT 和 AKT1-E17K 突变抑制剂，抑制 AKT1 、AKT2 和 AKT3 。 Vevorisertib trihydrochloride 可用于研究肝癌和晚期实体瘤。
T15704	Lagociclovir MIV-210	HBV	Microbiology/Virology
	Lagociclovir (MIV-210) 是一种核苷类似物，是一种可用治疗 HBV82的抗病毒化合物，可抑制野生型乙型肝炎病毒 (HBV) 在永久表达 HBV 的人肝癌细胞系中的复制。
T36848	Combretastatin A-1 Combretastatin A1	Akt; Microtubule Associated	Cytoskeletal Signaling; PI3K/Akt/mTOR signaling
	Combretastatin A-1 是一种有效的微管抑制剂，具有抗肿瘤和抗血管活性，通过微管蛋白解聚介导的 AKT 失活抑制 Wnt/β-catenin 通路发挥作用，可用于研究肝癌。
T76858	Ascrinvacumab PF-03446962	ALK; TGF-beta/Smad	Angiogenesis; Stem Cells; Tyrosine Kinase/Adaptors
	Ascrinvacumab (PF-03446962) 是一种针对 ALK-1 的高效人源化 IgG2 单克隆抗体。Ascrinvacumab 对人 ALK1 的 Kd 值为 7 nM。Ascrinvacumab 对 TGF-β 有抑制作用，可用于研究肝细胞癌 (HCC)。
T14997	Conteltinib SY-707,CT-707	FAK; PYK2; ALK	Angiogenesis; Cytoskeletal Signaling; Tyrosine Kinase/Adaptors
	Conteltinib (CT-707) 是一种靶向FAK、ALK 和 Pyk2 的酶抑制剂，具有抗肿瘤活性。Conteltinib 对 FAK 有明显的抑制作用，通过抑制 YAP 信号传导来克服肝细胞癌中缺氧介导的索拉非尼耐药性，可用于晚期 ALK 阳性非小细胞肺癌和淋巴癌。
T77149	Cobolimab TSR-022,GSK4069889	Others	Others
	Cobolimab (TSR-022) 是一种有效的 TIM-3 单克隆抗体。Cobolimab 诱导 TIM-3 的内化，IC50 值为 0.4464 nM。Cobolimab 具有抗肿瘤活性，可用于研究晚期/转移性黑色素瘤和晚期肝细胞癌。
T15367	Gadoxetate Disodium Gd-EOB-DTPA Disodium,钆塞酸二钠,ZK 139834	Others	Others
	Gadoxetate Disodium 是一种肝胆系统中磁共振成像 (MRI) 中的造影剂，能够在正常的功能性肝细胞中累积，可用于局灶性肝脏病变（如肝细胞癌或 T1 加权成像的肝转移）的研究。
T9842	5-HT2B antagonist-1
	5-HT2B antagonist-1 是一种具有口服活性的5-HT2B 受体拮抗剂，IC50值为 33.4 nM。5-HT2B antagonist-1可用于以 5-HT2B 受体信号传导为特征的疾病研究，如肝细胞癌、心血管疾病或胃肠道疾病。
T21297	Miriplatin hydrate SM-11355 (hydrate),Miripla,Miriplatin,SM 11355,SM11355,SM-11355,Miriplatin hydrate	DNA Alkylation	DNA Damage/DNA Repair
	Miriplatin hydrate (SM-11355 (hydrate)) (MPT)是一种用于TACE 的新型铂类化合物，在肝细胞癌(HCC)的治疗中显示出良好的前景。米铂是一种亲脂性铂复合物，容易悬浮在碘油中，并在肿瘤组织中逐渐释放活性铂化合物。
T11126	Durvalumab MEDI 4736	PD-1/PD-L1	Apoptosis; Cell Cycle/Checkpoint; Immunology/Inflammation
	Durvalumab (MEDI 4736) 是一种人源化的抗 PD-L1 蛋白单克隆抗体，可阻断 PD-L1 与 PD-1 和 CD80 结合的能力，其 IC50 分别为 0.1 和 0.04 nM。Durvalumab 常与铂类化合物联合一起用来治疗非小细胞肺癌和晚期肝癌细胞。
T7709	(E/Z)-GSK5182 GSK5182(Z/E)	Estrogen/progestogen Receptor; ROS	Endocrinology/Hormones; Immunology/Inflammation
	(E/Z)-GSK5182 (GSK5182(Z/E)) 是 (E)-GSK5182 和 (Z)-GSK5182 的外消旋体。GSK5182 是一种具有高效选择性和口服活性的ERRγ的反向激动剂，其IC50值为 79 nM。GSK5182 还诱导肝癌细胞中活性氧 (ROS)的产生。
T61428	4-PQBH	Others	Others
	4-PQBH 是一种有效的 Nur77 结合剂，具有抗肿瘤活性。4-PQBH通过 Nur77 介导的内质应激和自噬广泛诱导半胱天冬酶非依赖性细胞质空泡化和旁睑下垂，抑制异种移植肿瘤。4-PQBH 可用于研究肝癌。
T77651	Tubulin polymerization-IN-47	Microtubule Associated	Cytoskeletal Signaling
	Tubulin polymerization-IN-47 是一种 tubulin 聚合抑制剂和有丝分裂抑制剂，具有抗肿瘤活性，对神经母细胞瘤癌细胞增殖具有抑制作用，对 Chp-134 和 Kelly 细胞系的IC50 分别为 7 和 12 nM。Tubulin polymerization-IN-47 是治疗肝癌、结肠癌、肺癌和乳腺癌的候选化合物。
T62491	STAT3-IN-13	STAT	JAK/STAT signaling; Stem Cells
	STAT3-IN-13 是一种有效的 STAT3 抑制剂。STAT3-IN-13 具有抗增殖和抗癌活性，通过与 STAT3 SH2 结构域结合发挥作用。STAT3-IN-13 抑制 STAT3 Y705 的磷酸化，诱导细胞凋亡，抑制肿瘤细胞的生长和转移。STAT3-IN-13 可用于研究乳腺癌和肝癌。
T16538	PIN1 inhibitor API-1	Others	Others
	PIN1 inhibitor API-1 是特殊的 Pin1抑制剂，可直接特异性地与 Pin1 肽基脯氨酰异构酶结构域结合，并抑制 Pin1 顺反异构活性。它保留 pXPO5 的活性构象，恢复 pXPO5 将前 miRNA 从细胞核转运到细胞质的能力，从而上调抗癌 miRNA 的生物发生，抑制体内外肝癌的发生。
T3226	Paritaprevir ABT-450,Veruprevir,帕利瑞韦	HCV Protease	Microbiology/Virology; Proteases/Proteasome
	Paritaprevir (ABT-450) 是一种口服生物可利用的合成酰基磺酰胺抑制剂，可抑制丙型肝炎病毒 (HCV) 蛋白酶复合物，由非结构蛋白 3 和 4A (NS3/NS4A) 组成，对 HCV 基因型 1 具有潜在活性。给药后，paritaprevir 可逆地结合 HCV NS3/NS4A 蛋白酶的活性中心和结合位点，并阻止 NS3/NS4A 蛋白酶介导的多蛋白成熟。这会破坏病毒蛋白的加工和病毒复制复合物的形成，从而抑制病毒在 HCV 基因型 1 感染的宿主细胞中的复制。 NS3 是一种丝氨酸蛋白酶，对于 HCV 多蛋白内多个位点的蛋白水解切割至关重要，并且在 HCV 核糖核酸 (RNA) 复制过程中起关键作用。 NS4A 是 NS3 的激活因子。 HCV 是属于黄病毒科的一种小的、有包膜的单链 RNA 病毒，感染与肝细胞癌 (HCC) 的发展有关。
T28982	TLC 388 TLC-388,TLC388
	TLC 388, a DNA topoisomerase I inhibitor, is used potentially for the treatment of Renal carcinoma and Hepatocellular carcinoma
T34829	Tetrazanbigen TNBG
	Tetrazanbigen is an inducer of S phase arrest and apoptosis in hepatocellular carcinoma QGY-7701.
T24699	R1498 R-1498,R 1498
	R1498 is an inhibitor of cyclin-dependent kinase 2. It also acts by targeting angiogenesis and mitosis pathways. It is well-tolerated and orally active for hepatocellular carcinoma and gastric cancer treatment.
T37425	FGFR4-IN-5 FGFR4-IN-5
	FGFR4-IN-5, a covalent FGFR4 inhibitor, demonstrates potency and selectivity with an IC50 value of 6.5 nM. Exhibiting significant in vivo anti-tumor activity, it is applicable for research in hepatocellular carcinoma [1].
T68464	PABA/NO
	PABA/NO is a novel glutathione-S-transferase-p-activated nitric oxide donor, inhibiting proliferation and inducing apoptosis by targeting PI3K/AKT/mTOR and MEK/ERK pathways in hepatocellular carcinoma cells.
T61597	Nampt-IN-7
	Nampt-IN-7, also known as compound GF8, is a powerful NAMPT inhibitor exhibiting an IC50 value of 7.31 μM. It possesses significant cytotoxic effects against the human HepG2 hepatocellular carcinoma cell line, with an IC50 value of 24.28 μM [1].
T60277	2-Acetamidofluorene
	2-Acetamidofluorene 是一种强致癌物。2-Acetamidofluorene 可用于诱导肝细胞癌 (HCC) 和多原发肿瘤。
T62151	CHNQD-01255
	CHNQD-01255 是一种口服具有活力的 Arf-GEFs 抑制剂，能够有效地抵抗肝细胞癌 (HCC)。
T70318	AMG-337 monohydrate
	AMG-337 monohydrate is a highly selective small molecule MET inhibitor. Aberrant hepatocyte growth factor (HGF)/MET signaling has been implicated in hepatocarcinogenesis, suggesting that MET may serve as an attractive therapeutic target in hepatocellular carcinoma.
T63653	AKT-IN-11
	AKT-IN-11 是有效的抗人肝癌 Bel-7402 细胞株抗菌剂之一 (IC50: 1.15 μM)。
T77102	Nofazinlimab
	Nofazinlimab (CS1003) 是一种人源 IgG4抗PD-1单克隆抗体。Nofazinlimab 可用于不可切除肝细胞癌 (uHCC) 的研究。
T63662	FGFR4-IN-9
	FGFR4-IN-9 是 FGFR4 的选择性抑制剂 (IC50: 75.3 nM)，能够有效抑制肝癌细胞的生长和血管生成。
T33802	Ono 4007 Ono-4007,Ono4007
	ONO 4007 is a novel synthetic low-toxicity lipid A analog that stimulates the production of tumor necrosis factor-α in tumor tissues, resulting in the rejection of transplanted rat hepatocellular carcinoma cells. ONO-4007 has been shown to have a therapeu

化合物

Cat.No: T22661

Target: Apoptosis, Others, Microtubule Associated

Cat.No: T22830

Synonym: GYY 4137 morpholine salt

Target: Others

Cat.No: T7008

Synonym: Vacquinol 1

Target: JNK

Cat.No: T1785

Synonym: PD 0332991,帕博西尼,帕布昔利布

Target: CDK

Cat.No: T0334

Synonym: BRL49653,罗格列酮

Target: Ferroptosis, TRP/TRPV Channel, PPAR, Autophagy

Cat.No: T6481

Synonym: NS 41080,4-(4-氯-2-甲基苯氧基)-N-羟基丁酰胺

Target: Apoptosis, HDAC

Triglycidyl isocyanurate

Cat.No: T22443

Synonym: Tris(2,3-epoxypropyl) Isocyanurate,Teroxirone,TGIC,1,3,5-三缩水甘油-S-三嗪三酮,TGI

Target: Apoptosis

Cat.No: T9945

Synonym: 3-methyl-6-(naphthalen-1-yl)pyrimidine-2,4(1H,3H)-dione

Target: STAT

Rosiglitazone hydrochloride

Cat.No: T6646

Synonym: 盐酸罗格列酮,BRL-49653 HCl,Rosiglitazone HCl

Target: Ferroptosis, TRP/TRPV Channel, PPAR, Autophagy

Palbociclib monohydrochloride

Cat.No: T6239

Synonym: PD 0332991 hydrochloride,Palbociclib hydrochloride,帕布昔利布盐酸盐,Palbociclib (PD-0332991) HCl

Target: CDK

Palbociclib Isethionate

Cat.No: T6240

Synonym: Palbociclib (PD0332991) Isethionate,帕博西尼羟乙基磺酸盐,PD 0332991 isethionate,帕布昔利布羟乙基磺酸盐

Target: CDK

Cat.No: T77440

Synonym: RG-7686,RO5137382,GC33

Cat.No: TQ0090

Synonym: HCV-796

Target: HCV Protease

Cat.No: T7738

Target: FGFR

Cat.No: T4368

Synonym: 米铂,SM-11355

Target: DNA Alkylator/Crosslinker

Cat.No: T22289

Target: Kinesin

Cat.No: T64529

Synonym: MDL 800,MDL800

Target: Sirtuin

Glutaminase-IN-1

Cat.No: T11421

Synonym: CB839 derivative

Target: transporter

Cat.No: TP1472

Target: Others

Cat.No: T77466

Synonym: Ticilimumab,CP-675206

Target: Others

1-(4-Chloro-3-(trifluoromethyl)phenyl)-3-(4-(4-cyanophenoxy)phenyl)urea

Cat.No: T22424

Target: Apoptosis, STAT

Vevorisertib trihydrochloride

Cat.No: T38846

Synonym: ARQ 751 trihydrochloride

Target: Akt

Cat.No: T15704

Synonym: MIV-210

Target: HBV

Combretastatin A-1

Cat.No: T36848

Synonym: Combretastatin A1

Target: Akt, Microtubule Associated

Cat.No: T76858

Synonym: PF-03446962

Target: ALK, TGF-beta/Smad

Cat.No: T14997

Synonym: SY-707,CT-707

Target: FAK, PYK2, ALK

Cat.No: T77149

Synonym: TSR-022,GSK4069889

Target: Others

Gadoxetate Disodium

Cat.No: T15367

Synonym: Gd-EOB-DTPA Disodium,钆塞酸二钠,ZK 139834

Target: Others

5-HT2B antagonist-1

Cat.No: T9842

Miriplatin hydrate

Cat.No: T21297

Synonym: SM-11355 (hydrate),Miripla,Miriplatin,SM 11355,SM11355,SM-11355,Miriplatin hydrate

Target: DNA Alkylation

Cat.No: T11126

Synonym: MEDI 4736

Target: PD-1/PD-L1

Cat.No: T7709

Synonym: GSK5182(Z/E)

Target: Estrogen/progestogen Receptor, ROS

Cat.No: T61428

Target: Others

Tubulin polymerization-IN-47

Cat.No: T77651

Target: Microtubule Associated

Cat.No: T62491

Target: STAT

PIN1 inhibitor API-1

Cat.No: T16538

Target: Others

Cat.No: T3226

Synonym: ABT-450,Veruprevir,帕利瑞韦

Target: HCV Protease

Cat.No: T28982

Synonym: TLC-388,TLC388

Cat.No: T34829

Synonym: TNBG

Cat.No: T24699

Synonym: R-1498,R 1498

Cat.No: T37425

Synonym: FGFR4-IN-5

Cat.No: T68464

Cat.No: T61597

2-Acetamidofluorene

Cat.No: T60277

Cat.No: T62151

AMG-337 monohydrate

Cat.No: T70318

Cat.No: T63653

Cat.No: T77102

Cat.No: T63662

Cat.No: T33802

Synonym: Ono-4007,Ono4007

Cat. No.	Product Name	Target	Signaling Pathways
T6670	Silymarin Silybin B,水飞蓟素	SARS-CoV	Microbiology/Virology
	Silymarin (Silybin B) 是一种多酚类黄酮，是从水飞蓟或水飞蓟的种子中提取的一种 SARS-CoV-2 主蛋白酶抑制剂。它可降低肿瘤细胞的增殖，血管生成以及胰岛素抵抗，用于预防和治疗肝脏疾病，有潜力研究 COVID-19 。
TN1968	N-Feruloyloctopamine N-Feruloyloctopamine,N-阿魏酰章鱼胺	p38 MAPK; Akt	Cytoskeletal Signaling; MAPK; PI3K/Akt/mTOR signaling
	N-Feruloyloctopamine 是从木本曼陀罗提取的一种天然产物，有抗氧化作用，可显著降低Akt 和p38 MAPK 磷酸化水平。
T13741	Isoviolanthin 异佛莱心苷,异佛来心苷	Others	Others
	Isoviolanthin 是一种黄酮类苷类化合物，提取自铁皮石斛叶中。它能减少 TGF-β1 处理的 HCC 细胞的迁移和入侵能力，对正常细胞没有毒性影响，对转移性肝癌晚期具有潜在的研究价值。
TN1019	Beta-mangostin β-Mangostin,beta-倒捻子素	Apoptosis; Antibacterial; Parasite	Apoptosis; Microbiology/Virology
	Beta-mangostin (β-Mangostin) 是存在 Cratoxylum arborescens 中的一种氧杂蒽酮类天然产物，有抗癌和抗菌活性，对结核分枝杆菌的 MIC 值为 6.25 μg/mL。它在体外有抗疟活性，对恶性疟原虫的 IC50值为 3.00 μg/mL。
TN1013	Cucurbitacin D	IL Receptor; JNK; STAT	Immunology/Inflammation; JAK/STAT signaling; MAPK; Stem Cells
	Cucurbitacin D has anticancer effects, it induces apoptosis through caspase-3 and phosphorylation of JNK in hepatocellular carcinoma cells.
TN7217	4,6-Benzilidine-D-Glucose
	4,6-Benzilidine-D-Glucose 是一种临床抗肿瘤化合物，在化学诱导肝细胞癌大鼠中显示出抗肿瘤活性。
TN1644	Flavanomarein	Others	Others
	Flavanomarein 是Coreopsis tinctoria Nutt 的主要黄酮类化合物，对糖尿病性肾病具有保护作用。它具有很好的抗氧化，降糖，降压和降血脂作用。
T5S0506	Rotundic acid Rutundic acid,铁冬青酸	Apoptosis; Others; p38 MAPK; Akt; mTOR	Apoptosis; Cytoskeletal Signaling; MAPK; Others; PI3K/Akt/mTOR signaling
	Rotundic acid (Rutundic acid) 是一种从圆形肠球菌中获得的三萜类天然产物，具有抗炎和保护心脏的能力。它可通过 AKT/mTOR 和 MAPK 途径在肝细胞癌中诱导 DNA 损伤和细胞凋亡。
T6S0117	Avicularin Fenicularin,扁蓄苷	ERK	MAPK
	Avicularin (Fenicularin) 具有抗过敏、抗炎、保肝、抗氧化、抗肿瘤等活性。它能通过调节 NF-κB(p65)、COX-2 和 PPAR-γ 的活性来改善人类肝细胞癌。在 LPS 刺激的 RAW 264.7 巨噬细胞中，它通过抑制 ERK 信号通路产生抗炎活性。
T2S0837	Astragalus Polysacharin 2-(Chloromethyl)-4-(4-nitrophenyl)thiazole,黄芪多糖,89250-26-0	TAM Receptor	Tyrosine Kinase/Adaptors
	2-(Chloromethyl)-4-(4-nitrophenyl)thiazole 是一种从黄芪 (Astragalus propinquus) 中提取得到的天然产物。2-(Chloromethyl)-4-(4-nitrophenyl)thiazole 具有抗癌活性，通过抑制肿瘤相关巨噬细胞 (TAM) 的 M2 极化在肝细胞癌 (HCC) 中显示除抗肿瘤活性。
TN6694	5,6-Benzoflavone β-Naphthoflavone,beta-NF	Antioxidant	oxidation-reduction
	5,6-Benzoflavone (β-Naphthoflavone) 是芳烃受体的外源配体，可破坏人肝癌 HepG2 细胞中的锌稳态。5,6-Benzoflavone (β-Naphthoflavone) 具有抗炎和抗氧化活性，抑制通过 AKT/Nrf-2/HO-1-NF-kappaB 信号转导轴，抑制 LPS 诱导的炎症，抑制TNF-α诱导的ICAM-1和VCAM-1表达，可用于研究神经退行性疾病。
TN1880	Lucidenic acid B Lucidenicacid B	Apoptosis; Caspase	Apoptosis; Proteases/Proteasome
	Lucidenic acid B (Lucidenicacid B) 是从灵芝中提取得到的天然化合物，可诱导caspase-9 和 caspase-3 的活化和 PARP 的裂解，可通过线粒体介导诱导人白血病细胞凋亡。 Lucidenic acid B通过灭活MAPK / ERK信号转导途径和降低NF-kappaB和AP-1的结合活性来抑制PMA诱导的人肝癌细胞侵袭。。Lucidenic acid B 对细胞周期和坏死细胞没有影响。
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。
T4S0145	Corylifol A Corylinin,补骨脂异黄酮A	hCE; STAT; UGT	JAK/STAT signaling; Metabolism; Stem Cells
	Corylifol A (Corylinin) 是补骨脂中的一种天然产物，可抑制IL-6 诱导的STAT3激活和磷酸化，IC50值为0.81 μM。
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。
T24744	Rubone
	Rubone is the tumor suppressor miRNA-34a modulator that acts by inhibiting the growth of hepatocellular carcinoma.
T23774	Bauerenol NSC 147745,Baurenol
	Bauerenol is a triterpenoid from Indian Suregada angustifolia. It also induces reactive oxygen species-mediated P38MAPK activation and apoptosis in human hepatocellular carcinoma cells.
TN3740	Cyclocommunol	PAFR	GPCR/G Protein
	Cyclocommunol exhibits cytotoxicity against hepatocellular carcinoma (SMMC-7721) and gastric carcinoma (BGC-823 and SGC-7901) cell lines. It also shows strong inhibition of arachidonic acid (AA)- and collagen-induced platelet aggregation.
TN1156	(-)-Curine	p53	Apoptosis
	(-)-Curine can inhibit viability of hepatocellular carcinoma cells in regardless of p53 status.
TN1200	19-Oxocinobufotalin	Others	Others
	19-Oxocinobufotalin 3-adipoylarginine ester shows significant inhibition effect against human hepatocellular carcinoma cell line SMMC-7721 in vitro.
TN3931	ent-11alpha-Hydroxy-15-oxokaur-16-en-19-oic acid	ERK; BCL; p38 MAPK; NF-κB; Caspase; JNK; p53	Apoptosis; MAPK; NF-κB; Proteases/Proteasome
	Ent-11alpha-Hydroxy-15-oxokaur-16-en-19-oic acid has anti-cancer activity, it induces apoptosis of human malignant cancer cells, it also inhibits hepatocellular carcinoma in vitro and in vivo via stabilizing IkBα.
TN4496	Marginatoxin	Caspase; Fas/FasL	Apoptosis; Proteases/Proteasome
	Marginatoxin may be a promising chemopreventive agent for treating hepatocellular carcinoma, it induces human hepatoma BEL-7402 cells apoptosis in vitro and in vivo via activation of Fas/FasL-mediated apoptotic pathway.
T27282	Erucin AR 1G3839,AR-1G3839,CCRIS-9056,CCRIS9056,AR1G3839,CCRIS 9056
	Erucin is a sulforaphane analog found in cruciferous vegtables. Erucin is a telomerase inhibitor. It induces phase II enzyme activity, suppresses cellular proliferation in hepatocellular carcinoma cells, prevents 6-OHDA-induced neurodegenration, and inhib
T28122	Myrtenal NSC-54384,NSC 54384,NSC54384,Benihinal
	Myrtenal is a natural monoterpene. It is found to attenuate diethylnitrosamine-induced hepatocellular carcinoma in rats by stabilizing intrinsic antioxidants and modulating apoptotic and anti-apoptotic cascades. Myrtenal also inhibits acetylcholinesterase
TN6054	Norglaucine hydrochloride
	(+)-Norglaucine shows cytotoxic activity toward the tumor cell lines B16-F10 (mouse melanoma), HepG2 (human hepatocellular carcinoma), K562 (human chronic myelocytic leukemia) and HL-60 (human promyelocytic leukemia) and non-tumor peripheral blood mononuc
TN1549	Damnacanthal 丹宁卡	IL Receptor; Akt; Syk	Angiogenesis; Cytoskeletal Signaling; Immunology/Inflammation; PI3K/Akt/mTOR signaling; Tyrosine Kinase/Adaptors
	Damnacanthal possesses anti-cancer, immunomodulatory, antinociceptive and anti-inflammatory actions, it can treat or prevent hepatocellular carcinoma through its inhibitory effects on the HGF/c-Met axis.
TN1728	Hellebrigenin	PARP; Akt; CDK	Cell Cycle/Checkpoint; Chromatin/Epigenetic; Cytoskeletal Signaling; DNA Damage/DNA Repair; PI3K/Akt/mTOR signaling
	Hellebrigenin has anti-hepatoma activities, it induces cell cycle arrest and apoptosis in human hepatocellular carcinoma HepG2 cells through inhibition of Akt. Hellebrigenin exhibites moderate to strong activity against human HL-60, SF-295, MDA-MB-435, and HCT-8 cancer cell strains without hemolysis of mouse erythrocytes.
T75454	Penicitide A
	Penicitide A 是一种海洋次生代谢产物。Penicitide A 对病原体 A.brassicae 和人肝细胞肝癌 (HepG2) 细胞系显示中度细胞毒性。
T3425	Polyphyllin G 重楼皂苷VII,Polyphyllin VII,Polyphyllin VII,Y-0166,重楼皂苷G	Others	Others
	Polyphyllin G (Polyphyllin VII) 是从Paris yunnanensis 的根茎中分离出来的，具有抗菌活性，抑制革兰氏阳性和革兰氏阴性细菌的生长。它是polyphyllin 家族的主要成员，对肺癌、乳腺癌、结直肠癌、宫颈癌、肝细胞癌和骨肉瘤等多种癌症具有很强的抗癌活性。
TN1464	Camellianin A	RAAS	Endocrinology/Hormones
	Camellianin A has anticancer activity, it can inhibit the proliferation of the human hepatocellular liver carcinoma Hep G2 and human breast adenocarcinoma MCF-7 cell lines in a dose-dependent manner and induce the significant increase of the G0/G1 cell po
T75637	Demethylcantharidate disodium
	Demethylcantharidate disodium 是一种内源性代谢产物，能通过诱导内质网应激来促进肝癌细胞的凋亡，并且对多种类型的癌症展现出良好的抗癌活性。
TN1617	Ergosta-4,6,8(14),22-tetraen-3-one	BCL; Caspase; p53	Apoptosis; Proteases/Proteasome
	Ergosta-4,6,8(14),22-tetraen-3-one has cytotoxic activity against human gastric cancer cell, it can induce G2/M cell cycle arrest and apoptosis in human hepatocellular carcinoma HepG2 cells, these results would be useful for the further utilization of man
TN6458	Acetylshikonin
	Acetylshikonin can effectively inhibit tumor cells, it can be used to treat hepatocellular carcinoma cells expressing hepatitis B virus X protein (HBX) by inducing ER stress , an oncoprotein from hepatitis B virus. Acetylshikonin inhibits the production of eicosanoid, is due to the attenuation of cytosolic phospholipase A(2) membrane recruitment via the decrease in [Ca(2+)](i) and to the blockade of cyclooxygenase and 5-lipoxygenase activity.
TN5050	Sprengerinin C	NADPH-oxidase; VEGFR; p38 MAPK; ROS; Akt; PI3K; mTOR; p53	Angiogenesis; Apoptosis; Cytoskeletal Signaling; Immunology/Inflammation; MAPK; PI3K/Akt/mTOR signaling; Tyrosine Kinase/Adaptors
	Sprengerinin C exerts anti-tumorigenic effects in hepatocellular carcinoma via inhibition of proliferation and angiogenesis and induction of apoptosis, it can strongly suppress tumor angiogenesis in human umbilical vein endothelial cells, it blocks vascul
T64246	Cinchonine monohydrochloride hydrate
	Cinchonine ((8R,9S)-Cinchonine) monohydrochloride hydrate 是一种天然的、有效的抗疟剂，也是一种人血小板聚集的抑制剂。Cinchonine monohydrochloride hydrate 能够激活内质网应激，诱导的人肝癌细胞凋亡，并可抑制脂肪的生成。
TN1646	Flemiphilippinin A	Others	Others
	Flemiphilippin A has antioxidant activity, it shows DPPH radical scavenging activity with effective half maximal concentration (EC50) of 18.36 ug/mL. Flemiphilippinin A (5 ug/mL) exhibits some level of antitumor activity against human hepatocellular carci
T37452	Stephacidin B
	Stephacidin B is a fungal metabolite that has been found inA. ochraceus.1Dimeric stephacidin B is rapidly converted to a monomer, avrainvillamide ,in vitro.2Stephacidin B is cytotoxic to a variety of cancer cells, including testosterone-independent PC3 and -sensitive LNCaP prostate cancer cells (IC50s = 0.37 and 0.06 μM, respectively) and estradiol-independent SK-BR-3 and -sensitive MCF-7 breast cancer cells (IC50s = 0.32 and 0.27 μM, respectively).1It induces apoptosis in HepG2 and Huh7 hepatoc...
TN4300	Isojacareubin	MAPK; PKC; Antifection	Chromatin/Epigenetic; Cytoskeletal Signaling; MAPK; Microbiology/Virology
	Isojacareubin displays potent activity against H. pylori HP40 clinical isolate with MIC 23.9 uM, which is approximately two times greater than that of the standard drug amoxicillin. Isojacareubin is a potent inhibitor of protein kinase C (PKC), suppresses

天然产物

Cat.No: T6670

Synonym: Silybin B,水飞蓟素

Target: SARS-CoV

N-Feruloyloctopamine

Cat.No: TN1968

Synonym: N-Feruloyloctopamine,N-阿魏酰章鱼胺

Target: p38 MAPK, Akt

Cat.No: T13741

Synonym: 异佛莱心苷,异佛来心苷

Target: Others

Cat.No: TN1019

Synonym: β-Mangostin,beta-倒捻子素

Target: Apoptosis, Antibacterial, Parasite

Cat.No: TN1013

Target: IL Receptor, JNK, STAT

4,6-Benzilidine-D-Glucose

Cat.No: TN7217

Cat.No: TN1644

Target: Others

Cat.No: T5S0506

Synonym: Rutundic acid,铁冬青酸

Target: Apoptosis, Others, p38 MAPK, Akt, mTOR

Cat.No: T6S0117

Synonym: Fenicularin,扁蓄苷

Target: ERK

Astragalus Polysacharin

Cat.No: T2S0837

Synonym: 2-(Chloromethyl)-4-(4-nitrophenyl)thiazole,黄芪多糖,89250-26-0

Target: TAM Receptor

5,6-Benzoflavone

Cat.No: TN6694

Synonym: β-Naphthoflavone,beta-NF

Target: Antioxidant

Lucidenic acid B

Cat.No: TN1880

Synonym: Lucidenicacid B

Target: Apoptosis, Caspase

Cat.No: T6S1699

Synonym: [6]-Shogaol,姜烯酚,6-姜烯酚,6-Shogaol

Target: Lipoxygenase, Autophagy

Cat.No: T4S0145

Synonym: Corylinin,补骨脂异黄酮A

Target: hCE, STAT, UGT

Cat.No: T5S2343

Synonym: 乙酰紫草素,Acetyl shikonin

Target: Others, P450, AChE

Cat.No: T24744

Cat.No: T23774

Synonym: NSC 147745,Baurenol

Cat.No: TN3740

Target: PAFR

Cat.No: TN1156

Target: p53

19-Oxocinobufotalin

Cat.No: TN1200

Target: Others

ent-11alpha-Hydroxy-15-oxokaur-16-en-19-oic acid

Cat.No: TN3931

Target: ERK, BCL, p38 MAPK, NF-κB, Caspase, JNK, p53

Cat.No: TN4496

Target: Caspase, Fas/FasL

Cat.No: T27282

Synonym: AR 1G3839,AR-1G3839,CCRIS-9056,CCRIS9056,AR1G3839,CCRIS 9056

Cat.No: T28122

Synonym: NSC-54384,NSC 54384,NSC54384,Benihinal

Norglaucine hydrochloride

Cat.No: TN6054

Cat.No: TN1549

Synonym: 丹宁卡

Target: IL Receptor, Akt, Syk

Cat.No: TN1728

Target: PARP, Akt, CDK

Cat.No: T75454

Cat.No: T3425

Synonym: 重楼皂苷VII,Polyphyllin VII,Polyphyllin VII,Y-0166,重楼皂苷G

Target: Others

Cat.No: TN1464

Target: RAAS

Demethylcantharidate disodium

Cat.No: T75637

Ergosta-4,6,8(14),22-tetraen-3-one

Cat.No: TN1617

Target: BCL, Caspase, p53

Cat.No: TN6458

Cat.No: TN5050

Target: NADPH-oxidase, VEGFR, p38 MAPK, ROS, Akt, PI3K, mTOR, p53

Cinchonine monohydrochloride hydrate

Cat.No: T64246

Flemiphilippinin A

Cat.No: TN1646

Target: Others

Cat.No: T37452

Cat.No: TN4300

Target: MAPK, PKC, Antifection

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