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Search Results for " gastric cancer "

74

抑制剂 & 化合物

25

天然产物

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Cat. No.	Product Name	Target	Signaling Pathways
T9929	Ramucirumab	VEGFR	Angiogenesis; Tyrosine Kinase/Adaptors
	Ramucirumab 是一种人 VEGFR-2 拮抗剂，具有抗实体瘤活性。它是人源化单克隆抗体，能够与 VEGFR-2 结合，阻碍 VEGFR 配体 VEGF-A，VEGF-C 和 VEGF-D 结合。
T6540	Ibuprofen Lysine 布洛芬赖氨酸盐,Neoprofen	COX	Immunology/Inflammation; Neuroscience
	Ibuprofen Lysine (Neoprofen) 是一种非甾体抗炎药。
T1787	Levobupivacaine	Sodium Channel	Membrane transporter/Ion channel
	Levobupivacaine 是一种氨基酰胺类局麻药，属于n-alkylsubstituted pipecoloxylidide 家族。它是bupivacaine 的 S-对映异构体。
T2325	Neratinib HKI-272,来那替尼	EGFR; HER	Angiogenesis; JAK/STAT signaling; Tyrosine Kinase/Adaptors
	Neratinib (HKI-272) 是一种口服的、不可逆的酪氨酸激酶抑制剂，对 HER2 和 EGFR 的 IC50值分别为 59 和 92 nM。
T1394	Ibuprofen Brufen,(±)-Ibuprofe,布洛芬,Motrin,Advil	COX	Immunology/Inflammation; Neuroscience
	Ibuprofen (Advil) 是一种丙酸衍生物和非甾体抗炎药 (NSAID)，具有抗炎、镇痛和解热作用。它是COX-1和COX-2的抑制剂，IC50值分别为 13 和 370 μM，导致前列腺素和血栓素前体的形成减少。
T1756L	Ilaprazole IY81149,艾普拉唑,IY 81149,IY-81149	Proton pump; TOPK	MAPK; Membrane transporter/Ion channel
	Ilaprazole (IY-81149) 是一种具有口服活性质子泵抑制剂，以剂量依赖性方式不可逆地抑制H+/K+-ATPase，在兔壁细胞制剂中的IC50为 6 μM。它也是一种有效的T 细胞起源蛋白激酶(TOPK)抑制剂，用于胃溃疡的研究。
T1756	Ilaprazole sodium IY-81149 sodium,艾普拉唑钠	Proton pump; TOPK	MAPK; Membrane transporter/Ion channel
	Ilaprazole sodium (IY-81149 sodium) 是一种具有口服活性质子泵抑制剂，以剂量依赖性方式不可逆地抑制 H+/K+-ATPase，在兔壁细胞制剂中的 IC50为 6 μM。它也是一种有效的 T 细胞起源蛋白激酶(TOPK)抑制剂，用于胃溃疡的研究。
T1562	Rebamipide Proamipide,OPC12759,瑞巴派特	Free radical scavengers; COX; Prostaglandin Receptor	GPCR/G Protein; Immunology/Inflammation; Neuroscience; oxidation-reduction
	Rebamipide (OPC12759) 是一种粘膜保护剂，可诱导COX-2表达，增加PGE2水平，并以 COX-2 依赖性方式增强胃粘膜防御。
T11139	(E/Z)-BCI NSC 150117	Apoptosis; Phosphatase	Apoptosis; Metabolism
	(E/Z)-BCI (NSC-150117) 是一种DUSP6抑制剂，可通过激活 Nrf2 信号和抑制 NF-κB 通路，减弱 LPS 诱导的巨噬细胞炎症和 ROS 生成，具有抗炎活性。
T11826	LCH-7749944 GNF-PF-2356	Apoptosis; PAK	Apoptosis; Cytoskeletal Signaling
	LCH-7749944 (GNF-PF-2356) 是一种 PAK4抑制剂，IC50为 14.93 μM。它通过下调 PAK4/c-Src/EGFR/cyclin D1 途径有效抑制人胃癌细胞的增殖，并诱导凋亡。
T8505	SC-236 4-(5-(4-氯苯基)-3-(三氟甲基)-1H-,Sc 236	Apoptosis; COX; PPAR	Apoptosis; DNA Damage/DNA Repair; Immunology/Inflammation; Metabolism; Neuroscience
	SC-236 (Sc 236) 是一种具有口服活性的COX-2特异性抑制剂和PPARγ激动剂。它可通过 c-Jun 氨基端抑制激活蛋白-1活性，在小鼠模型中通过抑制 ERK 的磷酸化发挥抗炎作用。
T6566	Levobupivacaine hydrochloride Levobupivacaine HCl,(S)-(-)-Bupivacaine HCl,盐酸左布比卡因,(S)-(-)-Bupivacaine monohydrochloride	Sodium Channel	Membrane transporter/Ion channel
	Levobupivacaine hydrochloride ((S)-(-)-Bupivacaine monohydrochloride) 是有效的钠通道阻滞剂。
T11571	HLY78 4-Ethyl-5-methyl-5,6-dihydro-[1,3]dioxolo[4,5-j]phenanthridine	Wnt/beta-catenin	Cytoskeletal Signaling; Stem Cells
	HLY78 (4-Ethyl-5-methyl-5,6-dihydro-[1,3]dioxolo[4,5-j]phenanthridine) 是 Wnt/β-catenin 信号通路的激活剂，通过靶向通道中 Axin 的 DIX 域，增强 Axin-LRP6 交联，诱导 Wnt 信号转导。
TQ0157	EIPA L593754,MH 12-43	Sodium Channel; TRP/TRPV Channel	Membrane transporter/Ion channel
	EIPA (L593754) 是一种有效的TRPP3 channel 抑制剂，IC50为 10.5 μM。EIPA 对Na+/H+交换 (NHE) 和巨噬细胞也有抑制作用。
T6442	CH5138303	HSP	Cytoskeletal Signaling; Metabolism
	CH5138303 是一种可口服的 Hsp90 抑制剂，Kd 为 0.48 nM。
T7351	3-Methylcytidine	Nucleoside Antimetabolite/Analog	Cell Cycle/Checkpoint; DNA Damage/DNA Repair
	3-Methylcytidine 是一种尿核苷，作为四种不同类型癌症的生物标志物：肺癌、胃癌、结肠癌和乳腺癌。
T27259	Emitefur BOFA2,BOF A2,BOF-A2	Others	Others
	Emitefur (BOF-A 2)是一种有口服活性和有效性的 5-氟尿嘧啶衍生物，具有抗癌和抗肿瘤活性。Emitefur 可用于研究晚期胃癌、乳腺癌和代谢相关疾病。
T10655	c-Met inhibitor 1 3-[(2-甲基-2H-吲唑-5-基)硫基]-6-(1-甲基-1H-吡唑-4-基)-1,2,4-三唑并[4,3-B]哒嗪	c-Met/HGFR	Tyrosine Kinase/Adaptors
	c-Met inhibitor 1 是一种 c-Met 受体信号通路抑制剂，可用于癌症的治疗，包括胶质母细胞瘤、胃癌和胰腺癌。
T28994L	Topixantrone 2HCl Topixantrone 2HCl( 156090-18-5 Free base),BBR3576 2HCl	Topoisomerase	DNA Damage/DNA Repair
	Topixantrone 2HCl 是一种DNA 拓扑异构酶抑制剂，具有抗肿瘤活性，可用于研究胃癌和前列腺癌。
T77635	LSD1-IN-27	Histone Demethylase; PD-1/PD-L1	Apoptosis; Cell Cycle/Checkpoint; Chromatin/Epigenetic; Immunology/Inflammation
	LSD1-IN-27 是一种高效的 LSD1 抑制剂，IC50 值为 13 nM。LSD1-IN-27 对胃癌细胞的干细胞性和迁移有抑制作用。LSD1-IN-27 对 BGC-823 和 MFC 细胞中 PD-L1 的表达有抑制作用。LSD1-IN-27 可增强对胃癌的 T 细胞免疫反应。
T9912	Trastuzumab	EGFR	Angiogenesis; JAK/STAT signaling; Tyrosine Kinase/Adaptors
	Trastuzumab 是人源化单克隆抗体，以高亲和力与HER2选择性结合，可用于 HER2 阳性转移性乳腺癌和 HER2 阳性胃癌的研究。
T27704	K00135 K-00135,Imidazol[1,2-b]pyridazine 1,K 00135,IMIDAZOPYRIDAZIN 1	Pim	Chromatin/Epigenetic; JAK/STAT signaling
	K00135 (IMIDAZOPYRIDAZIN 1) 是 Pim 激酶的选择性抑制剂，可用于胃癌和抗白血病治疗的研究。
T39595	Disitamab vedotin RC 48,RC-48,RC48	EGFR	Angiogenesis; JAK/STAT signaling; Tyrosine Kinase/Adaptors
	Disitamab vedotin (RC-48) 是一种抗体-活性分子偶联物 (ADC)，包含抗人表皮生长因子受体2 (HER2) 的单克隆抗体，该单克隆抗体通过可降解连接子结合到细胞毒性剂 MMAE。Disitamab vedotin 在不同HER-2表达水平胃癌细胞中显示出抗肿瘤和抗增殖活性且抑制胃癌细胞中HER-2蛋白的表达。
T29017	TrxR1-IN-B19 TrxR1INB19,Go Y015,TrxR1 IN B19,Go-Y015	Others	Others
	TrxR1-IN-B19 (TrxR1 IN B19) 是一种 TrxR1 抑制剂，通过靶向 TrxR1 和 ROS 介导的 ER 应激激活，通过小分子选择性杀死胃癌细胞。
T61859	MK-28	Antiviral; PERK	Apoptosis; Immunology/Inflammation
	MK-28 是一种具有选择性的 PERK 激动剂，可降低亨廷顿病模型的毒性并延长生存期。MK-28 对MK28胃癌细胞有显著的杀伤作用。
T76758	Rilotumumab AMG 102	c-Met/HGFR	Tyrosine Kinase/Adaptors
	Rilotumumab (AMG 102) 是一种针对肝细胞生长因子的单克隆抗体，对 HGF/MET 驱动的信号传导有抑制作用。Rilotumumab 具有抗肿瘤作用，可用于研究去势抵抗性前列腺癌 (CRPC) 和胃癌。
T2283	PX-12 2-[(1-甲基丙基)二硫代]-1H-咪唑,IV-2,PX12	Thioredoxin	Metabolism
	PX-12 (PX12) 是一种可逆的硫氧还蛋白-1(Trx-1)抑制剂，能够抑制 MCF-7 细胞(IC50:1.9 μM)和HT-29 细胞(IC50:2.9 μM)的生长。
T16947	SU16f 3-substituted indolin-2-one 16f,SU-16F,SU 16F	PDGFR	Angiogenesis; Tyrosine Kinase/Adaptors
	SU16f (3-substituted indolin-2-one 16f) 是一种有效的，选择性 PDGFRβ 抑制剂，对 PDGFRβ，PDGFR1，PDGFR2 的 IC50 分别为 10 nM，140 nM，2.29 μM。SU16f 抑制 PDGFRβ 受体从而可以阻断胃癌来源的间充质干细胞 (GC-MSC) 条件培养基在胃癌细胞增殖和迁移中的促进作用。
T19710	Ciglitazone Ciglitazona,U 63287,ADD3878,ADD-3878,U-63287,ADD 3878	Apoptosis; p38 MAPK; PPAR	Apoptosis; DNA Damage/DNA Repair; MAPK; Metabolism
	Ciglitazone (ADD 3878) 是一种强效和选择性的PPARγ激动剂(EC50：3μM)和口服降糖药。Ciglitazone 抑制th17细胞的增殖和分化，降低胰岛素水平、血管内皮生长因子的产生和血压，诱导胃癌细胞的细胞周期停止。Ciglitazone 能诱导负鼠肾上皮细胞的凋亡，激活p38 MAPK 和凋亡诱导因子(AIF)的核转位。 Ciglitazone 在肥胖症和高血糖症的动物模型中表现出降血糖活性。
T28994	Topixantrone BBR3576,BBR-3576,BBR 3576
	Topixantrone, a DNA topoisomerase inhibitor, is used potentially for the treatment of gastric cancer and prostate cancer.
T27414	GL-331 W68,W 68,W-68,GL331
	GL-331, a DNA topoisomerase II inhibitor, is used potentially for the treatment of small cell lung cancer and gastric cancer.
T70894	Azamitosene
	Azamitosene is a DNA cleaving agent exhibiting G and A base specificity. Azamitosene may exhibit a growth inhibitory effect on human gastric cancer cells.
T71060	IST-622
	IST-622 is a unique topoisomerase inhibitor, showing significant growth-inhibitory effects against large-cell lung cancer (Lu-116) and gastric adenocarcinoma (St-4).
T12635L	Plevitrexed BGC9331,ZD 9331	Others	Others
	Plevitrexed is taken up via the α-folate receptor as well as the reduced folate carrier. Plevitrexed is an orally active and effective thymidylate synthase (TS) inhibitor (Ki: 0.44 nM). Plevitrexed is used for gastric cancer in clinical.
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.
T60416	CRM1 degrader 1
	CRM1 degrader 1 (1l) 是一种低毒的CRM1降解剂，可诱导胃癌细胞凋亡并选择性抑制胃癌细胞的增殖。
T69243	AK963
	AK963, also known as 40708899, is a potent PAK1 (p21-activated kinase 1) inhibitor, which suppresses the proliferation of human gastric cancer cells significantly by downregulation of PAK1-NFκB-CyclinB1 pathway.
T69162	Ki23057
	Ki23057 is a a FGFR2 inhibitor, which enhances the chemosensitivity of drug-resistant gastric cancer cell lines when used in combination with chemotherapeutic drugs. Ki23057 might be therapeutically promising for treating drug-resistant gastric cancer cells, especially when used in combination with SN38, PTX, or VP16. The apoptosis process might be the main mechanism underlying the synergistic effect of these combinations. The ERCC1 and p53 genes may play an integral role in the synergism betwee...
T61243	MAT2A-IN-5
	MAT2A-IN-5, a potent inhibitor of MAT2A, effectively targets the abnormally elevated expression of MAT2A found in various tumor types such as gastric, colon, liver, and pancreatic cancers. By reducing the proliferative activity of MTAP-deficient cancer cells, MAT2A-IN-5 exhibits potential in cancer research applications [1].
T21307	Heptaplatin NSC644591 NSCD644591 SKI2053R,Heptaplatin Sunpla,HTP
	Heptaplatin, a new platinum derivative with anticancer activity, is used against various cancer cell lines, including cisplatin-resistant cancer cell lines. It has been reported to have a response rate of 17% as a single agent, and tolerable toxicity in t
T61565	KDM5B-IN-3
	KDM5B-IN-3 (Compound 5) is an inhibitor of histone lysine-specific demethylase 5B (KDM5B) or JARID1B. It effectively inhibits the activity of KDM5B with an IC50 value of 9.32 μM. Consequently, KDM5B-IN-3 serves as a valuable tool in gastric cancer research [1].
T61672	MAT2A-IN-7
	MAT2A-IN-7, a potent inhibitor of the enzyme MAT2A, demonstrates efficacy in targeting the abnormally elevated expression of MAT2A observed in gastric, colon, liver, and pancreatic cancers. Furthermore, MAT2A-IN-7 effectively reduces the proliferative activity specifically in MTAP-deficient cancer cells, thus highlighting its potential for cancer research applications [1].
T61228	Pirenzepine
	Pirenzepine (LS 519 free base) is a selective antagonist of the M1 muscarinic acetylcholine receptor (mAChR). It effectively inhibits gastric acid secretion and reduces muscle spasm, making it a valuable compound for investigating peptic ulcers. Additionally, Pirenzepine exhibits anti-proliferative activity against cancer cells [1] [2].
T9665	Esuberaprost Sodium
	Famitinib (SHR1020) is a potent orally active multi-targeted kinase inhibitor that effectively inhibits the activity of c-kit, VEGFR-2, and PDGFRβ with IC50 values of 2.3 nM, 4.7 nM, and 6.6 nM, respectively [1]. It demonstrates remarkable antitumor properties in human gastric cancer cells and xenografts, inducing apoptosis [2].
T76004	Super-TDU TFA
	Super-TDU TFA 是一种特异性的 YAP 拮抗剂，可以靶向 YAP-TEAD 相互作用。Super-TDU TFA 可以抑制胃癌小鼠模型的肿瘤生长。
T60639	SLEC-11
	SLEC-11 可在E-钙粘蛋白缺陷细胞中作为合成致死(SL)的先导化合物出现，具有治疗胃癌的潜力。
T62041	XP5
	XP5 是一种有效的、具有口服活性的HDAC6抑制剂(IC50= 31 nM)。XP5高效抑制各种癌细胞系（包括抗 HDACi 的 YCC3/7 胃癌细胞）的增殖 (IC50=0.16-2.31 μM)。
T60584	Cimetidine hydrochloride
	Cimetidine (SKF-92334) hydrochloride 是一种具有口服活性的，可逆的组胺H2受体拮抗剂 (Ki = 0.6 μM)。Cimetidine hydrochloride 显示出抗癌和抗炎活性。Cimetidine hydrochloride 是一种胃酸减少剂，它可用于十二指肠和胃溃疡的相关研究。
T76971	Trastuzumab beta
	Trastuzumab beta (ABP 980)是Trastuzumab的生物仿制药，靶向人表皮生长因子受体2 (HER2) 的单克隆抗体 (McAb)。该药物适用于研究HER2阳性转移性乳腺癌、早期乳腺癌 (EBC) 和转移性胃癌。
T78155	MY-943
	MY-943是一种有效的tubulin聚合和LSD1抑制剂，展现出抗癌性能。它能够诱导G2/M期阻滞和细胞凋亡，同时抑制细胞迁移，适用于胃癌研究。

化合物

Cat.No: T9929

Target: VEGFR

Ibuprofen Lysine

Cat.No: T6540

Synonym: 布洛芬赖氨酸盐,Neoprofen

Target: COX

Levobupivacaine

Cat.No: T1787

Target: Sodium Channel

Cat.No: T2325

Synonym: HKI-272,来那替尼

Target: EGFR, HER

Cat.No: T1394

Synonym: Brufen,(±)-Ibuprofe,布洛芬,Motrin,Advil

Target: COX

Cat.No: T1756L

Synonym: IY81149,艾普拉唑,IY 81149,IY-81149

Target: Proton pump, TOPK

Ilaprazole sodium

Cat.No: T1756

Synonym: IY-81149 sodium,艾普拉唑钠

Target: Proton pump, TOPK

Cat.No: T1562

Synonym: Proamipide,OPC12759,瑞巴派特

Target: Free radical scavengers, COX, Prostaglandin Receptor

Cat.No: T11139

Synonym: NSC 150117

Target: Apoptosis, Phosphatase

Cat.No: T11826

Synonym: GNF-PF-2356

Target: Apoptosis, PAK

Cat.No: T8505

Synonym: 4-(5-(4-氯苯基)-3-(三氟甲基)-1H-,Sc 236

Target: Apoptosis, COX, PPAR

Levobupivacaine hydrochloride

Cat.No: T6566

Synonym: Levobupivacaine HCl,(S)-(-)-Bupivacaine HCl,盐酸左布比卡因,(S)-(-)-Bupivacaine monohydrochloride

Target: Sodium Channel

Cat.No: T11571

Synonym: 4-Ethyl-5-methyl-5,6-dihydro-[1,3]dioxolo[4,5-j]phenanthridine

Target: Wnt/beta-catenin

Cat.No: TQ0157

Synonym: L593754,MH 12-43

Target: Sodium Channel, TRP/TRPV Channel

Cat.No: T6442

Target: HSP

3-Methylcytidine

Cat.No: T7351

Target: Nucleoside Antimetabolite/Analog

Cat.No: T27259

Synonym: BOFA2,BOF A2,BOF-A2

Target: Others

c-Met inhibitor 1

Cat.No: T10655

Synonym: 3-[(2-甲基-2H-吲唑-5-基)硫基]-6-(1-甲基-1H-吡唑-4-基)-1,2,4-三唑并[4,3-B]哒嗪

Target: c-Met/HGFR

Topixantrone 2HCl

Cat.No: T28994L

Synonym: Topixantrone 2HCl( 156090-18-5 Free base),BBR3576 2HCl

Target: Topoisomerase

Cat.No: T77635

Target: Histone Demethylase, PD-1/PD-L1

Cat.No: T9912

Target: EGFR

Cat.No: T27704

Synonym: K-00135,Imidazol[1,2-b]pyridazine 1,K 00135,IMIDAZOPYRIDAZIN 1

Target: Pim

Disitamab vedotin

Cat.No: T39595

Synonym: RC 48,RC-48,RC48

Target: EGFR

Cat.No: T29017

Synonym: TrxR1INB19,Go Y015,TrxR1 IN B19,Go-Y015

Target: Others

Cat.No: T61859

Target: Antiviral, PERK

Cat.No: T76758

Synonym: AMG 102

Target: c-Met/HGFR

Cat.No: T2283

Synonym: 2-[(1-甲基丙基)二硫代]-1H-咪唑,IV-2,PX12

Target: Thioredoxin

Cat.No: T16947

Synonym: 3-substituted indolin-2-one 16f,SU-16F,SU 16F

Target: PDGFR

Cat.No: T19710

Synonym: Ciglitazona,U 63287,ADD3878,ADD-3878,U-63287,ADD 3878

Target: Apoptosis, p38 MAPK, PPAR

Cat.No: T28994

Synonym: BBR3576,BBR-3576,BBR 3576

Cat.No: T27414

Synonym: W68,W 68,W-68,GL331

Cat.No: T70894

Cat.No: T71060

Cat.No: T12635L

Synonym: BGC9331,ZD 9331

Target: Others

Cat.No: T24699

Synonym: R-1498,R 1498

CRM1 degrader 1

Cat.No: T60416

Cat.No: T69243

Cat.No: T69162

Cat.No: T61243

Cat.No: T21307

Synonym: NSC644591 NSCD644591 SKI2053R,Heptaplatin Sunpla,HTP

Cat.No: T61565

Cat.No: T61672

Cat.No: T61228

Esuberaprost Sodium

Cat.No: T9665

Cat.No: T76004

Cat.No: T60639

Cat.No: T62041

Cimetidine hydrochloride

Cat.No: T60584

Trastuzumab beta

Cat.No: T76971

Cat.No: T78155

Cat. No.	Product Name	Target	Signaling Pathways
T5043	Lentinan	Others	Others
	Lentinan 是一种 β-葡聚糖，从香菇中提取获得。它在日本已被批准用作胃癌的生物反应调节剂。
T3862	Irigenin	NF-κB; Integrin	Cytoskeletal Signaling; NF-κB
	Irigenin 可通过特异性和选择性地阻断 Extra Domain A 域的 C-C 环上α9β1和α4β1整合素结合位点，介导其抗转移作用。可通过增强胃癌细胞中促凋亡分子的表达来敏化 TRAIL 诱导的凋亡，具有抗癌作用。
T4034	Solamargine Solamargin,δ-Solanigrine,澳洲茄边碱	Apoptosis; p38 MAPK; P-gp; STAT	Apoptosis; JAK/STAT signaling; MAPK; Membrane transporter/Ion channel; Neuroscience; Stem Cells
	Solamargine (δ-Solanigrine) 是一种来源于茄属植物的类固醇 Solasodine 的衍生物，诱导非选择性细胞毒性和 P-gp 抑制作用。它通过下调 MMP-2 和 MMP-9 的表达和活性来显著抑制 HepG2 细胞的迁移和侵袭，在多种癌症中均表现出抗癌活性。
TC0039	Vasicinone	Others	Others
	Vasicinone 是一种喹唑啉类生物碱，分离自凡士林植物中。它是具有研究帕金森病和其他氧化应激相关神经退行性疾病的潜力。
T6S2038	Ziyuglycoside II	Apoptosis; Antioxidant; Reactive Oxygen Species	Apoptosis; Immunology/Inflammation; Metabolism; NF-κB; oxidation-reduction
	Ziyuglycoside II 是从地榆中提取的一种三萜皂苷，可诱导活性氧产生和凋亡，具有抗炎和抗癌作用。
TN1560	Dehydroeffusol 去氢厄弗酚,5-Ethenyl-1-Methylphenanthrene-2,7-Diol,Dehydro Effusol	MMP; ERK; GPR; Others	Endocrinology/Hormones; GPCR/G Protein; MAPK; Others; Proteases/Proteasome
	Dehydroeffusol (Dehydro Effusol) 通过选择性诱导肿瘤抑制性内质网应激和中度细胞凋亡来抑制胃癌细胞生长和致瘤性，具有抗癌、抗焦虑和镇静作用。
T2S1975	Ponicidin 冬凌草乙素,Rubescensine B	Apoptosis; JAK; STAT	Angiogenesis; Apoptosis; Chromatin/Epigenetic; JAK/STAT signaling; Stem Cells
	Ponicidin (Rubescensine B) 是来源于冬凌草的一种二萜，具有免疫调节、抗炎、抗病毒和抗癌作用。它可诱导胃癌细胞凋亡，降低 JAK2 和 STAT3 的磷酸化水平。
TN1103	Diphyllin 山荷叶素,二叶草素	ATPase; Proton pump; Influenza Virus; HIV Protease	Membrane transporter/Ion channel; Microbiology/Virology; Proteases/Proteasome
	Diphyllin 是一种从Justicia procumbens 中分离的芳基萘木脂素，是HIV-1的有效抑制剂，IC50 为 0.38 μM。它是V-ATPase 抑制剂，IC50值为 17 nM，可抑制人破骨细胞中的溶酶体酸化。它抑制NO 产生，IC50值为 50 μM ，具有抗癌和抗炎活性。
T6S1302	Carnosol	Nrf2; Endogenous Metabolite; S6 Kinase	Immunology/Inflammation; MAPK; Metabolism; PI3K/Akt/mTOR signaling
	Carnosol 是 Nrf2激活剂，增加 Nrf2 的水平以及能促进血红素氧合酶 1（HMOX1）表达。它是核糖体 S6激酶(RSK2)抑制剂，可用于胃癌相关研究，IC50值约为 5.5 μM。
T3S2312	Poncirin 枸橘苷,Isosakuranetin-7-neohesperidoside	Apoptosis; Others	Apoptosis; Others
	Poncirin (Isosakuranetin-7-neohesperidoside) 是从三叶草中分离出来的一种天然产物，具有抗炎活性。它防止脂肪生成，增强间充质干细胞中的成骨细胞分化，增加骨矿物质密度，改善小梁微结构，可能反映 GIO 小鼠的骨形成增加和骨吸收减少。
T3S2344	β,β-Dimethylacrylshikonin β,β-二甲基丙烯酰紫草素,Dimethylacrylshikonin,β, β-Dimethylacrylshikonin	ERK; HIF/HIF Prolyl-Hydroxylase	Chromatin/Epigenetic; MAPK; Metabolism
	β,β-Dimethylacrylshikonin (Dimethylacrylshikonin) 是一种萘醌衍生物，从 Arnebia nobilis 中提取得到。它利用 PI3K 通路诱导 eNOS、VEGF 和 HIF-1α 的表达，促进血管生成，具有抗肿瘤活性。
T4S0797	Berberine 小檗碱,Berberin,Umbellatine,黄连素	Reactive Oxygen Species; Topoisomerase; Endogenous Metabolite; Antibacterial; Antibiotic; Autophagy	Autophagy; DNA Damage/DNA Repair; Immunology/Inflammation; Metabolism; Microbiology/Virology; NF-κB
	Berberine (Umbellatine) 是从中草药黄连中分离出来的一种生物碱抗生素。它诱导活性氧生成并抑制 DNA 拓扑异构酶，具有抗肿瘤特性。
TN4932	Sageone	PARP; Akt; Caspase; Antifection	Apoptosis; Chromatin/Epigenetic; Cytoskeletal Signaling; DNA Damage/DNA Repair; Microbiology/Virology; PI3K/Akt/mTOR signaling; Proteases/Proteasome
	Sageone represents a promising anticancer agent against gastric cancer that warrants further study, it synergizes with cisplatin cytotoxicity in SNU-1 human gastric cancer cells.Sageone also shows antiviral activity.
TN1810	Jatropholone B	Others	Others
	Jatropholone B shows antiproliferative activity against cancer cell lines. It also has gastroprotective activity in preventing the gastric lesions in mice.
TN3495	Benzyl ferulate	TNF; Antifection	Apoptosis; Microbiology/Virology
	Benzyl ferulate has antimicrobial activity. It also shows good anti-proliferative against three gastro-intestinal cancer cell lines(HCT-116 colon carcinoma, KYSE-30 oesophageal squamous cancer, and NCI-N87 gastric carcinoma).
TN3852	Dihydrolicoisoflavone	Antifection	Microbiology/Virology
	Dihydrolicoisoflavone A possesses weaker anti-H. pylori activity, it may be useful chemopreventive agents for peptic ulcer or gastric cancer in H. pylori-infected individuals.
TN1302	6,8-Diprenylorobol 6,8-二异戊烯基香豌豆苷元	Others; HIV Protease; Antifection	Microbiology/Virology; Others; Proteases/Proteasome
	6,8-Diprenylorobol possesses weaker anti-H. pylori activity, it may be a useful chemopreventive agent for peptic ulcer or gastric cancer in H. pylori-infected individuals.
TN6010	Picrasidine S
	Picrasidine S shows the potent cytotoxicity against human HeLa cervical, gastric MKN-28, and mouse melanoma B-16 cancer cells, it also shows the potent antibacterial activity against two strains of pathogenic bacteria methicillin-resistant Staphylococcus
T83088	Anticancer agent 156
	Anticanceragent 156（compound 11）是一种基于Miliusanes的强效抗癌剂，有效抑制人源癌细胞生长，并对胃癌细胞展现出显著细胞毒性。
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
TN4113	Garcinone E	Antifection	Microbiology/Virology
	Garcinone E is active constituents in the anticomplement assay used. Garcinone E exhibits potent activity in vitro against Plasmodium falciparum chloroquine-resistant strain W2, with IC50 values below 3 µM. It has potent cytotoxic effect on all hepatocellular carcinomas cell lines as well as on the other gastric and lung cancer cell lines included in the screen, may be potentially useful for the treatment of certain types of cancer.
TN5369	Dehydroleucodine Dehydroleucodin
	Dehydroleucodine has antidiarrheal, anti-inflammatory, anti-microbial, embryotoxicity, gastric cytoprotective, anti-cancer activities. Dehydroleucodine has an important inhibitory effect in cellular pathways regulating adipocyte differentiation by modulat
T83320	4'-Demethylpodophyllotoxone
	4'-Demethylpodophyllotoxone为链格孢（Alternaria alternata）S-f6的生物转化中间产物，经4-(2,3,5,6-tetramethylpyrazine-1) (4-TMP)修饰后形成的新化合物，可有效抑制人胃癌细胞系（BGC-823）的生长。
TN3655	Cimiside E	ERK; TNF; ROS; Akt; PI3K; PKC; PPAR	Apoptosis; Chromatin/Epigenetic; Cytoskeletal Signaling; DNA Damage/DNA Repair; Immunology/Inflammation; MAPK; Metabolism; PI3K/Akt/mTOR signaling
	Cimiside E has anti-inflammatory activity, it selectively inhibits TNF-α-induced expression of VCAM-1 at least by upregulation of PPAR-γ, and signals for ERK1/2, PI3K, and PKC are involved in this effect.Cimiside E may be an effective chemopreventive agen
TN4223	Homopterocarpin	Antifection	Microbiology/Virology
	Homopterocarpin and Pterocarpus extract offer gastroprotection against indomethacin- induced ulcer by antioxidative mechanism and the modulation of gastric homeostasis, homopterocarpin may be responsible for, or contribute to the antiulcerogenic property

天然产物

Cat.No: T5043

Target: Others

Cat.No: T3862

Target: NF-κB, Integrin

Cat.No: T4034

Synonym: Solamargin,δ-Solanigrine,澳洲茄边碱

Target: Apoptosis, p38 MAPK, P-gp, STAT

Cat.No: TC0039

Target: Others

Ziyuglycoside II

Cat.No: T6S2038

Target: Apoptosis, Antioxidant, Reactive Oxygen Species

Cat.No: TN1560

Synonym: 去氢厄弗酚,5-Ethenyl-1-Methylphenanthrene-2,7-Diol,Dehydro Effusol

Target: MMP, ERK, GPR, Others

Cat.No: T2S1975

Synonym: 冬凌草乙素,Rubescensine B

Target: Apoptosis, JAK, STAT

Cat.No: TN1103

Synonym: 山荷叶素,二叶草素

Target: ATPase, Proton pump, Influenza Virus, HIV Protease

Cat.No: T6S1302

Target: Nrf2, Endogenous Metabolite, S6 Kinase

Cat.No: T3S2312

Synonym: 枸橘苷,Isosakuranetin-7-neohesperidoside

Target: Apoptosis, Others

β,β-Dimethylacrylshikonin

Cat.No: T3S2344

Synonym: β,β-二甲基丙烯酰紫草素,Dimethylacrylshikonin,β, β-Dimethylacrylshikonin

Target: ERK, HIF/HIF Prolyl-Hydroxylase

Cat.No: T4S0797

Synonym: 小檗碱,Berberin,Umbellatine,黄连素

Target: Reactive Oxygen Species, Topoisomerase, Endogenous Metabolite, Antibacterial, Antibiotic, Autophagy

Cat.No: TN4932

Target: PARP, Akt, Caspase, Antifection

Cat.No: TN1810

Target: Others

Benzyl ferulate

Cat.No: TN3495

Target: TNF, Antifection

Dihydrolicoisoflavone

Cat.No: TN3852

Target: Antifection

6,8-Diprenylorobol

Cat.No: TN1302

Synonym: 6,8-二异戊烯基香豌豆苷元

Target: Others, HIV Protease, Antifection

Cat.No: TN6010

Anticancer agent 156

Cat.No: T83088

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

Cat.No: TN1617

Target: BCL, Caspase, p53

Cat.No: TN4113

Target: Antifection

Dehydroleucodine

Cat.No: TN5369

Synonym: Dehydroleucodin

4'-Demethylpodophyllotoxone

Cat.No: T83320

Cat.No: TN3655

Target: ERK, TNF, ROS, Akt, PI3K, PKC, PPAR

Homopterocarpin

Cat.No: TN4223

Target: Antifection

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