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Search Results for " g1 phase "

104

抑制剂 & 化合物

19

天然产物

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Cat. No.	Product Name	Target	Signaling Pathways
T7969	Dipyrithione	Others	Others
	Dipyrithione 似乎具有新的细胞毒性和强大的广谱抗肿瘤活性。
T7057	Methylstat	Histone Demethylase; Others	Chromatin/Epigenetic; Others
	Methylstat 是一种含有 Jumonji C 结构域的组蛋白去甲基化酶 (JMJD) 抑制剂的甲酯前药，具有良好的细胞渗透性。在体外试验中，methylstat 的游离酸可抑制 JMJD2A、JMJD2C、JMJD2E、PHF8 和 JMJD3，IC50 值分别约为 4.3、3.4、5.9、10 和 43 µM。 Methylstat 抑制 JMJD2C 敏感的食管癌细胞系 KYSE150 的生长，GI50 为 5.1 µM，而 methylstat 的游离酸在高达 100 µM 时不抑制细胞生长。 Methylstat 以浓度依赖性方式在多个位点诱导组蛋白高甲基化（KYSE150 细胞中 H3K4me3 和 H3K9me3 的 EC50 = 10.3 和 8.6 µM，MCF-7 细胞中的 EC50 分别为 6.7 和 6.3 µM）。
T8616	Fasentin N-[4-chloro-3-(trifluoromethyl)phenyl]-3-oxobutanamide	transporter	Metabolism
	Fasentin (N-[4-chloro-3-(trifluoromethyl)phenyl]-3-oxobutanamide) 是葡萄糖摄取抑制剂，可抑制GLUT-1/GLUT-4转运蛋白，优先抑制 GLUT4，IC50为 68 μM。它是死亡受体刺激敏化剂，可敏化细胞对 FAS 诱导的细胞死亡，具有抗血管生成活性。
T4321	Indisulam E 7070	CDK; Carbonic Anhydrase	Cell Cycle/Checkpoint; Metabolism
	Indisulam (E 7070) 是碳酸酐酶抑制剂。它是细胞周期 G1期的靶向化合物，能够抑制 CDK2及周期蛋白 E 的激活，阻止 G1/S 的转化。它可以募集 DCAF15诱导RBM39降解来靶向剪接，具有抗癌作用。
T61884	C6 Ceramide N-hexanoylsphingosine,N-(hexanoyl)sphing-4-enine	Apoptosis	Apoptosis
	C6 Ceramide (N-hexanoylsphingosine) 是神经酰胺途径的一种激活剂，通过激活ERK使细胞停滞在G0/G1期，可以在多种癌细胞系中发挥作用。
T73577	TJ08	Apoptosis	Apoptosis
	TJ08 是一种具有抗癌的1,2,5-三取代苯并咪唑衍生物，能够有效诱导G1/S期阻滞，同时促进多种癌细胞的凋亡作用。
T61722	ZDLD20	Apoptosis	Apoptosis
	ZDLD20 是一种具有口服活性和选择性的CDK4抑制剂，是一种 β-咔啉类化合物，具有抗 HCT116 和抗癌活性，抑制集落形成、抑制侵袭和迁移、诱导细胞凋亡和阻止细胞周期的 G1 期。
T22317	DRB18	transporter	Metabolism
	DRB18 is a highly effective pan-class inhibitor of glucose transporter proteins (GLUT). It significantly modulates energy-related metabolism in A549 cells by inducing alterations in the abundance of metabolites associated with glucose-related pathways. DRB18 exerts its effects by promoting G1/S phase arrest, increasing oxidative stress, and prompting necrotic cell death, ultimately displaying notable anti-tumor activity [1].
T36082	Cysmethynil	Autophagy; Ras	Autophagy; GPCR/G Protein; MAPK
	Cysmethynil 是一种基于吲哚的 Icmt 时间依赖性抑制剂，具有抗肿瘤活性，对 RAS 膜结合和 EGF的信号转导有抑制作用。Cysmethynil 诱导细胞周期阻滞在 G1 期，诱导细胞自噬，可用于研究实体肿瘤。
T21872	CCT018159	Apoptosis; HSP	Apoptosis; Cytoskeletal Signaling; Metabolism
	CCT018159 是一种 3,4-二芳基吡唑间苯二酚，是一种 ATP 竞争性HSP90ATPase 抑制剂，对人 Hsp90β 和酵母 Hsp90 具有抑制作用，IC50分别为 3.2 和 6.6 μM。CCT018159 抑制与侵袭和血管生成有关的关键内皮细胞和肿瘤细胞功能。CCT018159 引起与 G1 期阻滞相关的细胞抑制并诱导细胞凋亡。
T16522	Phenoxodiol 脱氢雌马酚,Dehydroequol,Idronoxil,Haginin E	Apoptosis; IAP; Caspase; Topoisomerase; p53	Apoptosis; DNA Damage/DNA Repair; Proteases/Proteasome
	Phenoxodiol (Idronoxil) 是合成genestein 的类似物，激活线粒体caspase 系统，抑制XIAP，使癌细胞对fas 介导的凋亡敏感。它在细胞周期的G1/S 期诱导细胞周期阻滞，通过独立于p53的方式上调p21WAF1。它通过稳定可分裂复合物抑制DNA 拓扑异构酶II，从而阻止DNA 复制。
T35900	JAK2-IN-7 JAK2-IN-7	JAK	Angiogenesis; Chromatin/Epigenetic; JAK/STAT signaling; Stem Cells
	JAK2-IN-7 是一种选择性 JAK2抑制剂，对 JAK2，SET-2 和 Ba/F3V617F 细胞的IC50为 3、11.7 和 41 nM。 JAK2-IN-7 的选择性是 JAK1, JAK3，FLT3 的 14 倍以上。JAK2-IN-7 刺激细胞周期停滞在 G0/G1 期，并诱导肿瘤细胞凋亡 (apoptosis)，具有抗肿瘤活性。
T77697	BML-278 BML278,BML 278	Sirtuin; Histone Methyltransferase	Chromatin/Epigenetic; DNA Damage/DNA Repair
	BML-278 是一种 SIRT1 激活剂，EC150 值为 1 μM。BML-278 增加父本和母本原核中的 H3K9 甲基化并抑制 H3K9 乙酰化，可用于改善早期胚胎发育。BML-278 促使原代人间充质细胞的细胞周期停止在 G1/S 期，可用于延缓衰老。BML-278 减少 U937 细胞中的微管蛋白乙酰化，增加小鼠 C2C12 成肌细胞的线粒体密度。
T33380	MI-389
	MI-389 is a protein degrader, targeting the translation termination factor G1 to S phase transition 1 (GSPT1).
T26194	SKLB70326 SKLB 70326,SKLB-70326
	SKLB70326 is a cell-cycle progression inhibitor that acts by inducing G0/G1 phase arrest and apoptosis in human hepatic carcinoma cells.
T79474	GSPT1 degrader-1	Apoptosis	Apoptosis
	GSPT1 degrader-1 (compound 9q) 是通过泛素蛋白酶体系统有效实现 G1 至 S 相变 1 (GSPT1) 降解的化合物。此外，该化合物能诱导G0/G1 期细胞停滞及细胞凋亡 (apoptosis)。
T29026	Tylophorine NSC 76387,Tylophorin
	Tylophorine is a major alkaloid of Tylophora indica with anti-inflammatory and antitumor activity. Tylophorine arrests carcinoma cells at G1 phase by downregulating cyclin A2 expression.
T61719	DC-CPin711
	DC-CPin711, a potent and selective inhibitor of the bromodomain of CREB-binding protein (CBP) with an IC50 of 0.0626 μM, effectively halts the cell cycle at the G1 phase and promotes apoptosis [1].
T63594	Topoisomerase IIα-IN-3
	Topoisomerase IIα-IN-3 是 DNA 插入型 topoisomerase-Iiα 抑制剂，能够将细胞周期阻滞在 G0/G1 期，并诱导细胞凋亡 (apoptosis)。
T6844	GGTI298 Trifluoroacetate GGTI 298,GGTI 298 TFA salt	Apoptosis; Transferase; Ras	Apoptosis; GPCR/G Protein; MAPK; Metabolism
	GGTI298 Trifluoroacetate (GGTI 298 TFA salt) 是一种GGTase I 抑制剂，能够抑制Rap1A 且IC50值为3μM，对Ha-Ras 的作用很小IC50值 > 20 μM。
T72722	Physachenolide C	Epigenetic Reader Domain	Chromatin/Epigenetic
	Physachenolide C 是一种选择性BET抑制剂，具有诱导细胞凋亡(apoptosis)和引起细胞周期在G0-G1期停滞的抗肿瘤活性。
T61631	VEGFR-2-IN-23
	VEGFR-2-IN-23 (compound 11b) is a highly potent and selective inhibitor of VEGFR-2, with an impressive IC 50 value of 0.34 nM. This compound exhibits notable antitumor activity, capable of inducing apoptosis and cell cycle arrest specifically at the G1 phase [1].
T72411	Kobusine derivative-2
	Kobusine derivative-2，一种kobusine衍生物，对癌细胞显示出抗增殖活性，并能诱导MDA-MB-231细胞在亚G1期阻滞，表现出抗癌活性。
T61412	Anticancer agent 47
	Anticancer agent 47 (compound 4j) exhibits potent anticancer properties, demonstrating antiproliferative activities and inducing apoptosis as well as cell cycle arrest at G0/G1 phase. Moreover, Anticancer agent 47 has exhibited significant in vivo antitumor activities [1].
T74440	YM281
	YM281是高效EZH2抑制剂，具备诱导细胞凋亡(apoptosis)及使细胞周期在G0/G1期停滞的能力。在体内，YM281展现出对抗肿瘤的活性，并有研究淋巴瘤的潜力。
T74525	PROTAC EGFR degrader 6
	PROTACEGFRdegrader 6 是一种PROTACEGFR 降解剂，可有效降解 HCC827 细胞中的EGFRDel19，DC50为 45.2 nM。PROTACEGFRdegrader 6 显著诱导 HCC827 细胞凋亡 (apoptosis) 并将细胞阻滞在 G1 期。
T63002	VEGFR-2-IN-15
	VEGFR-2-IN-15 (Compound 14b) 是一种 VEGFR-2 的有效抑制剂。VEGFR-2-IN-15 能够抑制 HepG2 细胞在 Pre-G1 期的生长，诱导细胞凋亡。
T63360	DNA topoisomerase II inhibitor 1
	DNA topoisomerase II inhibitor 1 是 DNA 拓扑异构酶 II 的有效抑制剂，能够将细胞周期停滞在亚 G1 期，并诱导细胞凋亡 (apoptosis) ，具有抗增值作用。
T62439	VEGFR-2-IN-14
	VEGFR-2-IN-14 (Compound 5) 是一种 VEGFR-2 的有效抑制剂。VEGFR-2-IN-14 对 HepG2 细胞在 Pre-G1 期的生长具有抑制作用，并能够诱导细胞凋亡 (apoptosis)。
T61299	PAK4-IN-2
	PAK4-IN-2 is an exceptionally effective inhibitor of PAK4, exhibiting an IC 50 value of 2.7 nM. This compound is capable of arresting MV4-11 cells at the G0/G1 phase and inducing cell apoptosis. It holds significant potential in cancer research [1].
T36944	Ara-G	Nucleoside Antimetabolite/Analog	Cell Cycle/Checkpoint; DNA Damage/DNA Repair
	Ara-G 是一种脱氧鸟苷 (GdR) 类似物和核苷类似物，可被 T 淋巴谱系细胞迅速转化为其相应的阿拉伯糖基鸟嘌呤核苷酸三磷酸 (araGTP)，从而抑制 DNA 合成和对 T 淋巴母细胞的选择性体外毒性细胞系以及来自 T 细胞急性淋巴细胞白血病 (ALL) 患者的新鲜分离的白血病细胞。
T64026	ERα antagonist 1
	ERα antagonist 1 是选择性的、有效的、共价雌激素受体 α (ERα)拮抗剂。ERα antagonist 1 能够将 MCF-7 细胞的细胞周期阻滞在 G0/G1 期，并诱导其凋亡 (apoptosis)。
T83023	Antiproliferative agent-26
	Antiproliferative agent-26 (compound 4g) 是抗增殖药物，(10 μM) 对多种癌细胞如白血病、中枢神经系统肿瘤、黑色素瘤、肾癌和乳腺癌具有抑制效果。该药物能够阻止集落形成，并在(5 μM) 和 (25 μM) 浓度作用下导致细胞周期在G1期/S期停滞。
T82762	Cdc25A (80-93) (human)
	Cdc25A (80-93) (human)为调控细胞周期蛋白D1及G1/S转换中相关蛋白表达，进而控制细胞增殖与肿瘤发生的多肽。该化合物在癌症研究中具应用价值。
T63599	Anticancer agent 54
	Anticancer agent 54 是有效的抗癌剂，其抗癌活性取决于 DNA 嵌入和 ROS 生成。 Anticancer agent 54 能够将细胞周期阻滞在 G0/G1 期，并诱导细胞凋亡 (apoptosis)，具有抗增殖效果。
T73512	ZC0109
	ZC0109 是 IDO1和硫氧还蛋白还原酶 1 (TrxR1) 的双抑制剂，IC50分别为 50 nM 和 3.0 μM。ZC0109 诱导活性氧 (ROS) 积累，使细胞周期阻滞于 G1/S 期，导致癌细胞凋亡 (apoptosis)。
T74768	Antitumor agent-92	Apoptosis	Apoptosis
	Antitumor agent-92为一种淫羊藿素衍生物，能够引起细胞周期在G0/G1期的停滞，并诱导细胞凋亡。该化合物展现出在肝细胞癌(HCC)研究中的应用潜力。
TP1105	α-Factor Mating Pheromone, yeast (TFA) α-Factor Mating Pheromone, yeast (TFA)(59401-28-4,FREE),Mating Factor α (TFA)
	The alpha factor pheromone arrests yeast in the G1 phase of their cell cycle. Alpha Factor Mating Pheromone induces the expression of mating genes, changes in nuclear architecture, and polarzes growth toward the mating partner.
T61501	Topoisomerase I inhibitor 5
	Topoisomerase I inhibitor 5 is an efficient inhibitor of topoisomerase I, with an IC50 value. It effectively disrupts DNA and inhibits the activity of topoisomerase I. Moreover, it can induce apoptosis in MCF-7 cells and arrest the cell cycle at the G1 phase. Topoisomerase I inhibitor 5 also exhibits potency in reversing P-gp-mediated resistance to Adriamycin [1].
T63123	FAK inhibitor 6
	化合物26f 不仅优化了有效抑制酶（IC50= 28.2 nM），也表现出相对较少的细胞毒性（IC50= 3.32 μM），并以剂量依赖性方式诱导 MDA-MB-231细胞凋亡，有效阻断 G0/G1期MDA-MB-231细胞。
T78549	Ethylene glycol dimethacrylate	Reactive Oxygen Species	Immunology/Inflammation; Metabolism; NF-κB
	Ethylene glycol dimethacrylate 是一种具有细胞毒性和基因毒性作用的甲基丙烯酸酯单体。它可增加人牙龈成纤维细胞 (HGF) 内的活性氧 (ROS) 产生，引发 DNA 损伤和细胞凋亡 (apoptosis)，并使细胞周期在 G1/G0 期停滞。
T64222	Antitumor agent-55
	Antitumor agent-55 (compound 5q) 是一种有效的抗肿瘤剂，能够有效的抑制PC3 (IC50: 0.91 μM)。Antitumor agent-55 能够将 PC3 的细胞周期阻滞 G1/S 期，诱导其凋亡，抑制细胞迁移，阻碍 PC3 的形成。
T62917	MIR002
	MIR002 是一种有效的、口服具有活力的 DNA polymerase α (POLA1) 和 HDAC 11 双重抑制剂，具有显著的体内抗肿瘤活性。MIR002 能够诱导 p53 乙酰化、激活 p21，将细胞周期阻滞在 G1/S 期，并诱导细胞凋亡。
T79466	Antitumor agent-111	c-Met/HGFR	Tyrosine Kinase/Adaptors
	Antitumor agent-111（compound 46）是一款c-Met激酶抑制剂，IC50为46 nM，显示出抗肿瘤和抗增殖特性。该化合物能够导致细胞周期在G0/G1期停滞，并诱发细胞凋亡（apoptosis）。
T62916	GEM144
	GEM144 是一种有效的、口服具有活力的 DNA polymerase α(POLA1) 和HDAC 11 双重抑制剂。GEM144 能够诱导 p53 乙酰化、激活 p21，将细胞周期阻滞在 G1/S 期，并诱导细胞凋亡。
T63470	PI3K/mTOR Inhibitor-8
	PI3K/mTOR Inhibitor-8 是 PI3K (PI3Kα IC50: 0.46 nM) 和 mTOR (mTOR IC50: 12 nM) 双重抑制剂。PI3K/mTOR Inhibitor-8 能够将 HCT-116 细胞的细胞周期阻滞在G1/S 期，并诱导其凋亡 (apoptosis)。
T61596	EGFR/HER2/DHFR-IN-1
	EGFR/HER2/DHFR-IN-1 is a highly selective and potent anticancer compound specifically targeting MCF-7 breast cancer cells. It acts as a multi-inhibitor, targeting the EGFR/HER2 kinase and DHFR enzymes, with IC50 values of 0.153 μM, 0.108 μM, and 0.291 μM, respectively. Its mechanism of action involves cell cycle arrest at the G1/S phase and induction of apoptosis in cells [1].
T74524	PROTAC EGFR degrader 5
	PROTACEGFRdegrader 5 (Compound 10) 是一种 PROTACEGFR 降解剂，可有效降解 HCC827 细胞中的 EGFRDel19，DC50为 34.8 nM。PROTACEGFRdegrader 5 显著诱导 HCC827 细胞凋亡 (apoptosis) 并将细胞阻滞在 G1 期。
T63693	EGFR-IN-55
	EGFR-IN-55 是 EGFR 的有效抑制剂，能够作用于 EGFRWT (IC50: 70 nM) 和 EGFRL858R/T790M (IC50: 3.9 nM) 。EGFR-IN-55 能够将 NCI-H1975 细胞的细胞周期阻滞在 G0/G1 期，表现出抗癌效果。
T78942	HSP90-IN-23	HSP	Cytoskeletal Signaling; Metabolism
	HSP90-IN-23 (Comp 12-1)为热休克蛋白90 (HSP90)的抑制剂，具有9 nM的IC50值。该化合物能够诱导肿瘤细胞凋亡，并抑制肿瘤细胞在G0/G1期的细胞周期。HSP90-IN-23常用于肿瘤学领域的研究。

化合物

Cat.No: T7969

Target: Others

Cat.No: T7057

Target: Histone Demethylase, Others

Cat.No: T8616

Synonym: N-[4-chloro-3-(trifluoromethyl)phenyl]-3-oxobutanamide

Target: transporter

Cat.No: T4321

Synonym: E 7070

Target: CDK, Carbonic Anhydrase

Cat.No: T61884

Synonym: N-hexanoylsphingosine,N-(hexanoyl)sphing-4-enine

Target: Apoptosis

Cat.No: T73577

Target: Apoptosis

Cat.No: T61722

Target: Apoptosis

Cat.No: T22317

Target: transporter

Cat.No: T36082

Target: Autophagy, Ras

Cat.No: T21872

Target: Apoptosis, HSP

Cat.No: T16522

Synonym: 脱氢雌马酚,Dehydroequol,Idronoxil,Haginin E

Target: Apoptosis, IAP, Caspase, Topoisomerase, p53

Cat.No: T35900

Synonym: JAK2-IN-7

Target: JAK

Cat.No: T77697

Synonym: BML278,BML 278

Target: Sirtuin, Histone Methyltransferase

Cat.No: T33380

Cat.No: T26194

Synonym: SKLB 70326,SKLB-70326

GSPT1 degrader-1

Cat.No: T79474

Target: Apoptosis

Cat.No: T29026

Synonym: NSC 76387,Tylophorin

Cat.No: T61719

Topoisomerase IIα-IN-3

Cat.No: T63594

GGTI298 Trifluoroacetate

Cat.No: T6844

Synonym: GGTI 298,GGTI 298 TFA salt

Target: Apoptosis, Transferase, Ras

Physachenolide C

Cat.No: T72722

Target: Epigenetic Reader Domain

Cat.No: T61631

Kobusine derivative-2

Cat.No: T72411

Anticancer agent 47

Cat.No: T61412

Cat.No: T74440

PROTAC EGFR degrader 6

Cat.No: T74525

Cat.No: T63002

DNA topoisomerase II inhibitor 1

Cat.No: T63360

Cat.No: T62439

Cat.No: T61299

Cat.No: T36944

Target: Nucleoside Antimetabolite/Analog

ERα antagonist 1

Cat.No: T64026

Antiproliferative agent-26

Cat.No: T83023

Cdc25A (80-93) (human)

Cat.No: T82762

Anticancer agent 54

Cat.No: T63599

Cat.No: T73512

Antitumor agent-92

Cat.No: T74768

Target: Apoptosis

α-Factor Mating Pheromone, yeast (TFA)

Cat.No: TP1105

Synonym: α-Factor Mating Pheromone, yeast (TFA)(59401-28-4,FREE),Mating Factor α (TFA)

Topoisomerase I inhibitor 5

Cat.No: T61501

FAK inhibitor 6

Cat.No: T63123

Ethylene glycol dimethacrylate

Cat.No: T78549

Target: Reactive Oxygen Species

Antitumor agent-55

Cat.No: T64222

Cat.No: T62917

Antitumor agent-111

Cat.No: T79466

Target: c-Met/HGFR

Cat.No: T62916

PI3K/mTOR Inhibitor-8

Cat.No: T63470

EGFR/HER2/DHFR-IN-1

Cat.No: T61596

PROTAC EGFR degrader 5

Cat.No: T74524

Cat.No: T63693

Cat.No: T78942

Target: HSP

Cat. No.	Product Name	Target	Signaling Pathways
T3S1416	Decursin Decursinol angelate,前胡素,(+)-Decursin,紫花前胡素	Apoptosis; PKC	Apoptosis; Chromatin/Epigenetic; Cytoskeletal Signaling
	Decursin (Decursinol angelate) 是一种细胞毒性剂，是一种来自朝鲜当归根的有效蛋白激酶 C 激活剂。它通过 Hippo/YAP 信号通路抑制 HepG2 细胞的生长。它通过下调 CXCR7 表达来抑制胃癌中的肿瘤生长，迁移和侵袭。
T1882	Meisoindigo N-Methylisoindigotin,Methylisoindigotin,Natura-α,甲异靛,Dian III,异甲靛	Apoptosis	Apoptosis
	Meisoindigo (Natura-α) 是 Indirubin 的衍生物，可以造成急性髓细胞性白血病细胞周期在 G0/G1 期停滞，并诱导凋亡，具有高抗肿瘤活性。
T3805	Prim-O-glucosylcimifugin 升麻苷,Cimifugin beta-D-glucopyranoside,Cimifugin 7-glucoside	TNF; COX; JAK; NO Synthase	Angiogenesis; Apoptosis; Chromatin/Epigenetic; Immunology/Inflammation; JAK/STAT signaling; Neuroscience; Stem Cells
	Prim-O-glucosylcimifugin (Cimifugin 7-glucoside) 具有强效的抗炎作用。通过调节 JAK2/STAT3 信号传导可抑制iNOS 和COX-2表达。
T2996	Tetrandrine NSC-77037,d-Tetrandrine,Hanfangchin A,粉防己碱,Fanchinine,Sinomenine A,汉防己甲素	Potassium Channel; Calcium Channel	Membrane transporter/Ion channel; Metabolism
	Tetrandrine (Sinomenine A) 是来自粉防己的一种双苯基异喹啉生物碱，可抑制电压门控钙离子通道 (ICa) 和 Ca2+激活的钾离子通道。
TN1805	Isosilybin B	Apoptosis; Androgen Receptor	Apoptosis; Endocrinology/Hormones
	Isosilybin B 是一种从水飞蓟中提取的黄酮木脂素，具有抗前列腺癌 (PCA) 活性，对癌细胞增殖有抑制作用，促使 G1 期阻滞和凋亡。Isosilybin B 诱导雄激素受体降解。
T3314	Perillyl alcohol Isocarveol,Perilla alcohol,紫苏醇	Apoptosis; Endogenous Metabolite	Apoptosis; Metabolism
	Perillyl alcohol (Isocarveol) 是一种单萜，可在不影响正常细胞的情况下诱导肿瘤细胞凋亡。
T2S2043	Dracorhodin perchlorate Dracorhodin perochlorate,血竭素高氯酸盐,Dracohodin perochlorate	Apoptosis; Others	Apoptosis; Others
	Dracorhodin perchlorate 是来源于中药血竭的一种天然产物。它抑制细胞生长，并以剂量和时间依赖性方式诱导成纤维细胞凋亡，将细胞周期阻滞在 G1 期，可作为抗乳腺癌的候选药物。
T3386	Kaempferitrin Lespedin,Kaempferol,Lespenephryl,Lespenefril,Kaempferol 3,7-dirhamnoside,山奈苷	cell cycle arrest; Glucokinase; IGF-1R	Cell Cycle/Checkpoint; Metabolism; Tyrosine Kinase/Adaptors
	Kaempferitrin (Lespenephryl) 是天然黄酮苷类化合物，具有缓解疼痛、抗糖尿病、消炎、抗肿瘤和化疗作用，可激活胰岛素信号传导。
T37067	9-hydroxy Stearic Acid	HDAC	Chromatin/Epigenetic; DNA Damage/DNA Repair
	9-hydroxy Stearic Acid 是一种羟基脂肪酸，是9-PAHSA 的活性代谢物。9-hydroxy Stearic Acid 是由9-PAHSA 通过肝脏和胰腺的羧基酯脂肪酶形成的。9-hydroxy Stearic Acid (5 μM)抑制HT-29结肠癌细胞裂解物中组蛋白去乙酰化酶1 (HDAC1)的表达。3 .当浓度为100 μM.1时，可抑制HT-29细胞的增殖，并诱导细胞周期阻滞于G0/ g1期。
T6S1917	Schisandrol B Gomisin A,TJN-101,Besigomsin,五味子醇乙,Gamma-Schisandrin,戈米辛A,Schizandrol B,Wuweizi alcohol-B	P450; Reactive Oxygen Species; Autophagy	Autophagy; Immunology/Inflammation; Metabolism; NF-κB
	Schisandrol B (Besigomsin) 是华中五味子的主要活性成分，具有保肝、抗炎、抗糖尿病和抗氧化的作用。它抑制活性氧的产生，也抑制 P-糖蛋白和CYP3A 的活性。
T2S2215	Crebanine	Apoptosis; Others; Akt	Apoptosis; Cytoskeletal Signaling; Others; PI3K/Akt/mTOR signaling
	Crebanine 是来自于韦诺萨千金藤的一种生物碱，通过抑制 MAPKs 和 Akt 信号通路表现出抗炎活性，还具有抗心律失常的作用。它可诱导人类癌细胞的 G1阻滞和凋亡。
T16942	Sterigmatocystine	Others	Others
	Sterigmatocystine is an inhibitor of G1 Phase and DNA synthesis and is used to inhibit p21 activity. Sterigmatocystine is a precursor of aflatoxins and a mycotoxin produced by common mold strains from Aspergillus versicolor.
TMA0918	Neochamaejasmine A	Caspase	Apoptosis; Proteases/Proteasome
	Neochamaejasmin A can inhibit cellular (3)H-thymidine incorporation (IC 50 12.5 microg/mL) and subsequent proliferation of human prostate cancer LNCaP cells, it blocks cell cycle progression at the G1 phase by activating the p21 protein and ultimately pro
T75630	Ganoderic acid Mf
	Ganoderic acid Mf为具有抗肿瘤活性的三萜类化合物，能导致细胞周期在G1期停滞，并在正常细胞与癌细胞中显示高度选择性，通过线粒体介导途径促进细胞凋亡(apoptosis)。
T75621	Secalonic acid D
	Secalonic acid D 是一种抗肿瘤细胞的有毒化合物。Secalonic acid D 可以从Aspergillus aculeatus 的代谢产物中分离得到。Secalonic acid D 激活GSK3-β，并降解β-catenin。因此，Secalonic acid D 下调c-Myc 表达，使细胞周期停滞在 G1 期，诱导细胞凋亡 (apoptosis)。
T79971	Asparanin A	Apoptosis	Apoptosis
	Asparanin A 是一种具有抗癌活性的凋亡 (apoptosis) 诱导剂。它能够通过线粒体和 PI3K/AKT 信号通路使细胞周期在 G0/G1 期停滞，并有效抑制癌细胞生长。此外，Asparanin A 在小鼠Ishikawa子宫内膜癌异种移植模型中显示出显著的体内抑制肿瘤生长效力。
TN3719	Cristacarpin	p38 MAPK; ROS; CDK; Antifection; p53	Apoptosis; Cell Cycle/Checkpoint; Immunology/Inflammation; MAPK; Microbiology/Virology
	Cristacarpin exhibits moderate but selective activity towards DNA repair-deficient yeast mutants. It promotes endoplasmic reticulum (ER) stress, leading to sub-lethal reactive oxygen species (ROS) generation and which eventually terminates by triggering s
TN3587	Capillarisin	MMP; ERK; IL Receptor; BCL; VEGFR; TNF; NOS; NF-κB; TLR; MAPK; COX; DNA/RNA Synthesis; Prostaglandin Receptor; JNK; STAT	Angiogenesis; Apoptosis; Cell Cycle/Checkpoint; DNA Damage/DNA Repair; GPCR/G Protein; Immunology/Inflammation; JAK/STAT signaling; MAPK; Neuroscience; NF-κB; Proteases/Proteasome; Stem Cells; Tyrosine Kinase/Adaptors
	Capillarisin is a novel blocker of STAT3 activation and thus may have a potential in negative regulation of growth, metastasis, and chemoresistance of tumor cells, it inhibits cancer cell growth of osteosarcoma cells by inducing apoptosis accompanied with
T36954	Nemorosone
	Nemorosone is a polycyclic polyprenylated acylphloroglucinol (PPAP) originally isolated from C. rosea that has antiproliferative properties.1 Nemorosone inhibits growth of NB69, Kelly, SK-N-AS, and LAN-1 neuroblastoma cells (IC50s = 3.1-6.3 μM), including several drug-resistant clones, but not MRC-5 human embryonic fibroblasts (IC50 = >40 μM).2 It increases DNA fragmentation in LAN-1 cells in a dose-dependent manner, and decreases N-Myc protein levels and phosphorylation of ERK1/2 by MEK1/2. Nem...

天然产物

Cat.No: T3S1416

Synonym: Decursinol angelate,前胡素,(+)-Decursin,紫花前胡素

Target: Apoptosis, PKC

Cat.No: T1882

Synonym: N-Methylisoindigotin,Methylisoindigotin,Natura-α,甲异靛,Dian III,异甲靛

Target: Apoptosis

Prim-O-glucosylcimifugin

Cat.No: T3805

Synonym: 升麻苷,Cimifugin beta-D-glucopyranoside,Cimifugin 7-glucoside

Target: TNF, COX, JAK, NO Synthase

Cat.No: T2996

Synonym: NSC-77037,d-Tetrandrine,Hanfangchin A,粉防己碱,Fanchinine,Sinomenine A,汉防己甲素

Target: Potassium Channel, Calcium Channel

Cat.No: TN1805

Target: Apoptosis, Androgen Receptor

Perillyl alcohol

Cat.No: T3314

Synonym: Isocarveol,Perilla alcohol,紫苏醇

Target: Apoptosis, Endogenous Metabolite

Dracorhodin perchlorate

Cat.No: T2S2043

Synonym: Dracorhodin perochlorate,血竭素高氯酸盐,Dracohodin perochlorate

Target: Apoptosis, Others

Cat.No: T3386

Synonym: Lespedin,Kaempferol,Lespenephryl,Lespenefril,Kaempferol 3,7-dirhamnoside,山奈苷

Target: cell cycle arrest, Glucokinase, IGF-1R

9-hydroxy Stearic Acid

Cat.No: T37067

Target: HDAC

Cat.No: T6S1917

Synonym: Gomisin A,TJN-101,Besigomsin,五味子醇乙,Gamma-Schisandrin,戈米辛A,Schizandrol B,Wuweizi alcohol-B

Target: P450, Reactive Oxygen Species, Autophagy

Cat.No: T2S2215

Target: Apoptosis, Others, Akt

Sterigmatocystine

Cat.No: T16942

Target: Others

Neochamaejasmine A

Cat.No: TMA0918

Target: Caspase

Ganoderic acid Mf

Cat.No: T75630

Secalonic acid D

Cat.No: T75621

Cat.No: T79971

Target: Apoptosis

Cat.No: TN3719

Target: p38 MAPK, ROS, CDK, Antifection, p53

Cat.No: TN3587

Target: MMP, ERK, IL Receptor, BCL, VEGFR, TNF, NOS, NF-κB, TLR, MAPK, COX, DNA/RNA Synthesis, Prostaglandin Receptor, JNK, STAT

Cat.No: T36954

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