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Search Results for " cisplatin "

55

抑制剂 & 化合物

14

天然产物

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Cat. No.	Product Name	Target	Signaling Pathways
T1564	Cisplatin cis-Diaminodichloroplatinum,CDDP,顺铂	DNA Alkylator/Crosslinker; Ferroptosis; DNA/RNA Synthesis; Autophagy	Apoptosis; Autophagy; Cell Cycle/Checkpoint; DNA Damage/DNA Repair
	Cisplatin (CDDP) 是一种 DNA 交联剂。Cisplatin 具有抗肿瘤活性，能够通过在癌细胞中形成 DNA 加合物来抑制 DNA 合成。Cisplatin 还可激活铁死亡并诱导自噬。
T82715	Cisplatin-resistant cells-IN-1
	Cisplatin-resistant cells-IN-1（化合物8）对顽固的铂类药物抗性细胞具有较高的细胞毒性。在低纳摩尔浓度范围内（IC50：0.14–1.79 μM in A549/A549-R, K562/K562-R, and MCF-7/MCF-7TamR cells），该化合物能有效降低代谢活性。
T10777	CG347B	HDAC	Chromatin/Epigenetic; DNA Damage/DNA Repair
	CG347B 是一种选择性HDAC6抑制剂。
T6612	NU6027	ATM/ATR; DNA-PK; CDK	Cell Cycle/Checkpoint; DNA Damage/DNA Repair; PI3K/Akt/mTOR signaling
	NU6027 是一种有效的 ATR/CDK 抑制剂，抑制 CDK1/2、ATR 和 DNA-PK，Ki 为 2.5 μM/1.3 μM、0.4 μM 和 2.2 μM。它以 ATR 依赖性方式增强羟基脲和顺铂的细胞毒性。
T68105	monohydroxycisplatin
	monohydroxycisplatin 是一种有用的有机化合物，可用于生命科学领域的相关研究。其产品编号为 T68105，CAS号为 101311-26-6。
T35300	Zeniplatin Zeniplatinum	Others	Others
	Zeniplatin (Zeniplatinum) 是一种新顺铂复合物，具有抗癌活性，可用于治疗转移性黑色素瘤和肾癌。
T36404L	PRLX-93936 HCL PRLX-93936 hcl(903499-49-0 Free base)	Ferroptosis; Reactive Oxygen Species	Apoptosis; Immunology/Inflammation; Metabolism; NF-κB
	PRLX-93936 HCL 是 erastin 的类似物，并显示出与顺铂对非小细胞肺癌 (NSCLC) 细胞的协同作用。
T1058	Carboplatin NSC 241240,卡铂,CBDCA,JM-8	DNA Alkylator/Crosslinker; DNA/RNA Synthesis; Autophagy	Autophagy; Cell Cycle/Checkpoint; DNA Damage/DNA Repair
	Carboplatin (JM-8) 是一种顺铂衍生物，一种 DNA 合成抑制剂。Carboplatin 能够与 DNA 结合，抑制复制和转录并诱导细胞死亡。Carboplatin 具有抗肿瘤活性。
T6381	Amifostine trihydrate Ethyol trihydrate,WR2721,三水氨磷汀,Amifostine	Others; HIF/HIF Prolyl-Hydroxylase	Chromatin/Epigenetic; Metabolism; Others
	Amifostine trihydrate (WR2721) 是一种广谱细胞保护剂和辐射防护剂。它可选择性保护正常组织免受放射线和化学疗法造成的损害。它是有效的HIF-α1和p53诱导剂。它通过清除氧衍生的自由基来保护细胞免受损伤。它可降低肾脏毒性并具有抗血管生成作用。
T2410	Nedaplatin 奈达铂,NSC 375101D	DNA/RNA Synthesis	Cell Cycle/Checkpoint; DNA Damage/DNA Repair
	Nedaplatin (NSC-375101D) 是顺铂的衍生物，是肿瘤集落形成单位的 DNA 损伤剂，IC50为94 μM。
T1478	Ondansetron hydrochloride dihydrate 盐酸昂丹司琼,SN 307,NSC 665799,GR 38032,Ondansetron hydrochloride	5-HT Receptor	GPCR/G Protein; Neuroscience
	Ondansetron hydrochloride dihydrate (GR 38032) 是5- HT3受体拮抗剂，可治疗化疗后的恶心和呕吐，有抗焦虑和抗精神病作用。
T60904	ERCC1-XPF-IN-2	Others	Others
	ERCC1-XPF-IN-2 在核苷酸切除修复、顺铂增强和 γH2AX 测定中具有活性。ERCC1-XPF-IN-2 是 ERCC1-XPF 核酸内切酶的有效抑制剂，IC50值为 0.6 μM。
T4434	Tirapazamine Tirazone,Win59075,SR4233,替拉扎明,SR259075	Others	Others
	Tirapazamine (Win59075) 是抗癌剂，对实体瘤中的缺氧细胞具有选择性细胞毒性，促使 DNA 中的单链和双链断裂，碱基损伤和细胞死亡。
T8845	UTL-5g 3-Isoxazolecarboxamide, N-(2,4-dichlorophenyl)-5-methyl-,GBL-5g	TNF	Apoptosis
	UTL-5g (3-Isoxazolecarboxamide, N-(2,4-dichlorophenyl)-5-methyl-) 是一种抗炎性TNF-α抑制剂，可通过抑制 TNF-α 等因子降低顺铂引起的肝毒性、肾毒性和骨髓毒性，具有化学保护和肝脏放射保护作用。
T14919	CDKI-73	Apoptosis; CDK	Apoptosis; Cell Cycle/Checkpoint
	CDKI-73 是一种具有口服活性的 CDK9抑制剂，其对 CDK9、CDK1 和 CDK2 的Ki 值分别为 4 nM、4 nM 和 3 nM。CDKI-73 可下调 RNA 聚合酶 II 的磷酸化。CDKI-73 也是一种 Rab11 的抑制剂。
T7545	6-Aminonicotinamide	Others	Others
	6-Aminonicotinamide 是一种竞争性 NADP+依赖性酶，是一种烟酰胺抗代谢药，葡萄糖 6-磷酸脱氢酶抑制剂 (Ki=0.46 μM)。它干扰糖酵解，导致 ATP 耗竭，并与 DNA 交联化学疗法药物，如Cisplatin，协同杀死癌细胞。
T10936	D-I03 DI03	DNA/RNA Synthesis	Cell Cycle/Checkpoint; DNA Damage/DNA Repair
	D-I03 是一种选择性的RAD52 抑制剂，Kd 为 25.8 µM。D-I03 抑制 RAD52 依赖性单链退火 (SSA) 和 D 环形成，IC50 分别为 5 µM 和 8 µM。D-I03 抑制 BRCA1 和 BRCA2 缺陷细胞的生长，并抑制顺铂诱导的 RAD52 病灶形成，但对 RAD51 无影响。
T16328	Nitroaspirin 2-乙酰氧基苯甲酸-3-硝酸甲基苯酯,NCX 4016	Apoptosis; COX	Apoptosis; Immunology/Inflammation; Neuroscience
	Nitroaspirin (NCX 4016) 是一氧化氮供体和阿司匹林的硝基衍生物，与 Aspirin 结合可抑制环氧合酶=，可作为 COX-1 的直接和不可逆抑制剂。它通过下调 EGFR/PI3K/STAT3 信号传导和调节 Bcl-2 家族蛋白，显着诱导顺铂耐药人卵巢癌细胞的细胞周期停滞和凋亡，具有抗血栓和抗血小板特性。
T6924	Riviciclib hydrochloride P276-00	Apoptosis; CDK	Apoptosis; Cell Cycle/Checkpoint
	Riviciclib hydrochloride (P276-00) 是一种CDK 抑制剂，抑制CDK9-cyclinT1、CDK4-cyclin D1、CDK1-cyclinB 的IC50值分别为 20 nM、63 nM、79 nM。它对 Cisplatin 耐药性细胞具有抗肿瘤活性。
T24879	Thioxodihydroquinazolinone-19 Thioxodihydroquinazolinone19
	In platinum-resistant A2780cis human ovarian cancer cells, thioxodihydroquinazolinone-19 is an inducer of apoptotic cell death. It acts by exhibiting a strong inhibitory effect in ovarian CSC-LCs in combination with cisplatin.
T68804	LC28
	LC28 is a novel inhibitor of STAT3 signaling, suppressing survival of cisplatin-resistant ovarian cancer cells.
T75268	84-B10
	84-B10是一种3-苯基戊二酸衍生物，能够抑制cisplatin诱导的肾小管铁死亡，并减轻cisplatin引起的线粒体损伤和氧化应激，从而有效改善cisplatin诱导的急性肾损伤(AKI)。
T78217	(R)-Azasetron besylate SENS-401	Phosphatase	Metabolism
	(R)-Azasetron besylate (SENS-401)是一种口服活性的钙调神经磷酸酶抑制剂，能够减轻Cisplatin引发的听力损失和耳蜗损害。
T39594	AKR1B10-IN-1 AKR1B10-IN-1
	AKR1B10-IN-1, a powerful AKR1B10 (Aldo-Keto Reductase 1B10) inhibitor, demonstrates an IC50 value of 3.5 nM. This compound effectively curtails the proliferation, metastasis, and Cisplatin (CDDP) resistance of lung cancer cells.
T32189	Iproplatin JM-9,CHIP,Code name: JM9,JM 9
	Iproplatin is a synthetic second-generation platinum-containing compound related to cisplatin. Iproplatin binds to and forms DNA crosslinks and platinum-DNA adducts, resulting in DNA replication failure and cell death. Although less prone to glutathione i
T71655	KX1-141
	KX1-141 is an Src-protein tyrosine kinase inhibitor, which may reduce cisplatin ototoxicity while preserving its antitumor effect.
T28398	Phenanthriplatin cis-[Pt(NH3)2-(phenanthridine)Cl]NO3
	Phenanthriplatin, also known as cis-[Pt(NH3)2-(phenanthridine)Cl]NO3, is a new drug candidate. It belongs to a family of platinum(II)-based agents which includes cisplatin, oxaliplatin and carboplatin. Phenanthriplatin Acts As a Covalent Poison of Topoiso
T71401	Oxaliplatin-d10
	Oxaliplatin-d10 is intended for use as an internal standard for the quantification of oxaliplatin by GC- or LC-MS. Oxaliplatin is a platinum-containing DNA-crosslinking agent. It induces the formation of DNA inter- and intrastrand crosslinks and DNA-protein adducts, inhibits DNA and RNA synthesis, and induces apoptosis in cancer cells. Oxaliplatin is cytotoxic to cisplatin-sensitive A2780(1A9) and KB-3-1 cells and cisplatin-resistant A2780-E(80) and KB-CP20 cells (IC50s = 0.12, 0.39, 4.7, and 2....
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
T32404	KMH-233 KMH233
	KMH-233 is a potent selective LAT1 inhibitor 1 that inhibits the uptake of LAT1 substrate, L-leucine, and cell growth. Even at low concentrations (25 μM), it significantly enhanced the efficacy of betastatin and cisplatin.
T12737	Riviciclib P276-00 (free base)	Others	Others
	Riviciclib is a potent inhibitor of cyclin-dependent kinase (CDK)(CDK9-cyclinT1, CDK4-cyclin D1, and CDK1-cyclinB with IC50s of 20 nM, 63 nM, and 79 nM, respectively),with antitumor activity on cisplatin-resistant cells.
T81267	RIPK3-IN-4	RIP kinase	Apoptosis; NF-κB
	RIPK3-IN-4（Compound 42）是一种抑制RIPK3活性的化合物。它能有效减轻HK-2细胞的损伤和凋亡（necroptosis），同时降低急性肾损伤中（Cisplatin）以及缺血/再灌注（I/R）引起的肾脏损伤、炎症及坏死性凋亡现象。
T74681	NecroIr2
	NecroIr2 是一种铱 (III) 复合物，是顺铂 (Cisplatin) 耐药肺癌细胞 (A549R) 的坏死诱导剂。NecroIr2 选择性积累在线粒体中，导致氧化应激和线粒体膜电位 (MMP) 的损失。NecroIr2 能够激活受体相互作用的丝氨酸苏氨酸激酶 3 (RIPK3) 和混合谱系激酶结构域样假激酶 (MLKL)，调节CDK4表达。
T65440	Sodium Thiosulfate Pentahydrate
	Sodium thiosulfate (Pentahydrate) is an antioxidant and antifungal. Sodium thiosulfate protects against cisplatin-induced hearing loss in children and is not associated with serious adverse events attributed to its use[3]. The addition of sodium thiosulfate, administered 6 hours after cisplatin chemotherapy, resulted in a lower incidence of cisplatin-induced hearing loss among children with standard-risk hepatoblastoma, without jeopardizing overall or event-free survival[4]. Calciphylaxis is a p...
T78841	Nrf2-IN-3
	Nrf2-IN-3 (Compound R16) 为Nrf2抑制剂，与KEAP1突变体 (G333C mKEAP1) 结合，能够恢复受损的KEAP1/NRF2相互作用。该化合物通过修复mKEAP1/NRF2复合物，增加KEAP1突变癌细胞对Cisplatin和Gefitinib的敏感性。
T69596	SK-575
	SK-575 is a Highly Potent and Efficacious Proteolysis-Targeting Chimera Degrader of PARP1 for Treating Cancers. SK-575 potently inhibits the growth of cancer cells bearing BRCA1/2 mutations and induces potent and specific degradation of PARP1 in various human cancer cells even at low picomolar concentrations. SK-575 achieves durable tumor growth inhibition in mice when used as a single agent or in combination with cytotoxic agents, such as temozolomide and cisplatin.
T71099	LLL12
	LLL12 是一种 STAT3小分子抑制剂，抑制 STAT3磷酸化。LLL12 增强顺铂和紫杉醇对卵巢癌症细胞生成、迁徙、和生长的抑制作用。
T74501	NHEJ inhibitor-1
	NHEJ inhibitor-1 (Compound C2) 是一种三功能 Pt(II) 复合物，可缓解非同源末端连接 (NHEJ)/同源重组 (HR) 相关的双链断裂 (DSB) 修复，从而避免非小细胞肺对顺铂的耐药性。NHEJ inhibitor-1 抑制损伤修复蛋白 Ku70 和 Rad51，从而使肿瘤对活性分子重新敏感。NHEJ inhibitor-1 还诱导 ROS 产生和MMP 降低。
T36385	Ansatrienin A
	Ansatrienin A is an ansamycin antibiotic and antifungal agent first isolated from S. collinus and S. rishiriensis. In fetal rat long bones, it is an inhibitor of parathyroid hormone-induced calcium release (IC50 = 64 nM), which is a measure of bone resorption, and pp60c-srcM kinase (IC50 = 100 nM). It also inhibits TNF-α-induced expression of intercellular adhesion molecule-1 (ICAM-1; IC50 = 570 nM). Early in vitro studies showed that ansatrienin A potentiates the chemotherapeutic action of 5-fl...
T68708	Denibulin HCl
	Denibulin (MN-029) is a novel vascular-disrupting agent that reversibly inhibits microtubule assembly, resulting in disruption of the cytoskeleton of tumor vascular endothelial cells. The results of preclinical study demonstrated that MN-029 could cause rapid vascular shutdown in solid tumors, dose-dependent secondary tumor cell killing, and effective enhancement of the antitumor effects of radiation and cisplatin chemotherapy.
T74225	ROS-ERS inducer 1
	ROS-ERS inducer 1 是一种基于4,5-二芳基咪唑的Pt(II)-N-杂环卡宾 (Pt(II)-NHC) 复合物，属于 II 型免疫原性细胞死亡(ICD)诱导剂。它能促使内质网应激(ERS)并伴随活性氧(ROS)的生成，进而在HCC细胞中触发损伤相关分子模式(DAMP)的释放。相比Cisplatin，ROS-ERS inducer 1 表现出更高的抗癌效能。
T81962	Lactate transportor 1	Monocarboxylate transporter	Membrane transporter/Ion channel
	Lactate transporter 1 (compound 1) 作为一种活性乳酸运输蛋白，主要在活细胞内发挥作用。在Hela、CAL27、MCF7和MCF10A细胞系中，Lactate transporter 1 均显示出了明显的毒性，其半抑制浓度（IC50）值依次为3.36、3.27、5.58和7.66 μM。此外，在HeLa细胞中，Lactate transporter 1 与Cisplatin表现出了协同抑制的作用。
T71385	Aroplatin
	Aroplatin is a synthetic liposomal formulation of bis-neodecanoate diaminocyclohexane platinum (NDDP), a third-generation platinum complex analogue of cisplatin, with potential antineoplastic activity. After displacement of the 2 long-chain aliphatic leaving groups (neodecanoic acid), platinum diaminocyclohexane (DACH) complexes become highly reactive and alkylate macromolecules, forming both inter- and intra-strand DNA crosslinks and inhibiting DNA synthesis, which results in tumor cell cytotox...
T36745	cDPCP
	cDPCP is a platinum-containing DNA-crosslinking agent.1Unlike cisplatin or oxaliplatin , cDPCP forms monofunctional DNA adducts. It is transported into cells by organic cation transporter 1 (OCT1) and OCT2, inhibiting proliferation of MDCK cells expressing the human transporters with IC50values of 8.1 and 1.5 μM, respectively. cDPCP inhibits RNA polymerase II-mediated transcription in a reporter assay using HeLa cells. It increases survival in murine S180 sarcoma and P388 leukemia models when ad...
T74680	NecroIr1
	NecroIr1 是一种铱 (III) 复合物，是顺铂 (Cisplatin) 耐药肺癌细胞 (A549R) 的坏死诱导剂。NecroIr1 选择性积累在线粒体中，导致氧化应激和线粒体膜电位 (MMP) 的损失。NecroIr1 能够激活受体相互作用的丝氨酸苏氨酸激酶 3 (RIPK3) 和混合谱系激酶结构域样假激酶 (MLKL)，调节CDK4表达。
T71559	Melanotan II acetate
	Melanotan II acetate is an agonist of melanocortin receptor 1 (MC1R), MC3R, MC4R, and MC5R. It has been shown to improve recovery of sciatic nerve function after mechanical injury and increase cisplatin-induced decreases in sensory nerve conduction velocity. Melanotan II acetate increases oxygen consumption and protein levels of uncoupling protein 1 (UCP1) in brown adipose tissue homogenates and decreases food intake, body weight, and serum levels of leptin, glucose, insulin, and cholesterol.
T73550	CUR5g
	CUR5g 是一种有效的自噬 (autophagy) 抑制剂。CUR5g 通过阻断自噬体-溶酶体融合选择性地抑制癌细胞中的自噬体降解。CUR5g 通过依赖 UVRAG 的机制阻止 STX17 募集到自噬体，导致自噬体无法与溶酶体融合。CUR5g 可提高顺铂 (Cisplatin) 在体外和体内对 A549 细胞的抗癌作用。
T62298	PHD2/HDACs-IN-1
	PHD2/HDACs-IN-1 是一种有效的 PHD2/HDACs 混合抑制剂，能够作用于 PHD2 (IC50: 1.15 μM)、HDAC1 (IC50: 19.75 μM)、HDAC2 (IC50: 26.60 μM)、HDAC16 (IC50: 15.98 μM)。PHD2/HDACs-IN-1 是一种低毒性肾保护剂，能够用于顺铂诱导的急性肾损伤 (AKI) 的研究。
TP1551	Difopein TFA (396834-58-5 free base) Difopein TFA
	Difopein (TFA), a specific and competitive inhibitor of 14-3-3 protein (a highly conserved eukaryotic regulatory molecule), blocking the ability of 14-3-3 to bind to target proteins and inhibits 14-3-3/Ligand interactions. Difopein (TFA) leads to inductio
T62730	TDRL-X80
	TDRL-X80 是一种色素性干皮症蛋白 (XPA) 的有效抑制剂。TDRL-X80 能够抑制 XPA 的 DNA 结合活性。TDRL-X80 能够作用于单、双和顺铂损伤的 DNA，在荧光偏振 (FP) 分析中的 IC50 值为 18、20 和 29 μM，而 ELISA 分析中的 IC50为 21、39 和 28。

化合物

Cat.No: T1564

Synonym: cis-Diaminodichloroplatinum,CDDP,顺铂

Target: DNA Alkylator/Crosslinker, Ferroptosis, DNA/RNA Synthesis, Autophagy

Cisplatin-resistant cells-IN-1

Cat.No: T82715

Cat.No: T10777

Target: HDAC

Cat.No: T6612

Target: ATM/ATR, DNA-PK, CDK

monohydroxycisplatin

Cat.No: T68105

Cat.No: T35300

Synonym: Zeniplatinum

Target: Others

Cat.No: T36404L

Synonym: PRLX-93936 hcl(903499-49-0 Free base)

Target: Ferroptosis, Reactive Oxygen Species

Cat.No: T1058

Synonym: NSC 241240,卡铂,CBDCA,JM-8

Target: DNA Alkylator/Crosslinker, DNA/RNA Synthesis, Autophagy

Amifostine trihydrate

Cat.No: T6381

Synonym: Ethyol trihydrate,WR2721,三水氨磷汀,Amifostine

Target: Others, HIF/HIF Prolyl-Hydroxylase

Cat.No: T2410

Synonym: 奈达铂,NSC 375101D

Target: DNA/RNA Synthesis

Ondansetron hydrochloride dihydrate

Cat.No: T1478

Synonym: 盐酸昂丹司琼,SN 307,NSC 665799,GR 38032,Ondansetron hydrochloride

Target: 5-HT Receptor

Cat.No: T60904

Target: Others

Cat.No: T4434

Synonym: Tirazone,Win59075,SR4233,替拉扎明,SR259075

Target: Others

Cat.No: T8845

Synonym: 3-Isoxazolecarboxamide, N-(2,4-dichlorophenyl)-5-methyl-,GBL-5g

Target: TNF

Cat.No: T14919

Target: Apoptosis, CDK

6-Aminonicotinamide

Cat.No: T7545

Target: Others

Cat.No: T10936

Synonym: DI03

Target: DNA/RNA Synthesis

Cat.No: T16328

Synonym: 2-乙酰氧基苯甲酸-3-硝酸甲基苯酯,NCX 4016

Target: Apoptosis, COX

Riviciclib hydrochloride

Cat.No: T6924

Synonym: P276-00

Target: Apoptosis, CDK

Thioxodihydroquinazolinone-19

Cat.No: T24879

Synonym: Thioxodihydroquinazolinone19

Cat.No: T68804

Cat.No: T75268

(R)-Azasetron besylate

Cat.No: T78217

Synonym: SENS-401

Target: Phosphatase

Cat.No: T39594

Synonym: AKR1B10-IN-1

Cat.No: T32189

Synonym: JM-9,CHIP,Code name: JM9,JM 9

Cat.No: T71655

Phenanthriplatin

Cat.No: T28398

Synonym: cis-[Pt(NH3)2-(phenanthridine)Cl]NO3

Oxaliplatin-d10

Cat.No: T71401

Cat.No: T21307

Synonym: NSC644591 NSCD644591 SKI2053R,Heptaplatin Sunpla,HTP

Cat.No: T32404

Synonym: KMH233

Cat.No: T12737

Synonym: P276-00 (free base)

Target: Others

Cat.No: T81267

Target: RIP kinase

Cat.No: T74681

Sodium Thiosulfate Pentahydrate

Cat.No: T65440

Cat.No: T78841

Cat.No: T69596

Cat.No: T71099

NHEJ inhibitor-1

Cat.No: T74501

Cat.No: T36385

Cat.No: T68708

ROS-ERS inducer 1

Cat.No: T74225

Lactate transportor 1

Cat.No: T81962

Target: Monocarboxylate transporter

Cat.No: T71385

Cat.No: T36745

Cat.No: T74680

Melanotan II acetate

Cat.No: T71559

Cat.No: T73550

PHD2/HDACs-IN-1

Cat.No: T62298

Difopein TFA (396834-58-5 free base)

Cat.No: TP1551

Synonym: Difopein TFA

Cat.No: T62730

Cat. No.	Product Name	Target	Signaling Pathways
TN1621	Eriodictyol-7-O-glucoside	Nrf2	Immunology/Inflammation
	Eriodictyol-7-O-glucoside 是一种 Nrf2 激活剂，可防止顺铂诱导的毒性。 Eriodictyol-7-O-glucoside 是一种类黄酮和自由基清除剂，在开心果皮中具有抗氧化活性。
TN1637	Eurycomalactone	Anti-infection; NF-κB	Microbiology/Virology; NF-κB
	Eurycomalactone 是一种NF-κB 抑制剂，IC50=0.5 μM，是一种天然产物。它可抑制蛋白合成，降低 cyclin D1 蛋白水平，但对 TNFα 诱导的 IκBα 降解或 IKKα/β 和 IκBα 的磷酸化水平没有作用。
TQ0211	Brusatol (+)-Brusatol,鸦胆子苦醇,NSC 172924	Others; Ferroptosis; Nrf2	Apoptosis; Immunology/Inflammation; Others
	Brusatol (NSC-172924) 是一种从鸦胆子植物中分离出来的天然产物，抑制Nrf2通路，可使多种癌细胞对 Cisplatin 和其他化疗药物敏感。它可开发为辅助化疗化合物，可增加细胞凋亡。
T4943	Monoolein 1-Oleoyl-rac-glycerol,甘油单油酸酯	Others; Endogenous Metabolite	Metabolism; Others
	Monoolein (1-Oleoyl-rac-glycerol) 是内源性代谢产物的一种。
T6S1141	Ganoderic acid A 灵芝酸 A,灵芝酸A	Apoptosis; NF-κB; Endogenous Metabolite; Autophagy	Apoptosis; Autophagy; Metabolism; NF-κB
	Ganoderic acid A 能够抑制 JAK-STAT3信号通路，也能抑制细胞增殖，存活率和 ROS。它对人骨肉瘤 HOS 和MG-63细胞具有增殖抑制、凋亡和侵袭抑制作用。
TN3174	6-Methoxyflavanone NSC50184	GABA Receptor	Membrane transporter/Ion channel; Neuroscience
	6-Methoxyflavanone（6-MeOF）是人重组GABA A受体GABA反应的正变构调节剂，具有抗焦虑活性和抗炎活性，可用于减轻顺铂诱导的神经性疼痛。
T3795	Corilagin	Apoptosis; TLR; Reverse Transcriptase; Antibacterial; Autophagy	Apoptosis; Autophagy; Immunology/Inflammation; Microbiology/Virology
	Corilagin 是一种鞣酸，有抑制 RNA 肿瘤病毒逆转录酶的活性。它抑制金黄色葡萄球菌的生长，MIC 为 25 μg/mL。它有抗肿瘤活性，可用于肝癌和卵巢癌。
TN2211	Silybin B Silibinin B	Apoptosis; Beta Amyloid; Bcr-Abl	Angiogenesis; Apoptosis; Cytoskeletal Signaling; Neuroscience; Tyrosine Kinase/Adaptors
	Silybin B (Silibinin B) 是雷洛昔芬4′-和6-葡萄糖醛酸化的有效抑制剂，是水飞蓟素有效的抗纤维原性和抗低聚物成分，具有清除1,1-二苯基-2-吡啶酰肼(DPPH)自由基的活性，可通过减轻 DNA 损伤和细胞凋亡对顺铂诱导的神经毒性具有保护作用。Silybin B 对人慢性髓系白血病 K562细胞的生长抑制和诱导凋亡有较强的作用。
T6427	Butein 2’,3,4,4’-tetrahydroxy Chalcone,紫铆因	Apoptosis; EGFR; Others; PDE; Autophagy	Angiogenesis; Apoptosis; Autophagy; JAK/STAT signaling; Metabolism; Others; Tyrosine Kinase/Adaptors
	Butein (2’,3,4,4’-tetrahydroxy Chalcone) 是一种 cAMP 特异性PDE 抑制剂，也是蛋白酪氨酸激酶抑制剂，还是一种SIRT1激活剂。它通过 AKT 和 ERK/p38 MAPK 通路，靶向 FoxO3a 使 HeLa 细胞对 Cisplatin 敏感。
T75485	Dehydrobruceine B
	Dehydrobruceine B 是一种苦木素，可从鸦胆子 (Brucea javanica) 中分离得到。Dehydrobruceine B 与 Cisplatin 通过线粒体途径，协同诱导细胞凋亡 (apoptosis)。Dehydrobruceine B 还增加凋亡诱导因子 (AIF) 和 Bax 表达，抑制 Keap1-Nrf2。
TN3988	Ervamycine	Others	Others
	11-Methoxytabersonine(Ervamycine) exhibits inhibitory effects against five human cancer cell lines , with IC(50) values comparable to those of cisplatin and vinorelbine.
TN4284	Isodonal	Others	Others
	Isodonal shows abilities to inhibit K562 cells camparable to that of cisplatin.
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.
TN4382	Kazinol A	AMPK; mTOR	Chromatin/Epigenetic; PI3K/Akt/mTOR signaling
	Kazinol A shows strong inhibition of arachidonic acid (AA)-induced platelet aggregation. It also exhibits potent inhibition with IC50 values ranging 0.6-164 M against XOD. Kazinol A may be a candidate for the development of effective anti-cancer drug on h

天然产物

Eriodictyol-7-O-glucoside

Cat.No: TN1621

Target: Nrf2

Eurycomalactone

Cat.No: TN1637

Target: Anti-infection, NF-κB

Cat.No: TQ0211

Synonym: (+)-Brusatol,鸦胆子苦醇,NSC 172924

Target: Others, Ferroptosis, Nrf2

Cat.No: T4943

Synonym: 1-Oleoyl-rac-glycerol,甘油单油酸酯

Target: Others, Endogenous Metabolite

Ganoderic acid A

Cat.No: T6S1141

Synonym: 灵芝酸 A,灵芝酸A

Target: Apoptosis, NF-κB, Endogenous Metabolite, Autophagy

6-Methoxyflavanone

Cat.No: TN3174

Synonym: NSC50184

Target: GABA Receptor

Cat.No: T3795

Target: Apoptosis, TLR, Reverse Transcriptase, Antibacterial, Autophagy

Cat.No: TN2211

Synonym: Silibinin B

Target: Apoptosis, Beta Amyloid, Bcr-Abl

Cat.No: T6427

Synonym: 2’,3,4,4’-tetrahydroxy Chalcone,紫铆因

Target: Apoptosis, EGFR, Others, PDE, Autophagy

Dehydrobruceine B

Cat.No: T75485

Cat.No: TN3988

Target: Others

Cat.No: TN4284

Target: Others

Cat.No: TN4932

Target: PARP, Akt, Caspase, Antifection

Cat.No: TN4382

Target: AMPK, mTOR

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