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Search Results for " synergistic effect "

18

抑制剂 & 化合物

7

天然产物

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Cat. No.	Product Name	Target	Signaling Pathways
T26168	Rufigallol AI3 00865,AI3-00865,AI300865
	Rufigallol (AI3-00865) 是一种具有六个羟基的电子缺失的盘状分子，是诱导非平面AIE 分子形成DLC 的良好单元，是一种蒽醌衍生物。Rufigallol 诱导获得了DLC 特性，而TPE 基团的引入使分子结构在聚集状态下具有良好的荧光。Rufigallol 在体外的显著的协同抗疟作用，在体内与维生素C 和酮类化合物一起使用具有协同作用并显示出抗疟活性。
T70373	AS2575959
	AS2575959 is a novel GPR40 agonist, exhibiting glucose metabolism improvement and synergistic effect with sitagliptin on insulin and incretin secretion.
T27052	CMP3a CMP-3a,CMP 3a
	CMP3a is a NEK2 kinase inhibitor. CMP3a efficiently attenuated GBM growth in a mouse model and exhibited a synergistic effect with radiotherapy. Targeting NEK2 attenuates glioblastoma growth and radioresistance by destabilizing histone methyltransferase E
T30831	Cgp 43182 Cgp-43182,Cgp43182
	CGP 43182 is an effective inhibitor of group IIA secretory phospholipase A2 (Group IIA sPLA2) activity in vitro, which can be used to prevent the synergistic effect of pro-inflammatory genes stimulated by cytokines mediated by NFkappaB.
T79264	Z1078601926
	Z1078601926为hDAT (人多巴胺转运蛋白) 的变构抑制剂，且与诺米芬辛表现出协同效应。
T74318	18:0 EPC chloride
	18:0 EPC chloride为合成阳离子磷脂，(在临界协同浓度2.34-2.93 μM)可显著增强丁香酚对大肠杆菌的灭活效能。
T69935	L0909
	L0909 is an orally available inhibitors of Hepatitis C virus with a novel mechanism of action (EC50 = 0.022 μM, SI > 600). L0909 could block HCV replication by acting on the HCV entry stage. The high sensitivity to clinical resistant HCV mutants and synergistic effect with clinical drugs were observed for this compound. L0909 as a promising HCV entry inhibitor for single or combinational therapeutic potential.
T61751	DNA-PK-IN-3
	DNA-PK-IN-3 is a highly potent inhibitor of DNA-PK. This compound exerts a synergistic effect when combined with radiotherapy and chemotherapy, resulting in enhanced therapeutic outcomes and significant inhibition of tumor growth. Furthermore, DNA-PK-IN-3 demonstrates remarkable efficacy in reducing damage to normal cells, effectively minimizing adverse side effects. Due to these compelling properties, DNA-PK-IN-3 holds great potential for cancer research applications[1].
T76325	GHRF, bovine
	GHRF, bovine (bGRF(1-44)-NH2) 是牛生长激素 (GH) 释放因子 (GHRF)。GHRF, bovine 促牛生长激素释放，并受到Hydrocortisone 的促进作用。
T62553	JAK3/BTK-IN-4
	JAK3/BTK-IN-4 是一种 JAK3/BTK 的有效抑制剂。其中 BTK 和 JAK3 是自身免疫性疾病的两个重要靶点。同时抑制 BTK/JAK3 信号通路具有协同效应。JAK3/BTK-IN-4 具有潜力进行 JAK3 激酶和/或 BTK 相关疾病的研究。
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...
T62234	JAK3/BTK-IN-3
	JAK3/BTK-IN-3 是一种 JAK3/BTK 的有效抑制剂。其中 BTK 和 JAK3 是自身免疫性疾病的两个重要靶点。同时抑制 BTK/JAK3 信号通路具有协同效应。JAK3/BTK-IN-3 对 JAK3 激酶和/或 BTK 相关疾病表现出研究潜力。
T62153	JAK3/BTK-IN-5
	JAK3/BTK-IN-5 是一种 JAK3/BTK 的有效抑制剂。其中 BTK 和 JAK3 是自身免疫性疾病的两个关键的靶点。同时抑制 BTK/JAK3 信号通路具有协同效应。JAK3/BTK-IN-5 对 JAK3 激酶和/或 BTK 相关疾病具有潜在的研究价值。
T71361	CHS-828 nicotinate
	CHS-828 nicotinate is a CHS-828 salt with Nicotinic acid.. CHS-828 also known as GMX-1778, is a potent and selective NAMPT inhibitor. CHS-828 inhibits cellular synthesis of NAD. CHS 828 kill tumour cells by inhibiting the nuclear factor-kappaB translocation but unlikely through down-regulation of proteasome. CHS 828 has shown promising anticancer activity in experimental tumor models and primary cultures of cancer cells from patients. CHS 828 showed a synergistic effect with melphalan in 67%, ...
T78935	Quorum Sensing-IN-2
	Quorum Sensing-IN-2（compound 23e）是一款不影响细菌生长的群体感应抑制剂，具有减少细菌致病性的功能。该化合物在抑制细菌感染方面表现出效力，同时具有极低的溶血活性。在铜绿假单胞菌PAO1引起的菌血症模型中，Quorum Sensing-IN-2与环丙沙星共同作用，显示了协同效应。
T79407	HL23	Others	Others
	HL23是一种HDAC抑制剂，对抗HCC具有活性。通过增强TXNIP启动子乙酰化，此化合物上调TXNIP表达，进而介导钾通道活性并触发TXNIP依赖性钾剥夺，抑制HCC的进展和转移。HL23与Sorafenib联合应用时显示出协同作用，并且其效力超过Sorafenib与Vorinostat的联用。
T9813	JAK3/BTK-IN-2	JAK; BTK	Angiogenesis; Chromatin/Epigenetic; JAK/STAT signaling; Stem Cells; Tyrosine Kinase/Adaptors
	JAK3/BTK-IN-2 是一种有效的 JAK3/BTK 抑制剂。JAK3/BTK-IN-2对BTK 和 JAK3具有抑制作用（ BTK 和 JAK3是自身免疫性疾病的两个重要靶点）JAK3/BTK-IN-2同时抑制 BTK/JAK3 信号通路表现出协同效应。JAK3/BTK-IN-2 具有治疗 JAK3 和BTK 活性异常引起相关疾病的潜力。
T9814	JAK3/BTK-IN-1	JAK; BTK	Angiogenesis; Chromatin/Epigenetic; JAK/STAT signaling; Stem Cells; Tyrosine Kinase/Adaptors
	JAK3/BTK- in -1是一种特异性靶向和抑制Janus 激酶3 (JAK3)和布鲁顿酪氨酸激酶(BTK）的JAK3/BTK 双重抑制剂，BTK 和 JAK3 是自身免疫性疾病的两个重要靶点。JAK3/BTK- in -1同时抑制 BTK/JAK3 信号通路表现出协同效应。 JAK3/BTK- in -1是治疗免疫相关疾病(如自身免疫性疾病、某些类型的癌症(包括淋巴瘤和白血病)以及可能以免疫反应失调为特征的其他疾病)的潜在化合物。

化合物

Cat.No: T26168

Synonym: AI3 00865,AI3-00865,AI300865

Cat.No: T70373

Cat.No: T27052

Synonym: CMP-3a,CMP 3a

Cat.No: T30831

Synonym: Cgp-43182,Cgp43182

Cat.No: T79264

18:0 EPC chloride

Cat.No: T74318

Cat.No: T69935

Cat.No: T61751

Cat.No: T76325

Cat.No: T62553

Cat.No: T69162

Cat.No: T62234

Cat.No: T62153

CHS-828 nicotinate

Cat.No: T71361

Quorum Sensing-IN-2

Cat.No: T78935

Cat.No: T79407

Target: Others

Cat.No: T9813

Target: JAK, BTK

Cat.No: T9814

Target: JAK, BTK

Cat. No.	Product Name	Target	Signaling Pathways
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。
T4763	trans-Cyclohexane-1,2-diol trans-1,2-Cyclohexanediol,反式-1,2-环己二醇	Others; Endogenous Metabolite	Metabolism; Others
	trans-Cyclohexane-1,2-diol (trans-1,2-Cyclohexanediol) 是内源性代谢产物的一种。
TN3700	Corianin	Others	Others
	Corianin and coriatin demonstrate synergistic effect to insecticidal activity of tutin againstarmyworm.
TN3701	Coriatin	Others	Others
	Coriatin and corianin demonstrate synergistic effect to insecticidal activity of tutin againstarmyworm.
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。
TN4470	Lyoniside	Antifection	Microbiology/Virology
	Lyoniside and saracoside are cytotoxic to promastigotes and intracellular amastigotes, they demonstrate strong anti-leishmanial efficacies in BALB/c mice model of leishmaniasis, suggests that these two compounds potential anti-leishmanial candidates. The
TN1690	Glabrene	Others; Estrogen/progestogen Receptor; Tyrosinase	Endocrinology/Hormones; Others; Proteases/Proteasome
	Glabrene, Liquiritin apioside, neolicuroside, and 18α²-glycyrrhetic acid are the predominant phenolic derivatives partitioning at the interface and most likely the major contributors to the notable synergistic antioxidant activity when coupled with pea pr

天然产物

Cat.No: TQ0211

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

Target: Others, Ferroptosis, Nrf2

trans-Cyclohexane-1,2-diol

Cat.No: T4763

Synonym: trans-1,2-Cyclohexanediol,反式-1,2-环己二醇

Target: Others, Endogenous Metabolite

Cat.No: TN3700

Target: Others

Cat.No: TN3701

Target: Others

Dehydrobruceine B

Cat.No: T75485

Cat.No: TN4470

Target: Antifection

Cat.No: TN1690

Target: Others, Estrogen/progestogen Receptor, Tyrosinase

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