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抑制剂 & 化合物

天然产物

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Cat. No.	Product Name	Target	Signaling Pathways
T27998	MDK-4204 Anticancer AgentI,MDK 4204,Anticancer Agent I,MDK4204,Anticancer Agent-I
	MDK-4204, an anticancer agent, shows significant anti-cancer activity with IC50 values of 8.8 µM and 9.5 µM in PC-3 and DU-145 cells, respectively.
T7309	TAS-103 dihydrochloride 6-[[2-(二甲基氨基)乙基]氨基]-3-羟基-7H-茚并[2,1-C]喹啉-7-酮二盐酸盐,TAS-103 (dihydrochloride),BMS-247615 dihydrochloride	Topoisomerase	DNA Damage/DNA Repair
	TAS-103 dihydrochloride (BMS-247615 dihydrochloride) 是可用于癌症研究的一种 DNA 拓扑异构酶 I/II 双重抑制剂。
T61286	Glyoxalase I inhibitor 7
	Glyoxalase I inhibitor 7 (Compound 6) is a potent inhibitor of glyoxalase I (Glo-I) with an IC50 of 3.65 μM. It exhibits potential as an anticancer agent [1].
T61692	Glyoxalase I inhibitor 6
	Glyoxalase I inhibitor 6 (Compound 9j) is an inhibitor of glyoxalase I (Glo-I) with an IC50 value of 1.13 μM. This compound shows potential as an anticancer agent, demonstrating low toxicity [1].
T61103	Glyoxalase I inhibitor 5
	Glyoxalase I inhibitor 5 (Compound 9h) is a potent inhibitor of glyoxalase I (Glo-I), with an IC50 value of 1.28 μM. This compound holds promise as an anticancer agent [1].
T38474	CL2-MMT-SN38 CL2-MMT-SN38
	CL2-MMT-SN38 is a derivative of SN-38, which is a potent anticancer agent and the active metabolite of Irinotecan (CPT-11), a Topoisomerase I inhibitor.
T79557	fac-[Re(CO)3(L6)(H2O)][NO3]	Apoptosis	Apoptosis
	fac-[Re(CO)3(L6)(H2O)][NO3]（compound 6）是一种具有针对线粒体功能失调的抗癌活性的铼(I)三羰基水配合物。该化合物对前列腺癌细胞展现出显著的细胞毒性，具有50 nM的IC50值（PC-3细胞）。fac-[Re(CO)3(L6)(H2O)][NO3]能够主要集中在细胞核，抑制PC3细胞的ATP生成并诱导细胞凋亡，而不触发坏死、焦亡或自噬过程。
T79558	fac-[Re(CO)3(L3)(H2O)][NO3]
	fac-[Re(CO)3(L3)(H2O)][NO3]（简称compound 3），是一种与线粒体功能障碍相关的抗前列腺癌剂。这种铼(I)三羰基水配合物对前列腺癌细胞系(PC-3)表现出显著的细胞毒性，其IC50值为0.32 μM。研究表明，fac-[Re(CO)3(L3)(H2O)][NO3]主要在线粒体中积聚，能够降低PC-3细胞的ATP生成，进而触发细胞副凋亡(paraptosis)机制，而不通过引发坏死、凋亡或自噬途径作用。
T83898	S-(N-Methylsulfinylbutylthiocarbamoyl)-L-cysteine SFN-Cys,D,L-Sulforaphane-L-cysteine
	S-(N-Methylsulfinylbutylthiocarbamoyl)-L-cysteine (SFN-Cys) 是一种异硫氰酸酯衍生物及第一类和第二类组蛋白去乙酰化酶（HDAC）抑制剂和抗癌剂硫代硫酸烯醇醚的活性代谢产物。它通过巯基乙酸途径酶从硫代硫酸烯醇醚经DL-硫代硫酸烯醇醚谷胱甘肽和硫代硫酸烯醇醚半胱氨酸甘肽中间体形成。SFN-Cys (20 µM) 通过创伤愈合和腔室分析实验，分别减少了U87MG和U373 MG胶质母细胞瘤细胞的侵袭和迁移。在45 µM的浓度下，它降低了对紫杉醇耐药的A549肺癌细胞（A549/T）中的α-微管蛋白、βIII-微管蛋白、司他敏1和X连锁抑制剂的凋亡（XIAP）的水平，并减少了细胞密度。使用30 µM浓度的SFN-Cys诱导U87MG和U373 MG细胞凋亡和G2/M期细胞周期停滞。

化合物

MDK-4204

Cat.No: T27998

Synonym: Anticancer AgentI,MDK 4204,Anticancer Agent I,MDK4204,Anticancer Agent-I

Target:

TAS-103 dihydrochloride

Cat.No: T7309

Synonym: 6-[[2-(二甲基氨基)乙基]氨基]-3-羟基-7H-茚并[2,1-C]喹啉-7-酮二盐酸盐,TAS-103 (dihydrochloride),BMS-247615 dihydrochloride

Target: Topoisomerase

Glyoxalase I inhibitor 7

Cat.No: T61286

Synonym:

Target:

Glyoxalase I inhibitor 6

Cat.No: T61692

Synonym:

Target:

Glyoxalase I inhibitor 5

Synonym: CL2-MMT-SN38

Target:

fac-[Re(CO)3(L6)(H2O)][NO3]

Cat.No: T79557

Synonym:

Target: Apoptosis

fac-[Re(CO)3(L3)(H2O)][NO3]

Cat.No: T79558

Synonym:

Target:

S-(N-Methylsulfinylbutylthiocarbamoyl)-L-cysteine

Cat.No: T83898

Synonym: SFN-Cys,D,L-Sulforaphane-L-cysteine

Target:

Cat. No.	Product Name	Target	Signaling Pathways
T2830	Betulinic acid 白桦脂酸,桦木酸,ALS-357,Lupatic acid,Betulic acid	Apoptosis; Mitophagy; NF-κB; HIV Protease; Topoisomerase; Endogenous Metabolite; Aminopeptidase; Autophagy	Apoptosis; Autophagy; DNA Damage/DNA Repair; Metabolism; Microbiology/Virology; NF-κB; Proteases/Proteasome
	Betulinic acid (ALS-357) 是从白桦树皮中分离出来的一种五环三萜类天然产物，是真核细胞拓扑异构酶 I 的抑制剂，IC50值为 5 μM，具有抗逆转录病毒、抗疟疾、抗癌和抗炎特性。

天然产物

Betulinic acid

Cat.No: T2830

Synonym: 白桦脂酸,桦木酸,ALS-357,Lupatic acid,Betulic acid

Target: Apoptosis, Mitophagy, NF-κB, HIV Protease, Topoisomerase, Endogenous Metabolite, Aminopeptidase, Autophagy

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