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抑制剂 & 化合物

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Cat. No.	Product Name	Target	Signaling Pathways
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。
T68065	Enloplatin
	Enloplatin 是一种卡铂类似物，在治疗晚期卵巢癌有部分作用。
T77401	Bavituximab Anti-PS MAb 3G4	Others	Others
	Bavituximab (Anti-Human Phosphatidylserine Recombinant Antibody) 是一种针对磷脂酰丝氨酸 (PS) 的单克隆抗体，具有血管靶向和免疫调节特性，能够重新激活抗肿瘤免疫来抑制肿瘤生长。Bavituximab 具有抗癌活性，常联合Paclitaxel 和 Carboplatin 来研究非小细胞肺癌。
T27307L	Fasnall HCl Fasnall HCl（929978-58-5 Free base）	Fatty Acid Synthase	Metabolism
	Fasnall HCl 是一种FASN 选择性抑制剂，通过其辅助因子结合位点起作用。Fasnall HCl 在HER2(+)乳腺癌MMTV-Neu 模型中也显示出强大的抗肿瘤活性，特别是与卡铂联合使用时。
T9864	Debio-0123 WEE1-IN-5	Wee1	Cell Cycle/Checkpoint
	Debio-0123 (WEE1-IN-5) 是一种口服有效且高度特异性的WEE1抑制剂，IC50值在低纳摩尔范围内。Debio-0123 抑制磷酸化 CDC2。Debio-0123 可增强卡铂在体内的抗肿瘤活性，而这两种药物单独使用都没有活性。
T27307	Fasnall	Fatty Acid Synthase	Metabolism
	Fasnall 是一种选择性 FASN 抑制剂，通过其辅因子结合位点起作用。 Fasnall 在 HER2(+) 乳腺癌的 MMTV-Neu 模型中显示出有效的抗肿瘤活性，尤其是与卡铂联合使用时。
T38765	UBE2T/FANCL-IN-1 UBE2T/FANCL-IN-1
	UBE2T/FANCL-IN-1 is a highly effective inhibitor of UBE2T/FANCL-mediated FANCD2 monoubiquitylation. It greatly enhances the sensitivity of cells to Carboplatin, a DNA cross-linking agent.
T27790	Labradimil RMP-7,ALK-01-040,Receptor-mediated permeabiliser-7,DRG0182,DRG 0182,DRG-0182
	Labradimil is a bradykinin B2 receptor agonist. Labradimil increases the permeability of human brain microvascular endothelial cell monolayers. Labradimil enhances delivery of hydrophilic chemotherapeutics and increases survival in rats with metastatic tu
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

化合物

Carboplatin

Cat.No: T1058

Synonym: NSC 241240,卡铂,CBDCA,JM-8

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

Synonym: Anti-PS MAb 3G4

Target: Others

Fasnall HCl

Cat.No: T27307L

Synonym: Fasnall HCl（929978-58-5 Free base）

Target: Fatty Acid Synthase

Debio-0123

Cat.No: T9864

Synonym: WEE1-IN-5

Target: Fatty Acid Synthase

UBE2T/FANCL-IN-1

Cat.No: T38765

Synonym: UBE2T/FANCL-IN-1

Target:

Labradimil

Cat.No: T27790

Synonym: RMP-7,ALK-01-040,Receptor-mediated permeabiliser-7,DRG0182,DRG 0182,DRG-0182

Target:

Phenanthriplatin

Cat.No: T28398

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

Target:

Cat. No.	Product Name	Target	Signaling Pathways
T36893	4-oxo Withaferin A
	4-oxo Withaferin A is a derivative of the steroidal lactone withaferin A that has anticancer activity.1 It is cytotoxic to A2780 ovarian cancer cells and carboplatin-resistant A2780 (A2780/CP70) cells (IC50s = 7.3 and <1 μM, respectively) and is 4.4-fold selective for A2780 cells over non-cancerous ARPE19 cells.References1. Perestelo, N.R., Llanos, G.G., Reyes, C.P., et al. Expanding the chemical space of withaferin A by incorporating silicon to improve its clinical potential on human ovarian ca...
T35647	4-oxo-27-TBDMS Withaferin A
	4-oxo-27-TBDMS Withaferin A is a derivative of the steroidal lactone withaferin A that has anticancer activity.1 It is cytotoxic to A2780 ovarian cancer cells (IC50 = 17 μM) but not to carboplatin-resistant A2780 (A2780/CP70) cells (IC50 = >100 μM). It is selective for A2780 cells over non-cancerous ARPE19 cells (IC50 = 1,660 μM). 4-oxo-27-TBDMS Withaferin A induces DNA fragmentation in A2780 cells.References1. Perestelo, N.R., Llanos, G.G., Reyes, C.P., et al. Expanding the chemical space of wi...

天然产物

4-oxo-27-TBDMS Withaferin A

Cat.No: T35647

Synonym:

Target:

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