This compound is a customized synthesis product. We have a strong synthesis team with excellent synthesis technology and capabilities. However, due to various objective factors, there is a low probability that the synthesis will not be successful. If you need to learn more, please feel free to consult us, we will serve you wholeheartedly.
This compound is a customized synthesis product. We have a strong synthesis team with excellent synthesis technology and capabilities. However, due to various objective factors, there is a low probability that the synthesis will not be successful. If you need to learn more, please feel free to consult us, we will serve you wholeheartedly.
Antitumor agent-23
Catalog No. T39889 CAS
2355185-12-3
Antitumor agent-23 exhibits potent antitumoral activity, as demonstrated by its GI50 values of 38, 48, 5, 27, 80, and 28 nM against the lymphoma cell lines GRANTA-519, KARPAS-422, KARPAS-299, RAMOS, DAUDI, and RAJI respectively.
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Antitumor agent-23 exhibits potent antitumoral activity, as demonstrated by its GI50 values of 38, 48, 5, 27, 80, and 28 nM against the lymphoma cell lines GRANTA-519, KARPAS-422, KARPAS-299, RAMOS, DAUDI, and RAJI respectively.
In vitro
Antitumor agent-23, ranging from 0.001 to 100 μM over five days, effectively inhibits the proliferation of various lymphoma cell lines[1]. In HPV-positive cervical cancer cells, concentrations between 2 and 70 nM over 72 hours significantly upregulate p53 protein levels and induce acetylation at lysine 382 of p53 (K382Ac-p53)[1]. Detailed Cell Proliferation Assay findings reveal GI50 values of 38, 48, 5, 27, 80, and 28 nM for GRANTA-519, KARPAS-422, KARPAS-299, RAMOS, DAUDI, and RAJI cell lines, respectively, over a five-day period[1]. Western Blot Analysis conducted on the HPV16-positive cervical cancer cell line (CaSki) demonstrated noticeable p53 protein expression enhancement starting at 7 nM and noticeable acetylation at p53 lysine 382 starting at 20 nM over a 72-hour incubation period[1].
Molecular Weight
506.732
Formula
C28H50N4O4
CAS No.
2355185-12-3
Storage
Powder: -20°C for 3 years | In solvent: -80°C for 1 year
Method for preparing DMSO master liquid: mg
drug pre-dissolved in μL DMSO (Master liquid concentration
mg/mL),
Method for preparing in vivo formulation:Take μL
DMSO master liquid, next add μL PEG300, mix and clarify, next add μL
Tween 80,mix and clarify, next add μL ddH2O, mix and clarify.
Method for preparing in vivo formulation:Take μL
DMSO master liquid, next add μL Corn oil,mix and clarify.
Note:
Be sure to add the solvent(s) in order. Physical methods such as vortex, ultrasound or hot water bath can be used to aid dissolving.
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Tech Support
Please see Inhibitor Handling Instructions for more frequently ask questions. Topics include: how to prepare stock solutions, how to store products, and cautions on cell-based assays & animal experiments, etc.