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4,4-Dimethyl-2-cyclopenten-1-one Sale

(Synonyms: 4,4-二甲基-2-环戊烯-1-酮,4,4-Dimethylcyclopent-2-enone) 目录号 : GC61637

4,4-Dimethyl-2-cyclopenten-1-one是可来源于ApocynivenetiFolium的天然产物,对不同肿瘤细胞显示出高选择性的细胞毒性。

4,4-Dimethyl-2-cyclopenten-1-one Chemical Structure

Cas No.:22748-16-9

规格 价格 库存 购买数量
10 mg
¥450.00
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产品描述

4,4-Dimethyl-2-cyclopenten-1-one, a natural compound from Apocyniveneti Folium, displays higher tumor-specific cytotoxicity[1].

4,4-Dimethyl-2-cyclopenten-1-one selectively kills the tumor cells (HSC-2, HL-60). 4,4-Dimethyl-2-cyclopenten-1-one exhibits CC50 (50% cytotoxic concentration) values of 43.8 μg/mL, 152 μg/mL, 118 μg/mL, 14.0 μg/mL, 177 μg/mL and 123 μg/mL in HSC-2, HSC-3, HSG, HL-60, HGF and normal cells (HPC), respectively[1].

[1]. Tohru Nakayachi, et al. Structure-activity relationships of alpha, beta-unsaturated ketones as assessed by their cytotoxicity against oral tumor cells. Anticancer Res. Mar-Apr 2004;24(2B):737-42. [2]. Wei-WeiZhu, et al. Cornstalk liquefaction in methanol/water mixed solvents. Fuel Processing Technology Volume 117, January 2014, Pages 1-7.

Chemical Properties

Cas No. 22748-16-9 SDF
别名 4,4-二甲基-2-环戊烯-1-酮,4,4-Dimethylcyclopent-2-enone
Canonical SMILES O=C1C=CC(C)(C)C1
分子式 C7H10O 分子量 110.15
溶解度 储存条件 Store at -20°C
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1 mg 5 mg 10 mg
1 mM 9.0785 mL 45.3926 mL 90.7853 mL
5 mM 1.8157 mL 9.0785 mL 18.1571 mL
10 mM 0.9079 mL 4.5393 mL 9.0785 mL
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Research Update

Structure-activity relationships of alpha, beta-unsaturated ketones as assessed by their cytotoxicity against oral tumor cells

Anticancer Res 2004 Mar-Apr;24(2B):737-42.PMID:15161020doi

A series of simple alpha, beta-unsaturated carbonyl compounds (1-26) was characterized for their cytotoxic profiles against oral human normal and tumor cells. Several cycloalkenones showed potent cytotoxic activities against human oral squamous cell carcinoma HSC-2 cell line. Among them, 4,4-Dimethyl-2-cyclopenten-1-one (12) exhibited low cytotoxic activity against a normal human cell, gingival fibroblast HGF, and displayed higher tumor-specific cytotoxicity (SI value = CC50 (HGF)/CC50 (HSC-2) = 4.0). The cytotoxicities of the unsaturated lactones were moderately tumor-specific (SI = 1.5-1.9). Agarose gel electrophoresis showed that the induction of internucleosomal DNA fragmentation in human promyelocytic leukemia cell HL-60 is dependent on the structure of alpha, beta-unsaturated carbonyl compounds. Fluorometric protease assay showed that some, but not all compounds, activated the caspase 3 in a dose-dependent manner. All alpha, beta-unsaturated carbonyl compounds studied did not activate caspases 8 and 9. The cytotoxic activity of alpha, beta-unsaturated carbonyl compounds was profoundly reduced in the presence of N-acetylcysteine. The study suggests that the presence of a non sterically hindered Michael acceptor seems to be an essential structural requirement for the cytotoxic activity in alpha, beta-unsaturated ketones.