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UCM05

🥰Excellent
Catalog No. T21831Cas No. 1094451-90-7
Alias G28UCM

UCM05 (G28UCM) is a potent inhibitor of fatty acid synthase (FASN) with efficacy against HER2+ breast cancer xenografts, including cell lines resistant to anti-HER2 drugs [1]. Additionally, it functions as an inhibitor of the Filamentous temperature-sensitive protein Z (FtsZ), selectively inhibiting the growth of the Gram-positive bacterium B. subtilis with minimum inhibitory concentration (MIC) values of 100 μM, while showing no activity against the Gram-negative bacterium E. coli [2].

UCM05

UCM05

🥰Excellent
Purity: 99.11%
Catalog No. T21831Alias G28UCMCas No. 1094451-90-7
UCM05 (G28UCM) is a potent inhibitor of fatty acid synthase (FASN) with efficacy against HER2+ breast cancer xenografts, including cell lines resistant to anti-HER2 drugs [1]. Additionally, it functions as an inhibitor of the Filamentous temperature-sensitive protein Z (FtsZ), selectively inhibiting the growth of the Gram-positive bacterium B. subtilis with minimum inhibitory concentration (MIC) values of 100 μM, while showing no activity against the Gram-negative bacterium E. coli [2].
Pack SizePriceAvailabilityQuantity
1 mg$34In Stock
5 mg$80In Stock
10 mg$139In Stock
25 mg$289In Stock
50 mg$455In Stock
100 mg$672In Stock
1 mL x 10 mM (in DMSO)$82In Stock
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Purity:99.11%
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Product Introduction

Bioactivity
Description
UCM05 (G28UCM) is a potent inhibitor of fatty acid synthase (FASN) with efficacy against HER2+ breast cancer xenografts, including cell lines resistant to anti-HER2 drugs [1]. Additionally, it functions as an inhibitor of the Filamentous temperature-sensitive protein Z (FtsZ), selectively inhibiting the growth of the Gram-positive bacterium B. subtilis with minimum inhibitory concentration (MIC) values of 100 μM, while showing no activity against the Gram-negative bacterium E. coli [2].
In vitro
G28UCM shows cytotoxic activity in developed HER2 + and FASN + trastuzumab and lapatinib-resistant cells[1].
In vivo
G28UCM (40 mg/Kg; Daily i.p; for 45 days) inhibits the growth of BT474 xenografts and do not induce weight loss in vivo[1].
AliasG28UCM
Chemical Properties
Molecular Weight464.38
FormulaC24H16O10
Cas No.1094451-90-7
SmilesOc1cc(cc(O)c1O)C(=O)Oc1cc(OC(=O)c2cc(O)c(O)c(O)c2)c2ccccc2c1
Relative Density.1.652 g/cm3 (Predicted)
Storage & Solubility Information
StoragePowder: -20°C for 3 years | In solvent: -80°C for 1 year | Shipping with blue ice.
Solubility Information
DMSO: 90.0 mg/mL (193.8 mM), Sonication is recommended.
Ethanol: Soluble
Solution Preparation Table
DMSO
1mg5mg10mg50mg
1 mM2.1534 mL10.7670 mL21.5341 mL107.6704 mL
5 mM0.4307 mL2.1534 mL4.3068 mL21.5341 mL
10 mM0.2153 mL1.0767 mL2.1534 mL10.7670 mL
20 mM0.1077 mL0.5384 mL1.0767 mL5.3835 mL
50 mM0.0431 mL0.2153 mL0.4307 mL2.1534 mL
100 mM0.0215 mL0.1077 mL0.2153 mL1.0767 mL

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Mother liquor preparation method: 2 mg of drug dissolved in 50 μL DMSOTargetMol | reagent (mother liquor concentration of 40 mg/mL), if you need to configure a concentration that exceeds the solubility of the product, please contact us first.
Preparation method for in vivo formula: Take 50 μL DMSOTargetMol | reagent main solution, add 300 μLPEG300TargetMol | reagent mix well and clarify, then add 50 more μL Tween 80, mix well and clarify, then add 600 more μLddH2OTargetMol | reagent mix well and clarify
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