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JGB1741 (Synonyms: ILS-JGB-1741)

カタログ番号GC13062 Copy One-Click Copy Product Info

JGB1741(ILS-JGB-1741)は、IC50が約15μMの強力で特異的なSIRT1活性阻害剤です。 JGB1741 は弱い SIRT2 および SIRT3 阻害剤であり、すべての IC50 が 100 μM を超えています。 JGB1741は、アセチル化p53レベルを増加させ、Bax / Bcl2比、シトクロムcの放出、およびPARP切断の調節により、p53を介したアポトーシスを引き起こします。 JGB1741は乳がん研究の可能性を秘めています。

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JGB1741 化学構造

Cas No.: 1256375-38-8

サイズ 価格 在庫数 個数
1mg
$91.00
在庫あり
5mg
$319.00
在庫あり
10mg
$545.00
在庫あり
25mg
$1,137.00
在庫あり

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Sample solution is provided at 25 µL, 10mM.



Description of JGB1741

JGB1741 is a small molecule SIRT1 inhibitor [1].

Sirtuins or Sir2 (silent information regulator 2)-related enzymes have originally been defined as a family of nicotinamide adenine dinucleotide-dependent enzymes which are involved in deacetylating lysine residue on multiple proteins. The sirtuins show highly conservation from archaebacteria to eukaryotes. The mammalian sirtuins SIRT1–SIRT7 have been implicated in a variety of cellular functions, such as gene silencing, over the control of the cell cycle and apoptosis, to energy homeostasis [2].

In vitro: JGB1741 potently inhibited the proliferation of human metastatic breast cancer cells, MDA-MB 231. JGB1741 showed antitumor effects on three different cancer cell lines, K562, HepG2 and MDA-MB 231 with an IC50 of 1, 10 and 0.5 μM, respectively. JGB1741-induced apoptosis has been associated with increase in cytochrome c release, modulation in Bax/Bcl2 ratio and cleavage of PARP [1].

References:
[1] Kalle A M, Mallika A, Badiger J, et al.  Inhibition of SIRT1 by a small molecule induces apoptosis in breast cancer cells[J]. Biochemical and biophysical research communications, 2010, 401(1): 13-19.
[2] Yamamoto H, Schoonjans K, Auwerx J.  Sirtuin functions in health and disease[J]. Molecular Endocrinology, 2007, 21(8): 1745-1755.

Chemical Properties of JGB1741

Cas No. 1256375-38-8 SDF
同義語 ILS-JGB-1741
Chemical Name 4,5,6,7-tetrahydro-2-[(E)-[(2-hydroxy-1-naphthalenyl)methylene]amino]-N-(phenylmethyl)-benzo[b]thiophene-3-carboxamide
Canonical SMILES OC1=C(/C=N/C2=C(C(NCC3=CC=CC=C3)=O)C(CCCC4)=C4S2)C(C=CC=C5)=C5C=C1
Formula C27H24N2O2S M.Wt 440.6
溶解度 ≤0.2mg/ml in DMSO;0.14mg/ml in dimethyl formamide Storage Store at -20°C
General tips Please select the appropriate solvent to prepare the stock solution according to the solubility of the product in different solvents; once the solution is prepared, please store it in separate packages to avoid product failure caused by repeated freezing and thawing.Storage method and period of the stock solution: When stored at -80°C, please use it within 6 months; when stored at -20°C, please use it within 1 month.
To increase solubility, heat the tube to 37°C and then oscillate in an ultrasonic bath for some time.
Shipping Condition Evaluation sample solution: shipped with blue ice. All other sizes available: with RT, or with Blue Ice upon request.

Complete Stock Solution Preparation Table of JGB1741

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1 mg 5 mg 10 mg
1 mM 2.2696 mL 11.3482 mL 22.6963 mL
5 mM 453.9 μL 2.2696 mL 4.5393 mL
10 mM 227 μL 1.1348 mL 2.2696 mL
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Method for preparing DMSO master liquid: mg drug pre-dissolved in μL DMSO ( Master liquid concentration mg/mL, Please contact us first if the concentration exceeds the DMSO solubility of the batch of drug. )

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Method for preparing in vivo formulation: Take μL DMSO master liquid, next add μL Corn oil, mix and clarify.

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Average Rating: 5 ★★★★★ (Based on Reviews and 10 reference(s) in Google Scholar.)

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