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|---|---|---|---|---|---|---|---|
| {[ item.pr_size ]} | {[ getRatePriceInt(item.pr_rmb, 1,1) ]}{[ getRatePriceInt(item.pr_rmb_sale, 1,1) ]} {[ suihuo_tips(item.pr_tag_price, item.pr_am) ]} | {[ getRatePriceInt(item.pr_rmb, 1,1) ]}{[ getRatePriceInt(item.pr_rmb,item.pr_rate,1) ]} {[ suihuo_tips(item.pr_tag_price, item.pr_am) ]} | {[ getRatePriceInt(item.pr_rmb, 1,1) ]}{[ suihuo_tips(item.pr_tag_price, item.pr_am) ]} | {[ getRatePrice(item.pr_rmb_sale, 1,1,item.mem_isinteger) ]} {[ getRatePrice(item.pr_rmb,item.pr_rate,item.mem_rate,item.mem_isinteger) ]} {[ getRatePrice(item.pr_rmb,1,item.mem_rate,item.mem_isinteger) ]} | 现货 | 1周 咨询 | - + | 
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| 产品名称 | SIRT1 ↓ ↑ | SIRT2 ↓ ↑ | SIRT3 ↓ ↑ | SIRT5 ↓ ↑ | SIRT6 ↓ ↑ | SIRT7 ↓ ↑ | Sirtuin ↓ ↑ | 其他靶点 | 纯度 | ||||||||||
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| Selisistat | ++++ SIRT1, IC50: 38 nM | 99%+ | |||||||||||||||||
| Resveratrol | ✔ | 98% | |||||||||||||||||
| Inauhzin | ✔ | p53 | 99%+ | ||||||||||||||||
| Suramin sodium salt | +++ SirT1, IC50: 297 nM | ++ SirT5, IC50: 22 μM | 99%+ | ||||||||||||||||
| Salermide | ✔ | 99% | |||||||||||||||||
| Quercetin Dihydrate | ✔ | 95% | |||||||||||||||||
| Sirtinol | + SIRT1, IC50: 131 μM | ++ SIRT2, IC50: 38 μM | 98%+ | ||||||||||||||||
| AGK2 | +++ SIRT2, IC50: 3.5 μM | 99%+ | |||||||||||||||||
| Tenovin-3 | ✔ | p53 | 99%+ | ||||||||||||||||
| 3-TYP | ++++ SIRT1, IC50: 88 nM | ++++ SIRT2, IC50: 92 nM | ++++ SIRT3, IC50: 16 nM | 95% | |||||||||||||||
| Tenovin-6 | ++ SIRT1, IC50: 21 μM | ++ SIRT2, IC50: 10 μM | + SIRT3, IC50: 67 μM | p53 | 99%+ | ||||||||||||||
| SirReal2 | +++ SIRT2, IC50: 140 nM | 99%+ | |||||||||||||||||
| Thiomyristoyl | ++++ SIRT2, IC50: 28 nM | 99%+ | |||||||||||||||||
| Et-29 | ✔ | 98% | |||||||||||||||||
| OSS_128167 | + SIRT1, IC50: 1578 μM | + SIRT2, IC50: 751 μM | + SIRT6, IC50: 89 μM | 98% | |||||||||||||||
| SIRT7 inhibitor 97491 | +++ SIRT7, IC50: 325 nM | 97% | |||||||||||||||||
| Nicotinamide | ✔ | 99+% | |||||||||||||||||
| 1. 鼠标悬停在“+”上可以显示相关IC50的具体数值。"+"越多,抑制作用越强。2. "✔"表示该化合物对相应的亚型有抑制作用,但抑制强度暂时没有相关数据。 | |||||||||||||||||||
| 靶点 | 
 | 
| 描述 | 3-TYP is a selective SIRT3 inhibitor. | 
| Concentration | Treated Time | Description | References | |
| HK-2 cells | 50 μM | 3-TYP further aggravated LPS-induced PDHA1 hyperacetylation and PDH inactivation, and promoted lactate production. | Cell Death Dis. 2023 Jul 21;14(7):457. | |
| Primary mouse hippocampal neurons | 50 μM | 1 h | 3-TYP, as a SIRT3 inhibitor, was used to study its effect on the protective role of HKL in the hippocampal neuronal AD model. The results showed that 3-TYP treatment reversed the protective effect of HKL on the hippocampal neuronal AD model and inhibited the activation of mitochondrial autophagy. | CNS Neurosci Ther. 2024 Aug;30(8):e14878. | 
| H9c2 cells | 50 μM | 12 h | 3-TYP was used to inhibit SIRT3 activity to verify the role of SIRT3 in the regulation of mitochondrial homeostasis by omentin1. The results showed that 3-TYP treatment significantly reduced the expression of SIRT3 and inhibited the improvement effects of omentin1 on mitochondrial function, mitochondrial fusion-fission dynamics, and mitophagy. | J Transl Med. 2022 Oct 4;20(1):447. | 
| 3T3-L1 preadipocytes | 50 µM and 100 µM | 3-TYP inhibited adipogenesis in 3T3-L1 preadipocytes, reducing adipogenesis compared to the control. | Int J Mol Sci. 2022 Mar 29;23(7):3740. | |
| BMDMs | 50 µM | 1 h | To investigate the inhibitory effect of 3-TYP on SIRT3 and its impact on XBP1s expression. The results showed that 3-TYP significantly increased the production of XBP1s. | Front Immunol. 2023 May 19;14:1128543. | 
| THP-1 cells | 10 to 200 μM | Suppressed IFNβ and CXCL10 expression after VSV infection | Proc Natl Acad Sci U S A. 2024 Apr 23;121(17):e2314201121. | |
| A549 cells | 10 to 200 μM | Suppressed IFNβ, CXCL10, and ISG15 expression after VSV infection | Proc Natl Acad Sci U S A. 2024 Apr 23;121(17):e2314201121. | |
| H1299 cells | 10 to 200 μM | Suppressed IFNβ and CXCL10 expression after poly(I:C) LMW transfection | Proc Natl Acad Sci U S A. 2024 Apr 23;121(17):e2314201121. | 
| Administration | Dosage | Frequency | Description | References | ||
| C57BL/6 mice | Cecal ligation and puncture (CLP) model | Intraperitoneal injection | 5 mg/kg | Single dose, 0.5 h before CLP | Pretreatment with 3-TYP significantly increased CLP-induced PDHA1 hyperacetylation and PDH inactivation, and exacerbated the elevation of renal lactate levels. | Cell Death Dis. 2023 Jul 21;14(7):457. | 
| Mice | APP/PS1 mouse AD model | Intraperitoneal injection | 50 mg/kg | Once daily for 5 days | 3-TYP, as a SIRT3 inhibitor, was used to study its effect on the protective role of HKL in the AD mouse model. The results showed that 3-TYP treatment reversed the protective effect of HKL on the AD mouse model and inhibited the activation of hippocampal mitochondrial autophagy. | CNS Neurosci Ther. 2024 Aug;30(8):e14878. | 
| C57BL/6N mice | Sepsis model | Intraperitoneal injection | 5 mg/kg | Once daily for 3 days | To investigate the effect of 3-TYP on sepsis-associated acute lung injury, the results showed that 3-TYP reversed the protective effect of MK-4 on sepsis by inhibiting Sirt3 activity | J Inflamm Res. 2024 Oct 24;17:7675-7685 | 
| C57BL/6 mice | IMQ-induced psoriasis-like mouse model | Intraperitoneal injection | 50 mg/kg | Every 2 days for 7 days | To investigate the effect of 3-TYP on IMQ-induced psoriasis-like skin inflammation. The results showed that the 3-TYP group displayed accelerated psoriasis-like skin lesions. | Front Immunol. 2023 May 19;14:1128543. | 
| BALB/c mice | 786-O cell subcutaneous xenograft model | Intraperitoneal injection | 25 mg/kg | Every other day for 12 days | To verify the effect of MLT on RCC cell growth in vivo, the results showed that MLT significantly inhibited tumor growth in mice without affecting. | Redox Rep. 2023 Dec;28(1):2251234 | 
| 计算器 | ||||
| 存储液制备 |  | 1mg | 5mg | 10mg | 
| 1 mM 5 mM 10 mM | 6.84mL 1.37mL 0.68mL | 34.21mL 6.84mL 3.42mL | 68.42mL 13.68mL 6.84mL | |
| CAS号 | 120241-79-4 | 
| 分子式 | C7H6N4 | 
| 分子量 | 146.15 | 
| SMILES Code | C1(C2=CNN=N2)=CC=CN=C1 | 
| MDL No. | MFCD25956467 | 
| 别名 | |
| 运输 | 蓝冰 | 
| InChI Key | VYXFEFOIYPNBFK-UHFFFAOYSA-N | 
| Pubchem ID | 9833992 | 
| 存储条件 | In solvent -20°C: 3-6个月 -80°C: 12个月 Pure form Sealed in dry, 2-8°C | 
| 溶解方案 | DMSO: 120 mg/mL(821.08 mM),配合低频超声助溶,注意:DMSO长时间开封后,会吸水并导致溶解能力下降,请避免使用长期开封的DMSO H2O: 1 mg/mL(6.84 mM),配合低频超声,并水浴加热至45℃助溶 无水乙醇: 15 mg/mL(102.63 mM),配合低频超声助溶,注意:无水乙醇开封后,易挥发,也会吸收空气中的水分,导致溶解能力下降,请避免使用开封较久的乙醇 以下溶解方案都请先按照体外实验的方式配制澄清的储备液,再依次添加助溶剂: ——为保证实验结果的可靠性,澄清的储备液可以根据储存条件,适当保存;体内实验的工作液,建议现用现配,当天使用; 以下溶剂前显示的百分比是指该溶剂在终溶液中的体积占比;如在配制过程中出现沉淀、析出现象,可以通过加热和/或超声的方式助溶 
 
 
 
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