SIRT5 inhibitor 1 (compound 49) is a very potent human sirtuin 5 deacylase inhibitor, with an IC50 of 0.11 μM.
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Type | HazMat fee for 500 gram (Estimated) |
Excepted Quantity | USD 0.00 |
Limited Quantity | USD 15-60 |
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Inaccessible (Haz class 6.1), International | USD 150+ |
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Accessible (Haz class 3, 4, 5 or 8), International | USD 200+ |
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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。 |
描述 | Sirtuins are protein deacylases that regulate metabolism and stress responses and are implicated in aging-related diseases[1]. SIRT5 has drawn extensive attention due to its specific catalytic activity for low deacetylation activity but significant desuccinylation, demalonylation and deglutarylation activities[2]. SIRT5 inhibitor 1 (compound 49) is a very potent human sirtuin 5 deacylase inhibitor, with an IC50 of 0.11 μM, >100-fold from compound 1[3]. In vivo rat model of ischemia/reperfusion injury, SIRT5 inhibitor 1 (compound 49) reduced the ischemic area, showing a cardioprotective effect against myocardial injury that was higher than that exerted by diazoxide, used as reference cardioprotective drug, and maximum with compound 49[4]. |
计算器 | ||||
存储液制备 | ![]() |
1mg | 5mg | 10mg |
1 mM 5 mM 10 mM |
1.48mL 0.30mL 0.15mL |
7.41mL 1.48mL 0.74mL |
14.82mL 2.96mL 1.48mL |
CAS号 | 2166487-21-2 |
分子式 | C31H39FN6O6S2 |
分子量 | 674.81 |
SMILES Code | O=C(NC1CCC1)[C@@H](NC([C@@H](NS(C2=CC(F)=CC=C2)(=O)=O)CCCCNC(NCCC(O)=O)=S)=O)CC3=CNC4=CC=CC=C34 |
MDL No. | MFCD31746885 |
别名 | |
运输 | 蓝冰 |
InChI Key | NEJMWPNVCQYZKG-SVBPBHIXSA-N |
Pubchem ID | 134828254 |
存储条件 |
In solvent -20°C:3-6个月-80°C:12个月 Pure form Sealed in dry, store in freezer, under -20°C |