计算溶液所需的质量、体积或浓度。
活性类型 | 活性值-log(M) | 作用机制 | 期刊 | 参考文献(PubMed IDs) |
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货号 (SKU) | 包装规格 | 是否现货 | 价格 | 数量 |
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G129772-5mg |
5mg |
现货 ![]() |
| |
G129772-25mg |
25mg |
现货 ![]() |
| |
G129772-50mg |
50mg |
现货 ![]() |
| |
G129772-250mg |
250mg |
现货 ![]() |
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G129772-1g |
1g |
现货 ![]() |
|
别名 | 2-[2-甲基-4-[[[4-甲基-2-[4-(三氟甲基)苯基]-5-噻唑基]甲基]硫代]苯氧基]-乙酸 |
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英文别名 | HMS3744O09 | HY-10838 | 2-[2-Methyl-4-[[[4-methyl-2-[4-(trifluoromethyl)phenyl]-5-thiazolyl]methyl]thio]phenoxy]acetic Acid | CS-0438 | GW 501516 | SB19569 | AC-23001 | 2-{2-methyl-4-[({4-methyl-2-[4-(trifluoromethyl)phenyl]-1,3-thiazol-5-yl}methyl)sulfan |
规格或纯度 | Moligand™, ≥97% |
英文名称 | GW501516 |
生化机理 | GW501516 激活 PPARδ,可通过脂肪组织和骨骼肌中的脂肪酸分解代谢延缓体重增加。GW501516 可提高高密度脂蛋白胆固醇和载脂蛋白 A(apoA)的水平,降低低密度脂蛋白胆固醇、载脂蛋白 B 和甘油三酯的水平。 GW501516 是一种选择性过氧化物酶体增殖激活受体δ(PPARδ)激动剂,对 PPARδ 具有高亲和力(Ki = 1 nM)和效力(EC50 = 1 nM),对 PPARα 和 PPARγ 的选择性大于 1000 倍。GW501516 被证明能激活一些与运动激活的途径相同的途径,并被研究作为肥胖症、糖尿病、血脂异常和心血管疾病的潜在治疗药物。然而,GW501516 也显示会增加大鼠的癌症发病率。 |
储存温度 | -20°C储存 |
运输条件 | 超低温冰袋运输 |
作用类型 | 激动剂 |
作用机制 | 过氧化物酶体增殖激活受体δ激动剂 |
产品介绍 |
GW 501516 (GW 1516) 是 PPARδ 的激动剂,EC50 值为 1.1 nM。 GW501516 has been used to study its effect on mutation-driven colorectal tumorigenesis and tumor invasion using mouse model.
GW501516 has been used as a peroxisome proliferator-activated receptor (PPAR) δ agonist:
to treat the differentiated L6 myotubes to test its effect on free fatty acid (FFA) uptake under mild hypoxia conditions
in organoid culture medium to test its effect on self-renewal of PR domain containing 16 (Prdm16)-depleted intestinal stem cells
as a component in the defatting medium for primary human hepatocytes (PHH) culture |
ALogP | 5.9 |
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作用机制 | Action Type | target ID | Target Name | Target Type | Target Organism | Binding Site Name | 参考文献 |
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PubChem SID | 504764871 |
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分子类型 | 小分子 |
IUPAC Name | 2-[2-methyl-4-[[4-methyl-2-[4-(trifluoromethyl)phenyl]-1,3-thiazol-5-yl]methylsulfanyl]phenoxy]acetic acid |
INCHI | InChI=1S/C21H18F3NO3S2/c1-12-9-16(7-8-17(12)28-10-19(26)27)29-11-18-13(2)25-20(30-18)14-3-5-15(6-4-14)21(22,23)24/h3-9H,10-11H2,1-2H3,(H,26,27) |
InChi Key | YDBLKRPLXZNVNB-UHFFFAOYSA-N |
Canonical SMILES | CC1=C(C=CC(=C1)SCC2=C(N=C(S2)C3=CC=C(C=C3)C(F)(F)F)C)OCC(=O)O |
Isomeric SMILES | CC1=C(C=CC(=C1)SCC2=C(N=C(S2)C3=CC=C(C=C3)C(F)(F)F)C)OCC(=O)O |
RTECS | AI9105500 |
PubChem CID | 9803963 |
分子量 | 453.5 |
Beilstein号 | 18515150 |
溶解性 | 溶于DMSO, 最高浓度 (mg/mL): 45.35, 最高浓度(mM): 100;溶于ethanol, 最高浓度 (mg/mL): 22.68, 最高浓度(mM): 50 |
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分子量 | 453.500 g/mol |
XLogP3 | 5.900 |
氢键供体数Hydrogen Bond Donor Count | 1 |
氢键受体数Hydrogen Bond Acceptor Count | 9 |
可旋转键计数Rotatable Bond Count | 7 |
精确质量Exact Mass | 453.068 Da |
单同位素质量Monoisotopic Mass | 453.068 Da |
拓扑极表面积Topological Polar Surface Area | 113.000 Ų |
重原子数Heavy Atom Count | 30 |
形式电荷Formal Charge | 0 |
复杂度Complexity | 572.000 |
同位素原子数Isotope Atom Count | 0 |
定义的原子立体中心计数Defined Atom Stereocenter Count | 0 |
未定义的原子立体中心计数Undefined Atom Stereocenter Count | 0 |
定义的键立体中心计数Defined Bond Stereocenter Count | 0 |
未定义的键立体中心计数Undefined Bond Stereocenter Count | 0 |
所有立体化学键的总数The total count of all stereochemical bonds | 0 |
共价键合单元计数Covalently-Bonded Unit Count | 1 |
RTECS | AI9105500 |
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Purity | 97-100(%) |
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Appearance(G129772) | White to Yellow to Brown Powder and/or Chunks |
Infrared spectrum | Conforms to Structure |
NMR spectrum | Conforms to Structure |
1. Xian Sun, Yanqing Xie, Xiyang Zhang, Jiebing Song, Yuping Wu. (2023) Estimation of Per- and Polyfluorinated Alkyl Substance Induction Equivalency Factors for Humpback Dolphins by Transactivation Potencies of Peroxisome Proliferator-Activated Receptors. ENVIRONMENTAL SCIENCE & TECHNOLOGY, 57 (9): (3713–3721). [PMID:36812292] [10.1021/acs.est.2c05044] |
1. Xian Sun, Yanqing Xie, Xiyang Zhang, Jiebing Song, Yuping Wu. (2023) Estimation of Per- and Polyfluorinated Alkyl Substance Induction Equivalency Factors for Humpback Dolphins by Transactivation Potencies of Peroxisome Proliferator-Activated Receptors. ENVIRONMENTAL SCIENCE & TECHNOLOGY, 57 (9): (3713–3721). [PMID:36812292] [10.1021/acs.est.2c05044] |