Gomisin D
CAS No. 60546-10-3
Gomisin D ( —— )
产品货号. M29043 CAS No. 60546-10-3
Gomisin D is a natural product.Gomisin D is used as a quality marker of Shengmai San and shenqi Jiangtang Granule.Gomisin D is a potential antidiabetic and anti-Alzheimer’s agent.
纯度: >98% (HPLC)
规格 | 价格/人民币 | 库存 | 数量 |
5MG | ¥1320 | 有现货 |
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10MG | ¥1944 | 有现货 |
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25MG | ¥3183 | 有现货 |
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50MG | ¥4763 | 有现货 |
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100MG | 获取报价 | 有现货 |
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200MG | 获取报价 | 有现货 |
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500MG | 获取报价 | 有现货 |
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1G | 获取报价 | 有现货 |
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生物学信息
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产品名称Gomisin D
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注意事项本公司产品仅用于科研实验,不得用于人体或动物的临床与诊断
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产品简述Gomisin D is a natural product.Gomisin D is used as a quality marker of Shengmai San and shenqi Jiangtang Granule.Gomisin D is a potential antidiabetic and anti-Alzheimer’s agent.
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产品描述Gomisin D is a natural product.Gomisin D is used as a quality marker of Shengmai San and shenqi Jiangtang Granule.Gomisin D is a potential antidiabetic and anti-Alzheimer’s agent.(In Vitro):Using exhaustive chromatographic separation we have isolated (-)-tigloyl-deangeloyl-gomisin F as a novel dibenzocyclooctadiene lignan from schisandra chinensis. With the help of HPLC, we further isolated (+)-schisandrin, (+)-deoxyschisandrin, (+)-γ-schisandrin, (-)-gomisin J, (+)-gomisin A, (-)-gomisin N, (-)-tigloyl-gomisin P, (-)-wuweizisu C, (-)-Gomisin D, rubrisandrin A, (-)-gomisin G, (+)-gomisin K (3) and (-)-schisantherin C. A full NMR description of (-)-schisantherin C was carried out with the aim to confirm previous reports of its structure. Compounds isolated were identified on the basis of UV, IR, (1)H- and (13)C-NMR and MS. The cytotoxicity of lignans was tested for the BY-2 cell line alone and as a synergistic effect with the cytotoxic agent camptothecin.
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同义词——
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通路Others
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靶点Other Targets
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受体——
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研究领域——
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适应症——
化学信息
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CAS Number60546-10-3
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分子量530.6
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分子式C28H34O10
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纯度>98% (HPLC)
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溶解度——
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SMILESCOc1cc2C3OC(=O)C(C)(O)C(C)COc4c5OCOc5cc(C[C@H](C)[C@@]3(C)O)c4-c2c(OC)c1OC
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化学全称——
运输与储存
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储存条件(-20℃)
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运输条件With Ice Pack
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稳定性≥ 2 years
参考文献
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Amino-PEG14-alcohol
Amino-PEG14-alcohol is a PEG-based PROTAC linker that can be used in the synthesis of PROTACs.
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FIDAS-5
FIDAS-5 effectively competes against S-adenosylmethionine (SAM) for MAT2A binding.?FIDAS-5 has anticancer activities.?FIDAS-5 is a potent and orally active methionine S-adenosyltransferase 2A (MAT2A) inhibitor with an IC50 of 2.1 μM.FIDAS-5 induces the expression of cell cycle inhibitor, p21WAF1/CIP1. FIDAS-5 (3 μM; 36 h) treatment reduces the levels of both S-adenosylmethionine (SAM) and S-adenosylhomocysteine (SAH) in LS174T cells.FIDAS-5 (3 μM; 7 days; LS174T cells) treatment significantly inhibits the proliferation of LS174T cells.
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UM171
UM171 is able to stimulate the expansion ex vivo of human cord blood cells, which is capable of reconstituting human hematopoiesis in immunocompromised mice.