Enmein
CAS No. 3776-39-4
Enmein ( —— )
产品货号. M29061 CAS No. 3776-39-4
Enmein 对人肿瘤细胞 K562 有显着的抑制作用,IC(50) 值范围为 3.2 μg/ml 至 8.2 μg/ml。
纯度: >98% (HPLC)
COA
Datasheet
HNMR
HPLC
MSDS
Handing Instructions
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生物学信息
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产品名称Enmein
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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Enmein 对人肿瘤细胞 K562 有显着的抑制作用,IC(50) 值范围为 3.2 μg/ml 至 8.2 μg/ml。
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产品描述Enmein shows a significant inhibitory effect toward human tumor cell K562 with IC(50) values ranging from 3.2 μg/ml to 8.2 μg/ml.(In Vitro):Four new ent-kaurane diterpenoids, sculponeatins F-I (1-4), together with six known compounds, sculponeatin E (5), epi-nodosin (6), epi-nodosinol (7), Enmein (8), and macrocalyxoformins A and B (9 and 10), were isolated from the leaves of Isodon sculponeata. Also obtained were ursolic acid, 2alpha,3beta-dihydroxy-urs-12-en-28-oic acid, 2alpha,3beta,19alpha-trihydroxy-urs-12-en-28-oic acid, beta-sitosterol, daucosterol, quercetin, pedalitin, rosmarinic acid, caffeic acid and ethyl caffeic acid. Their structures were determined by spectral methods (1D-, 2D-NMR and MS). Some diterpenoids were tested for their cytotoxicity to inhibit three kinds of human tumor cells K562, A549 and T24.
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体外实验Enmein shows significant inhibitory effect toward K562 with an IC50 value ranging from 3.2 μg/ml to 8.2 μg/ml.Enmein (3.13-25 μg/ml; 48 hours) has inhibitory effect on lymphocytes with significant difference within concentration from 6.25 μg/ml to 25 μg/ml.Enmein (5.5-22 μg/ml; 48 hours) causes the percentage of S stage cells decreased from 19% to 6%, causes the percentage of G2/M stage cells to decrease from 2% to 0.4%. Cell Viability Assay Cell Line:Splenic lymphocyte cells Concentration:3.13, 6.25, 12.5, 25 μg/ml Incubation Time:48 hours Result:Exhibited an IC50 value of 17 μg/ml in splenic lymphocytes.Cell Cycle Analysis Cell Line:Splenic lymphocyte cells Concentration:5.5 μg/ml, 11 μg/ml, 22 μg/ml Incubation Time:48 hours Result:Caused S stage cells and G2/M stage cells decreased.
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体内实验Enmein (inject to ear; 6.52-13.04 mg/kg; 5 days) inhibits the xylene-induced ear swelling and inhibits IL-2 expression. Animal Model:Balb/c mice Dosage:6.52 mg/kg, 9.78 mg/kg or 13.04 mg/kg Administration:Injected to ear; 6.52 mg/kg, 9.78 mg/kg or 13.04 mg/kg; 5 days Result:Had inhibitory effect on IL-2 release in blood.
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同义词——
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通路Microbiology/Virology
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靶点Antifection
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受体Anti-infection
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研究领域——
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适应症——
化学信息
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CAS Number3776-39-4
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分子量362.422
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分子式C20H26O6
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纯度>98% (HPLC)
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溶解度——
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SMILESCC1(C)[C@H]2[C@H](O)OC[C@@]22[C@H](C[C@@H]1O)OC(=O)[C@@]13C[C@@H](CC[C@@H]21)C(=C)C3=O
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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
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