INUVISCOLIDE
Modify Date: 2024-04-05 08:01:36
INUVISCOLIDE structure
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Common Name | INUVISCOLIDE | ||
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| CAS Number | 63109-30-8 | Molecular Weight | 248.31700 | |
| Density | N/A | Boiling Point | N/A | |
| Molecular Formula | C15H20O3 | Melting Point | N/A | |
| MSDS | N/A | Flash Point | N/A | |
Use of INUVISCOLIDEInuviscolide is an apoptosis inducer. Inuviscolide can induce of G2/M arrest in human melanoma cell lines. Inuviscolide exhibits antineoplastic and anti-inflammatory activities[1][2][3]. |
| Name | (3aS,5aS,8R,8aR,9aR)-8-hydroxy-8-methyl-1,5-dimethylidene-3a,4,5a,6,7,8a,9,9a-octahydroazuleno[6,5-b]furan-2-one |
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| Synonym | More Synonyms |
| Description | Inuviscolide is an apoptosis inducer. Inuviscolide can induce of G2/M arrest in human melanoma cell lines. Inuviscolide exhibits antineoplastic and anti-inflammatory activities[1][2][3]. |
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| Related Catalog | |
| In Vitro | Inuviscolide (9-72 μM; 24 h) 抑制 SK-28，624 和 1363 黑色素瘤细胞的增殖，IC50 值分别为 37，41.1 和 39 μM[2]。 Inuviscolide (36-54 μM; 4-24 h) 导致 SK-28 细胞在 G2/M 期发生剂量依赖性积累[2]。 Inuviscolide (72 μM; 48 h) 导致约 70% 的 SK-28 细胞表现出早期凋亡标志物[2]。 Inuviscolide 在 100 μM 时抑制人白细胞弹性蛋白酶的释放 51%[1]。 Inuviscolide 抑制蜂毒分泌的 PLA2 (sPLA2)，IC50 值为 80.5 μM[1]。 Inuviscolide 在 50 μM 时抑制 COX-1 (40%)，而它对诱导型 COX-2 没有活性[1]。 Cell Proliferation Assay[2] Cell Line: SK-28, 624 and 1363 melanoma cells Concentration: 9-72 μM Incubation Time: 24 hours Result: Resulted in a dose-dependent inhibition of cellular proliferation, with no significant changes between the three cell lines. |
| In Vivo | Inuviscolide 减少了反复应用 12-O-tetradecanoylphorbol 13-acetate 诱导的皮炎小鼠皮肤白细胞浸润[1]。 |
| References |
| Molecular Formula | C15H20O3 |
|---|---|
| Molecular Weight | 248.31700 |
| Exact Mass | 248.14100 |
| PSA | 46.53000 |
| LogP | 2.21140 |
| Inuviscolide |
| (3aR,4aR,5R,7aS,9aS)-5-hydroxy-5-methyl-3,8-dimethylidenedecahydroazuleno[6,5-b]furan-2(3H)-one |