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Cat #: V34478 CAS #: 102115-79-7 Purity ≥ 99%
Description: Pseudoprotodioscin, a furostanoside, is natural product of the steroids class with diverse biological activities such as anticancer effects. It inhibits SREBP1/2 and microRNA 33a/b levels and reduces the gene expression regarding the synthesis of cholesterol and triglycerides.
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CAS No. | 102115-79-7 |
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SMILES Code | C[C@]12[C@]([H])([C@]3([C@]([H])(CC2)[C@]4(C)C(C[C@@H](O[C@H]5[C@H](O[C@H]6[C@H](O)[C@H](O)[C@@H](O)[C@H](C)O6)[C@@H](O)[C@H](O[C@H]7[C@H](O)[C@H](O)[C@@H](O)[C@H](C)O7)[C@@H](CO)O5)CC4)=CC3)[H])C[C@]8([C@@]1(C(C)=C(O8)CC[C@H](CO[C@H]9[C@@H]([C@H]([C@@H]([C@H](O9)CO)O)O)O)C)[H])[H] |
Protocol | In Vitro | In Hep G2 cells, Pseudoprotodioscin increases ABCA1 protein and mRNA levels, and promotes the effluxion of ApoA-1-mediated cholesterol. Pseudoprotodioscin inhibits SREBP1c and SREBP2 transcription by decreasing microRNA 33a/b levels. This procedure reciprocally lead to the increase of ABCA1 levels. In THP-1 macrophages, Pseudoprotodioscin shows the similar effect, which reduces HMGCR, FAS and ACC mRNA levels and promotes low density lipoprotein receptor by decreasing the PCSK9 levels[1]. |
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This equation is commonly abbreviated as: C1 V1 = C2 V2
- (1) Please be sure that the solution is clear before the addition of next solvent. Dissolution methods like vortex, ultrasound or warming and heat may be used to aid dissolving.
- (2) Be sure to add the solvent(s) in order.