CSNpharm

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Csnpharm is committed to providing you with high quality products and outstanding services. We supply over 5000 bioactive compounds in stock, including inhibitors, agonists and natural products for laboratory and scientific use. Csnpharm has always been committed to develop quality products that are validated by NMR, UPLC, LC-MS, GC, Chiral HPLC and so on. We have a professional technical support team for customer service with years of experience in life science. Csnpharm is your reliable partner for scientific research.

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Sesamin 25mg  | ≥99%

CSNpharm

Sesamin is a natural product derived from sesame seeds, acting as a potent serum lipid-lowering food component.

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Sesamin 100mg  | ≥99%

CSNpharm

Sesamin is a natural product derived from sesame seeds, acting as a potent serum lipid-lowering food component.

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Sesamin 50mg  | ≥99%

CSNpharm

Sesamin is a natural product derived from sesame seeds, acting as a potent serum lipid-lowering food component.

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Sesamol 25mg  | ≥99%

CSNpharm

Sesamol, a natural product isolated and purified from the seeds of Sesamum indicum, ameliorates inflammatory and oxidative damage by upregulating AMPK activation and Nrf2 signaling and blocking the NF-κB and MAPK signaling pathways.

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Sesamol 100mg  | ≥99%

CSNpharm

Sesamol, a natural product isolated and purified from the seeds of Sesamum indicum, ameliorates inflammatory and oxidative damage by upregulating AMPK activation and Nrf2 signaling and blocking the NF-κB and MAPK signaling pathways.

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SGC0946 1mg  | ≥99%

CSNpharm

SGC0946 is a selective inhibitor of DOT1L methyltransferase with IC50 of 0.3 nM and can kill mixed lineage leukaemia cells.

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SGC0946 5mg  | ≥99%

CSNpharm

SGC0946 is a selective inhibitor of DOT1L methyltransferase with IC50 of 0.3 nM and can kill mixed lineage leukaemia cells.

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SGC0946 50mg  | ≥99%

CSNpharm

SGC0946 is a selective inhibitor of DOT1L methyltransferase with IC50 of 0.3 nM and can kill mixed lineage leukaemia cells.

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SGC0946 10mg  | ≥99%

CSNpharm

SGC0946 is a selective inhibitor of DOT1L methyltransferase with IC50 of 0.3 nM and can kill mixed lineage leukaemia cells.

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SGN-2FF 5mg  | ≥98%

CSNpharm

SGN-2FF is an oral inhibitor of fucosylation, directly inhibits fucosyltransferase activity, and possesses antitumor activity.

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SGN-2FF 50mg  | ≥98%

CSNpharm

SGN-2FF is an oral inhibitor of fucosylation, directly inhibits fucosyltransferase activity, and possesses antitumor activity.

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SGN-2FF 100mg  | ≥98%

CSNpharm

SGN-2FF is an oral inhibitor of fucosylation, directly inhibits fucosyltransferase activity, and possesses antitumor activity.

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SGN-2FF 10mg  | ≥98%

CSNpharm

SGN-2FF is an oral inhibitor of fucosylation, directly inhibits fucosyltransferase activity, and possesses antitumor activity.

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SGN-2FF 25mg  | ≥98%

CSNpharm

SGN-2FF is an oral inhibitor of fucosylation, directly inhibits fucosyltransferase activity, and possesses antitumor activity.

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Shikimic Acid 100mg  | ≥99%

CSNpharm

Shikimic acid(Shikimate), more commonly known as its anionic form shikimate, is an important biochemical intermediate in plants and microorganisms.

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Shikonin 25mg  | ≥99%

CSNpharm

Shikonin is an inhibitor of TMEM16A chloride channel with IC50 of 6.5 μM, it’s a natural product isolated and purified from the roots of Lithosperraum erythrorhizon Sieb. et Zucc..

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Shikonin 100mg  | ≥99%

CSNpharm

Shikonin is an inhibitor of TMEM16A chloride channel with IC50 of 6.5 μM, it’s a natural product isolated and purified from the roots of Lithosperraum erythrorhizon Sieb. et Zucc..

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Shikonin 10mg  | ≥99%

CSNpharm

Shikonin is an inhibitor of TMEM16A chloride channel with IC50 of 6.5 μM, it’s a natural product isolated and purified from the roots of Lithosperraum erythrorhizon Sieb. et Zucc..

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Shikonin 50mg  | ≥99%

CSNpharm

Shikonin is an inhibitor of TMEM16A chloride channel with IC50 of 6.5 μM, it’s a natural product isolated and purified from the roots of Lithosperraum erythrorhizon Sieb. et Zucc..

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Shionone 5mg  | ≥98%

CSNpharm

Shionone, a natural product isolated and purified from the flower of Chrysanthemum morifolium, has anti-inflammatory effect, the mechanism is related to decrease the phosphorylation level of ERK1/2 protein and IκBα and the protein expression of i NOS, and can inhibit the activity of ubiquitin-specific protease 2 (USP2) and provide a lead compound for future development […]

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