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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6-Thioguanine 100mg  | ≥99%

CSNpharm

6-Thioguanine belongs to the thiopurine family of drugs that also include mercaptopurine and azathioprine, which are examples of antimetabolites, and is a purine analogue of the nucleobase guanine. It was found to inhibit SARS-CoV PLpro.

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6,8-Diprenylgenistein 5mg  | ≥98%

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6,8-Diprenylgenistein is a natural product isolated and purified from the roots of Lupinus mutabilis with antimicrobial activity against Gram-negative and Gram-positive bacteria.

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7-Amino-4-Methylcoumarin 50mg  | ≥99%

CSNpharm

7-Amino-4-methylcoumarin is a natural product isolated and purified from an endophytic Xylaria fungal species and exhibited strong antibacterial and antifungal activities in vitro against Aspergillus, Candida, Escherichia, Staphylococcus, Salmonella and Vibrio species, among others. It is also a reagent employed in the preparation of fluorogenic AMC-based substrates for the detection of proteolytic enzyme activity. AMC […]

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7-Amino-4-Methylcoumarin 10mg  | ≥99%

CSNpharm

7-Amino-4-methylcoumarin is a natural product isolated and purified from an endophytic Xylaria fungal species and exhibited strong antibacterial and antifungal activities in vitro against Aspergillus, Candida, Escherichia, Staphylococcus, Salmonella and Vibrio species, among others. It is also a reagent employed in the preparation of fluorogenic AMC-based substrates for the detection of proteolytic enzyme activity. AMC […]

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7-Chlorokynurenic acid 50mg  | ≥98%

CSNpharm

7-Chlorokynurenic acid is an antagonist of NMDA receptor acting at the glycine site. It can also act as competitive inhibitor of L-glutamate transport into synaptic vesicles.

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7-Chlorokynurenic acid 100mg  | ≥98%

CSNpharm

7-Chlorokynurenic acid is an antagonist of NMDA receptor acting at the glycine site. It can also act as competitive inhibitor of L-glutamate transport into synaptic vesicles.

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7-Chlorokynurenic acid 10mg  | ≥98%

CSNpharm

7-Chlorokynurenic acid is an antagonist of NMDA receptor acting at the glycine site. It can also act as competitive inhibitor of L-glutamate transport into synaptic vesicles.

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7-Ethylcamptothecin 100mg  | ≥99%

CSNpharm

7-Ethylcamptothecin is derived from Camptothecin with anti-cancer activity against various murine tumors through inhibition of Topo I (topoisomerase).

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7-Ethylcamptothecin 250mg  | ≥99%

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7-Ethylcamptothecin is derived from Camptothecin with anti-cancer activity against various murine tumors through inhibition of Topo I (topoisomerase).

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7-Ethylcamptothecin 25mg  | ≥99%

CSNpharm

7-Ethylcamptothecin is derived from Camptothecin with anti-cancer activity against various murine tumors through inhibition of Topo I (topoisomerase).

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7-Hydroxy-3,4-dihydrocarbostyril 100mg  | ≥99%

CSNpharm

7-​Hydroxy-​3,​4-​dihydro-​2(1H)​-​quinolinone (3,4-Dihydro-7-hydroxy-2(1H)-quinolinone) is a weak MAO-A inhibitor, with an IC50 of 183 μM, and has no effect on MAO-B.

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7-Methoxycoumarin 25mg  | ≥99%

CSNpharm

7-Methoxycoumarin, a natural product isolated and purified from the herbs of Citrus reticulata cv. Chachiensis, has potent antioxidant effect, strong hepatoprotective activity, and weak estrogenic activity.

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7-Methoxycoumarin 100mg  | ≥99%

CSNpharm

7-Methoxycoumarin, a natural product isolated and purified from the herbs of Citrus reticulata cv. Chachiensis, has potent antioxidant effect, strong hepatoprotective activity, and weak estrogenic activity.

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7,3′,4′-Trihydroxyflavone 10mg  | ≥95%

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7,3′,4′-Trihydroxyflavone, a natural product isolated and purified from the seeds of Cassia occidentalis, can markedly inhibit the receptor activator of nuclear factor kappa B ligand (RANKL) induced osteoclastic differentiation from mouse bone marrow derived macrophages (BMMs), it inhibits osteoclastogenesis via nuclear factor of activated T cells c1 (NFATc1).

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7,4′-Di-O-methylapigenin 2mg  | ≥99%

CSNpharm

7,4′-Di-O-methylapigenin, a flavonoid purified from aquilaria sinensis, can inhibit α-glucosidase, α-amylase enzymes and enhance 2-NBDG uptake in L6 cells. It has hypolipidemic effect.

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7,4′-Di-O-methylapigenin 5mg  | ≥99%

CSNpharm

7,4′-Di-O-methylapigenin, a flavonoid purified from aquilaria sinensis, can inhibit α-glucosidase, α-amylase enzymes and enhance 2-NBDG uptake in L6 cells. It has hypolipidemic effect.

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7,4′-Dihydroxy-8-Methylflavan 5mg  | ≥98%

CSNpharm

7,4’Dihydroxy-8-methylflavan, a natural product isolated and purified from the red resin of Dracaena cochinchinensis with free radical scavenging properties, can significantly promote mesenchymal stem cells (MSCs) osteogenic differentiation by increasing the levels of alkaline phosphatase (ALP) activity.

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7,4′-Dihydroxy-8-Methylflavan 1mg  | ≥98%

CSNpharm

7,4’Dihydroxy-8-methylflavan, a natural product isolated and purified from the red resin of Dracaena cochinchinensis with free radical scavenging properties, can significantly promote mesenchymal stem cells (MSCs) osteogenic differentiation by increasing the levels of alkaline phosphatase (ALP) activity.

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7ACC1 100mg  | ≥99%

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7ACC1 selectively interfere with lactate fluxes in the lactate-rich tumor microenvironment and inhibits lactate influx but not efflux in tumor cells expressing MCT1 and MCT4 transporters.

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7ACC1 250mg  | ≥99%

CSNpharm

7ACC1 selectively interfere with lactate fluxes in the lactate-rich tumor microenvironment and inhibits lactate influx but not efflux in tumor cells expressing MCT1 and MCT4 transporters.

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7ACC1 25mg  | ≥99%

CSNpharm

7ACC1 selectively interfere with lactate fluxes in the lactate-rich tumor microenvironment and inhibits lactate influx but not efflux in tumor cells expressing MCT1 and MCT4 transporters.

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