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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10058-F4 50mg  | 98%

CSNpharm

10058-F4 is a cell-permeable thiazolidinone that specificallly inhibits the c-Myc-Max interaction and prevents transactivation of c-Myc target gene expression and induces cell-cycle arrest and apoptosis.

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10058-F4 5mg  | 98%

CSNpharm

10058-F4 is a cell-permeable thiazolidinone that specificallly inhibits the c-Myc-Max interaction and prevents transactivation of c-Myc target gene expression and induces cell-cycle arrest and apoptosis.

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10058-F4 10mg  | 98%

CSNpharm

10058-F4 is a cell-permeable thiazolidinone that specificallly inhibits the c-Myc-Max interaction and prevents transactivation of c-Myc target gene expression and induces cell-cycle arrest and apoptosis.

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17-AAG 25mg  | 98%

CSNpharm

17-AAG is a potent HSP90 inhibitor with IC50 of 5 nM, having a 100-fold higher binding affinity for HSP90 derived from tumour cells than HSP90 from normal cells.

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17-AAG 5mg  | 98%

CSNpharm

17-AAG is a potent HSP90 inhibitor with IC50 of 5 nM, having a 100-fold higher binding affinity for HSP90 derived from tumour cells than HSP90 from normal cells.

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17-AAG 250mg  | 98%

CSNpharm

17-AAG is a potent HSP90 inhibitor with IC50 of 5 nM, having a 100-fold higher binding affinity for HSP90 derived from tumour cells than HSP90 from normal cells.

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17-AAG 100mg  | 98%

CSNpharm

17-AAG is a potent HSP90 inhibitor with IC50 of 5 nM, having a 100-fold higher binding affinity for HSP90 derived from tumour cells than HSP90 from normal cells.

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17-AAG 10mg  | 98%

CSNpharm

17-AAG is a potent HSP90 inhibitor with IC50 of 5 nM, having a 100-fold higher binding affinity for HSP90 derived from tumour cells than HSP90 from normal cells.

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1NM-PP1(PP1 Analog II) 1mg  | 98%

CSNpharm

1NM-PP1 is a cell-permeable PP1 analog that acts as a potent and selective inhibitor of mutant kinases over their wild-type progenitors with IC50 of 28 μM for vSrc and 4.2 nM for v-Src-as1 I338G.

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1NM-PP1(PP1 Analog II) 50mg  | 98%

CSNpharm

1NM-PP1 is a cell-permeable PP1 analog that acts as a potent and selective inhibitor of mutant kinases over their wild-type progenitors with IC50 of 28 μM for vSrc and 4.2 nM for v-Src-as1 I338G.

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1NM-PP1(PP1 Analog II) 10mg  | 98%

CSNpharm

1NM-PP1 is a cell-permeable PP1 analog that acts as a potent and selective inhibitor of mutant kinases over their wild-type progenitors with IC50 of 28 μM for vSrc and 4.2 nM for v-Src-as1 I338G.

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1NM-PP1(PP1 Analog II) 5mg  | 98%

CSNpharm

1NM-PP1 is a cell-permeable PP1 analog that acts as a potent and selective inhibitor of mutant kinases over their wild-type progenitors with IC50 of 28 μM for vSrc and 4.2 nM for v-Src-as1 I338G.

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2-(3,4-Dihydroxyphenyl)ethanol 50mg  | 98%

CSNpharm

2-(3,4-Dihydroxyphenyl)ethanol is a potent and specific inhibitor of lipoxygenase activities, inhibits platelet 12-LO activity with IC50 of 4.2 mM and PMNL 5-LO activity with IC50 of 13 mM. It’s a natural product isolated and purified from the herbs of Canarium album with antioxidant property.

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2-(3,4-Dihydroxyphenyl)ethanol 250mg  | 98%

CSNpharm

2-(3,4-Dihydroxyphenyl)ethanol is a potent and specific inhibitor of lipoxygenase activities, inhibits platelet 12-LO activity with IC50 of 4.2 mM and PMNL 5-LO activity with IC50 of 13 mM. It’s a natural product isolated and purified from the herbs of Canarium album with antioxidant property.

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2-(3,4-Dihydroxyphenyl)ethanol 10mg  | 98%

CSNpharm

2-(3,4-Dihydroxyphenyl)ethanol is a potent and specific inhibitor of lipoxygenase activities, inhibits platelet 12-LO activity with IC50 of 4.2 mM and PMNL 5-LO activity with IC50 of 13 mM. It’s a natural product isolated and purified from the herbs of Canarium album with antioxidant property.

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2-(4-Hydroxyphenyl)ethanol 25mg  | 99%

CSNpharm

2-(4-Hydroxyphenyl)ethanol is a natural product isolated and purified from the leaves of Canarium album, which significantly protects dopaminergic neurons from MPP(+)-induced degradation, and reveals potential neuroprotective mechanism of tyrosol.

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2-(4-Hydroxyphenyl)ethanol 100mg  | 99%

CSNpharm

2-(4-Hydroxyphenyl)ethanol is a natural product isolated and purified from the leaves of Canarium album, which significantly protects dopaminergic neurons from MPP(+)-induced degradation, and reveals potential neuroprotective mechanism of tyrosol.

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2-Cl-IB-MECA 50mg  | 99%

CSNpharm

2-Cl-IB-MECA is a highly selective A3 adenosine receptor agonist with Ki value of 0.33nM, displaying 2500- and 1400-fold selectivity over A1 and A2A receptors, respectively.

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2-Cl-IB-MECA 5mg  | 99%

CSNpharm

2-Cl-IB-MECA is a highly selective A3 adenosine receptor agonist with Ki value of 0.33nM, displaying 2500- and 1400-fold selectivity over A1 and A2A receptors, respectively.

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2-Cl-IB-MECA 2mg  | 99%

CSNpharm

2-Cl-IB-MECA is a highly selective A3 adenosine receptor agonist with Ki value of 0.33nM, displaying 2500- and 1400-fold selectivity over A1 and A2A receptors, respectively.

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2-Cl-IB-MECA 10mg  | 99%

CSNpharm

2-Cl-IB-MECA is a highly selective A3 adenosine receptor agonist with Ki value of 0.33nM, displaying 2500- and 1400-fold selectivity over A1 and A2A receptors, respectively.

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2-Cl-IB-MECA 100mg  | 99%

CSNpharm

2-Cl-IB-MECA is a highly selective A3 adenosine receptor agonist with Ki value of 0.33nM, displaying 2500- and 1400-fold selectivity over A1 and A2A receptors, respectively.

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2-Cl-IB-MECA 25mg  | 99%

CSNpharm

2-Cl-IB-MECA is a highly selective A3 adenosine receptor agonist with Ki value of 0.33nM, displaying 2500- and 1400-fold selectivity over A1 and A2A receptors, respectively.

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2-D08 10mg  | 98%

CSNpharm

2′,3′,4′-trihydroxyflavone interacts with amyloid β, showing an anti-aggregatory and neuroprotective effect.

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2-D08 25mg  | 98%

CSNpharm

2′,3′,4′-trihydroxyflavone interacts with amyloid β, showing an anti-aggregatory and neuroprotective effect.

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2-D08 100mg  | 98%

CSNpharm

2′,3′,4′-trihydroxyflavone interacts with amyloid β, showing an anti-aggregatory and neuroprotective effect.

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2-Hydroxy-6-methylbenzoic acid 5g  | 98%

CSNpharm

2-Hydroxy-6-Methylbenzoic Acid is a key structural moiety for many different antibiotic and anticancer agents, including chlorothricin, maduropeptin, neocarzinostatin, and terreic acid. It is a constituent of G. anandria, a well-known traditional Chinese medicinal herb, and also produced in various fungi, including P. patulum.

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2-Hydroxy-6-methylbenzoic acid 1g  | 98%

CSNpharm

2-Hydroxy-6-Methylbenzoic Acid is a key structural moiety for many different antibiotic and anticancer agents, including chlorothricin, maduropeptin, neocarzinostatin, and terreic acid. It is a constituent of G. anandria, a well-known traditional Chinese medicinal herb, and also produced in various fungi, including P. patulum.

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