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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V-9302 HCl 100mg  | ≥99%

CSNpharm

V-9302 HCl is a competitive and selective antagonist of transmembrane glutamine flux that selectively and potently targets the amino acid transporter ASCT2 with IC50 of 9.6 μM.

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V-9302 HCl 10mg  | ≥99%

CSNpharm

V-9302 HCl is a competitive and selective antagonist of transmembrane glutamine flux that selectively and potently targets the amino acid transporter ASCT2 with IC50 of 9.6 μM.

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V-9302 HCl 25mg  | ≥99%

CSNpharm

V-9302 HCl is a competitive and selective antagonist of transmembrane glutamine flux that selectively and potently targets the amino acid transporter ASCT2 with IC50 of 9.6 μM.

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V-9302 HCl 50mg  | ≥99%

CSNpharm

V-9302 HCl is a competitive and selective antagonist of transmembrane glutamine flux that selectively and potently targets the amino acid transporter ASCT2 with IC50 of 9.6 μM.

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Vacuolin-1 5mg  | ≥98%

CSNpharm

Vacuolin-1 is cell-permeable inhibitor of lysosomal exocytosis and can block the Ca2+-dependent exocytosis of lysosomes and prevents the release of lysosomal content without affecting the process of resealing. Vacuolin-1 is also PIKfyve inhibitor that inhibits late-stage autophagy by impairing lysosomal maturation.

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Vacuolin-1 10mg  | ≥98%

CSNpharm

Vacuolin-1 is cell-permeable inhibitor of lysosomal exocytosis and can block the Ca2+-dependent exocytosis of lysosomes and prevents the release of lysosomal content without affecting the process of resealing. Vacuolin-1 is also PIKfyve inhibitor that inhibits late-stage autophagy by impairing lysosomal maturation.

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VAL-083 25mg  | ≥98%

CSNpharm

VAL-083 is a bi-functional alkylating agent and inhibits U251 and SF188 cell growth in monolayer better than TMZ and caused apoptosis.

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VAL-083 10mg  | ≥98%

CSNpharm

VAL-083 is a bi-functional alkylating agent and inhibits U251 and SF188 cell growth in monolayer better than TMZ and caused apoptosis.

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VAL-083 50mg  | ≥98%

CSNpharm

VAL-083 is a bi-functional alkylating agent and inhibits U251 and SF188 cell growth in monolayer better than TMZ and caused apoptosis.

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VAL-083 5mg  | ≥98%

CSNpharm

VAL-083 is a bi-functional alkylating agent and inhibits U251 and SF188 cell growth in monolayer better than TMZ and caused apoptosis.

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VAL-083 1mg  | ≥98%

CSNpharm

VAL-083 is a bi-functional alkylating agent and inhibits U251 and SF188 cell growth in monolayer better than TMZ and caused apoptosis.

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Val-Cit-PAB-OH 50mg  | ≥99%

CSNpharm

Val-Cit-PAB-OH is a linker for ADC through cleaveage by catepsin B only present in lysosome at Val-Cit site, thus making ACD payload be released only in the cell.

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Val-Cit-PAB-OH 5mg  | ≥99%

CSNpharm

Val-Cit-PAB-OH is a linker for ADC through cleaveage by catepsin B only present in lysosome at Val-Cit site, thus making ACD payload be released only in the cell.

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Val-Cit-PAB-OH 100mg  | ≥99%

CSNpharm

Val-Cit-PAB-OH is a linker for ADC through cleaveage by catepsin B only present in lysosome at Val-Cit site, thus making ACD payload be released only in the cell.

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Val-Cit-PAB-OH 10mg  | ≥99%

CSNpharm

Val-Cit-PAB-OH is a linker for ADC through cleaveage by catepsin B only present in lysosome at Val-Cit site, thus making ACD payload be released only in the cell.

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Valacyclovir HCl 50mg  | ≥98%

CSNpharm

Valacyclovir HCl is a Herpes Simplex Virus and Herpes Zoster Virus nucleoside analog DNA polymerase inhibitor as it is a synthetic purine nucleoside analogue.

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Valacyclovir HCl 10mg  | ≥98%

CSNpharm

Valacyclovir HCl is a Herpes Simplex Virus and Herpes Zoster Virus nucleoside analog DNA polymerase inhibitor as it is a synthetic purine nucleoside analogue.

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Valganciclovir HCl 5mg  | ≥98%

CSNpharm

Valganciclovir HCl is the L-valyl ester of ganciclovir, is a prodrug for ganciclovir with antiviral activity used to treat cytomegalovirus infections.

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Valganciclovir HCl 100mg  | ≥98%

CSNpharm

Valganciclovir HCl is the L-valyl ester of ganciclovir, is a prodrug for ganciclovir with antiviral activity used to treat cytomegalovirus infections.

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Valganciclovir HCl 50mg  | ≥98%

CSNpharm

Valganciclovir HCl is the L-valyl ester of ganciclovir, is a prodrug for ganciclovir with antiviral activity used to treat cytomegalovirus infections.

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Valganciclovir HCl 10mg  | ≥98%

CSNpharm

Valganciclovir HCl is the L-valyl ester of ganciclovir, is a prodrug for ganciclovir with antiviral activity used to treat cytomegalovirus infections.

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Valiolamine 100mg  | ≥97%

CSNpharm

Valiolamine, an aminocyclitol has been isolated from the fermentation broth of Streptomyces hygroscopicus subsp. Valiolamine has potent alpha-glucosidase inhibitory activity against porcine intestinal sucrase, maltase and isomaltase.

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Valnemulin HCl 100mg  | ≥99%

CSNpharm

Valnemulin HCl is a pleuromutilin antibiotic used to treat swine dysentery, ileitis, colitis and pneumonia, and prevent intestinal infections of swine.

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Valnemulin HCl 50mg  | ≥99%

CSNpharm

Valnemulin HCl is a pleuromutilin antibiotic used to treat swine dysentery, ileitis, colitis and pneumonia, and prevent intestinal infections of swine.

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Valnemulin HCl 10mg  | ≥99%

CSNpharm

Valnemulin HCl is a pleuromutilin antibiotic used to treat swine dysentery, ileitis, colitis and pneumonia, and prevent intestinal infections of swine.

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Valproic Acid 1g  | ≥99%

CSNpharm

Valproic acid is a histone deacetylase (HDAC) inhibitor with IC50 of 10 μM in Hela cell with anticancer effect. It can be used in the treatment of epilepsy and bipolar disorder.

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Valproic Acid 5g  | ≥99%

CSNpharm

Valproic acid is a histone deacetylase (HDAC) inhibitor with IC50 of 10 μM in Hela cell with anticancer effect. It can be used in the treatment of epilepsy and bipolar disorder.

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Valpromide 50mg  | ≥98%

CSNpharm

Valpromide is a carboxamide derivative of valproic acid with anticonvulsant properties and used in the treatment of epilepsy and some affective disorders. It is also a potent inhibitor of liver microsomal epoxide hydrolase.

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Valpromide 100mg  | ≥98%

CSNpharm

Valpromide is a carboxamide derivative of valproic acid with anticonvulsant properties and used in the treatment of epilepsy and some affective disorders. It is also a potent inhibitor of liver microsomal epoxide hydrolase.

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Valpromide 10mg  | ≥98%

CSNpharm

Valpromide is a carboxamide derivative of valproic acid with anticonvulsant properties and used in the treatment of epilepsy and some affective disorders. It is also a potent inhibitor of liver microsomal epoxide hydrolase.

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Valsartan 100mg  | ≥99%

CSNpharm

Valsartan is a selective angiotensin II AT1 receptor antagonist with elimination half-life‎ of ‎6 hours.

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Valsartan 10mg  | ≥99%

CSNpharm

Valsartan is a selective angiotensin II AT1 receptor antagonist with elimination half-life‎ of ‎6 hours.

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Valsartan 50mg  | ≥99%

CSNpharm

Valsartan is a selective angiotensin II AT1 receptor antagonist with elimination half-life‎ of ‎6 hours.

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