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Enalaprilat is the first dicarboxylate-containing ACE inhibitor with IC50 of 1.94 nM, which is the active metabolite of enalapril.
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CSNpharm
Enalaprilat is the first dicarboxylate-containing ACE inhibitor with IC50 of 1.94 nM, which is the active metabolite of enalapril.
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CSNpharm
Enalaprilat is the first dicarboxylate-containing ACE inhibitor with IC50 of 1.94 nM, which is the active metabolite of enalapril.
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CSNpharm
CSNpharm
CSNpharm
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CSNpharm
Enoxacin Sesquihydrate is a broad-spectrum fluoroquinolone antibacterial agent used in the treatment of urinary tract infections and gonorrhea, working by inhibiting bacterial DNA gyrase and topoisomerase IV.
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Enoxacin Sesquihydrate is a broad-spectrum fluoroquinolone antibacterial agent used in the treatment of urinary tract infections and gonorrhea, working by inhibiting bacterial DNA gyrase and topoisomerase IV.
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CSNpharm
Entacapone is a specific, potent and peripherally acting catechol-O-methyltransferase (COMT) inhibitor with IC50 of 151 nM for PD treatment.
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CSNpharm
Entacapone is a specific, potent and peripherally acting catechol-O-methyltransferase (COMT) inhibitor with IC50 of 151 nM for PD treatment.
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CSNpharm
Entacapone is a specific, potent and peripherally acting catechol-O-methyltransferase (COMT) inhibitor with IC50 of 151 nM for PD treatment.
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CSNpharm
Entacapone is a specific, potent and peripherally acting catechol-O-methyltransferase (COMT) inhibitor with IC50 of 151 nM for PD treatment.
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CSNpharm
Entecavir is a guanosine analogue that inhibits reverse transcription, DNA replication and transcription in the viral replication process, and is a potent, orally-active and selective inhibitor of HBV with an EC50 of 3.75 nM in HepG2 cell.
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Entecavir is a guanosine analogue that inhibits reverse transcription, DNA replication and transcription in the viral replication process, and is a potent, orally-active and selective inhibitor of HBV with an EC50 of 3.75 nM in HepG2 cell.
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CSNpharm
Entecavir is a guanosine analogue that inhibits reverse transcription, DNA replication and transcription in the viral replication process, and is a potent, orally-active and selective inhibitor of HBV with an EC50 of 3.75 nM in HepG2 cell.
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CSNpharm
Entecavir, an analogue of guanosine, is reverse transcription inhibitor of HBV with EC50 of 3.75 nM in HepG2 cell.
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CSNpharm
Entecavir, an analogue of guanosine, is reverse transcription inhibitor of HBV with EC50 of 3.75 nM in HepG2 cell.
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CSNpharm
Entecavir, an analogue of guanosine, is reverse transcription inhibitor of HBV with EC50 of 3.75 nM in HepG2 cell.
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CSNpharm
Entecavir, an analogue of guanosine, is reverse transcription inhibitor of HBV with EC50 of 3.75 nM in HepG2 cell.
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CSNpharm
CSNpharm
Enterodiol is a mammalian lignan formed by the action of intestinal bacteria from plant lignan precursors present in the diet and is potential anti-cancer effect.
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Enzastaurin is a potent PKCβ selective inhibitor with IC50 of 6 nM, 6- to 20-fold selectivity against PKCα, PKCγ and PKCε.
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CSNpharm
Enzastaurin is a potent PKCβ selective inhibitor with IC50 of 6 nM, 6- to 20-fold selectivity against PKCα, PKCγ and PKCε.
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CSNpharm
Enzastaurin is a potent PKCβ selective inhibitor with IC50 of 6 nM, 6- to 20-fold selectivity against PKCα, PKCγ and PKCε.
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CSNpharm
Enzastaurin is a potent PKCβ selective inhibitor with IC50 of 6 nM, 6- to 20-fold selectivity against PKCα, PKCγ and PKCε.
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CSNpharm
Enzastaurin is a potent PKCβ selective inhibitor with IC50 of 6 nM, 6- to 20-fold selectivity against PKCα, PKCγ and PKCε.
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CSNpharm
CSNpharm
Epalrestat is an aldose reductase inhibitor with IC50 of 72 nM, and used for the treatment of diabetic neuropathy.
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Epalrestat is an aldose reductase inhibitor with IC50 of 72 nM, and used for the treatment of diabetic neuropathy.
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CSNpharm
Epalrestat is an aldose reductase inhibitor with IC50 of 72 nM, and used for the treatment of diabetic neuropathy.
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Eperisone HCl has very low bioavailability after oral administration in rats and extensively high oral clearance in humans. It undergoes extensive first-pass metabolism after oral administration in rats and humans because absorption of the drug is very high. The bioavailabilities in the intestine were 0.176 and 0.0879 at administration rates of 100 and 25 mg/h/kg, […]
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CSNpharm
Eperisone HCl has very low bioavailability after oral administration in rats and extensively high oral clearance in humans. It undergoes extensive first-pass metabolism after oral administration in rats and humans because absorption of the drug is very high. The bioavailabilities in the intestine were 0.176 and 0.0879 at administration rates of 100 and 25 mg/h/kg, […]
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