常州市存仁生物工程有限公司

GW791343 (HCL)

GW791343 (HCL)

Theoretical analysis:GW791343 (HCL)
Molecular Formula: C20H24F2N4O.3HCl
CAS No.: 1019779-04-4 
Availability and price:GW7...
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Rivastigmine tartrate

Rivastigmine tartrate

Theoretical analysis:Rivastigmine tartrate
MF: C18H28N2O8 
FW Weight: 400.42
CAS No.: 129101-54-8 
Availabili...
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Tropisetron

Tropisetron

Description of:Tropisetron
Tropisetron is a selective 5-HT3 receptor antagonist and α7-nicotinic receptor agonist with an IC50 of 70.1 &p...
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Solifenacin Succinate(YM905)

Solifenacin Succinate(YM905)

Description of:Solifenacin Succinate(YM905)
Solifenacin Succinate(YM905; Vesicare) is a muscarinic receptor antagonist.Solifenacin succinate (Y...
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A-740003

A-740003

Description of:A-740003
A-740003 is potent, selective and competitive P2X7 receptor antagonist (IC50 values are 18 and 40 nM for rat and human ...
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Tolterodine tartrate (Detrol LA)

Tolterodine tartrate (Detrol LA)

Description of:Tolterodine tartrate (Detrol LA)
Tolterodine tartrate (Detrol LA) is a tartrate salt of tolterodine that is a competitive muscar...
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PF3845

PF3845

Description of:PF3845
PF-3845 (PF 3845) is a selective fatty acid amide hydrolase (FAAH) inhibitor (Ki = 0.23 μM). PF-3845 (PF 3845) reduces...
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URB597

URB597

Description of:URB597
URB-597 is a relatively selective fatty acid amide hydrolase (FAAH) inhibitor with IC50 of 4.6 and 0.5 nM in brain membra...
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MK-0974(Telcagepant)

MK-0974(Telcagepant)

Description of:MK-0974(Telcagepant)
MK-0974 is a highly potent, selective, and orally bioavailable CGRP receptor antagonist, which may be valua...
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OSU-03012

OSU-03012

Description of:OSU-03012
OSU-03012 inhibited cell proliferation more effectively in both VS (IC50=3.1 μM ) and HMS-97 (IC50=2.6 μM )cells...
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