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Membrane Transporter Proteins

Membrane transport proteins, also known as membrane transport proteins, selectively transport small molecules across the plasma membrane that are not freely diffusing. Membrane transport proteins are membrane integral proteins, or large transmembrane molecular complexes, that function to participate in passive or active transport.
Cat. No. Product name
BP16081 NSC 139486
M-084 hydrochloride is a blocker of TRPC4/5 channel, with antidepressant and anxiolytic effects.
BP16082 M8-B Hydrochloride
M8-B Hydrochloride is a selective transient receptor potential melastatin-8 (TRPM8) channel antagonist.
BP16083 Mavatrep
Mavatrep is a selective antagonist of TRPV1 with Ki of 6.5 nM and can be used for studies about inflammatory pain.
BP16084 MDL-29951
MDL-29951 is a novel glycine antagonist of NMDA receptor activation.
BP16085 Mebeverine hydrochloride
Mebeverine hydrochloride, a β-phenylethylamine derivative, is a potent α1 repector inhibitor, relaxing the muscles in and around the gut.
BP16086 Menthol
Menthyl alcohol is an organic compound made synthetically or obtained from peppermint or mint oils with flavoring and local anesthetic properties.
BP16087 Mephenesin
Mephenesin is a centrally acting muscle relaxant with a short duration of action.
BP16088 Mepivacaine hydrochloride
Mepivacaine Hydrochloride is the hydrochloride salt form of mepivacaine, an amide derivative with local anesthetic properties.
BP16089 MIDD0301
MIDD0301 is a potent positive allosteric α5β3γ selective GABAA receptor (GABAAR) ligand with EC50 of 17 nM.
BP16090 Mirogabalin
Mirogabalin is a calcium channel blocker with analgesic effects.
BP16091 ML133 hydrochloride
ML133 HCl is a selective potassium channel inhibitor for Kir2.1 with IC50 of 1.8 μM (pH 7.4) and 290 nM (pH 8.5), has no effect on Kir1.1 and weak activity for Kir4.1 and Kir7.1.
BP16092 ML204
ML204 is a novel potent antagonist that selectively modulates native TRPC4/C5 ion channels.
BP16093 ML402
ML402 is an activator of TREK-1 and TREK-2 with EC50s of 13.7 μM and 5.9 μM.
BP16094 Myomodulin acetate(110570-93-9 free base)
Myomodulin acetate is present in two identified aplysia neurons that contain myomodulin A the ARC motor neuron B16 and the abdominal neuron L10.
BP16095 N4-benzyl-N2-methylquinazoline-2,4-diamine hydrochloride
N4-benzyl-N2-methylquinazoline-2,4-diamine hydrochloride is an inhibitor of TRPC4.
BP16096 Naspm trihydrochloride
Naspm trihydrochloride is a synthetic analogue of Joro spider toxin and is an antagonist of calcium permeable AMPA (CP-AMPA) receptors.
BP16097 NHE3-IN-1
NHE3-IN-1 is a inhibitor of Na+/H+-exchanger 3 (NHE-3).
BP16098 Nilvadipine
Nilvadipine, a calcium channel blocker (CCB), is utilized for treatment of hypertension.
BP16099 N-Me-aminopyrimidinone9
N-Me-aminopyrimidinone9 is a sodium channel antagonist
BP16100 NO-711ME
NO-711ME is a prodrug of NO-711. It also is a potent and selective GABA uptake inhibitor.
NSC 139486
BP16081
M-084 hydrochloride is a blocker of TRPC4/5 channel, with antidepressant and anxiolytic effects.
M8-B Hydrochloride
BP16082
M8-B Hydrochloride is a selective transient receptor potential melastatin-8 (TRPM8) channel antagonist.
Mavatrep
BP16083
Mavatrep is a selective antagonist of TRPV1 with Ki of 6.5 nM and can be used for studies about inflammatory pain.
MDL-29951
BP16084
MDL-29951 is a novel glycine antagonist of NMDA receptor activation.
Mebeverine hydrochloride
BP16085
Mebeverine hydrochloride, a β-phenylethylamine derivative, is a potent α1 repector inhibitor, relaxing the muscles in and around the gut.
Menthol
BP16086
Menthyl alcohol is an organic compound made synthetically or obtained from peppermint or mint oils with flavoring and local anesthetic properties.
Mephenesin
BP16087
Mephenesin is a centrally acting muscle relaxant with a short duration of action.
Mepivacaine hydrochloride
BP16088
Mepivacaine Hydrochloride is the hydrochloride salt form of mepivacaine, an amide derivative with local anesthetic properties.
MIDD0301
BP16089
MIDD0301 is a potent positive allosteric α5β3γ selective GABAA receptor (GABAAR) ligand with EC50 of 17 nM.
Mirogabalin
BP16090
Mirogabalin is a calcium channel blocker with analgesic effects.
ML133 hydrochloride
BP16091
ML133 HCl is a selective potassium channel inhibitor for Kir2.1 with IC50 of 1.8 μM (pH 7.4) and 290 nM (pH 8.5), has no effect on Kir1.1 and weak activity for Kir4.1 and Kir7.1.
ML204
BP16092
ML204 is a novel potent antagonist that selectively modulates native TRPC4/C5 ion channels.
ML402
BP16093
ML402 is an activator of TREK-1 and TREK-2 with EC50s of 13.7 μM and 5.9 μM.
Myomodulin acetate(110570-93-9 free base)
BP16094
Myomodulin acetate is present in two identified aplysia neurons that contain myomodulin A the ARC motor neuron B16 and the abdominal neuron L10.
N4-benzyl-N2-methylquinazoline-2,4-diamine hydrochloride
BP16095
N4-benzyl-N2-methylquinazoline-2,4-diamine hydrochloride is an inhibitor of TRPC4.
Naspm trihydrochloride
BP16096
Naspm trihydrochloride is a synthetic analogue of Joro spider toxin and is an antagonist of calcium permeable AMPA (CP-AMPA) receptors.
NHE3-IN-1
BP16097
NHE3-IN-1 is a inhibitor of Na+/H+-exchanger 3 (NHE-3).
Nilvadipine
BP16098
Nilvadipine, a calcium channel blocker (CCB), is utilized for treatment of hypertension.
N-Me-aminopyrimidinone9
BP16099
N-Me-aminopyrimidinone9 is a sodium channel antagonist
NO-711ME
BP16100
NO-711ME is a prodrug of NO-711. It also is a potent and selective GABA uptake inhibitor.