Membrane Transporter/Ion Channel
Research Areas
- AMPAR(55)
- Aquaporins(3)
- Piezo Channels(6)
- ATPase(79)
- Calcium Channel(354)
- Cannabinoid Transporters(6)
- CFTR(51)
- Chloride Channels(12)
- GABA Receptor(202)
- Glucose Transporters(17)
- Glutamate (EAAT) Transporters(18)
- Glycine Receptors(2)
- GlyT(19)
- GTPase(30)
- ICB(1)
- MCT2(2)
- Monoamine transporter(16)
- Monocarboxylate Transporters(14)
- Multidrug Transporters(4)
- Na+/Ca2+ Exchanger(16)
- NKCC(9)
- NMDA Receptor(77)
- Nucleoside Transporters(6)
- Pannexin-1(2)
- P2X purinergic receptor(70)
- P-gp(10)
- Proton Pump(59)
- Potassium Channel(335)
- Sodium Channel(224)
- TRP Channel(188)
- TRPV1(10)
- URAT1(14)
- Other Channel Modulators(10)
- MCT(3)
- Kainate Receptors(11)
- Ionophore(3)
- sodium-hydrogen exchanger(3)
- Chloride Channel(31)
- CRAC Channel(14)
- EAAT2(6)
- HCN Channel(10)
- Na+/HCO3- Cotransporter(1)
- Na+/K+ ATPase(31)
- P-glycoprotein(60)
- iGluR(179)
- nAChR(119)
- VDAC(3)
- GlyR(1)
- Ferroportin(4)
- Urea Transporter(1)
- Na+/H+ Exchanger (NHE)(2)
- NTPDase(4)
- EAAT(5)
- ASCT(3)
- Apical Sodium-Dependent Bile Acid Transporter(1)
- Sec61(2)
- ATP-binding cassette (ABC) transporters(5)
- SLC39 (Zinc Transporter)(2)
- Sodium Phosphate Cotransporter(1)
Products Related to Membrane Transporter/Ion Channel(2422)
- GC83750Octopamine-d 3CAS: 111988-19-3Purity: >99.50%
Octopamine -d3 ((±)-p-Octopamine-d3) is the deuterated-labeled Octopamine.
- GC83757Oleic acid- 13 C-1CAS: 2483735-58-4Purity: >99.50%
Oleic acid - 13 C-1 is the 13 C labeled Oleic acid.
- GC83781Oxybutynin-d 11 chlorideCAS: 1185151-95-4Purity: >97.00%
Oxybutynin-d 11 (chloride) is the deuterium labeled Oxybutynin chloride.
- GA10750L-Glutamic acidCAS: 56-86-0Purity: >99.00%
L-Glutamic acid is the main excitatory neurotransmitter in the mammalian central nervous system (CNS). L-Glutamic acid has two major types of receptors: ionotropic (NMDA-, AMPA-, and kainate-selective iGluRs) and metabotropic glutamate receptors. L-Glutamic acid induces excitotoxicity by activating the postsynaptic N-methyl-D-aspartate receptors, leading to neurodegenerative diseases.
- GA20775Anxiety PeptideCAS: 95237-86-8Purity: >98.00%
Anxiety Peptide, also known as Octadecaneuropeptide (ODN), is produced by trypsin digestion of diazepam binding inhibitor (DBI).
- GA22579H-Ile-Trp-OHCAS: 13589-06-5Purity: >98.00%
H-Ile-Trp-OH (H-Ile-Trp-OH) ist ein oral aktiver α7 nAChR negativer VerÄnderungsmodulator (NAM) ohne offensichtliche Nebenwirkungen.
- GA24016ω-Conotoxin MVIIACAS: 107452-89-1Purity: >98.00%
ω-Conotoxin MVIIA (SNX-111), ein Peptid, ist ein wirksamer und selektiver Blocker des N-Typ-Calciumkanal-Antagonisten.
- GC10101SR 95531 hydrobromideCAS: 104104-50-9Purity: >97.00%
SR 95531 hydrobromide (Gabazine) ist ein selektiver Antagonist an den GABA-Bindungsstäten der GABAA-Rezeptoren.
- GC101198-Bromo-cGMP, sodium saltCAS: 51116-01-9Purity: >98.00%
8-Bromo-cGMP, sodium salt ist ein zellgängiges cGMP-Analogon, das die PKG-Aktivierung induziert.
| Catalog No. | Product Name | CAS No. | Purity | Structure |
|---|---|---|---|---|
| GC83733 | NSC73306 | 79560-74-0 | >98.50% | |
NSC73306, a thiosemicarbazone, is a cell penetrant, cytotoxic agent that exhibits greater toxicity against cells expressing functional P-gp ( P-glycoprotein ) than against other cells [1] . | ||||
| GC83750 | Octopamine-d 3 | 111988-19-3 | >99.50% | |
Octopamine -d3 ((±)-p-Octopamine-d3) is the deuterated-labeled Octopamine. | ||||
| GC83757 | Oleic acid- 13 C-1 | 2483735-58-4 | >99.50% | |
Oleic acid - 13 C-1 is the 13 C labeled Oleic acid. | ||||
| GC83766 | Opakalim | 2376397-93-0 | >99.50% | |
Opakalim (BHV-7000) is a selective Kv7.2/7.3 potassium channels activator with an EC 50 of 0.6 μM. | ||||
| GC83781 | Oxybutynin-d 11 chloride | 1185151-95-4 | >97.00% | |
Oxybutynin-d 11 (chloride) is the deuterium labeled Oxybutynin chloride. | ||||
| GA10299 | H-Phe-OH | 63-91-2 | >99.00% | |
| GA10750 | L-Glutamic acid | 56-86-0 | >99.00% | |
L-Glutamic acid is the main excitatory neurotransmitter in the mammalian central nervous system (CNS). L-Glutamic acid has two major types of receptors: ionotropic (NMDA-, AMPA-, and kainate-selective iGluRs) and metabotropic glutamate receptors. L-Glutamic acid induces excitotoxicity by activating the postsynaptic N-methyl-D-aspartate receptors, leading to neurodegenerative diseases. | ||||
| GA10922 | H-Gly-OH | 56-40-6 | >99.50% | |
| GA11306 | H-D-Ser-OH | 312-84-5 | >99.00% | |
An NMDA co-agonist | ||||
| GA11338 | H-D-Asp-OH | 1783-96-6 | >99.00% | |
An amino acid and a precursor in NMDA biosynthesis | ||||
| GA20418 | 4-Hydroxy-hippuric acid | 2482-25-9 | >98.00% | |
Polyphenol metabolite. | ||||
| GA20775 | Anxiety Peptide | 95237-86-8 | >98.00% | |
Anxiety Peptide, also known as Octadecaneuropeptide (ODN), is produced by trypsin digestion of diazepam binding inhibitor (DBI). | ||||
| GA22579 | H-Ile-Trp-OH | 13589-06-5 | >98.00% | |
H-Ile-Trp-OH (H-Ile-Trp-OH) ist ein oral aktiver α7 nAChR negativer VerÄnderungsmodulator (NAM) ohne offensichtliche Nebenwirkungen. | ||||
| GA24016 | ω-Conotoxin MVIIA | 107452-89-1 | >98.00% | |
ω-Conotoxin MVIIA (SNX-111), ein Peptid, ist ein wirksamer und selektiver Blocker des N-Typ-Calciumkanal-Antagonisten. | ||||
| GC10038 | Vernakalant Hydrochloride | 748810-28-8 | >99.00% | |
| GC10043 | D-CPP-ene | 117414-74-1 | >98.00% | |
NMDA antagonist | ||||
| GC10065 | (-)-Bicuculline methiodide | 40709-69-1 | >98.00% | |
GABAA receptor antagonist | ||||
| GC10085 | DQP 1105 | 380560-89-4 | >98.00% | |
DQP 1105 ist ein potenter nichtkompetitiver NMDA-Rezeptorantagonist. | ||||
| GC10094 | BL 1249 | 18200-13-0 | >98.00% | |
BL 1249 ist ein nichtsteroidales Antirheumatikum (NSAID) und ein Kaliumkanalaktivator. | ||||
| GC10101 | SR 95531 hydrobromide | 104104-50-9 | >97.00% | |
SR 95531 hydrobromide (Gabazine) ist ein selektiver Antagonist an den GABA-Bindungsstäten der GABAA-Rezeptoren. | ||||
| GC10114 | Homoquinolinic acid | 490-75-5 | >98.00% | |
NMDA receptor agonist | ||||
| GC10119 | 8-Bromo-cGMP, sodium salt | 51116-01-9 | >98.00% | |
8-Bromo-cGMP, sodium salt ist ein zellgängiges cGMP-Analogon, das die PKG-Aktivierung induziert. | ||||
| GC10122 | CGP 37849 | 127910-31-0 | >99.00% | |
CGP 37849 ist ein potenter, kompetitiver und oral aktiver N-Methyl-D-Aspartat (NMDA)-Rezeptorantagonist. | ||||
| GC10152 | RO-3 | 1026582-88-6 | >98.00% | |
RO-3 ist ein potenter, ZNS-penetranter und oral aktiver P2X3- und P2X2/3-Antagonist mit pIC50-Werten von 5,9 und 7,0 fÜr humane homomultimere P2X3- bzw. heteromultimere P2X2/3-Rezeptoren. | ||||