Membrane Transporter/Ion Channel
Research Areas
- AMPAR(55)
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- ATPase(77)
- Calcium Channel(343)
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- Glycine Receptors(2)
- GlyT(19)
- GTPase(30)
- ICB(1)
- MCT2(2)
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- Nucleoside Transporters(5)
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- P2X purinergic receptor(69)
- P-gp(10)
- Proton Pump(58)
- Potassium Channel(324)
- Sodium Channel(216)
- TRP Channel(184)
- TRPV1(10)
- URAT1(14)
- Other Channel Modulators(10)
- MCT(3)
- Kainate Receptors(11)
- Ionophore(3)
- sodium-hydrogen exchanger(3)
- Chloride Channel(30)
- CRAC Channel(14)
- EAAT2(6)
- HCN Channel(9)
- Na+/HCO3- Cotransporter(1)
- Na+/K+ ATPase(30)
- P-glycoprotein(55)
- iGluR(171)
- nAChR(111)
- 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)(1)
- Sodium Phosphate Cotransporter(1)
Products Related to Membrane Transporter/Ion Channel(2353)
- GC819613,4,5-Trimethoxycinnamic acidCAS: 90-50-6Purity: >99.50%
3,4,5-Trimethoxycinnamic acid is a phenylpropanoid isolated from the roots of Polygala tenuifolia WILLD, with anti-stress effect, prolonging the sleeping time in animals [1] [2] . 3,4,5-Trimethoxycinnamic acid increases expression of GAD65 and γ-subunit of GABAA receptor, but shows no effect on the amounts of α-, β-subunits [2] .
- GC82077ABCA1 inducer 2CAS: 2451589-46-9Purity: >98.00%
ABCA1 inducer 2 is a non-lipotropic ABCA1 inducer.
- GC82112ADWX 1 TFAPurity: >98.00%
ADWX 1 TFA is a new peptide inhibitor that is potent and selective for Kv1.3 with an IC 50 value of 1.89 pM.
- GC82184Amlodipine-d 4 maleateCAS: 2714486-25-4
Amlodipine-d 4 (maleate) is the deuterium labeled Amlodipine maleate.
- GC82279AdimanebartCAS: 2966023-63-0Purity: >99.50%
ARGX-119 is a first-in-class humanized agonist monoclonal antibody specific for muscle-specific kinase ( MuSK ).
- 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%
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.
| Catalog No. | Product Name | CAS No. | Purity | Structure |
|---|---|---|---|---|
| GC81961 | 3,4,5-Trimethoxycinnamic acid | 90-50-6 | >99.50% | |
3,4,5-Trimethoxycinnamic acid is a phenylpropanoid isolated from the roots of Polygala tenuifolia WILLD, with anti-stress effect, prolonging the sleeping time in animals [1] [2] . 3,4,5-Trimethoxycinnamic acid increases expression of GAD65 and γ-subunit of GABAA receptor, but shows no effect on the amounts of α-, β-subunits [2] . | ||||
| GC82061 | 8-BuS-AMP | 344402-39-7 | >99.50% | |
8-BuS-AMP is a NTPDase1 inhibitor and a CD73/CD39 inhibitor, with an IC 50 of 35 μM and a K i value of 0.292 μM against human NTPDase1; its K i values against human CD73 and CD39 are 1.19 μM and 0.847 μM, respectively. | ||||
| GC82077 | ABCA1 inducer 2 | 2451589-46-9 | >98.00% | |
ABCA1 inducer 2 is a non-lipotropic ABCA1 inducer. | ||||
| GC82112 | ADWX 1 TFA | - | >98.00% | |
ADWX 1 TFA is a new peptide inhibitor that is potent and selective for Kv1.3 with an IC 50 value of 1.89 pM. | ||||
| GC82183 | Amlenetug | 2850367-41-6 | >99.50% | |
is an SNCA -targeting IgG1κ type human antibody, the recommed isotype control is Human IgG1 kappa, Isotype Control [1] . | ||||
| GC82184 | Amlodipine-d 4 maleate | 2714486-25-4 | - | |
Amlodipine-d 4 (maleate) is the deuterium labeled Amlodipine maleate. | ||||
| GC82195 | ANO1-IN-4 | 2098490-06-1 | >99.50% | |
ANO1-IN-4 (Compound 10bm) is a reversible inhibitor for calcium-activated chloride channel transmembrane protein 16A ( TMEM16A, also known as ANO1 ) with an IC 50 of 0.030 µM. | ||||
| GC82279 | Adimanebart | 2966023-63-0 | >99.50% | |
ARGX-119 is a first-in-class humanized agonist monoclonal antibody specific for muscle-specific kinase ( MuSK ). | ||||
| 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% | |
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% | |
NMDA antagonist | ||||
| GC10065 | (-)-Bicuculline methiodide | 40709-69-1 | >98% | |
GABAA receptor antagonist | ||||
| GC10085 | DQP 1105 | 380560-89-4 | >98% | |
DQP 1105 ist ein potenter nichtkompetitiver NMDA-Rezeptorantagonist. | ||||
| GC10094 | BL 1249 | 18200-13-0 | >98% | |
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% | |
NMDA receptor agonist | ||||