Membrane Transporter/Ion Channel
Membrane Transporter/Ion Channel(跨膜转运)
- AMPAR(58)
- ATPase(80)
- Calcium Channel(331)
- Cannabinoid Transporters(6)
- CFTR(45)
- Chloride Channels(13)
- GABA Receptor(239)
- Gardos Channel(1)
- Glucose Transporters(13)
- Glutamate (EAAT) Transporters(18)
- Glycine Receptors(2)
- GlyT(19)
- GTPase(32)
- Kv1.3(1)
- ICB(2)
- Lipophilic platinum complex(1)
- M2 ion Channel(1)
- MCT2(2)
- Monoamine transporter(18)
- Monocarboxylate Transporters(12)
- Multidrug Transporters(4)
- Na+/Ca2+ Exchanger(16)
- NKCC(7)
- NMDA Receptor(81)
- Nucleoside Transporters(4)
- Pannexin-1(2)
- P2X purinergic receptor(68)
- P-gp(11)
- Proton Pump(56)
- Potassium Channel(308)
- Sodium Channel(211)
- TRP Channel(165)
- TRPV1(10)
- URAT1(12)
- Other Channel Modulators(10)
- MCT(3)
- Kainate Receptors(12)
- Ionophore(3)
- sodium-hydrogen exchanger(3)
- Chloride Channel(27)
- CRAC Channel(13)
- EAAT2(6)
- HCN Channel(6)
- Na+/HCO3- Cotransporter(1)
- Na+/K+ ATPase(28)
- P-glycoprotein(49)
- iGluR(164)
- nAChR(103)
- VDAC(2)
- Aquaporins(1)
- Piezo Channels(1)
- GlyR(1)
- Ferroportin(1)
- Urea Transporter(1)
- Na+/H+ Exchanger (NHE)(1)
- NTPDase(1)
- EAAT(1)
- Piezo Channel(1)
- ASCT(2)
Membrane Transporter/Ion Channel 相关产品(2265)
- GC11109ATP disodium saltCAS: 987-65-5纯度: >98.00% / >99.00%
An essential energy substrate for cellular metabolism
- GC11210Vecuronium BromideCAS: 50700-72-6纯度: >98.00% / >99.50%
Vecuronium Bromide是一种非去极化神经肌肉阻断剂，特异性地作用于肌肉型乙酰胆碱受体，IC 50 为1-2nM。
- GC11216Ro 0437626CAS: 134362-79-1
Ro 0437626 是一种选择性嘌呤能 (P2X1) 受体拮抗剂 (IC50 = 3 μM)，但对 P2X2、P2X3 和 P2X2/3 受体的亲和力较低 (IC50 > 100 μM)。
- GC11259GYKI 47261 dihydrochlorideCAS: 220445-20-5
AMPA receptor antagonist, non-competitive and selective
- GC112672-HydroxysaclofenCAS: 117354-64-0
2-Hydroxysaclofen 是一种有效的 γ-amino-butyric-acid-B (GABAB) 受体拮抗剂。
- GC11271Oxybuprocaine HClCAS: 5987-82-6纯度: >99.00%
Oxybuprocaine HCl (Benoxinate hydrochloride) 可逆地阻断钠通道并防止疼痛的神经冲动在角膜、结膜和巩膜中传播。
| 货号 | 产品名称 | CAS号 | 纯度 | 结构 |
|---|---|---|---|---|
| GC11109 | ATP disodium salt | 987-65-5 | >98.00% / >99.00% | |
An essential energy substrate for cellular metabolism | ||||
| GC11124 | Lanicemine | 153322-05-5 | >95.00% | |
A low-trapping NMDA channel blocker | ||||
| GC11132 | Y-26763 | 127408-31-5 | >99.00% | |
An activator of K ATP channels | ||||
| GC11138 | (±)-HIP-A | 227619-64-9 | - | |
excitatory amino acid transporter (EAAT) blocker | ||||
| GC11143 | NS 11394 | 951650-22-9 | >99.50% | |
A subunit-selective positive allosteric modulator of the GABA A receptor | ||||
| GC11147 | Oleoyl Serotonin | 1002100-44-8 | - | |
TRPV1 antagonist | ||||
| GC11151 | SCH 28080 | 76081-98-6 | >99.00% | |
An inhibitor of H + /K + -ATPases | ||||
| GC11153 | CGP 35348 | 123690-79-9 | - | |
A brain-accessible GABA B receptor antagonist | ||||
| GC11156 | Ganaxolone | 38398-32-2 | >98.00% | |
A positive allosteric modulator of GABA A receptors | ||||
| GC11178 | A-7 hydrochloride | 79127-24-5 | - | |
A cell-permeable antagonist of calmodulin | ||||
| GC11185 | TCS 5861528 | 332117-28-9 | >99.00% | |
A TRPA1 channel blocker | ||||
| GC11200 | A23187 | 52665-69-7 | >98.00% / >98.50% | |
A23187自由酸是一种Ca2+离子载体。 | ||||
| GC11210 | Vecuronium Bromide | 50700-72-6 | >98.00% / >99.50% | |
Vecuronium Bromide是一种非去极化神经肌肉阻断剂，特异性地作用于肌肉型乙酰胆碱受体，IC 50 为1-2nM。 | ||||
| GC11213 | Trichlormethiazide | 133-67-5 | >99.00% | |
A thiazide diuretic | ||||
| GC11216 | Ro 0437626 | 134362-79-1 | - | |
Ro 0437626 是一种选择性嘌呤能 (P2X1) 受体拮抗剂 (IC50 = 3 μM)，但对 P2X2、P2X3 和 P2X2/3 受体的亲和力较低 (IC50 > 100 μM)。 | ||||
| GC11244 | pep2-AVKI | 1315378-69-8 | - | |
Inhibitor peptide that selectively disrupts binding of the GluR2 subunit(at the C-terminal PDZ site) to PICK1 | ||||
| GC11254 | Lithium carbonate | 554-13-2 | >98.00% / >99.00% | |
Na+/K+ ATPase pump inhibitor | ||||
| GC11259 | GYKI 47261 dihydrochloride | 220445-20-5 | - | |
AMPA receptor antagonist, non-competitive and selective | ||||
| GC11260 | W-9 hydrochloride | 69762-85-2 | - | |
calmodulin antagonist | ||||
| GC11267 | 2-Hydroxysaclofen | 117354-64-0 | - | |
2-Hydroxysaclofen 是一种有效的 γ-amino-butyric-acid-B (GABAB) 受体拮抗剂。 | ||||
| GC11271 | Oxybuprocaine HCl | 5987-82-6 | >99.00% | |
Oxybuprocaine HCl (Benoxinate hydrochloride) 可逆地阻断钠通道并防止疼痛的神经冲动在角膜、结膜和巩膜中传播。 | ||||
| GC11281 | N20C hydrochloride | 1177583-87-7 | - | |
NMDA receptor antagonist | ||||
| GC11284 | 6-(4-Methoxyphenyl)-3-pyridazinamine | 4776-87-8 | - | |
A GABA A receptor antagonist | ||||
| GC11286 | ACBC | 22264-50-2 | >98.00% | |
ACBC 是一种 NMDA 受体部分激动剂，作用于甘氨酸位点 NR1。 | ||||