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)
- GC4982010,11-dihydro-10,11-dihydroxy CarbamazepineCAS: 35079-97-1纯度: >95.00%
A metabolite of carbamazepine and oxcarbazepine
- GC50202SSR 180711 hydrochlorideCAS: 446031-79-4纯度: >99.50%
SSR 180711 hydrochloride 是一种具有口服活性、选择性和可逆的 α7 乙酰胆碱烟碱受体 (n-AChRs) 部分激动剂。
| 货号 | 产品名称 | CAS号 | 纯度 | 结构 |
|---|---|---|---|---|
| GC49820 | 10,11-dihydro-10,11-dihydroxy Carbamazepine | 35079-97-1 | >95.00% | |
A metabolite of carbamazepine and oxcarbazepine | ||||
| GC49866 | Desmethyl Carvedilol | 72956-44-6 | >90.00% | |
An active metabolite of carvedilol | ||||
| GC50058 | AMG 21629 | 939040-79-6 | - | |
Potent and selective TRPV1 antagonist | ||||
| GC50059 | Org 24598 | 372198-97-5 | - | |
Potent and selective inhibitor of the glial glycine transporter GlyT1b; active in vivo | ||||
| GC50064 | JTV 519 fumarate | 1883549-36-7 | >98.00% | |
Ryanodine receptor (RyR) inhibitor | ||||
| GC50068 | 8MDP | 29491-75-6 | - | |
Potent equilibrative nucleoside transporter (ENT) inhibitor | ||||
| GC50071 | NAV 26 | 1198160-14-3 | - | |
NAV 26 (compound 26) 是一种选择性电压门控钠通道 Nav1.7 阻滞剂，IC50 为 0.37 μM。 | ||||
| GC50088 | A 85380 dihydrochloride | 174740-86-4 | - | |
High affinity and selective α4β2 nAChR agonist | ||||
| GC50095 | QO 58 | 1259536-62-3 | - | |
QO 58 是 K(v)7 通道的有效调节剂。 | ||||
| GC50111 | CX 614 | 191744-13-5 | - | |
Positive allosteric modulator of AMPA receptors | ||||
| GC50115 | ASP 7663 | 1190217-35-6 | >99.00% | |
A TRPA1 agonist | ||||
| GC50126 | CC4 | 492-02-4 | - | |
High affinity and subtype-selective α6β2 and α4β2 nAChR partial agonist | ||||
| GC50127 | CLP 257 | 1181081-71-9 | - | |
A KCC2 cotransporter activator | ||||
| GC50147 | PK-THPP | 1332454-07-5 | - | |
An inhibitor of K 2P 9.1/TASK-3 | ||||
| GC50159 | TC AQP1 1 | 37710-81-9 | >98.00% | |
Aquaporin 1 (AQP1) channel blocker | ||||
| GC50163 | SR 13800 | 227321-12-2 | >99.00% | |
SR 13800 是一种有效的单羧酸转运蛋白 1 (MCT1) 抑制剂。 SR 13800 具有抗癌活性。 | ||||
| GC50167 | AAQ chloride | - | - | |
Photoswitchable Kv channel blocker | ||||
| GC50174 | QAQ dichloride | - | - | |
QAQ dichloride 是一种可光开关的电压门控 Nav 和 Kv 通道阻断剂，可阻断其反式（偶氮苯光电开关）的通道，但不阻断其顺式形式。 | ||||
| GC50179 | 5J 4 | 827001-82-1 | - | |
5J 4 是一种有效的 CRAC 抑制剂。 | ||||
| GC50188 | CIM 0216 | 1031496-06-6 | >99.50% | |
A TRPM3 channel activator | ||||
| GC50198 | Topiramate - d12 | 1279037-95-4 | - | |
An internal standard for the quantification of topiramate | ||||
| GC50200 | BX 430 | 688309-70-8 | >99.50% | |
A P2X 4 receptor antagonist | ||||
| GC50202 | SSR 180711 hydrochloride | 446031-79-4 | >99.50% | |
SSR 180711 hydrochloride 是一种具有口服活性、选择性和可逆的 α7 乙酰胆碱烟碱受体 (n-AChRs) 部分激动剂。 | ||||
| GC50207 | Lei-Dab 7 | 1061556-49-7 | >98.00% | |
Lei-Dab 7 是一种有效的选择性 SK2 (KCa2.2) 通道阻滞剂，Kd 为 3.8 nM。 | ||||