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)
- GC14484(-)-Xestospongin CCAS: 88903-69-9纯度: >90.00%
A membrane-permeable antagonist of the inositol-1,4,5-triphosphate receptor
- GC14487RanolazineCAS: 95635-55-5纯度: >99.00%
Ranolazine (CVT 303) 是一种抗心绞痛药物,通过抑制内向钠电流(INa 和 IKr,IC50 值分别为 6 μM 和 12 μM)的晚期而不影响心率或血压 (BP) 来实现其效果。
- GC14533Kynurenic acidCAS: 492-27-3纯度: >99.00% / >98.00%
Kynurenic acid 是一种内源性色氨酸代谢物,是一种针对 NMDA、谷氨酸、α7 烟碱乙酰胆碱受体的广谱拮抗剂。
- GC14641SKF 96365 hydrochlorideCAS: 130495-35-1纯度: >99.50%
SKF 96365 hydrochloride是一种具有口服活性的TRP通道/钙库操控性钙内流(SOCE)抑制剂,可阻断TRPC通道、电压门控钙通道及多种钾通道,并抑制STIM1介导的钙信号。
| 货号 | 产品名称 | CAS号 | 纯度 | 结构 |
|---|---|---|---|---|
| GC14410 | (±)-Epibatidine | 148152-66-3 | - | |
An agonist of α4β2 subunit-containing nAChRs | ||||
| GC14414 | CIQ | 486427-17-2 | >98.00% | |
A subunit-selective NMDA receptor potentiator | ||||
| GC14442 | TCS 46b | 302799-86-6 | - | |
NR1A/NR2B NMDA receptor antagonist,orally active | ||||
| GC14453 | cis-ACBD | 73550-55-7 | - | |
An NMDA receptor agonist | ||||
| GC14470 | Arcaine sulfate | 14923-17-2 | >95.00% | |
An NMDA receptor antagonist | ||||
| GC14477 | CI 966 hydrochloride | 110283-66-4 | >99.00% | |
GABA transporter GAT-1 inhibitor | ||||
| GC14480 | CNQX disodium salt | 479347-85-8 | >98.00% | |
A non-NMDA glutamate receptor antagonist | ||||
| GC14481 | A 887826 | 1266212-81-0 | - | |
A 887826 是一种有效的、选择性的、口服生物利用度和电压依赖性 Na(v)1.8 钠通道阻滞剂,IC50 为 11 nM。 | ||||
| GC14484 | (-)-Xestospongin C | 88903-69-9 | >90.00% | |
A membrane-permeable antagonist of the inositol-1,4,5-triphosphate receptor | ||||
| GC14487 | Ranolazine | 95635-55-5 | >99.00% | |
Ranolazine (CVT 303) 是一种抗心绞痛药物,通过抑制内向钠电流(INa 和 IKr,IC50 值分别为 6 μM 和 12 μM)的晚期而不影响心率或血压 (BP) 来实现其效果。 | ||||
| GC14492 | PF 4778574 | 1219633-99-4 | - | |
PF 4778574 是 AMPA 受体的正向变构调节剂,在不同细胞中的 EC50 为 45 至 919 nM。 | ||||
| GC14495 | CX 546 | 215923-54-9 | >99.00% | |
CX 546是一种强效的3-羟基-5-甲基-4-异唑丙酸(AMPA)受体激活剂,EC 50 值为93.2μM。 | ||||
| GC14515 | Azimilide | 149908-53-2 | - | |
A class III antiarrhythmic agent | ||||
| GC14533 | Kynurenic acid | 492-27-3 | >99.00% / >98.00% | |
Kynurenic acid 是一种内源性色氨酸代谢物,是一种针对 NMDA、谷氨酸、α7 烟碱乙酰胆碱受体的广谱拮抗剂。 | ||||
| GC14537 | AMTB hydrochloride | 926023-82-7 | - | |
A TRPM8 antagonist | ||||
| GC14547 | Quinolinic acid | 89-00-9 | >99.00% | |
An excitotoxic agonist at NMDA receptors | ||||
| GC14563 | Ketanserin | 74050-98-9 | >99.00% / >97.00% | |
A potent 5-HT 2 receptor antagonist | ||||
| GC14579 | NPEC-caged-(S)-AMPA | 1257323-84-4 | - | |
AMPA receptor agonist | ||||
| GC14598 | 5,7-Dichlorokynurenic acid sodium salt | 1184986-70-6 | - | |
An NMDA receptor antagonist | ||||
| GC14635 | RQ-00203078 | 1254205-52-1 | >99.00% | |
A TRPM8 antagonist | ||||
| GC14641 | SKF 96365 hydrochloride | 130495-35-1 | >99.50% | |
SKF 96365 hydrochloride是一种具有口服活性的TRP通道/钙库操控性钙内流(SOCE)抑制剂,可阻断TRPC通道、电压门控钙通道及多种钾通道,并抑制STIM1介导的钙信号。 | ||||
| GC14642 | 7ACC2 | 1472624-85-3 | >98.00% | |
An MCT1 and MPC inhibitor | ||||
| GC14646 | RuBi-4AP | 851956-02-0 | - | |
voltage-dependent K+ channel blocker | ||||
| GC14649 | Pyr3 | 1160514-60-2 | >99.50% | |
Pyr3是瞬时受体电位经典通道3(TRPC3)的一种强效、选择性抑制剂,对TRPC3介导的钙离子内流的IC 50 为700nM。 | ||||
