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)
- GC34049Aranidipine (MPC1304)CAS: 86780-90-7纯度: >99.00%
Aranidipine (MPC1304) (MPC1304) 是一种 Ca2+ 通道拮抗剂,具有强效和持久的抗高血压作用。
- GC34064Aminooxyacetic acid hemihydrochloride (Carboxymethoxylamine Hemihydrochloride)CAS: 2921-14-4纯度: >98.00%
Aminooxyacetic acid hemihydrochloride (Carboxymethoxylamine Hemihydrochloride)是一种苹果酸-天冬氨酸穿梭(MAS)抑制剂和γ-氨基丁酸转氨酶(GABA-T)抑制剂。
- GC34079Monepantel (AAD1566)CAS: 887148-69-8纯度: >99.50%
Monepantel (AAD1566)是一种氨基乙腈衍生物类驱虫药,Monepantel可抑制mTOR/p70S6K信号通路诱导自噬。
- GC34352NMDAR antagonist 1CAS: 2220162-06-9
NMDAR antagonist 1 is a potent and orally bioavailable NR2B-selective antagonist of NMDAR. It has neuroprotective activity.
- GC34532CFTR corrector 2CAS: 1628416-28-3纯度: >99.50%
FDL169 is a CFTR corrector that is designed to fix and restore the function of the defective CFTR protein.
- GC34638JNJ-61432059CAS: 2035814-50-5纯度: >99.00%
JNJ-61432059是具有口服活性的、选择性的AMPAR的负向调节剂,其对GluA1/γ-8的pIC50值为9.7。在老鼠的海马体中显示出具有时间和剂量依赖性的AMPA受体占用情况,在角膜点燃癫痫动物模型中显示出较强的保护作用。
- GC34828Tat-NR2B9c TFACAS: 1834571-04-8纯度: >99.50%
Tat-NR2B9c(TFA)是由20个氨基酸组成的多肽,为PSD-95的抑制剂,对PSD-95d2和PSD-95d1的EC50值分别为6.7nM和670nM。Tat-NR2B9c同时可降低NMDA诱导的p38的活化,具有神经保护作用。
- GC34912Levamlodipine besylateCAS: 150566-71-5纯度: >99.50%
Levamlodipine Besylate is a powerful dihydropyridine calcium channel blocker, possessing vasodilation properties and used in the treatment of hypertension and angina.
- GC34952(-)-Sparteine sulfate pentahydrateCAS: 6160-12-9纯度: >98.00%
Sparteine Sulfate, a quinolizidine alkaloid, is the sulfate form of sparteini, which is a sodium channel blocker used as an oxytocic and an anti-arrhythmia agent.
| 货号 | 产品名称 | CAS号 | 纯度 | 结构 |
|---|---|---|---|---|
| GC34049 | Aranidipine (MPC1304) | 86780-90-7 | >99.00% | |
Aranidipine (MPC1304) (MPC1304) 是一种 Ca2+ 通道拮抗剂,具有强效和持久的抗高血压作用。 | ||||
| GC34064 | Aminooxyacetic acid hemihydrochloride (Carboxymethoxylamine Hemihydrochloride) | 2921-14-4 | >98.00% | |
Aminooxyacetic acid hemihydrochloride (Carboxymethoxylamine Hemihydrochloride)是一种苹果酸-天冬氨酸穿梭(MAS)抑制剂和γ-氨基丁酸转氨酶(GABA-T)抑制剂。 | ||||
| GC34079 | Monepantel (AAD1566) | 887148-69-8 | >99.50% | |
Monepantel (AAD1566)是一种氨基乙腈衍生物类驱虫药,Monepantel可抑制mTOR/p70S6K信号通路诱导自噬。 | ||||
| GC34352 | NMDAR antagonist 1 | 2220162-06-9 | - | |
NMDAR antagonist 1 is a potent and orally bioavailable NR2B-selective antagonist of NMDAR. It has neuroprotective activity. | ||||
| GC34362 | SSD114 hydrochloride | 2319790-02-6 | >99.00% | |
SSD114hydrochloride是一种新型GABAB受体正变构调节剂。 | ||||
| GC34486 | BI 01383298 | 2227549-00-8 | >99.50% | |
An NaCT inhibitor | ||||
| GC34489 | BI-749327 | 2361241-23-6 | >98.00% | |
BI-749327是一种可口服利用的TRPC6拮抗剂, | ||||
| GC34492 | BI-9627 | 1204329-34-9 | >98.50% | |
An NHE1 inhibitor | ||||
| GC34494 | Bifenazate | 149877-41-8 | >99.50% | |
An acaricide | ||||
| GC34532 | CFTR corrector 2 | 1628416-28-3 | >99.50% | |
FDL169 is a CFTR corrector that is designed to fix and restore the function of the defective CFTR protein. | ||||
| GC34574 | Endovion | 265646-85-3 | >99.00% | |
Endovion (NS 3728, SCO-101) is a potent anion channel inhibitor that blocks the Volume Regulated Anion Channels (VRAC). | ||||
| GC34616 | HMR 1556 | 223749-46-0 | >99.50% | |
HMR1556,色氨醇衍生物,是一种IKs阻滞剂,在犬和豚鼠的左心室肌细胞中的IC50值分别为10.5nM、34nM。 | ||||
| GC34638 | JNJ-61432059 | 2035814-50-5 | >99.00% | |
JNJ-61432059是具有口服活性的、选择性的AMPAR的负向调节剂,其对GluA1/γ-8的pIC50值为9.7。在老鼠的海马体中显示出具有时间和剂量依赖性的AMPA受体占用情况,在角膜点燃癫痫动物模型中显示出较强的保护作用。 | ||||
| GC34665 | Metaflumizone | 139968-49-3 | - | |
Metaflumizone是一种缩氨基脲杀虫剂,为有效的钠离子通道(sodiumchannel)阻滞剂。 | ||||
| GC34745 | PTI-428 | 1953130-87-4 | >99.50% | |
PTI-428是一种可增强并稳定囊性纤维化跨膜传导调节因子(CFTR)蛋白功能的特异性调节剂。 | ||||
| GC34753 | Radiprodil | 496054-87-6 | >99.00% | |
An NMDA receptor antagonist | ||||
| GC34828 | Tat-NR2B9c TFA | 1834571-04-8 | >99.50% | |
Tat-NR2B9c(TFA)是由20个氨基酸组成的多肽,为PSD-95的抑制剂,对PSD-95d2和PSD-95d1的EC50值分别为6.7nM和670nM。Tat-NR2B9c同时可降低NMDA诱导的p38的活化,具有神经保护作用。 | ||||
| GC34833 | TC-I 2014 | 1221349-53-6 | >99.00% | |
TC-I2014(compound5)是一种强效的、苯并咪唑类的、TRPM8的拮抗剂,其对犬类、人和大鼠通道的IC50值分别为0.8nM,3.0nM和4.4nM。在疼痛动物模型中具有抗痛觉超敏作用。 | ||||
| GC34912 | Levamlodipine besylate | 150566-71-5 | >99.50% | |
Levamlodipine Besylate is a powerful dihydropyridine calcium channel blocker, possessing vasodilation properties and used in the treatment of hypertension and angina. | ||||
| GC34951 | (-)-Menthol | 2216-51-5 | >98.00% | |
A monoterpene with diverse biological activities | ||||
| GC34952 | (-)-Sparteine sulfate pentahydrate | 6160-12-9 | >98.00% | |
Sparteine Sulfate, a quinolizidine alkaloid, is the sulfate form of sparteini, which is a sodium channel blocker used as an oxytocic and an anti-arrhythmia agent. | ||||
| GC34954 | (+)-Borneol | 464-43-7 | >98.00% | |
A bicyclic monoterpene with diverse biological activities | ||||
| GC34959 | (+)-Sparteine | 492-08-0 | >98.60% | |
A quinolizidine alkaloid | ||||
| GC34986 | (R)-Baclofen hydrochloride | 63701-55-3 | >98.00% | |
A GABA B receptor agonist | ||||
