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)
- GC50586uPSEM 792 hydrochlorideCAS: 2341841-08-3
Highly potent PSAM4-GlyR and PSAM4-5-HT3 chimeric ion channel agonist; brain-penetrant
- GC50587uPSEM 817 tartrateCAS: 2341833-14-3
Highly potent and selective PSAM4-GlyR and PSAM4-5-HT3 chimeric ion channel agonist; brain-penetrant
- GC50702GoSlo SR 5-69CAS: 1363419-31-1纯度: >98.00%
GoSlo SR 5-69 是一种有效的大电导 Ca2+- 激活 K+ (BK) 通道激活剂,EC50 为 251 nM。
- GC52503FTase Inhibitor II (trifluoroacetate salt)纯度: >80.00%
A potent, selective inhibitor of farnesyltransferase
| 货号 | 产品名称 | CAS号 | 纯度 | 结构 |
|---|---|---|---|---|
| GC50536 | (2R/S)-6-PNG | 68682-01-9 | - | |
A flavonoid with diverse biological activities | ||||
| GC50547 | GI 530159 | 69563-88-8 | >98.00% | |
GI 530159 是 TREK1 和 TREK2 钾通道的选择性开放剂。 | ||||
| GC50557 | CBA | 351424-20-9 | >98.00% | |
A TRPM4 inhibitor | ||||
| GC50582 | TAT-GluA2 3Y | 1404188-93-7 | - | |
TAT-GluA2 3Y 是一种干扰肽,通过破坏 AMPAR 的内吞作用来阻断谷氨酸能突触的长期抑制 (LTD)。 | ||||
| GC50586 | uPSEM 792 hydrochloride | 2341841-08-3 | - | |
Highly potent PSAM4-GlyR and PSAM4-5-HT3 chimeric ion channel agonist; brain-penetrant | ||||
| GC50587 | uPSEM 817 tartrate | 2341833-14-3 | - | |
Highly potent and selective PSAM4-GlyR and PSAM4-5-HT3 chimeric ion channel agonist; brain-penetrant | ||||
| GC50590 | TRPC6-PAM-C20 | 667427-75-0 | - | |
TRPC6-PAM-C20 是 TRPC6 通道的选择性正变构调节剂 (PAM)。 | ||||
| GC50596 | ML 418 | 1928763-08-9 | >99.00% | |
ML 418 是第一个有效的、选择性的和 CNS 穿透性的 Kir7.1 钾通道 (IC50, 310 nM) 阻断剂,它也有效地抑制 Kir6.2/SUR1,并且表现出优于其他 Kir 通道的选择性。 | ||||
| GC50617 | BTD | 896684-04-1 | - | |
Selective TRPC5 activator | ||||
| GC50632 | A 1899 | 498577-46-1 | - | |
Potent K2P3.1 (TASK-1) and K2P9.1 (TASK-3) blocker | ||||
| GC50640 | OptoBI-1 | 2415272-11-4 | - | |
OptoBI-1 是一种光致变色 TRPC3 激动剂,可作为一种光药理学工具来控制神经元放电。 | ||||
| GC50641 | IA-Alkyne | 930800-38-7 | >99.00% | |
IA-Alkyne (Iodoacetamide-alkyne; N-Hex-5-ynyl-2-iodo-acetamide) 是一种 TRP 通道 (TRPC) 激动剂,具有研究呼吸道感染的潜力。 | ||||
| GC50649 | FFN 200 dihydrochloride | 2080306-27-8 | >98.00% | |
Selective fluorescent VMAT2 substrate | ||||
| GC50661 | BeKm 1 | 524962-01-4 | - | |
BeKm 1 是一种 HERG(人类 ether-a-go-go 相关基因)阻断化合物。 | ||||
| GC50664 | TRPV3 74a | 1432051-63-2 | >99.50% | |
TRPV3 74a 是一种有效的选择性 TRPV3 拮抗剂。 | ||||
| GC50667 | SET 2 | 2313525-20-9 | >98.00% | |
TRPV2 (transient receptor potential vanilloid type 2) antagonist (IC50 = 0 | ||||
| GC50670 | D-GsMTx4 | - | >98.00% | |
TRPC1/6 and Piezo2 inhibitor | ||||
| GC50678 | NS 383 | 309711-59-9 | - | |
NS 383 是一种有效且独特的选择性大鼠 ASIC 抑制剂,含有 1a 和/或 3 个亚基。 | ||||
| GC50702 | GoSlo SR 5-69 | 1363419-31-1 | >98.00% | |
GoSlo SR 5-69 是一种有效的大电导 Ca2+- 激活 K+ (BK) 通道激活剂,EC50 为 251 nM。 | ||||
| GC50707 | GX 201 | 1788071-27-1 | >99.00% | |
GX 201 是一种选择性 NaV1.7 抑制剂,对 hNaV1.7 的 IC50 \u003c3.2 nM。 | ||||
| GC52250 | Mevalonate (lithium salt) | 2618458-93-6 | >98.00% | |
Mevalonate (lithium salt)是甲羟戊酸途径的代谢前体。 | ||||
| GC52465 | ICR-1 AM | - | >90.00% | |
A cell-permeable fluorescent calcium indicator | ||||
| GC52466 | ICR-1 (potassium salt) | - | >90.00% | |
A cell-impermeable fluorescent calcium indicator | ||||
| GC52503 | FTase Inhibitor II (trifluoroacetate salt) | - | >80.00% | |
A potent, selective inhibitor of farnesyltransferase | ||||
