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)
- GC31184Phe-Met-Arg-Phe, amideCAS: 64190-70-1
Phe-Met-Arg-Phe,amide是一种神经肽,在肽能神经元中激活K+电流,ED50为23nM,这种作用具有剂量依赖性。
- GC31209Cyclodrine hydrochlorideCAS: 78853-39-1
Cyclodrinehydrochloride是一种胆碱能(毒蕈碱,烟碱)受体(mAChR和nAChR)拮抗剂。
- GC31216Nicainoprol (RU-42924)CAS: 76252-06-7纯度: >99.00%
Nicainoprol (RU-42924) 是一种快速钠通道阻断药,是一种有效的抗心律失常药物。
- GC31248β-Amino Acid Imagabalin Hydrochloride (PD-0332334)CAS: 610300-00-0
β-Amino Acid Imagabalin Hydrochloride (PD-0332334) (PD-0332334) 是 α2δ 的配体;电压依赖性钙通道的亚基。
- GC31257Rilmazafone hydrochloride (450191S)CAS: 85815-37-8纯度: >99.50%
Rilmazafone hydrochloride (450191S) (450191S) 是苯二氮卓 (omega) 配体。
- GC31282p-HydroxybenzaldehydeCAS: 123-08-0
p-Hydroxybenzaldehyde (4-Hydroxybenzaldehyde, 4-Formylphenol, p-Formylphenol), which can be found in the orchids Gastrodia elata, Galeola faberi and vanilla, is a hydroxybenzaldehyde that reacts with NAD+ and H2O to produce 4-hydroxybenzoate, NADH, and 2 protons. p-Hydroxybenzaldehyde at 101.7 μM can significantly reduce the GABA-induced chloride current of GABAA receptors(α1β2γ2S subtype) expressed.
- GC31301Darodipine (PY 108-068)CAS: 72803-02-2
Darodipine (PY 108-068) (PY 108-068, PY-108068) 是一种有效的钙通道拮抗剂。
- GC313096-Methoxy-2-naphthoic acid (Naproxen impurity O)CAS: 2471-70-7纯度: >98.00%
An active metabolite of nabumetone
- GC31387Rimeporide (EMD-87580)CAS: 187870-78-6纯度: >98.50%
Rimeporide(EMD-87580) is a sodium hydrogen exchanger (NHE-1) inhibitor indicated for patients with Duchenne muscular dystrophy.
- GC31426Bamaquimast (F 10126)CAS: 135779-82-7纯度: >98.00%
Bamaquimast (F 10126) (F 10126; L 0042) 是一种有效的平喘药。
- GC31431Amiloride (MK-870)CAS: 2609-46-3纯度: >98.00%
Amiloride (MK-870)是一种选择性T型钙通道阻滞剂、上皮钠通道(ENaC)和尿激酶型纤溶酶原激活物受体(uTPA)抑制剂,Ki =7 µM。
| 货号 | 产品名称 | CAS号 | 纯度 | 结构 |
|---|---|---|---|---|
| GC31184 | Phe-Met-Arg-Phe, amide | 64190-70-1 | - | |
Phe-Met-Arg-Phe,amide是一种神经肽,在肽能神经元中激活K+电流,ED50为23nM,这种作用具有剂量依赖性。 | ||||
| GC31196 | SX-3228 | 156364-04-4 | - | |
SX-3228是一种选择性苯二氮卓类(benzodiazepine1,BZ1)受体激动剂,IC50为17nM。 | ||||
| GC31200 | Myomodulin | 110570-93-9 | - | |
Myomodulin是存在于软体动物,昆虫和腹足动物中的神经多肽。 | ||||
| GC31206 | PF 04531083 | 1079400-07-9 | >98.00% | |
PF04531083是一种选择性的NaV1.8阻滞剂,能够用于神经性或炎症性疼痛的研究。 | ||||
| GC31209 | Cyclodrine hydrochloride | 78853-39-1 | - | |
Cyclodrinehydrochloride是一种胆碱能(毒蕈碱,烟碱)受体(mAChR和nAChR)拮抗剂。 | ||||
| GC31216 | Nicainoprol (RU-42924) | 76252-06-7 | >99.00% | |
Nicainoprol (RU-42924) 是一种快速钠通道阻断药,是一种有效的抗心律失常药物。 | ||||
| GC31224 | Carburazepam (RGH 3331) | 59009-93-7 | - | |
Carburazepam (RGH 3331) 是一种衍生自苯二氮卓类药物的药物。 | ||||
| GC31236 | JYL 1421 (SC 0030) | 401907-26-4 | - | |
A TRPV1 antagonist | ||||
| GC31248 | β-Amino Acid Imagabalin Hydrochloride (PD-0332334) | 610300-00-0 | - | |
β-Amino Acid Imagabalin Hydrochloride (PD-0332334) (PD-0332334) 是 α2δ 的配体;电压依赖性钙通道的亚基。 | ||||
| GC31257 | Rilmazafone hydrochloride (450191S) | 85815-37-8 | >99.50% | |
Rilmazafone hydrochloride (450191S) (450191S) 是苯二氮卓 (omega) 配体。 | ||||
| GC31270 | GNE 0723 | 1883518-31-7 | >98.50% / >97.00% | |
GNE 0723是一种选择性作用于GluN2A亚基且能穿透血脑屏障的N-甲基-D-天冬氨酸受体(NMDAR)正向变构调节剂(PAM),其半数有效浓度(EC 50 )为0.021μM,最大增强作用为152%。 | ||||
| GC31279 | Sodium ionophore III (ETH2120) | 81686-22-8 | >98.00% | |
钠离子载体 III (ETH2120) 是一种 Na+ 离子载体。 | ||||
| GC31282 | p-Hydroxybenzaldehyde | 123-08-0 | - | |
p-Hydroxybenzaldehyde (4-Hydroxybenzaldehyde, 4-Formylphenol, p-Formylphenol), which can be found in the orchids Gastrodia elata, Galeola faberi and vanilla, is a hydroxybenzaldehyde that reacts with NAD+ and H2O to produce 4-hydroxybenzoate, NADH, and 2 protons. p-Hydroxybenzaldehyde at 101.7 μM can significantly reduce the GABA-induced chloride current of GABAA receptors(α1β2γ2S subtype) expressed. | ||||
| GC31301 | Darodipine (PY 108-068) | 72803-02-2 | - | |
Darodipine (PY 108-068) (PY 108-068, PY-108068) 是一种有效的钙通道拮抗剂。 | ||||
| GC31302 | NHE3-IN-1 | 632355-68-1 | - | |
NHE3-IN-1是钠/质子交换类型3(sodium/protonexchangertype3(NHE-3))的抑制剂,来自专利WO2011019784A1。 | ||||
| GC31309 | 6-Methoxy-2-naphthoic acid (Naproxen impurity O) | 2471-70-7 | >98.00% | |
An active metabolite of nabumetone | ||||
| GC31313 | S16961 (S169611) | 153874-14-7 | - | |
S16961 (S169611) 是一种烟碱受体激动剂。 | ||||
| GC31332 | CDN1163 | 892711-75-0 | >98.50% / >98.00% | |
An allosteric activator of SERCA2 | ||||
| GC31340 | Encequidar (HM30181) | 849675-66-7 | >98.00% | |
An inhibitor of P-glycoprotein | ||||
| GC31347 | Ilaprazole (IY-81149) | 172152-36-2 | >98.00% | |
A gastric proton pump inhibitor | ||||
| GC31387 | Rimeporide (EMD-87580) | 187870-78-6 | >98.50% | |
Rimeporide(EMD-87580) is a sodium hydrogen exchanger (NHE-1) inhibitor indicated for patients with Duchenne muscular dystrophy. | ||||
| GC31405 | BMS-191095 | 166095-21-2 | >98.00% | |
BMS-191095是线粒体ATP敏感性(mitoKATP)的钾离子通道活化剂。 | ||||
| GC31426 | Bamaquimast (F 10126) | 135779-82-7 | >98.00% | |
Bamaquimast (F 10126) (F 10126; L 0042) 是一种有效的平喘药。 | ||||
| GC31431 | Amiloride (MK-870) | 2609-46-3 | >98.00% | |
Amiloride (MK-870)是一种选择性T型钙通道阻滞剂、上皮钠通道(ENaC)和尿激酶型纤溶酶原激活物受体(uTPA)抑制剂,Ki =7 µM。 | ||||
