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)
- GC605305-HydroxylansoprazoleCAS: 131926-98-2纯度: >99.50%
5-Hydroxylansoprazole(AG1908)是血浆中Lansoprazole的活性代谢产物。Lansoprazole由CYP2C19代谢形成5-Hydroxylansoprazole。Lansoprazole是一种胃质子泵(proton-pump)抑制剂,可有效研究各种消化系统疾病。
- GC60549ABT-418 hydrochlorideCAS: 147388-83-8纯度: >99.50%
ABT-418hydrochloride是一种高效、选择性的nAChRs激动剂,具有增强认知和抗焦虑的作用。ABT-418hydrochloride激活胆碱能通道,可用于阿尔茨海默病的研究。
- GC60596ArecaidineCAS: 499-04-7纯度: >98.00%
Arecaidine,一种吡啶生物碱,是一种有效的GABA吸收抑制剂。Arecaidine是H+偶联的氨基酸转运蛋白1(PAT1,SLC36A1)的底物,竞争性抑制L-脯氨酸的摄取。
- GC60718Cloperastine hydrochlorideCAS: 14984-68-0纯度: >99.00%
Cloperastine (HT-11) is a drug with a central antitussive effect, and is also endowed with an antihistaminic activity.
- GC60750Dehydrosoyasaponin ICAS: 117210-14-7纯度: >98.00%
DehydrosoyasaponinI(SoyasaponinBe;DHS-I),一种三萜糖苷,是一种有效且可逆的钙激活钾(maxi-K)通道激活剂。
- GC60834Fenamic acidCAS: 91-40-7纯度: >98.00%
Fenamic acid (N-Phenylanthranilic acid, 2-(Phenylamino)benzoic acid, 2-Anilinobenzoic acid, Diphenylamine-2-carboxylic acid) serves as a parent structure for several nonsteroidal anti-inflammatory drugs (NSAIDs), including mefenamic acid, tolfenamic acid, flufenamic acid, and meclofenamic acid.
- GC60862GABAA receptor agent 1CAS: 1571-87-5纯度: >98.50%
GABAA receptor agent 1 is a high affinity ligand for Gamma-aminobutyric acid A (GABAA) receptor that exerts potent anticonvulsant activity.
- GC60975Lansoprazole Sulfide D4CAS: 1216682-38-0
LansoprazoleSulfideD4是LansoprazoleSulfide的氘代物。LansoprazoleSulfide是质子泵抑制剂Lansoprazole的活性代谢产物。LansoprazoleSulfide是一种口服活性抗结核药,细胞内的IC50值为0.59µM,肉汤中的IC50值为0.46µM。
- GC61046Methocarbamol D5CAS: 1189699-70-4
An internal standard for the quantification of methocarbamol
- GC61066Minoxidil sulfateCAS: 83701-22-8纯度: >99.50%
Minoxidil (U-58838) is a potent direct-acting peripheral vasodilator that reduces peripheral resistance and produces a fall in blood pressure.
- GC61110Nav1.1 activator 1CAS: 2332897-85-3纯度: >98.00%
Nav1.1activator1(compound4)是强有效的、能透过血脑屏障的、Nav1.1激动剂,0.03μM可增加衰减Nav1.1电流的时间常数τ。对Nav1.2、Nav1.5、Nav1.6有显著的选择性。
- GC61139NothofaginCAS: 11023-94-2
Nothofagin是一种二氢查尔酮,是从如意宝(Aspalathuslinearis)中分离得到的。Nothofagin通过阻断钙(calcium)内流来下调NF-κB的转运。Nothofagin具有抗氧化活性,可改善各种炎症反应,例如脓毒症反应和血管炎症。
- GC61155Omeprazole sodiumCAS: 95510-70-6纯度: >98.00%
An irreversible inhibitor of the gastric proton pump
- GC61175PF-06305591 dihydrateCAS: 2703582-76-5纯度: >99.00%
PF-06305591dihydrate是一种有效的、高选择性的电压门控钠通道NaV1.8的阻断剂,其IC50值为15nM。具有良好的临床前体外ADME(吸收、分布、代谢和排泄)和安全性。
- GC61186PicrotoxininCAS: 17617-45-7纯度: >98.00%
Picrotoxinin是一种来源于天然植物的苦味毒素,存在于一种名为 Anamirta cocculus 的攀援植物的种子中,是一种氯离子通道阻断剂。Picrotoxinin是一种非竞争性的GABA A 受体拮抗剂,负向调节神经递质γ氨基丁酸(GABA)对GABA A 受体的作用。
- GC61248RO2959 monohydrochlorideCAS: 2309172-44-7纯度: >99.00%
RO2959monohydrochloride是一种有效的选择性CRAC通道抑制剂,IC50为402nM。RO2959monohydrochloride是由Orai1/Stim1通道介导的钙存储进入(SOCE)的有效阻滞剂,IC50为25nM。RO2959monohydrochloride还是人IL-2产生的有效抑制剂,有效阻断T细胞受体触发的基因表达和T细胞功能途径。
| 货号 | 产品名称 | CAS号 | 纯度 | 结构 |
|---|---|---|---|---|
| GC60530 | 5-Hydroxylansoprazole | 131926-98-2 | >99.50% | |
5-Hydroxylansoprazole(AG1908)是血浆中Lansoprazole的活性代谢产物。Lansoprazole由CYP2C19代谢形成5-Hydroxylansoprazole。Lansoprazole是一种胃质子泵(proton-pump)抑制剂,可有效研究各种消化系统疾病。 | ||||
| GC60542 | 8-Gingerol | 23513-08-8 | >99.50% / >99.00% | |
A natural TRPV1 agonist | ||||
| GC60545 | A2793 | 88349-90-0 | >99.50% | |
A2793 (Ethyl [(5-Chloroquinolin-8-yl)oxy]acetate) is an efficient inhibitor of TWIK-related spinal cord potassium channel (TRESK, K2P18, KCNK18) and TASK-1 (KCNK3) with IC50 of 6.8 μM for mouse TRESK. | ||||
| GC60549 | ABT-418 hydrochloride | 147388-83-8 | >99.50% | |
ABT-418hydrochloride是一种高效、选择性的nAChRs激动剂,具有增强认知和抗焦虑的作用。ABT-418hydrochloride激活胆碱能通道,可用于阿尔茨海默病的研究。 | ||||
| GC60596 | Arecaidine | 499-04-7 | >98.00% | |
Arecaidine,一种吡啶生物碱,是一种有效的GABA吸收抑制剂。Arecaidine是H+偶联的氨基酸转运蛋白1(PAT1,SLC36A1)的底物,竞争性抑制L-脯氨酸的摄取。 | ||||
| GC60642 | Bifenthrin | 82657-04-3 | >98.00% | |
Bifenthrin是一种拟除虫菊酯杀虫剂,其神经毒性作用的主要靶点是神经细胞膜的电压门控Na + 通道。 | ||||
| GC60709 | Cinnarizine D8 | 1185242-27-6 | - | |
An internal standard for the quantification of cinnarizine | ||||
| GC60718 | Cloperastine hydrochloride | 14984-68-0 | >99.00% | |
Cloperastine (HT-11) is a drug with a central antitussive effect, and is also endowed with an antihistaminic activity. | ||||
| GC60723 | COR659 | 544450-68-2 | >99.50% | |
COR659是GABAB的阳性变构调节剂(PAM)。COR659可缓解大鼠对酒精和巧克力的药物成瘾。 | ||||
| GC60750 | Dehydrosoyasaponin I | 117210-14-7 | >98.00% | |
DehydrosoyasaponinI(SoyasaponinBe;DHS-I),一种三萜糖苷,是一种有效且可逆的钙激活钾(maxi-K)通道激活剂。 | ||||
| GC60834 | Fenamic acid | 91-40-7 | >98.00% | |
Fenamic acid (N-Phenylanthranilic acid, 2-(Phenylamino)benzoic acid, 2-Anilinobenzoic acid, Diphenylamine-2-carboxylic acid) serves as a parent structure for several nonsteroidal anti-inflammatory drugs (NSAIDs), including mefenamic acid, tolfenamic acid, flufenamic acid, and meclofenamic acid. | ||||
| GC60862 | GABAA receptor agent 1 | 1571-87-5 | >98.50% | |
GABAA receptor agent 1 is a high affinity ligand for Gamma-aminobutyric acid A (GABAA) receptor that exerts potent anticonvulsant activity. | ||||
| GC60890 | Guvacine | 498-96-4 | - | |
An inhibitor of GABA uptake | ||||
| GC60929 | Ilaprazole sodium | 172152-50-0 | >98.50% | |
A gastric proton pump inhibitor | ||||
| GC60975 | Lansoprazole Sulfide D4 | 1216682-38-0 | - | |
LansoprazoleSulfideD4是LansoprazoleSulfide的氘代物。LansoprazoleSulfide是质子泵抑制剂Lansoprazole的活性代谢产物。LansoprazoleSulfide是一种口服活性抗结核药,细胞内的IC50值为0.59µM,肉汤中的IC50值为0.46µM。 | ||||
| GC61046 | Methocarbamol D5 | 1189699-70-4 | - | |
An internal standard for the quantification of methocarbamol | ||||
| GC61066 | Minoxidil sulfate | 83701-22-8 | >99.50% | |
Minoxidil (U-58838) is a potent direct-acting peripheral vasodilator that reduces peripheral resistance and produces a fall in blood pressure. | ||||
| GC61110 | Nav1.1 activator 1 | 2332897-85-3 | >98.00% | |
Nav1.1activator1(compound4)是强有效的、能透过血脑屏障的、Nav1.1激动剂,0.03μM可增加衰减Nav1.1电流的时间常数τ。对Nav1.2、Nav1.5、Nav1.6有显著的选择性。 | ||||
| GC61139 | Nothofagin | 11023-94-2 | - | |
Nothofagin是一种二氢查尔酮,是从如意宝(Aspalathuslinearis)中分离得到的。Nothofagin通过阻断钙(calcium)内流来下调NF-κB的转运。Nothofagin具有抗氧化活性,可改善各种炎症反应,例如脓毒症反应和血管炎症。 | ||||
| GC61141 | NSC 15364 | 4550-72-5 | >98.00% | |
NSC15364是一种VDAC1寡聚化和细胞凋亡(apoptosis)抑制剂。 | ||||
| GC61155 | Omeprazole sodium | 95510-70-6 | >98.00% | |
An irreversible inhibitor of the gastric proton pump | ||||
| GC61175 | PF-06305591 dihydrate | 2703582-76-5 | >99.00% | |
PF-06305591dihydrate是一种有效的、高选择性的电压门控钠通道NaV1.8的阻断剂,其IC50值为15nM。具有良好的临床前体外ADME(吸收、分布、代谢和排泄)和安全性。 | ||||
| GC61186 | Picrotoxinin | 17617-45-7 | >98.00% | |
Picrotoxinin是一种来源于天然植物的苦味毒素,存在于一种名为 Anamirta cocculus 的攀援植物的种子中,是一种氯离子通道阻断剂。Picrotoxinin是一种非竞争性的GABA A 受体拮抗剂,负向调节神经递质γ氨基丁酸(GABA)对GABA A 受体的作用。 | ||||
| GC61248 | RO2959 monohydrochloride | 2309172-44-7 | >99.00% | |
RO2959monohydrochloride是一种有效的选择性CRAC通道抑制剂,IC50为402nM。RO2959monohydrochloride是由Orai1/Stim1通道介导的钙存储进入(SOCE)的有效阻滞剂,IC50为25nM。RO2959monohydrochloride还是人IL-2产生的有效抑制剂,有效阻断T细胞受体触发的基因表达和T细胞功能途径。 | ||||
