Membrane Transporter/Ion Channel(跨膜转运)
- AMPAR(55)
- ATPase(78)
- Calcium Channel(322)
- Cannabinoid Transporters(6)
- CFTR(45)
- Chloride Channels(12)
- GABA Receptor(220)
- Glucose Transporters(13)
- Glutamate (EAAT) Transporters(18)
- Glycine Receptors(2)
- GlyT(18)
- GTPase(28)
- ICB(1)
- MCT2(2)
- Monoamine transporter(15)
- Monocarboxylate Transporters(12)
- Multidrug Transporters(4)
- Na+/Ca2+ Exchanger(15)
- NKCC(7)
- NMDA Receptor(76)
- Nucleoside Transporters(4)
- Pannexin-1(2)
- P2X purinergic receptor(65)
- P-gp(10)
- Proton Pump(55)
- Potassium Channel(302)
- Sodium Channel(204)
- TRP Channel(162)
- TRPV1(10)
- URAT1(12)
- Other Channel Modulators(10)
- MCT(3)
- Kainate Receptors(11)
- Ionophore(3)
- sodium-hydrogen exchanger(3)
- Chloride Channel(27)
- CRAC Channel(13)
- EAAT2(5)
- HCN Channel(6)
- Na+/HCO3- Cotransporter(1)
- Na+/K+ ATPase(27)
- P-glycoprotein(49)
- iGluR(156)
- nAChR(100)
- 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)
- Cat.No. 产品名称 Information
- 
                    
                     GC30986 
					
						
							Nicardipine (YC-93)							
                                                           尼卡地平; YC-93 free base Nicardipine is a potent calcium channel blockader with marked vasodilator action.  
- 
                    
                     GC30984 
					
						
							XEN907							
                            									            
                    XEN907是一种新型的螺羟吲哚类NaV1.7阻断剂,抑制hNaV1.7,IC50为3nM。           
					
					   
- 
                    
                     GC30983 
					
						
							alpha-Asarone (α-Asarone)							
                                                           α-细辛脑; α-Asarone; trans-Asarone An inhibitor of HMG-CoA reductase and CYP450 isoforms   
- 
                    
                     GC30977 
					
						
							Ca2+ channel agonist 1							
                            									            
                    Ca2+channelagonist1是一种N-型钙离子通道(N-typeCa2+channel)激动剂和Cdk2的抑制剂,EC50分别为14.23μM和3.34μM,对运动神经终端功能障碍有潜在疗效。           
					
					   
- 
                    
                     GC30973 
					
						
							Mephenesin							
                                                           甲酚甘油醚 Mephenesin (Decontractyl, Cresoxydiol, Memphenesin, Mephedan) is centrally acting muscle relaxant, a topical analgesic and may be an NMDA receptor antagonist.  
- 
                    
                     GC30961 
					
						
							Mirogabalin besylate (DS 5565 besylate)							
                                                           10928苯磺酸盐,DS 5565 besylate A calcium channel blocker   
- 
                    
                     GC30957 
					
						
							Propoxycaine hydrochloride							
                                                           盐酸丙氧卡因;丙氧卡因盐酸盐 Propoxycaine盐酸盐是一种局部麻醉剂,结合并抑制电压门控钠通道,抑制脉冲起始和传导所需的离子通量,从而导致感觉的丢失。   
- 
                    
                     GC30951 
					
						
							MDL 105519							
                                                           3-[(1E)-2-羧基-2-苯乙烯基]-4,6-二氯-1H-吲哚-2-羧酸 MDL105519是有效和选择性的甘氨酸与NMDA受体结合的拮抗剂。  
- 
                    
                     GC30950 
					
						
							TTA-Q6							
                            									            
                    TTA-Q6是T型Ca2+通道的选择性拮抗剂,可用于神经学研究。           
					
					   
- 
                    
                     GC30946 
					
						
							Procyclidine hydrochloride ((±)-Procyclidine hydrochlorid)							
                                                           丙环定盐酸盐; Tricyclamol hydrochloride; (±)-Procyclidine hydrochloride A muscarinic acetylcholine receptor antagonist  
- 
                    
                     GC30943 
					
						
							6,2'-Dihydroxyflavone							
                                                           6,2-二羟基黄酮 6,2'-Dihydroxyflavone是一个新型的GABAA受体拮抗剂。  
- 
                    
                     GC30933 
					
						
							(+)-Kavain							
                                                           醉椒素 A kavalactone with diverse biological activities  
- 
                    
                     GC30930 
					
						
							DAA-1106							
                                                           N-(2,5-二甲氧基苄基)-N-(5-氟-2-苯氧基苯基)乙酰胺 A TSPO agonist  
- 
                    
                     GC30927 
					
						
							Acevaltrate							
                                                           乙酰缬草三酯 Acevaltrate, an active component derived from the herbal plant Valeriana jatamansi Jones, is strikingly potent to induce GBM cell apoptosis. Acevaltrate inhibits the Na+/K+-ATPase activity in the rat kidney and brain hemispheres with IC50 of 22.8 μM and 42.3 μM, respectively.  
- 
                    
                     GC30917 
					
						
							AM-2099							
                            									            
                    AM-2099是电压门控钠通道Nav1.7的有效,选择性的抑制剂,对人类Nav1.7的IC50值为0.16μM。           
					
					   
- 
                    
                     GC30914 
					
						
							Butamben (Butyl 4-aminobenzoate)							
                                                           4-氨基苯甲酸丁酯,Butyl 4-aminobenzoate Butamben (Butyl 4-aminobenzoate) is a long-duration local anesthetic used for the treatment of chronic pain.  
- 
                    
                     GC30911 
					
						
							Apimostinel (NRX-1074)							
                                                           NRX-1074; AGN-241660 Apimostinel (NRX-1074) (NRX-1074; AGN-241660) 是一种具有口服活性的 NMDA 受体部分激动剂。   
- 
                    
                     GC30910 
					
						
							Eucalyptol (1,8-Cineole)							
                                                           NSC 6171 Eucalyptol是5-HT3受体,钾通道,TNF-α和IL-1β的抑制剂。  
- 
                    
                     GC30898 
					
						
							6-Methylflavone							
                                                           6-甲基黄酮 6-methylflavone是α1β2γ2L和α1β2GABAA受体的激活剂。  
- 
                    
                     GC30893 
					
						
							TRPM8 Antagonist							
                            									            
                    TRPM8 antagonist 2 (TRPM8 Antagonist) is a potent and selective antagonist of TRPM8 with IC50 of 0.2 nM that can be used for the pharmacological treatment of neuropathic pain syndromes.           
					
					   
- 
                    
                     GC30891 
					
						
							Almitrine mesylate (Almitrine bismesylate)							
                                                           甲磺酸阿米三嗪,Almitrine bismesylate; Almitrine bismethanesulfonate; Almitrine dimesylate Almitrine mesylate (Almitrine bismesylate, Almitrine dimethanesulfonate, Almitrine dimesylate), a pharmacologically unique respiratory stimulant, acts as an agonist of peripheral chemoreceptors located on the carotid bodies. Almitrine mesylate inhibits the activity of Ca2+-dependent K+ channel by decreasing its open probability with IC50 of 0.22 μM.  
- 
                    
                     GC30889 
					
						
							(-)-Securinine							
                                                           一叶秋碱 An alkaloid  
- 
                    
                     GC30873 
					
						
							Mirogabalin (DS5565)							
                                                           米洛巴林,DS5565 A calcium channel blocker  
- 
                    
                     GC30866 
					
						
							Anabasine ((S)-Anabasine)							
                                                           (+)-假木贼碱; (S)-Anabasine; (+)-Anabasine Anabasine ((S)-Anabasine) ((S)-Anabasine ((S)-Anabasine)) 是一种生物碱,在烟草 (Nicotiana) 中是一种微量成分。  
- 
                    
                     GC30865 
					
						
							TPA 023							
                            									            
                    TPA023是GABAAα2/α3的选择性的激动剂,Ki值为0.19-0.41nM。           
					
					   
- 
                    
                     GC30862 
					
						
							L-Cycloserine ((S)-4-Amino-3-isoxazolidone)							
                                                           环丝氨酸,(S)-Cycloserine; (S)-4-Amino-3-isoxazolidone An inhibitor of sphingolipid synthesis and aminotransferases  
- 
                    
                     GC30860 
					
						
							Neu2000							
                                                           Salfaprodil free base; Neu2000 Neu2000 (Salfaprodil free base) 是 N-甲基-D-天冬氨酸 (NMDA) 的 NR2B 选择性和非竞争性拮抗剂。  
- 
                    
                     GC30852 
					
						
							Org-26576							
                            									            
                    Org26576是AMPA受体的正变构调节剂。           
					
					   
- 
                    
                     GC30850 
					
						
							GV-58							
                                                           (2R)-2-[[6-[[(5-甲基噻吩-2-基)甲基]氨基]-9-丙基-9H-嘌呤-2-基]氨基]丁烷-1-醇 GV-58 is a novel, selective N-type and P/Q-type Ca2+ channels agonist with IC50s of 7.21 μM and 8.81 μM, respectively.  
- 
                    
                     GC30847 
					
						
							IC87201							
                            									            
                    An inhibitor of the nNOS-PSD-95 protein-protein interaction           
					
					   
- 
                    
                     GC30844 
					
						
							Afloqualone							
                                                           氟喹酮; HQ-495 An Analytical Reference Standard  
- 
                    
                     GC30839 
					
						
							Traxoprodil							
                                                           曲索罗地 An antagonist of NR2B subunit-containing NMDA receptors   
- 
                    
                     GC30837 
					
						
							A-1165442							
                            									            
                    A-1165442是有效,竞争性,有口服活性的TRPV1拮抗剂,对人TRPV1的IC50值为9nM。           
					
					   
- 
                    
                     GC30835 
					
						
							Rislenemdaz (MK-0657)							
                                                           MK-0657; CERC-301 Rislenemdaz (MK-0657) (CERC-301) 是一种口服生物可利用的选择性 N-甲基-D-天冬氨酸 (NMDA) 受体亚基 2B (GluN2B) 拮抗剂,其 Ki 和 IC 50 分别为 8.1 nM 和 3.6 nM。   
- 
                    
                     GC30827 
					
						
							Pipequaline (PK-8165)							
                                                           哌夸林,PK-8165 A partial agonist of central benzodiazepine receptors  
- 
                    
                     GC30818 
					
						
							ZL006							
                            									            
                    An nNOS/PSD-95 interaction inhibitor           
					
					   
- 
                    
                     GC30815 
					
						
							Synaptamide (Dehydroepiandrosteron(DHEA))							
                                                           DEA, DHEA, Synaptamide An endocannabinoid found in brain and retina   
- 
                    
                     GC30813 
					
						
							Raxatrigine hydrochloride (GSK-1014802 hydrochloride)							
                                                           GSK-1014802 hydrochloride; CNV1014802 hydrochloride An inhibitor of voltage-gated sodium channels  
- 
                    
                     GC30807 
					
						
							ZSET1446 (ST-101)							
                                                           ST-101 ZSET1446 (ST-101) 是一种新型认知增强剂,可显着改善各种类型的阿尔茨海默病 (AD) 模型中的学习缺陷。  
- 
                    
                     GC30805 
					
						
							PSB-12062 (N-(p-Methylphenylsulfonyl)phenoxazine)							
                                                           N-(p-Methylphenylsulfonyl)phenoxazine PSB-12062 (N-(p-Methylphenylsulfonyl)phenoxazine) 是一种有效的选择性 P2X4 拮抗剂,对人 P2X4 的 IC50 为 1.38 μM。  
- 
                    
                     GC30799 
					
						
							HC-070							
                            									            
                    HC-070是一种瞬时受体电位通道蛋白4/5(TRPC4/TRPC5)拮抗剂,在细胞中,对hTRPC5和hTRPC4的IC50值分别为9.3nM和46nM。           
					
					   
- 
                    
                     GC30788 
					
						
							L-Glutamic acid monosodium salt (Monosodium glutamate)							
                                                           谷氨酸单钠盐 L-Glutamic acid monosodium salt is the sodium salt of glutamic acid, found naturally in tomatoes, cheese and other foods. L-Glutamic acid monosodium salt acts as an excitatory transmitter and an agonist at all subtypes of glutamate receptors (metabotropic, kainate, NMDA, and AMPA). (S)-Glutamic acid shows a direct activating effect on the release of DA from dopaminergic terminals.  
- 
                    
                     GC30774 
					
						
							Tat-NR2B9c							
                                                           Tat-NR2Bct; NA-1 Tat-NR2B9c 旨在通过阻止突触后密度蛋白 95 (PSD-95) 与 N-甲基-D-天冬氨酸 (NMDA) 受体和神经元一氧化氮结合来阻止一氧化氮 (NO) 的产生氧化物合成酶。  
- 
                    
                     GC30725 
					
						
							TRPV antagonist 1							
                            									            
                    TRPVantagonist1是一种有效的瞬时受体电位V型(TRPV)拮抗剂,IC50值<250nM。   
- 
                    
                     GC30628 
					
						
							Funapide (TV 45070)							
                                                           TV 45070; XEN402 Funapide (TV 45070) (TV 45070; XEN402) 是一种有效的钠通道 Nav1.7 抑制剂。  
- 
                    
                     GC30555 
					
						
							H100							
                            									            
                    H100是一种氯离子运输(Cl-transport)抑制剂,可以部分抑制氯离子载体NaK2Clcotransporter和Band3anionexchanger,但是对KClcotransporter无作用。           
					
					   
- 
                    
                     GC30546 
					
						
							TRPC6-IN-1							
                            									            
                    TRPC6-IN-1是TRPC6的一个抑制剂,其EC50值为4.66μM。           
					
					   
- 
                    
                     GC30537 
					
						
							BPO-27 racemate							
                            									            
                    BPO-27racemate是有效的CFTR抑制剂,IC50值为8nM。           
					
					   
- 
                    
                     GC30535 
					
						
							Transdermal Peptide (TD 1 (peptide))							
                                                           透皮短肽 Transdermal Peptide (TD 1 (peptide)) 由 11 个氨基酸组成,是第一个通过噬菌体展示发现的透皮增强肽。   
- 
                    
                     GC30521 
					
						
							Broflanilide							
                                                           氟苯双酰胺 Broflanilide是一种杀虫剂,可以分解成desmethyl-broflanilide,为特异性的昆虫耐狄氏剂的GABAreceptor拮抗剂,抑制斜纹夜蛾RDLGABAR,IC50值为1.3nM。  
 
 
   
   
  