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(221)
- 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
-
GC30457
Zonampanel (YM 872)
唑南帕奈; YM 872
Zonampanel (YM 872) (YM 872) 是谷氨酸受体亚型 α;-氨基-3-羟基-5-甲基异恶唑-4-丙酸 (AMPA) 受体的选择性拮抗剂。 -
GC30433
Ru-32514
Ru-32514是一种苯二氮受体(benzodiazepinereceptor)激动剂。
-
GC30418
SKF96067
SKF96067是一种可逆的H+/K+-ATPase抑制剂。
-
GC30415
Propafenone D7 hydrochloride (SA-79 (D7 hydrochloride))
盐酸普罗帕酮 D7; SA-79 D7 hydrochloride
Propafenone D7 (SA-79 D7) hydrochloride 是氘标记的 Propafenone,是一种经典的抗心律失常药物。 -
GC30371
Alisol F
泽泻醇 F
A triterpene with anti-inflammatory and hepatoprotective activities -
GC30361
CRAC intermediate 2
4-(3,5-双(三氟甲基)-1H-吡唑-1-基)-苯胺
CRACintermediate2是摘自专利WO2013059666A1中用于CRAC系列抑制剂合成的中间体。 -
GC30322
PF-05241328
PF-05241328是有效的、人电压依赖性钠通道(Nav1.7)的选择性抑制剂,其IC50值为31nM。
-
GC30280
Chlorpromazine D6 hydrochloride
盐酸氯丙嗪 D6
An internal standard for the quantification of chlorpromazine -
GC30267
Pinacidil monohydrate
吡那地尔一水合物; P-1134 monohydrate
A potassium channel opener -
GC30212
(S)-Willardiine ((-)-Willardiine)
尿嘧啶基丙氨酸; (-)-Willardiine
(S)-Willardiine ((-)-Willardiine) 是一种有效的 AMPA/红藻氨酸受体激动剂,EC50 为 44.8 uM。 -
GC30130
Soraprazan (BYK61359)
BYK61359
Soraprazan (BYK61359) (BYK61359) 是一种选择性的、可逆的 K 竞争性 H,K-ATPase 抑制剂 (Ki=6.4 nM),在胃腺中的 IC50 为 0.19 μM。
-
GC30110
Oleic acid (9-cis-Octadecenoic acid)
油酸; 9-cis-Octadecenoic acid; 9Z-Octadecenoic acid
油酸(9-顺式-十八碳烯酸)是一种单不饱和的Omega-9脂肪酸,存在于植物和动物中。 -
GC30096
Pyr10
Pyr10是一种新型TRPC3选择性抑制剂,作用于转染YFP-TRPC3的HEK293细胞,抑制ROCE,IC50为0.72uM。
-
GC30088
Fluxametamide
4-[5-(3,5-二氯苯基)-4,5-二氢-5-(三氟甲基)-3-异恶唑基]-N-[(甲氧基氨基)亚甲基]-2-甲基苯甲酰胺
Fluxametamide是一种广谱的杀虫剂,为GABA-和谷氨酸门控氯离子通道(chloridechannel)拮抗剂,对M.domestica中GABACl和GluCl的IC50值分别为1.95?nM和225?nM。 -
GC30063
Eleclazine hydrochloride (GS 6615 hydrochloride)
GS 6615 hydrochloride
An inhibitor of the cardiac late INa -
GC30055
Pinaverium bromide
匹维溴铵
Pinaverium bromide (Icosapentaenoic acid) acts as a calcium channel blocker and is useful for functional gastrointestinal disorders. -
GC30054
Dantrolene sodium hemiheptahydrate (Dantrolene sodium hydrate)
丹曲林钠,Dantrolene sodium hydrate
Dantrolene sodium hemiheptahydrate (Dantrium) ia a skeletal muscle relaxant that acts by interfering with excitation-contraction coupling in the muscle fiber. -
GC30033
Sinapine thiocyanate
芥子碱硫氰酸盐
Sinapine thiocyanate is the thiocyanate salt form of Sinapine, which shows favorable biological activities such as antioxidant and radio-protective activities. -
GC19480
AUT1
A positive modulator of Kv3.1b, Kv3.2a, and Kv3.3
-
GC19438
TMB 8 (hydrochloride)
3,4,5-三甲氧基苯甲酸(8-二乙氨基正辛基)酯盐酸盐
A non-competitive antagonist of nAChRs and an inhibitor of intracellular calcium availability -
GC19422
Gefapixant
吉法匹生,AF219; MK-7264)
Gefapixant 是一种具有口服活性的强效嘌呤能 P2X3 受体 (P2X3R) 拮抗剂,与重组 hP2X3 同源三聚体相比,IC50 值约为 30 nM,对 hP2X2/3 异源三聚体受体的 IC50 值为 100-250 nM。 -
GC19373
Verinurad
维立诺雷; RDEA3170
A URAT1 inhibitor -
GC19370
Valbenazine
缬苯那嗪,NBI-98854
An inhibitor of VMAT2 -
GC19352
Tenapanor
AZD1722; RDX5791
A NHE-3 inhibitor -
GC19351
Tebanicline hydrochloride
ABT594盐酸盐
A potent agonist of neuronal α4β2 subunit-containing nAChRs -
GC19346
Talampanel
(8R)-7-乙酰基-5-(4-氨基苯基)-8,9-二氢-8-甲基-7H-1,3-二氧杂环戊烯并[4,5-H][2,3]苯并二氮杂卓,GYKI-53773; LY-300164
An allosteric AMPA receptor antagonist -
GC19318
SAGE-217
S-812217, SGE 797
A positive allosteric modulator of GABAA receptors -
GC19310
Ro 25-6981
A potent, NR2B-selective NMDA receptor antagonist
-
GC19291
PF-4840154
A TRPA1 channel agonist
-
GC19289
PF-06869206
An NaPi2a inhibitor
-
GC19281
PF-01247324
2-吡啶甲酰胺,6-氨基-N-甲基-5-(2,3,5-三氯苯基)-
An inhibitor of Nav1.8 channels -
GC19271
ONO-8590580
A negative allosteric modulator of α5 subunit-containing GABAA receptors
-
GC19252
MK-8998
MK-8998
MK-8998 (MK-8998; Compound 33) 是一种有效的选择性 T 型钙通道抑制剂。 -
GC19183
GSK369796 Dihydrochloride
N-tert-butyl Isoquine
An antimalarial agent -
GC19169
GLPG1837
ABBV-974
A CFTR potentiator -
GC19152
Fantofarone
泛托法隆,SR 33557
A calcium channel inhibitor -
GC19107
CM-4620
CM-4620
CM-4620 (CM-4620) 是一种钙释放激活的钙通道(CRAC 通道)抑制剂,对 Orai1/STIM1 和 Orai2/STIM1 通道的 IC50 分别为 119 nM 和 895 nM。 -
GC19057
Basmisanil
巴米沙尼,RG1662; RO5186582
A negative allosteric modulator of α5 subunit-containing GABAA receptors -
GC19025
AM-0902
AM-0902 是一种有效的选择性瞬时受体电位 A1 (TRPA1) 拮抗剂,对 rTRPA1 和 hTRPA1 的 IC50 分别为 71 和 131 nM。
-
GC19022
AF-353
Ro-4
A dual P2X3 and P2X2/3 receptor antagonist -
GC19021
Adjudin
男用口服避孕药,AF-2364
A derivative of lonidamine -
GC19016
ABT-639
A T-type calcium channel blocker
-
GC19004
SKA-121
A positive-gating modulator of IKCa1/KCa3.1 channels
-
GC19000
BAY-588
A glucose transporter inhibitor
-
GC18947
PF-05089771 (tosylate)
An Nav1.7 channel blocker
-
GC18890
Emamectin B1a
依马菌素B1A
An insecticide -
GC18827
Supercinnamaldehyde
A TRPA1 channel activator
-
GC18762
Remogliflozin A
Remogliflozin A
A potent inhibitor of SGLT2 -
GC18641
Ferutinin
An ERα agonist
-
GC18631
4BP-TQS
An agonist of α7 subunit-containing nAChRs