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
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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。
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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。
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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.
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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。
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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。
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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。
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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。
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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。
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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。
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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。