Home >> Signaling Pathways >> Membrane Transporter/Ion Channel

Membrane Transporter/Ion Channel(跨膜转运)

  1. Cat.No. 产品名称 Information
  2. GC30986 Nicardipine (YC-93)

    尼卡地平; YC-93 free base

    Nicardipine is a potent calcium channel blockader with marked vasodilator action.
  3. 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。
  4. GC30983 alpha-Asarone (α-Asarone)

    α-细辛脑; α-Asarone; trans-Asarone

    An inhibitor of HMG-CoA reductase and CYP450 isoforms
  5. 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。
  6. 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.
  7. GC30961 Mirogabalin besylate (DS 5565 besylate)

    10928苯磺酸盐,DS 5565 besylate

    A calcium channel blocker

  8. 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。

  9. 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。
  10. 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。
  11. GC30946 Procyclidine hydrochloride ((±)-Procyclidine hydrochlorid)

    丙环定盐酸盐; Tricyclamol hydrochloride; (±)-Procyclidine hydrochloride

    A muscarinic acetylcholine receptor antagonist
  12. 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。
  13. GC30933 (+)-Kavain

    醉椒素

    A kavalactone with diverse biological activities
  14. 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
  15. 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.
  16. 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。
  17. 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.
  18. 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。

  19. 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。
  20. GC30898 6-Methylflavone

    6-甲基黄酮

    6-methylflavone是α1β2γ2L和α1β2GABAA受体的激活剂。
  21. 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.
  22. 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.
  23. GC30889 (-)-Securinine

    一叶秋碱

    An alkaloid
  24. GC30873 Mirogabalin (DS5565)

    米洛巴林,DS5565

    A calcium channel blocker
  25. 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。
  26. GC30865 TPA 023 TPA023是GABAAα2/α3的选择性的激动剂,Ki值为0.19-0.41nM。
  27. 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
  28. 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。
  29. GC30852 Org-26576 Org26576是AMPA受体的正变构调节剂。
  30. 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.
  31. GC30847 IC87201 An inhibitor of the nNOS-PSD-95 protein-protein interaction
  32. GC30844 Afloqualone

    氟喹酮; HQ-495

    An Analytical Reference Standard
  33. GC30839 Traxoprodil

    曲索罗地

    An antagonist of NR2B subunit-containing NMDA receptors

  34. 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。
  35. 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。

  36. GC30827 Pipequaline (PK-8165)

    哌夸林,PK-8165

    A partial agonist of central benzodiazepine receptors
  37. GC30818 ZL006 An nNOS/PSD-95 interaction inhibitor
  38. GC30815 Synaptamide (Dehydroepiandrosteron(DHEA))

    DEA, DHEA, Synaptamide

    An endocannabinoid found in brain and retina

  39. GC30813 Raxatrigine hydrochloride (GSK-1014802 hydrochloride)

    GSK-1014802 hydrochloride; CNV1014802 hydrochloride

    An inhibitor of voltage-gated sodium channels
  40. 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。
  41. 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。
  42. 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。
  43. 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.
  44. 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。
  45. 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。

  46. 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。
  47. 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。
  48. GC30546 TRPC6-IN-1 TRPC6-IN-1是TRPC6的一个抑制剂,其EC50值为4.66μM。
  49. GC30537 BPO-27 racemate BPO-27racemate是有效的CFTR抑制剂,IC50值为8nM。
  50. 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。

  51. 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。

Items 1301 to 1350 of 2268 total

per page

Set Descending Direction