Membrane Transporter/Ion Channel

Membrane Transporter/Ion Channel(跨膜转运)

研究方向

Membrane Transporter/Ion Channel 相关产品(2265)

  • GC60530 structure
    GC605305-Hydroxylansoprazole
    CAS: 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。

  • GC60542 structure
    GC605428-Gingerol
    CAS: 23513-08-8
    纯度: >99.50% / >99.00%

    A natural TRPV1 agonist

  • GC60545 structure
    GC60545A2793
    CAS: 88349-90-0
    纯度: >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 structure
    GC60549ABT-418 hydrochloride
    CAS: 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。

  • GC60596 structure
    GC60596Arecaidine
    CAS: 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。

  • GC60642 structure
    GC60642Bifenthrin
    CAS: 82657-04-3
    纯度: >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 structure
    GC60709Cinnarizine D8
    CAS: 1185242-27-6

    An internal standard for the quantification of cinnarizine

  • GC60718 structure
    GC60718Cloperastine hydrochloride
    CAS: 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.

  • GC60723 structure
    GC60723COR659
    CAS: 544450-68-2
    纯度: >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 structure
    GC60750Dehydrosoyasaponin I
    CAS: 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。

  • GC60834 structure
    GC60834Fenamic acid
    CAS: 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.

  • GC60862 structure
    GC60862GABAA receptor agent 1
    CAS: 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.

  • GC60890 structure
    GC60890Guvacine
    CAS: 498-96-4

    An inhibitor of GABA uptake

  • GC60929 structure
    GC60929Ilaprazole sodium
    CAS: 172152-50-0
    纯度: >98.50%

    A gastric proton pump inhibitor

  • GC60975 structure
    GC60975Lansoprazole Sulfide D4
    CAS: 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 structure
    GC61046Methocarbamol D5
    CAS: 1189699-70-4

    An internal standard for the quantification of methocarbamol

  • GC61066 structure
    GC61066Minoxidil sulfate
    CAS: 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.

  • GC61110 structure
    GC61110Nav1.1 activator 1
    CAS: 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。

  • GC61139 structure
    GC61139Nothofagin
    CAS: 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 structure
    GC61141NSC 15364
    CAS: 4550-72-5
    纯度: >98.00%

    NSC15364是一种VDAC1寡聚化和细胞凋亡(apoptosis)抑制剂。

  • GC61155 structure
    GC61155Omeprazole sodium
    CAS: 95510-70-6
    纯度: >98.00%

    An irreversible inhibitor of the gastric proton pump

  • GC61175 structure
    GC61175PF-06305591 dihydrate
    CAS: 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。

  • GC61186 structure
    GC61186Picrotoxinin
    CAS: 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。

  • GC61248 structure
    GC61248RO2959 monohydrochloride
    CAS: 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。