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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)

  • GC16167 structure
    GC16167K 858
    CAS: 72926-24-0
    纯度: >99.50%

    An inhibitor of Eg5

  • GC16182 structure
    GC16182Co 102862
    CAS: 181144-66-1

    Co 102862 (V 102862) 是一种强效、广谱、依赖于状态的 Na+ 通道阻滞剂。

  • GC16188 structure
    GC16188CL 218872
    CAS: 66548-69-4

    An anxiolytic agent

  • GC16199 structure
    GC161998-pCPT-2-O-Me-cAMP-AM
    CAS: 1152197-23-3
    纯度: >97.00%

    Epac activator

  • GC16221 structure
    GC16221Oligomycin C
    CAS: 11052-72-5

    A mitochondrial F 1 F O ATP synthase inhibitor

  • GC16238 structure
    GC16238FGIN-1-43
    CAS: 145040-29-5

    ligand as probe for the mitochondial DBI receptor (peripheral benzodiazepine receptor)

  • GC16240 structure
    GC16240MNI-caged-NMDA
    CAS: 1227675-52-6

    NMDA caged with the photosensitive 4-methoxy-7-nitroindolinyl group

  • GC16254 structure
    GC16254Iberiotoxin
    CAS: 129203-60-7

    Selective blocker of K Ca 1.1/BK channels

  • GC16255 structure
    GC16255Decamethonium Bromide
    CAS: 541-22-0
    纯度: >98.00%

    A depolarizing neuromuscular blocking agent

  • GC16272 structure
    GC16272CGS 19755
    CAS: 110347-85-8
    纯度: >98.00%

    NMDA receptor antagonist

  • GC16300 structure
    GC16300ZK 200775
    CAS: 161605-73-8
    纯度: >99.00%

    ZK 200775 (ZK200775) 是一种高度选择性的 AMPA/红藻氨酸拮抗剂，对 NMDA 几乎没有活性； Ki 值分别为 3.2 nM、100 nM 和 8.5 μ；M 分别针对 quisqualate、红藻氨酸和 NMDA。

  • GC16311 structure
    GC16311Chlormethiazole hydrochloride
    CAS: 6001-74-7
    纯度: >98.00%

    A potentiator of GABA A receptors

  • GC16315 structure
    GC16315D-AP5
    CAS: 79055-68-8
    纯度: >98.00%

    D-AP5是一种选择性N-甲基-D-天门冬胺酸（NMDA）受体拮抗剂，K d 值为1.4μM。

  • GC16322 structure
    GC16322trans-Ned 19
    CAS: 1354235-96-3
    纯度: >99.50%

    An antagonist of NAADP receptors

  • GC16330 structure
    GC16330Ro 51
    CAS: 1050670-85-3

    Ro 51 是一种有效的选择性双重 P2X3/P2X2/3 拮抗剂，对 P2X3 和 P2X2/3 的 IC50 分别为 2 nM 和 5 nM。

  • GC16342 structure
    GC16342PPNDS
    CAS: 1021868-77-8

    PPNDS 是一种选择性和竞争性的 meprin ⋲；抑制剂 (IC50: 80 nM, Ki: 8 nM)，并且还抑制 ADAM10 (IC50: 1.2 μM)。

  • GC16353 structure
    GC16353N-ArachidonylGABA
    CAS: 128201-89-8
    纯度: >98.00%

    A natural arachidonoyl amino acid with analgesic activity

  • GC16354 structure
    GC16354Dequalinium Chloride
    CAS: 522-51-0
    纯度: >99.00%

    An ammonium cation with diverse biological activities

  • GC16356 structure
    GC16356SB 205384
    CAS: 160296-13-9

    positive GABAA receptor modulator

  • GC16359 structure
    GC16359Rosuvastatin
    CAS: 287714-41-4

    Rosuvastatin是一种竞争性HMG-CoA还原酶抑制剂，IC 50 值为11nM。

  • GC16360 structure
    GC16360TP 003
    CAS: 628690-75-5

    GABAA receptor (α3 subtype) partial agonist

  • GC16390 structure
    GC16390Ropivacaine hydrochloride monohydrate
    CAS: 132112-35-7
    纯度: >99.50%

    A sodium channel blocker

  • GC16409 structure
    GC16409Oligomycin B
    CAS: 11050-94-5
    纯度: >85.00%

    A nonselective inhibitor of the mitochondrial F 1 F O ATP synthase

  • GC16419 structure
    GC16419OMDM-2
    CAS: 616884-63-0

    An inhibitor of AEA uptake