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ROCK

ROCK

Los inhibidores de la quinasa asociada a Rho (ROCK) se dirigen a las quinasas ROCK, que están involucradas en la regulación del citoesqueleto, la forma celular y la motilidad. ROCK desempeña un papel significativo en el control de la división celular, particularmente en procesos como la citocinesis. Inhibir ROCK puede provocar cambios en la dinámica del ciclo celular, la motilidad celular y la apoptosis, lo que hace que estos inhibidores sean valiosos en la investigación del cáncer, la neurobiología y los estudios cardiovasculares. En CymitQuimica, ofrecemos una selección de inhibidores de ROCK de alta calidad para apoyar su investigación en biología celular, dinámica del citoesqueleto y mecanismos de enfermedades.

Se han encontrado 67 productos de "ROCK"

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  • GSK429286A

    CAS:
    <p>GSK429286A (RHO-15) is a specific inhibitor of ROCK1/2 (IC50: 14/63 nM).</p>
    Fórmula:C21H16F4N4O2
    Pureza:97.68% - 98.49%
    Forma y color:Solid
    Peso molecular:432.37
  • Y-27632 dihydrochloride

    CAS:
    <p>View and buy Y-27632 dihydrochloride from TargetMol.Y-27632 is a selective inhibitor of ROCKs.Cited in 10 publications.</p>
    Fórmula:C14H21N3O·2HCl
    Pureza:97.96% - 99.98%
    Forma y color:Solid
    Peso molecular:320.26
  • Hydroxyfasudil

    CAS:
    Hydroxyfasudil (Hydroxy-Fasudil) is a ROCK inhibitor(IC50s of 0.73 and 0.72 μM for ROCK1 and ROCK2, respectively).
    Fórmula:C14H17N3O3S
    Pureza:98.13%
    Forma y color:Solid
    Peso molecular:307.37
  • Y-33075

    CAS:
    Y-33075 (Y-39983 free base) is a ROCK inhibitor that lowers IOP, increases blood flow to ONH, and increases the number of RGCs with regenerating axons.
    Fórmula:C16H16N4O
    Pureza:98%
    Forma y color:Solid
    Peso molecular:280.32
  • SB-772077B dihydrochloride

    CAS:
    SB-772077B dihydrochloride is an aminofurazan-based Rho kinase inhibitor (IC50s: 5.6 nM and 6 nM toward ROCK1 and ROCK2, respectively).
    Fórmula:C15H20Cl2N8O2
    Pureza:98%
    Forma y color:Solid
    Peso molecular:415.28
  • CAY10746

    CAS:
    CAY10746 selectively inhibits ROCK I/II with IC50s: 0.014/0.003 μM, useful for diabetic retinopathy research.
    Fórmula:C26H23N3O5
    Pureza:99.71%
    Forma y color:Solid
    Peso molecular:457.48
  • H-1152

    CAS:
    <p>H-1152 is a potent, specific, ATP-competitive, and cell permeable ROCK inhibitor (Ki = 1.6 nM).</p>
    Fórmula:C16H21N3O2S
    Pureza:98%
    Forma y color:Solid
    Peso molecular:319.42
  • AS 1892802

    CAS:
    AS 1892802, a ROCK inhibitor: IC50 - 52nM (hROCK2), 57nM (rROCK2), 122nM (hROCK1). Fast antinociceptive effect similar to Tramadol, Diclofenac.
    Fórmula:C20H19N3O2
    Pureza:99.86%
    Forma y color:Solid
    Peso molecular:333.38
  • Rhodblock 6

    CAS:
    Rhodblock 6 is a Rho kinase inhibitor, blocking phosphorylated MRLC localization by targeting ROCK activity.
    Fórmula:C12H13N3O
    Pureza:99.87%
    Forma y color:Solid
    Peso molecular:215.25
  • CID-5056270

    CAS:
    <p>CID-5056270 has anticancer activity and can inhibit lung cancer, anal cancer, bladder cancer, cervical cancer, vulvar cancer, penile cancer, Burkitt's lymphoma</p>
    Fórmula:C17H13N3O3S
    Pureza:99.6%
    Forma y color:Solid
    Peso molecular:339.37
  • Rho-Kinase-IN-1

    CAS:
    Rho-Kinase-IN-1: ROCK inhibitor, Ki of 30.5 nM (ROCK1) & 3.9 nM (ROCK2), used in research for diseases linked to cell overgrowth and inflammation.
    Fórmula:C20H24N4S
    Pureza:99.8%
    Forma y color:Solid
    Peso molecular:352.5
  • CRT0066854 hydrochloride

    CAS:
    CRT0066854 HCl inhibits atypical PKCs; IC50: PKCι 132 nM, PKCζ 639 nM, ROCK-II 620 nM.
    Fórmula:C24H27Cl2N5S
    Pureza:99.63%
    Forma y color:Solid
    Peso molecular:488.48
  • ROCK-IN-7

    CAS:
    ROCK-IN-7 (compound 9) serves as a ROCK kinase inhibitor and is utilized in the investigation of ocular conditions, including glaucoma and retinal diseases [1].
    Fórmula:C17H17N3O2S
    Pureza:98%
    Forma y color:Solid
    Peso molecular:327.4
  • Chroman 1

    CAS:
    Chroman 1 is a potent inhibitor of ROCK1 (IC50 = 52 pM) and ROCK2 (IC50 = 1 pM).
    Fórmula:C24H28N4O4
    Pureza:99.67% - 99.84%
    Forma y color:Solid
    Peso molecular:436.5
  • ROCK-IN-9

    CAS:
    <p>ROCK-IN-9 (Compound T345), a ROCK inhibitor, exhibits cytotoxicity in HepG2 cells with an IC50 of 40.8 μM.</p>
    Fórmula:C20H20FN5O2
    Pureza:98%
    Forma y color:Solid
    Peso molecular:381.4
  • ROCK2-IN-6 hydrochloride

    CAS:
    ROCK2-IN-6 hydrochloride (Comp A)为一种选择性ROCK2抑制剂,适用于研究ROCK介导的疾病、自身免疫性病症与炎症。
    Fórmula:C26H22ClF2N7O
    Pureza:98%
    Forma y color:Solid
    Peso molecular:521.95
  • ROCK-IN-8

    CAS:
    ROCK-IN-8 (Example 4), a ROCK inhibitor, exhibits anti-inflammatory properties and is suitable for respiratory and gastro-intestinal disease research,
    Fórmula:C30H25FN4O4S
    Pureza:98%
    Forma y color:Solid
    Peso molecular:556.61
  • ROCK2-IN-2

    CAS:
    ROCK2-IN-2 is a selective inhibitor of ROCK2 (IC50 of <1 μM).
    Fórmula:C18H12N6OS
    Pureza:99.65%
    Forma y color:Solid
    Peso molecular:360.39
  • LX7101

    CAS:
    LX7101 is an effective inhibitor of LIMK and ROCK2 (IC50: 24, 1.6, and 10 nM for LIMK1, LIMK2, and ROCK2, respectively). It also inhibits PKA (IC50 <1 nM).
    Fórmula:C23H29N7O3
    Pureza:99.08%
    Forma y color:Solid
    Peso molecular:451.52
  • ROCK-IN-1

    CAS:
    <p>ROCK-IN-1 is a potent ROCK inhibitor that inhibits ROCK2-mediated signaling with an IC50 value of 1.2 nM.ROCK-IN-1 can be used in the study of neurological</p>
    Fórmula:C20H18FN3O
    Pureza:>99.99%
    Forma y color:Solid
    Peso molecular:335.37