1. Signaling Pathways
  2. PI3K/Akt/mTOR
  3. Akt
  4. Akt Isoform



Akt Related Products (89):

Cat. No. Product Name Effect Purity
  • HY-B0988
    Deferoxamine mesylate
    Activator 99.86%
    Deferoxamine mesylate (Deferoxamine B mesylate) is an iron chelator (binds to Fe(III) and many other metal cations), is widely used to reduce iron accumulation and deposition in tissues.
  • HY-N2117
    Inhibitor 99.73%
    Isoginkgetin is a pre-mRNA splicing inhibitor inhibitor.
  • HY-15457
    Inhibitor 99.81%
    Triciribine is a DNA synthesis inhibitor, also inhibits Akt and HIV-1/2 with IC50 of 130 nM, and 0.02-0.46 μM, respectively.
  • HY-18100A
    PRE-084 hydrochloride
    Activator 99.79%
    PRE-084 hydrochloride is a highly selective σ1 receptor (S1R) agonist, with an IC50 of 44 nM.
  • HY-B0789
    Inhibitor 98.05%
    SU6656 is a Src family kinases inhibitor with IC50s of 280, 20, 130, 170 nM for Src, Yes, Lyn, and Fyn, respectively.
  • HY-W016412
    Coenzyme Q0
    Inhibitor ≥99.0%
    Coenzyme Q0 (CoQ0) is a potent, oral active ubiquinone compound can be derived from Antrodia cinnamomea.
  • HY-119152
    CMX-2043 is a novel analogue of α-Lipoic Acid (HY-N0492).
  • HY-13065
    Inhibitor 99.01%
    Isobavachalcone (Corylifolinin) is derived from Psoralea corylifolia Linn.
  • HY-15477
    Activator 99.92%
    YS-49 is a PI3K/Akt (a downstream target of RhoA) activator, to reduce RhoA/PTEN activation in the 3-methylcholanthrene-treated cells.
  • HY-N0047
    Polyphyllin I
    Inhibitor 99.61%
    Polyphyllin I is a bioactive constituent extracted from Paris polyphylla, has strong anti-tumor activity.
  • HY-18686
    Inducer 99.90%
    AS1949490 is a potent, orally active, selective SHIP2 phosphatase inhibitor with IC50 values of 0.34, 0.62, 13, >50, >50, and >50 µM for Mouse SHIP2, Human SHIP2, Human SHIP1, Human PTEN, Human synaptojanin, and Human myotubularin, respectively.
  • HY-15985
    Inhibitor 99.46%
    CTX-0294885 is a broad spectrum kinase inhibitor that can capture 235 kinases from MDA-MB-231 cells, and can capture all members of the AKT family.
  • HY-14971
    (E)-Akt inhibitor-IV
    Inhibitor 98.61%
    (E)-Akt inhibitor-IV ((E)-AKTIV) is a PI3K-Akt inhibitor, with potent cytotoxic.
  • HY-N0261
    Aurantio-obtusin is an anthraquinone isolated from Semen Cassiae, with anti-Inflammatory, anti-oxidative, anti-coagulating and anti-hypertension activities.
  • HY-P0093A
    Sincalide ammonium
    Modulator 99.90%
    Sincalide ammonium (Cholecystokinin octapeptide ammonium, CCK-8 ammonium) is a rapid-acting amino acid polypeptide hormone analogue of cholecystokinin (CCK) for intravenous use in postevacuation cholecystography.
  • HY-15673
    Inhibitor 99.52%
    KP372-1 is an Akt inhibitor that inhibits proliferation and induces apoptosis and anoikis.
  • HY-P1844A
    Chemerin-9 (149-157) (TFA)
    Inducer 99.64%
    Chemerin-9 (149-157) TFA is a potent agonist of chemokine-like receptor 1 (CMKLR1) .
  • HY-N2110
    Phellopterin is a natural product isolated from Angelica dahurica.
  • HY-N0107
    Cyclovirobuxine D
    Inhibitor 99.36%
    Cyclovirobuxine D (CVB-D) is the main active component of the traditional Chinese medicine Buxus microphylla.
  • HY-124674A
    CCT365623 hydrochloride
    Inhibitor 98.11%
    CCT365623 hydrochloride is an orally active lysyl oxidase (LOX) inhibitor, with an IC50 of 0.89 μM.