TRAM-34

289905-88-0

C22H17ClN2

DMSO : >= 3.5 mg/mL (10.15 mM)

Membrane Transporter/Ion Channel

TRAM-34 is a highly selective blocker of intermediate-conductance calcium-activated K⁺ channel (IKCa1) (K_d=20 nM). IC50 & Target: Kd: 20 nM (IKCa1)^[1] In Vitro: TRAM-34 selectively blocks the IKCa1 current (K_d=25 nM), TRAM-34 also blocks IKCa1 currents in human T84 colonic epithelial cells with equivalent potency (K_d=22 nM). TRAM-34 inhibits the cloned and the native IKCa1 channel in human T lymphocytes with a K_d of 20-25 nM and is 200- to 1, 500-fold selective over other ion channels. The dose-response curve reveals a K_d of 20+/-3 nM and a Hill coefficient of 1.2 with 1 uM calcium in the pipette^[1]. TRAM-34, a specific inhibitor of K_Ca 3.1 channels increased or decreased cell proliferation depending on the concentration. At intermediate concentrations (3-10 uM) TRAM-34 increased cell proliferation, whereas at higher concentrations (20-100 uM) TRAM-34 decreased cell proliferation. The enhancement of cell proliferation caused by TRAM-34 is blocked by the oestrogen receptor antagonists ICI182, 780 and tamoxifen. TRAM-34 also increases progesterone receptor mRNA expression, decreased oestrogen receptor-alpha mRNA expression and reduced the binding of radiolabelled oestrogen to MCF-7 oestrogen receptor, in each case mimicking the effects of 17beta-oestradiol^[2]. In Vivo: Mice (n=5) injected intravenously with a single dose of TRAM-34 (0.5 mg/kg; 29 uM) appeared clinically normal during the 7-day study. The body-weight data of the TRAM-34-treated group (day 1:17.8 g; day 7: 27.0 g) are similar to control mice injected with the vehicle (day 1: 17.4 g; day 7: 23.4 g). Collectively, data from these limited toxicity studies suggest that TRAM-34 is not acutely toxic at ?500-1, 000 times the channel-blocking dose^[1].Treatment with TRAM-34 results in a significant reduction in hematoxylin & eosin (H&E) defined lesion area with the mean infarct size being reduced from 22.6+/-3.6% in the controls (n=8) to 11.3+/-2.8% in rats treated with 10 mg/kg TRAM-34 (n=6, mean+/-s.e.m., P=0.039) and to 8.1+/-1.9% in rats treated with 40 mg/kg TRAM-34 (n=8; P=0.004). The treatment also tended to reduce brain shrinkage. However, the results are only statistically significant with 40 mg/kg TRAM-34 (P=0.013), but not for the 10 mg/kg group (P=0.11)^[3].