GLPBio

SL-327

Catalog No.: GC15359Purity:>98.00%
SL-327 is a selective inhibitor of MEK1 and MEK2, with IC50 values of 0.18μM and 0.22μM, respectively.

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SL-327
Cas No.: 305350-87-2
10mM (in 1mL DMSO)In Stock
$30.00
1
5mgIn Stock
$28.00
1
10mgIn Stock
$35.00
1
25mgIn Stock
$56.00
1
50mgIn Stock
$84.00
1
100mgIn Stock
$140.00
1

Citations

1 publicationsPublications from researchers using this product

Description

SL-327 is a selective inhibitor of MEK1 and MEK2, with IC50 values of 0.18μM and 0.22μM, respectively[1]. SL-327 can be used to study the role of the MAPK signaling pathway in interictal spikes and behavior in epileptic rats[2]. SL-327 can penetrate the blood-brain barrier and produce neuroprotective effects in mice with ischemic brain injury[3].

In vitro, treatment of melanoma cells (MV3 and A375 cells) with SL-327 (1.25µM) for 48h restored the cell growth curve inhibited by TBMS1 treatment, restored the cell colony formation ability inhibited by TBMS1, and reversed the high expression levels of LC3B-II and p62 induced by TBMS1[4].

In vivo, SL-327 (20mg/kg) administered by intraperitoneal injection to male Swiss albino CD1 middle-aged mice blocked the positive effects of growth hormone (GH) on the mice in the radial arm maze test[5]. SL-327 (1, 5mg/kg) administered by intraperitoneal injection to Swiss mice followed by behavioral testing induced anxiolytic behavior in the mice, and the anxiolytic properties were particularly significant in combination with diazepam in the elevated plus maze (EPM) test[6].

References:
[1] Moranta D, Esteban S, García‐Sevilla J A. Acute, chronic and withdrawal effects of the cannabinoid receptor agonist WIN55212‐2 on the sequential activation of MAPK/Raf‐MEK‐ERK signaling in the rat cerebral frontal cortex: short‐term regulation by intrinsic and extrinsic pathways[J]. Journal of neuroscience research, 2007, 85(3): 656-667.
[2] Glazova M V, Nikitina L S, Hudik K A, et al. Inhibition of ERK 1/2 signaling prevents epileptiform behavior in rats prone to audiogenic seizures[J]. Journal of neurochemistry, 2015, 132(2): 218-229.
[3] Wang X, Wang H, Xu L, et al. Significant neuroprotection against ischemic brain injury by inhibition of the MEK1 protein kinase in mice: exploration of potential mechanism associated with apoptosis[J]. The Journal of pharmacology and experimental therapeutics, 2003, 304(1): 172-178.
[4] Du J, Dong Z, Tan L, et al. Tubeimoside I inhibits cell proliferation and induces a partly disrupted and cytoprotective autophagy through rapidly hyperactivation of MEK1/2-ERK1/2 cascade via promoting PTP1B in melanoma[J]. Frontiers in cell and developmental biology, 2020, 8: 607757.
[5] Ramis M, Sarubbo F, Sola J, et al. Cognitive improvement by acute growth hormone is mediated by NMDA and AMPA receptors and MEK pathway[J]. Progress in Neuro-Psychopharmacology and Biological Psychiatry, 2013, 45: 11-20.
[6] Michalak A, Wnorowski A, Berardinelli A, et al. Diazepam and SL-327 synergistically attenuate anxiety-like behaviours in mice–Possible hippocampal MAPKs specificity[J]. Neuropharmacology, 2020, 180: 108302.

Protocol

Animal experiment [1]:

Animal models

Male Swiss albino CD1 middle-age mice

Preparation Method

Male Swiss albino CD1 middle-age mice were used. Groups of mice were treated with saline and Growth hormone (GH) (1mg/kg i.p.) 1h before the working memory tests. A different group of mice was injected with the MEK inhibitor SL-327 (20mg/kg dissolved in dimethyl sulfoxide, i.p.) 30min before the administration of GH to compare with the effect of GH alone in mice.

Dosage form

20mg/kg; i.p.

Applications

Mice treated with GH showed a reduction in the number of errors (unvisited arms or re-visited arms) in the radial arm maze test. However, intraperitoneal injection of the MEK inhibitor SL-327 30min before GH administration blocked the positive effects of GH on the radial arm maze test.

References:
[1] Ramis M, Sarubbo F, Sola J, et al. Cognitive improvement by acute growth hormone is mediated by NMDA and AMPA receptors and MEK pathway[J]. Progress in Neuro-Psychopharmacology and Biological Psychiatry, 2013, 45: 11-20.

Product Documents

Purity:>98.00%Appearance:A solid

Chemical Properties

CAS No.
305350-87-2
Chemical Name
(Z)-3-amino-3-(4-aminophenyl)sulfanyl-2-[2-(trifluoromethyl)phenyl]prop-2-enenitrile
SMILES
C1=CC=C(C(=C1)C(=C(N)SC2=CC=C(C=C2)N)C#N)C(F)(F)F
Molecular Formula
C16H12F3N3S
Molecular Weight
335.35
Solubility
≥ 16.75mg/mL in DMSO
Storage
Store at -20°C
General tips
Select a suitable solvent according to the product solubility data. Once prepared, aliquot the stock solution to avoid repeated freeze-thaw cycles.
Use stock solutions within 6 months when stored at -80°C or within 1 month when stored at -20°C.
To improve solubility, warm the tube to 37°C and sonicate it for an appropriate period.
Shipping Condition
Evaluation samples are shipped with blue ice. Other available sizes are shipped at room temperature or with blue ice upon request.

CalculatorsMolarity / Dilution / Molecular Weight / Unit Conversion / In Vivo Formulation / Solubility

g/mol

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