Shopping Cart
  • Remove All
  • TargetMol
    Your shopping cart is currently empty

Otaplimastat HCl

🥰Excellent
Catalog No. T24817LCas No. 1176758-02-3
Alias SP8203 HCl, SP 8203 HCl, Otaplimastat HCl (1176758-04-5 Free base)

Otaplimastat HCl is a matrix metalloproteinase (MMP) inhibitor that blocks NMDA receptor-mediated excitotoxicity competitively and exhibits antioxidant activity,In oxygen-glucose-deprived endothelial cells, otaplimastat suppressed the activity rather than protein expression of MMPs by restoring the level of tissue inhibitor of metalloproteinase (TIMP) suppressed in ischemia, and consequently reduced vascular permeation. serving as a tool for research into brain ischemic injury and neuroprotection.

Otaplimastat HCl

Otaplimastat HCl

🥰Excellent
Purity: 100%
Catalog No. T24817LAlias SP8203 HCl, SP 8203 HCl, Otaplimastat HCl (1176758-04-5 Free base)Cas No. 1176758-02-3
Otaplimastat HCl is a matrix metalloproteinase (MMP) inhibitor that blocks NMDA receptor-mediated excitotoxicity competitively and exhibits antioxidant activity,In oxygen-glucose-deprived endothelial cells, otaplimastat suppressed the activity rather than protein expression of MMPs by restoring the level of tissue inhibitor of metalloproteinase (TIMP) suppressed in ischemia, and consequently reduced vascular permeation. serving as a tool for research into brain ischemic injury and neuroprotection.
Pack SizePriceAvailabilityQuantity
1 mg$195In Stock
5 mg$483In Stock
10 mg$691In Stock
25 mg$1,080In Stock
50 mg$1,490In Stock
100 mg$1,960In Stock
200 mg$2,680In Stock
Add to Cart
Add to Quotation
Bulk & Custom
All TargetMol products are for research purposes only and cannot be used for human consumption. We do not provide products or services to individuals. Please comply with the intended use and do not use TargetMol products for any other purpose.
Questions
View More

Batch Information

Select Batch
Purity:100%
Contact us for more batch information

Resource Download

Product Introduction

Bioactivity
Description
Otaplimastat HCl is a matrix metalloproteinase (MMP) inhibitor that blocks NMDA receptor-mediated excitotoxicity competitively and exhibits antioxidant activity,In oxygen-glucose-deprived endothelial cells, otaplimastat suppressed the activity rather than protein expression of MMPs by restoring the level of tissue inhibitor of metalloproteinase (TIMP) suppressed in ischemia, and consequently reduced vascular permeation. serving as a tool for research into brain ischemic injury and neuroprotection.
In vitro
Otaplimastat HCl (87.5-350 μM, 20 min) can protect neuronal cells through competitive action, preventing NMDA-induced cell death [1].
Otaplimastat HCl (350 μM) is capable of inhibiting calcium ion (Ca²⁺) influx triggered by NMDA receptor activation in primary cultured neurons [1].
When pretreated for 4 hours at concentrations of 2-200 μM, Otaplimastat HCl significantly suppresses hydrogen peroxide (H₂O₂)-induced cell death and reduces reactive oxygen species (ROS) generation [2].
In vivo
In the middle cerebral artery occlusion (MCAO) model, intraperitoneal injection of Otaplimastat HCl (10-20 mg/kg) (administered once 30 minutes before occlusion and once 1 hour after reperfusion) prevented ischemic neuronal death [1].
Daily intraperitoneal injection of Otaplimastat HCl (5-10 mg/kg) for 10 consecutive days alleviated stroke-induced motor function impairment [2].
SynonymsSP8203 HCl, SP 8203 HCl, Otaplimastat HCl (1176758-04-5 Free base)
Chemical Properties
Molecular Weight571.07
FormulaC28H35ClN6O5
Cas No.1176758-02-3
SmilesCl.O=C1NC=2C=CC=CC2C(=O)N1CCCNCCCCN(C(=O)C)CCCN3C(=O)NC=4C=CC=CC4C3=O
Relative Density.no data available
ColorWhite
AppearanceSolid
Storage & Solubility Information
Storagestore at low temperature | Powder: -20°C for 3 years | In solvent: -80°C for 1 year | Shipping with blue ice/Shipping at ambient temperature.

Calculator

  • Molarity Calculator
  • Dilution Calculator
  • Reconstitution Calculator
  • Molecular Weight Calculator

In Vivo Formulation Calculator (Clear solution)

Please enter your animal experiment information in the following box and click Calculate to obtain the mother liquor preparation method and in vivo formula preparation method:
TargetMol | Animal experimentsFor example, your dosage is 10 mg/kg Each animal weighs 20 g, and the dosage volume is 100 μL . TargetMol | Animal experiments A total of 10 animals were administered, and the formula you used is 5% TargetMol | reagent DMSO+30% PEG300+5% Tween 80+60% Saline/PBS/ddH2O. So your working solution concentration is 2 mg/mL。
Mother liquor preparation method: 2 mg of drug dissolved in 50 μL DMSOTargetMol | reagent (mother liquor concentration of 40 mg/mL), if you need to configure a concentration that exceeds the solubility of the product, please contact us first.
Preparation method for in vivo formula: Take 50 μL DMSOTargetMol | reagent main solution, add 300 μLPEG300TargetMol | reagent mix well and clarify, then add 50 more μL Tween 80, mix well and clarify, then add 600 more μLSaline/PBS/ddH2OTargetMol | reagent mix well and clarify
For Reference Only. Please develop an appropriate dissolution method based on your laboratory animals and route of administration.
All types of co-solvents required for the protocol, such asDMSO, PEG300/ PEG400, Tween 80, SBE-β-CD, corn oil are available for purchase on the TargetMol website with a simple click.
1 Enter information below:
mg/kg
g
μL
2 Enter the in vivo formulation:
% DMSO
%
% Tween 80
% Saline/PBS/ddH2O

Dose Conversion

You can also refer to dose conversion for different animals. More Dose Conversion

Sci Citations

Tech Support

Please see Inhibitor Handling Instructions for more frequently ask questions. Topics include: how to prepare stock solutions, how to store products, and cautions on cell-based assays & animal experiments, etc
Related Tags: buy Otaplimastat HCl | purchase Otaplimastat HCl | Otaplimastat HCl cost | order Otaplimastat HCl | Otaplimastat HCl chemical structure | Otaplimastat HCl in vivo | Otaplimastat HCl in vitro | Otaplimastat HCl formula | Otaplimastat HCl molecular weight