MD2-IN-1

MD2-IN-1 Suppliers list
Company Name: ATK CHEMICAL COMPANY LIMITED
Tel: +undefined-21-51877795
Email: ivan@atkchemical.com
Products Intro: Product Name:MD2-IN-1
CAS:111797-22-9
Purity:98% Package:10MG;50MG;100MG,1G,5G,10G.100G
Company Name: career henan chemical co
Tel: +86-0371-86658258 +8613203830695
Email: factory@coreychem.com
Products Intro: Product Name:MD2-IN-1
CAS:111797-22-9
Purity:99.99% Package:1g;1USD
Company Name: InvivoChem
Tel: +1-708-310-1919 +1-13798911105
Email: sales@invivochem.cn
Products Intro: Product Name:MD2-IN-1
CAS:111797-22-9
Purity:98% Package:5mg Remarks:V4032
Company Name: TargetMol Chemicals Inc.
Tel: +1-781-999-5354
Email: support@targetmol.com
Products Intro: Product Name:MD2-IN-1
CAS:111797-22-9
Package:1 mg;10 mg;100 mg;25 mg;5 mg;50 mg Remarks:REAGENT;FOR LABORATORY USE ONLY
Company Name: LEAPCHEM CO., LTD.
Tel: +86-852-30606658
Email: market18@leapchem.com
Products Intro: Product Name:MD2-IN-1
CAS:111797-22-9
Purity:0 Package:1g; 5g; 25g; 1kg; 5kg; 25kg Remarks:0

MD2-IN-1 manufacturers

  • MD2-IN-1
  • MD2-IN-1 pictures
  • $1.00 / 1g
  • 2019-12-24
  • CAS:111797-22-9
  • Min. Order: 1g
  • Purity: 99.99%
  • Supply Ability: 200kg
MD2-IN-1 Basic information
Product Name:MD2-IN-1
Synonyms:MD2-IN-1;MD2 inhibitor 1;MD2-IN-1; MDK7229; MDK 7229; MDK 7229;MDK 7229;MDK7229;2-Propen-1-one, 1-(3,4-dimethoxyphenyl)-3-(3,4,5-trimethoxyphenyl)-;inhibit,Inhibitor,MD2IN1,Toll-like Receptor (TLR),MD-2-IN-1,MD2 IN 1
CAS:111797-22-9
MF:C20H22O6
MW:358.39
EINECS:
Product Categories:
Mol File:111797-22-9.mol
MD2-IN-1 Structure
MD2-IN-1 Chemical Properties
Melting point 131-132 °C
Boiling point 521.3±50.0 °C(Predicted)
density 1.156±0.06 g/cm3(Predicted)
storage temp. Store at -20°C
solubility DMSO : 50 mg/mL (139.51 mM);Water : < 0.1 mg/mL (insoluble)
form Solid
color Light yellow to yellow
Safety Information
MSDS Information
MD2-IN-1 Usage And Synthesis
Biological ActivityMD2-IN-1 is an inhibitor of myeloid differentiation protein 2 (MD2) with a KD value of 189 μM.
in vitro

Myeloid differentiation protein 2 (MD2) is a co-receptor of TLR4. Among those derivatives, MD2-IN-1 (compound 20) shows the strongest inhibitory effect on LPS-induced expression of both TNF-α and IL-6. Compare to the vehicle, LPS alone largely increases the amount of TLR4/MD2 complex, while pretreatment with MD2-IN-1 inhibits the increase of TLR4/MD2 complex to the vehicle level. SPR analysis shows that MD2-IN- 1 exhibits recognizable binding to rhMD2 protein in a dose-dependent manner, with a KD value of 189 μM, while the KD value of xanthohumol binding to MD2 is 460 μM. Pre-treatment with different doses of MD2-IN-1 dose-dependently FITC-LPS binding to MD2 in cell surface membranes reduces FITC-LPS binding to MD2 in cell surface membranes, with a 65% inhibition at 10 μM in terms of mean fluorescence intensity. Pretreatment with MD2-IN-1 also dose-dependently blocks LPS-induced MAPK phosphorylation in the MPMs.

in vivo

Administration of MD2-IN-1 evidently reduces the LPS-induced increase in protein concentrations in BALF. The lung wet/dry weight ratio is markedly higher in the LPS-treated group than the control group, and MD2- IN-1 treatment reduces LPS-induced pulmonary edema. LPS also causes observable lung histopathologic changes, including areas of inflammatory infiltration, hemorrhage, interstitial edema, thickening of the alveolar wall, and lung tissue destruction. These histopathological changes are ameliorated in the MD2- IN-1 treatment group.

target
TargetValue
MD2
()
189 μM(Kd)
MD2-IN-1 Preparation Products And Raw materials
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