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6-ISOPROPOXY-9-XANTHONE-2-CARBOXYLIC ACID

6-ISOPROPOXY-9-XANTHONE-2-CARBOXYLIC ACID Structure
  • ₹12925.05
  • Product name: 6-ISOPROPOXY-9-XANTHONE-2-CARBOXYLIC ACID
  • CAS: 33458-93-4
  • MF: C17H14O5
  • MW: 298.29
  • EINECS:
  • MDL Number:MFCD08056083
  • Synonyms:6-ISOPROPOXY-9-OXOXANTHENE-2-CARBOXYLIC ACID;6-ISOPROPOXY-9-XANTHONE-2-CARBOXYLIC ACID;AH 6809;6-(1-Methylethoxy)-9-oxo-9H-xanthene-2-carboxylic acid;6-Isopropoxy-9-oxo-9H-xanthene-2-carboxylic acid;AH6809;AH-6809;9H-Xanthene-2-carboxylic acid, 6-(1-methylethoxy)-9-oxo-;Prostaglandin Receptor,AH-6809,inhibit,Inhibitor,AH6809,AH 6809
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Selected condition:

Brand

  • Sigma-Aldrich(India)

Package

  • 5MG
  • ManufacturerSigma-Aldrich(India)
  • Product numberA1221
  • Product descriptionAH6809 ≥98%, crystalline solid or supercooled liquid
  • Packaging5MG
  • Price₹12925.05
  • Updated2022-06-14
  • Buy
Manufacturer Product number Product description Packaging Price Updated Buy
Sigma-Aldrich(India) A1221 AH6809 ≥98%, crystalline solid or supercooled liquid 5MG ₹12925.05 2022-06-14 Buy

Properties

storage temp. :Sealed in dry,Room Temperature
solubility :ethanol: 2.5 mg/mL, soluble
form :crystalline solid or supercooled liquid
color :White
Stability :Stable for 1 year from date of purchase as supplied. Solutions in DMSO may be stored at -20°C for up to 6 months.

Safety Information

Symbol(GHS):
Signal word:
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Code Hazard statements Hazard class Category Signal word Pictogram P-Codes
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Description

AH 6809 is an EP and DP receptor antagonist with nearly equal affinity for the cloned human EP1, EP2, EP3-III, and DP1 receptors. AH 6809 blocks the PGE2-induced accumulation of cAMP in COS cells transfected with the human EP2 receptor. It also blocks the accumulation of Ca2+ in Xenopus oocytes expressing the human EP1 receptor. In the human and guinea pig, the activity profile of AH 6809 is similar to that of SC-19220, but it is somewhat more potent. In the mouse, AH 6809 has the highest affinity for the EP2 receptor, but also acts as a weak ligand at the murine EP1 and DP1 receptors. In whole human platelets, AH 6809 is an effective antagonist of the antiaggregatory actions of PGD2, but not PGI2, with an EC50 of about 5 x 10?5 M.

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