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AM 630

AM 630 Structure
  • ₹16161.73 - ₹63964.93
  • Product name: AM 630
  • CAS: 164178-33-0
  • MF: C23H25IN2O3
  • MW: 504.36
  • EINECS:
  • MDL Number:MFCD01861183
  • Synonyms:AM 630;6-IODO-2-METHYL-1-[[2-(4-MORPHOLINYL)ETHYL]-1H-INDOL-3-YL](4-METHOXYPHENYL)METHANONE;SC-200365(AM-630);1-[2-(Morpholin-4-yl)ethyl]-2-Methyl-3-(4-Methoxybenzoyl)-6-iodoindole;(6-iodo-2-Methyl-1-(2-Morpholinoethyl)-1H-indol-3-yl)(4-Methoxyphenyl)Methanone;AM630;AM 630;AM-630;Methanone, [6-iodo-2-methyl-1-[2-(4-morpholinyl)ethyl]-1H-indol-3-yl](4-methoxyphenyl)-;Iodopravadoline (AM630)
2 prices
Selected condition:

Brand

  • Sigma-Aldrich(India)

Package

  • 5MG
  • 25MG
  • ManufacturerSigma-Aldrich(India)
  • Product numberSML0327
  • Product descriptionAM630 ≥90% (HPLC)
  • Packaging25MG
  • Price₹63964.93
  • Updated2022-06-14
  • Buy
  • ManufacturerSigma-Aldrich(India)
  • Product numberSML0327
  • Product descriptionAM630 ≥90% (HPLC)
  • Packaging5MG
  • Price₹16161.73
  • Updated2022-06-14
  • Buy
Manufacturer Product number Product description Packaging Price Updated Buy
Sigma-Aldrich(India) SML0327 AM630 ≥90% (HPLC) 25MG ₹63964.93 2022-06-14 Buy
Sigma-Aldrich(India) SML0327 AM630 ≥90% (HPLC) 5MG ₹16161.73 2022-06-14 Buy

Properties

Boiling point :605.9±55.0 °C(Predicted)
Density :1.49±0.1 g/cm3(Predicted)
storage temp. :2-8°C
solubility :DMSO: >5mg/mL
pka :6.98±0.10(Predicted)
form :powder
color :white to beige

Safety Information

Symbol(GHS): GHS hazard pictograms
Signal word: Warning
Hazard statements:
Code Hazard statements Hazard class Category Signal word Pictogram P-Codes
H410 Very toxic to aquatic life with long lasting effects Hazardous to the aquatic environment, long-term hazard Category 1 Warning GHS hazard pictograms P273, P391, P501
Precautionary statements:
P273 Avoid release to the environment.
P501 Dispose of contents/container to..…

Description

AM-630 is a selective CB2 receptor antagonist that binds to CB1 and CB2 receptors with Ki values of 5.2 μM and 31.2 nM, respectively. AM630 has been shown to display 165-fold selectivity over CB1 receptors and behave as a weak partial/inverse agonist at CB1 receptors. AM-630 acts as an inverse agonist on cloned human CB1 receptors.

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