| Identification | Back Directory | [Name]
AM 630 | [CAS]
164178-33-0 | [Synonyms]
AM 630
CS-1545
AM630;AM 630
SC-200365(AM-630)
6-Iodopravadoline
AM630;AM 630;AM-630
Iodopravadoline (AM630)
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
6-IODO-2-METHYL-1-[[2-(4-MORPHOLINYL)ETHYL]-1H-INDOL-3-YL](4-METHOXYPHENYL)METHANONE
Methanone, [6-iodo-2-methyl-1-[2-(4-morpholinyl)ethyl]-1H-indol-3-yl](4-methoxyphenyl)- | [Molecular Formula]
C23H25IN2O3 | [MDL Number]
MFCD01861183 | [MOL File]
164178-33-0.mol | [Molecular Weight]
504.36 |
| Chemical Properties | Back Directory | [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 | [form ]
powder | [pka]
6.98±0.10(Predicted) | [color ]
white to beige | [InChI]
1S/C23H25IN2O3/c1-16-22(23(27)17-3-6-19(28-2)7-4-17)20-8-5-18(24)15-21(20)26(16)10-9-25-11-13-29-14-12-25/h3-8,15H,9-14H2,1-2H3 | [InChIKey]
JHOTYHDSLIUKCJ-UHFFFAOYSA-N | [SMILES]
COc1ccc(cc1)C(=O)c2c(C)n(CCN3CCOCC3)c4cc(I)ccc24 |
| Safety Data | Back Directory | [Hazard Codes ]
N | [Risk Statements ]
50 | [Safety Statements ]
61 | [RIDADR ]
UN 3077 9 / PGIII | [WGK Germany ]
3 | [Storage Class]
11 - Combustible Solids | [Hazard Classifications]
Aquatic Acute 1
Aquatic Chronic 1 |
| Hazard Information | Back Directory | [Uses]
AM 630 acts as a potential CB2 receptor cannabinoid antagonist with application towards human lung cancer treatment and angiogenesis induction. | [Definition]
ChEBI: [6-iodo-2-methyl-1-[2-(4-morpholinyl)ethyl]-3-indolyl]-(4-methoxyphenyl)methanone is a N-acylindole. | [Biological Activity]
CB 2 antagonist/inverse agonist (K i = 31.2 nM) that displays 165-fold selectivity over CB 1 receptors. Behaves as a weak partial/inverse agonist at CB 1 receptors. | [Biochem/physiol Actions]
AM630 is an aminoalkylindole and acts as a competitive antagonist of CP 55,940 and WIN 55,212-2. It also behaves as a competitive antagonist of anandamide and (R)-(+)-arachidonyl-1′-hydroxy-2′-propylamide (AM356). | [storage]
Desiccate at +4°C | [References]
1. ross r a, brockie h c, stevenson l a, et al. agonist-inverse agonist characterization at cb1 and cb2 cannabinoid receptors of l759633, l759656 and am630. british journal of pharmacology, 1999, 126(3): 665-672. 2. patil m, patwardhan a, salas m m, et al. cannabinoid receptor antagonists am251 and am630 activate trpa1 in sensory neurons. neuropharmacology, 2011, 61(4): 778-788. |
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J & K SCIENTIFIC LTD.
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China Langchem Inc.
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0086-21-58956006 |
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LETOPHARM LIMITED
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+86-21-5821 5861 |
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Sigma-Aldrich
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SPIRO PHARMA
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www.spiropharma.com.cn |
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parabiochem
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025-83453382-8005 |
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www.parabiochem.cn |
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