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1031206-36-6

1031206-36-6 Structure

1031206-36-6 Structure
IdentificationBack Directory
[Name]

3-[1-(3-Hydroxy-4-methoxyphenyl)-meth-(E)-ylidene]-6-methyl-chroman-4-one
[CAS]

1031206-36-6
[Synonyms]

IMS2186
IMS2186, 10 mM in DMSO
(E)-3-(3-Hydroxy-4-methoxybenzylidene)-6-methylchroman-4-one
3-[1-(3-Hydroxy-4-methoxyphenyl)-meth-(E)-ylidene]-6-methyl-chroman-4-one
(3E)-2,3-Dihydro-3-[(3-Hydroxy-4-Methoxyphenyl)Methylene]-6-Methyl-4H-1-Benzopyran-4-One
4H-1-Benzopyran-4-one, 2,3-dihydro-3-[(3-hydroxy-4-methoxyphenyl)methylene]-6-methyl-, (3E)-
[Molecular Formula]

C18H16O4
[MDL Number]

MFCD12912419
[MOL File]

1031206-36-6.mol
[Molecular Weight]

296.32
Chemical PropertiesBack Directory
[Boiling point ]

535.7±50.0 °C(Predicted)
[density ]

1.286±0.06 g/cm3(Predicted)
[storage temp. ]

room temp
[solubility ]

DMSO: >20mg/mL
[form ]

solid
[pka]

9.39±0.10(Predicted)
[color ]

white to off-white
Safety DataBack Directory
[Hazard Codes ]

N
[Risk Statements ]

50/53
[Safety Statements ]

60-61
[RIDADR ]

UN 3077 9 / PGIII
[WGK Germany ]

3
Hazard InformationBack Directory
[Uses]

IMS2186 is an anti-prileferative and anti-angiogenic compound.
[Biological Activity]

IMS2186 is an anti-proliferative and anti-angiogenic agent. Apparently IMS2186 blocks the cell cycle at G2 and inhibits the production of PGE2/TNF-α. IMS2186 inhibits cell growth in vitro in tumor cells, non-transformed fibroblasts, and retinal pigment epithelial cells. IMS2186 inhibits angiogenesis (IC50 = 0.1 μM) and cell migration. Intraocular injection of IMS2186 could be a long-lasting effective treatment for CNV (choroidal neovascularization) in AMD (age-related macular degeneration) with a reduction in scarring and related visual loss.
[in vivo]

IMS2186 (2.5 mg in 0.5 mL; intravitreal injection; single dose) has no ocular toxicity while applied to rabbit eyes[1].
IMS2186 (100 μg/eye, i.e. 2.0 μL of the solution of 50 μg/μL; single dose) shows anti-proliferative effect on laser-induced choroidal neovascularization (CNV) rat models[1].

Animal Model:Rat model of laser induced CNV[1]
Dosage:100 μg/eye, 2.0 μL of the solution of 50 μg/μL
Administration:Intravitreal injection; single dose
Result:Resulted 30% reduction of lesion area compared to PBS in the lesion area measurement.
Spectrum DetailBack Directory
[Spectrum Detail]

3-[1-(3-Hydroxy-4-methoxyphenyl)-meth-(E)-ylidene]-6-methyl-chroman-4-one(1031206-36-6)1HNMR
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