Compositions of small molecules, matrices, and isolated cells including methods of preparation, and methods for differentiation, trans-differentiation, and proliferation of animal cells into the osteoblast blast cell lineage were described. Examples of osteogenic materials that were administered to cells or co-cultured with cells are represented by compounds of Formula II, IV, and VI independently or preferably in combination with a matrix to afford bone cells. Small molecule-stimulated cells were also combined with a matrix, placed with a cellular adhesive or material carrier and implanted to a site in an animal for bone repair. Matrix pretreated with compounds of Formula II, IV, and VI were also used to cause cells to migrate to the matrix that is of use for therapeutic purposes.

Compositions of small molecules, matrices, and isolated cells including methods of preparation, and methods for differentiation, trans-differentiation, and proliferation of animal cells into the osteoblast blast cell lineage were described. Examples of osteogenic materials that were administered to cells or co-cultured with cells are represented by compounds of Formula II, IV, and VI independently or preferably in combination with a matrix to afford bone cells. Small molecule-stimulated cells were also combined with a matrix, placed with a cellular adhesive or material carrier and implanted to a site in an animal for bone repair. Matrix pretreated with compounds of Formula II, IV, and VI were also used to cause cells to migrate to the matrix that is of use for therapeutic purposes.

The present invention provides a fluorescent resveratrone [(E)-4-(6,8-dihydroxynaphthalen-2-yl)but-3-en-2-one] and its derivatives having Formula 1 and a method for preparing the same by a photochemical reaction of resveratrol and its derivatives which are not fluorescent having Formula 7 or Formula 8. The new fluorescent compounds of the present invention has single-photon absorptive characteristics and/or two-photon absorptive characteristics as well as no or little toxicity according to a cytotoxicity test and can be usefully utilized in the field of organic fluorescent element, display element, spectrometer, two-photon absorptive storing device, laser micro processing apparatus, photo dynamic therapy apparatus and the like.

The present invention provides a fluorescent resveratrone [(E)-4-(6,8-dihydroxynaphthalen-2-yl)but-3-en-2-one] and its derivatives having Formula 1 and a method for preparing the same by a photochemical reaction of resveratrol and its derivatives which are not fluorescent having Formula 7 or Formula 8. The new fluorescent compounds of the present invention has single-photon absorptive characteristics and/or two-photon absorptive characteristics as well as no or little toxicity according to a cytotoxicity test and can be usefully utilized in the field of organic fluorescent element, display element, spectrometer, two-photon absorptive storing device, laser micro processing apparatus, photo dynamic therapy apparatus and the like.

Provided herein are substituted 1,2,3,4-tetrahydro-1,1-biphenyl compounds and methods of making same.

Provided herein are substituted 1,2,3,4-tetrahydro-1,1-biphenyl compounds and methods of making same.

Provided are synthesis processes and intermediates for preparing cannabinoids and analogs.

Provided are synthesis processes and intermediates for preparing cannabinoids and analogs.

It is an object of the present invention to provide a composition having an anti-inflammatory action.

The anti-inflammatory composition of the present invention comprises, as an active ingredient, a compound represented by the following Formula 1. In the following Formula 1, R.sub.1 represents hydrogen or a hydroxy group, and A represents a phenyl group optionally substituted with a hydroxyl group or a methyl group, or a cyclohexenyl group substituted with a hydroxyl group and a methylene group.

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It is an object of the present invention to provide a composition having an anti-inflammatory action.

The anti-inflammatory composition of the present invention comprises, as an active ingredient, a compound represented by the following Formula 1. In the following Formula 1, R.sub.1 represents hydrogen or a hydroxy group, and A represents a phenyl group optionally substituted with a hydroxyl group or a methyl group, or a cyclohexenyl group substituted with a hydroxyl group and a methylene group.

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