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3-Hydroxy-1,5-diphenyl-1-pentanone

CAS# 60669-64-9

3-Hydroxy-1,5-diphenyl-1-pentanone

2D Structure

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3-Hydroxy-1,5-diphenyl-1-pentanone: 5mg Please Inquire In Stock
3-Hydroxy-1,5-diphenyl-1-pentanone: 10mg Please Inquire In Stock
3-Hydroxy-1,5-diphenyl-1-pentanone: 20mg Please Inquire Please Inquire
3-Hydroxy-1,5-diphenyl-1-pentanone: 50mg Please Inquire Please Inquire
3-Hydroxy-1,5-diphenyl-1-pentanone: 100mg Please Inquire Please Inquire
3-Hydroxy-1,5-diphenyl-1-pentanone: 200mg Please Inquire Please Inquire
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3D structure

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3-Hydroxy-1,5-diphenyl-1-pentanone

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Chemical Properties of 3-Hydroxy-1,5-diphenyl-1-pentanone

Cas No. 60669-64-9 SDF Download SDF
PubChem ID 11021438 Appearance Powder
Formula C17H18O2 M.Wt 254.3
Type of Compound Phenols Storage Desiccate at -20°C
Solubility Soluble in Chloroform,Dichloromethane,Ethyl Acetate,DMSO,Acetone,etc.
Chemical Name 3-hydroxy-1,5-diphenylpentan-1-one
SMILES C1=CC=C(C=C1)CCC(CC(=O)C2=CC=CC=C2)O
Standard InChIKey QJUWGGININGVSC-UHFFFAOYSA-N
General tips For obtaining a higher solubility , please warm the tube at 37 ℃ and shake it in the ultrasonic bath for a while.Stock solution can be stored below -20℃ for several months.
We recommend that you prepare and use the solution on the same day. However, if the test schedule requires, the stock solutions can be prepared in advance, and the stock solution must be sealed and stored below -20℃. In general, the stock solution can be kept for several months.
Before use, we recommend that you leave the vial at room temperature for at least an hour before opening it.
About Packaging 1. The packaging of the product may be reversed during transportation, cause the high purity compounds to adhere to the neck or cap of the vial.Take the vail out of its packaging and shake gently until the compounds fall to the bottom of the vial.
2. For liquid products, please centrifuge at 500xg to gather the liquid to the bottom of the vial.
3. Try to avoid loss or contamination during the experiment.
Shipping Condition Packaging according to customer requirements(5mg, 10mg, 20mg and more). Ship via FedEx, DHL, UPS, EMS or other couriers with RT, or blue ice upon request.

Source of 3-Hydroxy-1,5-diphenyl-1-pentanone

The roots of Daphne odora

Biological Activity of 3-Hydroxy-1,5-diphenyl-1-pentanone

Description1. (+)-3-Hydroxy-1,5-diphenyl-1-pentanone exhibits both immunomodulatory and anti-tumor activity.
TargetsImmunology & Inflammation related

3-Hydroxy-1,5-diphenyl-1-pentanone Dilution Calculator

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3-Hydroxy-1,5-diphenyl-1-pentanone Molarity Calculator

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Preparing Stock Solutions of 3-Hydroxy-1,5-diphenyl-1-pentanone

1 mg 5 mg 10 mg 20 mg 25 mg
1 mM 3.9324 mL 19.6618 mL 39.3236 mL 78.6473 mL 98.3091 mL
5 mM 0.7865 mL 3.9324 mL 7.8647 mL 15.7295 mL 19.6618 mL
10 mM 0.3932 mL 1.9662 mL 3.9324 mL 7.8647 mL 9.8309 mL
50 mM 0.0786 mL 0.3932 mL 0.7865 mL 1.5729 mL 1.9662 mL
100 mM 0.0393 mL 0.1966 mL 0.3932 mL 0.7865 mL 0.9831 mL
* Note: If you are in the process of experiment, it's necessary to make the dilution ratios of the samples. The dilution data above is only for reference. Normally, it's can get a better solubility within lower of Concentrations.

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References on 3-Hydroxy-1,5-diphenyl-1-pentanone

A new bicoumarin from Stellera chamaejasme L.[Pubmed:11783587]

J Asian Nat Prod Res. 2001;3(4):335-40.

Thirteen compounds were isolated from roots of Stellera chamaejasme L. (Thymelaeaceae). They are 3-sitosterol (2), simplexin (3), pimelea factor P2 (4), daucosterol (5), (+)-3-Hydroxy-1,5-diphenyl-1-pentanone (6), 4-ethoxy-benzoic acid (7), 2,4,6-Trimethoxy-benzoic acid (8), (+)-afzelechin (9), fumaric acid (10), N,N-dimethyl-L-aspartic acid (11), umbelliferone (12), daphniretin (13) and a novel bicoumarin named bicoumastechamin (1). Among the known compounds, 7, 8, 9, 10 and 11 were first isolated from this plant, and 6 was first isolated from the natural resources. Their structures have been elucidated on the basis of spectral data. In vitro bioassays showed that 4 inhibited cancer cell growth, 13 exhibited immunomodulatory activity, and 6 exhibited both immunomodulatory and anti-tumor activity.

Oleodaphnoic acid and coriaceol, two new natural products from the stem bark of Wikstroemia coriacea.[Pubmed:23462531]

Molecules. 2013 Mar 5;18(3):2988-96.

Fractionation of the chloroform extract of Wikstroemia coriacea led to the isolation of two new compounds, oleodaphnoic acid (1), a guaiane-type sesquiterpenoid, and coriaceol (2), an 1,5-diphenyl-1-pentanone analogue, together with nine known compounds. The structures of 1 and 2 were elucidated by extensive spectroscopic data analysis. The known compounds were oleodaphnal (3), indicanone (4), (5R,8R,8aR)-3,8-dimethyl-4,5,6,7,8,8a-hexahydro-5-(1-methylethenyl)-2(1H)-azuleno ne, (5), 1,5 diphenyl-1-pentanone (6), (+)-3-Hydroxy-1,5-diphenyl-1-pentanone (7), umbelliferone (8), daphnoretin (9), beta-sitostenone (10) and (-)-hinokinin (11).

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