5-hydroxy-1,7-diphenyl-3-heptanoneCAS# 55836-43-6 |
| Cas No. | 55836-43-6 | SDF | File under preparation. |
| PubChem ID | 562075.0 | Appearance | Powder |
| Formula | C19H22O2 | M.Wt | 282.4 |
| Type of Compound | N/A | Storage | Desiccate at -20°C |
| Solubility | Soluble in Chloroform,Dichloromethane,Ethyl Acetate,DMSO,Acetone,etc. | ||
| Chemical Name | 5-hydroxy-1,7-diphenylheptan-3-one | ||
| SMILES | C1=CC=C(C=C1)CCC(CC(=O)CCC2=CC=CC=C2)O | ||
| Standard InChIKey | CCNKTMMNRPJQHV-UHFFFAOYSA-N | ||
| Standard InChI | InChI=1S/C19H22O2/c20-18(13-11-16-7-3-1-4-8-16)15-19(21)14-12-17-9-5-2-6-10-17/h1-10,18,20H,11-15H2 | ||
| 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. |
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| 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. |
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| 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. | ||
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5-hydroxy-1,7-diphenyl-3-heptanone Dilution Calculator
5-hydroxy-1,7-diphenyl-3-heptanone Molarity Calculator
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5-Hydroxy-7-(4'-hydroxy-3'-methoxyphenyl)-1-phenyl-3-heptanone (DHPA)Catalog No.: BCN8791CAS No.: 79559-61-8 -
(R)-5-Hydroxy-7-(4-hydroxy-3-methoxyphenyl)-1-phenylheptan-3-oneCatalog No.: BCN0534CAS No.: 68622-73-1 -
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(S)-3-Hydroxy-1,5-diphenylpentan-1-oneCatalog No.: BCX0187CAS No.: 163086-00-8 -
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| 1 mg | 5 mg | 10 mg | 20 mg | 25 mg | |
| 1 mM | 3.5411 mL | 17.7054 mL | 35.4108 mL | 70.8215 mL | 88.5269 mL |
| 5 mM | 0.7082 mL | 3.5411 mL | 7.0822 mL | 14.1643 mL | 17.7054 mL |
| 10 mM | 0.3541 mL | 1.7705 mL | 3.5411 mL | 7.0822 mL | 8.8527 mL |
| 50 mM | 0.0708 mL | 0.3541 mL | 0.7082 mL | 1.4164 mL | 1.7705 mL |
| 100 mM | 0.0354 mL | 0.1771 mL | 0.3541 mL | 0.7082 mL | 0.8853 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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DPHC from Alpinia officinarum Hance specifically modulates the function of CENPU in the cell cycle and apoptosis to ameliorate hepatocellular carcinoma.[Pubmed:40058474]
J Ethnopharmacol. 2025 Apr 9;345:119598.
ETHNOPHARMACOLOGICAL RELEVANCE: Alpinia officinarum Hance (A. officinarum), a perennial herb used in the treatment of digestive system cancers, holds significant value for the Li people of Hainan as a traditional Chinese medicine. (R)-5-hydroxy-1,7-diphenyl-3-heptanone (DPHC), a diarylheptanoid component is derived from A. officinarum. Diarylheptanoids have demonstrated anti-proliferative effects on breast cancer cells, neuroblastoma cells, and other tumor cells. However, the pharmacological activity of DPHC in improving hepatocellular carcinoma (HCC) remains undefined. AIM OF THE STUDY: To elucidate the anti-HCC effects of DPHC derived from A. officinarum and explore its underlying mechanistic pathways both in vivo and in vitro. MATERIAL AND METHODS: The effects of DPHC on HCC cell lines were evaluated in vitro using cell counting kit-8, EdU cell proliferation assays, a wound healing assay, a three-dimensional tumor spheroid model, and flow cytometry. The ability of DPHC to ameliorate HCC was assessed in vivo via a nude mouse subcutaneous xenograft tumor model, serum biochemical marker detection, and hematoxylin-eosin staining. The molecular mechanism of DPHC in HCC was elucidated through a combination of transcriptome sequencing, cell transfection, immunohistochemistry assay, immunofluorescence staining, quantitative reverse transcription-PCR, and western blot analysis. RESULTS: DPHC induced significant G0/G1 phase arrest and apoptosis in HepG2 and HCCLM3 cells while also markedly inhibiting tumor growth in nude mice. Mechanically, DPHC directly interacted with centromere-associated protein U (CENPU) to suppress its expression. The reduced expression of CENPU results in decreased interaction with the transcription factor E2F6, thereby affecting the transcriptional activity of the transcription factor E2F1. This subsequently inhibits the expression of downstream cell cycle factors (CCND1, CDK4, and CDK1) and increases apoptosis factors (Caspase 3 and Caspase 9). CONCLUSIONS: DPHC from A. officinarum specifically modulates the function of CENPU in the cell cycle and apoptosis to ameliorate HCC. Our study revealed the anti-HCC effect and underlying mechanism of DPHC, offering new insights and potential targets for HCC treatment.
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