| Company Name: |
Tcichem, Inc. |
| Tel: |
13918644899 |
| Email: |
81587635@qq.com |
7-Methyl-juglone manufacturers
- Ramentaceone
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- $2380.00
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2026-05-21
- CAS:14787-38-3
- Purity:
- Supply Ability: 10g
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| | 7-Methyl-juglone Basic information |
| Product Name: | 7-Methyl-juglone | | Synonyms: | 5-Hydroxy-7-methyl-1,4-naphthoquinone;6-Methyl-8-hydroxy-1,4-naphthoquinone;7-Methyl-5-hydroxynaphthalene-1,4-dione;Ramentaceone;7-Methyl-5-hydroxy-1,4-naphthoquinone;5-Hydroxy-7-methyll-,1,4-naphtoquinone;Aids108047;Aids-108047 | | CAS: | 14787-38-3 | | MF: | C11H8O3 | | MW: | 188.18 | | EINECS: | | | Product Categories: | | | Mol File: | 14787-38-3.mol |  |
| | 7-Methyl-juglone Chemical Properties |
| Melting point | 125.5-126.5 °C | | Boiling point | 427.2±45.0 °C(Predicted) | | density | 1.44 g/cm3 | | storage temp. | 2-8°C | | pka | 6.66±0.20(Predicted) |
| | 7-Methyl-juglone Usage And Synthesis |
| Uses | Ramentaceone (7-Methyljuglon), a naphthoquinone that can be isolated from Drosera sp., inhibits PI3K activity. Ramentaceone (7-Methyljuglon) reduces the expression of the PI3K protein and inhibits the phosphorylation of the Akt protein in breast cancer cells. Ramentaceone (7-Methyljuglon) induces apoptosis[1]. | | Definition | ChEBI: Ramentaceone is a hydroxy-1,4-naphthoquinone. | | Synthesis Reference(s) | The Journal of Organic Chemistry, 49, p. 3766, 1984 DOI: 10.1021/jo00194a017 | | References | [1] Anna Kawiak, et al. Ramentaceone, a Naphthoquinone Derived from Drosera sp., Induces Apoptosis by Suppressing PI3K/Akt Signaling in Breast Cancer Cells. PLoS One. 2016 Feb 3;11(2):e0147718. DOI:10.1371/journal.pone.0147718 |
| | 7-Methyl-juglone Preparation Products And Raw materials |
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