DIDYMIN
Synonym(s):(S)-5,7-Dihydroxy-4′-methoxyflavanone-7-β-rutinoside;Isosakuranetin 7-O-rutinoside;Neoponcirin
- CAS NO.：14259-47-3
- Empirical Formula: C28H34O14
- Molecular Weight: 594.56
- MDL number: MFCD00151177
- EINECS: 238-139-6
- SAFETY DATA SHEET (SDS)
- Update Date: 2026-02-02 18:10:39
What is DIDYMIN?
The Uses of DIDYMIN
Neoponcirin is a flavonoid that was shown to exhibit anticancer properties by inducing apoptosis by inhibiting N-Myc and upregulating RKIP in neuroblastoma.
Definition
ChEBI: Didymin is a member of flavonoids and a glycoside.
Properties of DIDYMIN
| Melting point: | 211-213°C |
| Boiling point: | 896.6±65.0 °C(Predicted) |
| Density | 1.59±0.1 g/cm3(Predicted) |
| storage temp. | Inert atmosphere,Room Temperature |
| solubility | DMSO (Sparingly), Methanol (Slightly, Heated, Sonicated) |
| form | neat |
| pka | 7.17±0.40(Predicted) |
| form | Solid |
| color | White to Pale Beige |
| BRN | 1361217 |
| Stability: | Hygroscopic |
Safety information for DIDYMIN
Computed Descriptors for DIDYMIN
New Products
4-Iodo-3,5-dimethylbenzonitrile 2-fluoro-4-iodoaniline 2-(3-Methyl-1,2,4-oxadiazol-5-yl)acetic acid (as potassium salt) 6,6'-methylenebis(9-methyl-3-((2-methyl-1H-imidazol-1-yl)methyl)-2,3-dihydro-1H-carbazol-4(9H)-one) 3-Bromo-2-fluorobenzoic acid Quinuclidine-4-carbonitrile N,N CARBONYL DIIMIDAZOLE 2-Amino-5-bromo-4-(trifluoromethyl)pyridine（RM for Indian lab) (RS)-beta-Amino-beta-(4-bromophenyl)propionic acid Tetrabutylammonium perchlorate N,O-Dimethylhydroxylamine hydrochloride (R)-1-Benzyl-3-pyrrolidinecarbonitrile Bupropian related compound F Lantanoprost rc B Clidinium Bromide Impurity Noradrenaline EP Impurity D/Noradrenaline Methyl Ether Cetirizine EP Impurity A/Cetirizine CBHP Impurity N-Nitroso hydroxy Cetrizine EP Impurity-A 4-(5-amino-1-methyl-1h-benzoimidazol-2-yl)-butyric acid isopropyl ester. 1,4-bis(methylsulfonyl)butane 4-Cyano-N-Methacryloyl-3-Trifluoromethyl Aniline 5-Methyl-1,3-benzenediacetonitrile 4-Fluorothiophenol 1-methyl amino-2,4-dinitro benzeneRelated products of tetrahydrofuran
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