- DELPHINIDIN CHLORIDE
-
- $100.00
-
2019-07-06
- CAS:528-53-0
- Min. Order: 1MG
- Purity: 98%
- Supply Ability: 1KG /Month or Customized
- DELPHINIDIN CHLORIDE
-
- $100.00
-
2019-07-06
- CAS:528-53-0
- Min. Order: 1MG
- Purity: 98%
- Supply Ability: 1KG /Month or Customized
|
| | Delphinidin chloride Basic information |
| Product Name: | Delphinidin chloride | | Synonyms: | 3,5,7-trihydroxy-2-(3,4,5-trihydroxyphenyl)-1-benzopyryliuchloride;3,5,7-trihydroxy-2-(3,4,5-trihydroxyphenyl)-1-benzopyryliumchloride;3’,4’,5,5’,7-hexahydroxy-flavyliumchloride;delfinidolchloride;delphinidine;delphinidol;ephdine;2-(3,4,5-trihydroxyphenyl)-1-benzopyrylium-3,5,7-triol | | CAS: | 528-53-0 | | MF: | C15H11ClO7 | | MW: | 338.7 | | EINECS: | 208-437-0 | | Product Categories: | Flavonoids;Aromatics;Heterocycles;Intermediates & Fine Chemicals;Pharmaceuticals;Anthocyanins | | Mol File: | 528-53-0.mol |  |
| | Delphinidin chloride Chemical Properties |
| Melting point | >349.85°C | | Boiling point | 454.94°C (rough estimate) | | density | 1.3946 (rough estimate) | | refractive index | 1.4429 (estimate) | | storage temp. | −20°C | | solubility | Methanol (Slightly) | | form | Solid | | color | Blue-Red to Black | | Major Application | food and beverages | | InChI | InChI=1S/C15H10O7.ClH/c16-7-3-9(17)8-5-12(20)15(22-13(8)4-7)6-1-10(18)14(21)11(19)2-6;/h1-5H,(H5-,16,17,18,19,20,21);1H | | InChIKey | FFNDMZIBVDSQFI-UHFFFAOYSA-N | | SMILES | C1(=C(O)C=C2C(O)=CC(O)=CC2=[O+]1)C1=CC(=C(O)C(O)=C1)O.[Cl-] |
| WGK Germany | 3 | | RTECS | DK1310000 | | F | 10-21 | | HS Code | 29072990 | | Storage Class | 11 - Combustible Solids |
| | Delphinidin chloride Usage And Synthesis |
| Description | Delphinidin (chloride) is an anthocyanidin, a natural plant pigment which serves as the precursor of certain anthocyanins that provide the blue-red colors of flowers, fruits, and red wine. Delphinidin induces the release of nitric oxide by vascular endothelium, causing vasorelaxation. It also inhibits signaling through epithelial growth factor receptors, suppressing the expression of estrogen receptor α and inducing both apoptosis and autophagy at a dose of 1-40 μM. Delphinidin also inhibits the histone acetyltransferase activities of p300/CBP (IC50 = ~ 30 μM). | | Chemical Properties | Soluble in organic solvents such as methanol, ethanol, and DMSO, derived from rhododendron and raspberry. | | Uses | Delphinidin Chloride is an anthocyanidin; antioxidant. Delphinidin Chloride is a pigment found in grapes, cranberries, and pomegranates. | | Definition | ChEBI: Delphinidin chloride is an anthocyanidin chloride that has delphinidin as the cationic counterpart. It contains a delphinidin. | | Biotechnological Production | Methods for extracting delphinidin chloride from plants. Commonly used extraction methods include solvent extraction, ultrasonic extraction, and microwave-assisted extraction. Among these, solvent extraction is the most commonly used method, which utilizes organic solvents to extract delphinidin chloride from plants, followed by concentration and drying steps to obtain the pure product. | | target | VEGFR | | References | [1] TIMOTHY A. HOLTON. Cloning and expression of cytochrome P450 genes controlling flower colour[J]. Nature, 1993, 366 6452: 276-279. DOI:10.1038/366276a0.
[1] EMILE ANDRIAMBELOSON . Natural Dietary Polyphenolic Compounds Cause Endothelium-Dependent Vasorelaxation in Rat Thoracic Aorta12[J]. Journal of Nutrition, 1998, 128 12: Pages 2324-2333. DOI:10.1093/jn/128.12.2324.
[1] TUBA OZBAY Rita N. Delphinidin Inhibits HER2 and Erk1/2 Signaling and Suppresses Growth of HER2-Overexpressing and Triple Negative Breast Cancer Cell Lines.[J]. Breast Cancer : Basic and Clinical Research, 2011, 5: 143-154. DOI:10.4137/BCBCR.S7156.
[1] HARINI S. AIYER*. Influence of Berry Polyphenols on Receptor Signaling and Cell-Death Pathways: Implications for Breast Cancer Prevention[J]. Journal of Agricultural and Food Chemistry, 2012, 60 23: 5693-5708. DOI:10.1021/jf204084f.
[1] AH-REUM SEONG . Delphinidin, a specific inhibitor of histone acetyltransferase, suppresses inflammatory signaling via prevention of NF-κB acetylation in fibroblast-like synoviocyte MH7A cells[J]. Biochemical and biophysical research communications, 2011, 410 3: Pages 581-586. DOI:10.1016/j.bbrc.2011.06.029.
[1] B. GABETTA G. P P Morazzoni. Synthesis of Delphinidin Chloride (IdB 1056), A Potent Free-Radicals Scavenger Endowed with Microvascular Protective Activity[J]. Planta medica, 1990, 56 1: 694-695. DOI:10.1055/s-2006-961376. |
| | Delphinidin chloride Preparation Products And Raw materials |
| Raw materials | 5-(2-acetoxyacetyl)benzene-1,2,3-triyl triacetate-->Ethanone, 2-chloro-1-[3,4,5-tris(acetyloxy)phenyl]--->Benzoyl chloride, 3,4,5-tris(acetyloxy)--->3,4,5-TRIACETOXYBENZOIC ACID-->2-formyl-3,5-dihydroxyphenyl benzoate-->2,4,6-TRIHYDROXYBENZALDEHYDE-->Gallic acid | | Preparation Products | D-glucose |
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