Malvidin chloride structure
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Common Name | Malvidin chloride | ||
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| CAS Number | 643-84-5 | Molecular Weight | 366.75000 | |
| Density | 1.183 g/mL at 25 °C(lit.) | Boiling Point | 66-67 °C(lit.) | |
| Molecular Formula | C17H15ClO7 | Melting Point | N/A | |
| MSDS | Chinese USA | Flash Point | 30 °F | |
Use of Malvidin chlorideMalvidin (chloride) is a bioactive compound isolated from Oryza sativacv. Heugjinjubyeo. Malvidin shows cytotoxicity through the arrest of the G2/M phase of cell cycle and induction of apoptosis. Malvidin can be used for the research of cancer[1]. |
This table lists Chinese names, IUPAC names and various aliases of this chemical substance.
| Name | Malvidin chloride |
|---|---|
| Synonym | More Synonyms |
This table contains bioactivity, target information and biological‑assay experimental data of this compound.
| Description | Malvidin (chloride) is a bioactive compound isolated from Oryza sativacv. Heugjinjubyeo. Malvidin shows cytotoxicity through the arrest of the G2/M phase of cell cycle and induction of apoptosis. Malvidin can be used for the research of cancer[1]. |
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| Related Catalog | |
| In Vitro | Malvidin (0~80 μg/mL; 96 hours; U937 cells) shows cytotoxic activity in a dose-dependent pattern[1]. The IC50 value of Malvidin for U937 cells is 40 μg/mL. Malvidin (U937 cells) shows arrest at the G2/M phase of the cell cycle and increases sub G1 hypo-diploid population[1]. Cell Viability Assay[1] Cell Line: U937 cells Concentration: 0~80 μg/mL Incubation Time: 96 hours Result: Showed cytotoxic activity in a dose-dependent pattern. |
| References |
This table shows physicochemical parameters including melting point, boiling point, density, solubility and optical rotation. Missing data is marked as N/A.
| Density | 1.183 g/mL at 25 °C(lit.) |
|---|---|
| Boiling Point | 66-67 °C(lit.) |
| Molecular Formula | C17H15ClO7 |
| Molecular Weight | 366.75000 |
| Flash Point | 30 °F |
| Exact Mass | 366.05100 |
| PSA | 112.52000 |
| LogP | 0.22450 |
| Index of Refraction | n20/D 1.335(lit.) |
| InChIKey | KQIKOUUKQBTQBE-UHFFFAOYSA-N |
| SMILES | COc1cc(-c2[o+]c3cc(O)cc(O)c3cc2O)cc(OC)c1O.[Cl-] |
| Storage condition | ?20°C |
This table provides MSDS information including hazard classification, first‑aid, fire‑fighting, spill handling, operation and storage instructions.
This table summarizes toxicological test data, acute & chronic toxicity and ecological hazard parameters for this chemical.
CHEMICAL IDENTIFICATION
HEALTH HAZARD DATAACUTE TOXICITY DATA
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This table covers safety warnings, protective measures, incompatible substances and disposal guidelines for this compound.
| Personal Protective Equipment | Eyeshields;Gloves;type N95 (US);type P1 (EN143) respirator filter |
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| RIDADR | NONH for all modes of transport |
| WGK Germany | 3 |
| RTECS | LK9900000 |
| HS Code | 2909499000 |
This table presents publicly reported synthetic routes, reaction conditions, reactants and product information of the compound.
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Malvidin chloride CAS#:643-84-5 |
| Literature: Tetrahedron Letters, , vol. 23, # 38 p. 3963 - 3964 |
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Malvidin chloride CAS#:643-84-5 |
| Literature: Tetrahedron Letters, , vol. 23, # 38 p. 3963 - 3964 |
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Malvidin chloride CAS#:643-84-5 |
| Literature: Tetrahedron Letters, , vol. 23, # 38 p. 3963 - 3964 |
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Malvidin chloride CAS#:643-84-5 |
| Literature: Phytochemistry, , vol. 70, # 5 p. 672 - 674 |
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Malvidin chloride CAS#:643-84-5 |
| Literature: Phytochemistry, , vol. 70, # 5 p. 672 - 674 |
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Malvidin chloride CAS#:643-84-5 |
| Literature: Journal of the Chemical Society, , p. 1551 |
This table lists upstream starting materials and downstream derivative products related to this chemical.
| Precursor 5 | |
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| DownStream 2 | |
This table shows customs‑related data including HS‑code, tariff and regulatory conditions for import and export.
| HS Code | 2909499000 |
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| Summary | 2909499000. ether-alcohols and their halogenated, sulphonated, nitrated or nitrosated derivatives. VAT:17.0%. Tax rebate rate:9.0%. . MFN tariff:5.5%. General tariff:30.0% |
This table lists relevant public references with title, journal and publication metadata for this compound.
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A nicotinic receptor-mediated anti-inflammatory effect of the flavonoid rhamnetin in BV2 microglia.
Fitoterapia 98 , 11-21, (2014) The alpha7 nicotinic acetylcholine receptor (nAChR) is a potential target in neuroinflammation. Screening a plant extract library identified Solidago nemoralis as containing methyl-quercetin derivativ... |
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How subtle is the "terroir" effect? Chemistry-related signatures of two "climats de Bourgogne".
PLoS ONE 9(5) , e97615, (2014) The chemical composition of grape berries is influenced by various environmental conditions often considered to be representative of a "terroir". If grapes from a given terroir are assumed to reflect ... |
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Direct and indirect inactivation of tumor cell protective catalase by salicylic acid and anthocyanidins reactivates intercellular ROS signaling and allows for synergistic effects.
Carcinogenesis 36(3) , 400-11, (2015) Salicylic acid and anthocyanidins are known as plant-derived antioxidants, but also can provoke paradoxically seeming prooxidant effects in vitro. These prooxidant effects are connected to the potenti... |
This table contains target information, in‑vitro & in‑vivo assay data for this compound.
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Name: ABTS radical scavenging activity assessed as vitamin C equivalent antioxidant capacit...
Source: ChEMBL
Target: N/A
External Id: CHEMBL1070370
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Name: Antioxidant activity assessed as trolox equivalent by TEAC assay
Source: ChEMBL
Target: NON-PROTEIN TARGET
External Id: CHEMBL1070368
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Name: Inhibition of LPS-stimulated ROS production in mouse RAW264.7 cells preincubated for ...
Source: ChEMBL
Target: RAW264.7
External Id: CHEMBL4034120
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This table collects all English aliases, systematic names and CAS‑related synonyms of the compound.
| MFCD00017585 |
| 2-(4-hydroxy-3,5-dimethoxyphenyl)chromenylium-3,5,7-triol,chloride |
| EINECS 211-403-8 |
This section contains frequently‑asked‑questions about this compound, including basic parameters, properties, storage conditions and corresponding answers.
| Q: What is the polar surface area (PSA) of Malvidin chloride? |
| A: Polar surface area (PSA) of Malvidin chloride is 112.52000. |
| Q: What is the molecular weight of Malvidin chloride? |
| A: Molecular weight of Malvidin chloride is 366.75000. |
| Q: What is the CAS number of Malvidin chloride? |
| A: CAS number of Malvidin chloride is 643-84-5. |
| Q: What English synonyms does Malvidin chloride have? |
| A: English synonyms of Malvidin chloride: MFCD00017585, 2-(4-hydroxy-3,5-dimethoxyphenyl)chromenylium-3,5,7-triol,chloride, EINECS 211-403-8. |
| Q: What is the LogP of Malvidin chloride? |
| A: LogP of Malvidin chloride is 0.22450. |
| Q: What are the uses of Malvidin chloride? |
| A: Main uses of Malvidin chloride: Malvidin (chloride) is a bioactive compound isolated from Oryza sativacv. Heugjinjubyeo. Malvidin shows cytotoxicity through the arrest of the G2/M phase of cell cycle and induction of apoptosis. Malvidin can be used for the research of cancer[1]. |
| Q: What is the InChIKey of Malvidin chloride? |
| A: InChIKey of Malvidin chloride is KQIKOUUKQBTQBE-UHFFFAOYSA-N. |
| Q: What is the SMILES notation of Malvidin chloride? |
| A: SMILES notation of Malvidin chloride is COc1cc(-c2[o+]c3cc(O)cc(O)c3cc2O)cc(OC)c1O.[Cl-]. |
| Q: What is the English name of Malvidin chloride? |
| A: The English name of Malvidin chloride is Malvidin chloride. |
| Q: What are the downstream products of Malvidin chloride? |
| A: Related downstream products(CAS) of Malvidin chloride: 530-57-4;6318-20-3. |
This table lists manufacturers and suppliers of this compound, including vendor names and product supply reference information.
| Shanghai Nianxing Industrial Co., Ltd |
| Dayang Chem (Hangzhou) Co., Ltd. |
| naturewill |