Fraxetin structure
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Common Name | Fraxetin | ||
|---|---|---|---|---|
| CAS Number | 574-84-5 | Molecular Weight | 208.167 | |
| Density | 1.5±0.1 g/cm3 | Boiling Point | 472.0±45.0 °C at 760 mmHg | |
| Molecular Formula | C10H8O5 | Melting Point | 230-232°C | |
| MSDS | Chinese USA | Flash Point | 196.0±22.2 °C | |
| Symbol |
GHS07 |
Signal Word | Warning | |
Use of FraxetinFraxetin is isolated from Cortex Fraxini. Fraxetin has antitumor, anti-oxidation effects and anti-inflammory effects. Fraxetin induces apoptosis[1]. |
| Name | 7,8-dihydroxy-6-methoxychromen-2-one |
|---|---|
| Synonym | More Synonyms |
| Description | Fraxetin is isolated from Cortex Fraxini. Fraxetin has antitumor, anti-oxidation effects and anti-inflammory effects. Fraxetin induces apoptosis[1]. |
|---|---|
| Related Catalog | |
| References |
| Density | 1.5±0.1 g/cm3 |
|---|---|
| Boiling Point | 472.0±45.0 °C at 760 mmHg |
| Melting Point | 230-232°C |
| Molecular Formula | C10H8O5 |
| Molecular Weight | 208.167 |
| Flash Point | 196.0±22.2 °C |
| Exact Mass | 208.037170 |
| PSA | 79.90000 |
| LogP | 0.59 |
| Vapour Pressure | 0.0±1.2 mmHg at 25°C |
| Index of Refraction | 1.648 |
| InChIKey | HAVWRBANWNTOJX-UHFFFAOYSA-N |
| SMILES | COc1cc2ccc(=O)oc2c(O)c1O |
| Storage condition | 2~8°C |
| Symbol |
GHS07 |
|---|---|
| Signal Word | Warning |
| Hazard Statements | H302 + H312 + H332-H315-H319-H335 |
| Precautionary Statements | P261-P280-P305 + P351 + P338 |
| Personal Protective Equipment | dust mask type N95 (US);Eyeshields;Gloves |
| Hazard Codes | Xn: Harmful; |
| Risk Phrases | R20/21/22;R36/37/38 |
| Safety Phrases | S26-S36 |
| RIDADR | NONH for all modes of transport |
| HS Code | 2932209090 |
| Precursor 8 | |
|---|---|
| DownStream 6 | |
| HS Code | 2932209090 |
|---|---|
| Summary | 2932209090. other lactones. VAT:17.0%. Tax rebate rate:13.0%. . MFN tariff:6.5%. General tariff:20.0% |
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[Studies on chemical constituents from stem barks of Fraxinus paxiana].
Zhongguo Zhong Yao Za Zhi 33(16) , 1990-3, (2008) To investigate the chemical constituents of Fraxinus paxiana.The chemical constituents were isolated and purified by chromatographic techniques and the structures of the compounds were identified with... |
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Antihyperglycemic effect of fraxetin on hepatic key enzymes of carbohydrate metabolism in streptozotocin-induced diabetic rats.
Biochimie 95(10) , 1848-54, (2013) Epidemiological studies have demonstrated that the diabetes mellitus is a serious health burden for both governments and healthcare providers. The present study was hypothesized to evaluate the antihy... |
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[Coumarins from branch of Fraxinus sieboldiana and their antioxidative activity].
Zhongguo Zhong Yao Za Zhi 33(14) , 1708-10, (2008) To investigate the chemical constituents from the branch of Fraxinus sieboldiana, and evaluate their antioxidative activity.The chemical constituents were isolated and purified by chromatographic tech... |
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Name: Luminescence-based cell-based primary high throughput screening assay to identify ago...
Source: The Scripps Research Institute Molecular Screening Center
Target: mu-type opioid receptor isoform MOR-1 [Homo sapiens]
External Id: OPRM1-OPRD1_AG_LUMI_1536_1X%ACT PRUN
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Name: QFRET-based biochemical primary high throughput screening assay to identify exosite i...
Source: The Scripps Research Institute Molecular Screening Center
Target: disintegrin and metalloproteinase domain-containing protein 17 preproprotein [Homo sapiens]
External Id: ADAM17_INH_QFRET_1536_1X%INH PRUN
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Name: Induction of apoptosis in human U937 cells assessed as active 11 kDa fragment of casp...
Source: ChEMBL
Target: U-937
External Id: CHEMBL2209386
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Name: ERK5 transcriptional activity HTS
Source: 24565
Target: N/A
External Id: ERK5 transcriptional activity-HTS
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Name: Fluorescence-based cell-based primary high throughput screening assay to identify ago...
Source: The Scripps Research Institute Molecular Screening Center
Target: muscarinic acetylcholine receptor M1 [Homo sapiens]
External Id: CHRM1_AG_FLUO8_1536_1X%ACT PRUN
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Name: Fluorescence polarization to screen for inhibitor that competite the binding of FadD2...
Source: Broad Institute
Target: FATTY-ACID-CoA LIGASE FADD28 (FATTY-ACID-CoA SYNTHETASE)
External Id: 2147-01_Inhibitor_SinglePoint_HTS_Activity
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Name: Cytotoxicity against human U937 cells after 48 hrs by trypan blue assay
Source: ChEMBL
Target: U-937
External Id: CHEMBL2209398
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Name: Antiproliferative activity against human U937 cells assessed as incorporation of [3H]...
Source: ChEMBL
Target: U-937
External Id: CHEMBL2209399
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Name: Inhibition of clonogenic activity in human U937 cells assessed as reduction of colony...
Source: ChEMBL
Target: U-937
External Id: CHEMBL2209396
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Name: Cell cycle arrest in human U937 cells assessed as accumulation at sub-G0/G1 phase at ...
Source: ChEMBL
Target: U-937
External Id: CHEMBL2209397
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| EINECS 209-376-2 |
| 6-methoxy-7,8-dihydroxycoumarin |
| 7,8-Dihydroxy-6-methoxy-2H-chromen-2-one |
| 2H-1-Benzopyran-2-one,7,8-dihydroxy-6-methoxy |
| 7,8-Dihydroxy-6-methoxycoumarin |
| 7,8-dihydroxy-6-methoxy-benzopyran-2-one |
| 7,8-Dihydroxy-6-methoxy-2H-1-benzopyran-2-one |
| Fraxetin |
| MFCD00006873 |