Xanthoxylin structure
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Common Name | Xanthoxylin | ||
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CAS Number | 90-24-4 | Molecular Weight | 196.200 | |
Density | 1.2±0.1 g/cm3 | Boiling Point | 355.1±37.0 °C at 760 mmHg | |
Molecular Formula | C10H12O4 | Melting Point | 80-84 °C(lit.) | |
MSDS | Chinese USA | Flash Point | 141.2±20.0 °C |
Use of XanthoxylinXanthoxylin (Xanthoxyline) is isolated from Zanthoxylum simulans. Xanthoxylin (Xanthoxyline) has antifungal and antispasmodic activities[1][2]. |
Name | 4',6'-Dimethoxy-2'-hydroxyacetophenone |
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Synonym | More Synonyms |
Description | Xanthoxylin (Xanthoxyline) is isolated from Zanthoxylum simulans. Xanthoxylin (Xanthoxyline) has antifungal and antispasmodic activities[1][2]. |
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Related Catalog | |
References |
Density | 1.2±0.1 g/cm3 |
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Boiling Point | 355.1±37.0 °C at 760 mmHg |
Melting Point | 80-84 °C(lit.) |
Molecular Formula | C10H12O4 |
Molecular Weight | 196.200 |
Flash Point | 141.2±20.0 °C |
Exact Mass | 196.073563 |
PSA | 55.76000 |
LogP | 2.37 |
Vapour Pressure | 0.0±0.8 mmHg at 25°C |
Index of Refraction | 1.528 |
Personal Protective Equipment | Eyeshields;Gloves;type N95 (US);type P1 (EN143) respirator filter |
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Risk Phrases | R36/37/38 |
Safety Phrases | S26-S36/37/39 |
RIDADR | NONH for all modes of transport |
WGK Germany | 3 |
HS Code | 2914509090 |
Precursor 10 | |
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DownStream 10 | |
HS Code | 2914509090 |
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Summary | HS:2914509090 other ketones with other oxygen function VAT:17.0% Tax rebate rate:9.0% Supervision conditions:none MFN tariff:5.5% General tariff:30.0% |
Collateral sensitivity of resistant MRP1-overexpressing cells to flavonoids and derivatives through GSH efflux.
Biochem. Pharmacol. 90(3) , 235-45, (2014) The multidrug resistance protein 1 (MRP1) is involved in multidrug resistance of cancer cells by mediating drug efflux out of cells, often in co-transport with glutathione (GSH). GSH efflux mediated b... |
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Antinociceptive action of 2-(4-bromobenzoyl)-3-methyl-4,6-dimethoxy benzofuran, a novel xanthoxyline derivative on chemical and thermal models of nociception in mice.
J. Pharmacol. Exp. Ther. 278(1) , 304-12, (1996) The antinociceptive effect of the novel xanthoxyline derivative 2-(4-bromobenzoyl)-3-methyl-4-6-dimethoxy benzofuran) (BMDB), given i.p., p.o., s.c., subplantarly, intrathecally or by i.c.v. routes wa... |
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Synthesis of chalcone analogues with increased antileishmanial activity.
Bioorg. Med. Chem. 14(5) , 1538-45, (2006) Eighteen analogues of an active natural chalcone were synthesized using xanthoxyline and some derivatives, and these analogues were tested for selective activity against both promastigotes and intrace... |
2-HYDROXY-4,6-DIMETHOXYACETOPHENONE |
MFCD00017243 |
Brevifolin (VAN) |
EINECS 201-978-3 |
4,6-Dimethoxy-2-hydroxyacetophenone |
Phloracetophenone 4,6-Dimethyl Ether |
2,4-Dimethoxy-6-hydroxyacetophenone |
Acetophenone, 2'-hydroxy-4',6'-dimethoxy- |
Ethanone, 1-(2-hydroxy-4,6-dimethoxyphenyl)- |
1-(2-Hydroxy-4,6-dimethoxyphenyl)ethanone |