Imperatorin CAS 482-44-0

Introduction:Basic information about Imperatorin CAS 482-44-0, including its chemical name, molecular formula, synonyms, physicochemical properties, and safety information, etc.

Imperatorin Basic informationDescription References

Product Name:Imperatorin
Synonyms:2-g)(1)benzopyran-7-one,9-((3-methyl-2-butenyl)oxy)-7h-furo(;6-hydroxy-7-((3-methyl-2-butenyl)oxy)-5-benzofuranacrylicacidelta-lacto;6-hydroxy-7-((3-methyl-2-butenyl)oxy)-5-benzofuranacrylicacidelta-lactone;6-hydroxy-7-(3-methyl-2-butenyloxy)-5-benzofuranacrylicacidomega-lactone;8-isopentenyloxypsoralene;9-((3-methyl-2-butenyl)oxy)-7h-furo(3,2-g)(1)benzopyran-7-one;9-[(3-methyl-2-butenyl)oxy]-7h-furo[3,2-g][1]benzopyran-7-one;IMPERATORIN
CAS:482-44-0
MF:C16H14O4
MW:270.28
EINECS:207-581-1
Product Categories:Inhibitors;chemical reagent;pharmaceutical intermediate;phytochemical;reference standards from Chinese medicinal herbs (TCM).;standardized herbal extract;Coumarins;Intermediates & Fine Chemicals;Pharmaceuticals
Mol File:482-44-0.mol

Imperatorin Chemical Properties

Melting point 98-100°C
Boiling point 333.4°C (rough estimate)
density 1.1311 (rough estimate)
refractive index 1.4350 (estimate)
storage temp. -20°C
solubility DMSO: ≥5mg/mL
form powder
color off-white to light brown
λmax301nm(MeOH)(lit.)
Merck 14,4925
Major Applicationfood and beverages
InChIInChI=1S/C16H14O4/c1-10(2)5-7-19-16-14-12(6-8-18-14)9-11-3-4-13(17)20-15(11)16/h3-6,8-9H,7H2,1-2H3
InChIKeyOLOOJGVNMBJLLR-UHFFFAOYSA-N
SMILESC1(=O)OC2=C(OC/C=C(\C)/C)C3OC=CC=3C=C2C=C1
LogP2.983 (est)
CAS DataBase Reference482-44-0(CAS DataBase Reference)
NIST Chemistry Reference7H-furo[3,2-g][1]benzopyran-7-one, 9-[(3-methyl-2-butenyl)oxy]-(482-44-0)

Safety Information

Safety Statements 24/25
WGK Germany 3
RTECS LV1575000
HS Code 29419090
Storage Class11 - Combustible Solids
Hazard ClassificationsAcute Tox. 4 Oral
Eye Irrit. 2
Skin Irrit. 2
Skin Sens. 1
STOT SE 3
Hazardous Substances Data482-44-0(Hazardous Substances Data)

Imperatorin Usage And Synthesis

DescriptionImperatorin is a kind of furocoumarin and phytochemical that present in citrus fruits. It could be isolated from Urena lobata L. (Malvaceae). It is biosynthesized from Umbelliferae in vivo. It has been found that it has anti-hypertrophic and anti-convulsant effects, and is useful in the HIV-1 research. Previous studies have shown that Imperatorin requires the transcription factor Sp1 to exert its inhibitory effect on the HIV-1. It can further inhibit the expression of cyclin D1 to cause cell cycle arrest at G1 stage. Moreover, it can suppress the HIV-1 replication inside the primary T lymphocytes and transformed cell lines. This inhibitory effect on HIV-1 can also be effectively observed in the HeLa cells. In addition, it has also been shown that it can cause apoptosis of human promyelocytic leukaemia via the cytochrome c/caspase-9 pathway.
Referenceshttps://www.scbt.com/scbt/product/imperatorin-482-44-0
https://pubchem.ncbi.nlm.nih.gov/compound/imperatorin#section=Top
https://en.wikipedia.org/wiki/Imperatorin
Chemical PropertiesWhite Solid
UsesImperatorin (cas# 482-44-0) is a compound useful in organic synthesis.
DefinitionChEBI: A member of the class of psoralens that is psoralen substituted by a prenyloxy group at position 8. Isolated from Angelica dahurica and Angelica koreana, it acts as a acetylcholinesterase inhibitor.
General DescriptionThis substance is a primary reference substance with assigned absolute purity (considering chromatographic purity, water, residual solvents, inorganic impurities). The exact value can be found on the certificate. Produced by PhytoLab GmbH & Co. KG
Biochem/physiol ActionsImperatorin is a modulator of p38, ERK pathway. Imperatorin increases BMP-2 expression (mRNA) and increases bone density/volume and mineralization in vivo.

Imperatorin Preparation Products And Raw materials

Preparation Products6-Hydroxy-7-methoxy-4-(3-methyl-2-butenyl)-5-benzofuranacrylic acid δ-lactone-->5,8-Dioxopsoralen
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