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Imperatorin

Description References
Imperatorin
Imperatorin
CAS No.
482-44-0
Chemical Name:
Imperatorin
Synonyms
AMMIDIN;Marmelide;Pentosalen;MARMELOSIN;NSC 402949;IMPERATORIN;8-ISOAMYLEN;AKOS 214-72;Enoxypsoralen;Baizhi Extract
CBNumber:
CB5355754
Molecular Formula:
C16H14O4
Formula Weight:
270.28
MOL File:
482-44-0.mol

Imperatorin 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. 
2-8°C
solubility 
DMSO: ≥5mg/mL
form 
powder
color 
off-white to light brown
λmax
301nm(MeOH)(lit.)
Merck 
14,4925
CAS DataBase Reference
482-44-0(CAS DataBase Reference)
NIST Chemistry Reference
7H-furo[3,2-g][1]benzopyran-7-one, 9-[(3-methyl-2-butenyl)oxy]-(482-44-0)

SAFETY

Safety Statements  24/25
WGK Germany  3
RTECS  LV1575000
HS Code  29419090
Hazardous Substances Data 482-44-0(Hazardous Substances Data)

Imperatorin price More Price(10)

Manufacturer Product number Product description CAS number Packaging Price Updated Buy
Sigma-Aldrich I6659 Imperatorin ≥98% (HPLC), powder 482-44-0 5mg $114 2018-11-13 Buy
Sigma-Aldrich 55193 Imperatorin analytical standard 482-44-0 10mg $121 2018-11-13 Buy
TCI Chemical I0904 Imperatorin >98.0%(HPLC) 482-44-0 25mg $100 2018-11-22 Buy
TCI Chemical I0904 Imperatorin >98.0%(HPLC) 482-44-0 100mg $276 2018-11-22 Buy
Cayman Chemical 26070 Imperatorin ≥98% 482-44-0 10mg $60 2018-11-19 Buy

Imperatorin Chemical Properties,Uses,Production

Description

Imperatorin 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.

References

https://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 Properties

White Solid

Definition

ChEBI: 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.

Imperatorin Preparation Products And Raw materials

Raw materials

Preparation Products


Imperatorin Suppliers

Global( 156)Suppliers
Supplier Tel Fax Email Country ProdList Advantage
Shenzhen Sendi Biotechnology Co.Ltd.
0755-23311925 18102838259
0755-23311925 Abel@chembj.com CHINA 3217 55
Henan DaKen Chemical CO.,LTD.
+86-371-55531817
info@dakenchem.com CHINA 22049 58
Henan Tianfu Chemical Co.,Ltd.
0371-55170693
0371-55170693 info@tianfuchem.com CHINA 20786 55
Mainchem Co., Ltd.
+86-0592-6210733
+86-0592-6210733 sales@mainchem.com CHINA 32651 55
Hubei Jusheng Technology Co.,Ltd.
86-155-27864001
peter@hubeijusheng.com CHINA 18004 58
Chengdu Biopurify Phytochemicals Ltd.
18080483897
maggie@biopurify.com CHINA 2238 58
Shanghai Zheyan Biotech Co., Ltd.
18017610038
zheyansh@163.com CHINA 3624 58
ShangHai YuanYe Biotechnology Co., Ltd. 021-61312847 qq:2797782341
021-55068248 2797782341@qq.com China 7590 60
Sichuan Wei Keqi Biological Technology Co., Ltd. 028-81700200 QQ:2851167785
028-81705658 2851167785@qq.com China 2701 56
J & K SCIENTIFIC LTD. 400-666-7788 +86-10-82848833
+86-10-82849933 jkinfo@jkchemical.com;market6@jkchemical.com China 96815 76

482-44-0(Imperatorin)Related Search:


  • 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
  • MARMELOSIN
  • 8-ISOAMYLEN
  • 8-ISOAMYLENOXYPSORALEN
  • AKOS 214-72
  • AMMIDIN
  • Enoxypsoralen
  • Pentosalen
  • 8-Isopentenyloxypsoralen
  • 9-(3-Methylbut-2-enyloxy)-7H-furo[3,2-g]chromen-7-one
  • IMPERATORIN WITH HPLC
  • 9-[(3-Methyl-2-butenyl)-oxy]-7H-furo[3,2-γ],[1][benzopyran-7-one
  • 8-isopent-2-enyloxy-6,7-furanocoumarin
  • Marmelide
  • 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
  • 482-44-0
  • 482-4-0
  • C16H14O4
  • Coumarins
  • Intermediates & Fine Chemicals
  • Pharmaceuticals
  • chemical reagent
  • pharmaceutical intermediate
  • phytochemical
  • reference standards from Chinese medicinal herbs (TCM).
  • standardized herbal extract
  • Inhibitors
  • Ammidin, Marmelide, Marmelosin, NSC 402949, 9-[(3-Methyl-2-buten-1-yl)oxy]-7h-furo[3,2-g][1]benzopyran-7-one
  • Imperatorin,8-Isopentenyloxypsoralen
  • 9-(3-methylbut-2-enoxy)furo[3,2-g]chromen-7-one
  • MARMELOSIN (IMPERATORIN)(RG)
  • 9-[(3-Methyl-2-buten-1-yl)oxy]-7h-furo[3,2-g][1]benzopyran-7-one
  • NSC 402949
  • MARMELOSIN (IMPERATORIN)
  • AMMidin,8-Isopentenyloxypsoralen
  • Imperatorin, >=98%
  • Ammidin Marmelide Marmelosin NSC 402949
  • Baizhi Extract
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