CasNo.35825-57-1,factory lower price 35825-57-1,(35825-57-1) Suppliers

100 Kilogram	Negotiable

Min.Order :100 Kilogram
Purity: 99%
Payment Terms : L/C,D/A,D/P,T/T,Other

Keywords

(R)-1,2,6,7,8,9-Hexahydro-1,6,6-trimethyl-phenanthro(1,2-b)furan-10,11-dione 35825-57-1 C19H20O3

Quick Details

Appearance:powder
Application:35825-57-1
PackAge:Depended
ProductionCapacity:300|Kilogram|Month
Storage:Refrigerator
Transportation:by air or by sea

Superiority:

(R)-1,2,6,7,8,9-Hexahydro-1,6,6-trimethyl-phenanthro(1,2-b)furan-10,11-dione Basic information

Product Name:	(R)-1,2,6,7,8,9-Hexahydro-1,6,6-trimethyl-phenanthro(1,2-b)furan-10,11-dione
Synonyms:	CRYPTOTANSHINONE;(r)-1,2,6,7,8,9-hexahydro-1,6,6-trimethyl-phenanthro(1,2-b)furan-10,11-dione;TANSHINONE, CRYPTO;98% BY HPLC;CRYPTOTANSHINONE >;TANSHINONE, CRYPTO(P);hexahydro-1,6,6-trimethyl-,(R)-;Phenanthro[1,2-b]furan-10,11-dione,1,2,6,7,8,9-
CAS:	35825-57-1
MF:	C19H20O3
MW:	296.36
EINECS:
Product Categories:	Anthraquinones, Hydroquinones and Quinones;The group of Danshen;Herb extract;chemical reagent;pharmaceutical intermediate;phytochemical;reference standards from Chinese medicinal herbs (TCM).;standardized herbal extract;Inhibitors
Mol File:	35825-57-1.mol

(R)-1,2,6,7,8,9-Hexahydro-1,6,6-trimethyl-phenanthro(1,2-b)furan-10,11-dione Chemical Properties

storage temp.	Store at RT
CAS DataBase Reference	35825-57-1(CAS DataBase Reference)

Safety Information

Hazard Codes	T,N
Risk Statements	25-50/53
Safety Statements	45-60-61

MSDS Information

(R)-1,2,6,7,8,9-Hexahydro-1,6,6-trimethyl-phenanthro(1,2-b)furan-10,11-dione Usage And Synthesis

Chemical Properties	Orange powder
Usage	inhibits angiogenesis
Biological Activity	Major tanshinone isolated from Salvia miltiorrhiza that exhibits multiple activities. Exhibits antitumor activity via inhibition STAT3 activity (IC 50 = 4.6 μ ). Displays antibacterial and anti-inflammatory activity and acts as an antidiabetes and antiobesity agent via activation of AMP-activated protein kinase (AMPK). Also improves cognitive impairment in Alzheimer's disease transgenic mice by inhibition of acetylcholinesterase (IC 50 = 4.09 μ ) and reduction in A β peptide generation.

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