Catalogue Number
BN-O1627
Analysis Method
HPLC,NMR,MS
Specification
98%(HPLC)
Storage
-20℃
Molecular Weight
442.7
Appearance
Powder
Botanical Source
This product is isolated and purified from the herbs of Lycopodium serratum Thunb.
Structure Type
Triterpenoids
Category
Standards;Natural Pytochemical;API
SMILES
CC1(C2CCC(=C)C(C2(CCC1O)C)CCC3C(=C)CCC4C3(CCC(C4(C)C)O)C)C
Synonyms
(2S,4aR,5S,8aR,2'S,4a'R,5'S,8a'R)-5,5'-(1,2-Ethanediyl)bis(1,1,4a-trimethyl-6-methylenedecahydro-2-naphthalenol)/1-Hydroxymethylmidazolam/1'-Hydroxymidazolam/1-OH-midazolam/1'-hydroxy-MDZ/2-Naphthalenol, 5,5'-(1,2-ethanediyl)bis[decahydro-1,1,4a-trimethyl-6-methylene-, (2S,4aR,5S,8aR,2'S,4'aR,5'S,8'aR)-
IUPAC Name
(2S,4aR,5S,8aR)-5-[2-[(1S,4aR,6S,8aR)-6-hydroxy-5,5,8a-trimethyl-2-methylidene-3,4,4a,6,7,8-hexahydro-1H-naphthalen-1-yl]ethyl]-1,1,4a-trimethyl-6-methylidene-3,4,5,7,8,8a-hexahydro-2H-naphthalen-2-ol
Density
1.0±0.1 g/cm3
Solubility
Soluble in Chloroform,Dichloromethane,Ethyl Acetate,DMSO,Acetone,etc.
Flash Point
210.3±24.7 °C
Boiling Point
524.3±50.0 °C at 760 mmHg
Melting Point
InChl
InChl Key
GESZMTVZGWZBPW-IHIDZKKCSA-N
WGK Germany
RID/ADR
HS Code Reference
2906190000
Personal Projective Equipment
Correct Usage
For Reference Standard and R&D, Not for Human Use Directly.
Meta Tag
provides coniferyl ferulate(CAS#:511-01-3) MSDS, density, melting point, boiling point, structure, formula, molecular weight etc. Articles of coniferyl ferulate are included as well.>> amp version: coniferyl ferulate
No Technical Documents Available For This Product.
12677532
In order to find new acetylcholinesterase inhibitors from natural sources which have therapeutic potential in the treatment of Alzheimer’s disease, the chloroform : methanol (1 : 1) extracts of five Lycopodium species ( L. clavatum L., L. selago L., L. annotinum L., L. alpinum L., and L. complanatum ssp. chamaecyparissus A. (Br.) Doll.), growing in Turkey (Lycopodiaceae), were screened in vitro by the Ellman spectrophotometric method at 1 mg/ml concentration. Among these extracts, only the extract of L. clavatum was found to be active (49.85 %). Bioassay-guided fractionation of the chloroform extract of L. clavatum led to the isolation of alpha-onocerin (IC 50 = 5.2 microM), a well-known triterpenoid, as the responsible compound for the activity.
Alpha-onocerin: an acetylcholinesterase inhibitor from Lycopodium clavatum.
Orhan I1, Terzioglu S, Sener B
2003 Mar
10821066
A detailed NMR and MS analysis of alpha-onocerin was performed in order to provide precise phytochemical reference for structure identification and quality control of this analytical lead compound from Ononis spinosa the roots of which are widely used as a diuretic drug. Unambiguous 1H- and 13C-NMR assignments revealed that the linkage of two subunits were confirmed to possess identical stereochemistries in this triterpenoid.
Comprehensive spectroscopic investigation of alpha-onocerin
Pauli GF
2000 Apr
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