Picfeltarraenin IB

Modify Date: 2024-01-08 16:01:01

Picfeltarraenin IB Structure
Picfeltarraenin IB structure
Common Name Picfeltarraenin IB
CAS Number 97230-46-1 Molecular Weight 792.949
Density 1.4±0.1 g/cm3 Boiling Point 895.7±65.0 °C at 760 mmHg
Molecular Formula C42H64O14 Melting Point N/A
MSDS N/A Flash Point 264.0±27.8 °C

 Use of Picfeltarraenin IB


Picfeltarraenin IB, a triterpenoid obtained from Picriafel-terrae Lour (P.fel-terrae), is an acetylcholinesterase (AChE) inhibitor. Picfeltarraenin IB can be used for the treatment of herpes infections, cancer and inflammation[1].

 Names

Name Picfeltarraenin IB
Synonym More Synonyms

 Picfeltarraenin IB Biological Activity

Description Picfeltarraenin IB, a triterpenoid obtained from Picriafel-terrae Lour (P.fel-terrae), is an acetylcholinesterase (AChE) inhibitor. Picfeltarraenin IB can be used for the treatment of herpes infections, cancer and inflammation[1].
Related Catalog
Target

AChE[1]

References

[1]. Wen L, et al. Bioassay- and liquid chromatography/mass spectrometry-guided acetylcholinesterase inhibitors from Picriafel-terrae. Pharmacogn Mag. 2013 Oct;9(Suppl 1):S25-31.

 Chemical & Physical Properties

Density 1.4±0.1 g/cm3
Boiling Point 895.7±65.0 °C at 760 mmHg
Molecular Formula C42H64O14
Molecular Weight 792.949
Flash Point 264.0±27.8 °C
Exact Mass 792.429626
PSA 221.90000
LogP 5.14
Vapour Pressure 0.0±0.6 mmHg at 25°C
Index of Refraction 1.607

 Synonyms

(1R,4R,9β,16α)-16-Hydroxy-9,10,14-trimethyl-11,22-dioxo-20,24-epoxy-4,9-cyclo-9,10-secocholesta-5,23-dien-1-yl 2-O-(6-deoxy-α-L-mannopyranosyl)-β-D-glucopyranoside
(1R,4R,9β,16α)-16-Hydroxy-9,10,14-trimethyl-11,22-dioxo-21,24-epoxy-4,9-cyclo-9,10-secocholesta-5,23-dien-1-yl 2-O-(6-deoxy-α-L-mannopyranosyl)-β-D-glucopyranoside
19-Norlanosta-5,23-diene-11,22-dione, 3-[[2-O-(6-deoxy-α-L-mannopyranosyl)-β-D-glucopyranosyl]oxy]-20,24-epoxy-16-hydroxy-9-methyl-, (3α,9β,10α,16α)-
Estr-5-en-11-one, 3-[[2-O-(6-deoxy-α-L-mannopyranosyl)-β-D-glucopyranosyl]oxy]-17-[(3R)-3,4-dihydro-6-(1-methylethyl)-4-oxo-2H-pyran-3-yl]-16-hydroxy-4,4,9,14-tetramethyl-, (3α,9β,10alph ; a,16α,17β)-
estr-5-en-11-one, 3-[[2-O-(6-deoxy-α-L-mannopyranosyl)-β-D-glucopyranosyl]oxy]-17-[(2R)-2,3-dihydro-2-methyl-5-(1-methylethyl)-3-oxo-2-furanyl]-16-hydroxy-4,4,9,14-tetramethyl-, (3α,9β,10α,16α,17β)-
Estr-5-en-11-one, 3-[[2-O-(6-deoxy-α-L-mannopyranosyl)-β-D-glucopyranosyl]oxy]-17-[(2R)-2,3-dihydro-2-methyl-5-(1-methylethyl)-3-oxo-2-furanyl]-16-hydroxy-4,4,9,14-tetramethyl-, (3α,9β,1 ; 0α,16α,17β)-