Oligospirostanoside, pharmaceutical composition containing...

Details Oligospirostanoside, pharmaceutical composition containing... Oligospirostanoside, pharmaceutical composition containing...

2002-03-20

2003-11-18

Wilson, James O. (Department: 1623)

Organic compounds -- part of the class 532-570 series

Organic compounds

Carbohydrates or derivatives

C514S026000

Reexamination Certificate

active

06649745

ABSTRACT:

FIELD OF THE INVENTION
Accordingly, the present invention provides a novel oligospirostanoside of formula 1,3-0-[&agr;-L-rhamnopyranosyl-(1→2)-&agr;-L-rhamnopyranosyl-(1→4)-0-&bgr;-D-glucopyranosyl]-25(S)-5&bgr;-spirostan-3&bgr;-ol of the formula below:
BACKGROUND OF THE INVENTION
The Ayurvedic crude drug, Shatavari comprises decorticated roots of
Asparagus racemosus
wild [Kanitkar, U. K., Dange, P. S. and Pendse, G. S.
J. Res. Indian Med
. 3 (1969) 123
; Medicinal Plants of India
vol. 1, ed. by Satyavati, G. V., Raina, M. K. and Sharma, M. Indian Council of Medical Research, New Delhi (1976) 101].
Phytochemical investigations of the plant
Asparagus racemosus
, have resulted in isolation and characterization of steroidal glycosides [Ravikumar, P. R., Soman, R., Chetty, G. L. Pandey, R. C. and Sukhdev,
Indian J. Chem
. 26 B (1987) 1012, Kar, Deepak Kumar and Sen Sumitra,
Cell Chromosome Res
. 7 (1984) 10], a novel cage type pyrrolizidine alkaloid, asparaginine [Sekine, T., Fukasawa, N., Kashiwagi, Y., Ruangrungsi, N. and Murakoshi, I,
Chem. Pharm. Bull
. 42 (1994) 1360] and a 9,10-dihydrophenanthrene derivative [Sekine, T., Fukasawa, N., Murakoshi, I. and Ruangrungsi,
N. Phytochemistry
, 44 (1997) 763].
OBJECTS OF THE INVENTION
The main object of the present invention is to provide a novel oligospirostanoside.
Another object of the invention is to provide and characterize a novel sarsasapogenin glycoside Immunoside, an oligospirostanoside isolated from aqueous extract of
Asparagus racemosus
, present in the range of 0.0023-0.0045% w/w in the dried plant material.
Yet another object of the present invention is to provide a process for isolation of a novel oligospirostanoside from
Asparagus racemosus.
SUMMARY OF THE INVENTION
Accordingly, the present invention provides a novel oligospirostanoside of formula 1, 3-0-[&agr;-L-rhamnopyranosyl-(1→2)-&agr;-L-rhamnopyranosyl-(1→4)-0-&bgr;-D-glucopyranosyl]-25(S)-5&bgr;-spirostan-3&bgr;-ol of the formula 1 below:
The present invention also relates to a process for isolation of immunoside, 3-0-[&agr;-L-rhamnopyranosyl-(1→2)-&agr;-L-rhamnopyranosyl-(1→4)-0-&bgr;-D-glucopyranosyl]-25(S)-5&bgr;-spirostan-3&bgr;-ol of the formula 1 below which comprises:
In one embodiment of the invention, the clarified extract is obtained by filtering or centrifugation.
In another embodiment of the invention, the clarified extract is subjected to desolventation in a spray dryer, hot air oven or a rotavapour at 50±5° C.
In a further embodiment of the invention, the dry residue of step (e) is resolved into pure constituents in step (f) by adsorption, gel permeation chromatography using isotropic or graded elution, reverse phase purification on Lichroprep RP-8 or pooling and distillation of TLC homogeneous fractions (Rf 0.53, EtOAc:MeOH:H
2
O::75:13.5:10) under reduced pressure.
In a further embodiment of the invention, the dry residue obtained at the end of step (e) is repeatedly crystallised using methanol or ethanol to get pure immunoside.
The present invention also relates to a pharmaceutical composition comprising an effective amount of the novel oligospirostanoside 3-0-[&agr;-L-rhamnopyranosyl-(1→2)-&agr;-L-rhamnopyranosyl-(1&Dgr;4)-0-&bgr;-D-glucopyranosyl]-25(S)-5&bgr;-spirostan-3&bgr;-ol contained in a pharmaceutically acceptable carrier.
In one embodiment of the invention, the amount of 3-0-[&agr;-L-rhamnopyranosyl-(1→2)-&agr;-L-rhamnopyranosyl-(1→4)-0-&bgr;-D-glucopyranosyl]-25(S)-5&bgr;-spirostan-3&bgr;-ol is in the range of 0.006 to 0.0125 mg per kg of body weight of subject to be treated.
The present invention also provides a method for immunomodulation in a immune suppressed animal comprising administering a pharmaceutically effective amount of 3-0-[&agr;-L-rhamnopyranosyl-(1→2)-&agr;-L-rhamnopyranosyl-(1→4)-0-&bgr;-D-glucopyranosyl]-25(S)-5&bgr;-spirostan-3&bgr;-ol.
In one embodiment of the invention, the amount of 3-0-[&agr;-L-rhamnopyranosyl-(1→2)-&agr;-L-rhamnopyranosyl-(1→4)-0-&bgr;-D-glucopyranosyl]-25(S)-5&bgr;-spirostan-3&bgr;-ol administered to the said animal comprises 0.006 to 0.0125 mg per kilogram of body weight of the animal.
The invention also relates to use of 3-0-[&agr;-L-rhamnopyranosyl-(1→2)-&agr;-L-rhamnopyranosyl-(1→4)-0-&bgr;-D-glucopyranosyl]-25(S)-5&mgr;-spirostan-3&bgr;-ol for the preparation of a pharmaceutical composition for immunomodulation in animals.
DETAILED DESCRIPTION OF THE INVENTION
The process for isolation of a novel oligospirostanoside of formula 1 which comprises extraction of dried and powdered roots with a polar solvent with or without prior extraction with EtOAc, subjecting aqueous sol. of the desolvented extract to partitioning with CHCl
3
, EtOAc, n-BuOH and resolution of n-BuOH extract residue to adsorption/gel permeation chromatography using isotropic or graded elution, reverse phase purification on Lichroprep RP-8 and repeated crystallizations from methanol or ethanol. Physical constants and spectral data (
1
H-NMR,
13
C-NMR, MS and IR spectral data) are used for characterization of novel isolate. Corroboration of assigned structure is done by permethylation and hydrolysis to get aglycone and partially methylated sugars to confirm linkage site and sequence of sugar units.
Estimation of the compound in the dried plant material is carried out by HPTLC densitometer scanning (0.0023-0.0045%). The compound of the invention can be used for authentication of immunomodulatory formulation from
Asparagus racemosus
. The novel oligospirostanoside was evaluated for immunomodulatory activity and the results are given in Table 1, The compound of the invention is obtained as a white amorphous powder, mp 275° C., [&agr;]
D
21
−90.2[C 0.5% pyridine], molecular composition C
45
H
74
O
16
derived from FABM, MS (M+Na)
+
m/z 893, elemental analytical data and
13
C-NMR, CPD and DEPT spectral data. Immunoside responded positively to the Liebermann-Burchard Reaction [Liebermann, G. (1885)
Ber. Deut.Chem.Ges
.18, 1804; Burchard, H. (1890) Chem. Zentbl. 1, 25], negatively to the Ehrlich test [Kiyosawa, S and Hutoh, M. (1968)
Chem. Pharm. Bull
. 16, 1162; Tschesche, R; Siedel, L.; Sharma, S. C. and Wulff, G. (1972)
Chemische Berichte
, 105, 3397] and positively to Molisch's test indicating it to be spirostanol glycoside.


REFERENCES:
Shvets, S.A. et al “Steroidal glycosides of Nicotiana tabacum seeds II. Structure of Nicotianosides C and F.” English Abstract fo Khim Prir Soedin, 1995m 3, 396-401, XP-002210389, Chemical Abstracts, Columbus, Ohio, US, vol. 124, No. 17, 1996.*
Muruganandan, S. et al “Studies on the immunomodulant and antihepatotoxic activities of Asparagus racemosus root extract”, Journal of Medicinal and Aromatic Plant Sciences, vol. 22/4A and 23/1A, Oct. 200 to Mar. 2001.*
Ravikumar, P.R. et al “Chemistry of Ayurvedic Crude Drugs: Part VI-(Shatavari-1): Structure of Shatavarin-IV.”, Indian Journal of Chemistry, 1987, vol. 26B, pp. 1012-1017.*
Biochemical Nomenclature and Related Documents: Spirostans, 203, XP-002210388.*
U.K. Kanitkar et al.,J. Res. Indian Med., 1969, 3:123-137.
G.V. Satyavati et al.,Medicinal Plants of India, 1976, vol. 1, 101-106.
P.R. Ravikumar et al.,Indian J. Chem, 1987, 26B:1012-1017.
Dipak Kumar Kar et al.,Cell and Chromosome Res., 1984, 7(4):10-15.
T. Sekine et al,Chem Pharm Bull., 1994:42(6):1360-1362.
T. Sekine et al,Phytochemistry, 1997, 44(4):763-764.
S. Kiyosawa et al.,Chem Pharm Bull., 1968, 16(6):1162-1164.
Gong Wu et al.,Phytochemistry, 1996, 42(6):1677-1681.
X.C. Li et al.,Phytochemistry, 1990, 29(12):3899-3901.
S. Soe et al,J. Am. Chem. Soc., 1978, 100(11):3331-3339.
S. Hakomori,J. Biochem, 1964, 55(2) 205-208.
PCT International Search Report.
Shvets, S.A., et al., “Steroidal Glycosides of Nicotiana Tabacum Seeds. II Structure of Nicotianosides C and F”,Chemical Abstracts, 124 (17):847, 1996,

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