January 1990
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8 Reads
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27 Citations
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January 1990
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8 Reads
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27 Citations
August 1989
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12 Reads
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21 Citations
Indian Journal of Experimental Biology
The in vivo studies have been carried out in the rat brain for characterization of binding sites for potassium embelate (ex: Embelia ribes) a potent centrally acting analgesic compound. The results indicate that mixed mu and kappa binding sites in the brain may be involved in the analgesic action of this compound.
February 1989
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6 Reads
ChemInform
An alkaloid which was previously isolated from Crotalaria crispata and reported as crispatine despite data differing from that for the original crispatine (I) is reexamined.
September 1988
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6 Reads
ChemInform
A series of products, i.e. N1,N5-bis(α- and β-D-glucopyranosides) as well as N1-α-, N2-β- and N5-β-D-glucopyranosides are obtained from the reaction of allopurinol (II) with the glucopyranose (I) according to the conditions shown (yields given in mg) and tested for their in vivo xanthine oxidase inhibitory activity.
July 1988
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23 Reads
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52 Citations
Agents and Actions
Effect of alcoholic extract of salai guggal (AESG) was studied on cellular and humoral immune responses in mice and leucocyte migration in rats. Oral administration of AESG strongly inhibited the antibody production and cellular responses to sheep red blood cells in mice. It inhibited the infiltration of polymorphonuclear leucocytes and reduced the volume of pleural exudate in carrageenan induced pleurisy in rats. It showed no cytotoxic effect.
June 1988
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18 Reads
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46 Citations
Inflammation Research
Effect of alcoholic extract of salai guggal (AESG) was studied on cellular and humoral immune responses in mice and leucocyte migration in rats. Oral administration of AESG strongly inhibited the antibody production and cellular responses to sheep red blood cells in mice. It inhibited the infiltration of polymorphonuclear leucocytes and reduced the volume of pleural exudate in carrageenan induced pleurisy in rats. It showed no cytotoxic effect.
April 1988
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10 Reads
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8 Citations
An alkaloid of Crotalaria leschenaultii DC., previously reported as crispatine and now named crotaleschenine, has been re-investigated and shown to be (7β,8α-H,12α,13α,14α)-12β-hydroxy-1,2-didehydrocrotalane-11,15-dione.¹ Spectroscopic data are presented and the stereochemistry determined by X-ray crystallography. The esterifying acid of crotaleschenine is identical with that of retusine , which is thereby determined as (1a,7β,8α-H,12α,13α,14α)-12β- hydroxycrotalane-11,15-dione.
January 1988
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6 Reads
ChemInform
October 1987
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6 Reads
Indian Journal of Physiology and Pharmacology
August 1987
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8 Reads
Indian Journal of Experimental Biology
... Експериментально підтверджено здатність смоли Boswellia serrata інгібувати синтез глікозаміногліканів та запобігати деградації сполучної тканини при різних запальних процесах у суглобах. Також доведено здатність камеді (в експерименті на щурах) знижувати рівень холестерину та тригліцеридів у сироватці крові [18]. ...
January 1981
British Journal of Pharmacology
... Picrorhiza kurroa is one of the most commonly used medicinal plant in Asian countries especially in the Himalayan belt of India. This plant is used against a wide array of diseases and disorders like inflammation (Jayaweera;Nadkarni, 1954), treatment of bronchial asthma (Rajaram, 1976), infectious hepatitis (Mittal et al., 1978), and arthritic pain of bone joints (Langer, 1981). The root and leaf extracts are known to boost humoral and cell mediated immunity (Atal et al., 1986;Sharma et al., 1988). ...
January 1981
Indian Journal of Pharmacology
... Vanillin and 4-methylpentan-2-one reacts under Claisen-Schmidt conditions yielding corresponding enone compound (E)-1-(4-hydroxy-3-methoxyphenyl)-5-methylhex-1-en-3one, 2a in good yield, Scheme 1. Compound 2a was prepared according to slightly modified procedure [39]. A set of its O-alkyl derivatives, compounds 2b-g, was prepared by alkylation of free phenolic group in 2a with corresponding alkyl halides, according to the described literature procedures, [29,30,40], Scheme 2. Compounds 2a and 2b are known compounds and their chemical synthesis was published earlier [41,42]. Compounds 2c-g are new compound and their structure and spectral data are given. ...
February 1983
Chemischer Informationsdienst
... The mixture of these acids is known as D-003 [ Figure 2]. [17] Although fatty acid and fatty alcohol are reported as major constituents [18][19][20][21][22] various phytosterols (19 -22), steroids (23 -28), and higher terpenoids (29 -30) have also been reported in sugarcane wax [23,24] [ Figure 3]. ...
June 1985
... Kutajarista (200 mL; original pH 4.5) was treated using a published procedure for the enrichment of an alkaloid extract (Bhutani et al., 1984). The preparation was partitioned with chloroform (3 × 200 mL) to remove the neutral components, and the remaining aqueous portion of the formulation was basified by the addition of aqueous ammonium hydroxide (30%). ...
January 1984
INDIAN DRUGS
... 19 Atal et al. prepared five glycosylated psoralen derivatives including 9-b-D-arabinopyranosyl psoralen 3 and found that it caused dose dependent inhibition of spontaneous motor activity, prolongation of hexabarbitone, pentobarbitone, and ether hypnosis. 20 Considering that introducing sugar moieties into pharmacophores, natural products or prodrugs can improve their anticancer activities, 22e30 we embarked on the design and synthesis of glycosylated psoralen derivatives and the evaluation of their Scheme 1. Structures of some glycosidic psoralen derivatives. antiproliferative activities against several human tumor cell lines and antioxidant activities. ...
January 1987
... The procedures for its synthesis have been extensively studied and such studies have been stimulated by various promising applications, especially in the case of highly substituted 4-hydroxycoumarin derivatives. In fact, certain substituted chromene are used as antimicrobial, anticancer, anti-inflammatory, antidepressant, anticonvulsant, antihyperglycemic, antipyretic, antibacterial, antifungal activities, fungicidal, anti-arthritic activities [1][2][3][4].The knowledge of such applications has pointed out that substituted 4-hydroxycoumarin are important target to be prepared to our interest on synthesis and molecular structure determination of some types of 4-hydroxycoumarin [5]. ...
January 1990
... Different Boswellic acids have been identified including β-Boswellic acid, α-Boswellic acid and these belong to the family of pentacyclic triterpenes. Boswellic acids have been reported as inhibitors of 5lipoxygenase, the key enzyme for leukotriene biosynthesis in inflammatory disorders and human leukocyte elastase [1][2][3][4][5][6][7][8][9][10][11][12][13][14] . Docking studies of Boswellic acid is carried out on lipoxygenase target to identify the most potent inhibitor of lipoxygenase protein among Boswellic acids and their derivatives. ...
January 1987
INDIAN DRUGS
... It has been reported that allopolyploids from O. basilicum x O. americanum had higher herbage and essential oil content (Dhar, 1999). The cultivar 'Clocimum' resulted from the cross between O. gratissimum and O. basilicum, is reported to be a cheap source of eugenol (Sobti et al., 1982). Recently, Ben-Naim et al. (2018) (Maurya et al., 2022) or exhibited tolerance to cold (Dhawan et al., 2016). ...
January 1982
... It was revealed that no relevant data showed any abortion effect when the dose range was minimum, i.e., 10-80 mg. In contrast, it showed its abortion activity in 12 cases with the increasing dosage forms [215]. Furthermore, by the decoction procedure, the leaves were given to pregnant women to stimulate and heal the pain both in pre and post-delivery time whereas the roots helped to destroy the fetus and during birthing in Bihar [216]. ...
January 1983
INDIAN DRUGS