C.K. Atal’s research while affiliated with CSIRO BioFoundry and other places

What is this page?


This page lists works of an author who doesn't have a ResearchGate profile or hasn't added the works to their profile yet. It is automatically generated from public (personal) data to further our legitimate goal of comprehensive and accurate scientific recordkeeping. If you are this author and want this page removed, please let us know.

Publications (203)


Synthesis, anti-inflammatory and anti-arthritic activity of newer β-boswellic acid derivatives
  • Article

January 1990

·

8 Reads

·

27 Citations

·

V.N. Gupta

·

C.K. Atal

Possible interaction of potassium embelate, a putative analgesic agent, with opiate receptors

August 1989

·

12 Reads

·

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.



ChemInform Abstract: Glucopyranosides Derived from Allopurinol and Their Xanthine Oxidase Inhibitory Activity.

September 1988

·

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.


Effect of salai guggal ex-Boswellia serrata on cellular and humoral immune responses and leucocyte migration

July 1988

·

23 Reads

·

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.


Effect of salai guggal ex-Boswellia serrata on cellular and humoral immune responses and leucocyte migration

June 1988

·

18 Reads

·

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.


Crotaleschenine, an Alkaloid of Crotalaria leschenaultii
  • Article
  • Publisher preview available

April 1988

·

10 Reads

·

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.

View access options




Citations (64)


... 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]. ...

Reference:

The safety assessment of the dietary supplement “Rheumacаre Ultra”: the optimizing of dietary conditions for the functioning of joints
Salai guggal: A promising anti-arthritic and anti-hyperlipidaemic agent
  • Citing Article
  • 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). ...

Clinical trials on Picrorhiza kurroa
  • Citing Article
  • 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. ...

ChemInform Abstract: SYNTHESIS OF POTENTIAL ANTIINFLAMMATORY COMPOUNDS
  • Citing Article
  • 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]. ...

SUGARCANE PRESSMUD: A POTENTIAL SOURCE OF PHYTOSTEROLS, FATTY ALCOHOLS, FATTY ACIDS AND HARDWAX.
  • Citing Article
  • 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%). ...

Profile of kurchi in India
  • Citing Article
  • 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. ...

Synthesis of 9-β-D-glycopyranosyl xanthotoxol and CNS depressant activity of 9 β-D-arabinopyranosyl xanthotoxol
  • Citing Article
  • 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]. ...

Synthesis, anti-inflammatory and anti-arthritic activity of newer β-boswellic acid derivatives
  • Citing Article
  • 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. ...

Chemistry and Pharmacology of gum resin of boswellia serrata extract
  • Citing Article
  • 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). ...

Clocimum: a new hybrid strain of Ocimum gratissimum as a potential source of clove type oil, rich in eugenol
  • Citing Article
  • 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]. ...

The in vivo metabolism of vasicine - A potent uterotonic
  • Citing Article
  • January 1983

INDIAN DRUGS