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  • 1
    ISSN: 1520-6025
    Source: ACS Legacy Archives
    Topics: Chemistry and Pharmacology
    Type of Medium: Electronic Resource
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  • 2
    Electronic Resource
    Electronic Resource
    s.l. : American Chemical Society
    Journal of natural products 47 (1984), S. 482-496 
    ISSN: 1520-6025
    Source: ACS Legacy Archives
    Topics: Chemistry and Pharmacology
    Type of Medium: Electronic Resource
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  • 3
    Electronic Resource
    Electronic Resource
    Springer
    Cellular and molecular life sciences 37 (1981), S. 88-91 
    ISSN: 1420-9071
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology , Medicine
    Notes: Summary From the roots ofEuphorbia cyparissias L. a highly irritant diterpene ester fraction was isolated and further resolved into its constituents. Together with some less active and some inactive isomers, the pure Euphorbia factors were characterized as new diesters of 13-hydroxyingenol and as triesters of the new 13,19-dihydroxyingenol. The Euphorbia factorsCy 6,Cy 11 andCy 14 are the strongest irritants of the ingenane ester type hitherto known,Cy 11 being at least as active as the standard diterpene ester type irritant 12-O-tetradecanoylphorbol-13-acetate (TPA).
    Type of Medium: Electronic Resource
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  • 4
    ISSN: 1432-1335
    Keywords: Diterpene ; Tumorpromoter ; Plasminogen-Aktivator ; Blutplättchen-Aggregation ; Diterpene ; Tumor promoter ; Plasminogen activator ; Platelet aggregation
    Source: Springer Online Journal Archives 1860-2000
    Topics: Medicine
    Description / Table of Contents: Summary Phorbol and eight of its derivatives were investigated for their ability to stimulate the synthesis of the enzyme plasminogen activator in cultured chick embryo fibroblasts and to aggregate human blood platelets and have been assayed for tumor, promoting and skin, irritant activities. Over a range of concentrations, elevation in the levels of plasminogen activator activity induced by phorbol derivatives correlates well with their promoting and irritant properties. In the platelet aggregation assay however, the parallelism between the activities measured in different biological assays was less complete. While strong promoters, such as TPA, are potent aggregating agents, and weak promoters, such as PDA, are poor or ineffective inducers of aggregation, two derivatives, PDD and PDB, deviate from this general result. Platelets must be exposed to PDD in relatively high concentrations before they will aggregate, and PDB was found to be the most potent aggregating agent of all the derivatives tested.
    Notes: Zusammenfassung Phorbol und acht seiner Derivate wurden auf ihre Fähigkeit untersucht, die Synthese von Plasminogen-Aktivator in Zellkulturen von Hühnerembryo-Fibroblasten zu stimulieren und die Aggregation von Blutplättchen zu induzieren und auf ihre tumorpromovierende und hautirritierende Wirkung getestet. Die Erhöhung der Plasminogen-Aktivator Aktivität durch Phorbolderivate korreliert gut mit ihren irritierenden und promovierenden Eigenschaften. Im Test auf Blutplättchen-Aggregation ist die Korrelation nicht eindeutig: Sie gilt für starke Promotoren (wie TPA), die auch hochwirksame Induktoren der Aggregation sind, sowie für schwache Promotoren (wie PDA), die nur gering oder nicht induzieren; Ausnahmen sind PDD und PDB: PDD, ein starker Promoter, ist nur schwach wirksam, PDB, ein schwacher Promotor, ist dagegen das am stärksten aggregationsstimulierende Derivat.
    Type of Medium: Electronic Resource
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  • 5
    Electronic Resource
    Electronic Resource
    Springer
    Journal of cancer research and clinical oncology 99 (1981), S. 103-124 
    ISSN: 1432-1335
    Keywords: Cocarcinogens ; Carcinogenic risk factors ; Diterpene esters ; Euphorbiaceae ; Thymelaeaceae
    Source: Springer Online Journal Archives 1860-2000
    Topics: Medicine
    Notes: Summary In the last 15 years the hypothetical concept of cocarcinogenesis has been substantiated by chemical, biochemical, and biologic investigation of the polyfunctional, diterpene mono- and diester type promoters (and stimulators) of initiation, originating from plant species. Thus, the long suspected concept of amplification of carcinogenesis by non-carcinogens was finally established. In addition, the new principle of “cryptic” cocarcinogens was detected in the form of low activity 20-esters of corresponding highly active polyfunctional diterpene mono- and diesters. Cryptic cocarcinogens require metabolic activation by esterases or lipases to become directly acting promoters and/or stimulators of initiation. It is suspected that cocarcinogens of the diterpene ester type may play a role as possible carcinogenic risk factors of the human environment, especially as environmental promoters. Apart from certain officinal or folk medical drugs derived from Euphorbiaceae and Thymelaeaceae, three etiologic models of possible human exposure to polyfunctional diterpenes are presently investigated: (i) The utilization according to local habits of roots and other parts of Croton flavens L. Such utilization was suspected to be responsible for the unusually high incidence of esophageal cancer on the island of Curacao. Several polyfunctional diterpenes of the tigliane type were detected to be present in the roots of the plant. They were identified as highly active irritants and as cocarcinogens of the promoter type in mouse skin. (ii) It was shown that many, but not all, species of the Euphorbiaceae and Thymelaeceae families utilized as ornamental plants in family homes, gardens, and parks contain irritant and cocarcinogenic diterpene esters. Provided intensive contacts are avoided with skin and/or by ingestion of plant parts, it appears most likely that an actual carcinogenic risk does not exist by raising and maintenance of single species of such plants. However, it is suggested that the existence of a possible occupational risk in persons involved professionally in raising and maintaining of mass cultures of species of Euphorbiaceae and/or Thymelaeaceae be clarified by epidemiologic investigations. (iii) It was shown that nectar collected by honey bees from species of Euphorbiaceae growing abundantly in certain locations contain irritant polyfunctional diterpenes of the promoter type. The results presented demonstrate for the first time that in the etiology of human cancer, besides well defined environmental solitary carcinogens also well defined and highly active environmental cocarcinogens, i.e., non-carcinogenic amplifiers of carcinogenesis, may play an important role. Environmental cocarcinogens of the diterpene ester type are capable to amplify initiation in prototype processes of cocarcinogenesis, such as initiation/promotion and stimulated initiation/promotion, and therefore may be considered complete cocarcinogens. As compared to environmental solitary carcinogens, the classical first order carcinogenic risk factors, environmental cocarcinogens may be considered second order carcinogenic risk factors. In this way the risk of cancer by envionmental carcinogens of whatever origin and nature may be graded to allow for more refined risk/benefit evaluations and thus for more appropriate preventive legislation.
    Type of Medium: Electronic Resource
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  • 6
    Electronic Resource
    Electronic Resource
    Springer
    Naturwissenschaften 71 (1984), S. 259-261 
    ISSN: 1432-1904
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology , Chemistry and Pharmacology , Natural Sciences in General
    Type of Medium: Electronic Resource
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  • 7
    Electronic Resource
    Electronic Resource
    Springer
    Journal of cancer research and clinical oncology 103 (1982), S. 255-268 
    ISSN: 1432-1335
    Keywords: Cocarcinogenesis ; Tumor promoters ; Occupational cancer ; Ingenol ; Euphorbiaceae
    Source: Springer Online Journal Archives 1860-2000
    Topics: Medicine
    Notes: Summary The irritant and tumor-promoting principles of the latex of Euphorbia ingens E. Mey have been isolated together with several nonirritant compounds. The Euphorbia factors I1, I5, and I6 are esters of ingenane-type polyfunctional diterpene alcohols. Euphorbia factor I1 is characterized as the 3-hexadecanoate of the polyfunctional parent alcohol ingenol and Euphorbia factor I6 as the 3-deca-2.4.6-trienoic acid ester of ingenol. Euphorbia factor I5 is the 16-angelate-3-deca-2.4.6-trienoate of 16-hydroxyingenol. Nonirritant diterpenes of the latex are I2, the ingenol-20-hexadecanoate — an isomer of Euphorbia factor I1-and I4, the 3.7.12-triacetate-8-nicotinate of the macrocyclic lathyrane-type polyfunctional diterpene alcohol ingol. The diterpene alcohols ingenol and 16-hydroxyingenol are inactive as irritants and tumor promoters of mouse skin. Compared to croton oil factor A1 (TPA), the Euphorbia factor I1 exhibits about 1/10 of the irritant and tumor-promoting activity in mouse skin. I1 shows no reasonable tumorigenic activity. Compared with I1, Euphorbia factors I5 and I6 are more potent irritants and less potent tumor promoters.
    Type of Medium: Electronic Resource
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  • 8
    Electronic Resource
    Electronic Resource
    Springer
    Journal of cancer research and clinical oncology 108 (1984), S. 98-109 
    ISSN: 1432-1335
    Keywords: Cocarcinogenesis ; Tumor promoters ; Irritants ; Diterpene esters ; Euphorbia resinifera ; Euphorbium
    Source: Springer Online Journal Archives 1860-2000
    Topics: Medicine
    Notes: Summary The irritant and tumor-promoting principles were isolated from the latex of Euphorbia resinifera Berg. and from the resin derived from latex (euphorbium), which is commercially available as a drug. The irritant Euphorbia factors RL 5 (mixture), RL 6, RL 7, RL 8, and RL 10 were identified as tigliane-type 12-deoxyphorbol esters each bearing, in the 13 position, either long-chain, partially methylsubstituted acyl residues (10–16 carbon atoms) or short-chain acyl residues (4 or 5 carbon atoms) or a (substituted) phenylacetyl group with a 20-acetoxy group. Euphorbia factors RL 15 (mixture), RL 16, RL 17, RL 18, and RL 21 are the corresponding 20-deacetylated derivatives thereof. The irritant Euphorbia factors RL 11, RL 12, RL 22, RL 23 were characterized as esters of the tigliane type 12-deoxy-16-hydroxyphorbol, i.e., 13-0-phenylacetyl-16-0-benzoyl-12-deoxy 16-hydroxyphorobol-20-acetate (RL 11) and 13, 16-0-phenylacetyl, tigloyl-12-deoxy-16-hydroxy-phorbol-20-acetate (RL 12), RL 22 and RL 23 representing the respective 20-deacetylated derivatives. A mixture of irritant factors, RL 13, was shown to represent long-chain 3-esters of ingenane-type ingenol with similar acyl residues (10–16 carbon atoms, partially methyl-substituted) to RL 5 (RL 15) above. A further group of E. resinifera factors was of the daphnane type: RL 9 was identified as the extremely irritant 9,13,14-orthophenylacetate of resiniferonol-20-(4-hydroxy-3-methoxy)phenylacetate (Resiniferatoxin), RL 14 as the corresponding 9,13,14-orthophenylacetate of resiniferonol, and RL 20 as 14-0-phenylacetylresiniferonol-20-(4-hydroxy-3-methoxy)-phenylacetate (Proresiniferatoxin). The irritant factors specified below were accompanied by nonirritant esters of the tigliane type 12,20-dideoxyphorbol, i.e., RL 1 and RL 2, and of the lathyrane type ingol, i.e., RL 3 and RL 4. In tumor promotion experiments the mixture of homologous irritant factors RL 13 was equipotent with the standard tumor promoter TPA, but at 10 times the dose of TPA. Several others of the irritant factors had low activity as tumor promotors, but of the few tumors obtained in these experiments a high percentage was malignant. The very high irritant activity of the latex may be ascribed to resiniferatoxin (RL 9), representing a new class of rapidly acting skin irritants. No promoting activity was detected on administration of the highly irritant resiniferatoxin.
    Type of Medium: Electronic Resource
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  • 9
    Electronic Resource
    Electronic Resource
    Springer
    Journal of cancer research and clinical oncology 104 (1982), S. 31-39 
    ISSN: 1432-1335
    Keywords: Diterpene esters ; Irritant activity ; Structure-Activity relationships ; Tumor promoting activity ; Diterpenester ; irritierende Aktivität ; Strukturwirkungs-beziehungen ; tumorpromovierende Aktivität
    Source: Springer Online Journal Archives 1860-2000
    Topics: Medicine
    Description / Table of Contents: Zusammenfassung Die Kinetik der irritierenden Wirkung von einigen polyfunktionellen Diterpenestern auf dem Mausohr [Erythem-Auslösung, quantitativ gemessen als irritierende Dosis 50 (ID50)], und ihre Beziehung zur initiationspromovierenden Aktivität auf der Rückenhaut der NMRI-Maus wurde untersucht: 1) Ein sehr schnell einsetzendes, aber rasch abklingendes Erythem ist mit schwacher oder fehlender Promoter-Wirkung verbunden. 2) Ester, die ein schnell einsetzendes, aber langsam abklingendes Erythem verurschen, zeigen in den meisten Fällen mäßige bis starke initiationspromovierende Wirkung und 3) relativ spät einsetzende, aber anhaltende Erythem-Wirkung (bis mindestens 24 h) ist mit hoher promovierender Aktivität verbunden. Diese Ergebnisse weisen auf eine Beziehung zwischen der Kinetik der irritierenden Wirkung und der initiationspromovierenden Aktivität der Diterpenester hin. Die verhältnismäßig geringe promovierende Aktivität von Estern mit mehrfach ungesättigten Acylresten könnte auf den Einfluß von pharmakologischen Parametern wie Bioverfügbarkeit und Stabilität im biologischen System, Wirkstoff-Rezeptor-Wechselwirkung und “intrinsic activity” der Diterpeneser hinweisen.
    Notes: Summary The kinetics of the irritant response on the mouse ear [erythema measured quantitatively by the irritant dose 50 (ID50)] and its relation to the initiation-promoting activity on the back skin of NMRI mice of some polyfunctional diterpene esters were investigated: (1) A very rapid and transient erythema response is associated with low or absent promoting activity (2) an early and more persistent erythema response in most cases is associated with moderate-to-high promoting activity, and (3) a relatively late onset but persistence up to at least 24 h of the erythema response is associated with high promoting activity. These results may indicate a relationship between the kinetics of the erythema response and the initiation-promoting activity of diterpene esters. The comparatively low promoting activity of esters carrying polyunsaturated acyl functions may indicate that importance of pharmacological parameters such as biovailability and stability in the biological system, drug-receptor interaction, and “intrinsic activity” of the diterpene esters.
    Type of Medium: Electronic Resource
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  • 10
    Electronic Resource
    Electronic Resource
    Springer
    Journal of cancer research and clinical oncology 102 (1981), S. 127-139 
    ISSN: 1432-1335
    Keywords: Polycyclic aromatic hydrocarbons ; K-region oxides ; Gene conversion in yeast ; Tumor initiation in mouse skin ; Ultimate carcinogens ; Ultimate initiators ; Polycyclische aromatische Kohlenwasserstoffe ; K-Region-Oxide ; Genkonversion in Hefe ; Tumor-Initiation an der Mäusehaut ; Wirkformen von Carcinogenen ; Wirkformen von Initiatoren
    Source: Springer Online Journal Archives 1860-2000
    Topics: Medicine
    Description / Table of Contents: Zusammenfassung Am atmungsdefizienten diploiden Hefestamm D4-RDII wurde die konvertogene (mutagene) Wirkung von PAH, Urthan, einigen sauerstoffhaltigen PAH-Derivaten und des (aliphatischen) Epoxidhydrolase-Inhibitors TCPO untersucht. Als positive Kontrolle diente die konvertogene “Wirkform” des Rattenlebercarcinogens NOAcAAF. PAH und Urethan waren nicht konvertogen, TCPO zeigte eine geringe Wirkung, während elektrophile PAH-Derivate wie die K-Region-Oxide stark konvertogen wirkten. Einige konvertogene Schlüsselsubstanzen wurden zum Vergleich auf ihre tumorinitiierende Wirkung an der Mäusehaut im standardisierten Experiment mit TPA als Promoter geprüft. PAH erwiesen sich als stärkere Initiatoren als alle ihre entsprechenden sauerstoffhaltigen Derivate. TCPO allein zeigt—wenn überhaupt — nur geringe Wirkung. Wenn TCPO 5 min vor einem Initiator appliziert wurde, hatte es keinen nennenswerten Einfluß auf die Initiation. Auf Grund der mangelnden Korrelation zwischen konvertogener und initiierender Wirkung sind weitere Untersuchungen zum Problem der chemischen Natur der „Wirkformen” von Initiatoren der Carcinogenese der Mäusehaut erforderlich.
    Notes: Summary The diploid respiratory-deficient strain of yeast D4-RDII was used to assay PAH and urethane as well as some oxygenated derivatives of PAH and the (aliphatic) epoxide hydrolase inhibitor TCPO for convertogenic (mutagenic) activity. As a positive control, the convertogenic ultimate rat liver carcinogen NOAcAAF was used. PAH and urethane were found inactive as convertogens, TCPO was weakly active, whereas oxygenated electrophilic derivatives of PAH, such as K-region oxides, were found strong convertogens. For comparison, some convertogenic key compounds were assayed for their tumorinitiating activity in mouse skin in the standardized system using TPA as a promoter. PAH were stronger initiators than all oxygenated derivatives of PAH tested. TCPO alone exhibited very weak, if any, initiating activity. It was unable to modify initiation to any significant extent, if administered 5 min prior to administration of an initiator. In the absence of correlation between convertogenic and initiating activity the question of the chemical nature of “ultimate initiators” of mouse skin carcinogenesis awaits further investigation.
    Type of Medium: Electronic Resource
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