Literature DB >> 1923700

Allergic contact dermatitis caused by naturally occurring quinones.

J P Lepoittevin1, C Benezra.   

Abstract

Quinones play a major role in allergic contact dermatitis caused by plants. The principal allergens are benzoquinones or naphthoquinones but also compounds, such as catechols and other phenolic or flavonoid compounds, which are bioconverted into ortho-quinones or para-quinones. The high electrophilic reactivity of these compounds toward nucleophilic residues of proteins associated with lipophilic properties may explain that they are strong sensitizers. The more important allergens are reported and their structure-activity relationship is discussed.

Entities:  

Mesh:

Substances:

Year:  1991        PMID: 1923700     DOI: 10.1007/bf01981527

Source DB:  PubMed          Journal:  Pharm Weekbl Sci        ISSN: 0167-6555


  7 in total

1.  Enantiospecificity in allergic contact dermatitis. A review and new results in Frullania-sensitive patients.

Authors:  C Benezra; J L Stampf; P Barbier; G Ducombs
Journal:  Contact Dermatitis       Date:  1985-08       Impact factor: 6.600

2.  Delayed contact sensitivity to catechols. 3. The relationship of side-chain length to sensitizing potency of catechols chemically related to the active principles of poison ivy.

Authors:  H Baer; R C Watkins; A P Kurtz; J S Byck; C R Dawson
Journal:  J Immunol       Date:  1967-08       Impact factor: 5.422

3.  [On plant defensive agents. IV. Structure of the primrose poison].

Authors:  H Schildknecht; I Bayer; H Schmidt
Journal:  Z Naturforsch B       Date:  1967-01       Impact factor: 1.047

4.  True cross-sensitization, false cross-sensitization and otherwise.

Authors:  C Benezra; H Maibach
Journal:  Contact Dermatitis       Date:  1984-08       Impact factor: 6.600

5.  Allergic contact dermatitis to Ginkgo biloba L.: relationship with urushiol.

Authors:  J P Lepoittevin; C Benezra; Y Asakawa
Journal:  Arch Dermatol Res       Date:  1989       Impact factor: 3.017

6.  Regiospecific attack of nitrogen and sulfur nucleophiles on quinones derived from poison oak/ivy catechols (urushiols) and analogues as models for urushiol-protein conjugate formation.

Authors:  D J Liberato; V S Byers; R G Dennick; N Castagnoli
Journal:  J Med Chem       Date:  1981-01       Impact factor: 7.446

7.  The sensitizing capacity of naturally occurring quinones. Experimental studies in guinea pigs. I. Naphthoquinones and related compounds.

Authors:  K H Schulz; I Garbe; B M Hausen; M H Simatupang
Journal:  Arch Dermatol Res       Date:  1977-03-25       Impact factor: 3.017

  7 in total
  3 in total

Review 1.  Bioreductive activation of quinones: a mixed blessing.

Authors:  A S Koster
Journal:  Pharm Weekbl Sci       Date:  1991-06-21

2.  Comparison of various easy-to-use procedures for extraction of phenols from apricot fruits.

Authors:  Ondrej Zitka; Jiri Sochor; Otakar Rop; Sylvie Skalickova; Pavlina Sobrova; Josef Zehnalek; Miroslava Beklova; Boris Krska; Vojtech Adam; Rene Kizek
Journal:  Molecules       Date:  2011-04-04       Impact factor: 4.411

3.  Effects of several quinones on insulin aggregation.

Authors:  Hao Gong; Zihao He; Anlin Peng; Xin Zhang; Biao Cheng; Yue Sun; Ling Zheng; Kun Huang
Journal:  Sci Rep       Date:  2014-07-10       Impact factor: 4.379

  3 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.