Skip to search formSkip to main content
You are currently offline. Some features of the site may not work correctly.

Equilenin

Known as: Equilenin [Chemical/Ingredient], Estra-1,3,5,7,9-pentaen-17-one, 3-hydroxy- 
An estrogenic steroid produced by HORSES. It has a total of five double bonds in the A- and B-ring. High concentration of equilenin is found in the… Expand
National Institutes of Health

Papers overview

Semantic Scholar uses AI to extract papers important to this topic.
Highly Cited
2008
Highly Cited
2008
Sulfonyl chlorides substituted with functional groups having high proton affinity can serve as derivatization reagents to enhance… Expand
  • figure 1
  • figure 2
  • figure 3
  • figure 4
  • figure 5
2006
2006
Syntheses of novel heterocyclic derivatives of 18-nor-equilenin, namely, (12H-11-oxa-17-thia-15-aza-cyclopenta[a]phenanthrene-16… Expand
Highly Cited
1999
Highly Cited
1999
  • H. Cho, N. Ha, +7 authors B. Oh
  • The Journal of Biological Chemistry
  • 1999
  • Corpus ID: 28637892
Δ5-3-Ketosteroid isomerase from Pseudomonas testosteroni has been intensively studied as a prototype to understand an enzyme… Expand
  • figure 1
  • table I
  • figure 4
  • figure 3
  • table II
Review
1998
Review
1998
  • B. Bhavnani
  • Proceedings of the Society for Experimental…
  • 1998
  • Corpus ID: 45177839
Abstact Conjugated equine estrogens (Premarin), are used extensively for estrogen replacement therapy and prevention of… Expand
  • figure 1
  • table 1
  • table II
  • table 111
  • figure 2
Highly Cited
1995
Highly Cited
1995
Free radical generation by metabolic redox cycling between catechol estrogens and their quinones and subsequent hydroxyl radical… Expand
Highly Cited
1995
Highly Cited
1995
The therapeutic use of estrogens has been associated with an increased risk of some of the most predominant, as well as less… Expand
  • figure 1
  • table 1
  • table 2
  • figure 2
  • figure 3
Highly Cited
1986
Highly Cited
1986
The two-state excited-state proton-transfer process for d-equilenin [d-3-hydroxyestra-1,3,-5(10),6,8-pentaen-17-one] and… Expand
Highly Cited
1985
Highly Cited
1985
Estrogen 2- and 4-hydroxylase (ESH), a microsomal enzyme which mediates the formation of catechol estrogens, has been studied in… Expand
Highly Cited
1983
Highly Cited
1983
Both synthetic and natural estrogens have been studied for their ability to induce renal carcinomas in castrated male hamsters… Expand
  • table 1
  • table 2
Highly Cited
1959
Highly Cited
1959
  • F. Hisaw
  • Endocrinology
  • 1959
  • Corpus ID: 33796858
Five natural estrogens (estradiol-17B, estrone, estriol, equilin and equilenin) and one synthetic estrogen (diethylstilbestrol… Expand