Movatterモバイル変換


[0]ホーム

URL:


Jump to content
WikipediaThe Free Encyclopedia
Search

Etiocholanolone

From Wikipedia, the free encyclopedia
Chemical compound
Pharmaceutical compound
Etiocholanolone
Skeletal formula of etiocholanolone
Ball-and-stick model of the etiocholanolone molecule
Clinical data
Other namesAetiocholanolone
5-Isoandrosterone
ATC code
  • none
Identifiers
  • (3R,5R,8R,9S,10S,13S,14S)-3-Hydroxy-10,13-dimethyl-1,2,3,4,5,6,7,8,9,11,12,14,15,16-tetradecahydrocyclopenta[a]phenanthren-17-one
CAS Number
PubChemCID
DrugBank
ChemSpider
UNII
ChEBI
ChEMBL
CompTox Dashboard(EPA)
Chemical and physical data
FormulaC19H30O2
Molar mass290.447 g·mol−1
3D model (JSmol)
  • [H][C@]12CC[C@@]3([H])[C@]4([H])CCC(=O)[C@@]4(C)CC[C@]3([H])[C@@]1(C)CC[C@@H](O)C2
  • InChI=1S/C19H30O2/c1-18-9-7-13(20)11-12(18)3-4-14-15-5-6-17(21)19(15,2)10-8-16(14)18/h12-16,20H,3-11H2,1-2H3/t12-,13-,14+,15+,16+,18+,19+/m1/s1 ☒N
  • Key:QGXBDMJGAMFCBF-BNSUEQOYSA-N ☒N
 ☒NcheckY (what is this?)  (verify)

Etiocholanolone, also known as5β-androsterone, as well as3α-hydroxy-5β-androstan-17-one oretiocholan-3α-ol-17-one, is anetiocholane (5β-androstane)steroid as well as anendogenous17-ketosteroid that is produced from themetabolism oftestosterone. It causesfever,immunostimulation, andleukocytosis, and is used to evaluateadrenal cortex function,bone marrow performance, and inneoplastic disease to stimulate theimmune system. Etiocholanolone is also known to be aninhibitoryandrostaneneurosteroid,[1] acting as apositive allosteric modulator of theGABAA receptor,[2] and possessesanticonvulsant effects.[3] The unnatural enantiomer of etiocholanolone is more potent as a positive allosteric modulator of GABAA receptors and as an anticonvulsant than the natural form.[4]

Etiocholanolone has been studied as apyrogenic steroid in the so-called steroid fever (or etiocholanolone fever),[5][6] a condition similar tofamilial mediterranean fever (FMF). Etiocholanolone (likepregnanolone) activates thepyrininflammasome.[7] It is not known whether these endogenoussteroids play a role in triggeringFMF flares but they may make a link betweenstress,menstrual cycle and disease flares.[8][9]

Etiocholanolone is produced from5β-dihydrotestosterone, with3α,5β-androstanediol as anintermediate.

Chemistry

[edit]
See also:List of neurosteroids

See also

[edit]

References

[edit]
  1. ^Reddy DS (2010). "Neurosteroids".Sex Differences in the Human Brain, their Underpinnings and Implications. Progress in Brain Research. Vol. 186. pp. 113–37.doi:10.1016/B978-0-444-53630-3.00008-7.ISBN 978-0-444-53630-3.PMC 3139029.PMID 21094889.{{cite book}}:|journal= ignored (help)
  2. ^Li P, Bracamontes J, Katona BW, Covey DF, Steinbach JH, Akk G (June 2007)."Natural and enantiomeric etiocholanolone interact with distinct sites on the rat alpha1beta2gamma2L GABAA receptor".Molecular Pharmacology.71 (6):1582–1590.doi:10.1124/mol.106.033407.PMC 3788649.PMID 17341652.S2CID 44286086.
  3. ^Kaminski RM, Marini H, Kim WJ, Rogawski MA (June 2005)."Anticonvulsant activity of androsterone and etiocholanolone".Epilepsia.46 (6):819–827.doi:10.1111/j.1528-1167.2005.00705.x.PMC 1181535.PMID 15946323.
  4. ^Zolkowska D, Dhir A, Krishnan K, Covey DF, Rogawski MA (September 2014)."Anticonvulsant potencies of the enantiomers of the neurosteroids androsterone and etiocholanolone exceed those of the natural forms".Psychopharmacology.231 (17):3325–3332.doi:10.1007/s00213-014-3546-x.PMC 4134984.PMID 24705905.
  5. ^Heckel GP (April 1963). "Steroid fever".The Lancet.281 (7285):835–836.doi:10.1016/S0140-6736(63)91549-6.
  6. ^Kappas A, Palmer RH (July 1967). "Novel biological properties of steroid metabolites; fever-production in man".Journal of the Reticuloendothelial Society.4 (4):231–236.PMID 6056839.
  7. ^Magnotti F, Chirita D, Dalmon S, Martin A, Bronnec P, Sousa J, et al. (October 2022)."Steroid hormone catabolites activate the pyrin inflammasome through a non-canonical mechanism".Cell Reports.41 (2) 111472.bioRxiv 10.1101/2021.10.29.466454.doi:10.1016/j.celrep.2022.111472.PMC 9626387.PMID 36223753.S2CID 240345817.
  8. ^Karadag O, Tufan A, Yazisiz V, Ureten K, Yilmaz S, Cinar M, et al. (April 2013). "The factors considered as trigger for the attacks in patients with familial Mediterranean fever".Rheumatology International.33 (4):893–897.doi:10.1007/s00296-012-2453-x.PMID 22814791.S2CID 25599588.
  9. ^Akar S, Soyturk M, Onen F, Tunca M (May 2006). "The relations between attacks and menstrual periods and pregnancies of familial Mediterranean fever patients".Rheumatology International.26 (7):676–679.doi:10.1007/s00296-005-0041-z.PMID 16184383.S2CID 1617088.
Precursors
Corticosteroids
Glucocorticoids
Mineralocorticoids
Sex steroids
Androgens
Estrogens
Progestogens
Neurosteroids
Others
Alcohols
Barbiturates
Benzodiazepines
Carbamates
Flavonoids
Imidazoles
Kava constituents
Monoureides
Neuroactive steroids
Nonbenzodiazepines
Phenols
Piperidinediones
Pyrazolopyridines
Quinazolinones
Volatiles/gases
Others/unsorted
Retrieved from "https://en.wikipedia.org/w/index.php?title=Etiocholanolone&oldid=1314523149"
Categories:
Hidden categories:

[8]ページ先頭

©2009-2025 Movatter.jp