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Pregnenolone sulfate

From Wikipedia, the free encyclopedia
Pregnenolone sulfate
Skeletal formula
Ball-and-stick model of pregnenolone sulfate as an anion
Names
IUPAC name
20-Oxopregn-5-en-3β-yl hydrogen sulfate
Systematic IUPAC name
(1S,3aS,3bS,7S,9aR,9bS,11aS)-1-Acetyl-9a,11a-dimethyl-2,3,3a,3b,4,6,7,8,9,9a,9b,10,11,11a-tetradecahydro-1H-cyclopenta[a]phenanthren-7-yl hydrogen sulfate
Other names
Pregn-sulf; Pregnenolone monosulfate; Pregnenolone hydrogen sulfate; Pregnenolone 3β-sulfate; 5-Pregnen-3β-ol-20-one sulfate; (3β)-3-(Sulfooxy)pregn-5-en-20-one; 5-Pregnen-3β-sulfate-20-one; 20-Oxo-5-pregnen-3β-yl sulfate
Identifiers
3D model (JSmol)
ChEMBL
ChemSpider
UNII
  • InChI=1S/C21H32O5S/c1-13(22)17-6-7-18-16-5-4-14-12-15(26-27(23,24)25)8-10-20(14,2)19(16)9-11-21(17,18)3/h4,15-19H,5-12H2,1-3H3,(H,23,24,25)/t15-,16-,17+,18-,19-,20-,21+/m0/s1 ☒N
    Key: DIJBBUIOWGGQOP-QGVNFLHTSA-N ☒N
  • InChI=1/C21H32O5S/c1-13(22)17-6-7-18-16-5-4-14-12-15(26-27(23,24)25)8-10-20(14,2)19(16)9-11-21(17,18)3/h4,15-19H,5-12H2,1-3H3,(H,23,24,25)/t15-,16-,17+,18-,19-,20-,21+/m0/s1
    Key: DIJBBUIOWGGQOP-QGVNFLHTBX
  • CC(=O)[C@H]1CC[C@@H]2[C@@]1(CC[C@H]3[C@H]2CC=C4[C@@]3(CC[C@@H](C4)OS(=O)(=O)O)C)C
Properties
C21H32O5S
Molar mass396.54 g·mol−1
Except where otherwise noted, data are given for materials in theirstandard state (at 25 °C [77 °F], 100 kPa).
☒N verify (what is checkY☒N ?)
Chemical compound

Pregnenolone sulfate (PS,PREGS) is anendogenousexcitatoryneurosteroid that issynthesized frompregnenolone.[1][2] It is known to havecognitive andmemory-enhancing,antidepressant,anxiogenic, andproconvulsant effects.[2]

Biological activity

[edit]

Pregnenolone sulfate is a neurosteroid with excitatory effects in the brain, acting as a potentnegative allosteric modulator of theGABAA receptor and a weakpositive allosteric modulator of theNMDA receptor.[1][2] To a lesser extent, it also acts as a negative allosteric modulator of theAMPA,kainate, andglycine receptors,[3][4] and may interact with thenACh receptors as well.[1] In addition to its effects onligand-gated ion channels, pregnenolone sulfate is anagonist of thesigma receptor,[2] as well as anactivator of theTRPM1 andTRPM3 channels.[1] It may also interact withpotassium channels andvoltage-gated sodium channels[1] and has been found to inhibitvoltage-gated calcium channels.[5]

Biochemistry

[edit]
Steroidogenesis, with pregnenolone, the precursor of pregnenolone sulfate, at top left.

Biosynthesis

[edit]

Pregnenolone sulfate issynthesized frompregnenolone viasulfation. Pregnenolone itself is produced fromcholesterol viacholesterol side-chain cleavage enzyme.

Chemistry

[edit]
See also:List of neurosteroids

Pregnenolone sulfate, also known as pregn-5-en-3β-ol-20-one 3β-sulfate, is anaturally occurringpregnanesteroid and aderivative ofcholesterol. It is the C3βsulfateester ofpregnenolone. A closely related steroid isdehydroepiandrosterone sulfate (DHEA-S), which is the C3β sulfate ester ofdehydroepiandrosterone (DHEA).

References

[edit]
  1. ^abcdeHarteneck C (2013)."Pregnenolone sulfate: from steroid metabolite to TRP channel ligand".Molecules.18 (10):12012–28.doi:10.3390/molecules181012012.PMC 6270300.PMID 24084011.
  2. ^abcdReddy DS (2010)."Neurosteroids: endogenous role in the human brain and therapeutic potentials".Prog. Brain Res.186:113–37.doi:10.1016/B978-0-444-53630-3.00008-7.PMC 3139029.PMID 21094889.
  3. ^Park-Chung M, Wu FS, Farb DH (July 1994). "3 alpha-Hydroxy-5 beta-pregnan-20-one sulfate: a negative modulator of the NMDA-induced current in cultured neurons".Mol. Pharmacol.46 (1):146–50.PMID 7520124.
  4. ^Yaghoubi N, Malayev A, Russek SJ, Gibbs TT, Farb DH (August 1998)."Neurosteroid modulation of recombinant ionotropic glutamate receptors".Brain Res.803 (1–2):153–60.doi:10.1016/s0006-8993(98)00644-1.PMID 9729352.
  5. ^Mellon SH (2007)."Neurosteroid regulation of central nervous system development".Pharmacol. Ther.116 (1):107–24.doi:10.1016/j.pharmthera.2007.04.011.PMC 2386997.PMID 17651807.


Precursors
Corticosteroids
Glucocorticoids
Mineralocorticoids
Sex steroids
Androgens
Estrogens
Progestogens
Neurosteroids
Others
Ionotropic
GABAATooltip γ-Aminobutyric acid A receptor
GABAATooltip γ-Aminobutyric acid A-rho receptor
Metabotropic
GABABTooltip γ-Aminobutyric acid B receptor
Receptor
(ligands)
GlyRTooltip Glycine receptor
NMDARTooltip N-Methyl-D-aspartate receptor
Transporter
(blockers)
GlyT1Tooltip Glycine transporter 1
GlyT2Tooltip Glycine transporter 2
AMPARTooltip α-Amino-3-hydroxy-5-methyl-4-isoxazolepropionic acid receptor
KARTooltip Kainate receptor
NMDARTooltip N-Methyl-D-aspartate receptor
σ1
σ2
Unsorted
TRPA
Activators
Blockers
TRPC
Activators
Blockers
TRPM
Activators
Blockers
TRPML
Activators
Blockers
TRPP
Activators
Blockers
TRPV
Activators
Blockers
Retrieved from "https://en.wikipedia.org/w/index.php?title=Pregnenolone_sulfate&oldid=1316210787"
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