Basic information Safety Supplier Related

3-BETA,5-ALPHA-TETRAHYDRODEOSOXYCORTICOSTERONE

Basic information Safety Supplier Related

3-BETA,5-ALPHA-TETRAHYDRODEOSOXYCORTICOSTERONE Basic information

Product Name:
3-BETA,5-ALPHA-TETRAHYDRODEOSOXYCORTICOSTERONE
Synonyms:
  • 3-BETA,5-ALPHA-TETRAHYDRODEOSOXYCORTICOSTERONE
  • 5-A-pregnane-3-B-21-diol-20-one
  • 5-ALPHA-PREGNAN-3-BETA, 21-DIOL-20-ONE
  • 3-beta,5-alfa-Tetrahydrodeoxycorticosterone
  • 3β,5α-Tetrahydrodeoxycorticosterone
  • 1-[(1S,3aS,3bR,5aS,7S,9aS,9bS,11aS)-7-hydroxy-9 a,11a-dimethyl-hexadecahydro-1H-cyclopenta[a]p henanthren-1-yl]-2-hydroxyethan-1-one
  • "3β,5a-Tetrahydrodeoxycorticosterone"
  • 3β,5α-THDOC
CAS:
567-01-1
MF:
C21H34O3
MW:
334.49
Mol File:
567-01-1.mol
More
Less

3-BETA,5-ALPHA-TETRAHYDRODEOSOXYCORTICOSTERONE Chemical Properties

storage temp. 
Store at -20°C
solubility 
≤25mg/ml in ethanol;25mg/ml in DMSO;25mg/ml in dimethyl formamide
form 
crystalline solid
More
Less

3-BETA,5-ALPHA-TETRAHYDRODEOSOXYCORTICOSTERONE Usage And Synthesis

Description

3β,5α-THDOC is a neurosteroid. It inhibits seizures induced by pilocarpine, but not pentylenetetrazol (PTZ; ), in mice (ED50s = 45.9 and >100 mg/kg, respectively). 3β,5α-THDOC has been found in the urine of women during the third trimester of pregnancy.

Uses

3β,5α-Tetrahydrodeoxycorticosterone is a novel derivative of the steroid Dehydroepiandrosterone (DHEA), a known uncompetitive inhibitor of Glucose 6-Phosphate Dehydrogenase (G6PD). Studies have shown that 3β,5α-Tetrahydrodeoxycorticosterone may have potential function in the modulation of calcium and GABAA-gated chloride channel currents found in rat and guinea-pig neurons.

in vitro

epiallopregnanolone showed no effects on the gaba-mediated chloride flux through several types of recombinant gaba receptors. epiallopregnanolone inhibited the allopregnanolone-stimulated gaba-mediated chloride flux through gabaa receptors. epiallopregnanolone antagonized the inhibitory effects of allopregnanolone and ethanol on the population spike in the ca1 region of the hippocampal brain slices [1]. epiallopregnanolone selectively blocked the allopregnanolone inhibition of the population spike in the rat hippocampal ca1[3].

in vivo

in rats trained to discriminate either 0.8g/kg or 1.2 g/kg ethanol, 100 mg/kg epiallopregnanolone treatment decreased the maximum effect by 40% and 54% ethanol lever, respectively. epiallopregnanolone significantly decreased response rates when compared with control condition [1].

References

[1] ginsburg b c, lamb r j. alphaxalone and epiallopregnanolone in rats trained to discriminate ethanol[j]. alcoholism: clinical and experimental research, 2005, 29(9): 1621-1629.
[2] macdonald r l, olsen r w. gabaa receptor channels[j]. annual review of neuroscience, 1994, 17(1): 569-602.
[3] wang m, bckstrm t, landgren s. epiallopregnanolone selectively blocks the allopregnanolone inhibition of the population spike in the rat hippocampal ca1[j]. acta physiologica scandinavica, 1999, 167(2): a5-a5.

3-BETA,5-ALPHA-TETRAHYDRODEOSOXYCORTICOSTERONESupplier

J & K SCIENTIFIC LTD.
Tel
010-82848833 400-666-7788
Email
jkinfo@jkchemical.com
SynAsst Chemical.
Tel
021-60343070
BOC Sciences
Tel
16314854226
Email
info@bocsci.com
Shanghai EFE Biological Technology Co., Ltd.
Tel
021-65675885 18964387627
Email
info@efebio.com
Shenzhen Polymeri Biochemical Technology Co., Ltd.
Tel
+86-400-002-6226 +86-13028896684;
Email
sales@rrkchem.com