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Merck
CN

SMB01348

Dihydrocortisol

≥95% (HPLC)

Synonym(s):

5β-Pregnane-11β,17α,21-triol-3,20-dione, 11β,17,21-Trihydroxy-5β-pregnane-3,20-dione, 11β,17α,21-Trihydroxy-5β-pregnane-3,20-dione, 5β-Dihydrocortisol

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About This Item

Empirical Formula (Hill Notation):
C21H32O5
CAS Number:
Molecular Weight:
364.48
UNSPSC Code:
51420000
MDL number:
Assay:
≥95% (HPLC)
Form:
solid
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SMILES string

O[C@]1([C@@]2([C@H]([C@H]3[C@@H]([C@@]4([C@H](CC3)CC(=O)CC4)C)[C@H](C2)O)CC1)C)C(=O)CO

InChI

1S/C21H32O5/c1-19-7-5-13(23)9-12(19)3-4-14-15-6-8-21(26,17(25)11-22)20(15,2)10-16(24)18(14)19/h12,14-16,18,22,24,26H,3-11H2,1-2H3/t12-,14+,15+,16+,18-,19+,20+,21+/m1/s1

InChI key

ACSFOIGNUQUIGE-AIPUTVCKSA-N

assay

≥95% (HPLC)

form

solid

storage temp.

2-8°C

Quality Level

Related Categories

General description

5β-Dihydrocortisol is the product of the enzyme steroid 5-beta-reductase, which catalyzes the reduction of progesterone, androstenedione, 17-alpha-hydroxyprogesterone, testosterone, aldosterone, corticosterone, and cortisol to 5-beta-reduced metabolites. 5β-Dihydrocortisol has shown to potentiate the action of topically applied dexamethasone in raising the intraocular pressure in young rabbits.

Application

Metabolomics research

pictograms

Health hazard

signalword

Danger

Hazard Classifications

Repr. 1A - STOT RE 2

Storage Class

6.1C - Combustible acute toxic Cat.3 / toxic compounds or compounds which causing chronic effects

wgk

WGK 3

Regulatory Information

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A L Southren et al.
Investigative ophthalmology & visual science, 26(3), 393-395 (1985-03-01)
5 beta-dihydrocortisol potentiates the action of topically applied dexamethasone in raising the intraocular pressure (IOP) in young rabbits. Dexamethasone (0.06%) plus 5 beta-dihydrocortisol (0.1 and 1.0%) elevated the IOP 7-10 mmHg within 18 days of treatment. By contrast, 0.06% dexamethasone

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