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303-01-5

303-01-5 structure
303-01-5 structure
  • Name: Pregnane-3,20-dione,21-hydroxy-, (5b)-
  • Chemical Name: 5β-dihydrodeoxycorticosterone
  • CAS Number: 303-01-5
  • Molecular Formula: C21H32O3
  • Molecular Weight: 332.47700
  • Catalog: Research Areas Neurological Disease
  • Create Date: 2016-01-03 20:18:54
  • Modify Date: 2024-01-05 20:35:45
  • Hydroxydione has an effect of general anesthetic. Hydroxydione is a neuroactive steroid it can be used for anaesthesia related research[1][2].

Name 5β-dihydrodeoxycorticosterone
Synonyms 21-hydroxy-5|A-pregnan-3,20-dion
21-Hydroxy-5beta-pregnan-3,20-dion
hydroxydione
21-hydroxy-4-pregnen-3,20-dione
5beta-dihydrodeoxycorticosterone
(5R,8R,9S,10S,13S,14S,17S)-17-(2-hydroxyacetyl)-10,13-dimethyl-1,2,4,5,6,7,8,9,11,12,14,15,16,17-tetradecahydrocyclopenta[a]phenanthren-3-one
Description Hydroxydione has an effect of general anesthetic. Hydroxydione is a neuroactive steroid it can be used for anaesthesia related research[1][2].
Related Catalog
In Vivo Hydroxydione increases the duration of hexobarbital narcosis and repeats hexobarbital doses decrease the duration of hydroxydione narcosis[1]. Hydroxydione (5-100 mg/kg; i.v. once) produces a transient hypotension with little bradycardia and affects the respiration[2]. Animal Model: Cats with chloralose 60 to 80 mg/kg[2] Dosage: 5-100 mg/kg Administration: Intravenous injection; 5-100 mg/kg once Result: Produce severe respiratory depression, but showed no effect on the tibialis in response to excitation of its motor nerve under the condition of chloralose. Produced the usual substantial sustained hypotension seen in chloralosed cats to response the nictitating membrane topreganglionic excitation with a dose of 10 mg/kg. Repressed the respiration in chloralosed cats after a rapid injection.
Density 1.11g/cm3
Boiling Point 468.6ºC at 760 mmHg
Molecular Formula C21H32O3
Molecular Weight 332.47700
Flash Point 251.3ºC
Exact Mass 332.23500
PSA 54.37000
LogP 3.77580
Index of Refraction 1.531

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303-01-5 structure

303-01-5

Literature: Gelbart,A.; Thomas,R. Journal of Medicinal Chemistry, 1978 , vol. 21, p. 284 - 288

~28%

303-01-5 structure

303-01-5

Literature: Kluge; Schulz; Liebsch Tetrahedron, 1996 , vol. 52, # 8 p. 2957 - 2976

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303-01-5 structure

303-01-5

Literature: Upjohn Co. Patent: US2817670 , 1952 ;

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303-01-5 structure

303-01-5

Literature: Upjohn Co. Patent: US2817670 , 1952 ;
Precursor  2

DownStream  1