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2203-97-6

2203-97-6 structure
2203-97-6 structure
  • Name: Hydrocortisone hemisuccinate
  • Chemical Name: Hydrocortisone 21-hemisuccinate
  • CAS Number: 2203-97-6
  • Molecular Formula: C25H34O8
  • Molecular Weight: 462.533
  • Catalog: API Hormone and endocrine-regulating drugs Adrenal corticosteroids
  • Create Date: 2018-04-04 08:00:00
  • Modify Date: 2026-07-10 14:13:57
  • Hydrocortisone hemisuccinate (Hydrocortisone 21-hemisuccinate), a physiological glucocorticoid, and is an orally active steroidal anti-inflammatory drug (SAID). Hydrocortisone hemisuccinate inhibits proinflammatory cytokine activity, with IC50s of 6.7 and 21.4 μM for IL-6 and IL-3, respectively. Hydrocortisone hemisuccinate can be used for the research of ulcerative colitis (UC)[1][2][3].

Name Hydrocortisone 21-hemisuccinate
Synonyms HYDROCORTISONEHEMISUCCINATE(ANHYDROUS)
Cortisol 21-(4-oxo-4-hydroxybutanoate)
MFCD00046256
saxizon
21-(3-Cboxy-1-oxopropoxy)-11β,17-dihydroxypregn-4-ene-3,20-dione
20-dione 21-hemisuccinate
Butanedioic acid, mono(11,17-dihydroxy-3,20-dioxopregn-4-en-21-yl) ester
hydrocortisone hemisuccinate ester
C12888
2-oxoethoxy)
Hydrocortisone hydrogen succinate
11b,17a,21-Trihydroxy-4-pregnene-3,20-dione 21-hemisuccinate
4-PREGNEN-11-BETA, 17,21-TRIOL-3,20-DIONE 21-HEMISUCCINATE
Butanedioic acid, mono[(11α)-11,17-dihydroxy-3,20-dioxopregn-4-en-21-yl] ester
hydrocortisone21-hemisuccinate*freeacid
Pregn-4-ene-3,20-dione,21-(3-cboxy-1-oxopropoxy)-11,17-dihydroxy-, (11b)
4-[2-[(8S,9S,10R,11S,13S,14S,17R)-11,17-dihydroxy-10,13-dimethyl-3-oxo-2,6,7,8,9,11,12,14,15,16-decahydro-1H-cyclopenta[a]phenanthren-17-yl]-2-oxoethoxy]-4-oxobutanoic acid
Hydrocortisone 21-he
Hydrocortisone acetate half Kohaku
Hydrocortisone 21-hemisuccinate //BP
HYDROCORTISONE 21-HEMISUCCINATE
Hydrocortisone hydrogen succinate CRS
4-PREGNEN-11β, 17, 21-TRIOL-3, 20-DIONE 21-HEMISUCCINATE
4-{[(11α)-11,17-Dihydroxy-3,20-dioxopregn-4-en-21-yl]oxy}-4-oxobutanoic acid
Cortisol, 21-(hydrogen succinate) (8CI)
4-[(11,17-Dihydroxy-3,20-dioxopregn-4-en-21-yl)oxy]-4-oxobutanoic acid
hydrocortisone21-succinate
EINECS 218-612-3
21-Trihydroxy-4-pregnene-3
HYDROCORTISONE HEMISUCCINATE
4-(2-((8S,9S,10R,11S,13S,14S,17R)
Hydrocortisone Succinate RS
Hydrocortisone hemisuccinate anhydrous,Hydrocortisone 21-hemisuccinate
Hydrocortizone Succinate
HYDROCORTISONE HYDROGEN SUCCINATE
HYDROCORTISONE SUCCINATE
17-dihydroxy-20-dion(11-beta)-preg-4-ene-21-(3-cboxy-1-oxopropoxy)-11
Cortisol, hydrogen succinate (7CI)
cortisol,hydrogensuccinate
cortisolsuccinate
21-(3-Cboxy-1-oxopropoxy)-11β,17α-dihydroxypregn-4-ene-3,20-dione
11β,17α,21-trihydroxy-4-pregnene-3,20-dione 21-hemisuccinate
HYDROXYCORTISONE SUCCINATE
Pregn-4-ene-3,20-dione, 21-(3-cboxy-1-oxopropoxy)-11,17-dihydroxy-, (11β)
11beta,17,21-Trihydroxypregn-4-ene-3,20-dione21-(hydrogensuccinate)
CORTISOL 21-HEMISUCCINATE
hydrocortisone-21-O-hemisuccinate
4-(2-((8S,9S,10R,11S,13S,14S,17R)-11,17-Dihydroxy-10,13-dimethyl-3-oxo-2,3,6,7,8,9,10,11,12,13,14,15,16,17-tetradecahydro-1H-cyclopenta[a]phenanthren-17-yl)-2-oxoethoxy)-4-oxobutanoic acid
RMA-279
cortisol,21-(hydrogensuccinate)
4-PREGNEN-11BETA,17ALPHA,21-TRIOL-3,20-DIONE 21-HEMISUCCINATE
Hydrocortisone Hemisuccinate Monomer
hydrocortisone 21-(hydrogen succinate)
(11-beta)-21-(3-cboxy-1-oxopropoxy)-11,17-dihydroxypreg-4-ene-3,20-dione
11,17-Dihydroxy-10,13-dimethyl-3-oxo-2,3,6,7,8,9,10,11,12,13,14,15,16,17-tetradecahydro-1H-cyclopenta[a]phenanthren-17-yl)
CORTISOL HEMISUCCINATE
Hydrocortisone hemisuccinate, 10 mM in DMSO
11BETA,17ALPHA,21-TRIHYDROXY-4-PREGNENE-3,20-DIONE 21-HEMISUCCINATE
hydrocortisone 21-hemisuccinate*free acid
Description Hydrocortisone hemisuccinate (Hydrocortisone 21-hemisuccinate), a physiological glucocorticoid, and is an orally active steroidal anti-inflammatory drug (SAID). Hydrocortisone hemisuccinate inhibits proinflammatory cytokine activity, with IC50s of 6.7 and 21.4 μM for IL-6 and IL-3, respectively. Hydrocortisone hemisuccinate can be used for the research of ulcerative colitis (UC)[1][2][3].
Related Catalog
Target

IL-6:6.7 μM (IC50)

IL-3:21.4 μM (IC50)

In Vitro Hydrocortisone hemisuccinate inhibits IL-6 and IL-3 bioactivity, with IC50s of 6.7 and 21.4 μM, respectively, and shows no cytotoxic effects on IL-6-independent MH60 cells[3]. Hydrocortisone hemisuccinate (0.12-60 μM; 72 h) inhibits phytohemagglutinin (PHA) response in peripheral lymphocytes (PBL) and T-lymphocytes cultures[3].
In Vivo Hydrocortisone hemisuccinate (30 mg/kg; p.o. twice daily for 5 d) reduces the weight loss and increases the food intake in mice[2]. Animal Model: Male Sprague-Dawley rats (200-220 g, 10-11 weeks) are induced colitis[2] Dosage: 30 mg/kg Administration: P.o. twice daily for 5 days Result: Significantly decreased the disease activity index (DAI) scores and myeloperoxidase (MPO) activity compared to the 2, 4, 6-trinitrobenzenesulfonic acid (TNBS) group. Increased the body weight.
References

[1]. Kang BS, et, al. Inhibitory effects of anti-inflammatory drugs on interleukin-6 bioactivity. Biol Pharm Bull. 2001 Jun;24(6):701-3.

[2]. You YC, et, al. In vitro and in vivo application of pH-sensitive colon-targeting polysaccharide hydrogel used for ulcerative colitis therapy. Carbohydr Polym. 2015 Oct 5;130:243-53.

[3]. Langhoff E, et, al. The immunosuppressive potency in vitro of physiological and synthetic steroids on lymphocyte cultures. Int J Immunopharmacol. 1987;9(4):469-73.

Density 1.3±0.1 g/cm3
Boiling Point 685.5±55.0 °C at 760 mmHg
Molecular Formula C25H34O8
Molecular Weight 462.533
Flash Point 231.1±25.0 °C
Exact Mass 462.225372
PSA 138.20000
LogP 2.13
Vapour Pressure 0.0±4.8 mmHg at 25°C
Index of Refraction 1.587
Storage condition −20°C
Water Solubility Practically insoluble in water, freely soluble in acetone and in anhydrous ethanol. It dissolves in dilute solutions of alkali carbonates and alkali hydroxides.

CHEMICAL IDENTIFICATION

RTECS NUMBER :
TU5010147
CHEMICAL NAME :
Preg-4-ene-3,20-dione, 21-(3-carboxy-1-oxopropoxy)-11,17-dihydroxy-, (11-beta)-
CAS REGISTRY NUMBER :
2203-97-6
LAST UPDATED :
199504
DATA ITEMS CITED :
2
MOLECULAR FORMULA :
C25-H34-O8

HEALTH HAZARD DATA

ACUTE TOXICITY DATA

TYPE OF TEST :
TDLo - Lowest published toxic dose
ROUTE OF EXPOSURE :
Oral
SPECIES OBSERVED :
Rodent - rat
DOSE/DURATION :
4200 mg/kg/10W-C
TOXIC EFFECTS :
Immunological Including Allergic - decrease in humoral immune response
REFERENCE :
BECTA6 Bulletin of Environmental Contamination and Toxicology. (Springer-Verlag New York, Inc., Service Center, 44 Hartz Way, Secaucus, NJ 07094) V.1- 1966- Volume(issue)/page/year: 41,523,1988 *** NIOSH STANDARDS DEVELOPMENT AND SURVEILLANCE DATA *** NIOSH OCCUPATIONAL EXPOSURE SURVEY DATA : NOES - National Occupational Exposure Survey (1983) NOES Hazard Code - X4704 No. of Facilities: 114 (estimated) No. of Industries: 1 No. of Occupations: 5 No. of Employees: 16945 (estimated) No. of Female Employees: 15681 (estimated)
Personal Protective Equipment Eyeshields;Gloves;type N95 (US);type P1 (EN143) respirator filter
Hazard Codes Xi
Safety Phrases S22-S24/25
RIDADR NONH for all modes of transport
WGK Germany 3
RTECS TU5010147
Precursor  2

DownStream  1

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