Hydrocortisone hemisuccinate structure
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Common Name | Hydrocortisone hemisuccinate | ||
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CAS Number | 2203-97-6 | Molecular Weight | 462.533 | |
Density | 1.3±0.1 g/cm3 | Boiling Point | 685.5±55.0 °C at 760 mmHg | |
Molecular Formula | C25H34O8 | Melting Point | N/A | |
MSDS | USA | Flash Point | 231.1±25.0 °C |
Use of Hydrocortisone hemisuccinateHydrocortisone 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 |
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Synonym | More Synonyms |
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]. |
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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 |
Density | 1.3±0.1 g/cm3 |
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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
HEALTH HAZARD DATAACUTE TOXICITY DATA
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Personal Protective Equipment | Eyeshields;Gloves;type N95 (US);type P1 (EN143) respirator filter |
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Hazard Codes | Xi |
Safety Phrases | S22-S24/25 |
RIDADR | NONH for all modes of transport |
WGK Germany | 3 |
RTECS | TU5010147 |
~98% Hydrocortisone ... CAS#:2203-97-6 |
Literature: Wang, Chao; Zhao, Ming; Qiu, Xuecai; Peng, Shiqi Bioorganic and Medicinal Chemistry, 2004 , vol. 12, # 16 p. 4403 - 4421 |
Precursor 2 | |
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DownStream 1 | |
Daily endogenous cortisol production and hydrocortisone pharmacokinetics in adult horses and neonatal foals.
Am. J. Vet. Res. 73(1) , 68-75, (2012) To compare daily endogenous cortisol production rate and the pharmacokinetics of an i.v. bolus of hydrocortisone between neonatal foals and adult horses.10 healthy full-term 2- to 4-day-old foals and ... |
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The compatibility of a low concentration of hydrocortisone sodium succinate with selected drugs during a simulated Y-site administration.
Crit. Care Resusc. 15(1) , 63-6, (2013) Bolus dose concentrations of hydrocortisone (50mg/mL) are reported to be incompatible with midazolam and ciprofloxacin in Y-site mixing studies. We evaluated the physical and chemical compatibility of... |
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Glucocorticoids decrease serum adiponectin level and WAT adiponectin mRNA expression in rats.
Steroids 75(12) , 853-8, (2010) Accumulating evidence suggests that adiponectin plays an important role in the genesis of obesity and insulin resistance. Although it has been shown that glucocortocoids (GC) inhibit adiponectin expre... |
Hydrocortisone 21-he |
MFCD00046256 |
saxizon |
cortisol,hydrogensuccinate |
cortisolsuccinate |
Butanedioic acid, mono(11,17-dihydroxy-3,20-dioxopregn-4-en-21-yl) ester |
hydrocortisone hemisuccinate ester |
4-{[(11α)-11,17-Dihydroxy-3,20-dioxopregn-4-en-21-yl]oxy}-4-oxobutanoic acid |
CORTISOL HEMISUCCINATE |
Hydrocortisone hydrogen succinate |
4-[(11,17-Dihydroxy-3,20-dioxopregn-4-en-21-yl)oxy]-4-oxobutanoic acid |
Hydrocortisone hemisuccinate |
EINECS 218-612-3 |
CORTISOL 21-HEMISUCCINATE |
hydrocortisone-21-O-hemisuccinate |
Hydrocortizone Succinate |
Butanedioic acid, mono[(11α)-11,17-dihydroxy-3,20-dioxopregn-4-en-21-yl] ester |
hydrocortisone21-hemisuccinate*freeacid |
HYDROCORTISONE SUCCINATE |