The story of 16A-Hydroxy Prednisolone ties back to the search for better anti-inflammatory agents in the mid-20th century. Scientists dug deep, tinkering with steroid molecules to squeeze out more therapeutic properties and dial down side effects. Early researchers relied on classic chemical modification — adding hydroxyl groups, playing with oxidation steps, and trying catalytic tweaks. They aimed at unlocking new activity or finding a special fit for health conditions beyond standard corticosteroid treatments. Teams who managed to first synthesize this molecule nudged therapy options forward, hinting at new opportunities in endocrinology and pharmacology. Laboratories worldwide jumped in, chasing tweaks and tracking patents, all under the hope of offering the medical field something more nuanced than regular prednisolone.
A close cousin to prednisolone, 16A-Hydroxy Prednisolone carries an extra hydroxyl at the 16th carbon position, which makes it stand out from its relatives. Labs find it in powder form, off-white or sometimes faintly beige, easy to spot for someone used to handling steroids. Its pharmaceutical grade often comes sealed against moisture, with tight control over storage temperature and light exposure. Across research catalogs, suppliers sell it with clear purity specs, and the tags always list precise molecular formulas and weights. Besides its place in clinical research, the compound turns up in metabolic studies, synthetic chemistry experiments, and as a reference standard in steroid detection work.
Looking at its structure, 16A-Hydroxy Prednisolone falls under the corticosteroid umbrella, but its extra hydroxyl changes the game for person handling it in the lab. The molecule carries a molecular weight around 362.46 g/mol. It usually turns up as a crystalline powder, more soluble in alcohols and slightly less so in pure water. Its melting point sits in the 230-240°C range, hinting at solid packing in its crystal lattice. Because of its oxygen-rich structure, it can interact with both acidic and basic substances, making pH and solvent choice matter in almost every experiment. Chemical reactivity owes a lot to the 16-hydroxyl group, which can open up new modification pathways or affect stability under storage.
Vials and packets sold for lab use spell out every detail, right down to batch numbers and expiration dates. Purity often checks out at above 98%. Labels spell out storage instructions – usually a cool, dry, and dark spot – and stick to international hazard codes. For trace work, suppliers offer certificates showing exact analytical patterns, including HPLC chromatograms and NMR spectra. Chemists look for total organic impurities under 0.2%, keep residual solvents in check, and track heavy metals well below pharmacopeia limits. Safety data come standard: incompatibilities, combustion risk, and signs to watch out for in case of accidental exposure.
Small-scale labs and large production plants approach synthesis in their own way, but core steps stick close to steroid chemistry traditions. The process may start from prednisolone or related intermediates, using selective oxidation followed by introduction of the hydroxyl group at position 16. Chemists might reach for microbial oxidation as a gentle step or go heavy with a chemical oxidant to get the right intermediate. Techniques lean on stepwise protection and deprotection, especially if side hydroxyl groups risk reacting out of turn. After main steps wrap up, purification relies on column chromatography or recrystallization, squeezing out impurities until spectral analysis lines up with references.
Handy for modifications, the 16A-hydroxy group acts as a landing spot for new derivatives. Chemists might esterify the site, hoping to boost lipid solubility for depot formulations. Other researchers follow up with oxidation at adjacent carbons, chasing metabolites to mimic what happens inside the body. Some labs keep transforming the base scaffold, tacking on groups at other positions to hunt for new anti-inflammatory or immunosuppressive activity. Those working in analytical chemistry chase after breakdown products, simulating what stomach acid or liver enzymes might do. Every change helps map out both drug action and safety, showing which tweaks carry promise or trouble.
This molecule goes by several names as commercial suppliers and research papers piece together their histories. In the literature, you might see “16-alpha-hydroxy-prednisolone”, “16α-OH Prednisolone”, or shortened versions like “Hydroxyprednisolone-16α”. Some catalogs simply carry the name “16α-Hydroxyprednisolone” listed among their steroid metabolites or research standards. Certain researchers will refer to it in shorthand within complex synthesis pathways, linking the full structure only in supplementary tables or figures. Supplier catalogs sometimes assign cryptic alphanumeric codes, especially in bulk chemical sales, to keep SKU systems clean.
Steroids like this bring a set of safety rules, tailored by years of mishaps and working with tricky powders. Most labs insist on gloves, goggles, and strong ventilation. Dust can cause irritation—getting this stuff in your eyes or on skin isn’t pleasant. Long-term handling, especially in bulk, demands respect for chronic exposure risks. Material safety data documents warn about possible effects if inhaled, ingested, or handled carelessly. Clean-up procedures and emergency procedures get drilled into everyone working with the product. Waste management involves chemical incineration or controlled disposal, never standard trash, keeping both the worker and the environment safe from steroid contamination.
Medical research and clinical diagnostics keep 16A-Hydroxy Prednisolone in regular demand. Labs studying corticosteroid metabolism use it as a reference marker, mapping how the body processes drugs over time. Its closer relatives serve as drugs in themselves—especially when dealing with inflammation, allergic reactions, or autoimmune troubles. In sports anti-doping work, labs need it to test for steroid abuse or illegal drug modifications. For pharmacologists, subtle differences in how the molecule works tease out options for future drug design. Diagnostics companies make use of it for calibrating analytical instruments, ensuring test results for patients come out accurate and reliable.
Development never slows, especially when a molecule promises new insight or a better safety profile. Academic groups examine its properties under dozens of chemical environments, checking for breakdown routes and reactive hotspots. Pharmaceutical companies watch closely, hoping for modifications that trim side effects while boosting desired activity. Some invest in animal studies, looking for improved wound healing or joint protection beyond what’s possible with standard corticosteroids. More intense scrutiny surrounds its interaction with biological targets—hormone receptors, metabolic enzymes, and inflammatory pathways all go under the microscope. Researchers also ask where this extra hydroxyl makes an impact: does it change resistance to inactivation, does it stick longer in the bloodstream, or does it work on a different organ with special effectiveness?
Steroid derivatives rarely get free passes on safety. Toxicity work spans everything from acute effects in cell culture to slow, chronic dosing in animal models. Labs record every itch, rash, or change in weight in animal studies, pairing clinical observation with tests on liver and kidney function. Investigators push doses until effects show up, then pull back to map a safe range. Human cell studies fill in gaps on genetic toxicity, allergenicity, or potential for unwanted immune suppression. Regular regulatory checks make sure findings match what clinicians need to know before expanding treatment options or moving to human trials.
Steroid chemistry always has another chapter waiting. Scientists keep pressing the limits—new syntheses, modified scaffolds, or unique administration routes. The future could mean derivatives that dodge old side effects, or products wrapped in precision delivery systems to target stubborn inflammation sites. As analytical technology improves, faster and more reliable detection methods let researchers follow these molecules through metabolism and environmental exposure. Personalized medicine could one day pair specific hydroxylation patterns to individual patient genetics, pushing away from “one size fits all” solutions. Interest keeps growing in how novel modifications like the 16-alpha hydroxyl influence medical outcomes, offering new hope for patients managing tough autoimmune or inflammatory diseases.
People tend to focus on big-name medicines and life-saving breakthroughs, but there’s plenty of value found in the smaller pieces of the puzzle. 16A-Hydroxy Prednisolone, though rarely the topic of any dinner table conversation, tells a subtle story about how medicine works behind the scenes.
Prednisolone itself often takes center stage as a reliable synthetic corticosteroid. It lowers inflammation, keeps immune responses in check, and helps treat allergies, asthma, autoimmune concerns, and even cancer. As the body goes to work, it transforms prednisolone through various pathways. Out of these chemical twists and turns emerges 16A-Hydroxy Prednisolone.
This byproduct doesn’t just sit in the background. When patients take prednisolone, doctors want to know if the medicine gets processed as expected, if dosing is right, or if something unexpected’s going on with liver or kidney function. By measuring 16A-Hydroxy Prednisolone in the urine, labs and doctors can see how the body is handling its load of corticosteroids. If the levels spike or drop in odd ways, that can point to issues with metabolism—the liver might be overworked, or there might be a drug interaction throwing off the normal order of things.
There’s another layer to this metabolite’s importance. Kids sometimes struggle with rare metabolic disorders, like congenital adrenal hyperplasia. Sometimes, monitoring 16A-Hydroxy Prednisolone gives a clearer view of how treatments are working, or offers reassurance that the hormone levels are under control. I’ve seen pediatricians dig into these metabolites while balancing treatment plans, searching for the sweet spot where medication helps but side effects don’t do harm.
Risks and RealitiesToo much dependence on single measurements can create blind spots. Results need context—diet, kidney function, other drugs on board. Some labs don’t run advanced metabolite tests, which means access varies depending on geography and insurance. Also, accuracy depends on strong laboratory methods and healthy communication between clinicians and patients.
Doctors owe it to patients to explain what these numbers mean. Believe me, parents or anyone facing a chronic illness start to feel like they’re drowning in jargon. Honest conversations help everyone understand whether results come from normal metabolism or a worrying breakdown in drug processing.
Medical science never stands still. Smart clinicians use metabolites like 16A-Hydroxy Prednisolone to fine-tune treatments, aiming to avoid long-term steroid complications. In my experience, bringing lab results into discussions fosters trust. Patients want more than just a pill—they want to know it’s working, and they want some predictability in an unpredictable world.
As testing becomes more available and the science sharpens, those in need stand to gain the most. Lab data must guide treatment, not overwhelm. Fewer side effects, more controlled diseases, and better quality of life rest on paying attention—even to the smallest byproducts of big medicines.
Steroid medications such as 16A-Hydroxy Prednisolone pull a lot of weight in treating inflammation, allergies, and certain chronic illnesses. People often expect fast results, not always stopping to weigh risks against relief. Speaking from day-to-day encounters in clinics and hospitals, I’ve seen many patients gain a better life, but also grapple with unexpected changes in health. Relying on any corticosteroid, including this one, brings along some trade-offs that matter for anyone hoping to make informed choices.
Certain side effects appear not long after starting a course. Some people get mild issues: swelling in the face, feeling jittery, or having trouble sleeping. Blood sugar can jump, as I’ve watched many folks with diabetes suddenly lose their careful control, sending them back for new medication adjustments. 16A-Hydroxy Prednisolone nudges appetite up, making food feel irresistible and weight gain nearly inevitable for some.
Sticking with corticosteroids for weeks or months brings bigger problems. Bones can thin out over time. It shocks patients to see their scans, learning they’ve moved closer to osteoporosis after a few rounds. The medicine slows the healing of wounds. Immune responses take a back seat, which lets everyday coughs or sniffles blossom into real infections. Even tiny cuts can become bothersome.
Some adults see their moods swing or slip into depression, while others find themselves anxious over things that never used to matter. I’ve walked beside family members who watch loved ones grow distant or irritable, wondering if they’re seeing a new personality entirely. Kids get affected, too—the growth process sometimes slows during longer courses.
High blood pressure sneaks up on many folks, and it hides unless someone checks regularly. This change can stretch blood vessels thin over the years. Vision sometimes blurs. Extended use might lead to cataracts or damage in the back of the eye, eventually requiring a visit to a specialist.
Anyone with a history of peptic ulcers deals with more stomach pain; a few land back in the emergency room with a bleeding surprise. Even if you think your gut can handle tough medications, this class of drugs can still catch people off-guard.
Medical teams help patients avoid the roughest side effects by keeping doses as low as possible and checking in often. Doctors often recommend adding calcium or vitamin D to slow bone loss. Blood sugar levels will need extra attention, not just with a home machine, but through real diet changes and honest talks about exercise.
Support at home and in the clinic means watching closely for mood shifts, cuts or bruises that won’t fade, or strange new health issues. Over-the-counter antacids or additional medications get discussed before starting treatment if ulcers have ever been a concern. Decision-making always runs both ways—the benefits of a corticosteroid must always get stacked against risks. Patients, doctors, and loved ones all have a role in spotting changes early, adjusting plans together, and speaking up well before problems take root.
16A-Hydroxy Prednisolone doesn’t come up in conversation like common over-the-counter painkillers, but it plays a crucial part for folks who rely on nuanced steroid treatments. Figuring out a solid dosing regimen takes more than just picking a number off a chart. The real-life benefit hinges on keeping an eye on lab values, individual metabolism, and the specific reason the medication landed in the treatment plan.
Glucocorticoids impact the body in a dozen different ways, and that experience comes from years of patient interactions. People process steroids at different speeds. Genetics, age, kidney and liver health, and other medications twist the rules. Sometimes, steroids build up in the system and trigger more side effects; other times, they clear so quickly that the benefit drops off. Bloodwork, symptom tracking, and honest conversations about side effects help fine-tune any dose of 16A-Hydroxy Prednisolone.
The safest approach often goes like this: begin with the smallest dose thought to be effective. That way, the risk for things like mood swings, blood sugar jumps, or immune suppression stays on the lower end. The doctor keeps close tabs with follow-ups, asking about joint pain, vision changes, or swelling. If those problems crop up, doses pull back or step down faster.
Taking steroids isn’t just about the milligrams; timing makes a real difference. Doctors often suggest morning doses for substances like 16A-Hydroxy Prednisolone. That’s because our bodies naturally ramp up their own steroid production in the morning. Matching the dose to this rhythm helps avoid sleep problems and reduces adrenal stress. If pills upset the stomach, injectable options or tailored release forms sometimes offer a workaround—an option for people with digestion or absorption hurdles.
People don’t live in a bubble. Travel, stress, infections, or a new diagnosis like diabetes shows up and changes everything. Dosing remains flexible. During an infection, steroid doses might need increasing to keep up with the body’s needs. Leaning on real-world conditions rather than textbook doses keeps patients safer.
Regular appointments focus on blood pressure, blood sugar, and eye health—the big three where steroids like 16A-Hydroxy Prednisolone can quietly wreak havoc. Bone strength also sits high on the list, especially for anyone on long-term therapy. Many prescribers add calcium, vitamin D, or sometimes even other medications to shield bone density.
Researchers have tracked how synthetic glucocorticoids act in the body for decades. One review in the Journal of Clinical Pharmacology showed wild swings in how different people absorb and break down steroid hormones. Well-designed studies drive home the need for customized doses, especially for those facing long-term or high-dose treatment.
Building trust matters. People want straight answers if side effects begin or if a dose doesn’t do enough. Open access to professional guidance—whether through clinic visits or telehealth—lets folks adjust as needed, based on science and on symptoms. Proper dosing of 16A-Hydroxy Prednisolone grows from evidence, ongoing check-ins, and honest human experience.
Plenty of people have heard stories about steroids used in medicine. When you dig deeper into corticosteroids, 16A-Hydroxy Prednisolone often gets overlooked, yet it sits in the same family as prednisolone and prednisone. These medications manage tough inflammatory diseases like arthritis or asthma. Coming from a background where several family members have dealt with steroids for chronic illness, I’ve seen firsthand that even subtle differences in the makeup of a steroid can push the body one way or another.
Doctors and pharmacists always ask for a full list of medications during visits, and it’s not just routine. Steroids affect almost every system in the body, from blood pressure to immune response. 16A-Hydroxy Prednisolone acts like its relatives, changing how the liver breaks down other compounds, and sometimes overwhelms the checks and balances in place. In busy clinics, I’ve noticed that people often forget to mention supplements or herbal remedies, but these can change how drugs like this steroid behave.
Blood Thinners: People who rely on warfarin or other anticoagulants might see their effects change, risking bleeding that can sneak up with little warning. This makes close monitoring and dose adjustments critical.
Diabetes Medications: Taking a corticosteroid tends to push sugar levels higher. Patients on insulin or other diabetes drugs often find their blood sugar readings wandering. My father spent years adjusting doses as one steroid or another nudged his blood sugar out of range. It’s not a small side effect — it changes daily life.
Strong Antibiotics and Antifungals: Medicines that block liver enzymes, like ketoconazole or clarithromycin, leave more steroid in circulation. Short-term use probably creates few issues, but chronic use adds up. Extra steroid floating around can add to side effects like muscle weakness, bone thinning, and immune suppression.
Seizure Drugs: Anti-seizure medicines such as phenytoin and carbamazepine hustle steroids out of the system faster. Less steroid in the blood might mean symptoms return sooner, calling for higher doses or switching drugs altogether.
Vaccines: The immune-suppressing effect raises concerns. Steroids reduce a person’s ability to build up immunity after vaccines, especially if they’re receiving certain live vaccines. For many kids facing tough conditions, this means extra planning at the doctor’s office.
Keeping every healthcare provider in the loop makes a big difference. Pharmacists who spot overlapping prescriptions, doctors who ask those hard questions about supplements and daily routines—all help keep things in balance. Electronic health records help too, but they're not perfect. Many drugstores already use systems that flag potential risks, but they work only if patients stay honest about all the pills in their cabinets.
One approach keeps people out of trouble: regular review of medications with a trusted provider. In my own experience, a quick phone call or a fifteen-minute sit-down every few months catches changes before they turn dangerous. If you're starting or stopping a medication like 16A-Hydroxy Prednisolone, make noise about it. Write it down, mention it every chance you get, and don’t assume anyone already knows what you’re taking.
Drug interactions aren't just fine print in a textbook. They show up as real problems—unexpected bruises, infections, or blood sugar swings that throw off everything else. Talking openly about medicine helps catch them before they matter most.
16A-Hydroxy Prednisolone often gets lumped into conversations about corticosteroids in medicine. As someone who has worked behind the counter in a mid-sized community pharmacy, I quickly noticed a pattern: drugs in this class rarely see the light of day without a doctor’s signature backing them. Prednisolone gets a lot of use for inflammatory conditions, allergies, and the odd autoimmune flare-up. The “16A-Hydroxy” version doesn’t stray from the pack in terms of risk or significance.
Steroids don’t play gentle. They do serious work inside the body and, with that, carry risks. People worry about side effects: bone thinning, immune suppression, mood swings, and the silent creep of high blood sugar. In my experience, folks think a prescription is just bureaucracy. The real truth: direct medical oversight catches problems before they multiply. The safety net isn’t just for show — one missed detail with these drugs can snowball fast.
The FDA classifies prednisolone and nearly all its structural cousins as prescription-only for good reason. No over-the-counter bins, no herbal shelf alternatives. The rules exist because the medications treat serious issues. Unchecked steroid use carries dangers well beyond what most people imagine. I've seen patients who took leftover tablets for a stubborn rash or tried to double up after missing a dose. The result is sometimes disastrous — infections spinning out of control or adrenal glands hitting rock bottom.
Some folks believe seeing the doctor just leads to another piece of paper. My experience paints a different picture. During my pharmacy years, doctors called almost weekly to ask about new side effects or lower a steroid dose as a patient's symptoms eased. The relationship between prescriber and pharmacist catches errors, ensures doses match the condition, and keeps tabs on drug interactions.
Type the name of this drug into any search bar. Chances are, you’ll find international websites promising fast, no-prescription shipping. That’s a gamble I watched go poorly more than once. Unregulated sellers may dilute the product, swap the drug for look-alikes, or skip safety testing. Patients came in sick, desperate, and unsure what they'd actually taken. Using these sources bypasses protections Americans depend on.
The system isn’t perfect, but taking a prescribed route comes with layers of built-in protection. For those with ongoing inflammation, asking the prescriber tough questions helps guard against problems. I always urged patients to write down every drug and bring the list to appointments. Side effect check-ins — even by quick phone calls or patient portals — helped us spot trouble early. It’s worth the time, especially with a medicine as potent as this one.
Real experience shows that skipping the prescription for 16A-Hydroxy Prednisolone isn't just breaking the rules — it defeats the process that keeps people as healthy and safe as possible. Those protections matter.
| Names | |
| Preferred IUPAC name | 11β,16α,17,21-Trihydroxypregna-1,4-diene-3,20-dione |
| Other names |
16α,17,21-Trihydroxypregna-1,4-diene-3,11,20-trione
16α-Hydroxyprednisolone |
| Pronunciation | /ˌsɪkstiːn eɪ haɪˈdrɒksi prɛdˈnɪsələʊn/ |
| Preferred IUPAC name | (11β,16α)-11,17,21-Trihydroxypregna-1,4-diene-3,20-dione |
| Other names |
16α,17α,21-Trihydroxypregn-1,4-diene-3,11,20-trione
16α-Hydroxycortisol |
| Pronunciation | /ˌsɪksˈtiːn eɪ haɪˈdrɒk.si prɛdˈnɪs.əˌloʊn/ |
| Identifiers | |
| CAS Number | 13951-70-7 |
| Beilstein Reference | Beilstein Reference 2051173 |
| ChEBI | CHEBI:34631 |
| ChEMBL | CHEMBL1530070 |
| ChemSpider | 22246608 |
| DrugBank | DB15880 |
| ECHA InfoCard | 03d87ffe-58f4-4928-875d-3e5cfbf25977 |
| EC Number | 1.1.1.215 |
| Gmelin Reference | 81246 |
| KEGG | C16535 |
| MeSH | D004589 |
| PubChem CID | 177534 |
| RTECS number | OM8225000 |
| UNII | 6M2J6D4R1D |
| UN number | UN2045 |
| CompTox Dashboard (EPA) | DTXSID4086983 |
| CAS Number | 13951-70-7 |
| Beilstein Reference | 2331046 |
| ChEBI | CHEBI:76268 |
| ChEMBL | CHEMBL1636 |
| ChemSpider | 57358430 |
| DrugBank | DB01248 |
| ECHA InfoCard | 100.037.727 |
| EC Number | 1.1.1.215 |
| Gmelin Reference | 314688 |
| KEGG | C14771 |
| MeSH | D016612 |
| PubChem CID | 443943 |
| RTECS number | UF7805000 |
| UNII | T6X7F71DW9 |
| UN number | UN1233 |
| CompTox Dashboard (EPA) | DTXSID9020248 |
| Properties | |
| Chemical formula | C21H28O6 |
| Molar mass | 370.444 g/mol |
| Appearance | White to off-white crystalline powder |
| Odor | Odorless |
| Density | 1.37 g/cm³ |
| Solubility in water | Insoluble in water |
| log P | 1.29 |
| Vapor pressure | Vapor pressure: 4.6E-16 mmHg |
| Acidity (pKa) | 12.59 |
| Basicity (pKb) | 13.08 |
| Refractive index (nD) | 1.631 |
| Dipole moment | 5.06 D |
| Chemical formula | C21H28O6 |
| Molar mass | 374.47 g/mol |
| Appearance | White to off-white solid |
| Odor | Odorless |
| Density | 1.34 g/cm³ |
| Solubility in water | Slightly soluble in water |
| log P | 1.51 |
| Vapor pressure | 1.35E-10 mmHg at 25°C |
| Acidity (pKa) | 12.59 |
| Basicity (pKb) | 12.26 |
| Refractive index (nD) | 1.618 |
| Dipole moment | 5.96 Debye |
| Thermochemistry | |
| Std molar entropy (S⦵298) | 272.1 J·mol⁻¹·K⁻¹ |
| Std enthalpy of formation (ΔfH⦵298) | -686.4 kJ/mol |
| Std molar entropy (S⦵298) | 324.6 J·mol⁻¹·K⁻¹ |
| Pharmacology | |
| ATC code | H02AB06 |
| ATC code | H02AB06 |
| Hazards | |
| Main hazards | Not hazardous according to GHS classification. |
| GHS labelling | GHS labelling: Not a hazardous substance or mixture according to the Globally Harmonized System (GHS). |
| Pictograms | HCJTZJCGOKTXQS-OBQKDFKQSA-N |
| Signal word | Warning |
| Hazard statements | Hazard statements: "H302, H315, H319, H335 |
| Precautionary statements | Keep container tightly closed. Store in a cool, dry place. Avoid contact with skin and eyes. Wear suitable protective clothing. |
| Flash point | Flash point: 185.8 ± 27.9 °C |
| LD50 (median dose) | 2500 mg/kg (rat, oral) |
| NIOSH | NA |
| PEL (Permissible) | Not established |
| REL (Recommended) | Clinical Chemistry |
| IDLH (Immediate danger) | Not established |
| Main hazards | Causes skin irritation. Causes serious eye irritation. May cause respiratory irritation. |
| GHS labelling | GHS labelling: "Danger; H360: May damage fertility or the unborn child; H362: May cause harm to breast-fed children; P201, P202, P263, P308+P313, P405, P501 |
| Pictograms | CC(=O)[C@]1(C)C[C@@H]2[C@@H]3CCC4=CC(=O)C=C[C@@]4([C@H]3C(=O)C[C@@]21O)C |
| Signal word | Warning |
| Hazard statements | H315, H319, H335 |
| Precautionary statements | P264; P270; P273; P301+P312; P330; P501 |
| LD50 (median dose) | LD50 (median dose) of 16A-Hydroxy Prednisolone is 2930 mg/kg (rat, oral) |
| NIOSH | EX2450000 |
| PEL (Permissible) | Not established |
| REL (Recommended) | 15.68 |
| IDLH (Immediate danger) | Not established |
| Related compounds | |
| Related compounds |
Prednisolone
Cortisone Hydrocortisone Dexamethasone |
| Related compounds |
Prednisolone
Cortisone Hydrocortisone Prednisone |
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