Details
| Stereochemistry | ABSOLUTE |
| Molecular Formula | C22H30O5 |
| Molecular Weight | 374.4706 |
| Optical Activity | UNSPECIFIED |
| Defined Stereocenters | 8 / 8 |
| E/Z Centers | 0 |
| Charge | 0 |
SHOW SMILES / InChI
SMILES
C[C@H]1C[C@H]2[C@@H]3CC[C@](O)(C(=O)CO)[C@@]3(C)C[C@H](O)[C@@H]2[C@@]4(C)C=CC(=O)C=C14
InChI
InChIKey=VHRSUDSXCMQTMA-PJHHCJLFSA-N
InChI=1S/C22H30O5/c1-12-8-14-15-5-7-22(27,18(26)11-23)21(15,3)10-17(25)19(14)20(2)6-4-13(24)9-16(12)20/h4,6,9,12,14-15,17,19,23,25,27H,5,7-8,10-11H2,1-3H3/t12-,14-,15-,17-,19+,20-,21-,22-/m0/s1
| Molecular Formula | C22H30O5 |
| Molecular Weight | 374.4706 |
| Charge | 0 |
| Count |
|
| Stereochemistry | ABSOLUTE |
| Additional Stereochemistry | No |
| Defined Stereocenters | 8 / 8 |
| E/Z Centers | 0 |
| Optical Activity | UNSPECIFIED |
DescriptionSources: http://www.drugbank.ca/drugs/DB00959Curator's Comment: Description was created based on several sources, including https://www.drugs.com/pro/medrol.html
Sources: http://www.drugbank.ca/drugs/DB00959
Curator's Comment: Description was created based on several sources, including https://www.drugs.com/pro/medrol.html
Methylprednisolone is a prednisolone derivative with similar anti-inflammatory and immunosuppressive action. It is adjunctive therapy for short-term administration in rheumatoid arthritis. It is indicated in the following conditions: endocrine disorders, rheumatic disorders, collagen diseases, allergic states etc. Methylprednisolone is marketed in the USA and Canada under the brand names Medrol and Solu-Medrol. Methylprednisolone is a GR receptor agonist.
CNS Activity
Originator
Sources: http://adisinsight.springer.com/drugs/800003722
Curator's Comment: # Pfizer
Approval Year
Targets
| Primary Target | Pharmacology | Condition | Potency |
|---|---|---|---|
Target ID: CHEMBL2034 Sources: http://www.drugbank.ca/drugs/DB00959 |
2.4 nM [EC50] | ||
Target ID: CHEMBL2034 Sources: http://www.ampoule.org.hk/pdf/advantan.pdf |
|||
Target ID: CHEMBL2111332 Sources: https://www.ncbi.nlm.nih.gov/pubmed/15329590 |
1.07 nM [IC50] |
Conditions
| Condition | Modality | Targets | Highest Phase | Product |
|---|---|---|---|---|
| Primary | MEDROL Approved UseINDICATIONS AND USAGE
MEDROL Tablets are indicated in the following conditions:
1. Endocrine Disorders
Primary or secondary adrenocortical insufficiency (hydrocortisone or cortisone is the first choice; synthetic analogs may be used in conjunction with mineralocorticoids where applicable; in infancy mineralocorticoid supplementation is of particular importance).
Congenital adrenal hyperplasia
Nonsuppurative thyroiditis
Hypercalcemia associated with cancer
2. Rheumatic Disorders
As adjunctive therapy for short-term administration (to tide the patient over an acute episode or exacerbation) in:
Rheumatoid arthritis, including juvenile rheumatoid arthritis (selected cases may require low-dose maintenance therapy)
Ankylosing spondylitis
Acute and subacute bursitis
Synovitis of osteoarthritis
Acute nonspecific tenosynovitis
Post-traumatic osteoarthritis
Psoriatic arthritis
Epicondylitis
Acute gouty arthritis
3. Collagen Diseases
During an exacerbation or as maintenance therapy in selected cases of:
Systemic lupus erythematosus
Systemic dermatomyositis (polymyositis)
Acute rheumatic carditis
4. Dermatologic Diseases
Bullous dermatitis herpetiformis
Severe erythema multiforme (Stevens-Johnson syndrome)
Severe seborrheic dermatitis
Exfoliative dermatitis
Mycosis fungoides
Pemphigus
Severe psoriasis
5. Allergic States
Control of severe or incapacitating allergic conditions intractable to adequate trials of conventional treatment:
Seasonal or perennial allergic rhinitis
Drug hypersensitivity reactions
Serum sickness
Contact dermatitis
Bronchial asthma
Atopic dermatitis
6. Ophthalmic Diseases
Severe acute and chronic allergic and inflammatory processes involving the eye and its adnexa such as:
Allergic corneal marginal ulcers
Herpes zoster ophthalmicus
Anterior segment inflammation
Diffuse posterior uveitis and choroiditis
Sympathetic ophthalmia
Keratitis
Optic neuritis
Allergic conjunctivitis
Chorioretinitis
Iritis and iridocyclitis
7. Respiratory Diseases
Symptomatic sarcoidosis
Berylliosis
Loeffler's syndrome not manageable by other means
Fulminating or disseminated pulmonary tuberculosis when used concurrently with appropriate antituberculous chemotherapy
Aspiration pneumonitis
8. Hematologic Disorders
Idiopathic thrombocytopenic purpura in adults
Secondary thrombocytopenia in adults
Acquired (autoimmune) hemolytic anemia
Erythroblastopenia (RBC anemia)
Congenital (erythroid) hypoplastic anemia
9. Neoplastic Diseases
For palliative management of:
Leukemias and lymphomas in adults
Acute leukemia of childhood
10. Edematous States
To induce a diuresis or remission of proteinuria in the nephrotic syndrome, without uremia, of the idiopathic type or that due to lupus erythematosus.
11. Gastrointestinal Diseases
To tide the patient over a critical period of the disease in:
Ulcerative colitis
Regional enteritis
12. Nervous System
Acute exacerbations of multiple sclerosis
13. Miscellaneous
Tuberculous meningitis with subarachnoid block or impending block when used concurrently with appropriate antituberculous chemotherapy.
Trichinosis with neurologic or myocardial involvement. Launch Date1957 |
|||
| Primary | MEDROL Approved UseINDICATIONS AND USAGE
MEDROL Tablets are indicated in the following conditions:
1. Endocrine Disorders
Primary or secondary adrenocortical insufficiency (hydrocortisone or cortisone is the first choice; synthetic analogs may be used in conjunction with mineralocorticoids where applicable; in infancy mineralocorticoid supplementation is of particular importance).
Congenital adrenal hyperplasia
Nonsuppurative thyroiditis
Hypercalcemia associated with cancer
2. Rheumatic Disorders
As adjunctive therapy for short-term administration (to tide the patient over an acute episode or exacerbation) in:
Rheumatoid arthritis, including juvenile rheumatoid arthritis (selected cases may require low-dose maintenance therapy)
Ankylosing spondylitis
Acute and subacute bursitis
Synovitis of osteoarthritis
Acute nonspecific tenosynovitis
Post-traumatic osteoarthritis
Psoriatic arthritis
Epicondylitis
Acute gouty arthritis
3. Collagen Diseases
During an exacerbation or as maintenance therapy in selected cases of:
Systemic lupus erythematosus
Systemic dermatomyositis (polymyositis)
Acute rheumatic carditis
4. Dermatologic Diseases
Bullous dermatitis herpetiformis
Severe erythema multiforme (Stevens-Johnson syndrome)
Severe seborrheic dermatitis
Exfoliative dermatitis
Mycosis fungoides
Pemphigus
Severe psoriasis
5. Allergic States
Control of severe or incapacitating allergic conditions intractable to adequate trials of conventional treatment:
Seasonal or perennial allergic rhinitis
Drug hypersensitivity reactions
Serum sickness
Contact dermatitis
Bronchial asthma
Atopic dermatitis
6. Ophthalmic Diseases
Severe acute and chronic allergic and inflammatory processes involving the eye and its adnexa such as:
Allergic corneal marginal ulcers
Herpes zoster ophthalmicus
Anterior segment inflammation
Diffuse posterior uveitis and choroiditis
Sympathetic ophthalmia
Keratitis
Optic neuritis
Allergic conjunctivitis
Chorioretinitis
Iritis and iridocyclitis
7. Respiratory Diseases
Symptomatic sarcoidosis
Berylliosis
Loeffler's syndrome not manageable by other means
Fulminating or disseminated pulmonary tuberculosis when used concurrently with appropriate antituberculous chemotherapy
Aspiration pneumonitis
8. Hematologic Disorders
Idiopathic thrombocytopenic purpura in adults
Secondary thrombocytopenia in adults
Acquired (autoimmune) hemolytic anemia
Erythroblastopenia (RBC anemia)
Congenital (erythroid) hypoplastic anemia
9. Neoplastic Diseases
For palliative management of:
Leukemias and lymphomas in adults
Acute leukemia of childhood
10. Edematous States
To induce a diuresis or remission of proteinuria in the nephrotic syndrome, without uremia, of the idiopathic type or that due to lupus erythematosus.
11. Gastrointestinal Diseases
To tide the patient over a critical period of the disease in:
Ulcerative colitis
Regional enteritis
12. Nervous System
Acute exacerbations of multiple sclerosis
13. Miscellaneous
Tuberculous meningitis with subarachnoid block or impending block when used concurrently with appropriate antituberculous chemotherapy.
Trichinosis with neurologic or myocardial involvement. Launch Date1957 |
|||
| Primary | MEDROL Approved UseINDICATIONS AND USAGE
MEDROL Tablets are indicated in the following conditions:
1. Endocrine Disorders
Primary or secondary adrenocortical insufficiency (hydrocortisone or cortisone is the first choice; synthetic analogs may be used in conjunction with mineralocorticoids where applicable; in infancy mineralocorticoid supplementation is of particular importance).
Congenital adrenal hyperplasia
Nonsuppurative thyroiditis
Hypercalcemia associated with cancer
2. Rheumatic Disorders
As adjunctive therapy for short-term administration (to tide the patient over an acute episode or exacerbation) in:
Rheumatoid arthritis, including juvenile rheumatoid arthritis (selected cases may require low-dose maintenance therapy)
Ankylosing spondylitis
Acute and subacute bursitis
Synovitis of osteoarthritis
Acute nonspecific tenosynovitis
Post-traumatic osteoarthritis
Psoriatic arthritis
Epicondylitis
Acute gouty arthritis
3. Collagen Diseases
During an exacerbation or as maintenance therapy in selected cases of:
Systemic lupus erythematosus
Systemic dermatomyositis (polymyositis)
Acute rheumatic carditis
4. Dermatologic Diseases
Bullous dermatitis herpetiformis
Severe erythema multiforme (Stevens-Johnson syndrome)
Severe seborrheic dermatitis
Exfoliative dermatitis
Mycosis fungoides
Pemphigus
Severe psoriasis
5. Allergic States
Control of severe or incapacitating allergic conditions intractable to adequate trials of conventional treatment:
Seasonal or perennial allergic rhinitis
Drug hypersensitivity reactions
Serum sickness
Contact dermatitis
Bronchial asthma
Atopic dermatitis
6. Ophthalmic Diseases
Severe acute and chronic allergic and inflammatory processes involving the eye and its adnexa such as:
Allergic corneal marginal ulcers
Herpes zoster ophthalmicus
Anterior segment inflammation
Diffuse posterior uveitis and choroiditis
Sympathetic ophthalmia
Keratitis
Optic neuritis
Allergic conjunctivitis
Chorioretinitis
Iritis and iridocyclitis
7. Respiratory Diseases
Symptomatic sarcoidosis
Berylliosis
Loeffler's syndrome not manageable by other means
Fulminating or disseminated pulmonary tuberculosis when used concurrently with appropriate antituberculous chemotherapy
Aspiration pneumonitis
8. Hematologic Disorders
Idiopathic thrombocytopenic purpura in adults
Secondary thrombocytopenia in adults
Acquired (autoimmune) hemolytic anemia
Erythroblastopenia (RBC anemia)
Congenital (erythroid) hypoplastic anemia
9. Neoplastic Diseases
For palliative management of:
Leukemias and lymphomas in adults
Acute leukemia of childhood
10. Edematous States
To induce a diuresis or remission of proteinuria in the nephrotic syndrome, without uremia, of the idiopathic type or that due to lupus erythematosus.
11. Gastrointestinal Diseases
To tide the patient over a critical period of the disease in:
Ulcerative colitis
Regional enteritis
12. Nervous System
Acute exacerbations of multiple sclerosis
13. Miscellaneous
Tuberculous meningitis with subarachnoid block or impending block when used concurrently with appropriate antituberculous chemotherapy.
Trichinosis with neurologic or myocardial involvement. Launch Date1957 |
Cmax
| Value | Dose | Co-administered | Analyte | Population |
|---|---|---|---|---|
213 ng/mL EXPERIMENT https://www.ncbi.nlm.nih.gov/pubmed/12174030 |
32 mg single, intravenous dose: 32 mg route of administration: Intravenous experiment type: SINGLE co-administered: |
METHYLPREDNISOLONE plasma | Homo sapiens population: HEALTHY age: ADULT sex: MALE food status: UNKNOWN |
AUC
| Value | Dose | Co-administered | Analyte | Population |
|---|---|---|---|---|
931 ng × h/mL EXPERIMENT https://www.ncbi.nlm.nih.gov/pubmed/12174030 |
32 mg single, intravenous dose: 32 mg route of administration: Intravenous experiment type: SINGLE co-administered: |
METHYLPREDNISOLONE plasma | Homo sapiens population: HEALTHY age: ADULT sex: MALE food status: UNKNOWN |
T1/2
| Value | Dose | Co-administered | Analyte | Population |
|---|---|---|---|---|
2.3 h EXPERIMENT https://www.ncbi.nlm.nih.gov/pubmed/12174030 |
32 mg single, intravenous dose: 32 mg route of administration: Intravenous experiment type: SINGLE co-administered: |
METHYLPREDNISOLONE plasma | Homo sapiens population: HEALTHY age: ADULT sex: MALE food status: UNKNOWN |
Funbound
| Value | Dose | Co-administered | Analyte | Population |
|---|---|---|---|---|
23% |
METHYLPREDNISOLONE plasma | Homo sapiens population: HEALTHY age: ADULT sex: UNKNOWN food status: UNKNOWN |
Doses
| Dose | Population | Adverse events |
|---|---|---|
1000 mg/kg single, intravenous Highest studied dose Dose: 1000 mg/kg Route: intravenous Route: single Dose: 1000 mg/kg Sources: |
unhealthy, 0-15 years Health Status: unhealthy Age Group: 0-15 years Sex: M+F Sources: |
|
1250 mg 1 times / day multiple, oral Highest studied dose Dose: 1250 mg, 1 times / day Route: oral Route: multiple Dose: 1250 mg, 1 times / day Sources: |
unhealthy, 18–59 years Health Status: unhealthy Age Group: 18–59 years Sex: M+F Sources: |
|
120 mg 1 times / week multiple, intramuscular Highest studied dose Dose: 120 mg, 1 times / week Route: intramuscular Route: multiple Dose: 120 mg, 1 times / week Sources: |
unhealthy, adult Health Status: unhealthy Age Group: adult Sources: |
Overview
| CYP3A4 | CYP2C9 | CYP2D6 | hERG |
|---|---|---|---|
OverviewOther
| Other Inhibitor | Other Substrate | Other Inducer |
|---|---|---|
Drug as perpetrator
| Target | Modality | Activity | Metabolite | Clinical evidence |
|---|---|---|---|---|
Sources: https://pubs.acs.org/doi/abs/10.1021/mp900163d Page: - |
no | |||
Page: - |
yes | |||
Page: - |
yes |
Drug as victim
| Target | Modality | Activity | Metabolite | Clinical evidence |
|---|---|---|---|---|
Page: - |
yes | |||
Page: - |
yes | |||
Sources: http://epubs.surrey.ac.uk/855783/1/27606608.pdf Page: - |
yes | |||
Page: - |
yes |
PubMed
| Title | Date | PubMed |
|---|---|---|
| Reversible posterior leukoencephalopathy in a patient with minimal-change nephrotic syndrome. | 2001-04 |
|
| Lupus nephritis in a child with AIDS. | 2001-04 |
|
| Glucocorticosteroid dependent decrease in the activity of calcineurin in the peripheral blood mononuclear cells of patients with systemic lupus erythematosus. | 2001-04 |
|
| Intrathecal methylprednisolone for postherpetic neuralgia. | 2001-03-29 |
|
| Intrathecal methylprednisolone for postherpetic neuralgia. | 2001-03-29 |
|
| Intrathecal methylprednisolone for postherpetic neuralgia. | 2001-03-29 |
|
| Intrathecal methylprednisolone for postherpetic neuralgia. | 2001-03-29 |
|
| Intrathecal methylprednisolone for postherpetic neuralgia. | 2001-03-29 |
|
| Intrathecal methylprednisolone for postherpetic neuralgia. | 2001-03-29 |
|
| Preliminary results of a prospective randomized study of basiliximab in kidney transplantation. | 2001-03-27 |
|
| Peripheral administration of thymoglobulin for induction therapy in pancreas transplantation. | 2001-03-27 |
|
| Pharmacoeconomic study of tacrolimus-based versus cyclosporine-based immunosuppressive therapy following liver transplantation. | 2001-03-27 |
|
| Standard cyclosporine A-based versus completely steroid-free FK506-based immunosuppression after liver transplantation. | 2001-03-27 |
|
| Daclizumab induction therapy in combination with tacrolimus. | 2001-03-27 |
|
| Prospective randomized trial of tacrolimus and prednisone versus tacrolimus, prednisone, and mycophenolate mofetil: complete report on 350 primary adult liver transplantations. | 2001-03-27 |
|
| Canadian multicentre trial of tacrolimus/azathioprine/steroids versus tacrolimus/mycophenolate mofetil/steroids versus neoral/mycophenolate mofetil/steroids in renal transplantation. | 2001-03-27 |
|
| Successful withdrawal of steroid after renal transplantation. | 2001-03-27 |
|
| Prevention of bone loss in kidney graft recipients. | 2001-03-27 |
|
| Conversion at first rejection: a prospective trial comparing cyclosporine microemulsion with tacrolimus in renal transplant recipients. | 2001-03-27 |
|
| Daclizumab induction for primary kidney transplant recipients using tacrolimus, mycophenolate mofetil, and steroids as maintenance immunosuppression. | 2001-03-27 |
|
| Addition of steroids blocks the tolerogenic potential of donor-specific blood transfusion. | 2001-03-27 |
|
| Prospective experience with a 20-gauge Tuohy needle for lumbar epidural steroid injections: Is confirmation with fluoroscopy necessary? | 2001-03-17 |
|
| [Comparison of two different treatments of lateral humeral epicondylitis--"tennis elbow". A randomized controlled trial]. | 2001-03-05 |
|
| Recurrent orbital inflammation from metastatic orbital carcinoid tumor. | 2001-03 |
|
| [Intramural hematoma of the large intestine caused by cytomegalovirus vasculitis in a patient with SLE]. | 2001-03 |
|
| Pulmonary function in men after repeated sessions of oxygen breathing at 0.25 MPa for 90 min. | 2001-03 |
|
| [Value of methylprednisolone perfusions in the corticodependent forms of Horton's disease]. | 2001-03 |
|
| [Acute myelitis of an unusual cause in a child: the lymphocytic choriomeningitis virus]. | 2001-03 |
|
| Lymph draining from foot joints in rheumatoid arthritis provides insight into local cytokine and chemokine production and transport to lymph nodes. | 2001-03 |
|
| The impact of attaining a minimal disease state after high-dose melphalan and autologous transplantation for multiple myeloma. | 2001-03 |
|
| Use of daclizumab as initial immunosuppression in liver transplant recipients with impaired renal function. | 2001-03 |
|
| Chronic eosinophilic pneumonia presenting with recurrent massive bilateral pleural effusion : case report. | 2001-03 |
|
| Systemic glucocorticoids in severe exacerbations of COPD. | 2001-03 |
|
| Steroids for acute exacerbations of COPD : how long is enough? | 2001-03 |
|
| Methylprednisolone does not benefit patients undergoing coronary artery bypass grafting and early tracheal extubation. | 2001-03 |
|
| Improvement of atypical acute disseminated encephalomyelitis with steroids and intravenous immunoglobulins. | 2001-02 |
|
| Initial remission-inducing effect of very low-dose cyclosporin monotherapy for minimal-change nephrotic syndrome in Japanese adults. | 2001-02 |
|
| Severe renal impairment in the case of classic polyarteritis nodosa. | 2001-02 |
|
| Three cases of C-ANCA-positive vasculitis treated with immunoadsorption: possible benefit in early treatment. | 2001-02 |
|
| Morphological analysis of knee synovial membrane biopsies from a randomized controlled clinical study comparing the effects of sodium hyaluronate (Hyalgan) and methylprednisolone acetate (Depomedrol) in osteoarthritis. | 2001-02 |
|
| Steroid-resistant kidney transplant rejection: diagnosis and treatment. | 2001-02 |
|
| Selective involvement of the choroid plexus on cerebral magnetic resonance images: a new radiological sign in patients with systemic lupus erythematosus with neurological symptoms. | 2001-02 |
|
| [Contact allergy caused by poison ivy (Toxicodendron spp]. | 2001-02 |
|
| Lupus nephritis in children: prognostic significance of clinicopathological findings. | 2001-02 |
|
| [Psychological and behavioral disorders with good outcome in neurosarcoidosis]. | 2001-02 |
|
| [Value of abdominal-pelvic computed tomography in adult rheumatoid purpura]. | 2001-02 |
|
| Graft failure in a patient with systemic lupus erythematosus (SLE) treated with high-dose immunosuppression and autologous stem cell rescue. | 2001-01 |
|
| A three or more drug combination as effective therapy for moderate or severe chronic graft-versus-host disease. | 2001-01 |
|
| Corticosteroids for acute severe asthma in hospitalised patients. | 2001 |
|
| Sensorineural hearing loss in conjunction with aortic insufficiency in systemic lupus erythematosus. | 2001 |
Sample Use Guides
In Vivo Use Guide
Sources: https://www.drugs.com/pro/medrol.html
Each Medrol Tablet (methylprednisolone) for oral administration contains 2 mg, 4 mg, 8 mg, 16 mg or 32 mg of methylprednisolone. The initial dosage of Medrol Tablets may vary from 4 mg to 48 mg of methylprednisolone per day depending on the specific disease entity being treated.
Route of Administration:
Other
In Vitro Use Guide
Sources: https://www.ncbi.nlm.nih.gov/pubmed/26339357
Treatment with methylprednisolone concentrations above 50 uM could ignificantly reduce the proliferation activity of human CLL cell line MEC-1 by 23.34%, 30.73%, 30.57% after 24 h, and 28.48%, 42.35%, 44.56% after 48 h respectively
| Substance Class |
Chemical
Created
by
admin
on
Edited
Mon Mar 31 17:46:52 GMT 2025
by
admin
on
Mon Mar 31 17:46:52 GMT 2025
|
| Record UNII |
X4W7ZR7023
|
| Record Status |
Validated (UNII)
|
| Record Version |
|
-
Download
| Name | Type | Language | ||
|---|---|---|---|---|
|
Official Name | English | ||
|
Preferred Name | English | ||
|
Common Name | English | ||
|
Code | English | ||
|
Common Name | English | ||
|
Systematic Name | English | ||
|
Common Name | English | ||
|
Common Name | English | ||
|
Code | English | ||
|
Common Name | English | ||
|
Systematic Name | English | ||
|
Common Name | English | ||
|
Common Name | English | ||
|
Common Name | English | ||
|
Common Name | English | ||
|
Common Name | English | ||
|
Common Name | English | ||
|
Common Name | English | ||
|
Code | English | ||
|
Common Name | English | ||
|
Brand Name | English | ||
|
Common Name | English | ||
|
Common Name | English | ||
|
Common Name | English |
| Classification Tree | Code System | Code | ||
|---|---|---|---|---|
|
WHO-VATC |
QH02AB04
Created by
admin on Mon Mar 31 17:46:52 GMT 2025 , Edited by admin on Mon Mar 31 17:46:52 GMT 2025
|
||
|
FDA ORPHAN DRUG |
531816
Created by
admin on Mon Mar 31 17:46:52 GMT 2025 , Edited by admin on Mon Mar 31 17:46:52 GMT 2025
|
||
|
WHO-ATC |
S01CA08
Created by
admin on Mon Mar 31 17:46:52 GMT 2025 , Edited by admin on Mon Mar 31 17:46:52 GMT 2025
|
||
|
CFR |
21 CFR 520.1408
Created by
admin on Mon Mar 31 17:46:52 GMT 2025 , Edited by admin on Mon Mar 31 17:46:52 GMT 2025
|
||
|
WHO-ATC |
D07AA01
Created by
admin on Mon Mar 31 17:46:52 GMT 2025 , Edited by admin on Mon Mar 31 17:46:52 GMT 2025
|
||
|
CFR |
21 CFR 520.1409
Created by
admin on Mon Mar 31 17:46:52 GMT 2025 , Edited by admin on Mon Mar 31 17:46:52 GMT 2025
|
||
|
WHO-VATC |
QD07CA02
Created by
admin on Mon Mar 31 17:46:52 GMT 2025 , Edited by admin on Mon Mar 31 17:46:52 GMT 2025
|
||
|
NCI_THESAURUS |
C521
Created by
admin on Mon Mar 31 17:46:52 GMT 2025 , Edited by admin on Mon Mar 31 17:46:52 GMT 2025
|
||
|
WHO-VATC |
QH02BX01
Created by
admin on Mon Mar 31 17:46:52 GMT 2025 , Edited by admin on Mon Mar 31 17:46:52 GMT 2025
|
||
|
CFR |
21 CFR 522.1410
Created by
admin on Mon Mar 31 17:46:52 GMT 2025 , Edited by admin on Mon Mar 31 17:46:52 GMT 2025
|
||
|
NDF-RT |
N0000175576
Created by
admin on Mon Mar 31 17:46:52 GMT 2025 , Edited by admin on Mon Mar 31 17:46:52 GMT 2025
|
||
|
WHO-ATC |
H02BX01
Created by
admin on Mon Mar 31 17:46:52 GMT 2025 , Edited by admin on Mon Mar 31 17:46:52 GMT 2025
|
||
|
WHO-VATC |
QS01CA08
Created by
admin on Mon Mar 31 17:46:52 GMT 2025 , Edited by admin on Mon Mar 31 17:46:52 GMT 2025
|
||
|
WHO-ATC |
D07CA02
Created by
admin on Mon Mar 31 17:46:52 GMT 2025 , Edited by admin on Mon Mar 31 17:46:52 GMT 2025
|
||
|
WHO-ATC |
D07AC14
Created by
admin on Mon Mar 31 17:46:52 GMT 2025 , Edited by admin on Mon Mar 31 17:46:52 GMT 2025
|
||
|
WHO-VATC |
QD10AA02
Created by
admin on Mon Mar 31 17:46:52 GMT 2025 , Edited by admin on Mon Mar 31 17:46:52 GMT 2025
|
||
|
WHO-VATC |
QD07AA01
Created by
admin on Mon Mar 31 17:46:52 GMT 2025 , Edited by admin on Mon Mar 31 17:46:52 GMT 2025
|
||
|
WHO-ESSENTIAL MEDICINES LIST |
8.3
Created by
admin on Mon Mar 31 17:46:52 GMT 2025 , Edited by admin on Mon Mar 31 17:46:52 GMT 2025
|
||
|
WHO-ATC |
H02AB04
Created by
admin on Mon Mar 31 17:46:52 GMT 2025 , Edited by admin on Mon Mar 31 17:46:52 GMT 2025
|
||
|
NDF-RT |
N0000175450
Created by
admin on Mon Mar 31 17:46:52 GMT 2025 , Edited by admin on Mon Mar 31 17:46:52 GMT 2025
|
||
|
WHO-ATC |
D10AA02
Created by
admin on Mon Mar 31 17:46:52 GMT 2025 , Edited by admin on Mon Mar 31 17:46:52 GMT 2025
|
||
|
LIVERTOX |
626
Created by
admin on Mon Mar 31 17:46:52 GMT 2025 , Edited by admin on Mon Mar 31 17:46:52 GMT 2025
|
| Code System | Code | Type | Description | ||
|---|---|---|---|---|---|
|
1768
Created by
admin on Mon Mar 31 17:46:52 GMT 2025 , Edited by admin on Mon Mar 31 17:46:52 GMT 2025
|
PRIMARY | |||
|
D008775
Created by
admin on Mon Mar 31 17:46:52 GMT 2025 , Edited by admin on Mon Mar 31 17:46:52 GMT 2025
|
PRIMARY | |||
|
C647
Created by
admin on Mon Mar 31 17:46:52 GMT 2025 , Edited by admin on Mon Mar 31 17:46:52 GMT 2025
|
PRIMARY | |||
|
DB00959
Created by
admin on Mon Mar 31 17:46:52 GMT 2025 , Edited by admin on Mon Mar 31 17:46:52 GMT 2025
|
PRIMARY | |||
|
100000091803
Created by
admin on Mon Mar 31 17:46:52 GMT 2025 , Edited by admin on Mon Mar 31 17:46:52 GMT 2025
|
PRIMARY | |||
|
3127
Created by
admin on Mon Mar 31 17:46:52 GMT 2025 , Edited by admin on Mon Mar 31 17:46:52 GMT 2025
|
PRIMARY | |||
|
83-43-2
Created by
admin on Mon Mar 31 17:46:52 GMT 2025 , Edited by admin on Mon Mar 31 17:46:52 GMT 2025
|
PRIMARY | |||
|
732
Created by
admin on Mon Mar 31 17:46:52 GMT 2025 , Edited by admin on Mon Mar 31 17:46:52 GMT 2025
|
PRIMARY | |||
|
6741
Created by
admin on Mon Mar 31 17:46:52 GMT 2025 , Edited by admin on Mon Mar 31 17:46:52 GMT 2025
|
PRIMARY | |||
|
7088
Created by
admin on Mon Mar 31 17:46:52 GMT 2025 , Edited by admin on Mon Mar 31 17:46:52 GMT 2025
|
PRIMARY | |||
|
DTXSID7023300
Created by
admin on Mon Mar 31 17:46:52 GMT 2025 , Edited by admin on Mon Mar 31 17:46:52 GMT 2025
|
PRIMARY | |||
|
6902
Created by
admin on Mon Mar 31 17:46:52 GMT 2025 , Edited by admin on Mon Mar 31 17:46:52 GMT 2025
|
PRIMARY | RxNorm | ||
|
19987
Created by
admin on Mon Mar 31 17:46:52 GMT 2025 , Edited by admin on Mon Mar 31 17:46:52 GMT 2025
|
PRIMARY | |||
|
SUB08872MIG
Created by
admin on Mon Mar 31 17:46:52 GMT 2025 , Edited by admin on Mon Mar 31 17:46:52 GMT 2025
|
PRIMARY | |||
|
Methylprednisolone
Created by
admin on Mon Mar 31 17:46:52 GMT 2025 , Edited by admin on Mon Mar 31 17:46:52 GMT 2025
|
PRIMARY | |||
|
X4W7ZR7023
Created by
admin on Mon Mar 31 17:46:52 GMT 2025 , Edited by admin on Mon Mar 31 17:46:52 GMT 2025
|
PRIMARY | |||
|
201-476-4
Created by
admin on Mon Mar 31 17:46:52 GMT 2025 , Edited by admin on Mon Mar 31 17:46:52 GMT 2025
|
PRIMARY | |||
|
6888
Created by
admin on Mon Mar 31 17:46:52 GMT 2025 , Edited by admin on Mon Mar 31 17:46:52 GMT 2025
|
PRIMARY | |||
|
CHEMBL650
Created by
admin on Mon Mar 31 17:46:52 GMT 2025 , Edited by admin on Mon Mar 31 17:46:52 GMT 2025
|
PRIMARY | |||
|
X4W7ZR7023
Created by
admin on Mon Mar 31 17:46:52 GMT 2025 , Edited by admin on Mon Mar 31 17:46:52 GMT 2025
|
PRIMARY | |||
|
METHYLPREDNISOLONE
Created by
admin on Mon Mar 31 17:46:52 GMT 2025 , Edited by admin on Mon Mar 31 17:46:52 GMT 2025
|
PRIMARY | |||
|
1435003
Created by
admin on Mon Mar 31 17:46:52 GMT 2025 , Edited by admin on Mon Mar 31 17:46:52 GMT 2025
|
PRIMARY | |||
|
135864
Created by
admin on Mon Mar 31 17:46:52 GMT 2025 , Edited by admin on Mon Mar 31 17:46:52 GMT 2025
|
PRIMARY | |||
|
m7454
Created by
admin on Mon Mar 31 17:46:52 GMT 2025 , Edited by admin on Mon Mar 31 17:46:52 GMT 2025
|
PRIMARY | Merck Index |
| Related Record | Type | Details | ||
|---|---|---|---|---|
|
|
TRANSPORTER -> SUBSTRATE |
| Related Record | Type | Details | ||
|---|---|---|---|---|
|
METABOLITE -> PARENT |
MAJOR
URINE
|
||
|
METABOLITE -> PARENT | |||
|
METABOLITE -> PARENT |
MAJOR
URINE
|
||
|
METABOLITE -> PARENT | |||
|
METABOLITE -> PARENT |
MAJOR
URINE
|
||
|
METABOLITE -> PARENT | |||
|
METABOLITE -> PARENT |
URINE
|
||
|
METABOLITE -> PARENT |
MAJOR
URINE
|
||
|
METABOLITE -> PARENT |
MAJOR
URINE
|
| Related Record | Type | Details | ||
|---|---|---|---|---|
|
IMPURITY -> PARENT |
CHROMATOGRAPHIC PURITY (HPLC/UV)
EP
|
||
|
IMPURITY -> PARENT |
CHROMATOGRAPHIC PURITY (HPLC/UV)
EP
|
||
|
PARENT -> IMPURITY |
CHROMATOGRAPHIC PURITY (HPLC/UV)
EP
|
||
|
IMPURITY -> PARENT |
CHROMATOGRAPHIC PURITY (HPLC/UV)
EP
|
||
|
IMPURITY -> PARENT |
CHROMATOGRAPHIC PURITY (HPLC/UV)
EP
|
||
|
IMPURITY -> PARENT |
|
||
|
IMPURITY -> PARENT |
CHROMATOGRAPHIC PURITY (HPLC/UV)
EP
|
||
|
PARENT -> IMPURITY |
CHROMATOGRAPHIC PURITY (HPLC/UV)
EP
|
||
|
IMPURITY -> PARENT |
CHROMATOGRAPHIC PURITY (HPLC/UV)
EP
|
||
|
IMPURITY -> PARENT |
CHROMATOGRAPHIC PURITY (HPLC/UV)
EP
|
||
|
IMPURITY -> PARENT |
CHROMATOGRAPHIC PURITY (HPLC/UV)
EP
|
||
|
IMPURITY -> PARENT |
CHROMATOGRAPHIC PURITY (HPLC/UV)
EP
|
||
|
IMPURITY -> PARENT |
CHROMATOGRAPHIC PURITY (HPLC/UV)
EP
|
| Related Record | Type | Details | ||
|---|---|---|---|---|
|
|
ACTIVE MOIETY |
| Name | Property Type | Amount | Referenced Substance | Defining | Parameters | References |
|---|---|---|---|---|---|---|
| Volume of Distribution | PHARMACOKINETIC |
|
|
|||
| Biological Half-life | PHARMACOKINETIC |
|
|
|||