General
Preferred name
prednisolone
Synonyms
Metacortandralone ()
Hydroretrocortine ()
Predonine ()
Prednisolone (NSC-9900) ()
NSC-9900 ()
Precortisyl fte ()
Neo-Delta-Cortef ()
Deltacortril ()
Precortisyl ()
Fernisolone-p ()
Cortalone ()
NSC-9120 ()
Verdeso ()
Meti-derm ()
Delta-cortef ()
Scheriproct ()
Servisone ()
Meticortelone ()
Dilacort ()
Dekotil ()
Deltalone ()
Pevanti ()
Desowen ()
Tridesilon ()
Poly-Pred ()
Hydeltra ()
Pred-G ()
Prelone ()
Hydeltra-Tba ()
Sterane ()
P&D ID
PD002902
CAS
50-24-8
Tags
probe
natural product
drug
available
Approved by
FDA
First approval
1955
Drug Status
approved
vet_approved
Drug indication
Multiple sclerosis
Glucocorticoid
Solid tumour/cancer
Max Phase
Phase 4
Probe info
Probe type
experimental probe
Probe sources
Probe targets
Structure
Probe scores
P&D probe-likeness score
[[ v.score ]]%
Structure formats
[[ format ]]
[[ compound[format === 'MOL' ? 'molblock' : format.toLowerCase()] ]]
Description
(extracted from source data)
DESCRIPTION Prednisolone is a synthetic glucocorticoid. Marketed formulations may contain prednisolone sodium phosphate, prednisolone acetate, prednisolone hexanoate or prednisolone. (GtoPdb)
MOA Glucocorticoid competitive, Agonist (Chemical Probes.org)
Cell lines
8
Organisms
1
Compound Sets
25
Cayman Chemical Bioactives
CeMM library of unique drugs (CLOUD)
ChEMBL Approved Drugs
ChEMBL Drugs
Chemical Probes.org
Drug Repurposing Hub
DrugBank
DrugBank Approved Drugs
DrugCentral
DrugCentral Approved Drugs
DrugMAP
DrugMAP Approved Drugs
Enamine BioReference Compounds
EU-OPENSCREEN Bioactive Compound Library
Guide to Pharmacology
LSP-MoA library (Laboratory of Systems Pharmacology)
MedChem Express Bioactive Compound Library
NCATS Inxight Approved Drugs
NIH Clinical Collections (NCC)
NPC Screening Collection
Prestwick Chemical Library
ReFrame library
Selleckchem Bioactive Compound Library
TargetMol Bioactive Compound Library
External IDs
53
Properties
(calculated by RDKit )
Molecular Weight
360.19
Hydrogen Bond Acceptors
5
Hydrogen Bond Donors
3
Rotatable Bonds
2
Ring Count
4
Aromatic Ring Count
0
cLogP
1.56
TPSA
94.83
Fraction CSP3
0.71
Chiral centers
7.0
Largest ring
6.0
QED
0.69
Structural alerts
0
No structural alerts detected
Custom attributes
(extracted from source data)
MOA
Glucocorticoid Receptor agonist
Target
Glucocorticoid Receptor
NR3C1, NR3C2, SERPINA6
Endogenous Metabolite
Glucocorticoid Receptor,Immunology & Inflammation related
NR3C1
Pathway
Metabolism
Immunology/Inflammation
Metabolic Enzyme/Protease
Vitamin D Related/Nuclear Receptor
Disease Area
ophthalmology, dermatology, infectious disease
Indication
conjunctivitis, rosacea, punctate keratitis, shingles, iritis, cyclitis
Therapeutic Class
Anticancer Agents
Target class
Nuclear Receptor
Target subclass
Nuclear Hormone Receptor
Source data