Basic Information

Drug ID DDPD05676 ...
Drug Name Apremilast
Molecular Weight 460.5
Molecular Formula C22H24N2O7S
CAS Number 608141-41-9
SMILES CCOC1=CC(=CC=C1OC)[C@@H](CS(C)(=O)=O)N1C(=O)C2=CC=CC(NC(C)=O)=C2C1=O
External Links
DRUGBANK DB05676
PubChem Compound 11561674
Drugs.com Drugs.com Drug Page

Experimental Physicochemical Property

Property Name Property Value Unit Raw Value Raw Unit Reference
Boiling Point 741.3 741.3±60.0 http://www.chemspider.com/Chemical-Structure.9736448.html
Melting Point 156.1 156.1 http://www.guildlink.com.au/gc/ws/celgene/pi.cfm?product=cjpaprem
pKa 12.58 - 12.58 - https://pubchem.ncbi.nlm.nih.gov/compound/Apremilast#section=Solubility

Pharmacokinetic/ Toxicokinetic Property

Property Name Property Value Unit Raw Value Raw Unit Annotation Reference
Bioavailability 73.0 % 73 % PO, oral; DRUGBANK
C Max 584.0 ng/ml 584 ng/ml PO, oral; DRUGBANK
T Max 2.5 h 2.5 h PO, oral; DRUGBANK
Clearance 10.0 L/h 10.0 L/h Plasma clearance; normal,healthy; patients; DRUGBANK
Clearance 0.14 L/h/kg 2.38 ml/min/kg intravenous injection, IV; human, homo sapiens; Human Intravenous Pharmacokinetic Dataset
Volume of Distribution 87.0 L 87.0 L Average volume of distribution; DRUGBANK
Half-life 7.5 h 6-9 h elimination half-life; DRUGBANK
Half-life 6.0 h 6.03 h intravenous injection, IV; human, homo sapiens; Human Intravenous Pharmacokinetic Dataset
Toxicity LD50 2000.0 mg/kg >2000 mg/kg PO, oral; mouse; DRUGBANK
Toxicity LD50 2000.0 mg/kg 2000.0 mg/kg PO, oral; Male, men; Rattus, Rat; DRUGBANK
Toxicity LD50 300.0 mg/kg 300.0 mg/kg PO, oral;  Female, women; Rattus, Rat; DRUGBANK
Eliminate Route 3.0 % 3 % Urinary excretion; Unchanged drug; DRUGBANK
Eliminate Route 7.0 % 7 % Faeces excretion; Unchanged drug; DRUGBANK
Protein Binding 68.0 % ~68 % plasma proteins; DRUGBANK

Maximum Dosage

Not Available

Drug Property Radar Chart

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Note: Center: Q1-1.5*IQR, Edge: Q3+1.5*IQR; Q1: Quantile 1, Q3: Quantile 3, IQR: Q3-Q1