General
Preferred name
perindopril
Synonyms
PERINDOPRIL ERBUMINE ()
Perindopril tert-butylamine salt ()
S9490-3 ()
Perindopril Erbumine (Aceon) ()
PERINDOPRIL ARGININE ()
S-9490 ()
Perindopril (tert-butylamine salt) ()
S-9490 (erbumine) ()
IC980033 ()
Perindopril (erbumine) ()
NSC-758929 ()
Aceon ()
S-9490-3 ()
Perindopril tert-butylamine ()
McN-A-2833-109 ()
Coversyl ()
McN-A-2833 ()
P&D ID
PD009719
CAS
107133-36-8
82834-16-0
99149-83-4
Tags
available
drug candidate
drug
prodrug
Approved by
FDA
First approval
1993
2015
Drug indication
Discovery agent
Antihypertensive
Hypertension
Antihypertensive,Enzyme Inhibitor (angiotensin-converting)
Drug Status
approved
Max Phase
4.0
Probe control
Probe control not defined
Orthogonal probes
0
No orthogonal probes found
Similar probes
0
No structurally similar probes found
Structure formats
[[ format ]]
[[ compound[format === 'MOL' ? 'molblock' : format.toLowerCase()] ]]
Description
(extracted from source data)
DESCRIPTION
Prodrug metabolically converted to the drug perindoprilat. Perindopril erbumine [USAN] aka perindopril tert-butylamine, is PubChem CID 441313.
(GtoPdb)
DESCRIPTION
Soluble guanylyl cyclase (sGC) activator; induces G1 cell cycle arrest
(Tocris Bioactive Compound Library)
DESCRIPTION
Perindopril is a long-acting ACE inhibitor. It is used to treat patients with hypertension, diabetes mellitus type 2, coronary heart disease, chronic heart failure or stable coronary artery disease in form of perindopril arginine on the basis of a large evidence. lt has anticancer activity through the inhibition of tumor growth and angiogenesis in hepatocellular carcinoma cells. It suppresses angiotensin II production in vitro. In the in vitro cell proliferation assays, it does not show significant effect on the cell proliferation. In vivo assays demonstrate it can suppress the growth of SCC-VII cells. It is reported that 8 mg perindopril given orally can lower blood pressure without a change in heart rate. It was developed by Xoma.
(BOC Sciences Bioactive Compounds)
[[ p.pathway_name ]]
[[ compound.targets[tid].gene_name ]]
Compound Sets
22
AdooQ Bioactive Compound Library
BOC Sciences Bioactive Compounds
Cayman Chemical Bioactives
ChEMBL Approved Drugs
ChEMBL Drugs
CZ-OPENSCREEN Bioactive Library
Drug Repurposing Hub
DrugBank
DrugBank Approved Drugs
DrugCentral
DrugCentral Approved Drugs
DrugMAP Approved Drugs
Guide to Pharmacology
LSP-MoA library (Laboratory of Systems Pharmacology)
NCATS Inxight Approved Drugs
Prestwick Chemical Library
ReFrame library
TargetMol Bioactive Compound Library
The Spectrum Collection
Tocris Bioactive Compound Library
[[ a.name ]]
[[ ligand_id ]]
free of charge
External IDs
84
Properties
(calculated by RDKit )
Molecular Weight
368.23
Hydrogen Bond Acceptors
5
Hydrogen Bond Donors
2
Rotatable Bonds
8
Ring Count
2
Aromatic Ring Count
0
cLogP
1.94
TPSA
95.94
Fraction CSP3
0.84
Chiral centers
5.0
Largest ring
6.0
QED
0.64
Structural alerts
0
No structural alerts detected
Custom attributes
(extracted from source data)
Pathway
Endocrinology/Hormones
Immunology/Inflammation
Cell Cycle/DNA Damage
Epigenetics
JAK/STAT Signaling
Metabolic Enzyme/Protease
NF-κB
Stem Cell/Wnt
Target
MRP1
ACE
Angiotensin-converting Enzyme (ACE)
Sirtuin
STAT
Primary Target
Angiotensin-Converting Enzyme
MOA
MRP inhibitor
RAAS inhibitor
Inhibitor
angiotensin converting enzyme inhibitor
Indication
hypertension, myocardial infarction, coronary artery disease (CAD)
Therapeutic Class
Antihypertensive Agents
Solubility
Soluble in water, chloroform, methanol
Source data