General
Preferred name
INDAPAMIDE
Synonyms
Noranat ()
Veroxil ()
Tertensif ()
Indapamide (Lozol) ()
Indamide ()
Natrilix SR ()
Ipamix ()
Ethibide XL ()
Natrilix ()
Flubest ()
Flupamid ()
Indaflex ()
Bajaten ()
Varbim XL ()
Damide ()
NSC-757075 ()
Rawel XL ()
Arifon ()
Lozol ()
Indipam XL ()
Tandix ()
Natrix ()
Fludex ()
Mapemid XL ()
SE-1520 ()
Lorvas ()
Tensaid XL ()
Indaxa 2.5 ()
KYD-041 ()
S-1520 ()
Cardide SR ()
Fludin ()
Opumide 2.5 ()
Indamol ()
Nindaxa 2.5 ()
Indapamide ()
Indapamide-13C-d3 ()
P&D ID
PD002293
CAS
26807-65-8
2934053-07-1
Tags
natural product
drug
available
Approved by
FDA
First approval
1983
Drug Status
approved
Drug indication
Diuretic
Hypertension
Antihypertensive
Max Phase
Phase 4
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 Indapamide is a thiazide diuretic drug. (GtoPdb)
Compound Sets
25
AdooQ Bioactive Compound Library
A10470
Cayman Chemical Bioactives
21308
34244
ChEMBL Approved Drugs
CHEMBL406
ChEMBL Drugs
CHEMBL406
DrugBank
DB00808
DrugBank Approved Drugs
DB00808
DrugCentral
1433
DrugCentral Approved Drugs
1433
DrugMAP
DMGN1PW
DrugMAP Approved Drugs
DMGN1PW
DrugMatrix
Enamine BioReference Compounds
Guide to Pharmacology
7203
LSP-MoA library (Laboratory of Systems Pharmacology)
CHEMBL406
Mcule NIBR MoA Box Subset
MCULE-1549472772
MedChem Express Bioactive Compound Library
HY-B0259
NCATS Inxight Approved Drugs
F089I0511L
NIH Clinical Collections (NCC)
Novartis Chemogenetic Library (NIBR MoA Box)
NPC Screening Collection
Prestwick Chemical Library
ReFrame library
Selleckchem Bioactive Compound Library
Indapamide(Lozol)
TargetMol Bioactive Compound Library
T1498
The Spectrum Collection
External IDs
41
Properties
(calculated by RDKit )
Molecular Weight
365.06
Hydrogen Bond Acceptors
4
Hydrogen Bond Donors
2
Rotatable Bonds
3
Ring Count
3
Aromatic Ring Count
2
cLogP
2.08
TPSA
92.5
Fraction CSP3
0.19
Chiral centers
1.0
Largest ring
6.0
QED
0.87
Structural alerts
0
No structural alerts detected
Related compounds
Custom attributes
(extracted from source data)
Pathway
Membrane Transporter/Ion Channel
Target
Potassium Channel
Member status
member
MOA
Carbonic Anhydrase Type VII Inhibitors
Therapeutic Class
Antihypertensive Agents
Source data