General
Preferred name
SODIUM CITRATE
Synonyms
Trisodium citrate dihydrate ()
Citric acid trisodium salt dihydrate ()
Sodium citrate dihydrate ()
Sodium citrate (dihydrate) ()
Citric acid (trisodium) ()
Trisodium citrate (dihydrate) ()
Citric acid (trisodium salt dihydrate) ()
trisodium citrate anhydrous ()
Trisodium citrate dihydrate, Citric acid trisodium salt dihydrate ()
Citric acid, trisodium salt ()
Anhydrous trisodium citrate ()
Anhydrous sodium citrate ()
Sodium citrate, anhydrous ()
N-1560 ()
Cystemme ()
Relaxit ()
Sodium citrate anhydrous ()
E331 ()
INS-331(III) ()
Sod Cit ()
Sodium citrate hydrate ()
Cystocalm ()
Sodium citrate hydrous ()
E-331(III) ()
Isolyte E ()
Natrii citras, dehydrate ()
FEMA NO. 3026 ()
Citrosodine ()
INS NO.331(III) ()
Trisodium citrate, anhydrous ()
Anticoagulant Sodium Citrate ()
Micralax ()
Natrocitral ()
Cystoleve ()
Micolette ()
Urisal ()
Cymalon ()
Natrii citras ()
Canesten Oasis ()
Sodium citrate,anhydrous ()
FEMA NO. 3026, ANHYDROUS- ()
P&D ID
PD009021
CAS
6132-04-3
183748-56-3
68-04-2
Tags
available
drug
Drug Status
investigational
approved
Drug indication
Discovery agent
Alkalizer (systemic)
Max Phase
Phase 4
First approval
1983
Probe control
Probe control not defined
Orthogonal probes
0
No orthogonal probes found
Similar probes
0
No structurally similar probes found
Structure
P&D probe-likeness score
Structure formats
[[ format ]]
[[ compound[format === 'MOL' ? 'molblock' : format.toLowerCase()] ]]
Description
(extracted from source data)
TOXICITY
Overdose toxicity is mainly due to alkalosis as well as tetany or depressed heart function due to lack of free calcium [L790].;
PHARMACODYNAMICS
Citrate prevents activation of the clotting cascade by chelating calcium ions. Citrate neutralizes acid in the stomach and urine, raising the pH [L790].;
[[ p.pathway_name ]]
[[ compound.targets[tid].gene_name ]]
Compound Sets
9
ChEMBL Approved Drugs
ChEMBL Drugs
DrugBank
DrugBank Approved Drugs
DrugMAP
LSP-MoA library (Laboratory of Systems Pharmacology)
Selleckchem Bioactive Compound Library
TargetMol Bioactive Compound Library
[[ a.name ]]
[[ ligand_id ]]
free of charge
External IDs
40
Molecular Weight
257.97
Hydrogen Bond Acceptors
7
Hydrogen Bond Donors
1
Rotatable Bonds
5
Ring Count
0
Aromatic Ring Count
0
cLogP
-14.24
TPSA
140.62
Fraction CSP3
0.5
Chiral centers
0.0
Largest ring
0.0
QED
0.48
Structural alerts
0
No structural alerts detected
Related compounds
Custom attributes
(extracted from source data)
Pathway
Microbiology/virology
Anti-infection
Metabolic Enzyme/Protease
Apoptosis
Target
Bacterial
Endogenous Metabolite
Source data
