General
Preferred name
DITIOCARB
Synonyms
DITHIOCARB ()
Sodium diethyldithiocarbamate ()
Ditiocarb Zinc ()
Sodium Diethyldithiocarbamate Trihydrate ()
disulfiram, Ora Bio-2 ()
DITIOCARB SODIUM ()
Diethyl dithiocarbamate ()
Carbamodithioic acid, diethyl- ()
Carbamic acid, diethyldithio- ()
Ditiocarbo de sodio ()
Imuthiol ()
Thiocarb ()
NSC-38583 ()
Ditiocarbe sodique ()
Dedtc ()
P&D ID
PD007900
CAS
392-74-5
147-84-2
143189-63-3
20624-25-3
14324-55-1
148-18-5
Tags
available
drug
drug candidate
Drug Status
approved
experimental
investigational
Max Phase
2.0
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)
PRICE
750
DESCRIPTION
Ditiocarb sodium inhibits carbonic anhydrases from Porphyromonas gingivalis and Burkholderia pseudomallei. It also reduces the incidence of HIV infection.
(Enamine Bioactive Compounds)
DESCRIPTION
Ditiocarb sodium (Sodium diethyldithiocarbamate) (sodium diethiocarbamate) is a copper reagent, which reacts with Cu2 + solution to form a complex and improves the precipitation rate of copper replacement. Sodium diethyldidiocarbamate can reduce HIV infection.
(TargetMol Bioactive Compound Library)
[[ p.pathway_name ]]
[[ compound.targets[tid].gene_name ]]
Cell lines
2
Organisms
1
Compound Sets
16
ChEMBL Drugs
Drug Repurposing Hub
DrugBank Approved Drugs
DrugCentral
DrugCentral Approved Drugs
DrugMatrix
Enamine Bioactive Compounds
Enamine BioReference Compounds
EU-OPENSCREEN Bioactive Compound Library
NCATS Inxight Approved Drugs
NIH Mechanistic Set
NPC Screening Collection
Other bioactive compounds
ReFrame library
TargetMol Bioactive Compound Library
[[ a.name ]]
[[ ligand_id ]]
free of charge
External IDs
117
Molecular Weight
149.03
Hydrogen Bond Acceptors
1
Hydrogen Bond Donors
1
Rotatable Bonds
2
Ring Count
0
Aromatic Ring Count
0
cLogP
1.54
TPSA
3.24
Fraction CSP3
0.8
Chiral centers
0.0
Largest ring
0.0
QED
0.47
Structural alerts
0
No structural alerts detected
Related compounds
Custom attributes
(extracted from source data)
Target
HIV
CA1, CA2, CA4
MOA
immunostimulant
Pathway
Microbiology/virology
Proteases/Proteasome
Source data
