Home | Screening data | Screen comparisons | Search for compounds | Structure search

Compound InformationSONAR Target prediction
Name:

ETHOPROPAZINE HYDROCHLORIDE

Unique Identifier:SPE01500293
MolClass: Checkout models in ver1.5 and ver1.0
Molecular Formula:
Molecular Weight:323.735 g/mol
X log p:17.895  (online calculus)
Lipinksi Failures1
TPSA31.78
Hydrogen Bond Donor Count:0
Hydrogen Bond Acceptors Count:2
Rotatable Bond Count:5
Canonical Smiles:Cl.CCN(CC)C(C)CN1c2ccccc2Sc2ccccc12
Source:synthetic
Therapeutics:antiparkinsonian, anticholinergic
Generic_name:Ethopropazine
Chemical_iupac_name:N,N-diethyl-1-(10H-phenothiazin-10-yl)propan-2-amine
Drug_type:Approved Drug
Pharmgkb_id:PA449531
Drugbank_id:APRD00729
Melting_point:64.5 oC
H2o_solubility:0.693 mg/L
Logp:5.772
Cas_registry_number:08/02/1094
Mass_spectrum:http://webbook.nist.gov/cgi/cbook.cgi?Spec=C522009&Index=0&Type=Mass&Large=on
Drug_category:Antiparkinson Agents; Antidyskinetics
Indication:For use in the treatment of Parkinson-s disease and also used to control severe
reactions to certain medicines such as reserpine.
Pharmacology:Ethopropazine, a phenothiazine and antidyskinetic, is used in the treatment of
Parkinson-s disease. By improving muscle control and reducing stiffness, this drug
permits more normal movements of the body as the disease symptoms are reduced. It is
also used to control severe reactions to certain medicines such as reserpine,
phenothiazines, chlorprothixene, thiothixene, loxapine, and haloperidol. Unlike
other NMDA antagonists, ethopropazine — because of its anticholinergic action
— is largely devoid of neurotoxic side effects. Ethopropazine also has a
slight antihistaminic and local anesthetic effect.
Mechanism_of_action:Ethopropazine-s antiparkinson action can be attributed to its anticholinergic
properties. Ethopropazine partially blocks central (striatal) cholinergic receptors,
thereby helping to balance cholinergic and dopaminergic activity in the basal
ganglia; salivation may be decreased, and smooth muscle may be relaxed. Drug-induced
extrapyramidal symptoms and those due to parkinsonism may be relieved, but tardive
dyskinesia is not alleviated and may be aggravated by anticholinergic effects.
Ethopropazine-s local anesthetic effect is due to its antagonism of the NMDA
glutamate receptor. Glutamate is recognized as an important transmitter in
nociceptive pathways, and the N-methyl-D-aspartate (NMDA) subtype of the glutamate
receptor, in particular, has been implicated in the mediation of neuropathic pain.
Excessive release of glutamate at NMDA receptors on dorsal horn neurons of the
spinal cord results in hyperactivation and hypersensitivity of these receptors
(perceived as hyperalgesia), thought to be an integral feature of neuropathic pain.
Organisms_affected:Humans and other mammals

Found: 42 active | as graph: single | with analogs [1] << Back 11 12 13 14 15 16 17 18 19 20  Next >> [42]
Species: 4932
Condition: FKS1
Replicates: 2
Raw OD Value: r im 0.5489±0.0092631
Normalized OD Score: sc h 0.8791±0.0102396
Z-Score: -5.3195±0.639503
p-Value: 0.000000569474
Z-Factor: -0.00722566
Fitness Defect: 14.3786
Bioactivity Statement: Active
Experimental Conditions
Library:SPECMTS3
Plate Number and Position:7|E5
Drug Concentration:50.00 nM
OD Absorbance:600 nm
Robot Temperature:25.80 Celcius
Date:2008-06-04 YYYY-MM-DD
Plate CH Control (+):0.04045±0.00038
Plate DMSO Control (-):0.629025±0.01841
Plate Z-Factor:0.8955
png
ps
pdf

DBLink | Rows returned: 82 Next >> 
3290 N,N-diethyl-1-phenothiazin-10-yl-propan-2-amine
6074 ethyl-dimethyl-(1-phenothiazin-10-ylpropan-2-yl)azanium
120622 diethyl-methyl-(1-phenothiazin-10-ylpropan-2-yl)azanium
122824 N,N-diethyl-1-phenothiazin-10-yl-propan-2-amine hydrochloride
667534 (2S)-N,N-diethyl-1-phenothiazin-10-yl-propan-2-amine
688098 (2R)-N,N-diethyl-1-phenothiazin-10-yl-propan-2-amine

internal high similarity DBLink | Rows returned: 3
LOPAC 00147 0.9677
RH 01503 0.9677
SPE01500510 0.9677

nonactive | Cluster 7451 | Additional Members: 8 | Rows returned: 6
SPE01504095 0.388888888888889
SPE01500512 0.314814814814815
Prest195 0.266666666666667
SPE01500510 0
Prest1176 0
LOPAC 00147 0

Service provided by the Mike Tyers Laboratory