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Compound InformationSONAR Target prediction
Name:

Nortriptyline hydrochloride

Unique Identifier:LOPAC 00524
MolClass: Checkout models in ver1.5 and ver1.0
Molecular Formula:C19ClH22N
Molecular Weight:277.663 g/mol
X log p:19.851  (online calculus)
Lipinksi Failures1
TPSA0
Hydrogen Bond Donor Count:0
Hydrogen Bond Acceptors Count:1
Rotatable Bond Count:3
Canonical Smiles:Cl.CNCCC=C1c2ccccc2CCc2ccccc21
Class:Adrenoceptor
Action:Inhibitor
Selectivity:Uptake
Generic_name:Amitriptyline
Chemical_iupac_name:3-(10,11-dihydro-5H-dibenzo-[a,d]cyclohepten-5-ylidene)-N,N-dimethyl-1-propanamine
Drug_type:Approved Drug
Pharmgkb_id:PA448385
Kegg_compound_id:C06824
Drugbank_id:APRD00227
Melting_point:196-197 oC
H2o_solubility:9.7 mg/mL
Logp:4.612
Isoelectric_point:9.4
Cas_registry_number:50-48-6
Mass_spectrum:http://webbook.nist.gov/cgi/cbook.cgi?Spec=C50486&Index=0&Type=Mass&Large=on
Drug_category:Analgesics, Non-Narcotic; Antidepressive Agents, Tricyclic; Adrenergic Uptake
Inhibitors; ATC:N06AA09
Indication:For the treatment of anxiety, bipolar disorders, and depression.
Pharmacology:Amitriptyline, a tertiary amine tricyclic antidepressant, is structurally related to
both the skeletal muscle relaxant cyclobenzaprine and the thioxanthene
antipsychotics such as thiothixene. It is extremely sedating, and thus improvement
of sleep patterns can be the first benefit of treatment. Amitriptyline exhibits
strong anticholinergic activity, cardiovascular effects including orthostatic
hypotension, changes in heart rhythm and conduction, and a lowering of the seizure
threshold. As with other antidepressants, several weeks of therapy may be required
in order to realize the full clinical benefit of amitriptyline. Although not a
labelled indication, amitriptyline is widely used in the management of chronic
nonmalignant pain (e.g., post-herpetic neuralgia, fibromyalgia).
Mechanism_of_action:Amitriptyline is metabolized to nortriptyline which inhibits the reuptake of
norepinephrine and serotonin almost equally. Amitriptyline inhibits the membrane
pump mechanism responsible for uptake of norepinephrine and serotonin in adrenergic
and serotonergic neurons. Pharmacologically this action may potentiate or prolong
neuronal activity since reuptake of these biogenic amines is important
physiologically in terminating transmitting activity. This interference with the
reuptake of norepinephrine and/or serotonin is believed by some to underlie the
antidepressant activity of amitriptyline.
Organisms_affected:Humans and other mammals

Found: 24 nonactive as graph: single | with analogs [1] << Back 11 12 13 14 15 16 17 18 19 20  Next >> [24]
Species: 4932
Condition: NOP13
Replicates: 2
Raw OD Value: r im 0.6899±0.00523259
Normalized OD Score: sc h 1.0006±0.00183743
Z-Score: 0.0205±0.0828753
p-Value: 0.95328
Z-Factor: -13.4816
Fitness Defect: 0.0478
Bioactivity Statement: Nonactive
Experimental Conditions
Library:Lopac
Plate Number and Position:11|G9
Drug Concentration:50.00 nM
OD Absorbance:600 nm
Robot Temperature:0.00 Celcius
Date:2005-04-22 YYYY-MM-DD
Plate CH Control (+):0.046700000000000005±0.00112
Plate DMSO Control (-):0.671575±0.03263
Plate Z-Factor:0.8148
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DBLink | Rows returned: 12<< Back 1 2
171402
441358
657214
657376
3413420
5458370

internal high similarity DBLink | Rows returned: 3
LOPAC 00484 1.0000
SPE01500117 1.0000
SPE01500442 1.0000

active | Cluster 1654 | Additional Members: 10 | Rows returned: 2
SPE01500442 0.333333333333333
SPE01500117 0

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