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Compound InformationSONAR Target prediction
Name:

NORTRIPTYLINE

Unique Identifier:SPE01500442
MolClass: Checkout models in ver1.5 and ver1.0
Molecular Formula:
Molecular Weight:242.21 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:CNCCC=C1c2ccccc2CCc2ccccc21
Source:synthetic
Therapeutics:antidepressant
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: 2 active | as graph: single | with analogs 2 Next >> 
Species: 4932
Condition: DRS2
Replicates: 2
Raw OD Value: r im 0.5962±0.0238295
Normalized OD Score: sc h 0.8542±0.0227264
Z-Score: -6.2946±0.99589
p-Value: 0.0000000113287
Z-Factor: 0.0391777
Fitness Defect: 18.2959
Bioactivity Statement: Active
Experimental Conditions
Library:SPECMTS3
Plate Number and Position:6|G7
Drug Concentration:50.00 nM
OD Absorbance:600 nm
Robot Temperature:22.70 Celcius
Date:2008-01-11 YYYY-MM-DD
Plate CH Control (+):0.041975±0.00078
Plate DMSO Control (-):0.67105±0.01550
Plate Z-Factor:0.9088
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DBLink | Rows returned: 122 Next >> 
2160
4543
11065
13468
49402
49403

internal high similarity DBLink | Rows returned: 3
LOPAC 00484 1.0000
LOPAC 00524 1.0000
SPE01500117 1.0000

active | Cluster 1654 | Additional Members: 10 | Rows returned: 1
SPE01500117 0

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