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

Compound InformationSONAR Target prediction
Name:

NIFEDIPINE

Unique Identifier:SPE01500431
MolClass: Checkout models in ver1.5 and ver1.0
Molecular Formula:
Molecular Weight:328.192 g/mol
X log p:8.766  (online calculus)
Lipinksi Failures1
TPSA95.74
Hydrogen Bond Donor Count:0
Hydrogen Bond Acceptors Count:5
Rotatable Bond Count:6
Canonical Smiles:[O-][N+](=O)c1ccccc1C1C(=C(C)NC(C)=C1C(=O)OC)C(=O)OC
Source:synthetic
Therapeutics:antianginal, antihypertensive
Generic_name:Nifedipine
Chemical_iupac_name:dimethyl2,6-dimethyl-4-(2-nitrophenyl)-1,4-dihydropyridine-3,5-dicarboxylate
Drug_type:Approved Drug
Pharmgkb_id:PA450631
Kegg_compound_id:C07266
Drugbank_id:APRD00590
Melting_point:172 - 174 oC
H2o_solubility:Insoluble
Logp:2.343
Cas_registry_number:21829-25-4
Drug_category:Tocolytic Agents; Vasodilator Agents; Calcium Channel Blockers; Dihydropyridines;
ATC:C08CA05
Indication:For the management of vasospastic angina, chronic stable angina and hypertension.
Pharmacology:Nifedipine, the prototype of the dihydropyridine class of calcium-channel
antagonists, is similar to other dihydropyridines including amlodipine, felodipine,
isradipine, and nicardipine. Nifedipine is used to treat Prinzmetal-s angina,
hypertension, and other vascular disorders such as Raynaud-s phenomenon. By blocking
the calcium channels, Nifedipine inhibits the spasm of the coronary artery and
dilates the systemic arteries, results in a increase of myocardial oxygen supply and
a decrease in systemic blood pressure.
Mechanism_of_action:Nifedipine inhibits the influx of extracellular calcium through myocardial and
vascular membrane pores by physically plugging the channel. The decrease in
intracellular calcium inhibits the contractile processes of smooth muscle cells,
causing dilation of the coronary and systemic arteries, increased oxygen delivery to
the myocardial tissue, decreased total peripheral resistance, decreased systemic
blood pressure, and decreased afterload.
Organisms_affected:Humans and other mammals

Found: 110 active | as graph: single | with analogs [1] << Back 21 22 23 24 25 26 27 28 29 30  Next >> [110]
Species: 4932
Condition: BY4741-3rd
Replicates: 2
Raw OD Value: r im 0.5279±0.00997021
Normalized OD Score: sc h 0.7722±0.0104589
Z-Score: -9.1745±0.894271
p-Value: 6.58494e-18
Z-Factor: -3.57859
Fitness Defect: 39.5617
Bioactivity Statement: Active
Experimental Conditions
Library:Spectrum
Plate Number and Position:16|H10
Drug Concentration:50.00 nM
OD Absorbance:600 nm
Robot Temperature:26.60 Celcius
Date:2007-09-25 YYYY-MM-DD
Plate CH Control (+):0.040075±0.00075
Plate DMSO Control (-):0.671375±0.16491
Plate Z-Factor:0.1564
png
ps
pdf

DBLink | Rows returned: 3
4485 dimethyl 2,6-dimethyl-4-(2-nitrophenyl)-1,4-dihydropyridine-3,5-dicarboxylate
63011 dimethyl 2,6-dimethyl-4-(2-nitrophenyl)-1,4-dihydropyridine-3,5-dicarboxylate hydrochloride
451023 dimethyl 2,6-dimethyl-4-(2-nitrophenyl)-1,4-dihydropyridine-3,5-dicarboxylate

internal high similarity DBLink | Rows returned: 5
RJC 03441 0.9048
JFD 03269 0.9486
JFD 03311 0.9595
JFD 03307 1.0000
LOPAC 00213 1.0000

nonactive | Cluster 5071 | Additional Members: 12 | Rows returned: 2
SPE01505390 0.228070175438597
LOPAC 00213 0

Service provided by the Mike Tyers Laboratory