| 
 | Compound Information | SONAR Target prediction |  | Name: | PAPAVERINE HYDROCHLORIDE |  | Unique Identifier: | SPE01500459 |  | MolClass: | Checkout models in ver1.5 and ver1.0 |  | Molecular Formula: |  |  | Molecular Weight: | 353.671 g/mol |  | X log p: | 15.917  (online calculus) |  | Lipinksi Failures | 1 |  | TPSA | 49.28 |  | Hydrogen Bond Donor Count: | 0 |  | Hydrogen Bond Acceptors Count: | 5 |  | Rotatable Bond Count: | 6 |  | Canonical Smiles: | Cl.COc1ccc(Cc2nccc3cc(OC)c(OC)cc23)cc1OC |  | Class: | alkaloid |  | Source: | Papaver somniferum, Rauwolfia serpentina |  | Therapeutics: | muscle relaxant (smooth), cerebral vasodilator |  | Generic_name: | Papaverine |  | Chemical_iupac_name: | 1-[(3,4-dimethoxyphenyl)methyl]-6,7-dimethoxy-isoquinoline |  | Drug_type: | Approved Drug |  | Pharmgkb_id: | PA450779 |  | Drugbank_id: | APRD00628 |  | Logp: | 3.72 |  | Cas_registry_number: | 61-25-6 |  | Drug_category: | Vasodilator Agents; ATC:A03AD01; ATC:G04BE02 |  | Indication: | Impotence |  | Pharmacology: | Papaverine is a nonxanthine phosphodiesterase inhibitor for the relief of cerebral and peripheral ischemia associated with arterial spasm and myocardial ischemia
 complicated by arrhythmias. The main actions of Papaverine are exerted on cardiac
 and smooth muscle. Like qathidine, Papaverine acts directly on the heart muscle to
 depress conduction and prolong the refractory period. Papaverine relaxes various
 smooth muscles. This relaxation may be prominent if spasm exists. The muscle cell is
 not paralyzed by Papaverine and still responds to drugs and other stimuli causing
 contraction. The antispasmodic effect is a direct one, and unrelated to muscle
 innervation. Papaverine is practically devoid of effects on the central nervous
 system. Papaverine relaxes the smooth musculature of the larger blood vessels,
 especially coronary, systemic peripheral, and pulmonary arteries.
 |  | Mechanism_of_action: | Perhaps by its direct vasodilating action on cerebral blood vessels, Papaverine increases cerebral blood flow and decreases cerebral vascular resistance in normal
 subjects; oxygen consumption is unaltered. These effects may explain the benefit
 reported from the drug in cerebral vascular encephalopathy.
 |  | Organisms_affected: | Humans and other mammals | 
 
 
	
		| Species: | 4932 |  
		| Condition: | TOR1 |  
		| Replicates: | 2 |  
		| Raw OD Value: r im | 0.9429±0.000848528 |  
		| Normalized OD Score: sc h | 0.9749±0.00903567 |  
		| Z-Score: | 0.5635±0.243234 |  
		| p-Value: | 0.578734 |  
		| Z-Factor: | -3.01939 |  
		| Fitness Defect: | 0.5469 |  
		| Bioactivity Statement: | Nonactive |  | | Experimental Conditions |  |  | Library: | Spectrum_ED |  | Plate Number and Position: | 2|B8 |  | Drug Concentration: | 50.00 nM |  | OD Absorbance: | 595 nm |  | Robot Temperature: | 30.00 Celcius |  | Date: | 2012-09-18 YYYY-MM-DD |  | Plate CH Control (+): | 0.0005499999999999999±0.00192 |  | Plate DMSO Control (-): | 1.004±0.01932 |  | Plate Z-Factor: | 0.9291 | 
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		| 4680 | 1-[(3,4-dimethoxyphenyl)methyl]-6,7-dimethoxy-isoquinoline |  
		| 6084 | 1-[(3,4-dimethoxyphenyl)methyl]-6,7-dimethoxy-isoquinoline hydrochloride |  
		| 100248 | 4-[(6,7-dimethoxyisoquinolin-1-yl)methyl]-2-methoxy-phenol |  
		| 425899 | 3-[(3,4-dimethoxyphenyl)methyl]-6,7-dimethoxy-isoquinoline |  
		| 426677 | 1-[(3,4-dimethoxyphenyl)methyl]-5,6-dimethoxy-isoquinoline |  
		| 657373 | 1-[(3,4-dimethoxyphenyl)methyl]-6,7-dimethoxy-isoquinoline; hydrogen(+1) cation; chloride |  
 | internal high similarity DBLink  | Rows returned: 3 |  | 
 
 | active | Cluster 1145 | Additional Members: 7 | Rows returned: 2 |  | 
 
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