486-47-5,MFCD00221783
Catalog No.:AA00DDIX

486-47-5 | ethaverine

Pack Size
Purity
Availability
Price(USD)
Quantity
  
10mg
3 weeks  
$452.00   $316.00
- +
100mg
3 weeks  
$2,380.00   $1,666.00
- +
  • Technical Information
  • Properties
  • Literature
  • Request for Quotation
  • Download SDS
Technical Information
Catalog Number:
AA00DDIX
Chemical Name:
ethaverine
CAS Number:
486-47-5
Molecular Formula:
C24H29NO4
Molecular Weight:
395.4914
MDL Number:
MFCD00221783
SMILES:
CCOc1ccc(cc1OCC)Cc1nccc2c1cc(OCC)c(c2)OCC
Properties
Computed Properties
 
Complexity:
462  
Covalently-Bonded Unit Count:
1  
Defined Atom Stereocenter Count:
0  
Defined Bond Stereocenter Count:
0  
Formal Charge:
0  
Heavy Atom Count:
29  
Hydrogen Bond Acceptor Count:
5  
Hydrogen Bond Donor Count:
0  
Isotope Atom Count:
0  
Rotatable Bond Count:
10  
Undefined Atom Stereocenter Count:
0  
Undefined Bond Stereocenter Count:
0  
XLogP3:
5.4  

Literature

Title: Why are most phospholipidosis inducers also hERG blockers?

Journal: Archives of toxicology 20171201

Title: New PDE4 inhibitors based on pharmacophoric similarity between papaverine and tofisopam.

Journal: Bioorganic & medicinal chemistry letters 20111101

Title: A novel flow cytometric high throughput assay for a systematic study on molecular mechanisms underlying T cell receptor-mediated integrin activation.

Journal: PloS one 20090101

Title: Stereoselective total synthesis of bioactive styryllactones (+)-goniofufurone, (+)7-epi-goniofufurone, (+)-goniopypyrone, (+)-goniotriol, (+)-altholactone, and (-)-etharvensin.

Journal: The Journal of organic chemistry 20080104

Title: Simple isoquinoline and benzylisoquinoline alkaloids as potential antimicrobial, antimalarial, cytotoxic, and anti-HIV agents.

Journal: Bioorganic & medicinal chemistry 20011101

Title: Inhibitory effects of ethaverine, a homologue of papaverine, on monoamine oxidase activity in mouse brain.

Journal: Biological & pharmaceutical bulletin 20010701

Title: Characterization of TbPDE2A, a novel cyclic nucleotide-specific phosphodiesterase from the protozoan parasite Trypanosoma brucei.

Journal: The Journal of biological chemistry 20010413

Title: Inhibitory effects of ethaverine, a homologue of papaverine, on dopamine content in PC12 cells.

Journal: Biological & pharmaceutical bulletin 20010101

Title: Tumor- and drug-induced cutaneous neuro-phospholipidosis.

Journal: Journal of cutaneous pathology 19750101

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SDS
Tags:486-47-5 Molecular Formula|486-47-5 MDL|486-47-5 SMILES|486-47-5 ethaverine
Catalog No.: AA00DDIX
486-47-5,MFCD00221783
486-47-5 | ethaverine
Pack Size: 10mg
Purity:
3 weeks
$452.00 $316.00
Pack Size: 100mg
Purity:
3 weeks
$2,380.00 $1,666.00
Quantity
- +
Add to Card
Order Now
bulk Quotation Request
Technical Information
Catalog Number: AA00DDIX
Chemical Name: ethaverine
CAS Number: 486-47-5
Molecular Formula: C24H29NO4
Molecular Weight: 395.4914
MDL Number: MFCD00221783
SMILES: CCOc1ccc(cc1OCC)Cc1nccc2c1cc(OCC)c(c2)OCC
Properties
Complexity: 462  
Covalently-Bonded Unit Count: 1  
Defined Atom Stereocenter Count: 0  
Defined Bond Stereocenter Count: 0  
Formal Charge: 0  
Heavy Atom Count: 29  
Hydrogen Bond Acceptor Count: 5  
Hydrogen Bond Donor Count: 0  
Isotope Atom Count: 0  
Rotatable Bond Count: 10  
Undefined Atom Stereocenter Count: 0  
Undefined Bond Stereocenter Count: 0  
XLogP3: 5.4  
Literature fold

Title: Why are most phospholipidosis inducers also hERG blockers?

Journal: Archives of toxicology20171201

Title: New PDE4 inhibitors based on pharmacophoric similarity between papaverine and tofisopam.

Journal: Bioorganic & medicinal chemistry letters20111101

Title: A novel flow cytometric high throughput assay for a systematic study on molecular mechanisms underlying T cell receptor-mediated integrin activation.

Journal: PloS one20090101

Title: Stereoselective total synthesis of bioactive styryllactones (+)-goniofufurone, (+)7-epi-goniofufurone, (+)-goniopypyrone, (+)-goniotriol, (+)-altholactone, and (-)-etharvensin.

Journal: The Journal of organic chemistry20080104

Title: Simple isoquinoline and benzylisoquinoline alkaloids as potential antimicrobial, antimalarial, cytotoxic, and anti-HIV agents.

Journal: Bioorganic & medicinal chemistry20011101

Title: Inhibitory effects of ethaverine, a homologue of papaverine, on monoamine oxidase activity in mouse brain.

Journal: Biological & pharmaceutical bulletin20010701

Title: Characterization of TbPDE2A, a novel cyclic nucleotide-specific phosphodiesterase from the protozoan parasite Trypanosoma brucei.

Journal: The Journal of biological chemistry20010413

Title: Inhibitory effects of ethaverine, a homologue of papaverine, on dopamine content in PC12 cells.

Journal: Biological & pharmaceutical bulletin20010101

Title: Tumor- and drug-induced cutaneous neuro-phospholipidosis.

Journal: Journal of cutaneous pathology19750101

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