67469-75-4,MFCD00209830
Catalog No.:AA00FYPC

67469-75-4 | Piperazine, 1-[2-(diphenylmethoxy)ethyl]-4-(3-phenyl-2-propenyl)-,dihydrochloride

Pack Size
Purity
Availability
Price(USD)
Quantity
  
10mg
99%
in stock  
$234.00   $164.00
- +
50mg
99%
in stock  
$667.00   $467.00
- +
  • Technical Information
  • Properties
  • Literature
  • Request for Quotation
  • Download SDS
Technical Information
Catalog Number:
AA00FYPC
Chemical Name:
Piperazine, 1-[2-(diphenylmethoxy)ethyl]-4-(3-phenyl-2-propenyl)-,dihydrochloride
CAS Number:
67469-75-4
Molecular Formula:
C28H32N2O
Molecular Weight:
412.5665
MDL Number:
MFCD00209830
SMILES:
c1ccc(cc1)/C=C/CN1CCN(CC1)CCOC(c1ccccc1)c1ccccc1
Properties
Computed Properties
 
Complexity:
477  
Covalently-Bonded Unit Count:
3  
Defined Atom Stereocenter Count:
0  
Defined Bond Stereocenter Count:
1  
Formal Charge:
0  
Heavy Atom Count:
33  
Hydrogen Bond Acceptor Count:
3  
Hydrogen Bond Donor Count:
2  
Isotope Atom Count:
0  
Rotatable Bond Count:
9  
Undefined Atom Stereocenter Count:
0  
Undefined Bond Stereocenter Count:
0  

Literature

Title: A novel mechanism of cocaine to enhance dopamine d2-like receptor mediated neurochemical and behavioral effects. An in vivo and in vitro study.

Journal: Neuropsychopharmacology : official publication of the American College of Neuropsychopharmacology 20120701

Title: Pharmacological manipulation of the dopaminergic system affects wheel-running activity in differentially active mice.

Journal: Journal of biological regulators and homeostatic agents 20120101

Title: Synergistic activation of dopamine D1 and TrkB receptors mediate gain control of synaptic plasticity in the basolateral amygdala.

Journal: PloS one 20110101

Title: A new model of the disrupted latent inhibition in C57BL/6J mice after bupropion treatment.

Journal: Psychopharmacology 20100201

Title: Catecholamine reuptake inhibition causes weight loss by increasing locomotor activity and thermogenesis.

Journal: Neuropsychopharmacology : official publication of the American College of Neuropsychopharmacology 20080501

Title: Inhibition of dopamine and norepinephrine reuptake produces additive effects on energy balance in lean and obese mice.

Journal: Neuropsychopharmacology : official publication of the American College of Neuropsychopharmacology 20070401

Title: Comparisons between bupropion and dexamphetamine in a range of in vivo tests exploring dopaminergic transmission.

Journal: British journal of pharmacology 20070301

Title: Methylphenidate and MK-801, an N-methyl-d-aspartate receptor antagonist: shared biological properties.

Journal: Neuroscience 20040101

Title: Stimulation of postsynaptic alpha1b- and alpha2-adrenergic receptors amplifies dopamine-mediated locomotor activity in both rats and mice.

Journal: Synapse (New York, N.Y.) 20031215

Title: Critical role of alpha1-adrenergic receptors in acute and sensitized locomotor effects of D-amphetamine, cocaine, and GBR 12783: influence of preexposure conditions and pharmacological characteristics.

Journal: Synapse (New York, N.Y.) 20020101

Title: Nail-Boucherie K, et al. The specific dopamine uptake inhibitor GBR 12783 improves learning of inhibitory avoidance and increases hippocampal acetylcholine release. Brain Res Cogn Brain Res. 1998 Oct;7(2):203-5.

Title: Bonnet JJ, et al. GBR 12783, a potent and selective inhibitor of dopamine uptake: biochemical studies in vivo and ex vivo. Eur J Pharmacol. 1986 Feb 18;121(2):199-209.

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Tags:67469-75-4 Molecular Formula|67469-75-4 MDL|67469-75-4 SMILES|67469-75-4 Piperazine, 1-[2-(diphenylmethoxy)ethyl]-4-(3-phenyl-2-propenyl)-,dihydrochloride
Catalog No.: AA00FYPC
67469-75-4,MFCD00209830
67469-75-4 | Piperazine, 1-[2-(diphenylmethoxy)ethyl]-4-(3-phenyl-2-propenyl)-,dihydrochloride
Pack Size: 10mg
Purity: 99%
in stock
$234.00 $164.00
Pack Size: 50mg
Purity: 99%
in stock
$667.00 $467.00
Quantity
- +
Add to Card
Order Now
bulk Quotation Request
Technical Information
Catalog Number: AA00FYPC
Chemical Name: Piperazine, 1-[2-(diphenylmethoxy)ethyl]-4-(3-phenyl-2-propenyl)-,dihydrochloride
CAS Number: 67469-75-4
Molecular Formula: C28H32N2O
Molecular Weight: 412.5665
MDL Number: MFCD00209830
SMILES: c1ccc(cc1)/C=C/CN1CCN(CC1)CCOC(c1ccccc1)c1ccccc1
Properties
Complexity: 477  
Covalently-Bonded Unit Count: 3  
Defined Atom Stereocenter Count: 0  
Defined Bond Stereocenter Count: 1  
Formal Charge: 0  
Heavy Atom Count: 33  
Hydrogen Bond Acceptor Count: 3  
Hydrogen Bond Donor Count: 2  
Isotope Atom Count: 0  
Rotatable Bond Count: 9  
Undefined Atom Stereocenter Count: 0  
Undefined Bond Stereocenter Count: 0  
Literature fold

Title: A novel mechanism of cocaine to enhance dopamine d2-like receptor mediated neurochemical and behavioral effects. An in vivo and in vitro study.

Journal: Neuropsychopharmacology : official publication of the American College of Neuropsychopharmacology20120701

Title: Pharmacological manipulation of the dopaminergic system affects wheel-running activity in differentially active mice.

Journal: Journal of biological regulators and homeostatic agents20120101

Title: Synergistic activation of dopamine D1 and TrkB receptors mediate gain control of synaptic plasticity in the basolateral amygdala.

Journal: PloS one20110101

Title: A new model of the disrupted latent inhibition in C57BL/6J mice after bupropion treatment.

Journal: Psychopharmacology20100201

Title: Catecholamine reuptake inhibition causes weight loss by increasing locomotor activity and thermogenesis.

Journal: Neuropsychopharmacology : official publication of the American College of Neuropsychopharmacology20080501

Title: Inhibition of dopamine and norepinephrine reuptake produces additive effects on energy balance in lean and obese mice.

Journal: Neuropsychopharmacology : official publication of the American College of Neuropsychopharmacology20070401

Title: Comparisons between bupropion and dexamphetamine in a range of in vivo tests exploring dopaminergic transmission.

Journal: British journal of pharmacology20070301

Title: Methylphenidate and MK-801, an N-methyl-d-aspartate receptor antagonist: shared biological properties.

Journal: Neuroscience20040101

Title: Stimulation of postsynaptic alpha1b- and alpha2-adrenergic receptors amplifies dopamine-mediated locomotor activity in both rats and mice.

Journal: Synapse (New York, N.Y.)20031215

Title: Critical role of alpha1-adrenergic receptors in acute and sensitized locomotor effects of D-amphetamine, cocaine, and GBR 12783: influence of preexposure conditions and pharmacological characteristics.

Journal: Synapse (New York, N.Y.)20020101

Title: Nail-Boucherie K, et al. The specific dopamine uptake inhibitor GBR 12783 improves learning of inhibitory avoidance and increases hippocampal acetylcholine release. Brain Res Cogn Brain Res. 1998 Oct;7(2):203-5.

Title: Bonnet JJ, et al. GBR 12783, a potent and selective inhibitor of dopamine uptake: biochemical studies in vivo and ex vivo. Eur J Pharmacol. 1986 Feb 18;121(2):199-209.

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