Details
Stereochemistry | ACHIRAL |
Molecular Formula | C14H15N |
Molecular Weight | 197.2756 |
Optical Activity | NONE |
Defined Stereocenters | 0 / 0 |
E/Z Centers | 0 |
Charge | 0 |
SHOW SMILES / InChI
SMILES
C(NCC1=CC=CC=C1)C2=CC=CC=C2
InChI
InChIKey=BWLUMTFWVZZZND-UHFFFAOYSA-N
InChI=1S/C14H15N/c1-3-7-13(8-4-1)11-15-12-14-9-5-2-6-10-14/h1-10,15H,11-12H2
Molecular Formula | C14H15N |
Molecular Weight | 197.2756 |
Charge | 0 |
Count |
|
Stereochemistry | ACHIRAL |
Additional Stereochemistry | No |
Defined Stereocenters | 0 / 0 |
E/Z Centers | 0 |
Optical Activity | NONE |
Approval Year
PubMed
Title | Date | PubMed |
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Dibenzylamine--a novel blocker of the voltage-dependent K+ current in myocardial mouse cells. | 2001 Jul |
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Dichlorobis(dibenzylamino)bis(tetrahydrofuran)zirconium(IV) toluene hemisolvate. | 2001 Jun |
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Acetoacetate, acetone, and dibenzylamine (a contaminant in l-(+)-beta-hydroxybutyrate) exhibit direct anticonvulsant actions in vivo. | 2002 Apr |
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Design, synthesis, and evaluation of new chemosensitizers in multi-drug-resistant Plasmodium falciparum. | 2002 Jun 20 |
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Probing polyvalency in artificial systems exhibiting molecular recognition. | 2002 Nov 15 |
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Ion pairing and host-guest complexation in low dielectric constant solvents. | 2003 Jun 11 |
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[Reactions of iminodibenzyl with 2,6-dichloro-1,4-benzoquinone-4-chlorimide]. | 2003 Mar |
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Controlling multivalent interactions in triply-threaded two-component superbundles. | 2003 Nov 7 |
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Voltage-dependent block of N-methyl-D-aspartate receptors by the novel anticonvulsant dibenzylamine, a bioactive constituent of L-(+)-beta-hydroxybutyrate. | 2003 Oct |
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Stevens-Johnson syndrome-toxic epidermal necrolysis (SJS-TEN) overlap associated with carbamazepine use. | 2005 Apr |
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A chimeric ligand approach leading to potent antiprion active acridine derivatives: design, synthesis, and biological investigations. | 2006 Nov 2 |
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Competitive interactions of two ion-paired salts with a neutral host to form two non-ion-paired complexes. | 2007 Aug 17 |
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Enhancing the reactivity of 1,2,3-triazoles in "click" macrocycles by face-to-face dibenzylammonium ion binding. | 2007 Dec 7 |
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Singlet oxygen promoted carbon-heteroatom bond cleavage in dibenzyl sulfides and tertiary dibenzylamines. Structural effects and the role of exciplexes. | 2007 Dec 7 |
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Synthesis and antibacterial activities of new quinolone derivatives utilizing 1-azabicyclo[1.1.0]butane. | 2007 Feb 15 |
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Asymmetric synthesis of beta2-amino acids: 2-substituted-3-aminopropanoic acids from N-acryloyl SuperQuat derivatives. | 2007 Sep 7 |
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An anthracene-based photochromic macrocycle as a key ring component to switch a frequency of threading motion. | 2008 |
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Coordination-driven self-assembly of cavity-cored multiple crown ether derivatives and poly[2]pseudorotaxanes. | 2008 Apr 16 |
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Synthesis of New Quinolone Antibiotics Utilizing Azetidine Derivatives Obtained from 1-Azabicyclo[1.1.0]butane. | 2008 Mar |
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Searching for anthropogenic contaminants in human breast adipose tissues using gas chromatography-time-of-flight mass spectrometry. | 2009 Jan |
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Neuroprotection by acetoacetate and β-hydroxybutyrate against NMDA-induced RGC damage in rat--possible involvement of kynurenic acid. | 2010 Dec |
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Bis(tribenzyl-ammonium) tetra-chloridoaurate(III) chloride. | 2010 Jan 30 |
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Reversible photoswitching of rotaxane character and interplay of thermodynamic stability and kinetic lability in a self-assembling ring-axle molecular system. | 2010 Oct 11 |
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The discovery of an orally efficacious positive allosteric modulator of the calcium sensing receptor containing a dibenzylamine core. | 2010 Sep 15 |
Patents
Substance Class |
Chemical
Created
by
admin
on
Edited
Fri Dec 15 19:43:38 GMT 2023
by
admin
on
Fri Dec 15 19:43:38 GMT 2023
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Record UNII |
3G0YFX01C6
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Record Status |
Validated (UNII)
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Record Version |
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4811
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203-117-7
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103-49-1
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7656
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3G0YFX01C6
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C005051
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DTXSID6044355
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m4286
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PRIMARY | Merck Index |
Related Record | Type | Details | ||
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SALT/SOLVATE -> PARENT |
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SALT/SOLVATE -> PARENT | |||
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SALT/SOLVATE -> PARENT |
Related Record | Type | Details | ||
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PARENT -> IMPURITY |
CHROMATOGRAPHIC PURITY (HPLC/UV)
EP
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