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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
Structure of DIBENZYLAMINE

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

HIDE SMILES / InChI

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

PubMed

TitleDatePubMed
Dibenzylamine--a novel blocker of the voltage-dependent K+ current in myocardial mouse cells.
2001 Jul
Dichlorobis(dibenzylamino)bis(tetrahydrofuran)zirconium(IV) toluene hemisolvate.
2001 Jun
Acetoacetate, acetone, and dibenzylamine (a contaminant in l-(+)-beta-hydroxybutyrate) exhibit direct anticonvulsant actions in vivo.
2002 Apr
Design, synthesis, and evaluation of new chemosensitizers in multi-drug-resistant Plasmodium falciparum.
2002 Jun 20
Probing polyvalency in artificial systems exhibiting molecular recognition.
2002 Nov 15
Ion pairing and host-guest complexation in low dielectric constant solvents.
2003 Jun 11
[Reactions of iminodibenzyl with 2,6-dichloro-1,4-benzoquinone-4-chlorimide].
2003 Mar
Controlling multivalent interactions in triply-threaded two-component superbundles.
2003 Nov 7
Voltage-dependent block of N-methyl-D-aspartate receptors by the novel anticonvulsant dibenzylamine, a bioactive constituent of L-(+)-beta-hydroxybutyrate.
2003 Oct
Stevens-Johnson syndrome-toxic epidermal necrolysis (SJS-TEN) overlap associated with carbamazepine use.
2005 Apr
A chimeric ligand approach leading to potent antiprion active acridine derivatives: design, synthesis, and biological investigations.
2006 Nov 2
Competitive interactions of two ion-paired salts with a neutral host to form two non-ion-paired complexes.
2007 Aug 17
Enhancing the reactivity of 1,2,3-triazoles in "click" macrocycles by face-to-face dibenzylammonium ion binding.
2007 Dec 7
Singlet oxygen promoted carbon-heteroatom bond cleavage in dibenzyl sulfides and tertiary dibenzylamines. Structural effects and the role of exciplexes.
2007 Dec 7
Synthesis and antibacterial activities of new quinolone derivatives utilizing 1-azabicyclo[1.1.0]butane.
2007 Feb 15
Asymmetric synthesis of beta2-amino acids: 2-substituted-3-aminopropanoic acids from N-acryloyl SuperQuat derivatives.
2007 Sep 7
An anthracene-based photochromic macrocycle as a key ring component to switch a frequency of threading motion.
2008
Coordination-driven self-assembly of cavity-cored multiple crown ether derivatives and poly[2]pseudorotaxanes.
2008 Apr 16
Synthesis of New Quinolone Antibiotics Utilizing Azetidine Derivatives Obtained from 1-Azabicyclo[1.1.0]butane.
2008 Mar
Searching for anthropogenic contaminants in human breast adipose tissues using gas chromatography-time-of-flight mass spectrometry.
2009 Jan
Neuroprotection by acetoacetate and β-hydroxybutyrate against NMDA-induced RGC damage in rat--possible involvement of kynurenic acid.
2010 Dec
Bis(tribenzyl-ammonium) tetra-chloridoaurate(III) chloride.
2010 Jan 30
Reversible photoswitching of rotaxane character and interplay of thermodynamic stability and kinetic lability in a self-assembling ring-axle molecular system.
2010 Oct 11
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 Fri Dec 15 19:43:38 GMT 2023
Edited
by admin
on Fri Dec 15 19:43:38 GMT 2023
Record UNII
3G0YFX01C6
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
DIBENZYLAMINE
MI  
Systematic Name English
N-(PHENYLMETHYL)BENZENEMETHANAMINE
Systematic Name English
NORADRENALINE TARTRATE IMPURITY F [EP IMPURITY]
Common Name English
N-BENZYL-1-PHENYLMETHANAMINE
Systematic Name English
NSC-4811
Code English
DIBENZYLAMINE [MI]
Common Name English
Code System Code Type Description
NSC
4811
Created by admin on Fri Dec 15 19:43:38 GMT 2023 , Edited by admin on Fri Dec 15 19:43:38 GMT 2023
PRIMARY
ECHA (EC/EINECS)
203-117-7
Created by admin on Fri Dec 15 19:43:38 GMT 2023 , Edited by admin on Fri Dec 15 19:43:38 GMT 2023
PRIMARY
CAS
103-49-1
Created by admin on Fri Dec 15 19:43:38 GMT 2023 , Edited by admin on Fri Dec 15 19:43:38 GMT 2023
PRIMARY
PUBCHEM
7656
Created by admin on Fri Dec 15 19:43:38 GMT 2023 , Edited by admin on Fri Dec 15 19:43:38 GMT 2023
PRIMARY
FDA UNII
3G0YFX01C6
Created by admin on Fri Dec 15 19:43:38 GMT 2023 , Edited by admin on Fri Dec 15 19:43:38 GMT 2023
PRIMARY
MESH
C005051
Created by admin on Fri Dec 15 19:43:38 GMT 2023 , Edited by admin on Fri Dec 15 19:43:38 GMT 2023
PRIMARY
EPA CompTox
DTXSID6044355
Created by admin on Fri Dec 15 19:43:38 GMT 2023 , Edited by admin on Fri Dec 15 19:43:38 GMT 2023
PRIMARY
MERCK INDEX
m4286
Created by admin on Fri Dec 15 19:43:38 GMT 2023 , Edited by admin on Fri Dec 15 19:43:38 GMT 2023
PRIMARY Merck Index
Related Record Type Details
SALT/SOLVATE -> PARENT
SALT/SOLVATE -> PARENT
SALT/SOLVATE -> PARENT
Related Record Type Details
PARENT -> IMPURITY
CHROMATOGRAPHIC PURITY (HPLC/UV)
EP