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Molecule
ID:118517
Structure
Similarity
Functional Group
Text
General Information
Structure
Molecular Formula
C₁₃H₁₈N₂
Molecular Mass
202.29542
Exact Mass
202.14699859
Charge
0
InChI
InChI=1S/C13H18N2/c1-2-4-11(5-3-1)8-15-9-12-6-7-13(10-15)14-12/h1-5,12-14H,6-10H2
InChIKey
QXMPIEOTDBYZDL-UHFFFAOYSA-N
Canonic Smiles
C1CC2NC1CN(C2)Cc1ccccc1
Isomeric Smiles
N1(CC2NC(C1)CC2)Cc1ccccc1
Calculated Properties
JChem
H Acceptors
2
H Donor
1
LogD (pH = 5.5)
-1.3656421
LogD (pH = 7.4)
-0.7718595
Log P
1.9040458
Molar Refractivity
62.2375
Polarizability
24.857315
Polar Surface Area
15.27
Rotatable Bonds
2
Lipinski's Rule of Five
true
Data Source
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Names and Identifiers
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Registration numbers
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Properties
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Related Proteins
No Data Available
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Molecular Spectra
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Molecule Details
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References
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Bioactivity
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General Information
Calculated Properties
•
RDKit
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JChem
Data Source
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Commercial Catalog
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Academic Data
Names and Identifiers
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IUPAC name
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Synonyms
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IUPAC Traditional name
Registration numbers
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MDL Number
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CAS Number
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PubChem CID
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PubChem SID
Properties
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Product Information
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Physical Property
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Safety Information
Related Proteins
Molecular Spectra
Molecule Details
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TRC
References
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PubChem Literature
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From Data Sources
Bioactivity
•
PubChem BioAssay
Data Source
Commercial Catalog
Life Chemicals
F2196-0005
TRC
B251290
Enamine
EN300-90563
Academic Data
PubChem
12430594
Names and Identifiers
IUPAC name
3-benzyl-3,8-diazabicyclo[3.2.1]octane
Synonyms
3-benzyl-3,8-diazabicyclo[3.2.1]octane dihydrochloride
3-Benzyl-3,8-diazabicyclo[3.2.1]octane
3-(Phenylmethyl)-3,8-diazabicyclo[3.2.1]octane
IUPAC Traditional name
3-benzyl-3,8-diazabicyclo[3.2.1]octane
Registration numbers
MDL Number
MFCD20441694
CAS Number
67571-90-8
PubChem CID
12430594
PubChem SID
162106907
Molecule Details
TRC
B251290
A novel substituted diazabicyclooctane derivative as monoamine neurotransmitter re-uptake inhibitors.
References
PubChem Literature
From Data Sources
•
Maeda, K, et al.: J. Biol. Chem., 276, 35194 (2001) Castonguay, L, et al.: Biochem., 42, 1544 (2003)
•
Dorr, P, et al.: Antimicrob. Agents Chemother., 49, 4721 (2003)
Bioactivity
PubChem BioAssay
Properties
Product Information
Purity
95+%
Source
95%
Source
Salt Data
2 HCl
Source
Certificate of Analysis
Download link
Source
Physical Property
Partition Coefficient
1.986
Source
2.189
Source
Safety Information
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Source
Hydrophobicity(logP)
MSDS Link