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Molecule
ID:4177
Structure
Similarity
Functional Group
Text
General Information
Structure
Molecular Formula
C₃₂H₄₄N₄O
Molecular Mass
500.71796
Exact Mass
500.35151205
Charge
0
InChI
InChI=1S/C32H44N4O/c37-31-21-20-24-27(18-13-19-28(24)36-31)33-22-11-5-3-1-2-4-6-12-23-34-32-25-14-7-9-16-29(25)35-30-17-10-8-15-26(30)32/h7,9,14,16,20-21,27,33H,1-6,8,10-13,15,17-19,22-23H2,(H,34,35)(H,36,37)/t27-/m1/s1
InChIKey
ROTFGKJJMRTWBD-HHHXNRCGSA-N
Canonic Smiles
O=c1ccc2c([nH]1)CCC[C@H]2NCCCCCCCCCCNc1c2CCCCc2nc2c1cccc2
Isomeric Smiles
O=c1[nH]c2c(cc1)[C@@H](CCC2)NCCCCCCCCCCNc1c2CCCCc2nc2ccccc12
Calculated Properties
JChem
Acid pKa
11.334502
H Acceptors
4
H Donor
3
LogD (pH = 5.5)
1.0526994
LogD (pH = 7.4)
2.2801619
Log P
5.8759212
Molar Refractivity
155.7953
Polarizability
60.4132
Polar Surface Area
66.05
Rotatable Bonds
13
Lipinski's Rule of Five
false
ALOGPS 2.1
Log P
6.89
LOG S
-5.82
Solubility (Water)
7.51e-04 g/l
Data Source
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Properties
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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
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RDKit
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JChem
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ALOGPS 2.1
Data Source
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Academic Data
Names and Identifiers
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IUPAC Traditional name
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IUPAC name
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Synonyms
Registration numbers
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PubChem SID
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PubChem CID
Properties
Related Proteins
Molecular Spectra
Molecule Details
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DrugBank
References
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PubChem Literature
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From Data Sources
Bioactivity
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PubChem BioAssay
Data Source
Academic Data
PubChem
5326966
DrugBank
DB04614
Names and Identifiers
IUPAC Traditional name
@(R)-tacrine(10)-hupyridone
IUPAC name
(5R)-5-({10-[(1,2,3,4-tetrahydroacridin-9-yl)amino]decyl}amino)-1,2,5,6,7,8-hexahydroquinolin-2-one
Synonyms
(R)-tacrine(10)-hupyridone
Registration numbers
PubChem SID
46505238
160967609
PubChem CID
5326966
Molecule Details
DrugBank
DB04614
Drug information: experimental
References
PubChem Literature
No Data Available
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Bioactivity
PubChem BioAssay