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Molecule
ID:118992
Structure
Similarity
Functional Group
Text
General Information
Structure
Molecular Formula
C₁₀H₂₀ClNO
Molecular Mass
205.7249
Exact Mass
205.12334195
Charge
0
InChI
InChI=1S/C10H19NO.ClH/c12-8-9-4-3-7-11-6-2-1-5-10(9)11;/h9-10,12H,1-8H2;1H/t9-,10+;/m0./s1
InChIKey
ZKXVUMSVQBQBCR-BAUSSPIASA-N
Canonic Smiles
OC[C@@H]1CCCN2[C@@H]1CCCC2.Cl
Isomeric Smiles
N12[C@@H]([C@H](CO)CCC1)CCCC2.Cl
Calculated Properties
JChem
Acid pKa
15.422514
H Acceptors
2
H Donor
1
LogD (pH = 5.5)
-2.526804
LogD (pH = 7.4)
-1.5202918
Log P
0.9205197
Molar Refractivity
50.2438
Polarizability
19.837076
Polar Surface Area
23.47
Rotatable Bonds
1
Lipinski's Rule of Five
true
Data Source
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Related Proteins
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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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Academic Data
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Synonyms
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IUPAC name
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IUPAC Traditional name
Registration numbers
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PubChem SID
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PubChem CID
Properties
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Product Information
Related Proteins
Molecular Spectra
Molecule Details
References
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PubChem Literature
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From Data Sources
Bioactivity
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PubChem BioAssay
Data Source
Commercial Catalog
InterBioScreen
BB_NC-0121
STOCK1N-06600
Academic Data
PubChem
24721130
Names and Identifiers
Synonyms
((1R,9aR)-octahydro-1H-quinolizin-1-yl)methanol hydrochloride
IUPAC name
(1R,9aR)-octahydro-1H-quinolizin-1-ylmethanol hydrochloride
IUPAC Traditional name
(-)-lupinine hydrochloride
Registration numbers
PubChem SID
162107230
PubChem CID
24721130
Properties
Product Information
Salt Data
HCl
Source
Classification
Genuine Natural Compounds
Source
References
PubChem Literature
No Data Available
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Bioactivity
PubChem BioAssay