Record No. 1 of 8

ID1944
NameCorydaline
Pubchem ID101301
KEGG IDC15530
SourceCorydalis cava
TypeNatural
FunctionAcetylcholinesterase inhibitor
Drug Like PropertiesYes
Molecular Weight369.45
Exact mass369.194008
Molecular formulaC22H27NO4
XlogP3.6
Topological Polar Surface Area40.2
H-Bond Donor0
H-Bond Acceptor5
Rotational Bond Count4
IUPAC Name(13S,13aR)-2,3,9,10-tetramethoxy-13-methyl-6,8,13,13a-tetrahydro-5H-isoquinolino[3,2-a]isoquinoline
Structure
   
SDF file
MOL file
PDB file
Canonical SMILECC1C2C3=CC(=C(C=C3CCN2CC4=C1C=CC(=C4OC)OC)OC)OC
Isomeric SMILEC[C@@H]1[C@@H]2C3=CC(=C(C=C3CCN2CC4=C1C=CC(=C4OC)OC)OC)OC
Drugpediawiki
References1. Source  
2. Function  
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Record No. 2 of 8

ID1945
NameCorydaline
Pubchem ID101301
KEGG IDC15530
SourceCorydalis intermedia
TypeNatural
FunctionAcetylcholinesterase inhibitor
Drug Like PropertiesYes
Molecular Weight369.45
Exact mass369.194008
Molecular formulaC22H27NO4
XlogP3.6
Topological Polar Surface Area40.2
H-Bond Donor0
H-Bond Acceptor5
Rotational Bond Count4
IUPAC Name(13S,13aR)-2,3,9,10-tetramethoxy-13-methyl-6,8,13,13a-tetrahydro-5H-isoquinolino[3,2-a]isoquinoline
Structure
   
SDF file
MOL file
PDB file
Canonical SMILECC1C2C3=CC(=C(C=C3CCN2CC4=C1C=CC(=C4OC)OC)OC)OC
Isomeric SMILEC[C@@H]1[C@@H]2C3=CC(=C(C=C3CCN2CC4=C1C=CC(=C4OC)OC)OC)OC
Drugpediawiki
References1. Slavik,Collect.Czech.Chem.Commun.,54,(1989),2009
2. Harborne,Phytochemical Dictionary Second Edition,Taylor and Francis,(1999),Chapter21
3. Source  
4. Function  
5. All Records  
Record No. 3 of 8

ID1946
NameCorydaline
Pubchem ID101301
KEGG IDC15530
SourceCorydalis nobilis
TypeNatural
FunctionAcetylcholinesterase inhibitor
Drug Like PropertiesYes
Molecular Weight369.45
Exact mass369.194008
Molecular formulaC22H27NO4
XlogP3.6
Topological Polar Surface Area40.2
H-Bond Donor0
H-Bond Acceptor5
Rotational Bond Count4
IUPAC Name(13S,13aR)-2,3,9,10-tetramethoxy-13-methyl-6,8,13,13a-tetrahydro-5H-isoquinolino[3,2-a]isoquinoline
Structure
   
SDF file
MOL file
PDB file
Canonical SMILECC1C2C3=CC(=C(C=C3CCN2CC4=C1C=CC(=C4OC)OC)OC)OC
Isomeric SMILEC[C@@H]1[C@@H]2C3=CC(=C(C=C3CCN2CC4=C1C=CC(=C4OC)OC)OC)OC
Drugpediawiki
References1. Slavik,Collect.Czech.Chem.Commun.,54,(1989),2009
2. Harborne,Phytochemical Dictionary Second Edition,Taylor and Francis,(1999),Chapter21
3. Source  
4. Function  
5. All Records  
Record No. 4 of 8

ID1947
NameCorydaline
Pubchem ID101301
KEGG IDC15530
SourceCorydalis ochroleuca
TypeNatural
FunctionAcetylcholinesterase inhibitor
Drug Like PropertiesYes
Molecular Weight369.45
Exact mass369.194008
Molecular formulaC22H27NO4
XlogP3.6
Topological Polar Surface Area40.2
H-Bond Donor0
H-Bond Acceptor5
Rotational Bond Count4
IUPAC Name(13S,13aR)-2,3,9,10-tetramethoxy-13-methyl-6,8,13,13a-tetrahydro-5H-isoquinolino[3,2-a]isoquinoline
Structure
   
SDF file
MOL file
PDB file
Canonical SMILECC1C2C3=CC(=C(C=C3CCN2CC4=C1C=CC(=C4OC)OC)OC)OC
Isomeric SMILEC[C@@H]1[C@@H]2C3=CC(=C(C=C3CCN2CC4=C1C=CC(=C4OC)OC)OC)OC
Drugpediawiki
References1. Ribar,Bull.Acad.Serbe Sci.Arts.Cl.Sci.Math.Nat.Sci.Nat.,40,(2003),95
2. Harborne,Phytochemical Dictionary Second Edition,Taylor and Francis,(1999),Chapter21
3. Source  
4. Function  
5. All Records  
Record No. 5 of 8

ID1948
NameCorydaline
Pubchem ID101301
KEGG IDC15530
SourceCorydalis solida
TypeNatural
FunctionAcetylcholinesterase inhibitor
Drug Like PropertiesYes
Molecular Weight369.45
Exact mass369.194008
Molecular formulaC22H27NO4
XlogP3.6
Topological Polar Surface Area40.2
H-Bond Donor0
H-Bond Acceptor5
Rotational Bond Count4
IUPAC Name(13S,13aR)-2,3,9,10-tetramethoxy-13-methyl-6,8,13,13a-tetrahydro-5H-isoquinolino[3,2-a]isoquinoline
Structure
   
SDF file
MOL file
PDB file
Canonical SMILECC1C2C3=CC(=C(C=C3CCN2CC4=C1C=CC(=C4OC)OC)OC)OC
Isomeric SMILEC[C@@H]1[C@@H]2C3=CC(=C(C=C3CCN2CC4=C1C=CC(=C4OC)OC)OC)OC
Drugpediawiki
References1. Source  
2. Function  
3. All Records  
Record No. 6 of 8

ID1949
NameCorydaline
Pubchem ID101301
KEGG IDC15530
SourceCorydalis turtschaninowii
TypeNatural
FunctionAcetylcholinesterase inhibitor
Drug Like PropertiesYes
Molecular Weight369.45
Exact mass369.194008
Molecular formulaC22H27NO4
XlogP3.6
Topological Polar Surface Area40.2
H-Bond Donor0
H-Bond Acceptor5
Rotational Bond Count4
IUPAC Name(13S,13aR)-2,3,9,10-tetramethoxy-13-methyl-6,8,13,13a-tetrahydro-5H-isoquinolino[3,2-a]isoquinoline
Structure
   
SDF file
MOL file
PDB file
Canonical SMILECC1C2C3=CC(=C(C=C3CCN2CC4=C1C=CC(=C4OC)OC)OC)OC
Isomeric SMILEC[C@@H]1[C@@H]2C3=CC(=C(C=C3CCN2CC4=C1C=CC(=C4OC)OC)OC)OC
Drugpediawiki
References1. Jo,Choson Minjujuui Inmin Konghwaguk Kwahagwon Tongbo,(2002),52
2. Harborne,Phytochemical Dictionary Second Edition,Taylor and Francis,(1999),Chapter21
3. Source  
4. Function  
5. All Records  
Record No. 7 of 8

ID1950
NameCorydaline
Pubchem ID101301
KEGG IDC15530
SourceCorydalis yanhusuo
TypeNatural
FunctionAcetylcholinesterase inhibitor
Drug Like PropertiesYes
Molecular Weight369.45
Exact mass369.194008
Molecular formulaC22H27NO4
XlogP3.6
Topological Polar Surface Area40.2
H-Bond Donor0
H-Bond Acceptor5
Rotational Bond Count4
IUPAC Name(13S,13aR)-2,3,9,10-tetramethoxy-13-methyl-6,8,13,13a-tetrahydro-5H-isoquinolino[3,2-a]isoquinoline
Structure
   
SDF file
MOL file
PDB file
Canonical SMILECC1C2C3=CC(=C(C=C3CCN2CC4=C1C=CC(=C4OC)OC)OC)OC
Isomeric SMILEC[C@@H]1[C@@H]2C3=CC(=C(C=C3CCN2CC4=C1C=CC(=C4OC)OC)OC)OC
Drugpediawiki
References1. Xu,Zhongguo Yaoke Daxue Xuebao,33,(2002),483
2. Harborne,Phytochemical Dictionary Second Edition,Taylor and Francis,(1999),Chapter21
3. Source  
4. Function  
5. All Records  
Record No. 8 of 8

ID1956
NameCorynoline
Pubchem ID177014
KEGG IDN/A
SourceCorydalis incisa
TypeNatural
FunctionAcetylcholinesterase inhibitor
Drug Like PropertiesYes
Molecular Weight367.40
Exact mass367.141973
Molecular formulaC21H21NO5
XlogP2.7
Topological Polar Surface Area60.4
H-Bond Donor1
H-Bond Acceptor6
Rotational Bond Count0
IUPAC NameN/A
Structure
   
SDF file
MOL file
PDB file
Canonical SMILECC12C(CC3=CC4=C(C=C3C1N(CC5=C2C=CC6=C5OCO6)C)OCO4)O
Isomeric SMILEC[C@]12[C@H](CC3=CC4=C(C=C3[C@H]1N(CC5=C2C=CC6=C5OCO6)C)OCO4)O
Drugpediawiki
References1. Source  
2. Function  
3. All Records