NP-MRD: Showing NP-Card for (-)-Cycleaneonine (NP0067787)

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Record Information

Version

2.0

Created at

2022-04-28 12:38:09 UTC

Updated at

2022-04-28 12:38:09 UTC

NP-MRD ID

NP0067787

Secondary Accession Numbers

None

Natural Product Identification

Common Name

(-)-Cycleaneonine

Description

(1S,16R)-9,10,25-trimethoxy-15,30-dimethyl-7,23-dioxa-15,30-diazaheptacyclo[22.6.2.2³,⁶.2¹⁸,²¹.1⁸,¹².0²⁷,³¹.0¹⁶,³⁵]Heptatriaconta-3,5,8(35),9,11,18,20,24,26,31,33,36-dodecaen-32-ol belongs to the class of organic compounds known as diarylethers. These are organic compounds containing the dialkyl ether functional group, with the formula ROR', where R and R' are aryl groups. (-)-Cycleaneonine is found in Cyclea racemosa and Cyclea sutchuenensis Gagnep.. Based on a literature review very few articles have been published on (1S,16R)-9,10,25-trimethoxy-15,30-dimethyl-7,23-dioxa-15,30-diazaheptacyclo[22.6.2.2³,⁶.2¹⁸,²¹.1⁸,¹².0²⁷,³¹.0¹⁶,³⁵]Heptatriaconta-3,5,8(35),9,11,18,20,24,26,31,33,36-dodecaen-32-ol.

Structure

MOL 3D MOL SDF PDB SMILES InChI


  Mrv1652304282214382D          

 46 52  0  0  1  0            999 V2000
   10.3948    2.6149    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   11.1896    2.3292    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
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   10.8538    0.9433    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   10.0453    1.1376    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    9.7874    1.9466    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.9927    1.5696    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    8.2123    1.1894    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.9756    1.9970    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.1746    2.1968    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.5518    1.6513    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
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   11.8867   -0.0441    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  2  0  0  0  0
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M  END

     RDKit          3D

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M  END


  Mrv1652304282214382D          

 46 52  0  0  1  0            999 V2000
   10.3948    2.6149    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
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    8.9927    1.5696    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    8.2123    1.1894    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.9756    1.9970    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.1746    2.1968    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.5518    1.6513    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.8016    0.8474    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.6027    0.6007    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.9013    2.2276    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.2112    2.7614    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    4.4920    2.3064    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    3.7481    2.6756    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.6901    3.4956    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.3784    3.9703    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.1492    3.6322    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.7979    4.2111    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.6927    5.0560    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.8869    5.3011    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.2363    4.7871    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.7338    6.1117    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.9552    6.3844    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.3264    5.6559    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    7.0760    6.0705    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.9481    5.9888    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.9087    5.1441    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.5994    4.6943    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    9.3716    4.9985    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    9.8178    4.2286    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   10.3604    3.5190    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
   11.0848    3.9717    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
   11.8271    3.6116    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   11.8833    2.7951    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   11.0408    4.7955    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    9.3875    5.8483    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.7174    6.3487    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.5703    3.9211    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.5346    1.4825    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    9.4836    0.5333    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    8.6795    0.7177    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   11.0852    0.1515    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   11.8867   -0.0441    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  2  0  0  0  0
  2  3  1  0  0  0  0
  3  4  2  0  0  0  0
  4  5  1  0  0  0  0
  5  6  2  0  0  0  0
  1  6  1  0  0  0  0
  6  7  1  0  0  0  0
  7  8  1  0  0  0  0
  8  9  2  0  0  0  0
  9 10  1  0  0  0  0
 10 11  2  0  0  0  0
 11 12  1  0  0  0  0
 12 13  2  0  0  0  0
  8 13  1  0  0  0  0
 11 14  1  0  0  0  0
 14 15  1  0  0  0  0
 15 16  1  6  0  0  0
 16 17  1  0  0  0  0
 17 18  1  0  0  0  0
 18 19  1  0  0  0  0
 19 20  2  0  0  0  0
 15 20  1  0  0  0  0
 20 21  1  0  0  0  0
 21 22  2  0  0  0  0
 22 23  1  0  0  0  0
 23 24  2  0  0  0  0
 19 24  1  0  0  0  0
 23 25  1  0  0  0  0
 25 26  1  0  0  0  0
 22 27  1  0  0  0  0
 27 28  1  0  0  0  0
 28 29  1  0  0  0  0
 29 30  2  0  0  0  0
 30 31  1  0  0  0  0
 31 32  2  0  0  0  0
 32 33  1  0  0  0  0
 33 34  1  0  0  0  0
  1 34  1  0  0  0  0
 34 35  1  1  0  0  0
 35 36  1  0  0  0  0
 36 37  1  0  0  0  0
  2 37  1  0  0  0  0
 35 38  1  0  0  0  0
 32 39  1  0  0  0  0
 39 40  2  0  0  0  0
 29 40  1  0  0  0  0
 21 41  1  0  0  0  0
 16 42  1  0  0  0  0
  5 43  1  0  0  0  0
 43 44  1  0  0  0  0
  4 45  1  0  0  0  0
 45 46  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0067787

> <DATABASE_NAME>
NP-MRD

> <SMILES>
COC1=CC2=C3[C@@H](CC4=CC=C(COC5=C(O)C6=C(CCN(C)[C@H]6CC6=CC=C(OC3=C1OC)C=C6)C=C5OC)C=C4)N(C)CC2

> <INCHI_IDENTIFIER>
InChI=1S/C38H42N2O6/c1-39-16-14-26-20-31(42-3)36-35(41)33(26)29(39)18-24-10-12-28(13-11-24)46-38-34-27(21-32(43-4)37(38)44-5)15-17-40(2)30(34)19-23-6-8-25(9-7-23)22-45-36/h6-13,20-21,29-30,41H,14-19,22H2,1-5H3/t29-,30+/m0/s1

> <INCHI_KEY>
BPJPWJSSKSLGNM-XZWHSSHBSA-N

> <FORMULA>
C38H42N2O6

> <MOLECULAR_WEIGHT>
622.762

> <EXACT_MASS>
622.30428708

> <JCHEM_ACCEPTOR_COUNT>
7

> <JCHEM_ATOM_COUNT>
88

> <JCHEM_AVERAGE_POLARIZABILITY>
68.8243695525704

> <JCHEM_BIOAVAILABILITY>
0

> <JCHEM_DONOR_COUNT>
1

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
0

> <JCHEM_IUPAC>
(1S,16R)-9,10,25-trimethoxy-15,30-dimethyl-7,23-dioxa-15,30-diazaheptacyclo[22.6.2.2^{3,6}.2^{18,21}.1^{8,12}.0^{27,31}.0^{16,35}]heptatriaconta-3,5,8,10,12(35),18,20,24(32),25,27(31),33,36-dodecaen-32-ol

> <ALOGPS_LOGP>
5.63

> <JCHEM_LOGP>
5.859114662420942

> <ALOGPS_LOGS>
-5.05

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
7

> <JCHEM_PHYSIOLOGICAL_CHARGE>
2

> <JCHEM_PKA_STRONGEST_ACIDIC>
8.610026807172153

> <JCHEM_PKA_STRONGEST_BASIC>
9.549833020069785

> <JCHEM_POLAR_SURFACE_AREA>
72.86000000000001

> <JCHEM_REFRACTIVITY>
180.4672999999999

> <JCHEM_ROTATABLE_BOND_COUNT>
3

> <JCHEM_RULE_OF_FIVE>
0

> <ALOGPS_SOLUBILITY>
5.50e-03 g/l

> <JCHEM_TRADITIONAL_IUPAC>
(1S,16R)-9,10,25-trimethoxy-15,30-dimethyl-7,23-dioxa-15,30-diazaheptacyclo[22.6.2.2^{3,6}.2^{18,21}.1^{8,12}.0^{27,31}.0^{16,35}]heptatriaconta-3,5,8,10,12(35),18,20,24(32),25,27(31),33,36-dodecaen-32-ol

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 28-APR-22   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   28-APR-22         0                                  
HETATM    1  C   UNK     0      19.404   4.881   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0      20.887   4.348   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0      21.323   2.865   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0      20.260   1.761   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0      18.751   2.123   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0      18.270   3.634   0.000  0.00  0.00           C+0
HETATM    7  O   UNK     0      16.786   2.930   0.000  0.00  0.00           O+0
HETATM    8  C   UNK     0      15.330   2.220   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0      14.888   3.728   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0      13.393   4.101   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0      12.230   3.082   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0      12.696   1.582   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0      14.192   1.121   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0      11.016   4.158   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0       9.728   5.155   0.000  0.00  0.00           C+0
HETATM   16  N   UNK     0       8.385   4.305   0.000  0.00  0.00           N+0
HETATM   17  C   UNK     0       6.996   4.994   0.000  0.00  0.00           C+0
HETATM   18  C   UNK     0       6.888   6.525   0.000  0.00  0.00           C+0
HETATM   19  C   UNK     0       8.173   7.411   0.000  0.00  0.00           C+0
HETATM   20  C   UNK     0       9.612   6.780   0.000  0.00  0.00           C+0
HETATM   21  C   UNK     0      10.823   7.861   0.000  0.00  0.00           C+0
HETATM   22  C   UNK     0      10.626   9.438   0.000  0.00  0.00           C+0
HETATM   23  C   UNK     0       9.122   9.895   0.000  0.00  0.00           C+0
HETATM   24  C   UNK     0       7.908   8.936   0.000  0.00  0.00           C+0
HETATM   25  O   UNK     0       8.836  11.409   0.000  0.00  0.00           O+0
HETATM   26  C   UNK     0       7.383  11.918   0.000  0.00  0.00           C+0
HETATM   27  O   UNK     0      11.809  10.558   0.000  0.00  0.00           O+0
HETATM   28  C   UNK     0      13.208  11.332   0.000  0.00  0.00           C+0
HETATM   29  C   UNK     0      14.837  11.179   0.000  0.00  0.00           C+0
HETATM   30  C   UNK     0      14.763   9.602   0.000  0.00  0.00           C+0
HETATM   31  C   UNK     0      16.052   8.763   0.000  0.00  0.00           C+0
HETATM   32  C   UNK     0      17.494   9.331   0.000  0.00  0.00           C+0
HETATM   33  C   UNK     0      18.327   7.893   0.000  0.00  0.00           C+0
HETATM   34  C   UNK     0      19.339   6.569   0.000  0.00  0.00           C+0
HETATM   35  N   UNK     0      20.692   7.414   0.000  0.00  0.00           N+0
HETATM   36  C   UNK     0      22.077   6.742   0.000  0.00  0.00           C+0
HETATM   37  C   UNK     0      22.182   5.217   0.000  0.00  0.00           C+0
HETATM   38  C   UNK     0      20.609   8.952   0.000  0.00  0.00           C+0
HETATM   39  C   UNK     0      17.523  10.917   0.000  0.00  0.00           C+0
HETATM   40  C   UNK     0      16.272  11.851   0.000  0.00  0.00           C+0
HETATM   41  O   UNK     0      12.265   7.319   0.000  0.00  0.00           O+0
HETATM   42  C   UNK     0       8.465   2.767   0.000  0.00  0.00           C+0
HETATM   43  O   UNK     0      17.703   0.996   0.000  0.00  0.00           O+0
HETATM   44  C   UNK     0      16.202   1.340   0.000  0.00  0.00           C+0
HETATM   45  O   UNK     0      20.692   0.283   0.000  0.00  0.00           O+0
HETATM   46  C   UNK     0      22.188  -0.082   0.000  0.00  0.00           C+0
CONECT    1    2    6   34                                                  
CONECT    2    1    3   37                                                  
CONECT    3    2    4                                                       
CONECT    4    3    5   45                                                  
CONECT    5    4    6   43                                                  
CONECT    6    5    1    7                                                  
CONECT    7    6    8                                                       
CONECT    8    7    9   13                                                  
CONECT    9    8   10                                                       
CONECT   10    9   11                                                       
CONECT   11   10   12   14                                                  
CONECT   12   11   13                                                       
CONECT   13   12    8                                                       
CONECT   14   11   15                                                       
CONECT   15   14   16   20                                                  
CONECT   16   15   17   42                                                  
CONECT   17   16   18                                                       
CONECT   18   17   19                                                       
CONECT   19   18   20   24                                                  
CONECT   20   19   15   21                                                  
CONECT   21   20   22   41                                                  
CONECT   22   21   23   27                                                  
CONECT   23   22   24   25                                                  
CONECT   24   23   19                                                       
CONECT   25   23   26                                                       
CONECT   26   25                                                            
CONECT   27   22   28                                                       
CONECT   28   27   29                                                       
CONECT   29   28   30   40                                                  
CONECT   30   29   31                                                       
CONECT   31   30   32                                                       
CONECT   32   31   33   39                                                  
CONECT   33   32   34                                                       
CONECT   34   33    1   35                                                  
CONECT   35   34   36   38                                                  
CONECT   36   35   37                                                       
CONECT   37   36    2                                                       
CONECT   38   35                                                            
CONECT   39   32   40                                                       
CONECT   40   39   29                                                       
CONECT   41   21                                                            
CONECT   42   16                                                            
CONECT   43    5   44                                                       
CONECT   44   43                                                            
CONECT   45    4   46                                                       
CONECT   46   45                                                            
MASTER        0    0    0    0    0    0    0    0   46    0  104    0
END

View in JSmol

Synonyms

Not Available

Chemical Formula

C₃₈H₄₂N₂O₆

Average Mass

622.7620 Da

Monoisotopic Mass

622.30429 Da

IUPAC Name

(1S,16R)-9,10,25-trimethoxy-15,30-dimethyl-7,23-dioxa-15,30-diazaheptacyclo[22.6.2.2^{3,6}.2^{18,21}.1^{8,12}.0^{27,31}.0^{16,35}]heptatriaconta-3,5,8,10,12(35),18,20,24(32),25,27(31),33,36-dodecaen-32-ol

Traditional Name

CAS Registry Number

Not Available

SMILES

COC1=CC2=C3[C@@H](CC4=CC=C(COC5=C(O)C6=C(CCN(C)[C@H]6CC6=CC=C(OC3=C1OC)C=C6)C=C5OC)C=C4)N(C)CC2

InChI Identifier

InChI=1S/C38H42N2O6/c1-39-16-14-26-20-31(42-3)36-35(41)33(26)29(39)18-24-10-12-28(13-11-24)46-38-34-27(21-32(43-4)37(38)44-5)15-17-40(2)30(34)19-23-6-8-25(9-7-23)22-45-36/h6-13,20-21,29-30,41H,14-19,22H2,1-5H3/t29-,30+/m0/s1

InChI Key

BPJPWJSSKSLGNM-XZWHSSHBSA-N

Experimental Spectra

Not Available

Predicted Spectra

Spectrum Type	Description	Depositor ID	Depositor Organization	Depositor	Deposition Date	View
1D NMR	¹³C NMR Spectrum (1D, 25 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 100 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 252 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 1000 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 50 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 200 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 75 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 300 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 101 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 400 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 126 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 500 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 151 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 600 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 176 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 700 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 201 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 800 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 226 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 900 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum

Chemical Shift Submissions

Not Available

Species

Species of Origin

Species Name	Source	Reference
Cyclea racemosa	LOTUS Database	35616633
Cyclea sutchuenensis Gagnep.	Plant	KNApSAcK

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as diarylethers. These are organic compounds containing the dialkyl ether functional group, with the formula ROR', where R and R' are aryl groups.

Kingdom

Organic compounds

Super Class

Organic oxygen compounds

Class

Organooxygen compounds

Sub Class

Ethers

Direct Parent

Diarylethers

Alternative Parents

Substituents

Diaryl ether
Tetrahydroisoquinoline
Anisole
Alkyl aryl ether
1-hydroxy-4-unsubstituted benzenoid
Aralkylamine
Benzenoid
Tertiary aliphatic amine
Tertiary amine
Organoheterocyclic compound
Oxacycle
Azacycle
Organic nitrogen compound
Organonitrogen compound
Hydrocarbon derivative
Organopnictogen compound
Amine
Aromatic heteropolycyclic compound

Molecular Framework

Aromatic heteropolycyclic compounds

External Descriptors

Not Available

Physical Properties

State

Not Available

Experimental Properties

Property	Value	Reference
Melting Point	Not Available	Not Available
Boiling Point	Not Available	Not Available
Water Solubility	Not Available	Not Available
LogP	Not Available	Not Available

Predicted Properties

Property	Value	Source
logP	5.63	ALOGPS
logP	5.86	ChemAxon
logS	-5	ALOGPS
pKa (Strongest Acidic)	8.61	ChemAxon
pKa (Strongest Basic)	9.55	ChemAxon
Physiological Charge	2	ChemAxon
Hydrogen Acceptor Count	7	ChemAxon
Hydrogen Donor Count	1	ChemAxon
Polar Surface Area	72.86 Å²	ChemAxon
Rotatable Bond Count	3	ChemAxon
Refractivity	180.47 m³·mol⁻¹	ChemAxon
Polarizability	68.82 Å³	ChemAxon
Number of Rings	7	ChemAxon
Bioavailability	No	ChemAxon
Rule of Five	No	ChemAxon
Ghose Filter	No	ChemAxon
Veber's Rule	No	ChemAxon
MDDR-like Rule	No	ChemAxon

External Links

HMDB ID

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DrugBank ID

Not Available

Phenol Explorer Compound ID

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FoodDB ID

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KNApSAcK ID

Not Available

Chemspider ID

Not Available

KEGG Compound ID

Not Available

BioCyc ID

Not Available

BiGG ID

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Wikipedia Link

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METLIN ID

Not Available

PubChem Compound

162914406

PDB ID

Not Available

ChEBI ID

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Good Scents ID

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References

General References

Not Available

Showing NP-Card for (-)-Cycleaneonine (NP0067787)

MOL for NP0067787 ((-)-Cycleaneonine)

3D MOL for NP0067787 ((-)-Cycleaneonine)

3D SDF for NP0067787 ((-)-Cycleaneonine)

3D-SDF for NP0067787 ((-)-Cycleaneonine)

PDB for NP0067787 ((-)-Cycleaneonine)

3D PDB for NP0067787 ((-)-Cycleaneonine)

SMILES for NP0067787 ((-)-Cycleaneonine)

INCHI for NP0067787 ((-)-Cycleaneonine)

Structure for NP0067787 ((-)-Cycleaneonine)

3D Structure for NP0067787 ((-)-Cycleaneonine)