NP-MRD: Showing NP-Card for 12-methyl-6-methylidene-17-oxa-14-azahexacyclo[10.6.3.1⁵,⁸.0¹,¹¹.0²,⁸.0¹⁴,¹⁸]docosan-7-yl acetate (NP0157980)

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Record Information

Version

2.0

Created at

2022-09-02 15:29:29 UTC

Updated at

2022-09-02 15:29:29 UTC

NP-MRD ID

NP0157980

Secondary Accession Numbers

None

Natural Product Identification

Common Name

12-methyl-6-methylidene-17-oxa-14-azahexacyclo[10.6.3.1⁵,⁸.0¹,¹¹.0²,⁸.0¹⁴,¹⁸]docosan-7-yl acetate

Description

12-Methyl-6-methylidene-17-oxa-14-azahexacyclo[10.6.3.1⁵,⁸.0¹,¹¹.0²,⁸.0¹⁴,¹⁸]Docosan-7-yl acetate belongs to the class of organic compounds known as veatchine-type diterpenoid alkaloids. These are alkaloid diterpenoids with a structure based on the veatchine skeleton, a pentacyclic compound, in which the carbon skeleton is the same as kaurane. 12-methyl-6-methylidene-17-oxa-14-azahexacyclo[10.6.3.1⁵,⁸.0¹,¹¹.0²,⁸.0¹⁴,¹⁸]docosan-7-yl acetate is found in Garrya ovata. 12-Methyl-6-methylidene-17-oxa-14-azahexacyclo[10.6.3.1⁵,⁸.0¹,¹¹.0²,⁸.0¹⁴,¹⁸]Docosan-7-yl acetate is a very strong basic compound (based on its pKa).

Structure

MOL 3D MOL SDF PDB SMILES InChI


  Mrv1533004171511282D          

 28 33  0  0  0  0            999 V2000
   -0.1481   -2.1555    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.2049   -1.4098    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2644   -0.7313    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.0272   -1.3427    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.3802   -0.5970    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.9414    0.1586    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.1207    0.2420    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.5178    0.8047    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.2440    1.2783    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.0109    0.8995    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.0059    0.0309    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.2682   -0.4533    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.4265   -1.2909    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.2262   -1.7363    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.8564   -1.1299    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.4796   -2.0498    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.7628   -2.8247    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.6553   -2.0150    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.0971   -1.4075    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.1320   -0.5832    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.7395   -0.0250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.5637   -0.0599    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.9690    0.6587    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.7777    0.4954    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.8722   -0.3242    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.1219   -0.6673    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    5.0871   -1.4916    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.9320    0.1897    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0  0  0  0
  2  3  2  0  0  0  0
  2  4  1  0  0  0  0
  4  5  1  0  0  0  0
  5  6  1  0  0  0  0
  6  7  2  0  0  0  0
  6  8  1  0  0  0  0
  8  9  1  0  0  0  0
  9 10  1  0  0  0  0
 10 11  1  0  0  0  0
 11 12  1  0  0  0  0
  5 12  1  0  0  0  0
 12 13  1  0  0  0  0
 13 14  1  0  0  0  0
 14 15  1  0  0  0  0
 15 16  1  0  0  0  0
 16 17  1  0  0  0  0
 16 18  1  0  0  0  0
 18 19  1  0  0  0  0
 19 20  1  0  0  0  0
 20 21  1  0  0  0  0
 11 21  1  0  0  0  0
 15 21  1  0  0  0  0
 21 22  1  0  0  0  0
 22 23  1  0  0  0  0
 23 24  1  0  0  0  0
 24 25  1  0  0  0  0
 25 26  1  0  0  0  0
 22 26  1  0  0  0  0
 26 27  1  0  0  0  0
 16 27  1  0  0  0  0
 12 28  1  0  0  0  0
  8 28  1  0  0  0  0
M  END

     RDKit          3D

 63 68  0  0  0  0  0  0  0  0999 V2000
   -2.9875    2.5139   -1.8211 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6885    1.2826   -1.4781 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8175    0.0170   -2.2528 C   0  0  1  0  0  0  0  0  0  0  0  0
   -1.5909   -0.0530   -3.1377 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4024    0.3683   -2.2525 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3745   -0.6786   -1.1513 C   0  0  2  0  0  0  0  0  0  0  0  0
   -1.5927   -0.5098   -0.3354 C   0  0  2  0  0  0  0  0  0  0  0  0
   -1.4909   -1.3098    0.9235 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2558   -1.0840    1.7085 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.8065   -0.3104    1.0180 C   0  0  2  0  0  0  0  0  0  0  0  0
    0.9193   -0.7688   -0.4104 C   0  0  1  0  0  0  0  0  0  0  0  0
    1.4272   -2.1823   -0.4043 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.6981   -2.4252    0.2944 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.7001   -1.8337    1.6837 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1451   -0.4563    1.7129 C   0  0  2  0  0  0  0  0  0  0  0  0
    2.0846    0.0081    3.1450 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.0879    0.5167    0.9887 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.2044    0.1603   -0.3891 N   0  0  0  0  0  0  0  0  0  0  0  0
    3.8608    1.2795   -1.0826 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.7103    1.9892   -1.7942 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.5909    1.4184   -1.1903 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.9595    0.0846   -1.1035 C   0  0  2  0  0  0  0  0  0  0  0  0
   -2.7538   -1.0790   -1.1788 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1193    0.8637   -0.1536 C   0  0  2  0  0  0  0  0  0  0  0  0
   -3.2695    0.7416    0.7024 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.4329    1.4759    1.8402 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.6692    1.2606    2.6470 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5774    2.2973    2.1911 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8351    3.3337   -1.1415 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.3958    2.7537   -2.7924 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.7549   -0.0395   -2.8230 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4184   -1.1414   -3.3460 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6837    0.5522   -4.0281 H   0  0  0  0  0  0  0  0  0  0  0  0
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    3.6209   -2.1763   -0.2816 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.7780   -3.5433    0.4556 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.1354   -2.4770    2.3880 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.7363   -1.8083    2.0297 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.7634    0.8567    3.3616 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.0802    0.3045    3.4751 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.4063   -0.8075    3.8573 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.0792    0.5278    1.4386 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.6178    1.5144    1.0819 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.3949    1.9295   -0.3918 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.5383    0.8044   -1.8345 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.7490    3.0753   -1.6629 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.7300    1.6873   -2.8695 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.2077   -0.3599   -2.1084 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.6908   -1.0648   -0.6227 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4895   -2.0274   -1.6413 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4884    1.6088    0.2934 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.2331    2.2136    2.7998 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.3556    0.5609    2.1672 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.4402    0.8598    3.6563 H   0  0  0  0  0  0  0  0  0  0  0  0
 27 26  1  0
 26 28  2  0
 26 25  1  0
 25 24  1  0
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  2  1  2  3
  2  3  1  0
  3 23  1  0
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 22 57  1  6
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 17 51  1  0
 17 52  1  0
  6 36  1  6
  5 34  1  0
  5 35  1  0
  4 32  1  0
  4 33  1  0
M  END


  Mrv1533004171511282D          

 28 33  0  0  0  0            999 V2000
   -0.1481   -2.1555    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.2049   -1.4098    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2644   -0.7313    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.0272   -1.3427    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.3802   -0.5970    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.9414    0.1586    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.1207    0.2420    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.5178    0.8047    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.2440    1.2783    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.0109    0.8995    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.0059    0.0309    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.2682   -0.4533    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.4265   -1.2909    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.2262   -1.7363    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
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    4.7628   -2.8247    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
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    4.9690    0.6587    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.7777    0.4954    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.8722   -0.3242    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.1219   -0.6673    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    5.0871   -1.4916    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.9320    0.1897    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0  0  0  0
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  2  4  1  0  0  0  0
  4  5  1  0  0  0  0
  5  6  1  0  0  0  0
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  6  8  1  0  0  0  0
  8  9  1  0  0  0  0
  9 10  1  0  0  0  0
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  5 12  1  0  0  0  0
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 15 16  1  0  0  0  0
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 18 19  1  0  0  0  0
 19 20  1  0  0  0  0
 20 21  1  0  0  0  0
 11 21  1  0  0  0  0
 15 21  1  0  0  0  0
 21 22  1  0  0  0  0
 22 23  1  0  0  0  0
 23 24  1  0  0  0  0
 24 25  1  0  0  0  0
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 22 26  1  0  0  0  0
 26 27  1  0  0  0  0
 16 27  1  0  0  0  0
 12 28  1  0  0  0  0
  8 28  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0157980

> <DATABASE_NAME>
NP-MRD

> <SMILES>
CC(=O)OC1C(=C)C2CC11CCC3C4(C)CCCC3(C3OCCN3C4)C1CC2

> <INCHI_IDENTIFIER>
InChI=1S/C24H35NO3/c1-15-17-5-6-19-23(13-17,20(15)28-16(2)26)10-7-18-22(3)8-4-9-24(18,19)21-25(14-22)11-12-27-21/h17-21H,1,4-14H2,2-3H3

> <INCHI_KEY>
YHPDTHOCMSACJY-UHFFFAOYSA-N

> <FORMULA>
C24H35NO3

> <MOLECULAR_WEIGHT>
385.548

> <EXACT_MASS>
385.261693991

> <JCHEM_ACCEPTOR_COUNT>
3

> <JCHEM_ATOM_COUNT>
63

> <JCHEM_AVERAGE_POLARIZABILITY>
43.9118279381144

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
0

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
1

> <JCHEM_IUPAC>
12-methyl-6-methylidene-17-oxa-14-azahexacyclo[10.6.3.1⁵,⁸.0¹,¹¹.0²,⁸.0¹⁴,¹⁸]docosan-7-yl acetate

> <ALOGPS_LOGP>
3.43

> <JCHEM_LOGP>
3.755518877

> <ALOGPS_LOGS>
-5.00

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
6

> <JCHEM_PHYSIOLOGICAL_CHARGE>
1

> <JCHEM_PKA_STRONGEST_BASIC>
7.731189835598734

> <JCHEM_POLAR_SURFACE_AREA>
38.77

> <JCHEM_REFRACTIVITY>
106.98639999999999

> <JCHEM_ROTATABLE_BOND_COUNT>
2

> <JCHEM_RULE_OF_FIVE>
1

> <ALOGPS_SOLUBILITY>
3.90e-03 g/l

> <JCHEM_TRADITIONAL_IUPAC>
12-methyl-6-methylidene-17-oxa-14-azahexacyclo[10.6.3.1⁵,⁸.0¹,¹¹.0²,⁸.0¹⁴,¹⁸]docosan-7-yl acetate

> <JCHEM_VEBER_RULE>
1

$$$$

HEADER    PROTEIN                                 17-APR-15   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   17-APR-15         0                                  
HETATM    1  C   UNK     0      -0.276  -4.024   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0       0.382  -2.632   0.000  0.00  0.00           C+0
HETATM    3  O   UNK     0      -0.493  -1.365   0.000  0.00  0.00           O+0
HETATM    4  O   UNK     0       1.917  -2.506   0.000  0.00  0.00           O+0
HETATM    5  C   UNK     0       2.576  -1.114   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0       1.757   0.296   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0       0.225   0.452   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0       2.833   1.502   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0       4.189   2.386   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0       5.620   1.679   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0       5.611   0.058   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0       4.234  -0.846   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0       4.529  -2.410   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0       6.022  -3.241   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0       7.199  -2.109   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0       8.362  -3.826   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0       8.891  -5.273   0.000  0.00  0.00           C+0
HETATM   18  C   UNK     0       6.823  -3.761   0.000  0.00  0.00           C+0
HETATM   19  C   UNK     0       5.781  -2.627   0.000  0.00  0.00           C+0
HETATM   20  C   UNK     0       5.846  -1.089   0.000  0.00  0.00           C+0
HETATM   21  C   UNK     0       6.980  -0.047   0.000  0.00  0.00           C+0
HETATM   22  C   UNK     0       8.519  -0.112   0.000  0.00  0.00           C+0
HETATM   23  O   UNK     0       9.275   1.230   0.000  0.00  0.00           O+0
HETATM   24  C   UNK     0      10.785   0.925   0.000  0.00  0.00           C+0
HETATM   25  C   UNK     0      10.961  -0.605   0.000  0.00  0.00           C+0
HETATM   26  N   UNK     0       9.561  -1.246   0.000  0.00  0.00           N+0
HETATM   27  C   UNK     0       9.496  -2.784   0.000  0.00  0.00           C+0
HETATM   28  C   UNK     0       3.606   0.354   0.000  0.00  0.00           C+0
CONECT    1    2                                                            
CONECT    2    1    3    4                                                  
CONECT    3    2                                                            
CONECT    4    2    5                                                       
CONECT    5    4    6   12                                                  
CONECT    6    5    7    8                                                  
CONECT    7    6                                                            
CONECT    8    6    9   28                                                  
CONECT    9    8   10                                                       
CONECT   10    9   11                                                       
CONECT   11   10   12   21                                                  
CONECT   12   11    5   13   28                                             
CONECT   13   12   14                                                       
CONECT   14   13   15                                                       
CONECT   15   14   16   21                                                  
CONECT   16   15   17   18   27                                             
CONECT   17   16                                                            
CONECT   18   16   19                                                       
CONECT   19   18   20                                                       
CONECT   20   19   21                                                       
CONECT   21   20   11   15   22                                             
CONECT   22   21   23   26                                                  
CONECT   23   22   24                                                       
CONECT   24   23   25                                                       
CONECT   25   24   26                                                       
CONECT   26   25   22   27                                                  
CONECT   27   26   16                                                       
CONECT   28   12    8                                                       
MASTER        0    0    0    0    0    0    0    0   28    0   66    0
END

View in JSmol

Synonyms

Value	Source
12-Methyl-6-methylidene-17-oxa-14-azahexacyclo[10.6.3.1,.0,.0,.0,]docosan-7-yl acetic acid	Generator
12-Methyl-6-methylidene-17-oxa-14-azahexacyclo[10.6.3.1⁵,⁸.0¹,¹¹.0²,⁸.0¹⁴,¹⁸]docosan-7-yl acetic acid	Generator

Chemical Formula

C₂₄H₃₅NO₃

Average Mass

385.5480 Da

Monoisotopic Mass

385.26169 Da

IUPAC Name

12-methyl-6-methylidene-17-oxa-14-azahexacyclo[10.6.3.1⁵,⁸.0¹,¹¹.0²,⁸.0¹⁴,¹⁸]docosan-7-yl acetate

Traditional Name

12-methyl-6-methylidene-17-oxa-14-azahexacyclo[10.6.3.1⁵,⁸.0¹,¹¹.0²,⁸.0¹⁴,¹⁸]docosan-7-yl acetate

CAS Registry Number

Not Available

SMILES

CC(=O)OC1C(=C)C2CC11CCC3C4(C)CCCC3(C3OCCN3C4)C1CC2

InChI Identifier

InChI=1S/C24H35NO3/c1-15-17-5-6-19-23(13-17,20(15)28-16(2)26)10-7-18-22(3)8-4-9-24(18,19)21-25(14-22)11-12-27-21/h17-21H,1,4-14H2,2-3H3

InChI Key

YHPDTHOCMSACJY-UHFFFAOYSA-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, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 100 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 252 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 1000 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 50 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 200 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 75 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 300 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 101 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 400 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 126 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 500 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 151 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 600 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 176 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 700 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 201 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 800 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 226 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 900 MHz, H₂O, 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
Garrya ovata	LOTUS Database	35616633

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as veatchine-type diterpenoid alkaloids. These are alkaloid diterpenoids with a structure based on the veatchine skeleton, a pentacyclic compound, in which the carbon skeleton is the same as kaurane.

Kingdom

Organic compounds

Super Class

Lipids and lipid-like molecules

Class

Prenol lipids

Sub Class

Diterpenoids

Direct Parent

Veatchine-type diterpenoid alkaloids

Alternative Parents

Substituents

Veatchine-type diterpenoid alkaloid
Alkaloid or derivatives
Piperidine
Oxazolidine
Carboxylic acid ester
Hemiaminal
Carboxylic acid derivative
Monocarboxylic acid or derivatives
Organoheterocyclic compound
Oxacycle
Azacycle
Organopnictogen compound
Organooxygen compound
Organonitrogen compound
Carbonyl group
Organic oxide
Hydrocarbon derivative
Organic nitrogen compound
Organic oxygen compound
Aliphatic heteropolycyclic compound

Molecular Framework

Aliphatic 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	3.43	ALOGPS
logP	3.76	ChemAxon
logS	-5	ALOGPS
pKa (Strongest Basic)	7.73	ChemAxon
Physiological Charge	1	ChemAxon
Hydrogen Acceptor Count	3	ChemAxon
Hydrogen Donor Count	0	ChemAxon
Polar Surface Area	38.77 Å²	ChemAxon
Rotatable Bond Count	2	ChemAxon
Refractivity	106.99 m³·mol⁻¹	ChemAxon
Polarizability	43.91 Å³	ChemAxon
Number of Rings	6	ChemAxon
Bioavailability	Yes	ChemAxon
Rule of Five	Yes	ChemAxon
Ghose Filter	Yes	ChemAxon
Veber's Rule	Yes	ChemAxon
MDDR-like Rule	No	ChemAxon

External Links

HMDB ID

Not Available

DrugBank ID

Not Available

Phenol Explorer Compound ID

Not Available

FoodDB ID

Not Available

KNApSAcK ID

Not Available

Chemspider ID

Not Available

KEGG Compound ID

Not Available

BioCyc ID

Not Available

BiGG ID

Not Available

Wikipedia Link

Not Available

METLIN ID

Not Available

PubChem Compound

431672

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

LOTUS database [Link]

Showing NP-Card for 12-methyl-6-methylidene-17-oxa-14-azahexacyclo[10.6.3.1⁵,⁸.0¹,¹¹.0²,⁸.0¹⁴,¹⁸]docosan-7-yl acetate (NP0157980)

MOL for NP0157980 (12-methyl-6-methylidene-17-oxa-14-azahexacyclo[10.6.3.1⁵,⁸.0¹,¹¹.0²,⁸.0¹⁴,¹⁸]docosan-7-yl acetate)

3D MOL for NP0157980 (12-methyl-6-methylidene-17-oxa-14-azahexacyclo[10.6.3.1⁵,⁸.0¹,¹¹.0²,⁸.0¹⁴,¹⁸]docosan-7-yl acetate)

3D SDF for NP0157980 (12-methyl-6-methylidene-17-oxa-14-azahexacyclo[10.6.3.1⁵,⁸.0¹,¹¹.0²,⁸.0¹⁴,¹⁸]docosan-7-yl acetate)

3D-SDF for NP0157980 (12-methyl-6-methylidene-17-oxa-14-azahexacyclo[10.6.3.1⁵,⁸.0¹,¹¹.0²,⁸.0¹⁴,¹⁸]docosan-7-yl acetate)

PDB for NP0157980 (12-methyl-6-methylidene-17-oxa-14-azahexacyclo[10.6.3.1⁵,⁸.0¹,¹¹.0²,⁸.0¹⁴,¹⁸]docosan-7-yl acetate)

3D PDB for NP0157980 (12-methyl-6-methylidene-17-oxa-14-azahexacyclo[10.6.3.1⁵,⁸.0¹,¹¹.0²,⁸.0¹⁴,¹⁸]docosan-7-yl acetate)

SMILES for NP0157980 (12-methyl-6-methylidene-17-oxa-14-azahexacyclo[10.6.3.1⁵,⁸.0¹,¹¹.0²,⁸.0¹⁴,¹⁸]docosan-7-yl acetate)

INCHI for NP0157980 (12-methyl-6-methylidene-17-oxa-14-azahexacyclo[10.6.3.1⁵,⁸.0¹,¹¹.0²,⁸.0¹⁴,¹⁸]docosan-7-yl acetate)

Structure for NP0157980 (12-methyl-6-methylidene-17-oxa-14-azahexacyclo[10.6.3.1⁵,⁸.0¹,¹¹.0²,⁸.0¹⁴,¹⁸]docosan-7-yl acetate)

3D Structure for NP0157980 (12-methyl-6-methylidene-17-oxa-14-azahexacyclo[10.6.3.1⁵,⁸.0¹,¹¹.0²,⁸.0¹⁴,¹⁸]docosan-7-yl acetate)