NP-MRD: Showing NP-Card for 11-ethyl-7-methyl-3-(4-methyl-5-oxooxolan-2-yl)-9,17-dioxa-2-azapentacyclo[10.5.0.0¹,⁵.0²,¹⁶.0⁶,¹⁰]heptadecan-8-one (NP0175853)

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Record Information

Version

2.0

Created at

2022-09-03 13:25:14 UTC

Updated at

2022-09-03 13:25:14 UTC

NP-MRD ID

NP0175853

Secondary Accession Numbers

None

Natural Product Identification

Common Name

11-ethyl-7-methyl-3-(4-methyl-5-oxooxolan-2-yl)-9,17-dioxa-2-azapentacyclo[10.5.0.0¹,⁵.0²,¹⁶.0⁶,¹⁰]heptadecan-8-one

Description

11-Ethyl-7-methyl-3-(4-methyl-5-oxooxolan-2-yl)-9,17-dioxa-2-azapentacyclo[10.5.0.0¹,⁵.0²,¹⁶.0⁶,¹⁰]Heptadecan-8-one belongs to the class of organic compounds known as indoles and derivatives. These are organic compounds containing an indole, which is a bicyclic ring system made up of a six-membered benzene ring fused to a five-membered nitrogen-containing pyrrole ring. 11-ethyl-7-methyl-3-(4-methyl-5-oxooxolan-2-yl)-9,17-dioxa-2-azapentacyclo[10.5.0.0¹,⁵.0²,¹⁶.0⁶,¹⁰]heptadecan-8-one is found in Stemona sessilifolia. 11-Ethyl-7-methyl-3-(4-methyl-5-oxooxolan-2-yl)-9,17-dioxa-2-azapentacyclo[10.5.0.0¹,⁵.0²,¹⁶.0⁶,¹⁰]Heptadecan-8-one is a strong basic compound (based on its pKa).

Structure

MOL 3D MOL SDF PDB SMILES InChI


  Mrv1533004161518272D          

 28 33  0  0  0  0            999 V2000
    4.2172    1.7272    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5458    1.2477    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.6255    0.4265    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.3988    0.1104    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.2016    0.3007    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.6306   -0.4040    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.4528   -0.4712    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.0929   -1.0298    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.2831   -1.8326    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.3317   -0.7118    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.6075   -1.1643    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.8809   -1.9718    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.0902   -2.2624    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8840   -3.0612    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.4090   -3.6976    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.9661   -4.3936    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.2688   -5.1610    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1672   -4.1873    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.5309   -4.7124    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.1165   -3.3639    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.5298   -1.6149    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    1.8629   -0.8982    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.3352   -0.2262    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.6083    0.5612    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.4453    0.6696    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.9145   -0.0406    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.7499   -0.9074    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.0104   -1.5866    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0  0  0  0
  2  3  1  0  0  0  0
  3  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
  8 10  1  0  0  0  0
  4 10  1  0  0  0  0
 10 11  1  0  0  0  0
 11 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
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  3 26  1  0  0  0  0
 26 27  1  0  0  0  0
 11 27  1  0  0  0  0
 21 27  1  0  0  0  0
 27 28  1  0  0  0  0
 22 28  1  0  0  0  0
M  END

     RDKit          3D

 59 64  0  0  0  0  0  0  0  0999 V2000
   -3.9087   -0.5317    2.7109 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.3878   -1.2643    1.4950 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1958   -0.5252    0.8993 C   0  0  1  0  0  0  0  0  0  0  0  0
   -1.6236   -1.2536   -0.2896 C   0  0  2  0  0  0  0  0  0  0  0  0
   -1.3239   -2.6564    0.0941 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0914   -3.2874   -0.4150 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.3274   -2.9781   -1.7985 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.8202   -1.5209   -1.8163 C   0  0  1  0  0  0  0  0  0  0  0  0
   -0.2861   -0.7672   -2.2768 O   0  0  0  0  0  0  0  0  0  0  0  0
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    0.5692    1.2282    0.2939 C   0  0  0  0  0  0  0  0  0  0  0  0
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    3.6981   -0.3961   -1.1770 C   0  0  0  0  0  0  0  0  0  0  0  0
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    5.3638    2.1740    0.6544 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.2715    1.7267   -0.3156 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.7870   -0.9677   -0.5445 N   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8313    1.6055   -0.3915 C   0  0  2  0  0  0  0  0  0  0  0  0
   -1.6361    2.9838    0.2116 C   0  0  1  0  0  0  0  0  0  0  0  0
   -1.7934    4.0584   -0.8207 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7778    3.0010    1.1947 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.4846    4.0036    1.5276 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8633    1.6875    1.6339 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6863    0.8278    0.5234 C   0  0  2  0  0  0  0  0  0  0  0  0
   -3.1063   -0.0369    3.2917 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.4593   -1.2607    3.3329 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.5773    0.2786    2.3569 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.2518   -1.2652    0.7665 H   0  0  0  0  0  0  0  0  0  0  0  0
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    0.8019   -3.1053    0.2508 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2275   -4.4072   -0.3501 H   0  0  0  0  0  0  0  0  0  0  0  0
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   -0.4917   -3.1573   -2.5029 H   0  0  0  0  0  0  0  0  0  0  0  0
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    1.0473    2.2187    0.1508 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.2338    1.1680    1.3246 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.0186   -0.1839    0.8922 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.2883    1.0005   -1.9325 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.9267   -0.5629   -2.2354 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.3646   -1.3766   -0.7261 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.8279   -0.0251   -0.9680 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.1238   -0.8379    1.1724 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.4883   -0.2973    1.7393 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.6614   -1.8108    0.7734 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3811    1.7725   -1.3574 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7182    3.0707    0.8005 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1599    4.9449   -0.6448 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8818    4.3289   -0.9153 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5220    3.6096   -1.8146 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.7222    0.6905    0.0922 H   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0
  2  3  1  0
  3 28  1  0
 28 27  1  0
 27 25  1  0
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 21  8  1  0
  8  7  1  0
  7  6  1  0
  6  5  1  0
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  4 10  1  0
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  4  3  1  0
 22 28  1  0
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  9  8  1  0
  1 29  1  0
  1 30  1  0
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 23 55  1  1
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 16 50  1  6
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  8 42  1  6
  7 40  1  0
  7 41  1  0
  6 38  1  0
  6 39  1  0
  5 36  1  0
  5 37  1  0
  4 35  1  6
M  END


  Mrv1533004161518272D          

 28 33  0  0  0  0            999 V2000
    4.2172    1.7272    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5458    1.2477    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.6255    0.4265    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.3988    0.1104    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.2016    0.3007    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.6306   -0.4040    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.4528   -0.4712    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.0929   -1.0298    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.2831   -1.8326    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.3317   -0.7118    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.6075   -1.1643    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.8809   -1.9718    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.0902   -2.2624    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8840   -3.0612    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.4090   -3.6976    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.9661   -4.3936    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.2688   -5.1610    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1672   -4.1873    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.5309   -4.7124    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.1165   -3.3639    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.5298   -1.6149    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    1.8629   -0.8982    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.3352   -0.2262    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.6083    0.5612    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.4453    0.6696    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.9145   -0.0406    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.7499   -0.9074    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.0104   -1.5866    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0  0  0  0
  2  3  1  0  0  0  0
  3  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
  8 10  1  0  0  0  0
  4 10  1  0  0  0  0
 10 11  1  0  0  0  0
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 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
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 18 20  1  0  0  0  0
 14 20  1  0  0  0  0
 13 21  1  0  0  0  0
 21 22  1  0  0  0  0
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 24 25  1  0  0  0  0
 25 26  1  0  0  0  0
  3 26  1  0  0  0  0
 26 27  1  0  0  0  0
 11 27  1  0  0  0  0
 21 27  1  0  0  0  0
 27 28  1  0  0  0  0
 22 28  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0175853

> <DATABASE_NAME>
NP-MRD

> <SMILES>
CCC1C2OC(=O)C(C)C2C2CC(C3CC(C)C(=O)O3)N3C4CCCC1C23O4

> <INCHI_IDENTIFIER>
InChI=1S/C22H31NO5/c1-4-12-13-6-5-7-17-23-15(16-8-10(2)20(24)26-16)9-14(22(13,23)28-17)18-11(3)21(25)27-19(12)18/h10-19H,4-9H2,1-3H3

> <INCHI_KEY>
RRHMLMRBONYJOT-UHFFFAOYSA-N

> <FORMULA>
C22H31NO5

> <MOLECULAR_WEIGHT>
389.492

> <EXACT_MASS>
389.220223102

> <JCHEM_ACCEPTOR_COUNT>
4

> <JCHEM_ATOM_COUNT>
59

> <JCHEM_AVERAGE_POLARIZABILITY>
42.635378789727255

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
0

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
1

> <JCHEM_IUPAC>
11-ethyl-7-methyl-3-(4-methyl-5-oxooxolan-2-yl)-9,17-dioxa-2-azapentacyclo[10.5.0.0¹,⁵.0²,¹⁶.0⁶,¹⁰]heptadecan-8-one

> <ALOGPS_LOGP>
2.53

> <JCHEM_LOGP>
3.571976745333332

> <ALOGPS_LOGS>
-2.87

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
6

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA_STRONGEST_BASIC>
3.0594319521793722

> <JCHEM_POLAR_SURFACE_AREA>
65.07000000000001

> <JCHEM_REFRACTIVITY>
99.70859999999999

> <JCHEM_ROTATABLE_BOND_COUNT>
2

> <JCHEM_RULE_OF_FIVE>
1

> <ALOGPS_SOLUBILITY>
5.29e-01 g/l

> <JCHEM_TRADITIONAL_IUPAC>
11-ethyl-7-methyl-3-(4-methyl-5-oxooxolan-2-yl)-9,17-dioxa-2-azapentacyclo[10.5.0.0¹,⁵.0²,¹⁶.0⁶,¹⁰]heptadecan-8-one

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 16-APR-15   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   16-APR-15         0                                  
HETATM    1  C   UNK     0       7.872   3.224   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0       6.619   2.329   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0       6.768   0.796   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0       8.211   0.206   0.000  0.00  0.00           C+0
HETATM    5  O   UNK     0       9.710   0.561   0.000  0.00  0.00           O+0
HETATM    6  C   UNK     0      10.510  -0.754   0.000  0.00  0.00           C+0
HETATM    7  O   UNK     0      12.045  -0.880   0.000  0.00  0.00           O+0
HETATM    8  C   UNK     0       9.507  -1.922   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0       9.862  -3.421   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0       8.086  -1.329   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0       6.734  -2.173   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0       7.244  -3.681   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0       5.768  -4.223   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0       5.383  -5.714   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0       6.364  -6.902   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0       5.537  -8.201   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0       6.102  -9.634   0.000  0.00  0.00           C+0
HETATM   18  C   UNK     0       4.046  -7.816   0.000  0.00  0.00           C+0
HETATM   19  O   UNK     0       2.858  -8.796   0.000  0.00  0.00           O+0
HETATM   20  O   UNK     0       3.951  -6.279   0.000  0.00  0.00           O+0
HETATM   21  N   UNK     0       4.722  -3.014   0.000  0.00  0.00           N+0
HETATM   22  C   UNK     0       3.477  -1.677   0.000  0.00  0.00           C+0
HETATM   23  C   UNK     0       2.492  -0.422   0.000  0.00  0.00           C+0
HETATM   24  C   UNK     0       3.002   1.048   0.000  0.00  0.00           C+0
HETATM   25  C   UNK     0       4.565   1.250   0.000  0.00  0.00           C+0
HETATM   26  C   UNK     0       5.440  -0.076   0.000  0.00  0.00           C+0
HETATM   27  C   UNK     0       5.133  -1.694   0.000  0.00  0.00           C+0
HETATM   28  O   UNK     0       3.753  -2.962   0.000  0.00  0.00           O+0
CONECT    1    2                                                            
CONECT    2    1    3                                                       
CONECT    3    2    4   26                                                  
CONECT    4    3    5   10                                                  
CONECT    5    4    6                                                       
CONECT    6    5    7    8                                                  
CONECT    7    6                                                            
CONECT    8    6    9   10                                                  
CONECT    9    8                                                            
CONECT   10    8    4   11                                                  
CONECT   11   10   12   27                                                  
CONECT   12   11   13                                                       
CONECT   13   12   14   21                                                  
CONECT   14   13   15   20                                                  
CONECT   15   14   16                                                       
CONECT   16   15   17   18                                                  
CONECT   17   16                                                            
CONECT   18   16   19   20                                                  
CONECT   19   18                                                            
CONECT   20   18   14                                                       
CONECT   21   13   22   27                                                  
CONECT   22   21   23   28                                                  
CONECT   23   22   24                                                       
CONECT   24   23   25                                                       
CONECT   25   24   26                                                       
CONECT   26   25    3   27                                                  
CONECT   27   26   11   21   28                                             
CONECT   28   27   22                                                       
MASTER        0    0    0    0    0    0    0    0   28    0   66    0
END

View in JSmol

Synonyms

Not Available

Chemical Formula

C₂₂H₃₁NO₅

Average Mass

389.4920 Da

Monoisotopic Mass

389.22022 Da

IUPAC Name

11-ethyl-7-methyl-3-(4-methyl-5-oxooxolan-2-yl)-9,17-dioxa-2-azapentacyclo[10.5.0.0¹,⁵.0²,¹⁶.0⁶,¹⁰]heptadecan-8-one

Traditional Name

11-ethyl-7-methyl-3-(4-methyl-5-oxooxolan-2-yl)-9,17-dioxa-2-azapentacyclo[10.5.0.0¹,⁵.0²,¹⁶.0⁶,¹⁰]heptadecan-8-one

CAS Registry Number

Not Available

SMILES

CCC1C2OC(=O)C(C)C2C2CC(C3CC(C)C(=O)O3)N3C4CCCC1C23O4

InChI Identifier

InChI=1S/C22H31NO5/c1-4-12-13-6-5-7-17-23-15(16-8-10(2)20(24)26-16)9-14(22(13,23)28-17)18-11(3)21(25)27-19(12)18/h10-19H,4-9H2,1-3H3

InChI Key

RRHMLMRBONYJOT-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
Stemona sessilifolia	LOTUS Database	35616633

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as indoles and derivatives. These are organic compounds containing an indole, which is a bicyclic ring system made up of a six-membered benzene ring fused to a five-membered nitrogen-containing pyrrole ring.

Kingdom

Organic compounds

Super Class

Organoheterocyclic compounds

Class

Indoles and derivatives

Sub Class

Not Available

Direct Parent

Indoles and derivatives

Alternative Parents

Substituents

Indole or derivatives
Meta-oxazepine
Azepane
Oxepane
Dicarboxylic acid or derivatives
Gamma butyrolactone
N-alkylpyrrolidine
Tetrahydrofuran
Pyrrolidine
Carboxylic acid ester
Lactone
Carboxylic acid derivative
Oxacycle
Azacycle
Hydrocarbon derivative
Organic oxide
Organopnictogen compound
Organic nitrogen compound
Carbonyl group
Organic oxygen compound
Organonitrogen compound
Organooxygen 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	2.53	ALOGPS
logP	3.57	ChemAxon
logS	-2.9	ALOGPS
pKa (Strongest Basic)	3.06	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	4	ChemAxon
Hydrogen Donor Count	0	ChemAxon
Polar Surface Area	65.07 Å²	ChemAxon
Rotatable Bond Count	2	ChemAxon
Refractivity	99.71 m³·mol⁻¹	ChemAxon
Polarizability	42.64 Å³	ChemAxon
Number of Rings	6	ChemAxon
Bioavailability	Yes	ChemAxon
Rule of Five	Yes	ChemAxon
Ghose Filter	Yes	ChemAxon
Veber's Rule	No	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

124222278

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

LOTUS database [Link]

Showing NP-Card for 11-ethyl-7-methyl-3-(4-methyl-5-oxooxolan-2-yl)-9,17-dioxa-2-azapentacyclo[10.5.0.0¹,⁵.0²,¹⁶.0⁶,¹⁰]heptadecan-8-one (NP0175853)

MOL for NP0175853 (11-ethyl-7-methyl-3-(4-methyl-5-oxooxolan-2-yl)-9,17-dioxa-2-azapentacyclo[10.5.0.0¹,⁵.0²,¹⁶.0⁶,¹⁰]heptadecan-8-one)

3D MOL for NP0175853 (11-ethyl-7-methyl-3-(4-methyl-5-oxooxolan-2-yl)-9,17-dioxa-2-azapentacyclo[10.5.0.0¹,⁵.0²,¹⁶.0⁶,¹⁰]heptadecan-8-one)

3D SDF for NP0175853 (11-ethyl-7-methyl-3-(4-methyl-5-oxooxolan-2-yl)-9,17-dioxa-2-azapentacyclo[10.5.0.0¹,⁵.0²,¹⁶.0⁶,¹⁰]heptadecan-8-one)

3D-SDF for NP0175853 (11-ethyl-7-methyl-3-(4-methyl-5-oxooxolan-2-yl)-9,17-dioxa-2-azapentacyclo[10.5.0.0¹,⁵.0²,¹⁶.0⁶,¹⁰]heptadecan-8-one)

PDB for NP0175853 (11-ethyl-7-methyl-3-(4-methyl-5-oxooxolan-2-yl)-9,17-dioxa-2-azapentacyclo[10.5.0.0¹,⁵.0²,¹⁶.0⁶,¹⁰]heptadecan-8-one)

3D PDB for NP0175853 (11-ethyl-7-methyl-3-(4-methyl-5-oxooxolan-2-yl)-9,17-dioxa-2-azapentacyclo[10.5.0.0¹,⁵.0²,¹⁶.0⁶,¹⁰]heptadecan-8-one)

SMILES for NP0175853 (11-ethyl-7-methyl-3-(4-methyl-5-oxooxolan-2-yl)-9,17-dioxa-2-azapentacyclo[10.5.0.0¹,⁵.0²,¹⁶.0⁶,¹⁰]heptadecan-8-one)

INCHI for NP0175853 (11-ethyl-7-methyl-3-(4-methyl-5-oxooxolan-2-yl)-9,17-dioxa-2-azapentacyclo[10.5.0.0¹,⁵.0²,¹⁶.0⁶,¹⁰]heptadecan-8-one)

Structure for NP0175853 (11-ethyl-7-methyl-3-(4-methyl-5-oxooxolan-2-yl)-9,17-dioxa-2-azapentacyclo[10.5.0.0¹,⁵.0²,¹⁶.0⁶,¹⁰]heptadecan-8-one)

3D Structure for NP0175853 (11-ethyl-7-methyl-3-(4-methyl-5-oxooxolan-2-yl)-9,17-dioxa-2-azapentacyclo[10.5.0.0¹,⁵.0²,¹⁶.0⁶,¹⁰]heptadecan-8-one)