NP-MRD: Showing NP-Card for Neotuberostemonone (NP0138993)

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Record Information

Version

1.0

Created at

2022-06-29 19:34:52 UTC

Updated at

2022-06-29 19:34:52 UTC

NP-MRD ID

NP0138993

Secondary Accession Numbers

None

Natural Product Identification

Common Name

Neotuberostemonone

Description

2-Ethyl-6-methyl-10-(4-methyl-5-oxooxolan-2-yl)-4-oxa-11-azatricyclo[9.4.1.0³,⁷]Hexadecane-5,8,16-trione belongs to the class of organic compounds known as caprolactams. These are cyclic amides of caproic acid. Caproic acid is the carboxylic acid derived from hexane with the general formula C5H11COOH. Neotuberostemonone is found in Stemona mairei, Stemona sessilifolia and Stemona tuberosa. 2-Ethyl-6-methyl-10-(4-methyl-5-oxooxolan-2-yl)-4-oxa-11-azatricyclo[9.4.1.0³,⁷]Hexadecane-5,8,16-trione is an extremely weak basic (essentially neutral) compound (based on its pKa).

Structure

MOL 3D MOL SDF PDB SMILES InChI


  Mrv1533004171522162D          

 29 32  0  0  0  0            999 V2000
    4.2400   -0.2377    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.4603    0.0318    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.3038    0.8418    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.0473    1.2498    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.6916    0.7346    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.3807    1.1882    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.1527    0.8973    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.1623    1.9837    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.6775    2.6281    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.3381    2.0218    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.0564    2.8131    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.6834    3.3493    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.3156    3.2158    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.4863    3.0384    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.0752    3.7536    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.2548    3.8414    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.0848    4.6487    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.3318    4.9857    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.8001    5.0599    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.8878    5.8802    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.4121    4.5067    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.9026    2.3966    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    1.0531    2.2484    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.5860    1.5314    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.8806    0.7398    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.7028    0.5026    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.4425    0.9459    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.2087    1.6847    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.9819    1.9724    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  2  0  0  0  0
 11 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
 17 18  1  0  0  0  0
 17 19  1  0  0  0  0
 19 20  2  0  0  0  0
 19 21  1  0  0  0  0
 15 21  1  0  0  0  0
 14 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
 26 27  1  0  0  0  0
  3 27  1  0  0  0  0
 27 28  1  0  0  0  0
 22 28  1  0  0  0  0
 28 29  2  0  0  0  0
M  END

     RDKit          3D

 60 63  0  0  0  0  0  0  0  0999 V2000
   -4.0638   -1.6266    1.8463 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.8688   -0.4713    0.8984 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3796   -0.2988    0.6809 C   0  0  1  0  0  0  0  0  0  0  0  0
   -1.7548   -1.5732    0.1442 C   0  0  1  0  0  0  0  0  0  0  0  0
   -2.1317   -1.8228   -1.2239 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1287   -2.0592   -2.2809 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0147   -2.9548   -1.9998 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.1723   -2.0651   -1.5473 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7308   -1.0868   -0.5132 N   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2664   -1.3733    0.4214 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1190   -1.5212    1.6760 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.5222    0.0705   -0.7811 C   0  0  2  0  0  0  0  0  0  0  0  0
    2.9577   -0.0454   -0.2944 C   0  0  1  0  0  0  0  0  0  0  0  0
    3.1490   -0.0437    1.1689 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.5496   -0.6652    1.3004 C   0  0  2  0  0  0  0  0  0  0  0  0
    5.5349    0.4669    1.1952 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.6399   -1.4719    0.0693 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.4724   -2.4081   -0.1841 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.6691   -1.0881   -0.8437 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.0486    1.4138   -0.4252 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.1252    1.5781    0.6904 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.5113    1.4689    1.8437 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3179    1.8841    0.5239 C   0  0  1  0  0  0  0  0  0  0  0  0
   -1.5588    3.1209   -0.3038 C   0  0  2  0  0  0  0  0  0  0  0  0
   -1.4739    4.3462    0.5798 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.9657    2.8970   -0.7284 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.7900    3.7575   -1.1116 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.2410    1.5449   -0.6343 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0718    0.8395   -0.2592 C   0  0  2  0  0  0  0  0  0  0  0  0
   -3.1756   -1.7954    2.4970 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.9363   -1.3820    2.4839 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.2255   -2.5856    1.3044 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.2423    0.4828    1.3203 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.4217   -0.6681   -0.0203 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9380   -0.1411    1.6963 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1624   -2.3751    0.8243 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8600   -2.6949   -1.2755 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7908   -0.9816   -1.6072 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7268   -1.0942   -2.6790 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6574   -2.4997   -3.1842 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.3732   -3.4985   -2.8697 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2126   -3.6285   -1.1277 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.4105   -1.5012   -2.5044 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.9905   -2.6920   -1.2264 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.6628    0.0886   -1.9192 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.4532    0.9022   -0.6762 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.1982    1.0033    1.5972 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.4335   -0.5804    1.7828 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.6470   -1.2483    2.2200 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.1636    1.3901    1.7047 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.4888    0.2115    1.7037 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.7984    0.7095    0.1461 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.9394    2.0979   -0.2703 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.5753    1.8944   -1.3396 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8494    2.0234    1.4712 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9655    3.2011   -1.2117 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1825    5.1296    0.2366 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7589    4.0930    1.6179 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4462    4.7627    0.5677 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5483    0.5638   -1.1703 H   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0
  2  3  1  0
  3 29  1  0
 29 28  1  0
 28 26  1  0
 26 27  2  0
 26 24  1  0
 24 25  1  0
 24 23  1  0
 23 21  1  0
 21 22  2  0
 21 20  1  0
 20 12  1  0
 12 13  1  0
 13 14  1  0
 14 15  1  0
 15 16  1  0
 15 17  1  0
 17 18  2  0
 17 19  1  0
 12  9  1  0
  9  8  1  0
  8  7  1  0
  7  6  1  0
  6  5  1  0
  5  4  1  0
  4 10  1  0
 10 11  2  0
  4  3  1  0
 23 29  1  0
 19 13  1  0
 10  9  1  0
  1 30  1  0
  1 31  1  0
  1 32  1  0
  2 33  1  0
  2 34  1  0
  3 35  1  1
 29 60  1  6
 24 56  1  6
 25 57  1  0
 25 58  1  0
 25 59  1  0
 23 55  1  1
 20 53  1  0
 20 54  1  0
 12 45  1  6
 13 46  1  6
 14 47  1  0
 14 48  1  0
 15 49  1  1
 16 50  1  0
 16 51  1  0
 16 52  1  0
  8 43  1  0
  8 44  1  0
  7 41  1  0
  7 42  1  0
  6 39  1  0
  6 40  1  0
  5 37  1  0
  5 38  1  0
  4 36  1  1
M  END


  Mrv1533004171522162D          

 29 32  0  0  0  0            999 V2000
    4.2400   -0.2377    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.4603    0.0318    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.3038    0.8418    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.0473    1.2498    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.6916    0.7346    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.3807    1.1882    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.1527    0.8973    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.1623    1.9837    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.6775    2.6281    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.3381    2.0218    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.0564    2.8131    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.6834    3.3493    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.3156    3.2158    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.4863    3.0384    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.0752    3.7536    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.2548    3.8414    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.0848    4.6487    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.3318    4.9857    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.8001    5.0599    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.8878    5.8802    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.4121    4.5067    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.9026    2.3966    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    1.0531    2.2484    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.5860    1.5314    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.8806    0.7398    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.7028    0.5026    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.4425    0.9459    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.2087    1.6847    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.9819    1.9724    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  2  0  0  0  0
 11 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
 17 18  1  0  0  0  0
 17 19  1  0  0  0  0
 19 20  2  0  0  0  0
 19 21  1  0  0  0  0
 15 21  1  0  0  0  0
 14 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
 26 27  1  0  0  0  0
  3 27  1  0  0  0  0
 27 28  1  0  0  0  0
 22 28  1  0  0  0  0
 28 29  2  0  0  0  0
M  END
> <DATABASE_ID>
NP0138993

> <DATABASE_NAME>
NP-MRD

> <SMILES>
CCC1C2OC(=O)C(C)C2C(=O)CC(C2CC(C)C(=O)O2)N2CCCCC1C2=O

> <INCHI_IDENTIFIER>
InChI=1S/C22H31NO6/c1-4-13-14-7-5-6-8-23(20(14)25)15(17-9-11(2)21(26)28-17)10-16(24)18-12(3)22(27)29-19(13)18/h11-15,17-19H,4-10H2,1-3H3

> <INCHI_KEY>
CHQGOWAOLJKTQX-UHFFFAOYSA-N

> <FORMULA>
C22H31NO6

> <MOLECULAR_WEIGHT>
405.491

> <EXACT_MASS>
405.215137722

> <JCHEM_ACCEPTOR_COUNT>
4

> <JCHEM_ATOM_COUNT>
60

> <JCHEM_AVERAGE_POLARIZABILITY>
42.92615645979336

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
0

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
1

> <JCHEM_IUPAC>
2-ethyl-6-methyl-10-(4-methyl-5-oxooxolan-2-yl)-4-oxa-11-azatricyclo[9.4.1.0³,⁷]hexadecane-5,8,16-trione

> <ALOGPS_LOGP>
1.62

> <JCHEM_LOGP>
2.451669673666666

> <ALOGPS_LOGS>
-2.52

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
4

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA_STRONGEST_ACIDIC>
15.985906801664115

> <JCHEM_PKA_STRONGEST_BASIC>
0.7696155165798456

> <JCHEM_POLAR_SURFACE_AREA>
89.97999999999999

> <JCHEM_REFRACTIVITY>
102.85619999999999

> <JCHEM_ROTATABLE_BOND_COUNT>
2

> <JCHEM_RULE_OF_FIVE>
1

> <ALOGPS_SOLUBILITY>
1.24e+00 g/l

> <JCHEM_TRADITIONAL_IUPAC>
2-ethyl-6-methyl-10-(4-methyl-5-oxooxolan-2-yl)-4-oxa-11-azatricyclo[9.4.1.0³,⁷]hexadecane-5,8,16-trione

> <JCHEM_VEBER_RULE>
0

$$$$

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       7.915  -0.444   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0       6.459   0.059   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0       6.167   1.571   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0       7.555   2.333   0.000  0.00  0.00           C+0
HETATM    5  O   UNK     0       8.758   1.371   0.000  0.00  0.00           O+0
HETATM    6  C   UNK     0      10.044   2.218   0.000  0.00  0.00           C+0
HETATM    7  O   UNK     0      11.485   1.675   0.000  0.00  0.00           O+0
HETATM    8  C   UNK     0       9.636   3.703   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0      10.598   4.906   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0       8.098   3.774   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0       7.572   5.251   0.000  0.00  0.00           C+0
HETATM   12  O   UNK     0       8.742   6.252   0.000  0.00  0.00           O+0
HETATM   13  C   UNK     0       6.189   6.003   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0       4.641   5.672   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0       3.874   7.007   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0       2.342   7.171   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0       2.025   8.678   0.000  0.00  0.00           C+0
HETATM   18  C   UNK     0       0.619   9.307   0.000  0.00  0.00           C+0
HETATM   19  C   UNK     0       3.360   9.445   0.000  0.00  0.00           C+0
HETATM   20  O   UNK     0       3.524  10.976   0.000  0.00  0.00           O+0
HETATM   21  O   UNK     0       4.503   8.412   0.000  0.00  0.00           O+0
HETATM   22  N   UNK     0       3.551   4.474   0.000  0.00  0.00           N+0
HETATM   23  C   UNK     0       1.966   4.197   0.000  0.00  0.00           C+0
HETATM   24  C   UNK     0       1.094   2.859   0.000  0.00  0.00           C+0
HETATM   25  C   UNK     0       1.644   1.381   0.000  0.00  0.00           C+0
HETATM   26  C   UNK     0       3.179   0.938   0.000  0.00  0.00           C+0
HETATM   27  C   UNK     0       4.559   1.766   0.000  0.00  0.00           C+0
HETATM   28  C   UNK     0       4.123   3.145   0.000  0.00  0.00           C+0
HETATM   29  O   UNK     0       5.566   3.682   0.000  0.00  0.00           O+0
CONECT    1    2                                                            
CONECT    2    1    3                                                       
CONECT    3    2    4   27                                                  
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   13                                                  
CONECT   12   11                                                            
CONECT   13   11   14                                                       
CONECT   14   13   15   22                                                  
CONECT   15   14   16   21                                                  
CONECT   16   15   17                                                       
CONECT   17   16   18   19                                                  
CONECT   18   17                                                            
CONECT   19   17   20   21                                                  
CONECT   20   19                                                            
CONECT   21   19   15                                                       
CONECT   22   14   23   28                                                  
CONECT   23   22   24                                                       
CONECT   24   23   25                                                       
CONECT   25   24   26                                                       
CONECT   26   25   27                                                       
CONECT   27   26    3   28                                                  
CONECT   28   27   22   29                                                  
CONECT   29   28                                                            
MASTER        0    0    0    0    0    0    0    0   29    0   64    0
END

View in JSmol

Synonyms

Not Available

Chemical Formula

C₂₂H₃₁NO₆

Average Mass

405.4910 Da

Monoisotopic Mass

405.21514 Da

IUPAC Name

2-ethyl-6-methyl-10-(4-methyl-5-oxooxolan-2-yl)-4-oxa-11-azatricyclo[9.4.1.0³,⁷]hexadecane-5,8,16-trione

Traditional Name

2-ethyl-6-methyl-10-(4-methyl-5-oxooxolan-2-yl)-4-oxa-11-azatricyclo[9.4.1.0³,⁷]hexadecane-5,8,16-trione

CAS Registry Number

Not Available

SMILES

CCC1C2OC(=O)C(C)C2C(=O)CC(C2CC(C)C(=O)O2)N2CCCCC1C2=O

InChI Identifier

InChI=1S/C22H31NO6/c1-4-13-14-7-5-6-8-23(20(14)25)15(17-9-11(2)21(26)28-17)10-16(24)18-12(3)22(27)29-19(13)18/h11-15,17-19H,4-10H2,1-3H3

InChI Key

CHQGOWAOLJKTQX-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 mairei	LOTUS Database	35616633
Stemona sessilifolia	LOTUS Database	35616633
Stemona tuberosa	LOTUS Database	35616633

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as caprolactams. These are cyclic amides of caproic acid. Caproic acid is the carboxylic acid derived from hexane with the general formula C5H11COOH.

Kingdom

Organic compounds

Super Class

Organoheterocyclic compounds

Class

Lactams

Sub Class

Caprolactams

Direct Parent

Caprolactams

Alternative Parents

Substituents

Caprolactam
Azepane
Dicarboxylic acid or derivatives
Gamma butyrolactone
Tertiary carboxylic acid amide
Oxolane
Carboxamide group
Carboxylic acid ester
Ketone
Lactone
Carboxylic acid derivative
Oxacycle
Azacycle
Organic nitrogen compound
Hydrocarbon derivative
Organic oxide
Organopnictogen compound
Carbonyl group
Organic oxygen compound
Organooxygen compound
Organonitrogen 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	1.62	ALOGPS
logP	2.45	ChemAxon
logS	-2.5	ALOGPS
pKa (Strongest Acidic)	15.99	ChemAxon
pKa (Strongest Basic)	0.77	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	4	ChemAxon
Hydrogen Donor Count	0	ChemAxon
Polar Surface Area	89.98 Å²	ChemAxon
Rotatable Bond Count	2	ChemAxon
Refractivity	102.86 m³·mol⁻¹	ChemAxon
Polarizability	42.93 Å³	ChemAxon
Number of Rings	4	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

78385648

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

Not Available

Showing NP-Card for Neotuberostemonone (NP0138993)

MOL for NP0138993 (Neotuberostemonone)

3D MOL for NP0138993 (Neotuberostemonone)

3D SDF for NP0138993 (Neotuberostemonone)

3D-SDF for NP0138993 (Neotuberostemonone)

PDB for NP0138993 (Neotuberostemonone)

3D PDB for NP0138993 (Neotuberostemonone)

SMILES for NP0138993 (Neotuberostemonone)

INCHI for NP0138993 (Neotuberostemonone)

Structure for NP0138993 (Neotuberostemonone)

3D Structure for NP0138993 (Neotuberostemonone)