NP-MRD: Showing NP-Card for 1,4',4',12',14'-pentamethyl-9',14'-diazaspiro[pyrrolidine-3,5'-tetracyclo[5.5.2.0¹,⁹.0³,⁷]tetradecane]-2,5,10',13'-tetrone (NP0214240)

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Record Information

Version

2.0

Created at

2022-09-05 13:28:59 UTC

Updated at

2022-09-05 13:28:59 UTC

NP-MRD ID

NP0214240

Secondary Accession Numbers

None

Natural Product Identification

Common Name

1,4',4',12',14'-pentamethyl-9',14'-diazaspiro[pyrrolidine-3,5'-tetracyclo[5.5.2.0¹,⁹.0³,⁷]tetradecane]-2,5,10',13'-tetrone

Description

1,4',4',12',14'-Pentamethyl-9',14'-diazaspiro[pyrrolidine-3,5'-tetracyclo[5.5.2.0¹,⁹.0³,⁷]Tetradecane]-2,5,10',13'-tetrone belongs to the class of organic compounds known as azaspirodecane derivatives. These are organic compounds containing a spirodecane moiety with at least one nitrogen atom. 1,4',4',12',14'-Pentamethyl-9',14'-diazaspiro[pyrrolidine-3,5'-tetracyclo[5.5.2.0¹,⁹.0³,⁷]Tetradecane]-2,5,10',13'-tetrone is an extremely weak basic (essentially neutral) compound (based on its pKa).

Structure

MOL 3D MOL SDF PDB SMILES InChI


  Mrv1533005011512462D          

 27 31  0  0  0  0            999 V2000
   -0.2697   -0.6696    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0170    0.1040    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4968    0.7694    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0284    1.4235    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2238    2.2090    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.8531    1.1929    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    1.6299    1.7051    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.3732    1.1610    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.1950    1.3822    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.7331    0.7390    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.2042    1.4163    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.9939    1.1776    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.6512    1.6762    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.0109    0.3528    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    5.6882   -0.1183    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.2317    0.0817    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.9930   -0.7080    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.2203    0.0740    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.9416   -0.3265    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.9321   -0.6990    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.3824    0.2498    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.6136   -0.2620    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.8574    0.2775    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.6355    0.3452    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.2599   -0.1940    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.5907    1.0977    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    0.9679    1.6388    0.0000 C   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  2  0  0  0  0
  4  6  1  0  0  0  0
  6  7  1  0  0  0  0
  7  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
 12 13  2  0  0  0  0
 12 14  1  0  0  0  0
 14 15  1  0  0  0  0
 14 16  1  0  0  0  0
 10 16  1  0  0  0  0
 16 17  2  0  0  0  0
 10 18  1  0  0  0  0
 18 19  1  0  0  0  0
 18 20  1  0  0  0  0
 18 21  1  0  0  0  0
  8 21  1  0  0  0  0
 21 22  1  0  0  0  0
 22 23  1  0  0  0  0
  2 23  1  0  0  0  0
  6 23  1  0  0  0  0
 23 24  1  0  0  0  0
 24 25  2  0  0  0  0
 24 26  1  0  0  0  0
  8 26  1  0  0  0  0
 26 27  1  0  0  0  0
M  END

     RDKit          3D

 54 58  0  0  0  0  0  0  0  0999 V2000
   -3.2977    1.4102    2.4159 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5702    0.4317    1.3105 C   0  0  1  0  0  0  0  0  0  0  0  0
   -4.4854    1.0057    0.2383 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5626    1.3548   -0.8927 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.8385    2.0998   -1.8664 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3397    0.7163   -0.6908 N   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0552    0.5885   -1.3930 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4395   -0.7055   -0.9089 C   0  0  1  0  0  0  0  0  0  0  0  0
    0.7979   -1.1130   -1.5769 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.9042   -0.4798   -0.7534 C   0  0  1  0  0  0  0  0  0  0  0  0
    3.1260   -1.3854   -0.7102 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.2212   -0.4392   -0.4283 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.3464   -0.6411    0.1390 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.7870    0.8312   -0.9296 N   0  0  0  0  0  0  0  0  0  0  0  0
    4.5939    2.0539   -0.9136 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.4649    0.7142   -1.4382 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.9702    1.4999   -2.2816 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.3541   -0.1803    0.6093 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.5929    1.2457    1.0393 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.0552   -1.0477    1.6666 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0619   -0.6064    0.5778 C   0  0  1  0  0  0  0  0  0  0  0  0
   -1.0554    0.2977    1.2289 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3965   -0.0082    0.5671 C   0  0  1  0  0  0  0  0  0  0  0  0
   -2.4554   -1.4560    0.1168 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.2368   -2.2842    0.6000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5019   -1.6888   -0.9099 N   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5389   -2.7541   -1.8580 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.2555    1.8824    2.7186 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.9057    0.8649    3.2879 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5359    2.1626    2.1286 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.0871   -0.4500    1.7592 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.9611    1.9197    0.6671 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.2257    0.2649   -0.1208 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4904    1.4903   -1.0824 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1939    0.5059   -2.4730 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.7987   -0.7283   -2.6277 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.9188   -2.2122   -1.6526 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.0402   -2.2125   -0.0106 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.2687   -1.7301   -1.7728 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.5087    1.9451   -1.5296 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.8897    2.1903    0.1601 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.9782    2.9188   -1.1759 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.0193    1.4122    1.9726 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.4179    1.9949    0.2695 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.6742    1.2813    1.3679 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.6323   -0.7409    2.6659 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.1229   -0.8716    1.7297 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.7518   -2.1122    1.5604 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2057   -1.6145    1.0753 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7577    1.3576    0.9811 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1079    0.2065    2.3257 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7854   -3.5231   -1.5393 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5425   -3.2500   -1.7718 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3452   -2.4119   -2.8940 H   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0
  2  3  1  0
  3  4  1  0
  4  5  2  0
  4  6  1  0
  6  7  1  0
  7  8  1  0
  8  9  1  6
  9 10  1  0
 10 11  1  0
 11 12  1  0
 12 13  2  0
 12 14  1  0
 14 15  1  0
 14 16  1  0
 16 17  2  0
 10 18  1  0
 18 19  1  0
 18 20  1  0
 18 21  1  0
 21 22  1  0
 22 23  1  0
 23 24  1  6
 24 25  2  0
 24 26  1  0
 26 27  1  0
 23  2  1  0
 23  6  1  0
 21  8  1  0
 26  8  1  0
 10 16  1  6
  1 28  1  0
  1 29  1  0
  1 30  1  0
  2 31  1  1
  3 32  1  0
  3 33  1  0
  7 34  1  0
  7 35  1  0
  9 36  1  0
  9 37  1  0
 11 38  1  0
 11 39  1  0
 15 40  1  0
 15 41  1  0
 15 42  1  0
 19 43  1  0
 19 44  1  0
 19 45  1  0
 20 46  1  0
 20 47  1  0
 20 48  1  0
 21 49  1  1
 22 50  1  0
 22 51  1  0
 27 52  1  0
 27 53  1  0
 27 54  1  0
M  END


  Mrv1533005011512462D          

 27 31  0  0  0  0            999 V2000
   -0.2697   -0.6696    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0170    0.1040    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4968    0.7694    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0284    1.4235    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2238    2.2090    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.8531    1.1929    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    1.6299    1.7051    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.3732    1.1610    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.1950    1.3822    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.7331    0.7390    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.2042    1.4163    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.9939    1.1776    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.6512    1.6762    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.0109    0.3528    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    5.6882   -0.1183    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.2317    0.0817    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.9930   -0.7080    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.2203    0.0740    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.9416   -0.3265    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.9321   -0.6990    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.3824    0.2498    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.6136   -0.2620    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.8574    0.2775    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.6355    0.3452    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.2599   -0.1940    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.5907    1.0977    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    0.9679    1.6388    0.0000 C   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  2  0  0  0  0
  4  6  1  0  0  0  0
  6  7  1  0  0  0  0
  7  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
 12 13  2  0  0  0  0
 12 14  1  0  0  0  0
 14 15  1  0  0  0  0
 14 16  1  0  0  0  0
 10 16  1  0  0  0  0
 16 17  2  0  0  0  0
 10 18  1  0  0  0  0
 18 19  1  0  0  0  0
 18 20  1  0  0  0  0
 18 21  1  0  0  0  0
  8 21  1  0  0  0  0
 21 22  1  0  0  0  0
 22 23  1  0  0  0  0
  2 23  1  0  0  0  0
  6 23  1  0  0  0  0
 23 24  1  0  0  0  0
 24 25  2  0  0  0  0
 24 26  1  0  0  0  0
  8 26  1  0  0  0  0
 26 27  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0214240

> <DATABASE_NAME>
NP-MRD

> <SMILES>
CC1CC(=O)N2CC34CC5(CC(=O)N(C)C5=O)C(C)(C)C3CC12C(=O)N4C

> <INCHI_IDENTIFIER>
InChI=1S/C20H27N3O4/c1-11-6-13(24)23-10-19-9-18(8-14(25)21(4)15(18)26)17(2,3)12(19)7-20(11,23)16(27)22(19)5/h11-12H,6-10H2,1-5H3

> <INCHI_KEY>
YAYKUKWEFJDSJG-UHFFFAOYSA-N

> <FORMULA>
C20H27N3O4

> <MOLECULAR_WEIGHT>
373.453

> <EXACT_MASS>
373.200156361

> <JCHEM_ACCEPTOR_COUNT>
4

> <JCHEM_ATOM_COUNT>
54

> <JCHEM_AVERAGE_POLARIZABILITY>
39.38256848143027

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
0

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
0

> <JCHEM_IUPAC>
1,4',4',12',14'-pentamethyl-9',14'-diazaspiro[pyrrolidine-3,5'-tetracyclo[5.5.2.0¹,⁹.0³,⁷]tetradecane]-2,5,10',13'-tetrone

> <ALOGPS_LOGP>
1.20

> <JCHEM_LOGP>
-0.4674283773333342

> <ALOGPS_LOGS>
-1.79

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
5

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA_STRONGEST_ACIDIC>
19.649389481674735

> <JCHEM_PKA_STRONGEST_BASIC>
-0.9231331344521235

> <JCHEM_POLAR_SURFACE_AREA>
78.0

> <JCHEM_REFRACTIVITY>
95.78229999999999

> <JCHEM_ROTATABLE_BOND_COUNT>
0

> <JCHEM_RULE_OF_FIVE>
1

> <ALOGPS_SOLUBILITY>
6.08e+00 g/l

> <JCHEM_TRADITIONAL_IUPAC>
1,4',4',12',14'-pentamethyl-9',14'-diazaspiro[pyrrolidine-3,5'-tetracyclo[5.5.2.0¹,⁹.0³,⁷]tetradecane]-2,5,10',13'-tetrone

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 01-MAY-15   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   01-MAY-15         0                                  
HETATM    1  C   UNK     0      -0.503  -1.250   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0       0.032   0.194   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0      -0.927   1.436   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0       0.053   2.657   0.000  0.00  0.00           C+0
HETATM    5  O   UNK     0      -0.418   4.124   0.000  0.00  0.00           O+0
HETATM    6  N   UNK     0       1.592   2.227   0.000  0.00  0.00           N+0
HETATM    7  C   UNK     0       3.043   3.183   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0       4.430   2.167   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0       5.964   2.580   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0       6.969   1.379   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0       7.848   2.644   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0       9.322   2.198   0.000  0.00  0.00           C+0
HETATM   13  O   UNK     0      10.549   3.129   0.000  0.00  0.00           O+0
HETATM   14  N   UNK     0       9.354   0.658   0.000  0.00  0.00           N+0
HETATM   15  C   UNK     0      10.618  -0.221   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0       7.899   0.152   0.000  0.00  0.00           C+0
HETATM   17  O   UNK     0       7.454  -1.322   0.000  0.00  0.00           O+0
HETATM   18  C   UNK     0       6.011   0.138   0.000  0.00  0.00           C+0
HETATM   19  C   UNK     0       7.358  -0.609   0.000  0.00  0.00           C+0
HETATM   20  C   UNK     0       5.473  -1.305   0.000  0.00  0.00           C+0
HETATM   21  C   UNK     0       4.447   0.466   0.000  0.00  0.00           C+0
HETATM   22  C   UNK     0       3.012  -0.489   0.000  0.00  0.00           C+0
HETATM   23  C   UNK     0       1.600   0.518   0.000  0.00  0.00           C+0
HETATM   24  C   UNK     0       3.053   0.644   0.000  0.00  0.00           C+0
HETATM   25  O   UNK     0       4.218  -0.362   0.000  0.00  0.00           O+0
HETATM   26  N   UNK     0       2.969   2.049   0.000  0.00  0.00           N+0
HETATM   27  C   UNK     0       1.807   3.059   0.000  0.00  0.00           C+0
CONECT    1    2                                                            
CONECT    2    1    3   23                                                  
CONECT    3    2    4                                                       
CONECT    4    3    5    6                                                  
CONECT    5    4                                                            
CONECT    6    4    7   23                                                  
CONECT    7    6    8                                                       
CONECT    8    7    9   21   26                                             
CONECT    9    8   10                                                       
CONECT   10    9   11   16   18                                             
CONECT   11   10   12                                                       
CONECT   12   11   13   14                                                  
CONECT   13   12                                                            
CONECT   14   12   15   16                                                  
CONECT   15   14                                                            
CONECT   16   14   10   17                                                  
CONECT   17   16                                                            
CONECT   18   10   19   20   21                                             
CONECT   19   18                                                            
CONECT   20   18                                                            
CONECT   21   18    8   22                                                  
CONECT   22   21   23                                                       
CONECT   23   22    2    6   24                                             
CONECT   24   23   25   26                                                  
CONECT   25   24                                                            
CONECT   26   24    8   27                                                  
CONECT   27   26                                                            
MASTER        0    0    0    0    0    0    0    0   27    0   62    0
END

View in JSmol

Synonyms

Not Available

Chemical Formula

C₂₀H₂₇N₃O₄

Average Mass

373.4530 Da

Monoisotopic Mass

373.20016 Da

IUPAC Name

1,4',4',12',14'-pentamethyl-9',14'-diazaspiro[pyrrolidine-3,5'-tetracyclo[5.5.2.0¹,⁹.0³,⁷]tetradecane]-2,5,10',13'-tetrone

Traditional Name

1,4',4',12',14'-pentamethyl-9',14'-diazaspiro[pyrrolidine-3,5'-tetracyclo[5.5.2.0¹,⁹.0³,⁷]tetradecane]-2,5,10',13'-tetrone

CAS Registry Number

Not Available

SMILES

CC1CC(=O)N2CC34CC5(CC(=O)N(C)C5=O)C(C)(C)C3CC12C(=O)N4C

InChI Identifier

InChI=1S/C20H27N3O4/c1-11-6-13(24)23-10-19-9-18(8-14(25)21(4)15(18)26)17(2,3)12(19)7-20(11,23)16(27)22(19)5/h11-12H,6-10H2,1-5H3

InChI Key

YAYKUKWEFJDSJG-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

Not Available

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as azaspirodecane derivatives. These are organic compounds containing a spirodecane moiety with at least one nitrogen atom.

Kingdom

Organic compounds

Super Class

Organoheterocyclic compounds

Class

Azaspirodecane derivatives

Sub Class

Not Available

Direct Parent

Azaspirodecane derivatives

Alternative Parents

Substituents

Alpha-amino acid or derivatives
Azaspirodecane
Indolizidine
Delta-lactam
N-alkylpiperazine
N-methylpiperazine
Piperidinone
1,4-diazinane
N-alkylpyrrolidine
Carboxylic acid imide, n-substituted
Piperazine
2-pyrrolidone
Pyrrolidone
Piperidine
Carboxylic acid imide
Dicarboximide
Tertiary carboxylic acid amide
Pyrrolidine
Lactam
Carboxamide group
Tertiary amine
Amino acid or derivatives
Azacycle
Carboxylic acid derivative
Amine
Organic nitrogen compound
Hydrocarbon derivative
Organic oxide
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	1.2	ALOGPS
logP	-0.47	ChemAxon
logS	-1.8	ALOGPS
pKa (Strongest Acidic)	19.65	ChemAxon
pKa (Strongest Basic)	-0.92	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	4	ChemAxon
Hydrogen Donor Count	0	ChemAxon
Polar Surface Area	78 Å²	ChemAxon
Rotatable Bond Count	0	ChemAxon
Refractivity	95.78 m³·mol⁻¹	ChemAxon
Polarizability	39.38 Å³	ChemAxon
Number of Rings	5	ChemAxon
Bioavailability	Yes	ChemAxon
Rule of Five	Yes	ChemAxon
Ghose Filter	No	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

46829795

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

LOTUS database [Link]

Showing NP-Card for 1,4',4',12',14'-pentamethyl-9',14'-diazaspiro[pyrrolidine-3,5'-tetracyclo[5.5.2.0¹,⁹.0³,⁷]tetradecane]-2,5,10',13'-tetrone (NP0214240)

MOL for NP0214240 (1,4',4',12',14'-pentamethyl-9',14'-diazaspiro[pyrrolidine-3,5'-tetracyclo[5.5.2.0¹,⁹.0³,⁷]tetradecane]-2,5,10',13'-tetrone)

3D MOL for NP0214240 (1,4',4',12',14'-pentamethyl-9',14'-diazaspiro[pyrrolidine-3,5'-tetracyclo[5.5.2.0¹,⁹.0³,⁷]tetradecane]-2,5,10',13'-tetrone)

3D SDF for NP0214240 (1,4',4',12',14'-pentamethyl-9',14'-diazaspiro[pyrrolidine-3,5'-tetracyclo[5.5.2.0¹,⁹.0³,⁷]tetradecane]-2,5,10',13'-tetrone)

3D-SDF for NP0214240 (1,4',4',12',14'-pentamethyl-9',14'-diazaspiro[pyrrolidine-3,5'-tetracyclo[5.5.2.0¹,⁹.0³,⁷]tetradecane]-2,5,10',13'-tetrone)

PDB for NP0214240 (1,4',4',12',14'-pentamethyl-9',14'-diazaspiro[pyrrolidine-3,5'-tetracyclo[5.5.2.0¹,⁹.0³,⁷]tetradecane]-2,5,10',13'-tetrone)

3D PDB for NP0214240 (1,4',4',12',14'-pentamethyl-9',14'-diazaspiro[pyrrolidine-3,5'-tetracyclo[5.5.2.0¹,⁹.0³,⁷]tetradecane]-2,5,10',13'-tetrone)

SMILES for NP0214240 (1,4',4',12',14'-pentamethyl-9',14'-diazaspiro[pyrrolidine-3,5'-tetracyclo[5.5.2.0¹,⁹.0³,⁷]tetradecane]-2,5,10',13'-tetrone)

INCHI for NP0214240 (1,4',4',12',14'-pentamethyl-9',14'-diazaspiro[pyrrolidine-3,5'-tetracyclo[5.5.2.0¹,⁹.0³,⁷]tetradecane]-2,5,10',13'-tetrone)

Structure for NP0214240 (1,4',4',12',14'-pentamethyl-9',14'-diazaspiro[pyrrolidine-3,5'-tetracyclo[5.5.2.0¹,⁹.0³,⁷]tetradecane]-2,5,10',13'-tetrone)

3D Structure for NP0214240 (1,4',4',12',14'-pentamethyl-9',14'-diazaspiro[pyrrolidine-3,5'-tetracyclo[5.5.2.0¹,⁹.0³,⁷]tetradecane]-2,5,10',13'-tetrone)