NP-MRD: Showing NP-Card for (1'r,3s,3's,7'r,12's)-1,4',4',12',14'-pentamethyl-9',14'-diazaspiro[pyrrolidine-3,5'-tetracyclo[5.5.2.0¹,⁹.0³,⁷]tetradecane]-2,5,13'-trione (NP0177859)

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Record Information

Version

2.0

Created at

2022-09-03 15:45:25 UTC

Updated at

2022-09-03 15:45:25 UTC

NP-MRD ID

NP0177859

Secondary Accession Numbers

None

Natural Product Identification

Common Name

(1'r,3s,3's,7'r,12's)-1,4',4',12',14'-pentamethyl-9',14'-diazaspiro[pyrrolidine-3,5'-tetracyclo[5.5.2.0¹,⁹.0³,⁷]tetradecane]-2,5,13'-trione

Description

Asperparaline A, also known as aspergillimide, 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'r,3s,3's,7'r,12's)-1,4',4',12',14'-pentamethyl-9',14'-diazaspiro[pyrrolidine-3,5'-tetracyclo[5.5.2.0¹,⁹.0³,⁷]tetradecane]-2,5,13'-trione was first documented in 2003 (PMID: 14640629). Based on a literature review a small amount of articles have been published on Asperparaline A (PMID: 30363149) (PMID: 21483774).

Structure

MOL 3D MOL SDF PDB SMILES InChI


  Mrv1652309032217452D          

 26 30  0  0  1  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  1  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
    0.8531    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  1  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  1  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  2  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  2  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
  2  1  1  1  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  1  0  0  0  0
  7  8  1  6  0  0  0
  9  8  1  1  0  0  0
  9 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
 13 15  1  0  0  0  0
  9 15  1  0  0  0  0
 15 16  2  0  0  0  0
  9 17  1  0  0  0  0
 17 18  1  0  0  0  0
 17 19  1  0  0  0  0
 17 20  1  0  0  0  0
  7 20  1  0  0  0  0
 20 21  1  6  0  0  0
 21 22  1  0  0  0  0
  2 22  1  0  0  0  0
 22  5  1  6  0  0  0
 22 23  1  0  0  0  0
 23 24  2  0  0  0  0
 23 25  1  0  0  0  0
  7 25  1  0  0  0  0
 25 26  1  0  0  0  0
M  END

     RDKit          2D

 55 59  0  0  0  0  0  0  0  0999 V2000
    2.3907    1.0037    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.2760    0.0000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.3943    1.2135    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0323    0.7500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0323   -0.7500    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1470   -1.7537    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8351   -3.2209    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7168   -4.4344    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8351   -5.6480    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9535   -6.8615    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8351   -8.0750    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3716   -9.5016    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.2617   -7.6115    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
   -4.4752   -8.4932    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.2617   -6.1115    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.5737   -5.3843    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4086   -5.1844    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0967   -6.6517    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.0832   -5.0277    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4086   -3.6844    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0404   -2.4644    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.3943   -1.2135    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1827   -1.8009    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1328   -3.1443    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1906   -2.7085    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0967   -5.1517    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5054    2.0074    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.3944   -0.1110    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.5304    2.2324    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.3907   -1.0037    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2158    2.5838    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.5922    2.1163    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5241    0.5932    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3442    2.2172    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5378   -2.3156    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.9419   -0.4816    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.8315   -3.4307    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.9456   -5.2948    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.4470   -6.3241    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.0306   -7.9936    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.6888   -9.3748    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5936   -9.7067    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.3569   -7.2796    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.3917   -8.0699    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.3976   -6.5210    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4448   -7.3093    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.5750   -4.8709    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.4207   -6.4892    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.2921   -3.5423    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.0894   -3.7628    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.0969   -2.1188    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.9042   -3.5834    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.7204   -6.4096    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4448   -5.8093    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.3452   -5.5653    0.0000 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  1  0
  5  6  1  0
  6  7  1  0
  7  8  1  1
  8  9  1  0
  9 10  1  0
 10 11  1  0
 11 12  2  0
 11 13  1  0
 13 14  1  0
 13 15  1  0
 15 16  2  0
  9 17  1  0
 17 18  1  0
 17 19  1  0
 17 20  1  0
 20 21  1  0
 21 22  1  0
 22 23  1  6
 23 24  2  0
 23 25  1  0
 25 26  1  0
 22  2  1  0
 22  5  1  0
 20  7  1  0
 25  7  1  0
  9 15  1  6
  1 27  1  0
  1 28  1  0
  1 29  1  0
  2 30  1  1
  3 31  1  0
  3 32  1  0
  4 33  1  0
  4 34  1  0
  6 35  1  0
  6 36  1  0
  8 37  1  0
  8 38  1  0
 10 39  1  0
 10 40  1  0
 14 41  1  0
 14 42  1  0
 14 43  1  0
 18 44  1  0
 18 45  1  0
 18 46  1  0
 19 47  1  0
 19 48  1  0
 19 49  1  0
 20 50  1  6
 21 51  1  0
 21 52  1  0
 26 53  1  0
 26 54  1  0
 26 55  1  0
M  END


  Mrv1652309032217452D          

 26 30  0  0  1  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  1  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
    0.8531    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  1  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  1  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  2  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  2  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
  2  1  1  1  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  1  0  0  0  0
  7  8  1  6  0  0  0
  9  8  1  1  0  0  0
  9 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
 13 15  1  0  0  0  0
  9 15  1  0  0  0  0
 15 16  2  0  0  0  0
  9 17  1  0  0  0  0
 17 18  1  0  0  0  0
 17 19  1  0  0  0  0
 17 20  1  0  0  0  0
  7 20  1  0  0  0  0
 20 21  1  6  0  0  0
 21 22  1  0  0  0  0
  2 22  1  0  0  0  0
 22  5  1  6  0  0  0
 22 23  1  0  0  0  0
 23 24  2  0  0  0  0
 23 25  1  0  0  0  0
  7 25  1  0  0  0  0
 25 26  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0177859

> <DATABASE_NAME>
NP-MRD

> <SMILES>
C[C@H]1CCN2C[C@@]34C[C@]5(CC(=O)N(C)C5=O)C(C)(C)[C@@H]3C[C@]12C(=O)N4C

> <INCHI_IDENTIFIER>
InChI=1S/C20H29N3O3/c1-12-6-7-23-11-19-10-18(9-14(24)21(4)15(18)25)17(2,3)13(19)8-20(12,23)16(26)22(19)5/h12-13H,6-11H2,1-5H3/t12-,13-,18-,19-,20+/m0/s1

> <INCHI_KEY>
RTNMRJRMTGSUAE-ASTIPKKCSA-N

> <FORMULA>
C20H29N3O3

> <MOLECULAR_WEIGHT>
359.47

> <EXACT_MASS>
359.220891806

> <JCHEM_ACCEPTOR_COUNT>
4

> <JCHEM_ATOM_COUNT>
55

> <JCHEM_AVERAGE_POLARIZABILITY>
70.06158080655749

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
0

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
1

> <JCHEM_IUPAC>
(1'R,3S,3'S,7'R,12'S)-1,4',4',12',14'-pentamethyl-9',14'-diazaspiro[pyrrolidine-3,5'-tetracyclo[5.5.2.0^{1,9}.0^{3,7}]tetradecane]-2,5,13'-trione

> <JCHEM_LOGP>
0.4844717876666657

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
5

> <JCHEM_PHYSIOLOGICAL_CHARGE>
1

> <JCHEM_PKA_STRONGEST_ACIDIC>
19.649398262179815

> <JCHEM_PKA_STRONGEST_BASIC>
8.828187005356707

> <JCHEM_POLAR_SURFACE_AREA>
60.93

> <JCHEM_REFRACTIVITY>
96.15679999999996

> <JCHEM_ROTATABLE_BOND_COUNT>
0

> <JCHEM_RULE_OF_FIVE>
1

> <JCHEM_TRADITIONAL_IUPAC>
(1'R,3S,3'S,7'R,12'S)-1,4',4',12',14'-pentamethyl-9',14'-diazaspiro[pyrrolidine-3,5'-tetracyclo[5.5.2.0^{1,9}.0^{3,7}]tetradecane]-2,5,13'-trione

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 03-SEP-22   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   03-SEP-22         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  N   UNK     0       1.592   2.227   0.000  0.00  0.00           N+0
HETATM    6  C   UNK     0       3.043   3.183   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0       4.430   2.167   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0       5.964   2.580   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0       6.969   1.379   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0       7.848   2.644   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0       9.322   2.198   0.000  0.00  0.00           C+0
HETATM   12  O   UNK     0      10.549   3.129   0.000  0.00  0.00           O+0
HETATM   13  N   UNK     0       9.354   0.658   0.000  0.00  0.00           N+0
HETATM   14  C   UNK     0      10.618  -0.221   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0       7.899   0.152   0.000  0.00  0.00           C+0
HETATM   16  O   UNK     0       7.454  -1.322   0.000  0.00  0.00           O+0
HETATM   17  C   UNK     0       6.011   0.138   0.000  0.00  0.00           C+0
HETATM   18  C   UNK     0       7.358  -0.609   0.000  0.00  0.00           C+0
HETATM   19  C   UNK     0       5.473  -1.305   0.000  0.00  0.00           C+0
HETATM   20  C   UNK     0       4.447   0.466   0.000  0.00  0.00           C+0
HETATM   21  C   UNK     0       3.012  -0.489   0.000  0.00  0.00           C+0
HETATM   22  C   UNK     0       1.600   0.518   0.000  0.00  0.00           C+0
HETATM   23  C   UNK     0       3.053   0.644   0.000  0.00  0.00           C+0
HETATM   24  O   UNK     0       4.218  -0.362   0.000  0.00  0.00           O+0
HETATM   25  N   UNK     0       2.969   2.049   0.000  0.00  0.00           N+0
HETATM   26  C   UNK     0       1.807   3.059   0.000  0.00  0.00           C+0
CONECT    1    2                                                            
CONECT    2    1    3   22                                                  
CONECT    3    2    4                                                       
CONECT    4    3    5                                                       
CONECT    5    4    6   22                                                  
CONECT    6    5    7                                                       
CONECT    7    6    8   20   25                                             
CONECT    8    7    9                                                       
CONECT    9    8   10   15   17                                             
CONECT   10    9   11                                                       
CONECT   11   10   12   13                                                  
CONECT   12   11                                                            
CONECT   13   11   14   15                                                  
CONECT   14   13                                                            
CONECT   15   13    9   16                                                  
CONECT   16   15                                                            
CONECT   17    9   18   19   20                                             
CONECT   18   17                                                            
CONECT   19   17                                                            
CONECT   20   17    7   21                                                  
CONECT   21   20   22                                                       
CONECT   22   21    2    5   23                                             
CONECT   23   22   24   25                                                  
CONECT   24   23                                                            
CONECT   25   23    7   26                                                  
CONECT   26   25                                                            
MASTER        0    0    0    0    0    0    0    0   26    0   60    0
END

View in JSmol

Synonyms

Value	Source
Aspergillimide	MeSH

Chemical Formula

C₂₀H₂₉N₃O₃

Average Mass

359.4700 Da

Monoisotopic Mass

359.22089 Da

IUPAC Name

Not Available

Traditional Name

Not Available

CAS Registry Number

Not Available

SMILES

C[C@H]1CCN2C[C@@]34C[C@]5(CC(=O)N(C)C5=O)C(C)(C)[C@@H]3C[C@]12C(=O)N4C

InChI Identifier

InChI=1S/C20H29N3O3/c1-12-6-7-23-11-19-10-18(9-14(24)21(4)15(18)25)17(2,3)13(19)8-20(12,23)16(26)22(19)5/h12-13H,6-11H2,1-5H3/t12-,13-,18-,19-,20+/m0/s1

InChI Key

RTNMRJRMTGSUAE-ASTIPKKCSA-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
Carboxylic acid imide, n-substituted
N-alkylpyrrolidine
Piperazine
Piperidine
2-pyrrolidone
Pyrrolidone
Carboxylic acid imide
Dicarboximide
Tertiary carboxylic acid amide
Pyrrolidine
Amino acid or derivatives
Tertiary amine
Lactam
Tertiary aliphatic amine
Carboxamide group
Azacycle
Carboxylic acid derivative
Organooxygen compound
Organopnictogen compound
Organic oxide
Organic nitrogen compound
Carbonyl group
Organic oxygen compound
Hydrocarbon derivative
Amine
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

External Links

HMDB ID

Not Available

DrugBank ID

Not Available

Phenol Explorer Compound ID

Not Available

FoodDB ID

Not Available

KNApSAcK ID

C00016379

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

139585852

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

Hirata K: Studies on the mode of action of neurotoxic insecticides. J Pestic Sci. 2016 Aug 20;41(3):87-94. doi: 10.1584/jpestics.J16-01. [PubMed:30363149 ]
Hirata K, Kataoka S, Furutani S, Hayashi H, Matsuda K: A fungal metabolite asperparaline a strongly and selectively blocks insect nicotinic acetylcholine receptors: the first report on the mode of action. PLoS One. 2011 Apr 1;6(4):e18354. doi: 10.1371/journal.pone.0018354. [PubMed:21483774 ]
Gray CR, Sanz-Cervera JF, Silks LA, Williams RM: Studies on the biosynthesis of asperparaline A: origin of the spirosuccinimde ring system. J Am Chem Soc. 2003 Dec 3;125(48):14692-3. doi: 10.1021/ja037687i. [PubMed:14640629 ]
LOTUS database [Link]

Showing NP-Card for (1'r,3s,3's,7'r,12's)-1,4',4',12',14'-pentamethyl-9',14'-diazaspiro[pyrrolidine-3,5'-tetracyclo[5.5.2.0¹,⁹.0³,⁷]tetradecane]-2,5,13'-trione (NP0177859)

MOL for NP0177859 ((1'r,3s,3's,7'r,12's)-1,4',4',12',14'-pentamethyl-9',14'-diazaspiro[pyrrolidine-3,5'-tetracyclo[5.5.2.0¹,⁹.0³,⁷]tetradecane]-2,5,13'-trione)

3D MOL for NP0177859 ((1'r,3s,3's,7'r,12's)-1,4',4',12',14'-pentamethyl-9',14'-diazaspiro[pyrrolidine-3,5'-tetracyclo[5.5.2.0¹,⁹.0³,⁷]tetradecane]-2,5,13'-trione)

3D SDF for NP0177859 ((1'r,3s,3's,7'r,12's)-1,4',4',12',14'-pentamethyl-9',14'-diazaspiro[pyrrolidine-3,5'-tetracyclo[5.5.2.0¹,⁹.0³,⁷]tetradecane]-2,5,13'-trione)

3D-SDF for NP0177859 ((1'r,3s,3's,7'r,12's)-1,4',4',12',14'-pentamethyl-9',14'-diazaspiro[pyrrolidine-3,5'-tetracyclo[5.5.2.0¹,⁹.0³,⁷]tetradecane]-2,5,13'-trione)

PDB for NP0177859 ((1'r,3s,3's,7'r,12's)-1,4',4',12',14'-pentamethyl-9',14'-diazaspiro[pyrrolidine-3,5'-tetracyclo[5.5.2.0¹,⁹.0³,⁷]tetradecane]-2,5,13'-trione)

3D PDB for NP0177859 ((1'r,3s,3's,7'r,12's)-1,4',4',12',14'-pentamethyl-9',14'-diazaspiro[pyrrolidine-3,5'-tetracyclo[5.5.2.0¹,⁹.0³,⁷]tetradecane]-2,5,13'-trione)

SMILES for NP0177859 ((1'r,3s,3's,7'r,12's)-1,4',4',12',14'-pentamethyl-9',14'-diazaspiro[pyrrolidine-3,5'-tetracyclo[5.5.2.0¹,⁹.0³,⁷]tetradecane]-2,5,13'-trione)

INCHI for NP0177859 ((1'r,3s,3's,7'r,12's)-1,4',4',12',14'-pentamethyl-9',14'-diazaspiro[pyrrolidine-3,5'-tetracyclo[5.5.2.0¹,⁹.0³,⁷]tetradecane]-2,5,13'-trione)

Structure for NP0177859 ((1'r,3s,3's,7'r,12's)-1,4',4',12',14'-pentamethyl-9',14'-diazaspiro[pyrrolidine-3,5'-tetracyclo[5.5.2.0¹,⁹.0³,⁷]tetradecane]-2,5,13'-trione)

3D Structure for NP0177859 ((1'r,3s,3's,7'r,12's)-1,4',4',12',14'-pentamethyl-9',14'-diazaspiro[pyrrolidine-3,5'-tetracyclo[5.5.2.0¹,⁹.0³,⁷]tetradecane]-2,5,13'-trione)