NP-MRD: Showing NP-Card for 2,13'-dihydroxy-4',4'-dimethyl-9',14'-diazaspiro[indole-3,5'-tetracyclo[5.5.2.0¹,⁹.0³,⁷]tetradecan]-13'-en-8'-one (NP0215548)

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Record Information

Version

2.0

Created at

2022-09-05 15:12:22 UTC

Updated at

2022-09-05 15:12:22 UTC

NP-MRD ID

NP0215548

Secondary Accession Numbers

None

Natural Product Identification

Common Name

2,13'-dihydroxy-4',4'-dimethyl-9',14'-diazaspiro[indole-3,5'-tetracyclo[5.5.2.0¹,⁹.0³,⁷]tetradecan]-13'-en-8'-one

Description

2,13'-Dihydroxy-4',4'-dimethyl-9',14'-diazaspiro[indole-3,5'-tetracyclo[5.5.2.0¹,⁹.0³,⁷]Tetradecan]-13'-en-8'-one 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. 2,13'-dihydroxy-4',4'-dimethyl-9',14'-diazaspiro[indole-3,5'-tetracyclo[5.5.2.0¹,⁹.0³,⁷]tetradecan]-13'-en-8'-one is found in Penicillium brevicompactum. Based on a literature review very few articles have been published on 2,13'-dihydroxy-4',4'-dimethyl-9',14'-diazaspiro[indole-3,5'-tetracyclo[5.5.2.0¹,⁹.0³,⁷]Tetradecan]-13'-en-8'-one.

Structure

MOL 3D MOL SDF PDB SMILES InChI


  Mrv1652309052217122D          

 27 32  0  0  0  0            999 V2000
    6.3728    1.2848    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.5774    1.5038    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.4672    0.6861    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.7211    1.5032    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.1114    0.8002    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.2488    1.1233    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.5173    0.6884    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.8255    1.1625    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1397    1.9412    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.9939    1.9982    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    3.5960    2.6986    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.3861    3.4964    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.4698    2.3834    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.2321    2.7774    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.9065    2.2754    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.2016    3.0459    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.7517    3.7374    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    7.0255    3.0033    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    7.2396    2.2066    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.9750    1.8326    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.0188    1.0088    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.3272    0.5589    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.5919    0.9329    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.5480    1.7567    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.7389    2.1081    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    3.9851    1.3956    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.7309    1.0428    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
  2  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  0  0  0  0
  8  9  1  0  0  0  0
  9 10  1  0  0  0  0
  6 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
  4 13  1  0  0  0  0
 13 14  1  0  0  0  0
 14 15  1  0  0  0  0
  2 15  1  0  0  0  0
 15 16  1  0  0  0  0
 16 17  1  0  0  0  0
 16 18  2  0  0  0  0
 18 19  1  0  0  0  0
 19 20  2  0  0  0  0
 20 21  1  0  0  0  0
 21 22  2  0  0  0  0
 22 23  1  0  0  0  0
 23 24  2  0  0  0  0
 19 24  1  0  0  0  0
 15 24  1  0  0  0  0
 13 25  1  0  0  0  0
 25 26  2  0  0  0  0
  6 26  1  0  0  0  0
 26 27  1  0  0  0  0
M  END

     RDKit          3D

 50 55  0  0  0  0  0  0  0  0999 V2000
   -1.6810   -1.6469   -0.7214 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8078   -0.8047    0.1971 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5423   -1.6094    1.4207 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.3667   -0.3056   -0.5324 C   0  0  2  0  0  0  0  0  0  0  0  0
    1.5899   -1.1368   -0.5303 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.7807   -0.1669   -0.5379 C   0  0  2  0  0  0  0  0  0  0  0  0
    4.0695   -0.8087   -0.8045 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.9930   -0.1906    0.2238 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.0842    0.0011    1.4458 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8233    0.3390    0.8545 N   0  0  0  0  0  0  0  0  0  0  0  0
    1.6104    1.0020    1.1779 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.3171    1.5013    2.2717 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.6491    1.0661    0.0504 C   0  0  2  0  0  0  0  0  0  0  0  0
   -0.6486    1.6368    0.3237 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5800    0.4673    0.5496 C   0  0  2  0  0  0  0  0  0  0  0  0
   -2.0761    0.4169    1.9422 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3858    0.2835    3.1416 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.3555    0.5214    1.9196 N   0  0  0  0  0  0  0  0  0  0  0  0
   -3.8457    0.6468    0.5935 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.1501    0.7801    0.1571 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.3755    0.8872   -1.2161 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.3060    0.8572   -2.0817 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.0133    0.7228   -1.6137 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7816    0.6175   -0.2757 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4230    1.7259   -1.0232 N   0  0  0  0  0  0  0  0  0  0  0  0
    2.4694    1.0277   -1.3657 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.2658    1.3768   -2.4558 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7509   -1.4983   -0.5279 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4035   -1.4834   -1.7954 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4649   -2.7262   -0.5259 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2525   -2.6610    1.1755 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.1499   -1.1637    2.1396 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5296   -1.7237    1.9588 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.0656   -0.1434   -1.6064 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.7004   -1.7983    0.3496 H   0  0  0  0  0  0  0  0  0  0  0  0
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    4.0072   -1.8899   -0.5626 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.2887    0.8115   -0.1889 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.8708   -0.7899    0.4460 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.4750    0.8069    2.0924 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.0727   -0.9697    1.9800 H   0  0  0  0  0  0  0  0  0  0  0  0
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   -1.7125   -0.2609    3.9169 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.9872    0.8027    0.8486 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.4001    0.9896   -1.5225 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.5158    0.9439   -3.1598 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2200    0.7067   -2.3503 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.2729    0.7440   -3.2491 H   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0
  2  3  1  0
  2  4  1  0
  4  5  1  0
  5  6  1  0
  6  7  1  6
  7  8  1  0
  8  9  1  0
  9 10  1  0
 10 11  1  0
 11 12  2  0
 11 13  1  0
 13 14  1  1
 14 15  1  0
 15 16  1  1
 16 17  1  0
 16 18  2  0
 18 19  1  0
 19 20  2  0
 20 21  1  0
 21 22  2  0
 22 23  1  0
 23 24  2  0
 13 25  1  0
 25 26  2  0
 26 27  1  0
 15  2  1  0
 24 15  1  0
 13  4  1  0
 24 19  1  0
 10  6  1  0
 26  6  1  0
  1 28  1  0
  1 29  1  0
  1 30  1  0
  3 31  1  0
  3 32  1  0
  3 33  1  0
  4 34  1  6
  5 35  1  0
  5 36  1  0
  7 37  1  0
  7 38  1  0
  8 39  1  0
  8 40  1  0
  9 41  1  0
  9 42  1  0
 14 43  1  0
 14 44  1  0
 17 45  1  0
 20 46  1  0
 21 47  1  0
 22 48  1  0
 23 49  1  0
 27 50  1  0
M  END


  Mrv1652309052217122D          

 27 32  0  0  0  0            999 V2000
    6.3728    1.2848    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.5774    1.5038    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.4672    0.6861    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.7211    1.5032    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.1114    0.8002    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.2488    1.1233    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.5173    0.6884    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.8255    1.1625    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1397    1.9412    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.9939    1.9982    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    3.5960    2.6986    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.3861    3.4964    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.4698    2.3834    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.2321    2.7774    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.9065    2.2754    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.2016    3.0459    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.7517    3.7374    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    7.0255    3.0033    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    7.2396    2.2066    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.9750    1.8326    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.0188    1.0088    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.3272    0.5589    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.5919    0.9329    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.5480    1.7567    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.7389    2.1081    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    3.9851    1.3956    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.7309    1.0428    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
  2  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  0  0  0  0
  8  9  1  0  0  0  0
  9 10  1  0  0  0  0
  6 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
  4 13  1  0  0  0  0
 13 14  1  0  0  0  0
 14 15  1  0  0  0  0
  2 15  1  0  0  0  0
 15 16  1  0  0  0  0
 16 17  1  0  0  0  0
 16 18  2  0  0  0  0
 18 19  1  0  0  0  0
 19 20  2  0  0  0  0
 20 21  1  0  0  0  0
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 15 24  1  0  0  0  0
 13 25  1  0  0  0  0
 25 26  2  0  0  0  0
  6 26  1  0  0  0  0
 26 27  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0215548

> <DATABASE_NAME>
NP-MRD

> <SMILES>
CC1(C)C2CC34CCCN3C(=O)C2(CC11C(O)=NC2=CC=CC=C12)N=C4O

> <INCHI_IDENTIFIER>
InChI=1S/C21H23N3O3/c1-18(2)14-10-19-8-5-9-24(19)17(27)21(14,23-15(19)25)11-20(18)12-6-3-4-7-13(12)22-16(20)26/h3-4,6-7,14H,5,8-11H2,1-2H3,(H,22,26)(H,23,25)

> <INCHI_KEY>
PZTOWERCGLXQSU-UHFFFAOYSA-N

> <FORMULA>
C21H23N3O3

> <MOLECULAR_WEIGHT>
365.433

> <EXACT_MASS>
365.173941613

> <JCHEM_ACCEPTOR_COUNT>
5

> <JCHEM_ATOM_COUNT>
50

> <JCHEM_AVERAGE_POLARIZABILITY>
38.55898533453288

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
2

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
1

> <JCHEM_IUPAC>
2,13'-dihydroxy-4',4'-dimethyl-9',14'-diazaspiro[indole-3,5'-tetracyclo[5.5.2.0^{1,9}.0^{3,7}]tetradecan]-13'-en-8'-one

> <JCHEM_LOGP>
2.6888561143333325

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
6

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA>
4.712122369322139

> <JCHEM_PKA_STRONGEST_ACIDIC>
3.9854937678388

> <JCHEM_PKA_STRONGEST_BASIC>
1.2505190895151042

> <JCHEM_POLAR_SURFACE_AREA>
85.49000000000001

> <JCHEM_REFRACTIVITY>
100.30340000000001

> <JCHEM_ROTATABLE_BOND_COUNT>
0

> <JCHEM_RULE_OF_FIVE>
1

> <JCHEM_TRADITIONAL_IUPAC>
2,13'-dihydroxy-4',4'-dimethyl-9',14'-diazaspiro[indole-3,5'-tetracyclo[5.5.2.0^{1,9}.0^{3,7}]tetradecan]-13'-en-8'-one

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 05-SEP-22   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   05-SEP-22         0                                  
HETATM    1  C   UNK     0      11.896   2.398   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0      10.411   2.807   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0      10.205   1.281   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0       8.813   2.806   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0       7.675   1.494   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0       6.064   2.097   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0       4.699   1.285   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0       3.408   2.170   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0       3.994   3.624   0.000  0.00  0.00           C+0
HETATM   10  N   UNK     0       5.589   3.730   0.000  0.00  0.00           N+0
HETATM   11  C   UNK     0       6.712   5.037   0.000  0.00  0.00           C+0
HETATM   12  O   UNK     0       6.321   6.527   0.000  0.00  0.00           O+0
HETATM   13  C   UNK     0       8.344   4.449   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0       9.767   5.184   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0      11.025   4.247   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0      11.576   5.686   0.000  0.00  0.00           C+0
HETATM   17  O   UNK     0      10.737   6.977   0.000  0.00  0.00           O+0
HETATM   18  N   UNK     0      13.114   5.606   0.000  0.00  0.00           N+0
HETATM   19  C   UNK     0      13.514   4.119   0.000  0.00  0.00           C+0
HETATM   20  C   UNK     0      14.887   3.421   0.000  0.00  0.00           C+0
HETATM   21  C   UNK     0      14.968   1.883   0.000  0.00  0.00           C+0
HETATM   22  C   UNK     0      13.677   1.043   0.000  0.00  0.00           C+0
HETATM   23  C   UNK     0      12.305   1.741   0.000  0.00  0.00           C+0
HETATM   24  C   UNK     0      12.223   3.279   0.000  0.00  0.00           C+0
HETATM   25  N   UNK     0       6.979   3.935   0.000  0.00  0.00           N+0
HETATM   26  C   UNK     0       7.439   2.605   0.000  0.00  0.00           C+0
HETATM   27  O   UNK     0       8.831   1.947   0.000  0.00  0.00           O+0
CONECT    1    2                                                            
CONECT    2    1    3    4   15                                             
CONECT    3    2                                                            
CONECT    4    2    5   13                                                  
CONECT    5    4    6                                                       
CONECT    6    5    7   10   26                                             
CONECT    7    6    8                                                       
CONECT    8    7    9                                                       
CONECT    9    8   10                                                       
CONECT   10    9    6   11                                                  
CONECT   11   10   12   13                                                  
CONECT   12   11                                                            
CONECT   13   11    4   14   25                                             
CONECT   14   13   15                                                       
CONECT   15   14    2   16   24                                             
CONECT   16   15   17   18                                                  
CONECT   17   16                                                            
CONECT   18   16   19                                                       
CONECT   19   18   20   24                                                  
CONECT   20   19   21                                                       
CONECT   21   20   22                                                       
CONECT   22   21   23                                                       
CONECT   23   22   24                                                       
CONECT   24   23   19   15                                                  
CONECT   25   13   26                                                       
CONECT   26   25    6   27                                                  
CONECT   27   26                                                            
MASTER        0    0    0    0    0    0    0    0   27    0   64    0
END

View in JSmol

Synonyms

Not Available

Chemical Formula

C₂₁H₂₃N₃O₃

Average Mass

365.4330 Da

Monoisotopic Mass

365.17394 Da

IUPAC Name

Not Available

Traditional Name

Not Available

CAS Registry Number

Not Available

SMILES

CC1(C)C2CC34CCCN3C(=O)C2(CC11C(O)=NC2=CC=CC=C12)N=C4O

InChI Identifier

InChI=1S/C21H23N3O3/c1-18(2)14-10-19-8-5-9-24(19)17(27)21(14,23-15(19)25)11-20(18)12-6-3-4-7-13(12)22-16(20)26/h3-4,6-7,14H,5,8-11H2,1-2H3,(H,22,26)(H,23,25)

InChI Key

PZTOWERCGLXQSU-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
Penicillium brevicompactum	LOTUS Database	35616633

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

Azaspirodecane
Alpha-amino acid or derivatives
Indolizidine
Dihydroindole
Indole or derivatives
2,5-dioxopiperazine
Dioxopiperazine
N-alkylpiperazine
Piperidinone
Delta-lactam
Benzenoid
Piperidine
Piperazine
1,4-diazinane
Tertiary carboxylic acid amide
Pyrrolidine
Secondary carboxylic acid amide
Lactam
Carboxamide group
Azacycle
Carboxylic acid derivative
Organic nitrogen compound
Organic oxygen compound
Organopnictogen compound
Organic oxide
Hydrocarbon derivative
Organooxygen compound
Organonitrogen compound
Carbonyl group
Aromatic heteropolycyclic compound

Molecular Framework

Aromatic 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

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

162815428

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

LOTUS database [Link]

Showing NP-Card for 2,13'-dihydroxy-4',4'-dimethyl-9',14'-diazaspiro[indole-3,5'-tetracyclo[5.5.2.0¹,⁹.0³,⁷]tetradecan]-13'-en-8'-one (NP0215548)

MOL for NP0215548 (2,13'-dihydroxy-4',4'-dimethyl-9',14'-diazaspiro[indole-3,5'-tetracyclo[5.5.2.0¹,⁹.0³,⁷]tetradecan]-13'-en-8'-one)

3D MOL for NP0215548 (2,13'-dihydroxy-4',4'-dimethyl-9',14'-diazaspiro[indole-3,5'-tetracyclo[5.5.2.0¹,⁹.0³,⁷]tetradecan]-13'-en-8'-one)

3D SDF for NP0215548 (2,13'-dihydroxy-4',4'-dimethyl-9',14'-diazaspiro[indole-3,5'-tetracyclo[5.5.2.0¹,⁹.0³,⁷]tetradecan]-13'-en-8'-one)

3D-SDF for NP0215548 (2,13'-dihydroxy-4',4'-dimethyl-9',14'-diazaspiro[indole-3,5'-tetracyclo[5.5.2.0¹,⁹.0³,⁷]tetradecan]-13'-en-8'-one)

PDB for NP0215548 (2,13'-dihydroxy-4',4'-dimethyl-9',14'-diazaspiro[indole-3,5'-tetracyclo[5.5.2.0¹,⁹.0³,⁷]tetradecan]-13'-en-8'-one)

3D PDB for NP0215548 (2,13'-dihydroxy-4',4'-dimethyl-9',14'-diazaspiro[indole-3,5'-tetracyclo[5.5.2.0¹,⁹.0³,⁷]tetradecan]-13'-en-8'-one)

SMILES for NP0215548 (2,13'-dihydroxy-4',4'-dimethyl-9',14'-diazaspiro[indole-3,5'-tetracyclo[5.5.2.0¹,⁹.0³,⁷]tetradecan]-13'-en-8'-one)

INCHI for NP0215548 (2,13'-dihydroxy-4',4'-dimethyl-9',14'-diazaspiro[indole-3,5'-tetracyclo[5.5.2.0¹,⁹.0³,⁷]tetradecan]-13'-en-8'-one)

Structure for NP0215548 (2,13'-dihydroxy-4',4'-dimethyl-9',14'-diazaspiro[indole-3,5'-tetracyclo[5.5.2.0¹,⁹.0³,⁷]tetradecan]-13'-en-8'-one)

3D Structure for NP0215548 (2,13'-dihydroxy-4',4'-dimethyl-9',14'-diazaspiro[indole-3,5'-tetracyclo[5.5.2.0¹,⁹.0³,⁷]tetradecan]-13'-en-8'-one)