NP-MRD: Showing NP-Card for 2-(hydroxymethyl)-1'-methyl-3-(2-oxopropyl)-8-azaspiro[bicyclo[3.2.1]octane-6,3'-indol]-2'-one (NP0153448)

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Record Information

Version

2.0

Created at

2022-09-02 10:06:20 UTC

Updated at

2022-09-02 10:06:20 UTC

NP-MRD ID

NP0153448

Secondary Accession Numbers

None

Natural Product Identification

Common Name

2-(hydroxymethyl)-1'-methyl-3-(2-oxopropyl)-8-azaspiro[bicyclo[3.2.1]octane-6,3'-indol]-2'-one

Description

2-(Hydroxymethyl)-1'-methyl-3-(2-oxopropyl)-1',2'-dihydro-8-azaspiro[bicyclo[3.2.1]Octane-6,3'-indole]-2'-one belongs to the class of organic compounds known as beta amino acids and derivatives. These are amino acids having a (-NH2) group attached to the beta carbon atom. 2-(hydroxymethyl)-1'-methyl-3-(2-oxopropyl)-8-azaspiro[bicyclo[3.2.1]octane-6,3'-indol]-2'-one is found in Alstonia angustifolia and Alstonia macrophylla. 2-(Hydroxymethyl)-1'-methyl-3-(2-oxopropyl)-1',2'-dihydro-8-azaspiro[bicyclo[3.2.1]Octane-6,3'-indole]-2'-one is a very strong basic compound (based on its pKa).

Structure

MOL 3D MOL SDF PDB SMILES InChI

     RDKit          3D

 48 51  0  0  0  0  0  0  0  0999 V2000
    4.6933    2.8605    0.0584 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5898    1.8992    0.4305 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.9478    2.1878    1.4239 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.3540    0.6973   -0.4024 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1873   -0.0582    0.0624 C   0  0  1  0  0  0  0  0  0  0  0  0
    0.8532    0.7067    0.0100 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1458    0.0087    0.8916 C   0  0  2  0  0  0  0  0  0  0  0  0
    0.4624   -1.2681    1.2471 N   0  0  0  0  0  0  0  0  0  0  0  0
    0.6039   -1.8724   -0.0582 C   0  0  1  0  0  0  0  0  0  0  0  0
   -0.5978   -1.4019   -0.8921 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3067   -0.4913    0.0613 C   0  0  1  0  0  0  0  0  0  0  0  0
   -2.2033   -1.3533    0.8762 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9652   -2.5129    1.3788 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.4222   -0.6721    1.0218 N   0  0  0  0  0  0  0  0  0  0  0  0
   -4.5343   -1.0595    1.8951 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.3822    0.4731    0.1599 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.3957    1.3848   -0.1157 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.2525    2.3735   -1.0563 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.0552    2.4402   -1.7339 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0389    1.5276   -1.4563 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1765    0.5228   -0.5001 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.9099   -1.3483   -0.6859 C   0  0  2  0  0  0  0  0  0  0  0  0
    3.0019   -2.3520   -0.5178 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.6533   -3.5468   -1.1406 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.2600    3.8607   -0.0231 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.4348    2.8801    0.8808 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.1838    2.4956   -0.8537 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.3152    0.1084   -0.3405 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.2868    0.9604   -1.4844 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.2902   -0.3570    1.1373 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.0254    1.7198    0.3972 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.6006    0.7119   -1.0576 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4395    0.5964    1.7581 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.0603   -1.7898    1.9879 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.6560   -2.9614    0.0157 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2847   -0.8855   -1.7818 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2235   -2.2930   -1.1458 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.4502   -0.9263    1.2829 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.4631   -2.1551    2.1215 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.5387   -0.5241    2.8434 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.3171    1.3114    0.4252 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.0697    3.0550   -1.2310 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.9361    3.2225   -2.4829 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1413    1.6367   -2.0356 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.6856   -1.1135   -1.7363 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.9350   -2.0068   -0.9603 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.1316   -2.5184    0.5717 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.2179   -4.1732   -0.4820 H   0  0  0  0  0  0  0  0  0  0  0  0
 15 14  1  0
 14 12  1  0
 12 13  2  0
 11 12  1  1
 11 10  1  0
 10  9  1  0
  9  8  1  0
  8  7  1  0
  7  6  1  0
  6  5  1  0
  5  4  1  0
  4  2  1  0
  2  1  1  0
  2  3  2  0
  5 22  1  0
 22 23  1  0
 23 24  1  0
 11 21  1  0
 21 20  2  0
 20 19  1  0
 19 18  2  0
 18 17  1  0
 17 16  2  0
 16 14  1  0
  7 11  1  0
 16 21  1  0
 22  9  1  0
 15 38  1  0
 15 39  1  0
 15 40  1  0
 10 36  1  0
 10 37  1  0
  9 35  1  1
  8 34  1  0
  7 33  1  1
  6 31  1  0
  6 32  1  0
  5 30  1  1
  4 28  1  0
  4 29  1  0
  1 25  1  0
  1 26  1  0
  1 27  1  0
 22 45  1  6
 23 46  1  0
 23 47  1  0
 24 48  1  0
 20 44  1  0
 19 43  1  0
 18 42  1  0
 17 41  1  0
M  END


  Mrv1533004191513532D          

 24 27  0  0  0  0            999 V2000
   -0.1197    0.6764    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.2130   -0.0786    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    1.0193   -0.2532    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.6345    0.2965    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.1024   -1.0740    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.0376   -1.8964    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.6402   -2.4598    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.9440   -1.5540    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    1.7858   -0.6118    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.5732   -0.8580    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8717   -1.6271    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.6942   -1.6919    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.0493   -2.4365    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.8717   -2.5013    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.5820   -3.1164    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.4565   -2.3400    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.9186   -3.0234    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.5579   -3.7653    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.3474   -1.4067    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0895   -2.1903    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7181   -2.3588    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2678   -1.7436    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0099   -0.9599    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2023   -0.7915    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  2  0  0  0  0
  3  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
  5  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  1  0  0  0  0
 13 14  2  0  0  0  0
 13 15  1  0  0  0  0
 11 16  1  0  0  0  0
  7 16  1  0  0  0  0
 16 17  1  0  0  0  0
 17 18  1  0  0  0  0
  5 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
  2 24  1  0  0  0  0
 19 24  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0153448

> <DATABASE_NAME>
NP-MRD

> <SMILES>
CN1C(=O)C2(CC3NC2CC(CC(C)=O)C3CO)C2=CC=CC=C12

> <INCHI_IDENTIFIER>
InChI=1S/C19H24N2O3/c1-11(23)7-12-8-17-19(9-15(20-17)13(12)10-22)14-5-3-4-6-16(14)21(2)18(19)24/h3-6,12-13,15,17,20,22H,7-10H2,1-2H3

> <INCHI_KEY>
OBKLTAKGMJSCGE-UHFFFAOYSA-N

> <FORMULA>
C19H24N2O3

> <MOLECULAR_WEIGHT>
328.412

> <EXACT_MASS>
328.178692641

> <JCHEM_ACCEPTOR_COUNT>
4

> <JCHEM_ATOM_COUNT>
48

> <JCHEM_AVERAGE_POLARIZABILITY>
35.81736328358431

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
2

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
1

> <JCHEM_IUPAC>
2-(hydroxymethyl)-1'-methyl-3-(2-oxopropyl)-1',2'-dihydro-8-azaspiro[bicyclo[3.2.1]octane-6,3'-indole]-2'-one

> <ALOGPS_LOGP>
0.64

> <JCHEM_LOGP>
0.2872341206666667

> <ALOGPS_LOGS>
-2.63

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
4

> <JCHEM_PHYSIOLOGICAL_CHARGE>
1

> <JCHEM_PKA>
19.20552669413404

> <JCHEM_PKA_STRONGEST_ACIDIC>
15.413187806337113

> <JCHEM_PKA_STRONGEST_BASIC>
9.810329545518163

> <JCHEM_POLAR_SURFACE_AREA>
69.64

> <JCHEM_REFRACTIVITY>
90.40150000000001

> <JCHEM_ROTATABLE_BOND_COUNT>
3

> <JCHEM_RULE_OF_FIVE>
1

> <ALOGPS_SOLUBILITY>
7.77e-01 g/l

> <JCHEM_TRADITIONAL_IUPAC>
2-(hydroxymethyl)-1'-methyl-3-(2-oxopropyl)-8-azaspiro[bicyclo[3.2.1]octane-6,3'-indole]-2'-one

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 19-APR-15   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   19-APR-15         0                                  
HETATM    1  C   UNK     0      -0.224   1.263   0.000  0.00  0.00           C+0
HETATM    2  N   UNK     0       0.398  -0.147   0.000  0.00  0.00           N+0
HETATM    3  C   UNK     0       1.903  -0.473   0.000  0.00  0.00           C+0
HETATM    4  O   UNK     0       3.051   0.554   0.000  0.00  0.00           O+0
HETATM    5  C   UNK     0       2.058  -2.005   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0       1.937  -3.540   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0       3.062  -4.592   0.000  0.00  0.00           C+0
HETATM    8  N   UNK     0       3.629  -2.901   0.000  0.00  0.00           N+0
HETATM    9  C   UNK     0       3.333  -1.142   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0       4.803  -1.602   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0       5.361  -3.037   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0       6.896  -3.158   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0       7.559  -4.548   0.000  0.00  0.00           C+0
HETATM   14  O   UNK     0       9.094  -4.669   0.000  0.00  0.00           O+0
HETATM   15  C   UNK     0       6.686  -5.817   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0       4.585  -4.368   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0       5.448  -5.644   0.000  0.00  0.00           C+0
HETATM   18  O   UNK     0       4.775  -7.029   0.000  0.00  0.00           O+0
HETATM   19  C   UNK     0       0.649  -2.626   0.000  0.00  0.00           C+0
HETATM   20  C   UNK     0       0.167  -4.089   0.000  0.00  0.00           C+0
HETATM   21  C   UNK     0      -1.340  -4.403   0.000  0.00  0.00           C+0
HETATM   22  C   UNK     0      -2.367  -3.255   0.000  0.00  0.00           C+0
HETATM   23  C   UNK     0      -1.885  -1.792   0.000  0.00  0.00           C+0
HETATM   24  C   UNK     0      -0.378  -1.477   0.000  0.00  0.00           C+0
CONECT    1    2                                                            
CONECT    2    1    3   24                                                  
CONECT    3    2    4    5                                                  
CONECT    4    3                                                            
CONECT    5    3    6    9   19                                             
CONECT    6    5    7                                                       
CONECT    7    6    8   16                                                  
CONECT    8    7    9                                                       
CONECT    9    8    5   10                                                  
CONECT   10    9   11                                                       
CONECT   11   10   12   16                                                  
CONECT   12   11   13                                                       
CONECT   13   12   14   15                                                  
CONECT   14   13                                                            
CONECT   15   13                                                            
CONECT   16   11    7   17                                                  
CONECT   17   16   18                                                       
CONECT   18   17                                                            
CONECT   19    5   20   24                                                  
CONECT   20   19   21                                                       
CONECT   21   20   22                                                       
CONECT   22   21   23                                                       
CONECT   23   22   24                                                       
CONECT   24   23    2   19                                                  
MASTER        0    0    0    0    0    0    0    0   24    0   54    0
END

View in JSmol

Synonyms

Not Available

Chemical Formula

C₁₉H₂₄N₂O₃

Average Mass

328.4120 Da

Monoisotopic Mass

328.17869 Da

IUPAC Name

2-(hydroxymethyl)-1'-methyl-3-(2-oxopropyl)-1',2'-dihydro-8-azaspiro[bicyclo[3.2.1]octane-6,3'-indole]-2'-one

Traditional Name

2-(hydroxymethyl)-1'-methyl-3-(2-oxopropyl)-8-azaspiro[bicyclo[3.2.1]octane-6,3'-indole]-2'-one

CAS Registry Number

Not Available

SMILES

CN1C(=O)C2(CC3NC2CC(CC(C)=O)C3CO)C2=CC=CC=C12

InChI Identifier

InChI=1S/C19H24N2O3/c1-11(23)7-12-8-17-19(9-15(20-17)13(12)10-22)14-5-3-4-6-16(14)21(2)18(19)24/h3-6,12-13,15,17,20,22H,7-10H2,1-2H3

InChI Key

OBKLTAKGMJSCGE-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
Alstonia angustifolia	LOTUS Database	35616633
Alstonia macrophylla	LOTUS Database	35616633

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as beta amino acids and derivatives. These are amino acids having a (-NH2) group attached to the beta carbon atom.

Kingdom

Organic compounds

Super Class

Organic acids and derivatives

Class

Carboxylic acids and derivatives

Sub Class

Amino acids, peptides, and analogues

Direct Parent

Beta amino acids and derivatives

Alternative Parents

Substituents

Beta amino acid or derivatives
Indole or derivatives
Aralkylamine
Piperidine
Benzenoid
1,3-aminoalcohol
Pyrrolidine
Tertiary carboxylic acid amide
Carboxamide group
Ketone
Lactam
Secondary aliphatic amine
Azacycle
Secondary amine
Organoheterocyclic compound
Primary alcohol
Hydrocarbon derivative
Organooxygen compound
Organonitrogen compound
Amine
Alcohol
Organic oxide
Organic nitrogen compound
Carbonyl group
Organic oxygen compound
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
logP	0.64	ALOGPS
logP	0.29	ChemAxon
logS	-2.6	ALOGPS
pKa (Strongest Acidic)	15.41	ChemAxon
pKa (Strongest Basic)	9.81	ChemAxon
Physiological Charge	1	ChemAxon
Hydrogen Acceptor Count	4	ChemAxon
Hydrogen Donor Count	2	ChemAxon
Polar Surface Area	69.64 Å²	ChemAxon
Rotatable Bond Count	3	ChemAxon
Refractivity	90.4 m³·mol⁻¹	ChemAxon
Polarizability	35.82 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

85448529

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

LOTUS database [Link]

Showing NP-Card for 2-(hydroxymethyl)-1'-methyl-3-(2-oxopropyl)-8-azaspiro[bicyclo[3.2.1]octane-6,3'-indol]-2'-one (NP0153448)

MOL for NP0153448 (2-(hydroxymethyl)-1'-methyl-3-(2-oxopropyl)-8-azaspiro[bicyclo[3.2.1]octane-6,3'-indol]-2'-one)

3D MOL for NP0153448 (2-(hydroxymethyl)-1'-methyl-3-(2-oxopropyl)-8-azaspiro[bicyclo[3.2.1]octane-6,3'-indol]-2'-one)

3D SDF for NP0153448 (2-(hydroxymethyl)-1'-methyl-3-(2-oxopropyl)-8-azaspiro[bicyclo[3.2.1]octane-6,3'-indol]-2'-one)

3D-SDF for NP0153448 (2-(hydroxymethyl)-1'-methyl-3-(2-oxopropyl)-8-azaspiro[bicyclo[3.2.1]octane-6,3'-indol]-2'-one)

PDB for NP0153448 (2-(hydroxymethyl)-1'-methyl-3-(2-oxopropyl)-8-azaspiro[bicyclo[3.2.1]octane-6,3'-indol]-2'-one)

3D PDB for NP0153448 (2-(hydroxymethyl)-1'-methyl-3-(2-oxopropyl)-8-azaspiro[bicyclo[3.2.1]octane-6,3'-indol]-2'-one)

SMILES for NP0153448 (2-(hydroxymethyl)-1'-methyl-3-(2-oxopropyl)-8-azaspiro[bicyclo[3.2.1]octane-6,3'-indol]-2'-one)

INCHI for NP0153448 (2-(hydroxymethyl)-1'-methyl-3-(2-oxopropyl)-8-azaspiro[bicyclo[3.2.1]octane-6,3'-indol]-2'-one)

Structure for NP0153448 (2-(hydroxymethyl)-1'-methyl-3-(2-oxopropyl)-8-azaspiro[bicyclo[3.2.1]octane-6,3'-indol]-2'-one)

3D Structure for NP0153448 (2-(hydroxymethyl)-1'-methyl-3-(2-oxopropyl)-8-azaspiro[bicyclo[3.2.1]octane-6,3'-indol]-2'-one)