NP-MRD: Showing NP-Card for (1's,2'r,7'r,9's)-6'-acetyl-1-methyl-2-oxo-4'-oxa-12'-azaspiro[indole-3,10'-tricyclo[7.2.1.0²,⁷]dodecan]-5'-ene-12'-carbaldehyde (NP0246297)

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Record Information

Version

2.0

Created at

2022-09-07 07:43:03 UTC

Updated at

2022-09-07 07:43:03 UTC

NP-MRD ID

NP0246297

Secondary Accession Numbers

None

Natural Product Identification

Common Name

(1's,2'r,7'r,9's)-6'-acetyl-1-methyl-2-oxo-4'-oxa-12'-azaspiro[indole-3,10'-tricyclo[7.2.1.0²,⁷]dodecan]-5'-ene-12'-carbaldehyde

Description

(1'S,2'R,7'R,9'S)-6'-acetyl-1-methyl-2-oxo-1,2-dihydro-4'-oxa-12'-azaspiro[indole-3,10'-tricyclo[7.2.1.0²,⁷]Dodecan]-5'-ene-12'-carbaldehyde belongs to the class of organic compounds known as indoles and derivatives. These are organic compounds containing an indole, which is a bicyclic ring system made up of a six-membered benzene ring fused to a five-membered nitrogen-containing pyrrole ring. (1's,2'r,7'r,9's)-6'-acetyl-1-methyl-2-oxo-4'-oxa-12'-azaspiro[indole-3,10'-tricyclo[7.2.1.0²,⁷]dodecan]-5'-ene-12'-carbaldehyde is found in Alstonia angustifolia. Based on a literature review very few articles have been published on (1'S,2'R,7'R,9'S)-6'-acetyl-1-methyl-2-oxo-1,2-dihydro-4'-oxa-12'-azaspiro[indole-3,10'-tricyclo[7.2.1.0²,⁷]Dodecan]-5'-ene-12'-carbaldehyde.

Structure

MOL 3D MOL SDF PDB SMILES InChI


  Mrv1652309072209432D          

 27 31  0  0  1  0            999 V2000
   -1.1728    2.8551    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3478    2.0086    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1671    2.2481    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9779    1.1943    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5232    0.5753    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2599   -0.2065    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4511   -0.3693    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0943    0.2497    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    0.8698   -0.0318    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    1.5734    0.3989    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.6753    1.2176    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.9218    2.0049    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.6931    2.8493    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.7467    2.0138    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    3.0620    2.8374    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.0101    1.2320    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.7674    0.9046    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.8624    0.0851    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.2003   -0.4070    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.4430   -0.0796    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.3479    0.7399    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.0988    1.8077    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    0.2779    1.7249    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1691    1.0315    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    1.2142    0.8593    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    2.1395    1.1449    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.7950    1.6077    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0  0  0  0
  2  3  2  0  0  0  0
  2  4  1  0  0  0  0
  4  5  2  0  0  0  0
  5  6  1  0  0  0  0
  6  7  1  0  0  0  0
  8  7  1  6  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
 16 17  2  0  0  0  0
 17 18  1  0  0  0  0
 18 19  2  0  0  0  0
 19 20  1  0  0  0  0
 20 21  2  0  0  0  0
 16 21  1  0  0  0  0
 11 21  1  0  0  0  0
 11 22  1  0  0  0  0
 22 23  1  0  0  0  0
 24 23  1  6  0  0  0
  4 24  1  0  0  0  0
  8 24  1  0  0  0  0
 22 25  1  6  0  0  0
  9 25  1  6  0  0  0
 25 26  1  0  0  0  0
 26 27  2  0  0  0  0
M  END

     RDKit          3D

 49 53  0  0  0  0  0  0  0  0999 V2000
    5.1103    0.6952    1.5015 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.7190    0.9808    1.0727 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.0752    1.8954    1.6221 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.0886    0.1801   -0.0106 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.7689   -0.7875   -0.5971 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.1732   -1.5208   -1.6107 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.3393   -0.7528   -2.4696 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.2059   -0.2492   -1.6087 C   0  0  1  0  0  0  0  0  0  0  0  0
    0.3420   -1.4596   -1.3107 C   0  0  2  0  0  0  0  0  0  0  0  0
   -1.1347   -1.0806   -1.4591 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4422   -0.5050   -0.0905 C   0  0  2  0  0  0  0  0  0  0  0  0
   -2.4980   -1.3409    0.5419 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4475   -2.5802    0.7417 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5649   -0.4800    0.8743 N   0  0  0  0  0  0  0  0  0  0  0  0
   -4.8265   -0.8447    1.5487 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.2208    0.8355    0.4430 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.9659    2.0226    0.5342 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.4881    3.2157    0.0436 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2629    3.2378   -0.5432 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5223    2.0532   -0.6326 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9788    0.8496   -0.1490 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2119   -0.6820    0.7525 C   0  0  2  0  0  0  0  0  0  0  0  0
    0.7489    0.4450    0.7547 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.6990    0.4807   -0.4280 C   0  0  1  0  0  0  0  0  0  0  0  0
    0.4268   -1.8029    0.0924 N   0  0  0  0  0  0  0  0  0  0  0  0
    1.0073   -2.9698    0.6285 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.5290   -3.8640   -0.0750 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.3360    1.2446    2.4131 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.8291    0.8649    0.6694 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.1444   -0.4174    1.6937 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.7938   -0.9622   -0.2399 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.9586   -1.4031   -3.2923 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.8823    0.1173   -2.8818 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.5890    0.4397   -2.2606 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.5595   -2.3159   -1.9808 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2825   -0.3482   -2.2734 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6693   -2.0372   -1.6459 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.5986   -1.5592    2.3910 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.2544    0.0643    1.9717 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.4395   -1.3453    0.7888 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.9346    2.0139    0.9962 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.0557    4.1450    0.1077 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8895    4.1684   -0.9266 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5693    2.1724   -1.1172 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4766   -0.9793    1.8005 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.4076    0.2895    1.6673 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.2572    1.4149    0.9628 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.7320    1.5798   -0.7156 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.0117   -3.1185    1.7044 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  2  0
  4 24  1  0
 24 23  1  0
 23 22  1  0
 22 25  1  0
 25 26  1  0
 26 27  2  0
  4  2  1  0
  2  1  1  0
  2  3  2  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
 22 11  1  0
 16 21  1  0
 25  9  1  0
 24  8  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  6
  8 34  1  6
  7 32  1  0
  7 33  1  0
  5 31  1  0
 24 48  1  6
 23 46  1  0
 23 47  1  0
 22 45  1  1
 26 49  1  0
  1 28  1  0
  1 29  1  0
  1 30  1  0
 20 44  1  0
 19 43  1  0
 18 42  1  0
 17 41  1  0
M  END


  Mrv1652309072209432D          

 27 31  0  0  1  0            999 V2000
   -1.1728    2.8551    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3478    2.0086    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1671    2.2481    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9779    1.1943    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5232    0.5753    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2599   -0.2065    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4511   -0.3693    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0943    0.2497    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    0.8698   -0.0318    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    1.5734    0.3989    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.6753    1.2176    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.9218    2.0049    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.6931    2.8493    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.7467    2.0138    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    3.0620    2.8374    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.0101    1.2320    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.7674    0.9046    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.8624    0.0851    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.2003   -0.4070    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.4430   -0.0796    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.3479    0.7399    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.0988    1.8077    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    0.2779    1.7249    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1691    1.0315    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    1.2142    0.8593    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    2.1395    1.1449    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.7950    1.6077    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0  0  0  0
  2  3  2  0  0  0  0
  2  4  1  0  0  0  0
  4  5  2  0  0  0  0
  5  6  1  0  0  0  0
  6  7  1  0  0  0  0
  8  7  1  6  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
 16 17  2  0  0  0  0
 17 18  1  0  0  0  0
 18 19  2  0  0  0  0
 19 20  1  0  0  0  0
 20 21  2  0  0  0  0
 16 21  1  0  0  0  0
 11 21  1  0  0  0  0
 11 22  1  0  0  0  0
 22 23  1  0  0  0  0
 24 23  1  6  0  0  0
  4 24  1  0  0  0  0
  8 24  1  0  0  0  0
 22 25  1  6  0  0  0
  9 25  1  6  0  0  0
 25 26  1  0  0  0  0
 26 27  2  0  0  0  0
M  END
> <DATABASE_ID>
NP0246297

> <DATABASE_NAME>
NP-MRD

> <SMILES>
CN1C(=O)C2(C[C@H]3[C@@H]4COC=C([C@@H]4C[C@@H]2N3C=O)C(C)=O)C2=CC=CC=C12

> <INCHI_IDENTIFIER>
InChI=1S/C21H22N2O4/c1-12(25)14-9-27-10-15-13(14)7-19-21(8-18(15)23(19)11-24)16-5-3-4-6-17(16)22(2)20(21)26/h3-6,9,11,13,15,18-19H,7-8,10H2,1-2H3/t13-,15+,18-,19-,21?/m0/s1

> <INCHI_KEY>
SANFAUSBJXJGKX-HZGCYMHYSA-N

> <FORMULA>
C21H22N2O4

> <MOLECULAR_WEIGHT>
366.417

> <EXACT_MASS>
366.157957196

> <JCHEM_ACCEPTOR_COUNT>
4

> <JCHEM_ATOM_COUNT>
49

> <JCHEM_AVERAGE_POLARIZABILITY>
38.171759869975105

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
0

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
1

> <JCHEM_IUPAC>
(1'S,2'R,7'R,9'S)-6'-acetyl-1-methyl-2-oxo-1,2-dihydro-4'-oxa-12'-azaspiro[indole-3,10'-tricyclo[7.2.1.0^{2,7}]dodecan]-5'-ene-12'-carbaldehyde

> <JCHEM_LOGP>
0.34077732400000005

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
5

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA_STRONGEST_ACIDIC>
19.217744149236502

> <JCHEM_PKA_STRONGEST_BASIC>
-0.8562246787315541

> <JCHEM_POLAR_SURFACE_AREA>
66.92000000000002

> <JCHEM_REFRACTIVITY>
98.32239999999999

> <JCHEM_ROTATABLE_BOND_COUNT>
1

> <JCHEM_RULE_OF_FIVE>
1

> <JCHEM_TRADITIONAL_IUPAC>
(1'S,2'R,7'R,9'S)-6'-acetyl-1-methyl-2-oxo-4'-oxa-12'-azaspiro[indole-3,10'-tricyclo[7.2.1.0^{2,7}]dodecan]-5'-ene-12'-carbaldehyde

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 07-SEP-22   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   07-SEP-22         0                                  
HETATM    1  C   UNK     0      -2.189   5.330   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0      -2.516   3.749   0.000  0.00  0.00           C+0
HETATM    3  O   UNK     0      -4.045   4.197   0.000  0.00  0.00           O+0
HETATM    4  C   UNK     0      -1.825   2.229   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0      -2.843   1.074   0.000  0.00  0.00           C+0
HETATM    6  O   UNK     0      -2.352  -0.385   0.000  0.00  0.00           O+0
HETATM    7  C   UNK     0      -0.842  -0.689   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0       0.176   0.466   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0       1.624  -0.059   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0       2.937   0.745   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0       3.127   2.273   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0       3.587   3.743   0.000  0.00  0.00           C+0
HETATM   13  O   UNK     0       3.160   5.319   0.000  0.00  0.00           O+0
HETATM   14  N   UNK     0       5.127   3.759   0.000  0.00  0.00           N+0
HETATM   15  C   UNK     0       5.716   5.296   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0       5.619   2.300   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0       7.032   1.689   0.000  0.00  0.00           C+0
HETATM   18  C   UNK     0       7.210   0.159   0.000  0.00  0.00           C+0
HETATM   19  C   UNK     0       5.974  -0.760   0.000  0.00  0.00           C+0
HETATM   20  C   UNK     0       4.560  -0.149   0.000  0.00  0.00           C+0
HETATM   21  C   UNK     0       4.383   1.381   0.000  0.00  0.00           C+0
HETATM   22  C   UNK     0       2.051   3.374   0.000  0.00  0.00           C+0
HETATM   23  C   UNK     0       0.519   3.220   0.000  0.00  0.00           C+0
HETATM   24  C   UNK     0      -0.316   1.925   0.000  0.00  0.00           C+0
HETATM   25  N   UNK     0       2.267   1.604   0.000  0.00  0.00           N+0
HETATM   26  C   UNK     0       3.994   2.137   0.000  0.00  0.00           C+0
HETATM   27  O   UNK     0       5.217   3.001   0.000  0.00  0.00           O+0
CONECT    1    2                                                            
CONECT    2    1    3    4                                                  
CONECT    3    2                                                            
CONECT    4    2    5   24                                                  
CONECT    5    4    6                                                       
CONECT    6    5    7                                                       
CONECT    7    6    8                                                       
CONECT    8    7    9   24                                                  
CONECT    9    8   10   25                                                  
CONECT   10    9   11                                                       
CONECT   11   10   12   21   22                                             
CONECT   12   11   13   14                                                  
CONECT   13   12                                                            
CONECT   14   12   15   16                                                  
CONECT   15   14                                                            
CONECT   16   14   17   21                                                  
CONECT   17   16   18                                                       
CONECT   18   17   19                                                       
CONECT   19   18   20                                                       
CONECT   20   19   21                                                       
CONECT   21   20   16   11                                                  
CONECT   22   11   23   25                                                  
CONECT   23   22   24                                                       
CONECT   24   23    4    8                                                  
CONECT   25   22    9   26                                                  
CONECT   26   25   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

C₂₁H₂₂N₂O₄

Average Mass

366.4170 Da

Monoisotopic Mass

366.15796 Da

IUPAC Name

Not Available

Traditional Name

Not Available

CAS Registry Number

Not Available

SMILES

CN1C(=O)C2(C[C@H]3[C@@H]4COC=C([C@@H]4C[C@@H]2N3C=O)C(C)=O)C2=CC=CC=C12

InChI Identifier

InChI=1S/C21H22N2O4/c1-12(25)14-9-27-10-15-13(14)7-19-21(8-18(15)23(19)11-24)16-5-3-4-6-17(16)22(2)20(21)26/h3-6,9,11,13,15,18-19H,7-8,10H2,1-2H3/t13-,15+,18-,19-,21?/m0/s1

InChI Key

SANFAUSBJXJGKX-HZGCYMHYSA-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

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as indoles and derivatives. These are organic compounds containing an indole, which is a bicyclic ring system made up of a six-membered benzene ring fused to a five-membered nitrogen-containing pyrrole ring.

Kingdom

Organic compounds

Super Class

Organoheterocyclic compounds

Class

Indoles and derivatives

Sub Class

Not Available

Direct Parent

Indoles and derivatives

Alternative Parents

Substituents

Indole or derivatives
Benzenoid
Piperidine
Vinylogous ester
Tertiary carboxylic acid amide
Pyrrolidine
Lactam
Ketone
Carboxamide group
Oxacycle
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

163188321

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

LOTUS database [Link]

Showing NP-Card for (1's,2'r,7'r,9's)-6'-acetyl-1-methyl-2-oxo-4'-oxa-12'-azaspiro[indole-3,10'-tricyclo[7.2.1.0²,⁷]dodecan]-5'-ene-12'-carbaldehyde (NP0246297)

MOL for NP0246297 ((1's,2'r,7'r,9's)-6'-acetyl-1-methyl-2-oxo-4'-oxa-12'-azaspiro[indole-3,10'-tricyclo[7.2.1.0²,⁷]dodecan]-5'-ene-12'-carbaldehyde)

3D MOL for NP0246297 ((1's,2'r,7'r,9's)-6'-acetyl-1-methyl-2-oxo-4'-oxa-12'-azaspiro[indole-3,10'-tricyclo[7.2.1.0²,⁷]dodecan]-5'-ene-12'-carbaldehyde)

3D SDF for NP0246297 ((1's,2'r,7'r,9's)-6'-acetyl-1-methyl-2-oxo-4'-oxa-12'-azaspiro[indole-3,10'-tricyclo[7.2.1.0²,⁷]dodecan]-5'-ene-12'-carbaldehyde)

3D-SDF for NP0246297 ((1's,2'r,7'r,9's)-6'-acetyl-1-methyl-2-oxo-4'-oxa-12'-azaspiro[indole-3,10'-tricyclo[7.2.1.0²,⁷]dodecan]-5'-ene-12'-carbaldehyde)

PDB for NP0246297 ((1's,2'r,7'r,9's)-6'-acetyl-1-methyl-2-oxo-4'-oxa-12'-azaspiro[indole-3,10'-tricyclo[7.2.1.0²,⁷]dodecan]-5'-ene-12'-carbaldehyde)

3D PDB for NP0246297 ((1's,2'r,7'r,9's)-6'-acetyl-1-methyl-2-oxo-4'-oxa-12'-azaspiro[indole-3,10'-tricyclo[7.2.1.0²,⁷]dodecan]-5'-ene-12'-carbaldehyde)

SMILES for NP0246297 ((1's,2'r,7'r,9's)-6'-acetyl-1-methyl-2-oxo-4'-oxa-12'-azaspiro[indole-3,10'-tricyclo[7.2.1.0²,⁷]dodecan]-5'-ene-12'-carbaldehyde)

INCHI for NP0246297 ((1's,2'r,7'r,9's)-6'-acetyl-1-methyl-2-oxo-4'-oxa-12'-azaspiro[indole-3,10'-tricyclo[7.2.1.0²,⁷]dodecan]-5'-ene-12'-carbaldehyde)

Structure for NP0246297 ((1's,2'r,7'r,9's)-6'-acetyl-1-methyl-2-oxo-4'-oxa-12'-azaspiro[indole-3,10'-tricyclo[7.2.1.0²,⁷]dodecan]-5'-ene-12'-carbaldehyde)

3D Structure for NP0246297 ((1's,2'r,7'r,9's)-6'-acetyl-1-methyl-2-oxo-4'-oxa-12'-azaspiro[indole-3,10'-tricyclo[7.2.1.0²,⁷]dodecan]-5'-ene-12'-carbaldehyde)