NP-MRD: Showing NP-Card for (1'r,3s,4's,8'r,9's)-1,6-dimethoxy-2-oxo-11'-oxa-5'-azaspiro[indole-3,2'-tricyclo[6.3.1.0⁴,⁹]dodecan]-6'-ene-7'-carbaldehyde (NP0284096)

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Record Information

Version

2.0

Created at

2022-09-09 11:39:18 UTC

Updated at

2022-09-09 11:39:18 UTC

NP-MRD ID

NP0284096

Secondary Accession Numbers

None

Natural Product Identification

Common Name

(1'r,3s,4's,8'r,9's)-1,6-dimethoxy-2-oxo-11'-oxa-5'-azaspiro[indole-3,2'-tricyclo[6.3.1.0⁴,⁹]dodecan]-6'-ene-7'-carbaldehyde

Description

CHEMBL3590534 belongs to the class of organic compounds known as gelsemium alkaloids. These are alkaloids with a structure that is based on the tetracyclic gelsemium skeleton. These alkaloids contain an oxindole function and a cage-like, hydroaromatic residue which is believed to arise from an intermediate related to anhydrovobasinediol by formation of a 6,20 bond and rearrangement to an oxindole. The major alkaloids in this group are related to Gelsemine; however, a smaller group, characterized by Gelsedine, lack the 6,20 bond, and have also lost C-21. (1'r,3s,4's,8'r,9's)-1,6-dimethoxy-2-oxo-11'-oxa-5'-azaspiro[indole-3,2'-tricyclo[6.3.1.0⁴,⁹]dodecan]-6'-ene-7'-carbaldehyde is found in Gelsemium elegans. Based on a literature review very few articles have been published on CHEMBL3590534.

Structure

MOL 3D MOL SDF PDB SMILES InChI


  Mrv1652309092213392D          

 27 31  0  0  1  0            999 V2000
    5.6932    0.9203    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.2825    0.1717    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.4092    0.1154    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.9478    0.7994    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.1249    0.7417    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.7633    0.0002    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.2247   -0.6837    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.0476   -0.6261    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.7168   -1.3339    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    2.9804   -2.2010    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.7877   -2.4733    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.9415   -1.0518    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.2635   -1.6564    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.9702   -0.2273    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    2.1614    0.6316    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.5238    1.2994    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    0.8640    1.9646    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    1.6702    1.8158    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.5715    0.7894    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.3144    0.1558    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.4529   -0.7704    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.6965    0.5473    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    0.6218   -0.4202    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.1661   -0.6074    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    0.1132   -0.5637    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1950    0.3485    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.4482    1.0423    0.0000 C   0  0  2  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
  4  5  1  0  0  0  0
  5  6  2  0  0  0  0
  6  7  1  0  0  0  0
  7  8  2  0  0  0  0
  3  8  1  0  0  0  0
  7  9  1  0  0  0  0
  9 10  1  0  0  0  0
 10 11  1  0  0  0  0
  9 12  1  0  0  0  0
 12 13  2  0  0  0  0
 14 12  1  1  0  0  0
  6 14  1  0  0  0  0
 14 15  1  0  0  0  0
 15 16  1  0  0  0  0
 16 17  1  1  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
 19 22  1  0  0  0  0
 22 23  1  6  0  0  0
 24 23  1  1  0  0  0
 14 24  1  0  0  0  0
 24 25  1  0  0  0  0
 25 26  1  0  0  0  0
 27 26  1  6  0  0  0
 16 27  1  0  0  0  0
 22 27  1  0  0  0  0
M  END

     RDKit          3D

 49 53  0  0  0  0  0  0  0  0999 V2000
    6.0511   -1.2594    1.2620 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.4615   -0.2336    0.5148 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.1004   -0.2528    0.2615 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.2904   -1.2631    0.7191 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.9295   -1.2278    0.4390 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.3412   -0.1933   -0.3000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1423    0.8068   -0.7607 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5027    0.7641   -0.4734 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.3910    1.7243   -1.5639 N   0  0  0  0  0  0  0  0  0  0  0  0
    1.9154    2.8319   -2.1650 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.0775    3.8217   -1.1705 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0684    1.2484   -1.5968 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8373    1.7388   -2.3400 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0609    0.1315   -0.6550 C   0  0  1  0  0  0  0  0  0  0  0  0
   -0.8295   -0.9804   -1.2707 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8057   -1.7257   -0.4822 C   0  0  2  0  0  0  0  0  0  0  0  0
   -3.0657   -1.8793   -1.2456 N   0  0  0  0  0  0  0  0  0  0  0  0
   -4.2107   -1.1245   -0.9478 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.2801   -0.2865    0.0823 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.5348    0.3281    0.4838 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.6042    1.1248    1.4590 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.0656    0.0242    0.8282 C   0  0  2  0  0  0  0  0  0  0  0  0
   -2.1707    1.0546    0.2163 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7546    0.7253    0.5678 C   0  0  1  0  0  0  0  0  0  0  0  0
   -0.5329    0.0492    1.7266 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1948   -1.1285    1.9148 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2256   -1.2626    0.8519 C   0  0  2  0  0  0  0  0  0  0  0  0
    7.0368   -0.8740    1.6702 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.2009   -2.1789    0.6635 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.4323   -1.5253    2.1500 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.6989   -2.1034    1.2995 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.3273   -2.0500    0.8058 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.1232    1.5651   -0.8442 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.2163    4.5195   -1.2465 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.0533    4.3136   -1.2526 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.0054    3.3395   -0.1617 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0985   -1.6724   -1.7455 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3629   -0.5365   -2.1698 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4643   -2.7970   -0.3416 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.0735   -2.5657   -2.0120 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.1128   -1.1867   -1.5579 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.4350    0.1114   -0.0493 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.2143    0.2874    1.8972 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3754    0.9994   -0.8935 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4610    2.0945    0.4815 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2599    1.7433    0.7227 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7579   -0.9850    2.9049 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6062   -2.0240    2.0941 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.9708   -2.0309    1.2295 H   0  0  0  0  0  0  0  0  0  0  0  0
 11 10  1  0
 10  9  1  0
  9 12  1  0
 12 13  2  0
 14 12  1  6
 14 15  1  0
 15 16  1  0
 16 17  1  0
 17 18  1  0
 18 19  2  0
 19 20  1  0
 20 21  2  0
 19 22  1  0
 22 23  1  0
 23 24  1  0
 24 25  1  0
 25 26  1  0
 26 27  1  0
 14  6  1  0
  6  5  2  0
  5  4  1  0
  4  3  2  0
  3  2  1  0
  2  1  1  0
  3  8  1  0
  8  7  2  0
  7  9  1  0
 24 14  1  0
  7  6  1  0
 27 16  1  0
 27 22  1  0
 11 34  1  0
 11 35  1  0
 11 36  1  0
 15 37  1  0
 15 38  1  0
 16 39  1  1
 17 40  1  0
 18 41  1  0
 20 42  1  0
 22 43  1  1
 23 44  1  0
 23 45  1  0
 24 46  1  1
 26 47  1  0
 26 48  1  0
 27 49  1  1
  5 32  1  0
  4 31  1  0
  1 28  1  0
  1 29  1  0
  1 30  1  0
  8 33  1  0
M  END


  Mrv1652309092213392D          

 27 31  0  0  1  0            999 V2000
    5.6932    0.9203    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.2825    0.1717    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.4092    0.1154    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.9478    0.7994    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.1249    0.7417    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.7633    0.0002    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.2247   -0.6837    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.0476   -0.6261    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.7168   -1.3339    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    2.9804   -2.2010    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.7877   -2.4733    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.9415   -1.0518    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.2635   -1.6564    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.9702   -0.2273    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    2.1614    0.6316    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.5238    1.2994    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    0.8640    1.9646    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    1.6702    1.8158    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.5715    0.7894    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.3144    0.1558    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.4529   -0.7704    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.6965    0.5473    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    0.6218   -0.4202    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.1661   -0.6074    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    0.1132   -0.5637    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1950    0.3485    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.4482    1.0423    0.0000 C   0  0  2  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
  4  5  1  0  0  0  0
  5  6  2  0  0  0  0
  6  7  1  0  0  0  0
  7  8  2  0  0  0  0
  3  8  1  0  0  0  0
  7  9  1  0  0  0  0
  9 10  1  0  0  0  0
 10 11  1  0  0  0  0
  9 12  1  0  0  0  0
 12 13  2  0  0  0  0
 14 12  1  1  0  0  0
  6 14  1  0  0  0  0
 14 15  1  0  0  0  0
 15 16  1  0  0  0  0
 16 17  1  1  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
 19 22  1  0  0  0  0
 22 23  1  6  0  0  0
 24 23  1  1  0  0  0
 14 24  1  0  0  0  0
 24 25  1  0  0  0  0
 25 26  1  0  0  0  0
 27 26  1  6  0  0  0
 16 27  1  0  0  0  0
 22 27  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0284096

> <DATABASE_NAME>
NP-MRD

> <SMILES>
CON1C(=O)[C@@]2(C[C@@H]3NC=C(C=O)[C@@H]4C[C@H]2OC[C@H]34)C2=CC=C(OC)C=C12

> <INCHI_IDENTIFIER>
InChI=1S/C20H22N2O5/c1-25-12-3-4-15-17(5-12)22(26-2)19(24)20(15)7-16-14-10-27-18(20)6-13(14)11(9-23)8-21-16/h3-5,8-9,13-14,16,18,21H,6-7,10H2,1-2H3/t13-,14-,16-,18+,20-/m0/s1

> <INCHI_KEY>
HICAXUMNKFUXNW-RSXWSOLBSA-N

> <FORMULA>
C20H22N2O5

> <MOLECULAR_WEIGHT>
370.405

> <EXACT_MASS>
370.152871816

> <JCHEM_ACCEPTOR_COUNT>
6

> <JCHEM_ATOM_COUNT>
49

> <JCHEM_AVERAGE_POLARIZABILITY>
37.785645051850096

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
1

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
1

> <JCHEM_IUPAC>
(1'R,3S,4'S,8'R,9'S)-1,6-dimethoxy-2-oxo-1,2-dihydro-11'-oxa-5'-azaspiro[indole-3,2'-tricyclo[6.3.1.0^{4,9}]dodecan]-6'-ene-7'-carbaldehyde

> <JCHEM_LOGP>
0.28472364600000005

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
5

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA_STRONGEST_BASIC>
-3.3727541774372853

> <JCHEM_POLAR_SURFACE_AREA>
77.10000000000001

> <JCHEM_REFRACTIVITY>
96.58389999999999

> <JCHEM_ROTATABLE_BOND_COUNT>
3

> <JCHEM_RULE_OF_FIVE>
1

> <JCHEM_TRADITIONAL_IUPAC>
(1'R,3S,4'S,8'R,9'S)-1,6-dimethoxy-2-oxo-11'-oxa-5'-azaspiro[indole-3,2'-tricyclo[6.3.1.0^{4,9}]dodecan]-6'-ene-7'-carbaldehyde

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 09-SEP-22   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   09-SEP-22         0                                  
HETATM    1  C   UNK     0      10.627   1.718   0.000  0.00  0.00           C+0
HETATM    2  O   UNK     0       9.861   0.320   0.000  0.00  0.00           O+0
HETATM    3  C   UNK     0       8.231   0.215   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0       7.369   1.492   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0       5.833   1.385   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0       5.158   0.000   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0       6.019  -1.276   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0       7.556  -1.169   0.000  0.00  0.00           C+0
HETATM    9  N   UNK     0       5.071  -2.490   0.000  0.00  0.00           N+0
HETATM   10  O   UNK     0       5.563  -4.109   0.000  0.00  0.00           O+0
HETATM   11  C   UNK     0       7.070  -4.617   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0       3.624  -1.963   0.000  0.00  0.00           C+0
HETATM   13  O   UNK     0       2.359  -3.092   0.000  0.00  0.00           O+0
HETATM   14  C   UNK     0       3.678  -0.424   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0       4.035   1.179   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0       2.844   2.426   0.000  0.00  0.00           C+0
HETATM   17  N   UNK     0       1.613   3.667   0.000  0.00  0.00           N+0
HETATM   18  C   UNK     0       3.118   3.389   0.000  0.00  0.00           C+0
HETATM   19  C   UNK     0       2.933   1.473   0.000  0.00  0.00           C+0
HETATM   20  C   UNK     0       4.320   0.291   0.000  0.00  0.00           C+0
HETATM   21  O   UNK     0       4.579  -1.438   0.000  0.00  0.00           O+0
HETATM   22  C   UNK     0       1.300   1.022   0.000  0.00  0.00           C+0
HETATM   23  C   UNK     0       1.161  -0.784   0.000  0.00  0.00           C+0
HETATM   24  C   UNK     0       2.177  -1.134   0.000  0.00  0.00           C+0
HETATM   25  O   UNK     0       0.211  -1.052   0.000  0.00  0.00           O+0
HETATM   26  C   UNK     0      -0.364   0.651   0.000  0.00  0.00           C+0
HETATM   27  C   UNK     0       0.837   1.946   0.000  0.00  0.00           C+0
CONECT    1    2                                                            
CONECT    2    1    3                                                       
CONECT    3    2    4    8                                                  
CONECT    4    3    5                                                       
CONECT    5    4    6                                                       
CONECT    6    5    7   14                                                  
CONECT    7    6    8    9                                                  
CONECT    8    7    3                                                       
CONECT    9    7   10   12                                                  
CONECT   10    9   11                                                       
CONECT   11   10                                                            
CONECT   12    9   13   14                                                  
CONECT   13   12                                                            
CONECT   14   12    6   15   24                                             
CONECT   15   14   16                                                       
CONECT   16   15   17   27                                                  
CONECT   17   16   18                                                       
CONECT   18   17   19                                                       
CONECT   19   18   20   22                                                  
CONECT   20   19   21                                                       
CONECT   21   20                                                            
CONECT   22   19   23   27                                                  
CONECT   23   22   24                                                       
CONECT   24   23   14   25                                                  
CONECT   25   24   26                                                       
CONECT   26   25   27                                                       
CONECT   27   26   16   22                                                  
MASTER        0    0    0    0    0    0    0    0   27    0   62    0
END

View in JSmol

Synonyms

Not Available

Chemical Formula

C₂₀H₂₂N₂O₅

Average Mass

370.4050 Da

Monoisotopic Mass

370.15287 Da

IUPAC Name

(1'R,3S,4'S,8'R,9'S)-1,6-dimethoxy-2-oxo-1,2-dihydro-11'-oxa-5'-azaspiro[indole-3,2'-tricyclo[6.3.1.0^{4,9}]dodecan]-6'-ene-7'-carbaldehyde

Traditional Name

(1'R,3S,4'S,8'R,9'S)-1,6-dimethoxy-2-oxo-11'-oxa-5'-azaspiro[indole-3,2'-tricyclo[6.3.1.0^{4,9}]dodecan]-6'-ene-7'-carbaldehyde

CAS Registry Number

Not Available

SMILES

CON1C(=O)[C@@]2(C[C@@H]3NC=C(C=O)[C@@H]4C[C@H]2OC[C@H]34)C2=CC=C(OC)C=C12

InChI Identifier

InChI=1S/C20H22N2O5/c1-25-12-3-4-15-17(5-12)22(26-2)19(24)20(15)7-16-14-10-27-18(20)6-13(14)11(9-23)8-21-16/h3-5,8-9,13-14,16,18,21H,6-7,10H2,1-2H3/t13-,14-,16-,18+,20-/m0/s1

InChI Key

HICAXUMNKFUXNW-RSXWSOLBSA-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
Gelsemium elegans	LOTUS Database	35616633

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as gelsemium alkaloids. These are alkaloids with a structure that is based on the tetracyclic gelsemium skeleton. These alkaloids contain an oxindole function and a cage-like, hydroaromatic residue which is believed to arise from an intermediate related to anhydrovobasinediol by formation of a 6,20 bond and rearrangement to an oxindole. The major alkaloids in this group are related to Gelsemine; however, a smaller group, characterized by Gelsedine, lack the 6,20 bond, and have also lost C-21.

Kingdom

Organic compounds

Super Class

Alkaloids and derivatives

Class

Gelsemium alkaloids

Sub Class

Not Available

Direct Parent

Gelsemium alkaloids

Alternative Parents

Substituents

Gelsemium skeleton
Indole or derivatives
Anisole
Alkyl aryl ether
Oxepane
Tetrahydropyridine
Aralkylamine
Oxane
Benzenoid
Vinylogous amide
Amino acid or derivatives
Carboxylic acid derivative
Dialkyl ether
Secondary aliphatic amine
Enamine
Ether
Allylamine
Secondary amine
Oxacycle
Azacycle
Organoheterocyclic compound
Organic oxygen compound
Organopnictogen compound
Organic oxide
Organonitrogen compound
Organooxygen compound
Hydrocarbon derivative
Carbonyl group
Aldehyde
Organic nitrogen compound
Amine
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	0.28	ChemAxon
pKa (Strongest Basic)	-3.4	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	6	ChemAxon
Hydrogen Donor Count	1	ChemAxon
Polar Surface Area	77.1 Å²	ChemAxon
Rotatable Bond Count	3	ChemAxon
Refractivity	96.58 m³·mol⁻¹	ChemAxon
Polarizability	37.79 Å³	ChemAxon
Number of Rings	5	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

59002831

KEGG Compound ID

Not Available

BioCyc ID

Not Available

BiGG ID

Not Available

Wikipedia Link

Not Available

METLIN ID

Not Available

PubChem Compound

122181683

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

LOTUS database [Link]

Showing NP-Card for (1'r,3s,4's,8'r,9's)-1,6-dimethoxy-2-oxo-11'-oxa-5'-azaspiro[indole-3,2'-tricyclo[6.3.1.0⁴,⁹]dodecan]-6'-ene-7'-carbaldehyde (NP0284096)

MOL for NP0284096 ((1'r,3s,4's,8'r,9's)-1,6-dimethoxy-2-oxo-11'-oxa-5'-azaspiro[indole-3,2'-tricyclo[6.3.1.0⁴,⁹]dodecan]-6'-ene-7'-carbaldehyde)

3D MOL for NP0284096 ((1'r,3s,4's,8'r,9's)-1,6-dimethoxy-2-oxo-11'-oxa-5'-azaspiro[indole-3,2'-tricyclo[6.3.1.0⁴,⁹]dodecan]-6'-ene-7'-carbaldehyde)

3D SDF for NP0284096 ((1'r,3s,4's,8'r,9's)-1,6-dimethoxy-2-oxo-11'-oxa-5'-azaspiro[indole-3,2'-tricyclo[6.3.1.0⁴,⁹]dodecan]-6'-ene-7'-carbaldehyde)

3D-SDF for NP0284096 ((1'r,3s,4's,8'r,9's)-1,6-dimethoxy-2-oxo-11'-oxa-5'-azaspiro[indole-3,2'-tricyclo[6.3.1.0⁴,⁹]dodecan]-6'-ene-7'-carbaldehyde)

PDB for NP0284096 ((1'r,3s,4's,8'r,9's)-1,6-dimethoxy-2-oxo-11'-oxa-5'-azaspiro[indole-3,2'-tricyclo[6.3.1.0⁴,⁹]dodecan]-6'-ene-7'-carbaldehyde)

3D PDB for NP0284096 ((1'r,3s,4's,8'r,9's)-1,6-dimethoxy-2-oxo-11'-oxa-5'-azaspiro[indole-3,2'-tricyclo[6.3.1.0⁴,⁹]dodecan]-6'-ene-7'-carbaldehyde)

SMILES for NP0284096 ((1'r,3s,4's,8'r,9's)-1,6-dimethoxy-2-oxo-11'-oxa-5'-azaspiro[indole-3,2'-tricyclo[6.3.1.0⁴,⁹]dodecan]-6'-ene-7'-carbaldehyde)

INCHI for NP0284096 ((1'r,3s,4's,8'r,9's)-1,6-dimethoxy-2-oxo-11'-oxa-5'-azaspiro[indole-3,2'-tricyclo[6.3.1.0⁴,⁹]dodecan]-6'-ene-7'-carbaldehyde)

Structure for NP0284096 ((1'r,3s,4's,8'r,9's)-1,6-dimethoxy-2-oxo-11'-oxa-5'-azaspiro[indole-3,2'-tricyclo[6.3.1.0⁴,⁹]dodecan]-6'-ene-7'-carbaldehyde)

3D Structure for NP0284096 ((1'r,3s,4's,8'r,9's)-1,6-dimethoxy-2-oxo-11'-oxa-5'-azaspiro[indole-3,2'-tricyclo[6.3.1.0⁴,⁹]dodecan]-6'-ene-7'-carbaldehyde)