NP-MRD: Showing NP-Card for 1-{3-[(1r,8s,9r)-11-methyl-10-(prop-2-en-1-yl)-7,11-diazatricyclo[7.3.1.0²,⁷]tridecan-8-yl]-5,6-dihydro-4h-pyridin-1-yl}ethanone (NP0219131)

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Record Information

Version

2.0

Created at

2022-09-05 20:02:05 UTC

Updated at

2022-09-05 20:02:05 UTC

NP-MRD ID

NP0219131

Secondary Accession Numbers

None

Natural Product Identification

Common Name

1-{3-[(1r,8s,9r)-11-methyl-10-(prop-2-en-1-yl)-7,11-diazatricyclo[7.3.1.0²,⁷]tridecan-8-yl]-5,6-dihydro-4h-pyridin-1-yl}ethanone

Description

1-{5-[(1R,8S,9R)-11-methyl-10-(prop-2-en-1-yl)-7,11-diazatricyclo[7.3.1.0²,⁷]Tridecan-8-yl]-1,2,3,4-tetrahydropyridin-1-yl}ethan-1-one belongs to the class of organic compounds known as quinolizidines. Quinolizidines are compounds containing a quinolizidine moiety, which is a octahydro-2H-quinolizine derivative. Based on a literature review very few articles have been published on 1-{5-[(1R,8S,9R)-11-methyl-10-(prop-2-en-1-yl)-7,11-diazatricyclo[7.3.1.0²,⁷]Tridecan-8-yl]-1,2,3,4-tetrahydropyridin-1-yl}ethan-1-one.

Structure

MOL 3D MOL SDF PDB SMILES InChI


  Mrv1652309052222022D          

 26 29  0  0  1  0            999 V2000
    7.5278    1.3664    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.7951    0.9872    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.1004    1.4322    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.3677    1.0530    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.7370    1.5848    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    4.6672    0.4759    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.0838   -0.4697    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    4.9058   -0.3998    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.4376    0.2309    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    6.2238   -0.0190    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.4531    0.0621    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.7761   -0.4095    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.0293   -0.0591    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.9593    0.7629    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.6362    1.2345    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.3831    0.8841    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    3.9149    1.5148    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    3.5357    2.2475    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.7116    2.2854    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.3324    3.0181    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    1.5083    3.0561    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.0633    2.3613    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.1291    3.7888    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.7773    3.7129    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.6014    3.6749    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.9806    2.9422    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  2  0  0  0  0
  2  3  1  0  0  0  0
  3  4  1  0  0  0  0
  4  5  1  0  0  0  0
  5  6  1  6  0  0  0
  7  6  1  1  0  0  0
  7  8  1  0  0  0  0
  8  9  1  0  0  0  0
  4  9  1  0  0  0  0
  9 10  1  0  0  0  0
  7 11  1  0  0  0  0
 11 12  1  0  0  0  0
 12 13  1  0  0  0  0
 13 14  1  0  0  0  0
 14 15  1  0  0  0  0
 15 16  1  0  0  0  0
 11 16  1  0  0  0  0
 16 17  1  0  0  0  0
  5 17  1  0  0  0  0
 17 18  1  6  0  0  0
 18 19  2  0  0  0  0
 19 20  1  0  0  0  0
 20 21  1  0  0  0  0
 21 22  1  0  0  0  0
 21 23  2  0  0  0  0
 20 24  1  0  0  0  0
 24 25  1  0  0  0  0
 25 26  1  0  0  0  0
 18 26  1  0  0  0  0
M  END

     RDKit          3D

 61 64  0  0  0  0  0  0  0  0999 V2000
   -1.9919   -3.5623    2.3183 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7604   -3.5725    1.0212 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5476   -2.7261    0.1065 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7466   -1.7079   -0.6640 C   0  0  2  0  0  0  0  0  0  0  0  0
   -1.1303   -0.6425    0.0120 C   0  0  1  0  0  0  0  0  0  0  0  0
   -2.3064    0.0900    0.6650 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3765    1.2319   -0.3524 C   0  0  2  0  0  0  0  0  0  0  0  0
   -2.5084    0.4388   -1.6301 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7694   -0.9952   -1.4952 N   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8105   -1.5321   -2.8174 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9629    1.7976   -0.1065 C   0  0  1  0  0  0  0  0  0  0  0  0
   -1.2291    3.2388    0.3056 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0719    3.9456    0.8762 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7552    3.1841    1.8578 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.1528    1.8304    2.0672 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1948    1.2069    0.8936 N   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0295   -0.2693    0.8315 C   0  0  2  0  0  0  0  0  0  0  0  0
    1.2711   -0.6269    0.2665 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.2178    0.2430   -0.0515 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.4798   -0.1246   -0.6008 N   0  0  0  0  0  0  0  0  0  0  0  0
    4.6336    0.7058   -0.4727 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.5933    2.0070    0.2416 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.7179    0.3244   -0.9801 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.5886   -1.3866   -1.3127 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.3151   -2.1627   -1.3023 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.5760   -2.0471    0.0188 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7732   -2.9302    2.7730 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4411   -4.1661    3.0342 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9939   -4.2082    0.6272 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.0206   -3.4687   -0.6218 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.4143   -2.3243    0.6557 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1377   -2.2902   -1.4180 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7007   -0.1393   -0.9424 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1472    0.4225    1.6842 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.2668   -0.3972    0.6201 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.1806    1.9145   -0.1411 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.4979    0.7965   -2.0668 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7917    0.6924   -2.4175 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2742   -2.5254   -2.7937 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.8584   -1.7576   -3.1022 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2738   -0.9169   -3.5504 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4919    1.8737   -1.1197 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5989    3.7935   -0.5769 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0770    3.2492    1.0512 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4728    4.8508    1.4231 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.5650    4.4043    0.0626 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.7997    3.6905    2.8627 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.7999    3.1912    1.5041 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.8138    1.1714    2.6707 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7460    2.0088    2.7304 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0277   -0.5811    1.9033 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.0453    1.2830    0.1028 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.5260    2.8732   -0.4327 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.8275    1.9911    1.0305 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.5871    2.0902    0.7716 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.4204   -2.0184   -0.9126 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.8578   -1.2050   -2.3892 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.5004   -3.2474   -1.4564 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.5958   -1.8521   -2.0962 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.7395   -2.7270   -0.0158 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.2432   -2.4302    0.8498 H   0  0  0  0  0  0  0  0  0  0  0  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  3  1  0
  3  2  1  0
  2  1  2  3
  5 17  1  0
 17 16  1  0
 16 15  1  0
 15 14  1  0
 14 13  1  0
 13 12  1  0
 12 11  1  0
 17 18  1  0
 18 19  2  0
 19 20  1  0
 20 24  1  0
 24 25  1  0
 25 26  1  0
 20 21  1  0
 21 22  1  0
 21 23  2  0
  4  9  1  0
 11 16  1  0
 26 18  1  0
 11  7  1  0
 10 39  1  0
 10 40  1  0
 10 41  1  0
  8 37  1  0
  8 38  1  0
  7 36  1  1
  6 34  1  0
  6 35  1  0
  5 33  1  6
  4 32  1  6
  3 30  1  0
  3 31  1  0
  2 29  1  0
  1 27  1  0
  1 28  1  0
 17 51  1  1
 15 49  1  0
 15 50  1  0
 14 47  1  0
 14 48  1  0
 13 45  1  0
 13 46  1  0
 12 43  1  0
 12 44  1  0
 11 42  1  6
 19 52  1  0
 24 56  1  0
 24 57  1  0
 25 58  1  0
 25 59  1  0
 26 60  1  0
 26 61  1  0
 22 53  1  0
 22 54  1  0
 22 55  1  0
M  END


  Mrv1652309052222022D          

 26 29  0  0  1  0            999 V2000
    7.5278    1.3664    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.7951    0.9872    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.1004    1.4322    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.3677    1.0530    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.7370    1.5848    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    4.6672    0.4759    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.0838   -0.4697    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    4.9058   -0.3998    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.4376    0.2309    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    6.2238   -0.0190    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.4531    0.0621    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.7761   -0.4095    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.0293   -0.0591    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.9593    0.7629    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.6362    1.2345    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.3831    0.8841    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    3.9149    1.5148    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    3.5357    2.2475    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.7116    2.2854    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.3324    3.0181    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    1.5083    3.0561    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.0633    2.3613    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.1291    3.7888    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.7773    3.7129    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.6014    3.6749    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.9806    2.9422    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  2  0  0  0  0
  2  3  1  0  0  0  0
  3  4  1  0  0  0  0
  4  5  1  0  0  0  0
  5  6  1  6  0  0  0
  7  6  1  1  0  0  0
  7  8  1  0  0  0  0
  8  9  1  0  0  0  0
  4  9  1  0  0  0  0
  9 10  1  0  0  0  0
  7 11  1  0  0  0  0
 11 12  1  0  0  0  0
 12 13  1  0  0  0  0
 13 14  1  0  0  0  0
 14 15  1  0  0  0  0
 15 16  1  0  0  0  0
 11 16  1  0  0  0  0
 16 17  1  0  0  0  0
  5 17  1  0  0  0  0
 17 18  1  6  0  0  0
 18 19  2  0  0  0  0
 19 20  1  0  0  0  0
 20 21  1  0  0  0  0
 21 22  1  0  0  0  0
 21 23  2  0  0  0  0
 20 24  1  0  0  0  0
 24 25  1  0  0  0  0
 25 26  1  0  0  0  0
 18 26  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0219131

> <DATABASE_NAME>
NP-MRD

> <SMILES>
CN1C[C@H]2C[C@H](C1CC=C)[C@H](N1CCCCC21)C1=CN(CCC1)C(C)=O

> <INCHI_IDENTIFIER>
InChI=1S/C22H35N3O/c1-4-8-21-19-13-18(14-23(21)3)20-10-5-6-12-25(20)22(19)17-9-7-11-24(15-17)16(2)26/h4,15,18-22H,1,5-14H2,2-3H3/t18-,19-,20?,21?,22-/m1/s1

> <INCHI_KEY>
NGYQGPQSBNFVQF-WWOKZEJKSA-N

> <FORMULA>
C22H35N3O

> <MOLECULAR_WEIGHT>
357.542

> <EXACT_MASS>
357.278012759

> <ALOGPS_LOGP>
2.47

> <ALOGPS_LOGS>
-2.69

> <ALOGPS_SOLUBILITY>
7.32e-01 g/l

$$$$

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      14.052   2.551   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0      12.684   1.843   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0      11.387   2.673   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0      10.020   1.966   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0       8.842   2.958   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0       8.712   0.888   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0       7.623  -0.877   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0       9.158  -0.746   0.000  0.00  0.00           C+0
HETATM    9  N   UNK     0      10.150   0.431   0.000  0.00  0.00           N+0
HETATM   10  C   UNK     0      11.618  -0.036   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0       6.446   0.116   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0       5.182  -0.764   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0       3.788  -0.110   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0       3.657   1.424   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0       4.921   2.304   0.000  0.00  0.00           C+0
HETATM   16  N   UNK     0       6.315   1.650   0.000  0.00  0.00           N+0
HETATM   17  C   UNK     0       7.308   2.828   0.000  0.00  0.00           C+0
HETATM   18  C   UNK     0       6.600   4.195   0.000  0.00  0.00           C+0
HETATM   19  C   UNK     0       5.062   4.266   0.000  0.00  0.00           C+0
HETATM   20  N   UNK     0       4.354   5.634   0.000  0.00  0.00           N+0
HETATM   21  C   UNK     0       2.815   5.705   0.000  0.00  0.00           C+0
HETATM   22  C   UNK     0       1.985   4.408   0.000  0.00  0.00           C+0
HETATM   23  O   UNK     0       2.108   7.072   0.000  0.00  0.00           O+0
HETATM   24  C   UNK     0       5.184   6.931   0.000  0.00  0.00           C+0
HETATM   25  C   UNK     0       6.723   6.860   0.000  0.00  0.00           C+0
HETATM   26  C   UNK     0       7.431   5.492   0.000  0.00  0.00           C+0
CONECT    1    2                                                            
CONECT    2    1    3                                                       
CONECT    3    2    4                                                       
CONECT    4    3    5    9                                                  
CONECT    5    4    6   17                                                  
CONECT    6    5    7                                                       
CONECT    7    6    8   11                                                  
CONECT    8    7    9                                                       
CONECT    9    8    4   10                                                  
CONECT   10    9                                                            
CONECT   11    7   12   16                                                  
CONECT   12   11   13                                                       
CONECT   13   12   14                                                       
CONECT   14   13   15                                                       
CONECT   15   14   16                                                       
CONECT   16   15   11   17                                                  
CONECT   17   16    5   18                                                  
CONECT   18   17   19   26                                                  
CONECT   19   18   20                                                       
CONECT   20   19   21   24                                                  
CONECT   21   20   22   23                                                  
CONECT   22   21                                                            
CONECT   23   21                                                            
CONECT   24   20   25                                                       
CONECT   25   24   26                                                       
CONECT   26   25   18                                                       
MASTER        0    0    0    0    0    0    0    0   26    0   58    0
END

View in JSmol

Synonyms

Not Available

Chemical Formula

C₂₂H₃₅N₃O

Average Mass

357.5420 Da

Monoisotopic Mass

357.27801 Da

IUPAC Name

Not Available

Traditional Name

Not Available

CAS Registry Number

Not Available

SMILES

CN1C[C@H]2C[C@H](C1CC=C)[C@H](N1CCCCC21)C1=CN(CCC1)C(C)=O

InChI Identifier

InChI=1S/C22H35N3O/c1-4-8-21-19-13-18(14-23(21)3)20-10-5-6-12-25(20)22(19)17-9-7-11-24(15-17)16(2)26/h4,15,18-22H,1,5-14H2,2-3H3/t18-,19-,20?,21?,22-/m1/s1

InChI Key

NGYQGPQSBNFVQF-WWOKZEJKSA-N

Experimental Spectra

Not Available

Predicted Spectra

Spectrum Type	Description	Depositor ID	Depositor Organization	Depositor	Deposition Date	View
1D NMR	¹³C NMR Spectrum (1D, 25 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 100 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 252 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 1000 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 50 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 200 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 75 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 300 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 101 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 400 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 126 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 500 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 151 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 600 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 176 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 700 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 201 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 800 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 226 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 900 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum

Chemical Shift Submissions

Not Available

Species

Species of Origin

Not Available

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as quinolizidines. Quinolizidines are compounds containing a quinolizidine moiety, which is a octahydro-2H-quinolizine derivative.

Kingdom

Organic compounds

Super Class

Organoheterocyclic compounds

Class

Quinolizidines

Sub Class

Not Available

Direct Parent

Quinolizidines

Alternative Parents

Substituents

Quinolizidine
Tetrahydropyridine
Piperidine
Hydropyridine
Acetamide
Tertiary carboxylic acid amide
Tertiary aliphatic amine
Tertiary amine
Carboxamide group
Amino acid or derivatives
Azacycle
Carboxylic acid derivative
Organic nitrogen compound
Organic oxygen compound
Organopnictogen compound
Organic oxide
Hydrocarbon derivative
Organooxygen compound
Organonitrogen compound
Carbonyl group
Amine
Aliphatic heteropolycyclic compound

Molecular Framework

Aliphatic heteropolycyclic compounds

External Descriptors

Not Available

Physical Properties

State

Not Available

Experimental Properties

Property	Value	Reference
Melting Point	Not Available	Not Available
Boiling Point	Not Available	Not Available
Water Solubility	Not Available	Not Available
LogP	Not Available	Not Available

Predicted Properties

Property	Value	Source

External Links

HMDB ID

Not Available

DrugBank ID

Not Available

Phenol Explorer Compound ID

Not Available

FoodDB ID

Not Available

KNApSAcK ID

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

162855339

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

LOTUS database [Link]

Showing NP-Card for 1-{3-[(1r,8s,9r)-11-methyl-10-(prop-2-en-1-yl)-7,11-diazatricyclo[7.3.1.0²,⁷]tridecan-8-yl]-5,6-dihydro-4h-pyridin-1-yl}ethanone (NP0219131)

MOL for NP0219131 (1-{3-[(1r,8s,9r)-11-methyl-10-(prop-2-en-1-yl)-7,11-diazatricyclo[7.3.1.0²,⁷]tridecan-8-yl]-5,6-dihydro-4h-pyridin-1-yl}ethanone)

3D MOL for NP0219131 (1-{3-[(1r,8s,9r)-11-methyl-10-(prop-2-en-1-yl)-7,11-diazatricyclo[7.3.1.0²,⁷]tridecan-8-yl]-5,6-dihydro-4h-pyridin-1-yl}ethanone)

3D SDF for NP0219131 (1-{3-[(1r,8s,9r)-11-methyl-10-(prop-2-en-1-yl)-7,11-diazatricyclo[7.3.1.0²,⁷]tridecan-8-yl]-5,6-dihydro-4h-pyridin-1-yl}ethanone)

3D-SDF for NP0219131 (1-{3-[(1r,8s,9r)-11-methyl-10-(prop-2-en-1-yl)-7,11-diazatricyclo[7.3.1.0²,⁷]tridecan-8-yl]-5,6-dihydro-4h-pyridin-1-yl}ethanone)

PDB for NP0219131 (1-{3-[(1r,8s,9r)-11-methyl-10-(prop-2-en-1-yl)-7,11-diazatricyclo[7.3.1.0²,⁷]tridecan-8-yl]-5,6-dihydro-4h-pyridin-1-yl}ethanone)

3D PDB for NP0219131 (1-{3-[(1r,8s,9r)-11-methyl-10-(prop-2-en-1-yl)-7,11-diazatricyclo[7.3.1.0²,⁷]tridecan-8-yl]-5,6-dihydro-4h-pyridin-1-yl}ethanone)

SMILES for NP0219131 (1-{3-[(1r,8s,9r)-11-methyl-10-(prop-2-en-1-yl)-7,11-diazatricyclo[7.3.1.0²,⁷]tridecan-8-yl]-5,6-dihydro-4h-pyridin-1-yl}ethanone)

INCHI for NP0219131 (1-{3-[(1r,8s,9r)-11-methyl-10-(prop-2-en-1-yl)-7,11-diazatricyclo[7.3.1.0²,⁷]tridecan-8-yl]-5,6-dihydro-4h-pyridin-1-yl}ethanone)

Structure for NP0219131 (1-{3-[(1r,8s,9r)-11-methyl-10-(prop-2-en-1-yl)-7,11-diazatricyclo[7.3.1.0²,⁷]tridecan-8-yl]-5,6-dihydro-4h-pyridin-1-yl}ethanone)

3D Structure for NP0219131 (1-{3-[(1r,8s,9r)-11-methyl-10-(prop-2-en-1-yl)-7,11-diazatricyclo[7.3.1.0²,⁷]tridecan-8-yl]-5,6-dihydro-4h-pyridin-1-yl}ethanone)