NP-MRD: Showing NP-Card for methyl 3-[(1s,2s,7r,10s,13r,14r)-14-isopropyl-1-methyl-12-azatetracyclo[8.6.0.0²,¹³.0³,⁷]hexadeca-3,11-dien-2-yl]propanoate (NP0211618)

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Record Information

Version

2.0

Created at

2022-09-05 09:58:54 UTC

Updated at

2022-09-05 09:58:54 UTC

NP-MRD ID

NP0211618

Secondary Accession Numbers

None

Natural Product Identification

Common Name

methyl 3-[(1s,2s,7r,10s,13r,14r)-14-isopropyl-1-methyl-12-azatetracyclo[8.6.0.0²,¹³.0³,⁷]hexadeca-3,11-dien-2-yl]propanoate

Description

Daphnezomine L methyl ester belongs to the class of organic compounds known as sesquiterpenoids. These are terpenes with three consecutive isoprene units. methyl 3-[(1s,2s,7r,10s,13r,14r)-14-isopropyl-1-methyl-12-azatetracyclo[8.6.0.0²,¹³.0³,⁷]hexadeca-3,11-dien-2-yl]propanoate was first documented in 2009 (PMID: 19739650). Based on a literature review very few articles have been published on Daphnezomine L methyl ester.

Structure

MOL 3D MOL SDF PDB SMILES InChI


  Mrv1652309052211582D          

 26 29  0  0  1  0            999 V2000
   -1.0832    2.6531    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3716    3.0705    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.3611    2.6541    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1052    1.9736    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.3244    2.5797    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4949    1.7321    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.5746    0.7458    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    2.6157    0.6071    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.0316   -0.1054    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.8377    0.0699    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.9201    0.8908    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.1648    1.2228    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    2.8694    1.9792    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.0305    2.1009    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.7153    1.2149    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    2.2340    0.2558    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.9315   -0.4665    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    1.2295   -0.1315    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    0.4498   -0.2696    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    0.1239   -1.0773    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.5099   -1.8385    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7355   -1.2567    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0234    0.4084    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.2641    1.1907    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.0873    1.2780    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    0.7221    2.1235    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
  7  6  1  6  0  0  0
  7  8  1  0  0  0  0
  8  9  2  0  0  0  0
  9 10  1  0  0  0  0
 10 11  1  0  0  0  0
 12 11  1  1  0  0  0
  8 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  6  0  0  0
 16 17  2  0  0  0  0
 18 17  1  6  0  0  0
  7 18  1  0  0  0  0
 18 19  1  0  0  0  0
 19 20  1  1  0  0  0
 20 21  1  0  0  0  0
 20 22  1  0  0  0  0
 19 23  1  0  0  0  0
 23 24  1  0  0  0  0
 24 25  1  0  0  0  0
 15 25  1  0  0  0  0
  7 25  1  0  0  0  0
 25 26  1  6  0  0  0
M  END

     RDKit          2D

 61 64  0  0  0  0  0  0  0  0999 V2000
   -5.2500   -6.4952    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.5000   -5.1962    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.0000   -5.1962    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2500   -6.4952    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2500   -3.8971    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5000   -2.5981    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7500   -1.2990    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2124   -1.7376    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7395   -3.1420    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.2379   -3.0747    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.6370   -1.6288    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.3851   -0.8024    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.3851    0.6976    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2124    1.6328    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7500    1.2990    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7500    1.2990    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.5000    0.0000    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    0.7500   -1.2990    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0000   -2.5981    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4095   -3.1111    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8191   -3.6241    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.8965   -4.5206    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5000   -2.5981    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2500   -1.2990    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5000    0.0000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.0000    0.0000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.0000   -7.7942    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.5490   -5.7452    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.9510   -7.2452    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.7491   -3.8449    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0521   -4.7999    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.9672   -2.9102    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7053   -3.8702    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4167   -4.6069    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.7177   -3.3204    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.5132   -4.5492    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.7593   -0.6335    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.0333   -2.1768    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.7828   -0.2579    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.1958    1.9596    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.8700    0.9102    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7312    3.0535    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.2624    2.7040    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3361    2.6798    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.5000    2.5981    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.7920   -2.3780    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0785   -4.0960    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.9226   -1.7016    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.2286   -4.1372    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.4817   -5.0857    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.3321   -2.2146    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.3835   -5.9302    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.2330   -5.2017    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5953   -4.3639    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0614   -4.0325    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8365   -3.2791    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5080   -2.1160    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.3991   -0.3349    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.4888    0.1828    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.0000    1.5000    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.0039   -1.1146    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0
  2  3  1  0
  3  4  2  0
  3  5  1  0
  5  6  1  0
  7  6  1  1
  7 18  1  0
 18 17  1  0
 17 16  2  0
 16 15  1  0
 15 14  1  0
 14 13  1  0
 13 12  1  0
 12 11  1  0
 11 10  1  0
 10  9  1  0
  9  8  2  0
 15 25  1  0
 25 26  1  6
 25 24  1  0
 24 23  1  0
 23 19  1  0
 19 20  1  0
 20 21  1  0
 20 22  1  0
  8  7  1  0
 25  7  1  0
 19 18  1  0
  8 12  1  0
  1 27  1  0
  1 28  1  0
  1 29  1  0
  5 30  1  0
  5 31  1  0
  6 32  1  0
  6 33  1  0
 18 46  1  1
 16 45  1  0
 15 44  1  1
 14 42  1  0
 14 43  1  0
 13 40  1  0
 13 41  1  0
 12 39  1  1
 11 37  1  0
 11 38  1  0
 10 35  1  0
 10 36  1  0
  9 34  1  0
 26 59  1  0
 26 60  1  0
 26 61  1  0
 24 57  1  0
 24 58  1  0
 23 55  1  0
 23 56  1  0
 19 47  1  6
 20 48  1  0
 21 49  1  0
 21 50  1  0
 21 51  1  0
 22 52  1  0
 22 53  1  0
 22 54  1  0
M  END


  Mrv1652309052211582D          

 26 29  0  0  1  0            999 V2000
   -1.0832    2.6531    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3716    3.0705    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.3611    2.6541    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1052    1.9736    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.3244    2.5797    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4949    1.7321    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.5746    0.7458    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    2.6157    0.6071    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.0316   -0.1054    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.8377    0.0699    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.9201    0.8908    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.1648    1.2228    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    2.8694    1.9792    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.0305    2.1009    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.7153    1.2149    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    2.2340    0.2558    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.9315   -0.4665    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    1.2295   -0.1315    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    0.4498   -0.2696    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    0.1239   -1.0773    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.5099   -1.8385    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7355   -1.2567    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0234    0.4084    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.2641    1.1907    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.0873    1.2780    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    0.7221    2.1235    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
  7  6  1  6  0  0  0
  7  8  1  0  0  0  0
  8  9  2  0  0  0  0
  9 10  1  0  0  0  0
 10 11  1  0  0  0  0
 12 11  1  1  0  0  0
  8 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  6  0  0  0
 16 17  2  0  0  0  0
 18 17  1  6  0  0  0
  7 18  1  0  0  0  0
 18 19  1  0  0  0  0
 19 20  1  1  0  0  0
 20 21  1  0  0  0  0
 20 22  1  0  0  0  0
 19 23  1  0  0  0  0
 23 24  1  0  0  0  0
 24 25  1  0  0  0  0
 15 25  1  0  0  0  0
  7 25  1  0  0  0  0
 25 26  1  6  0  0  0
M  END
> <DATABASE_ID>
NP0211618

> <DATABASE_NAME>
NP-MRD

> <SMILES>
COC(=O)CC[C@@]12[C@@H]3N=C[C@@H](CC[C@H]4CCC=C14)[C@]2(C)CC[C@@H]3C(C)C

> <INCHI_IDENTIFIER>
InChI=1S/C23H35NO2/c1-15(2)18-10-12-22(3)17-9-8-16-6-5-7-19(16)23(22,21(18)24-14-17)13-11-20(25)26-4/h7,14-18,21H,5-6,8-13H2,1-4H3/t16-,17-,18-,21-,22+,23+/m1/s1

> <INCHI_KEY>
CPDMKDOXBXJZGN-QNWULWIJSA-N

> <FORMULA>
C23H35NO2

> <MOLECULAR_WEIGHT>
357.538

> <EXACT_MASS>
357.266779371

> <JCHEM_ACCEPTOR_COUNT>
2

> <JCHEM_ATOM_COUNT>
61

> <JCHEM_AVERAGE_POLARIZABILITY>
36.80167432990486

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
0

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
1

> <JCHEM_IUPAC>
methyl 3-[(1S,2S,7R,10S,13R,14R)-1-methyl-14-(propan-2-yl)-12-azatetracyclo[8.6.0.0^{2,13}.0^{3,7}]hexadeca-3,11-dien-2-yl]propanoate

> <JCHEM_LOGP>
4.260408039000001

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
4

> <JCHEM_PHYSIOLOGICAL_CHARGE>
1

> <JCHEM_PKA_STRONGEST_BASIC>
8.577417455492

> <JCHEM_POLAR_SURFACE_AREA>
38.66

> <JCHEM_REFRACTIVITY>
105.1804

> <JCHEM_ROTATABLE_BOND_COUNT>
5

> <JCHEM_RULE_OF_FIVE>
1

> <JCHEM_TRADITIONAL_IUPAC>
methyl 3-[(1S,2S,7R,10S,13R,14R)-14-isopropyl-1-methyl-12-azatetracyclo[8.6.0.0^{2,13}.0^{3,7}]hexadeca-3,11-dien-2-yl]propanoate

> <JCHEM_VEBER_RULE>
1

$$$$

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      -2.022   4.952   0.000  0.00  0.00           C+0
HETATM    2  O   UNK     0      -0.694   5.732   0.000  0.00  0.00           O+0
HETATM    3  C   UNK     0       0.674   4.954   0.000  0.00  0.00           C+0
HETATM    4  O   UNK     0      -0.196   3.684   0.000  0.00  0.00           O+0
HETATM    5  C   UNK     0       2.472   4.815   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0       2.790   3.233   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0       2.939   1.392   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0       4.883   1.133   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0       5.659  -0.197   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0       7.164   0.130   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0       7.318   1.663   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0       5.908   2.282   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0       5.356   3.694   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0       3.790   3.922   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0       3.202   2.268   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0       4.170   0.478   0.000  0.00  0.00           C+0
HETATM   17  N   UNK     0       3.605  -0.871   0.000  0.00  0.00           N+0
HETATM   18  C   UNK     0       2.295  -0.245   0.000  0.00  0.00           C+0
HETATM   19  C   UNK     0       0.840  -0.503   0.000  0.00  0.00           C+0
HETATM   20  C   UNK     0       0.231  -2.011   0.000  0.00  0.00           C+0
HETATM   21  C   UNK     0       0.952  -3.432   0.000  0.00  0.00           C+0
HETATM   22  C   UNK     0      -1.373  -2.346   0.000  0.00  0.00           C+0
HETATM   23  C   UNK     0      -0.044   0.762   0.000  0.00  0.00           C+0
HETATM   24  C   UNK     0       0.493   2.223   0.000  0.00  0.00           C+0
HETATM   25  C   UNK     0       2.030   2.386   0.000  0.00  0.00           C+0
HETATM   26  C   UNK     0       1.348   3.964   0.000  0.00  0.00           C+0
CONECT    1    2                                                            
CONECT    2    1    3                                                       
CONECT    3    2    4    5                                                  
CONECT    4    3                                                            
CONECT    5    3    6                                                       
CONECT    6    5    7                                                       
CONECT    7    6    8   18   25                                             
CONECT    8    7    9   12                                                  
CONECT    9    8   10                                                       
CONECT   10    9   11                                                       
CONECT   11   10   12                                                       
CONECT   12   11    8   13                                                  
CONECT   13   12   14                                                       
CONECT   14   13   15                                                       
CONECT   15   14   16   25                                                  
CONECT   16   15   17                                                       
CONECT   17   16   18                                                       
CONECT   18   17    7   19                                                  
CONECT   19   18   20   23                                                  
CONECT   20   19   21   22                                                  
CONECT   21   20                                                            
CONECT   22   20                                                            
CONECT   23   19   24                                                       
CONECT   24   23   25                                                       
CONECT   25   24   15    7   26                                             
CONECT   26   25                                                            
MASTER        0    0    0    0    0    0    0    0   26    0   58    0
END

View in JSmol

Synonyms

Not Available

Chemical Formula

C₂₃H₃₅NO₂

Average Mass

357.5380 Da

Monoisotopic Mass

357.26678 Da

IUPAC Name

Not Available

Traditional Name

Not Available

CAS Registry Number

Not Available

SMILES

COC(=O)CC[C@@]12[C@@H]3N=C[C@@H](CC[C@H]4CCC=C14)[C@]2(C)CC[C@@H]3C(C)C

InChI Identifier

InChI=1S/C23H35NO2/c1-15(2)18-10-12-22(3)17-9-8-16-6-5-7-19(16)23(22,21(18)24-14-17)13-11-20(25)26-4/h7,14-18,21H,5-6,8-13H2,1-4H3/t16-,17-,18-,21-,22+,23+/m1/s1

InChI Key

CPDMKDOXBXJZGN-QNWULWIJSA-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 sesquiterpenoids. These are terpenes with three consecutive isoprene units.

Kingdom

Organic compounds

Super Class

Lipids and lipid-like molecules

Class

Prenol lipids

Sub Class

Sesquiterpenoids

Direct Parent

Sesquiterpenoids

Alternative Parents

Substituents

Sesquiterpenoid
Fatty acid ester
Tetrahydropyridine
Fatty acyl
Methyl ester
Carboxylic acid ester
Azacycle
Carboxylic acid derivative
Organoheterocyclic compound
Organic 1,3-dipolar compound
Propargyl-type 1,3-dipolar organic compound
Monocarboxylic acid or derivatives
Hydrocarbon derivative
Organooxygen compound
Organonitrogen compound
Organic oxygen compound
Imine
Organic nitrogen compound
Organic oxide
Carbonyl group
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

24655452

KEGG Compound ID

Not Available

BioCyc ID

Not Available

BiGG ID

Not Available

Wikipedia Link

Not Available

METLIN ID

Not Available

PubChem Compound

46882263

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

Zhang CR, Liu HB, Feng T, Zhu JY, Geng MY, Yue JM: Alkaloids from the leaves of Daphniphyllum subverticillatum. J Nat Prod. 2009 Sep;72(9):1669-72. doi: 10.1021/np9003799. [PubMed:19739650 ]
LOTUS database [Link]

Showing NP-Card for methyl 3-[(1s,2s,7r,10s,13r,14r)-14-isopropyl-1-methyl-12-azatetracyclo[8.6.0.0²,¹³.0³,⁷]hexadeca-3,11-dien-2-yl]propanoate (NP0211618)

MOL for NP0211618 (methyl 3-[(1s,2s,7r,10s,13r,14r)-14-isopropyl-1-methyl-12-azatetracyclo[8.6.0.0²,¹³.0³,⁷]hexadeca-3,11-dien-2-yl]propanoate)

3D MOL for NP0211618 (methyl 3-[(1s,2s,7r,10s,13r,14r)-14-isopropyl-1-methyl-12-azatetracyclo[8.6.0.0²,¹³.0³,⁷]hexadeca-3,11-dien-2-yl]propanoate)

3D SDF for NP0211618 (methyl 3-[(1s,2s,7r,10s,13r,14r)-14-isopropyl-1-methyl-12-azatetracyclo[8.6.0.0²,¹³.0³,⁷]hexadeca-3,11-dien-2-yl]propanoate)

3D-SDF for NP0211618 (methyl 3-[(1s,2s,7r,10s,13r,14r)-14-isopropyl-1-methyl-12-azatetracyclo[8.6.0.0²,¹³.0³,⁷]hexadeca-3,11-dien-2-yl]propanoate)

PDB for NP0211618 (methyl 3-[(1s,2s,7r,10s,13r,14r)-14-isopropyl-1-methyl-12-azatetracyclo[8.6.0.0²,¹³.0³,⁷]hexadeca-3,11-dien-2-yl]propanoate)

3D PDB for NP0211618 (methyl 3-[(1s,2s,7r,10s,13r,14r)-14-isopropyl-1-methyl-12-azatetracyclo[8.6.0.0²,¹³.0³,⁷]hexadeca-3,11-dien-2-yl]propanoate)

SMILES for NP0211618 (methyl 3-[(1s,2s,7r,10s,13r,14r)-14-isopropyl-1-methyl-12-azatetracyclo[8.6.0.0²,¹³.0³,⁷]hexadeca-3,11-dien-2-yl]propanoate)

INCHI for NP0211618 (methyl 3-[(1s,2s,7r,10s,13r,14r)-14-isopropyl-1-methyl-12-azatetracyclo[8.6.0.0²,¹³.0³,⁷]hexadeca-3,11-dien-2-yl]propanoate)

Structure for NP0211618 (methyl 3-[(1s,2s,7r,10s,13r,14r)-14-isopropyl-1-methyl-12-azatetracyclo[8.6.0.0²,¹³.0³,⁷]hexadeca-3,11-dien-2-yl]propanoate)

3D Structure for NP0211618 (methyl 3-[(1s,2s,7r,10s,13r,14r)-14-isopropyl-1-methyl-12-azatetracyclo[8.6.0.0²,¹³.0³,⁷]hexadeca-3,11-dien-2-yl]propanoate)