NP-MRD: Showing NP-Card for (-)-3-O-Methylepivobasinol (NP0081508)

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Record Information

Version

2.0

Created at

2022-04-29 02:30:57 UTC

Updated at

2022-04-29 02:30:57 UTC

NP-MRD ID

NP0081508

Secondary Accession Numbers

None

Natural Product Identification

Common Name

(-)-3-O-Methylepivobasinol

Description

Methyl (1S,12R,14R,15E,18R)-15-ethylidene-12-methoxy-17-methyl-10,17-diazatetracyclo[12.3.1.0³,¹¹.0⁴,⁹]Octadeca-3(11),4,6,8-tetraene-18-carboxylate belongs to the class of organic compounds known as vobasan alkaloids. These are alkaloids containing the vobasan skeleton. (-)-3-O-Methylepivobasinol is found in Hunteria zeylanica . Based on a literature review very few articles have been published on methyl (1S,12R,14R,15E,18R)-15-ethylidene-12-methoxy-17-methyl-10,17-diazatetracyclo[12.3.1.0³,¹¹.0⁴,⁹]Octadeca-3(11),4,6,8-tetraene-18-carboxylate.

Structure

MOL 3D MOL SDF PDB SMILES InChI


  Mrv1652304292204312D          

 27 30  0  0  1  0            999 V2000
    6.0161    0.3797    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.4657    1.0714    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.0915    1.8067    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.2677    1.8503    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.8180    1.1586    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.1922    0.4233    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.0213    1.3725    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.9785    2.1963    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.7488    2.4916    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    3.3320    2.7523    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    2.4823    2.6509    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.8865    2.0127    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    1.1297    1.5909    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.3999    2.0621    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.3205    2.9090    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.0483    0.7495    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.7699    0.3092    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    2.5616    0.6610    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    3.4298    0.7540    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.2837    1.3666    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    2.9211    1.7680    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5024    1.2369    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.9946    2.5206    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.8665    3.0113    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.7125   -0.5455    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.4800    3.7217    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.0331    4.4670    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  2  0  0  0  0
  4  5  1  0  0  0  0
  5  6  2  0  0  0  0
  1  6  1  0  0  0  0
  5  7  1  0  0  0  0
  7  8  2  0  0  0  0
  8  9  1  0  0  0  0
  4  9  1  0  0  0  0
  8 10  1  0  0  0  0
 10 11  1  0  0  0  0
 11 12  1  0  0  0  0
 12 13  1  6  0  0  0
 13 14  2  0  0  0  0
 14 15  1  0  0  0  0
 13 16  1  0  0  0  0
 16 17  1  0  0  0  0
 18 17  1  6  0  0  0
 18 19  1  0  0  0  0
  7 19  1  0  0  0  0
 18 20  1  0  0  0  0
 12 20  1  0  0  0  0
 20 21  1  1  0  0  0
 21 22  2  0  0  0  0
 21 23  1  0  0  0  0
 23 24  1  0  0  0  0
 17 25  1  0  0  0  0
 10 26  1  1  0  0  0
 26 27  1  0  0  0  0
M  END

     RDKit          3D

 55 58  0  0  0  0  0  0  0  0999 V2000
   -3.0227    2.9120   -0.0460 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4341    2.0035   -1.0703 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6880    0.9361   -0.7359 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1410    0.0838   -1.7990 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0284   -1.2697   -1.4379 N   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0160   -2.1299   -2.0572 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6783   -1.6219   -0.1174 C   0  0  1  0  0  0  0  0  0  0  0  0
    0.7713   -1.8702    0.1215 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.7042   -0.7972   -0.0399 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.7480    0.5779    0.0114 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.0077    0.9515   -0.2543 N   0  0  0  0  0  0  0  0  0  0  0  0
    3.8090   -0.1040   -0.4806 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.1651   -0.2261   -0.7894 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.7432   -1.4608   -0.9730 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.9317   -2.5637   -0.8400 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5924   -2.4440   -0.5352 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.9940   -1.2026   -0.3467 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.8171    1.6835    0.2709 C   0  0  2  0  0  0  0  0  0  0  0  0
    1.5616    2.7205    0.8856 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.5041    3.8972    0.1880 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2590    1.3502    1.2730 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4341    0.6404    0.6838 C   0  0  2  0  0  0  0  0  0  0  0  0
   -1.3075   -0.8222    0.9825 C   0  0  1  0  0  0  0  0  0  0  0  0
   -2.6099   -1.3837    1.4266 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.1074   -2.3122    0.7458 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.2690   -0.9304    2.5296 O   0  0  0  0  0  0  0  0  0  0  0  0
   -4.5155   -1.4418    2.9856 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.7520    2.2886    0.5419 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2509    3.3753    0.5673 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.6553    3.6531   -0.5913 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5906    2.1756   -2.1464 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1736    0.4487   -2.2292 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8535    0.1442   -2.6770 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9921   -3.1403   -1.6241 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8168   -2.1680   -3.1495 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.0076   -1.6412   -1.9164 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1318   -2.6609    0.0193 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.8707   -2.3177    1.1436 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.0505   -2.7132   -0.5790 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.3817    1.9453   -0.2940 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.7978    0.6433   -0.8926 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.8106   -1.5584   -1.2161 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.3476   -3.5382   -0.9759 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.9758   -3.3291   -0.4353 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.3841    2.1452   -0.6397 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.9076    3.7606   -0.8287 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.4996    4.3707    0.1881 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.1784    4.6148    0.6989 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5628    2.2570    1.8479 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.2401    0.6949    2.0466 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3427    1.0005    1.2504 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6225   -0.9592    1.8748 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.2609   -1.5171    2.1709 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.4012   -2.4214    3.4951 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.8688   -0.7291    3.7689 H   0  0  0  0  0  0  0  0  0  0  0  0
 20 19  1  0
 19 18  1  0
 18 21  1  0
 21 22  1  0
 22 23  1  0
 23  7  1  0
  7  8  1  0
  8  9  1  0
  9 10  2  0
 10 11  1  0
 11 12  1  0
 12 13  2  0
 13 14  1  0
 14 15  2  0
 15 16  1  0
 16 17  2  0
  7  5  1  0
  5  6  1  0
  5  4  1  0
  4  3  1  0
  3  2  2  0
  2  1  1  0
 23 24  1  0
 24 25  2  0
 24 26  1  0
 26 27  1  0
 10 18  1  0
 17 12  1  0
  3 22  1  0
 17  9  1  0
 20 46  1  0
 20 47  1  0
 20 48  1  0
 18 45  1  6
 21 49  1  0
 21 50  1  0
 22 51  1  1
 23 52  1  1
  7 37  1  1
  8 38  1  0
  8 39  1  0
 11 40  1  0
 13 41  1  0
 14 42  1  0
 15 43  1  0
 16 44  1  0
  6 34  1  0
  6 35  1  0
  6 36  1  0
  4 32  1  0
  4 33  1  0
  2 31  1  0
  1 28  1  0
  1 29  1  0
  1 30  1  0
 27 53  1  0
 27 54  1  0
 27 55  1  0
M  END


  Mrv1652304292204312D          

 27 30  0  0  1  0            999 V2000
    6.0161    0.3797    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.4657    1.0714    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.0915    1.8067    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.2677    1.8503    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.8180    1.1586    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.1922    0.4233    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.0213    1.3725    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.9785    2.1963    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.7488    2.4916    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    3.3320    2.7523    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    2.4823    2.6509    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.8865    2.0127    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    1.1297    1.5909    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.3999    2.0621    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.3205    2.9090    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.0483    0.7495    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.7699    0.3092    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    2.5616    0.6610    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    3.4298    0.7540    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.2837    1.3666    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    2.9211    1.7680    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5024    1.2369    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.9946    2.5206    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.8665    3.0113    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.7125   -0.5455    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.4800    3.7217    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.0331    4.4670    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  2  0  0  0  0
  4  5  1  0  0  0  0
  5  6  2  0  0  0  0
  1  6  1  0  0  0  0
  5  7  1  0  0  0  0
  7  8  2  0  0  0  0
  8  9  1  0  0  0  0
  4  9  1  0  0  0  0
  8 10  1  0  0  0  0
 10 11  1  0  0  0  0
 11 12  1  0  0  0  0
 12 13  1  6  0  0  0
 13 14  2  0  0  0  0
 14 15  1  0  0  0  0
 13 16  1  0  0  0  0
 16 17  1  0  0  0  0
 18 17  1  6  0  0  0
 18 19  1  0  0  0  0
  7 19  1  0  0  0  0
 18 20  1  0  0  0  0
 12 20  1  0  0  0  0
 20 21  1  1  0  0  0
 21 22  2  0  0  0  0
 21 23  1  0  0  0  0
 23 24  1  0  0  0  0
 17 25  1  0  0  0  0
 10 26  1  1  0  0  0
 26 27  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0081508

> <DATABASE_NAME>
NP-MRD

> <SMILES>
CO[C@@H]1C[C@@H]2[C@H]([C@H](CC3=C1NC1=CC=CC=C31)N(C)C\C2=C\C)C(=O)OC

> <INCHI_IDENTIFIER>
InChI=1S/C22H28N2O3/c1-5-13-12-24(2)18-10-16-14-8-6-7-9-17(14)23-21(16)19(26-3)11-15(13)20(18)22(25)27-4/h5-9,15,18-20,23H,10-12H2,1-4H3/b13-5-/t15-,18-,19+,20+/m0/s1

> <INCHI_KEY>
FPYWPRHZJJOPJP-XOXQQVMWSA-N

> <FORMULA>
C22H28N2O3

> <MOLECULAR_WEIGHT>
368.477

> <EXACT_MASS>
368.20999277

> <JCHEM_ACCEPTOR_COUNT>
3

> <JCHEM_ATOM_COUNT>
55

> <JCHEM_AVERAGE_POLARIZABILITY>
41.403741834848184

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
1

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
1

> <JCHEM_IUPAC>
methyl (1S,12R,14R,15E,18R)-15-ethylidene-12-methoxy-17-methyl-10,17-diazatetracyclo[12.3.1.0^{3,11}.0^{4,9}]octadeca-3(11),4,6,8-tetraene-18-carboxylate

> <ALOGPS_LOGP>
3.52

> <JCHEM_LOGP>
2.8876918953333317

> <ALOGPS_LOGS>
-3.69

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
4

> <JCHEM_PHYSIOLOGICAL_CHARGE>
1

> <JCHEM_PKA_STRONGEST_ACIDIC>
15.007731837135559

> <JCHEM_PKA_STRONGEST_BASIC>
7.498928428365432

> <JCHEM_POLAR_SURFACE_AREA>
54.56

> <JCHEM_REFRACTIVITY>
106.88679999999997

> <JCHEM_ROTATABLE_BOND_COUNT>
3

> <JCHEM_RULE_OF_FIVE>
1

> <ALOGPS_SOLUBILITY>
7.44e-02 g/l

> <JCHEM_TRADITIONAL_IUPAC>
methyl (1S,12R,14R,15E,18R)-15-ethylidene-12-methoxy-17-methyl-10,17-diazatetracyclo[12.3.1.0^{3,11}.0^{4,9}]octadeca-3(11),4,6,8-tetraene-18-carboxylate

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 29-APR-22   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   29-APR-22         0                                  
HETATM    1  C   UNK     0      11.230   0.709   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0      12.069   2.000   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0      11.371   3.372   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0       9.833   3.454   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0       8.994   2.163   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0       9.692   0.790   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0       7.506   2.562   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0       7.426   4.100   0.000  0.00  0.00           C+0
HETATM    9  N   UNK     0       8.864   4.651   0.000  0.00  0.00           N+0
HETATM   10  C   UNK     0       6.220   5.138   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0       4.634   4.948   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0       3.521   3.757   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0       2.109   2.970   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0       0.746   3.849   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0       0.598   5.430   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0       1.957   1.399   0.000  0.00  0.00           C+0
HETATM   17  N   UNK     0       3.304   0.577   0.000  0.00  0.00           N+0
HETATM   18  C   UNK     0       4.782   1.234   0.000  0.00  0.00           C+0
HETATM   19  C   UNK     0       6.402   1.407   0.000  0.00  0.00           C+0
HETATM   20  C   UNK     0       4.263   2.551   0.000  0.00  0.00           C+0
HETATM   21  C   UNK     0       5.453   3.300   0.000  0.00  0.00           C+0
HETATM   22  O   UNK     0       6.538   2.309   0.000  0.00  0.00           O+0
HETATM   23  O   UNK     0       5.590   4.705   0.000  0.00  0.00           O+0
HETATM   24  C   UNK     0       7.217   5.621   0.000  0.00  0.00           C+0
HETATM   25  C   UNK     0       3.197  -1.018   0.000  0.00  0.00           C+0
HETATM   26  O   UNK     0       6.496   6.947   0.000  0.00  0.00           O+0
HETATM   27  C   UNK     0       5.662   8.338   0.000  0.00  0.00           C+0
CONECT    1    2    6                                                       
CONECT    2    1    3                                                       
CONECT    3    2    4                                                       
CONECT    4    3    5    9                                                  
CONECT    5    4    6    7                                                  
CONECT    6    5    1                                                       
CONECT    7    5    8   19                                                  
CONECT    8    7    9   10                                                  
CONECT    9    8    4                                                       
CONECT   10    8   11   26                                                  
CONECT   11   10   12                                                       
CONECT   12   11   13   20                                                  
CONECT   13   12   14   16                                                  
CONECT   14   13   15                                                       
CONECT   15   14                                                            
CONECT   16   13   17                                                       
CONECT   17   16   18   25                                                  
CONECT   18   17   19   20                                                  
CONECT   19   18    7                                                       
CONECT   20   18   12   21                                                  
CONECT   21   20   22   23                                                  
CONECT   22   21                                                            
CONECT   23   21   24                                                       
CONECT   24   23                                                            
CONECT   25   17                                                            
CONECT   26   10   27                                                       
CONECT   27   26                                                            
MASTER        0    0    0    0    0    0    0    0   27    0   60    0
END

View in JSmol

Synonyms

Value	Source
Methyl (1S,12R,14R,15E,18R)-15-ethylidene-12-methoxy-17-methyl-10,17-diazatetracyclo[12.3.1.0,.0,]octadeca-3(11),4,6,8-tetraene-18-carboxylic acid	Generator

Chemical Formula

C₂₂H₂₈N₂O₃

Average Mass

368.4770 Da

Monoisotopic Mass

368.20999 Da

IUPAC Name

methyl (1S,12R,14R,15E,18R)-15-ethylidene-12-methoxy-17-methyl-10,17-diazatetracyclo[12.3.1.0^{3,11}.0^{4,9}]octadeca-3(11),4,6,8-tetraene-18-carboxylate

Traditional Name

methyl (1S,12R,14R,15E,18R)-15-ethylidene-12-methoxy-17-methyl-10,17-diazatetracyclo[12.3.1.0^{3,11}.0^{4,9}]octadeca-3(11),4,6,8-tetraene-18-carboxylate

CAS Registry Number

Not Available

SMILES

CO[C@@H]1C[C@@H]2[C@H]([C@H](CC3=C1NC1=CC=CC=C31)N(C)C\C2=C\C)C(=O)OC

InChI Identifier

InChI=1S/C22H28N2O3/c1-5-13-12-24(2)18-10-16-14-8-6-7-9-17(14)23-21(16)19(26-3)11-15(13)20(18)22(25)27-4/h5-9,15,18-20,23H,10-12H2,1-4H3/b13-5-/t15-,18-,19+,20+/m0/s1

InChI Key

FPYWPRHZJJOPJP-XOXQQVMWSA-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, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 100 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 252 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 1000 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 50 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 200 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 75 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 300 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 101 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 400 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 126 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 500 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 151 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 600 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 176 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 700 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 201 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 800 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 226 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 900 MHz, D₂O, 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
Hunteria zeylanica	Plant	KNApSAcK

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as vobasan alkaloids. These are alkaloids containing the vobasan skeleton.

Kingdom

Organic compounds

Super Class

Alkaloids and derivatives

Class

Vobasan alkaloids

Sub Class

Not Available

Direct Parent

Vobasan alkaloids

Alternative Parents

Substituents

Vobasan skeleton
3-alkylindole
Piperidinecarboxylic acid
Indole or derivatives
Indole
Aralkylamine
Benzenoid
Piperidine
Heteroaromatic compound
Methyl ester
Pyrrole
Tertiary aliphatic amine
Tertiary amine
Carboxylic acid ester
Amino acid or derivatives
Azacycle
Organoheterocyclic compound
Monocarboxylic acid or derivatives
Ether
Dialkyl ether
Carboxylic acid derivative
Organic nitrogen compound
Organic oxygen compound
Organopnictogen compound
Organic oxide
Hydrocarbon derivative
Organooxygen compound
Organonitrogen compound
Carbonyl group
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	3.52	ALOGPS
logP	2.89	ChemAxon
logS	-3.7	ALOGPS
pKa (Strongest Acidic)	15.01	ChemAxon
pKa (Strongest Basic)	7.5	ChemAxon
Physiological Charge	1	ChemAxon
Hydrogen Acceptor Count	3	ChemAxon
Hydrogen Donor Count	1	ChemAxon
Polar Surface Area	54.56 Å²	ChemAxon
Rotatable Bond Count	3	ChemAxon
Refractivity	106.89 m³·mol⁻¹	ChemAxon
Polarizability	41.4 Å³	ChemAxon
Number of Rings	4	ChemAxon
Bioavailability	Yes	ChemAxon
Rule of Five	Yes	ChemAxon
Ghose Filter	Yes	ChemAxon
Veber's Rule	No	ChemAxon
MDDR-like Rule	No	ChemAxon

External Links

HMDB ID

Not Available

DrugBank ID

Not Available

Phenol Explorer Compound ID

Not Available

FoodDB ID

Not Available

KNApSAcK ID

Not Available

Chemspider ID

Not Available

KEGG Compound ID

Not Available

BioCyc ID

Not Available

BiGG ID

Not Available

Wikipedia Link

Not Available

METLIN ID

Not Available

PubChem Compound

163038030

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

Not Available

Showing NP-Card for (-)-3-O-Methylepivobasinol (NP0081508)

MOL for NP0081508 ((-)-3-O-Methylepivobasinol)

3D MOL for NP0081508 ((-)-3-O-Methylepivobasinol)

3D SDF for NP0081508 ((-)-3-O-Methylepivobasinol)

3D-SDF for NP0081508 ((-)-3-O-Methylepivobasinol)

PDB for NP0081508 ((-)-3-O-Methylepivobasinol)

3D PDB for NP0081508 ((-)-3-O-Methylepivobasinol)

SMILES for NP0081508 ((-)-3-O-Methylepivobasinol)

INCHI for NP0081508 ((-)-3-O-Methylepivobasinol)

Structure for NP0081508 ((-)-3-O-Methylepivobasinol)

3D Structure for NP0081508 ((-)-3-O-Methylepivobasinol)