NP-MRD: Showing NP-Card for Nervosanin B (NP0081651)

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Record Information

Version

2.0

Created at

2022-04-29 02:39:52 UTC

Updated at

2022-04-29 02:39:52 UTC

NP-MRD ID

NP0081651

Secondary Accession Numbers

None

Natural Product Identification

Common Name

Nervosanin B

Description

Nervosanin B belongs to the class of organic compounds known as kaurane diterpenoids. These are diterpene alkaloids with a structure that is based on the kaurane skeleton. Kaurane is a tetracyclic compound that arises by cyclisation of a pimarane precursor followed by rearrangement. It possesses a [3,2,1]-bicyclic ring system with C15-C16 bridge connected to C13, forming the five-membered ring D. Nervosanin B is found in Isodon nervosus, Isodon sculponeatus and Rabdosia nervosa. Nervosanin B was first documented in 2010 (PMID: 21579763). Based on a literature review very few articles have been published on Nervosanin B.

Structure

MOL 3D MOL SDF PDB SMILES InChI


  Mrv1652304292204392D          

 26 30  0  0  1  0            999 V2000
    7.3349   -0.7720    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.6004    0.0200    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.9763    0.5828    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.1341    0.4235    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    5.8274   -0.4538    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    6.5193   -0.9618    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    6.3535   -1.7700    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.9206   -0.6791    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    4.3622    0.1026    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    4.7341    0.9050    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    5.6118    1.1973    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    5.8774    1.9784    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.4550    0.6284    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.1273   -0.0775    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.1845    1.5203    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.5366    0.3968    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    2.8222   -0.0464    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.0491    0.2416    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.0821   -0.8796    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    3.5820   -1.5689    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.4244   -1.3877    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    4.8806   -2.0751    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.8131   -0.5412    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.4488    1.2171    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    7.5371    1.1879    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.8120    1.3912    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
  4  3  1  6  0  0  0
  4  5  1  0  0  0  0
  5  6  1  0  0  0  0
  1  6  1  0  0  0  0
  6  7  1  6  0  0  0
  5  8  1  0  0  0  0
  8  9  1  6  0  0  0
  9 10  1  0  0  0  0
 10 11  1  0  0  0  0
  4 11  1  0  0  0  0
 11 12  1  1  0  0  0
 10 13  1  0  0  0  0
 13 14  1  0  0  0  0
  5 14  1  6  0  0  0
 10 15  1  6  0  0  0
  9 16  1  0  0  0  0
 16 17  1  0  0  0  0
 17 18  2  0  0  0  0
 17 19  1  0  0  0  0
 19 20  1  0  0  0  0
 20 21  1  0  0  0  0
  8 21  1  0  0  0  0
 21 22  1  6  0  0  0
 19 23  1  6  0  0  0
  9 23  1  6  0  0  0
 16 24  1  1  0  0  0
  3 25  1  0  0  0  0
  3 26  1  0  0  0  0
M  END

     RDKit          3D

 56 60  0  0  0  0  0  0  0  0999 V2000
   -4.2749   -0.9571    1.7564 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5047   -0.3206    0.9134 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5659   -0.4625   -0.5835 C   0  0  2  0  0  0  0  0  0  0  0  0
   -2.9243   -1.7678   -0.9237 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4348   -1.7694   -0.9036 C   0  0  1  0  0  0  0  0  0  0  0  0
   -1.0084   -1.8365   -2.2484 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7976   -0.6997   -0.1224 C   0  0  1  0  0  0  0  0  0  0  0  0
    0.6109   -0.3288   -0.5955 C   0  0  1  0  0  0  0  0  0  0  0  0
    0.5279    0.6520   -1.7705 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2951    1.7156   -1.5421 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6865    1.7772   -0.1961 C   0  0  2  0  0  0  0  0  0  0  0  0
   -1.4092    2.9038    0.0955 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.5578    1.7575    0.6288 C   0  0  1  0  0  0  0  0  0  0  0  0
    0.3380    2.1319    1.9509 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.2436    0.3895    0.5565 C   0  0  2  0  0  0  0  0  0  0  0  0
    2.7109    0.4595    0.5910 C   0  0  2  0  0  0  0  0  0  0  0  0
    3.2439    0.0804    1.9865 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.2790    1.8673    0.3562 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.4308   -0.4424   -0.3710 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.6988   -1.7372   -0.4166 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.3694   -1.5198   -1.0788 C   0  0  2  0  0  0  0  0  0  0  0  0
    1.6244   -1.4660   -2.4707 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5646    0.5700    0.0115 C   0  0  1  0  0  0  0  0  0  0  0  0
   -2.6130    0.6178   -1.1103 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4316    0.6527    1.2196 C   0  0  2  0  0  0  0  0  0  0  0  0
   -1.7719    0.3670    2.4055 O   0  0  0  0  0  0  0  0  0  0  0  0
   -4.1480   -0.7822    2.8180 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.0371   -1.6540    1.4429 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.5723   -0.3631   -0.9791 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.3676   -2.5338   -0.2204 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.3377   -2.0756   -1.9296 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1426   -2.7757   -0.4758 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5267   -2.5578   -2.6837 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6367   -1.0877    0.9282 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.1744    0.1229   -2.7017 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.5280    1.0138   -1.9952 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8810    3.6684    0.4221 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.2566    2.5002    0.1929 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.5790    3.0995    2.0975 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.8950   -0.1347    1.4968 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.5266   -0.6960    2.3699 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.2307   -0.3992    1.9217 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.1897    0.9295    2.6797 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.0368    2.5510    1.1789 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.0914    2.2359   -0.6490 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.3982    1.7170    0.4213 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.6098    0.0117   -1.3637 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.4571   -0.6527    0.0361 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.2779   -2.4447   -1.0601 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.6126   -2.1296    0.6066 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.8127   -2.4920   -0.9464 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.7792   -2.3727   -2.8244 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.1308    1.5812   -1.1350 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1476    0.3150   -2.0573 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.9035    1.6586    1.2330 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9770    1.1124    3.0370 H   0  0  0  0  0  0  0  0  0  0  0  0
 16 17  1  1
 16 18  1  0
 16 19  1  0
 19 20  1  0
 20 21  1  0
 21 22  1  0
 21  8  1  0
  8  9  1  6
  9 10  1  0
 10 11  1  0
 11 12  1  6
 11 13  1  0
 13 14  1  0
 13 15  1  0
 11 23  1  0
 23 24  1  6
 24  3  1  0
  3  4  1  0
  4  5  1  0
  5  6  1  0
  5  7  1  0
  3  2  1  0
  2  1  2  3
  2 25  1  0
 25 26  1  0
 15 16  1  0
  7 23  1  0
 15  8  1  0
 25 23  1  0
  7  8  1  0
 17 41  1  0
 17 42  1  0
 17 43  1  0
 18 44  1  0
 18 45  1  0
 18 46  1  0
 19 47  1  0
 19 48  1  0
 20 49  1  0
 20 50  1  0
 21 51  1  6
 22 52  1  0
  9 35  1  0
  9 36  1  0
 12 37  1  0
 13 38  1  6
 14 39  1  0
 15 40  1  1
 24 53  1  0
 24 54  1  0
  3 29  1  6
  4 30  1  0
  4 31  1  0
  5 32  1  1
  6 33  1  0
  7 34  1  1
  1 27  1  0
  1 28  1  0
 25 55  1  1
 26 56  1  0
M  END


  Mrv1652304292204392D          

 26 30  0  0  1  0            999 V2000
    7.3349   -0.7720    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.6004    0.0200    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.9763    0.5828    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.1341    0.4235    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    5.8274   -0.4538    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    6.5193   -0.9618    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    6.3535   -1.7700    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.9206   -0.6791    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    4.3622    0.1026    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    4.7341    0.9050    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    5.6118    1.1973    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    5.8774    1.9784    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.4550    0.6284    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.1273   -0.0775    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.1845    1.5203    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.5366    0.3968    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    2.8222   -0.0464    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.0491    0.2416    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.0821   -0.8796    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    3.5820   -1.5689    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.4244   -1.3877    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    4.8806   -2.0751    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.8131   -0.5412    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.4488    1.2171    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    7.5371    1.1879    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.8120    1.3912    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
  4  3  1  6  0  0  0
  4  5  1  0  0  0  0
  5  6  1  0  0  0  0
  1  6  1  0  0  0  0
  6  7  1  6  0  0  0
  5  8  1  0  0  0  0
  8  9  1  6  0  0  0
  9 10  1  0  0  0  0
 10 11  1  0  0  0  0
  4 11  1  0  0  0  0
 11 12  1  1  0  0  0
 10 13  1  0  0  0  0
 13 14  1  0  0  0  0
  5 14  1  6  0  0  0
 10 15  1  6  0  0  0
  9 16  1  0  0  0  0
 16 17  1  0  0  0  0
 17 18  2  0  0  0  0
 17 19  1  0  0  0  0
 19 20  1  0  0  0  0
 20 21  1  0  0  0  0
  8 21  1  0  0  0  0
 21 22  1  6  0  0  0
 19 23  1  6  0  0  0
  9 23  1  6  0  0  0
 16 24  1  1  0  0  0
  3 25  1  0  0  0  0
  3 26  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0081651

> <DATABASE_NAME>
NP-MRD

> <SMILES>
CC1(C)CC[C@H](O)[C@]23CO[C@](O)([C@@H](O)[C@H]12)[C@@]12C[C@@H](C[C@@H](O)[C@@H]31)C(=C)[C@H]2O

> <INCHI_IDENTIFIER>
InChI=1S/C20H30O6/c1-9-10-6-11(21)13-18-8-26-20(25,19(13,7-10)15(9)23)16(24)14(18)17(2,3)5-4-12(18)22/h10-16,21-25H,1,4-8H2,2-3H3/t10-,11-,12+,13+,14-,15-,16+,18+,19+,20-/m1/s1

> <INCHI_KEY>
DSHJJLKUJOADCV-RATWNWGVSA-N

> <FORMULA>
C20H30O6

> <MOLECULAR_WEIGHT>
366.454

> <EXACT_MASS>
366.204238686

> <JCHEM_ACCEPTOR_COUNT>
6

> <JCHEM_ATOM_COUNT>
56

> <JCHEM_AVERAGE_POLARIZABILITY>
38.48819474161801

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
5

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
0

> <JCHEM_IUPAC>
(1S,2S,3R,5S,7R,8S,9S,10S,11R,15S)-12,12-dimethyl-6-methylidene-17-oxapentacyclo[7.6.2.1^{5,8}.0^{1,11}.0^{2,8}]octadecane-3,7,9,10,15-pentol

> <ALOGPS_LOGP>
-0.22

> <JCHEM_LOGP>
-0.5348538756666663

> <ALOGPS_LOGS>
-1.30

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
5

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA>
13.555210974934493

> <JCHEM_PKA_STRONGEST_ACIDIC>
10.688698748557456

> <JCHEM_PKA_STRONGEST_BASIC>
-2.8549343050931464

> <JCHEM_POLAR_SURFACE_AREA>
110.38000000000001

> <JCHEM_REFRACTIVITY>
92.64779999999999

> <JCHEM_ROTATABLE_BOND_COUNT>
0

> <JCHEM_RULE_OF_FIVE>
1

> <ALOGPS_SOLUBILITY>
1.82e+01 g/l

> <JCHEM_TRADITIONAL_IUPAC>
(1S,2S,3R,5S,7R,8S,9S,10S,11R,15S)-12,12-dimethyl-6-methylidene-17-oxapentacyclo[7.6.2.1^{5,8}.0^{1,11}.0^{2,8}]octadecane-3,7,9,10,15-pentol

> <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      13.692  -1.441   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0      14.187   0.037   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0      13.022   1.088   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0      11.450   0.790   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0      10.878  -0.847   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0      12.169  -1.795   0.000  0.00  0.00           C+0
HETATM    7  O   UNK     0      11.860  -3.304   0.000  0.00  0.00           O+0
HETATM    8  C   UNK     0       9.185  -1.268   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0       8.143   0.192   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0       8.837   1.689   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0      10.475   2.235   0.000  0.00  0.00           C+0
HETATM   12  O   UNK     0      10.971   3.693   0.000  0.00  0.00           O+0
HETATM   13  O   UNK     0      10.183   1.173   0.000  0.00  0.00           O+0
HETATM   14  C   UNK     0       9.571  -0.145   0.000  0.00  0.00           C+0
HETATM   15  O   UNK     0       7.811   2.838   0.000  0.00  0.00           O+0
HETATM   16  C   UNK     0       6.602   0.741   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0       5.268  -0.087   0.000  0.00  0.00           C+0
HETATM   18  C   UNK     0       3.825   0.451   0.000  0.00  0.00           C+0
HETATM   19  C   UNK     0       5.753  -1.642   0.000  0.00  0.00           C+0
HETATM   20  C   UNK     0       6.686  -2.929   0.000  0.00  0.00           C+0
HETATM   21  C   UNK     0       8.259  -2.590   0.000  0.00  0.00           C+0
HETATM   22  O   UNK     0       9.110  -3.874   0.000  0.00  0.00           O+0
HETATM   23  C   UNK     0       7.118  -1.010   0.000  0.00  0.00           C+0
HETATM   24  O   UNK     0       6.438   2.272   0.000  0.00  0.00           O+0
HETATM   25  C   UNK     0      14.069   2.217   0.000  0.00  0.00           C+0
HETATM   26  C   UNK     0      12.716   2.597   0.000  0.00  0.00           C+0
CONECT    1    2    6                                                       
CONECT    2    1    3                                                       
CONECT    3    2    4   25   26                                             
CONECT    4    3    5   11                                                  
CONECT    5    4    6    8   14                                             
CONECT    6    5    1    7                                                  
CONECT    7    6                                                            
CONECT    8    5    9   21                                                  
CONECT    9    8   10   16   23                                             
CONECT   10    9   11   13   15                                             
CONECT   11   10    4   12                                                  
CONECT   12   11                                                            
CONECT   13   10   14                                                       
CONECT   14   13    5                                                       
CONECT   15   10                                                            
CONECT   16    9   17   24                                                  
CONECT   17   16   18   19                                                  
CONECT   18   17                                                            
CONECT   19   17   20   23                                                  
CONECT   20   19   21                                                       
CONECT   21   20    8   22                                                  
CONECT   22   21                                                            
CONECT   23   19    9                                                       
CONECT   24   16                                                            
CONECT   25    3                                                            
CONECT   26    3                                                            
MASTER        0    0    0    0    0    0    0    0   26    0   60    0
END

View in JSmol

Synonyms

Not Available

Chemical Formula

C₂₀H₃₀O₆

Average Mass

366.4540 Da

Monoisotopic Mass

366.20424 Da

IUPAC Name

(1S,2S,3R,5S,7R,8S,9S,10S,11R,15S)-12,12-dimethyl-6-methylidene-17-oxapentacyclo[7.6.2.1^{5,8}.0^{1,11}.0^{2,8}]octadecane-3,7,9,10,15-pentol

Traditional Name

(1S,2S,3R,5S,7R,8S,9S,10S,11R,15S)-12,12-dimethyl-6-methylidene-17-oxapentacyclo[7.6.2.1^{5,8}.0^{1,11}.0^{2,8}]octadecane-3,7,9,10,15-pentol

CAS Registry Number

Not Available

SMILES

CC1(C)CC[C@H](O)[C@]23CO[C@](O)([C@@H](O)[C@H]12)[C@@]12C[C@@H](C[C@@H](O)[C@@H]31)C(=C)[C@H]2O

InChI Identifier

InChI=1S/C20H30O6/c1-9-10-6-11(21)13-18-8-26-20(25,19(13,7-10)15(9)23)16(24)14(18)17(2,3)5-4-12(18)22/h10-16,21-25H,1,4-8H2,2-3H3/t10-,11-,12+,13+,14-,15-,16+,18+,19+,20-/m1/s1

InChI Key

DSHJJLKUJOADCV-RATWNWGVSA-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
Isodon nervosus	LOTUS Database	35616633
Isodon sculponeatus	Plant	KNApSAcK
Rabdosia nervosa	Plant	KNApSAcK

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as kaurane diterpenoids. These are diterpene alkaloids with a structure that is based on the kaurane skeleton. Kaurane is a tetracyclic compound that arises by cyclisation of a pimarane precursor followed by rearrangement. It possesses a [3,2,1]-bicyclic ring system with C15-C16 bridge connected to C13, forming the five-membered ring D.

Kingdom

Organic compounds

Super Class

Lipids and lipid-like molecules

Class

Prenol lipids

Sub Class

Diterpenoids

Direct Parent

Kaurane diterpenoids

Alternative Parents

Substituents

Kaurane diterpenoid
Oxane
Cyclic alcohol
Secondary alcohol
Hemiacetal
Oxacycle
Organoheterocyclic compound
Polyol
Organic oxygen compound
Hydrocarbon derivative
Organooxygen compound
Alcohol
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
logP	-0.22	ALOGPS
logP	-0.53	ChemAxon
logS	-1.3	ALOGPS
pKa (Strongest Acidic)	10.69	ChemAxon
pKa (Strongest Basic)	-2.9	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	6	ChemAxon
Hydrogen Donor Count	5	ChemAxon
Polar Surface Area	110.38 Å²	ChemAxon
Rotatable Bond Count	0	ChemAxon
Refractivity	92.65 m³·mol⁻¹	ChemAxon
Polarizability	38.49 Å³	ChemAxon
Number of Rings	5	ChemAxon
Bioavailability	Yes	ChemAxon
Rule of Five	Yes	ChemAxon
Ghose Filter	No	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

C00048018

Chemspider ID

24744261

KEGG Compound ID

Not Available

BioCyc ID

Not Available

BiGG ID

Not Available

Wikipedia Link

Not Available

METLIN ID

Not Available

PubChem Compound

101677459

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

Feng C, Guo LQ, Yan FL, Cui JM, Di XM: 1alpha,6beta,7beta,11alpha,15beta-Penta-hydr-oxy-7alpha,20-ep-oxy-ent-kaur-16-ene . Acta Crystallogr Sect E Struct Rep Online. 2010 Jan 13;66(Pt 2):o334. doi: 10.1107/S1600536810000619. [PubMed:21579763 ]

Showing NP-Card for Nervosanin B (NP0081651)

MOL for NP0081651 (Nervosanin B)

3D MOL for NP0081651 (Nervosanin B)

3D SDF for NP0081651 (Nervosanin B)

3D-SDF for NP0081651 (Nervosanin B)

PDB for NP0081651 (Nervosanin B)

3D PDB for NP0081651 (Nervosanin B)

SMILES for NP0081651 (Nervosanin B)

INCHI for NP0081651 (Nervosanin B)

Structure for NP0081651 (Nervosanin B)

3D Structure for NP0081651 (Nervosanin B)