NP-MRD: Showing NP-Card for 5-(hydroxymethyl)-5,9,14-trimethyl-15-oxapentacyclo[11.3.1.0¹,¹⁰.0⁴,⁹.0¹⁴,¹⁶]heptadecan-2-yl acetate (NP0210105)

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Record Information

Version

2.0

Created at

2022-09-05 07:47:11 UTC

Updated at

2022-09-05 07:47:12 UTC

NP-MRD ID

NP0210105

Secondary Accession Numbers

None

Natural Product Identification

Common Name

5-(hydroxymethyl)-5,9,14-trimethyl-15-oxapentacyclo[11.3.1.0¹,¹⁰.0⁴,⁹.0¹⁴,¹⁶]heptadecan-2-yl acetate

Description

Epoxysiderol 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. Epoxysiderol is isolated from Sideritis species. Epoxysiderol is an extremely weak basic (essentially neutral) compound (based on its pKa).

Structure

MOL 3D MOL SDF PDB SMILES InChI


  Mrv0541 05061309172D          

 26 30  0  0  0  0            999 V2000
    1.3105    4.8688    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.1143    3.6568    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.4374    1.0423    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0425    1.2440    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.9933    1.5899    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.9410    0.3920    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.7357    0.7080    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.1453    2.4008    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.2151    1.3162    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.1168    3.2103    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.7163    1.5030    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.1568    3.4614    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.9129    4.3051    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.2549    0.9230    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8010    1.5747    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.7409    2.6641    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.3284    2.9379    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.2307    2.3295    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.5191    2.9379    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5888    1.8533    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7593    1.6524    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1039    2.1150    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.0223    4.2753    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.7023    4.5450    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.7260    3.5016    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.4086    2.3992    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
  7  6  1  0  0  0  0
  8  5  1  0  0  0  0
  9  5  1  0  0  0  0
 13  1  1  0  0  0  0
 14  6  1  0  0  0  0
 14 11  1  0  0  0  0
 15  7  1  0  0  0  0
 16 10  1  0  0  0  0
 17 10  1  0  0  0  0
 19  2  1  0  0  0  0
 19  8  1  0  0  0  0
 19 12  1  0  0  0  0
 19 16  1  0  0  0  0
 20  3  1  0  0  0  0
 20  9  1  0  0  0  0
 20 15  1  0  0  0  0
 20 16  1  0  0  0  0
 21  4  1  0  0  0  0
 21 14  1  0  0  0  0
 21 18  1  0  0  0  0
 22 11  1  0  0  0  0
 22 15  1  0  0  0  0
 22 17  1  0  0  0  0
 22 18  1  0  0  0  0
 23 12  1  0  0  0  0
 24 13  2  0  0  0  0
 25 13  1  0  0  0  0
 25 17  1  0  0  0  0
 26 18  1  0  0  0  0
 26 21  1  0  0  0  0
M  END

     RDKit          3D

 60 64  0  0  0  0  0  0  0  0999 V2000
   -3.2246    3.8826   -0.7895 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2855    3.0637    0.0254 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0821    3.2641    1.2492 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6136    2.0467   -0.5872 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6856    1.1738    0.0416 C   0  0  2  0  0  0  0  0  0  0  0  0
    0.6443    1.3673   -0.5491 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.6167    0.2363   -0.4281 C   0  0  1  0  0  0  0  0  0  0  0  0
    3.0216    0.6251   -0.1836 C   0  0  1  0  0  0  0  0  0  0  0  0
    3.3814    1.6699   -1.2535 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.4188    1.1343    1.1233 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.7869    2.2833    1.5602 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.9113   -0.5818   -0.5129 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.4573   -1.7978    0.2634 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.0159   -2.1230   -0.0253 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.0983   -0.9441    0.3367 C   0  0  1  0  0  0  0  0  0  0  0  0
    1.0616   -0.8385    1.7958 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2369   -1.2669   -0.2795 C   0  0  1  0  0  0  0  0  0  0  0  0
   -0.7374   -2.6459   -0.0310 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0368   -2.8158   -0.7822 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.9409   -1.6380   -0.7649 C   0  0  2  0  0  0  0  0  0  0  0  0
   -2.2509   -0.3434   -1.2114 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2655   -0.2003   -0.0351 C   0  0  2  0  0  0  0  0  0  0  0  0
   -2.1599   -0.4121    1.1266 C   0  0  2  0  0  0  0  0  0  0  0  0
   -2.5470   -1.6073    1.6359 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.3697   -1.2135    0.6225 C   0  0  2  0  0  0  0  0  0  0  0  0
   -4.6765   -0.5449    0.8454 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.1952    3.3472   -0.9457 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.4408    4.8572   -0.3477 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8008    3.9991   -1.8238 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6648    1.5357    1.1137 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.1145    2.2725   -0.0609 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.5014    1.7227   -1.6152 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.6576   -0.1925   -1.4892 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.9513    2.6477   -0.9383 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.4588    1.7000   -1.4467 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.8506    1.3690   -2.1799 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.5145    1.4214    1.0575 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.4132    0.3485    1.9076 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.2967    3.1130    1.3374 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.9217   -0.3096   -0.1383 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.9216   -0.7963   -1.5808 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.0639   -2.6453   -0.0789 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.6453   -1.6799    1.3458 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.8998   -2.2574   -1.1196 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.7180   -3.0287    0.5039 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.8611   -1.4245    2.2992 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.1171   -1.3188    2.1555 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.0427    0.1839    2.2197 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0362   -1.2254   -1.3974 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0098   -3.3472   -0.5441 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7645   -2.9706    1.0064 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8785   -3.1152   -1.8330 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5733   -3.6563   -0.2969 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.7670   -1.8131   -1.4504 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.0020    0.4438   -1.1902 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7157   -0.4677   -2.1557 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3765    0.4609    1.8028 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.9678   -0.0107   -0.1013 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.4678   -1.2210    1.1844 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.5902    0.2842    1.6072 H   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0
  2  3  2  0
  2  4  1  0
  4  5  1  0
  5  6  1  0
  6  7  1  0
  7  8  1  0
  8  9  1  6
  8 10  1  0
 10 11  1  0
  8 12  1  0
 12 13  1  0
 13 14  1  0
 14 15  1  0
 15 16  1  1
 15 17  1  0
 17 18  1  0
 18 19  1  0
 19 20  1  0
 20 21  1  0
 22 21  1  6
 22 23  1  0
 23 24  1  0
 24 25  1  0
 25 26  1  1
 22  5  1  0
 25 23  1  0
 15  7  1  0
 22 17  1  0
 25 20  1  0
  1 27  1  0
  1 28  1  0
  1 29  1  0
  5 30  1  1
  6 31  1  0
  6 32  1  0
  7 33  1  6
  9 34  1  0
  9 35  1  0
  9 36  1  0
 10 37  1  0
 10 38  1  0
 11 39  1  0
 12 40  1  0
 12 41  1  0
 13 42  1  0
 13 43  1  0
 14 44  1  0
 14 45  1  0
 16 46  1  0
 16 47  1  0
 16 48  1  0
 17 49  1  6
 18 50  1  0
 18 51  1  0
 19 52  1  0
 19 53  1  0
 20 54  1  6
 21 55  1  0
 21 56  1  0
 23 57  1  1
 26 58  1  0
 26 59  1  0
 26 60  1  0
M  END


  Mrv0541 05061309172D          

 26 30  0  0  0  0            999 V2000
    1.3105    4.8688    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.1143    3.6568    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.4374    1.0423    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0425    1.2440    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.9933    1.5899    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.9410    0.3920    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.7357    0.7080    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.1453    2.4008    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.2151    1.3162    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.1168    3.2103    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.7163    1.5030    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.1568    3.4614    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.9129    4.3051    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.2549    0.9230    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8010    1.5747    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.7409    2.6641    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.3284    2.9379    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.2307    2.3295    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.5191    2.9379    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5888    1.8533    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7593    1.6524    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1039    2.1150    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.0223    4.2753    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.7023    4.5450    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.7260    3.5016    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.4086    2.3992    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
  7  6  1  0  0  0  0
  8  5  1  0  0  0  0
  9  5  1  0  0  0  0
 13  1  1  0  0  0  0
 14  6  1  0  0  0  0
 14 11  1  0  0  0  0
 15  7  1  0  0  0  0
 16 10  1  0  0  0  0
 17 10  1  0  0  0  0
 19  2  1  0  0  0  0
 19  8  1  0  0  0  0
 19 12  1  0  0  0  0
 19 16  1  0  0  0  0
 20  3  1  0  0  0  0
 20  9  1  0  0  0  0
 20 15  1  0  0  0  0
 20 16  1  0  0  0  0
 21  4  1  0  0  0  0
 21 14  1  0  0  0  0
 21 18  1  0  0  0  0
 22 11  1  0  0  0  0
 22 15  1  0  0  0  0
 22 17  1  0  0  0  0
 22 18  1  0  0  0  0
 23 12  1  0  0  0  0
 24 13  2  0  0  0  0
 25 13  1  0  0  0  0
 25 17  1  0  0  0  0
 26 18  1  0  0  0  0
 26 21  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0210105

> <DATABASE_NAME>
NP-MRD

> <SMILES>
CC(=O)OC1CC2C(C)(CO)CCCC2(C)C2CCC3CC12C1OC31C

> <INCHI_IDENTIFIER>
InChI=1S/C22H34O4/c1-13(24)25-17-10-16-19(2,12-23)8-5-9-20(16,3)15-7-6-14-11-22(15,17)18-21(14,4)26-18/h14-18,23H,5-12H2,1-4H3

> <INCHI_KEY>
YSPZBZPFWJQSQN-UHFFFAOYSA-N

> <FORMULA>
C22H34O4

> <MOLECULAR_WEIGHT>
362.503

> <EXACT_MASS>
362.245709576

> <JCHEM_ACCEPTOR_COUNT>
3

> <JCHEM_AVERAGE_POLARIZABILITY>
41.023684045453436

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
1

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
1

> <JCHEM_IUPAC>
5-(hydroxymethyl)-5,9,14-trimethyl-15-oxapentacyclo[11.3.1.0¹,¹⁰.0⁴,⁹.0¹⁴,¹⁶]heptadecan-2-yl acetate

> <ALOGPS_LOGP>
3.00

> <JCHEM_LOGP>
2.8208273633333336

> <ALOGPS_LOGS>
-4.85

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
5

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA_STRONGEST_ACIDIC>
18.592292898998593

> <JCHEM_PKA_STRONGEST_BASIC>
-1.2271000001535488

> <JCHEM_POLAR_SURFACE_AREA>
59.06

> <JCHEM_REFRACTIVITY>
97.69009999999997

> <JCHEM_ROTATABLE_BOND_COUNT>
3

> <JCHEM_RULE_OF_FIVE>
1

> <ALOGPS_SOLUBILITY>
5.07e-03 g/l

> <JCHEM_TRADITIONAL_IUPAC>
5-(hydroxymethyl)-5,9,14-trimethyl-15-oxapentacyclo[11.3.1.0¹,¹⁰.0⁴,⁹.0¹⁴,¹⁶]heptadecan-2-yl acetate

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 06-MAY-13   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   06-MAY-13         0                                  
HETATM    1  C   UNK     0       2.446   9.088   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0       7.680   6.826   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0       6.416   1.946   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0       0.079   2.322   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0       9.321   2.968   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0       3.623   0.732   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0       5.107   1.322   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0       9.605   4.481   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0       7.868   2.457   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0       5.818   5.993   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0       3.204   2.806   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0       9.626   6.461   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0       3.571   8.036   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0       2.342   1.723   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0       5.229   2.939   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0       6.983   4.973   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0       4.346   5.484   0.000  0.00  0.00           C+0
HETATM   18  C   UNK     0       2.297   4.348   0.000  0.00  0.00           C+0
HETATM   19  C   UNK     0       8.436   5.484   0.000  0.00  0.00           C+0
HETATM   20  C   UNK     0       6.699   3.459   0.000  0.00  0.00           C+0
HETATM   21  C   UNK     0       1.417   3.084   0.000  0.00  0.00           C+0
HETATM   22  C   UNK     0       3.927   3.948   0.000  0.00  0.00           C+0
HETATM   23  O   UNK     0       9.375   7.981   0.000  0.00  0.00           O+0
HETATM   24  O   UNK     0       5.044   8.484   0.000  0.00  0.00           O+0
HETATM   25  O   UNK     0       3.222   6.536   0.000  0.00  0.00           O+0
HETATM   26  O   UNK     0       0.763   4.479   0.000  0.00  0.00           O+0
CONECT    1   13                                                            
CONECT    2   19                                                            
CONECT    3   20                                                            
CONECT    4   21                                                            
CONECT    5    8    9                                                       
CONECT    6    7   14                                                       
CONECT    7    6   15                                                       
CONECT    8    5   19                                                       
CONECT    9    5   20                                                       
CONECT   10   16   17                                                       
CONECT   11   14   22                                                       
CONECT   12   19   23                                                       
CONECT   13    1   24   25                                                  
CONECT   14    6   11   21                                                  
CONECT   15    7   20   22                                                  
CONECT   16   10   19   20                                                  
CONECT   17   10   22   25                                                  
CONECT   18   21   22   26                                                  
CONECT   19    2    8   12   16                                             
CONECT   20    3    9   15   16                                             
CONECT   21    4   14   18   26                                             
CONECT   22   11   15   17   18                                             
CONECT   23   12                                                            
CONECT   24   13                                                            
CONECT   25   13   17                                                       
CONECT   26   18   21                                                       
MASTER        0    0    0    0    0    0    0    0   26    0   60    0
END

View in JSmol

Synonyms

Value	Source
5-(Hydroxymethyl)-5,9,14-trimethyl-15-oxapentacyclo[11.3.1.0¹,¹⁰.0⁴,⁹.0¹⁴,¹⁶]heptadecan-2-yl acetic acid	Generator

Chemical Formula

C₂₂H₃₄O₄

Average Mass

362.5030 Da

Monoisotopic Mass

362.24571 Da

IUPAC Name

5-(hydroxymethyl)-5,9,14-trimethyl-15-oxapentacyclo[11.3.1.0¹,¹⁰.0⁴,⁹.0¹⁴,¹⁶]heptadecan-2-yl acetate

Traditional Name

5-(hydroxymethyl)-5,9,14-trimethyl-15-oxapentacyclo[11.3.1.0¹,¹⁰.0⁴,⁹.0¹⁴,¹⁶]heptadecan-2-yl acetate

CAS Registry Number

Not Available

SMILES

CC(=O)OC1CC2C(C)(CO)CCCC2(C)C2CCC3CC12C1OC31C

InChI Identifier

InChI=1S/C22H34O4/c1-13(24)25-17-10-16-19(2,12-23)8-5-9-20(16,3)15-7-6-14-11-22(15,17)18-21(14,4)26-18/h14-18,23H,5-12H2,1-4H3

InChI Key

YSPZBZPFWJQSQN-UHFFFAOYSA-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 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

Not Available

Substituents

Not Available

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	3	ALOGPS
logP	2.82	ChemAxon
logS	-4.8	ALOGPS
pKa (Strongest Acidic)	18.59	ChemAxon
pKa (Strongest Basic)	-1.2	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	3	ChemAxon
Hydrogen Donor Count	1	ChemAxon
Polar Surface Area	59.06 Å²	ChemAxon
Rotatable Bond Count	3	ChemAxon
Refractivity	97.69 m³·mol⁻¹	ChemAxon
Polarizability	41.02 Å³	ChemAxon
Number of Rings	5	ChemAxon
Bioavailability	Yes	ChemAxon
Rule of Five	Yes	ChemAxon
Ghose Filter	Yes	ChemAxon
Veber's Rule	No	ChemAxon
MDDR-like Rule	No	ChemAxon

External Links

HMDB ID

HMDB0036704

DrugBank ID

Not Available

Phenol Explorer Compound ID

Not Available

FoodDB ID

FDB015640

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

131752043

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

LOTUS database [Link]

Showing NP-Card for 5-(hydroxymethyl)-5,9,14-trimethyl-15-oxapentacyclo[11.3.1.0¹,¹⁰.0⁴,⁹.0¹⁴,¹⁶]heptadecan-2-yl acetate (NP0210105)

MOL for NP0210105 (5-(hydroxymethyl)-5,9,14-trimethyl-15-oxapentacyclo[11.3.1.0¹,¹⁰.0⁴,⁹.0¹⁴,¹⁶]heptadecan-2-yl acetate)

3D MOL for NP0210105 (5-(hydroxymethyl)-5,9,14-trimethyl-15-oxapentacyclo[11.3.1.0¹,¹⁰.0⁴,⁹.0¹⁴,¹⁶]heptadecan-2-yl acetate)

3D SDF for NP0210105 (5-(hydroxymethyl)-5,9,14-trimethyl-15-oxapentacyclo[11.3.1.0¹,¹⁰.0⁴,⁹.0¹⁴,¹⁶]heptadecan-2-yl acetate)

3D-SDF for NP0210105 (5-(hydroxymethyl)-5,9,14-trimethyl-15-oxapentacyclo[11.3.1.0¹,¹⁰.0⁴,⁹.0¹⁴,¹⁶]heptadecan-2-yl acetate)

PDB for NP0210105 (5-(hydroxymethyl)-5,9,14-trimethyl-15-oxapentacyclo[11.3.1.0¹,¹⁰.0⁴,⁹.0¹⁴,¹⁶]heptadecan-2-yl acetate)

3D PDB for NP0210105 (5-(hydroxymethyl)-5,9,14-trimethyl-15-oxapentacyclo[11.3.1.0¹,¹⁰.0⁴,⁹.0¹⁴,¹⁶]heptadecan-2-yl acetate)

SMILES for NP0210105 (5-(hydroxymethyl)-5,9,14-trimethyl-15-oxapentacyclo[11.3.1.0¹,¹⁰.0⁴,⁹.0¹⁴,¹⁶]heptadecan-2-yl acetate)

INCHI for NP0210105 (5-(hydroxymethyl)-5,9,14-trimethyl-15-oxapentacyclo[11.3.1.0¹,¹⁰.0⁴,⁹.0¹⁴,¹⁶]heptadecan-2-yl acetate)

Structure for NP0210105 (5-(hydroxymethyl)-5,9,14-trimethyl-15-oxapentacyclo[11.3.1.0¹,¹⁰.0⁴,⁹.0¹⁴,¹⁶]heptadecan-2-yl acetate)

3D Structure for NP0210105 (5-(hydroxymethyl)-5,9,14-trimethyl-15-oxapentacyclo[11.3.1.0¹,¹⁰.0⁴,⁹.0¹⁴,¹⁶]heptadecan-2-yl acetate)