NP-MRD: Showing NP-Card for 14,19-dihydroxy-11,16,16-trimethyl-6-methylidene-10,12,21-trioxahexacyclo[11.6.2.0¹,¹⁵.0²,⁸.0⁵,⁹.0⁸,¹³]henicosan-7-one (NP0304767)

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Record Information

Version

2.0

Created at

2022-09-10 20:05:46 UTC

Updated at

2022-09-10 20:05:47 UTC

NP-MRD ID

NP0304767

Secondary Accession Numbers

None

Natural Product Identification

Common Name

14,19-dihydroxy-11,16,16-trimethyl-6-methylidene-10,12,21-trioxahexacyclo[11.6.2.0¹,¹⁵.0²,⁸.0⁵,⁹.0⁸,¹³]henicosan-7-one

Description

14,19-Dihydroxy-11,16,16-trimethyl-6-methylidene-10,12,21-trioxahexacyclo[11.6.2.0¹,¹⁵.0²,⁸.0⁵,⁹.0⁸,¹³]Henicosan-7-one 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. 14,19-dihydroxy-11,16,16-trimethyl-6-methylidene-10,12,21-trioxahexacyclo[11.6.2.0¹,¹⁵.0²,⁸.0⁵,⁹.0⁸,¹³]henicosan-7-one is found in Isodon nervosus. 14,19-Dihydroxy-11,16,16-trimethyl-6-methylidene-10,12,21-trioxahexacyclo[11.6.2.0¹,¹⁵.0²,⁸.0⁵,⁹.0⁸,¹³]Henicosan-7-one is an extremely weak basic (essentially neutral) compound (based on its pKa).

Structure

MOL 3D MOL SDF PDB SMILES InChI


  Mrv1533004161522482D          

 28 33  0  0  0  0            999 V2000
    1.5679   -1.1698    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.0084   -0.4723    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.6644    0.2964    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.9838    1.0933    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.0164    2.1097    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.2891    2.9166    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.1109    2.6809    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.4572    1.9331    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.3739    1.9661    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.1405    1.2741    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.4423    1.0258    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.0403    0.3934    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8478   -0.4525    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.9538    0.3989    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.2491   -0.3714    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.6583    1.0247    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.4632    0.7326    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.0846   -0.0004    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.1416    0.2630    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.0361    1.3673    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.7866    2.1725    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.0333    2.5276    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.9244    3.3454    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.7735    1.3165    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.8877    1.5954    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.5408    0.8469    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.1767    2.0441    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.3759    2.2422    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  1  0  0  0  0
  4  5  1  0  0  0  0
  5  6  1  0  0  0  0
  6  7  1  0  0  0  0
  7  8  1  0  0  0  0
  8  9  1  0  0  0  0
  9 10  1  0  0  0  0
 10 11  1  0  0  0  0
 11 12  1  0  0  0  0
 12 13  1  0  0  0  0
  2 13  1  0  0  0  0
 12 14  1  0  0  0  0
 14 15  1  0  0  0  0
 14 16  1  0  0  0  0
  9 16  1  0  0  0  0
 16 17  1  0  0  0  0
 17 18  1  0  0  0  0
 17 19  1  0  0  0  0
 17 20  1  0  0  0  0
 20 21  1  0  0  0  0
 21 22  1  0  0  0  0
  9 22  1  0  0  0  0
 22 23  1  0  0  0  0
 12 24  1  0  0  0  0
  4 24  1  0  0  0  0
  8 24  1  0  0  0  0
 24 25  1  0  0  0  0
 25 26  2  0  0  0  0
 25 27  1  0  0  0  0
  5 27  1  0  0  0  0
 27 28  2  0  0  0  0
M  END

     RDKit          3D

 58 63  0  0  0  0  0  0  0  0999 V2000
    3.9582   -0.4462    2.1685 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.0924   -0.4341    1.2033 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.8113    0.2828    1.0778 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.3714    0.8822    2.1133 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.3217    0.1288   -0.2794 C   0  0  2  0  0  0  0  0  0  0  0  0
    2.6312   -0.1580   -1.0363 C   0  0  1  0  0  0  0  0  0  0  0  0
    3.3269    0.9843   -1.1159 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.7350    2.1447   -0.7398 C   0  0  1  0  0  0  0  0  0  0  0  0
    3.4955    3.2866   -1.4422 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4216    2.3323   -1.0069 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.5831    1.2738   -0.8515 C   0  0  1  0  0  0  0  0  0  0  0  0
    0.0844    0.9182   -2.1037 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9411    0.0009   -2.0619 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9496   -0.7698   -0.7192 C   0  0  1  0  0  0  0  0  0  0  0  0
   -1.3684    0.2702    0.2854 C   0  0  1  0  0  0  0  0  0  0  0  0
   -0.6253    1.5383    0.0292 C   0  0  2  0  0  0  0  0  0  0  0  0
   -1.3702    2.5063   -0.6414 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8202    0.3901    0.5119 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.7265    0.7803   -0.5630 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.0104    1.3438    1.7012 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.2550   -0.9847    1.0320 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.9183   -2.1095    0.1384 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8325   -1.9418   -0.8348 C   0  0  1  0  0  0  0  0  0  0  0  0
   -2.3407   -2.0414   -2.1581 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.4902   -1.1173   -0.5470 C   0  0  2  0  0  0  0  0  0  0  0  0
    0.9126   -2.0916    0.4697 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.3715   -2.4113    0.0760 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.2053   -1.1956   -0.0869 C   0  0  2  0  0  0  0  0  0  0  0  0
    4.8650   -1.0303    2.1142 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.8071    0.1291    3.0683 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.4064   -0.6111   -2.0197 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.9906    2.3185    0.3479 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.0045    4.2183   -1.0632 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.4412    3.1896   -2.5304 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.5053    3.2742   -1.0255 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6659   -0.8020   -2.8101 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9182    0.3563   -2.3549 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9845   -0.1603    1.2662 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3251    2.0306    1.0011 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3777    3.3771   -0.2143 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.4921    1.6808   -1.1373 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.7218    1.0220   -0.0726 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.0140   -0.0505   -1.2736 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.8130    0.9619    2.3640 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.2928    2.3427    1.2985 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0689    1.4582    2.2757 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.3336   -0.9840    1.2912 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7142   -1.0918    2.0165 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7507   -3.0111    0.8061 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.8718   -2.3956   -0.4033 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1690   -2.8609   -0.7786 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6656   -2.9546   -2.3380 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.7835   -1.5855   -1.5440 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.9966   -1.6216    1.4882 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.4013   -3.0472    0.5051 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.8130   -3.0480    0.8384 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.2897   -2.9828   -0.8790 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.2207   -1.4843   -0.3154 H   0  0  0  0  0  0  0  0  0  0  0  0
  9  8  1  0
  8  7  1  0
  7  6  1  0
  6 28  1  0
 28 27  1  0
 27 26  1  0
 26 25  1  0
 25  5  1  0
  5  3  1  1
  3  4  2  0
  3  2  1  0
  2  1  2  3
  5 11  1  0
 11 12  1  0
 12 13  1  0
 14 13  1  6
 14 23  1  0
 23 24  1  0
 23 22  1  0
 22 21  1  0
 21 18  1  0
 18 19  1  0
 18 20  1  0
 18 15  1  0
 15 16  1  0
 16 17  1  0
 11 10  1  6
 10  8  1  0
  5  6  1  0
 16 11  1  0
  2 28  1  0
 15 14  1  0
 14 25  1  0
  9 33  1  0
  9 34  1  0
  9 35  1  0
  8 32  1  1
  6 31  1  6
 28 58  1  6
 27 56  1  0
 27 57  1  0
 26 54  1  0
 26 55  1  0
 25 53  1  6
  1 29  1  0
  1 30  1  0
 13 36  1  0
 13 37  1  0
 23 51  1  1
 24 52  1  0
 22 49  1  0
 22 50  1  0
 21 47  1  0
 21 48  1  0
 19 41  1  0
 19 42  1  0
 19 43  1  0
 20 44  1  0
 20 45  1  0
 20 46  1  0
 15 38  1  1
 16 39  1  1
 17 40  1  0
M  END


  Mrv1533004161522482D          

 28 33  0  0  0  0            999 V2000
    1.5679   -1.1698    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.0084   -0.4723    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.6644    0.2964    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.9838    1.0933    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.0164    2.1097    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.2891    2.9166    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.1109    2.6809    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.4572    1.9331    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.3739    1.9661    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.1405    1.2741    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.4423    1.0258    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.0403    0.3934    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8478   -0.4525    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.9538    0.3989    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.2491   -0.3714    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.6583    1.0247    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.4632    0.7326    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.0846   -0.0004    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.1416    0.2630    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.0361    1.3673    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.7866    2.1725    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.0333    2.5276    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.9244    3.3454    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.7735    1.3165    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.8877    1.5954    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.5408    0.8469    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.1767    2.0441    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.3759    2.2422    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  1  0  0  0  0
  4  5  1  0  0  0  0
  5  6  1  0  0  0  0
  6  7  1  0  0  0  0
  7  8  1  0  0  0  0
  8  9  1  0  0  0  0
  9 10  1  0  0  0  0
 10 11  1  0  0  0  0
 11 12  1  0  0  0  0
 12 13  1  0  0  0  0
  2 13  1  0  0  0  0
 12 14  1  0  0  0  0
 14 15  1  0  0  0  0
 14 16  1  0  0  0  0
  9 16  1  0  0  0  0
 16 17  1  0  0  0  0
 17 18  1  0  0  0  0
 17 19  1  0  0  0  0
 17 20  1  0  0  0  0
 20 21  1  0  0  0  0
 21 22  1  0  0  0  0
  9 22  1  0  0  0  0
 22 23  1  0  0  0  0
 12 24  1  0  0  0  0
  4 24  1  0  0  0  0
  8 24  1  0  0  0  0
 24 25  1  0  0  0  0
 25 26  2  0  0  0  0
 25 27  1  0  0  0  0
  5 27  1  0  0  0  0
 27 28  2  0  0  0  0
M  END
> <DATABASE_ID>
NP0304767

> <DATABASE_NAME>
NP-MRD

> <SMILES>
CC1OC2C3CCC4C2(C(=O)C3=C)C2(OCC43C(O)CCC(C)(C)C3C2O)O1

> <INCHI_IDENTIFIER>
InChI=1S/C22H30O6/c1-10-12-5-6-13-20-9-26-22(17(25)15(20)19(3,4)8-7-14(20)23)21(13,16(10)24)18(12)27-11(2)28-22/h11-15,17-18,23,25H,1,5-9H2,2-4H3

> <INCHI_KEY>
PRNDKTYPVUYEHT-UHFFFAOYSA-N

> <FORMULA>
C22H30O6

> <MOLECULAR_WEIGHT>
390.476

> <EXACT_MASS>
390.204238686

> <JCHEM_ACCEPTOR_COUNT>
6

> <JCHEM_ATOM_COUNT>
58

> <JCHEM_AVERAGE_POLARIZABILITY>
41.185324000951596

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
2

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
1

> <JCHEM_IUPAC>
14,19-dihydroxy-11,16,16-trimethyl-6-methylidene-10,12,21-trioxahexacyclo[11.6.2.0¹,¹⁵.0²,⁸.0⁵,⁹.0⁸,¹³]henicosan-7-one

> <ALOGPS_LOGP>
1.63

> <JCHEM_LOGP>
1.9949700840000002

> <ALOGPS_LOGS>
-2.37

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
6

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA>
14.623102063592764

> <JCHEM_PKA_STRONGEST_ACIDIC>
12.952821060553443

> <JCHEM_PKA_STRONGEST_BASIC>
-2.97052092989433

> <JCHEM_POLAR_SURFACE_AREA>
85.22

> <JCHEM_REFRACTIVITY>
99.06249999999999

> <JCHEM_ROTATABLE_BOND_COUNT>
0

> <JCHEM_RULE_OF_FIVE>
1

> <ALOGPS_SOLUBILITY>
1.67e+00 g/l

> <JCHEM_TRADITIONAL_IUPAC>
14,19-dihydroxy-11,16,16-trimethyl-6-methylidene-10,12,21-trioxahexacyclo[11.6.2.0¹,¹⁵.0²,⁸.0⁵,⁹.0⁸,¹³]henicosan-7-one

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 16-APR-15   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   16-APR-15         0                                  
HETATM    1  C   UNK     0       2.927  -2.184   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0       3.749  -0.882   0.000  0.00  0.00           C+0
HETATM    3  O   UNK     0       3.107   0.553   0.000  0.00  0.00           O+0
HETATM    4  C   UNK     0       3.703   2.041   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0       3.764   3.938   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0       4.273   5.444   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0       5.807   5.004   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0       6.453   3.609   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0       8.165   3.670   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0       7.729   2.378   0.000  0.00  0.00           C+0
HETATM   11  O   UNK     0       6.426   1.915   0.000  0.00  0.00           O+0
HETATM   12  C   UNK     0       5.675   0.734   0.000  0.00  0.00           C+0
HETATM   13  O   UNK     0       5.316  -0.845   0.000  0.00  0.00           O+0
HETATM   14  C   UNK     0       7.380   0.745   0.000  0.00  0.00           C+0
HETATM   15  O   UNK     0       7.932  -0.693   0.000  0.00  0.00           O+0
HETATM   16  C   UNK     0       8.696   1.913   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0      10.198   1.367   0.000  0.00  0.00           C+0
HETATM   18  C   UNK     0       9.491  -0.001   0.000  0.00  0.00           C+0
HETATM   19  C   UNK     0      11.464   0.491   0.000  0.00  0.00           C+0
HETATM   20  C   UNK     0      11.267   2.552   0.000  0.00  0.00           C+0
HETATM   21  C   UNK     0      10.802   4.055   0.000  0.00  0.00           C+0
HETATM   22  C   UNK     0       9.395   4.718   0.000  0.00  0.00           C+0
HETATM   23  O   UNK     0       9.192   6.245   0.000  0.00  0.00           O+0
HETATM   24  C   UNK     0       5.177   2.457   0.000  0.00  0.00           C+0
HETATM   25  C   UNK     0       3.524   2.978   0.000  0.00  0.00           C+0
HETATM   26  O   UNK     0       2.876   1.581   0.000  0.00  0.00           O+0
HETATM   27  C   UNK     0       2.197   3.816   0.000  0.00  0.00           C+0
HETATM   28  C   UNK     0       0.702   4.185   0.000  0.00  0.00           C+0
CONECT    1    2                                                            
CONECT    2    1    3   13                                                  
CONECT    3    2    4                                                       
CONECT    4    3    5   24                                                  
CONECT    5    4    6   27                                                  
CONECT    6    5    7                                                       
CONECT    7    6    8                                                       
CONECT    8    7    9   24                                                  
CONECT    9    8   10   16   22                                             
CONECT   10    9   11                                                       
CONECT   11   10   12                                                       
CONECT   12   11   13   14   24                                             
CONECT   13   12    2                                                       
CONECT   14   12   15   16                                                  
CONECT   15   14                                                            
CONECT   16   14    9   17                                                  
CONECT   17   16   18   19   20                                             
CONECT   18   17                                                            
CONECT   19   17                                                            
CONECT   20   17   21                                                       
CONECT   21   20   22                                                       
CONECT   22   21    9   23                                                  
CONECT   23   22                                                            
CONECT   24   12    4    8   25                                             
CONECT   25   24   26   27                                                  
CONECT   26   25                                                            
CONECT   27   25    5   28                                                  
CONECT   28   27                                                            
MASTER        0    0    0    0    0    0    0    0   28    0   66    0
END

View in JSmol

Synonyms

Not Available

Chemical Formula

C₂₂H₃₀O₆

Average Mass

390.4760 Da

Monoisotopic Mass

390.20424 Da

IUPAC Name

14,19-dihydroxy-11,16,16-trimethyl-6-methylidene-10,12,21-trioxahexacyclo[11.6.2.0¹,¹⁵.0²,⁸.0⁵,⁹.0⁸,¹³]henicosan-7-one

Traditional Name

14,19-dihydroxy-11,16,16-trimethyl-6-methylidene-10,12,21-trioxahexacyclo[11.6.2.0¹,¹⁵.0²,⁸.0⁵,⁹.0⁸,¹³]henicosan-7-one

CAS Registry Number

Not Available

SMILES

CC1OC2C3CCC4C2(C(=O)C3=C)C2(OCC43C(O)CCC(C)(C)C3C2O)O1

InChI Identifier

InChI=1S/C22H30O6/c1-10-12-5-6-13-20-9-26-22(17(25)15(20)19(3,4)8-7-14(20)23)21(13,16(10)24)18(12)27-11(2)28-22/h11-15,17-18,23,25H,1,5-9H2,2-4H3

InChI Key

PRNDKTYPVUYEHT-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

Species Name	Source	Reference
Isodon nervosus	LOTUS Database	35616633

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
Ketal
Meta-dioxane
Oxane
Cyclic alcohol
Ketone
Secondary alcohol
Acetal
Oxacycle
Organoheterocyclic compound
Hydrocarbon derivative
Organic oxide
Carbonyl group
Organooxygen compound
Organic oxygen 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	1.63	ALOGPS
logP	1.99	ChemAxon
logS	-2.4	ALOGPS
pKa (Strongest Acidic)	12.95	ChemAxon
pKa (Strongest Basic)	-3	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	6	ChemAxon
Hydrogen Donor Count	2	ChemAxon
Polar Surface Area	85.22 Å²	ChemAxon
Rotatable Bond Count	0	ChemAxon
Refractivity	99.06 m³·mol⁻¹	ChemAxon
Polarizability	41.19 Å³	ChemAxon
Number of Rings	6	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

Not Available

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

LOTUS database [Link]

Showing NP-Card for 14,19-dihydroxy-11,16,16-trimethyl-6-methylidene-10,12,21-trioxahexacyclo[11.6.2.0¹,¹⁵.0²,⁸.0⁵,⁹.0⁸,¹³]henicosan-7-one (NP0304767)

MOL for NP0304767 (14,19-dihydroxy-11,16,16-trimethyl-6-methylidene-10,12,21-trioxahexacyclo[11.6.2.0¹,¹⁵.0²,⁸.0⁵,⁹.0⁸,¹³]henicosan-7-one)

3D MOL for NP0304767 (14,19-dihydroxy-11,16,16-trimethyl-6-methylidene-10,12,21-trioxahexacyclo[11.6.2.0¹,¹⁵.0²,⁸.0⁵,⁹.0⁸,¹³]henicosan-7-one)

3D SDF for NP0304767 (14,19-dihydroxy-11,16,16-trimethyl-6-methylidene-10,12,21-trioxahexacyclo[11.6.2.0¹,¹⁵.0²,⁸.0⁵,⁹.0⁸,¹³]henicosan-7-one)

3D-SDF for NP0304767 (14,19-dihydroxy-11,16,16-trimethyl-6-methylidene-10,12,21-trioxahexacyclo[11.6.2.0¹,¹⁵.0²,⁸.0⁵,⁹.0⁸,¹³]henicosan-7-one)

PDB for NP0304767 (14,19-dihydroxy-11,16,16-trimethyl-6-methylidene-10,12,21-trioxahexacyclo[11.6.2.0¹,¹⁵.0²,⁸.0⁵,⁹.0⁸,¹³]henicosan-7-one)

3D PDB for NP0304767 (14,19-dihydroxy-11,16,16-trimethyl-6-methylidene-10,12,21-trioxahexacyclo[11.6.2.0¹,¹⁵.0²,⁸.0⁵,⁹.0⁸,¹³]henicosan-7-one)

SMILES for NP0304767 (14,19-dihydroxy-11,16,16-trimethyl-6-methylidene-10,12,21-trioxahexacyclo[11.6.2.0¹,¹⁵.0²,⁸.0⁵,⁹.0⁸,¹³]henicosan-7-one)

INCHI for NP0304767 (14,19-dihydroxy-11,16,16-trimethyl-6-methylidene-10,12,21-trioxahexacyclo[11.6.2.0¹,¹⁵.0²,⁸.0⁵,⁹.0⁸,¹³]henicosan-7-one)

Structure for NP0304767 (14,19-dihydroxy-11,16,16-trimethyl-6-methylidene-10,12,21-trioxahexacyclo[11.6.2.0¹,¹⁵.0²,⁸.0⁵,⁹.0⁸,¹³]henicosan-7-one)

3D Structure for NP0304767 (14,19-dihydroxy-11,16,16-trimethyl-6-methylidene-10,12,21-trioxahexacyclo[11.6.2.0¹,¹⁵.0²,⁸.0⁵,⁹.0⁸,¹³]henicosan-7-one)