NP-MRD: Showing NP-Card for 17-hydroxy-17-(hydroxymethyl)-9-methoxy-12-methyl-8-oxapentacyclo[14.2.1.0¹,¹³.0⁴,¹².0⁵,⁹]nonadec-5-en-7-one (NP0315711)

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Record Information

Version

2.0

Created at

2022-09-11 14:28:51 UTC

Updated at

2022-09-11 14:28:51 UTC

NP-MRD ID

NP0315711

Secondary Accession Numbers

None

Natural Product Identification

Common Name

17-hydroxy-17-(hydroxymethyl)-9-methoxy-12-methyl-8-oxapentacyclo[14.2.1.0¹,¹³.0⁴,¹².0⁵,⁹]nonadec-5-en-7-one

Description

17-Hydroxy-17-(hydroxymethyl)-9-methoxy-12-methyl-8-oxapentacyclo[14.2.1.0¹,¹³.0⁴,¹².0⁵,⁹]Nonadec-5-en-7-one belongs to the class of organic compounds known as diterpene lactones. These are diterpenoids containing a lactone moiety. 17-hydroxy-17-(hydroxymethyl)-9-methoxy-12-methyl-8-oxapentacyclo[14.2.1.0¹,¹³.0⁴,¹².0⁵,⁹]nonadec-5-en-7-one is found in Diplospora dubia. 17-Hydroxy-17-(hydroxymethyl)-9-methoxy-12-methyl-8-oxapentacyclo[14.2.1.0¹,¹³.0⁴,¹².0⁵,⁹]Nonadec-5-en-7-one is an extremely weak basic (essentially neutral) compound (based on its pKa).

Structure

MOL 3D MOL SDF PDB SMILES InChI


  Mrv1533004171515192D          

 26 30  0  0  0  0            999 V2000
    3.7779    1.8713    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.1121    1.1171    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.6260    0.4505    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.2148    1.1657    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.3898    1.1671    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.9760    0.4534    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.5709    1.1721    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.3873   -0.2618    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.9815   -0.9909    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.1553   -1.0010    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.6887   -0.2979    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.1103    0.1208    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5522    0.4524    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1462    1.2161    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7137    1.2419    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.1341    0.4692    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7588   -0.3858    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5347   -0.1055    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1188   -1.1281    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6560   -1.8110    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0205   -0.8451    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.2123   -0.2632    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.7632   -0.8773    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.5175   -0.5431    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.2312   -0.9568    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.4327    0.2776    0.0000 O   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
  6  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
 13 14  1  0  0  0  0
 14 15  1  0  0  0  0
 15 16  1  0  0  0  0
  6 16  1  0  0  0  0
 11 16  1  0  0  0  0
 13 17  1  0  0  0  0
 17 18  1  0  0  0  0
 17 19  1  0  0  0  0
 19 20  1  0  0  0  0
 17 21  1  0  0  0  0
 11 21  1  0  0  0  0
  8 22  1  0  0  0  0
  3 22  1  0  0  0  0
 22 23  2  0  0  0  0
 23 24  1  0  0  0  0
 24 25  2  0  0  0  0
 24 26  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
    5.3574   -0.2941    0.1662 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.1258   -0.1374    0.7462 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.3116    0.7907    0.0955 C   0  0  1  0  0  0  0  0  0  0  0  0
    2.8350    0.2803   -1.2396 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.3050    0.1372   -1.2839 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.8499   -0.8844   -0.2249 C   0  0  1  0  0  0  0  0  0  0  0  0
    1.6853   -2.1309   -0.5820 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.3332   -0.4020    1.0899 C   0  0  2  0  0  0  0  0  0  0  0  0
    0.3248   -0.1961    2.1580 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8677   -1.1513    2.0613 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4870   -0.8260    0.7258 C   0  0  2  0  0  0  0  0  0  0  0  0
   -2.7910   -1.6002    0.5050 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.4262   -0.6774   -0.5479 C   0  0  2  0  0  0  0  0  0  0  0  0
   -2.6311   -0.7145   -1.7911 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1686   -0.5514   -1.6687 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5784   -1.1689   -0.3977 C   0  0  1  0  0  0  0  0  0  0  0  0
   -3.3561    0.6254    0.1995 C   0  0  2  0  0  0  0  0  0  0  0  0
   -4.2573    0.5399    1.2607 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.6332    1.8220   -0.6677 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5074    2.9541    0.1666 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9525    0.6086    0.7378 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.0867    0.9035    0.9497 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.9710    2.1266    1.3654 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.0951    2.8970    0.8212 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.2269    4.1305    1.0738 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.8770    2.0642    0.0639 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.8704    0.6881    0.1845 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.2260   -0.6375   -0.8737 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.9089   -1.0477    0.7879 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.3129   -0.6440   -1.5695 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.0648    1.0540   -2.0088 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.0704   -0.1756   -2.2966 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.9093    1.1167   -0.9813 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.9926   -3.0004   -0.3785 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.5220   -2.2710    0.1151 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.9528   -2.1613   -1.6394 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.1246   -1.0816    1.5383 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0116    0.8573    2.1683 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.7495   -0.3818    3.1789 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4795   -2.1729    2.1057 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5519   -0.8888    2.8693 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6082   -2.5904    0.0708 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.4346   -1.5859    1.3872 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.4458   -1.0165   -0.7431 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.0114    0.1084   -2.4655 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.9066   -1.6548   -2.3439 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8502    0.4890   -1.8024 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7021   -1.1432   -2.5128 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7152   -2.2809   -0.5731 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.0105   -0.0696    1.0781 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8450    1.9277   -1.4386 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.6560    1.8441   -1.0640 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.1167    2.7742    0.9491 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0035    1.0333    1.7731 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2682    1.2771    0.1798 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.1847    2.4885    1.9948 H   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0
  3  2  1  1
  3  4  1  0
  4  5  1  0
  5  6  1  0
  6  7  1  6
  6  8  1  0
  8  9  1  0
  9 10  1  0
 11 10  1  1
 11 12  1  0
 12 13  1  0
 13 14  1  0
 14 15  1  0
 15 16  1  0
 13 17  1  0
 17 18  1  1
 17 19  1  0
 19 20  1  0
 17 21  1  0
  8 22  1  0
 22 23  2  0
 23 24  1  0
 24 25  2  0
 24 26  1  0
 22  3  1  0
 26  3  1  0
 16  6  1  0
 16 11  1  0
 21 11  1  0
  1 27  1  0
  1 28  1  0
  1 29  1  0
  4 30  1  0
  4 31  1  0
  5 32  1  0
  5 33  1  0
  7 34  1  0
  7 35  1  0
  7 36  1  0
  8 37  1  1
  9 38  1  0
  9 39  1  0
 10 40  1  0
 10 41  1  0
 12 42  1  0
 12 43  1  0
 13 44  1  6
 14 45  1  0
 14 46  1  0
 15 47  1  0
 15 48  1  0
 16 49  1  6
 18 50  1  0
 19 51  1  0
 19 52  1  0
 20 53  1  0
 21 54  1  0
 21 55  1  0
 23 56  1  0
M  END


  Mrv1533004171515192D          

 26 30  0  0  0  0            999 V2000
    3.7779    1.8713    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.1121    1.1171    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.6260    0.4505    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.2148    1.1657    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.3898    1.1671    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.9760    0.4534    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.5709    1.1721    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.3873   -0.2618    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.9815   -0.9909    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.1553   -1.0010    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.6887   -0.2979    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.1103    0.1208    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5522    0.4524    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1462    1.2161    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7137    1.2419    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.1341    0.4692    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7588   -0.3858    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5347   -0.1055    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1188   -1.1281    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6560   -1.8110    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0205   -0.8451    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.2123   -0.2632    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.7632   -0.8773    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.5175   -0.5431    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.2312   -0.9568    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.4327    0.2776    0.0000 O   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
  6  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
 13 14  1  0  0  0  0
 14 15  1  0  0  0  0
 15 16  1  0  0  0  0
  6 16  1  0  0  0  0
 11 16  1  0  0  0  0
 13 17  1  0  0  0  0
 17 18  1  0  0  0  0
 17 19  1  0  0  0  0
 19 20  1  0  0  0  0
 17 21  1  0  0  0  0
 11 21  1  0  0  0  0
  8 22  1  0  0  0  0
  3 22  1  0  0  0  0
 22 23  2  0  0  0  0
 23 24  1  0  0  0  0
 24 25  2  0  0  0  0
 24 26  1  0  0  0  0
  3 26  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0315711

> <DATABASE_NAME>
NP-MRD

> <SMILES>
COC12CCC3(C)C(CCC45CC(CCC34)C(O)(CO)C5)C1=CC(=O)O2

> <INCHI_IDENTIFIER>
InChI=1S/C21H30O5/c1-18-7-8-21(25-2)15(9-17(23)26-21)14(18)5-6-19-10-13(3-4-16(18)19)20(24,11-19)12-22/h9,13-14,16,22,24H,3-8,10-12H2,1-2H3

> <INCHI_KEY>
WGZVRWCVRXZGME-UHFFFAOYSA-N

> <FORMULA>
C21H30O5

> <MOLECULAR_WEIGHT>
362.466

> <EXACT_MASS>
362.209324066

> <JCHEM_ACCEPTOR_COUNT>
4

> <JCHEM_ATOM_COUNT>
56

> <JCHEM_AVERAGE_POLARIZABILITY>
39.71115821288593

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
2

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
1

> <JCHEM_IUPAC>
17-hydroxy-17-(hydroxymethyl)-9-methoxy-12-methyl-8-oxapentacyclo[14.2.1.0¹,¹³.0⁴,¹².0⁵,⁹]nonadec-5-en-7-one

> <ALOGPS_LOGP>
1.57

> <JCHEM_LOGP>
2.271846616666666

> <ALOGPS_LOGS>
-4.19

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
5

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA>
15.306117084580855

> <JCHEM_PKA_STRONGEST_ACIDIC>
13.68534777326245

> <JCHEM_PKA_STRONGEST_BASIC>
-3.0757507495331193

> <JCHEM_POLAR_SURFACE_AREA>
75.99

> <JCHEM_REFRACTIVITY>
96.06489999999997

> <JCHEM_ROTATABLE_BOND_COUNT>
2

> <JCHEM_RULE_OF_FIVE>
1

> <ALOGPS_SOLUBILITY>
2.35e-02 g/l

> <JCHEM_TRADITIONAL_IUPAC>
17-hydroxy-17-(hydroxymethyl)-9-methoxy-12-methyl-8-oxapentacyclo[14.2.1.0¹,¹³.0⁴,¹².0⁵,⁹]nonadec-5-en-7-one

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 17-APR-15   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   17-APR-15         0                                  
HETATM    1  C   UNK     0       7.052   3.493   0.000  0.00  0.00           C+0
HETATM    2  O   UNK     0       7.676   2.085   0.000  0.00  0.00           O+0
HETATM    3  C   UNK     0       6.769   0.841   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0       6.001   2.176   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0       4.461   2.179   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0       3.689   0.846   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0       2.932   2.188   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0       4.456  -0.489   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0       3.699  -1.850   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0       2.156  -1.868   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0       1.286  -0.556   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0       0.206   0.226   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0      -1.031   0.844   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0      -0.273   2.270   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0       1.332   2.318   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0       2.117   0.876   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0      -1.416  -0.720   0.000  0.00  0.00           C+0
HETATM   18  O   UNK     0      -2.865  -0.197   0.000  0.00  0.00           O+0
HETATM   19  C   UNK     0      -2.088  -2.106   0.000  0.00  0.00           C+0
HETATM   20  O   UNK     0      -1.224  -3.381   0.000  0.00  0.00           O+0
HETATM   21  C   UNK     0      -0.038  -1.578   0.000  0.00  0.00           C+0
HETATM   22  C   UNK     0       5.996  -0.491   0.000  0.00  0.00           C+0
HETATM   23  C   UNK     0       7.025  -1.638   0.000  0.00  0.00           C+0
HETATM   24  C   UNK     0       8.433  -1.014   0.000  0.00  0.00           C+0
HETATM   25  O   UNK     0       9.765  -1.786   0.000  0.00  0.00           O+0
HETATM   26  O   UNK     0       8.274   0.518   0.000  0.00  0.00           O+0
CONECT    1    2                                                            
CONECT    2    1    3                                                       
CONECT    3    2    4   22   26                                             
CONECT    4    3    5                                                       
CONECT    5    4    6                                                       
CONECT    6    5    7    8   16                                             
CONECT    7    6                                                            
CONECT    8    6    9   22                                                  
CONECT    9    8   10                                                       
CONECT   10    9   11                                                       
CONECT   11   10   12   16   21                                             
CONECT   12   11   13                                                       
CONECT   13   12   14   17                                                  
CONECT   14   13   15                                                       
CONECT   15   14   16                                                       
CONECT   16   15    6   11                                                  
CONECT   17   13   18   19   21                                             
CONECT   18   17                                                            
CONECT   19   17   20                                                       
CONECT   20   19                                                            
CONECT   21   17   11                                                       
CONECT   22    8    3   23                                                  
CONECT   23   22   24                                                       
CONECT   24   23   25   26                                                  
CONECT   25   24                                                            
CONECT   26   24    3                                                       
MASTER        0    0    0    0    0    0    0    0   26    0   60    0
END

View in JSmol

Synonyms

Not Available

Chemical Formula

C₂₁H₃₀O₅

Average Mass

362.4660 Da

Monoisotopic Mass

362.20932 Da

IUPAC Name

17-hydroxy-17-(hydroxymethyl)-9-methoxy-12-methyl-8-oxapentacyclo[14.2.1.0¹,¹³.0⁴,¹².0⁵,⁹]nonadec-5-en-7-one

Traditional Name

17-hydroxy-17-(hydroxymethyl)-9-methoxy-12-methyl-8-oxapentacyclo[14.2.1.0¹,¹³.0⁴,¹².0⁵,⁹]nonadec-5-en-7-one

CAS Registry Number

Not Available

SMILES

COC12CCC3(C)C(CCC45CC(CCC34)C(O)(CO)C5)C1=CC(=O)O2

InChI Identifier

InChI=1S/C21H30O5/c1-18-7-8-21(25-2)15(9-17(23)26-21)14(18)5-6-19-10-13(3-4-16(18)19)20(24,11-19)12-22/h9,13-14,16,22,24H,3-8,10-12H2,1-2H3

InChI Key

WGZVRWCVRXZGME-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
Diplospora dubia	LOTUS Database	35616633

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as diterpene lactones. These are diterpenoids containing a lactone moiety.

Kingdom

Organic compounds

Super Class

Lipids and lipid-like molecules

Class

Prenol lipids

Sub Class

Terpene lactones

Direct Parent

Diterpene lactones

Alternative Parents

Substituents

Diterpene lactone
Diterpenoid
Steroid
17-oxasteroid
Ketal
2-furanone
Cyclic alcohol
Dihydrofuran
Alpha,beta-unsaturated carboxylic ester
Enoate ester
Tertiary alcohol
1,2-diol
Carboxylic acid ester
Lactone
Acetal
Carboxylic acid derivative
Oxacycle
Organoheterocyclic compound
Monocarboxylic acid or derivatives
Hydrocarbon derivative
Organic oxygen compound
Carbonyl group
Alcohol
Primary alcohol
Organooxygen compound
Organic oxide
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	1.57	ALOGPS
logP	2.27	ChemAxon
logS	-4.2	ALOGPS
pKa (Strongest Acidic)	13.69	ChemAxon
pKa (Strongest Basic)	-3.1	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	4	ChemAxon
Hydrogen Donor Count	2	ChemAxon
Polar Surface Area	75.99 Å²	ChemAxon
Rotatable Bond Count	2	ChemAxon
Refractivity	96.06 m³·mol⁻¹	ChemAxon
Polarizability	39.71 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

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

72983482

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

LOTUS database [Link]

Showing NP-Card for 17-hydroxy-17-(hydroxymethyl)-9-methoxy-12-methyl-8-oxapentacyclo[14.2.1.0¹,¹³.0⁴,¹².0⁵,⁹]nonadec-5-en-7-one (NP0315711)

MOL for NP0315711 (17-hydroxy-17-(hydroxymethyl)-9-methoxy-12-methyl-8-oxapentacyclo[14.2.1.0¹,¹³.0⁴,¹².0⁵,⁹]nonadec-5-en-7-one)

3D MOL for NP0315711 (17-hydroxy-17-(hydroxymethyl)-9-methoxy-12-methyl-8-oxapentacyclo[14.2.1.0¹,¹³.0⁴,¹².0⁵,⁹]nonadec-5-en-7-one)

3D SDF for NP0315711 (17-hydroxy-17-(hydroxymethyl)-9-methoxy-12-methyl-8-oxapentacyclo[14.2.1.0¹,¹³.0⁴,¹².0⁵,⁹]nonadec-5-en-7-one)

3D-SDF for NP0315711 (17-hydroxy-17-(hydroxymethyl)-9-methoxy-12-methyl-8-oxapentacyclo[14.2.1.0¹,¹³.0⁴,¹².0⁵,⁹]nonadec-5-en-7-one)

PDB for NP0315711 (17-hydroxy-17-(hydroxymethyl)-9-methoxy-12-methyl-8-oxapentacyclo[14.2.1.0¹,¹³.0⁴,¹².0⁵,⁹]nonadec-5-en-7-one)

3D PDB for NP0315711 (17-hydroxy-17-(hydroxymethyl)-9-methoxy-12-methyl-8-oxapentacyclo[14.2.1.0¹,¹³.0⁴,¹².0⁵,⁹]nonadec-5-en-7-one)

SMILES for NP0315711 (17-hydroxy-17-(hydroxymethyl)-9-methoxy-12-methyl-8-oxapentacyclo[14.2.1.0¹,¹³.0⁴,¹².0⁵,⁹]nonadec-5-en-7-one)

INCHI for NP0315711 (17-hydroxy-17-(hydroxymethyl)-9-methoxy-12-methyl-8-oxapentacyclo[14.2.1.0¹,¹³.0⁴,¹².0⁵,⁹]nonadec-5-en-7-one)

Structure for NP0315711 (17-hydroxy-17-(hydroxymethyl)-9-methoxy-12-methyl-8-oxapentacyclo[14.2.1.0¹,¹³.0⁴,¹².0⁵,⁹]nonadec-5-en-7-one)

3D Structure for NP0315711 (17-hydroxy-17-(hydroxymethyl)-9-methoxy-12-methyl-8-oxapentacyclo[14.2.1.0¹,¹³.0⁴,¹².0⁵,⁹]nonadec-5-en-7-one)