NP-MRD: Showing NP-Card for 10,11,16-trihydroxy-17-methoxy-13,13-dimethyl-6-methylidene-4,18-dioxapentacyclo[8.6.2.1³,⁷.0¹,¹².0²,⁹]nonadecan-5-one (NP0256859)

Jump To Section:

Identification Spectra BioTaxonomy ChemoTaxonomy Physical properties Links References XML

Record Information

Version

2.0

Created at

2022-09-07 21:49:19 UTC

Updated at

2022-09-07 21:49:19 UTC

NP-MRD ID

NP0256859

Secondary Accession Numbers

None

Natural Product Identification

Common Name

10,11,16-trihydroxy-17-methoxy-13,13-dimethyl-6-methylidene-4,18-dioxapentacyclo[8.6.2.1³,⁷.0¹,¹².0²,⁹]nonadecan-5-one

Description

10,11,16-Trihydroxy-17-methoxy-13,13-dimethyl-6-methylidene-4,18-dioxapentacyclo[8.6.2.1³,⁷.0¹,¹².0²,⁹]Nonadecan-5-one belongs to the class of organic compounds known as diterpene lactones. These are diterpenoids containing a lactone moiety. 10,11,16-trihydroxy-17-methoxy-13,13-dimethyl-6-methylidene-4,18-dioxapentacyclo[8.6.2.1³,⁷.0¹,¹².0²,⁹]nonadecan-5-one is found in Isodon rubescens. 10,11,16-Trihydroxy-17-methoxy-13,13-dimethyl-6-methylidene-4,18-dioxapentacyclo[8.6.2.1³,⁷.0¹,¹².0²,⁹]Nonadecan-5-one is an extremely weak basic (essentially neutral) compound (based on its pKa).

Structure

MOL 3D MOL SDF PDB SMILES InChI


  Mrv1533004241503362D          

 28 32  0  0  0  0            999 V2000
    3.7867    1.7863    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.7580    0.9041    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.9357   -0.1229    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.5212   -0.7186    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.8410   -1.3836    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.2590   -2.2495    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.0611   -1.3391    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.6801   -2.1400    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.4528   -0.7082    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.5831   -0.7394    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4124   -1.5912    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7379   -0.9917    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.1422   -0.0236    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4877    0.7414    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.3277    0.6152    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.2429    1.4734    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.9738    0.0020    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.6308    0.3922    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.2747    0.9080    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.3165   -0.2023    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.8759   -1.1623    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.0559   -1.0717    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5401   -0.4278    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.5198   -0.6466    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.3182   -1.0038    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.6105    0.1734    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.4274    0.4884    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.0947    0.8173    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
  5  7  1  0  0  0  0
  7  8  1  0  0  0  0
  7  9  1  0  0  0  0
  9 10  1  0  0  0  0
 10 11  1  0  0  0  0
 10 12  1  0  0  0  0
 10 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
 15 17  1  0  0  0  0
  3 17  1  0  0  0  0
  9 17  1  0  0  0  0
 17 18  1  0  0  0  0
 18 19  1  0  0  0  0
 19 20  1  0  0  0  0
 20 21  1  0  0  0  0
 21 22  1  0  0  0  0
 22 23  1  0  0  0  0
  5 23  1  0  0  0  0
 18 23  1  0  0  0  0
 21 24  1  0  0  0  0
 24 25  2  0  0  0  0
 24 26  1  0  0  0  0
 26 27  2  0  0  0  0
 26 28  1  0  0  0  0
 19 28  1  0  0  0  0
M  END

     RDKit          3D

 58 62  0  0  0  0  0  0  0  0999 V2000
    4.3319   -1.9665   -1.3762 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5373   -1.4457   -0.4820 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.7788   -2.2980    0.4090 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8911   -3.5499    0.3477 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.8926   -1.7629    1.3715 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.6231   -0.3487    1.3608 C   0  0  1  0  0  0  0  0  0  0  0  0
    2.9947    0.2782    1.0650 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.4015    0.0182   -0.3673 C   0  0  2  0  0  0  0  0  0  0  0  0
    2.4199    0.5912   -1.3644 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.2883    1.1693   -0.5660 C   0  0  2  0  0  0  0  0  0  0  0  0
    0.7256    0.0226    0.2510 C   0  0  2  0  0  0  0  0  0  0  0  0
   -0.6959    0.3782    0.6143 C   0  0  2  0  0  0  0  0  0  0  0  0
   -1.2054   -0.4032    1.7750 C   0  0  1  0  0  0  0  0  0  0  0  0
   -0.8760    0.2240    2.9594 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7076   -0.5462    1.7112 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.1472   -1.3511    0.5148 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2434   -1.1846   -0.6698 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.1966   -1.1017   -1.8861 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4105   -2.3954   -0.9406 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5708    0.1214   -0.6327 C   0  0  2  0  0  0  0  0  0  0  0  0
   -0.7284    0.4653   -1.8116 C   0  0  1  0  0  0  0  0  0  0  0  0
   -1.5511    0.9635   -2.8455 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.1347    1.6614   -1.3887 C   0  0  2  0  0  0  0  0  0  0  0  0
    0.4896    2.3408   -2.5152 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6341    2.4391   -0.5337 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7568    1.8721    0.7592 C   0  0  2  0  0  0  0  0  0  0  0  0
    0.0615    2.4598    1.6581 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5002    3.3064    2.5744 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.4898   -3.0220   -1.5275 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.9098   -1.3193   -2.0550 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.3260   -0.0779    2.3677 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.0490    1.3219    1.3649 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.7115   -0.2838    1.7005 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.3569    0.5565   -0.5232 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.0008   -0.2880   -1.9281 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.8748    1.2871   -2.0731 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.6679    1.9942    0.0263 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.6978   -0.8501   -0.4661 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6964   -1.3930    1.7711 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6761   -0.3905    3.6977 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.1374    0.4674    1.7354 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.0261   -1.0849    2.6276 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.1950   -2.4325    0.8045 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.1950   -1.0560    0.3033 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.8638   -1.9802   -1.8222 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.7864   -0.1746   -1.8367 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5645   -1.1855   -2.7745 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1301   -3.1901   -1.3125 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7496   -2.2157   -1.8046 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9245   -2.8553   -0.0835 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4181    0.8804   -0.6479 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1362   -0.3321   -2.2485 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1917    1.5922   -2.3915 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.8925    3.2192   -2.3752 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8258    2.1402    1.0168 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2495    2.8308    3.1909 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.3147    3.6805    3.2444 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8721    4.2038    2.0276 H   0  0  0  0  0  0  0  0  0  0  0  0
 28 27  1  0
 27 26  1  0
 26 25  1  0
 25 23  1  0
 23 24  1  6
 23 21  1  0
 21 22  1  0
 21 20  1  0
 20 17  1  0
 17 18  1  0
 17 19  1  0
 17 16  1  0
 16 15  1  0
 15 13  1  0
 13 14  1  0
 12 13  1  1
 12 11  1  0
 11  6  1  0
  6  7  1  0
  7  8  1  0
  8  9  1  0
  9 10  1  0
  8  2  1  0
  2  1  2  3
  2  3  1  0
  3  4  2  0
  3  5  1  0
 12 26  1  0
 10 11  1  0
 10 23  1  0
 12 20  1  0
  5  6  1  0
 28 56  1  0
 28 57  1  0
 28 58  1  0
 26 55  1  1
 24 54  1  0
 21 52  1  6
 22 53  1  0
 20 51  1  1
 18 45  1  0
 18 46  1  0
 18 47  1  0
 19 48  1  0
 19 49  1  0
 19 50  1  0
 16 43  1  0
 16 44  1  0
 15 41  1  0
 15 42  1  0
 13 39  1  1
 14 40  1  0
 11 38  1  6
  6 31  1  1
  7 32  1  0
  7 33  1  0
  8 34  1  6
  9 35  1  0
  9 36  1  0
 10 37  1  1
  1 29  1  0
  1 30  1  0
M  END


  Mrv1533004241503362D          

 28 32  0  0  0  0            999 V2000
    3.7867    1.7863    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.7580    0.9041    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.9357   -0.1229    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.5212   -0.7186    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.8410   -1.3836    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.2590   -2.2495    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.0611   -1.3391    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.6801   -2.1400    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.4528   -0.7082    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.5831   -0.7394    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4124   -1.5912    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7379   -0.9917    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.1422   -0.0236    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4877    0.7414    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.3277    0.6152    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.2429    1.4734    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.9738    0.0020    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.6308    0.3922    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.2747    0.9080    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.3165   -0.2023    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.8759   -1.1623    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.0559   -1.0717    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5401   -0.4278    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.5198   -0.6466    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.3182   -1.0038    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.6105    0.1734    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.4274    0.4884    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.0947    0.8173    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
  5  7  1  0  0  0  0
  7  8  1  0  0  0  0
  7  9  1  0  0  0  0
  9 10  1  0  0  0  0
 10 11  1  0  0  0  0
 10 12  1  0  0  0  0
 10 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
 15 17  1  0  0  0  0
  3 17  1  0  0  0  0
  9 17  1  0  0  0  0
 17 18  1  0  0  0  0
 18 19  1  0  0  0  0
 19 20  1  0  0  0  0
 20 21  1  0  0  0  0
 21 22  1  0  0  0  0
 22 23  1  0  0  0  0
  5 23  1  0  0  0  0
 18 23  1  0  0  0  0
 21 24  1  0  0  0  0
 24 25  2  0  0  0  0
 24 26  1  0  0  0  0
 26 27  2  0  0  0  0
 26 28  1  0  0  0  0
 19 28  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0256859

> <DATABASE_NAME>
NP-MRD

> <SMILES>
COC1OC2(O)C(O)C3C(C)(C)CCC(O)C13C1C3CC(CC21)C(=C)C(=O)O3

> <INCHI_IDENTIFIER>
InChI=1S/C21H30O7/c1-9-10-7-11-14(12(8-10)27-17(9)24)20-13(22)5-6-19(2,3)15(20)16(23)21(11,25)28-18(20)26-4/h10-16,18,22-23,25H,1,5-8H2,2-4H3

> <INCHI_KEY>
NUYJBFSDWBBTBE-UHFFFAOYSA-N

> <FORMULA>
C21H30O7

> <MOLECULAR_WEIGHT>
394.464

> <EXACT_MASS>
394.199153306

> <JCHEM_ACCEPTOR_COUNT>
6

> <JCHEM_ATOM_COUNT>
58

> <JCHEM_AVERAGE_POLARIZABILITY>
40.57700119753203

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
3

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
1

> <JCHEM_IUPAC>
10,11,16-trihydroxy-17-methoxy-13,13-dimethyl-6-methylidene-4,18-dioxapentacyclo[8.6.2.1³,⁷.0¹,¹².0²,⁹]nonadecan-5-one

> <ALOGPS_LOGP>
0.76

> <JCHEM_LOGP>
1.3243923349999998

> <ALOGPS_LOGS>
-1.90

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
5

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA>
13.73507362235016

> <JCHEM_PKA_STRONGEST_ACIDIC>
10.870421144033397

> <JCHEM_PKA_STRONGEST_BASIC>
-3.008754704314355

> <JCHEM_POLAR_SURFACE_AREA>
105.45

> <JCHEM_REFRACTIVITY>
97.35269999999997

> <JCHEM_ROTATABLE_BOND_COUNT>
1

> <JCHEM_RULE_OF_FIVE>
1

> <ALOGPS_SOLUBILITY>
5.01e+00 g/l

> <JCHEM_TRADITIONAL_IUPAC>
10,11,16-trihydroxy-17-methoxy-13,13-dimethyl-6-methylidene-4,18-dioxapentacyclo[8.6.2.1³,⁷.0¹,¹².0²,⁹]nonadecan-5-one

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 24-APR-15   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   24-APR-15         0                                  
HETATM    1  C   UNK     0       7.068   3.334   0.000  0.00  0.00           C+0
HETATM    2  O   UNK     0       7.015   1.688   0.000  0.00  0.00           O+0
HETATM    3  C   UNK     0       7.347  -0.229   0.000  0.00  0.00           C+0
HETATM    4  O   UNK     0       8.440  -1.341   0.000  0.00  0.00           O+0
HETATM    5  C   UNK     0       7.170  -2.583   0.000  0.00  0.00           C+0
HETATM    6  O   UNK     0       7.950  -4.199   0.000  0.00  0.00           O+0
HETATM    7  C   UNK     0       5.714  -2.500   0.000  0.00  0.00           C+0
HETATM    8  O   UNK     0       5.003  -3.995   0.000  0.00  0.00           O+0
HETATM    9  C   UNK     0       4.579  -1.322   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0       2.955  -1.380   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0       2.637  -2.970   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0       1.377  -1.851   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0       2.132  -0.044   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0       2.777   1.384   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0       4.345   1.148   0.000  0.00  0.00           C+0
HETATM   16  O   UNK     0       4.187   2.750   0.000  0.00  0.00           O+0
HETATM   17  C   UNK     0       5.551   0.004   0.000  0.00  0.00           C+0
HETATM   18  C   UNK     0       6.777   0.732   0.000  0.00  0.00           C+0
HETATM   19  C   UNK     0       7.979   1.695   0.000  0.00  0.00           C+0
HETATM   20  C   UNK     0       8.057  -0.378   0.000  0.00  0.00           C+0
HETATM   21  C   UNK     0       9.102  -2.170   0.000  0.00  0.00           C+0
HETATM   22  C   UNK     0       7.571  -2.001   0.000  0.00  0.00           C+0
HETATM   23  C   UNK     0       6.608  -0.799   0.000  0.00  0.00           C+0
HETATM   24  C   UNK     0      10.304  -1.207   0.000  0.00  0.00           C+0
HETATM   25  C   UNK     0      11.794  -1.874   0.000  0.00  0.00           C+0
HETATM   26  C   UNK     0      10.473   0.324   0.000  0.00  0.00           C+0
HETATM   27  O   UNK     0      11.998   0.912   0.000  0.00  0.00           O+0
HETATM   28  O   UNK     0       9.510   1.526   0.000  0.00  0.00           O+0
CONECT    1    2                                                            
CONECT    2    1    3                                                       
CONECT    3    2    4   17                                                  
CONECT    4    3    5                                                       
CONECT    5    4    6    7   23                                             
CONECT    6    5                                                            
CONECT    7    5    8    9                                                  
CONECT    8    7                                                            
CONECT    9    7   10   17                                                  
CONECT   10    9   11   12   13                                             
CONECT   11   10                                                            
CONECT   12   10                                                            
CONECT   13   10   14                                                       
CONECT   14   13   15                                                       
CONECT   15   14   16   17                                                  
CONECT   16   15                                                            
CONECT   17   15    3    9   18                                             
CONECT   18   17   19   23                                                  
CONECT   19   18   20   28                                                  
CONECT   20   19   21                                                       
CONECT   21   20   22   24                                                  
CONECT   22   21   23                                                       
CONECT   23   22    5   18                                                  
CONECT   24   21   25   26                                                  
CONECT   25   24                                                            
CONECT   26   24   27   28                                                  
CONECT   27   26                                                            
CONECT   28   26   19                                                       
MASTER        0    0    0    0    0    0    0    0   28    0   64    0
END

View in JSmol

Synonyms

Not Available

Chemical Formula

C₂₁H₃₀O₇

Average Mass

394.4640 Da

Monoisotopic Mass

394.19915 Da

IUPAC Name

10,11,16-trihydroxy-17-methoxy-13,13-dimethyl-6-methylidene-4,18-dioxapentacyclo[8.6.2.1³,⁷.0¹,¹².0²,⁹]nonadecan-5-one

Traditional Name

10,11,16-trihydroxy-17-methoxy-13,13-dimethyl-6-methylidene-4,18-dioxapentacyclo[8.6.2.1³,⁷.0¹,¹².0²,⁹]nonadecan-5-one

CAS Registry Number

Not Available

SMILES

COC1OC2(O)C(O)C3C(C)(C)CCC(O)C13C1C3CC(CC21)C(=C)C(=O)O3

InChI Identifier

InChI=1S/C21H30O7/c1-9-10-7-11-14(12(8-10)27-17(9)24)20-13(22)5-6-19(2,3)15(20)16(23)21(11,25)28-18(20)26-4/h10-16,18,22-23,25H,1,5-8H2,2-4H3

InChI Key

NUYJBFSDWBBTBE-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 rubescens	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
Kaurane diterpenoid
Delta valerolactone
Delta_valerolactone
Oxane
Cyclic alcohol
Enoate ester
Alpha,beta-unsaturated carboxylic ester
Secondary alcohol
Carboxylic acid ester
Hemiacetal
Lactone
Polyol
Carboxylic acid derivative
Organoheterocyclic compound
Acetal
Oxacycle
Monocarboxylic acid or derivatives
Carbonyl group
Organic oxygen compound
Organic oxide
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	0.76	ALOGPS
logP	1.32	ChemAxon
logS	-1.9	ALOGPS
pKa (Strongest Acidic)	10.87	ChemAxon
pKa (Strongest Basic)	-3	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	6	ChemAxon
Hydrogen Donor Count	3	ChemAxon
Polar Surface Area	105.45 Å²	ChemAxon
Rotatable Bond Count	1	ChemAxon
Refractivity	97.35 m³·mol⁻¹	ChemAxon
Polarizability	40.58 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

72966947

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

LOTUS database [Link]

Showing NP-Card for 10,11,16-trihydroxy-17-methoxy-13,13-dimethyl-6-methylidene-4,18-dioxapentacyclo[8.6.2.1³,⁷.0¹,¹².0²,⁹]nonadecan-5-one (NP0256859)

MOL for NP0256859 (10,11,16-trihydroxy-17-methoxy-13,13-dimethyl-6-methylidene-4,18-dioxapentacyclo[8.6.2.1³,⁷.0¹,¹².0²,⁹]nonadecan-5-one)

3D MOL for NP0256859 (10,11,16-trihydroxy-17-methoxy-13,13-dimethyl-6-methylidene-4,18-dioxapentacyclo[8.6.2.1³,⁷.0¹,¹².0²,⁹]nonadecan-5-one)

3D SDF for NP0256859 (10,11,16-trihydroxy-17-methoxy-13,13-dimethyl-6-methylidene-4,18-dioxapentacyclo[8.6.2.1³,⁷.0¹,¹².0²,⁹]nonadecan-5-one)

3D-SDF for NP0256859 (10,11,16-trihydroxy-17-methoxy-13,13-dimethyl-6-methylidene-4,18-dioxapentacyclo[8.6.2.1³,⁷.0¹,¹².0²,⁹]nonadecan-5-one)

PDB for NP0256859 (10,11,16-trihydroxy-17-methoxy-13,13-dimethyl-6-methylidene-4,18-dioxapentacyclo[8.6.2.1³,⁷.0¹,¹².0²,⁹]nonadecan-5-one)

3D PDB for NP0256859 (10,11,16-trihydroxy-17-methoxy-13,13-dimethyl-6-methylidene-4,18-dioxapentacyclo[8.6.2.1³,⁷.0¹,¹².0²,⁹]nonadecan-5-one)

SMILES for NP0256859 (10,11,16-trihydroxy-17-methoxy-13,13-dimethyl-6-methylidene-4,18-dioxapentacyclo[8.6.2.1³,⁷.0¹,¹².0²,⁹]nonadecan-5-one)

INCHI for NP0256859 (10,11,16-trihydroxy-17-methoxy-13,13-dimethyl-6-methylidene-4,18-dioxapentacyclo[8.6.2.1³,⁷.0¹,¹².0²,⁹]nonadecan-5-one)

Structure for NP0256859 (10,11,16-trihydroxy-17-methoxy-13,13-dimethyl-6-methylidene-4,18-dioxapentacyclo[8.6.2.1³,⁷.0¹,¹².0²,⁹]nonadecan-5-one)

3D Structure for NP0256859 (10,11,16-trihydroxy-17-methoxy-13,13-dimethyl-6-methylidene-4,18-dioxapentacyclo[8.6.2.1³,⁷.0¹,¹².0²,⁹]nonadecan-5-one)