NP-MRD: Showing NP-Card for (1r,2r,5s,6r,7r,8s,9r,10s,11r,18r)-7,9,10,18-tetrahydroxy-6,12,12-trimethyl-17-oxapentacyclo[7.6.2.1⁵,⁸.0¹,¹¹.0²,⁸]octadecan-16-one (NP0190428)

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Record Information

Version

2.0

Created at

2022-09-04 07:05:50 UTC

Updated at

2022-09-04 07:05:50 UTC

NP-MRD ID

NP0190428

Secondary Accession Numbers

None

Natural Product Identification

Common Name

(1r,2r,5s,6r,7r,8s,9r,10s,11r,18r)-7,9,10,18-tetrahydroxy-6,12,12-trimethyl-17-oxapentacyclo[7.6.2.1⁵,⁸.0¹,¹¹.0²,⁸]octadecan-16-one

Description

CHEMBL2407380 belongs to the class of organic compounds known as diterpene lactones. These are diterpenoids containing a lactone moiety. (1r,2r,5s,6r,7r,8s,9r,10s,11r,18r)-7,9,10,18-tetrahydroxy-6,12,12-trimethyl-17-oxapentacyclo[7.6.2.1⁵,⁸.0¹,¹¹.0²,⁸]octadecan-16-one is found in Isodon rosthornii. Based on a literature review very few articles have been published on CHEMBL2407380.

Structure

MOL 3D MOL SDF PDB SMILES InChI


  Mrv1652309042209052D          

 26 30  0  0  1  0            999 V2000
    7.8983    1.0612    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.1268    0.7689    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    6.9810   -0.0777    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    6.3817   -0.6935    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.5315   -0.6530    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.1641    0.1233    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    5.6724    0.9371    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    6.2666    0.3273    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    5.7627   -0.3259    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    6.4656    1.2990    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    6.5676    2.1177    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.3375    1.7931    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    5.8736    2.4202    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.6926    1.4405    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.8761    0.7027    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.6431    0.3987    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.2390    0.2923    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    3.5545   -0.2303    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.7903    0.1204    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.6476    0.9516    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.2055    1.5818    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.5445    2.0755    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.6427    2.2814    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.9665    1.1899    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    4.4350    1.9919    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    4.1041    2.7476    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
  2  1  1  6  0  0  0
  2  3  1  0  0  0  0
  3  4  1  6  0  0  0
  4  5  1  0  0  0  0
  6  5  1  1  0  0  0
  6  7  1  0  0  0  0
  7  8  1  1  0  0  0
  3  8  1  0  0  0  0
  8  9  1  1  0  0  0
  7 10  1  0  0  0  0
  2 10  1  0  0  0  0
 10 11  1  6  0  0  0
  7 12  1  0  0  0  0
 12 13  1  6  0  0  0
 12 14  1  0  0  0  0
 14 15  1  0  0  0  0
 15 16  2  0  0  0  0
 17 15  1  1  0  0  0
  6 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
 21 23  1  0  0  0  0
 24 21  1  1  0  0  0
 17 24  1  0  0  0  0
 24 25  1  0  0  0  0
 12 25  1  0  0  0  0
 25 26  1  6  0  0  0
M  END

     RDKit          2D

 56 60  0  0  0  0  0  0  0  0999 V2000
   -3.0000   -4.6055    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8853   -3.6018    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.0000   -2.5981    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.7500   -1.2990    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.0000    0.0000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5000    0.0000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7500   -1.2990    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5000   -2.5981    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7605   -4.0753    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5862   -2.8518    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0239   -4.2221    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.7500   -1.2990    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.5000   -2.5981    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.5000    0.0000    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.7500    1.2990    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.1634    2.7410    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7500    1.2990    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5000    2.5981    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7500    3.8971    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7500    3.8971    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.5000    2.5981    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.6491    1.6339    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.6491    3.5623    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7500    1.2990    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.5000   -0.0000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.6491   -0.9642    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -4.1147   -5.6092    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9963   -5.7202    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.1321   -3.6214    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8623   -4.6988    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.9028   -3.7960    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.8991   -0.3349    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.8991   -2.2632    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.1047    1.4963    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.4095    0.5130    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2500    1.2990    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2565   -3.4369    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7375   -5.1723    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.9101   -2.7472    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.5156   -4.3789    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.0000   -2.5981    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6491    3.5623    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8482    1.9406    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4895    5.3743    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1595    4.4101    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.0865    4.5781    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.4895    5.3743    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.7981    0.6697    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.7461    2.6569    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.6849    0.4848    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.7981    4.5264    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.7461    2.5393    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.8321    4.8203    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.2388    1.1162    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.9183    0.4882    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.0586   -0.4512    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0
  2  3  1  0
  3  4  1  0
  4  5  1  0
  5  6  1  0
  6  7  1  0
  7 10  1  0
 10 11  1  0
  7  8  1  0
  8  9  1  0
  7 12  1  1
 12 13  1  6
 12 14  1  0
 14 15  1  0
 15 16  2  0
 15 17  1  0
 17 18  1  6
 18 19  1  0
 19 20  1  0
 20 21  1  0
 21 22  1  0
 21 23  1  0
 21 24  1  0
 24 25  1  0
 25 26  1  0
 10  2  1  0
 25 12  1  0
  8  3  1  0
 24 17  1  0
 17  6  1  0
  1 27  1  0
  1 28  1  0
  1 29  1  0
  2 30  1  1
  3 31  1  1
  4 32  1  0
  4 33  1  0
  5 34  1  0
  5 35  1  0
  6 36  1  6
 10 39  1  1
 11 40  1  0
  8 37  1  1
  9 38  1  0
 13 41  1  0
 18 42  1  0
 18 43  1  0
 19 44  1  0
 19 45  1  0
 20 46  1  0
 20 47  1  0
 22 48  1  0
 22 49  1  0
 22 50  1  0
 23 51  1  0
 23 52  1  0
 23 53  1  0
 24 54  1  6
 25 55  1  1
 26 56  1  0
M  END


  Mrv1652309042209052D          

 26 30  0  0  1  0            999 V2000
    7.8983    1.0612    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.1268    0.7689    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    6.9810   -0.0777    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    6.3817   -0.6935    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.5315   -0.6530    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.1641    0.1233    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    5.6724    0.9371    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    6.2666    0.3273    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    5.7627   -0.3259    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    6.4656    1.2990    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    6.5676    2.1177    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.3375    1.7931    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    5.8736    2.4202    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.6926    1.4405    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.8761    0.7027    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.6431    0.3987    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.2390    0.2923    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    3.5545   -0.2303    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.7903    0.1204    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.6476    0.9516    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.2055    1.5818    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.5445    2.0755    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.6427    2.2814    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.9665    1.1899    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    4.4350    1.9919    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    4.1041    2.7476    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
  2  1  1  6  0  0  0
  2  3  1  0  0  0  0
  3  4  1  6  0  0  0
  4  5  1  0  0  0  0
  6  5  1  1  0  0  0
  6  7  1  0  0  0  0
  7  8  1  1  0  0  0
  3  8  1  0  0  0  0
  8  9  1  1  0  0  0
  7 10  1  0  0  0  0
  2 10  1  0  0  0  0
 10 11  1  6  0  0  0
  7 12  1  0  0  0  0
 12 13  1  6  0  0  0
 12 14  1  0  0  0  0
 14 15  1  0  0  0  0
 15 16  2  0  0  0  0
 17 15  1  1  0  0  0
  6 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
 21 23  1  0  0  0  0
 24 21  1  1  0  0  0
 17 24  1  0  0  0  0
 24 25  1  0  0  0  0
 12 25  1  0  0  0  0
 25 26  1  6  0  0  0
M  END
> <DATABASE_ID>
NP0190428

> <DATABASE_NAME>
NP-MRD

> <SMILES>
C[C@@H]1[C@@H]2CC[C@@H]3[C@]([C@@H]1O)([C@@H]2O)[C@@]1(O)OC(=O)[C@]32CCCC(C)(C)[C@H]2[C@@H]1O

> <INCHI_IDENTIFIER>
InChI=1S/C20H30O6/c1-9-10-5-6-11-18-8-4-7-17(2,3)12(18)15(23)20(25,26-16(18)24)19(11,13(9)21)14(10)22/h9-15,21-23,25H,4-8H2,1-3H3/t9-,10+,11+,12-,13-,14-,15+,18-,19+,20+/m1/s1

> <INCHI_KEY>
HZXNJXNYQASOMR-IPJVHAIESA-N

> <FORMULA>
C20H30O6

> <MOLECULAR_WEIGHT>
366.454

> <EXACT_MASS>
366.204238686

> <JCHEM_ACCEPTOR_COUNT>
5

> <JCHEM_ATOM_COUNT>
56

> <JCHEM_AVERAGE_POLARIZABILITY>
28.78376073687963

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
4

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
1

> <JCHEM_IUPAC>
(1R,2R,5S,6R,7R,8S,9R,10S,11R,18R)-7,9,10,18-tetrahydroxy-6,12,12-trimethyl-17-oxapentacyclo[7.6.2.1^{5,8}.0^{1,11}.0^{2,8}]octadecan-16-one

> <JCHEM_LOGP>
1.0967880403333328

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
5

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA>
13.574853831190342

> <JCHEM_PKA_STRONGEST_ACIDIC>
10.472233201118181

> <JCHEM_PKA_STRONGEST_BASIC>
-3.138374288753866

> <JCHEM_POLAR_SURFACE_AREA>
107.22000000000001

> <JCHEM_REFRACTIVITY>
91.23819999999999

> <JCHEM_ROTATABLE_BOND_COUNT>
0

> <JCHEM_RULE_OF_FIVE>
1

> <JCHEM_TRADITIONAL_IUPAC>
(1R,2R,5S,6R,7R,8S,9R,10S,11R,18R)-7,9,10,18-tetrahydroxy-6,12,12-trimethyl-17-oxapentacyclo[7.6.2.1^{5,8}.0^{1,11}.0^{2,8}]octadecan-16-one

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 04-SEP-22   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   04-SEP-22         0                                  
HETATM    1  C   UNK     0      14.743   1.981   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0      13.303   1.435   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0      13.031  -0.145   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0      11.913  -1.295   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0      10.326  -1.219   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0       9.640   0.230   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0      10.588   1.749   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0      11.698   0.611   0.000  0.00  0.00           C+0
HETATM    9  O   UNK     0      10.757  -0.608   0.000  0.00  0.00           O+0
HETATM   10  C   UNK     0      12.069   2.425   0.000  0.00  0.00           C+0
HETATM   11  O   UNK     0      12.259   3.953   0.000  0.00  0.00           O+0
HETATM   12  C   UNK     0       9.963   3.347   0.000  0.00  0.00           C+0
HETATM   13  O   UNK     0      10.964   4.518   0.000  0.00  0.00           O+0
HETATM   14  O   UNK     0       8.759   2.689   0.000  0.00  0.00           O+0
HETATM   15  C   UNK     0       9.102   1.312   0.000  0.00  0.00           C+0
HETATM   16  O   UNK     0      10.534   0.744   0.000  0.00  0.00           O+0
HETATM   17  C   UNK     0       7.913   0.546   0.000  0.00  0.00           C+0
HETATM   18  C   UNK     0       6.635  -0.430   0.000  0.00  0.00           C+0
HETATM   19  C   UNK     0       5.209   0.225   0.000  0.00  0.00           C+0
HETATM   20  C   UNK     0       4.942   1.776   0.000  0.00  0.00           C+0
HETATM   21  C   UNK     0       5.984   2.953   0.000  0.00  0.00           C+0
HETATM   22  C   UNK     0       4.750   3.874   0.000  0.00  0.00           C+0
HETATM   23  C   UNK     0       6.800   4.259   0.000  0.00  0.00           C+0
HETATM   24  C   UNK     0       7.404   2.221   0.000  0.00  0.00           C+0
HETATM   25  C   UNK     0       8.279   3.718   0.000  0.00  0.00           C+0
HETATM   26  O   UNK     0       7.661   5.129   0.000  0.00  0.00           O+0
CONECT    1    2                                                            
CONECT    2    1    3   10                                                  
CONECT    3    2    4    8                                                  
CONECT    4    3    5                                                       
CONECT    5    4    6                                                       
CONECT    6    5    7   17                                                  
CONECT    7    6    8   10   12                                             
CONECT    8    7    3    9                                                  
CONECT    9    8                                                            
CONECT   10    7    2   11                                                  
CONECT   11   10                                                            
CONECT   12    7   13   14   25                                             
CONECT   13   12                                                            
CONECT   14   12   15                                                       
CONECT   15   14   16   17                                                  
CONECT   16   15                                                            
CONECT   17   15    6   18   24                                             
CONECT   18   17   19                                                       
CONECT   19   18   20                                                       
CONECT   20   19   21                                                       
CONECT   21   20   22   23   24                                             
CONECT   22   21                                                            
CONECT   23   21                                                            
CONECT   24   21   17   25                                                  
CONECT   25   24   12   26                                                  
CONECT   26   25                                                            
MASTER        0    0    0    0    0    0    0    0   26    0   60    0
END

View in JSmol

Synonyms

Not Available

Chemical Formula

C₂₀H₃₀O₆

Average Mass

366.4540 Da

Monoisotopic Mass

366.20424 Da

IUPAC Name

Not Available

Traditional Name

Not Available

CAS Registry Number

Not Available

SMILES

C[C@@H]1[C@@H]2CC[C@@H]3[C@]([C@@H]1O)([C@@H]2O)[C@@]1(O)OC(=O)[C@]32CCCC(C)(C)[C@H]2[C@@H]1O

InChI Identifier

InChI=1S/C20H30O6/c1-9-10-5-6-11-18-8-4-7-17(2,3)12(18)15(23)20(25,26-16(18)24)19(11,13(9)21)14(10)22/h9-15,21-23,25H,4-8H2,1-3H3/t9-,10+,11+,12-,13-,14-,15+,18-,19+,20+/m1/s1

InChI Key

HZXNJXNYQASOMR-IPJVHAIESA-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 rosthornii	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
Carboxylic acid ester
Hemiacetal
Lactone
Secondary alcohol
Organoheterocyclic compound
Oxacycle
Monocarboxylic acid or derivatives
Carboxylic acid derivative
Polyol
Carbonyl group
Hydrocarbon derivative
Organic oxide
Organic oxygen compound
Alcohol
Organooxygen compound
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

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

30821329

KEGG Compound ID

Not Available

BioCyc ID

Not Available

BiGG ID

Not Available

Wikipedia Link

Not Available

METLIN ID

Not Available

PubChem Compound

71745896

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

LOTUS database [Link]

Showing NP-Card for (1r,2r,5s,6r,7r,8s,9r,10s,11r,18r)-7,9,10,18-tetrahydroxy-6,12,12-trimethyl-17-oxapentacyclo[7.6.2.1⁵,⁸.0¹,¹¹.0²,⁸]octadecan-16-one (NP0190428)

MOL for NP0190428 ((1r,2r,5s,6r,7r,8s,9r,10s,11r,18r)-7,9,10,18-tetrahydroxy-6,12,12-trimethyl-17-oxapentacyclo[7.6.2.1⁵,⁸.0¹,¹¹.0²,⁸]octadecan-16-one)

3D MOL for NP0190428 ((1r,2r,5s,6r,7r,8s,9r,10s,11r,18r)-7,9,10,18-tetrahydroxy-6,12,12-trimethyl-17-oxapentacyclo[7.6.2.1⁵,⁸.0¹,¹¹.0²,⁸]octadecan-16-one)

3D SDF for NP0190428 ((1r,2r,5s,6r,7r,8s,9r,10s,11r,18r)-7,9,10,18-tetrahydroxy-6,12,12-trimethyl-17-oxapentacyclo[7.6.2.1⁵,⁸.0¹,¹¹.0²,⁸]octadecan-16-one)

3D-SDF for NP0190428 ((1r,2r,5s,6r,7r,8s,9r,10s,11r,18r)-7,9,10,18-tetrahydroxy-6,12,12-trimethyl-17-oxapentacyclo[7.6.2.1⁵,⁸.0¹,¹¹.0²,⁸]octadecan-16-one)

PDB for NP0190428 ((1r,2r,5s,6r,7r,8s,9r,10s,11r,18r)-7,9,10,18-tetrahydroxy-6,12,12-trimethyl-17-oxapentacyclo[7.6.2.1⁵,⁸.0¹,¹¹.0²,⁸]octadecan-16-one)

3D PDB for NP0190428 ((1r,2r,5s,6r,7r,8s,9r,10s,11r,18r)-7,9,10,18-tetrahydroxy-6,12,12-trimethyl-17-oxapentacyclo[7.6.2.1⁵,⁸.0¹,¹¹.0²,⁸]octadecan-16-one)

SMILES for NP0190428 ((1r,2r,5s,6r,7r,8s,9r,10s,11r,18r)-7,9,10,18-tetrahydroxy-6,12,12-trimethyl-17-oxapentacyclo[7.6.2.1⁵,⁸.0¹,¹¹.0²,⁸]octadecan-16-one)

INCHI for NP0190428 ((1r,2r,5s,6r,7r,8s,9r,10s,11r,18r)-7,9,10,18-tetrahydroxy-6,12,12-trimethyl-17-oxapentacyclo[7.6.2.1⁵,⁸.0¹,¹¹.0²,⁸]octadecan-16-one)

Structure for NP0190428 ((1r,2r,5s,6r,7r,8s,9r,10s,11r,18r)-7,9,10,18-tetrahydroxy-6,12,12-trimethyl-17-oxapentacyclo[7.6.2.1⁵,⁸.0¹,¹¹.0²,⁸]octadecan-16-one)

3D Structure for NP0190428 ((1r,2r,5s,6r,7r,8s,9r,10s,11r,18r)-7,9,10,18-tetrahydroxy-6,12,12-trimethyl-17-oxapentacyclo[7.6.2.1⁵,⁸.0¹,¹¹.0²,⁸]octadecan-16-one)