NP-MRD: Showing NP-Card for (1s,2s,5s,8r,9r,10s,11r,15s,18r)-9,10,18-trihydroxy-12,12-dimethyl-6-methylidene-7-oxo-17-oxapentacyclo[7.6.2.1⁵,⁸.0¹,¹¹.0²,⁸]octadecan-15-yl acetate (NP0329923)

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Record Information

Version

2.0

Created at

2022-09-12 14:47:33 UTC

Updated at

2022-09-12 14:47:33 UTC

NP-MRD ID

NP0329923

Secondary Accession Numbers

None

Natural Product Identification

Common Name

(1s,2s,5s,8r,9r,10s,11r,15s,18r)-9,10,18-trihydroxy-12,12-dimethyl-6-methylidene-7-oxo-17-oxapentacyclo[7.6.2.1⁵,⁸.0¹,¹¹.0²,⁸]octadecan-15-yl acetate

Description

Lasiokaurin 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. (1s,2s,5s,8r,9r,10s,11r,15s,18r)-9,10,18-trihydroxy-12,12-dimethyl-6-methylidene-7-oxo-17-oxapentacyclo[7.6.2.1⁵,⁸.0¹,¹¹.0²,⁸]octadecan-15-yl acetate is found in Isodon adenolomus, Isodon japonicus and Isodon rosthornii. (1s,2s,5s,8r,9r,10s,11r,15s,18r)-9,10,18-trihydroxy-12,12-dimethyl-6-methylidene-7-oxo-17-oxapentacyclo[7.6.2.1⁵,⁸.0¹,¹¹.0²,⁸]octadecan-15-yl acetate was first documented in 2005 (PMID: 16142643). Based on a literature review a significant number of articles have been published on Lasiokaurin (PMID: 30989952) (PMID: 29320879) (PMID: 28110416) (PMID: 22743545) (PMID: 18491868) (PMID: 19606380).

Structure

MOL 3D MOL SDF PDB SMILES InChI


  Mrv1652309122216472D          

 29 33  0  0  1  0            999 V2000
    7.8690    0.3782    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.0976    0.6705    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.4364    0.1404    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.5383   -0.6783    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.6431    0.5023    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    5.1349    1.3161    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    5.5023    2.0925    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.3525    2.1330    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.9517    1.5171    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    6.2374    1.1121    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    5.7335    1.7654    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.2098    1.1472    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    4.8469    0.7367    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.6633   -0.0011    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.3082   -0.3537    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    5.8443   -0.9808    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.4058   -0.5525    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    4.0749   -1.3082    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.9373    0.2496    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    3.1762   -0.1423    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.5153   -0.6361    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.6135   -0.8420    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.6183    0.4878    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.7611    1.3190    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5253    1.6697    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    3.6166    2.4897    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.9521    2.9787    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1964    2.6478    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.0434    3.7986    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  2  0  0  0  0
  2  3  1  0  0  0  0
  3  4  2  0  0  0  0
  5  3  1  1  0  0  0
  5  6  1  0  0  0  0
  6  7  1  6  0  0  0
  7  8  1  0  0  0  0
  8  9  1  0  0  0  0
  9  2  1  1  0  0  0
  9 10  1  0  0  0  0
  5 10  1  0  0  0  0
 10 11  1  6  0  0  0
  6 12  1  0  0  0  0
 12 13  1  6  0  0  0
 13 14  1  0  0  0  0
 14 15  1  0  0  0  0
  5 15  1  0  0  0  0
 15 16  1  1  0  0  0
 15 17  1  0  0  0  0
 17 18  1  1  0  0  0
 19 17  1  6  0  0  0
 12 19  1  0  0  0  0
 19 20  1  0  0  0  0
 20 21  1  0  0  0  0
 20 22  1  0  0  0  0
 20 23  1  0  0  0  0
 23 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
 26 27  1  0  0  0  0
 27 28  1  0  0  0  0
 27 29  2  0  0  0  0
M  END

     RDKit          2D

 59 63  0  0  0  0  0  0  0  0999 V2000
   -1.8940    5.0080    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7372    3.5163    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4381    2.7663    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.9322    3.3764    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    0.0000    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
   -3.7500    1.2990    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
   -1.5000    2.5981    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0905    3.1111    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    0.0000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7500    1.2990    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 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
    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
    2.6491   -3.5623    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
    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 O   0  0  0  0  0  0  0  0  0  0  0  0
   -4.0586   -2.1469    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.2077   -1.1827    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.3191   -3.6241    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6804    5.8897    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.2643    5.6181    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5420   -1.0790    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.4616   -0.3374    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.4637   -1.4265    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
   -4.7730    0.2020    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.7500    3.8971    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3953    4.0944    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.1700    4.5883    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6491   -0.9642    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6491    0.9642    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
    2.9183   -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
    2.2388   -1.1162    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
    1.8321   -4.8203    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
    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
    1.9916   -0.2857    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
    2.0865   -4.5781    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
   -0.4895   -5.3743    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
   -6.3567   -0.2186    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.1719   -2.3318    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.2435   -0.0337    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
 28 27  1  0
 27 29  2  0
 27 26  1  0
 26 25  1  0
 25 24  1  0
 24 23  1  0
 23 20  1  0
 20 21  1  0
 20 22  1  0
 20 19  1  0
 19 17  1  0
 17 18  1  0
 17 15  1  0
 15 16  1  1
 15 14  1  0
 14 13  1  0
 12 13  1  1
 12  6  1  0
  6  7  1  0
  7  8  1  0
  8  9  1  0
  9 10  1  0
 10 11  1  0
 10  5  1  0
  5  3  1  1
  3  4  2  0
  3  2  1  0
  2  1  2  3
 12 25  1  0
  5  6  1  0
 12 19  1  0
  2  9  1  0
  5 15  1  0
 28 57  1  0
 28 58  1  0
 28 59  1  0
 25 56  1  1
 24 54  1  0
 24 55  1  0
 23 52  1  0
 23 53  1  0
 21 46  1  0
 21 47  1  0
 21 48  1  0
 22 49  1  0
 22 50  1  0
 22 51  1  0
 19 45  1  1
 17 43  1  6
 18 44  1  0
 16 42  1  0
 13 40  1  0
 13 41  1  0
  6 32  1  1
  7 33  1  0
  7 34  1  0
  8 35  1  0
  8 36  1  0
  9 37  1  6
 10 38  1  6
 11 39  1  0
  1 30  1  0
  1 31  1  0
M  END


  Mrv1652309122216472D          

 29 33  0  0  1  0            999 V2000
    7.8690    0.3782    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.0976    0.6705    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.4364    0.1404    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.5383   -0.6783    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.6431    0.5023    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    5.1349    1.3161    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    5.5023    2.0925    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.3525    2.1330    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.9517    1.5171    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    6.2374    1.1121    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    5.7335    1.7654    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.2098    1.1472    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    4.8469    0.7367    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.6633   -0.0011    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.3082   -0.3537    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    5.8443   -0.9808    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.4058   -0.5525    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    4.0749   -1.3082    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.9373    0.2496    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    3.1762   -0.1423    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.5153   -0.6361    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.6135   -0.8420    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.6183    0.4878    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.7611    1.3190    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5253    1.6697    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    3.6166    2.4897    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.9521    2.9787    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1964    2.6478    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.0434    3.7986    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  2  0  0  0  0
  2  3  1  0  0  0  0
  3  4  2  0  0  0  0
  5  3  1  1  0  0  0
  5  6  1  0  0  0  0
  6  7  1  6  0  0  0
  7  8  1  0  0  0  0
  8  9  1  0  0  0  0
  9  2  1  1  0  0  0
  9 10  1  0  0  0  0
  5 10  1  0  0  0  0
 10 11  1  6  0  0  0
  6 12  1  0  0  0  0
 12 13  1  6  0  0  0
 13 14  1  0  0  0  0
 14 15  1  0  0  0  0
  5 15  1  0  0  0  0
 15 16  1  1  0  0  0
 15 17  1  0  0  0  0
 17 18  1  1  0  0  0
 19 17  1  6  0  0  0
 12 19  1  0  0  0  0
 19 20  1  0  0  0  0
 20 21  1  0  0  0  0
 20 22  1  0  0  0  0
 20 23  1  0  0  0  0
 23 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
 26 27  1  0  0  0  0
 27 28  1  0  0  0  0
 27 29  2  0  0  0  0
M  END
> <DATABASE_ID>
NP0329923

> <DATABASE_NAME>
NP-MRD

> <SMILES>
CC(=O)O[C@H]1CCC(C)(C)[C@H]2[C@H](O)[C@]3(O)OC[C@@]12[C@@H]1CC[C@@H]2[C@@H](O)[C@]31C(=O)C2=C

> <INCHI_IDENTIFIER>
InChI=1S/C22H30O7/c1-10-12-5-6-13-20-9-28-22(27,21(13,16(10)24)17(12)25)18(26)15(20)19(3,4)8-7-14(20)29-11(2)23/h12-15,17-18,25-27H,1,5-9H2,2-4H3/t12-,13-,14-,15+,17+,18-,20+,21-,22-/m0/s1

> <INCHI_KEY>
DJQLJZNVICMJRV-VPKUEDJQSA-N

> <FORMULA>
C22H30O7

> <MOLECULAR_WEIGHT>
406.475

> <EXACT_MASS>
406.199153306

> <ALOGPS_LOGP>
1.01

> <ALOGPS_LOGS>
-2.22

> <ALOGPS_SOLUBILITY>
2.43e+00 g/l

$$$$

HEADER    PROTEIN                                 12-SEP-22   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   12-SEP-22         0                                  
HETATM    1  C   UNK     0      14.689   0.706   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0      13.249   1.252   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0      12.015   0.262   0.000  0.00  0.00           C+0
HETATM    4  O   UNK     0      12.205  -1.266   0.000  0.00  0.00           O+0
HETATM    5  C   UNK     0      10.534   0.938   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0       9.585   2.457   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0      10.271   3.906   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0      11.858   3.982   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0      12.977   2.832   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0      11.643   2.076   0.000  0.00  0.00           C+0
HETATM   11  O   UNK     0      10.703   3.295   0.000  0.00  0.00           O+0
HETATM   12  C   UNK     0       7.858   2.141   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0       9.047   1.375   0.000  0.00  0.00           C+0
HETATM   14  O   UNK     0       8.705  -0.002   0.000  0.00  0.00           O+0
HETATM   15  C   UNK     0       9.909  -0.660   0.000  0.00  0.00           C+0
HETATM   16  O   UNK     0      10.909  -1.831   0.000  0.00  0.00           O+0
HETATM   17  C   UNK     0       8.224  -1.031   0.000  0.00  0.00           C+0
HETATM   18  O   UNK     0       7.607  -2.442   0.000  0.00  0.00           O+0
HETATM   19  C   UNK     0       7.350   0.466   0.000  0.00  0.00           C+0
HETATM   20  C   UNK     0       5.929  -0.266   0.000  0.00  0.00           C+0
HETATM   21  C   UNK     0       4.695  -1.187   0.000  0.00  0.00           C+0
HETATM   22  C   UNK     0       6.745  -1.572   0.000  0.00  0.00           C+0
HETATM   23  C   UNK     0       4.888   0.911   0.000  0.00  0.00           C+0
HETATM   24  C   UNK     0       5.154   2.462   0.000  0.00  0.00           C+0
HETATM   25  C   UNK     0       6.581   3.117   0.000  0.00  0.00           C+0
HETATM   26  O   UNK     0       6.751   4.647   0.000  0.00  0.00           O+0
HETATM   27  C   UNK     0       5.511   5.560   0.000  0.00  0.00           C+0
HETATM   28  C   UNK     0       4.100   4.943   0.000  0.00  0.00           C+0
HETATM   29  O   UNK     0       5.681   7.091   0.000  0.00  0.00           O+0
CONECT    1    2                                                            
CONECT    2    1    3    9                                                  
CONECT    3    2    4    5                                                  
CONECT    4    3                                                            
CONECT    5    3    6   10   15                                             
CONECT    6    5    7   12                                                  
CONECT    7    6    8                                                       
CONECT    8    7    9                                                       
CONECT    9    8    2   10                                                  
CONECT   10    9    5   11                                                  
CONECT   11   10                                                            
CONECT   12    6   13   19   25                                             
CONECT   13   12   14                                                       
CONECT   14   13   15                                                       
CONECT   15   14    5   16   17                                             
CONECT   16   15                                                            
CONECT   17   15   18   19                                                  
CONECT   18   17                                                            
CONECT   19   17   12   20                                                  
CONECT   20   19   21   22   23                                             
CONECT   21   20                                                            
CONECT   22   20                                                            
CONECT   23   20   24                                                       
CONECT   24   23   25                                                       
CONECT   25   24   12   26                                                  
CONECT   26   25   27                                                       
CONECT   27   26   28   29                                                  
CONECT   28   27                                                            
CONECT   29   27                                                            
MASTER        0    0    0    0    0    0    0    0   29    0   66    0
END

View in JSmol

Synonyms

Not Available

Chemical Formula

C₂₂H₃₀O₇

Average Mass

406.4750 Da

Monoisotopic Mass

406.19915 Da

IUPAC Name

Not Available

Traditional Name

Not Available

CAS Registry Number

Not Available

SMILES

CC(=O)O[C@H]1CCC(C)(C)[C@H]2[C@H](O)[C@]3(O)OC[C@@]12[C@@H]1CC[C@@H]2[C@@H](O)[C@]31C(=O)C2=C

InChI Identifier

InChI=1S/C22H30O7/c1-10-12-5-6-13-20-9-28-22(27,21(13,16(10)24)17(12)25)18(26)15(20)19(3,4)8-7-14(20)29-11(2)23/h12-15,17-18,25-27H,1,5-9H2,2-4H3/t12-,13-,14-,15+,17+,18-,20+,21-,22-/m0/s1

InChI Key

DJQLJZNVICMJRV-VPKUEDJQSA-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 adenolomus	LOTUS Database	35616633
Isodon japonicus	LOTUS Database	35616633
Isodon rosthornii	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
Oxane
Cyclic alcohol
Carboxylic acid ester
Hemiacetal
Ketone
Secondary alcohol
Polyol
Monocarboxylic acid or derivatives
Carboxylic acid derivative
Organoheterocyclic compound
Oxacycle
Organic oxide
Organooxygen compound
Carbonyl group
Organic oxygen compound
Alcohol
Hydrocarbon derivative
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

C00039604

Chemspider ID

30845927

KEGG Compound ID

Not Available

BioCyc ID

Not Available

BiGG ID

Not Available

Wikipedia Link

Not Available

METLIN ID

Not Available

PubChem Compound

73348360

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

Zhang LX, Liu YL, Wu H, Chen SQ, Dai LP: [Studies on chemical constituents of Isodon henryi]. Zhongguo Zhong Yao Za Zhi. 2019 Jan;44(2):319-323. doi: 10.19540/j.cnki.cjcmm.20181101.009. [PubMed:30989952 ]
Dai LP, Zhang LX, Liu YL, Wu H, Liu RX, Zhao M, Tian SS, Jiang X, Chen SQ: Isolation and purification of diterpenoids from the aerial parts of Isodon excisoides target-guided by UPLC-LTQ-Orbitrap-MS. Nat Prod Res. 2018 Oct;32(20):2424-2430. doi: 10.1080/14786419.2017.1419225. Epub 2018 Jan 10. [PubMed:29320879 ]
Li DH, Hu P, Xu ST, Fang CY, Tang S, Wang XY, Sun XY, Li H, Xu Y, Gu XK, Xu JY: Lasiokaurin derivatives: synthesis, antimicrobial and antitumor biological evaluation, and apoptosis-inducing effects. Arch Pharm Res. 2017 Jul;40(7):796-806. doi: 10.1007/s12272-016-0867-9. Epub 2017 Jan 21. [PubMed:28110416 ]
Zhao W, Wang WG, Li XN, Du X, Zhan R, Zou J, Li Y, Zhang HB, He F, Pu JX, Sun HD: Neoadenoloside A, a highly functionalized diterpene C-glycoside, from Isodon adenolomus. Chem Commun (Camb). 2012 Aug 11;48(62):7723-5. doi: 10.1039/c2cc33656a. Epub 2012 Jun 28. [PubMed:22743545 ]
Bai SP, Wei QY, Jin XL, Wu QX, Yang L: Two novel ent-kauranoid diterpenoids from Isodon japonica leaves. Planta Med. 2005 Aug;71(8):764-9. doi: 10.1055/s-2005-871246. [PubMed:16142643 ]
Hong SS, Lee SA, Han XH, Hwang JS, Lee C, Lee D, Hong JT, Kim Y, Lee H, Hwang BY: ent-Kaurane diterpenoids from Isodon japonicus. J Nat Prod. 2008 Jun;71(6):1055-8. doi: 10.1021/np0705965. Epub 2008 May 21. [PubMed:18491868 ]
Ding L, Zhou Q, Wang L, Wang W, Zhang S, Liu B: Comparison of cytotoxicity and DNA damage potential induced by ent-kaurene diterpenoids from Isodon plant. Nat Prod Res. 2011 Sep;25(15):1402-11. doi: 10.1080/14786410802267734. Epub 2011 Jul 8. [PubMed:19606380 ]
Du Y, Liu P, Zhu H, Shi X, Zhao C, Wang N, Zhang L: A sensitive analysis method for 7 diterpenoids in rat plasma by liquid chromatography-electrospray ionization mass spectrometry and its application to pharmacokinetic study of Isodon serra extract. J Chromatogr A. 2011 Oct 28;1218(43):7771-80. doi: 10.1016/j.chroma.2011.08.033. Epub 2011 Aug 17. [PubMed:21930275 ]
Zhang HB, Pu JX, Wang YY, He F, Zhao Y, Li XN, Luo X, Xiao WL, Li Y, Sun HD: Four new ent-kauranoids from Isodon rubescens var. lushanensis and data reassignment of dayecrystal B. Chem Pharm Bull (Tokyo). 2010 Jan;58(1):56-60. doi: 10.1248/cpb.58.56. [PubMed:20045967 ]
LOTUS database [Link]

Showing NP-Card for (1s,2s,5s,8r,9r,10s,11r,15s,18r)-9,10,18-trihydroxy-12,12-dimethyl-6-methylidene-7-oxo-17-oxapentacyclo[7.6.2.1⁵,⁸.0¹,¹¹.0²,⁸]octadecan-15-yl acetate (NP0329923)

MOL for NP0329923 ((1s,2s,5s,8r,9r,10s,11r,15s,18r)-9,10,18-trihydroxy-12,12-dimethyl-6-methylidene-7-oxo-17-oxapentacyclo[7.6.2.1⁵,⁸.0¹,¹¹.0²,⁸]octadecan-15-yl acetate)

3D MOL for NP0329923 ((1s,2s,5s,8r,9r,10s,11r,15s,18r)-9,10,18-trihydroxy-12,12-dimethyl-6-methylidene-7-oxo-17-oxapentacyclo[7.6.2.1⁵,⁸.0¹,¹¹.0²,⁸]octadecan-15-yl acetate)

3D SDF for NP0329923 ((1s,2s,5s,8r,9r,10s,11r,15s,18r)-9,10,18-trihydroxy-12,12-dimethyl-6-methylidene-7-oxo-17-oxapentacyclo[7.6.2.1⁵,⁸.0¹,¹¹.0²,⁸]octadecan-15-yl acetate)

3D-SDF for NP0329923 ((1s,2s,5s,8r,9r,10s,11r,15s,18r)-9,10,18-trihydroxy-12,12-dimethyl-6-methylidene-7-oxo-17-oxapentacyclo[7.6.2.1⁵,⁸.0¹,¹¹.0²,⁸]octadecan-15-yl acetate)

PDB for NP0329923 ((1s,2s,5s,8r,9r,10s,11r,15s,18r)-9,10,18-trihydroxy-12,12-dimethyl-6-methylidene-7-oxo-17-oxapentacyclo[7.6.2.1⁵,⁸.0¹,¹¹.0²,⁸]octadecan-15-yl acetate)

3D PDB for NP0329923 ((1s,2s,5s,8r,9r,10s,11r,15s,18r)-9,10,18-trihydroxy-12,12-dimethyl-6-methylidene-7-oxo-17-oxapentacyclo[7.6.2.1⁵,⁸.0¹,¹¹.0²,⁸]octadecan-15-yl acetate)

SMILES for NP0329923 ((1s,2s,5s,8r,9r,10s,11r,15s,18r)-9,10,18-trihydroxy-12,12-dimethyl-6-methylidene-7-oxo-17-oxapentacyclo[7.6.2.1⁵,⁸.0¹,¹¹.0²,⁸]octadecan-15-yl acetate)

INCHI for NP0329923 ((1s,2s,5s,8r,9r,10s,11r,15s,18r)-9,10,18-trihydroxy-12,12-dimethyl-6-methylidene-7-oxo-17-oxapentacyclo[7.6.2.1⁵,⁸.0¹,¹¹.0²,⁸]octadecan-15-yl acetate)

Structure for NP0329923 ((1s,2s,5s,8r,9r,10s,11r,15s,18r)-9,10,18-trihydroxy-12,12-dimethyl-6-methylidene-7-oxo-17-oxapentacyclo[7.6.2.1⁵,⁸.0¹,¹¹.0²,⁸]octadecan-15-yl acetate)

3D Structure for NP0329923 ((1s,2s,5s,8r,9r,10s,11r,15s,18r)-9,10,18-trihydroxy-12,12-dimethyl-6-methylidene-7-oxo-17-oxapentacyclo[7.6.2.1⁵,⁸.0¹,¹¹.0²,⁸]octadecan-15-yl acetate)