NP-MRD: Showing NP-Card for maoesin d (NP0306264)

Jump To Section:

Identification Spectra BioTaxonomy ChemoTaxonomy Physical properties Links References XML

Record Information

Version

2.0

Created at

2022-09-10 22:37:45 UTC

Updated at

2022-09-10 22:37:45 UTC

NP-MRD ID

NP0306264

Secondary Accession Numbers

None

Natural Product Identification

Common Name

maoesin d

Description

Maoesin D 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. maoesin d is found in Isodon eriocalyx. Based on a literature review very few articles have been published on Maoesin D.

Structure

MOL 3D MOL SDF PDB SMILES InChI


  Mrv1652309112200372D          

 32 36  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  2  0  0  0  0  0  0  0  0  0
    6.2374    1.1121    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.9517    1.5171    0.0000 C   0  0  1  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
    5.5023    2.0925    0.0000 C   0  0  0  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
    4.2098    1.1472    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    3.5253    1.6697    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
    2.6183    0.4878    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    1.8249    0.2619    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.2325    0.8362    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.4390    0.6103    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4337    1.6363    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.1762   -0.1423    0.0000 C   0  0  1  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
    3.2262   -1.5704    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.6634   -2.2700    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.4879   -2.2412    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.2762   -2.9985    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.9373    0.2496    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    4.4058   -0.5525    0.0000 C   0  0  2  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
    5.3082   -0.3537    0.0000 C   0  0  1  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
    4.6633   -0.0011    0.0000 O   0  0  0  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
  1  2  2  0  0  0  0
  2  3  1  0  0  0  0
  3  4  2  0  0  0  0
  3  5  1  0  0  0  0
  5  6  1  6  0  0  0
  7  6  1  6  0  0  0
  2  7  1  0  0  0  0
  7  8  1  0  0  0  0
  8  9  2  0  0  0  0
 10  9  1  6  0  0  0
  5 10  1  0  0  0  0
 10 11  1  0  0  0  0
 11 12  1  6  0  0  0
 12 13  1  0  0  0  0
 13 14  1  0  0  0  0
 14 15  1  1  0  0  0
 15 16  1  0  0  0  0
 16 17  1  0  0  0  0
 16 18  2  0  0  0  0
 14 19  1  0  0  0  0
 19 20  1  1  0  0  0
 19 21  1  6  0  0  0
 21 22  1  0  0  0  0
 22 23  1  0  0  0  0
 23 24  1  0  0  0  0
 23 25  2  0  0  0  0
 26 19  1  6  0  0  0
 11 26  1  0  0  0  0
 26 27  1  0  0  0  0
 27 28  1  1  0  0  0
 27 29  1  0  0  0  0
  5 29  1  0  0  0  0
 29 30  1  1  0  0  0
 29 31  1  0  0  0  0
 31 32  1  0  0  0  0
 11 32  1  0  0  0  0
M  END

     RDKit          2D

 62 66  0  0  0  0  0  0  0  0999 V2000
    2.0421    5.0936    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
    0.5862    2.8518    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7841    3.4619    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
    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
    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
   -2.1595   -4.4101    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4200   -5.8874    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.8296   -6.4004    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2709   -6.8515    0.0000 O   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
   -3.7981   -4.5264    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -5.2077   -4.0134    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.3567   -4.9776    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.4681   -2.5362    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
   -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 O   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
    1.5000    0.0000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.4124    5.7037    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.8286    5.9752    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
    0.2565    3.4369    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
    5.2500    1.2990    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.7500   -1.2990    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
    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
   -0.4895   -5.3743    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.1660   -7.0814    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.3165   -7.8099    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.6684   -5.1569    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.9071   -0.8170    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
   -3.7461   -2.5393    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9916   -4.9105    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
   -7.5058   -5.9418    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
   -7.3209   -3.8285    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.5398   -6.2356    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
   -2.6491    0.9642    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.9856   -0.2832    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    0.9642    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.8482   -0.6575    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
 24 23  1  0
 23 25  2  0
 23 22  1  0
 22 21  1  0
 19 21  1  1
 19 20  1  0
 19 14  1  0
 14 13  1  0
 13 12  1  0
 11 12  1  6
 11 32  1  0
 32 31  1  0
 31 29  1  0
 29 30  1  1
 29 27  1  0
 27 28  1  0
 27 26  1  0
 29  5  1  0
  5  6  1  0
  6  7  1  0
  7  8  1  0
  8  9  2  0
  9 10  1  0
  7  2  1  0
  2  1  2  3
  2  3  1  0
  3  4  2  0
 14 15  1  0
 15 16  1  0
 16 17  1  0
 16 18  2  0
 26 19  1  0
 10  5  1  0
 26 11  1  0
  5  3  1  6
 10 11  1  0
 24 54  1  0
 24 55  1  0
 24 56  1  0
 21 52  1  0
 21 53  1  0
 20 49  1  0
 20 50  1  0
 20 51  1  0
 14 45  1  1
 13 43  1  0
 13 44  1  0
 12 41  1  0
 12 42  1  0
 32 61  1  0
 32 62  1  0
 30 60  1  0
 27 58  1  1
 28 59  1  0
 26 57  1  6
  6 35  1  0
  6 36  1  0
  7 37  1  1
  8 38  1  0
  9 39  1  0
 10 40  1  6
  1 33  1  0
  1 34  1  0
 17 46  1  0
 17 47  1  0
 17 48  1  0
M  END


  Mrv1652309112200372D          

 32 36  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  2  0  0  0  0  0  0  0  0  0
    6.2374    1.1121    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.9517    1.5171    0.0000 C   0  0  1  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
    5.5023    2.0925    0.0000 C   0  0  0  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
    4.2098    1.1472    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    3.5253    1.6697    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
    2.6183    0.4878    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    1.8249    0.2619    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.2325    0.8362    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.4390    0.6103    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4337    1.6363    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.1762   -0.1423    0.0000 C   0  0  1  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
    3.2262   -1.5704    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.6634   -2.2700    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.4879   -2.2412    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.2762   -2.9985    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.9373    0.2496    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    4.4058   -0.5525    0.0000 C   0  0  2  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
    5.3082   -0.3537    0.0000 C   0  0  1  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
    4.6633   -0.0011    0.0000 O   0  0  0  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
  1  2  2  0  0  0  0
  2  3  1  0  0  0  0
  3  4  2  0  0  0  0
  3  5  1  0  0  0  0
  5  6  1  6  0  0  0
  7  6  1  6  0  0  0
  2  7  1  0  0  0  0
  7  8  1  0  0  0  0
  8  9  2  0  0  0  0
 10  9  1  6  0  0  0
  5 10  1  0  0  0  0
 10 11  1  0  0  0  0
 11 12  1  6  0  0  0
 12 13  1  0  0  0  0
 13 14  1  0  0  0  0
 14 15  1  1  0  0  0
 15 16  1  0  0  0  0
 16 17  1  0  0  0  0
 16 18  2  0  0  0  0
 14 19  1  0  0  0  0
 19 20  1  1  0  0  0
 19 21  1  6  0  0  0
 21 22  1  0  0  0  0
 22 23  1  0  0  0  0
 23 24  1  0  0  0  0
 23 25  2  0  0  0  0
 26 19  1  6  0  0  0
 11 26  1  0  0  0  0
 26 27  1  0  0  0  0
 27 28  1  1  0  0  0
 27 29  1  0  0  0  0
  5 29  1  0  0  0  0
 29 30  1  1  0  0  0
 29 31  1  0  0  0  0
 31 32  1  0  0  0  0
 11 32  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0306264

> <DATABASE_NAME>
NP-MRD

> <SMILES>
CC(=O)OC[C@]1(C)[C@H](CC[C@]23CO[C@@](O)([C@@H](O)[C@H]12)[C@@]12C[C@@H](C=C[C@@H]31)C(=C)C2=O)OC(C)=O

> <INCHI_IDENTIFIER>
InChI=1S/C24H30O8/c1-12-15-5-6-16-22-8-7-17(32-14(3)26)21(4,10-30-13(2)25)18(22)20(28)24(29,31-11-22)23(16,9-15)19(12)27/h5-6,15-18,20,28-29H,1,7-11H2,2-4H3/t15-,16+,17+,18-,20+,21-,22-,23+,24+/m1/s1

> <INCHI_KEY>
FUWZKRPAEKGTSW-MIWKWXCYSA-N

> <FORMULA>
C24H30O8

> <MOLECULAR_WEIGHT>
446.496

> <EXACT_MASS>
446.194067926

> <JCHEM_ACCEPTOR_COUNT>
6

> <JCHEM_ATOM_COUNT>
62

> <JCHEM_AVERAGE_POLARIZABILITY>
69.49576753247221

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
2

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
1

> <JCHEM_IUPAC>
[(1R,2S,5S,8S,9R,10S,11S,12R,13S)-13-(acetyloxy)-9,10-dihydroxy-12-methyl-6-methylidene-7-oxo-17-oxapentacyclo[7.6.2.1^{5,8}.0^{1,11}.0^{2,8}]octadec-3-en-12-yl]methyl acetate

> <JCHEM_LOGP>
0.9330235383333345

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
5

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA>
13.790458136086308

> <JCHEM_PKA_STRONGEST_ACIDIC>
10.582779568596292

> <JCHEM_PKA_STRONGEST_BASIC>
-3.6854763813790914

> <JCHEM_POLAR_SURFACE_AREA>
119.36000000000003

> <JCHEM_REFRACTIVITY>
111.63309999999998

> <JCHEM_ROTATABLE_BOND_COUNT>
5

> <JCHEM_RULE_OF_FIVE>
1

> <JCHEM_TRADITIONAL_IUPAC>
[(1R,2S,5S,8S,9R,10S,11S,12R,13S)-13-(acetyloxy)-9,10-dihydroxy-12-methyl-6-methylidene-7-oxo-17-oxapentacyclo[7.6.2.1^{5,8}.0^{1,11}.0^{2,8}]octadec-3-en-12-yl]methyl acetate

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 11-SEP-22   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   11-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      11.643   2.076   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0      12.977   2.832   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      10.271   3.906   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0       9.585   2.457   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0       7.858   2.141   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0       6.581   3.117   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0       5.154   2.462   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0       4.888   0.911   0.000  0.00  0.00           C+0
HETATM   15  O   UNK     0       3.406   0.489   0.000  0.00  0.00           O+0
HETATM   16  C   UNK     0       2.301   1.561   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0       0.820   1.139   0.000  0.00  0.00           C+0
HETATM   18  O   UNK     0       2.676   3.054   0.000  0.00  0.00           O+0
HETATM   19  C   UNK     0       5.929  -0.266   0.000  0.00  0.00           C+0
HETATM   20  C   UNK     0       4.695  -1.187   0.000  0.00  0.00           C+0
HETATM   21  C   UNK     0       6.745  -1.572   0.000  0.00  0.00           C+0
HETATM   22  O   UNK     0       6.022  -2.931   0.000  0.00  0.00           O+0
HETATM   23  C   UNK     0       6.838  -4.237   0.000  0.00  0.00           C+0
HETATM   24  C   UNK     0       8.377  -4.184   0.000  0.00  0.00           C+0
HETATM   25  O   UNK     0       6.116  -5.597   0.000  0.00  0.00           O+0
HETATM   26  C   UNK     0       7.350   0.466   0.000  0.00  0.00           C+0
HETATM   27  C   UNK     0       8.224  -1.031   0.000  0.00  0.00           C+0
HETATM   28  O   UNK     0       7.607  -2.442   0.000  0.00  0.00           O+0
HETATM   29  C   UNK     0       9.909  -0.660   0.000  0.00  0.00           C+0
HETATM   30  O   UNK     0      10.909  -1.831   0.000  0.00  0.00           O+0
HETATM   31  O   UNK     0       8.705  -0.002   0.000  0.00  0.00           O+0
HETATM   32  C   UNK     0       9.047   1.375   0.000  0.00  0.00           C+0
CONECT    1    2                                                            
CONECT    2    1    3    7                                                  
CONECT    3    2    4    5                                                  
CONECT    4    3                                                            
CONECT    5    3    6   10   29                                             
CONECT    6    5    7                                                       
CONECT    7    6    2    8                                                  
CONECT    8    7    9                                                       
CONECT    9    8   10                                                       
CONECT   10    9    5   11                                                  
CONECT   11   10   12   26   32                                             
CONECT   12   11   13                                                       
CONECT   13   12   14                                                       
CONECT   14   13   15   19                                                  
CONECT   15   14   16                                                       
CONECT   16   15   17   18                                                  
CONECT   17   16                                                            
CONECT   18   16                                                            
CONECT   19   14   20   21   26                                             
CONECT   20   19                                                            
CONECT   21   19   22                                                       
CONECT   22   21   23                                                       
CONECT   23   22   24   25                                                  
CONECT   24   23                                                            
CONECT   25   23                                                            
CONECT   26   19   11   27                                                  
CONECT   27   26   28   29                                                  
CONECT   28   27                                                            
CONECT   29   27    5   30   31                                             
CONECT   30   29                                                            
CONECT   31   29   32                                                       
CONECT   32   31   11                                                       
MASTER        0    0    0    0    0    0    0    0   32    0   72    0
END

View in JSmol

Synonyms

Not Available

Chemical Formula

C₂₄H₃₀O₈

Average Mass

446.4960 Da

Monoisotopic Mass

446.19407 Da

IUPAC Name

Not Available

Traditional Name

Not Available

CAS Registry Number

Not Available

SMILES

CC(=O)OC[C@]1(C)[C@H](CC[C@]23CO[C@@](O)([C@@H](O)[C@H]12)[C@@]12C[C@@H](C=C[C@@H]31)C(=C)C2=O)OC(C)=O

InChI Identifier

InChI=1S/C24H30O8/c1-12-15-5-6-16-22-8-7-17(32-14(3)26)21(4,10-30-13(2)25)18(22)20(28)24(29,31-11-22)23(16,9-15)19(12)27/h5-6,15-18,20,28-29H,1,7-11H2,2-4H3/t15-,16+,17+,18-,20+,21-,22-,23+,24+/m1/s1

InChI Key

FUWZKRPAEKGTSW-MIWKWXCYSA-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 eriocalyx	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
Steroid
Dicarboxylic acid or derivatives
Oxane
Cyclic alcohol
Carboxylic acid ester
Hemiacetal
Ketone
Secondary alcohol
Carboxylic acid derivative
Oxacycle
Organoheterocyclic compound
Organooxygen compound
Carbonyl group
Organic oxide
Organic oxygen compound
Alcohol
Hydrocarbon derivative
Aliphatic heteropolycyclic compound

Molecular Framework

Aliphatic heteropolycyclic compounds

External Descriptors

kaurane diterpenoid (CHEBI:70366 )

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

26375671

KEGG Compound ID

Not Available

BioCyc ID

Not Available

BiGG ID

Not Available

Wikipedia Link

Not Available

METLIN ID

Not Available

PubChem Compound

50901151

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

LOTUS database [Link]

Showing NP-Card for maoesin d (NP0306264)

MOL for NP0306264 (maoesin d)

3D MOL for NP0306264 (maoesin d)

3D SDF for NP0306264 (maoesin d)

3D-SDF for NP0306264 (maoesin d)

PDB for NP0306264 (maoesin d)

3D PDB for NP0306264 (maoesin d)

SMILES for NP0306264 (maoesin d)

INCHI for NP0306264 (maoesin d)

Structure for NP0306264 (maoesin d)

3D Structure for NP0306264 (maoesin d)