NP-MRD: Showing NP-Card for (-)-Leoheteronone A (NP0072200)

Jump To Section:

Identification Spectra BioTaxonomy ChemoTaxonomy Physical properties Links References XML

Record Information

Version

2.0

Created at

2022-04-28 17:34:19 UTC

Updated at

2022-04-28 17:34:19 UTC

NP-MRD ID

NP0072200

Secondary Accession Numbers

None

Natural Product Identification

Common Name

(-)-Leoheteronone A

Description

(1S,2R,4aS,5'R,5''R,8aS)-5''-methoxy-2,5,5,8a-tetramethyl-4-methylidene-3-oxo-octahydro-2H-dispiro[naphthalene-1,2':5',3''-Bis(oxolane)]-2-yl acetate belongs to the class of organic compounds known as diterpenoids. These are terpene compounds formed by four isoprene units. (-)-Leoheteronone A is found in Leonurus japonicus. Based on a literature review very few articles have been published on (1S,2R,4aS,5'R,5''R,8aS)-5''-methoxy-2,5,5,8a-tetramethyl-4-methylidene-3-oxo-octahydro-2H-dispiro[naphthalene-1,2':5',3''-Bis(oxolane)]-2-yl acetate.

Structure

MOL 3D MOL SDF PDB SMILES InChI


  Mrv1652304282219342D          

 30 33  0  0  1  0            999 V2000
    2.4565    1.6463    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.0861    2.1794    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.9393    2.9912    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1628    3.2700    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    1.5332    2.7369    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    1.6800    1.9251    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7567    3.0156    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    0.6098    3.8275    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    1.2395    4.3605    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.0927    5.1724    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.0160    4.0818    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.6456    4.6149    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0551    4.4381    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.3066    5.2239    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.0193    5.6395    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2481    5.8345    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2066    3.7091    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.8178    2.1929    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0543    1.8805    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4788    2.5102    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
   -0.0447    3.2117    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9129    1.8086    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7143    2.0047    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
   -1.7754    2.8274    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0119    3.1398    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3439    1.4716    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.1204    1.7504    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.0990    2.0353    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.2450    3.7575    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.7455    3.1663    0.0000 C   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
  1  6  1  0  0  0  0
  5  7  1  0  0  0  0
  7  8  1  0  0  0  0
  8  9  1  0  0  0  0
  9 10  2  0  0  0  0
  9 11  1  0  0  0  0
  4 11  1  1  0  0  0
 11 12  2  0  0  0  0
  8 13  1  1  0  0  0
 13 14  1  0  0  0  0
 14 15  2  0  0  0  0
 14 16  1  0  0  0  0
  8 17  1  6  0  0  0
  7 18  1  0  0  0  0
 18 19  1  0  0  0  0
 19 20  1  0  0  0  0
 20 21  1  6  0  0  0
  7 21  1  6  0  0  0
 20 22  1  0  0  0  0
 22 23  1  0  0  0  0
 23 24  1  0  0  0  0
 24 25  1  0  0  0  0
 20 25  1  0  0  0  0
 23 26  1  6  0  0  0
 26 27  1  0  0  0  0
  5 28  1  1  0  0  0
  3 29  1  0  0  0  0
  3 30  1  0  0  0  0
M  END

     RDKit          3D

 66 69  0  0  0  0  0  0  0  0999 V2000
   -3.9888    1.0854    0.4884 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7472    0.7249    0.6499 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8445    1.6829    1.2412 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2462    2.6375    1.9966 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3775    1.6449    1.0249 C   0  0  2  0  0  0  0  0  0  0  0  0
    0.2286    1.6151    2.4401 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0934    2.9685    0.5967 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5651    3.6073   -0.5105 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1493    5.0200   -0.8586 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3677    2.9903   -1.2524 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.1294    0.5614    0.1367 C   0  0  1  0  0  0  0  0  0  0  0  0
    1.0099    1.1749   -0.9014 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.2206    0.2911   -0.9633 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.3124   -0.0028    0.5184 C   0  0  2  0  0  0  0  0  0  0  0  0
    3.2135    1.0590    1.1104 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.5094    0.6342    0.9303 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.5341   -0.5963    0.3169 C   0  0  1  0  0  0  0  0  0  0  0  0
    5.5497   -1.4202    0.7976 O   0  0  0  0  0  0  0  0  0  0  0  0
    6.3541   -1.8780   -0.2716 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.2279   -1.2136    0.7546 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.0729   -0.1008    0.9911 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8181   -0.4694   -0.3646 C   0  0  1  0  0  0  0  0  0  0  0  0
   -1.0048   -0.4340   -1.8706 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2143   -1.8739   -0.1270 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1964   -2.9191    0.2133 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5186   -2.9217   -0.4156 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.1273   -1.5204   -0.2073 C   0  0  1  0  0  0  0  0  0  0  0  0
   -3.8892   -1.2186   -1.4315 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.1538   -1.7212    0.9300 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1405   -0.5625    0.3125 C   0  0  2  0  0  0  0  0  0  0  0  0
   -4.2879    2.0960    0.7951 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.8046    0.5132    0.0854 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.6293    0.6366    2.6889 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5390    1.9774    3.1658 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.0587    2.3493    2.5365 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0283    5.5293   -1.2765 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.7298    5.0247   -1.5072 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.0563    5.5099    0.1356 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.4039    2.1387   -0.5104 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.5804    1.4050   -1.8766 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.1386   -0.6480   -1.4825 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.1210    0.8238   -1.3354 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.0534    1.0895    2.2183 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.0946    2.0490    0.6475 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.5825   -0.4842   -0.7889 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.1471   -2.5273    0.1493 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.8581   -1.0381   -0.7820 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.6738   -2.4407   -0.9436 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.2520   -1.3814    1.8328 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.9256   -2.0714    0.1486 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5516    0.4570   -2.1984 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0389   -0.4116   -2.4202 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4240   -1.3921   -2.2432 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.4645   -1.8584    0.7694 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.3813   -2.2025   -1.0008 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7067   -3.9054   -0.0114 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3651   -2.9782    1.3321 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6071   -3.2733   -1.4545 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.1294   -3.7003    0.1403 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.7066   -1.9690   -2.2693 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.7967   -0.2435   -1.8895 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.9984   -1.3832   -1.2628 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.0286   -1.0086    1.7450 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.1868   -1.7830    0.5420 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.0044   -2.7312    1.4229 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8664   -1.0127    1.3434 H   0  0  0  0  0  0  0  0  0  0  0  0
 19 18  1  0
 18 17  1  0
 17 20  1  0
 20 14  1  0
 14 13  1  0
 13 12  1  0
 12 11  1  0
 11 21  1  1
 11 22  1  0
 22 23  1  6
 22 24  1  0
 24 25  1  0
 25 26  1  0
 26 27  1  0
 27 28  1  6
 27 29  1  0
 27 30  1  0
 30  2  1  0
  2  1  2  3
  2  3  1  0
  3  4  2  0
  3  5  1  0
  5  6  1  0
  5  7  1  6
  7  8  1  0
  8  9  1  0
  8 10  2  0
 14 15  1  0
 15 16  1  0
 16 17  1  0
 14 21  1  1
 30 22  1  0
  5 11  1  0
 19 46  1  0
 19 47  1  0
 19 48  1  0
 17 45  1  6
 20 49  1  0
 20 50  1  0
 13 41  1  0
 13 42  1  0
 12 39  1  0
 12 40  1  0
 23 51  1  0
 23 52  1  0
 23 53  1  0
 24 54  1  0
 24 55  1  0
 25 56  1  0
 25 57  1  0
 26 58  1  0
 26 59  1  0
 28 60  1  0
 28 61  1  0
 28 62  1  0
 29 63  1  0
 29 64  1  0
 29 65  1  0
 30 66  1  1
  1 31  1  0
  1 32  1  0
  6 33  1  0
  6 34  1  0
  6 35  1  0
  9 36  1  0
  9 37  1  0
  9 38  1  0
 15 43  1  0
 15 44  1  0
M  END


  Mrv1652304282219342D          

 30 33  0  0  1  0            999 V2000
    2.4565    1.6463    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.0861    2.1794    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.9393    2.9912    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1628    3.2700    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    1.5332    2.7369    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    1.6800    1.9251    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7567    3.0156    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    0.6098    3.8275    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    1.2395    4.3605    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.0927    5.1724    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.0160    4.0818    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.6456    4.6149    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0551    4.4381    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.3066    5.2239    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.0193    5.6395    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2481    5.8345    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2066    3.7091    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.8178    2.1929    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0543    1.8805    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4788    2.5102    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
   -0.0447    3.2117    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9129    1.8086    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7143    2.0047    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
   -1.7754    2.8274    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0119    3.1398    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3439    1.4716    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.1204    1.7504    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.0990    2.0353    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.2450    3.7575    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.7455    3.1663    0.0000 C   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
  1  6  1  0  0  0  0
  5  7  1  0  0  0  0
  7  8  1  0  0  0  0
  8  9  1  0  0  0  0
  9 10  2  0  0  0  0
  9 11  1  0  0  0  0
  4 11  1  1  0  0  0
 11 12  2  0  0  0  0
  8 13  1  1  0  0  0
 13 14  1  0  0  0  0
 14 15  2  0  0  0  0
 14 16  1  0  0  0  0
  8 17  1  6  0  0  0
  7 18  1  0  0  0  0
 18 19  1  0  0  0  0
 19 20  1  0  0  0  0
 20 21  1  6  0  0  0
  7 21  1  6  0  0  0
 20 22  1  0  0  0  0
 22 23  1  0  0  0  0
 23 24  1  0  0  0  0
 24 25  1  0  0  0  0
 20 25  1  0  0  0  0
 23 26  1  6  0  0  0
 26 27  1  0  0  0  0
  5 28  1  1  0  0  0
  3 29  1  0  0  0  0
  3 30  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0072200

> <DATABASE_NAME>
NP-MRD

> <SMILES>
CO[C@H]1C[C@]2(CC[C@]3(O2)[C@@]2(C)CCCC(C)(C)[C@@H]2C(=C)C(=O)[C@]3(C)OC(C)=O)CO1

> <INCHI_IDENTIFIER>
InChI=1S/C24H36O6/c1-15-18-20(3,4)9-8-10-21(18,5)24(22(6,19(15)26)29-16(2)25)12-11-23(30-24)13-17(27-7)28-14-23/h17-18H,1,8-14H2,2-7H3/t17-,18+,21+,22+,23-,24+/m1/s1

> <INCHI_KEY>
MMHWBOSXIUOOSO-BDADTYDISA-N

> <FORMULA>
C24H36O6

> <MOLECULAR_WEIGHT>
420.546

> <EXACT_MASS>
420.251188879

> <JCHEM_ACCEPTOR_COUNT>
5

> <JCHEM_ATOM_COUNT>
66

> <JCHEM_AVERAGE_POLARIZABILITY>
46.063775471551544

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
0

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
1

> <JCHEM_IUPAC>
(1S,2R,4aS,5'R,5''R,8aS)-5''-methoxy-2,5,5,8a-tetramethyl-4-methylidene-3-oxo-octahydro-2H-dispiro[naphthalene-1,2':5',3''-bis(oxolane)]-2-yl acetate

> <ALOGPS_LOGP>
3.35

> <JCHEM_LOGP>
4.196827798000001

> <ALOGPS_LOGS>
-5.25

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
4

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA_STRONGEST_BASIC>
-3.8142012110344585

> <JCHEM_POLAR_SURFACE_AREA>
71.06000000000002

> <JCHEM_REFRACTIVITY>
110.23460000000001

> <JCHEM_ROTATABLE_BOND_COUNT>
3

> <JCHEM_RULE_OF_FIVE>
1

> <ALOGPS_SOLUBILITY>
2.39e-03 g/l

> <JCHEM_TRADITIONAL_IUPAC>
(1S,2R,4aS,5'R,5''R,8aS)-5''-methoxy-2,5,5,8a-tetramethyl-4-methylidene-3-oxo-tetrahydrodispiro[naphthalene-1,2':5',3''-bis(oxolane)]-2-yl acetate

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 28-APR-22   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   28-APR-22         0                                  
HETATM    1  C   UNK     0       4.585   3.073   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0       5.761   4.068   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0       5.487   5.584   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0       4.037   6.104   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0       2.862   5.109   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0       3.136   3.593   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0       1.412   5.629   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0       1.138   7.145   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0       2.314   8.140   0.000  0.00  0.00           C+0
HETATM   10  O   UNK     0       2.040   9.655   0.000  0.00  0.00           O+0
HETATM   11  C   UNK     0       3.763   7.619   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0       4.939   8.614   0.000  0.00  0.00           C+0
HETATM   13  O   UNK     0       0.103   8.285   0.000  0.00  0.00           O+0
HETATM   14  C   UNK     0       0.572   9.751   0.000  0.00  0.00           C+0
HETATM   15  O   UNK     0       1.903  10.527   0.000  0.00  0.00           O+0
HETATM   16  C   UNK     0      -0.463  10.891   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0      -0.386   6.924   0.000  0.00  0.00           C+0
HETATM   18  C   UNK     0       1.527   4.093   0.000  0.00  0.00           C+0
HETATM   19  C   UNK     0       0.101   3.510   0.000  0.00  0.00           C+0
HETATM   20  C   UNK     0      -0.894   4.686   0.000  0.00  0.00           C+0
HETATM   21  O   UNK     0      -0.083   5.995   0.000  0.00  0.00           O+0
HETATM   22  C   UNK     0      -1.704   3.376   0.000  0.00  0.00           C+0
HETATM   23  C   UNK     0      -3.200   3.742   0.000  0.00  0.00           C+0
HETATM   24  O   UNK     0      -3.314   5.278   0.000  0.00  0.00           O+0
HETATM   25  C   UNK     0      -1.889   5.861   0.000  0.00  0.00           C+0
HETATM   26  O   UNK     0      -4.375   2.747   0.000  0.00  0.00           O+0
HETATM   27  C   UNK     0      -5.825   3.267   0.000  0.00  0.00           C+0
HETATM   28  C   UNK     0       2.052   3.799   0.000  0.00  0.00           C+0
HETATM   29  C   UNK     0       6.057   7.014   0.000  0.00  0.00           C+0
HETATM   30  C   UNK     0       6.992   5.910   0.000  0.00  0.00           C+0
CONECT    1    2    6                                                       
CONECT    2    1    3                                                       
CONECT    3    2    4   29   30                                             
CONECT    4    3    5   11                                                  
CONECT    5    4    6    7   28                                             
CONECT    6    5    1                                                       
CONECT    7    5    8   18   21                                             
CONECT    8    7    9   13   17                                             
CONECT    9    8   10   11                                                  
CONECT   10    9                                                            
CONECT   11    9    4   12                                                  
CONECT   12   11                                                            
CONECT   13    8   14                                                       
CONECT   14   13   15   16                                                  
CONECT   15   14                                                            
CONECT   16   14                                                            
CONECT   17    8                                                            
CONECT   18    7   19                                                       
CONECT   19   18   20                                                       
CONECT   20   19   21   22   25                                             
CONECT   21   20    7                                                       
CONECT   22   20   23                                                       
CONECT   23   22   24   26                                                  
CONECT   24   23   25                                                       
CONECT   25   24   20                                                       
CONECT   26   23   27                                                       
CONECT   27   26                                                            
CONECT   28    5                                                            
CONECT   29    3                                                            
CONECT   30    3                                                            
MASTER        0    0    0    0    0    0    0    0   30    0   66    0
END

View in JSmol

Synonyms

Value	Source
(1S,2R,4AS,5'r,5''r,8as)-5''-methoxy-2,5,5,8a-tetramethyl-4-methylidene-3-oxo-octahydro-2H-dispiro[naphthalene-1,2':5',3''-bis(oxolane)]-2-yl acetic acid	Generator

Chemical Formula

C₂₄H₃₆O₆

Average Mass

420.5460 Da

Monoisotopic Mass

420.25119 Da

IUPAC Name

(1S,2R,4aS,5'R,5''R,8aS)-5''-methoxy-2,5,5,8a-tetramethyl-4-methylidene-3-oxo-octahydro-2H-dispiro[naphthalene-1,2':5',3''-bis(oxolane)]-2-yl acetate

Traditional Name

(1S,2R,4aS,5'R,5''R,8aS)-5''-methoxy-2,5,5,8a-tetramethyl-4-methylidene-3-oxo-tetrahydrodispiro[naphthalene-1,2':5',3''-bis(oxolane)]-2-yl acetate

CAS Registry Number

Not Available

SMILES

CO[C@H]1C[C@]2(CC[C@]3(O2)[C@@]2(C)CCCC(C)(C)[C@@H]2C(=C)C(=O)[C@]3(C)OC(C)=O)CO1

InChI Identifier

InChI=1S/C24H36O6/c1-15-18-20(3,4)9-8-10-21(18,5)24(22(6,19(15)26)29-16(2)25)12-11-23(30-24)13-17(27-7)28-14-23/h17-18H,1,8-14H2,2-7H3/t17-,18+,21+,22+,23-,24+/m1/s1

InChI Key

MMHWBOSXIUOOSO-BDADTYDISA-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, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 100 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 252 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 1000 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 50 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 200 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 75 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 300 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 101 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 400 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 126 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 500 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 151 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 600 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 176 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 700 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 201 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 800 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 226 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 900 MHz, D₂O, 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
Leonurus japonicus	LOTUS Database	35616633

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as diterpenoids. These are terpene compounds formed by four isoprene units.

Kingdom

Organic compounds

Super Class

Lipids and lipid-like molecules

Class

Prenol lipids

Sub Class

Diterpenoids

Direct Parent

Diterpenoids

Alternative Parents

Substituents

Grindelane diterpenoid
Diterpenoid
Alpha-acyloxy ketone
Tetrahydrofuran
Cyclic ketone
Ketone
Carboxylic acid ester
Oxacycle
Organoheterocyclic compound
Monocarboxylic acid or derivatives
Ether
Dialkyl ether
Carboxylic acid derivative
Acetal
Organic oxygen compound
Organic oxide
Hydrocarbon derivative
Organooxygen compound
Carbonyl group
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	3.35	ALOGPS
logP	4.2	ChemAxon
logS	-5.2	ALOGPS
pKa (Strongest Basic)	-3.8	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	5	ChemAxon
Hydrogen Donor Count	0	ChemAxon
Polar Surface Area	71.06 Å²	ChemAxon
Rotatable Bond Count	3	ChemAxon
Refractivity	110.23 m³·mol⁻¹	ChemAxon
Polarizability	46.06 Å³	ChemAxon
Number of Rings	4	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

163105058

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

Not Available

Showing NP-Card for (-)-Leoheteronone A (NP0072200)

MOL for NP0072200 ((-)-Leoheteronone A)

3D MOL for NP0072200 ((-)-Leoheteronone A)

3D SDF for NP0072200 ((-)-Leoheteronone A)

3D-SDF for NP0072200 ((-)-Leoheteronone A)

PDB for NP0072200 ((-)-Leoheteronone A)

3D PDB for NP0072200 ((-)-Leoheteronone A)

SMILES for NP0072200 ((-)-Leoheteronone A)

INCHI for NP0072200 ((-)-Leoheteronone A)

Structure for NP0072200 ((-)-Leoheteronone A)

3D Structure for NP0072200 ((-)-Leoheteronone A)