NP-MRD: Showing NP-Card for Leoheteronone E (NP0072201)

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Record Information

Version

2.0

Created at

2022-04-28 17:34:22 UTC

Updated at

2022-04-28 17:34:22 UTC

NP-MRD ID

NP0072201

Secondary Accession Numbers

None

Natural Product Identification

Common Name

Leoheteronone E

Description

Leoheteronone E belongs to the class of organic compounds known as diterpenoids. These are terpene compounds formed by four isoprene units. Leoheteronone E is found in Leonurus heterophyllus SW. and Leonurus japonicus. Based on a literature review very few articles have been published on Leoheteronone E.

Structure

MOL 3D MOL SDF PDB SMILES InChI


  Mrv1652304282219342D          

 28 31  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
    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
   -0.2481    5.8345    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.0193    5.6395    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  2  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
    1.0990    2.0353    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
    3.2450    3.7575    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
  8 12  1  1  0  0  0
 12 13  1  0  0  0  0
 13 14  2  0  0  0  0
 13 15  1  0  0  0  0
  8 16  1  6  0  0  0
  7 17  1  0  0  0  0
 17 18  1  0  0  0  0
 18 19  1  0  0  0  0
 19 20  1  1  0  0  0
  7 20  1  6  0  0  0
 19 21  1  0  0  0  0
 21 22  1  0  0  0  0
 22 23  1  0  0  0  0
 23 24  1  0  0  0  0
 19 24  1  0  0  0  0
 22 25  1  6  0  0  0
  5 26  1  1  0  0  0
  3 27  1  0  0  0  0
  3 28  1  0  0  0  0
M  END

     RDKit          3D

 62 65  0  0  0  0  0  0  0  0999 V2000
   -0.2358    4.9350    0.9808 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2666    3.8417   -0.0383 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0577    4.1917   -1.2394 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5090    2.5164    0.2997 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5295    1.4940   -0.7140 C   0  0  1  0  0  0  0  0  0  0  0  0
   -1.6033    1.8573   -1.6738 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7678    1.6677   -1.4267 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.8675    2.1126   -2.5582 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.0359    1.2858   -0.7474 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.7592   -0.1381   -0.3004 C   0  0  1  0  0  0  0  0  0  0  0  0
    3.0329   -0.7544    0.0861 C   0  0  1  0  0  0  0  0  0  0  0  0
    3.9049   -0.8202   -1.1803 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.8363    0.0010    1.1009 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.9121   -2.1840    0.5685 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.8451   -2.2113    1.6089 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.5382   -1.6587    1.1175 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.6407   -0.2130    0.6833 C   0  0  1  0  0  0  0  0  0  0  0  0
    0.8641    0.6065    1.9262 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6736    0.1929   -0.0051 C   0  0  1  0  0  0  0  0  0  0  0  0
   -1.7161    0.4132    1.0938 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.9757   -0.0719    0.4070 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4204   -1.1897   -0.3996 C   0  0  1  0  0  0  0  0  0  0  0  0
   -2.6881   -2.4583    0.3542 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5178   -3.4189   -0.6304 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.4948   -3.0107   -1.5518 C   0  0  1  0  0  0  0  0  0  0  0  0
   -4.7442   -3.2577   -0.9400 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.2797   -1.5134   -1.6365 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1496   -0.8742   -0.6930 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7802    5.8298    0.5745 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.8072    5.1778    1.1849 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8031    4.5671    1.8619 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0802    1.0370   -2.2049 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3842    2.5290   -1.2020 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2109    2.5237   -2.5082 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.8858    1.2414   -1.4385 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.2802    1.9713    0.0572 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.3917   -0.6643   -1.2320 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.4769   -1.7580   -1.2277 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.2695   -0.7611   -2.0888 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.6211    0.0327   -1.2071 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.5539   -0.2328    2.1543 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.8971   -0.3800    1.0099 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.9076    1.0849    0.9072 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.7188   -2.8921   -0.2622 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.8832   -2.4323    1.0860 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.6609   -3.2760    1.8774 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.2112   -1.7221    2.5256 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1334   -1.6560    2.0183 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.1966   -2.2883    0.2979 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0281    1.2342    2.1928 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.7141    1.2839    1.8873 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.0212   -0.0361    2.8418 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5639   -0.2138    1.9693 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8558    1.4843    1.3126 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5059    0.6941   -0.1529 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.6794   -0.4264    1.2063 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1890   -2.6185    1.2818 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.7992   -2.4517    0.5744 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.4016   -3.5099   -2.5224 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.2718   -2.4135   -0.8608 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.2385   -0.9781   -1.5891 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7143   -1.3216   -2.5709 H   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0
  2  3  2  0
  2  4  1  0
  5  4  1  1
  5  6  1  0
  5  7  1  0
  7  8  2  0
  7  9  1  0
  9 10  1  0
 10 11  1  0
 11 12  1  6
 11 13  1  0
 11 14  1  0
 14 15  1  0
 15 16  1  0
 16 17  1  0
 17 18  1  1
 17 19  1  0
 19 20  1  0
 20 21  1  0
 21 22  1  0
 22 23  1  0
 23 24  1  0
 24 25  1  0
 25 26  1  0
 25 27  1  0
 22 28  1  6
 19  5  1  0
 19 28  1  6
 17 10  1  0
 27 22  1  0
  1 29  1  0
  1 30  1  0
  1 31  1  0
  6 32  1  0
  6 33  1  0
  6 34  1  0
  9 35  1  0
  9 36  1  0
 10 37  1  6
 12 38  1  0
 12 39  1  0
 12 40  1  0
 13 41  1  0
 13 42  1  0
 13 43  1  0
 14 44  1  0
 14 45  1  0
 15 46  1  0
 15 47  1  0
 16 48  1  0
 16 49  1  0
 18 50  1  0
 18 51  1  0
 18 52  1  0
 20 53  1  0
 20 54  1  0
 21 55  1  0
 21 56  1  0
 23 57  1  0
 23 58  1  0
 25 59  1  6
 26 60  1  0
 27 61  1  0
 27 62  1  0
M  END


  Mrv1652304282219342D          

 28 31  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
    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
   -0.2481    5.8345    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.0193    5.6395    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  2  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
    1.0990    2.0353    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
    3.2450    3.7575    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
  8 12  1  1  0  0  0
 12 13  1  0  0  0  0
 13 14  2  0  0  0  0
 13 15  1  0  0  0  0
  8 16  1  6  0  0  0
  7 17  1  0  0  0  0
 17 18  1  0  0  0  0
 18 19  1  0  0  0  0
 19 20  1  1  0  0  0
  7 20  1  6  0  0  0
 19 21  1  0  0  0  0
 21 22  1  0  0  0  0
 22 23  1  0  0  0  0
 23 24  1  0  0  0  0
 19 24  1  0  0  0  0
 22 25  1  6  0  0  0
  5 26  1  1  0  0  0
  3 27  1  0  0  0  0
  3 28  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0072201

> <DATABASE_NAME>
NP-MRD

> <SMILES>
CC(=O)O[C@@]1(C)C(=O)C[C@H]2C(C)(C)CCC[C@]2(C)[C@@]11CC[C@]2(CO[C@@H](O)C2)O1

> <INCHI_IDENTIFIER>
InChI=1S/C22H34O6/c1-14(23)27-20(5)16(24)11-15-18(2,3)7-6-8-19(15,4)22(20)10-9-21(28-22)12-17(25)26-13-21/h15,17,25H,6-13H2,1-5H3/t15-,17+,19-,20-,21-,22-/m0/s1

> <INCHI_KEY>
PYWYXDQVIHVOOS-VLIPQZQPSA-N

> <FORMULA>
C22H34O6

> <MOLECULAR_WEIGHT>
394.508

> <EXACT_MASS>
394.235538815

> <JCHEM_ACCEPTOR_COUNT>
5

> <JCHEM_ATOM_COUNT>
62

> <JCHEM_AVERAGE_POLARIZABILITY>
42.39608837895546

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
1

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
1

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

> <ALOGPS_LOGP>
2.20

> <JCHEM_LOGP>
3.102393645

> <ALOGPS_LOGS>
-4.57

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
4

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA>
18.037516690560263

> <JCHEM_PKA_STRONGEST_ACIDIC>
12.375611381468211

> <JCHEM_PKA_STRONGEST_BASIC>
-3.946707167974954

> <JCHEM_POLAR_SURFACE_AREA>
82.06000000000002

> <JCHEM_REFRACTIVITY>
101.10549999999999

> <JCHEM_ROTATABLE_BOND_COUNT>
2

> <JCHEM_RULE_OF_FIVE>
1

> <ALOGPS_SOLUBILITY>
1.07e-02 g/l

> <JCHEM_TRADITIONAL_IUPAC>
(1S,2R,4aS,5'S,5''R,8aS)-5''-hydroxy-2,5,5,8a-tetramethyl-3-oxo-tetrahydro-4H-dispiro[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  O   UNK     0       0.103   8.285   0.000  0.00  0.00           O+0
HETATM   13  C   UNK     0       0.572   9.751   0.000  0.00  0.00           C+0
HETATM   14  O   UNK     0      -0.463  10.891   0.000  0.00  0.00           O+0
HETATM   15  C   UNK     0       1.903  10.527   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0      -0.386   6.924   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0       1.527   4.093   0.000  0.00  0.00           C+0
HETATM   18  C   UNK     0       0.101   3.510   0.000  0.00  0.00           C+0
HETATM   19  C   UNK     0      -0.894   4.686   0.000  0.00  0.00           C+0
HETATM   20  O   UNK     0      -0.083   5.995   0.000  0.00  0.00           O+0
HETATM   21  C   UNK     0      -1.704   3.376   0.000  0.00  0.00           C+0
HETATM   22  C   UNK     0      -3.200   3.742   0.000  0.00  0.00           C+0
HETATM   23  O   UNK     0      -3.314   5.278   0.000  0.00  0.00           O+0
HETATM   24  C   UNK     0      -1.889   5.861   0.000  0.00  0.00           C+0
HETATM   25  O   UNK     0      -4.375   2.747   0.000  0.00  0.00           O+0
HETATM   26  C   UNK     0       2.052   3.799   0.000  0.00  0.00           C+0
HETATM   27  C   UNK     0       6.992   5.910   0.000  0.00  0.00           C+0
HETATM   28  C   UNK     0       6.057   7.014   0.000  0.00  0.00           C+0
CONECT    1    2    6                                                       
CONECT    2    1    3                                                       
CONECT    3    2    4   27   28                                             
CONECT    4    3    5   11                                                  
CONECT    5    4    6    7   26                                             
CONECT    6    5    1                                                       
CONECT    7    5    8   17   20                                             
CONECT    8    7    9   12   16                                             
CONECT    9    8   10   11                                                  
CONECT   10    9                                                            
CONECT   11    9    4                                                       
CONECT   12    8   13                                                       
CONECT   13   12   14   15                                                  
CONECT   14   13                                                            
CONECT   15   13                                                            
CONECT   16    8                                                            
CONECT   17    7   18                                                       
CONECT   18   17   19                                                       
CONECT   19   18   20   21   24                                             
CONECT   20   19    7                                                       
CONECT   21   19   22                                                       
CONECT   22   21   23   25                                                  
CONECT   23   22   24                                                       
CONECT   24   23   19                                                       
CONECT   25   22                                                            
CONECT   26    5                                                            
CONECT   27    3                                                            
CONECT   28    3                                                            
MASTER        0    0    0    0    0    0    0    0   28    0   62    0
END

View in JSmol

Synonyms

Not Available

Chemical Formula

C₂₂H₃₄O₆

Average Mass

394.5080 Da

Monoisotopic Mass

394.23554 Da

IUPAC Name

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

Traditional Name

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

CAS Registry Number

Not Available

SMILES

CC(=O)O[C@@]1(C)C(=O)C[C@H]2C(C)(C)CCC[C@]2(C)[C@@]11CC[C@]2(CO[C@@H](O)C2)O1

InChI Identifier

InChI=1S/C22H34O6/c1-14(23)27-20(5)16(24)11-15-18(2,3)7-6-8-19(15,4)22(20)10-9-21(28-22)12-17(25)26-13-21/h15,17,25H,6-13H2,1-5H3/t15-,17+,19-,20-,21-,22-/m0/s1

InChI Key

PYWYXDQVIHVOOS-VLIPQZQPSA-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 heterophyllus Sw.	Plant	KNApSAcK
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

Diterpenoid
Grindelane diterpenoid
Alpha-acyloxy ketone
Tetrahydrofuran
Carboxylic acid ester
Hemiacetal
Ketone
Cyclic ketone
Carboxylic acid derivative
Dialkyl ether
Ether
Oxacycle
Organoheterocyclic compound
Monocarboxylic acid or derivatives
Hydrocarbon derivative
Organic oxygen compound
Carbonyl group
Organic oxide
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
logP	2.2	ALOGPS
logP	3.1	ChemAxon
logS	-4.6	ALOGPS
pKa (Strongest Acidic)	12.38	ChemAxon
pKa (Strongest Basic)	-3.9	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	5	ChemAxon
Hydrogen Donor Count	1	ChemAxon
Polar Surface Area	82.06 Å²	ChemAxon
Rotatable Bond Count	2	ChemAxon
Refractivity	101.11 m³·mol⁻¹	ChemAxon
Polarizability	42.4 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

C00031509

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

101774202

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

Not Available

Showing NP-Card for Leoheteronone E (NP0072201)

MOL for NP0072201 (Leoheteronone E)

3D MOL for NP0072201 (Leoheteronone E)

3D SDF for NP0072201 (Leoheteronone E)

3D-SDF for NP0072201 (Leoheteronone E)

PDB for NP0072201 (Leoheteronone E)

3D PDB for NP0072201 (Leoheteronone E)

SMILES for NP0072201 (Leoheteronone E)

INCHI for NP0072201 (Leoheteronone E)

Structure for NP0072201 (Leoheteronone E)

3D Structure for NP0072201 (Leoheteronone E)