NP-MRD: Showing NP-Card for (1r,2s,4as,5s,6s,8r,8ar)-5-[2-(furan-3-yl)ethyl]-2,4a,8-trihydroxy-8a-(hydroxymethyl)-5,6-dimethyl-tetrahydro-2h-spiro[naphthalene-1,2'-oxiran]-7-one (NP0301759)

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Record Information

Version

2.0

Created at

2022-09-10 14:55:04 UTC

Updated at

2022-09-10 14:55:04 UTC

NP-MRD ID

NP0301759

Secondary Accession Numbers

None

Natural Product Identification

Common Name

(1r,2s,4as,5s,6s,8r,8ar)-5-[2-(furan-3-yl)ethyl]-2,4a,8-trihydroxy-8a-(hydroxymethyl)-5,6-dimethyl-tetrahydro-2h-spiro[naphthalene-1,2'-oxiran]-7-one

Description

Teucrolivin C belongs to the class of organic compounds known as heteroaromatic compounds. Heteroaromatic compounds are compounds containing an aromatic ring where a carbon atom is linked to an hetero atom. (1r,2s,4as,5s,6s,8r,8ar)-5-[2-(furan-3-yl)ethyl]-2,4a,8-trihydroxy-8a-(hydroxymethyl)-5,6-dimethyl-tetrahydro-2h-spiro[naphthalene-1,2'-oxiran]-7-one is found in Teucrium oliverianum and Teucrium orientale. Based on a literature review very few articles have been published on Teucrolivin C.

Structure

MOL 3D MOL SDF PDB SMILES InChI


  Mrv1652309102216552D          

 27 30  0  0  1  0            999 V2000
    5.3861    0.1140    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.5801   -0.0621    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    4.0246    0.5479    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.2751    1.3339    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.2186    0.3718    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    2.6632    0.9818    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.9681   -0.4142    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    2.4127    0.1957    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.6571    0.5270    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.5236   -1.0242    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    4.0791   -1.6342    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.2731   -1.8103    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.4671   -1.9863    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.9116   -1.3764    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    1.1057   -1.5525    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.1622   -0.5903    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    1.3761   -0.3398    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.9861    0.2157    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.3296   -0.8481    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    4.5337   -1.6475    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.1064   -1.1259    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.2543   -1.9376    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.6253   -2.4714    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.6875   -3.2941    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.9243   -3.6074    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.3905   -2.9784    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.8237   -2.2764    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
  2  1  1  1  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  1  0  0  0
  5  7  1  0  0  0  0
  7  8  1  1  0  0  0
  8  9  1  0  0  0  0
  7 10  1  0  0  0  0
 10 11  1  6  0  0  0
 10 12  1  0  0  0  0
 12 13  1  0  0  0  0
 13 14  1  0  0  0  0
 14 15  1  6  0  0  0
 14 16  1  0  0  0  0
  7 16  1  0  0  0  0
 16 17  1  0  0  0  0
 17 18  1  0  0  0  0
 16 18  1  1  0  0  0
 10 19  1  0  0  0  0
  2 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
 24 25  2  0  0  0  0
 25 26  1  0  0  0  0
 26 27  1  0  0  0  0
 23 27  2  0  0  0  0
M  END

     RDKit          3D

 55 58  0  0  0  0  0  0  0  0999 V2000
   -0.0680    3.0760   -0.9788 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.6073    1.7218   -0.9431 C   0  0  2  0  0  0  0  0  0  0  0  0
    0.3302    0.9340   -2.1941 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.5488    1.4460   -3.2764 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2030   -0.4537   -2.1692 C   0  0  2  0  0  0  0  0  0  0  0  0
   -0.7562   -0.7412   -3.3980 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2911   -0.4406   -1.1333 C   0  0  2  0  0  0  0  0  0  0  0  0
   -2.4253    0.3761   -1.7108 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8136   -0.2994   -2.8971 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8384   -0.0125    0.2162 C   0  0  2  0  0  0  0  0  0  0  0  0
   -0.4189   -1.1760    0.9045 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0653    0.4198    0.9899 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.9605   -0.7795    1.1064 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.1016   -1.6592   -0.0580 C   0  0  2  0  0  0  0  0  0  0  0  0
   -3.4108   -2.9604    0.4218 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9066   -1.8330   -0.9357 C   0  0  2  0  0  0  0  0  0  0  0  0
   -1.0246   -2.9992   -0.7735 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8827   -2.7429   -1.9395 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.3160    0.9370    0.2780 C   0  0  2  0  0  0  0  0  0  0  0  0
    0.0623    1.9256    1.4416 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.5706    0.2143    0.7026 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.7393    1.0748    1.0477 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.8315    0.1424    1.4502 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.0895   -0.3256    2.7172 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.1933   -1.1666    2.6412 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.5573   -1.1858    1.3943 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.7824   -0.4245    0.6386 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0780    3.0566   -0.5256 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2160    3.3315   -2.0493 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.5216    3.8727   -0.5153 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.6854    1.9559   -1.0152 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.5802   -1.2063   -1.9686 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0610   -0.6669   -4.0975 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.3162    0.4397   -1.0968 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1042    1.3734   -2.0877 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.7691   -0.0917   -3.0757 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5389   -0.9919    1.8682 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7233    0.6432    2.0239 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5417    1.3167    0.6060 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6708   -1.3882    2.0126 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.9823   -0.3821    1.3777 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.0313   -1.4022   -0.6497 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.0175   -3.0513    1.3429 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.0434   -2.9015   -0.9691 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4149   -3.8204   -0.1281 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.1394    1.3490    2.3819 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.8404    2.7218    1.3988 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9162    2.3890    1.3978 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.9350   -0.4536   -0.1388 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.3950   -0.4568    1.5710 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.1322    1.6503    0.2046 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.5641    1.7131    1.9428 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.5497   -0.1012    3.6389 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.6680   -1.7039    3.4400 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.8652   -0.2624   -0.4328 H   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0
  2  3  1  0
  3  4  2  0
  3  5  1  0
  5  6  1  0
  5  7  1  0
  7  8  1  6
  8  9  1  0
  7 16  1  0
 16 17  1  0
 17 18  1  0
 16 14  1  0
 14 15  1  0
 14 13  1  0
 13 12  1  0
 12 10  1  0
 10 11  1  1
 10 19  1  0
 19 20  1  1
 19 21  1  0
 21 22  1  0
 22 23  1  0
 23 27  2  0
 27 26  1  0
 26 25  1  0
 25 24  2  0
 19  2  1  0
 24 23  1  0
 10  7  1  0
 16 18  1  6
  1 28  1  0
  1 29  1  0
  1 30  1  0
  2 31  1  1
  5 32  1  1
  6 33  1  0
  8 34  1  0
  8 35  1  0
  9 36  1  0
 17 44  1  0
 17 45  1  0
 14 42  1  6
 15 43  1  0
 13 40  1  0
 13 41  1  0
 12 38  1  0
 12 39  1  0
 11 37  1  0
 20 46  1  0
 20 47  1  0
 20 48  1  0
 21 49  1  0
 21 50  1  0
 22 51  1  0
 22 52  1  0
 27 55  1  0
 25 54  1  0
 24 53  1  0
M  END


  Mrv1652309102216552D          

 27 30  0  0  1  0            999 V2000
    5.3861    0.1140    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.5801   -0.0621    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    4.0246    0.5479    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.2751    1.3339    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.2186    0.3718    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    2.6632    0.9818    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.9681   -0.4142    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    2.4127    0.1957    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.6571    0.5270    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.5236   -1.0242    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    4.0791   -1.6342    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.2731   -1.8103    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.4671   -1.9863    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.9116   -1.3764    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    1.1057   -1.5525    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.1622   -0.5903    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    1.3761   -0.3398    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.9861    0.2157    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.3296   -0.8481    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    4.5337   -1.6475    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.1064   -1.1259    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.2543   -1.9376    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.6253   -2.4714    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.6875   -3.2941    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.9243   -3.6074    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.3905   -2.9784    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.8237   -2.2764    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
  2  1  1  1  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  1  0  0  0
  5  7  1  0  0  0  0
  7  8  1  1  0  0  0
  8  9  1  0  0  0  0
  7 10  1  0  0  0  0
 10 11  1  6  0  0  0
 10 12  1  0  0  0  0
 12 13  1  0  0  0  0
 13 14  1  0  0  0  0
 14 15  1  6  0  0  0
 14 16  1  0  0  0  0
  7 16  1  0  0  0  0
 16 17  1  0  0  0  0
 17 18  1  0  0  0  0
 16 18  1  1  0  0  0
 10 19  1  0  0  0  0
  2 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
 24 25  2  0  0  0  0
 25 26  1  0  0  0  0
 26 27  1  0  0  0  0
 23 27  2  0  0  0  0
M  END
> <DATABASE_ID>
NP0301759

> <DATABASE_NAME>
NP-MRD

> <SMILES>
C[C@@H]1C(=O)[C@H](O)[C@@]2(CO)[C@@]3(CO3)[C@@H](O)CC[C@]2(O)[C@@]1(C)CCC1=COC=C1

> <INCHI_IDENTIFIER>
InChI=1S/C20H28O7/c1-12-15(23)16(24)18(10-21)19(11-27-19)14(22)4-7-20(18,25)17(12,2)6-3-13-5-8-26-9-13/h5,8-9,12,14,16,21-22,24-25H,3-4,6-7,10-11H2,1-2H3/t12-,14+,16+,17+,18+,19-,20+/m1/s1

> <INCHI_KEY>
PJRUENLEOUUHSU-UURCZBSZSA-N

> <FORMULA>
C20H28O7

> <MOLECULAR_WEIGHT>
380.437

> <EXACT_MASS>
380.183503242

> <JCHEM_ACCEPTOR_COUNT>
6

> <JCHEM_ATOM_COUNT>
55

> <JCHEM_AVERAGE_POLARIZABILITY>
39.19951992118655

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
4

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
1

> <JCHEM_IUPAC>
(1R,2S,4aS,5S,6S,8R,8aR)-5-[2-(furan-3-yl)ethyl]-2,4a,8-trihydroxy-8a-(hydroxymethyl)-5,6-dimethyl-octahydro-2H-spiro[naphthalene-1,2'-oxirane]-7-one

> <JCHEM_LOGP>
0.1712639999999997

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
4

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA>
14.050533691423155

> <JCHEM_PKA_STRONGEST_ACIDIC>
10.413938301476911

> <JCHEM_PKA_STRONGEST_BASIC>
-2.7688773424848354

> <JCHEM_POLAR_SURFACE_AREA>
123.66000000000001

> <JCHEM_REFRACTIVITY>
94.6639

> <JCHEM_ROTATABLE_BOND_COUNT>
4

> <JCHEM_RULE_OF_FIVE>
1

> <JCHEM_TRADITIONAL_IUPAC>
(1R,2S,4aS,5S,6S,8R,8aR)-5-[2-(furan-3-yl)ethyl]-2,4a,8-trihydroxy-8a-(hydroxymethyl)-5,6-dimethyl-tetrahydro-2H-spiro[naphthalene-1,2'-oxirane]-7-one

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 10-SEP-22   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   10-SEP-22         0                                  
HETATM    1  C   UNK     0      10.054   0.213   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0       8.550  -0.116   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0       7.513   1.023   0.000  0.00  0.00           C+0
HETATM    4  O   UNK     0       7.980   2.490   0.000  0.00  0.00           O+0
HETATM    5  C   UNK     0       6.008   0.694   0.000  0.00  0.00           C+0
HETATM    6  O   UNK     0       4.971   1.833   0.000  0.00  0.00           O+0
HETATM    7  C   UNK     0       5.541  -0.773   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0       4.504   0.365   0.000  0.00  0.00           C+0
HETATM    9  O   UNK     0       3.093   0.984   0.000  0.00  0.00           O+0
HETATM   10  C   UNK     0       6.577  -1.912   0.000  0.00  0.00           C+0
HETATM   11  O   UNK     0       7.614  -3.050   0.000  0.00  0.00           O+0
HETATM   12  C   UNK     0       6.110  -3.379   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0       4.605  -3.708   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0       3.568  -2.569   0.000  0.00  0.00           C+0
HETATM   15  O   UNK     0       2.064  -2.898   0.000  0.00  0.00           O+0
HETATM   16  C   UNK     0       4.036  -1.102   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0       2.569  -0.634   0.000  0.00  0.00           C+0
HETATM   18  O   UNK     0       3.707   0.403   0.000  0.00  0.00           O+0
HETATM   19  C   UNK     0       8.082  -1.583   0.000  0.00  0.00           C+0
HETATM   20  C   UNK     0       8.463  -3.075   0.000  0.00  0.00           C+0
HETATM   21  C   UNK     0       9.532  -2.102   0.000  0.00  0.00           C+0
HETATM   22  C   UNK     0       9.808  -3.617   0.000  0.00  0.00           C+0
HETATM   23  C   UNK     0       8.634  -4.613   0.000  0.00  0.00           C+0
HETATM   24  C   UNK     0       8.750  -6.149   0.000  0.00  0.00           C+0
HETATM   25  C   UNK     0       7.325  -6.734   0.000  0.00  0.00           C+0
HETATM   26  O   UNK     0       6.329  -5.560   0.000  0.00  0.00           O+0
HETATM   27  C   UNK     0       7.138  -4.249   0.000  0.00  0.00           C+0
CONECT    1    2                                                            
CONECT    2    1    3   19                                                  
CONECT    3    2    4    5                                                  
CONECT    4    3                                                            
CONECT    5    3    6    7                                                  
CONECT    6    5                                                            
CONECT    7    5    8   10   16                                             
CONECT    8    7    9                                                       
CONECT    9    8                                                            
CONECT   10    7   11   12   19                                             
CONECT   11   10                                                            
CONECT   12   10   13                                                       
CONECT   13   12   14                                                       
CONECT   14   13   15   16                                                  
CONECT   15   14                                                            
CONECT   16   14    7   17   18                                             
CONECT   17   16   18                                                       
CONECT   18   17   16                                                       
CONECT   19   10    2   20   21                                             
CONECT   20   19                                                            
CONECT   21   19   22                                                       
CONECT   22   21   23                                                       
CONECT   23   22   24   27                                                  
CONECT   24   23   25                                                       
CONECT   25   24   26                                                       
CONECT   26   25   27                                                       
CONECT   27   26   23                                                       
MASTER        0    0    0    0    0    0    0    0   27    0   60    0
END

View in JSmol

Synonyms

Not Available

Chemical Formula

C₂₀H₂₈O₇

Average Mass

380.4370 Da

Monoisotopic Mass

380.18350 Da

IUPAC Name

Not Available

Traditional Name

Not Available

CAS Registry Number

Not Available

SMILES

C[C@@H]1C(=O)[C@H](O)[C@@]2(CO)[C@@]3(CO3)[C@@H](O)CC[C@]2(O)[C@@]1(C)CCC1=COC=C1

InChI Identifier

InChI=1S/C20H28O7/c1-12-15(23)16(24)18(10-21)19(11-27-19)14(22)4-7-20(18,25)17(12,2)6-3-13-5-8-26-9-13/h5,8-9,12,14,16,21-22,24-25H,3-4,6-7,10-11H2,1-2H3/t12-,14+,16+,17+,18+,19-,20+/m1/s1

InChI Key

PJRUENLEOUUHSU-UURCZBSZSA-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
Teucrium oliverianum	LOTUS Database	35616633
Teucrium orientale	LOTUS Database	35616633

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as heteroaromatic compounds. Heteroaromatic compounds are compounds containing an aromatic ring where a carbon atom is linked to an hetero atom.

Kingdom

Organic compounds

Super Class

Organoheterocyclic compounds

Class

Heteroaromatic compounds

Sub Class

Not Available

Direct Parent

Heteroaromatic compounds

Alternative Parents

Substituents

Heteroaromatic compound
Tertiary alcohol
Furan
Cyclic alcohol
Cyclic ketone
Secondary alcohol
Ketone
Oxacycle
Polyol
Ether
Oxirane
Dialkyl ether
Organic oxygen compound
Organic oxide
Hydrocarbon derivative
Primary alcohol
Organooxygen compound
Carbonyl group
Alcohol
Aromatic heteropolycyclic compound

Molecular Framework

Aromatic 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

C00032313

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

101594600

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

LOTUS database [Link]

Showing NP-Card for (1r,2s,4as,5s,6s,8r,8ar)-5-[2-(furan-3-yl)ethyl]-2,4a,8-trihydroxy-8a-(hydroxymethyl)-5,6-dimethyl-tetrahydro-2h-spiro[naphthalene-1,2'-oxiran]-7-one (NP0301759)

MOL for NP0301759 ((1r,2s,4as,5s,6s,8r,8ar)-5-[2-(furan-3-yl)ethyl]-2,4a,8-trihydroxy-8a-(hydroxymethyl)-5,6-dimethyl-tetrahydro-2h-spiro[naphthalene-1,2'-oxiran]-7-one)

3D MOL for NP0301759 ((1r,2s,4as,5s,6s,8r,8ar)-5-[2-(furan-3-yl)ethyl]-2,4a,8-trihydroxy-8a-(hydroxymethyl)-5,6-dimethyl-tetrahydro-2h-spiro[naphthalene-1,2'-oxiran]-7-one)

3D SDF for NP0301759 ((1r,2s,4as,5s,6s,8r,8ar)-5-[2-(furan-3-yl)ethyl]-2,4a,8-trihydroxy-8a-(hydroxymethyl)-5,6-dimethyl-tetrahydro-2h-spiro[naphthalene-1,2'-oxiran]-7-one)

3D-SDF for NP0301759 ((1r,2s,4as,5s,6s,8r,8ar)-5-[2-(furan-3-yl)ethyl]-2,4a,8-trihydroxy-8a-(hydroxymethyl)-5,6-dimethyl-tetrahydro-2h-spiro[naphthalene-1,2'-oxiran]-7-one)

PDB for NP0301759 ((1r,2s,4as,5s,6s,8r,8ar)-5-[2-(furan-3-yl)ethyl]-2,4a,8-trihydroxy-8a-(hydroxymethyl)-5,6-dimethyl-tetrahydro-2h-spiro[naphthalene-1,2'-oxiran]-7-one)

3D PDB for NP0301759 ((1r,2s,4as,5s,6s,8r,8ar)-5-[2-(furan-3-yl)ethyl]-2,4a,8-trihydroxy-8a-(hydroxymethyl)-5,6-dimethyl-tetrahydro-2h-spiro[naphthalene-1,2'-oxiran]-7-one)

SMILES for NP0301759 ((1r,2s,4as,5s,6s,8r,8ar)-5-[2-(furan-3-yl)ethyl]-2,4a,8-trihydroxy-8a-(hydroxymethyl)-5,6-dimethyl-tetrahydro-2h-spiro[naphthalene-1,2'-oxiran]-7-one)

INCHI for NP0301759 ((1r,2s,4as,5s,6s,8r,8ar)-5-[2-(furan-3-yl)ethyl]-2,4a,8-trihydroxy-8a-(hydroxymethyl)-5,6-dimethyl-tetrahydro-2h-spiro[naphthalene-1,2'-oxiran]-7-one)

Structure for NP0301759 ((1r,2s,4as,5s,6s,8r,8ar)-5-[2-(furan-3-yl)ethyl]-2,4a,8-trihydroxy-8a-(hydroxymethyl)-5,6-dimethyl-tetrahydro-2h-spiro[naphthalene-1,2'-oxiran]-7-one)

3D Structure for NP0301759 ((1r,2s,4as,5s,6s,8r,8ar)-5-[2-(furan-3-yl)ethyl]-2,4a,8-trihydroxy-8a-(hydroxymethyl)-5,6-dimethyl-tetrahydro-2h-spiro[naphthalene-1,2'-oxiran]-7-one)