NP-MRD: Showing NP-Card for Luffarin R (NP0080271)

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Record Information

Version

2.0

Created at

2022-04-29 01:19:08 UTC

Updated at

2022-04-29 01:19:08 UTC

NP-MRD ID

NP0080271

Secondary Accession Numbers

None

Natural Product Identification

Common Name

Luffarin R

Description

4-[(1S,3E,7E)-1-hydroxy-4,8-dimethyl-11-[(3E,5R)-5-(2-methylprop-1-en-1-yl)-2-oxooxolan-3-ylidene]undeca-3,7-dien-1-yl]-2,5-dihydrofuran-2-one belongs to the class of organic compounds known as diterpene lactones. These are diterpenoids containing a lactone moiety. Luffarin R is found in Thorectandra sp. Based on a literature review very few articles have been published on 4-[(1S,3E,7E)-1-hydroxy-4,8-dimethyl-11-[(3E,5R)-5-(2-methylprop-1-en-1-yl)-2-oxooxolan-3-ylidene]undeca-3,7-dien-1-yl]-2,5-dihydrofuran-2-one.

Structure

MOL 3D MOL SDF PDB SMILES InChI


  Mrv1652304292203192D          

 30 31  0  0  1  0            999 V2000
   -0.8001   -8.9459    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0550   -9.7305    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
   -1.8800   -9.7305    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1350   -8.9459    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.9196   -8.6910    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5327   -9.2430    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.3173   -8.9881    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.9304   -9.5401    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.7150   -9.2851    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.3281   -9.8372    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -7.1127   -9.5822    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -7.7258  -10.1343    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -8.5105   -9.8793    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -9.1235  -10.4314    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -9.9082  -10.1764    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
  -10.0797   -9.3695    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
  -10.5213  -10.7285    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
  -10.4350  -11.5489    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
  -11.1887  -11.8845    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
  -11.3602  -12.6915    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
  -11.7407  -11.2714    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
  -11.3282  -10.5569    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -7.5543  -10.9412    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.7589  -10.3471    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4675   -8.4610    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4675   -7.6360    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5701  -10.3980    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9057  -11.1516    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4207  -11.8191    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7261  -11.2379    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  2  0  0  0  0
  5  6  1  0  0  0  0
  6  7  1  0  0  0  0
  7  8  1  0  0  0  0
  8  9  2  0  0  0  0
  9 10  1  0  0  0  0
 10 11  1  0  0  0  0
 11 12  1  0  0  0  0
 12 13  2  0  0  0  0
 13 14  1  0  0  0  0
 14 15  1  0  0  0  0
 15 16  1  1  0  0  0
 15 17  1  0  0  0  0
 17 18  2  0  0  0  0
 18 19  1  0  0  0  0
 19 20  2  0  0  0  0
 19 21  1  0  0  0  0
 21 22  1  0  0  0  0
 17 22  1  0  0  0  0
 12 23  1  0  0  0  0
  8 24  1  0  0  0  0
  4 25  1  0  0  0  0
  1 25  1  0  0  0  0
 25 26  2  0  0  0  0
  2 27  1  1  0  0  0
 27 28  2  0  0  0  0
 28 29  1  0  0  0  0
 28 30  1  0  0  0  0
M  END

     RDKit          3D

 64 65  0  0  0  0  0  0  0  0999 V2000
    7.2672    3.0849    1.2816 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.2960    1.5997    1.2946 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.5477    0.8103    1.4269 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.1512    0.9139    1.1850 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.1080   -0.5676    1.1906 C   0  0  1  0  0  0  0  0  0  0  0  0
    4.8006   -0.9726    0.4857 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.1999   -1.0511   -0.9196 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.4140   -1.1987   -1.9578 C   0  0  0  0  0  0  0  0  0  0  0  0
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    0.6867   -1.3631   -1.1392 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.2816   -2.6906   -1.6569 C   0  0  0  0  0  0  0  0  0  0  0  0
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   -4.2668   -2.0296   -1.0131 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.7884    0.2558   -0.3258 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.1955   -0.0242   -0.7419 C   0  0  0  0  0  0  0  0  0  0  0  0
   -7.1439    0.1480    0.4053 C   0  0  2  0  0  0  0  0  0  0  0  0
   -8.4299   -0.1649   -0.0868 O   0  0  0  0  0  0  0  0  0  0  0  0
   -7.2830    1.5865    0.8354 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.7990    2.6777    0.3104 C   0  0  0  0  0  0  0  0  0  0  0  0
   -7.2517    3.8039    1.1464 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.9704    5.0058    0.9324 O   0  0  0  0  0  0  0  0  0  0  0  0
   -8.0129    3.2992    2.1667 O   0  0  0  0  0  0  0  0  0  0  0  0
   -8.1221    1.9133    2.0355 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.6792   -0.9449   -0.9329 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.3705   -0.7079   -1.9489 O   0  0  0  0  0  0  0  0  0  0  0  0
    7.1088   -1.1599    0.3879 O   0  0  0  0  0  0  0  0  0  0  0  0
    7.2485    3.5168    2.2982 H   0  0  0  0  0  0  0  0  0  0  0  0
    8.1344    3.5196    0.7398 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.3542    3.4525    0.7630 H   0  0  0  0  0  0  0  0  0  0  0  0
    8.8352    0.4105    0.4487 H   0  0  0  0  0  0  0  0  0  0  0  0
    8.3012   -0.0786    2.0767 H   0  0  0  0  0  0  0  0  0  0  0  0
    9.3521    1.4117    1.9008 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.1970    1.4527    1.0887 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.1060   -0.9884    2.2170 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.5582   -2.0004    0.8742 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.0412   -0.2225    0.7271 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.9997   -1.2276   -2.9253 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.7657   -2.3173   -2.5291 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.5322   -0.5968   -2.8066 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.4180   -1.8126   -0.0019 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.1675   -0.0739   -0.4350 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.1261   -3.4060   -1.6867 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2136   -2.5934   -2.6543 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4898   -3.1795   -0.9986 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.1314    0.5926   -0.5686 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9939    0.0724   -2.0470 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7195   -1.6791   -1.6268 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3687    0.5528    0.3871 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2476   -1.1814    0.7429 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.6961   -1.8996   -2.0468 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.3853   -2.6871   -1.0205 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.0558   -2.5333   -0.4162 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.5362    1.2294    0.0783 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.2966   -1.0689   -1.0981 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.4811    0.6046   -1.6215 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.8697   -0.4275    1.2959 H   0  0  0  0  0  0  0  0  0  0  0  0
   -8.4662   -0.0810   -1.0718 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.1896    2.7489   -0.5731 H   0  0  0  0  0  0  0  0  0  0  0  0
   -7.6692    1.3538    2.8786 H   0  0  0  0  0  0  0  0  0  0  0  0
   -9.1616    1.5751    1.8491 H   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0
  2  3  1  0
  2  4  2  3
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 22 23  2  0
 23 24  1  0
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 26 27  1  0
  7 28  1  0
 28 29  2  0
 28 30  1  0
 30  5  1  0
 27 22  1  0
  1 31  1  0
  1 32  1  0
  1 33  1  0
  3 34  1  0
  3 35  1  0
  3 36  1  0
  4 37  1  0
  5 38  1  1
  6 39  1  0
  6 40  1  0
  8 41  1  0
  9 42  1  0
  9 43  1  0
 10 44  1  0
 10 45  1  0
 12 46  1  0
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 20 60  1  1
 21 61  1  0
 23 62  1  0
 27 63  1  0
 27 64  1  0
M  END


  Mrv1652304292203192D          

 30 31  0  0  1  0            999 V2000
   -0.8001   -8.9459    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0550   -9.7305    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
   -1.8800   -9.7305    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1350   -8.9459    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.9196   -8.6910    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5327   -9.2430    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.3173   -8.9881    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.9304   -9.5401    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.7150   -9.2851    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.3281   -9.8372    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -7.1127   -9.5822    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
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   -0.4207  -11.8191    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
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  1  2  1  0  0  0  0
  2  3  1  0  0  0  0
  3  4  1  0  0  0  0
  4  5  2  0  0  0  0
  5  6  1  0  0  0  0
  6  7  1  0  0  0  0
  7  8  1  0  0  0  0
  8  9  2  0  0  0  0
  9 10  1  0  0  0  0
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 28 30  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0080271

> <DATABASE_NAME>
NP-MRD

> <SMILES>
CC(C)=C[C@H]1C\C(=C/CC\C(C)=C\CC\C(C)=C\C[C@H](O)C2=CC(=O)OC2)C(=O)O1

> <INCHI_IDENTIFIER>
InChI=1S/C25H34O5/c1-17(2)13-22-14-20(25(28)30-22)10-6-9-18(3)7-5-8-19(4)11-12-23(26)21-15-24(27)29-16-21/h7,10-11,13,15,22-23,26H,5-6,8-9,12,14,16H2,1-4H3/b18-7+,19-11+,20-10+/t22-,23-/m0/s1

> <INCHI_KEY>
VKOBTBGPXFPMMX-RDKPZERASA-N

> <FORMULA>
C25H34O5

> <MOLECULAR_WEIGHT>
414.542

> <EXACT_MASS>
414.240624195

> <JCHEM_ACCEPTOR_COUNT>
3

> <JCHEM_ATOM_COUNT>
64

> <JCHEM_AVERAGE_POLARIZABILITY>
47.99340969045147

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
1

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
1

> <JCHEM_IUPAC>
4-[(1S,3E,7E)-1-hydroxy-4,8-dimethyl-11-[(3E,5R)-5-(2-methylprop-1-en-1-yl)-2-oxooxolan-3-ylidene]undeca-3,7-dien-1-yl]-2,5-dihydrofuran-2-one

> <ALOGPS_LOGP>
4.63

> <JCHEM_LOGP>
5.0467088833333325

> <ALOGPS_LOGS>
-5.07

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
2

> <JCHEM_PHYSIOLOGICAL_CHARGE>
-1

> <JCHEM_PKA>
15.001020279891879

> <JCHEM_PKA_STRONGEST_ACIDIC>
5.727795103959595

> <JCHEM_PKA_STRONGEST_BASIC>
-3.049607924702441

> <JCHEM_POLAR_SURFACE_AREA>
72.83000000000001

> <JCHEM_REFRACTIVITY>
121.99579999999997

> <JCHEM_ROTATABLE_BOND_COUNT>
10

> <JCHEM_RULE_OF_FIVE>
0

> <ALOGPS_SOLUBILITY>
3.55e-03 g/l

> <JCHEM_TRADITIONAL_IUPAC>
4-[(1S,3E,7E)-1-hydroxy-4,8-dimethyl-11-[(3E,5R)-5-(2-methylprop-1-en-1-yl)-2-oxooxolan-3-ylidene]undeca-3,7-dien-1-yl]-5H-furan-2-one

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 29-APR-22   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   29-APR-22         0                                  
HETATM    1  O   UNK     0      -1.493 -16.699   0.000  0.00  0.00           O+0
HETATM    2  C   UNK     0      -1.969 -18.164   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0      -3.509 -18.164   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0      -3.985 -16.699   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0      -5.450 -16.223   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0      -6.594 -17.254   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0      -8.059 -16.778   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0      -9.203 -17.808   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0     -10.668 -17.332   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0     -11.812 -18.363   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0     -13.277 -17.887   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0     -14.422 -18.917   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0     -15.886 -18.441   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0     -17.031 -19.472   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0     -18.495 -18.996   0.000  0.00  0.00           C+0
HETATM   16  O   UNK     0     -18.815 -17.490   0.000  0.00  0.00           O+0
HETATM   17  C   UNK     0     -19.640 -20.026   0.000  0.00  0.00           C+0
HETATM   18  C   UNK     0     -19.479 -21.558   0.000  0.00  0.00           C+0
HETATM   19  C   UNK     0     -20.886 -22.184   0.000  0.00  0.00           C+0
HETATM   20  O   UNK     0     -21.206 -23.691   0.000  0.00  0.00           O+0
HETATM   21  O   UNK     0     -21.916 -21.040   0.000  0.00  0.00           O+0
HETATM   22  C   UNK     0     -21.146 -19.706   0.000  0.00  0.00           C+0
HETATM   23  C   UNK     0     -14.101 -20.424   0.000  0.00  0.00           C+0
HETATM   24  C   UNK     0      -8.883 -19.315   0.000  0.00  0.00           C+0
HETATM   25  C   UNK     0      -2.739 -15.794   0.000  0.00  0.00           C+0
HETATM   26  O   UNK     0      -2.739 -14.254   0.000  0.00  0.00           O+0
HETATM   27  C   UNK     0      -1.064 -19.410   0.000  0.00  0.00           C+0
HETATM   28  C   UNK     0      -1.691 -20.816   0.000  0.00  0.00           C+0
HETATM   29  C   UNK     0      -0.785 -22.062   0.000  0.00  0.00           C+0
HETATM   30  C   UNK     0      -3.222 -20.977   0.000  0.00  0.00           C+0
CONECT    1    2   25                                                       
CONECT    2    1    3   27                                                  
CONECT    3    2    4                                                       
CONECT    4    3    5   25                                                  
CONECT    5    4    6                                                       
CONECT    6    5    7                                                       
CONECT    7    6    8                                                       
CONECT    8    7    9   24                                                  
CONECT    9    8   10                                                       
CONECT   10    9   11                                                       
CONECT   11   10   12                                                       
CONECT   12   11   13   23                                                  
CONECT   13   12   14                                                       
CONECT   14   13   15                                                       
CONECT   15   14   16   17                                                  
CONECT   16   15                                                            
CONECT   17   15   18   22                                                  
CONECT   18   17   19                                                       
CONECT   19   18   20   21                                                  
CONECT   20   19                                                            
CONECT   21   19   22                                                       
CONECT   22   21   17                                                       
CONECT   23   12                                                            
CONECT   24    8                                                            
CONECT   25    4    1   26                                                  
CONECT   26   25                                                            
CONECT   27    2   28                                                       
CONECT   28   27   29   30                                                  
CONECT   29   28                                                            
CONECT   30   28                                                            
MASTER        0    0    0    0    0    0    0    0   30    0   62    0
END

View in JSmol

Synonyms

Not Available

Chemical Formula

C₂₅H₃₄O₅

Average Mass

414.5420 Da

Monoisotopic Mass

414.24062 Da

IUPAC Name

4-[(1S,3E,7E)-1-hydroxy-4,8-dimethyl-11-[(3E,5R)-5-(2-methylprop-1-en-1-yl)-2-oxooxolan-3-ylidene]undeca-3,7-dien-1-yl]-2,5-dihydrofuran-2-one

Traditional Name

4-[(1S,3E,7E)-1-hydroxy-4,8-dimethyl-11-[(3E,5R)-5-(2-methylprop-1-en-1-yl)-2-oxooxolan-3-ylidene]undeca-3,7-dien-1-yl]-5H-furan-2-one

CAS Registry Number

Not Available

SMILES

CC(C)=C[C@H]1C\C(=C/CC\C(C)=C\CC\C(C)=C\C[C@H](O)C2=CC(=O)OC2)C(=O)O1

InChI Identifier

InChI=1S/C25H34O5/c1-17(2)13-22-14-20(25(28)30-22)10-6-9-18(3)7-5-8-19(4)11-12-23(26)21-15-24(27)29-16-21/h7,10-11,13,15,22-23,26H,5-6,8-9,12,14,16H2,1-4H3/b18-7+,19-11+,20-10+/t22-,23-/m0/s1

InChI Key

VKOBTBGPXFPMMX-RDKPZERASA-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
Thorectandra sp.	-	KNApSAcK

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as diterpene lactones. These are diterpenoids containing a lactone moiety.

Kingdom

Organic compounds

Super Class

Lipids and lipid-like molecules

Class

Prenol lipids

Sub Class

Terpene lactones

Direct Parent

Diterpene lactones

Alternative Parents

Substituents

Diterpenoid
Diterpene lactone
Long chain fatty alcohol
Fatty alcohol
Fatty acyl
Gamma butyrolactone
Dicarboxylic acid or derivatives
2-furanone
Alpha,beta-unsaturated carboxylic ester
Enoate ester
Tetrahydrofuran
Dihydrofuran
Secondary alcohol
Lactone
Carboxylic acid ester
Oxacycle
Organoheterocyclic compound
Carboxylic acid derivative
Organic oxygen compound
Organic oxide
Hydrocarbon derivative
Organooxygen compound
Carbonyl group
Alcohol
Aliphatic heteromonocyclic compound

Molecular Framework

Aliphatic heteromonocyclic 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	4.63	ALOGPS
logP	5.05	ChemAxon
logS	-5.1	ALOGPS
pKa (Strongest Acidic)	5.73	ChemAxon
pKa (Strongest Basic)	-3	ChemAxon
Physiological Charge	-1	ChemAxon
Hydrogen Acceptor Count	3	ChemAxon
Hydrogen Donor Count	1	ChemAxon
Polar Surface Area	72.83 Å²	ChemAxon
Rotatable Bond Count	10	ChemAxon
Refractivity	122 m³·mol⁻¹	ChemAxon
Polarizability	47.99 Å³	ChemAxon
Number of Rings	2	ChemAxon
Bioavailability	Yes	ChemAxon
Rule of Five	No	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

163066530

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

Not Available

Showing NP-Card for Luffarin R (NP0080271)

MOL for NP0080271 (Luffarin R)

3D MOL for NP0080271 (Luffarin R)

3D SDF for NP0080271 (Luffarin R)

3D-SDF for NP0080271 (Luffarin R)

PDB for NP0080271 (Luffarin R)

3D PDB for NP0080271 (Luffarin R)

SMILES for NP0080271 (Luffarin R)

INCHI for NP0080271 (Luffarin R)

Structure for NP0080271 (Luffarin R)

3D Structure for NP0080271 (Luffarin R)