NP-MRD: Showing NP-Card for lantalucratin A (NP0026031)

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Record Information

Version

2.0

Created at

2021-06-19 17:59:46 UTC

Updated at

2021-06-29 23:51:19 UTC

NP-MRD ID

NP0026031

Secondary Accession Numbers

None

Natural Product Identification

Common Name

lantalucratin A

Provided By

JEOL Database JEOL Logo

Description

lantalucratin A is found in Lantana involucrata. lantalucratin A was first documented in 2004 (Hayashi, K., et al.). Based on a literature review very few articles have been published on (2S)-6-methoxy-2-(prop-1-en-2-yl)-2H,3H,4H,5H-naphtho[1,2-b]furan-4,5-dione.

Structure

MOL 3D MOL SDF 3D SDF PDB SMILES InChI


  Mrv1652306192119593D          

 34 36  0  0  0  0            999 V2000
    5.0667   -1.0715   -1.1675 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.8858   -0.4471   -1.3208 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.8194    1.0357   -1.5716 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.5723   -1.1991   -1.2354 C   0  0  2  0  0  0  0  0  0  0  0  0
    1.8347   -1.3371   -2.5847 C   0  0  2  0  0  0  0  0  0  0  0  0
    0.4910   -0.8779   -2.2042 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.4824   -0.4440   -0.9548 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.6960   -0.5193   -0.2908 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6866    0.1359   -0.3052 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5975    0.6636    0.9917 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7097    1.2460    1.5989 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.9211    1.3057    0.9159 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.0313    0.7615   -0.3673 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.2272    0.9171   -1.0150 O   0  0  0  0  0  0  0  0  0  0  0  0
   -5.1378   -0.1216   -0.6506 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9173    0.1816   -0.9919 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0007   -0.4126   -2.3604 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.0596   -0.6158   -2.9374 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6992   -0.8386   -3.0433 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6552   -1.1456   -4.2244 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.1306   -2.1391   -0.9783 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.0073   -0.5302   -1.2217 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.2966    1.5419   -0.7539 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.2927    1.2490   -2.5066 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.8167    1.4821   -1.6490 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.7425   -2.2028   -0.8214 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.8361   -2.3789   -2.9219 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.2645   -0.7192   -3.3793 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.3455    0.6365    1.5360 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6264    1.6668    2.5984 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.7796    1.7881    1.3772 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.6892   -1.1155   -0.7587 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.4941    0.0214    0.3750 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.0001   -0.0623   -1.3214 H   0  0  0  0  0  0  0  0  0  0  0  0
  9 10  2  0  0  0  0
 10 11  1  0  0  0  0
  9 16  1  0  0  0  0
 12 13  1  0  0  0  0
  6  5  1  0  0  0  0
  5  4  1  0  0  0  0
  4  8  1  0  0  0  0
  8  7  1  0  0  0  0
 13 16  2  0  0  0  0
  4  2  1  0  0  0  0
 11 12  2  0  0  0  0
  2  1  2  3  0  0  0
  9  7  1  0  0  0  0
  2  3  1  0  0  0  0
 16 17  1  0  0  0  0
 13 14  1  0  0  0  0
 17 19  1  0  0  0  0
 14 15  1  0  0  0  0
 19  6  1  0  0  0  0
 17 18  2  0  0  0  0
  7  6  2  0  0  0  0
 19 20  2  0  0  0  0
 11 30  1  0  0  0  0
 12 31  1  0  0  0  0
 10 29  1  0  0  0  0
  5 27  1  0  0  0  0
  5 28  1  0  0  0  0
  4 26  1  1  0  0  0
  1 21  1  0  0  0  0
  1 22  1  0  0  0  0
  3 23  1  0  0  0  0
  3 24  1  0  0  0  0
  3 25  1  0  0  0  0
 15 32  1  0  0  0  0
 15 33  1  0  0  0  0
 15 34  1  0  0  0  0
M  END

     RDKit          3D

 34 36  0  0  0  0  0  0  0  0999 V2000
    5.0667   -1.0715   -1.1675 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.8858   -0.4471   -1.3208 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.8194    1.0357   -1.5716 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.5723   -1.1991   -1.2354 C   0  0  2  0  0  0  0  0  0  0  0  0
    1.8347   -1.3371   -2.5847 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.4910   -0.8779   -2.2042 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.4824   -0.4440   -0.9548 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.6960   -0.5193   -0.2908 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6866    0.1359   -0.3052 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5975    0.6636    0.9917 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7097    1.2460    1.5989 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.9211    1.3057    0.9159 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.0313    0.7615   -0.3673 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.2272    0.9171   -1.0150 O   0  0  0  0  0  0  0  0  0  0  0  0
   -5.1378   -0.1216   -0.6506 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9173    0.1816   -0.9919 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0007   -0.4126   -2.3604 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.0596   -0.6158   -2.9374 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6992   -0.8386   -3.0433 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6552   -1.1456   -4.2244 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.1306   -2.1391   -0.9783 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.0073   -0.5302   -1.2217 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.2966    1.5419   -0.7539 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.2927    1.2490   -2.5066 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.8167    1.4821   -1.6490 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.7425   -2.2028   -0.8214 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.8361   -2.3789   -2.9219 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.2645   -0.7192   -3.3793 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.3455    0.6365    1.5360 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6264    1.6668    2.5984 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.7796    1.7881    1.3772 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.6892   -1.1155   -0.7587 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.4941    0.0214    0.3750 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.0001   -0.0623   -1.3214 H   0  0  0  0  0  0  0  0  0  0  0  0
  9 10  2  0
 10 11  1  0
  9 16  1  0
 12 13  1  0
  6  5  1  0
  5  4  1  0
  4  8  1  0
  8  7  1  0
 13 16  2  0
  4  2  1  0
 11 12  2  0
  2  1  2  3
  9  7  1  0
  2  3  1  0
 16 17  1  0
 13 14  1  0
 17 19  1  0
 14 15  1  0
 19  6  1  0
 17 18  2  0
  7  6  2  0
 19 20  2  0
 11 30  1  0
 12 31  1  0
 10 29  1  0
  5 27  1  0
  5 28  1  0
  4 26  1  1
  1 21  1  0
  1 22  1  0
  3 23  1  0
  3 24  1  0
  3 25  1  0
 15 32  1  0
 15 33  1  0
 15 34  1  0
M  END


  Mrv1652306192119593D          

 34 36  0  0  0  0            999 V2000
    5.0667   -1.0715   -1.1675 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.8858   -0.4471   -1.3208 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.8194    1.0357   -1.5716 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.5723   -1.1991   -1.2354 C   0  0  2  0  0  0  0  0  0  0  0  0
    1.8347   -1.3371   -2.5847 C   0  0  2  0  0  0  0  0  0  0  0  0
    0.4910   -0.8779   -2.2042 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.4824   -0.4440   -0.9548 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.6960   -0.5193   -0.2908 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6866    0.1359   -0.3052 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5975    0.6636    0.9917 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7097    1.2460    1.5989 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.9211    1.3057    0.9159 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.0313    0.7615   -0.3673 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.2272    0.9171   -1.0150 O   0  0  0  0  0  0  0  0  0  0  0  0
   -5.1378   -0.1216   -0.6506 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9173    0.1816   -0.9919 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0007   -0.4126   -2.3604 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.0596   -0.6158   -2.9374 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6992   -0.8386   -3.0433 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6552   -1.1456   -4.2244 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.1306   -2.1391   -0.9783 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.0073   -0.5302   -1.2217 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.2966    1.5419   -0.7539 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.2927    1.2490   -2.5066 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.8167    1.4821   -1.6490 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.7425   -2.2028   -0.8214 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.8361   -2.3789   -2.9219 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.2645   -0.7192   -3.3793 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.3455    0.6365    1.5360 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6264    1.6668    2.5984 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.7796    1.7881    1.3772 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.6892   -1.1155   -0.7587 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.4941    0.0214    0.3750 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.0001   -0.0623   -1.3214 H   0  0  0  0  0  0  0  0  0  0  0  0
  9 10  2  0  0  0  0
 10 11  1  0  0  0  0
  9 16  1  0  0  0  0
 12 13  1  0  0  0  0
  6  5  1  0  0  0  0
  5  4  1  0  0  0  0
  4  8  1  0  0  0  0
  8  7  1  0  0  0  0
 13 16  2  0  0  0  0
  4  2  1  0  0  0  0
 11 12  2  0  0  0  0
  2  1  2  3  0  0  0
  9  7  1  0  0  0  0
  2  3  1  0  0  0  0
 16 17  1  0  0  0  0
 13 14  1  0  0  0  0
 17 19  1  0  0  0  0
 14 15  1  0  0  0  0
 19  6  1  0  0  0  0
 17 18  2  0  0  0  0
  7  6  2  0  0  0  0
 19 20  2  0  0  0  0
 11 30  1  0  0  0  0
 12 31  1  0  0  0  0
 10 29  1  0  0  0  0
  5 27  1  0  0  0  0
  5 28  1  0  0  0  0
  4 26  1  1  0  0  0
  1 21  1  0  0  0  0
  1 22  1  0  0  0  0
  3 23  1  0  0  0  0
  3 24  1  0  0  0  0
  3 25  1  0  0  0  0
 15 32  1  0  0  0  0
 15 33  1  0  0  0  0
 15 34  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0026031

> <DATABASE_NAME>
NP-MRD

> <SMILES>
[H]C([H])=C(C([H])([H])[H])[C@@]1([H])OC2=C(C(=O)C(=O)C3=C(OC([H])([H])[H])C([H])=C([H])C([H])=C23)C1([H])[H]

> <INCHI_IDENTIFIER>
InChI=1S/C16H14O4/c1-8(2)12-7-10-14(17)15(18)13-9(16(10)20-12)5-4-6-11(13)19-3/h4-6,12H,1,7H2,2-3H3/t12-/m0/s1

> <INCHI_KEY>
ICDFLJCHILFMDR-LBPRGKRZSA-N

> <FORMULA>
C16H14O4

> <MOLECULAR_WEIGHT>
270.284

> <EXACT_MASS>
270.089208931

> <JCHEM_ACCEPTOR_COUNT>
4

> <JCHEM_ATOM_COUNT>
34

> <JCHEM_AVERAGE_POLARIZABILITY>
28.406442909825188

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
0

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
1

> <JCHEM_IUPAC>
(2S)-6-methoxy-2-(prop-1-en-2-yl)-2H,3H,4H,5H-naphtho[1,2-b]furan-4,5-dione

> <ALOGPS_LOGP>
2.00

> <JCHEM_LOGP>
2.364304156666666

> <ALOGPS_LOGS>
-3.15

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
3

> <JCHEM_PHYSIOLOGICAL_CHARGE>
-1

> <JCHEM_PKA_STRONGEST_BASIC>
-4.590256895287101

> <JCHEM_POLAR_SURFACE_AREA>
52.6

> <JCHEM_REFRACTIVITY>
75.01209999999999

> <JCHEM_ROTATABLE_BOND_COUNT>
2

> <JCHEM_RULE_OF_FIVE>
1

> <ALOGPS_SOLUBILITY>
1.91e-01 g/l

> <JCHEM_TRADITIONAL_IUPAC>
(2S)-6-methoxy-2-(prop-1-en-2-yl)-2H,3H-naphtho[1,2-b]furan-4,5-dione

> <JCHEM_VEBER_RULE>
0

$$$$

     RDKit          3D

 34 36  0  0  0  0  0  0  0  0999 V2000
    5.0667   -1.0715   -1.1675 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.8858   -0.4471   -1.3208 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.8194    1.0357   -1.5716 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.5723   -1.1991   -1.2354 C   0  0  2  0  0  0  0  0  0  0  0  0
    1.8347   -1.3371   -2.5847 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.4910   -0.8779   -2.2042 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.4824   -0.4440   -0.9548 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.6960   -0.5193   -0.2908 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6866    0.1359   -0.3052 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5975    0.6636    0.9917 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7097    1.2460    1.5989 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.9211    1.3057    0.9159 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.0313    0.7615   -0.3673 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.2272    0.9171   -1.0150 O   0  0  0  0  0  0  0  0  0  0  0  0
   -5.1378   -0.1216   -0.6506 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9173    0.1816   -0.9919 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0007   -0.4126   -2.3604 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.0596   -0.6158   -2.9374 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6992   -0.8386   -3.0433 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6552   -1.1456   -4.2244 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.1306   -2.1391   -0.9783 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.0073   -0.5302   -1.2217 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.2966    1.5419   -0.7539 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.2927    1.2490   -2.5066 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.8167    1.4821   -1.6490 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.7425   -2.2028   -0.8214 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.8361   -2.3789   -2.9219 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.2645   -0.7192   -3.3793 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.3455    0.6365    1.5360 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6264    1.6668    2.5984 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.7796    1.7881    1.3772 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.6892   -1.1155   -0.7587 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.4941    0.0214    0.3750 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.0001   -0.0623   -1.3214 H   0  0  0  0  0  0  0  0  0  0  0  0
  9 10  2  0
 10 11  1  0
  9 16  1  0
 12 13  1  0
  6  5  1  0
  5  4  1  0
  4  8  1  0
  8  7  1  0
 13 16  2  0
  4  2  1  0
 11 12  2  0
  2  1  2  3
  9  7  1  0
  2  3  1  0
 16 17  1  0
 13 14  1  0
 17 19  1  0
 14 15  1  0
 19  6  1  0
 17 18  2  0
  7  6  2  0
 19 20  2  0
 11 30  1  0
 12 31  1  0
 10 29  1  0
  5 27  1  0
  5 28  1  0
  4 26  1  1
  1 21  1  0
  1 22  1  0
  3 23  1  0
  3 24  1  0
  3 25  1  0
 15 32  1  0
 15 33  1  0
 15 34  1  0
M  END

HEADER    PROTEIN                                 19-JUN-21   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   19-JUN-21         0                                  
HETATM    1  C   UNK     0       5.067  -1.071  -1.167  0.00  0.00           C+0
HETATM    2  C   UNK     0       3.886  -0.447  -1.321  0.00  0.00           C+0
HETATM    3  C   UNK     0       3.819   1.036  -1.572  0.00  0.00           C+0
HETATM    4  C   UNK     0       2.572  -1.199  -1.235  0.00  0.00           C+0
HETATM    5  C   UNK     0       1.835  -1.337  -2.585  0.00  0.00           C+0
HETATM    6  C   UNK     0       0.491  -0.878  -2.204  0.00  0.00           C+0
HETATM    7  C   UNK     0       0.482  -0.444  -0.955  0.00  0.00           C+0
HETATM    8  O   UNK     0       1.696  -0.519  -0.291  0.00  0.00           O+0
HETATM    9  C   UNK     0      -0.687   0.136  -0.305  0.00  0.00           C+0
HETATM   10  C   UNK     0      -0.598   0.664   0.992  0.00  0.00           C+0
HETATM   11  C   UNK     0      -1.710   1.246   1.599  0.00  0.00           C+0
HETATM   12  C   UNK     0      -2.921   1.306   0.916  0.00  0.00           C+0
HETATM   13  C   UNK     0      -3.031   0.762  -0.367  0.00  0.00           C+0
HETATM   14  O   UNK     0      -4.227   0.917  -1.015  0.00  0.00           O+0
HETATM   15  C   UNK     0      -5.138  -0.122  -0.651  0.00  0.00           C+0
HETATM   16  C   UNK     0      -1.917   0.182  -0.992  0.00  0.00           C+0
HETATM   17  C   UNK     0      -2.001  -0.413  -2.360  0.00  0.00           C+0
HETATM   18  O   UNK     0      -3.060  -0.616  -2.937  0.00  0.00           O+0
HETATM   19  C   UNK     0      -0.699  -0.839  -3.043  0.00  0.00           C+0
HETATM   20  O   UNK     0      -0.655  -1.146  -4.224  0.00  0.00           O+0
HETATM   21  H   UNK     0       5.131  -2.139  -0.978  0.00  0.00           H+0
HETATM   22  H   UNK     0       6.007  -0.530  -1.222  0.00  0.00           H+0
HETATM   23  H   UNK     0       3.297   1.542  -0.754  0.00  0.00           H+0
HETATM   24  H   UNK     0       3.293   1.249  -2.507  0.00  0.00           H+0
HETATM   25  H   UNK     0       4.817   1.482  -1.649  0.00  0.00           H+0
HETATM   26  H   UNK     0       2.743  -2.203  -0.821  0.00  0.00           H+0
HETATM   27  H   UNK     0       1.836  -2.379  -2.922  0.00  0.00           H+0
HETATM   28  H   UNK     0       2.264  -0.719  -3.379  0.00  0.00           H+0
HETATM   29  H   UNK     0       0.346   0.637   1.536  0.00  0.00           H+0
HETATM   30  H   UNK     0      -1.626   1.667   2.598  0.00  0.00           H+0
HETATM   31  H   UNK     0      -3.780   1.788   1.377  0.00  0.00           H+0
HETATM   32  H   UNK     0      -4.689  -1.115  -0.759  0.00  0.00           H+0
HETATM   33  H   UNK     0      -5.494   0.021   0.375  0.00  0.00           H+0
HETATM   34  H   UNK     0      -6.000  -0.062  -1.321  0.00  0.00           H+0
CONECT    1    2   21   22                                                  
CONECT    2    4    1    3                                                  
CONECT    3    2   23   24   25                                             
CONECT    4    5    8    2   26                                             
CONECT    5    6    4   27   28                                             
CONECT    6    5   19    7                                                  
CONECT    7    8    9    6                                                  
CONECT    8    4    7                                                       
CONECT    9   10   16    7                                                  
CONECT   10    9   11   29                                                  
CONECT   11   10   12   30                                                  
CONECT   12   13   11   31                                                  
CONECT   13   12   16   14                                                  
CONECT   14   13   15                                                       
CONECT   15   14   32   33   34                                             
CONECT   16    9   13   17                                                  
CONECT   17   16   19   18                                                  
CONECT   18   17                                                            
CONECT   19   17    6   20                                                  
CONECT   20   19                                                            
CONECT   21    1                                                            
CONECT   22    1                                                            
CONECT   23    3                                                            
CONECT   24    3                                                            
CONECT   25    3                                                            
CONECT   26    4                                                            
CONECT   27    5                                                            
CONECT   28    5                                                            
CONECT   29   10                                                            
CONECT   30   11                                                            
CONECT   31   12                                                            
CONECT   32   15                                                            
CONECT   33   15                                                            
CONECT   34   15                                                            
MASTER        0    0    0    0    0    0    0    0   34    0   72    0
END

RDKit          3D

34 36  0  0  0  0  0  0  0  0999 V2000
    5.0667   -1.0715   -1.1675 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.8858   -0.4471   -1.3208 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.8194    1.0357   -1.5716 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.5723   -1.1991   -1.2354 C   0  0  2  0  0  0  0  0  0  0  0  0
    1.8347   -1.3371   -2.5847 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.4910   -0.8779   -2.2042 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.4824   -0.4440   -0.9548 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.6960   -0.5193   -0.2908 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6866    0.1359   -0.3052 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5975    0.6636    0.9917 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7097    1.2460    1.5989 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.9211    1.3057    0.9159 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.0313    0.7615   -0.3673 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.2272    0.9171   -1.0150 O   0  0  0  0  0  0  0  0  0  0  0  0
   -5.1378   -0.1216   -0.6506 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9173    0.1816   -0.9919 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0007   -0.4126   -2.3604 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.0596   -0.6158   -2.9374 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6992   -0.8386   -3.0433 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6552   -1.1456   -4.2244 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.1306   -2.1391   -0.9783 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.0073   -0.5302   -1.2217 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.2966    1.5419   -0.7539 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.2927    1.2490   -2.5066 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.8167    1.4821   -1.6490 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.7425   -2.2028   -0.8214 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.8361   -2.3789   -2.9219 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.2645   -0.7192   -3.3793 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.3455    0.6365    1.5360 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6264    1.6668    2.5984 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.7796    1.7881    1.3772 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.6892   -1.1155   -0.7587 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.4941    0.0214    0.3750 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.0001   -0.0623   -1.3214 H   0  0  0  0  0  0  0  0  0  0  0  0
  9 10  2  0
 10 11  1  0
  9 16  1  0
 12 13  1  0
  6  5  1  0
  5  4  1  0
  4  8  1  0
  8  7  1  0
 13 16  2  0
  4  2  1  0
 11 12  2  0
  2  1  2  3
  9  7  1  0
  2  3  1  0
 16 17  1  0
 13 14  1  0
 17 19  1  0
 14 15  1  0
 19  6  1  0
 17 18  2  0
  7  6  2  0
 19 20  2  0
 11 30  1  0
 12 31  1  0
 10 29  1  0
  5 27  1  0
  5 28  1  0
  4 26  1  1
  1 21  1  0
  1 22  1  0
  3 23  1  0
  3 24  1  0
  3 25  1  0
 15 32  1  0
 15 33  1  0
 15 34  1  0
M  END

View in JSmol

Synonyms

Value	Source
2a-Isopropenyl-6-methoxy-2,3-dihydronaphtho[1,2-b]furan-4,5-dione	Generator
2Α-isopropenyl-6-methoxy-2,3-dihydronaphtho[1,2-b]furan-4,5-dione	Generator

Chemical Formula

C₁₆H₁₄O₄

Average Mass

270.2840 Da

Monoisotopic Mass

270.08921 Da

IUPAC Name

(2S)-6-methoxy-2-(prop-1-en-2-yl)-2H,3H,4H,5H-naphtho[1,2-b]furan-4,5-dione

Traditional Name

(2S)-6-methoxy-2-(prop-1-en-2-yl)-2H,3H-naphtho[1,2-b]furan-4,5-dione

CAS Registry Number

Not Available

SMILES

[H]C([H])=C(C([H])([H])[H])[C@@]1([H])OC2=C(C(=O)C(=O)C3=C(OC([H])([H])[H])C([H])=C([H])C([H])=C23)C1([H])[H]

InChI Identifier

InChI=1S/C16H14O4/c1-8(2)12-7-10-14(17)15(18)13-9(16(10)20-12)5-4-6-11(13)19-3/h4-6,12H,1,7H2,2-3H3/t12-/m0/s1

InChI Key

ICDFLJCHILFMDR-LBPRGKRZSA-N

Experimental Spectra

Spectrum Type	Description	Depositor Email	Depositor Organization	Depositor	Deposition Date	View
1D NMR	¹³C NMR Spectrum (1D, 500 MHz, CDCl₃, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 500 MHz, CDCl₃, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 100 MHz, CDCl₃, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 100 MHz, CDCl₃, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 200 MHz, CDCl₃, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 200 MHz, CDCl₃, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 300 MHz, CDCl₃, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 300 MHz, CDCl₃, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 400 MHz, CDCl₃, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 400 MHz, CDCl₃, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 600 MHz, CDCl₃, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 600 MHz, CDCl₃, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 700 MHz, CDCl₃, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 700 MHz, CDCl₃, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 800 MHz, CDCl₃, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 800 MHz, CDCl₃, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 900 MHz, CDCl₃, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 900 MHz, CDCl₃, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 1000 MHz, CDCl₃, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 1000 MHz, CDCl₃, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum

Predicted Spectra

Not Available

Chemical Shift Submissions

Not Available

Species

Species of Origin

Species Name	Source	Reference
Lantana involucrata	JEOL database	Hayashi, K., et al, J. Nat. Prod. 67, 990 (2004)

Chemical Taxonomy

Classification

Not classified

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	ALOGPS
logP	2.36	ChemAxon
logS	-3.2	ALOGPS
pKa (Strongest Basic)	-4.6	ChemAxon
Physiological Charge	-1	ChemAxon
Hydrogen Acceptor Count	4	ChemAxon
Hydrogen Donor Count	0	ChemAxon
Polar Surface Area	52.6 Å²	ChemAxon
Rotatable Bond Count	2	ChemAxon
Refractivity	75.01 m³·mol⁻¹	ChemAxon
Polarizability	28.41 Å³	ChemAxon
Number of Rings	3	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

102222642

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

Hayashi, K., et al. (2004). Hayashi, K., et al, J. Nat. Prod. 67, 990 (2004). J. Nat. Prod..

Showing NP-Card for lantalucratin A (NP0026031)

MOL for NP0026031 (lantalucratin A)

3D MOL for NP0026031 (lantalucratin A)

3D SDF for NP0026031 (lantalucratin A)

3D-SDF for NP0026031 (lantalucratin A)

PDB for NP0026031 (lantalucratin A)

3D PDB for NP0026031 (lantalucratin A)

SMILES for NP0026031 (lantalucratin A)

INCHI for NP0026031 (lantalucratin A)

Structure for NP0026031 (lantalucratin A)

3D Structure for NP0026031 (lantalucratin A)