NP-MRD: Showing NP-Card for (4s,4as,5s,8ar,9ar)-9a-methoxy-3,4a-dimethyl-4-{[(2z)-2-methylbut-2-enoyl]oxy}-2-oxo-4h,5h,6h,7h,8h,8ah,9h-naphtho[2,3-b]furan-5-carboxylic acid (NP0240880)

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Record Information

Version

2.0

Created at

2022-09-07 00:48:11 UTC

Updated at

2022-09-07 00:48:11 UTC

NP-MRD ID

NP0240880

Secondary Accession Numbers

None

Natural Product Identification

Common Name

(4s,4as,5s,8ar,9ar)-9a-methoxy-3,4a-dimethyl-4-{[(2z)-2-methylbut-2-enoyl]oxy}-2-oxo-4h,5h,6h,7h,8h,8ah,9h-naphtho[2,3-b]furan-5-carboxylic acid

Description

(4S,4aS,5S,8aR,9aR)-9a-methoxy-3,4a-dimethyl-4-{[(2Z)-2-methylbut-2-enoyl]oxy}-2-oxo-2H,4H,4aH,5H,6H,7H,8H,8aH,9H,9aH-naphtho[2,3-b]furan-5-carboxylic acid belongs to the class of organic compounds known as terpene lactones. These are prenol lipids containing a lactone ring. (4s,4as,5s,8ar,9ar)-9a-methoxy-3,4a-dimethyl-4-{[(2z)-2-methylbut-2-enoyl]oxy}-2-oxo-4h,5h,6h,7h,8h,8ah,9h-naphtho[2,3-b]furan-5-carboxylic acid is found in Ligularia dolichobotrys and Ligularia intermedia. Based on a literature review very few articles have been published on (4S,4aS,5S,8aR,9aR)-9a-methoxy-3,4a-dimethyl-4-{[(2Z)-2-methylbut-2-enoyl]oxy}-2-oxo-2H,4H,4aH,5H,6H,7H,8H,8aH,9H,9aH-naphtho[2,3-b]furan-5-carboxylic acid.

Structure

MOL 3D MOL SDF PDB SMILES InChI


  Mrv1652309072202482D          

 28 30  0  0  1  0            999 V2000
    4.2868    3.3000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5724    3.7125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8579    3.3000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1434    3.7125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8579    2.4750    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5724    2.0625    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.1434    2.0625    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.1434    1.2375    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    2.8579    0.8250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.6425    1.0799    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.8974    1.8646    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.1274    0.4125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.9524    0.4125    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.6425   -0.2549    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.8579    0.0000    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    2.9441   -0.8205    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.6978   -1.1560    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1434   -0.4125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4289    0.0000    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    0.7145   -0.4125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0000    0.0000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0000    0.8250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7145    1.2375    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    0.7145    2.0625    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4289    2.4750    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.0000    2.4750    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.4289    0.8250    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    1.4289    1.6500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0  0  0  0
  2  3  2  0  0  0  0
  3  4  1  0  0  0  0
  3  5  1  0  0  0  0
  5  6  2  0  0  0  0
  5  7  1  0  0  0  0
  8  7  1  6  0  0  0
  8  9  1  0  0  0  0
  9 10  2  0  0  0  0
 10 11  1  0  0  0  0
 10 12  1  0  0  0  0
 12 13  2  0  0  0  0
 12 14  1  0  0  0  0
 14 15  1  0  0  0  0
  9 15  1  0  0  0  0
 15 16  1  1  0  0  0
 16 17  1  0  0  0  0
 15 18  1  0  0  0  0
 19 18  1  1  0  0  0
 19 20  1  0  0  0  0
 20 21  1  0  0  0  0
 21 22  1  0  0  0  0
 22 23  1  0  0  0  0
 23 24  1  6  0  0  0
 24 25  2  0  0  0  0
 24 26  1  0  0  0  0
 23 27  1  0  0  0  0
  8 27  1  0  0  0  0
 19 27  1  0  0  0  0
 27 28  1  6  0  0  0
M  END

     RDKit          3D

 56 58  0  0  0  0  0  0  0  0999 V2000
    3.1819   -1.3346   -3.7426 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.0240   -1.1259   -2.5428 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.4497   -0.7046   -1.4352 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.2857   -0.4926   -0.2277 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.0386   -0.4507   -1.3830 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.2240   -0.5863   -2.3159 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.4270   -0.0052   -0.2153 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.0758    0.2667   -0.0654 C   0  0  2  0  0  0  0  0  0  0  0  0
   -0.2283    1.7068    0.2146 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.5386    2.7453    0.0514 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.9590    2.7457   -0.4986 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1814    3.9104    0.5338 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.2899    5.1140    0.5172 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3896    3.4902    0.9821 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5228    2.1346    0.7642 C   0  0  1  0  0  0  0  0  0  0  0  0
   -2.5199    2.0845   -0.2521 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.6976    2.6660    0.1007 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8744    1.3012    1.9396 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7609   -0.1604    1.6160 C   0  0  1  0  0  0  0  0  0  0  0  0
   -2.9555   -0.7807    0.9708 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7561   -1.2526   -0.4307 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5487   -2.1268   -0.6140 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5598   -1.9981    0.5129 C   0  0  2  0  0  0  0  0  0  0  0  0
   -0.8319   -3.0329    1.5055 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1286   -2.8613    2.7057 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7533   -4.3596    1.0712 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4553   -0.6079    1.0506 C   0  0  1  0  0  0  0  0  0  0  0  0
    0.5604   -0.6310    2.1871 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.4086   -2.1261   -3.5929 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.6969   -0.4098   -4.1061 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.8493   -1.6776   -4.5821 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.1030   -1.3215   -2.5879 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.1689    0.1291   -0.5131 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.7108   -0.0272    0.5972 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.6321   -1.4932    0.1071 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4081    0.0585   -1.0354 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.9701    2.4917   -1.5556 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.5722    2.0131    0.0503 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.3665    3.7531   -0.3177 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5636    3.7468    0.3467 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.3576    2.6422   -0.7988 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.2066    2.2032    0.9368 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1888    1.5344    2.7854 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.9133    1.4892    2.2550 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7802   -0.6224    2.6718 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.3491   -1.6871    1.5332 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.8146   -0.0918    0.9987 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7366   -0.4717   -1.2056 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.6561   -1.8883   -0.6863 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8385   -3.2183   -0.6646 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0537   -1.9352   -1.5911 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.4491   -2.2335    0.0612 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4415   -4.8227    0.5311 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.1083   -0.8817    3.1492 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.4534   -1.2342    1.9364 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.9281    0.4270    2.2770 H   0  0  0  0  0  0  0  0  0  0  0  0
 17 16  1  0
 15 16  1  6
 15 18  1  0
 18 19  1  0
 19 20  1  0
 20 21  1  0
 21 22  1  0
 22 23  1  0
 23 24  1  0
 24 26  1  0
 24 25  2  0
 23 27  1  0
 27 28  1  1
 27  8  1  0
  8  7  1  0
  7  5  1  0
  5  6  2  0
  5  3  1  0
  3  4  1  0
  3  2  2  0
  2  1  1  0
  8  9  1  0
  9 10  2  0
 10 11  1  0
 10 12  1  0
 12 13  2  0
 12 14  1  0
  9 15  1  0
 14 15  1  0
 27 19  1  0
 17 40  1  0
 17 41  1  0
 17 42  1  0
 18 43  1  0
 18 44  1  0
 19 45  1  1
 20 46  1  0
 20 47  1  0
 21 48  1  0
 21 49  1  0
 22 50  1  0
 22 51  1  0
 23 52  1  6
 26 53  1  0
 28 54  1  0
 28 55  1  0
 28 56  1  0
  8 36  1  6
  4 33  1  0
  4 34  1  0
  4 35  1  0
  2 32  1  0
  1 29  1  0
  1 30  1  0
  1 31  1  0
 11 37  1  0
 11 38  1  0
 11 39  1  0
M  END


  Mrv1652309072202482D          

 28 30  0  0  1  0            999 V2000
    4.2868    3.3000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5724    3.7125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8579    3.3000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1434    3.7125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8579    2.4750    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5724    2.0625    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.1434    2.0625    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.1434    1.2375    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    2.8579    0.8250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.6425    1.0799    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.8974    1.8646    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.1274    0.4125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.9524    0.4125    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.6425   -0.2549    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.8579    0.0000    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    2.9441   -0.8205    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.6978   -1.1560    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1434   -0.4125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4289    0.0000    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    0.7145   -0.4125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0000    0.0000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0000    0.8250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7145    1.2375    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    0.7145    2.0625    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4289    2.4750    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.0000    2.4750    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.4289    0.8250    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    1.4289    1.6500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0  0  0  0
  2  3  2  0  0  0  0
  3  4  1  0  0  0  0
  3  5  1  0  0  0  0
  5  6  2  0  0  0  0
  5  7  1  0  0  0  0
  8  7  1  6  0  0  0
  8  9  1  0  0  0  0
  9 10  2  0  0  0  0
 10 11  1  0  0  0  0
 10 12  1  0  0  0  0
 12 13  2  0  0  0  0
 12 14  1  0  0  0  0
 14 15  1  0  0  0  0
  9 15  1  0  0  0  0
 15 16  1  1  0  0  0
 16 17  1  0  0  0  0
 15 18  1  0  0  0  0
 19 18  1  1  0  0  0
 19 20  1  0  0  0  0
 20 21  1  0  0  0  0
 21 22  1  0  0  0  0
 22 23  1  0  0  0  0
 23 24  1  6  0  0  0
 24 25  2  0  0  0  0
 24 26  1  0  0  0  0
 23 27  1  0  0  0  0
  8 27  1  0  0  0  0
 19 27  1  0  0  0  0
 27 28  1  6  0  0  0
M  END
> <DATABASE_ID>
NP0240880

> <DATABASE_NAME>
NP-MRD

> <SMILES>
CO[C@@]12C[C@H]3CCC[C@H](C(O)=O)[C@@]3(C)[C@H](OC(=O)C(\C)=C/C)C1=C(C)C(=O)O2

> <INCHI_IDENTIFIER>
InChI=1S/C21H28O7/c1-6-11(2)18(24)27-16-15-12(3)19(25)28-21(15,26-5)10-13-8-7-9-14(17(22)23)20(13,16)4/h6,13-14,16H,7-10H2,1-5H3,(H,22,23)/b11-6-/t13-,14-,16-,20+,21-/m1/s1

> <INCHI_KEY>
PLUOSPXAEMKKRW-GVHGUOPMSA-N

> <FORMULA>
C21H28O7

> <MOLECULAR_WEIGHT>
392.448

> <EXACT_MASS>
392.183503242

> <JCHEM_ACCEPTOR_COUNT>
5

> <JCHEM_ATOM_COUNT>
56

> <JCHEM_AVERAGE_POLARIZABILITY>
40.17182970268847

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
1

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
1

> <JCHEM_IUPAC>
(4S,4aS,5S,8aR,9aR)-9a-methoxy-3,4a-dimethyl-4-{[(2Z)-2-methylbut-2-enoyl]oxy}-2-oxo-2H,4H,4aH,5H,6H,7H,8H,8aH,9H,9aH-naphtho[2,3-b]furan-5-carboxylic acid

> <JCHEM_LOGP>
3.980483408666667

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
3

> <JCHEM_PHYSIOLOGICAL_CHARGE>
-1

> <JCHEM_PKA_STRONGEST_ACIDIC>
4.279390873012894

> <JCHEM_PKA_STRONGEST_BASIC>
-4.339737906763609

> <JCHEM_POLAR_SURFACE_AREA>
99.13000000000001

> <JCHEM_REFRACTIVITY>
100.36030000000001

> <JCHEM_ROTATABLE_BOND_COUNT>
5

> <JCHEM_RULE_OF_FIVE>
1

> <JCHEM_TRADITIONAL_IUPAC>
(4S,4aS,5S,8aR,9aR)-9a-methoxy-3,4a-dimethyl-4-{[(2Z)-2-methylbut-2-enoyl]oxy}-2-oxo-4H,5H,6H,7H,8H,8aH,9H-naphtho[2,3-b]furan-5-carboxylic acid

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 07-SEP-22   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   07-SEP-22         0                                  
HETATM    1  C   UNK     0       8.002   6.160   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0       6.668   6.930   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0       5.335   6.160   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0       4.001   6.930   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0       5.335   4.620   0.000  0.00  0.00           C+0
HETATM    6  O   UNK     0       6.668   3.850   0.000  0.00  0.00           O+0
HETATM    7  O   UNK     0       4.001   3.850   0.000  0.00  0.00           O+0
HETATM    8  C   UNK     0       4.001   2.310   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0       5.335   1.540   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0       6.799   2.016   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0       7.275   3.481   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0       7.705   0.770   0.000  0.00  0.00           C+0
HETATM   13  O   UNK     0       9.245   0.770   0.000  0.00  0.00           O+0
HETATM   14  O   UNK     0       6.799  -0.476   0.000  0.00  0.00           O+0
HETATM   15  C   UNK     0       5.335   0.000   0.000  0.00  0.00           C+0
HETATM   16  O   UNK     0       5.496  -1.532   0.000  0.00  0.00           O+0
HETATM   17  C   UNK     0       6.903  -2.158   0.000  0.00  0.00           C+0
HETATM   18  C   UNK     0       4.001  -0.770   0.000  0.00  0.00           C+0
HETATM   19  C   UNK     0       2.667   0.000   0.000  0.00  0.00           C+0
HETATM   20  C   UNK     0       1.334  -0.770   0.000  0.00  0.00           C+0
HETATM   21  C   UNK     0       0.000   0.000   0.000  0.00  0.00           C+0
HETATM   22  C   UNK     0       0.000   1.540   0.000  0.00  0.00           C+0
HETATM   23  C   UNK     0       1.334   2.310   0.000  0.00  0.00           C+0
HETATM   24  C   UNK     0       1.334   3.850   0.000  0.00  0.00           C+0
HETATM   25  O   UNK     0       2.667   4.620   0.000  0.00  0.00           O+0
HETATM   26  O   UNK     0       0.000   4.620   0.000  0.00  0.00           O+0
HETATM   27  C   UNK     0       2.667   1.540   0.000  0.00  0.00           C+0
HETATM   28  C   UNK     0       2.667   3.080   0.000  0.00  0.00           C+0
CONECT    1    2                                                            
CONECT    2    1    3                                                       
CONECT    3    2    4    5                                                  
CONECT    4    3                                                            
CONECT    5    3    6    7                                                  
CONECT    6    5                                                            
CONECT    7    5    8                                                       
CONECT    8    7    9   27                                                  
CONECT    9    8   10   15                                                  
CONECT   10    9   11   12                                                  
CONECT   11   10                                                            
CONECT   12   10   13   14                                                  
CONECT   13   12                                                            
CONECT   14   12   15                                                       
CONECT   15   14    9   16   18                                             
CONECT   16   15   17                                                       
CONECT   17   16                                                            
CONECT   18   15   19                                                       
CONECT   19   18   20   27                                                  
CONECT   20   19   21                                                       
CONECT   21   20   22                                                       
CONECT   22   21   23                                                       
CONECT   23   22   24   27                                                  
CONECT   24   23   25   26                                                  
CONECT   25   24                                                            
CONECT   26   24                                                            
CONECT   27   23    8   19   28                                             
CONECT   28   27                                                            
MASTER        0    0    0    0    0    0    0    0   28    0   60    0
END

View in JSmol

Synonyms

Value	Source
(4S,4AS,5S,8ar,9ar)-9a-methoxy-3,4a-dimethyl-4-{[(2Z)-2-methylbut-2-enoyl]oxy}-2-oxo-2H,4H,4ah,5H,6H,7H,8H,8ah,9H,9ah-naphtho[2,3-b]furan-5-carboxylate	Generator

Chemical Formula

C₂₁H₂₈O₇

Average Mass

392.4480 Da

Monoisotopic Mass

392.18350 Da

IUPAC Name

Not Available

Traditional Name

Not Available

CAS Registry Number

Not Available

SMILES

CO[C@@]12C[C@H]3CCC[C@H](C(O)=O)[C@@]3(C)[C@H](OC(=O)C(\C)=C/C)C1=C(C)C(=O)O2

InChI Identifier

InChI=1S/C21H28O7/c1-6-11(2)18(24)27-16-15-12(3)19(25)28-21(15,26-5)10-13-8-7-9-14(17(22)23)20(13,16)4/h6,13-14,16H,7-10H2,1-5H3,(H,22,23)/b11-6-/t13-,14-,16-,20+,21-/m1/s1

InChI Key

PLUOSPXAEMKKRW-GVHGUOPMSA-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
Ligularia dolichobotrys	LOTUS Database	35616633
Ligularia intermedia	LOTUS Database	35616633

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as terpene lactones. These are prenol lipids containing a lactone ring.

Kingdom

Organic compounds

Super Class

Lipids and lipid-like molecules

Class

Prenol lipids

Sub Class

Terpene lactones

Direct Parent

Terpene lactones

Alternative Parents

Substituents

Terpene lactone
Eremophilanolide or secoeremophilanolide
Sesquiterpenoid
Naphthofuran
Tricarboxylic acid or derivatives
Ketal
Fatty acid ester
2-furanone
Fatty acyl
Dihydrofuran
Alpha,beta-unsaturated carboxylic ester
Enoate ester
Carboxylic acid ester
Lactone
Acetal
Carboxylic acid derivative
Carboxylic acid
Oxacycle
Organoheterocyclic compound
Organic oxide
Organic oxygen compound
Hydrocarbon derivative
Carbonyl group
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

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

9328671

KEGG Compound ID

Not Available

BioCyc ID

Not Available

BiGG ID

Not Available

Wikipedia Link

Not Available

METLIN ID

Not Available

PubChem Compound

11153563

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

LOTUS database [Link]

Showing NP-Card for (4s,4as,5s,8ar,9ar)-9a-methoxy-3,4a-dimethyl-4-{[(2z)-2-methylbut-2-enoyl]oxy}-2-oxo-4h,5h,6h,7h,8h,8ah,9h-naphtho[2,3-b]furan-5-carboxylic acid (NP0240880)

MOL for NP0240880 ((4s,4as,5s,8ar,9ar)-9a-methoxy-3,4a-dimethyl-4-{[(2z)-2-methylbut-2-enoyl]oxy}-2-oxo-4h,5h,6h,7h,8h,8ah,9h-naphtho[2,3-b]furan-5-carboxylic acid)

3D MOL for NP0240880 ((4s,4as,5s,8ar,9ar)-9a-methoxy-3,4a-dimethyl-4-{[(2z)-2-methylbut-2-enoyl]oxy}-2-oxo-4h,5h,6h,7h,8h,8ah,9h-naphtho[2,3-b]furan-5-carboxylic acid)

3D SDF for NP0240880 ((4s,4as,5s,8ar,9ar)-9a-methoxy-3,4a-dimethyl-4-{[(2z)-2-methylbut-2-enoyl]oxy}-2-oxo-4h,5h,6h,7h,8h,8ah,9h-naphtho[2,3-b]furan-5-carboxylic acid)

3D-SDF for NP0240880 ((4s,4as,5s,8ar,9ar)-9a-methoxy-3,4a-dimethyl-4-{[(2z)-2-methylbut-2-enoyl]oxy}-2-oxo-4h,5h,6h,7h,8h,8ah,9h-naphtho[2,3-b]furan-5-carboxylic acid)

PDB for NP0240880 ((4s,4as,5s,8ar,9ar)-9a-methoxy-3,4a-dimethyl-4-{[(2z)-2-methylbut-2-enoyl]oxy}-2-oxo-4h,5h,6h,7h,8h,8ah,9h-naphtho[2,3-b]furan-5-carboxylic acid)

3D PDB for NP0240880 ((4s,4as,5s,8ar,9ar)-9a-methoxy-3,4a-dimethyl-4-{[(2z)-2-methylbut-2-enoyl]oxy}-2-oxo-4h,5h,6h,7h,8h,8ah,9h-naphtho[2,3-b]furan-5-carboxylic acid)

SMILES for NP0240880 ((4s,4as,5s,8ar,9ar)-9a-methoxy-3,4a-dimethyl-4-{[(2z)-2-methylbut-2-enoyl]oxy}-2-oxo-4h,5h,6h,7h,8h,8ah,9h-naphtho[2,3-b]furan-5-carboxylic acid)

INCHI for NP0240880 ((4s,4as,5s,8ar,9ar)-9a-methoxy-3,4a-dimethyl-4-{[(2z)-2-methylbut-2-enoyl]oxy}-2-oxo-4h,5h,6h,7h,8h,8ah,9h-naphtho[2,3-b]furan-5-carboxylic acid)

Structure for NP0240880 ((4s,4as,5s,8ar,9ar)-9a-methoxy-3,4a-dimethyl-4-{[(2z)-2-methylbut-2-enoyl]oxy}-2-oxo-4h,5h,6h,7h,8h,8ah,9h-naphtho[2,3-b]furan-5-carboxylic acid)

3D Structure for NP0240880 ((4s,4as,5s,8ar,9ar)-9a-methoxy-3,4a-dimethyl-4-{[(2z)-2-methylbut-2-enoyl]oxy}-2-oxo-4h,5h,6h,7h,8h,8ah,9h-naphtho[2,3-b]furan-5-carboxylic acid)