NP-MRD: Showing NP-Card for (4s,4as,5s,8s,8as)-8,8a-dihydroxy-3,4a,5-trimethyl-9-oxo-4h,5h,6h,7h,8h-naphtho[2,3-b]furan-4-yl (2z)-2-methylbut-2-enoate (NP0285608)

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Record Information

Version

2.0

Created at

2022-09-09 13:51:22 UTC

Updated at

2022-09-09 13:51:22 UTC

NP-MRD ID

NP0285608

Secondary Accession Numbers

None

Natural Product Identification

Common Name

(4s,4as,5s,8s,8as)-8,8a-dihydroxy-3,4a,5-trimethyl-9-oxo-4h,5h,6h,7h,8h-naphtho[2,3-b]furan-4-yl (2z)-2-methylbut-2-enoate

Description

6Beta-Angeloyloxy-2,3-didesoxyhiliardinol belongs to the class of organic compounds known as eremophilane, 8,9-secoeremophilane and furoeremophilane sesquiterpenoids. These are sesquiterpenoids with a structure based either on the eremophilane skeleton, its 8,9-seco derivative, or the furoeremophilane skeleton. Eremophilanes have been shown to be derived from eudesmanes by migration of the methyl group at C-10 to C-5. (4s,4as,5s,8s,8as)-8,8a-dihydroxy-3,4a,5-trimethyl-9-oxo-4h,5h,6h,7h,8h-naphtho[2,3-b]furan-4-yl (2z)-2-methylbut-2-enoate is found in Ligularia atroviolacea. Based on a literature review very few articles have been published on 6beta-Angeloyloxy-2,3-didesoxyhiliardinol.

Structure

MOL 3D MOL SDF PDB SMILES InChI


  Mrv1652309092215512D          

 26 28  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
    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  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
    2.1434   -1.2375    0.0000 O   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
    1.4289   -0.8250    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.7145   -0.4125    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    0.7145   -1.2375    0.0000 O   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    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  1  0  0  0  0
 10 11  1  0  0  0  0
 10 12  2  0  0  0  0
 12 13  1  0  0  0  0
 13 14  1  0  0  0  0
  9 14  2  0  0  0  0
 14 15  1  0  0  0  0
 15 16  2  0  0  0  0
 15 17  1  0  0  0  0
 17 18  1  6  0  0  0
 17 19  1  0  0  0  0
 19 20  1  1  0  0  0
 19 21  1  0  0  0  0
 21 22  1  0  0  0  0
 22 23  1  0  0  0  0
 23 24  1  6  0  0  0
 23 25  1  0  0  0  0
  8 25  1  0  0  0  0
 17 25  1  0  0  0  0
 25 26  1  6  0  0  0
M  END

     RDKit          3D

 52 54  0  0  0  0  0  0  0  0999 V2000
    4.9978    0.7233    1.0887 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.3955   -0.1243    2.1381 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.0864   -0.3283    2.0919 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.4966   -1.1769    3.1458 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.2760    0.2645    1.0416 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.7167    0.9802    0.1380 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.9166    0.0163    1.0453 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.0098    0.5211    0.0953 C   0  0  2  0  0  0  0  0  0  0  0  0
   -1.0215    1.3814    0.6535 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1722    2.7215    0.7982 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2418    3.8350    0.3970 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3952    2.9307    1.4132 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.9629    1.7571    1.6321 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1506    0.7950    1.1806 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2316   -0.6525    1.1454 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8185   -1.2501    2.0819 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6200   -1.3775    0.0063 C   0  0  1  0  0  0  0  0  0  0  0  0
   -1.0017   -2.5170    0.5980 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6929   -1.9972   -0.8630 C   0  0  1  0  0  0  0  0  0  0  0  0
   -3.7462   -2.4239   -0.0945 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.2099   -1.0301   -1.8995 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0340   -0.7696   -2.8094 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0010   -0.0292   -2.0341 C   0  0  2  0  0  0  0  0  0  0  0  0
    0.1445    0.2468   -2.9757 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5782   -0.6297   -0.7320 C   0  0  1  0  0  0  0  0  0  0  0  0
    0.5384   -1.6254   -1.0787 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.6774    1.7727    1.1156 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.1070    0.7571    1.3026 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.9265    0.2409    0.0939 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.0076   -0.5756    2.9365 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.1592   -2.1183    2.6623 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.1537   -1.3371    3.9989 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.5420   -0.6622    3.4593 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.6154    1.1264   -0.6089 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7859    4.7195    0.0480 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.4652    3.5295   -0.3751 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.2710    4.1490    1.3509 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8494    3.8878    1.6876 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5503   -2.2910    1.4293 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2169   -2.8393   -1.4070 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.7142   -3.4258   -0.0185 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5716   -0.0884   -1.4891 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.9742   -1.5777   -2.4929 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6654   -1.7019   -3.2757 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3761   -0.1183   -3.6288 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4469    0.9785   -1.7815 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1639    1.1009   -3.6178 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.3245   -0.5945   -3.6780 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.0774    0.5599   -2.4737 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.7370   -2.2750   -0.1760 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.4447   -1.1436   -1.4277 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.1057   -2.3147   -1.8379 H   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0
  2  3  2  0
  3  4  1  0
  3  5  1  0
  5  6  2  0
  5  7  1  0
  7  8  1  0
  8  9  1  0
  9 14  2  0
 14 13  1  0
 13 12  1  0
 12 10  2  0
 10 11  1  0
 14 15  1  0
 15 16  2  0
 15 17  1  0
 17 18  1  1
 17 19  1  0
 19 20  1  0
 19 21  1  0
 21 22  1  0
 22 23  1  0
 23 24  1  0
 23 25  1  0
 25 26  1  6
 25  8  1  0
 10  9  1  0
 25 17  1  0
  1 27  1  0
  1 28  1  0
  1 29  1  0
  2 30  1  0
  4 31  1  0
  4 32  1  0
  4 33  1  0
  8 34  1  6
 12 38  1  0
 11 35  1  0
 11 36  1  0
 11 37  1  0
 18 39  1  0
 19 40  1  6
 20 41  1  0
 21 42  1  0
 21 43  1  0
 22 44  1  0
 22 45  1  0
 23 46  1  1
 24 47  1  0
 24 48  1  0
 24 49  1  0
 26 50  1  0
 26 51  1  0
 26 52  1  0
M  END


  Mrv1652309092215512D          

 26 28  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
    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  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
    2.1434   -1.2375    0.0000 O   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
    1.4289   -0.8250    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.7145   -0.4125    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    0.7145   -1.2375    0.0000 O   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    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  1  0  0  0  0
 10 11  1  0  0  0  0
 10 12  2  0  0  0  0
 12 13  1  0  0  0  0
 13 14  1  0  0  0  0
  9 14  2  0  0  0  0
 14 15  1  0  0  0  0
 15 16  2  0  0  0  0
 15 17  1  0  0  0  0
 17 18  1  6  0  0  0
 17 19  1  0  0  0  0
 19 20  1  1  0  0  0
 19 21  1  0  0  0  0
 21 22  1  0  0  0  0
 22 23  1  0  0  0  0
 23 24  1  6  0  0  0
 23 25  1  0  0  0  0
  8 25  1  0  0  0  0
 17 25  1  0  0  0  0
 25 26  1  6  0  0  0
M  END
> <DATABASE_ID>
NP0285608

> <DATABASE_NAME>
NP-MRD

> <SMILES>
C\C=C(\C)C(=O)O[C@@H]1C2=C(OC=C2C)C(=O)[C@@]2(O)[C@@H](O)CC[C@H](C)[C@@]12C

> <INCHI_IDENTIFIER>
InChI=1S/C20H26O6/c1-6-10(2)18(23)26-17-14-11(3)9-25-15(14)16(22)20(24)13(21)8-7-12(4)19(17,20)5/h6,9,12-13,17,21,24H,7-8H2,1-5H3/b10-6-/t12-,13-,17+,19-,20-/m0/s1

> <INCHI_KEY>
OVZYDQPLJDOTDE-IFVLMOTPSA-N

> <FORMULA>
C20H26O6

> <MOLECULAR_WEIGHT>
362.422

> <EXACT_MASS>
362.172938557

> <JCHEM_ACCEPTOR_COUNT>
4

> <JCHEM_ATOM_COUNT>
52

> <JCHEM_AVERAGE_POLARIZABILITY>
37.91886870333346

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
2

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
1

> <JCHEM_IUPAC>
(4S,4aS,5S,8S,8aS)-8,8a-dihydroxy-3,4a,5-trimethyl-9-oxo-4H,4aH,5H,6H,7H,8H,8aH,9H-naphtho[2,3-b]furan-4-yl (2Z)-2-methylbut-2-enoate

> <JCHEM_LOGP>
3.012980617666666

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
3

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA>
14.581803622736832

> <JCHEM_PKA_STRONGEST_ACIDIC>
11.488292593190716

> <JCHEM_PKA_STRONGEST_BASIC>
-2.9656714444575756

> <JCHEM_POLAR_SURFACE_AREA>
96.97

> <JCHEM_REFRACTIVITY>
95.25819999999997

> <JCHEM_ROTATABLE_BOND_COUNT>
3

> <JCHEM_RULE_OF_FIVE>
1

> <JCHEM_TRADITIONAL_IUPAC>
(4S,4aS,5S,8S,8aS)-8,8a-dihydroxy-3,4a,5-trimethyl-9-oxo-4H,5H,6H,7H,8H-naphtho[2,3-b]furan-4-yl (2Z)-2-methylbut-2-enoate

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 09-SEP-22   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   09-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       6.799  -0.476   0.000  0.00  0.00           O+0
HETATM   14  C   UNK     0       5.335   0.000   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0       4.001  -0.770   0.000  0.00  0.00           C+0
HETATM   16  O   UNK     0       4.001  -2.310   0.000  0.00  0.00           O+0
HETATM   17  C   UNK     0       2.667   0.000   0.000  0.00  0.00           C+0
HETATM   18  O   UNK     0       2.667  -1.540   0.000  0.00  0.00           O+0
HETATM   19  C   UNK     0       1.334  -0.770   0.000  0.00  0.00           C+0
HETATM   20  O   UNK     0       1.334  -2.310   0.000  0.00  0.00           O+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  C   UNK     0       2.667   1.540   0.000  0.00  0.00           C+0
HETATM   26  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   25                                                  
CONECT    9    8   10   14                                                  
CONECT   10    9   11   12                                                  
CONECT   11   10                                                            
CONECT   12   10   13                                                       
CONECT   13   12   14                                                       
CONECT   14   13    9   15                                                  
CONECT   15   14   16   17                                                  
CONECT   16   15                                                            
CONECT   17   15   18   19   25                                             
CONECT   18   17                                                            
CONECT   19   17   20   21                                                  
CONECT   20   19                                                            
CONECT   21   19   22                                                       
CONECT   22   21   23                                                       
CONECT   23   22   24   25                                                  
CONECT   24   23                                                            
CONECT   25   23    8   17   26                                             
CONECT   26   25                                                            
MASTER        0    0    0    0    0    0    0    0   26    0   56    0
END

View in JSmol

Synonyms

Value	Source
6b-Angeloyloxy-2,3-didesoxyhiliardinol	Generator
6Β-angeloyloxy-2,3-didesoxyhiliardinol	Generator

Chemical Formula

C₂₀H₂₆O₆

Average Mass

362.4220 Da

Monoisotopic Mass

362.17294 Da

IUPAC Name

Not Available

Traditional Name

Not Available

CAS Registry Number

Not Available

SMILES

C\C=C(\C)C(=O)O[C@@H]1C2=C(OC=C2C)C(=O)[C@@]2(O)[C@@H](O)CC[C@H](C)[C@@]12C

InChI Identifier

InChI=1S/C20H26O6/c1-6-10(2)18(23)26-17-14-11(3)9-25-15(14)16(22)20(24)13(21)8-7-12(4)19(17,20)5/h6,9,12-13,17,21,24H,7-8H2,1-5H3/b10-6-/t12-,13-,17+,19-,20-/m0/s1

InChI Key

OVZYDQPLJDOTDE-IFVLMOTPSA-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 atroviolacea	LOTUS Database	35616633

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as eremophilane, 8,9-secoeremophilane and furoeremophilane sesquiterpenoids. These are sesquiterpenoids with a structure based either on the eremophilane skeleton, its 8,9-seco derivative, or the furoeremophilane skeleton. Eremophilanes have been shown to be derived from eudesmanes by migration of the methyl group at C-10 to C-5.

Kingdom

Organic compounds

Super Class

Lipids and lipid-like molecules

Class

Prenol lipids

Sub Class

Sesquiterpenoids

Direct Parent

Eremophilane, 8,9-secoeremophilane and furoeremophilane sesquiterpenoids

Alternative Parents

Substituents

Furoeremophilane sesquiterpenoid
Naphthofuran
Benzofuran
Aryl alkyl ketone
Aryl ketone
Fatty acid ester
Fatty acyl
Cyclic alcohol
Heteroaromatic compound
Furan
Alpha,beta-unsaturated carboxylic ester
Enoate ester
Tertiary alcohol
1,2-diol
Carboxylic acid ester
Ketone
Secondary alcohol
Oxacycle
Carboxylic acid derivative
Monocarboxylic acid or derivatives
Organoheterocyclic compound
Hydrocarbon derivative
Organic oxide
Alcohol
Carbonyl group
Organooxygen compound
Organic oxygen compound
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

Not Available

Chemspider ID

10219141

KEGG Compound ID

Not Available

BioCyc ID

Not Available

BiGG ID

Not Available

Wikipedia Link

Not Available

METLIN ID

Not Available

PubChem Compound

21595083

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,8s,8as)-8,8a-dihydroxy-3,4a,5-trimethyl-9-oxo-4h,5h,6h,7h,8h-naphtho[2,3-b]furan-4-yl (2z)-2-methylbut-2-enoate (NP0285608)

MOL for NP0285608 ((4s,4as,5s,8s,8as)-8,8a-dihydroxy-3,4a,5-trimethyl-9-oxo-4h,5h,6h,7h,8h-naphtho[2,3-b]furan-4-yl (2z)-2-methylbut-2-enoate)

3D MOL for NP0285608 ((4s,4as,5s,8s,8as)-8,8a-dihydroxy-3,4a,5-trimethyl-9-oxo-4h,5h,6h,7h,8h-naphtho[2,3-b]furan-4-yl (2z)-2-methylbut-2-enoate)

3D SDF for NP0285608 ((4s,4as,5s,8s,8as)-8,8a-dihydroxy-3,4a,5-trimethyl-9-oxo-4h,5h,6h,7h,8h-naphtho[2,3-b]furan-4-yl (2z)-2-methylbut-2-enoate)

3D-SDF for NP0285608 ((4s,4as,5s,8s,8as)-8,8a-dihydroxy-3,4a,5-trimethyl-9-oxo-4h,5h,6h,7h,8h-naphtho[2,3-b]furan-4-yl (2z)-2-methylbut-2-enoate)

PDB for NP0285608 ((4s,4as,5s,8s,8as)-8,8a-dihydroxy-3,4a,5-trimethyl-9-oxo-4h,5h,6h,7h,8h-naphtho[2,3-b]furan-4-yl (2z)-2-methylbut-2-enoate)

3D PDB for NP0285608 ((4s,4as,5s,8s,8as)-8,8a-dihydroxy-3,4a,5-trimethyl-9-oxo-4h,5h,6h,7h,8h-naphtho[2,3-b]furan-4-yl (2z)-2-methylbut-2-enoate)

SMILES for NP0285608 ((4s,4as,5s,8s,8as)-8,8a-dihydroxy-3,4a,5-trimethyl-9-oxo-4h,5h,6h,7h,8h-naphtho[2,3-b]furan-4-yl (2z)-2-methylbut-2-enoate)

INCHI for NP0285608 ((4s,4as,5s,8s,8as)-8,8a-dihydroxy-3,4a,5-trimethyl-9-oxo-4h,5h,6h,7h,8h-naphtho[2,3-b]furan-4-yl (2z)-2-methylbut-2-enoate)

Structure for NP0285608 ((4s,4as,5s,8s,8as)-8,8a-dihydroxy-3,4a,5-trimethyl-9-oxo-4h,5h,6h,7h,8h-naphtho[2,3-b]furan-4-yl (2z)-2-methylbut-2-enoate)

3D Structure for NP0285608 ((4s,4as,5s,8s,8as)-8,8a-dihydroxy-3,4a,5-trimethyl-9-oxo-4h,5h,6h,7h,8h-naphtho[2,3-b]furan-4-yl (2z)-2-methylbut-2-enoate)