NP-MRD: Showing NP-Card for (3s,3as,6as,9s,10r)-4-formyl-3,10-dihydroxy-7,7-dimethyl-1-oxo-3h,3ah,6h,6ah,8h,9h,10h-naphtho[1,8a-c]furan-9-yl 2-hydroxyoctanoate (NP0239001)

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Record Information

Version

2.0

Created at

2022-09-06 22:29:57 UTC

Updated at

2022-09-06 22:29:57 UTC

NP-MRD ID

NP0239001

Secondary Accession Numbers

None

Natural Product Identification

Common Name

(3s,3as,6as,9s,10r)-4-formyl-3,10-dihydroxy-7,7-dimethyl-1-oxo-3h,3ah,6h,6ah,8h,9h,10h-naphtho[1,8a-c]furan-9-yl 2-hydroxyoctanoate

Description

Mniopetal C belongs to the class of organic compounds known as sugar acids and derivatives. Sugar acids and derivatives are compounds containing a saccharide unit which bears a carboxylic acid group. Based on a literature review very few articles have been published on Mniopetal C.

Structure

MOL 3D MOL SDF PDB SMILES InChI


  Mrv1652309072200292D          

 31 33  0  0  1  0            999 V2000
    3.5787   -5.4895    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.2580   -5.0214    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.0209   -5.3841    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.7225   -4.9127    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.4498   -5.3563    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.1034   -4.8282    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.7434   -5.3694    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.6328   -6.1870    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    8.5006   -5.0589    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.3987   -4.2402    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    9.2702   -5.3841    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   10.0311   -4.7745    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    9.9998   -3.9501    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   10.6980   -3.5108    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   10.2594   -2.7645    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   11.0782   -2.7138    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   11.4277   -3.8958    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
   12.1259   -3.4565    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   12.8556   -3.8415    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   12.8869   -4.6659    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   13.6747   -5.0161    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   14.4434   -4.6572    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   12.1887   -5.1053    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
   12.0480   -5.9182    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
   12.6081   -6.5764    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   11.2313   -6.0355    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   10.9018   -5.4066    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    9.9885   -5.4223    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   11.4590   -4.7202    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   10.7608   -5.1596    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
   10.4305   -6.0428    0.0000 O   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  1  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
  7  9  1  0  0  0  0
  9 10  2  0  0  0  0
  9 11  1  0  0  0  0
 12 11  1  1  0  0  0
 12 13  1  0  0  0  0
 13 14  1  0  0  0  0
 14 15  1  0  0  0  0
 14 16  1  0  0  0  0
 14 17  1  0  0  0  0
 17 18  1  6  0  0  0
 18 19  1  0  0  0  0
 19 20  2  0  0  0  0
 20 21  1  0  0  0  0
 21 22  2  0  0  0  0
 23 20  1  6  0  0  0
 23 24  1  0  0  0  0
 24 25  1  1  0  0  0
 24 26  1  0  0  0  0
 26 27  1  0  0  0  0
 27 28  2  0  0  0  0
 27 29  1  0  0  0  0
 23 29  1  0  0  0  0
 17 29  1  0  0  0  0
 29 30  1  0  0  0  0
 12 30  1  0  0  0  0
 30 31  1  1  0  0  0
M  END

     RDKit          3D

 65 67  0  0  0  0  0  0  0  0999 V2000
    5.9643   -0.0828   -1.7327 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.0251    0.2822   -0.7614 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.7033    0.1596    0.6817 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.3437   -1.1753    1.2023 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.0984   -1.8176    0.7281 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.8490   -1.0174    1.1081 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.6203   -1.6988    0.5837 C   0  0  2  0  0  0  0  0  0  0  0  0
    2.7146   -1.7843   -0.8070 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.3769   -1.0227    0.9653 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.0937   -0.8407    2.1796 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.4918   -0.5713    0.0273 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7402    0.0967    0.3283 C   0  0  1  0  0  0  0  0  0  0  0  0
   -0.7626    1.4432   -0.2435 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0292    1.9642   -0.8165 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7209    2.5104   -2.2271 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6164    3.1326   -0.0634 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.0803    0.9012   -1.0390 C   0  0  2  0  0  0  0  0  0  0  0  0
   -4.3471    1.4523   -1.5685 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.5267    1.0340   -0.8039 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.5499   -0.1185   -0.1689 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.7602   -0.4530    0.5607 C   0  0  0  0  0  0  0  0  0  0  0  0
   -7.7121    0.4092    0.5349 O   0  0  0  0  0  0  0  0  0  0  0  0
   -4.3608   -1.0229   -0.2114 C   0  0  2  0  0  0  0  0  0  0  0  0
   -4.3188   -1.8297    1.0435 C   0  0  1  0  0  0  0  0  0  0  0  0
   -3.6269   -3.0340    0.8943 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.7623   -0.9705    2.0111 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.3594    0.2419    1.3986 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.2768    1.2564    2.1116 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.1547   -0.1229    0.0158 C   0  0  2  0  0  0  0  0  0  0  0  0
   -1.8330   -0.8640   -0.0616 C   0  0  1  0  0  0  0  0  0  0  0  0
   -1.5914   -1.3973   -1.3192 O   0  0  0  0  0  0  0  0  0  0  0  0
    6.1094   -1.1003   -2.1739 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.1018    0.5992   -2.6431 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.9532    0.0890   -1.3433 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.3103    1.3587   -0.9610 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.9835   -0.2832   -1.0193 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.8862    0.9061    0.9287 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.5814    0.5839    1.2703 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.3892   -1.2219    2.3274 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.1904   -1.8789    0.8998 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.0084   -2.7901    1.3231 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.0637   -2.0537   -0.3404 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.9427   -0.0190    0.7072 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.7836   -1.0123    2.2426 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.6288   -2.7693    0.9432 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.7637   -0.8874   -1.2240 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7548    0.1324    1.4603 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4517    2.1752    0.5646 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.0852    1.5298   -0.9862 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7466    3.0382   -2.1877 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5945    1.6721   -2.9412 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4832    3.2340   -2.5364 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0198    3.3473    0.8746 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.6951    3.0636    0.1347 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5140    4.1089   -0.6278 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6420    0.3202   -1.9343 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.5759    1.1137   -2.6347 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.3146    2.5752   -1.7098 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.3667    1.7043   -0.7841 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.9669   -1.3309    1.1214 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.2981   -1.6006   -1.1340 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.3112   -2.1204    1.4220 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.2713   -3.6510    0.4314 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8438   -1.6629    0.6720 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0827   -2.2303   -1.2947 H   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0
  2  3  1  0
  3  4  1  0
  4  5  1  0
  5  6  1  0
  6  7  1  0
  7  8  1  0
  7  9  1  0
  9 10  2  0
  9 11  1  0
 11 12  1  0
 12 13  1  0
 13 14  1  0
 14 15  1  0
 14 16  1  0
 14 17  1  0
 17 18  1  0
 18 19  1  0
 19 20  2  0
 20 21  1  0
 21 22  2  0
 20 23  1  0
 23 24  1  0
 24 25  1  0
 24 26  1  0
 26 27  1  0
 27 28  2  0
 29 27  1  1
 29 30  1  0
 30 31  1  0
 30 12  1  0
 29 17  1  0
 29 23  1  0
  1 32  1  0
  1 33  1  0
  1 34  1  0
  2 35  1  0
  2 36  1  0
  3 37  1  0
  3 38  1  0
  4 39  1  0
  4 40  1  0
  5 41  1  0
  5 42  1  0
  6 43  1  0
  6 44  1  0
  7 45  1  1
  8 46  1  0
 12 47  1  1
 13 48  1  0
 13 49  1  0
 15 50  1  0
 15 51  1  0
 15 52  1  0
 16 53  1  0
 16 54  1  0
 16 55  1  0
 17 56  1  6
 18 57  1  0
 18 58  1  0
 19 59  1  0
 21 60  1  0
 23 61  1  6
 24 62  1  1
 25 63  1  0
 30 64  1  1
 31 65  1  0
M  END


  Mrv1652309072200292D          

 31 33  0  0  1  0            999 V2000
    3.5787   -5.4895    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.2580   -5.0214    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.0209   -5.3841    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.7225   -4.9127    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.4498   -5.3563    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.1034   -4.8282    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.7434   -5.3694    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.6328   -6.1870    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    8.5006   -5.0589    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.3987   -4.2402    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    9.2702   -5.3841    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   10.0311   -4.7745    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    9.9998   -3.9501    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   10.6980   -3.5108    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   10.2594   -2.7645    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   11.0782   -2.7138    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   11.4277   -3.8958    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
   12.1259   -3.4565    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   12.8556   -3.8415    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   12.8869   -4.6659    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   13.6747   -5.0161    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   14.4434   -4.6572    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   12.1887   -5.1053    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
   12.0480   -5.9182    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
   12.6081   -6.5764    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   11.2313   -6.0355    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   10.9018   -5.4066    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    9.9885   -5.4223    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   11.4590   -4.7202    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   10.7608   -5.1596    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
   10.4305   -6.0428    0.0000 O   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  1  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
  7  9  1  0  0  0  0
  9 10  2  0  0  0  0
  9 11  1  0  0  0  0
 12 11  1  1  0  0  0
 12 13  1  0  0  0  0
 13 14  1  0  0  0  0
 14 15  1  0  0  0  0
 14 16  1  0  0  0  0
 14 17  1  0  0  0  0
 17 18  1  6  0  0  0
 18 19  1  0  0  0  0
 19 20  2  0  0  0  0
 20 21  1  0  0  0  0
 21 22  2  0  0  0  0
 23 20  1  6  0  0  0
 23 24  1  0  0  0  0
 24 25  1  1  0  0  0
 24 26  1  0  0  0  0
 26 27  1  0  0  0  0
 27 28  2  0  0  0  0
 27 29  1  0  0  0  0
 23 29  1  0  0  0  0
 17 29  1  0  0  0  0
 29 30  1  0  0  0  0
 12 30  1  0  0  0  0
 30 31  1  1  0  0  0
M  END
> <DATABASE_ID>
NP0239001

> <DATABASE_NAME>
NP-MRD

> <SMILES>
CCCCCCC(O)C(=O)O[C@H]1CC(C)(C)[C@@H]2CC=C(C=O)[C@@H]3[C@@H](O)OC(=O)C23[C@H]1O

> <INCHI_IDENTIFIER>
InChI=1S/C23H34O8/c1-4-5-6-7-8-14(25)19(27)30-15-11-22(2,3)16-10-9-13(12-24)17-20(28)31-21(29)23(16,17)18(15)26/h9,12,14-18,20,25-26,28H,4-8,10-11H2,1-3H3/t14?,15-,16-,17+,18-,20-,23?/m0/s1

> <INCHI_KEY>
DSJKYHXDKAFGAJ-JGDXHKBCSA-N

> <FORMULA>
C23H34O8

> <MOLECULAR_WEIGHT>
438.517

> <EXACT_MASS>
438.225368055

> <JCHEM_ACCEPTOR_COUNT>
6

> <JCHEM_ATOM_COUNT>
65

> <JCHEM_AVERAGE_POLARIZABILITY>
45.94441001800229

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
3

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
1

> <JCHEM_IUPAC>
(3S,6aS,9S,10R,10bS)-4-formyl-3,10-dihydroxy-7,7-dimethyl-1-oxo-1H,3H,6H,6aH,7H,8H,9H,10H,10bH-naphtho[1,8a-c]furan-9-yl 2-hydroxyoctanoate

> <JCHEM_LOGP>
1.9620981543333338

> <JCHEM_MDDR_LIKE_RULE>
1

> <JCHEM_NUMBER_OF_RINGS>
3

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA>
12.69904742370596

> <JCHEM_PKA_STRONGEST_ACIDIC>
11.842895285205866

> <JCHEM_PKA_STRONGEST_BASIC>
-3.4805454213775295

> <JCHEM_POLAR_SURFACE_AREA>
130.35999999999999

> <JCHEM_REFRACTIVITY>
110.65519999999997

> <JCHEM_ROTATABLE_BOND_COUNT>
9

> <JCHEM_RULE_OF_FIVE>
1

> <JCHEM_TRADITIONAL_IUPAC>
(3S,6aS,9S,10R,10bS)-4-formyl-3,10-dihydroxy-7,7-dimethyl-1-oxo-3H,6H,6aH,8H,9H,10H,10bH-naphtho[1,8a-c]furan-9-yl 2-hydroxyoctanoate

> <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       6.680 -10.247   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0       7.948  -9.373   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0       9.372 -10.050   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0      10.682  -9.170   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0      12.040  -9.998   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0      13.260  -9.013   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0      14.454 -10.023   0.000  0.00  0.00           C+0
HETATM    8  O   UNK     0      14.248 -11.549   0.000  0.00  0.00           O+0
HETATM    9  C   UNK     0      15.868  -9.443   0.000  0.00  0.00           C+0
HETATM   10  O   UNK     0      15.678  -7.915   0.000  0.00  0.00           O+0
HETATM   11  O   UNK     0      17.304 -10.050   0.000  0.00  0.00           O+0
HETATM   12  C   UNK     0      18.725  -8.912   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0      18.666  -7.374   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0      19.970  -6.553   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0      19.151  -5.160   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0      20.679  -5.066   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0      21.332  -7.272   0.000  0.00  0.00           C+0
HETATM   18  C   UNK     0      22.635  -6.452   0.000  0.00  0.00           C+0
HETATM   19  C   UNK     0      23.997  -7.171   0.000  0.00  0.00           C+0
HETATM   20  C   UNK     0      24.056  -8.710   0.000  0.00  0.00           C+0
HETATM   21  C   UNK     0      25.526  -9.363   0.000  0.00  0.00           C+0
HETATM   22  O   UNK     0      26.961  -8.694   0.000  0.00  0.00           O+0
HETATM   23  C   UNK     0      22.752  -9.530   0.000  0.00  0.00           C+0
HETATM   24  C   UNK     0      22.490 -11.047   0.000  0.00  0.00           C+0
HETATM   25  O   UNK     0      23.535 -12.276   0.000  0.00  0.00           O+0
HETATM   26  O   UNK     0      20.965 -11.266   0.000  0.00  0.00           O+0
HETATM   27  C   UNK     0      20.350 -10.092   0.000  0.00  0.00           C+0
HETATM   28  O   UNK     0      18.645 -10.122   0.000  0.00  0.00           O+0
HETATM   29  C   UNK     0      21.390  -8.811   0.000  0.00  0.00           C+0
HETATM   30  C   UNK     0      20.087  -9.631   0.000  0.00  0.00           C+0
HETATM   31  O   UNK     0      19.470 -11.280   0.000  0.00  0.00           O+0
CONECT    1    2                                                            
CONECT    2    1    3                                                       
CONECT    3    2    4                                                       
CONECT    4    3    5                                                       
CONECT    5    4    6                                                       
CONECT    6    5    7                                                       
CONECT    7    6    8    9                                                  
CONECT    8    7                                                            
CONECT    9    7   10   11                                                  
CONECT   10    9                                                            
CONECT   11    9   12                                                       
CONECT   12   11   13   30                                                  
CONECT   13   12   14                                                       
CONECT   14   13   15   16   17                                             
CONECT   15   14                                                            
CONECT   16   14                                                            
CONECT   17   14   18   29                                                  
CONECT   18   17   19                                                       
CONECT   19   18   20                                                       
CONECT   20   19   21   23                                                  
CONECT   21   20   22                                                       
CONECT   22   21                                                            
CONECT   23   20   24   29                                                  
CONECT   24   23   25   26                                                  
CONECT   25   24                                                            
CONECT   26   24   27                                                       
CONECT   27   26   28   29                                                  
CONECT   28   27                                                            
CONECT   29   27   23   17   30                                             
CONECT   30   29   12   31                                                  
CONECT   31   30                                                            
MASTER        0    0    0    0    0    0    0    0   31    0   66    0
END

View in JSmol

Synonyms

Not Available

Chemical Formula

C₂₃H₃₄O₈

Average Mass

438.5170 Da

Monoisotopic Mass

438.22537 Da

IUPAC Name

Not Available

Traditional Name

Not Available

CAS Registry Number

Not Available

SMILES

CCCCCCC(O)C(=O)O[C@H]1CC(C)(C)[C@@H]2CC=C(C=O)[C@@H]3[C@@H](O)OC(=O)C23[C@H]1O

InChI Identifier

InChI=1S/C23H34O8/c1-4-5-6-7-8-14(25)19(27)30-15-11-22(2,3)16-10-9-13(12-24)17-20(28)31-21(29)23(16,17)18(15)26/h9,12,14-18,20,25-26,28H,4-8,10-11H2,1-3H3/t14?,15-,16-,17+,18-,20-,23?/m0/s1

InChI Key

DSJKYHXDKAFGAJ-JGDXHKBCSA-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

Not Available

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as sugar acids and derivatives. Sugar acids and derivatives are compounds containing a saccharide unit which bears a carboxylic acid group.

Kingdom

Organic compounds

Super Class

Organic oxygen compounds

Class

Organooxygen compounds

Sub Class

Carbohydrates and carbohydrate conjugates

Direct Parent

Sugar acids and derivatives

Alternative Parents

Substituents

Octose monosaccharide
Naphthofuran
Fatty alcohol
Sugar acid
Fatty acid ester
Fatty acyl
Monosaccharide
Gamma butyrolactone
Dicarboxylic acid or derivatives
Tetrahydrofuran
Cyclic alcohol
Secondary alcohol
Lactone
Hemiacetal
Carboxylic acid ester
Oxacycle
Organoheterocyclic compound
Carboxylic acid derivative
Organic oxide
Hydrocarbon derivative
Carbonyl group
Aldehyde
Alcohol
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

C00016641

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

101666702

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

LOTUS database [Link]

Showing NP-Card for (3s,3as,6as,9s,10r)-4-formyl-3,10-dihydroxy-7,7-dimethyl-1-oxo-3h,3ah,6h,6ah,8h,9h,10h-naphtho[1,8a-c]furan-9-yl 2-hydroxyoctanoate (NP0239001)

MOL for NP0239001 ((3s,3as,6as,9s,10r)-4-formyl-3,10-dihydroxy-7,7-dimethyl-1-oxo-3h,3ah,6h,6ah,8h,9h,10h-naphtho[1,8a-c]furan-9-yl 2-hydroxyoctanoate)

3D MOL for NP0239001 ((3s,3as,6as,9s,10r)-4-formyl-3,10-dihydroxy-7,7-dimethyl-1-oxo-3h,3ah,6h,6ah,8h,9h,10h-naphtho[1,8a-c]furan-9-yl 2-hydroxyoctanoate)

3D SDF for NP0239001 ((3s,3as,6as,9s,10r)-4-formyl-3,10-dihydroxy-7,7-dimethyl-1-oxo-3h,3ah,6h,6ah,8h,9h,10h-naphtho[1,8a-c]furan-9-yl 2-hydroxyoctanoate)

3D-SDF for NP0239001 ((3s,3as,6as,9s,10r)-4-formyl-3,10-dihydroxy-7,7-dimethyl-1-oxo-3h,3ah,6h,6ah,8h,9h,10h-naphtho[1,8a-c]furan-9-yl 2-hydroxyoctanoate)

PDB for NP0239001 ((3s,3as,6as,9s,10r)-4-formyl-3,10-dihydroxy-7,7-dimethyl-1-oxo-3h,3ah,6h,6ah,8h,9h,10h-naphtho[1,8a-c]furan-9-yl 2-hydroxyoctanoate)

3D PDB for NP0239001 ((3s,3as,6as,9s,10r)-4-formyl-3,10-dihydroxy-7,7-dimethyl-1-oxo-3h,3ah,6h,6ah,8h,9h,10h-naphtho[1,8a-c]furan-9-yl 2-hydroxyoctanoate)

SMILES for NP0239001 ((3s,3as,6as,9s,10r)-4-formyl-3,10-dihydroxy-7,7-dimethyl-1-oxo-3h,3ah,6h,6ah,8h,9h,10h-naphtho[1,8a-c]furan-9-yl 2-hydroxyoctanoate)

INCHI for NP0239001 ((3s,3as,6as,9s,10r)-4-formyl-3,10-dihydroxy-7,7-dimethyl-1-oxo-3h,3ah,6h,6ah,8h,9h,10h-naphtho[1,8a-c]furan-9-yl 2-hydroxyoctanoate)

Structure for NP0239001 ((3s,3as,6as,9s,10r)-4-formyl-3,10-dihydroxy-7,7-dimethyl-1-oxo-3h,3ah,6h,6ah,8h,9h,10h-naphtho[1,8a-c]furan-9-yl 2-hydroxyoctanoate)

3D Structure for NP0239001 ((3s,3as,6as,9s,10r)-4-formyl-3,10-dihydroxy-7,7-dimethyl-1-oxo-3h,3ah,6h,6ah,8h,9h,10h-naphtho[1,8a-c]furan-9-yl 2-hydroxyoctanoate)