NP-MRD: Showing NP-Card for methyl (3r)-5-[(6ar,7r,8s,10as)-7,8-dimethyl-3,9-dioxo-1h,5h,6h,6ah,8h,10h-naphtho[4,4a-c]furan-7-yl]-3-(hydroxymethyl)pentanoate (NP0257532)

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Record Information

Version

2.0

Created at

2022-09-07 22:40:50 UTC

Updated at

2022-09-07 22:40:51 UTC

NP-MRD ID

NP0257532

Secondary Accession Numbers

None

Natural Product Identification

Common Name

methyl (3r)-5-[(6ar,7r,8s,10as)-7,8-dimethyl-3,9-dioxo-1h,5h,6h,6ah,8h,10h-naphtho[4,4a-c]furan-7-yl]-3-(hydroxymethyl)pentanoate

Description

Methyl (3R)-5-[(6aR,7R,8S,10aS)-7,8-dimethyl-3,9-dioxo-1H,3H,5H,6H,6aH,7H,8H,9H,10H-naphtho[4,4a-c]furan-7-yl]-3-(hydroxymethyl)pentanoate belongs to the class of organic compounds known as diterpene lactones. These are diterpenoids containing a lactone moiety. Based on a literature review very few articles have been published on methyl (3R)-5-[(6aR,7R,8S,10aS)-7,8-dimethyl-3,9-dioxo-1H,3H,5H,6H,6aH,7H,8H,9H,10H-naphtho[4,4a-c]furan-7-yl]-3-(hydroxymethyl)pentanoate.

Structure

MOL 3D MOL SDF PDB SMILES InChI


  Mrv1652309082200402D          

 27 29  0  0  1  0            999 V2000
    4.2125    0.4217    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.9269    0.0092    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.6414    0.4217    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.6414    1.2467    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    6.3559    0.0092    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.0704    0.4217    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    7.0704    1.2467    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.7848    1.6592    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    7.7848    0.0092    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.4993    0.4217    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    9.2138    0.0092    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    8.6835   -0.6228    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    9.4959    0.7844    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    8.9656    1.4164    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   10.3084    0.9277    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   10.5906    1.7029    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   10.7401    0.5072    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   10.5565   -0.4795    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
   10.9937    0.2201    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   11.7942    0.0205    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   11.8518   -0.8025    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   12.5514   -1.2397    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   11.0868   -1.1115    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   10.8047   -1.8868    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    9.9922   -2.0300    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    9.4619   -1.3980    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    9.7441   -0.6228    0.0000 C   0  0  2  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  2  0  0  0  0
  3  5  1  0  0  0  0
  6  5  1  6  0  0  0
  6  7  1  0  0  0  0
  7  8  1  0  0  0  0
  6  9  1  0  0  0  0
  9 10  1  0  0  0  0
 11 10  1  1  0  0  0
 11 12  1  6  0  0  0
 11 13  1  0  0  0  0
 13 14  1  6  0  0  0
 13 15  1  0  0  0  0
 15 16  2  0  0  0  0
 15 17  1  0  0  0  0
 17 18  1  0  0  0  0
 18 19  1  6  0  0  0
 19 20  1  0  0  0  0
 20 21  1  0  0  0  0
 21 22  2  0  0  0  0
 21 23  1  0  0  0  0
 18 23  1  0  0  0  0
 23 24  2  0  0  0  0
 24 25  1  0  0  0  0
 25 26  1  0  0  0  0
 27 26  1  6  0  0  0
 18 27  1  0  0  0  0
 11 27  1  0  0  0  0
M  END

     RDKit          3D

 57 59  0  0  0  0  0  0  0  0999 V2000
    3.9852    1.8583    1.9360 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.2643    0.6619    1.7144 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.8488   -0.4798    1.2308 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.0887   -0.4569    0.9728 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.0559   -1.7089    1.0142 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.6883   -1.9347   -0.4221 C   0  0  2  0  0  0  0  0  0  0  0  0
    3.9223   -2.0716   -1.2993 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.7071   -3.1474   -0.8897 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.7859   -0.8281   -0.9435 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.5461   -0.8191   -0.1180 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4866    0.2175   -0.5142 C   0  0  1  0  0  0  0  0  0  0  0  0
    0.1005    1.5703   -0.3705 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9106    0.0179   -1.9654 C   0  0  2  0  0  0  0  0  0  0  0  0
   -0.1877    0.8899   -2.9320 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3745    0.0627   -2.1481 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8181   -0.4993   -3.1558 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.3636    0.6968   -1.2726 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8218    0.8819    0.1364 C   0  0  1  0  0  0  0  0  0  0  0  0
   -2.6707    2.3437    0.3671 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.0656    2.7511    0.2605 O   0  0  0  0  0  0  0  0  0  0  0  0
   -4.8092    1.7423    0.8666 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.0366    1.7759    1.1233 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.8801    0.6195    1.1535 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.8773   -0.3394    2.0376 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7309   -1.3273    2.1184 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4783   -0.4900    1.7194 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7229   -0.0517    0.3210 C   0  0  2  0  0  0  0  0  0  0  0  0
    5.0720    1.6745    2.0146 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.6205    2.3209    2.8664 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.7822    2.5056    1.0344 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.1856   -1.7511    1.6907 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.7225   -2.5506    1.3921 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.1526   -2.9050   -0.4752 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.5127   -1.1583   -1.1783 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.6409   -2.2717   -2.3479 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.1832   -3.8727   -0.4772 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.3971    0.0751   -0.9271 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.5623   -1.0202   -2.0348 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.8950   -0.4668    0.9058 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.1377   -1.8462   -0.0950 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0654    2.2625   -1.2247 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.2053    1.5195   -0.2681 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2464    1.9907    0.5984 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6084   -1.0432   -2.2186 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1242    0.4287   -3.9588 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.8268    1.1663   -2.6725 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7779    1.8177   -3.0793 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.6751    1.6726   -1.6792 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.2679    0.0627   -1.1812 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3955    2.6497    1.3801 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1960    2.9310   -0.4134 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.7019   -0.4284    2.7173 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5741   -1.6690    3.1436 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8746   -2.1373    1.3814 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3780    0.3254    2.4558 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6660   -1.1931    1.8872 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1040   -1.0250   -0.1773 H   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0
  2  3  1  0
  3  4  2  0
  3  5  1  0
  5  6  1  0
  6  7  1  0
  7  8  1  0
  6  9  1  0
  9 10  1  0
 11 10  1  1
 11 12  1  0
 11 13  1  0
 13 14  1  0
 13 15  1  0
 15 16  2  0
 15 17  1  0
 18 17  1  6
 18 19  1  0
 19 20  1  0
 20 21  1  0
 21 22  2  0
 21 23  1  0
 23 24  2  0
 24 25  1  0
 25 26  1  0
 26 27  1  0
 27 11  1  0
 23 18  1  0
 27 18  1  0
  1 28  1  0
  1 29  1  0
  1 30  1  0
  5 31  1  0
  5 32  1  0
  6 33  1  1
  7 34  1  0
  7 35  1  0
  8 36  1  0
  9 37  1  0
  9 38  1  0
 10 39  1  0
 10 40  1  0
 12 41  1  0
 12 42  1  0
 12 43  1  0
 13 44  1  6
 14 45  1  0
 14 46  1  0
 14 47  1  0
 17 48  1  0
 17 49  1  0
 19 50  1  0
 19 51  1  0
 24 52  1  0
 25 53  1  0
 25 54  1  0
 26 55  1  0
 26 56  1  0
 27 57  1  6
M  END


  Mrv1652309082200402D          

 27 29  0  0  1  0            999 V2000
    4.2125    0.4217    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.9269    0.0092    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.6414    0.4217    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.6414    1.2467    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    6.3559    0.0092    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.0704    0.4217    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    7.0704    1.2467    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.7848    1.6592    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    7.7848    0.0092    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.4993    0.4217    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    9.2138    0.0092    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    8.6835   -0.6228    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    9.4959    0.7844    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    8.9656    1.4164    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   10.3084    0.9277    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   10.5906    1.7029    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   10.7401    0.5072    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   10.5565   -0.4795    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
   10.9937    0.2201    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   11.7942    0.0205    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   11.8518   -0.8025    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   12.5514   -1.2397    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   11.0868   -1.1115    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   10.8047   -1.8868    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    9.9922   -2.0300    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    9.4619   -1.3980    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    9.7441   -0.6228    0.0000 C   0  0  2  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  2  0  0  0  0
  3  5  1  0  0  0  0
  6  5  1  6  0  0  0
  6  7  1  0  0  0  0
  7  8  1  0  0  0  0
  6  9  1  0  0  0  0
  9 10  1  0  0  0  0
 11 10  1  1  0  0  0
 11 12  1  6  0  0  0
 11 13  1  0  0  0  0
 13 14  1  6  0  0  0
 13 15  1  0  0  0  0
 15 16  2  0  0  0  0
 15 17  1  0  0  0  0
 17 18  1  0  0  0  0
 18 19  1  6  0  0  0
 19 20  1  0  0  0  0
 20 21  1  0  0  0  0
 21 22  2  0  0  0  0
 21 23  1  0  0  0  0
 18 23  1  0  0  0  0
 23 24  2  0  0  0  0
 24 25  1  0  0  0  0
 25 26  1  0  0  0  0
 27 26  1  6  0  0  0
 18 27  1  0  0  0  0
 11 27  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0257532

> <DATABASE_NAME>
NP-MRD

> <SMILES>
COC(=O)C[C@H](CO)CC[C@@]1(C)[C@H](C)C(=O)C[C@@]23COC(=O)C2=CCC[C@H]13

> <INCHI_IDENTIFIER>
InChI=1S/C21H30O6/c1-13-16(23)10-21-12-27-19(25)15(21)5-4-6-17(21)20(13,2)8-7-14(11-22)9-18(24)26-3/h5,13-14,17,22H,4,6-12H2,1-3H3/t13-,14-,17-,20+,21-/m1/s1

> <INCHI_KEY>
LOJULOSPWTXYPL-JKIZDXAZSA-N

> <FORMULA>
C21H30O6

> <MOLECULAR_WEIGHT>
378.465

> <EXACT_MASS>
378.204238686

> <JCHEM_ACCEPTOR_COUNT>
4

> <JCHEM_ATOM_COUNT>
57

> <JCHEM_AVERAGE_POLARIZABILITY>
40.65277385784803

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
1

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
1

> <JCHEM_IUPAC>
methyl (3R)-5-[(6aR,7R,8S,10aS)-7,8-dimethyl-3,9-dioxo-1H,3H,5H,6H,6aH,7H,8H,9H,10H-naphtho[4,4a-c]furan-7-yl]-3-(hydroxymethyl)pentanoate

> <JCHEM_LOGP>
2.1401301753333337

> <JCHEM_MDDR_LIKE_RULE>
1

> <JCHEM_NUMBER_OF_RINGS>
3

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA>
17.56916556428132

> <JCHEM_PKA_STRONGEST_ACIDIC>
15.44756114244283

> <JCHEM_PKA_STRONGEST_BASIC>
-2.601584516676888

> <JCHEM_POLAR_SURFACE_AREA>
89.9

> <JCHEM_REFRACTIVITY>
99.45479999999998

> <JCHEM_ROTATABLE_BOND_COUNT>
7

> <JCHEM_RULE_OF_FIVE>
1

> <JCHEM_TRADITIONAL_IUPAC>
methyl (3R)-5-[(6aR,7R,8S,10aS)-7,8-dimethyl-3,9-dioxo-1H,5H,6H,6aH,8H,10H-naphtho[4,4a-c]furan-7-yl]-3-(hydroxymethyl)pentanoate

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 08-SEP-22   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   08-SEP-22         0                                  
HETATM    1  C   UNK     0       7.863   0.787   0.000  0.00  0.00           C+0
HETATM    2  O   UNK     0       9.197   0.017   0.000  0.00  0.00           O+0
HETATM    3  C   UNK     0      10.531   0.787   0.000  0.00  0.00           C+0
HETATM    4  O   UNK     0      10.531   2.327   0.000  0.00  0.00           O+0
HETATM    5  C   UNK     0      11.864   0.017   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0      13.198   0.787   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0      13.198   2.327   0.000  0.00  0.00           C+0
HETATM    8  O   UNK     0      14.532   3.097   0.000  0.00  0.00           O+0
HETATM    9  C   UNK     0      14.532   0.017   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0      15.865   0.787   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0      17.199   0.017   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0      16.209  -1.163   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0      17.726   1.464   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0      16.736   2.644   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0      19.242   1.732   0.000  0.00  0.00           C+0
HETATM   16  O   UNK     0      19.769   3.179   0.000  0.00  0.00           O+0
HETATM   17  C   UNK     0      20.048   0.947   0.000  0.00  0.00           C+0
HETATM   18  C   UNK     0      19.706  -0.895   0.000  0.00  0.00           C+0
HETATM   19  C   UNK     0      20.522   0.411   0.000  0.00  0.00           C+0
HETATM   20  O   UNK     0      22.016   0.038   0.000  0.00  0.00           O+0
HETATM   21  C   UNK     0      22.123  -1.498   0.000  0.00  0.00           C+0
HETATM   22  O   UNK     0      23.429  -2.314   0.000  0.00  0.00           O+0
HETATM   23  C   UNK     0      20.695  -2.075   0.000  0.00  0.00           C+0
HETATM   24  C   UNK     0      20.169  -3.522   0.000  0.00  0.00           C+0
HETATM   25  C   UNK     0      18.652  -3.789   0.000  0.00  0.00           C+0
HETATM   26  C   UNK     0      17.662  -2.610   0.000  0.00  0.00           C+0
HETATM   27  C   UNK     0      18.189  -1.163   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                                                       
CONECT    6    5    7    9                                                  
CONECT    7    6    8                                                       
CONECT    8    7                                                            
CONECT    9    6   10                                                       
CONECT   10    9   11                                                       
CONECT   11   10   12   13   27                                             
CONECT   12   11                                                            
CONECT   13   11   14   15                                                  
CONECT   14   13                                                            
CONECT   15   13   16   17                                                  
CONECT   16   15                                                            
CONECT   17   15   18                                                       
CONECT   18   17   19   23   27                                             
CONECT   19   18   20                                                       
CONECT   20   19   21                                                       
CONECT   21   20   22   23                                                  
CONECT   22   21                                                            
CONECT   23   21   18   24                                                  
CONECT   24   23   25                                                       
CONECT   25   24   26                                                       
CONECT   26   25   27                                                       
CONECT   27   26   18   11                                                  
MASTER        0    0    0    0    0    0    0    0   27    0   58    0
END

View in JSmol

Synonyms

Value	Source
Methyl (3R)-5-[(6ar,7R,8S,10as)-7,8-dimethyl-3,9-dioxo-1H,3H,5H,6H,6ah,7H,8H,9H,10H-naphtho[4,4a-c]furan-7-yl]-3-(hydroxymethyl)pentanoic acid	Generator

Chemical Formula

C₂₁H₃₀O₆

Average Mass

378.4650 Da

Monoisotopic Mass

378.20424 Da

IUPAC Name

methyl (3R)-5-[(6aR,7R,8S,10aS)-7,8-dimethyl-3,9-dioxo-1H,3H,5H,6H,6aH,7H,8H,9H,10H-naphtho[4,4a-c]furan-7-yl]-3-(hydroxymethyl)pentanoate

Traditional Name

methyl (3R)-5-[(6aR,7R,8S,10aS)-7,8-dimethyl-3,9-dioxo-1H,5H,6H,6aH,8H,10H-naphtho[4,4a-c]furan-7-yl]-3-(hydroxymethyl)pentanoate

CAS Registry Number

Not Available

SMILES

COC(=O)C[C@H](CO)CC[C@@]1(C)[C@H](C)C(=O)C[C@@]23COC(=O)C2=CCC[C@H]13

InChI Identifier

InChI=1S/C21H30O6/c1-13-16(23)10-21-12-27-19(25)15(21)5-4-6-17(21)20(13,2)8-7-14(11-22)9-18(24)26-3/h5,13-14,17,22H,4,6-12H2,1-3H3/t13-,14-,17-,20+,21-/m1/s1

InChI Key

LOJULOSPWTXYPL-JKIZDXAZSA-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 diterpene lactones. These are diterpenoids containing a lactone moiety.

Kingdom

Organic compounds

Super Class

Lipids and lipid-like molecules

Class

Prenol lipids

Sub Class

Terpene lactones

Direct Parent

Diterpene lactones

Alternative Parents

Substituents

Diterpene lactone
Diterpenoid
Clerodane diterpenoid
Naphthofuran
Fatty alcohol
Fatty acid ester
Fatty acid methyl ester
Dicarboxylic acid or derivatives
Fatty acyl
Gamma butyrolactone
Alpha,beta-unsaturated carboxylic ester
Enoate ester
Tetrahydrofuran
Methyl ester
Lactone
Ketone
Carboxylic acid ester
Cyclic ketone
Organoheterocyclic compound
Oxacycle
Carboxylic acid derivative
Organooxygen compound
Alcohol
Hydrocarbon derivative
Organic oxide
Organic oxygen compound
Primary alcohol
Carbonyl group
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
logP	2.14	ChemAxon
pKa (Strongest Acidic)	15.45	ChemAxon
pKa (Strongest Basic)	-2.6	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	4	ChemAxon
Hydrogen Donor Count	1	ChemAxon
Polar Surface Area	89.9 Å²	ChemAxon
Rotatable Bond Count	7	ChemAxon
Refractivity	99.45 m³·mol⁻¹	ChemAxon
Polarizability	40.65 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	Yes	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

162962974

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

LOTUS database [Link]

Showing NP-Card for methyl (3r)-5-[(6ar,7r,8s,10as)-7,8-dimethyl-3,9-dioxo-1h,5h,6h,6ah,8h,10h-naphtho[4,4a-c]furan-7-yl]-3-(hydroxymethyl)pentanoate (NP0257532)

MOL for NP0257532 (methyl (3r)-5-[(6ar,7r,8s,10as)-7,8-dimethyl-3,9-dioxo-1h,5h,6h,6ah,8h,10h-naphtho[4,4a-c]furan-7-yl]-3-(hydroxymethyl)pentanoate)

3D MOL for NP0257532 (methyl (3r)-5-[(6ar,7r,8s,10as)-7,8-dimethyl-3,9-dioxo-1h,5h,6h,6ah,8h,10h-naphtho[4,4a-c]furan-7-yl]-3-(hydroxymethyl)pentanoate)

3D SDF for NP0257532 (methyl (3r)-5-[(6ar,7r,8s,10as)-7,8-dimethyl-3,9-dioxo-1h,5h,6h,6ah,8h,10h-naphtho[4,4a-c]furan-7-yl]-3-(hydroxymethyl)pentanoate)

3D-SDF for NP0257532 (methyl (3r)-5-[(6ar,7r,8s,10as)-7,8-dimethyl-3,9-dioxo-1h,5h,6h,6ah,8h,10h-naphtho[4,4a-c]furan-7-yl]-3-(hydroxymethyl)pentanoate)

PDB for NP0257532 (methyl (3r)-5-[(6ar,7r,8s,10as)-7,8-dimethyl-3,9-dioxo-1h,5h,6h,6ah,8h,10h-naphtho[4,4a-c]furan-7-yl]-3-(hydroxymethyl)pentanoate)

3D PDB for NP0257532 (methyl (3r)-5-[(6ar,7r,8s,10as)-7,8-dimethyl-3,9-dioxo-1h,5h,6h,6ah,8h,10h-naphtho[4,4a-c]furan-7-yl]-3-(hydroxymethyl)pentanoate)

SMILES for NP0257532 (methyl (3r)-5-[(6ar,7r,8s,10as)-7,8-dimethyl-3,9-dioxo-1h,5h,6h,6ah,8h,10h-naphtho[4,4a-c]furan-7-yl]-3-(hydroxymethyl)pentanoate)

INCHI for NP0257532 (methyl (3r)-5-[(6ar,7r,8s,10as)-7,8-dimethyl-3,9-dioxo-1h,5h,6h,6ah,8h,10h-naphtho[4,4a-c]furan-7-yl]-3-(hydroxymethyl)pentanoate)

Structure for NP0257532 (methyl (3r)-5-[(6ar,7r,8s,10as)-7,8-dimethyl-3,9-dioxo-1h,5h,6h,6ah,8h,10h-naphtho[4,4a-c]furan-7-yl]-3-(hydroxymethyl)pentanoate)

3D Structure for NP0257532 (methyl (3r)-5-[(6ar,7r,8s,10as)-7,8-dimethyl-3,9-dioxo-1h,5h,6h,6ah,8h,10h-naphtho[4,4a-c]furan-7-yl]-3-(hydroxymethyl)pentanoate)