NP-MRD: Showing NP-Card for (5r)-4-[(2s,3ar,5as,9as,9br)-3a-(hydroxymethyl)-6,6,9a-trimethyl-octahydro-1h-naphtho[2,1-b]furan-2-yl]-5-hydroxy-5h-furan-2-one (NP0153608)

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Record Information

Version

2.0

Created at

2022-09-02 10:17:50 UTC

Updated at

2022-09-02 10:17:50 UTC

NP-MRD ID

NP0153608

Secondary Accession Numbers

None

Natural Product Identification

Common Name

(5r)-4-[(2s,3ar,5as,9as,9br)-3a-(hydroxymethyl)-6,6,9a-trimethyl-octahydro-1h-naphtho[2,1-b]furan-2-yl]-5-hydroxy-5h-furan-2-one

Description

Acuminolide belongs to the class of organic compounds known as diterpene lactones. These are diterpenoids containing a lactone moiety. (5r)-4-[(2s,3ar,5as,9as,9br)-3a-(hydroxymethyl)-6,6,9a-trimethyl-octahydro-1h-naphtho[2,1-b]furan-2-yl]-5-hydroxy-5h-furan-2-one is found in Neo-uvaria acuminatissima. (5r)-4-[(2s,3ar,5as,9as,9br)-3a-(hydroxymethyl)-6,6,9a-trimethyl-octahydro-1h-naphtho[2,1-b]furan-2-yl]-5-hydroxy-5h-furan-2-one was first documented in 2014 (PMID: 25259727). Based on a literature review a small amount of articles have been published on Acuminolide (PMID: 28049908) (PMID: 26034885).

Structure

MOL 3D MOL SDF PDB SMILES InChI


  Mrv1652309022212172D          

 25 28  0  0  1  0            999 V2000
    5.5018   -0.6207    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.7358   -0.3145    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.5672   -1.1221    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.1704    0.3867    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.7804    1.1137    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.9558    1.1395    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5212    0.4383    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    3.1312    1.1653    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.9112   -0.2887    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    3.4766   -0.9900    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.6520   -0.9642    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.2620   -0.2372    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    1.7565   -0.8892    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.9391   -0.7774    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.4608   -0.0406    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.4002    0.7822    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    0.6989    1.2168    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0648    0.9050    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5975    1.5350    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4202    1.4744    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1628    2.2362    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.6384    2.0396    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    1.2684    2.5722    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.1640    1.0941    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.6966    0.4640    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
  2  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  6  0  0  0
  7  9  1  0  0  0  0
  2  9  1  0  0  0  0
  9 10  1  6  0  0  0
 10 11  1  0  0  0  0
 11 12  1  0  0  0  0
 12 13  1  6  0  0  0
 13 14  1  0  0  0  0
 12 15  1  0  0  0  0
 15 16  1  0  0  0  0
 16 17  1  6  0  0  0
 17 18  2  0  0  0  0
 18 19  1  0  0  0  0
 19 20  2  0  0  0  0
 19 21  1  0  0  0  0
 21 22  1  0  0  0  0
 17 22  1  0  0  0  0
 22 23  1  1  0  0  0
 16 24  1  0  0  0  0
 25 24  1  6  0  0  0
  7 25  1  0  0  0  0
 12 25  1  0  0  0  0
M  END

     RDKit          3D

 55 58  0  0  0  0  0  0  0  0999 V2000
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   -3.2477    0.4168    0.1062 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5184    1.7159   -0.5915 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.8354   -0.6951   -0.6853 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.9246   -1.2611   -1.7353 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5183   -1.4277   -1.3092 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9173   -0.1792   -0.6670 C   0  0  1  0  0  0  0  0  0  0  0  0
   -0.8432    0.8404   -1.7275 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8517    0.1479    0.4780 C   0  0  1  0  0  0  0  0  0  0  0  0
   -1.2557    1.1783    1.4252 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0399    0.5514    2.0649 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.9525    0.2747    0.9970 C   0  0  1  0  0  0  0  0  0  0  0  0
    1.6960    1.4723    0.6030 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.0499    2.5614    0.1270 O   0  0  0  0  0  0  0  0  0  0  0  0
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    4.9665   -1.3120    0.9656 C   0  0  1  0  0  0  0  0  0  0  0  0
    4.8553   -0.4835    2.0791 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.5120   -0.9587   -0.8542 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.3361   -0.5922   -0.0279 C   0  0  2  0  0  0  0  0  0  0  0  0
   -3.7015   -0.2744    2.1335 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.1075    0.3237    1.1131 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.9691    1.5245    1.7847 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.6140    1.9439   -0.4144 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.9790    2.5774   -0.1802 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.4535    1.6381   -1.7073 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.2613   -1.4930   -0.0320 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.7296   -0.2780   -1.2355 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.3202   -2.2968   -1.9573 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.0502   -0.7109   -2.6976 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9141   -1.7441   -2.1712 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4820   -2.2230   -0.5254 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.1915    0.8701   -2.1825 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0803    1.8651   -1.4587 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4924    0.6029   -2.6240 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8695   -0.7961    1.0846 H   0  0  0  0  0  0  0  0  0  0  0  0
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   -1.0613    2.1323    0.9208 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3971   -0.4320    2.4891 H   0  0  0  0  0  0  0  0  0  0  0  0
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    2.2714    1.8122    1.5213 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.2960    3.4276    0.5469 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.2899   -2.3806    0.5167 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.8429   -0.4752   -2.0387 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.0068   -2.3935    1.2638 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.7379   -0.3338    2.4994 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.2970   -1.8750   -1.4438 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.9049   -0.1627   -1.4885 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.0882   -1.5466    0.5486 H   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0
  2  3  1  0
  2  4  1  0
  4  5  1  0
  5  6  1  0
  6  7  1  0
  7  8  1  6
  7 25  1  0
 25 24  1  0
 24 16  1  0
 16 15  1  0
 15 12  1  0
 12 13  1  6
 13 14  1  0
 12 11  1  0
 11 10  1  0
 10  9  1  0
 16 17  1  0
 17 18  2  0
 18 19  1  0
 19 20  2  0
 19 21  1  0
 21 22  1  0
 22 23  1  0
  9  2  1  0
 22 17  1  0
  9  7  1  0
 12 25  1  0
  1 26  1  0
  1 27  1  0
  1 28  1  0
  3 29  1  0
  3 30  1  0
  3 31  1  0
  4 32  1  0
  4 33  1  0
  5 34  1  0
  5 35  1  0
  6 36  1  0
  6 37  1  0
  8 38  1  0
  8 39  1  0
  8 40  1  0
 25 55  1  1
 24 53  1  0
 24 54  1  0
 16 49  1  1
 13 46  1  0
 13 47  1  0
 14 48  1  0
 11 44  1  0
 11 45  1  0
 10 42  1  0
 10 43  1  0
  9 41  1  1
 18 50  1  0
 22 51  1  1
 23 52  1  0
M  END


  Mrv1652309022212172D          

 25 28  0  0  1  0            999 V2000
    5.5018   -0.6207    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.7358   -0.3145    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.5672   -1.1221    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.1704    0.3867    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.7804    1.1137    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.9558    1.1395    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5212    0.4383    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    3.1312    1.1653    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.9112   -0.2887    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    3.4766   -0.9900    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.6520   -0.9642    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.2620   -0.2372    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    1.7565   -0.8892    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.9391   -0.7774    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.4608   -0.0406    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.4002    0.7822    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    0.6989    1.2168    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0648    0.9050    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5975    1.5350    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4202    1.4744    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1628    2.2362    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.6384    2.0396    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    1.2684    2.5722    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.1640    1.0941    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.6966    0.4640    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
  2  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  6  0  0  0
  7  9  1  0  0  0  0
  2  9  1  0  0  0  0
  9 10  1  6  0  0  0
 10 11  1  0  0  0  0
 11 12  1  0  0  0  0
 12 13  1  6  0  0  0
 13 14  1  0  0  0  0
 12 15  1  0  0  0  0
 15 16  1  0  0  0  0
 16 17  1  6  0  0  0
 17 18  2  0  0  0  0
 18 19  1  0  0  0  0
 19 20  2  0  0  0  0
 19 21  1  0  0  0  0
 21 22  1  0  0  0  0
 17 22  1  0  0  0  0
 22 23  1  1  0  0  0
 16 24  1  0  0  0  0
 25 24  1  6  0  0  0
  7 25  1  0  0  0  0
 12 25  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0153608

> <DATABASE_NAME>
NP-MRD

> <SMILES>
CC1(C)CCC[C@]2(C)[C@H]3C[C@H](O[C@]3(CO)CC[C@@H]12)C1=CC(=O)O[C@H]1O

> <INCHI_IDENTIFIER>
InChI=1S/C20H30O5/c1-18(2)6-4-7-19(3)14(18)5-8-20(11-21)15(19)10-13(25-20)12-9-16(22)24-17(12)23/h9,13-15,17,21,23H,4-8,10-11H2,1-3H3/t13-,14-,15+,17+,19-,20-/m0/s1

> <INCHI_KEY>
KRFXWKURJSADKH-OUERMZRPSA-N

> <FORMULA>
C20H30O5

> <MOLECULAR_WEIGHT>
350.455

> <EXACT_MASS>
350.209324066

> <JCHEM_ACCEPTOR_COUNT>
4

> <JCHEM_ATOM_COUNT>
55

> <JCHEM_AVERAGE_POLARIZABILITY>
38.28267810914574

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
2

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
1

> <JCHEM_IUPAC>
(5R)-4-[(2S,3aR,5aS,9aS,9bR)-3a-(hydroxymethyl)-6,6,9a-trimethyl-dodecahydronaphtho[2,1-b]furan-2-yl]-5-hydroxy-2,5-dihydrofuran-2-one

> <ALOGPS_LOGP>
2.12

> <JCHEM_LOGP>
2.6488154686666663

> <ALOGPS_LOGS>
-3.58

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
4

> <JCHEM_PHYSIOLOGICAL_CHARGE>
-1

> <JCHEM_PKA>
11.73145287450128

> <JCHEM_PKA_STRONGEST_ACIDIC>
5.524351136518355

> <JCHEM_PKA_STRONGEST_BASIC>
-3.080530091797975

> <JCHEM_POLAR_SURFACE_AREA>
75.99000000000001

> <JCHEM_REFRACTIVITY>
92.6873

> <JCHEM_ROTATABLE_BOND_COUNT>
2

> <JCHEM_RULE_OF_FIVE>
1

> <ALOGPS_SOLUBILITY>
9.13e-02 g/l

> <JCHEM_TRADITIONAL_IUPAC>
(5R)-4-[(2S,3aR,5aS,9aS,9bR)-3a-(hydroxymethyl)-6,6,9a-trimethyl-octahydro-1H-naphtho[2,1-b]furan-2-yl]-5-hydroxy-5H-furan-2-one

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 02-SEP-22   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   02-SEP-22         0                                  
HETATM    1  C   UNK     0      10.270  -1.159   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0       8.840  -0.587   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0       8.525  -2.095   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0       9.651   0.722   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0       8.923   2.079   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0       7.384   2.127   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0       6.573   0.818   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0       5.845   2.175   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0       7.301  -0.539   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0       6.490  -1.848   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0       4.950  -1.800   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0       4.222  -0.443   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0       3.279  -1.660   0.000  0.00  0.00           C+0
HETATM   14  O   UNK     0       1.753  -1.451   0.000  0.00  0.00           O+0
HETATM   15  O   UNK     0       2.727  -0.076   0.000  0.00  0.00           O+0
HETATM   16  C   UNK     0       2.614   1.460   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0       1.305   2.271   0.000  0.00  0.00           C+0
HETATM   18  C   UNK     0      -0.121   1.689   0.000  0.00  0.00           C+0
HETATM   19  C   UNK     0      -1.115   2.865   0.000  0.00  0.00           C+0
HETATM   20  O   UNK     0      -2.651   2.752   0.000  0.00  0.00           O+0
HETATM   21  O   UNK     0      -0.304   4.174   0.000  0.00  0.00           O+0
HETATM   22  C   UNK     0       1.192   3.807   0.000  0.00  0.00           C+0
HETATM   23  O   UNK     0       2.368   4.801   0.000  0.00  0.00           O+0
HETATM   24  C   UNK     0       4.039   2.042   0.000  0.00  0.00           C+0
HETATM   25  C   UNK     0       5.034   0.866   0.000  0.00  0.00           C+0
CONECT    1    2                                                            
CONECT    2    1    3    4    9                                             
CONECT    3    2                                                            
CONECT    4    2    5                                                       
CONECT    5    4    6                                                       
CONECT    6    5    7                                                       
CONECT    7    6    8    9   25                                             
CONECT    8    7                                                            
CONECT    9    7    2   10                                                  
CONECT   10    9   11                                                       
CONECT   11   10   12                                                       
CONECT   12   11   13   15   25                                             
CONECT   13   12   14                                                       
CONECT   14   13                                                            
CONECT   15   12   16                                                       
CONECT   16   15   17   24                                                  
CONECT   17   16   18   22                                                  
CONECT   18   17   19                                                       
CONECT   19   18   20   21                                                  
CONECT   20   19                                                            
CONECT   21   19   22                                                       
CONECT   22   21   17   23                                                  
CONECT   23   22                                                            
CONECT   24   16   25                                                       
CONECT   25   24    7   12                                                  
MASTER        0    0    0    0    0    0    0    0   25    0   56    0
END

View in JSmol

Synonyms

Not Available

Chemical Formula

C₂₀H₃₀O₅

Average Mass

350.4550 Da

Monoisotopic Mass

350.20932 Da

IUPAC Name

Not Available

Traditional Name

Not Available

CAS Registry Number

Not Available

SMILES

CC1(C)CCC[C@]2(C)[C@H]3C[C@H](O[C@]3(CO)CC[C@@H]12)C1=CC(=O)O[C@H]1O

InChI Identifier

InChI=1S/C20H30O5/c1-18(2)6-4-7-19(3)14(18)5-8-20(11-21)15(19)10-13(25-20)12-9-16(22)24-17(12)23/h9,13-15,17,21,23H,4-8,10-11H2,1-3H3/t13-,14-,15+,17+,19-,20-/m0/s1

InChI Key

KRFXWKURJSADKH-OUERMZRPSA-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
Neo-uvaria acuminatissima	LOTUS Database	35616633

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
2-furanone
Dihydrofuran
Alpha,beta-unsaturated carboxylic ester
Enoate ester
Oxolane
Carboxylic acid ester
Hemiacetal
Lactone
Carboxylic acid derivative
Dialkyl ether
Oxacycle
Organoheterocyclic compound
Ether
Monocarboxylic acid or derivatives
Hydrocarbon derivative
Organic oxygen compound
Carbonyl group
Alcohol
Primary alcohol
Organooxygen compound
Organic oxide
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

8535985

KEGG Compound ID

Not Available

BioCyc ID

Not Available

BiGG ID

Not Available

Wikipedia Link

Not Available

METLIN ID

Not Available

PubChem Compound

10360536

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

Rasyid FA, Fukuyoshi S, Ando H, Miyake K, Atsumi T, Fujie T, Saito Y, Goto M, Shinya T, Mikage M, Sasaki Y, Nakagawa-Goto K: A Novel Clerodane Diterpene from Vitex cofassus. Chem Pharm Bull (Tokyo). 2017;65(1):116-120. doi: 10.1248/cpb.c16-00775. [PubMed:28049908 ]
Corlay N, Lecso-Bornet M, Leborgne E, Blanchard F, Cachet X, Bignon J, Roussi F, Butel MJ, Awang K, Litaudon M: Antibacterial Labdane Diterpenoids from Vitex vestita. J Nat Prod. 2015 Jun 26;78(6):1348-56. doi: 10.1021/acs.jnatprod.5b00206. Epub 2015 Jun 2. [PubMed:26034885 ]
Hwang BS, Kim HS, Yih W, Jeong EJ, Rho JR: Acuminolide A: structure and bioactivity of a new polyether macrolide from dinoflagellate Dinophysis acuminata. Org Lett. 2014 Oct 17;16(20):5362-5. doi: 10.1021/ol502567g. Epub 2014 Sep 26. [PubMed:25259727 ]
LOTUS database [Link]

Showing NP-Card for (5r)-4-[(2s,3ar,5as,9as,9br)-3a-(hydroxymethyl)-6,6,9a-trimethyl-octahydro-1h-naphtho[2,1-b]furan-2-yl]-5-hydroxy-5h-furan-2-one (NP0153608)

MOL for NP0153608 ((5r)-4-[(2s,3ar,5as,9as,9br)-3a-(hydroxymethyl)-6,6,9a-trimethyl-octahydro-1h-naphtho[2,1-b]furan-2-yl]-5-hydroxy-5h-furan-2-one)

3D MOL for NP0153608 ((5r)-4-[(2s,3ar,5as,9as,9br)-3a-(hydroxymethyl)-6,6,9a-trimethyl-octahydro-1h-naphtho[2,1-b]furan-2-yl]-5-hydroxy-5h-furan-2-one)

3D SDF for NP0153608 ((5r)-4-[(2s,3ar,5as,9as,9br)-3a-(hydroxymethyl)-6,6,9a-trimethyl-octahydro-1h-naphtho[2,1-b]furan-2-yl]-5-hydroxy-5h-furan-2-one)

3D-SDF for NP0153608 ((5r)-4-[(2s,3ar,5as,9as,9br)-3a-(hydroxymethyl)-6,6,9a-trimethyl-octahydro-1h-naphtho[2,1-b]furan-2-yl]-5-hydroxy-5h-furan-2-one)

PDB for NP0153608 ((5r)-4-[(2s,3ar,5as,9as,9br)-3a-(hydroxymethyl)-6,6,9a-trimethyl-octahydro-1h-naphtho[2,1-b]furan-2-yl]-5-hydroxy-5h-furan-2-one)

3D PDB for NP0153608 ((5r)-4-[(2s,3ar,5as,9as,9br)-3a-(hydroxymethyl)-6,6,9a-trimethyl-octahydro-1h-naphtho[2,1-b]furan-2-yl]-5-hydroxy-5h-furan-2-one)

SMILES for NP0153608 ((5r)-4-[(2s,3ar,5as,9as,9br)-3a-(hydroxymethyl)-6,6,9a-trimethyl-octahydro-1h-naphtho[2,1-b]furan-2-yl]-5-hydroxy-5h-furan-2-one)

INCHI for NP0153608 ((5r)-4-[(2s,3ar,5as,9as,9br)-3a-(hydroxymethyl)-6,6,9a-trimethyl-octahydro-1h-naphtho[2,1-b]furan-2-yl]-5-hydroxy-5h-furan-2-one)

Structure for NP0153608 ((5r)-4-[(2s,3ar,5as,9as,9br)-3a-(hydroxymethyl)-6,6,9a-trimethyl-octahydro-1h-naphtho[2,1-b]furan-2-yl]-5-hydroxy-5h-furan-2-one)

3D Structure for NP0153608 ((5r)-4-[(2s,3ar,5as,9as,9br)-3a-(hydroxymethyl)-6,6,9a-trimethyl-octahydro-1h-naphtho[2,1-b]furan-2-yl]-5-hydroxy-5h-furan-2-one)