NP-MRD: Showing NP-Card for (1s,3br,5ar,6s,9ar,9br)-1-methoxy-3b,6,9a-trimethyl-3-oxo-1h,4h,5h,5ah,7h,8h,9h,9bh,10h,11h-phenanthro[1,2-c]furan-6-carboxylic acid (NP0292908)

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Record Information

Version

2.0

Created at

2022-09-10 00:39:37 UTC

Updated at

2022-09-10 00:39:37 UTC

NP-MRD ID

NP0292908

Secondary Accession Numbers

None

Natural Product Identification

Common Name

(1s,3br,5ar,6s,9ar,9br)-1-methoxy-3b,6,9a-trimethyl-3-oxo-1h,4h,5h,5ah,7h,8h,9h,9bh,10h,11h-phenanthro[1,2-c]furan-6-carboxylic acid

Description

16Beta-Methoxy-15-oxospongi-13-en-19-oic acid belongs to the class of organic compounds known as diterpene lactones. These are diterpenoids containing a lactone moiety. (1s,3br,5ar,6s,9ar,9br)-1-methoxy-3b,6,9a-trimethyl-3-oxo-1h,4h,5h,5ah,7h,8h,9h,9bh,10h,11h-phenanthro[1,2-c]furan-6-carboxylic acid is found in Spongia matamata. Based on a literature review very few articles have been published on 16beta-Methoxy-15-oxospongi-13-en-19-oic acid.

Structure

MOL 3D MOL SDF PDB SMILES InChI


  Mrv1652309102202392D          

 26 29  0  0  1  0            999 V2000
    6.1111    1.5050    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.2939    1.6179    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.7875    0.9666    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    5.0168    0.1741    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.3340   -0.2889    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.3072   -1.1135    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.6826    0.2174    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.9629    0.9934    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.4311    1.6241    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.6190    1.4789    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.3387    0.7029    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    2.8705    0.0722    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    3.4023   -0.5585    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.5902   -0.7037    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.7781   -0.8489    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.2463   -0.2182    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    0.4342   -0.3634    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    0.7182   -1.1380    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2793   -0.7776    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2773   -1.6026    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9948   -0.3669    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0976    0.2673    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.1827    1.0432    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.9948    1.1884    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.5266    0.5577    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    1.8069    1.3336    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0  0  0  0
  3  2  1  1  0  0  0
  3  4  1  0  0  0  0
  4  5  1  0  0  0  0
  5  6  2  0  0  0  0
  5  7  1  0  0  0  0
  7  8  2  0  0  0  0
  3  8  1  0  0  0  0
  8  9  1  0  0  0  0
  9 10  1  0  0  0  0
 11 10  1  1  0  0  0
 11 12  1  0  0  0  0
  7 12  1  0  0  0  0
 12 13  1  1  0  0  0
 12 14  1  0  0  0  0
 14 15  1  0  0  0  0
 16 15  1  1  0  0  0
 16 17  1  0  0  0  0
 17 18  1  6  0  0  0
 17 19  1  1  0  0  0
 19 20  2  0  0  0  0
 19 21  1  0  0  0  0
 17 22  1  0  0  0  0
 22 23  1  0  0  0  0
 23 24  1  0  0  0  0
 24 25  1  0  0  0  0
 16 25  1  0  0  0  0
 11 25  1  0  0  0  0
 25 26  1  1  0  0  0
M  END

     RDKit          3D

 56 59  0  0  0  0  0  0  0  0999 V2000
    5.9043    0.4450   -1.7365 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.3421    0.4985   -0.4763 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.3673   -0.4360   -0.2544 C   0  0  1  0  0  0  0  0  0  0  0  0
    4.6288   -1.2907    0.8394 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.3565   -1.7189    1.2646 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.1384   -2.7822    1.9214 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.3899   -0.7235    0.8086 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.0688    0.1957    0.1743 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.6220    1.5808   -0.0615 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.2389    1.7202    0.5975 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.4480    0.5359    0.1860 C   0  0  1  0  0  0  0  0  0  0  0  0
    0.8907   -0.6552    0.9718 C   0  0  2  0  0  0  0  0  0  0  0  0
    0.6260   -0.6133    2.4342 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.2682   -1.9131    0.4247 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2385   -1.7613    0.3991 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5854   -0.5564   -0.4588 C   0  0  1  0  0  0  0  0  0  0  0  0
   -2.9984   -0.5206   -0.8964 C   0  0  1  0  0  0  0  0  0  0  0  0
   -3.0846   -0.8427   -2.4001 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.8762   -1.5099   -0.2250 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.3650   -2.4787   -0.8554 O   0  0  0  0  0  0  0  0  0  0  0  0
   -4.2104   -1.4335    1.1203 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.6506    0.8310   -0.7416 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7955    1.9655   -1.1752 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3312    1.7989   -0.9094 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0456    0.7250    0.1336 C   0  0  2  0  0  0  0  0  0  0  0  0
   -1.6469    1.1567    1.4118 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.6772    1.2505   -1.7889 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.4493   -0.5015   -1.9281 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.2079    0.5977   -2.5594 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.1990   -1.0856   -1.1491 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.3178    2.3458    0.3206 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.4239    1.6855   -1.1549 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.8200    2.7004    0.3712 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.4772    1.7502    1.7017 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.7373    0.3098   -0.8867 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.0208    0.2403    2.9814 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4456   -0.8199    2.7058 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.1678   -1.5098    2.8674 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.4963   -2.8003    1.0189 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.6198   -2.0499   -0.6040 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6327   -2.6504   -0.1399 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6987   -1.7398    1.3839 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9391   -0.7054   -1.3790 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.0318   -1.9421   -2.5559 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2207   -0.3302   -2.8661 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.0022   -0.3926   -2.8188 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.2096   -1.5344    1.3386 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.0736    0.9099    0.2798 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.5541    0.8197   -1.4221 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.9082    2.0969   -2.2874 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.2053    2.8982   -0.7326 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7839    1.4781   -1.8262 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9378    2.7874   -0.6335 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2647    2.0979    1.3009 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3097    0.3993    1.8258 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8582    1.4774    2.1574 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  2  0
  5  7  1  0
  7  8  2  0
  8  9  1  0
  9 10  1  0
 10 11  1  0
 11 25  1  0
 25 26  1  1
 25 24  1  0
 24 23  1  0
 23 22  1  0
 22 17  1  0
 17 18  1  0
 17 16  1  0
 16 15  1  0
 15 14  1  0
 14 12  1  0
 12 13  1  1
 17 19  1  1
 19 21  1  0
 19 20  2  0
  8  3  1  0
 12 11  1  0
 12  7  1  0
 16 25  1  0
  1 27  1  0
  1 28  1  0
  1 29  1  0
  3 30  1  6
  9 31  1  0
  9 32  1  0
 10 33  1  0
 10 34  1  0
 11 35  1  6
 26 54  1  0
 26 55  1  0
 26 56  1  0
 24 52  1  0
 24 53  1  0
 23 50  1  0
 23 51  1  0
 22 48  1  0
 22 49  1  0
 18 44  1  0
 18 45  1  0
 18 46  1  0
 16 43  1  6
 15 41  1  0
 15 42  1  0
 14 39  1  0
 14 40  1  0
 13 36  1  0
 13 37  1  0
 13 38  1  0
 21 47  1  0
M  END


  Mrv1652309102202392D          

 26 29  0  0  1  0            999 V2000
    6.1111    1.5050    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.2939    1.6179    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.7875    0.9666    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    5.0168    0.1741    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.3340   -0.2889    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.3072   -1.1135    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.6826    0.2174    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.9629    0.9934    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.4311    1.6241    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.6190    1.4789    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.3387    0.7029    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    2.8705    0.0722    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    3.4023   -0.5585    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.5902   -0.7037    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.7781   -0.8489    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.2463   -0.2182    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    0.4342   -0.3634    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    0.7182   -1.1380    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2793   -0.7776    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2773   -1.6026    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9948   -0.3669    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0976    0.2673    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.1827    1.0432    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.9948    1.1884    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.5266    0.5577    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    1.8069    1.3336    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0  0  0  0
  3  2  1  1  0  0  0
  3  4  1  0  0  0  0
  4  5  1  0  0  0  0
  5  6  2  0  0  0  0
  5  7  1  0  0  0  0
  7  8  2  0  0  0  0
  3  8  1  0  0  0  0
  8  9  1  0  0  0  0
  9 10  1  0  0  0  0
 11 10  1  1  0  0  0
 11 12  1  0  0  0  0
  7 12  1  0  0  0  0
 12 13  1  1  0  0  0
 12 14  1  0  0  0  0
 14 15  1  0  0  0  0
 16 15  1  1  0  0  0
 16 17  1  0  0  0  0
 17 18  1  6  0  0  0
 17 19  1  1  0  0  0
 19 20  2  0  0  0  0
 19 21  1  0  0  0  0
 17 22  1  0  0  0  0
 22 23  1  0  0  0  0
 23 24  1  0  0  0  0
 24 25  1  0  0  0  0
 16 25  1  0  0  0  0
 11 25  1  0  0  0  0
 25 26  1  1  0  0  0
M  END
> <DATABASE_ID>
NP0292908

> <DATABASE_NAME>
NP-MRD

> <SMILES>
CO[C@H]1OC(=O)C2=C1CC[C@@H]1[C@@]3(C)CCC[C@@](C)([C@@H]3CC[C@@]21C)C(O)=O

> <INCHI_IDENTIFIER>
InChI=1S/C21H30O5/c1-19-9-5-10-21(3,18(23)24)14(19)8-11-20(2)13(19)7-6-12-15(20)16(22)26-17(12)25-4/h13-14,17H,5-11H2,1-4H3,(H,23,24)/t13-,14-,17+,19-,20-,21+/m1/s1

> <INCHI_KEY>
TVJZRHHUGFVBCQ-SOEYYFHNSA-N

> <FORMULA>
C21H30O5

> <MOLECULAR_WEIGHT>
362.466

> <EXACT_MASS>
362.209324066

> <JCHEM_ACCEPTOR_COUNT>
4

> <JCHEM_ATOM_COUNT>
56

> <JCHEM_AVERAGE_POLARIZABILITY>
39.90652368354846

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
1

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
1

> <JCHEM_IUPAC>
(1R,2R,6S,7R,10R,14S)-14-methoxy-2,6,10-trimethyl-12-oxo-13-oxatetracyclo[8.7.0.0^{2,7}.0^{11,15}]heptadec-11(15)-ene-6-carboxylic acid

> <JCHEM_LOGP>
4.257593634333334

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
4

> <JCHEM_PHYSIOLOGICAL_CHARGE>
-1

> <JCHEM_PKA>
13.284296244687972

> <JCHEM_PKA_STRONGEST_ACIDIC>
4.348443354727813

> <JCHEM_PKA_STRONGEST_BASIC>
-4.324263873627218

> <JCHEM_POLAR_SURFACE_AREA>
72.83

> <JCHEM_REFRACTIVITY>
95.75249999999998

> <JCHEM_ROTATABLE_BOND_COUNT>
2

> <JCHEM_RULE_OF_FIVE>
1

> <JCHEM_TRADITIONAL_IUPAC>
(1R,2R,6S,7R,10R,14S)-14-methoxy-2,6,10-trimethyl-12-oxo-13-oxatetracyclo[8.7.0.0^{2,7}.0^{11,15}]heptadec-11(15)-ene-6-carboxylic acid

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 10-SEP-22   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   10-SEP-22         0                                  
HETATM    1  C   UNK     0      11.407   2.809   0.000  0.00  0.00           C+0
HETATM    2  O   UNK     0       9.882   3.020   0.000  0.00  0.00           O+0
HETATM    3  C   UNK     0       8.937   1.804   0.000  0.00  0.00           C+0
HETATM    4  O   UNK     0       9.365   0.325   0.000  0.00  0.00           O+0
HETATM    5  C   UNK     0       8.090  -0.539   0.000  0.00  0.00           C+0
HETATM    6  O   UNK     0       8.040  -2.078   0.000  0.00  0.00           O+0
HETATM    7  C   UNK     0       6.874   0.406   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0       7.398   1.854   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0       6.405   3.032   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0       4.889   2.761   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0       4.366   1.312   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0       5.358   0.135   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0       6.351  -1.043   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0       4.835  -1.314   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0       3.319  -1.585   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0       2.326  -0.407   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0       0.810  -0.678   0.000  0.00  0.00           C+0
HETATM   18  C   UNK     0       1.341  -2.124   0.000  0.00  0.00           C+0
HETATM   19  C   UNK     0      -0.521  -1.452   0.000  0.00  0.00           C+0
HETATM   20  O   UNK     0      -0.518  -2.992   0.000  0.00  0.00           O+0
HETATM   21  O   UNK     0      -1.857  -0.685   0.000  0.00  0.00           O+0
HETATM   22  C   UNK     0      -0.182   0.499   0.000  0.00  0.00           C+0
HETATM   23  C   UNK     0       0.341   1.947   0.000  0.00  0.00           C+0
HETATM   24  C   UNK     0       1.857   2.218   0.000  0.00  0.00           C+0
HETATM   25  C   UNK     0       2.850   1.041   0.000  0.00  0.00           C+0
HETATM   26  C   UNK     0       3.373   2.489   0.000  0.00  0.00           C+0
CONECT    1    2                                                            
CONECT    2    1    3                                                       
CONECT    3    2    4    8                                                  
CONECT    4    3    5                                                       
CONECT    5    4    6    7                                                  
CONECT    6    5                                                            
CONECT    7    5    8   12                                                  
CONECT    8    7    3    9                                                  
CONECT    9    8   10                                                       
CONECT   10    9   11                                                       
CONECT   11   10   12   25                                                  
CONECT   12   11    7   13   14                                             
CONECT   13   12                                                            
CONECT   14   12   15                                                       
CONECT   15   14   16                                                       
CONECT   16   15   17   25                                                  
CONECT   17   16   18   19   22                                             
CONECT   18   17                                                            
CONECT   19   17   20   21                                                  
CONECT   20   19                                                            
CONECT   21   19                                                            
CONECT   22   17   23                                                       
CONECT   23   22   24                                                       
CONECT   24   23   25                                                       
CONECT   25   24   16   11   26                                             
CONECT   26   25                                                            
MASTER        0    0    0    0    0    0    0    0   26    0   58    0
END

View in JSmol

Synonyms

Value	Source
16b-Methoxy-15-oxospongi-13-en-19-Oate	Generator
16b-Methoxy-15-oxospongi-13-en-19-Oic acid	Generator
16beta-Methoxy-15-oxospongi-13-en-19-Oate	Generator
16Β-methoxy-15-oxospongi-13-en-19-Oate	Generator
16Β-methoxy-15-oxospongi-13-en-19-Oic acid	Generator

Chemical Formula

C₂₁H₃₀O₅

Average Mass

362.4660 Da

Monoisotopic Mass

362.20932 Da

IUPAC Name

(1R,2R,6S,7R,10R,14S)-14-methoxy-2,6,10-trimethyl-12-oxo-13-oxatetracyclo[8.7.0.0^{2,7}.0^{11,15}]heptadec-11(15)-ene-6-carboxylic acid

Traditional Name

(1R,2R,6S,7R,10R,14S)-14-methoxy-2,6,10-trimethyl-12-oxo-13-oxatetracyclo[8.7.0.0^{2,7}.0^{11,15}]heptadec-11(15)-ene-6-carboxylic acid

CAS Registry Number

Not Available

SMILES

CO[C@H]1OC(=O)C2=C1CC[C@@H]1[C@@]3(C)CCC[C@@](C)([C@@H]3CC[C@@]21C)C(O)=O

InChI Identifier

InChI=1S/C21H30O5/c1-19-9-5-10-21(3,18(23)24)14(19)8-11-20(2)13(19)7-6-12-15(20)16(22)26-17(12)25-4/h13-14,17H,5-11H2,1-4H3,(H,23,24)/t13-,14-,17+,19-,20-,21+/m1/s1

InChI Key

TVJZRHHUGFVBCQ-SOEYYFHNSA-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
Spongia matamata	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
4-carboxy steroid
Steroid acid
Spongiane diterpenoid
Steroid
16-oxasteroid
2-furanone
Dicarboxylic acid or derivatives
Dihydrofuran
Alpha,beta-unsaturated carboxylic ester
Enoate ester
Carboxylic acid ester
Lactone
Organoheterocyclic compound
Oxacycle
Carboxylic acid
Acetal
Carboxylic acid derivative
Hydrocarbon derivative
Organic oxide
Carbonyl group
Organic oxygen compound
Organooxygen compound
Aliphatic heteropolycyclic compound

Molecular Framework

Aliphatic heteropolycyclic compounds

External Descriptors

Not Available

Physical Properties

State

Not Available

Experimental Properties

Property	Value	Reference
Melting Point	Not Available	Not Available
Boiling Point	Not Available	Not Available
Water Solubility	Not Available	Not Available
LogP	Not Available	Not Available

Predicted Properties

Property	Value	Source
logP	4.26	ChemAxon
pKa (Strongest Acidic)	4.35	ChemAxon
pKa (Strongest Basic)	-4.3	ChemAxon
Physiological Charge	-1	ChemAxon
Hydrogen Acceptor Count	4	ChemAxon
Hydrogen Donor Count	1	ChemAxon
Polar Surface Area	72.83 Å²	ChemAxon
Rotatable Bond Count	2	ChemAxon
Refractivity	95.75 m³·mol⁻¹	ChemAxon
Polarizability	39.91 Å³	ChemAxon
Number of Rings	4	ChemAxon
Bioavailability	Yes	ChemAxon
Rule of Five	Yes	ChemAxon
Ghose Filter	Yes	ChemAxon
Veber's Rule	No	ChemAxon
MDDR-like Rule	No	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

10197344

KEGG Compound ID

Not Available

BioCyc ID

Not Available

BiGG ID

Not Available

Wikipedia Link

Not Available

METLIN ID

Not Available

PubChem Compound

21582645

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

LOTUS database [Link]

Showing NP-Card for (1s,3br,5ar,6s,9ar,9br)-1-methoxy-3b,6,9a-trimethyl-3-oxo-1h,4h,5h,5ah,7h,8h,9h,9bh,10h,11h-phenanthro[1,2-c]furan-6-carboxylic acid (NP0292908)

MOL for NP0292908 ((1s,3br,5ar,6s,9ar,9br)-1-methoxy-3b,6,9a-trimethyl-3-oxo-1h,4h,5h,5ah,7h,8h,9h,9bh,10h,11h-phenanthro[1,2-c]furan-6-carboxylic acid)

3D MOL for NP0292908 ((1s,3br,5ar,6s,9ar,9br)-1-methoxy-3b,6,9a-trimethyl-3-oxo-1h,4h,5h,5ah,7h,8h,9h,9bh,10h,11h-phenanthro[1,2-c]furan-6-carboxylic acid)

3D SDF for NP0292908 ((1s,3br,5ar,6s,9ar,9br)-1-methoxy-3b,6,9a-trimethyl-3-oxo-1h,4h,5h,5ah,7h,8h,9h,9bh,10h,11h-phenanthro[1,2-c]furan-6-carboxylic acid)

3D-SDF for NP0292908 ((1s,3br,5ar,6s,9ar,9br)-1-methoxy-3b,6,9a-trimethyl-3-oxo-1h,4h,5h,5ah,7h,8h,9h,9bh,10h,11h-phenanthro[1,2-c]furan-6-carboxylic acid)

PDB for NP0292908 ((1s,3br,5ar,6s,9ar,9br)-1-methoxy-3b,6,9a-trimethyl-3-oxo-1h,4h,5h,5ah,7h,8h,9h,9bh,10h,11h-phenanthro[1,2-c]furan-6-carboxylic acid)

3D PDB for NP0292908 ((1s,3br,5ar,6s,9ar,9br)-1-methoxy-3b,6,9a-trimethyl-3-oxo-1h,4h,5h,5ah,7h,8h,9h,9bh,10h,11h-phenanthro[1,2-c]furan-6-carboxylic acid)

SMILES for NP0292908 ((1s,3br,5ar,6s,9ar,9br)-1-methoxy-3b,6,9a-trimethyl-3-oxo-1h,4h,5h,5ah,7h,8h,9h,9bh,10h,11h-phenanthro[1,2-c]furan-6-carboxylic acid)

INCHI for NP0292908 ((1s,3br,5ar,6s,9ar,9br)-1-methoxy-3b,6,9a-trimethyl-3-oxo-1h,4h,5h,5ah,7h,8h,9h,9bh,10h,11h-phenanthro[1,2-c]furan-6-carboxylic acid)

Structure for NP0292908 ((1s,3br,5ar,6s,9ar,9br)-1-methoxy-3b,6,9a-trimethyl-3-oxo-1h,4h,5h,5ah,7h,8h,9h,9bh,10h,11h-phenanthro[1,2-c]furan-6-carboxylic acid)

3D Structure for NP0292908 ((1s,3br,5ar,6s,9ar,9br)-1-methoxy-3b,6,9a-trimethyl-3-oxo-1h,4h,5h,5ah,7h,8h,9h,9bh,10h,11h-phenanthro[1,2-c]furan-6-carboxylic acid)