NP-MRD: Showing NP-Card for (1r,2s,5r,6r,9r,13r,14s,16s)-6-(furan-3-yl)-9,13-dihydroxy-16-(2-methoxy-2-oxoethyl)-1,5,15,15-tetramethyl-8,17-dioxo-7-oxatetracyclo[11.3.1.0²,¹¹.0⁵,¹⁰]heptadec-10-en-14-yl (2e)-2-methylbut-2-enoate (NP0226614)

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Record Information

Version

2.0

Created at

2022-09-06 05:42:50 UTC

Updated at

2022-09-06 05:42:50 UTC

NP-MRD ID

NP0226614

Secondary Accession Numbers

None

Natural Product Identification

Common Name

(1r,2s,5r,6r,9r,13r,14s,16s)-6-(furan-3-yl)-9,13-dihydroxy-16-(2-methoxy-2-oxoethyl)-1,5,15,15-tetramethyl-8,17-dioxo-7-oxatetracyclo[11.3.1.0²,¹¹.0⁵,¹⁰]heptadec-10-en-14-yl (2e)-2-methylbut-2-enoate

Description

Swietmanin E belongs to the class of organic compounds known as limonoids. These are highly oxygenated, modified terpenoids with a prototypical structure either containing or derived from a precursor with a 4,4,8-trimethyl-17-furanylsteroid skeleton. All naturally occurring citrus limonoids contain a furan ring attached to the D-ring, at C-17, as well as oxygen containing functional groups at C-3, C-4, C-7, C-16 and C-17. (1r,2s,5r,6r,9r,13r,14s,16s)-6-(furan-3-yl)-9,13-dihydroxy-16-(2-methoxy-2-oxoethyl)-1,5,15,15-tetramethyl-8,17-dioxo-7-oxatetracyclo[11.3.1.0²,¹¹.0⁵,¹⁰]heptadec-10-en-14-yl (2e)-2-methylbut-2-enoate is found in Swietenia mahagoni. Based on a literature review very few articles have been published on Swietmanin E.

Structure

MOL SDF PDB SMILES InChI


  Mrv1652309062207422D          

 42 46  0  0  1  0            999 V2000
   -1.5900    3.2351    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0472    2.6138    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2378    2.7732    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0289    3.5539    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.3050    2.1519    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.1144    2.3113    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.0383    1.3712    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.5811    0.7499    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    0.2148    0.0106    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4045    0.5558    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4721   -0.4464    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.4785   -0.7711    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
   -0.1428   -1.3139    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0166   -2.1233    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7973   -2.3900    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6047   -2.6661    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4453   -3.4755    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.2177   -1.1374    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    1.1622   -1.9605    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.0214   -0.0438    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.3881    0.4850    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.3628    1.0136    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    1.4183    1.8367    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.1020    0.6473    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.3657   -0.1345    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.1891   -0.0821    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5554    0.6571    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    3.0983    1.3440    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.3787    0.7095    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.7450    1.4487    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.8357    0.0227    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.4694   -0.7165    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    4.9265   -1.4034    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.7508   -1.4373    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.9732   -2.2318    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.2863   -2.6888    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.6394   -2.1768    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.6461   -0.7689    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    4.1031   -1.4558    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.2798   -1.5081    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.4564   -1.5605    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.9994   -0.8737    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
  1  2  1  0  0  0  0
  2  3  2  0  0  0  0
  3  4  1  0  0  0  0
  3  5  1  0  0  0  0
  5  6  2  0  0  0  0
  5  7  1  0  0  0  0
  8  7  1  6  0  0  0
  8  9  1  0  0  0  0
  9 10  1  0  0  0  0
  9 11  1  0  0  0  0
  9 12  1  0  0  0  0
 12 13  1  1  0  0  0
 13 14  1  0  0  0  0
 14 15  2  0  0  0  0
 14 16  1  0  0  0  0
 16 17  1  0  0  0  0
 12 18  1  0  0  0  0
 18 19  1  1  0  0  0
 18 20  1  0  0  0  0
 20 21  2  0  0  0  0
 20 22  1  0  0  0  0
  8 22  1  0  0  0  0
 22 23  1  1  0  0  0
 22 24  1  0  0  0  0
 24 25  1  0  0  0  0
 25 26  2  0  0  0  0
 26 27  1  0  0  0  0
 27 28  1  1  0  0  0
 27 29  1  0  0  0  0
 29 30  2  0  0  0  0
 29 31  1  0  0  0  0
 31 32  1  0  0  0  0
 32 33  1  1  0  0  0
 33 34  1  0  0  0  0
 34 35  2  0  0  0  0
 35 36  1  0  0  0  0
 36 37  1  0  0  0  0
 33 37  2  0  0  0  0
 32 38  1  0  0  0  0
 26 38  1  0  0  0  0
 38 39  1  1  0  0  0
 38 40  1  0  0  0  0
 40 41  1  0  0  0  0
 42 41  1  6  0  0  0
 25 42  1  0  0  0  0
 18 42  1  0  0  0  0
M  END


  Mrv1652309062207422D          

 42 46  0  0  1  0            999 V2000
   -1.5900    3.2351    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0472    2.6138    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2378    2.7732    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0289    3.5539    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.3050    2.1519    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.1144    2.3113    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.0383    1.3712    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.5811    0.7499    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    0.2148    0.0106    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4045    0.5558    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4721   -0.4464    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.4785   -0.7711    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
   -0.1428   -1.3139    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0166   -2.1233    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7973   -2.3900    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6047   -2.6661    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4453   -3.4755    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.2177   -1.1374    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    1.1622   -1.9605    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.0214   -0.0438    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.3881    0.4850    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.3628    1.0136    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    1.4183    1.8367    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.1020    0.6473    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.3657   -0.1345    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.1891   -0.0821    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5554    0.6571    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    3.0983    1.3440    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.3787    0.7095    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.7450    1.4487    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.8357    0.0227    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.4694   -0.7165    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    4.9265   -1.4034    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.7508   -1.4373    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.9732   -2.2318    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.2863   -2.6888    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.6394   -2.1768    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.6461   -0.7689    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    4.1031   -1.4558    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.2798   -1.5081    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.4564   -1.5605    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.9994   -0.8737    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
  1  2  1  0  0  0  0
  2  3  2  0  0  0  0
  3  4  1  0  0  0  0
  3  5  1  0  0  0  0
  5  6  2  0  0  0  0
  5  7  1  0  0  0  0
  8  7  1  6  0  0  0
  8  9  1  0  0  0  0
  9 10  1  0  0  0  0
  9 11  1  0  0  0  0
  9 12  1  0  0  0  0
 12 13  1  1  0  0  0
 13 14  1  0  0  0  0
 14 15  2  0  0  0  0
 14 16  1  0  0  0  0
 16 17  1  0  0  0  0
 12 18  1  0  0  0  0
 18 19  1  1  0  0  0
 18 20  1  0  0  0  0
 20 21  2  0  0  0  0
 20 22  1  0  0  0  0
  8 22  1  0  0  0  0
 22 23  1  1  0  0  0
 22 24  1  0  0  0  0
 24 25  1  0  0  0  0
 25 26  2  0  0  0  0
 26 27  1  0  0  0  0
 27 28  1  1  0  0  0
 27 29  1  0  0  0  0
 29 30  2  0  0  0  0
 29 31  1  0  0  0  0
 31 32  1  0  0  0  0
 32 33  1  1  0  0  0
 33 34  1  0  0  0  0
 34 35  2  0  0  0  0
 35 36  1  0  0  0  0
 36 37  1  0  0  0  0
 33 37  2  0  0  0  0
 32 38  1  0  0  0  0
 26 38  1  0  0  0  0
 38 39  1  1  0  0  0
 38 40  1  0  0  0  0
 40 41  1  0  0  0  0
 42 41  1  6  0  0  0
 25 42  1  0  0  0  0
 18 42  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0226614

> <DATABASE_NAME>
NP-MRD

> <SMILES>
COC(=O)C[C@H]1C(C)(C)[C@H](OC(=O)C(\C)=C\C)[C@]2(O)CC3=C4[C@@H](O)C(=O)O[C@@H](C5=COC=C5)[C@]4(C)CC[C@@H]3[C@@]1(C)C2=O

> <INCHI_IDENTIFIER>
InChI=1S/C32H40O10/c1-8-16(2)25(35)42-28-29(3,4)20(13-21(33)39-7)31(6)19-9-11-30(5)22(18(19)14-32(28,38)27(31)37)23(34)26(36)41-24(30)17-10-12-40-15-17/h8,10,12,15,19-20,23-24,28,34,38H,9,11,13-14H2,1-7H3/b16-8+/t19-,20-,23+,24-,28-,30+,31+,32-/m0/s1

> <INCHI_KEY>
RXMGRXIKBAZANJ-FNYDSEDVSA-N

> <FORMULA>
C32H40O10

> <MOLECULAR_WEIGHT>
584.662

> <EXACT_MASS>
584.262147488

> <JCHEM_ACCEPTOR_COUNT>
6

> <JCHEM_ATOM_COUNT>
82

> <JCHEM_AVERAGE_POLARIZABILITY>
60.024313657358

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
2

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
0

> <JCHEM_IUPAC>
(1R,2S,5R,6R,9R,13R,14S,16S)-6-(furan-3-yl)-9,13-dihydroxy-16-(2-methoxy-2-oxoethyl)-1,5,15,15-tetramethyl-8,17-dioxo-7-oxatetracyclo[11.3.1.0^{2,11}.0^{5,10}]heptadec-10-en-14-yl (2E)-2-methylbut-2-enoate

> <JCHEM_LOGP>
3.787590400666666

> <JCHEM_MDDR_LIKE_RULE>
1

> <JCHEM_NUMBER_OF_RINGS>
5

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA>
12.354299021660914

> <JCHEM_PKA_STRONGEST_ACIDIC>
11.745023836710935

> <JCHEM_PKA_STRONGEST_BASIC>
-2.888845371017653

> <JCHEM_POLAR_SURFACE_AREA>
149.57

> <JCHEM_REFRACTIVITY>
149.23129999999998

> <JCHEM_ROTATABLE_BOND_COUNT>
7

> <JCHEM_RULE_OF_FIVE>
0

> <JCHEM_TRADITIONAL_IUPAC>
(1R,2S,5R,6R,9R,13R,14S,16S)-6-(furan-3-yl)-9,13-dihydroxy-16-(2-methoxy-2-oxoethyl)-1,5,15,15-tetramethyl-8,17-dioxo-7-oxatetracyclo[11.3.1.0^{2,11}.0^{5,10}]heptadec-10-en-14-yl (2E)-2-methylbut-2-enoate

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 06-SEP-22   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   06-SEP-22         0                                  
HETATM    1  C   UNK     0      -2.968   6.039   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0      -1.955   4.879   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0      -0.444   5.177   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0       0.054   6.634   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0       0.569   4.017   0.000  0.00  0.00           C+0
HETATM    6  O   UNK     0       2.080   4.314   0.000  0.00  0.00           O+0
HETATM    7  O   UNK     0       0.071   2.560   0.000  0.00  0.00           O+0
HETATM    8  C   UNK     0       1.085   1.400   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0       0.401   0.020   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0      -0.755   1.037   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0      -0.881  -0.833   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0       0.893  -1.439   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0      -0.267  -2.453   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0       0.031  -3.964   0.000  0.00  0.00           C+0
HETATM   15  O   UNK     0       1.488  -4.461   0.000  0.00  0.00           O+0
HETATM   16  O   UNK     0      -1.129  -4.977   0.000  0.00  0.00           O+0
HETATM   17  C   UNK     0      -0.831  -6.488   0.000  0.00  0.00           C+0
HETATM   18  C   UNK     0       2.273  -2.123   0.000  0.00  0.00           C+0
HETATM   19  C   UNK     0       2.169  -3.660   0.000  0.00  0.00           C+0
HETATM   20  C   UNK     0       1.907  -0.082   0.000  0.00  0.00           C+0
HETATM   21  O   UNK     0       0.724   0.905   0.000  0.00  0.00           O+0
HETATM   22  C   UNK     0       2.544   1.892   0.000  0.00  0.00           C+0
HETATM   23  O   UNK     0       2.648   3.428   0.000  0.00  0.00           O+0
HETATM   24  C   UNK     0       3.924   1.208   0.000  0.00  0.00           C+0
HETATM   25  C   UNK     0       4.416  -0.251   0.000  0.00  0.00           C+0
HETATM   26  C   UNK     0       5.953  -0.153   0.000  0.00  0.00           C+0
HETATM   27  C   UNK     0       6.637   1.227   0.000  0.00  0.00           C+0
HETATM   28  O   UNK     0       5.784   2.509   0.000  0.00  0.00           O+0
HETATM   29  C   UNK     0       8.174   1.324   0.000  0.00  0.00           C+0
HETATM   30  O   UNK     0       8.857   2.704   0.000  0.00  0.00           O+0
HETATM   31  O   UNK     0       9.027   0.042   0.000  0.00  0.00           O+0
HETATM   32  C   UNK     0       8.343  -1.338   0.000  0.00  0.00           C+0
HETATM   33  C   UNK     0       9.196  -2.620   0.000  0.00  0.00           C+0
HETATM   34  C   UNK     0      10.735  -2.683   0.000  0.00  0.00           C+0
HETATM   35  C   UNK     0      11.150  -4.166   0.000  0.00  0.00           C+0
HETATM   36  O   UNK     0       9.868  -5.019   0.000  0.00  0.00           O+0
HETATM   37  C   UNK     0       8.660  -4.063   0.000  0.00  0.00           C+0
HETATM   38  C   UNK     0       6.806  -1.435   0.000  0.00  0.00           C+0
HETATM   39  C   UNK     0       7.659  -2.717   0.000  0.00  0.00           C+0
HETATM   40  C   UNK     0       6.122  -2.815   0.000  0.00  0.00           C+0
HETATM   41  C   UNK     0       4.585  -2.913   0.000  0.00  0.00           C+0
HETATM   42  C   UNK     0       3.732  -1.631   0.000  0.00  0.00           C+0
CONECT    1    2                                                            
CONECT    2    1    3                                                       
CONECT    3    2    4    5                                                  
CONECT    4    3                                                            
CONECT    5    3    6    7                                                  
CONECT    6    5                                                            
CONECT    7    5    8                                                       
CONECT    8    7    9   22                                                  
CONECT    9    8   10   11   12                                             
CONECT   10    9                                                            
CONECT   11    9                                                            
CONECT   12    9   13   18                                                  
CONECT   13   12   14                                                       
CONECT   14   13   15   16                                                  
CONECT   15   14                                                            
CONECT   16   14   17                                                       
CONECT   17   16                                                            
CONECT   18   12   19   20   42                                             
CONECT   19   18                                                            
CONECT   20   18   21   22                                                  
CONECT   21   20                                                            
CONECT   22   20    8   23   24                                             
CONECT   23   22                                                            
CONECT   24   22   25                                                       
CONECT   25   24   26   42                                                  
CONECT   26   25   27   38                                                  
CONECT   27   26   28   29                                                  
CONECT   28   27                                                            
CONECT   29   27   30   31                                                  
CONECT   30   29                                                            
CONECT   31   29   32                                                       
CONECT   32   31   33   38                                                  
CONECT   33   32   34   37                                                  
CONECT   34   33   35                                                       
CONECT   35   34   36                                                       
CONECT   36   35   37                                                       
CONECT   37   36   33                                                       
CONECT   38   32   26   39   40                                             
CONECT   39   38                                                            
CONECT   40   38   41                                                       
CONECT   41   40   42                                                       
CONECT   42   41   25   18                                                  
MASTER        0    0    0    0    0    0    0    0   42    0   92    0
END

View in JSmol

Synonyms

Not Available

Chemical Formula

C₃₂H₄₀O₁₀

Average Mass

584.6620 Da

Monoisotopic Mass

584.26215 Da

IUPAC Name

(1R,2S,5R,6R,9R,13R,14S,16S)-6-(furan-3-yl)-9,13-dihydroxy-16-(2-methoxy-2-oxoethyl)-1,5,15,15-tetramethyl-8,17-dioxo-7-oxatetracyclo[11.3.1.0^{2,11}.0^{5,10}]heptadec-10-en-14-yl (2E)-2-methylbut-2-enoate

Traditional Name

CAS Registry Number

Not Available

SMILES

COC(=O)C[C@H]1C(C)(C)[C@H](OC(=O)C(\C)=C\C)[C@]2(O)CC3=C4[C@@H](O)C(=O)O[C@@H](C5=COC=C5)[C@]4(C)CC[C@@H]3[C@@]1(C)C2=O

InChI Identifier

InChI=1S/C32H40O10/c1-8-16(2)25(35)42-28-29(3,4)20(13-21(33)39-7)31(6)19-9-11-30(5)22(18(19)14-32(28,38)27(31)37)23(34)26(36)41-24(30)17-10-12-40-15-17/h8,10,12,15,19-20,23-24,28,34,38H,9,11,13-14H2,1-7H3/b16-8+/t19-,20-,23+,24-,28-,30+,31+,32-/m0/s1

InChI Key

RXMGRXIKBAZANJ-FNYDSEDVSA-N

Experimental Spectra

Not Available

Predicted Spectra

Not Available

Chemical Shift Submissions

Not Available

Species

Species of Origin

Species Name	Source	Reference
Swietenia mahagoni	LOTUS Database	35616633

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as limonoids. These are highly oxygenated, modified terpenoids with a prototypical structure either containing or derived from a precursor with a 4,4,8-trimethyl-17-furanylsteroid skeleton. All naturally occurring citrus limonoids contain a furan ring attached to the D-ring, at C-17, as well as oxygen containing functional groups at C-3, C-4, C-7, C-16 and C-17.

Kingdom

Organic compounds

Super Class

Lipids and lipid-like molecules

Class

Prenol lipids

Sub Class

Triterpenoids

Direct Parent

Limonoids

Alternative Parents

Substituents

Limonoid skeleton
Mexicanolide
Steroid lactone
12-hydroxysteroid
Hydroxysteroid
12-alpha-hydroxysteroid
Steroid
Naphthopyran
Naphthalene
Tricarboxylic acid or derivatives
Delta valerolactone
Fatty acid ester
Delta_valerolactone
Fatty acyl
Oxane
Pyran
Cyclic alcohol
Furan
Heteroaromatic compound
Alpha,beta-unsaturated carboxylic ester
Enoate ester
Methyl ester
Tertiary alcohol
Lactone
Ketone
Carboxylic acid ester
Secondary alcohol
Oxacycle
Organoheterocyclic compound
Carboxylic acid derivative
Carbonyl group
Hydrocarbon derivative
Organic oxide
Alcohol
Organooxygen compound
Organic oxygen compound
Aromatic heteropolycyclic compound

Molecular Framework

Aromatic heteropolycyclic compounds

External Descriptors

Not Available

Physical Properties

State

Not Available

Experimental Properties

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

Predicted Properties

Property	Value	Source
logP	3.79	ChemAxon
pKa (Strongest Acidic)	11.75	ChemAxon
pKa (Strongest Basic)	-2.9	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	6	ChemAxon
Hydrogen Donor Count	2	ChemAxon
Polar Surface Area	149.57 Å²	ChemAxon
Rotatable Bond Count	7	ChemAxon
Refractivity	149.23 m³·mol⁻¹	ChemAxon
Polarizability	60.02 Å³	ChemAxon
Number of Rings	5	ChemAxon
Bioavailability	Yes	ChemAxon
Rule of Five	No	ChemAxon
Ghose Filter	No	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

C00048180

Chemspider ID

24664741

KEGG Compound ID

Not Available

BioCyc ID

Not Available

BiGG ID

Not Available

Wikipedia Link

Not Available

METLIN ID

Not Available

PubChem Compound

44613544

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

LOTUS database [Link]

Showing NP-Card for (1r,2s,5r,6r,9r,13r,14s,16s)-6-(furan-3-yl)-9,13-dihydroxy-16-(2-methoxy-2-oxoethyl)-1,5,15,15-tetramethyl-8,17-dioxo-7-oxatetracyclo[11.3.1.0²,¹¹.0⁵,¹⁰]heptadec-10-en-14-yl (2e)-2-methylbut-2-enoate (NP0226614)

MOL for NP0226614 ((1r,2s,5r,6r,9r,13r,14s,16s)-6-(furan-3-yl)-9,13-dihydroxy-16-(2-methoxy-2-oxoethyl)-1,5,15,15-tetramethyl-8,17-dioxo-7-oxatetracyclo[11.3.1.0²,¹¹.0⁵,¹⁰]heptadec-10-en-14-yl (2e)-2-methylbut-2-enoate)

3D MOL for NP0226614 ((1r,2s,5r,6r,9r,13r,14s,16s)-6-(furan-3-yl)-9,13-dihydroxy-16-(2-methoxy-2-oxoethyl)-1,5,15,15-tetramethyl-8,17-dioxo-7-oxatetracyclo[11.3.1.0²,¹¹.0⁵,¹⁰]heptadec-10-en-14-yl (2e)-2-methylbut-2-enoate)

3D SDF for NP0226614 ((1r,2s,5r,6r,9r,13r,14s,16s)-6-(furan-3-yl)-9,13-dihydroxy-16-(2-methoxy-2-oxoethyl)-1,5,15,15-tetramethyl-8,17-dioxo-7-oxatetracyclo[11.3.1.0²,¹¹.0⁵,¹⁰]heptadec-10-en-14-yl (2e)-2-methylbut-2-enoate)

3D-SDF for NP0226614 ((1r,2s,5r,6r,9r,13r,14s,16s)-6-(furan-3-yl)-9,13-dihydroxy-16-(2-methoxy-2-oxoethyl)-1,5,15,15-tetramethyl-8,17-dioxo-7-oxatetracyclo[11.3.1.0²,¹¹.0⁵,¹⁰]heptadec-10-en-14-yl (2e)-2-methylbut-2-enoate)

PDB for NP0226614 ((1r,2s,5r,6r,9r,13r,14s,16s)-6-(furan-3-yl)-9,13-dihydroxy-16-(2-methoxy-2-oxoethyl)-1,5,15,15-tetramethyl-8,17-dioxo-7-oxatetracyclo[11.3.1.0²,¹¹.0⁵,¹⁰]heptadec-10-en-14-yl (2e)-2-methylbut-2-enoate)

3D PDB for NP0226614 ((1r,2s,5r,6r,9r,13r,14s,16s)-6-(furan-3-yl)-9,13-dihydroxy-16-(2-methoxy-2-oxoethyl)-1,5,15,15-tetramethyl-8,17-dioxo-7-oxatetracyclo[11.3.1.0²,¹¹.0⁵,¹⁰]heptadec-10-en-14-yl (2e)-2-methylbut-2-enoate)

SMILES for NP0226614 ((1r,2s,5r,6r,9r,13r,14s,16s)-6-(furan-3-yl)-9,13-dihydroxy-16-(2-methoxy-2-oxoethyl)-1,5,15,15-tetramethyl-8,17-dioxo-7-oxatetracyclo[11.3.1.0²,¹¹.0⁵,¹⁰]heptadec-10-en-14-yl (2e)-2-methylbut-2-enoate)

INCHI for NP0226614 ((1r,2s,5r,6r,9r,13r,14s,16s)-6-(furan-3-yl)-9,13-dihydroxy-16-(2-methoxy-2-oxoethyl)-1,5,15,15-tetramethyl-8,17-dioxo-7-oxatetracyclo[11.3.1.0²,¹¹.0⁵,¹⁰]heptadec-10-en-14-yl (2e)-2-methylbut-2-enoate)

Structure for NP0226614 ((1r,2s,5r,6r,9r,13r,14s,16s)-6-(furan-3-yl)-9,13-dihydroxy-16-(2-methoxy-2-oxoethyl)-1,5,15,15-tetramethyl-8,17-dioxo-7-oxatetracyclo[11.3.1.0²,¹¹.0⁵,¹⁰]heptadec-10-en-14-yl (2e)-2-methylbut-2-enoate)

3D Structure for NP0226614 ((1r,2s,5r,6r,9r,13r,14s,16s)-6-(furan-3-yl)-9,13-dihydroxy-16-(2-methoxy-2-oxoethyl)-1,5,15,15-tetramethyl-8,17-dioxo-7-oxatetracyclo[11.3.1.0²,¹¹.0⁵,¹⁰]heptadec-10-en-14-yl (2e)-2-methylbut-2-enoate)