NP-MRD: Showing NP-Card for methyl (3s)-3-[(1r,2r,4s,7s,8s,11r,12r,16r)-7-(furan-3-yl)-1,8,15,15-tetramethyl-5,18-dioxo-3,6,14-trioxapentacyclo[9.7.0.0²,⁴.0²,⁸.0¹²,¹⁶]octadecan-12-yl]-3-hydroxypropanoate (NP0271448)

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Record Information

Version

2.0

Created at

2022-09-08 17:44:40 UTC

Updated at

2022-09-08 17:44:40 UTC

NP-MRD ID

NP0271448

Secondary Accession Numbers

None

Natural Product Identification

Common Name

methyl (3s)-3-[(1r,2r,4s,7s,8s,11r,12r,16r)-7-(furan-3-yl)-1,8,15,15-tetramethyl-5,18-dioxo-3,6,14-trioxapentacyclo[9.7.0.0²,⁴.0²,⁸.0¹²,¹⁶]octadecan-12-yl]-3-hydroxypropanoate

Description

Methyl (3S)-3-[(1R,2R,4S,7R,8S,11R,12R,16R)-7-(furan-3-yl)-1,8,15,15-tetramethyl-5,18-dioxo-3,6,14-trioxapentacyclo[9.7.0.0²,⁴.0²,⁸.0¹²,¹⁶]Octadecan-12-yl]-3-hydroxypropanoate belongs to the class of organic compounds known as steroid lactones. These are sterol lipids containing a lactone moiety linked to the steroid skeleton. methyl (3s)-3-[(1r,2r,4s,7s,8s,11r,12r,16r)-7-(furan-3-yl)-1,8,15,15-tetramethyl-5,18-dioxo-3,6,14-trioxapentacyclo[9.7.0.0²,⁴.0²,⁸.0¹²,¹⁶]octadecan-12-yl]-3-hydroxypropanoate is found in Citrus aurantium. Based on a literature review very few articles have been published on methyl (3S)-3-[(1R,2R,4S,7R,8S,11R,12R,16R)-7-(furan-3-yl)-1,8,15,15-tetramethyl-5,18-dioxo-3,6,14-trioxapentacyclo[9.7.0.0²,⁴.0²,⁸.0¹²,¹⁶]Octadecan-12-yl]-3-hydroxypropanoate.

Structure

MOL 3D MOL SDF PDB SMILES InChI


  Mrv1652309082219442D          

 36 41  0  0  1  0            999 V2000
    4.2793   -3.3288    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.4770   -2.5278    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.8822   -1.9562    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.0897   -2.1855    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.0798   -1.1552    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.4850   -0.5835    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    2.8021   -1.0465    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.6826    0.2174    0.0000 C   0  0  1  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
    5.0168    0.1741    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.7875    0.9666    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.5996    1.1118    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.7280    1.7894    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.9629    0.9934    0.0000 C   0  0  2  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
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    0.1827    1.0432    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3492    1.6739    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.9948    1.1884    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    1.8069    1.3336    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
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  1  2  1  0  0  0  0
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  9 10  1  0  0  0  0
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  8 14  1  0  0  0  0
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  8 20  1  0  0  0  0
 20 21  1  1  0  0  0
 21 22  1  0  0  0  0
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 23 24  1  6  0  0  0
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 36 35  1  1  0  0  0
 34 36  1  0  0  0  0
 23 36  1  0  0  0  0
 18 36  1  0  0  0  0
M  END

     RDKit          3D

 70 75  0  0  0  0  0  0  0  0999 V2000
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   -4.1923   -0.5682   -2.8315 H   0  0  0  0  0  0  0  0  0  0  0  0
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M  END


  Mrv1652309082219442D          

 36 41  0  0  1  0            999 V2000
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  2  3  1  0  0  0  0
  3  4  2  0  0  0  0
  3  5  1  0  0  0  0
  5  6  1  0  0  0  0
  6  7  1  6  0  0  0
  8  6  1  6  0  0  0
  8  9  1  0  0  0  0
  9 10  1  0  0  0  0
 10 11  1  0  0  0  0
 11 12  1  0  0  0  0
 11 13  1  0  0  0  0
 11 14  1  0  0  0  0
  8 14  1  0  0  0  0
 14 15  1  1  0  0  0
 15 16  1  0  0  0  0
 16 17  2  0  0  0  0
 16 18  1  0  0  0  0
 18 19  1  1  0  0  0
 18 20  1  0  0  0  0
  8 20  1  0  0  0  0
 20 21  1  1  0  0  0
 21 22  1  0  0  0  0
 22 23  1  0  0  0  0
 23 24  1  6  0  0  0
 23 25  1  0  0  0  0
 25 26  1  6  0  0  0
 26 27  1  0  0  0  0
 27 28  2  0  0  0  0
 28 29  1  0  0  0  0
 29 30  1  0  0  0  0
 26 30  2  0  0  0  0
 25 31  1  0  0  0  0
 31 32  1  0  0  0  0
 32 33  2  0  0  0  0
 32 34  1  0  0  0  0
 34 35  1  1  0  0  0
 36 35  1  1  0  0  0
 34 36  1  0  0  0  0
 23 36  1  0  0  0  0
 18 36  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0271448

> <DATABASE_NAME>
NP-MRD

> <SMILES>
COC(=O)C[C@H](O)[C@@]12COC(C)(C)[C@@H]1CC(=O)[C@]1(C)[C@@H]2CC[C@@]2(C)[C@@H](OC(=O)[C@H]3O[C@@]123)C1=COC=C1

> <INCHI_IDENTIFIER>
InChI=1S/C27H34O9/c1-23(2)16-10-17(28)25(4)15(26(16,13-34-23)18(29)11-19(30)32-5)6-8-24(3)20(14-7-9-33-12-14)35-22(31)21-27(24,25)36-21/h7,9,12,15-16,18,20-21,29H,6,8,10-11,13H2,1-5H3/t15-,16-,18-,20-,21+,24-,25-,26+,27+/m0/s1

> <INCHI_KEY>
WHVCPXKLXGUSKV-QGBLDOQRSA-N

> <FORMULA>
C27H34O9

> <MOLECULAR_WEIGHT>
502.56

> <EXACT_MASS>
502.220282675

> <JCHEM_ACCEPTOR_COUNT>
6

> <JCHEM_ATOM_COUNT>
70

> <JCHEM_AVERAGE_POLARIZABILITY>
51.63147980336261

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
1

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
0

> <JCHEM_IUPAC>
methyl (3S)-3-[(1R,2R,4S,7R,8S,11R,12R,16R)-7-(furan-3-yl)-1,8,15,15-tetramethyl-5,18-dioxo-3,6,14-trioxapentacyclo[9.7.0.0^{2,4}.0^{2,8}.0^{12,16}]octadecan-12-yl]-3-hydroxypropanoate

> <JCHEM_LOGP>
1.9386140723333318

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
6

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA>
17.273608370302245

> <JCHEM_PKA_STRONGEST_ACIDIC>
14.338097737794211

> <JCHEM_PKA_STRONGEST_BASIC>
-2.8513646229741574

> <JCHEM_POLAR_SURFACE_AREA>
124.80000000000001

> <JCHEM_REFRACTIVITY>
122.9805

> <JCHEM_ROTATABLE_BOND_COUNT>
5

> <JCHEM_RULE_OF_FIVE>
0

> <JCHEM_TRADITIONAL_IUPAC>
methyl (3S)-3-[(1R,2R,4S,7R,8S,11R,12R,16R)-7-(furan-3-yl)-1,8,15,15-tetramethyl-5,18-dioxo-3,6,14-trioxapentacyclo[9.7.0.0^{2,4}.0^{2,8}.0^{12,16}]octadecan-12-yl]-3-hydroxypropanoate

> <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       7.988  -6.214   0.000  0.00  0.00           C+0
HETATM    2  O   UNK     0       8.357  -4.719   0.000  0.00  0.00           O+0
HETATM    3  C   UNK     0       7.247  -3.652   0.000  0.00  0.00           C+0
HETATM    4  O   UNK     0       5.767  -4.080   0.000  0.00  0.00           O+0
HETATM    5  C   UNK     0       7.616  -2.156   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0       6.505  -1.089   0.000  0.00  0.00           C+0
HETATM    7  O   UNK     0       5.231  -1.953   0.000  0.00  0.00           O+0
HETATM    8  C   UNK     0       6.874   0.406   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0       8.090  -0.539   0.000  0.00  0.00           C+0
HETATM   10  O   UNK     0       9.365   0.325   0.000  0.00  0.00           O+0
HETATM   11  C   UNK     0       8.937   1.804   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0      10.453   2.075   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0       8.826   3.340   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0       7.398   1.854   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0       6.405   3.032   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0       4.889   2.761   0.000  0.00  0.00           C+0
HETATM   17  O   UNK     0       3.896   3.938   0.000  0.00  0.00           O+0
HETATM   18  C   UNK     0       4.366   1.312   0.000  0.00  0.00           C+0
HETATM   19  C   UNK     0       4.254   2.848   0.000  0.00  0.00           C+0
HETATM   20  C   UNK     0       5.358   0.135   0.000  0.00  0.00           C+0
HETATM   21  C   UNK     0       4.835  -1.314   0.000  0.00  0.00           C+0
HETATM   22  C   UNK     0       3.319  -1.585   0.000  0.00  0.00           C+0
HETATM   23  C   UNK     0       2.326  -0.407   0.000  0.00  0.00           C+0
HETATM   24  C   UNK     0       1.803  -1.856   0.000  0.00  0.00           C+0
HETATM   25  C   UNK     0       0.810  -0.678   0.000  0.00  0.00           C+0
HETATM   26  C   UNK     0       0.287  -2.127   0.000  0.00  0.00           C+0
HETATM   27  C   UNK     0       1.151  -3.401   0.000  0.00  0.00           C+0
HETATM   28  C   UNK     0       0.206  -4.617   0.000  0.00  0.00           C+0
HETATM   29  O   UNK     0      -1.242  -4.094   0.000  0.00  0.00           O+0
HETATM   30  C   UNK     0      -1.192  -2.555   0.000  0.00  0.00           C+0
HETATM   31  O   UNK     0      -0.182   0.499   0.000  0.00  0.00           O+0
HETATM   32  C   UNK     0       0.341   1.947   0.000  0.00  0.00           C+0
HETATM   33  O   UNK     0      -0.652   3.125   0.000  0.00  0.00           O+0
HETATM   34  C   UNK     0       1.857   2.218   0.000  0.00  0.00           C+0
HETATM   35  O   UNK     0       3.373   2.489   0.000  0.00  0.00           O+0
HETATM   36  C   UNK     0       2.850   1.041   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    8                                                  
CONECT    7    6                                                            
CONECT    8    6    9   14   20                                             
CONECT    9    8   10                                                       
CONECT   10    9   11                                                       
CONECT   11   10   12   13   14                                             
CONECT   12   11                                                            
CONECT   13   11                                                            
CONECT   14   11    8   15                                                  
CONECT   15   14   16                                                       
CONECT   16   15   17   18                                                  
CONECT   17   16                                                            
CONECT   18   16   19   20   36                                             
CONECT   19   18                                                            
CONECT   20   18    8   21                                                  
CONECT   21   20   22                                                       
CONECT   22   21   23                                                       
CONECT   23   22   24   25   36                                             
CONECT   24   23                                                            
CONECT   25   23   26   31                                                  
CONECT   26   25   27   30                                                  
CONECT   27   26   28                                                       
CONECT   28   27   29                                                       
CONECT   29   28   30                                                       
CONECT   30   29   26                                                       
CONECT   31   25   32                                                       
CONECT   32   31   33   34                                                  
CONECT   33   32                                                            
CONECT   34   32   35   36                                                  
CONECT   35   34   36                                                       
CONECT   36   35   34   23   18                                             
MASTER        0    0    0    0    0    0    0    0   36    0   82    0
END

View in JSmol

Synonyms

Value	Source
Methyl (3S)-3-[(1R,2R,4S,7R,8S,11R,12R,16R)-7-(furan-3-yl)-1,8,15,15-tetramethyl-5,18-dioxo-3,6,14-trioxapentacyclo[9.7.0.0,.0,.0,]octadecan-12-yl]-3-hydroxypropanoic acid	Generator

Chemical Formula

C₂₇H₃₄O₉

Average Mass

502.5600 Da

Monoisotopic Mass

502.22028 Da

IUPAC Name

methyl (3S)-3-[(1R,2R,4S,7R,8S,11R,12R,16R)-7-(furan-3-yl)-1,8,15,15-tetramethyl-5,18-dioxo-3,6,14-trioxapentacyclo[9.7.0.0^{2,4}.0^{2,8}.0^{12,16}]octadecan-12-yl]-3-hydroxypropanoate

Traditional Name

methyl (3S)-3-[(1R,2R,4S,7R,8S,11R,12R,16R)-7-(furan-3-yl)-1,8,15,15-tetramethyl-5,18-dioxo-3,6,14-trioxapentacyclo[9.7.0.0^{2,4}.0^{2,8}.0^{12,16}]octadecan-12-yl]-3-hydroxypropanoate

CAS Registry Number

Not Available

SMILES

COC(=O)C[C@H](O)[C@@]12COC(C)(C)[C@@H]1CC(=O)[C@]1(C)[C@@H]2CC[C@@]2(C)[C@@H](OC(=O)[C@H]3O[C@@]123)C1=COC=C1

InChI Identifier

InChI=1S/C27H34O9/c1-23(2)16-10-17(28)25(4)15(26(16,13-34-23)18(29)11-19(30)32-5)6-8-24(3)20(14-7-9-33-12-14)35-22(31)21-27(24,25)36-21/h7,9,12,15-16,18,20-21,29H,6,8,10-11,13H2,1-5H3/t15-,16-,18-,20-,21+,24-,25-,26+,27+/m0/s1

InChI Key

WHVCPXKLXGUSKV-QGBLDOQRSA-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
Citrus aurantium	LOTUS Database	35616633

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as steroid lactones. These are sterol lipids containing a lactone moiety linked to the steroid skeleton.

Kingdom

Organic compounds

Super Class

Lipids and lipid-like molecules

Class

Steroids and steroid derivatives

Sub Class

Steroid lactones

Direct Parent

Steroid lactones

Alternative Parents

Substituents

Steroid lactone
11-oxosteroid
Oxosteroid
2-oxosteroid
Naphthopyran
Naphthalene
Fatty acid ester
Delta_valerolactone
1,4-dioxepane
Beta-hydroxy acid
Dioxepane
Delta valerolactone
Fatty acyl
Hydroxy acid
Dicarboxylic acid or derivatives
Oxane
Pyran
Tetrahydrofuran
Furan
Methyl ester
Heteroaromatic compound
Secondary alcohol
Lactone
Ketone
Carboxylic acid ester
Organoheterocyclic compound
Oxacycle
Carboxylic acid derivative
Dialkyl ether
Oxirane
Ether
Hydrocarbon derivative
Organic oxide
Alcohol
Organooxygen compound
Organic oxygen compound
Carbonyl group
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	1.94	ChemAxon
pKa (Strongest Acidic)	14.34	ChemAxon
pKa (Strongest Basic)	-2.9	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	6	ChemAxon
Hydrogen Donor Count	1	ChemAxon
Polar Surface Area	124.8 Å²	ChemAxon
Rotatable Bond Count	5	ChemAxon
Refractivity	122.98 m³·mol⁻¹	ChemAxon
Polarizability	51.63 Å³	ChemAxon
Number of Rings	6	ChemAxon
Bioavailability	Yes	ChemAxon
Rule of Five	No	ChemAxon
Ghose Filter	No	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

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

163006631

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

LOTUS database [Link]

Showing NP-Card for methyl (3s)-3-[(1r,2r,4s,7s,8s,11r,12r,16r)-7-(furan-3-yl)-1,8,15,15-tetramethyl-5,18-dioxo-3,6,14-trioxapentacyclo[9.7.0.0²,⁴.0²,⁸.0¹²,¹⁶]octadecan-12-yl]-3-hydroxypropanoate (NP0271448)

MOL for NP0271448 (methyl (3s)-3-[(1r,2r,4s,7s,8s,11r,12r,16r)-7-(furan-3-yl)-1,8,15,15-tetramethyl-5,18-dioxo-3,6,14-trioxapentacyclo[9.7.0.0²,⁴.0²,⁸.0¹²,¹⁶]octadecan-12-yl]-3-hydroxypropanoate)

3D MOL for NP0271448 (methyl (3s)-3-[(1r,2r,4s,7s,8s,11r,12r,16r)-7-(furan-3-yl)-1,8,15,15-tetramethyl-5,18-dioxo-3,6,14-trioxapentacyclo[9.7.0.0²,⁴.0²,⁸.0¹²,¹⁶]octadecan-12-yl]-3-hydroxypropanoate)

3D SDF for NP0271448 (methyl (3s)-3-[(1r,2r,4s,7s,8s,11r,12r,16r)-7-(furan-3-yl)-1,8,15,15-tetramethyl-5,18-dioxo-3,6,14-trioxapentacyclo[9.7.0.0²,⁴.0²,⁸.0¹²,¹⁶]octadecan-12-yl]-3-hydroxypropanoate)

3D-SDF for NP0271448 (methyl (3s)-3-[(1r,2r,4s,7s,8s,11r,12r,16r)-7-(furan-3-yl)-1,8,15,15-tetramethyl-5,18-dioxo-3,6,14-trioxapentacyclo[9.7.0.0²,⁴.0²,⁸.0¹²,¹⁶]octadecan-12-yl]-3-hydroxypropanoate)

PDB for NP0271448 (methyl (3s)-3-[(1r,2r,4s,7s,8s,11r,12r,16r)-7-(furan-3-yl)-1,8,15,15-tetramethyl-5,18-dioxo-3,6,14-trioxapentacyclo[9.7.0.0²,⁴.0²,⁸.0¹²,¹⁶]octadecan-12-yl]-3-hydroxypropanoate)

3D PDB for NP0271448 (methyl (3s)-3-[(1r,2r,4s,7s,8s,11r,12r,16r)-7-(furan-3-yl)-1,8,15,15-tetramethyl-5,18-dioxo-3,6,14-trioxapentacyclo[9.7.0.0²,⁴.0²,⁸.0¹²,¹⁶]octadecan-12-yl]-3-hydroxypropanoate)

SMILES for NP0271448 (methyl (3s)-3-[(1r,2r,4s,7s,8s,11r,12r,16r)-7-(furan-3-yl)-1,8,15,15-tetramethyl-5,18-dioxo-3,6,14-trioxapentacyclo[9.7.0.0²,⁴.0²,⁸.0¹²,¹⁶]octadecan-12-yl]-3-hydroxypropanoate)

INCHI for NP0271448 (methyl (3s)-3-[(1r,2r,4s,7s,8s,11r,12r,16r)-7-(furan-3-yl)-1,8,15,15-tetramethyl-5,18-dioxo-3,6,14-trioxapentacyclo[9.7.0.0²,⁴.0²,⁸.0¹²,¹⁶]octadecan-12-yl]-3-hydroxypropanoate)

Structure for NP0271448 (methyl (3s)-3-[(1r,2r,4s,7s,8s,11r,12r,16r)-7-(furan-3-yl)-1,8,15,15-tetramethyl-5,18-dioxo-3,6,14-trioxapentacyclo[9.7.0.0²,⁴.0²,⁸.0¹²,¹⁶]octadecan-12-yl]-3-hydroxypropanoate)

3D Structure for NP0271448 (methyl (3s)-3-[(1r,2r,4s,7s,8s,11r,12r,16r)-7-(furan-3-yl)-1,8,15,15-tetramethyl-5,18-dioxo-3,6,14-trioxapentacyclo[9.7.0.0²,⁴.0²,⁸.0¹²,¹⁶]octadecan-12-yl]-3-hydroxypropanoate)