NP-MRD: Showing NP-Card for (1s,2s,5s,6s,8r,10r,11s,12r,14r,15r,16r,19s,21r)-6-(furan-3-yl)-12,16,19-trihydroxy-5,11,15-trimethyl-3-oxo-9,17-dioxahexacyclo[13.3.3.0¹,¹⁴.0²,¹¹.0⁵,¹⁰.0⁸,¹⁰]henicosan-21-yl acetate (NP0287558)

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Record Information

Version

2.0

Created at

2022-09-09 16:45:15 UTC

Updated at

2022-09-09 16:45:16 UTC

NP-MRD ID

NP0287558

Secondary Accession Numbers

None

Natural Product Identification

Common Name

(1s,2s,5s,6s,8r,10r,11s,12r,14r,15r,16r,19s,21r)-6-(furan-3-yl)-12,16,19-trihydroxy-5,11,15-trimethyl-3-oxo-9,17-dioxahexacyclo[13.3.3.0¹,¹⁴.0²,¹¹.0⁵,¹⁰.0⁸,¹⁰]henicosan-21-yl acetate

Description

(1S,2S,5S,6R,8R,10R,11S,12R,14R,15R,16R,19S,21R)-6-(furan-3-yl)-12,16,19-trihydroxy-5,11,15-trimethyl-3-oxo-9,17-dioxahexacyclo[13.3.3.0¹,¹⁴.0²,¹¹.0⁵,¹⁰.0⁸,¹⁰]Henicosan-21-yl acetate 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. (1s,2s,5s,6s,8r,10r,11s,12r,14r,15r,16r,19s,21r)-6-(furan-3-yl)-12,16,19-trihydroxy-5,11,15-trimethyl-3-oxo-9,17-dioxahexacyclo[13.3.3.0¹,¹⁴.0²,¹¹.0⁵,¹⁰.0⁸,¹⁰]henicosan-21-yl acetate is found in Pterorhachis zenkeri. Based on a literature review very few articles have been published on (1S,2S,5S,6R,8R,10R,11S,12R,14R,15R,16R,19S,21R)-6-(furan-3-yl)-12,16,19-trihydroxy-5,11,15-trimethyl-3-oxo-9,17-dioxahexacyclo[13.3.3.0¹,¹⁴.0²,¹¹.0⁵,¹⁰.0⁸,¹⁰]Henicosan-21-yl acetate.

Structure

MOL 3D MOL SDF PDB SMILES InChI


  Mrv1652309092218452D          

 37 43  0  0  1  0            999 V2000
    4.6181    3.8463    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
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    2.9940    0.6156    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
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  9 22  1  0  0  0  0
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M  END

     RDKit          3D

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M  END


  Mrv1652309092218452D          

 37 43  0  0  1  0            999 V2000
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    0.4155   -0.9024    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0635   -0.0756    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
   -0.5294   -0.6493    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4137   -1.4661    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1548   -1.8286    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7285   -1.2358    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3420   -0.5069    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0522    0.7413    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.6889    1.1038    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    1.4891    1.3042    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.2626    0.5109    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
  2  4  1  0  0  0  0
  5  4  1  1  0  0  0
  5  6  1  0  0  0  0
  6  7  1  0  0  0  0
  7  8  1  1  0  0  0
  7  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
 12 14  1  0  0  0  0
  5 14  1  0  0  0  0
 14 15  1  1  0  0  0
 14 16  1  0  0  0  0
  9 16  1  0  0  0  0
 16 17  1  1  0  0  0
 17 18  1  0  0  0  0
 18 19  1  6  0  0  0
 18 20  1  0  0  0  0
 20 21  1  1  0  0  0
 20 22  1  0  0  0  0
  9 22  1  0  0  0  0
 22 23  1  6  0  0  0
 23 24  2  0  0  0  0
 23 25  1  0  0  0  0
 25 26  1  0  0  0  0
 26 27  1  6  0  0  0
 26 28  1  0  0  0  0
 28 29  1  6  0  0  0
 29 30  1  0  0  0  0
 30 31  2  0  0  0  0
 31 32  1  0  0  0  0
 32 33  1  0  0  0  0
 29 33  2  0  0  0  0
 28 34  1  0  0  0  0
 34 35  1  0  0  0  0
 35 36  1  1  0  0  0
 37 36  1  1  0  0  0
 35 37  1  0  0  0  0
 26 37  1  0  0  0  0
 20 37  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0287558

> <DATABASE_NAME>
NP-MRD

> <SMILES>
CC(=O)O[C@@H]1C[C@H](O)[C@@]23CO[C@@H](O)[C@]1(C)[C@@H]2C[C@@H](O)[C@]1(C)[C@H]3C(=O)C[C@@]2(C)[C@@H](C[C@H]3O[C@@]123)C1=COC=C1

> <INCHI_IDENTIFIER>
InChI=1S/C28H36O9/c1-13(29)36-20-9-19(32)27-12-35-23(33)25(20,3)17(27)8-18(31)26(4)22(27)16(30)10-24(2)15(14-5-6-34-11-14)7-21-28(24,26)37-21/h5-6,11,15,17-23,31-33H,7-10,12H2,1-4H3/t15-,17-,18+,19-,20+,21+,22+,23+,24-,25+,26+,27+,28+/m0/s1

> <INCHI_KEY>
DTKVYFQSFHHKAR-PPQCXHAGSA-N

> <FORMULA>
C28H36O9

> <MOLECULAR_WEIGHT>
516.587

> <EXACT_MASS>
516.235932739

> <JCHEM_ACCEPTOR_COUNT>
7

> <JCHEM_ATOM_COUNT>
73

> <JCHEM_AVERAGE_POLARIZABILITY>
53.18430166816377

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
3

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
0

> <JCHEM_IUPAC>
(1S,2S,5S,6R,8R,10R,11S,12R,14R,15R,16R,19S,21R)-6-(furan-3-yl)-12,16,19-trihydroxy-5,11,15-trimethyl-3-oxo-9,17-dioxahexacyclo[13.3.3.0^{1,14}.0^{2,11}.0^{5,10}.0^{8,10}]henicosan-21-yl acetate

> <JCHEM_LOGP>
0.3414609883333334

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
7

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA>
13.205791521193337

> <JCHEM_PKA_STRONGEST_ACIDIC>
11.855641968227067

> <JCHEM_PKA_STRONGEST_BASIC>
-2.8442402702706673

> <JCHEM_POLAR_SURFACE_AREA>
138.96

> <JCHEM_REFRACTIVITY>
126.71839999999997

> <JCHEM_ROTATABLE_BOND_COUNT>
3

> <JCHEM_RULE_OF_FIVE>
0

> <JCHEM_TRADITIONAL_IUPAC>
(1S,2S,5S,6R,8R,10R,11S,12R,14R,15R,16R,19S,21R)-6-(furan-3-yl)-12,16,19-trihydroxy-5,11,15-trimethyl-3-oxo-9,17-dioxahexacyclo[13.3.3.0^{1,14}.0^{2,11}.0^{5,10}.0^{8,10}]henicosan-21-yl acetate

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 09-SEP-22   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   09-SEP-22         0                                  
HETATM    1  C   UNK     0       8.620   7.180   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0       8.702   5.642   0.000  0.00  0.00           C+0
HETATM    3  O   UNK     0      10.074   4.943   0.000  0.00  0.00           O+0
HETATM    4  O   UNK     0       7.411   4.803   0.000  0.00  0.00           O+0
HETATM    5  C   UNK     0       7.492   3.265   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0       5.754   2.863   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0       5.589   1.149   0.000  0.00  0.00           C+0
HETATM    8  O   UNK     0       4.101   1.547   0.000  0.00  0.00           O+0
HETATM    9  C   UNK     0       6.252  -0.241   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0       7.704  -0.754   0.000  0.00  0.00           C+0
HETATM   11  O   UNK     0       9.094  -0.090   0.000  0.00  0.00           O+0
HETATM   12  C   UNK     0       9.607   1.362   0.000  0.00  0.00           C+0
HETATM   13  O   UNK     0      11.145   1.443   0.000  0.00  0.00           O+0
HETATM   14  C   UNK     0       8.944   2.751   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0       9.974   3.896   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0       7.224   1.592   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0       6.156   2.425   0.000  0.00  0.00           C+0
HETATM   18  C   UNK     0       4.617   2.370   0.000  0.00  0.00           C+0
HETATM   19  O   UNK     0       3.800   3.675   0.000  0.00  0.00           O+0
HETATM   20  C   UNK     0       3.896   1.009   0.000  0.00  0.00           C+0
HETATM   21  C   UNK     0       3.522   2.503   0.000  0.00  0.00           C+0
HETATM   22  C   UNK     0       4.713  -0.296   0.000  0.00  0.00           C+0
HETATM   23  C   UNK     0       3.992  -1.656   0.000  0.00  0.00           C+0
HETATM   24  O   UNK     0       4.809  -2.962   0.000  0.00  0.00           O+0
HETATM   25  C   UNK     0       2.453  -1.712   0.000  0.00  0.00           C+0
HETATM   26  C   UNK     0       1.635  -0.407   0.000  0.00  0.00           C+0
HETATM   27  C   UNK     0       0.776  -1.684   0.000  0.00  0.00           C+0
HETATM   28  C   UNK     0       0.118  -0.141   0.000  0.00  0.00           C+0
HETATM   29  C   UNK     0      -0.988  -1.212   0.000  0.00  0.00           C+0
HETATM   30  C   UNK     0      -0.772  -2.737   0.000  0.00  0.00           C+0
HETATM   31  C   UNK     0      -2.156  -3.413   0.000  0.00  0.00           C+0
HETATM   32  O   UNK     0      -3.227  -2.307   0.000  0.00  0.00           O+0
HETATM   33  C   UNK     0      -2.505  -0.946   0.000  0.00  0.00           C+0
HETATM   34  C   UNK     0      -0.098   1.384   0.000  0.00  0.00           C+0
HETATM   35  C   UNK     0       1.286   2.060   0.000  0.00  0.00           C+0
HETATM   36  O   UNK     0       2.780   2.435   0.000  0.00  0.00           O+0
HETATM   37  C   UNK     0       2.357   0.954   0.000  0.00  0.00           C+0
CONECT    1    2                                                            
CONECT    2    1    3    4                                                  
CONECT    3    2                                                            
CONECT    4    2    5                                                       
CONECT    5    4    6   14                                                  
CONECT    6    5    7                                                       
CONECT    7    6    8    9                                                  
CONECT    8    7                                                            
CONECT    9    7   10   16   22                                             
CONECT   10    9   11                                                       
CONECT   11   10   12                                                       
CONECT   12   11   13   14                                                  
CONECT   13   12                                                            
CONECT   14   12    5   15   16                                             
CONECT   15   14                                                            
CONECT   16   14    9   17                                                  
CONECT   17   16   18                                                       
CONECT   18   17   19   20                                                  
CONECT   19   18                                                            
CONECT   20   18   21   22   37                                             
CONECT   21   20                                                            
CONECT   22   20    9   23                                                  
CONECT   23   22   24   25                                                  
CONECT   24   23                                                            
CONECT   25   23   26                                                       
CONECT   26   25   27   28   37                                             
CONECT   27   26                                                            
CONECT   28   26   29   34                                                  
CONECT   29   28   30   33                                                  
CONECT   30   29   31                                                       
CONECT   31   30   32                                                       
CONECT   32   31   33                                                       
CONECT   33   32   29                                                       
CONECT   34   28   35                                                       
CONECT   35   34   36   37                                                  
CONECT   36   35   37                                                       
CONECT   37   36   35   26   20                                             
MASTER        0    0    0    0    0    0    0    0   37    0   86    0
END

View in JSmol

Synonyms

Value	Source
(1S,2S,5S,6R,8R,10R,11S,12R,14R,15R,16R,19S,21R)-6-(Furan-3-yl)-12,16,19-trihydroxy-5,11,15-trimethyl-3-oxo-9,17-dioxahexacyclo[13.3.3.0,.0,.0,.0,]henicosan-21-yl acetic acid	Generator

Chemical Formula

C₂₈H₃₆O₉

Average Mass

516.5870 Da

Monoisotopic Mass

516.23593 Da

IUPAC Name

(1S,2S,5S,6R,8R,10R,11S,12R,14R,15R,16R,19S,21R)-6-(furan-3-yl)-12,16,19-trihydroxy-5,11,15-trimethyl-3-oxo-9,17-dioxahexacyclo[13.3.3.0^{1,14}.0^{2,11}.0^{5,10}.0^{8,10}]henicosan-21-yl acetate

Traditional Name

(1S,2S,5S,6R,8R,10R,11S,12R,14R,15R,16R,19S,21R)-6-(furan-3-yl)-12,16,19-trihydroxy-5,11,15-trimethyl-3-oxo-9,17-dioxahexacyclo[13.3.3.0^{1,14}.0^{2,11}.0^{5,10}.0^{8,10}]henicosan-21-yl acetate

CAS Registry Number

Not Available

SMILES

CC(=O)O[C@@H]1C[C@H](O)[C@@]23CO[C@@H](O)[C@]1(C)[C@@H]2C[C@@H](O)[C@]1(C)[C@H]3C(=O)C[C@@]2(C)[C@@H](C[C@H]3O[C@@]123)C1=COC=C1

InChI Identifier

InChI=1S/C28H36O9/c1-13(29)36-20-9-19(32)27-12-35-23(33)25(20,3)17(27)8-18(31)26(4)22(27)16(30)10-24(2)15(14-5-6-34-11-14)7-21-28(24,26)37-21/h5-6,11,15,17-23,31-33H,7-10,12H2,1-4H3/t15-,17-,18+,19-,20+,21+,22+,23+,24-,25+,26+,27+,28+/m0/s1

InChI Key

DTKVYFQSFHHKAR-PPQCXHAGSA-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
Pterorhachis zenkeri	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
17-furanylsteroid skeleton
Steroid ester
Naphthopyran
Naphthalene
Pyran
Oxane
Cyclic alcohol
Heteroaromatic compound
Furan
Carboxylic acid ester
Hemiacetal
Secondary alcohol
Ketone
Carboxylic acid derivative
Dialkyl ether
Oxirane
Ether
Oxacycle
Organoheterocyclic compound
Polyol
Monocarboxylic acid or derivatives
Carbonyl group
Organic oxygen compound
Organic oxide
Hydrocarbon derivative
Organooxygen compound
Alcohol
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	0.34	ChemAxon
pKa (Strongest Acidic)	11.86	ChemAxon
pKa (Strongest Basic)	-2.8	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	7	ChemAxon
Hydrogen Donor Count	3	ChemAxon
Polar Surface Area	138.96 Å²	ChemAxon
Rotatable Bond Count	3	ChemAxon
Refractivity	126.72 m³·mol⁻¹	ChemAxon
Polarizability	53.18 Å³	ChemAxon
Number of Rings	7	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

162946249

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

LOTUS database [Link]

Showing NP-Card for (1s,2s,5s,6s,8r,10r,11s,12r,14r,15r,16r,19s,21r)-6-(furan-3-yl)-12,16,19-trihydroxy-5,11,15-trimethyl-3-oxo-9,17-dioxahexacyclo[13.3.3.0¹,¹⁴.0²,¹¹.0⁵,¹⁰.0⁸,¹⁰]henicosan-21-yl acetate (NP0287558)

MOL for NP0287558 ((1s,2s,5s,6s,8r,10r,11s,12r,14r,15r,16r,19s,21r)-6-(furan-3-yl)-12,16,19-trihydroxy-5,11,15-trimethyl-3-oxo-9,17-dioxahexacyclo[13.3.3.0¹,¹⁴.0²,¹¹.0⁵,¹⁰.0⁸,¹⁰]henicosan-21-yl acetate)

3D MOL for NP0287558 ((1s,2s,5s,6s,8r,10r,11s,12r,14r,15r,16r,19s,21r)-6-(furan-3-yl)-12,16,19-trihydroxy-5,11,15-trimethyl-3-oxo-9,17-dioxahexacyclo[13.3.3.0¹,¹⁴.0²,¹¹.0⁵,¹⁰.0⁸,¹⁰]henicosan-21-yl acetate)

3D SDF for NP0287558 ((1s,2s,5s,6s,8r,10r,11s,12r,14r,15r,16r,19s,21r)-6-(furan-3-yl)-12,16,19-trihydroxy-5,11,15-trimethyl-3-oxo-9,17-dioxahexacyclo[13.3.3.0¹,¹⁴.0²,¹¹.0⁵,¹⁰.0⁸,¹⁰]henicosan-21-yl acetate)

3D-SDF for NP0287558 ((1s,2s,5s,6s,8r,10r,11s,12r,14r,15r,16r,19s,21r)-6-(furan-3-yl)-12,16,19-trihydroxy-5,11,15-trimethyl-3-oxo-9,17-dioxahexacyclo[13.3.3.0¹,¹⁴.0²,¹¹.0⁵,¹⁰.0⁸,¹⁰]henicosan-21-yl acetate)

PDB for NP0287558 ((1s,2s,5s,6s,8r,10r,11s,12r,14r,15r,16r,19s,21r)-6-(furan-3-yl)-12,16,19-trihydroxy-5,11,15-trimethyl-3-oxo-9,17-dioxahexacyclo[13.3.3.0¹,¹⁴.0²,¹¹.0⁵,¹⁰.0⁸,¹⁰]henicosan-21-yl acetate)

3D PDB for NP0287558 ((1s,2s,5s,6s,8r,10r,11s,12r,14r,15r,16r,19s,21r)-6-(furan-3-yl)-12,16,19-trihydroxy-5,11,15-trimethyl-3-oxo-9,17-dioxahexacyclo[13.3.3.0¹,¹⁴.0²,¹¹.0⁵,¹⁰.0⁸,¹⁰]henicosan-21-yl acetate)

SMILES for NP0287558 ((1s,2s,5s,6s,8r,10r,11s,12r,14r,15r,16r,19s,21r)-6-(furan-3-yl)-12,16,19-trihydroxy-5,11,15-trimethyl-3-oxo-9,17-dioxahexacyclo[13.3.3.0¹,¹⁴.0²,¹¹.0⁵,¹⁰.0⁸,¹⁰]henicosan-21-yl acetate)

INCHI for NP0287558 ((1s,2s,5s,6s,8r,10r,11s,12r,14r,15r,16r,19s,21r)-6-(furan-3-yl)-12,16,19-trihydroxy-5,11,15-trimethyl-3-oxo-9,17-dioxahexacyclo[13.3.3.0¹,¹⁴.0²,¹¹.0⁵,¹⁰.0⁸,¹⁰]henicosan-21-yl acetate)

Structure for NP0287558 ((1s,2s,5s,6s,8r,10r,11s,12r,14r,15r,16r,19s,21r)-6-(furan-3-yl)-12,16,19-trihydroxy-5,11,15-trimethyl-3-oxo-9,17-dioxahexacyclo[13.3.3.0¹,¹⁴.0²,¹¹.0⁵,¹⁰.0⁸,¹⁰]henicosan-21-yl acetate)

3D Structure for NP0287558 ((1s,2s,5s,6s,8r,10r,11s,12r,14r,15r,16r,19s,21r)-6-(furan-3-yl)-12,16,19-trihydroxy-5,11,15-trimethyl-3-oxo-9,17-dioxahexacyclo[13.3.3.0¹,¹⁴.0²,¹¹.0⁵,¹⁰.0⁸,¹⁰]henicosan-21-yl acetate)