NP-MRD: Showing NP-Card for (1r,2r,5s,6s,9r,11s,12s,13s,14r,17r,18r,20s,21r)-20-(acetyloxy)-6-(furan-3-yl)-13-hydroxy-1,5,12,17-tetramethyl-8-oxo-7,10,15-trioxahexacyclo[12.6.1.0²,¹².0⁵,¹¹.0⁹,¹¹.0¹⁷,²¹]henicosan-18-yl acetate (NP0253002)

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Record Information

Version

2.0

Created at

2022-09-07 16:43:44 UTC

Updated at

2022-09-07 16:43:44 UTC

NP-MRD ID

NP0253002

Secondary Accession Numbers

None

Natural Product Identification

Common Name

(1r,2r,5s,6s,9r,11s,12s,13s,14r,17r,18r,20s,21r)-20-(acetyloxy)-6-(furan-3-yl)-13-hydroxy-1,5,12,17-tetramethyl-8-oxo-7,10,15-trioxahexacyclo[12.6.1.0²,¹².0⁵,¹¹.0⁹,¹¹.0¹⁷,²¹]henicosan-18-yl acetate

Description

Cipadesin J 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,2r,5s,6s,9r,11s,12s,13s,14r,17r,18r,20s,21r)-20-(acetyloxy)-6-(furan-3-yl)-13-hydroxy-1,5,12,17-tetramethyl-8-oxo-7,10,15-trioxahexacyclo[12.6.1.0²,¹².0⁵,¹¹.0⁹,¹¹.0¹⁷,²¹]henicosan-18-yl acetate is found in Cipadessa baccifera. Based on a literature review very few articles have been published on Cipadesin J.

Structure

MOL 3D MOL SDF PDB SMILES InChI


  Mrv1652309072218432D          

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 40 16  1  6  0  0  0
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M  END

     RDKit          3D

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M  END


  Mrv1652309072218432D          

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    3.6515   -1.4930    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.4663   -1.6227    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.9859   -0.9819    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    5.2810   -1.7524    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.8007   -1.1116    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    6.0958   -1.8820    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.8925   -2.0962    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.9350   -2.9201    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.1646   -3.2151    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.6459   -2.5736    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.3204   -0.4709    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    6.0253    0.2996    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.5450    0.9403    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.2106    0.4293    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    4.3958    0.5589    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.6909   -0.2115    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    2.3751   -0.6374    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    2.6163   -1.4264    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.2466    0.1775    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
  8  9  1  0  0  0  0
  9 10  1  0  0  0  0
  9 11  2  0  0  0  0
  7 12  1  0  0  0  0
 12 13  1  6  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  1  0  0  0
 17 19  1  0  0  0  0
 19 20  1  6  0  0  0
 19 21  1  0  0  0  0
 21 22  1  6  0  0  0
 22 23  1  0  0  0  0
 23 24  1  0  0  0  0
 24 25  1  1  0  0  0
 24 26  1  0  0  0  0
 26 27  1  1  0  0  0
 27 28  1  0  0  0  0
 28 29  2  0  0  0  0
 29 30  1  0  0  0  0
 30 31  1  0  0  0  0
 27 31  2  0  0  0  0
 26 32  1  0  0  0  0
 32 33  1  0  0  0  0
 33 34  2  0  0  0  0
 33 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
 24 37  1  0  0  0  0
 19 37  1  0  0  0  0
 21 38  1  0  0  0  0
  5 38  1  0  0  0  0
 38 39  1  6  0  0  0
 38 40  1  0  0  0  0
 40 16  1  6  0  0  0
 12 40  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0253002

> <DATABASE_NAME>
NP-MRD

> <SMILES>
CC(=O)O[C@@H]1C[C@H](OC(C)=O)[C@@]2(C)[C@H]3[C@@H](OC[C@]13C)[C@@H](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/C30H38O10/c1-14(31)37-18-11-19(38-15(2)32)28(5)17-7-9-27(4)23(16-8-10-35-12-16)39-25(34)24-30(27,40-24)29(17,6)22(33)20-21(28)26(18,3)13-36-20/h8,10,12,17-24,33H,7,9,11,13H2,1-6H3/t17-,18-,19+,20-,21+,22-,23+,24+,26-,27+,28+,29+,30+/m1/s1

> <INCHI_KEY>
LVAGOWFLIUIEFT-LAFZNRGESA-N

> <FORMULA>
C30H38O10

> <MOLECULAR_WEIGHT>
558.624

> <EXACT_MASS>
558.246497424

> <JCHEM_ACCEPTOR_COUNT>
6

> <JCHEM_ATOM_COUNT>
78

> <JCHEM_AVERAGE_POLARIZABILITY>
56.85727906359685

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
1

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
0

> <JCHEM_IUPAC>
(1R,2R,5S,6R,9R,11S,12S,13S,14R,17R,18R,20S,21R)-20-(acetyloxy)-6-(furan-3-yl)-13-hydroxy-1,5,12,17-tetramethyl-8-oxo-7,10,15-trioxahexacyclo[12.6.1.0^{2,12}.0^{5,11}.0^{9,11}.0^{17,21}]henicosan-18-yl acetate

> <JCHEM_LOGP>
1.7601359936666678

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
7

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA_STRONGEST_ACIDIC>
13.64901366209003

> <JCHEM_PKA_STRONGEST_BASIC>
-2.851265951777052

> <JCHEM_POLAR_SURFACE_AREA>
134.03

> <JCHEM_REFRACTIVITY>
134.89450000000002

> <JCHEM_ROTATABLE_BOND_COUNT>
5

> <JCHEM_RULE_OF_FIVE>
0

> <JCHEM_TRADITIONAL_IUPAC>
(1R,2R,5S,6R,9R,11S,12S,13S,14R,17R,18R,20S,21R)-20-(acetyloxy)-6-(furan-3-yl)-13-hydroxy-1,5,12,17-tetramethyl-8-oxo-7,10,15-trioxahexacyclo[12.6.1.0^{2,12}.0^{5,11}.0^{9,11}.0^{17,21}]henicosan-18-yl acetate

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 07-SEP-22   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   07-SEP-22         0                                  
HETATM    1  C   UNK     0       0.841  -4.095   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0       2.278  -4.648   0.000  0.00  0.00           C+0
HETATM    3  O   UNK     0       2.518  -6.169   0.000  0.00  0.00           O+0
HETATM    4  O   UNK     0       3.476  -3.679   0.000  0.00  0.00           O+0
HETATM    5  C   UNK     0       3.236  -2.158   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0       1.799  -1.605   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0       1.559  -0.084   0.000  0.00  0.00           C+0
HETATM    8  O   UNK     0       0.122   0.469   0.000  0.00  0.00           O+0
HETATM    9  C   UNK     0      -1.076  -0.499   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0      -0.836  -2.020   0.000  0.00  0.00           C+0
HETATM   11  O   UNK     0      -2.513   0.054   0.000  0.00  0.00           O+0
HETATM   12  C   UNK     0       2.756   0.884   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0       1.385   1.585   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0       2.838   2.422   0.000  0.00  0.00           C+0
HETATM   15  O   UNK     0       4.326   2.820   0.000  0.00  0.00           O+0
HETATM   16  C   UNK     0       5.164   1.527   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0       6.685   1.285   0.000  0.00  0.00           C+0
HETATM   18  O   UNK     0       7.655   2.481   0.000  0.00  0.00           O+0
HETATM   19  C   UNK     0       7.235  -0.153   0.000  0.00  0.00           C+0
HETATM   20  C   UNK     0       7.317   1.385   0.000  0.00  0.00           C+0
HETATM   21  C   UNK     0       6.265  -1.349   0.000  0.00  0.00           C+0
HETATM   22  C   UNK     0       6.816  -2.787   0.000  0.00  0.00           C+0
HETATM   23  C   UNK     0       8.337  -3.029   0.000  0.00  0.00           C+0
HETATM   24  C   UNK     0       9.307  -1.833   0.000  0.00  0.00           C+0
HETATM   25  C   UNK     0       9.858  -3.271   0.000  0.00  0.00           C+0
HETATM   26  C   UNK     0      10.828  -2.075   0.000  0.00  0.00           C+0
HETATM   27  C   UNK     0      11.379  -3.513   0.000  0.00  0.00           C+0
HETATM   28  C   UNK     0      12.866  -3.913   0.000  0.00  0.00           C+0
HETATM   29  C   UNK     0      12.945  -5.451   0.000  0.00  0.00           C+0
HETATM   30  O   UNK     0      11.507  -6.002   0.000  0.00  0.00           O+0
HETATM   31  C   UNK     0      10.539  -4.804   0.000  0.00  0.00           C+0
HETATM   32  O   UNK     0      11.798  -0.879   0.000  0.00  0.00           O+0
HETATM   33  C   UNK     0      11.247   0.559   0.000  0.00  0.00           C+0
HETATM   34  O   UNK     0      12.217   1.755   0.000  0.00  0.00           O+0
HETATM   35  C   UNK     0       9.726   0.801   0.000  0.00  0.00           C+0
HETATM   36  O   UNK     0       8.206   1.043   0.000  0.00  0.00           O+0
HETATM   37  C   UNK     0       8.756  -0.395   0.000  0.00  0.00           C+0
HETATM   38  C   UNK     0       4.433  -1.190   0.000  0.00  0.00           C+0
HETATM   39  C   UNK     0       4.884  -2.663   0.000  0.00  0.00           C+0
HETATM   40  C   UNK     0       4.194   0.331   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   38                                                  
CONECT    6    5    7                                                       
CONECT    7    6    8   12                                                  
CONECT    8    7    9                                                       
CONECT    9    8   10   11                                                  
CONECT   10    9                                                            
CONECT   11    9                                                            
CONECT   12    7   13   14   40                                             
CONECT   13   12                                                            
CONECT   14   12   15                                                       
CONECT   15   14   16                                                       
CONECT   16   15   17   40                                                  
CONECT   17   16   18   19                                                  
CONECT   18   17                                                            
CONECT   19   17   20   21   37                                             
CONECT   20   19                                                            
CONECT   21   19   22   38                                                  
CONECT   22   21   23                                                       
CONECT   23   22   24                                                       
CONECT   24   23   25   26   37                                             
CONECT   25   24                                                            
CONECT   26   24   27   32                                                  
CONECT   27   26   28   31                                                  
CONECT   28   27   29                                                       
CONECT   29   28   30                                                       
CONECT   30   29   31                                                       
CONECT   31   30   27                                                       
CONECT   32   26   33                                                       
CONECT   33   32   34   35                                                  
CONECT   34   33                                                            
CONECT   35   33   36   37                                                  
CONECT   36   35   37                                                       
CONECT   37   36   35   24   19                                             
CONECT   38   21    5   39   40                                             
CONECT   39   38                                                            
CONECT   40   38   16   12                                                  
MASTER        0    0    0    0    0    0    0    0   40    0   92    0
END

View in JSmol

Synonyms

Not Available

Chemical Formula

C₃₀H₃₈O₁₀

Average Mass

558.6240 Da

Monoisotopic Mass

558.24650 Da

IUPAC Name

Not Available

Traditional Name

Not Available

CAS Registry Number

Not Available

SMILES

CC(=O)O[C@@H]1C[C@H](OC(C)=O)[C@@]2(C)[C@H]3[C@@H](OC[C@]13C)[C@@H](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/C30H38O10/c1-14(31)37-18-11-19(38-15(2)32)28(5)17-7-9-27(4)23(16-8-10-35-12-16)39-25(34)24-30(27,40-24)29(17,6)22(33)20-21(28)26(18,3)13-36-20/h8,10,12,17-24,33H,7,9,11,13H2,1-6H3/t17-,18-,19+,20-,21+,22-,23+,24+,26-,27+,28+,29+,30+/m1/s1

InChI Key

LVAGOWFLIUIEFT-LAFZNRGESA-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
Cipadessa baccifera	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
Naphthopyran
Naphthofuran
Naphthalene
Tricarboxylic acid or derivatives
1,4-dioxepane
Delta valerolactone
Dioxepane
Delta_valerolactone
Pyran
Oxane
Tetrahydrofuran
Heteroaromatic compound
Cyclic alcohol
Furan
Secondary alcohol
Carboxylic acid ester
Lactone
Organoheterocyclic compound
Oxacycle
Carboxylic acid derivative
Dialkyl ether
Oxirane
Ether
Organic oxygen compound
Alcohol
Hydrocarbon derivative
Organooxygen compound
Organic oxide
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

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

25052845

KEGG Compound ID

Not Available

BioCyc ID

Not Available

BiGG ID

Not Available

Wikipedia Link

Not Available

METLIN ID

Not Available

PubChem Compound

46918555

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

LOTUS database [Link]

Showing NP-Card for (1r,2r,5s,6s,9r,11s,12s,13s,14r,17r,18r,20s,21r)-20-(acetyloxy)-6-(furan-3-yl)-13-hydroxy-1,5,12,17-tetramethyl-8-oxo-7,10,15-trioxahexacyclo[12.6.1.0²,¹².0⁵,¹¹.0⁹,¹¹.0¹⁷,²¹]henicosan-18-yl acetate (NP0253002)

MOL for NP0253002 ((1r,2r,5s,6s,9r,11s,12s,13s,14r,17r,18r,20s,21r)-20-(acetyloxy)-6-(furan-3-yl)-13-hydroxy-1,5,12,17-tetramethyl-8-oxo-7,10,15-trioxahexacyclo[12.6.1.0²,¹².0⁵,¹¹.0⁹,¹¹.0¹⁷,²¹]henicosan-18-yl acetate)

3D MOL for NP0253002 ((1r,2r,5s,6s,9r,11s,12s,13s,14r,17r,18r,20s,21r)-20-(acetyloxy)-6-(furan-3-yl)-13-hydroxy-1,5,12,17-tetramethyl-8-oxo-7,10,15-trioxahexacyclo[12.6.1.0²,¹².0⁵,¹¹.0⁹,¹¹.0¹⁷,²¹]henicosan-18-yl acetate)

3D SDF for NP0253002 ((1r,2r,5s,6s,9r,11s,12s,13s,14r,17r,18r,20s,21r)-20-(acetyloxy)-6-(furan-3-yl)-13-hydroxy-1,5,12,17-tetramethyl-8-oxo-7,10,15-trioxahexacyclo[12.6.1.0²,¹².0⁵,¹¹.0⁹,¹¹.0¹⁷,²¹]henicosan-18-yl acetate)

3D-SDF for NP0253002 ((1r,2r,5s,6s,9r,11s,12s,13s,14r,17r,18r,20s,21r)-20-(acetyloxy)-6-(furan-3-yl)-13-hydroxy-1,5,12,17-tetramethyl-8-oxo-7,10,15-trioxahexacyclo[12.6.1.0²,¹².0⁵,¹¹.0⁹,¹¹.0¹⁷,²¹]henicosan-18-yl acetate)

PDB for NP0253002 ((1r,2r,5s,6s,9r,11s,12s,13s,14r,17r,18r,20s,21r)-20-(acetyloxy)-6-(furan-3-yl)-13-hydroxy-1,5,12,17-tetramethyl-8-oxo-7,10,15-trioxahexacyclo[12.6.1.0²,¹².0⁵,¹¹.0⁹,¹¹.0¹⁷,²¹]henicosan-18-yl acetate)

3D PDB for NP0253002 ((1r,2r,5s,6s,9r,11s,12s,13s,14r,17r,18r,20s,21r)-20-(acetyloxy)-6-(furan-3-yl)-13-hydroxy-1,5,12,17-tetramethyl-8-oxo-7,10,15-trioxahexacyclo[12.6.1.0²,¹².0⁵,¹¹.0⁹,¹¹.0¹⁷,²¹]henicosan-18-yl acetate)

SMILES for NP0253002 ((1r,2r,5s,6s,9r,11s,12s,13s,14r,17r,18r,20s,21r)-20-(acetyloxy)-6-(furan-3-yl)-13-hydroxy-1,5,12,17-tetramethyl-8-oxo-7,10,15-trioxahexacyclo[12.6.1.0²,¹².0⁵,¹¹.0⁹,¹¹.0¹⁷,²¹]henicosan-18-yl acetate)

INCHI for NP0253002 ((1r,2r,5s,6s,9r,11s,12s,13s,14r,17r,18r,20s,21r)-20-(acetyloxy)-6-(furan-3-yl)-13-hydroxy-1,5,12,17-tetramethyl-8-oxo-7,10,15-trioxahexacyclo[12.6.1.0²,¹².0⁵,¹¹.0⁹,¹¹.0¹⁷,²¹]henicosan-18-yl acetate)

Structure for NP0253002 ((1r,2r,5s,6s,9r,11s,12s,13s,14r,17r,18r,20s,21r)-20-(acetyloxy)-6-(furan-3-yl)-13-hydroxy-1,5,12,17-tetramethyl-8-oxo-7,10,15-trioxahexacyclo[12.6.1.0²,¹².0⁵,¹¹.0⁹,¹¹.0¹⁷,²¹]henicosan-18-yl acetate)

3D Structure for NP0253002 ((1r,2r,5s,6s,9r,11s,12s,13s,14r,17r,18r,20s,21r)-20-(acetyloxy)-6-(furan-3-yl)-13-hydroxy-1,5,12,17-tetramethyl-8-oxo-7,10,15-trioxahexacyclo[12.6.1.0²,¹².0⁵,¹¹.0⁹,¹¹.0¹⁷,²¹]henicosan-18-yl acetate)