NP-MRD: Showing NP-Card for (1's,2r,5s,6s,10'z,12'e,14'r,16'e,19'r)-6-[(2e)-but-2-en-2-yl]-7'-hydroxy-10'-(hydroxymethyl)-5,6',14',16'-tetramethyl-2',20'-dioxaspiro[oxane-2,21'-tricyclo[17.3.1.0⁴,⁹]tricosane]-4',6',8',10',12',16'-hexaen-3'-one (NP0288386)

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Record Information

Version

2.0

Created at

2022-09-09 18:03:58 UTC

Updated at

2022-09-09 18:03:58 UTC

NP-MRD ID

NP0288386

Secondary Accession Numbers

None

Natural Product Identification

Common Name

(1's,2r,5s,6s,10'z,12'e,14'r,16'e,19'r)-6-[(2e)-but-2-en-2-yl]-7'-hydroxy-10'-(hydroxymethyl)-5,6',14',16'-tetramethyl-2',20'-dioxaspiro[oxane-2,21'-tricyclo[17.3.1.0⁴,⁹]tricosane]-4',6',8',10',12',16'-hexaen-3'-one

Description

VM54339 belongs to the class of organic compounds known as milbemycins. These are a group of macrolides with a structure containing a 16-membered lactone ring fused to a 1,7-dioxaspiroundecane ring system and to either a benzofuran (or hydrogenated derivative thereof). In some cases (e.G. Milbemycin E), the tetrahydrofuranyl ring is missing. Milbemycins can be o-glycosylated at C13 to form Avermectins. Milbemycins are produced by Streptomyces species. Based on a literature review very few articles have been published on VM54339.

Structure

MOL 3D MOL SDF PDB SMILES InChI


  Mrv1652309092220032D          

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M  END

     RDKit          3D

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M  END


  Mrv1652309092220032D          

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    8.1208   -2.6414    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.1886   -3.4636    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.9345   -3.8160    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.5104   -3.9335    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.7645   -3.5811    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    6.0863   -4.0509    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.6967   -2.7589    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.9507   -2.4065    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.8829   -1.5843    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.1369   -1.2319    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.4588   -1.7017    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.7128   -1.3494    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.0691   -0.4097    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.3232   -0.0573    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.2553    0.7649    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5094    1.1172    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.9335    1.2347    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.8657    2.0569    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.6794    0.8823    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.7473    0.0601    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.4932   -0.2922    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.5610   -1.1145    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    7.1714    0.1776    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    9.4092   -0.8795    0.0000 O   0  0  0  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
  5  3  1  1  0  0  0
  5  6  1  0  0  0  0
  7  6  1  1  0  0  0
  7  8  1  0  0  0  0
  8  9  1  0  0  0  0
  9 10  1  0  0  0  0
  5 10  1  0  0  0  0
 10 11  1  6  0  0  0
  7 12  1  0  0  0  0
 12 13  1  0  0  0  0
 13 14  1  6  0  0  0
 15 14  1  6  0  0  0
 15 16  1  0  0  0  0
 16 17  1  0  0  0  0
 17 18  2  0  0  0  0
 18 19  1  0  0  0  0
 18 20  1  0  0  0  0
 20 21  1  0  0  0  0
 21 22  1  1  0  0  0
 21 23  1  0  0  0  0
 23 24  2  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  0  0  0  0
 26 29  1  0  0  0  0
 29 30  2  0  0  0  0
 30 31  1  0  0  0  0
 31 32  1  0  0  0  0
 31 33  2  0  0  0  0
 33 34  1  0  0  0  0
 33 35  1  0  0  0  0
 35 36  2  0  0  0  0
 29 36  1  0  0  0  0
 36 37  1  0  0  0  0
 37 38  2  0  0  0  0
 37 39  1  0  0  0  0
 13 39  1  0  0  0  0
 15 40  1  0  0  0  0
  7 40  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0288386

> <DATABASE_NAME>
NP-MRD

> <SMILES>
C\C=C(/C)[C@H]1O[C@]2(CC[C@@H]1C)C[C@@H]1C[C@@H](C\C=C(C)\C[C@@H](C)\C=C\C=C(CO)\C3=CC(O)=C(C)C=C3C(=O)O1)O2

> <INCHI_IDENTIFIER>
InChI=1S/C34H46O6/c1-7-23(4)32-24(5)13-14-34(40-32)19-28-17-27(39-34)12-11-22(3)15-21(2)9-8-10-26(20-35)29-18-31(36)25(6)16-30(29)33(37)38-28/h7-11,16,18,21,24,27-28,32,35-36H,12-15,17,19-20H2,1-6H3/b9-8+,22-11+,23-7+,26-10+/t21-,24-,27+,28-,32+,34+/m0/s1

> <INCHI_KEY>
KOPYOPABTFQTRP-WMDGEUCHSA-N

> <FORMULA>
C34H46O6

> <MOLECULAR_WEIGHT>
550.736

> <EXACT_MASS>
550.329439201

> <JCHEM_ACCEPTOR_COUNT>
5

> <JCHEM_ATOM_COUNT>
86

> <JCHEM_AVERAGE_POLARIZABILITY>
62.45547893045307

> <JCHEM_BIOAVAILABILITY>
0

> <JCHEM_DONOR_COUNT>
2

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
0

> <JCHEM_IUPAC>
(1'S,2R,5S,6S,10'Z,12'E,14'R,16'E,19'R)-6-[(2E)-but-2-en-2-yl]-7'-hydroxy-10'-(hydroxymethyl)-5,6',14',16'-tetramethyl-2',20'-dioxaspiro[oxane-2,21'-tricyclo[17.3.1.0^{4,9}]tricosane]-4'(9'),5',7',10',12',16'-hexaen-3'-one

> <JCHEM_LOGP>
7.281112252333332

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
4

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA>
14.96791158369319

> <JCHEM_PKA_STRONGEST_ACIDIC>
8.734764929804024

> <JCHEM_PKA_STRONGEST_BASIC>
-2.828843944484734

> <JCHEM_POLAR_SURFACE_AREA>
85.22000000000001

> <JCHEM_REFRACTIVITY>
162.59330000000003

> <JCHEM_ROTATABLE_BOND_COUNT>
2

> <JCHEM_RULE_OF_FIVE>
0

> <JCHEM_TRADITIONAL_IUPAC>
(1'S,2R,5S,6S,10'Z,12'E,14'R,16'E,19'R)-6-[(2E)-but-2-en-2-yl]-7'-hydroxy-10'-(hydroxymethyl)-5,6',14',16'-tetramethyl-2',20'-dioxaspiro[oxane-2,21'-tricyclo[17.3.1.0^{4,9}]tricosane]-4'(9'),5',7',10',12',16'-hexaen-3'-one

> <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      23.007  -2.738   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0      21.615  -2.080   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0      21.488  -0.546   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0      22.754   0.331   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0      20.096   0.112   0.000  0.00  0.00           C+0
HETATM    6  O   UNK     0      18.830  -0.765   0.000  0.00  0.00           O+0
HETATM    7  C   UNK     0      17.437  -0.107   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0      17.311   1.428   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0      18.577   2.305   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0      19.969   1.647   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0      21.235   2.524   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0      16.045   0.551   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0      14.779  -0.326   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0      14.906  -1.861   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0      16.298  -2.519   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0      16.425  -4.054   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0      15.159  -4.931   0.000  0.00  0.00           C+0
HETATM   18  C   UNK     0      15.285  -6.465   0.000  0.00  0.00           C+0
HETATM   19  C   UNK     0      16.678  -7.123   0.000  0.00  0.00           C+0
HETATM   20  C   UNK     0      14.019  -7.342   0.000  0.00  0.00           C+0
HETATM   21  C   UNK     0      12.627  -6.685   0.000  0.00  0.00           C+0
HETATM   22  C   UNK     0      11.361  -7.562   0.000  0.00  0.00           C+0
HETATM   23  C   UNK     0      12.500  -5.150   0.000  0.00  0.00           C+0
HETATM   24  C   UNK     0      11.108  -4.492   0.000  0.00  0.00           C+0
HETATM   25  C   UNK     0      10.981  -2.957   0.000  0.00  0.00           C+0
HETATM   26  C   UNK     0       9.589  -2.300   0.000  0.00  0.00           C+0
HETATM   27  C   UNK     0       8.323  -3.177   0.000  0.00  0.00           C+0
HETATM   28  O   UNK     0       6.931  -2.519   0.000  0.00  0.00           O+0
HETATM   29  C   UNK     0       9.462  -0.765   0.000  0.00  0.00           C+0
HETATM   30  C   UNK     0       8.070  -0.107   0.000  0.00  0.00           C+0
HETATM   31  C   UNK     0       7.943   1.428   0.000  0.00  0.00           C+0
HETATM   32  O   UNK     0       6.551   2.086   0.000  0.00  0.00           O+0
HETATM   33  C   UNK     0       9.209   2.305   0.000  0.00  0.00           C+0
HETATM   34  C   UNK     0       9.083   3.840   0.000  0.00  0.00           C+0
HETATM   35  C   UNK     0      10.602   1.647   0.000  0.00  0.00           C+0
HETATM   36  C   UNK     0      10.728   0.112   0.000  0.00  0.00           C+0
HETATM   37  C   UNK     0      12.121  -0.546   0.000  0.00  0.00           C+0
HETATM   38  O   UNK     0      12.247  -2.080   0.000  0.00  0.00           O+0
HETATM   39  O   UNK     0      13.387   0.331   0.000  0.00  0.00           O+0
HETATM   40  O   UNK     0      17.564  -1.642   0.000  0.00  0.00           O+0
CONECT    1    2                                                            
CONECT    2    1    3                                                       
CONECT    3    2    4    5                                                  
CONECT    4    3                                                            
CONECT    5    3    6   10                                                  
CONECT    6    5    7                                                       
CONECT    7    6    8   12   40                                             
CONECT    8    7    9                                                       
CONECT    9    8   10                                                       
CONECT   10    9    5   11                                                  
CONECT   11   10                                                            
CONECT   12    7   13                                                       
CONECT   13   12   14   39                                                  
CONECT   14   13   15                                                       
CONECT   15   14   16   40                                                  
CONECT   16   15   17                                                       
CONECT   17   16   18                                                       
CONECT   18   17   19   20                                                  
CONECT   19   18                                                            
CONECT   20   18   21                                                       
CONECT   21   20   22   23                                                  
CONECT   22   21                                                            
CONECT   23   21   24                                                       
CONECT   24   23   25                                                       
CONECT   25   24   26                                                       
CONECT   26   25   27   29                                                  
CONECT   27   26   28                                                       
CONECT   28   27                                                            
CONECT   29   26   30   36                                                  
CONECT   30   29   31                                                       
CONECT   31   30   32   33                                                  
CONECT   32   31                                                            
CONECT   33   31   34   35                                                  
CONECT   34   33                                                            
CONECT   35   33   36                                                       
CONECT   36   35   29   37                                                  
CONECT   37   36   38   39                                                  
CONECT   38   37                                                            
CONECT   39   37   13                                                       
CONECT   40   15    7                                                       
MASTER        0    0    0    0    0    0    0    0   40    0   86    0
END

View in JSmol

Synonyms

Not Available

Chemical Formula

C₃₄H₄₆O₆

Average Mass

550.7360 Da

Monoisotopic Mass

550.32944 Da

IUPAC Name

(1'S,2R,5S,6S,10'Z,12'E,14'R,16'E,19'R)-6-[(2E)-but-2-en-2-yl]-7'-hydroxy-10'-(hydroxymethyl)-5,6',14',16'-tetramethyl-2',20'-dioxaspiro[oxane-2,21'-tricyclo[17.3.1.0^{4,9}]tricosane]-4'(9'),5',7',10',12',16'-hexaen-3'-one

Traditional Name

CAS Registry Number

Not Available

SMILES

C\C=C(/C)[C@H]1O[C@]2(CC[C@@H]1C)C[C@@H]1C[C@@H](C\C=C(C)\C[C@@H](C)\C=C\C=C(CO)\C3=CC(O)=C(C)C=C3C(=O)O1)O2

InChI Identifier

InChI=1S/C34H46O6/c1-7-23(4)32-24(5)13-14-34(40-32)19-28-17-27(39-34)12-11-22(3)15-21(2)9-8-10-26(20-35)29-18-31(36)25(6)16-30(29)33(37)38-28/h7-11,16,18,21,24,27-28,32,35-36H,12-15,17,19-20H2,1-6H3/b9-8+,22-11+,23-7+,26-10+/t21-,24-,27+,28-,32+,34+/m0/s1

InChI Key

KOPYOPABTFQTRP-WMDGEUCHSA-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

Not Available

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as milbemycins. These are a group of macrolides with a structure containing a 16-membered lactone ring fused to a 1,7-dioxaspiroundecane ring system and to either a benzofuran (or hydrogenated derivative thereof). In some cases (e.G. Milbemycin E), the tetrahydrofuranyl ring is missing. Milbemycins can be o-glycosylated at C13 to form Avermectins. Milbemycins are produced by Streptomyces species.

Kingdom

Organic compounds

Super Class

Phenylpropanoids and polyketides

Class

Macrolides and analogues

Sub Class

Milbemycins

Direct Parent

Milbemycins

Alternative Parents

Substituents

Milbemycin
1-hydroxy-2-unsubstituted benzenoid
Ketal
Oxane
Benzenoid
Carboxylic acid ester
Lactone
Monocarboxylic acid or derivatives
Acetal
Carboxylic acid derivative
Organoheterocyclic compound
Oxacycle
Hydrocarbon derivative
Primary alcohol
Organic oxide
Organooxygen compound
Organic oxygen 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	7.28	ChemAxon
pKa (Strongest Acidic)	8.73	ChemAxon
pKa (Strongest Basic)	-2.8	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	5	ChemAxon
Hydrogen Donor Count	2	ChemAxon
Polar Surface Area	85.22 Å²	ChemAxon
Rotatable Bond Count	2	ChemAxon
Refractivity	162.59 m³·mol⁻¹	ChemAxon
Polarizability	62.46 Å³	ChemAxon
Number of Rings	4	ChemAxon
Bioavailability	No	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

8849580

KEGG Compound ID

Not Available

BioCyc ID

Not Available

BiGG ID

Not Available

Wikipedia Link

Not Available

METLIN ID

Not Available

PubChem Compound

10674230

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

LOTUS database [Link]

Showing NP-Card for (1's,2r,5s,6s,10'z,12'e,14'r,16'e,19'r)-6-[(2e)-but-2-en-2-yl]-7'-hydroxy-10'-(hydroxymethyl)-5,6',14',16'-tetramethyl-2',20'-dioxaspiro[oxane-2,21'-tricyclo[17.3.1.0⁴,⁹]tricosane]-4',6',8',10',12',16'-hexaen-3'-one (NP0288386)

MOL for NP0288386 ((1's,2r,5s,6s,10'z,12'e,14'r,16'e,19'r)-6-[(2e)-but-2-en-2-yl]-7'-hydroxy-10'-(hydroxymethyl)-5,6',14',16'-tetramethyl-2',20'-dioxaspiro[oxane-2,21'-tricyclo[17.3.1.0⁴,⁹]tricosane]-4',6',8',10',12',16'-hexaen-3'-one)

3D MOL for NP0288386 ((1's,2r,5s,6s,10'z,12'e,14'r,16'e,19'r)-6-[(2e)-but-2-en-2-yl]-7'-hydroxy-10'-(hydroxymethyl)-5,6',14',16'-tetramethyl-2',20'-dioxaspiro[oxane-2,21'-tricyclo[17.3.1.0⁴,⁹]tricosane]-4',6',8',10',12',16'-hexaen-3'-one)

3D SDF for NP0288386 ((1's,2r,5s,6s,10'z,12'e,14'r,16'e,19'r)-6-[(2e)-but-2-en-2-yl]-7'-hydroxy-10'-(hydroxymethyl)-5,6',14',16'-tetramethyl-2',20'-dioxaspiro[oxane-2,21'-tricyclo[17.3.1.0⁴,⁹]tricosane]-4',6',8',10',12',16'-hexaen-3'-one)

3D-SDF for NP0288386 ((1's,2r,5s,6s,10'z,12'e,14'r,16'e,19'r)-6-[(2e)-but-2-en-2-yl]-7'-hydroxy-10'-(hydroxymethyl)-5,6',14',16'-tetramethyl-2',20'-dioxaspiro[oxane-2,21'-tricyclo[17.3.1.0⁴,⁹]tricosane]-4',6',8',10',12',16'-hexaen-3'-one)

PDB for NP0288386 ((1's,2r,5s,6s,10'z,12'e,14'r,16'e,19'r)-6-[(2e)-but-2-en-2-yl]-7'-hydroxy-10'-(hydroxymethyl)-5,6',14',16'-tetramethyl-2',20'-dioxaspiro[oxane-2,21'-tricyclo[17.3.1.0⁴,⁹]tricosane]-4',6',8',10',12',16'-hexaen-3'-one)

3D PDB for NP0288386 ((1's,2r,5s,6s,10'z,12'e,14'r,16'e,19'r)-6-[(2e)-but-2-en-2-yl]-7'-hydroxy-10'-(hydroxymethyl)-5,6',14',16'-tetramethyl-2',20'-dioxaspiro[oxane-2,21'-tricyclo[17.3.1.0⁴,⁹]tricosane]-4',6',8',10',12',16'-hexaen-3'-one)

SMILES for NP0288386 ((1's,2r,5s,6s,10'z,12'e,14'r,16'e,19'r)-6-[(2e)-but-2-en-2-yl]-7'-hydroxy-10'-(hydroxymethyl)-5,6',14',16'-tetramethyl-2',20'-dioxaspiro[oxane-2,21'-tricyclo[17.3.1.0⁴,⁹]tricosane]-4',6',8',10',12',16'-hexaen-3'-one)

INCHI for NP0288386 ((1's,2r,5s,6s,10'z,12'e,14'r,16'e,19'r)-6-[(2e)-but-2-en-2-yl]-7'-hydroxy-10'-(hydroxymethyl)-5,6',14',16'-tetramethyl-2',20'-dioxaspiro[oxane-2,21'-tricyclo[17.3.1.0⁴,⁹]tricosane]-4',6',8',10',12',16'-hexaen-3'-one)

Structure for NP0288386 ((1's,2r,5s,6s,10'z,12'e,14'r,16'e,19'r)-6-[(2e)-but-2-en-2-yl]-7'-hydroxy-10'-(hydroxymethyl)-5,6',14',16'-tetramethyl-2',20'-dioxaspiro[oxane-2,21'-tricyclo[17.3.1.0⁴,⁹]tricosane]-4',6',8',10',12',16'-hexaen-3'-one)

3D Structure for NP0288386 ((1's,2r,5s,6s,10'z,12'e,14'r,16'e,19'r)-6-[(2e)-but-2-en-2-yl]-7'-hydroxy-10'-(hydroxymethyl)-5,6',14',16'-tetramethyl-2',20'-dioxaspiro[oxane-2,21'-tricyclo[17.3.1.0⁴,⁹]tricosane]-4',6',8',10',12',16'-hexaen-3'-one)