NP-MRD: Showing NP-Card for (1s,4s,8s,9r,11r)-9-tert-butyl-7,9-dihydroxy-3,5,12-trioxatetracyclo[6.6.0.0¹,¹¹.0⁴,⁸]tetradecane-2,6,13-trione (NP0229718)

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Record Information

Version

2.0

Created at

2022-09-06 09:54:04 UTC

Updated at

2022-09-06 09:54:04 UTC

NP-MRD ID

NP0229718

Secondary Accession Numbers

None

Natural Product Identification

Common Name

(1s,4s,8s,9r,11r)-9-tert-butyl-7,9-dihydroxy-3,5,12-trioxatetracyclo[6.6.0.0¹,¹¹.0⁴,⁸]tetradecane-2,6,13-trione

Description

Bilobalide belongs to the class of organic compounds known as ginkgolides and bilobalides. These are diterpene lactones with a structure based either on the gingkolide or the bilobalide skeleton. The ginkgolide skeleton is a very rigid structure consisting of hexacyclic C20 trilactone. The cis-fused F/A/D/C ring junction forms an empty semi-ball hole, the D ring contains a cage form tetrahydrofuran ring which occupies the center of the empty hole, and the oxygen atoms of the D,C and F ring and 10-hydroxyl group consist of an analogous crown ether structure. (1s,4s,8s,9r,11r)-9-tert-butyl-7,9-dihydroxy-3,5,12-trioxatetracyclo[6.6.0.0¹,¹¹.0⁴,⁸]tetradecane-2,6,13-trione is found in Ginkgo biloba. Based on a literature review very few articles have been published on Bilobalide.

Structure

MOL 3D MOL SDF PDB SMILES InChI

     RDKit          3D

 41 44  0  0  0  0  0  0  0  0999 V2000
    2.4172   -0.7782    1.7010 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.7466    0.1030    0.6175 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.3309    1.4643    0.9374 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.3252   -0.3744   -0.6573 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.2964   -0.0407    0.8195 C   0  0  2  0  0  0  0  0  0  0  0  0
   -0.0097    0.4181    2.1197 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0730   -1.5479    0.9298 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5156   -1.8198   -0.4322 C   0  0  1  0  0  0  0  0  0  0  0  0
   -1.5029   -2.7973   -0.6470 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1596   -2.3464   -1.7950 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8182   -2.9947   -2.6433 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9598   -0.8423   -1.8975 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4585   -0.6040   -0.5773 C   0  0  1  0  0  0  0  0  0  0  0  0
   -2.4755   -0.8698    0.5052 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.2457   -1.8894    0.5820 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3967    0.2194    1.3919 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8857    1.2042    0.6427 C   0  0  1  0  0  0  0  0  0  0  0  0
   -1.3449    2.3575    1.0613 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7086    2.8763   -0.0647 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4465    4.1007   -0.2641 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4261    1.6902   -0.9345 C   0  0  2  0  0  0  0  0  0  0  0  0
   -1.4424    1.7410   -1.9253 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6878    0.5303   -0.1048 C   0  0  1  0  0  0  0  0  0  0  0  0
    3.3916   -0.3566    2.0249 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.7167   -1.7742    1.2577 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.7887   -0.8711    2.5797 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.2630    1.7164    2.0311 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.4503    1.3042    0.8131 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.0889    2.2691    0.2732 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.3649    0.0568   -0.7777 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.8003   -0.1388   -1.5715 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.5100   -1.4897   -0.6868 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.3051    1.3087    2.3155 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.7317   -2.1530    1.3110 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9385   -1.6827    1.6217 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.2064   -1.8894   -1.2219 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1642   -0.7151   -2.6588 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.9040   -0.3499   -2.2076 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5947    1.4215   -0.2140 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.4968    1.8647   -1.4351 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0718    1.6793   -2.8196 H   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0
  2  3  1  0
  2  4  1  0
  2  5  1  0
  5  6  1  1
  5  7  1  0
  7  8  1  0
  8  9  1  0
  9 10  1  0
 10 11  2  0
 10 12  1  0
 12 13  1  0
 13 14  1  1
 14 15  2  0
 14 16  1  0
 16 17  1  0
 17 18  1  0
 18 19  1  0
 19 20  2  0
 19 21  1  0
 21 22  1  0
 21 23  1  0
 23  5  1  1
 13  8  1  0
 23 13  1  0
 23 17  1  0
  1 24  1  0
  1 25  1  0
  1 26  1  0
  3 27  1  0
  3 28  1  0
  3 29  1  0
  4 30  1  0
  4 31  1  0
  4 32  1  0
  6 33  1  0
  7 34  1  0
  7 35  1  0
  8 36  1  6
 12 37  1  0
 12 38  1  0
 17 39  1  6
 21 40  1  6
 22 41  1  0
M  END


  Mrv1652309062211542D          

 23 26  0  0  1  0            999 V2000
    1.4667    3.9411    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.7191    3.0199    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.8617    3.2772    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.6200    3.4456    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.0880    1.9806    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    1.2717    2.3457    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.8379    2.3246    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.3968    1.7178    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    4.2056    1.5554    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.3011    0.7359    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.1305    0.5364    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.5512    0.3919    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.9923    0.9987    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    3.0878    0.1793    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.8799   -0.3325    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.3380   -0.1648    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.7791    0.4421    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    0.9702    0.6045    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.8747    1.4240    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0803    1.4907    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.6246    1.7680    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.0778    2.5678    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.1835    1.1612    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
  1  2  1  0  0  0  0
  2  3  1  0  0  0  0
  2  4  1  0  0  0  0
  5  2  1  6  0  0  0
  5  6  1  1  0  0  0
  5  7  1  0  0  0  0
  7  8  1  0  0  0  0
  8  9  1  1  0  0  0
  9 10  1  0  0  0  0
 10 11  2  0  0  0  0
 10 12  1  0  0  0  0
 13 12  1  6  0  0  0
  8 13  1  0  0  0  0
 13 14  1  0  0  0  0
 14 15  2  0  0  0  0
 14 16  1  0  0  0  0
 17 16  1  1  0  0  0
 17 18  1  0  0  0  0
 18 19  1  0  0  0  0
 19 20  2  0  0  0  0
 19 21  1  0  0  0  0
 21 22  1  0  0  0  0
 23 21  1  6  0  0  0
 17 23  1  0  0  0  0
 13 23  1  0  0  0  0
  5 23  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0229718

> <DATABASE_NAME>
NP-MRD

> <SMILES>
CC(C)(C)[C@]1(O)C[C@H]2OC(=O)C[C@@]22C(=O)O[C@H]3OC(=O)C(O)[C@]123

> <INCHI_IDENTIFIER>
InChI=1S/C15H18O8/c1-12(2,3)14(20)4-6-13(5-7(16)21-6)10(19)23-11-15(13,14)8(17)9(18)22-11/h6,8,11,17,20H,4-5H2,1-3H3/t6-,8?,11-,13+,14-,15-/m1/s1

> <INCHI_KEY>
MOLPUWBMSBJXER-MJLURTQYSA-N

> <FORMULA>
C15H18O8

> <MOLECULAR_WEIGHT>
326.301

> <EXACT_MASS>
326.10016754

> <JCHEM_ACCEPTOR_COUNT>
5

> <JCHEM_ATOM_COUNT>
41

> <JCHEM_AVERAGE_POLARIZABILITY>
30.0960460243725

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
2

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
0

> <JCHEM_IUPAC>
(1S,4S,8S,9R,11R)-9-tert-butyl-7,9-dihydroxy-3,5,12-trioxatetracyclo[6.6.0.0^{1,11}.0^{4,8}]tetradecane-2,6,13-trione

> <JCHEM_LOGP>
-0.5177614286666664

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
4

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA>
13.776747765035385

> <JCHEM_PKA_STRONGEST_ACIDIC>
11.974249820349915

> <JCHEM_PKA_STRONGEST_BASIC>
-3.37953725747988

> <JCHEM_POLAR_SURFACE_AREA>
119.36

> <JCHEM_REFRACTIVITY>
69.98790000000002

> <JCHEM_ROTATABLE_BOND_COUNT>
1

> <JCHEM_RULE_OF_FIVE>
1

> <JCHEM_TRADITIONAL_IUPAC>
(1S,4S,8S,9R,11R)-9-tert-butyl-7,9-dihydroxy-3,5,12-trioxatetracyclo[6.6.0.0^{1,11}.0^{4,8}]tetradecane-2,6,13-trione

> <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       2.738   7.357   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0       3.209   5.637   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0       1.609   6.117   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0       4.891   6.432   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0       3.898   3.697   0.000  0.00  0.00           C+0
HETATM    6  O   UNK     0       2.374   4.379   0.000  0.00  0.00           O+0
HETATM    7  C   UNK     0       5.297   4.339   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0       6.341   3.207   0.000  0.00  0.00           C+0
HETATM    9  O   UNK     0       7.850   2.903   0.000  0.00  0.00           O+0
HETATM   10  C   UNK     0       8.029   1.374   0.000  0.00  0.00           C+0
HETATM   11  O   UNK     0       9.577   1.001   0.000  0.00  0.00           O+0
HETATM   12  C   UNK     0       6.629   0.732   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0       5.586   1.864   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0       5.764   0.335   0.000  0.00  0.00           C+0
HETATM   15  O   UNK     0       7.243  -0.621   0.000  0.00  0.00           O+0
HETATM   16  O   UNK     0       4.364  -0.308   0.000  0.00  0.00           O+0
HETATM   17  C   UNK     0       3.321   0.825   0.000  0.00  0.00           C+0
HETATM   18  O   UNK     0       1.811   1.128   0.000  0.00  0.00           O+0
HETATM   19  C   UNK     0       1.633   2.658   0.000  0.00  0.00           C+0
HETATM   20  O   UNK     0      -0.150   2.783   0.000  0.00  0.00           O+0
HETATM   21  C   UNK     0       3.033   3.300   0.000  0.00  0.00           C+0
HETATM   22  O   UNK     0       3.879   4.793   0.000  0.00  0.00           O+0
HETATM   23  C   UNK     0       4.076   2.167   0.000  0.00  0.00           C+0
CONECT    1    2                                                            
CONECT    2    1    3    4    5                                             
CONECT    3    2                                                            
CONECT    4    2                                                            
CONECT    5    2    6    7   23                                             
CONECT    6    5                                                            
CONECT    7    5    8                                                       
CONECT    8    7    9   13                                                  
CONECT    9    8   10                                                       
CONECT   10    9   11   12                                                  
CONECT   11   10                                                            
CONECT   12   10   13                                                       
CONECT   13   12    8   14   23                                             
CONECT   14   13   15   16                                                  
CONECT   15   14                                                            
CONECT   16   14   17                                                       
CONECT   17   16   18   23                                                  
CONECT   18   17   19                                                       
CONECT   19   18   20   21                                                  
CONECT   20   19                                                            
CONECT   21   19   22   23                                                  
CONECT   22   21                                                            
CONECT   23   21   17   13    5                                             
MASTER        0    0    0    0    0    0    0    0   23    0   52    0
END

View in JSmol

Synonyms

Value	Source
(-)-Bilobalide	MeSH

Chemical Formula

C₁₅H₁₈O₈

Average Mass

326.3010 Da

Monoisotopic Mass

326.10017 Da

IUPAC Name

(1S,4S,8S,9R,11R)-9-tert-butyl-7,9-dihydroxy-3,5,12-trioxatetracyclo[6.6.0.0^{1,11}.0^{4,8}]tetradecane-2,6,13-trione

Traditional Name

(1S,4S,8S,9R,11R)-9-tert-butyl-7,9-dihydroxy-3,5,12-trioxatetracyclo[6.6.0.0^{1,11}.0^{4,8}]tetradecane-2,6,13-trione

CAS Registry Number

Not Available

SMILES

CC(C)(C)[C@]1(O)C[C@H]2OC(=O)C[C@@]22C(=O)O[C@H]3OC(=O)C(O)[C@]123

InChI Identifier

InChI=1S/C15H18O8/c1-12(2,3)14(20)4-6-13(5-7(16)21-6)10(19)23-11-15(13,14)8(17)9(18)22-11/h6,8,11,17,20H,4-5H2,1-3H3/t6-,8?,11-,13+,14-,15-/m1/s1

InChI Key

MOLPUWBMSBJXER-MJLURTQYSA-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
Ginkgo biloba	LOTUS Database	35616633

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as ginkgolides and bilobalides. These are diterpene lactones with a structure based either on the gingkolide or the bilobalide skeleton. The ginkgolide skeleton is a very rigid structure consisting of hexacyclic C20 trilactone. The cis-fused F/A/D/C ring junction forms an empty semi-ball hole, the D ring contains a cage form tetrahydrofuran ring which occupies the center of the empty hole, and the oxygen atoms of the D,C and F ring and 10-hydroxyl group consist of an analogous crown ether structure.

Kingdom

Organic compounds

Super Class

Lipids and lipid-like molecules

Class

Prenol lipids

Sub Class

Terpene lactones

Direct Parent

Ginkgolides and bilobalides

Alternative Parents

Substituents

Bilobalide
Diterpenoid
Tricarboxylic acid or derivatives
Furofuran
Acylal
Gamma butyrolactone
Tetrahydrofuran
Tertiary alcohol
Cyclic alcohol
Secondary alcohol
Lactone
Carboxylic acid ester
Oxacycle
Organoheterocyclic compound
Carboxylic acid derivative
Acetal
Organic oxygen compound
Organic oxide
Hydrocarbon derivative
Organooxygen compound
Carbonyl group
Alcohol
Aliphatic heteropolycyclic compound

Molecular Framework

Aliphatic 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	-0.52	ChemAxon
pKa (Strongest Acidic)	11.97	ChemAxon
pKa (Strongest Basic)	-3.4	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	5	ChemAxon
Hydrogen Donor Count	2	ChemAxon
Polar Surface Area	119.36 Å²	ChemAxon
Rotatable Bond Count	1	ChemAxon
Refractivity	69.99 m³·mol⁻¹	ChemAxon
Polarizability	30.1 Å³	ChemAxon
Number of Rings	4	ChemAxon
Bioavailability	Yes	ChemAxon
Rule of Five	Yes	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

C00011512

Chemspider ID

Not Available

KEGG Compound ID

Not Available

BioCyc ID

Not Available

BiGG ID

Not Available

Wikipedia Link

Bilobalide

METLIN ID

Not Available

PubChem Compound

138107786

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

LOTUS database [Link]

Showing NP-Card for (1s,4s,8s,9r,11r)-9-tert-butyl-7,9-dihydroxy-3,5,12-trioxatetracyclo[6.6.0.0¹,¹¹.0⁴,⁸]tetradecane-2,6,13-trione (NP0229718)

MOL for NP0229718 ((1s,4s,8s,9r,11r)-9-tert-butyl-7,9-dihydroxy-3,5,12-trioxatetracyclo[6.6.0.0¹,¹¹.0⁴,⁸]tetradecane-2,6,13-trione)

3D MOL for NP0229718 ((1s,4s,8s,9r,11r)-9-tert-butyl-7,9-dihydroxy-3,5,12-trioxatetracyclo[6.6.0.0¹,¹¹.0⁴,⁸]tetradecane-2,6,13-trione)

3D SDF for NP0229718 ((1s,4s,8s,9r,11r)-9-tert-butyl-7,9-dihydroxy-3,5,12-trioxatetracyclo[6.6.0.0¹,¹¹.0⁴,⁸]tetradecane-2,6,13-trione)

3D-SDF for NP0229718 ((1s,4s,8s,9r,11r)-9-tert-butyl-7,9-dihydroxy-3,5,12-trioxatetracyclo[6.6.0.0¹,¹¹.0⁴,⁸]tetradecane-2,6,13-trione)

PDB for NP0229718 ((1s,4s,8s,9r,11r)-9-tert-butyl-7,9-dihydroxy-3,5,12-trioxatetracyclo[6.6.0.0¹,¹¹.0⁴,⁸]tetradecane-2,6,13-trione)

3D PDB for NP0229718 ((1s,4s,8s,9r,11r)-9-tert-butyl-7,9-dihydroxy-3,5,12-trioxatetracyclo[6.6.0.0¹,¹¹.0⁴,⁸]tetradecane-2,6,13-trione)

SMILES for NP0229718 ((1s,4s,8s,9r,11r)-9-tert-butyl-7,9-dihydroxy-3,5,12-trioxatetracyclo[6.6.0.0¹,¹¹.0⁴,⁸]tetradecane-2,6,13-trione)

INCHI for NP0229718 ((1s,4s,8s,9r,11r)-9-tert-butyl-7,9-dihydroxy-3,5,12-trioxatetracyclo[6.6.0.0¹,¹¹.0⁴,⁸]tetradecane-2,6,13-trione)

Structure for NP0229718 ((1s,4s,8s,9r,11r)-9-tert-butyl-7,9-dihydroxy-3,5,12-trioxatetracyclo[6.6.0.0¹,¹¹.0⁴,⁸]tetradecane-2,6,13-trione)

3D Structure for NP0229718 ((1s,4s,8s,9r,11r)-9-tert-butyl-7,9-dihydroxy-3,5,12-trioxatetracyclo[6.6.0.0¹,¹¹.0⁴,⁸]tetradecane-2,6,13-trione)