NP-MRD: Showing NP-Card for 17,17-dimethyl-8-(3-methylbut-2-en-1-yl)-4,12,18-trioxapentacyclo[11.8.0.0²,¹¹.0⁵,¹⁰.0¹⁴,¹⁹]henicosa-1(21),5(10),6,8,13,19-hexaene-7,16-diol (NP0194622)

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Record Information

Version

2.0

Created at

2022-09-04 12:18:37 UTC

Updated at

2022-09-04 12:18:37 UTC

NP-MRD ID

NP0194622

Secondary Accession Numbers

None

Natural Product Identification

Common Name

17,17-dimethyl-8-(3-methylbut-2-en-1-yl)-4,12,18-trioxapentacyclo[11.8.0.0²,¹¹.0⁵,¹⁰.0¹⁴,¹⁹]henicosa-1(21),5(10),6,8,13,19-hexaene-7,16-diol

Description

17,17-Dimethyl-8-(3-methylbut-2-en-1-yl)-4,12,18-trioxapentacyclo[11.8.0.0²,¹¹.0⁵,¹⁰.0¹⁴,¹⁹]Henicosa-1(13),5(10),6,8,14(19),20-hexaene-7,16-diol belongs to the class of organic compounds known as pterocarpans. These are benzo-pyrano-furano-benzene compounds, containing the 6H-[1]benzofuro[3,2-c]chromene skeleton. They are derivatives of isoflavonoids. 17,17-dimethyl-8-(3-methylbut-2-en-1-yl)-4,12,18-trioxapentacyclo[11.8.0.0²,¹¹.0⁵,¹⁰.0¹⁴,¹⁹]henicosa-1(21),5(10),6,8,13,19-hexaene-7,16-diol is found in Erythrina abyssinica, Erythrina lysistemon and Erythrina suberosa. 17,17-Dimethyl-8-(3-methylbut-2-en-1-yl)-4,12,18-trioxapentacyclo[11.8.0.0²,¹¹.0⁵,¹⁰.0¹⁴,¹⁹]Henicosa-1(13),5(10),6,8,14(19),20-hexaene-7,16-diol is an extremely weak basic (essentially neutral) compound (based on its pKa).

Structure

MOL 3D MOL SDF PDB SMILES InChI


  Mrv1533004241515052D          

 30 34  0  0  0  0            999 V2000
   -2.6129   -1.3536    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8060   -1.5252    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5510   -2.3098    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7441   -2.4813    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4891   -3.2659    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.3179   -3.4375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.5728   -4.2221    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.3798   -4.3936    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.0472   -3.9087    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.7146   -4.3936    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5216   -4.2221    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.7766   -3.4375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.5835   -3.2659    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.8385   -2.4813    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.1356   -3.8790    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.6435   -3.2289    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.8640   -4.2663    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.8806   -4.6637    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.0736   -4.8352    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.8187   -5.6198    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.0117   -5.7913    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.4597   -5.1782    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.6347   -5.1782    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.0827   -5.7913    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.2757   -5.6198    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.0208   -4.8352    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7862   -4.6637    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0412   -3.8790    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8481   -3.7075    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2539   -0.9121    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
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M  END

     RDKit          3D

 58 62  0  0  0  0  0  0  0  0999 V2000
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    0.6789   -0.3664    0.1706 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1117   -1.3541    0.8320 C   0  0  1  0  0  0  0  0  0  0  0  0
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    6.1552    1.9601   -1.3750 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.6290    1.6237    1.0448 C   0  0  0  0  0  0  0  0  0  0  0  0
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   -0.2004   -1.0139    1.8847 H   0  0  0  0  0  0  0  0  0  0  0  0
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M  END


  Mrv1533004241515052D          

 30 34  0  0  0  0            999 V2000
   -2.6129   -1.3536    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8060   -1.5252    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5510   -2.3098    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7441   -2.4813    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4891   -3.2659    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.3179   -3.4375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.5728   -4.2221    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.3798   -4.3936    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.0472   -3.9087    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.7146   -4.3936    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5216   -4.2221    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.7766   -3.4375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.5835   -3.2659    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.8385   -2.4813    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.1356   -3.8790    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.6435   -3.2289    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.8640   -4.2663    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
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M  END
> <DATABASE_ID>
NP0194622

> <DATABASE_NAME>
NP-MRD

> <SMILES>
CC(C)=CCC1=CC2=C(OCC3C2OC2=C4CC(O)C(C)(C)OC4=CC=C32)C=C1O

> <INCHI_IDENTIFIER>
InChI=1S/C25H28O5/c1-13(2)5-6-14-9-16-21(11-19(14)26)28-12-18-15-7-8-20-17(23(15)29-24(16)18)10-22(27)25(3,4)30-20/h5,7-9,11,18,22,24,26-27H,6,10,12H2,1-4H3

> <INCHI_KEY>
UNODSKHATHZQGW-UHFFFAOYSA-N

> <FORMULA>
C25H28O5

> <MOLECULAR_WEIGHT>
408.494

> <EXACT_MASS>
408.193674002

> <JCHEM_ACCEPTOR_COUNT>
5

> <JCHEM_ATOM_COUNT>
58

> <JCHEM_AVERAGE_POLARIZABILITY>
44.25602639959017

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
2

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
1

> <JCHEM_IUPAC>
17,17-dimethyl-8-(3-methylbut-2-en-1-yl)-4,12,18-trioxapentacyclo[11.8.0.0²,¹¹.0⁵,¹⁰.0¹⁴,¹⁹]henicosa-1(21),5(10),6,8,13,19-hexaene-7,16-diol

> <ALOGPS_LOGP>
4.26

> <JCHEM_LOGP>
4.344495652999999

> <ALOGPS_LOGS>
-4.90

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
5

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA>
13.77144743246146

> <JCHEM_PKA_STRONGEST_ACIDIC>
9.22098322122496

> <JCHEM_PKA_STRONGEST_BASIC>
-3.336174244475802

> <JCHEM_POLAR_SURFACE_AREA>
68.15

> <JCHEM_REFRACTIVITY>
115.633

> <JCHEM_ROTATABLE_BOND_COUNT>
2

> <JCHEM_RULE_OF_FIVE>
1

> <ALOGPS_SOLUBILITY>
5.09e-03 g/l

> <JCHEM_TRADITIONAL_IUPAC>
17,17-dimethyl-8-(3-methylbut-2-en-1-yl)-4,12,18-trioxapentacyclo[11.8.0.0²,¹¹.0⁵,¹⁰.0¹⁴,¹⁹]henicosa-1(21),5(10),6,8,13,19-hexaene-7,16-diol

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 24-APR-15   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   24-APR-15         0                                  
HETATM    1  C   UNK     0      -4.877  -2.527   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0      -3.371  -2.847   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0      -2.895  -4.312   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0      -1.389  -4.632   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0      -0.913  -6.096   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0       0.593  -6.417   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0       1.069  -7.881   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0       2.576  -8.201   0.000  0.00  0.00           C+0
HETATM    9  O   UNK     0       3.821  -7.296   0.000  0.00  0.00           O+0
HETATM   10  C   UNK     0       5.067  -8.201   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0       6.574  -7.881   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0       7.050  -6.417   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0       8.556  -6.096   0.000  0.00  0.00           C+0
HETATM   14  O   UNK     0       9.032  -4.632   0.000  0.00  0.00           O+0
HETATM   15  C   UNK     0       9.586  -7.241   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0      10.534  -6.027   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0      10.946  -7.964   0.000  0.00  0.00           C+0
HETATM   18  O   UNK     0       9.110  -8.705   0.000  0.00  0.00           O+0
HETATM   19  C   UNK     0       7.604  -9.026   0.000  0.00  0.00           C+0
HETATM   20  C   UNK     0       7.128 -10.490   0.000  0.00  0.00           C+0
HETATM   21  C   UNK     0       5.622 -10.810   0.000  0.00  0.00           C+0
HETATM   22  C   UNK     0       4.591  -9.666   0.000  0.00  0.00           C+0
HETATM   23  C   UNK     0       3.051  -9.666   0.000  0.00  0.00           C+0
HETATM   24  C   UNK     0       2.021 -10.810   0.000  0.00  0.00           C+0
HETATM   25  O   UNK     0       0.515 -10.490   0.000  0.00  0.00           O+0
HETATM   26  C   UNK     0       0.039  -9.026   0.000  0.00  0.00           C+0
HETATM   27  C   UNK     0      -1.468  -8.705   0.000  0.00  0.00           C+0
HETATM   28  C   UNK     0      -1.943  -7.241   0.000  0.00  0.00           C+0
HETATM   29  O   UNK     0      -3.450  -6.921   0.000  0.00  0.00           O+0
HETATM   30  C   UNK     0      -2.341  -1.703   0.000  0.00  0.00           C+0
CONECT    1    2                                                            
CONECT    2    1    3   30                                                  
CONECT    3    2    4                                                       
CONECT    4    3    5                                                       
CONECT    5    4    6   28                                                  
CONECT    6    5    7                                                       
CONECT    7    6    8   26                                                  
CONECT    8    7    9   23                                                  
CONECT    9    8   10                                                       
CONECT   10    9   11   22                                                  
CONECT   11   10   12   19                                                  
CONECT   12   11   13                                                       
CONECT   13   12   14   15                                                  
CONECT   14   13                                                            
CONECT   15   13   16   17   18                                             
CONECT   16   15                                                            
CONECT   17   15                                                            
CONECT   18   15   19                                                       
CONECT   19   18   11   20                                                  
CONECT   20   19   21                                                       
CONECT   21   20   22                                                       
CONECT   22   21   10   23                                                  
CONECT   23   22    8   24                                                  
CONECT   24   23   25                                                       
CONECT   25   24   26                                                       
CONECT   26   25    7   27                                                  
CONECT   27   26   28                                                       
CONECT   28   27    5   29                                                  
CONECT   29   28                                                            
CONECT   30    2                                                            
MASTER        0    0    0    0    0    0    0    0   30    0   68    0
END

View in JSmol

Synonyms

Not Available

Chemical Formula

C₂₅H₂₈O₅

Average Mass

408.4940 Da

Monoisotopic Mass

408.19367 Da

IUPAC Name

17,17-dimethyl-8-(3-methylbut-2-en-1-yl)-4,12,18-trioxapentacyclo[11.8.0.0²,¹¹.0⁵,¹⁰.0¹⁴,¹⁹]henicosa-1(21),5(10),6,8,13,19-hexaene-7,16-diol

Traditional Name

17,17-dimethyl-8-(3-methylbut-2-en-1-yl)-4,12,18-trioxapentacyclo[11.8.0.0²,¹¹.0⁵,¹⁰.0¹⁴,¹⁹]henicosa-1(21),5(10),6,8,13,19-hexaene-7,16-diol

CAS Registry Number

Not Available

SMILES

CC(C)=CCC1=CC2=C(OCC3C2OC2=C4CC(O)C(C)(C)OC4=CC=C32)C=C1O

InChI Identifier

InChI=1S/C25H28O5/c1-13(2)5-6-14-9-16-21(11-19(14)26)28-12-18-15-7-8-20-17(23(15)29-24(16)18)10-22(27)25(3,4)30-20/h5,7-9,11,18,22,24,26-27H,6,10,12H2,1-4H3

InChI Key

UNODSKHATHZQGW-UHFFFAOYSA-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
Erythrina abyssinica	LOTUS Database	35616633
Erythrina lysistemon	LOTUS Database	35616633
Erythrina suberosa	LOTUS Database	35616633

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as pterocarpans. These are benzo-pyrano-furano-benzene compounds, containing the 6H-[1]benzofuro[3,2-c]chromene skeleton. They are derivatives of isoflavonoids.

Kingdom

Organic compounds

Super Class

Phenylpropanoids and polyketides

Class

Isoflavonoids

Sub Class

Furanoisoflavonoids

Direct Parent

Pterocarpans

Alternative Parents

Substituents

Isoflavanol
Neolignan skeleton
Pterocarpan
Isoflavan
2,2-dimethyl-1-benzopyran
Chromane
Benzopyran
1-benzopyran
Coumaran
Benzofuran
1-hydroxy-2-unsubstituted benzenoid
Alkyl aryl ether
Benzenoid
Secondary alcohol
Ether
Oxacycle
Organoheterocyclic compound
Hydrocarbon derivative
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	4.26	ALOGPS
logP	4.34	ChemAxon
logS	-4.9	ALOGPS
pKa (Strongest Acidic)	9.22	ChemAxon
pKa (Strongest Basic)	-3.3	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	5	ChemAxon
Hydrogen Donor Count	2	ChemAxon
Polar Surface Area	68.15 Å²	ChemAxon
Rotatable Bond Count	2	ChemAxon
Refractivity	115.63 m³·mol⁻¹	ChemAxon
Polarizability	44.26 Å³	ChemAxon
Number of Rings	5	ChemAxon
Bioavailability	Yes	ChemAxon
Rule of Five	Yes	ChemAxon
Ghose Filter	Yes	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

Not Available

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

LOTUS database [Link]

Showing NP-Card for 17,17-dimethyl-8-(3-methylbut-2-en-1-yl)-4,12,18-trioxapentacyclo[11.8.0.0²,¹¹.0⁵,¹⁰.0¹⁴,¹⁹]henicosa-1(21),5(10),6,8,13,19-hexaene-7,16-diol (NP0194622)

MOL for NP0194622 (17,17-dimethyl-8-(3-methylbut-2-en-1-yl)-4,12,18-trioxapentacyclo[11.8.0.0²,¹¹.0⁵,¹⁰.0¹⁴,¹⁹]henicosa-1(21),5(10),6,8,13,19-hexaene-7,16-diol)

3D MOL for NP0194622 (17,17-dimethyl-8-(3-methylbut-2-en-1-yl)-4,12,18-trioxapentacyclo[11.8.0.0²,¹¹.0⁵,¹⁰.0¹⁴,¹⁹]henicosa-1(21),5(10),6,8,13,19-hexaene-7,16-diol)

3D SDF for NP0194622 (17,17-dimethyl-8-(3-methylbut-2-en-1-yl)-4,12,18-trioxapentacyclo[11.8.0.0²,¹¹.0⁵,¹⁰.0¹⁴,¹⁹]henicosa-1(21),5(10),6,8,13,19-hexaene-7,16-diol)

3D-SDF for NP0194622 (17,17-dimethyl-8-(3-methylbut-2-en-1-yl)-4,12,18-trioxapentacyclo[11.8.0.0²,¹¹.0⁵,¹⁰.0¹⁴,¹⁹]henicosa-1(21),5(10),6,8,13,19-hexaene-7,16-diol)

PDB for NP0194622 (17,17-dimethyl-8-(3-methylbut-2-en-1-yl)-4,12,18-trioxapentacyclo[11.8.0.0²,¹¹.0⁵,¹⁰.0¹⁴,¹⁹]henicosa-1(21),5(10),6,8,13,19-hexaene-7,16-diol)

3D PDB for NP0194622 (17,17-dimethyl-8-(3-methylbut-2-en-1-yl)-4,12,18-trioxapentacyclo[11.8.0.0²,¹¹.0⁵,¹⁰.0¹⁴,¹⁹]henicosa-1(21),5(10),6,8,13,19-hexaene-7,16-diol)

SMILES for NP0194622 (17,17-dimethyl-8-(3-methylbut-2-en-1-yl)-4,12,18-trioxapentacyclo[11.8.0.0²,¹¹.0⁵,¹⁰.0¹⁴,¹⁹]henicosa-1(21),5(10),6,8,13,19-hexaene-7,16-diol)

INCHI for NP0194622 (17,17-dimethyl-8-(3-methylbut-2-en-1-yl)-4,12,18-trioxapentacyclo[11.8.0.0²,¹¹.0⁵,¹⁰.0¹⁴,¹⁹]henicosa-1(21),5(10),6,8,13,19-hexaene-7,16-diol)

Structure for NP0194622 (17,17-dimethyl-8-(3-methylbut-2-en-1-yl)-4,12,18-trioxapentacyclo[11.8.0.0²,¹¹.0⁵,¹⁰.0¹⁴,¹⁹]henicosa-1(21),5(10),6,8,13,19-hexaene-7,16-diol)

3D Structure for NP0194622 (17,17-dimethyl-8-(3-methylbut-2-en-1-yl)-4,12,18-trioxapentacyclo[11.8.0.0²,¹¹.0⁵,¹⁰.0¹⁴,¹⁹]henicosa-1(21),5(10),6,8,13,19-hexaene-7,16-diol)