NP-MRD: Showing NP-Card for (-)-(7S,8R,1’R,3’R,4’R,5’S)-delta8’-4’-hydroxy-3,4-methylenedioxy-,5,3’,5’-trimethoxy-1’,2’,3’,4,’5’,6’,-hexahydro-6’-oxo-7.3’,8.5’-neolignan (NP0332324)

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Record Information

Version

2.0

Created at

2024-01-04 04:45:22 UTC

Updated at

2024-09-03 04:18:48 UTC

NP-MRD ID

NP0332324

Natural Product DOI

https://doi.org/10.57994/1526

Secondary Accession Numbers

None

Natural Product Identification

Common Name

(-)-(7S,8R,1’R,3’R,4’R,5’S)-delta8’-4’-hydroxy-3,4-methylenedioxy-,5,3’,5’-trimethoxy-1’,2’,3’,4,’5’,6’,-hexahydro-6’-oxo-7.3’,8.5’-neolignan

Description

(-)-(7S,8R,1’R,3’R,4’R,5’S)-delta8’-4’-hydroxy-3,4-methylenedioxy-,5,3’,5’-trimethoxy-1’,2’,3’,4,’5’,6’,-hexahydro-6’-oxo-7.3’,8.5’-neolignan was first documented in 2024 (PMID: 38395785). Based on a literature review very few articles have been published on (-)-(7S,8R,1’R,3’R,4’R,5’S)-delta8’-4’-hydroxy-3,4-methylenedioxy-,5,3’,5’-trimethoxy-1’,2’,3’,4,’5’,6’,-hexahydro-6’-oxo-7.3’,8.5’-Neolignan.

Structure

MOL SDF PDB SMILES InChI


  Mrv2104 01042404452D          

 29 32  0  0  1  0            999 V2000
    1.8319   -1.2419    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.9549   -0.4262    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.7229   -0.1248    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    3.6192    0.2059    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    4.2719   -0.2987    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.2545    0.9195    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    4.5559    0.1515    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.3786    0.0899    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.8157    1.5243    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.6200    1.3407    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.4662    1.1627    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    3.3432    1.9785    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.3276   -0.6859    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.1434   -0.5629    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    4.6082   -1.2446    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.2502   -1.9879    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.4275   -2.0495    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.7845    0.6979    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    2.0701    1.1104    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.3556    0.6979    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.6411    1.1104    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1435    0.8555    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6284    1.5229    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1435    2.1904    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.6411    1.9354    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.3556    2.3479    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.3556    3.1729    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.0701    3.5854    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.0701    1.9354    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0  0  0  0
  3  2  1  6  0  0  0
  3  4  1  0  0  0  0
  4  5  1  6  0  0  0
  4  6  1  0  0  0  0
  6  7  1  0  0  0  0
  7  8  2  0  0  0  0
  6  9  1  6  0  0  0
  9 10  1  0  0  0  0
  6 11  1  0  0  0  0
 11 12  1  1  0  0  0
  3 13  1  0  0  0  0
 14 13  1  0  0  0  0
 14  7  1  0  0  0  0
 14 15  1  6  0  0  0
 15 16  1  0  0  0  0
 16 17  2  0  0  0  0
  3 18  1  0  0  0  0
 18 11  1  0  0  0  0
 18 19  1  6  0  0  0
 19 20  2  0  0  0  0
 20 21  1  0  0  0  0
 21 22  1  0  0  0  0
 22 23  1  0  0  0  0
 23 24  1  0  0  0  0
 21 25  2  0  0  0  0
 24 25  1  0  0  0  0
 25 26  1  0  0  0  0
 26 27  1  0  0  0  0
 27 28  1  0  0  0  0
 26 29  2  0  0  0  0
 19 29  1  0  0  0  0
M  END


  Mrv2104 01042404452D          

 29 32  0  0  1  0            999 V2000
    1.8319   -1.2419    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.9549   -0.4262    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.7229   -0.1248    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    3.6192    0.2059    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    4.2719   -0.2987    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.2545    0.9195    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    4.5559    0.1515    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.3786    0.0899    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.8157    1.5243    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.6200    1.3407    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.4662    1.1627    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    3.3432    1.9785    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.3276   -0.6859    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.1434   -0.5629    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    4.6082   -1.2446    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.2502   -1.9879    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.4275   -2.0495    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.7845    0.6979    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    2.0701    1.1104    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.3556    0.6979    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.6411    1.1104    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1435    0.8555    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6284    1.5229    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1435    2.1904    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.6411    1.9354    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.3556    2.3479    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.3556    3.1729    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.0701    3.5854    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.0701    1.9354    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0  0  0  0
  3  2  1  6  0  0  0
  3  4  1  0  0  0  0
  4  5  1  6  0  0  0
  4  6  1  0  0  0  0
  6  7  1  0  0  0  0
  7  8  2  0  0  0  0
  6  9  1  6  0  0  0
  9 10  1  0  0  0  0
  6 11  1  0  0  0  0
 11 12  1  1  0  0  0
  3 13  1  0  0  0  0
 14 13  1  0  0  0  0
 14  7  1  0  0  0  0
 14 15  1  6  0  0  0
 15 16  1  0  0  0  0
 16 17  2  0  0  0  0
  3 18  1  0  0  0  0
 18 11  1  0  0  0  0
 18 19  1  6  0  0  0
 19 20  2  0  0  0  0
 20 21  1  0  0  0  0
 21 22  1  0  0  0  0
 22 23  1  0  0  0  0
 23 24  1  0  0  0  0
 21 25  2  0  0  0  0
 24 25  1  0  0  0  0
 25 26  1  0  0  0  0
 26 27  1  0  0  0  0
 27 28  1  0  0  0  0
 26 29  2  0  0  0  0
 19 29  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0332324

> <DATABASE_NAME>
NP-MRD

> <SMILES>
COC1=CC(=CC2=C1OCO2)[C@@H]1[C@@H](C)[C@]2(OC)[C@H](O)[C@]1(C[C@@H](CC=C)C2=O)OC

> <INCHI_IDENTIFIER>
InChI=1S/C22H28O7/c1-6-7-13-10-21(26-4)17(12(2)22(27-5,19(13)23)20(21)24)14-8-15(25-3)18-16(9-14)28-11-29-18/h6,8-9,12-13,17,20,24H,1,7,10-11H2,2-5H3/t12-,13-,17+,20-,21-,22-/m1/s1

> <INCHI_KEY>
QFHBVMNSSOLQFS-ROQUPQEXSA-N

> <FORMULA>
C22H28O7

> <MOLECULAR_WEIGHT>
404.459

> <EXACT_MASS>
404.183503242

> <JCHEM_ACCEPTOR_COUNT>
7

> <JCHEM_ATOM_COUNT>
57

> <JCHEM_AVERAGE_POLARIZABILITY>
42.627337535734085

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
1

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
1

> <JCHEM_IUPAC>
(1S,3R,5R,6S,7R,8R)-8-hydroxy-1,5-dimethoxy-6-(7-methoxy-2H-1,3-benzodioxol-5-yl)-7-methyl-3-(prop-2-en-1-yl)bicyclo[3.2.1]octan-2-one

> <JCHEM_LOGP>
2.6165456983333337

> <JCHEM_MDDR_LIKE_RULE>
1

> <JCHEM_NUMBER_OF_RINGS>
4

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA_STRONGEST_ACIDIC>
12.716291306865827

> <JCHEM_PKA_STRONGEST_BASIC>
-3.7976941733889267

> <JCHEM_POLAR_SURFACE_AREA>
83.45000000000002

> <JCHEM_REFRACTIVITY>
104.4492

> <JCHEM_ROTATABLE_BOND_COUNT>
6

> <JCHEM_RULE_OF_FIVE>
1

> <JCHEM_TRADITIONAL_IUPAC>
(1S,3R,5R,6S,7R,8R)-8-hydroxy-1,5-dimethoxy-6-(7-methoxy-2H-1,3-benzodioxol-5-yl)-7-methyl-3-(prop-2-en-1-yl)bicyclo[3.2.1]octan-2-one

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 04-JAN-24   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   04-JAN-24         0                                  
HETATM    1  C   UNK     0       3.420  -2.318   0.000  0.00  0.00           C+0
HETATM    2  O   UNK     0       3.649  -0.795   0.000  0.00  0.00           O+0
HETATM    3  C   UNK     0       5.083  -0.233   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0       6.756   0.384   0.000  0.00  0.00           C+0
HETATM    5  O   UNK     0       7.974  -0.558   0.000  0.00  0.00           O+0
HETATM    6  C   UNK     0       7.942   1.716   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0       8.504   0.283   0.000  0.00  0.00           C+0
HETATM    8  O   UNK     0      10.040   0.168   0.000  0.00  0.00           O+0
HETATM    9  O   UNK     0       8.989   2.845   0.000  0.00  0.00           O+0
HETATM   10  C   UNK     0      10.491   2.503   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0       6.470   2.170   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0       6.241   3.693   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0       6.212  -1.280   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0       7.734  -1.051   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0       8.602  -2.323   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0       7.934  -3.711   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0       6.398  -3.826   0.000  0.00  0.00           C+0
HETATM   18  C   UNK     0       5.198   1.303   0.000  0.00  0.00           C+0
HETATM   19  C   UNK     0       3.864   2.073   0.000  0.00  0.00           C+0
HETATM   20  C   UNK     0       2.530   1.303   0.000  0.00  0.00           C+0
HETATM   21  C   UNK     0       1.197   2.073   0.000  0.00  0.00           C+0
HETATM   22  O   UNK     0      -0.268   1.597   0.000  0.00  0.00           O+0
HETATM   23  C   UNK     0      -1.173   2.843   0.000  0.00  0.00           C+0
HETATM   24  O   UNK     0      -0.268   4.089   0.000  0.00  0.00           O+0
HETATM   25  C   UNK     0       1.197   3.613   0.000  0.00  0.00           C+0
HETATM   26  C   UNK     0       2.530   4.383   0.000  0.00  0.00           C+0
HETATM   27  O   UNK     0       2.530   5.923   0.000  0.00  0.00           O+0
HETATM   28  C   UNK     0       3.864   6.693   0.000  0.00  0.00           C+0
HETATM   29  C   UNK     0       3.864   3.613   0.000  0.00  0.00           C+0
CONECT    1    2                                                            
CONECT    2    1    3                                                       
CONECT    3    2    4   13   18                                             
CONECT    4    3    5    6                                                  
CONECT    5    4                                                            
CONECT    6    4    7    9   11                                             
CONECT    7    6    8   14                                                  
CONECT    8    7                                                            
CONECT    9    6   10                                                       
CONECT   10    9                                                            
CONECT   11    6   12   18                                                  
CONECT   12   11                                                            
CONECT   13    3   14                                                       
CONECT   14   13    7   15                                                  
CONECT   15   14   16                                                       
CONECT   16   15   17                                                       
CONECT   17   16                                                            
CONECT   18    3   11   19                                                  
CONECT   19   18   20   29                                                  
CONECT   20   19   21                                                       
CONECT   21   20   22   25                                                  
CONECT   22   21   23                                                       
CONECT   23   22   24                                                       
CONECT   24   23   25                                                       
CONECT   25   21   24   26                                                  
CONECT   26   25   27   29                                                  
CONECT   27   26   28                                                       
CONECT   28   27                                                            
CONECT   29   26   19                                                       
MASTER        0    0    0    0    0    0    0    0   29    0   64    0
END

View in JSmol

Synonyms

Value	Source
(-)-(7S,8R,1’R,3’r,4’r,5’s)-δ8’-4’-hydroxy-3,4-methylenedioxy-,5,3’,5’-trimethoxy-1’,2’,3’,4,’5’,6’,-hexahydro-6’-oxo-7.3’,8.5’-neolignan	Generator

Chemical Formula

C₂₂H₂₈O₇

Average Mass

404.4590 Da

Monoisotopic Mass

404.18350 Da

IUPAC Name

(1S,3R,5R,6S,7R,8R)-8-hydroxy-1,5-dimethoxy-6-(7-methoxy-2H-1,3-benzodioxol-5-yl)-7-methyl-3-(prop-2-en-1-yl)bicyclo[3.2.1]octan-2-one

Traditional Name

(1S,3R,5R,6S,7R,8R)-8-hydroxy-1,5-dimethoxy-6-(7-methoxy-2H-1,3-benzodioxol-5-yl)-7-methyl-3-(prop-2-en-1-yl)bicyclo[3.2.1]octan-2-one

CAS Registry Number

Not Available

SMILES

COC1=CC(=CC2=C1OCO2)[C@@H]1[C@@H](C)[C@]2(OC)[C@H](O)[C@]1(C[C@@H](CC=C)C2=O)OC

InChI Identifier

InChI=1S/C22H28O7/c1-6-7-13-10-21(26-4)17(12(2)22(27-5,19(13)23)20(21)24)14-8-15(25-3)18-16(9-14)28-11-29-18/h6,8-9,12-13,17,20,24H,1,7,10-11H2,2-5H3/t12-,13-,17+,20-,21-,22-/m1/s1

InChI Key

QFHBVMNSSOLQFS-ROQUPQEXSA-N

Experimental Spectra

Spectrum Type	Description	Depositor Email	Depositor Organization	Depositor	Deposition Date	View
COSY NMR	[¹H, ¹H] NMR Spectrum (2D, 500 MHz, CDCl3, experimental)	[email protected]	Federal University of Sao Paulo - UNIFESP	Joao M Batista Jr	2024-05-03	View Spectrum
HSQC NMR	[¹H, ¹³C] NMR Spectrum (2D, 500 MHz, CDCl3, experimental)	[email protected]	Federal University of Sao Paulo - UNIFESP	Joao M Batista Jr	2024-05-03	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 75 MHz, CDCl3, experimental)	[email protected]	Federal University of Sao Paulo - UNIFESP	Joao M Batista Jr	2024-05-03	View Spectrum
NOESY NMR	[¹H, ¹H] NMR Spectrum (2D, 500 MHz, CDCl3, experimental)	[email protected]	Federal University of Sao Paulo - UNIFESP	Joao M Batista Jr	2024-05-03	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 300 MHz, CDCl3, experimental)	[email protected]	Federal University of Sao Paulo - UNIFESP	Joao M Batista Jr	2024-05-03	View Spectrum
HMBC NMR	[¹H, ¹³C] NMR Spectrum (2D, 500 MHz, CDCl3, experimental)	[email protected]	Federal University of Sao Paulo - UNIFESP	Joao M Batista Jr	2024-05-03	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 75 MHz, CDCl3, experimental)	[email protected]	Federal University of Sao Paulo - UNIFESP	Joao M Batista Jr	2024-05-03	View Spectrum

Predicted Spectra

Spectrum Type	Description	Depositor ID	Depositor Organization	Depositor	Deposition Date	View

Chemical Shift Submissions

Not Available

Species

Species of Origin

Species Name	Source	Reference
Ocotea aciphylla		Not Available

Chemical Taxonomy

Classification

Not classified

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	2.62	ChemAxon
pKa (Strongest Acidic)	12.72	ChemAxon
pKa (Strongest Basic)	-3.8	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	7	ChemAxon
Hydrogen Donor Count	1	ChemAxon
Polar Surface Area	83.45 Å²	ChemAxon
Rotatable Bond Count	6	ChemAxon
Refractivity	104.45 m³·mol⁻¹	ChemAxon
Polarizability	42.63 Å³	ChemAxon
Number of Rings	4	ChemAxon
Bioavailability	Yes	ChemAxon
Rule of Five	Yes	ChemAxon
Ghose Filter	Yes	ChemAxon
Veber's Rule	No	ChemAxon
MDDR-like Rule	Yes	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

Showing NP-Card for (-)-(7S,8R,1’R,3’R,4’R,5’S)-delta8’-4’-hydroxy-3,4-methylenedioxy-,5,3’,5’-trimethoxy-1’,2’,3’,4,’5’,6’,-hexahydro-6’-oxo-7.3’,8.5’-neolignan (NP0332324)

MOL for NP0332324 ((-)-(7S,8R,1’R,3’R,4’R,5’S)-delta8’-4’-hydroxy-3,4-methylenedioxy-,5,3’,5’-trimethoxy-1’,2’,3’,4,’5’,6’,-hexahydro-6’-oxo-7.3’,8.5’-neolignan)

3D MOL for NP0332324 ((-)-(7S,8R,1’R,3’R,4’R,5’S)-delta8’-4’-hydroxy-3,4-methylenedioxy-,5,3’,5’-trimethoxy-1’,2’,3’,4,’5’,6’,-hexahydro-6’-oxo-7.3’,8.5’-neolignan)

3D SDF for NP0332324 ((-)-(7S,8R,1’R,3’R,4’R,5’S)-delta8’-4’-hydroxy-3,4-methylenedioxy-,5,3’,5’-trimethoxy-1’,2’,3’,4,’5’,6’,-hexahydro-6’-oxo-7.3’,8.5’-neolignan)

3D-SDF for NP0332324 ((-)-(7S,8R,1’R,3’R,4’R,5’S)-delta8’-4’-hydroxy-3,4-methylenedioxy-,5,3’,5’-trimethoxy-1’,2’,3’,4,’5’,6’,-hexahydro-6’-oxo-7.3’,8.5’-neolignan)

PDB for NP0332324 ((-)-(7S,8R,1’R,3’R,4’R,5’S)-delta8’-4’-hydroxy-3,4-methylenedioxy-,5,3’,5’-trimethoxy-1’,2’,3’,4,’5’,6’,-hexahydro-6’-oxo-7.3’,8.5’-neolignan)

3D PDB for NP0332324 ((-)-(7S,8R,1’R,3’R,4’R,5’S)-delta8’-4’-hydroxy-3,4-methylenedioxy-,5,3’,5’-trimethoxy-1’,2’,3’,4,’5’,6’,-hexahydro-6’-oxo-7.3’,8.5’-neolignan)

SMILES for NP0332324 ((-)-(7S,8R,1’R,3’R,4’R,5’S)-delta8’-4’-hydroxy-3,4-methylenedioxy-,5,3’,5’-trimethoxy-1’,2’,3’,4,’5’,6’,-hexahydro-6’-oxo-7.3’,8.5’-neolignan)

INCHI for NP0332324 ((-)-(7S,8R,1’R,3’R,4’R,5’S)-delta8’-4’-hydroxy-3,4-methylenedioxy-,5,3’,5’-trimethoxy-1’,2’,3’,4,’5’,6’,-hexahydro-6’-oxo-7.3’,8.5’-neolignan)

Structure for NP0332324 ((-)-(7S,8R,1’R,3’R,4’R,5’S)-delta8’-4’-hydroxy-3,4-methylenedioxy-,5,3’,5’-trimethoxy-1’,2’,3’,4,’5’,6’,-hexahydro-6’-oxo-7.3’,8.5’-neolignan)

3D Structure for NP0332324 ((-)-(7S,8R,1’R,3’R,4’R,5’S)-delta8’-4’-hydroxy-3,4-methylenedioxy-,5,3’,5’-trimethoxy-1’,2’,3’,4,’5’,6’,-hexahydro-6’-oxo-7.3’,8.5’-neolignan)