NP-MRD: Showing NP-Card for 10,11-dihydroxy-14-(2-hydroxy-3,4-dimethoxyphenyl)-8-methoxy-n,n-dimethyl-13-phenyl-4,6,15-trioxatetracyclo[7.6.0.0³,⁷.0¹⁰,¹⁴]pentadeca-1,3(7),8-triene-12-carboxamide (NP0295908)

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Record Information

Version

2.0

Created at

2022-09-10 05:10:56 UTC

Updated at

2022-09-10 05:10:56 UTC

NP-MRD ID

NP0295908

Secondary Accession Numbers

None

Natural Product Identification

Common Name

10,11-dihydroxy-14-(2-hydroxy-3,4-dimethoxyphenyl)-8-methoxy-n,n-dimethyl-13-phenyl-4,6,15-trioxatetracyclo[7.6.0.0³,⁷.0¹⁰,¹⁴]pentadeca-1,3(7),8-triene-12-carboxamide

Description

10,11-Dihydroxy-14-(2-hydroxy-3,4-dimethoxyphenyl)-8-methoxy-N,N-dimethyl-13-phenyl-4,6,15-trioxatetracyclo[7.6.0.0³,⁷.0¹⁰,¹⁴]Pentadeca-1,3(7),8-triene-12-carboxamide belongs to the class of organic compounds known as flavaglines. These are heterocyclic compounds with a structure characterized by a cyclopenta[b]benzofuran skeleton. 10,11-dihydroxy-14-(2-hydroxy-3,4-dimethoxyphenyl)-8-methoxy-n,n-dimethyl-13-phenyl-4,6,15-trioxatetracyclo[7.6.0.0³,⁷.0¹⁰,¹⁴]pentadeca-1,3(7),8-triene-12-carboxamide is found in Aglaia elaeagnoidea and Aglaia oligophylla. 10,11-Dihydroxy-14-(2-hydroxy-3,4-dimethoxyphenyl)-8-methoxy-N,N-dimethyl-13-phenyl-4,6,15-trioxatetracyclo[7.6.0.0³,⁷.0¹⁰,¹⁴]Pentadeca-1,3(7),8-triene-12-carboxamide is an extremely weak basic (essentially neutral) compound (based on its pKa).

Structure

MOL 3D MOL SDF PDB SMILES InChI


  Mrv1533004251503362D          

 41 46  0  0  0  0            999 V2000
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M  END

     RDKit          3D

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M  END


  Mrv1533004251503362D          

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    1.7577   -1.4581    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.9129   -0.6478    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.3487   -0.0460    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.5453   -0.2337    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0189    0.3682    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.2202    1.1578    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.0236    1.3455    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.5878    0.7436    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.0109   -1.8087    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.3339   -1.3373    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.9412   -2.6308    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    1.6183   -3.1022    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.1944   -2.9814    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0  0  0  0
  2  3  1  0  0  0  0
  3  4  2  0  0  0  0
  4  5  1  0  0  0  0
  5  6  2  0  0  0  0
  6  7  1  0  0  0  0
  7  8  1  0  0  0  0
  7  9  2  0  0  0  0
  3  9  1  0  0  0  0
  9 10  1  0  0  0  0
 10 11  1  0  0  0  0
  6 12  1  0  0  0  0
 12 13  1  0  0  0  0
 13 14  1  0  0  0  0
 14 15  2  0  0  0  0
 15 16  1  0  0  0  0
 16 17  1  0  0  0  0
 17 18  1  0  0  0  0
 18 19  1  0  0  0  0
 19 20  1  0  0  0  0
 16 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
 21 24  2  0  0  0  0
 14 24  1  0  0  0  0
 24 25  1  0  0  0  0
 12 25  1  0  0  0  0
 25 26  1  0  0  0  0
 25 27  1  0  0  0  0
 27 28  1  0  0  0  0
 27 29  1  0  0  0  0
 29 30  1  0  0  0  0
 12 30  1  0  0  0  0
 30 31  1  0  0  0  0
 31 32  2  0  0  0  0
 32 33  1  0  0  0  0
 33 34  2  0  0  0  0
 34 35  1  0  0  0  0
 35 36  2  0  0  0  0
 31 36  1  0  0  0  0
 29 37  1  0  0  0  0
 37 38  2  0  0  0  0
 37 39  1  0  0  0  0
 39 40  1  0  0  0  0
 39 41  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0295908

> <DATABASE_NAME>
NP-MRD

> <SMILES>
COC1=CC=C(C(O)=C1OC)C12OC3=CC4=C(OCO4)C(OC)=C3C1(O)C(O)C(C2C1=CC=CC=C1)C(=O)N(C)C

> <INCHI_IDENTIFIER>
InChI=1S/C30H31NO10/c1-31(2)28(34)20-21(15-9-7-6-8-10-15)30(16-11-12-17(36-3)24(37-4)23(16)32)29(35,27(20)33)22-18(41-30)13-19-25(26(22)38-5)40-14-39-19/h6-13,20-21,27,32-33,35H,14H2,1-5H3

> <INCHI_KEY>
ASMWUNIIUGWPST-UHFFFAOYSA-N

> <FORMULA>
C30H31NO10

> <MOLECULAR_WEIGHT>
565.575

> <EXACT_MASS>
565.194796202

> <JCHEM_ACCEPTOR_COUNT>
10

> <JCHEM_ATOM_COUNT>
72

> <JCHEM_AVERAGE_POLARIZABILITY>
57.491487378670556

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
3

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
0

> <JCHEM_IUPAC>
10,11-dihydroxy-14-(2-hydroxy-3,4-dimethoxyphenyl)-8-methoxy-N,N-dimethyl-13-phenyl-4,6,15-trioxatetracyclo[7.6.0.0³,⁷.0¹⁰,¹⁴]pentadeca-1,3(7),8-triene-12-carboxamide

> <ALOGPS_LOGP>
3.01

> <JCHEM_LOGP>
1.7081996879999994

> <ALOGPS_LOGS>
-3.51

> <JCHEM_MDDR_LIKE_RULE>
1

> <JCHEM_NUMBER_OF_RINGS>
6

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA>
11.597952593835585

> <JCHEM_PKA_STRONGEST_ACIDIC>
9.518119892639508

> <JCHEM_PKA_STRONGEST_BASIC>
-1.6803751109668568

> <JCHEM_POLAR_SURFACE_AREA>
136.38000000000002

> <JCHEM_REFRACTIVITY>
144.0093

> <JCHEM_ROTATABLE_BOND_COUNT>
6

> <JCHEM_RULE_OF_FIVE>
0

> <ALOGPS_SOLUBILITY>
1.76e-01 g/l

> <JCHEM_TRADITIONAL_IUPAC>
10,11-dihydroxy-14-(2-hydroxy-3,4-dimethoxyphenyl)-8-methoxy-N,N-dimethyl-13-phenyl-4,6,15-trioxatetracyclo[7.6.0.0³,⁷.0¹⁰,¹⁴]pentadeca-1,3(7),8-triene-12-carboxamide

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 25-APR-15   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   25-APR-15         0                                  
HETATM    1  C   UNK     0       5.559   6.025   0.000  0.00  0.00           C+0
HETATM    2  O   UNK     0       4.332   5.095   0.000  0.00  0.00           O+0
HETATM    3  C   UNK     0       4.524   3.567   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0       3.296   2.636   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0       3.488   1.108   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0       4.907   0.510   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0       6.135   1.441   0.000  0.00  0.00           C+0
HETATM    8  O   UNK     0       7.554   0.843   0.000  0.00  0.00           O+0
HETATM    9  C   UNK     0       5.943   2.969   0.000  0.00  0.00           C+0
HETATM   10  O   UNK     0       7.170   3.899   0.000  0.00  0.00           O+0
HETATM   11  C   UNK     0       6.978   5.427   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0       5.099  -1.018   0.000  0.00  0.00           C+0
HETATM   13  O   UNK     0       6.222   0.036   0.000  0.00  0.00           O+0
HETATM   14  C   UNK     0       7.571  -0.707   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0       9.026  -0.202   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0      10.191  -1.209   0.000  0.00  0.00           C+0
HETATM   17  O   UNK     0      11.719  -1.018   0.000  0.00  0.00           O+0
HETATM   18  C   UNK     0      12.373  -2.411   0.000  0.00  0.00           C+0
HETATM   19  O   UNK     0      11.250  -3.465   0.000  0.00  0.00           O+0
HETATM   20  C   UNK     0       9.901  -2.722   0.000  0.00  0.00           C+0
HETATM   21  C   UNK     0       8.446  -3.227   0.000  0.00  0.00           C+0
HETATM   22  O   UNK     0       8.157  -4.739   0.000  0.00  0.00           O+0
HETATM   23  C   UNK     0       9.321  -5.747   0.000  0.00  0.00           C+0
HETATM   24  C   UNK     0       7.281  -2.220   0.000  0.00  0.00           C+0
HETATM   25  C   UNK     0       5.753  -2.411   0.000  0.00  0.00           C+0
HETATM   26  O   UNK     0       6.408  -3.805   0.000  0.00  0.00           O+0
HETATM   27  C   UNK     0       4.630  -3.465   0.000  0.00  0.00           C+0
HETATM   28  O   UNK     0       4.822  -4.993   0.000  0.00  0.00           O+0
HETATM   29  C   UNK     0       3.281  -2.722   0.000  0.00  0.00           C+0
HETATM   30  C   UNK     0       3.571  -1.209   0.000  0.00  0.00           C+0
HETATM   31  C   UNK     0       2.518  -0.086   0.000  0.00  0.00           C+0
HETATM   32  C   UNK     0       1.018  -0.436   0.000  0.00  0.00           C+0
HETATM   33  C   UNK     0      -0.035   0.687   0.000  0.00  0.00           C+0
HETATM   34  C   UNK     0       0.411   2.161   0.000  0.00  0.00           C+0
HETATM   35  C   UNK     0       1.911   2.512   0.000  0.00  0.00           C+0
HETATM   36  C   UNK     0       2.964   1.388   0.000  0.00  0.00           C+0
HETATM   37  C   UNK     0       1.887  -3.376   0.000  0.00  0.00           C+0
HETATM   38  O   UNK     0       0.623  -2.496   0.000  0.00  0.00           O+0
HETATM   39  N   UNK     0       1.757  -4.911   0.000  0.00  0.00           N+0
HETATM   40  C   UNK     0       3.021  -5.791   0.000  0.00  0.00           C+0
HETATM   41  C   UNK     0       0.363  -5.565   0.000  0.00  0.00           C+0
CONECT    1    2                                                            
CONECT    2    1    3                                                       
CONECT    3    2    4    9                                                  
CONECT    4    3    5                                                       
CONECT    5    4    6                                                       
CONECT    6    5    7   12                                                  
CONECT    7    6    8    9                                                  
CONECT    8    7                                                            
CONECT    9    7    3   10                                                  
CONECT   10    9   11                                                       
CONECT   11   10                                                            
CONECT   12    6   13   25   30                                             
CONECT   13   12   14                                                       
CONECT   14   13   15   24                                                  
CONECT   15   14   16                                                       
CONECT   16   15   17   20                                                  
CONECT   17   16   18                                                       
CONECT   18   17   19                                                       
CONECT   19   18   20                                                       
CONECT   20   19   16   21                                                  
CONECT   21   20   22   24                                                  
CONECT   22   21   23                                                       
CONECT   23   22                                                            
CONECT   24   21   14   25                                                  
CONECT   25   24   12   26   27                                             
CONECT   26   25                                                            
CONECT   27   25   28   29                                                  
CONECT   28   27                                                            
CONECT   29   27   30   37                                                  
CONECT   30   29   12   31                                                  
CONECT   31   30   32   36                                                  
CONECT   32   31   33                                                       
CONECT   33   32   34                                                       
CONECT   34   33   35                                                       
CONECT   35   34   36                                                       
CONECT   36   35   31                                                       
CONECT   37   29   38   39                                                  
CONECT   38   37                                                            
CONECT   39   37   40   41                                                  
CONECT   40   39                                                            
CONECT   41   39                                                            
MASTER        0    0    0    0    0    0    0    0   41    0   92    0
END

View in JSmol

Synonyms

Not Available

Chemical Formula

C₃₀H₃₁NO₁₀

Average Mass

565.5750 Da

Monoisotopic Mass

565.19480 Da

IUPAC Name

10,11-dihydroxy-14-(2-hydroxy-3,4-dimethoxyphenyl)-8-methoxy-N,N-dimethyl-13-phenyl-4,6,15-trioxatetracyclo[7.6.0.0³,⁷.0¹⁰,¹⁴]pentadeca-1,3(7),8-triene-12-carboxamide

Traditional Name

10,11-dihydroxy-14-(2-hydroxy-3,4-dimethoxyphenyl)-8-methoxy-N,N-dimethyl-13-phenyl-4,6,15-trioxatetracyclo[7.6.0.0³,⁷.0¹⁰,¹⁴]pentadeca-1,3(7),8-triene-12-carboxamide

CAS Registry Number

Not Available

SMILES

COC1=CC=C(C(O)=C1OC)C12OC3=CC4=C(OCO4)C(OC)=C3C1(O)C(O)C(C2C1=CC=CC=C1)C(=O)N(C)C

InChI Identifier

InChI=1S/C30H31NO10/c1-31(2)28(34)20-21(15-9-7-6-8-10-15)30(16-11-12-17(36-3)24(37-4)23(16)32)29(35,27(20)33)22-18(41-30)13-19-25(26(22)38-5)40-14-39-19/h6-13,20-21,27,32-33,35H,14H2,1-5H3

InChI Key

ASMWUNIIUGWPST-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
Aglaia elaeagnoidea	LOTUS Database	35616633
Aglaia oligophylla	LOTUS Database	35616633

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as flavaglines. These are heterocyclic compounds with a structure characterized by a cyclopenta[b]benzofuran skeleton.

Kingdom

Organic compounds

Super Class

Organoheterocyclic compounds

Class

Benzofurans

Sub Class

Flavaglines

Direct Parent

Flavaglines

Alternative Parents

Substituents

Flavagline skeleton
Stilbene
Methoxyphenol
Dimethoxybenzene
O-dimethoxybenzene
Benzodioxole
Coumaran
Phenol ether
Phenoxy compound
Anisole
Methoxybenzene
1-hydroxy-4-unsubstituted benzenoid
Alkyl aryl ether
Phenol
Benzenoid
Monocyclic benzene moiety
Tertiary carboxylic acid amide
Tertiary alcohol
Cyclic alcohol
1,2-diol
Carboxamide group
Secondary alcohol
Oxacycle
Ether
Carboxylic acid derivative
Acetal
Hydrocarbon derivative
Carbonyl group
Organic oxide
Organopnictogen compound
Organic oxygen compound
Organic nitrogen compound
Alcohol
Organonitrogen compound
Organooxygen compound
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	3.01	ALOGPS
logP	1.71	ChemAxon
logS	-3.5	ALOGPS
pKa (Strongest Acidic)	9.52	ChemAxon
pKa (Strongest Basic)	-1.7	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	10	ChemAxon
Hydrogen Donor Count	3	ChemAxon
Polar Surface Area	136.38 Å²	ChemAxon
Rotatable Bond Count	6	ChemAxon
Refractivity	144.01 m³·mol⁻¹	ChemAxon
Polarizability	57.49 Å³	ChemAxon
Number of Rings	6	ChemAxon
Bioavailability	Yes	ChemAxon
Rule of Five	No	ChemAxon
Ghose Filter	No	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

LOTUS database [Link]

Showing NP-Card for 10,11-dihydroxy-14-(2-hydroxy-3,4-dimethoxyphenyl)-8-methoxy-n,n-dimethyl-13-phenyl-4,6,15-trioxatetracyclo[7.6.0.0³,⁷.0¹⁰,¹⁴]pentadeca-1,3(7),8-triene-12-carboxamide (NP0295908)

MOL for NP0295908 (10,11-dihydroxy-14-(2-hydroxy-3,4-dimethoxyphenyl)-8-methoxy-n,n-dimethyl-13-phenyl-4,6,15-trioxatetracyclo[7.6.0.0³,⁷.0¹⁰,¹⁴]pentadeca-1,3(7),8-triene-12-carboxamide)

3D MOL for NP0295908 (10,11-dihydroxy-14-(2-hydroxy-3,4-dimethoxyphenyl)-8-methoxy-n,n-dimethyl-13-phenyl-4,6,15-trioxatetracyclo[7.6.0.0³,⁷.0¹⁰,¹⁴]pentadeca-1,3(7),8-triene-12-carboxamide)

3D SDF for NP0295908 (10,11-dihydroxy-14-(2-hydroxy-3,4-dimethoxyphenyl)-8-methoxy-n,n-dimethyl-13-phenyl-4,6,15-trioxatetracyclo[7.6.0.0³,⁷.0¹⁰,¹⁴]pentadeca-1,3(7),8-triene-12-carboxamide)

3D-SDF for NP0295908 (10,11-dihydroxy-14-(2-hydroxy-3,4-dimethoxyphenyl)-8-methoxy-n,n-dimethyl-13-phenyl-4,6,15-trioxatetracyclo[7.6.0.0³,⁷.0¹⁰,¹⁴]pentadeca-1,3(7),8-triene-12-carboxamide)

PDB for NP0295908 (10,11-dihydroxy-14-(2-hydroxy-3,4-dimethoxyphenyl)-8-methoxy-n,n-dimethyl-13-phenyl-4,6,15-trioxatetracyclo[7.6.0.0³,⁷.0¹⁰,¹⁴]pentadeca-1,3(7),8-triene-12-carboxamide)

3D PDB for NP0295908 (10,11-dihydroxy-14-(2-hydroxy-3,4-dimethoxyphenyl)-8-methoxy-n,n-dimethyl-13-phenyl-4,6,15-trioxatetracyclo[7.6.0.0³,⁷.0¹⁰,¹⁴]pentadeca-1,3(7),8-triene-12-carboxamide)

SMILES for NP0295908 (10,11-dihydroxy-14-(2-hydroxy-3,4-dimethoxyphenyl)-8-methoxy-n,n-dimethyl-13-phenyl-4,6,15-trioxatetracyclo[7.6.0.0³,⁷.0¹⁰,¹⁴]pentadeca-1,3(7),8-triene-12-carboxamide)

INCHI for NP0295908 (10,11-dihydroxy-14-(2-hydroxy-3,4-dimethoxyphenyl)-8-methoxy-n,n-dimethyl-13-phenyl-4,6,15-trioxatetracyclo[7.6.0.0³,⁷.0¹⁰,¹⁴]pentadeca-1,3(7),8-triene-12-carboxamide)

Structure for NP0295908 (10,11-dihydroxy-14-(2-hydroxy-3,4-dimethoxyphenyl)-8-methoxy-n,n-dimethyl-13-phenyl-4,6,15-trioxatetracyclo[7.6.0.0³,⁷.0¹⁰,¹⁴]pentadeca-1,3(7),8-triene-12-carboxamide)

3D Structure for NP0295908 (10,11-dihydroxy-14-(2-hydroxy-3,4-dimethoxyphenyl)-8-methoxy-n,n-dimethyl-13-phenyl-4,6,15-trioxatetracyclo[7.6.0.0³,⁷.0¹⁰,¹⁴]pentadeca-1,3(7),8-triene-12-carboxamide)