NP-MRD: Showing NP-Card for 3-(3,4-dihydroxyphenyl)-2-[(3-{4,13,14-trihydroxy-2-oxatricyclo[9.4.0.0³,⁸]pentadeca-1(15),3(8),4,6,9,11,13-heptaen-7-yl}prop-2-enoyl)oxy]propanoic acid (NP0324005)

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Record Information

Version

2.0

Created at

2022-09-12 03:48:13 UTC

Updated at

2022-09-12 03:48:13 UTC

NP-MRD ID

NP0324005

Secondary Accession Numbers

None

Natural Product Identification

Common Name

3-(3,4-dihydroxyphenyl)-2-[(3-{4,13,14-trihydroxy-2-oxatricyclo[9.4.0.0³,⁸]pentadeca-1(15),3(8),4,6,9,11,13-heptaen-7-yl}prop-2-enoyl)oxy]propanoic acid

Description

3-(3,4-Dihydroxyphenyl)-2-[(3-{4,13,14-trihydroxy-2-oxatricyclo[9.4.0.0³,⁸]Pentadeca-1(11),3,5,7,9,12,14-heptaen-7-yl}prop-2-enoyl)oxy]propanoic acid belongs to the class of organic compounds known as dibenzoxepines. Dibenzoxepines are compounds containing a dibenzoxepine moiety, which consists of two benzene connected by an oxazepine ring. 3-(3,4-dihydroxyphenyl)-2-[(3-{4,13,14-trihydroxy-2-oxatricyclo[9.4.0.0³,⁸]pentadeca-1(15),3(8),4,6,9,11,13-heptaen-7-yl}prop-2-enoyl)oxy]propanoic acid is found in Salvia chinensis and Salvia prionitis. 3-(3,4-Dihydroxyphenyl)-2-[(3-{4,13,14-trihydroxy-2-oxatricyclo[9.4.0.0³,⁸]Pentadeca-1(11),3,5,7,9,12,14-heptaen-7-yl}prop-2-enoyl)oxy]propanoic acid is an extremely weak basic (essentially neutral) compound (based on its pKa).

Structure

MOL 3D MOL SDF PDB SMILES InChI


  Mrv1533004231521222D          

 36 39  0  0  0  0            999 V2000
    0.2883   -5.1407    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5001   -5.3839    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6837   -6.1882    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1049   -4.8228    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8932   -5.0659    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0768   -5.8702    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4720   -6.4314    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6556   -7.2357    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4439   -7.4789    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6275   -8.2832    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.0487   -6.9177    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.8371   -7.1609    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8651   -6.1134    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9213   -4.0184    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1329   -3.7753    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.4718   -4.3364    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
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    0.8390   -2.7278    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.0226   -1.9235    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.4178   -1.3623    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.6014   -0.5580    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.3897   -0.3148    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.5733    0.4895    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
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    3.6647   -1.6803    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.1503   -2.3253    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
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    1.8109   -1.6803    0.0000 C   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
  2  4  1  0  0  0  0
  4  5  1  0  0  0  0
  5  6  1  0  0  0  0
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  9 10  1  0  0  0  0
  9 11  1  0  0  0  0
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  6 13  1  0  0  0  0
  4 14  1  0  0  0  0
 14 15  1  0  0  0  0
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 22 23  1  0  0  0  0
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 33 34  1  0  0  0  0
 34 35  2  0  0  0  0
 35 36  1  0  0  0  0
 19 36  1  0  0  0  0
 24 36  2  0  0  0  0
M  END

     RDKit          3D

 56 59  0  0  0  0  0  0  0  0999 V2000
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   -6.2609    1.2978   -2.2702 H   0  0  0  0  0  0  0  0  0  0  0  0
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    3.5670   -1.8441   -0.1444 H   0  0  0  0  0  0  0  0  0  0  0  0
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M  END


  Mrv1533004231521222D          

 36 39  0  0  0  0            999 V2000
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M  END
> <DATABASE_ID>
NP0324005

> <DATABASE_NAME>
NP-MRD

> <SMILES>
OC(=O)C(CC1=CC=C(O)C(O)=C1)OC(=O)C=CC1=CC=C(O)C2=C1C=CC1=CC(O)=C(O)C=C1O2

> <INCHI_IDENTIFIER>
InChI=1S/C26H20O10/c27-17-6-1-13(9-19(17)29)10-23(26(33)34)35-24(32)8-4-14-3-7-18(28)25-16(14)5-2-15-11-20(30)21(31)12-22(15)36-25/h1-9,11-12,23,27-31H,10H2,(H,33,34)

> <INCHI_KEY>
AVGRZVZQTALJJF-UHFFFAOYSA-N

> <FORMULA>
C26H20O10

> <MOLECULAR_WEIGHT>
492.436

> <EXACT_MASS>
492.105646844

> <JCHEM_ACCEPTOR_COUNT>
8

> <JCHEM_ATOM_COUNT>
56

> <JCHEM_AVERAGE_POLARIZABILITY>
48.01533453198408

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
6

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
0

> <JCHEM_IUPAC>
3-(3,4-dihydroxyphenyl)-2-[(3-{4,13,14-trihydroxy-2-oxatricyclo[9.4.0.0³,⁸]pentadeca-1(15),3(8),4,6,9,11,13-heptaen-7-yl}prop-2-enoyl)oxy]propanoic acid

> <ALOGPS_LOGP>
3.88

> <JCHEM_LOGP>
4.567443361666666

> <ALOGPS_LOGS>
-4.75

> <JCHEM_MDDR_LIKE_RULE>
1

> <JCHEM_NUMBER_OF_RINGS>
4

> <JCHEM_PHYSIOLOGICAL_CHARGE>
-1

> <JCHEM_PKA>
8.234438774425191

> <JCHEM_PKA_STRONGEST_ACIDIC>
3.1175912944220827

> <JCHEM_PKA_STRONGEST_BASIC>
-3.7466276720321354

> <JCHEM_POLAR_SURFACE_AREA>
173.98

> <JCHEM_REFRACTIVITY>
128.5686

> <JCHEM_ROTATABLE_BOND_COUNT>
7

> <JCHEM_RULE_OF_FIVE>
0

> <ALOGPS_SOLUBILITY>
8.77e-03 g/l

> <JCHEM_TRADITIONAL_IUPAC>
3-(3,4-dihydroxyphenyl)-2-[(3-{4,13,14-trihydroxy-2-oxatricyclo[9.4.0.0³,⁸]pentadeca-1(15),3(8),4,6,9,11,13-heptaen-7-yl}prop-2-enoyl)oxy]propanoic acid

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 23-APR-15   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   23-APR-15         0                                  
HETATM    1  O   UNK     0       0.538  -9.596   0.000  0.00  0.00           O+0
HETATM    2  C   UNK     0      -0.934 -10.050   0.000  0.00  0.00           C+0
HETATM    3  O   UNK     0      -1.276 -11.551   0.000  0.00  0.00           O+0
HETATM    4  C   UNK     0      -2.062  -9.002   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0      -3.534  -9.456   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0      -3.877 -10.958   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0      -2.748 -12.005   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0      -3.090 -13.507   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0      -4.562 -13.961   0.000  0.00  0.00           C+0
HETATM   10  O   UNK     0      -4.905 -15.462   0.000  0.00  0.00           O+0
HETATM   11  C   UNK     0      -5.691 -12.913   0.000  0.00  0.00           C+0
HETATM   12  O   UNK     0      -7.163 -13.367   0.000  0.00  0.00           O+0
HETATM   13  C   UNK     0      -5.348 -11.412   0.000  0.00  0.00           C+0
HETATM   14  O   UNK     0      -1.720  -7.501   0.000  0.00  0.00           O+0
HETATM   15  C   UNK     0      -0.248  -7.047   0.000  0.00  0.00           C+0
HETATM   16  O   UNK     0       0.881  -8.095   0.000  0.00  0.00           O+0
HETATM   17  C   UNK     0       0.095  -5.546   0.000  0.00  0.00           C+0
HETATM   18  C   UNK     0       1.566  -5.092   0.000  0.00  0.00           C+0
HETATM   19  C   UNK     0       1.909  -3.590   0.000  0.00  0.00           C+0
HETATM   20  C   UNK     0       0.780  -2.543   0.000  0.00  0.00           C+0
HETATM   21  C   UNK     0       1.123  -1.042   0.000  0.00  0.00           C+0
HETATM   22  C   UNK     0       2.594  -0.588   0.000  0.00  0.00           C+0
HETATM   23  O   UNK     0       2.937   0.914   0.000  0.00  0.00           O+0
HETATM   24  C   UNK     0       3.723  -1.635   0.000  0.00  0.00           C+0
HETATM   25  O   UNK     0       5.111  -0.967   0.000  0.00  0.00           O+0
HETATM   26  C   UNK     0       6.498  -1.635   0.000  0.00  0.00           C+0
HETATM   27  C   UNK     0       7.627  -0.588   0.000  0.00  0.00           C+0
HETATM   28  C   UNK     0       9.099  -1.042   0.000  0.00  0.00           C+0
HETATM   29  O   UNK     0      10.227   0.006   0.000  0.00  0.00           O+0
HETATM   30  C   UNK     0       9.441  -2.543   0.000  0.00  0.00           C+0
HETATM   31  O   UNK     0      10.913  -2.997   0.000  0.00  0.00           O+0
HETATM   32  C   UNK     0       8.312  -3.590   0.000  0.00  0.00           C+0
HETATM   33  C   UNK     0       6.841  -3.137   0.000  0.00  0.00           C+0
HETATM   34  C   UNK     0       5.881  -4.341   0.000  0.00  0.00           C+0
HETATM   35  C   UNK     0       4.341  -4.341   0.000  0.00  0.00           C+0
HETATM   36  C   UNK     0       3.380  -3.137   0.000  0.00  0.00           C+0
CONECT    1    2                                                            
CONECT    2    1    3    4                                                  
CONECT    3    2                                                            
CONECT    4    2    5   14                                                  
CONECT    5    4    6                                                       
CONECT    6    5    7   13                                                  
CONECT    7    6    8                                                       
CONECT    8    7    9                                                       
CONECT    9    8   10   11                                                  
CONECT   10    9                                                            
CONECT   11    9   12   13                                                  
CONECT   12   11                                                            
CONECT   13   11    6                                                       
CONECT   14    4   15                                                       
CONECT   15   14   16   17                                                  
CONECT   16   15                                                            
CONECT   17   15   18                                                       
CONECT   18   17   19                                                       
CONECT   19   18   20   36                                                  
CONECT   20   19   21                                                       
CONECT   21   20   22                                                       
CONECT   22   21   23   24                                                  
CONECT   23   22                                                            
CONECT   24   22   25   36                                                  
CONECT   25   24   26                                                       
CONECT   26   25   27   33                                                  
CONECT   27   26   28                                                       
CONECT   28   27   29   30                                                  
CONECT   29   28                                                            
CONECT   30   28   31   32                                                  
CONECT   31   30                                                            
CONECT   32   30   33                                                       
CONECT   33   32   26   34                                                  
CONECT   34   33   35                                                       
CONECT   35   34   36                                                       
CONECT   36   35   19   24                                                  
MASTER        0    0    0    0    0    0    0    0   36    0   78    0
END

View in JSmol

Synonyms

Value	Source
3-(3,4-Dihydroxyphenyl)-2-[(3-{4,13,14-trihydroxy-2-oxatricyclo[9.4.0.0,]pentadeca-1(11),3,5,7,9,12,14-heptaen-7-yl}prop-2-enoyl)oxy]propanoate	Generator
3-(3,4-Dihydroxyphenyl)-2-[(3-{4,13,14-trihydroxy-2-oxatricyclo[9.4.0.0³,⁸]pentadeca-1(11),3,5,7,9,12,14-heptaen-7-yl}prop-2-enoyl)oxy]propanoate	Generator

Chemical Formula

C₂₆H₂₀O₁₀

Average Mass

492.4360 Da

Monoisotopic Mass

492.10565 Da

IUPAC Name

3-(3,4-dihydroxyphenyl)-2-[(3-{4,13,14-trihydroxy-2-oxatricyclo[9.4.0.0³,⁸]pentadeca-1(15),3(8),4,6,9,11,13-heptaen-7-yl}prop-2-enoyl)oxy]propanoic acid

Traditional Name

3-(3,4-dihydroxyphenyl)-2-[(3-{4,13,14-trihydroxy-2-oxatricyclo[9.4.0.0³,⁸]pentadeca-1(15),3(8),4,6,9,11,13-heptaen-7-yl}prop-2-enoyl)oxy]propanoic acid

CAS Registry Number

Not Available

SMILES

OC(=O)C(CC1=CC=C(O)C(O)=C1)OC(=O)C=CC1=CC=C(O)C2=C1C=CC1=CC(O)=C(O)C=C1O2

InChI Identifier

InChI=1S/C26H20O10/c27-17-6-1-13(9-19(17)29)10-23(26(33)34)35-24(32)8-4-14-3-7-18(28)25-16(14)5-2-15-11-20(30)21(31)12-22(15)36-25/h1-9,11-12,23,27-31H,10H2,(H,33,34)

InChI Key

AVGRZVZQTALJJF-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
Salvia chinensis	LOTUS Database	35616633
Salvia prionitis	LOTUS Database	35616633

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as dibenzoxepines. Dibenzoxepines are compounds containing a dibenzoxepine moiety, which consists of two benzene connected by an oxazepine ring.

Kingdom

Organic compounds

Super Class

Organoheterocyclic compounds

Class

Benzoxepines

Sub Class

Dibenzoxepines

Direct Parent

Dibenzoxepines

Alternative Parents

Substituents

Dibenzoxepine
Cinnamic acid or derivatives
Coumaric acid or derivatives
Cinnamic acid ester
Diaryl ether
3-phenylpropanoic-acid
Catechol
Styrene
1-hydroxy-4-unsubstituted benzenoid
1-hydroxy-2-unsubstituted benzenoid
Fatty acid ester
Phenol
Dicarboxylic acid or derivatives
Benzenoid
Fatty acyl
Monocyclic benzene moiety
Alpha,beta-unsaturated carboxylic ester
Enoate ester
Carboxylic acid ester
Polyol
Oxacycle
Carboxylic acid derivative
Ether
Carboxylic acid
Organooxygen compound
Organic oxygen compound
Organic oxide
Hydrocarbon derivative
Carbonyl group
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	3.88	ALOGPS
logP	4.57	ChemAxon
logS	-4.8	ALOGPS
pKa (Strongest Acidic)	3.12	ChemAxon
pKa (Strongest Basic)	-3.7	ChemAxon
Physiological Charge	-1	ChemAxon
Hydrogen Acceptor Count	8	ChemAxon
Hydrogen Donor Count	6	ChemAxon
Polar Surface Area	173.98 Å²	ChemAxon
Rotatable Bond Count	7	ChemAxon
Refractivity	128.57 m³·mol⁻¹	ChemAxon
Polarizability	48.02 Å³	ChemAxon
Number of Rings	4	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

75072247

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

LOTUS database [Link]

Showing NP-Card for 3-(3,4-dihydroxyphenyl)-2-[(3-{4,13,14-trihydroxy-2-oxatricyclo[9.4.0.0³,⁸]pentadeca-1(15),3(8),4,6,9,11,13-heptaen-7-yl}prop-2-enoyl)oxy]propanoic acid (NP0324005)

MOL for NP0324005 (3-(3,4-dihydroxyphenyl)-2-[(3-{4,13,14-trihydroxy-2-oxatricyclo[9.4.0.0³,⁸]pentadeca-1(15),3(8),4,6,9,11,13-heptaen-7-yl}prop-2-enoyl)oxy]propanoic acid)

3D MOL for NP0324005 (3-(3,4-dihydroxyphenyl)-2-[(3-{4,13,14-trihydroxy-2-oxatricyclo[9.4.0.0³,⁸]pentadeca-1(15),3(8),4,6,9,11,13-heptaen-7-yl}prop-2-enoyl)oxy]propanoic acid)

3D SDF for NP0324005 (3-(3,4-dihydroxyphenyl)-2-[(3-{4,13,14-trihydroxy-2-oxatricyclo[9.4.0.0³,⁸]pentadeca-1(15),3(8),4,6,9,11,13-heptaen-7-yl}prop-2-enoyl)oxy]propanoic acid)

3D-SDF for NP0324005 (3-(3,4-dihydroxyphenyl)-2-[(3-{4,13,14-trihydroxy-2-oxatricyclo[9.4.0.0³,⁸]pentadeca-1(15),3(8),4,6,9,11,13-heptaen-7-yl}prop-2-enoyl)oxy]propanoic acid)

PDB for NP0324005 (3-(3,4-dihydroxyphenyl)-2-[(3-{4,13,14-trihydroxy-2-oxatricyclo[9.4.0.0³,⁸]pentadeca-1(15),3(8),4,6,9,11,13-heptaen-7-yl}prop-2-enoyl)oxy]propanoic acid)

3D PDB for NP0324005 (3-(3,4-dihydroxyphenyl)-2-[(3-{4,13,14-trihydroxy-2-oxatricyclo[9.4.0.0³,⁸]pentadeca-1(15),3(8),4,6,9,11,13-heptaen-7-yl}prop-2-enoyl)oxy]propanoic acid)

SMILES for NP0324005 (3-(3,4-dihydroxyphenyl)-2-[(3-{4,13,14-trihydroxy-2-oxatricyclo[9.4.0.0³,⁸]pentadeca-1(15),3(8),4,6,9,11,13-heptaen-7-yl}prop-2-enoyl)oxy]propanoic acid)

INCHI for NP0324005 (3-(3,4-dihydroxyphenyl)-2-[(3-{4,13,14-trihydroxy-2-oxatricyclo[9.4.0.0³,⁸]pentadeca-1(15),3(8),4,6,9,11,13-heptaen-7-yl}prop-2-enoyl)oxy]propanoic acid)

Structure for NP0324005 (3-(3,4-dihydroxyphenyl)-2-[(3-{4,13,14-trihydroxy-2-oxatricyclo[9.4.0.0³,⁸]pentadeca-1(15),3(8),4,6,9,11,13-heptaen-7-yl}prop-2-enoyl)oxy]propanoic acid)

3D Structure for NP0324005 (3-(3,4-dihydroxyphenyl)-2-[(3-{4,13,14-trihydroxy-2-oxatricyclo[9.4.0.0³,⁸]pentadeca-1(15),3(8),4,6,9,11,13-heptaen-7-yl}prop-2-enoyl)oxy]propanoic acid)