NP-MRD: Showing NP-Card for artoindonesianin b (NP0228563)

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Record Information

Version

2.0

Created at

2022-09-06 08:16:14 UTC

Updated at

2022-09-06 08:16:14 UTC

NP-MRD ID

NP0228563

Secondary Accession Numbers

None

Natural Product Identification

Common Name

artoindonesianin b

Description

Artoindonesianin b belongs to the class of organic compounds known as benzoxepines. These are organic compounds containing a benzene ring fused to an oxepine ring (an unsaturated seven-membered heterocycle with one oxygen atom replacing a carbon atom). Thus, artoindonesianin b is considered to be a flavonoid. artoindonesianin b is found in Artocarpus integer. artoindonesianin b was first documented in 2016 (PMID: 27590167). Based on a literature review very few articles have been published on Artoindonesianin b.

Structure

MOL 3D MOL SDF PDB SMILES InChI


  Mrv1652309062210162D          

 34 37  0  0  0  0            999 V2000
    7.7329    0.9973    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.9116    1.0754    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    6.4334    0.4031    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.6121    0.4811    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.1339   -0.1911    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.3126   -0.1131    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.8343   -0.7854    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.1774   -1.5356    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.9987   -1.6137    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.3418   -2.3639    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.4769   -0.9414    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.2982   -1.0194    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.6413   -1.7697    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    6.7765   -0.3472    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.5978   -0.4252    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.9408   -1.1755    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.7621   -1.2535    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    9.1052   -2.0038    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    9.2404   -0.5812    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.8047   -2.2717    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.9969   -2.4392    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.7974   -3.2397    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
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    2.5978   -4.0402    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
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    2.3623   -1.9121    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
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    3.0338   -0.5858    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
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  7 34  1  0  0  0  0
M  END

     RDKit          3D

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   -3.6513    0.9758   -0.2192 C   0  0  2  0  0  0  0  0  0  0  0  0
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M  END


  Mrv1652309062210162D          

 34 37  0  0  0  0            999 V2000
    7.7329    0.9973    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.9116    1.0754    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
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M  END
> <DATABASE_ID>
NP0228563

> <DATABASE_NAME>
NP-MRD

> <SMILES>
COC1=C(\C=C\C(C)C)C(O)=C2C(=O)C3=C(OC2=C1)C1=CC=C(O)C=C1OC(C3)C(C)(C)OO

> <INCHI_IDENTIFIER>
InChI=1S/C26H28O8/c1-13(2)6-8-15-18(31-5)12-20-22(23(15)28)24(29)17-11-21(26(3,4)34-30)32-19-10-14(27)7-9-16(19)25(17)33-20/h6-10,12-13,21,27-28,30H,11H2,1-5H3/b8-6+

> <INCHI_KEY>
UYYZSBJGWJNBMX-SOFGYWHQSA-N

> <FORMULA>
C26H28O8

> <MOLECULAR_WEIGHT>
468.502

> <EXACT_MASS>
468.178417862

> <JCHEM_ACCEPTOR_COUNT>
8

> <JCHEM_ATOM_COUNT>
62

> <JCHEM_AVERAGE_POLARIZABILITY>
50.666076027342015

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
3

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
1

> <JCHEM_IUPAC>
9-(2-hydroperoxypropan-2-yl)-5,14-dihydroxy-16-methoxy-15-[(1E)-3-methylbut-1-en-1-yl]-8,19-dioxatetracyclo[9.8.0.0^{2,7}.0^{13,18}]nonadeca-1(11),2,4,6,13,15,17-heptaen-12-one

> <JCHEM_LOGP>
4.988006482666666

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
4

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA>
8.769299705764265

> <JCHEM_PKA_STRONGEST_ACIDIC>
7.281158569692792

> <JCHEM_PKA_STRONGEST_BASIC>
-4.23904657664118

> <JCHEM_POLAR_SURFACE_AREA>
114.68000000000002

> <JCHEM_REFRACTIVITY>
127.364

> <JCHEM_ROTATABLE_BOND_COUNT>
5

> <JCHEM_RULE_OF_FIVE>
1

> <JCHEM_TRADITIONAL_IUPAC>
9-(2-hydroperoxypropan-2-yl)-5,14-dihydroxy-16-methoxy-15-[(1E)-3-methylbut-1-en-1-yl]-8,19-dioxatetracyclo[9.8.0.0^{2,7}.0^{13,18}]nonadeca-1(11),2,4,6,13,15,17-heptaen-12-one

> <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      14.435   1.862   0.000  0.00  0.00           C+0
HETATM    2  O   UNK     0      12.902   2.007   0.000  0.00  0.00           O+0
HETATM    3  C   UNK     0      12.009   0.752   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0      10.476   0.898   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0       9.583  -0.357   0.000  0.00  0.00           C+0
HETATM    6  O   UNK     0       8.050  -0.211   0.000  0.00  0.00           O+0
HETATM    7  C   UNK     0       7.157  -1.466   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0       7.798  -2.867   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0       9.331  -3.012   0.000  0.00  0.00           C+0
HETATM   10  O   UNK     0       9.971  -4.413   0.000  0.00  0.00           O+0
HETATM   11  C   UNK     0      10.224  -1.757   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0      11.757  -1.903   0.000  0.00  0.00           C+0
HETATM   13  O   UNK     0      12.397  -3.303   0.000  0.00  0.00           O+0
HETATM   14  C   UNK     0      12.649  -0.648   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0      14.182  -0.794   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0      14.823  -2.194   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0      16.356  -2.340   0.000  0.00  0.00           C+0
HETATM   18  C   UNK     0      16.996  -3.740   0.000  0.00  0.00           C+0
HETATM   19  C   UNK     0      17.249  -1.085   0.000  0.00  0.00           C+0
HETATM   20  C   UNK     0       7.102  -4.240   0.000  0.00  0.00           C+0
HETATM   21  C   UNK     0       5.594  -4.553   0.000  0.00  0.00           C+0
HETATM   22  C   UNK     0       5.222  -6.047   0.000  0.00  0.00           C+0
HETATM   23  C   UNK     0       6.716  -6.420   0.000  0.00  0.00           C+0
HETATM   24  C   UNK     0       3.727  -5.675   0.000  0.00  0.00           C+0
HETATM   25  O   UNK     0       4.849  -7.542   0.000  0.00  0.00           O+0
HETATM   26  O   UNK     0       3.369  -7.966   0.000  0.00  0.00           O+0
HETATM   27  O   UNK     0       4.410  -3.569   0.000  0.00  0.00           O+0
HETATM   28  C   UNK     0       4.440  -2.029   0.000  0.00  0.00           C+0
HETATM   29  C   UNK     0       3.018  -1.438   0.000  0.00  0.00           C+0
HETATM   30  C   UNK     0       2.819   0.089   0.000  0.00  0.00           C+0
HETATM   31  O   UNK     0       1.397   0.680   0.000  0.00  0.00           O+0
HETATM   32  C   UNK     0       4.042   1.025   0.000  0.00  0.00           C+0
HETATM   33  C   UNK     0       5.464   0.434   0.000  0.00  0.00           C+0
HETATM   34  C   UNK     0       5.663  -1.093   0.000  0.00  0.00           C+0
CONECT    1    2                                                            
CONECT    2    1    3                                                       
CONECT    3    2    4   14                                                  
CONECT    4    3    5                                                       
CONECT    5    4    6   11                                                  
CONECT    6    5    7                                                       
CONECT    7    6    8   34                                                  
CONECT    8    7    9   20                                                  
CONECT    9    8   10   11                                                  
CONECT   10    9                                                            
CONECT   11    9    5   12                                                  
CONECT   12   11   13   14                                                  
CONECT   13   12                                                            
CONECT   14   12    3   15                                                  
CONECT   15   14   16                                                       
CONECT   16   15   17                                                       
CONECT   17   16   18   19                                                  
CONECT   18   17                                                            
CONECT   19   17                                                            
CONECT   20    8   21                                                       
CONECT   21   20   22   27                                                  
CONECT   22   21   23   24   25                                             
CONECT   23   22                                                            
CONECT   24   22                                                            
CONECT   25   22   26                                                       
CONECT   26   25                                                            
CONECT   27   21   28                                                       
CONECT   28   27   29   34                                                  
CONECT   29   28   30                                                       
CONECT   30   29   31   32                                                  
CONECT   31   30                                                            
CONECT   32   30   33                                                       
CONECT   33   32   34                                                       
CONECT   34   33   28    7                                                  
MASTER        0    0    0    0    0    0    0    0   34    0   74    0
END

View in JSmol

Synonyms

Value	Source
Artoindonesianin-b	MeSH

Chemical Formula

C₂₆H₂₈O₈

Average Mass

468.5020 Da

Monoisotopic Mass

468.17842 Da

IUPAC Name

9-(2-hydroperoxypropan-2-yl)-5,14-dihydroxy-16-methoxy-15-[(1E)-3-methylbut-1-en-1-yl]-8,19-dioxatetracyclo[9.8.0.0^{2,7}.0^{13,18}]nonadeca-1(11),2,4,6,13,15,17-heptaen-12-one

Traditional Name

9-(2-hydroperoxypropan-2-yl)-5,14-dihydroxy-16-methoxy-15-[(1E)-3-methylbut-1-en-1-yl]-8,19-dioxatetracyclo[9.8.0.0^{2,7}.0^{13,18}]nonadeca-1(11),2,4,6,13,15,17-heptaen-12-one

CAS Registry Number

Not Available

SMILES

COC1=C(\C=C\C(C)C)C(O)=C2C(=O)C3=C(OC2=C1)C1=CC=C(O)C=C1OC(C3)C(C)(C)OO

InChI Identifier

InChI=1S/C26H28O8/c1-13(2)6-8-15-18(31-5)12-20-22(23(15)28)24(29)17-11-21(26(3,4)34-30)32-19-10-14(27)7-9-16(19)25(17)33-20/h6-10,12-13,21,27-28,30H,11H2,1-5H3/b8-6+

InChI Key

UYYZSBJGWJNBMX-SOFGYWHQSA-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
Artocarpus champeden	LOTUS Database	35616633

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as benzoxepines. These are organic compounds containing a benzene ring fused to an oxepine ring (an unsaturated seven-membered heterocycle with one oxygen atom replacing a carbon atom).

Kingdom

Organic compounds

Super Class

Organoheterocyclic compounds

Class

Benzoxepines

Sub Class

Not Available

Direct Parent

Benzoxepines

Alternative Parents

Substituents

Benzoxepine
Chromone
Benzopyran
1-benzopyran
Anisole
Phenol ether
Styrene
1-hydroxy-4-unsubstituted benzenoid
1-hydroxy-2-unsubstituted benzenoid
Alkyl aryl ether
Phenol
Pyranone
Benzenoid
Pyran
Heteroaromatic compound
Vinylogous acid
Hydroperoxide
Peroxol
Ether
Oxacycle
Alkyl hydroperoxide
Organooxygen compound
Organic oxygen compound
Hydrocarbon derivative
Organic oxide
Aromatic heteropolycyclic compound

Molecular Framework

Aromatic heteropolycyclic compounds

External Descriptors

Flavones and Flavonols (LMPK12111537 )

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	4.99	ChemAxon
pKa (Strongest Acidic)	7.28	ChemAxon
pKa (Strongest Basic)	-4.2	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	8	ChemAxon
Hydrogen Donor Count	3	ChemAxon
Polar Surface Area	114.68 Å²	ChemAxon
Rotatable Bond Count	5	ChemAxon
Refractivity	127.36 m³·mol⁻¹	ChemAxon
Polarizability	50.67 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	No	ChemAxon

External Links

HMDB ID

Not Available

DrugBank ID

Not Available

Phenol Explorer Compound ID

Not Available

FoodDB ID

Not Available

KNApSAcK ID

C00013496

Chemspider ID

8271706

KEGG Compound ID

Not Available

BioCyc ID

Not Available

BiGG ID

Not Available

Wikipedia Link

Not Available

METLIN ID

Not Available

PubChem Compound

10096171

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

Lang L, Dong N, Wu D, Yao X, Lu W, Zhang C, Ouyang P, Zhu J, Tang Y, Wang W, Li J, Huang J: 2-Arylbenzo[b]furan derivatives as potent human lipoxygenase inhibitors. J Enzyme Inhib Med Chem. 2016;31(sup4):98-105. doi: 10.1080/14756366.2016.1220376. Epub 2016 Sep 2. [PubMed:27590167 ]
LOTUS database [Link]

Showing NP-Card for artoindonesianin b (NP0228563)

MOL for NP0228563 (artoindonesianin b)

3D MOL for NP0228563 (artoindonesianin b)

3D SDF for NP0228563 (artoindonesianin b)

3D-SDF for NP0228563 (artoindonesianin b)

PDB for NP0228563 (artoindonesianin b)

3D PDB for NP0228563 (artoindonesianin b)

SMILES for NP0228563 (artoindonesianin b)

INCHI for NP0228563 (artoindonesianin b)

Structure for NP0228563 (artoindonesianin b)

3D Structure for NP0228563 (artoindonesianin b)