NP-MRD: Showing NP-Card for (5s,7s,10as,13s,13as,14s,16as)-14-benzyl-5,16-dihydroxy-5,7,12,13-tetramethyl-6h,7h,8h,10ah,13h,13ah,14h-oxacyclododeca[3,2-d]isoindol-2-one (NP0202846)

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Record Information

Version

2.0

Created at

2022-09-04 22:09:35 UTC

Updated at

2022-09-04 22:09:36 UTC

NP-MRD ID

NP0202846

Secondary Accession Numbers

None

Natural Product Identification

Common Name

(5s,7s,10as,13s,13as,14s,16as)-14-benzyl-5,16-dihydroxy-5,7,12,13-tetramethyl-6h,7h,8h,10ah,13h,13ah,14h-oxacyclododeca[3,2-d]isoindol-2-one

Description

7-Deoxy-cytochalasin Z9 belongs to the class of organic compounds known as isoindolones. These are aromatic polycyclic compounds that an isoindole bearing a ketone. (5s,7s,10as,13s,13as,14s,16as)-14-benzyl-5,16-dihydroxy-5,7,12,13-tetramethyl-6h,7h,8h,10ah,13h,13ah,14h-oxacyclododeca[3,2-d]isoindol-2-one is found in Mariannaea elegans. Based on a literature review very few articles have been published on 7-deoxy-cytochalasin Z9.

Structure

MOL 3D MOL SDF PDB SMILES InChI


  Mrv1652309052200092D          

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M  END

     RDKit          3D

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M  END


  Mrv1652309052200092D          

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M  END
> <DATABASE_ID>
NP0202846

> <DATABASE_NAME>
NP-MRD

> <SMILES>
C[C@H]1[C@H]2[C@H](CC3=CC=CC=C3)N=C(O)[C@@]22OC(=O)\C=C/[C@@](C)(O)C[C@@H](C)C\C=C/[C@H]2C=C1C

> <INCHI_IDENTIFIER>
InChI=1S/C28H35NO4/c1-18-9-8-12-22-15-19(2)20(3)25-23(16-21-10-6-5-7-11-21)29-26(31)28(22,25)33-24(30)13-14-27(4,32)17-18/h5-8,10-15,18,20,22-23,25,32H,9,16-17H2,1-4H3,(H,29,31)/b12-8-,14-13-/t18-,20+,22-,23-,25-,27+,28-/m0/s1

> <INCHI_KEY>
PYGFBTSCVYWQCJ-GETIBZEOSA-N

> <FORMULA>
C28H35NO4

> <MOLECULAR_WEIGHT>
449.591

> <EXACT_MASS>
449.256608611

> <JCHEM_ACCEPTOR_COUNT>
4

> <JCHEM_ATOM_COUNT>
68

> <JCHEM_AVERAGE_POLARIZABILITY>
50.0847778919873

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
2

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
0

> <JCHEM_IUPAC>
(5S,7S,13S,13aS,14S,16aS,16bS)-14-benzyl-5,16-dihydroxy-5,7,12,13-tetramethyl-2H,5H,6H,7H,8H,13H,13aH,14H,16bH-oxacyclododeca[3,2-e]isoindol-2-one

> <JCHEM_LOGP>
4.025968649291996

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
4

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA>
14.615954670458855

> <JCHEM_PKA_STRONGEST_ACIDIC>
1.9828750272901

> <JCHEM_PKA_STRONGEST_BASIC>
4.887287460972175

> <JCHEM_POLAR_SURFACE_AREA>
79.12

> <JCHEM_REFRACTIVITY>
132.0307

> <JCHEM_ROTATABLE_BOND_COUNT>
2

> <JCHEM_RULE_OF_FIVE>
1

> <JCHEM_TRADITIONAL_IUPAC>
(5S,7S,13S,13aS,14S,16aS,16bS)-14-benzyl-5,16-dihydroxy-5,7,12,13-tetramethyl-6H,7H,8H,13H,13aH,14H,16bH-oxacyclododeca[3,2-e]isoindol-2-one

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 05-SEP-22   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   05-SEP-22         0                                  
HETATM    1  C   UNK     0      -1.904  -1.345   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0      -0.567  -2.109   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0       0.764  -1.334   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0       2.100  -2.098   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0       2.865  -0.761   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0       4.195   0.014   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0       5.735   0.021   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0       7.072  -0.744   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0       8.157   0.350   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0       7.848  -2.074   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0       7.854  -3.614   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0       9.299  -3.081   0.000  0.00  0.00           C+0
HETATM   13  O   UNK     0       8.849  -4.790   0.000  0.00  0.00           O+0
HETATM   14  C   UNK     0       7.090  -4.951   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0       5.759  -5.727   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0       4.219  -5.733   0.000  0.00  0.00           C+0
HETATM   17  O   UNK     0       3.827  -7.222   0.000  0.00  0.00           O+0
HETATM   18  O   UNK     0       2.827  -5.179   0.000  0.00  0.00           O+0
HETATM   19  C   UNK     0       2.107  -3.638   0.000  0.00  0.00           C+0
HETATM   20  C   UNK     0       3.256  -4.664   0.000  0.00  0.00           C+0
HETATM   21  O   UNK     0       4.761  -4.337   0.000  0.00  0.00           O+0
HETATM   22  N   UNK     0       2.635  -6.073   0.000  0.00  0.00           N+0
HETATM   23  C   UNK     0       1.103  -5.919   0.000  0.00  0.00           C+0
HETATM   24  C   UNK     0       0.077  -7.067   0.000  0.00  0.00           C+0
HETATM   25  C   UNK     0      -1.430  -6.753   0.000  0.00  0.00           C+0
HETATM   26  C   UNK     0      -2.456  -7.902   0.000  0.00  0.00           C+0
HETATM   27  C   UNK     0      -3.964  -7.588   0.000  0.00  0.00           C+0
HETATM   28  C   UNK     0      -4.446  -6.126   0.000  0.00  0.00           C+0
HETATM   29  C   UNK     0      -3.420  -4.977   0.000  0.00  0.00           C+0
HETATM   30  C   UNK     0      -1.912  -5.291   0.000  0.00  0.00           C+0
HETATM   31  C   UNK     0       0.776  -4.414   0.000  0.00  0.00           C+0
HETATM   32  C   UNK     0      -0.560  -3.649   0.000  0.00  0.00           C+0
HETATM   33  C   UNK     0      -1.891  -4.425   0.000  0.00  0.00           C+0
CONECT    1    2                                                            
CONECT    2    1    3   32                                                  
CONECT    3    2    4                                                       
CONECT    4    3    5   19                                                  
CONECT    5    4    6                                                       
CONECT    6    5    7                                                       
CONECT    7    6    8                                                       
CONECT    8    7    9   10                                                  
CONECT    9    8                                                            
CONECT   10    8   11                                                       
CONECT   11   10   12   13   14                                             
CONECT   12   11                                                            
CONECT   13   11                                                            
CONECT   14   11   15                                                       
CONECT   15   14   16                                                       
CONECT   16   15   17   18                                                  
CONECT   17   16                                                            
CONECT   18   16   19                                                       
CONECT   19   18    4   20   31                                             
CONECT   20   19   21   22                                                  
CONECT   21   20                                                            
CONECT   22   20   23                                                       
CONECT   23   22   24   31                                                  
CONECT   24   23   25                                                       
CONECT   25   24   26   30                                                  
CONECT   26   25   27                                                       
CONECT   27   26   28                                                       
CONECT   28   27   29                                                       
CONECT   29   28   30                                                       
CONECT   30   29   25                                                       
CONECT   31   23   19   32                                                  
CONECT   32   31    2   33                                                  
CONECT   33   32                                                            
MASTER        0    0    0    0    0    0    0    0   33    0   72    0
END

View in JSmol

Synonyms

Not Available

Chemical Formula

C₂₈H₃₅NO₄

Average Mass

449.5910 Da

Monoisotopic Mass

449.25661 Da

IUPAC Name

(5S,7S,13S,13aS,14S,16aS,16bS)-14-benzyl-5,16-dihydroxy-5,7,12,13-tetramethyl-2H,5H,6H,7H,8H,13H,13aH,14H,16bH-oxacyclododeca[3,2-e]isoindol-2-one

Traditional Name

(5S,7S,13S,13aS,14S,16aS,16bS)-14-benzyl-5,16-dihydroxy-5,7,12,13-tetramethyl-6H,7H,8H,13H,13aH,14H,16bH-oxacyclododeca[3,2-e]isoindol-2-one

CAS Registry Number

Not Available

SMILES

C[C@H]1[C@H]2[C@H](CC3=CC=CC=C3)N=C(O)[C@@]22OC(=O)\C=C/[C@@](C)(O)C[C@@H](C)C\C=C/[C@H]2C=C1C

InChI Identifier

InChI=1S/C28H35NO4/c1-18-9-8-12-22-15-19(2)20(3)25-23(16-21-10-6-5-7-11-21)29-26(31)28(22,25)33-24(30)13-14-27(4,32)17-18/h5-8,10-15,18,20,22-23,25,32H,9,16-17H2,1-4H3,(H,29,31)/b12-8-,14-13-/t18-,20+,22-,23-,25-,27+,28-/m0/s1

InChI Key

PYGFBTSCVYWQCJ-GETIBZEOSA-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
Mariannaea elegans	LOTUS Database	35616633

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as isoindolones. These are aromatic polycyclic compounds that an isoindole bearing a ketone.

Kingdom

Organic compounds

Super Class

Organoheterocyclic compounds

Class

Isoindoles and derivatives

Sub Class

Isoindolines

Direct Parent

Isoindolones

Alternative Parents

Substituents

Isoindolone
Isoindole
Benzenoid
Monocyclic benzene moiety
Cyclic carboximidic acid
Alpha,beta-unsaturated carboxylic ester
Enoate ester
Tertiary alcohol
Pyrroline
Lactone
Carboxylic acid ester
Oxacycle
Azacycle
Organic 1,3-dipolar compound
Propargyl-type 1,3-dipolar organic compound
Monocarboxylic acid or derivatives
Carboxylic acid derivative
Organic nitrogen compound
Organic oxygen compound
Organopnictogen compound
Organic oxide
Hydrocarbon derivative
Organooxygen compound
Organonitrogen compound
Carbonyl group
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	4.03	ChemAxon
pKa (Strongest Acidic)	1.98	ChemAxon
pKa (Strongest Basic)	4.89	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	4	ChemAxon
Hydrogen Donor Count	2	ChemAxon
Polar Surface Area	79.12 Å²	ChemAxon
Rotatable Bond Count	2	ChemAxon
Refractivity	132.03 m³·mol⁻¹	ChemAxon
Polarizability	50.08 Å³	ChemAxon
Number of Rings	4	ChemAxon
Bioavailability	Yes	ChemAxon
Rule of Five	Yes	ChemAxon
Ghose Filter	No	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

78440902

KEGG Compound ID

Not Available

BioCyc ID

Not Available

BiGG ID

Not Available

Wikipedia Link

Not Available

METLIN ID

Not Available

PubChem Compound

139584631

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

LOTUS database [Link]

Showing NP-Card for (5s,7s,10as,13s,13as,14s,16as)-14-benzyl-5,16-dihydroxy-5,7,12,13-tetramethyl-6h,7h,8h,10ah,13h,13ah,14h-oxacyclododeca[3,2-d]isoindol-2-one (NP0202846)

MOL for NP0202846 ((5s,7s,10as,13s,13as,14s,16as)-14-benzyl-5,16-dihydroxy-5,7,12,13-tetramethyl-6h,7h,8h,10ah,13h,13ah,14h-oxacyclododeca[3,2-d]isoindol-2-one)

3D MOL for NP0202846 ((5s,7s,10as,13s,13as,14s,16as)-14-benzyl-5,16-dihydroxy-5,7,12,13-tetramethyl-6h,7h,8h,10ah,13h,13ah,14h-oxacyclododeca[3,2-d]isoindol-2-one)

3D SDF for NP0202846 ((5s,7s,10as,13s,13as,14s,16as)-14-benzyl-5,16-dihydroxy-5,7,12,13-tetramethyl-6h,7h,8h,10ah,13h,13ah,14h-oxacyclododeca[3,2-d]isoindol-2-one)

3D-SDF for NP0202846 ((5s,7s,10as,13s,13as,14s,16as)-14-benzyl-5,16-dihydroxy-5,7,12,13-tetramethyl-6h,7h,8h,10ah,13h,13ah,14h-oxacyclododeca[3,2-d]isoindol-2-one)

PDB for NP0202846 ((5s,7s,10as,13s,13as,14s,16as)-14-benzyl-5,16-dihydroxy-5,7,12,13-tetramethyl-6h,7h,8h,10ah,13h,13ah,14h-oxacyclododeca[3,2-d]isoindol-2-one)

3D PDB for NP0202846 ((5s,7s,10as,13s,13as,14s,16as)-14-benzyl-5,16-dihydroxy-5,7,12,13-tetramethyl-6h,7h,8h,10ah,13h,13ah,14h-oxacyclododeca[3,2-d]isoindol-2-one)

SMILES for NP0202846 ((5s,7s,10as,13s,13as,14s,16as)-14-benzyl-5,16-dihydroxy-5,7,12,13-tetramethyl-6h,7h,8h,10ah,13h,13ah,14h-oxacyclododeca[3,2-d]isoindol-2-one)

INCHI for NP0202846 ((5s,7s,10as,13s,13as,14s,16as)-14-benzyl-5,16-dihydroxy-5,7,12,13-tetramethyl-6h,7h,8h,10ah,13h,13ah,14h-oxacyclododeca[3,2-d]isoindol-2-one)

Structure for NP0202846 ((5s,7s,10as,13s,13as,14s,16as)-14-benzyl-5,16-dihydroxy-5,7,12,13-tetramethyl-6h,7h,8h,10ah,13h,13ah,14h-oxacyclododeca[3,2-d]isoindol-2-one)

3D Structure for NP0202846 ((5s,7s,10as,13s,13as,14s,16as)-14-benzyl-5,16-dihydroxy-5,7,12,13-tetramethyl-6h,7h,8h,10ah,13h,13ah,14h-oxacyclododeca[3,2-d]isoindol-2-one)