NP-MRD: Showing NP-Card for 3-benzyl-1,12-dihydroxy-5-(hydroxymethyl)-13-methoxy-4,10,12-trimethyl-3h,3ah,4h,6ah,9h,10h,11h,13h,14h-cycloundeca[d]isoindol-15-one (NP0318644)

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Record Information

Version

2.0

Created at

2022-09-11 19:15:30 UTC

Updated at

2022-09-11 19:15:31 UTC

NP-MRD ID

NP0318644

Secondary Accession Numbers

None

Natural Product Identification

Common Name

3-benzyl-1,12-dihydroxy-5-(hydroxymethyl)-13-methoxy-4,10,12-trimethyl-3h,3ah,4h,6ah,9h,10h,11h,13h,14h-cycloundeca[d]isoindol-15-one

Description

3-Benzyl-1,12-dihydroxy-5-(hydroxymethyl)-13-methoxy-4,10,12-trimethyl-3H,4H,6aH,9H,10H,11H,12H,13H,14H,15H,15bH-cycloundeca[e]isoindol-15-one belongs to the class of organic compounds known as cytochalasans. These are fungal metabolites structurally characterized by the presence of an isoindolone nucleus fused to a macrocyclic ring, which can either a lactone, as in cytochalasin B, a carbonate, as in cytochalasin E, or a carbocycle, as in cytochalasin D, H, and K. Based on a literature review very few articles have been published on 3-benzyl-1,12-dihydroxy-5-(hydroxymethyl)-13-methoxy-4,10,12-trimethyl-3H,4H,6aH,9H,10H,11H,12H,13H,14H,15H,15bH-cycloundeca[e]isoindol-15-one.

Structure

MOL 3D MOL SDF PDB SMILES InChI


  Mrv1652309112221152D          

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M  END

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  Mrv1652309112221152D          

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 14 15  1  0  0  0  0
 15 16  2  0  0  0  0
 16 17  1  0  0  0  0
 17 18  2  0  0  0  0
 13 18  1  0  0  0  0
 11 19  1  0  0  0  0
  7 19  1  0  0  0  0
 19 20  1  0  0  0  0
 20 21  1  0  0  0  0
 20 22  1  0  0  0  0
 22 23  1  0  0  0  0
 23 24  1  0  0  0  0
 22 25  2  0  0  0  0
 25 26  1  0  0  0  0
  7 26  1  0  0  0  0
 27 26  1  4  0  0  0
 27 28  2  0  0  0  0
 28 29  1  0  0  0  0
 29 30  1  0  0  0  0
 30 31  1  0  0  0  0
 30 32  1  0  0  0  0
 32 33  1  0  0  0  0
  3 33  1  0  0  0  0
 33 34  1  0  0  0  0
 33 35  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0318644

> <DATABASE_NAME>
NP-MRD

> <SMILES>
COC1CC(=O)C23C(C(CC4=CC=CC=C4)N=C2O)C(C)C(CO)=CC3C=CCC(C)CC1(C)O

> <INCHI_IDENTIFIER>
InChI=1S/C29H39NO5/c1-18-9-8-12-22-14-21(17-31)19(2)26-23(13-20-10-6-5-7-11-20)30-27(33)29(22,26)24(32)15-25(35-4)28(3,34)16-18/h5-8,10-12,14,18-19,22-23,25-26,31,34H,9,13,15-17H2,1-4H3,(H,30,33)

> <INCHI_KEY>
DTQYSDBDFRRYKL-UHFFFAOYSA-N

> <FORMULA>
C29H39NO5

> <MOLECULAR_WEIGHT>
481.633

> <EXACT_MASS>
481.28282336

> <JCHEM_ACCEPTOR_COUNT>
6

> <JCHEM_ATOM_COUNT>
74

> <JCHEM_AVERAGE_POLARIZABILITY>
54.12518894741783

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
3

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
0

> <JCHEM_IUPAC>
3-benzyl-1,12-dihydroxy-5-(hydroxymethyl)-13-methoxy-4,10,12-trimethyl-3H,4H,6aH,9H,10H,11H,12H,13H,14H,15H,15bH-cycloundeca[e]isoindol-15-one

> <JCHEM_LOGP>
2.7484034533788604

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
4

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA>
13.985787445171539

> <JCHEM_PKA_STRONGEST_ACIDIC>
2.825662299029282

> <JCHEM_PKA_STRONGEST_BASIC>
5.49449583029092

> <JCHEM_POLAR_SURFACE_AREA>
99.35000000000001

> <JCHEM_REFRACTIVITY>
138.0644

> <JCHEM_ROTATABLE_BOND_COUNT>
4

> <JCHEM_RULE_OF_FIVE>
1

> <JCHEM_TRADITIONAL_IUPAC>
3-benzyl-1,12-dihydroxy-5-(hydroxymethyl)-13-methoxy-4,10,12-trimethyl-3H,4H,6aH,9H,10H,11H,13H,14H,15bH-cycloundeca[e]isoindol-15-one

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 11-SEP-22   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   11-SEP-22         0                                  
HETATM    1  C   UNK     0       4.704  -3.483   0.000  0.00  0.00           C+0
HETATM    2  O   UNK     0       5.474  -2.149   0.000  0.00  0.00           O+0
HETATM    3  C   UNK     0       4.704  -0.816   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0       3.164  -0.816   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0       2.258   0.606   0.000  0.00  0.00           C+0
HETATM    6  O   UNK     0       3.201   1.823   0.000  0.00  0.00           O+0
HETATM    7  C   UNK     0       0.794   1.082   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0       1.938   0.051   0.000  0.00  0.00           C+0
HETATM    9  O   UNK     0       3.445   0.371   0.000  0.00  0.00           O+0
HETATM   10  N   UNK     0       1.312  -1.356   0.000  0.00  0.00           N+0
HETATM   11  C   UNK     0      -0.220  -1.195   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0      -1.250  -2.339   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0      -0.774  -3.804   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0       0.732  -4.124   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0       1.208  -5.588   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0       0.177  -6.733   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0      -1.329  -6.413   0.000  0.00  0.00           C+0
HETATM   18  C   UNK     0      -1.805  -4.948   0.000  0.00  0.00           C+0
HETATM   19  C   UNK     0      -0.540   0.312   0.000  0.00  0.00           C+0
HETATM   20  C   UNK     0      -1.874   1.082   0.000  0.00  0.00           C+0
HETATM   21  C   UNK     0      -3.207   0.312   0.000  0.00  0.00           C+0
HETATM   22  C   UNK     0      -1.874   2.622   0.000  0.00  0.00           C+0
HETATM   23  C   UNK     0      -3.207   3.392   0.000  0.00  0.00           C+0
HETATM   24  O   UNK     0      -3.207   4.932   0.000  0.00  0.00           O+0
HETATM   25  C   UNK     0      -0.540   3.392   0.000  0.00  0.00           C+0
HETATM   26  C   UNK     0       0.794   2.622   0.000  0.00  0.00           C+0
HETATM   27  C   UNK     0       2.258   3.098   0.000  0.00  0.00           C+0
HETATM   28  C   UNK     0       3.164   4.519   0.000  0.00  0.00           C+0
HETATM   29  C   UNK     0       4.704   4.519   0.000  0.00  0.00           C+0
HETATM   30  C   UNK     0       5.474   3.185   0.000  0.00  0.00           C+0
HETATM   31  C   UNK     0       7.014   3.185   0.000  0.00  0.00           C+0
HETATM   32  C   UNK     0       4.704   1.852   0.000  0.00  0.00           C+0
HETATM   33  C   UNK     0       5.474   0.518   0.000  0.00  0.00           C+0
HETATM   34  C   UNK     0       6.833   1.241   0.000  0.00  0.00           C+0
HETATM   35  O   UNK     0       6.833  -0.205   0.000  0.00  0.00           O+0
CONECT    1    2                                                            
CONECT    2    1    3                                                       
CONECT    3    2    4   33                                                  
CONECT    4    3    5                                                       
CONECT    5    4    6    7                                                  
CONECT    6    5                                                            
CONECT    7    5    8   19   26                                             
CONECT    8    7    9   10                                                  
CONECT    9    8                                                            
CONECT   10    8   11                                                       
CONECT   11   10   12   19                                                  
CONECT   12   11   13                                                       
CONECT   13   12   14   18                                                  
CONECT   14   13   15                                                       
CONECT   15   14   16                                                       
CONECT   16   15   17                                                       
CONECT   17   16   18                                                       
CONECT   18   17   13                                                       
CONECT   19   11    7   20                                                  
CONECT   20   19   21   22                                                  
CONECT   21   20                                                            
CONECT   22   20   23   25                                                  
CONECT   23   22   24                                                       
CONECT   24   23                                                            
CONECT   25   22   26                                                       
CONECT   26   25    7   27                                                  
CONECT   27   26   28                                                       
CONECT   28   27   29                                                       
CONECT   29   28   30                                                       
CONECT   30   29   31   32                                                  
CONECT   31   30                                                            
CONECT   32   30   33                                                       
CONECT   33   32    3   34   35                                             
CONECT   34   33                                                            
CONECT   35   33                                                            
MASTER        0    0    0    0    0    0    0    0   35    0   76    0
END

View in JSmol

Synonyms

Not Available

Chemical Formula

C₂₉H₃₉NO₅

Average Mass

481.6330 Da

Monoisotopic Mass

481.28282 Da

IUPAC Name

Not Available

Traditional Name

Not Available

CAS Registry Number

Not Available

SMILES

COC1CC(=O)C23C(C(CC4=CC=CC=C4)N=C2O)C(C)C(CO)=CC3C=CCC(C)CC1(C)O

InChI Identifier

InChI=1S/C29H39NO5/c1-18-9-8-12-22-14-21(17-31)19(2)26-23(13-20-10-6-5-7-11-20)30-27(33)29(22,26)24(32)15-25(35-4)28(3,34)16-18/h5-8,10-12,14,18-19,22-23,25-26,31,34H,9,13,15-17H2,1-4H3,(H,30,33)

InChI Key

DTQYSDBDFRRYKL-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

Not Available

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as cytochalasans. These are fungal metabolites structurally characterized by the presence of an isoindolone nucleus fused to a macrocyclic ring, which can either a lactone, as in cytochalasin B, a carbonate, as in cytochalasin E, or a carbocycle, as in cytochalasin D, H, and K.

Kingdom

Organic compounds

Super Class

Alkaloids and derivatives

Class

Cytochalasans

Sub Class

Not Available

Direct Parent

Cytochalasans

Alternative Parents

Substituents

Carbocyclic cytochalasan skeleton
Cytochalasan
Isoindolone
Isoindoline
Isoindole
Isoindole or derivatives
Monocyclic benzene moiety
Benzenoid
2-pyrrolidone
Pyrrolidone
Tertiary alcohol
Pyrrolidine
Carboxamide group
Secondary carboxylic acid amide
Ketone
Lactam
Carboxylic acid derivative
Dialkyl ether
Ether
Azacycle
Organoheterocyclic compound
Hydrocarbon derivative
Organic nitrogen compound
Organic oxide
Organopnictogen compound
Alcohol
Carbonyl group
Organic oxygen compound
Primary alcohol
Organooxygen compound
Organonitrogen 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

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

163030288

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

LOTUS database [Link]

Showing NP-Card for 3-benzyl-1,12-dihydroxy-5-(hydroxymethyl)-13-methoxy-4,10,12-trimethyl-3h,3ah,4h,6ah,9h,10h,11h,13h,14h-cycloundeca[d]isoindol-15-one (NP0318644)

MOL for NP0318644 (3-benzyl-1,12-dihydroxy-5-(hydroxymethyl)-13-methoxy-4,10,12-trimethyl-3h,3ah,4h,6ah,9h,10h,11h,13h,14h-cycloundeca[d]isoindol-15-one)

3D MOL for NP0318644 (3-benzyl-1,12-dihydroxy-5-(hydroxymethyl)-13-methoxy-4,10,12-trimethyl-3h,3ah,4h,6ah,9h,10h,11h,13h,14h-cycloundeca[d]isoindol-15-one)

3D SDF for NP0318644 (3-benzyl-1,12-dihydroxy-5-(hydroxymethyl)-13-methoxy-4,10,12-trimethyl-3h,3ah,4h,6ah,9h,10h,11h,13h,14h-cycloundeca[d]isoindol-15-one)

3D-SDF for NP0318644 (3-benzyl-1,12-dihydroxy-5-(hydroxymethyl)-13-methoxy-4,10,12-trimethyl-3h,3ah,4h,6ah,9h,10h,11h,13h,14h-cycloundeca[d]isoindol-15-one)

PDB for NP0318644 (3-benzyl-1,12-dihydroxy-5-(hydroxymethyl)-13-methoxy-4,10,12-trimethyl-3h,3ah,4h,6ah,9h,10h,11h,13h,14h-cycloundeca[d]isoindol-15-one)

3D PDB for NP0318644 (3-benzyl-1,12-dihydroxy-5-(hydroxymethyl)-13-methoxy-4,10,12-trimethyl-3h,3ah,4h,6ah,9h,10h,11h,13h,14h-cycloundeca[d]isoindol-15-one)

SMILES for NP0318644 (3-benzyl-1,12-dihydroxy-5-(hydroxymethyl)-13-methoxy-4,10,12-trimethyl-3h,3ah,4h,6ah,9h,10h,11h,13h,14h-cycloundeca[d]isoindol-15-one)

INCHI for NP0318644 (3-benzyl-1,12-dihydroxy-5-(hydroxymethyl)-13-methoxy-4,10,12-trimethyl-3h,3ah,4h,6ah,9h,10h,11h,13h,14h-cycloundeca[d]isoindol-15-one)

Structure for NP0318644 (3-benzyl-1,12-dihydroxy-5-(hydroxymethyl)-13-methoxy-4,10,12-trimethyl-3h,3ah,4h,6ah,9h,10h,11h,13h,14h-cycloundeca[d]isoindol-15-one)

3D Structure for NP0318644 (3-benzyl-1,12-dihydroxy-5-(hydroxymethyl)-13-methoxy-4,10,12-trimethyl-3h,3ah,4h,6ah,9h,10h,11h,13h,14h-cycloundeca[d]isoindol-15-one)