NP-MRD: Showing NP-Card for 3-benzyl-1,5,6,12-tetrahydroxy-4,5,10,12-tetramethyl-11-oxo-3h,3ah,4h,6h,6ah,9h,10h,15h-cycloundeca[d]isoindol-15-yl acetate (NP0230638)

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Record Information

Version

2.0

Created at

2022-09-06 11:09:21 UTC

Updated at

2022-09-06 11:09:22 UTC

NP-MRD ID

NP0230638

Secondary Accession Numbers

None

Natural Product Identification

Common Name

3-benzyl-1,5,6,12-tetrahydroxy-4,5,10,12-tetramethyl-11-oxo-3h,3ah,4h,6h,6ah,9h,10h,15h-cycloundeca[d]isoindol-15-yl acetate

Description

3-Benzyl-1,5,6,12-tetrahydroxy-4,5,10,12-tetramethyl-11-oxo-3H,4H,5H,6H,6aH,9H,10H,11H,12H,15H,15bH-cycloundeca[e]isoindol-15-yl acetate 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. 3-Benzyl-1,5,6,12-tetrahydroxy-4,5,10,12-tetramethyl-11-oxo-3H,4H,5H,6H,6aH,9H,10H,11H,12H,15H,15bH-cycloundeca[e]isoindol-15-yl acetate is an extremely weak basic (essentially neutral) compound (based on its pKa).

Structure

MOL 3D MOL SDF PDB SMILES InChI


  Mrv1533004241507262D          

 38 41  0  0  0  0            999 V2000
    6.5020    0.6472    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
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    2.9653    0.8320    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
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  1  2  1  0  0  0  0
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 34 37  1  0  0  0  0
  2 37  1  0  0  0  0
 37 38  2  0  0  0  0
M  END

     RDKit          3D

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M  END


  Mrv1533004241507262D          

 38 41  0  0  0  0            999 V2000
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    4.9293    2.3381    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.5840    2.8401    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.3461    2.5241    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.8286    3.2556    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.2366    2.5625    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    6.4535    1.7062    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.3317    1.5332    0.0000 O   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
  4  3  1  4  0  0  0
  4  5  2  0  0  0  0
  5  6  1  0  0  0  0
  6  7  1  0  0  0  0
  7  8  1  0  0  0  0
  7  9  1  0  0  0  0
  9 10  1  0  0  0  0
  9 11  1  0  0  0  0
  9 12  1  0  0  0  0
 12 13  1  0  0  0  0
 12 14  1  0  0  0  0
 14 15  1  0  0  0  0
 15 16  1  0  0  0  0
 16 17  1  0  0  0  0
 17 18  2  0  0  0  0
 18 19  1  0  0  0  0
 19 20  2  0  0  0  0
 20 21  1  0  0  0  0
 21 22  2  0  0  0  0
 17 22  1  0  0  0  0
 15 23  1  0  0  0  0
 23 24  1  0  0  0  0
 24 25  2  0  0  0  0
 24 26  1  0  0  0  0
  6 26  1  0  0  0  0
 14 26  1  0  0  0  0
 26 27  1  0  0  0  0
 27 28  1  0  0  0  0
 28 29  1  0  0  0  0
 29 30  2  0  0  0  0
 29 31  1  0  0  0  0
 32 27  1  4  0  0  0
 32 33  2  0  0  0  0
 33 34  1  0  0  0  0
 34 35  1  0  0  0  0
 34 36  1  0  0  0  0
 34 37  1  0  0  0  0
  2 37  1  0  0  0  0
 37 38  2  0  0  0  0
M  END
> <DATABASE_ID>
NP0230638

> <DATABASE_NAME>
NP-MRD

> <SMILES>
CC1C2C(CC3=CC=CC=C3)NC(=O)C22C(C=CCC(C)C(=O)C(C)(O)C=CC2OC(C)=O)C(O)C1(C)O

> <INCHI_IDENTIFIER>
InChI=1S/C30H39NO7/c1-17-10-9-13-21-26(34)29(5,37)18(2)24-22(16-20-11-7-6-8-12-20)31-27(35)30(21,24)23(38-19(3)32)14-15-28(4,36)25(17)33/h6-9,11-15,17-18,21-24,26,34,36-37H,10,16H2,1-5H3,(H,31,35)

> <INCHI_KEY>
KPIFCQLJNVZJNN-UHFFFAOYSA-N

> <FORMULA>
C30H39NO7

> <MOLECULAR_WEIGHT>
525.642

> <EXACT_MASS>
525.2726526

> <JCHEM_ACCEPTOR_COUNT>
6

> <JCHEM_ATOM_COUNT>
77

> <JCHEM_AVERAGE_POLARIZABILITY>
55.72084086461139

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
4

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
0

> <JCHEM_IUPAC>
3-benzyl-5,6,12-trihydroxy-4,5,10,12-tetramethyl-1,11-dioxo-1H,2H,3H,4H,5H,6H,6aH,9H,10H,11H,12H,15H,15bH-cycloundeca[e]isoindol-15-yl acetate

> <ALOGPS_LOGP>
2.35

> <JCHEM_LOGP>
2.3035863356666644

> <ALOGPS_LOGS>
-4.29

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
4

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA>
13.486635901050924

> <JCHEM_PKA_STRONGEST_ACIDIC>
12.763266565934021

> <JCHEM_PKA_STRONGEST_BASIC>
-0.354250955029337

> <JCHEM_POLAR_SURFACE_AREA>
133.16000000000003

> <JCHEM_REFRACTIVITY>
143.2734

> <JCHEM_ROTATABLE_BOND_COUNT>
4

> <JCHEM_RULE_OF_FIVE>
0

> <ALOGPS_SOLUBILITY>
2.67e-02 g/l

> <JCHEM_TRADITIONAL_IUPAC>
3-benzyl-5,6,12-trihydroxy-4,5,10,12-tetramethyl-1,11-dioxo-2H,3H,4H,6H,6aH,9H,10H,15H,15bH-cycloundeca[e]isoindol-15-yl acetate

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 24-APR-15   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   24-APR-15         0                                  
HETATM    1  C   UNK     0      12.137   1.208   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0      10.755   2.102   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0      10.474   0.588   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0       8.947   0.388   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0       8.285   1.778   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0       6.757   2.490   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0       5.535   1.553   0.000  0.00  0.00           C+0
HETATM    8  O   UNK     0       5.808  -0.032   0.000  0.00  0.00           O+0
HETATM    9  C   UNK     0       4.113   2.143   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0       2.483   2.047   0.000  0.00  0.00           C+0
HETATM   11  O   UNK     0       3.603   0.592   0.000  0.00  0.00           O+0
HETATM   12  C   UNK     0       3.912   3.670   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0       2.454   4.356   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0       5.134   4.607   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0       5.256   6.142   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0       3.979   7.141   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0       4.366   8.657   0.000  0.00  0.00           C+0
HETATM   18  C   UNK     0       3.264   9.733   0.000  0.00  0.00           C+0
HETATM   19  C   UNK     0       3.645  11.225   0.000  0.00  0.00           C+0
HETATM   20  C   UNK     0       5.128  11.641   0.000  0.00  0.00           C+0
HETATM   21  C   UNK     0       6.230  10.565   0.000  0.00  0.00           C+0
HETATM   22  C   UNK     0       5.849   9.073   0.000  0.00  0.00           C+0
HETATM   23  N   UNK     0       6.753   6.501   0.000  0.00  0.00           N+0
HETATM   24  C   UNK     0       7.125   5.245   0.000  0.00  0.00           C+0
HETATM   25  O   UNK     0       8.882   5.388   0.000  0.00  0.00           O+0
HETATM   26  C   UNK     0       6.557   4.017   0.000  0.00  0.00           C+0
HETATM   27  C   UNK     0       7.779   4.954   0.000  0.00  0.00           C+0
HETATM   28  O   UNK     0       8.262   6.837   0.000  0.00  0.00           O+0
HETATM   29  C   UNK     0       9.343   8.002   0.000  0.00  0.00           C+0
HETATM   30  O   UNK     0       8.888   9.474   0.000  0.00  0.00           O+0
HETATM   31  C   UNK     0      10.844   7.660   0.000  0.00  0.00           C+0
HETATM   32  C   UNK     0       9.201   4.364   0.000  0.00  0.00           C+0
HETATM   33  C   UNK     0      10.423   5.302   0.000  0.00  0.00           C+0
HETATM   34  C   UNK     0      11.846   4.712   0.000  0.00  0.00           C+0
HETATM   35  C   UNK     0      12.747   6.077   0.000  0.00  0.00           C+0
HETATM   36  O   UNK     0      13.508   4.783   0.000  0.00  0.00           O+0
HETATM   37  C   UNK     0      12.047   3.185   0.000  0.00  0.00           C+0
HETATM   38  O   UNK     0      13.686   2.862   0.000  0.00  0.00           O+0
CONECT    1    2                                                            
CONECT    2    1    3   37                                                  
CONECT    3    2    4                                                       
CONECT    4    3    5                                                       
CONECT    5    4    6                                                       
CONECT    6    5    7   26                                                  
CONECT    7    6    8    9                                                  
CONECT    8    7                                                            
CONECT    9    7   10   11   12                                             
CONECT   10    9                                                            
CONECT   11    9                                                            
CONECT   12    9   13   14                                                  
CONECT   13   12                                                            
CONECT   14   12   15   26                                                  
CONECT   15   14   16   23                                                  
CONECT   16   15   17                                                       
CONECT   17   16   18   22                                                  
CONECT   18   17   19                                                       
CONECT   19   18   20                                                       
CONECT   20   19   21                                                       
CONECT   21   20   22                                                       
CONECT   22   21   17                                                       
CONECT   23   15   24                                                       
CONECT   24   23   25   26                                                  
CONECT   25   24                                                            
CONECT   26   24    6   14   27                                             
CONECT   27   26   28   32                                                  
CONECT   28   27   29                                                       
CONECT   29   28   30   31                                                  
CONECT   30   29                                                            
CONECT   31   29                                                            
CONECT   32   27   33                                                       
CONECT   33   32   34                                                       
CONECT   34   33   35   36   37                                             
CONECT   35   34                                                            
CONECT   36   34                                                            
CONECT   37   34    2   38                                                  
CONECT   38   37                                                            
MASTER        0    0    0    0    0    0    0    0   38    0   82    0
END

View in JSmol

Synonyms

Value	Source
3-Benzyl-1,5,6,12-tetrahydroxy-4,5,10,12-tetramethyl-11-oxo-3H,4H,5H,6H,6ah,9H,10H,11H,12H,15H,15BH-cycloundeca[e]isoindol-15-yl acetic acid	Generator

Chemical Formula

C₃₀H₃₉NO₇

Average Mass

525.6420 Da

Monoisotopic Mass

525.27265 Da

IUPAC Name

3-benzyl-5,6,12-trihydroxy-4,5,10,12-tetramethyl-1,11-dioxo-1H,2H,3H,4H,5H,6H,6aH,9H,10H,11H,12H,15H,15bH-cycloundeca[e]isoindol-15-yl acetate

Traditional Name

3-benzyl-5,6,12-trihydroxy-4,5,10,12-tetramethyl-1,11-dioxo-2H,3H,4H,6H,6aH,9H,10H,15H,15bH-cycloundeca[e]isoindol-15-yl acetate

CAS Registry Number

Not Available

SMILES

CC1C2C(CC3=CC=CC=C3)NC(=O)C22C(C=CCC(C)C(=O)C(C)(O)C=CC2OC(C)=O)C(O)C1(C)O

InChI Identifier

InChI=1S/C30H39NO7/c1-17-10-9-13-21-26(34)29(5,37)18(2)24-22(16-20-11-7-6-8-12-20)31-27(35)30(21,24)23(38-19(3)32)14-15-28(4,36)25(17)33/h6-9,11-15,17-18,21-24,26,34,36-37H,10,16H2,1-5H3,(H,31,35)

InChI Key

KPIFCQLJNVZJNN-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
Acyloin
Monocyclic benzene moiety
Benzenoid
2-pyrrolidone
Pyrrolidone
Cyclic alcohol
Tertiary alcohol
Pyrrolidine
Carboxamide group
Carboxylic acid ester
Cyclic ketone
Secondary carboxylic acid amide
Ketone
Lactam
Secondary alcohol
Organoheterocyclic compound
Azacycle
Monocarboxylic acid or derivatives
Polyol
Carboxylic acid derivative
Organic oxygen compound
Hydrocarbon derivative
Organic oxide
Organopnictogen compound
Alcohol
Carbonyl group
Organic nitrogen compound
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	2.35	ALOGPS
logP	2.3	ChemAxon
logS	-4.3	ALOGPS
pKa (Strongest Acidic)	12.76	ChemAxon
pKa (Strongest Basic)	-0.35	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	6	ChemAxon
Hydrogen Donor Count	4	ChemAxon
Polar Surface Area	133.16 Å²	ChemAxon
Rotatable Bond Count	4	ChemAxon
Refractivity	143.27 m³·mol⁻¹	ChemAxon
Polarizability	55.72 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	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

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

2923

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-1,5,6,12-tetrahydroxy-4,5,10,12-tetramethyl-11-oxo-3h,3ah,4h,6h,6ah,9h,10h,15h-cycloundeca[d]isoindol-15-yl acetate (NP0230638)

MOL for NP0230638 (3-benzyl-1,5,6,12-tetrahydroxy-4,5,10,12-tetramethyl-11-oxo-3h,3ah,4h,6h,6ah,9h,10h,15h-cycloundeca[d]isoindol-15-yl acetate)

3D MOL for NP0230638 (3-benzyl-1,5,6,12-tetrahydroxy-4,5,10,12-tetramethyl-11-oxo-3h,3ah,4h,6h,6ah,9h,10h,15h-cycloundeca[d]isoindol-15-yl acetate)

3D SDF for NP0230638 (3-benzyl-1,5,6,12-tetrahydroxy-4,5,10,12-tetramethyl-11-oxo-3h,3ah,4h,6h,6ah,9h,10h,15h-cycloundeca[d]isoindol-15-yl acetate)

3D-SDF for NP0230638 (3-benzyl-1,5,6,12-tetrahydroxy-4,5,10,12-tetramethyl-11-oxo-3h,3ah,4h,6h,6ah,9h,10h,15h-cycloundeca[d]isoindol-15-yl acetate)

PDB for NP0230638 (3-benzyl-1,5,6,12-tetrahydroxy-4,5,10,12-tetramethyl-11-oxo-3h,3ah,4h,6h,6ah,9h,10h,15h-cycloundeca[d]isoindol-15-yl acetate)

3D PDB for NP0230638 (3-benzyl-1,5,6,12-tetrahydroxy-4,5,10,12-tetramethyl-11-oxo-3h,3ah,4h,6h,6ah,9h,10h,15h-cycloundeca[d]isoindol-15-yl acetate)

SMILES for NP0230638 (3-benzyl-1,5,6,12-tetrahydroxy-4,5,10,12-tetramethyl-11-oxo-3h,3ah,4h,6h,6ah,9h,10h,15h-cycloundeca[d]isoindol-15-yl acetate)

INCHI for NP0230638 (3-benzyl-1,5,6,12-tetrahydroxy-4,5,10,12-tetramethyl-11-oxo-3h,3ah,4h,6h,6ah,9h,10h,15h-cycloundeca[d]isoindol-15-yl acetate)

Structure for NP0230638 (3-benzyl-1,5,6,12-tetrahydroxy-4,5,10,12-tetramethyl-11-oxo-3h,3ah,4h,6h,6ah,9h,10h,15h-cycloundeca[d]isoindol-15-yl acetate)

3D Structure for NP0230638 (3-benzyl-1,5,6,12-tetrahydroxy-4,5,10,12-tetramethyl-11-oxo-3h,3ah,4h,6h,6ah,9h,10h,15h-cycloundeca[d]isoindol-15-yl acetate)