NP-MRD: Showing NP-Card for 17-benzyl-2,5,19-trihydroxy-5,7,14,15-tetramethyl-13-oxa-18-azatetracyclo[9.8.0.0¹,¹⁶.0¹²,¹⁴]nonadeca-3,9,18-trien-6-one (NP0166693)

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Record Information

Version

2.0

Created at

2022-09-03 02:07:14 UTC

Updated at

2022-09-03 02:07:14 UTC

NP-MRD ID

NP0166693

Secondary Accession Numbers

None

Natural Product Identification

Common Name

17-benzyl-2,5,19-trihydroxy-5,7,14,15-tetramethyl-13-oxa-18-azatetracyclo[9.8.0.0¹,¹⁶.0¹²,¹⁴]nonadeca-3,9,18-trien-6-one

Description

17-Benzyl-2,5,19-trihydroxy-5,7,14,15-tetramethyl-13-oxa-18-azatetracyclo[9.8.0.0¹,¹⁶.0¹²,¹⁴]Nonadeca-3,9,18-trien-6-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 17-benzyl-2,5,19-trihydroxy-5,7,14,15-tetramethyl-13-oxa-18-azatetracyclo[9.8.0.0¹,¹⁶.0¹²,¹⁴]Nonadeca-3,9,18-trien-6-one.

Structure

MOL 3D MOL SDF PDB SMILES InChI


  Mrv1652309032204072D          

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M  END

     RDKit          3D

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M  END


  Mrv1652309032204072D          

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 30 32  1  0  0  0  0
 30 33  1  0  0  0  0
  2 33  1  0  0  0  0
 33 34  2  0  0  0  0
M  END
> <DATABASE_ID>
NP0166693

> <DATABASE_NAME>
NP-MRD

> <SMILES>
CC1C2C(CC3=CC=CC=C3)N=C(O)C22C(C=CCC(C)C(=O)C(C)(O)C=CC2O)C2OC12C

> <INCHI_IDENTIFIER>
InChI=1S/C28H35NO5/c1-16-9-8-12-19-24-27(4,34-24)17(2)22-20(15-18-10-6-5-7-11-18)29-25(32)28(19,22)21(30)13-14-26(3,33)23(16)31/h5-8,10-14,16-17,19-22,24,30,33H,9,15H2,1-4H3,(H,29,32)

> <INCHI_KEY>
RERIIFVZOREWKX-UHFFFAOYSA-N

> <FORMULA>
C28H35NO5

> <MOLECULAR_WEIGHT>
465.59

> <EXACT_MASS>
465.251523231

> <JCHEM_ACCEPTOR_COUNT>
6

> <JCHEM_ATOM_COUNT>
69

> <JCHEM_AVERAGE_POLARIZABILITY>
50.64423493998578

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
3

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
0

> <JCHEM_IUPAC>
17-benzyl-2,5,19-trihydroxy-5,7,14,15-tetramethyl-13-oxa-18-azatetracyclo[9.8.0.0^{1,16}.0^{12,14}]nonadeca-3,9,18-trien-6-one

> <ALOGPS_LOGP>
3.48

> <JCHEM_LOGP>
2.9862736254135442

> <ALOGPS_LOGS>
-4.95

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
5

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA>
12.86780275284218

> <JCHEM_PKA_STRONGEST_ACIDIC>
3.2197061407690866

> <JCHEM_PKA_STRONGEST_BASIC>
5.594756646910429

> <JCHEM_POLAR_SURFACE_AREA>
102.65

> <JCHEM_REFRACTIVITY>
131.13350000000003

> <JCHEM_ROTATABLE_BOND_COUNT>
2

> <JCHEM_RULE_OF_FIVE>
1

> <ALOGPS_SOLUBILITY>
5.22e-03 g/l

> <JCHEM_TRADITIONAL_IUPAC>
17-benzyl-2,5,19-trihydroxy-5,7,14,15-tetramethyl-13-oxa-18-azatetracyclo[9.8.0.0^{1,16}.0^{12,14}]nonadeca-3,9,18-trien-6-one

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 03-SEP-22   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   03-SEP-22         0                                  
HETATM    1  C   UNK     0       0.888   2.553   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0       1.893   1.257   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0       2.656   2.594   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0       4.164   2.281   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0       4.333   0.750   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0       5.541  -0.425   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0       7.003   0.058   0.000  0.00  0.00           C+0
HETATM    8  O   UNK     0       8.465   0.541   0.000  0.00  0.00           O+0
HETATM    9  C   UNK     0       8.152  -0.967   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0       9.766  -1.150   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0       7.839  -2.474   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0       9.048  -3.539   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0       6.377  -2.957   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0       5.758  -4.367   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0       6.632  -5.734   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0       5.771  -7.035   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0       6.458  -8.413   0.000  0.00  0.00           C+0
HETATM   18  C   UNK     0       5.607  -9.697   0.000  0.00  0.00           C+0
HETATM   19  C   UNK     0       4.070  -9.603   0.000  0.00  0.00           C+0
HETATM   20  C   UNK     0       3.383  -8.224   0.000  0.00  0.00           C+0
HETATM   21  C   UNK     0       4.234  -6.940   0.000  0.00  0.00           C+0
HETATM   22  N   UNK     0       4.225  -4.214   0.000  0.00  0.00           N+0
HETATM   23  C   UNK     0       4.287  -2.905   0.000  0.00  0.00           C+0
HETATM   24  O   UNK     0       2.585  -2.471   0.000  0.00  0.00           O+0
HETATM   25  C   UNK     0       5.228  -1.933   0.000  0.00  0.00           C+0
HETATM   26  C   UNK     0       3.765  -2.416   0.000  0.00  0.00           C+0
HETATM   27  O   UNK     0       2.716  -3.885   0.000  0.00  0.00           O+0
HETATM   28  C   UNK     0       2.616  -1.391   0.000  0.00  0.00           C+0
HETATM   29  C   UNK     0       1.154  -1.874   0.000  0.00  0.00           C+0
HETATM   30  C   UNK     0       0.004  -0.849   0.000  0.00  0.00           C+0
HETATM   31  C   UNK     0      -1.219  -1.922   0.000  0.00  0.00           C+0
HETATM   32  O   UNK     0      -1.651  -0.612   0.000  0.00  0.00           O+0
HETATM   33  C   UNK     0       0.317   0.659   0.000  0.00  0.00           C+0
HETATM   34  O   UNK     0      -0.938   1.698   0.000  0.00  0.00           O+0
CONECT    1    2                                                            
CONECT    2    1    3   33                                                  
CONECT    3    2    4                                                       
CONECT    4    3    5                                                       
CONECT    5    4    6                                                       
CONECT    6    5    7   25                                                  
CONECT    7    6    8    9                                                  
CONECT    8    7    9                                                       
CONECT    9    8    7   10   11                                             
CONECT   10    9                                                            
CONECT   11    9   12   13                                                  
CONECT   12   11                                                            
CONECT   13   11   14   25                                                  
CONECT   14   13   15   22                                                  
CONECT   15   14   16                                                       
CONECT   16   15   17   21                                                  
CONECT   17   16   18                                                       
CONECT   18   17   19                                                       
CONECT   19   18   20                                                       
CONECT   20   19   21                                                       
CONECT   21   20   16                                                       
CONECT   22   14   23                                                       
CONECT   23   22   24   25                                                  
CONECT   24   23                                                            
CONECT   25   23    6   13   26                                             
CONECT   26   25   27   28                                                  
CONECT   27   26                                                            
CONECT   28   26   29                                                       
CONECT   29   28   30                                                       
CONECT   30   29   31   32   33                                             
CONECT   31   30                                                            
CONECT   32   30                                                            
CONECT   33   30    2   34                                                  
CONECT   34   33                                                            
MASTER        0    0    0    0    0    0    0    0   34    0   76    0
END

View in JSmol

Synonyms

Not Available

Chemical Formula

C₂₈H₃₅NO₅

Average Mass

465.5900 Da

Monoisotopic Mass

465.25152 Da

IUPAC Name

17-benzyl-2,5,19-trihydroxy-5,7,14,15-tetramethyl-13-oxa-18-azatetracyclo[9.8.0.0^{1,16}.0^{12,14}]nonadeca-3,9,18-trien-6-one

Traditional Name

17-benzyl-2,5,19-trihydroxy-5,7,14,15-tetramethyl-13-oxa-18-azatetracyclo[9.8.0.0^{1,16}.0^{12,14}]nonadeca-3,9,18-trien-6-one

CAS Registry Number

Not Available

SMILES

CC1C2C(CC3=CC=CC=C3)N=C(O)C22C(C=CCC(C)C(=O)C(C)(O)C=CC2O)C2OC12C

InChI Identifier

InChI=1S/C28H35NO5/c1-16-9-8-12-19-24-27(4,34-24)17(2)22-20(15-18-10-6-5-7-11-18)29-25(32)28(19,22)21(30)13-14-26(3,33)23(16)31/h5-8,10-14,16-17,19-22,24,30,33H,9,15H2,1-4H3,(H,29,32)

InChI Key

RERIIFVZOREWKX-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
Isoindole or derivatives
Isoindoline
Oxepane
Acyloin
Pyrrolidone
2-pyrrolidone
Benzenoid
Monocyclic benzene moiety
Tertiary alcohol
Pyrrolidine
Secondary carboxylic acid amide
Secondary alcohol
Lactam
Cyclic ketone
Ketone
Carboxamide group
Carboxylic acid derivative
Dialkyl ether
Oxirane
Ether
Oxacycle
Azacycle
Organoheterocyclic compound
Alcohol
Hydrocarbon derivative
Organic oxide
Organic oxygen compound
Carbonyl group
Organopnictogen compound
Organic nitrogen compound
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
logP	3.48	ALOGPS
logP	2.99	ChemAxon
logS	-5	ALOGPS
pKa (Strongest Acidic)	3.22	ChemAxon
pKa (Strongest Basic)	5.59	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	6	ChemAxon
Hydrogen Donor Count	3	ChemAxon
Polar Surface Area	102.65 Å²	ChemAxon
Rotatable Bond Count	2	ChemAxon
Refractivity	131.13 m³·mol⁻¹	ChemAxon
Polarizability	50.64 Å³	ChemAxon
Number of Rings	5	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

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

76143921

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

LOTUS database [Link]

Showing NP-Card for 17-benzyl-2,5,19-trihydroxy-5,7,14,15-tetramethyl-13-oxa-18-azatetracyclo[9.8.0.0¹,¹⁶.0¹²,¹⁴]nonadeca-3,9,18-trien-6-one (NP0166693)

MOL for NP0166693 (17-benzyl-2,5,19-trihydroxy-5,7,14,15-tetramethyl-13-oxa-18-azatetracyclo[9.8.0.0¹,¹⁶.0¹²,¹⁴]nonadeca-3,9,18-trien-6-one)

3D MOL for NP0166693 (17-benzyl-2,5,19-trihydroxy-5,7,14,15-tetramethyl-13-oxa-18-azatetracyclo[9.8.0.0¹,¹⁶.0¹²,¹⁴]nonadeca-3,9,18-trien-6-one)

3D SDF for NP0166693 (17-benzyl-2,5,19-trihydroxy-5,7,14,15-tetramethyl-13-oxa-18-azatetracyclo[9.8.0.0¹,¹⁶.0¹²,¹⁴]nonadeca-3,9,18-trien-6-one)

3D-SDF for NP0166693 (17-benzyl-2,5,19-trihydroxy-5,7,14,15-tetramethyl-13-oxa-18-azatetracyclo[9.8.0.0¹,¹⁶.0¹²,¹⁴]nonadeca-3,9,18-trien-6-one)

PDB for NP0166693 (17-benzyl-2,5,19-trihydroxy-5,7,14,15-tetramethyl-13-oxa-18-azatetracyclo[9.8.0.0¹,¹⁶.0¹²,¹⁴]nonadeca-3,9,18-trien-6-one)

3D PDB for NP0166693 (17-benzyl-2,5,19-trihydroxy-5,7,14,15-tetramethyl-13-oxa-18-azatetracyclo[9.8.0.0¹,¹⁶.0¹²,¹⁴]nonadeca-3,9,18-trien-6-one)

SMILES for NP0166693 (17-benzyl-2,5,19-trihydroxy-5,7,14,15-tetramethyl-13-oxa-18-azatetracyclo[9.8.0.0¹,¹⁶.0¹²,¹⁴]nonadeca-3,9,18-trien-6-one)

INCHI for NP0166693 (17-benzyl-2,5,19-trihydroxy-5,7,14,15-tetramethyl-13-oxa-18-azatetracyclo[9.8.0.0¹,¹⁶.0¹²,¹⁴]nonadeca-3,9,18-trien-6-one)

Structure for NP0166693 (17-benzyl-2,5,19-trihydroxy-5,7,14,15-tetramethyl-13-oxa-18-azatetracyclo[9.8.0.0¹,¹⁶.0¹²,¹⁴]nonadeca-3,9,18-trien-6-one)

3D Structure for NP0166693 (17-benzyl-2,5,19-trihydroxy-5,7,14,15-tetramethyl-13-oxa-18-azatetracyclo[9.8.0.0¹,¹⁶.0¹²,¹⁴]nonadeca-3,9,18-trien-6-one)