NP-MRD: Showing NP-Card for 18-benzyl-7,20-dihydroxy-6,8,15,16-tetramethyl-2,14-dioxa-19-azatetracyclo[10.8.0.0¹,¹⁷.0¹³,¹⁵]icosa-4,10,19-trien-3-one (NP0281092)

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Record Information

Version

2.0

Created at

2022-09-09 07:14:00 UTC

Updated at

2022-09-09 07:14:00 UTC

NP-MRD ID

NP0281092

Secondary Accession Numbers

None

Natural Product Identification

Common Name

18-benzyl-7,20-dihydroxy-6,8,15,16-tetramethyl-2,14-dioxa-19-azatetracyclo[10.8.0.0¹,¹⁷.0¹³,¹⁵]icosa-4,10,19-trien-3-one

Description

18-Benzyl-7,20-dihydroxy-6,8,15,16-tetramethyl-2,14-dioxa-19-azatetracyclo[10.8.0.0¹,¹⁷.0¹³,¹⁵]Icosa-4,10,19-trien-3-one belongs to the class of organic compounds known as macrolide lactams. These are cyclic polyketides containing both a cyclic amide and a cyclic ester group. Based on a literature review very few articles have been published on 18-benzyl-7,20-dihydroxy-6,8,15,16-tetramethyl-2,14-dioxa-19-azatetracyclo[10.8.0.0¹,¹⁷.0¹³,¹⁵]Icosa-4,10,19-trien-3-one.

Structure

MOL 3D MOL SDF PDB SMILES InChI


  Mrv1652309092209142D          

 34 38  0  0  0  0            999 V2000
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M  END

     RDKit          3D

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M  END


  Mrv1652309092209142D          

 34 38  0  0  0  0            999 V2000
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M  END
> <DATABASE_ID>
NP0281092

> <DATABASE_NAME>
NP-MRD

> <SMILES>
CC1C2C(CC3=CC=CC=C3)N=C(O)C22OC(=O)C=CC(C)C(O)C(C)CC=CC2C2OC12C

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

> <INCHI_KEY>
JDIDLBCBCVLVMU-UHFFFAOYSA-N

> <FORMULA>
C28H35NO5

> <MOLECULAR_WEIGHT>
465.59

> <EXACT_MASS>
465.251523231

> <JCHEM_ACCEPTOR_COUNT>
5

> <JCHEM_ATOM_COUNT>
69

> <JCHEM_AVERAGE_POLARIZABILITY>
51.42252052398817

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
2

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
0

> <JCHEM_IUPAC>
18-benzyl-7,20-dihydroxy-6,8,15,16-tetramethyl-2,14-dioxa-19-azatetracyclo[10.8.0.0^{1,17}.0^{13,15}]icosa-4,10,19-trien-3-one

> <JCHEM_LOGP>
3.276550190405064

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
5

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA>
17.79063678524875

> <JCHEM_PKA_STRONGEST_ACIDIC>
1.8948929211384469

> <JCHEM_PKA_STRONGEST_BASIC>
4.780396148257632

> <JCHEM_POLAR_SURFACE_AREA>
91.65

> <JCHEM_REFRACTIVITY>
130.52580000000006

> <JCHEM_ROTATABLE_BOND_COUNT>
2

> <JCHEM_RULE_OF_FIVE>
1

> <JCHEM_TRADITIONAL_IUPAC>
18-benzyl-7,20-dihydroxy-6,8,15,16-tetramethyl-2,14-dioxa-19-azatetracyclo[10.8.0.0^{1,17}.0^{13,15}]icosa-4,10,19-trien-3-one

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 09-SEP-22   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   09-SEP-22         0                                  
HETATM    1  C   UNK     0       2.677   0.005   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0       1.143   0.137   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0       0.489   1.531   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0       1.371   2.794   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0       2.905   2.663   0.000  0.00  0.00           C+0
HETATM    6  O   UNK     0       3.786   3.926   0.000  0.00  0.00           O+0
HETATM    7  O   UNK     0       3.596   1.054   0.000  0.00  0.00           O+0
HETATM    8  C   UNK     0       5.093   1.136   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0       3.619   1.584   0.000  0.00  0.00           C+0
HETATM   10  O   UNK     0       2.391   0.655   0.000  0.00  0.00           O+0
HETATM   11  N   UNK     0       3.590   3.124   0.000  0.00  0.00           N+0
HETATM   12  C   UNK     0       5.045   3.628   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0       5.493   5.101   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0       4.441   6.226   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0       2.941   5.877   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0       1.888   7.001   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0       2.336   8.475   0.000  0.00  0.00           C+0
HETATM   18  C   UNK     0       3.836   8.824   0.000  0.00  0.00           C+0
HETATM   19  C   UNK     0       4.888   7.699   0.000  0.00  0.00           C+0
HETATM   20  C   UNK     0       5.974   2.399   0.000  0.00  0.00           C+0
HETATM   21  C   UNK     0       7.508   2.268   0.000  0.00  0.00           C+0
HETATM   22  C   UNK     0       8.389   3.531   0.000  0.00  0.00           C+0
HETATM   23  C   UNK     0       8.161   0.873   0.000  0.00  0.00           C+0
HETATM   24  C   UNK     0       9.556   1.526   0.000  0.00  0.00           C+0
HETATM   25  O   UNK     0       8.814  -0.522   0.000  0.00  0.00           O+0
HETATM   26  C   UNK     0       7.280  -0.390   0.000  0.00  0.00           C+0
HETATM   27  C   UNK     0       5.746  -0.258   0.000  0.00  0.00           C+0
HETATM   28  C   UNK     0       4.865  -1.521   0.000  0.00  0.00           C+0
HETATM   29  C   UNK     0       3.330  -1.390   0.000  0.00  0.00           C+0
HETATM   30  C   UNK     0       2.449  -2.653   0.000  0.00  0.00           C+0
HETATM   31  C   UNK     0       0.915  -2.521   0.000  0.00  0.00           C+0
HETATM   32  C   UNK     0       0.033  -3.784   0.000  0.00  0.00           C+0
HETATM   33  C   UNK     0       0.261  -1.126   0.000  0.00  0.00           C+0
HETATM   34  O   UNK     0      -1.273  -0.995   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    7                                                  
CONECT    6    5                                                            
CONECT    7    5    8                                                       
CONECT    8    7    9   20   27                                             
CONECT    9    8   10   11                                                  
CONECT   10    9                                                            
CONECT   11    9   12                                                       
CONECT   12   11   13   20                                                  
CONECT   13   12   14                                                       
CONECT   14   13   15   19                                                  
CONECT   15   14   16                                                       
CONECT   16   15   17                                                       
CONECT   17   16   18                                                       
CONECT   18   17   19                                                       
CONECT   19   18   14                                                       
CONECT   20   12    8   21                                                  
CONECT   21   20   22   23                                                  
CONECT   22   21                                                            
CONECT   23   21   24   25   26                                             
CONECT   24   23                                                            
CONECT   25   23   26                                                       
CONECT   26   25   23   27                                                  
CONECT   27   26    8   28                                                  
CONECT   28   27   29                                                       
CONECT   29   28   30                                                       
CONECT   30   29   31                                                       
CONECT   31   30   32   33                                                  
CONECT   32   31                                                            
CONECT   33   31    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

18-benzyl-7,20-dihydroxy-6,8,15,16-tetramethyl-2,14-dioxa-19-azatetracyclo[10.8.0.0^{1,17}.0^{13,15}]icosa-4,10,19-trien-3-one

Traditional Name

18-benzyl-7,20-dihydroxy-6,8,15,16-tetramethyl-2,14-dioxa-19-azatetracyclo[10.8.0.0^{1,17}.0^{13,15}]icosa-4,10,19-trien-3-one

CAS Registry Number

Not Available

SMILES

CC1C2C(CC3=CC=CC=C3)N=C(O)C22OC(=O)C=CC(C)C(O)C(C)CC=CC2C2OC12C

InChI Identifier

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

InChI Key

JDIDLBCBCVLVMU-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 macrolide lactams. These are cyclic polyketides containing both a cyclic amide and a cyclic ester group.

Kingdom

Organic compounds

Super Class

Phenylpropanoids and polyketides

Class

Macrolide lactams

Sub Class

Not Available

Direct Parent

Macrolide lactams

Alternative Parents

Substituents

Macrolide lactam
Macrolide
Macrolactam
Isoindolone
Isoindoline
Isoindole or derivatives
Oxepane
Monocyclic benzene moiety
Pyrrolidone
2-pyrrolidone
Benzenoid
Pyrrolidine
Enoate ester
Alpha,beta-unsaturated carboxylic ester
Secondary carboxylic acid amide
Secondary alcohol
Carboxylic acid ester
Carboxamide group
Lactam
Lactone
Carboxylic acid derivative
Dialkyl ether
Oxirane
Ether
Oxacycle
Azacycle
Organoheterocyclic compound
Monocarboxylic acid or derivatives
Carbonyl group
Organic nitrogen compound
Organic oxide
Hydrocarbon derivative
Organic oxygen compound
Alcohol
Organopnictogen 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	3.28	ChemAxon
pKa (Strongest Acidic)	1.89	ChemAxon
pKa (Strongest Basic)	4.78	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	5	ChemAxon
Hydrogen Donor Count	2	ChemAxon
Polar Surface Area	91.65 Å²	ChemAxon
Rotatable Bond Count	2	ChemAxon
Refractivity	130.53 m³·mol⁻¹	ChemAxon
Polarizability	51.42 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

73814009

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

LOTUS database [Link]

Showing NP-Card for 18-benzyl-7,20-dihydroxy-6,8,15,16-tetramethyl-2,14-dioxa-19-azatetracyclo[10.8.0.0¹,¹⁷.0¹³,¹⁵]icosa-4,10,19-trien-3-one (NP0281092)

MOL for NP0281092 (18-benzyl-7,20-dihydroxy-6,8,15,16-tetramethyl-2,14-dioxa-19-azatetracyclo[10.8.0.0¹,¹⁷.0¹³,¹⁵]icosa-4,10,19-trien-3-one)

3D MOL for NP0281092 (18-benzyl-7,20-dihydroxy-6,8,15,16-tetramethyl-2,14-dioxa-19-azatetracyclo[10.8.0.0¹,¹⁷.0¹³,¹⁵]icosa-4,10,19-trien-3-one)

3D SDF for NP0281092 (18-benzyl-7,20-dihydroxy-6,8,15,16-tetramethyl-2,14-dioxa-19-azatetracyclo[10.8.0.0¹,¹⁷.0¹³,¹⁵]icosa-4,10,19-trien-3-one)

3D-SDF for NP0281092 (18-benzyl-7,20-dihydroxy-6,8,15,16-tetramethyl-2,14-dioxa-19-azatetracyclo[10.8.0.0¹,¹⁷.0¹³,¹⁵]icosa-4,10,19-trien-3-one)

PDB for NP0281092 (18-benzyl-7,20-dihydroxy-6,8,15,16-tetramethyl-2,14-dioxa-19-azatetracyclo[10.8.0.0¹,¹⁷.0¹³,¹⁵]icosa-4,10,19-trien-3-one)

3D PDB for NP0281092 (18-benzyl-7,20-dihydroxy-6,8,15,16-tetramethyl-2,14-dioxa-19-azatetracyclo[10.8.0.0¹,¹⁷.0¹³,¹⁵]icosa-4,10,19-trien-3-one)

SMILES for NP0281092 (18-benzyl-7,20-dihydroxy-6,8,15,16-tetramethyl-2,14-dioxa-19-azatetracyclo[10.8.0.0¹,¹⁷.0¹³,¹⁵]icosa-4,10,19-trien-3-one)

INCHI for NP0281092 (18-benzyl-7,20-dihydroxy-6,8,15,16-tetramethyl-2,14-dioxa-19-azatetracyclo[10.8.0.0¹,¹⁷.0¹³,¹⁵]icosa-4,10,19-trien-3-one)

Structure for NP0281092 (18-benzyl-7,20-dihydroxy-6,8,15,16-tetramethyl-2,14-dioxa-19-azatetracyclo[10.8.0.0¹,¹⁷.0¹³,¹⁵]icosa-4,10,19-trien-3-one)

3D Structure for NP0281092 (18-benzyl-7,20-dihydroxy-6,8,15,16-tetramethyl-2,14-dioxa-19-azatetracyclo[10.8.0.0¹,¹⁷.0¹³,¹⁵]icosa-4,10,19-trien-3-one)