NP-MRD: Showing NP-Card for 3,12-dibenzyl-5,14,17-trihydroxy-15-methyl-1,4,10,13,16-pentaazatricyclo[16.3.0.0⁶,¹⁰]henicosa-4,13,16-triene-2,11-dione (NP0228431)

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Record Information

Version

2.0

Created at

2022-09-06 08:05:15 UTC

Updated at

2022-09-06 08:05:15 UTC

NP-MRD ID

NP0228431

Secondary Accession Numbers

None

Natural Product Identification

Common Name

3,12-dibenzyl-5,14,17-trihydroxy-15-methyl-1,4,10,13,16-pentaazatricyclo[16.3.0.0⁶,¹⁰]henicosa-4,13,16-triene-2,11-dione

Description

3,12-Dibenzyl-5,14,17-trihydroxy-15-methyl-1,4,10,13,16-pentaazatricyclo[16.3.0.0⁶,¹⁰]Henicosa-4,13,16-triene-2,11-dione belongs to the class of organic compounds known as cyclic peptides. Cyclic peptides are compounds containing a cyclic moiety bearing a peptide backbone. Based on a literature review very few articles have been published on 3,12-dibenzyl-5,14,17-trihydroxy-15-methyl-1,4,10,13,16-pentaazatricyclo[16.3.0.0⁶,¹⁰]Henicosa-4,13,16-triene-2,11-dione.

Structure

MOL 3D MOL SDF PDB SMILES InChI


  Mrv1652309062210052D          

 41 45  0  0  0  0            999 V2000
    6.9342   -2.8816    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
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 40 41  1  0  0  0  0
M  END

     RDKit          3D

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M  END


  Mrv1652309062210052D          

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    3.8423   -0.4284    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.5707   -0.0411    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    4.0627   -0.6912    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.2458   -0.5763    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.3717   -1.4561    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.8637   -2.1062    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.0468   -1.9913    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.5388   -2.6413    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.7218   -2.5264    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4128   -1.7615    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.9208   -1.1114    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.7378   -1.2263    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.1887   -1.5710    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    5.6499   -2.2551    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.2882   -2.9965    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0  0  0  0
  3  2  1  4  0  0  0
  3  4  2  0  0  0  0
  4  5  1  0  0  0  0
  4  6  1  0  0  0  0
  6  7  1  0  0  0  0
  7  8  1  0  0  0  0
  8  9  1  0  0  0  0
  9 10  1  0  0  0  0
  6 10  1  0  0  0  0
 10 11  1  0  0  0  0
 11 12  2  0  0  0  0
 11 13  1  0  0  0  0
 13 14  1  0  0  0  0
 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
 18 19  1  0  0  0  0
 19 20  2  0  0  0  0
 15 20  1  0  0  0  0
 21 13  1  4  0  0  0
 21 22  2  0  0  0  0
 22 23  1  0  0  0  0
 22 24  1  0  0  0  0
 24 25  1  0  0  0  0
 25 26  1  0  0  0  0
 26 27  1  0  0  0  0
 27 28  1  0  0  0  0
 24 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
 31 32  1  0  0  0  0
 32 33  1  0  0  0  0
 33 34  2  0  0  0  0
 34 35  1  0  0  0  0
 35 36  2  0  0  0  0
 36 37  1  0  0  0  0
 37 38  2  0  0  0  0
 33 38  1  0  0  0  0
 39 31  1  4  0  0  0
 39 40  2  0  0  0  0
  2 40  1  0  0  0  0
 40 41  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0228431

> <DATABASE_NAME>
NP-MRD

> <SMILES>
CC1N=C(O)C2CCCN2C(=O)C(CC2=CC=CC=C2)N=C(O)C2CCCN2C(=O)C(CC2=CC=CC=C2)N=C1O

> <INCHI_IDENTIFIER>
InChI=1S/C31H37N5O5/c1-20-27(37)33-23(18-21-10-4-2-5-11-21)30(40)36-17-9-15-26(36)29(39)34-24(19-22-12-6-3-7-13-22)31(41)35-16-8-14-25(35)28(38)32-20/h2-7,10-13,20,23-26H,8-9,14-19H2,1H3,(H,32,38)(H,33,37)(H,34,39)

> <INCHI_KEY>
WEORCYBDFCLEEX-UHFFFAOYSA-N

> <FORMULA>
C31H37N5O5

> <MOLECULAR_WEIGHT>
559.667

> <EXACT_MASS>
559.279469311

> <JCHEM_ACCEPTOR_COUNT>
8

> <JCHEM_ATOM_COUNT>
78

> <JCHEM_AVERAGE_POLARIZABILITY>
59.062977906566466

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
3

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
0

> <JCHEM_IUPAC>
3,12-dibenzyl-5,14,17-trihydroxy-15-methyl-1,4,10,13,16-pentaazatricyclo[16.3.0.0^{6,10}]henicosa-4,13,16-triene-2,11-dione

> <JCHEM_LOGP>
1.2092736350514774

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
5

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA>
3.3657769940003077

> <JCHEM_PKA_STRONGEST_ACIDIC>
1.8766447536466928

> <JCHEM_PKA_STRONGEST_BASIC>
7.146235899964151

> <JCHEM_POLAR_SURFACE_AREA>
138.39000000000001

> <JCHEM_REFRACTIVITY>
152.66829999999996

> <JCHEM_ROTATABLE_BOND_COUNT>
4

> <JCHEM_RULE_OF_FIVE>
0

> <JCHEM_TRADITIONAL_IUPAC>
3,12-dibenzyl-5,14,17-trihydroxy-15-methyl-1,4,10,13,16-pentaazatricyclo[16.3.0.0^{6,10}]henicosa-4,13,16-triene-2,11-dione

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 06-SEP-22   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   06-SEP-22         0                                  
HETATM    1  C   UNK     0      12.944  -5.379   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0      12.083  -4.102   0.000  0.00  0.00           C+0
HETATM    3  N   UNK     0      12.758  -2.718   0.000  0.00  0.00           N+0
HETATM    4  C   UNK     0      14.238  -2.294   0.000  0.00  0.00           C+0
HETATM    5  O   UNK     0      15.346  -3.364   0.000  0.00  0.00           O+0
HETATM    6  C   UNK     0      14.611  -0.800   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0      15.971  -0.077   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0      15.704   1.440   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0      14.179   1.654   0.000  0.00  0.00           C+0
HETATM   10  N   UNK     0      13.503   0.270   0.000  0.00  0.00           N+0
HETATM   11  C   UNK     0      13.557   1.809   0.000  0.00  0.00           C+0
HETATM   12  O   UNK     0      14.917   2.532   0.000  0.00  0.00           O+0
HETATM   13  C   UNK     0      12.252   2.626   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0      12.305   4.165   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0      13.665   4.887   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0      13.719   6.427   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0      15.079   7.149   0.000  0.00  0.00           C+0
HETATM   18  C   UNK     0      16.385   6.333   0.000  0.00  0.00           C+0
HETATM   19  C   UNK     0      16.331   4.794   0.000  0.00  0.00           C+0
HETATM   20  C   UNK     0      14.971   4.071   0.000  0.00  0.00           C+0
HETATM   21  N   UNK     0      10.892   1.903   0.000  0.00  0.00           N+0
HETATM   22  C   UNK     0       9.445   2.430   0.000  0.00  0.00           C+0
HETATM   23  O   UNK     0       9.177   3.946   0.000  0.00  0.00           O+0
HETATM   24  C   UNK     0       8.265   1.440   0.000  0.00  0.00           C+0
HETATM   25  C   UNK     0       6.740   1.654   0.000  0.00  0.00           C+0
HETATM   26  C   UNK     0       6.065   0.270   0.000  0.00  0.00           C+0
HETATM   27  C   UNK     0       7.172  -0.800   0.000  0.00  0.00           C+0
HETATM   28  N   UNK     0       8.532  -0.077   0.000  0.00  0.00           N+0
HETATM   29  C   UNK     0       7.584  -1.290   0.000  0.00  0.00           C+0
HETATM   30  O   UNK     0       6.059  -1.076   0.000  0.00  0.00           O+0
HETATM   31  C   UNK     0       8.161  -2.718   0.000  0.00  0.00           C+0
HETATM   32  C   UNK     0       7.212  -3.932   0.000  0.00  0.00           C+0
HETATM   33  C   UNK     0       5.687  -3.717   0.000  0.00  0.00           C+0
HETATM   34  C   UNK     0       4.739  -4.930   0.000  0.00  0.00           C+0
HETATM   35  C   UNK     0       3.214  -4.716   0.000  0.00  0.00           C+0
HETATM   36  C   UNK     0       2.637  -3.288   0.000  0.00  0.00           C+0
HETATM   37  C   UNK     0       3.586  -2.075   0.000  0.00  0.00           C+0
HETATM   38  C   UNK     0       5.111  -2.289   0.000  0.00  0.00           C+0
HETATM   39  N   UNK     0       9.686  -2.933   0.000  0.00  0.00           N+0
HETATM   40  C   UNK     0      10.547  -4.209   0.000  0.00  0.00           C+0
HETATM   41  O   UNK     0       9.871  -5.594   0.000  0.00  0.00           O+0
CONECT    1    2                                                            
CONECT    2    1    3   40                                                  
CONECT    3    2    4                                                       
CONECT    4    3    5    6                                                  
CONECT    5    4                                                            
CONECT    6    4    7   10                                                  
CONECT    7    6    8                                                       
CONECT    8    7    9                                                       
CONECT    9    8   10                                                       
CONECT   10    9    6   11                                                  
CONECT   11   10   12   13                                                  
CONECT   12   11                                                            
CONECT   13   11   14   21                                                  
CONECT   14   13   15                                                       
CONECT   15   14   16   20                                                  
CONECT   16   15   17                                                       
CONECT   17   16   18                                                       
CONECT   18   17   19                                                       
CONECT   19   18   20                                                       
CONECT   20   19   15                                                       
CONECT   21   13   22                                                       
CONECT   22   21   23   24                                                  
CONECT   23   22                                                            
CONECT   24   22   25   28                                                  
CONECT   25   24   26                                                       
CONECT   26   25   27                                                       
CONECT   27   26   28                                                       
CONECT   28   27   24   29                                                  
CONECT   29   28   30   31                                                  
CONECT   30   29                                                            
CONECT   31   29   32   39                                                  
CONECT   32   31   33                                                       
CONECT   33   32   34   38                                                  
CONECT   34   33   35                                                       
CONECT   35   34   36                                                       
CONECT   36   35   37                                                       
CONECT   37   36   38                                                       
CONECT   38   37   33                                                       
CONECT   39   31   40                                                       
CONECT   40   39    2   41                                                  
CONECT   41   40                                                            
MASTER        0    0    0    0    0    0    0    0   41    0   90    0
END

View in JSmol

Synonyms

Not Available

Chemical Formula

C₃₁H₃₇N₅O₅

Average Mass

559.6670 Da

Monoisotopic Mass

559.27947 Da

IUPAC Name

3,12-dibenzyl-5,14,17-trihydroxy-15-methyl-1,4,10,13,16-pentaazatricyclo[16.3.0.0^{6,10}]henicosa-4,13,16-triene-2,11-dione

Traditional Name

3,12-dibenzyl-5,14,17-trihydroxy-15-methyl-1,4,10,13,16-pentaazatricyclo[16.3.0.0^{6,10}]henicosa-4,13,16-triene-2,11-dione

CAS Registry Number

Not Available

SMILES

CC1N=C(O)C2CCCN2C(=O)C(CC2=CC=CC=C2)N=C(O)C2CCCN2C(=O)C(CC2=CC=CC=C2)N=C1O

InChI Identifier

InChI=1S/C31H37N5O5/c1-20-27(37)33-23(18-21-10-4-2-5-11-21)30(40)36-17-9-15-26(36)29(39)34-24(19-22-12-6-3-7-13-22)31(41)35-16-8-14-25(35)28(38)32-20/h2-7,10-13,20,23-26H,8-9,14-19H2,1H3,(H,32,38)(H,33,37)(H,34,39)

InChI Key

WEORCYBDFCLEEX-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 cyclic peptides. Cyclic peptides are compounds containing a cyclic moiety bearing a peptide backbone.

Kingdom

Organic compounds

Super Class

Organic acids and derivatives

Class

Carboxylic acids and derivatives

Sub Class

Amino acids, peptides, and analogues

Direct Parent

Cyclic peptides

Alternative Parents

Substituents

Cyclic alpha peptide
Alpha-amino acid or derivatives
Monocyclic benzene moiety
Benzenoid
Pyrrolidine
Tertiary carboxylic acid amide
Cyclic carboximidic acid
Lactam
Carboxamide group
Organic 1,3-dipolar compound
Propargyl-type 1,3-dipolar organic compound
Polyol
Organoheterocyclic compound
Azacycle
Organic oxygen compound
Organic oxide
Organic nitrogen compound
Organooxygen compound
Organonitrogen compound
Organopnictogen compound
Carbonyl group
Hydrocarbon derivative
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	1.21	ChemAxon
pKa (Strongest Acidic)	1.88	ChemAxon
pKa (Strongest Basic)	7.15	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	8	ChemAxon
Hydrogen Donor Count	3	ChemAxon
Polar Surface Area	138.39 Å²	ChemAxon
Rotatable Bond Count	4	ChemAxon
Refractivity	152.67 m³·mol⁻¹	ChemAxon
Polarizability	59.06 Å³	ChemAxon
Number of Rings	5	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

76166833

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

LOTUS database [Link]

Showing NP-Card for 3,12-dibenzyl-5,14,17-trihydroxy-15-methyl-1,4,10,13,16-pentaazatricyclo[16.3.0.0⁶,¹⁰]henicosa-4,13,16-triene-2,11-dione (NP0228431)

MOL for NP0228431 (3,12-dibenzyl-5,14,17-trihydroxy-15-methyl-1,4,10,13,16-pentaazatricyclo[16.3.0.0⁶,¹⁰]henicosa-4,13,16-triene-2,11-dione)

3D MOL for NP0228431 (3,12-dibenzyl-5,14,17-trihydroxy-15-methyl-1,4,10,13,16-pentaazatricyclo[16.3.0.0⁶,¹⁰]henicosa-4,13,16-triene-2,11-dione)

3D SDF for NP0228431 (3,12-dibenzyl-5,14,17-trihydroxy-15-methyl-1,4,10,13,16-pentaazatricyclo[16.3.0.0⁶,¹⁰]henicosa-4,13,16-triene-2,11-dione)

3D-SDF for NP0228431 (3,12-dibenzyl-5,14,17-trihydroxy-15-methyl-1,4,10,13,16-pentaazatricyclo[16.3.0.0⁶,¹⁰]henicosa-4,13,16-triene-2,11-dione)

PDB for NP0228431 (3,12-dibenzyl-5,14,17-trihydroxy-15-methyl-1,4,10,13,16-pentaazatricyclo[16.3.0.0⁶,¹⁰]henicosa-4,13,16-triene-2,11-dione)

3D PDB for NP0228431 (3,12-dibenzyl-5,14,17-trihydroxy-15-methyl-1,4,10,13,16-pentaazatricyclo[16.3.0.0⁶,¹⁰]henicosa-4,13,16-triene-2,11-dione)

SMILES for NP0228431 (3,12-dibenzyl-5,14,17-trihydroxy-15-methyl-1,4,10,13,16-pentaazatricyclo[16.3.0.0⁶,¹⁰]henicosa-4,13,16-triene-2,11-dione)

INCHI for NP0228431 (3,12-dibenzyl-5,14,17-trihydroxy-15-methyl-1,4,10,13,16-pentaazatricyclo[16.3.0.0⁶,¹⁰]henicosa-4,13,16-triene-2,11-dione)

Structure for NP0228431 (3,12-dibenzyl-5,14,17-trihydroxy-15-methyl-1,4,10,13,16-pentaazatricyclo[16.3.0.0⁶,¹⁰]henicosa-4,13,16-triene-2,11-dione)

3D Structure for NP0228431 (3,12-dibenzyl-5,14,17-trihydroxy-15-methyl-1,4,10,13,16-pentaazatricyclo[16.3.0.0⁶,¹⁰]henicosa-4,13,16-triene-2,11-dione)