NP-MRD: Showing NP-Card for [(2-{[5-(4-bromobuta-1,3-dien-1-yl)-1-hydroxy-2,7,10,10-tetramethyl-3,9-dioxo-4,15-dioxabicyclo[9.3.1]pentadec-7-en-13-yl]oxy}-3,5-dimethoxy-6-methyloxan-4-yl)oxy]methanimidic acid (NP0188145)

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Record Information

Version

2.0

Created at

2022-09-04 04:25:28 UTC

Updated at

2022-09-04 04:25:28 UTC

NP-MRD ID

NP0188145

Secondary Accession Numbers

None

Natural Product Identification

Common Name

[(2-{[5-(4-bromobuta-1,3-dien-1-yl)-1-hydroxy-2,7,10,10-tetramethyl-3,9-dioxo-4,15-dioxabicyclo[9.3.1]pentadec-7-en-13-yl]oxy}-3,5-dimethoxy-6-methyloxan-4-yl)oxy]methanimidic acid

Description

[(2-{[5-(4-Bromobuta-1,3-dien-1-yl)-1-hydroxy-2,7,10,10-tetramethyl-3,9-dioxo-4,15-dioxabicyclo[9.3.1]Pentadec-7-en-13-yl]oxy}-3,5-dimethoxy-6-methyloxan-4-yl)oxy]methanimidic acid belongs to the class of organic compounds known as o-glycosyl compounds. These are glycoside in which a sugar group is bonded through one carbon to another group via a O-glycosidic bond. [(2-{[5-(4-bromobuta-1,3-dien-1-yl)-1-hydroxy-2,7,10,10-tetramethyl-3,9-dioxo-4,15-dioxabicyclo[9.3.1]pentadec-7-en-13-yl]oxy}-3,5-dimethoxy-6-methyloxan-4-yl)oxy]methanimidic acid is found in Dolabella auricularia. Based on a literature review very few articles have been published on [(2-{[5-(4-bromobuta-1,3-dien-1-yl)-1-hydroxy-2,7,10,10-tetramethyl-3,9-dioxo-4,15-dioxabicyclo[9.3.1]Pentadec-7-en-13-yl]oxy}-3,5-dimethoxy-6-methyloxan-4-yl)oxy]methanimidic acid.

Structure

MOL 3D MOL SDF PDB SMILES InChI


  Mrv1652309042206252D          

 43 45  0  0  0  0            999 V2000
   -4.1250   -3.6829    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.3000   -3.6829    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
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   -3.3000   -2.2539    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
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M  END

     RDKit          3D

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M  END


  Mrv1652309042206252D          

 43 45  0  0  0  0            999 V2000
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   -3.3000   -3.6829    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
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   -1.6500   -0.8250    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8250   -0.8250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4125   -1.5395    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.4125   -1.5395    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.8250   -0.8250    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.4125   -0.1105    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0000    0.6039    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4125   -0.1105    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.8250    0.6039    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.4125    1.3184    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.6500    0.6039    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.0625    1.3184    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.0625   -0.1105    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.8875   -0.1105    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.3000    0.6039    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.1250    0.6039    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.5375    1.3184    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.3625    1.3184    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.7750    0.6039    0.0000 Br  0  0  0  0  0  0  0  0  0  0  0  0
    3.3000   -0.8250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8875   -1.5395    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.3000   -2.2539    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.0625   -1.5395    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.6500   -2.2539    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.0625   -2.9684    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.8250   -2.2539    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7962   -3.0784    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.1254   -2.6911    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6500   -2.2539    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8250   -2.2539    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4125   -2.9684    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0625   -2.9684    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6500   -3.6829    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0625   -4.3974    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8875   -4.3974    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6500   -5.1118    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
  3  4  1  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
 10 11  1  0  0  0  0
 11 12  1  0  0  0  0
 12 13  1  0  0  0  0
 13 14  1  0  0  0  0
 13 15  1  0  0  0  0
  9 15  1  0  0  0  0
 13 16  1  0  0  0  0
 16 17  1  0  0  0  0
 16 18  1  0  0  0  0
 18 19  2  0  0  0  0
 18 20  1  0  0  0  0
 20 21  1  0  0  0  0
 22 21  1  4  0  0  0
 22 23  2  0  0  0  0
 23 24  1  0  0  0  0
 24 25  2  0  0  0  0
 25 26  1  4  0  0  0
 21 27  1  0  0  0  0
 27 28  1  0  0  0  0
 28 29  1  0  0  0  0
 28 30  2  0  0  0  0
 30 31  1  4  0  0  0
 31 32  2  0  0  0  0
 31 33  1  0  0  0  0
 11 33  1  0  0  0  0
 33 34  1  0  0  0  0
 33 35  1  0  0  0  0
  7 36  1  0  0  0  0
 36 37  1  0  0  0  0
 37 38  1  0  0  0  0
 36 39  1  0  0  0  0
  3 39  1  0  0  0  0
 39 40  1  0  0  0  0
 40 41  1  0  0  0  0
 41 42  2  0  0  0  0
 41 43  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0188145

> <DATABASE_NAME>
NP-MRD

> <SMILES>
COC1C(C)OC(OC2CC3OC(O)(C2)C(C)C(=O)OC(CC(C)=CC(=O)C3(C)C)C=CC=CBr)C(OC)C1OC(O)=N

> <INCHI_IDENTIFIER>
InChI=1S/C30H44BrNO11/c1-16-12-19(10-8-9-11-31)40-26(34)17(2)30(36)15-20(14-22(43-30)29(4,5)21(33)13-16)41-27-25(38-7)24(42-28(32)35)23(37-6)18(3)39-27/h8-11,13,17-20,22-25,27,36H,12,14-15H2,1-7H3,(H2,32,35)

> <INCHI_KEY>
WLCFFJMAWFMKPH-UHFFFAOYSA-N

> <FORMULA>
C30H44BrNO11

> <MOLECULAR_WEIGHT>
674.582

> <EXACT_MASS>
673.209774

> <JCHEM_ACCEPTOR_COUNT>
10

> <JCHEM_ATOM_COUNT>
87

> <JCHEM_AVERAGE_POLARIZABILITY>
65.78468607361215

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
3

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
0

> <JCHEM_IUPAC>
[(2-{[5-(4-bromobuta-1,3-dien-1-yl)-1-hydroxy-2,7,10,10-tetramethyl-3,9-dioxo-4,15-dioxabicyclo[9.3.1]pentadec-7-en-13-yl]oxy}-3,5-dimethoxy-6-methyloxan-4-yl)oxy]methanimidic acid

> <JCHEM_LOGP>
2.654714017243063

> <JCHEM_MDDR_LIKE_RULE>
1

> <JCHEM_NUMBER_OF_RINGS>
3

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA>
11.550839118021516

> <JCHEM_PKA_STRONGEST_ACIDIC>
-4.70118225871077

> <JCHEM_PKA_STRONGEST_BASIC>
10.46642565437486

> <JCHEM_POLAR_SURFACE_AREA>
163.06

> <JCHEM_REFRACTIVITY>
169.71749999999997

> <JCHEM_ROTATABLE_BOND_COUNT>
8

> <JCHEM_RULE_OF_FIVE>
0

> <JCHEM_TRADITIONAL_IUPAC>
[(2-{[5-(4-bromobuta-1,3-dien-1-yl)-1-hydroxy-2,7,10,10-tetramethyl-3,9-dioxo-4,15-dioxabicyclo[9.3.1]pentadec-7-en-13-yl]oxy}-3,5-dimethoxy-6-methyloxan-4-yl)oxy]methanimidic acid

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 04-SEP-22   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   04-SEP-22         0                                  
HETATM    1  C   UNK     0      -7.700  -6.875   0.000  0.00  0.00           C+0
HETATM    2  O   UNK     0      -6.160  -6.875   0.000  0.00  0.00           O+0
HETATM    3  C   UNK     0      -5.390  -5.541   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0      -6.160  -4.207   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0      -7.700  -4.207   0.000  0.00  0.00           C+0
HETATM    6  O   UNK     0      -5.390  -2.874   0.000  0.00  0.00           O+0
HETATM    7  C   UNK     0      -3.850  -2.874   0.000  0.00  0.00           C+0
HETATM    8  O   UNK     0      -3.080  -1.540   0.000  0.00  0.00           O+0
HETATM    9  C   UNK     0      -1.540  -1.540   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0      -0.770  -2.874   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0       0.770  -2.874   0.000  0.00  0.00           C+0
HETATM   12  O   UNK     0       1.540  -1.540   0.000  0.00  0.00           O+0
HETATM   13  C   UNK     0       0.770  -0.206   0.000  0.00  0.00           C+0
HETATM   14  O   UNK     0       0.000   1.127   0.000  0.00  0.00           O+0
HETATM   15  C   UNK     0      -0.770  -0.206   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0       1.540   1.127   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0       0.770   2.461   0.000  0.00  0.00           C+0
HETATM   18  C   UNK     0       3.080   1.127   0.000  0.00  0.00           C+0
HETATM   19  O   UNK     0       3.850   2.461   0.000  0.00  0.00           O+0
HETATM   20  O   UNK     0       3.850  -0.206   0.000  0.00  0.00           O+0
HETATM   21  C   UNK     0       5.390  -0.206   0.000  0.00  0.00           C+0
HETATM   22  C   UNK     0       6.160   1.127   0.000  0.00  0.00           C+0
HETATM   23  C   UNK     0       7.700   1.127   0.000  0.00  0.00           C+0
HETATM   24  C   UNK     0       8.470   2.461   0.000  0.00  0.00           C+0
HETATM   25  C   UNK     0      10.010   2.461   0.000  0.00  0.00           C+0
HETATM   26 Br   UNK     0      10.780   1.127   0.000  0.00  0.00          Br+0
HETATM   27  C   UNK     0       6.160  -1.540   0.000  0.00  0.00           C+0
HETATM   28  C   UNK     0       5.390  -2.874   0.000  0.00  0.00           C+0
HETATM   29  C   UNK     0       6.160  -4.207   0.000  0.00  0.00           C+0
HETATM   30  C   UNK     0       3.850  -2.874   0.000  0.00  0.00           C+0
HETATM   31  C   UNK     0       3.080  -4.207   0.000  0.00  0.00           C+0
HETATM   32  O   UNK     0       3.850  -5.541   0.000  0.00  0.00           O+0
HETATM   33  C   UNK     0       1.540  -4.207   0.000  0.00  0.00           C+0
HETATM   34  C   UNK     0       1.486  -5.746   0.000  0.00  0.00           C+0
HETATM   35  C   UNK     0       0.234  -5.023   0.000  0.00  0.00           C+0
HETATM   36  C   UNK     0      -3.080  -4.207   0.000  0.00  0.00           C+0
HETATM   37  O   UNK     0      -1.540  -4.207   0.000  0.00  0.00           O+0
HETATM   38  C   UNK     0      -0.770  -5.541   0.000  0.00  0.00           C+0
HETATM   39  C   UNK     0      -3.850  -5.541   0.000  0.00  0.00           C+0
HETATM   40  O   UNK     0      -3.080  -6.875   0.000  0.00  0.00           O+0
HETATM   41  C   UNK     0      -3.850  -8.208   0.000  0.00  0.00           C+0
HETATM   42  N   UNK     0      -5.390  -8.208   0.000  0.00  0.00           N+0
HETATM   43  O   UNK     0      -3.080  -9.542   0.000  0.00  0.00           O+0
CONECT    1    2                                                            
CONECT    2    1    3                                                       
CONECT    3    2    4   39                                                  
CONECT    4    3    5    6                                                  
CONECT    5    4                                                            
CONECT    6    4    7                                                       
CONECT    7    6    8   36                                                  
CONECT    8    7    9                                                       
CONECT    9    8   10   15                                                  
CONECT   10    9   11                                                       
CONECT   11   10   12   33                                                  
CONECT   12   11   13                                                       
CONECT   13   12   14   15   16                                             
CONECT   14   13                                                            
CONECT   15   13    9                                                       
CONECT   16   13   17   18                                                  
CONECT   17   16                                                            
CONECT   18   16   19   20                                                  
CONECT   19   18                                                            
CONECT   20   18   21                                                       
CONECT   21   20   22   27                                                  
CONECT   22   21   23                                                       
CONECT   23   22   24                                                       
CONECT   24   23   25                                                       
CONECT   25   24   26                                                       
CONECT   26   25                                                            
CONECT   27   21   28                                                       
CONECT   28   27   29   30                                                  
CONECT   29   28                                                            
CONECT   30   28   31                                                       
CONECT   31   30   32   33                                                  
CONECT   32   31                                                            
CONECT   33   31   11   34   35                                             
CONECT   34   33                                                            
CONECT   35   33                                                            
CONECT   36    7   37   39                                                  
CONECT   37   36   38                                                       
CONECT   38   37                                                            
CONECT   39   36    3   40                                                  
CONECT   40   39   41                                                       
CONECT   41   40   42   43                                                  
CONECT   42   41                                                            
CONECT   43   41                                                            
MASTER        0    0    0    0    0    0    0    0   43    0   90    0
END

View in JSmol

Synonyms

Value	Source
[(2-{[5-(4-bromobuta-1,3-dien-1-yl)-1-hydroxy-2,7,10,10-tetramethyl-3,9-dioxo-4,15-dioxabicyclo[9.3.1]pentadec-7-en-13-yl]oxy}-3,5-dimethoxy-6-methyloxan-4-yl)oxy]methanimidate	Generator

Chemical Formula

C₃₀H₄₄BrNO₁₁

Average Mass

674.5820 Da

Monoisotopic Mass

673.20977 Da

IUPAC Name

[(2-{[5-(4-bromobuta-1,3-dien-1-yl)-1-hydroxy-2,7,10,10-tetramethyl-3,9-dioxo-4,15-dioxabicyclo[9.3.1]pentadec-7-en-13-yl]oxy}-3,5-dimethoxy-6-methyloxan-4-yl)oxy]methanimidic acid

Traditional Name

[(2-{[5-(4-bromobuta-1,3-dien-1-yl)-1-hydroxy-2,7,10,10-tetramethyl-3,9-dioxo-4,15-dioxabicyclo[9.3.1]pentadec-7-en-13-yl]oxy}-3,5-dimethoxy-6-methyloxan-4-yl)oxy]methanimidic acid

CAS Registry Number

Not Available

SMILES

COC1C(C)OC(OC2CC3OC(O)(C2)C(C)C(=O)OC(CC(C)=CC(=O)C3(C)C)C=CC=CBr)C(OC)C1OC(O)=N

InChI Identifier

InChI=1S/C30H44BrNO11/c1-16-12-19(10-8-9-11-31)40-26(34)17(2)30(36)15-20(14-22(43-30)29(4,5)21(33)13-16)41-27-25(38-7)24(42-28(32)35)23(37-6)18(3)39-27/h8-11,13,17-20,22-25,27,36H,12,14-15H2,1-7H3,(H2,32,35)

InChI Key

WLCFFJMAWFMKPH-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

Species Name	Source	Reference
Dolabella auricularia	LOTUS Database	35616633

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as o-glycosyl compounds. These are glycoside in which a sugar group is bonded through one carbon to another group via a O-glycosidic bond.

Kingdom

Organic compounds

Super Class

Organic oxygen compounds

Class

Organooxygen compounds

Sub Class

Carbohydrates and carbohydrate conjugates

Direct Parent

O-glycosyl compounds

Alternative Parents

Substituents

Hexose monosaccharide
O-glycosyl compound
Monosaccharide
Oxane
Carboxylic acid ester
Hemiacetal
Ketone
Lactone
Cyclic ketone
Acetal
Carboximidic acid derivative
Carboxylic acid derivative
Dialkyl ether
Ether
Oxacycle
Monocarboxylic acid or derivatives
Bromoalkene
Haloalkene
Organoheterocyclic compound
Vinyl bromide
Vinyl halide
Hydrocarbon derivative
Organic nitrogen compound
Carbonyl group
Aldehyde
Organohalogen compound
Organobromide
Organonitrogen compound
Organopnictogen compound
Organic oxide
Imine
Aliphatic heteropolycyclic compound

Molecular Framework

Aliphatic 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	2.65	ChemAxon
pKa (Strongest Acidic)	-4.7	ChemAxon
pKa (Strongest Basic)	10.47	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	10	ChemAxon
Hydrogen Donor Count	3	ChemAxon
Polar Surface Area	163.06 Å²	ChemAxon
Rotatable Bond Count	8	ChemAxon
Refractivity	169.72 m³·mol⁻¹	ChemAxon
Polarizability	65.78 Å³	ChemAxon
Number of Rings	3	ChemAxon
Bioavailability	Yes	ChemAxon
Rule of Five	No	ChemAxon
Ghose Filter	No	ChemAxon
Veber's Rule	No	ChemAxon
MDDR-like Rule	Yes	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

73836359

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

LOTUS database [Link]

Showing NP-Card for [(2-{[5-(4-bromobuta-1,3-dien-1-yl)-1-hydroxy-2,7,10,10-tetramethyl-3,9-dioxo-4,15-dioxabicyclo[9.3.1]pentadec-7-en-13-yl]oxy}-3,5-dimethoxy-6-methyloxan-4-yl)oxy]methanimidic acid (NP0188145)

MOL for NP0188145 ([(2-{[5-(4-bromobuta-1,3-dien-1-yl)-1-hydroxy-2,7,10,10-tetramethyl-3,9-dioxo-4,15-dioxabicyclo[9.3.1]pentadec-7-en-13-yl]oxy}-3,5-dimethoxy-6-methyloxan-4-yl)oxy]methanimidic acid)

3D MOL for NP0188145 ([(2-{[5-(4-bromobuta-1,3-dien-1-yl)-1-hydroxy-2,7,10,10-tetramethyl-3,9-dioxo-4,15-dioxabicyclo[9.3.1]pentadec-7-en-13-yl]oxy}-3,5-dimethoxy-6-methyloxan-4-yl)oxy]methanimidic acid)

3D SDF for NP0188145 ([(2-{[5-(4-bromobuta-1,3-dien-1-yl)-1-hydroxy-2,7,10,10-tetramethyl-3,9-dioxo-4,15-dioxabicyclo[9.3.1]pentadec-7-en-13-yl]oxy}-3,5-dimethoxy-6-methyloxan-4-yl)oxy]methanimidic acid)

3D-SDF for NP0188145 ([(2-{[5-(4-bromobuta-1,3-dien-1-yl)-1-hydroxy-2,7,10,10-tetramethyl-3,9-dioxo-4,15-dioxabicyclo[9.3.1]pentadec-7-en-13-yl]oxy}-3,5-dimethoxy-6-methyloxan-4-yl)oxy]methanimidic acid)

PDB for NP0188145 ([(2-{[5-(4-bromobuta-1,3-dien-1-yl)-1-hydroxy-2,7,10,10-tetramethyl-3,9-dioxo-4,15-dioxabicyclo[9.3.1]pentadec-7-en-13-yl]oxy}-3,5-dimethoxy-6-methyloxan-4-yl)oxy]methanimidic acid)

3D PDB for NP0188145 ([(2-{[5-(4-bromobuta-1,3-dien-1-yl)-1-hydroxy-2,7,10,10-tetramethyl-3,9-dioxo-4,15-dioxabicyclo[9.3.1]pentadec-7-en-13-yl]oxy}-3,5-dimethoxy-6-methyloxan-4-yl)oxy]methanimidic acid)

SMILES for NP0188145 ([(2-{[5-(4-bromobuta-1,3-dien-1-yl)-1-hydroxy-2,7,10,10-tetramethyl-3,9-dioxo-4,15-dioxabicyclo[9.3.1]pentadec-7-en-13-yl]oxy}-3,5-dimethoxy-6-methyloxan-4-yl)oxy]methanimidic acid)

INCHI for NP0188145 ([(2-{[5-(4-bromobuta-1,3-dien-1-yl)-1-hydroxy-2,7,10,10-tetramethyl-3,9-dioxo-4,15-dioxabicyclo[9.3.1]pentadec-7-en-13-yl]oxy}-3,5-dimethoxy-6-methyloxan-4-yl)oxy]methanimidic acid)

Structure for NP0188145 ([(2-{[5-(4-bromobuta-1,3-dien-1-yl)-1-hydroxy-2,7,10,10-tetramethyl-3,9-dioxo-4,15-dioxabicyclo[9.3.1]pentadec-7-en-13-yl]oxy}-3,5-dimethoxy-6-methyloxan-4-yl)oxy]methanimidic acid)

3D Structure for NP0188145 ([(2-{[5-(4-bromobuta-1,3-dien-1-yl)-1-hydroxy-2,7,10,10-tetramethyl-3,9-dioxo-4,15-dioxabicyclo[9.3.1]pentadec-7-en-13-yl]oxy}-3,5-dimethoxy-6-methyloxan-4-yl)oxy]methanimidic acid)