NP-MRD: Showing NP-Card for 14-hydroxy-18,19-dimethoxy-13,14-dimethyl-12-[(2-methylbut-2-enoyl)oxy]-20-oxo-3,6,8-trioxapentacyclo[9.9.1.0¹,¹⁶.0⁴,²¹.0⁵,⁹]henicosa-4(21),5(9),10,16,18-pentaen-15-yl 2-methylbut-2-enoate (NP0153283)

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Record Information

Version

2.0

Created at

2022-09-02 09:54:42 UTC

Updated at

2022-09-02 09:54:43 UTC

NP-MRD ID

NP0153283

Secondary Accession Numbers

None

Natural Product Identification

Common Name

14-hydroxy-18,19-dimethoxy-13,14-dimethyl-12-[(2-methylbut-2-enoyl)oxy]-20-oxo-3,6,8-trioxapentacyclo[9.9.1.0¹,¹⁶.0⁴,²¹.0⁵,⁹]henicosa-4(21),5(9),10,16,18-pentaen-15-yl 2-methylbut-2-enoate

Description

Kadsulignan D belongs to the class of organic compounds known as hydrolyzable tannins. These are tannins with a structure characterized by either of the following models. In model 1, the structure contains galloyl units (in some cases, shikimic acid units) that are linked to diverse polyol carbohydrate-, catechin-, or triterpenoid units. In model 2, contains at least two galloyl units C-C coupled to each other, and do not contain a glycosidically linked catechin unit. 14-hydroxy-18,19-dimethoxy-13,14-dimethyl-12-[(2-methylbut-2-enoyl)oxy]-20-oxo-3,6,8-trioxapentacyclo[9.9.1.0¹,¹⁶.0⁴,²¹.0⁵,⁹]henicosa-4(21),5(9),10,16,18-pentaen-15-yl 2-methylbut-2-enoate is found in Kadsura philippinensis. Kadsulignan D is an extremely weak basic (essentially neutral) compound (based on its pKa).

Structure

MOL 3D MOL SDF PDB SMILES InChI


  Mrv1533004161522462D          

 43 47  0  0  0  0            999 V2000
   -2.2527   -1.5933    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
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  3 42  1  0  0  0  0
 19 43  2  0  0  0  0
  9 43  1  0  0  0  0
 12 43  1  0  0  0  0
M  END

     RDKit          3D

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M  END


  Mrv1533004161522462D          

 43 47  0  0  0  0            999 V2000
   -2.2527   -1.5933    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
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    1.6939    0.5575    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4631    1.3495    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1065    1.8659    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.9811    2.6813    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.2122    2.9803    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.6245    3.1976    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.4991    4.0130    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.7302    4.3121    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.3934    2.8985    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7398    1.7464    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.8297    2.5665    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0523    1.5156    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0702    2.3404    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8536    1.7118    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4491    0.7923    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2692    0.8822    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7571    0.2169    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4249   -0.5382    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5772    0.3068    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.0651   -0.3585    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.8852   -0.2686    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.9094    1.0620    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2183    0.0003    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9520   -0.4432    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.2970   -0.1658    0.0000 C   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  2  0  0  0  0
  4  5  1  0  0  0  0
  5  6  1  0  0  0  0
  4  7  1  0  0  0  0
  7  8  2  0  0  0  0
  7  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  2  0  0  0  0
 13 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
 13 17  1  0  0  0  0
 17 18  2  0  0  0  0
 18 19  1  0  0  0  0
 19 20  1  0  0  0  0
 20 21  1  0  0  0  0
 21 22  1  0  0  0  0
 22 23  2  0  0  0  0
 22 24  1  0  0  0  0
 24 25  2  0  0  0  0
 25 26  1  4  0  0  0
 24 27  1  0  0  0  0
 20 28  1  0  0  0  0
 28 29  1  0  0  0  0
 28 30  1  0  0  0  0
 30 31  1  0  0  0  0
 30 32  1  0  0  0  0
 30 33  1  0  0  0  0
 33 34  1  0  0  0  0
 34 35  1  0  0  0  0
 35 36  2  0  0  0  0
 35 37  1  0  0  0  0
 37 38  2  0  0  0  0
 38 39  1  4  0  0  0
 37 40  1  0  0  0  0
 33 41  1  0  0  0  0
  9 41  1  0  0  0  0
 41 42  2  0  0  0  0
  3 42  1  0  0  0  0
 19 43  2  0  0  0  0
  9 43  1  0  0  0  0
 12 43  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0153283

> <DATABASE_NAME>
NP-MRD

> <SMILES>
COC1=C(OC)C(=O)C23COC4=C5OCOC5=CC(C(OC(=O)C(C)=CC)C(C)C(C)(O)C(OC(=O)C(C)=CC)C2=C1)=C34

> <INCHI_IDENTIFIER>
InChI=1S/C32H36O11/c1-9-15(3)29(34)42-23-17(5)31(6,36)28(43-30(35)16(4)10-2)19-12-20(37-7)25(38-8)27(33)32(19)13-39-26-22(32)18(23)11-21-24(26)41-14-40-21/h9-12,17,23,28,36H,13-14H2,1-8H3

> <INCHI_KEY>
CFIUOXCHUGBSDK-UHFFFAOYSA-N

> <FORMULA>
C32H36O11

> <MOLECULAR_WEIGHT>
596.629

> <EXACT_MASS>
596.225761979

> <JCHEM_ACCEPTOR_COUNT>
9

> <JCHEM_ATOM_COUNT>
79

> <JCHEM_AVERAGE_POLARIZABILITY>
61.70595220723071

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
1

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
0

> <JCHEM_IUPAC>
14-hydroxy-18,19-dimethoxy-13,14-dimethyl-15-[(2-methylbut-2-enoyl)oxy]-20-oxo-3,6,8-trioxapentacyclo[9.9.1.0¹,¹⁶.0⁴,²¹.0⁵,⁹]henicosa-4,9,11(21),16,18-pentaen-12-yl 2-methylbut-2-enoate

> <ALOGPS_LOGP>
3.47

> <JCHEM_LOGP>
3.8550680013333327

> <ALOGPS_LOGS>
-4.67

> <JCHEM_MDDR_LIKE_RULE>
1

> <JCHEM_NUMBER_OF_RINGS>
5

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA_STRONGEST_ACIDIC>
13.644332214674641

> <JCHEM_PKA_STRONGEST_BASIC>
-3.391769089301312

> <JCHEM_POLAR_SURFACE_AREA>
136.05

> <JCHEM_REFRACTIVITY>
156.51950000000005

> <JCHEM_ROTATABLE_BOND_COUNT>
8

> <JCHEM_RULE_OF_FIVE>
0

> <ALOGPS_SOLUBILITY>
1.28e-02 g/l

> <JCHEM_TRADITIONAL_IUPAC>
14-hydroxy-18,19-dimethoxy-13,14-dimethyl-15-[(2-methylbut-2-enoyl)oxy]-20-oxo-3,6,8-trioxapentacyclo[9.9.1.0¹,¹⁶.0⁴,²¹.0⁵,⁹]henicosa-4,9,11(21),16,18-pentaen-12-yl 2-methylbut-2-enoate

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 16-APR-15   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   16-APR-15         0                                  
HETATM    1  C   UNK     0      -4.205  -2.974   0.000  0.00  0.00           C+0
HETATM    2  O   UNK     0      -2.734  -3.429   0.000  0.00  0.00           O+0
HETATM    3  C   UNK     0      -1.604  -2.383   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0      -0.044  -2.678   0.000  0.00  0.00           C+0
HETATM    5  O   UNK     0       0.127  -4.208   0.000  0.00  0.00           O+0
HETATM    6  C   UNK     0      -1.112  -5.122   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0       1.657  -1.937   0.000  0.00  0.00           C+0
HETATM    8  O   UNK     0       3.123  -2.408   0.000  0.00  0.00           O+0
HETATM    9  C   UNK     0       0.943  -0.740   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0       0.895  -2.280   0.000  0.00  0.00           C+0
HETATM   11  O   UNK     0       2.345  -2.800   0.000  0.00  0.00           O+0
HETATM   12  C   UNK     0       3.220  -1.626   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0       4.760  -1.593   0.000  0.00  0.00           C+0
HETATM   14  O   UNK     0       5.815  -2.714   0.000  0.00  0.00           O+0
HETATM   15  C   UNK     0       7.208  -2.058   0.000  0.00  0.00           C+0
HETATM   16  O   UNK     0       7.013  -0.530   0.000  0.00  0.00           O+0
HETATM   17  C   UNK     0       5.500  -0.243   0.000  0.00  0.00           C+0
HETATM   18  C   UNK     0       4.702   1.074   0.000  0.00  0.00           C+0
HETATM   19  C   UNK     0       3.162   1.041   0.000  0.00  0.00           C+0
HETATM   20  C   UNK     0       2.731   2.519   0.000  0.00  0.00           C+0
HETATM   21  O   UNK     0       3.932   3.483   0.000  0.00  0.00           O+0
HETATM   22  C   UNK     0       3.698   5.005   0.000  0.00  0.00           C+0
HETATM   23  O   UNK     0       2.263   5.563   0.000  0.00  0.00           O+0
HETATM   24  C   UNK     0       4.899   5.969   0.000  0.00  0.00           C+0
HETATM   25  C   UNK     0       4.665   7.491   0.000  0.00  0.00           C+0
HETATM   26  C   UNK     0       3.230   8.049   0.000  0.00  0.00           C+0
HETATM   27  C   UNK     0       6.334   5.411   0.000  0.00  0.00           C+0
HETATM   28  C   UNK     0       1.381   3.260   0.000  0.00  0.00           C+0
HETATM   29  C   UNK     0       1.549   4.791   0.000  0.00  0.00           C+0
HETATM   30  C   UNK     0      -0.098   2.829   0.000  0.00  0.00           C+0
HETATM   31  C   UNK     0      -0.131   4.369   0.000  0.00  0.00           C+0
HETATM   32  O   UNK     0      -1.593   3.195   0.000  0.00  0.00           O+0
HETATM   33  C   UNK     0      -0.838   1.479   0.000  0.00  0.00           C+0
HETATM   34  O   UNK     0      -2.369   1.647   0.000  0.00  0.00           O+0
HETATM   35  C   UNK     0      -3.280   0.405   0.000  0.00  0.00           C+0
HETATM   36  O   UNK     0      -2.660  -1.005   0.000  0.00  0.00           O+0
HETATM   37  C   UNK     0      -4.811   0.573   0.000  0.00  0.00           C+0
HETATM   38  C   UNK     0      -5.721  -0.669   0.000  0.00  0.00           C+0
HETATM   39  C   UNK     0      -7.252  -0.501   0.000  0.00  0.00           C+0
HETATM   40  C   UNK     0      -5.431   1.982   0.000  0.00  0.00           C+0
HETATM   41  C   UNK     0      -0.408   0.001   0.000  0.00  0.00           C+0
HETATM   42  C   UNK     0      -1.777  -0.827   0.000  0.00  0.00           C+0
HETATM   43  C   UNK     0       2.421  -0.309   0.000  0.00  0.00           C+0
CONECT    1    2                                                            
CONECT    2    1    3                                                       
CONECT    3    2    4   42                                                  
CONECT    4    3    5    7                                                  
CONECT    5    4    6                                                       
CONECT    6    5                                                            
CONECT    7    4    8    9                                                  
CONECT    8    7                                                            
CONECT    9    7   10   41   43                                             
CONECT   10    9   11                                                       
CONECT   11   10   12                                                       
CONECT   12   11   13   43                                                  
CONECT   13   12   14   17                                                  
CONECT   14   13   15                                                       
CONECT   15   14   16                                                       
CONECT   16   15   17                                                       
CONECT   17   16   13   18                                                  
CONECT   18   17   19                                                       
CONECT   19   18   20   43                                                  
CONECT   20   19   21   28                                                  
CONECT   21   20   22                                                       
CONECT   22   21   23   24                                                  
CONECT   23   22                                                            
CONECT   24   22   25   27                                                  
CONECT   25   24   26                                                       
CONECT   26   25                                                            
CONECT   27   24                                                            
CONECT   28   20   29   30                                                  
CONECT   29   28                                                            
CONECT   30   28   31   32   33                                             
CONECT   31   30                                                            
CONECT   32   30                                                            
CONECT   33   30   34   41                                                  
CONECT   34   33   35                                                       
CONECT   35   34   36   37                                                  
CONECT   36   35                                                            
CONECT   37   35   38   40                                                  
CONECT   38   37   39                                                       
CONECT   39   38                                                            
CONECT   40   37                                                            
CONECT   41   33    9   42                                                  
CONECT   42   41    3                                                       
CONECT   43   19    9   12                                                  
MASTER        0    0    0    0    0    0    0    0   43    0   94    0
END

View in JSmol

Synonyms

Value	Source
14-Hydroxy-18,19-dimethoxy-13,14-dimethyl-15-[(2-methylbut-2-enoyl)oxy]-20-oxo-3,6,8-trioxapentacyclo[9.9.1.0¹,¹⁶.0⁴,²¹.0⁵,⁹]henicosa-4(21),5(9),10,16,18-pentaen-12-yl 2-methylbut-2-enoic acid	Generator

Chemical Formula

C₃₂H₃₆O₁₁

Average Mass

596.6290 Da

Monoisotopic Mass

596.22576 Da

IUPAC Name

14-hydroxy-18,19-dimethoxy-13,14-dimethyl-15-[(2-methylbut-2-enoyl)oxy]-20-oxo-3,6,8-trioxapentacyclo[9.9.1.0¹,¹⁶.0⁴,²¹.0⁵,⁹]henicosa-4,9,11(21),16,18-pentaen-12-yl 2-methylbut-2-enoate

Traditional Name

14-hydroxy-18,19-dimethoxy-13,14-dimethyl-15-[(2-methylbut-2-enoyl)oxy]-20-oxo-3,6,8-trioxapentacyclo[9.9.1.0¹,¹⁶.0⁴,²¹.0⁵,⁹]henicosa-4,9,11(21),16,18-pentaen-12-yl 2-methylbut-2-enoate

CAS Registry Number

Not Available

SMILES

COC1=C(OC)C(=O)C23COC4=C5OCOC5=CC(C(OC(=O)C(C)=CC)C(C)C(C)(O)C(OC(=O)C(C)=CC)C2=C1)=C34

InChI Identifier

InChI=1S/C32H36O11/c1-9-15(3)29(34)42-23-17(5)31(6,36)28(43-30(35)16(4)10-2)19-12-20(37-7)25(38-8)27(33)32(19)13-39-26-22(32)18(23)11-21-24(26)41-14-40-21/h9-12,17,23,28,36H,13-14H2,1-8H3

InChI Key

CFIUOXCHUGBSDK-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
Kadsura philippinensis	LOTUS Database	35616633

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as hydrolyzable tannins. These are tannins with a structure characterized by either of the following models. In model 1, the structure contains galloyl units (in some cases, shikimic acid units) that are linked to diverse polyol carbohydrate-, catechin-, or triterpenoid units. In model 2, contains at least two galloyl units C-C coupled to each other, and do not contain a glycosidically linked catechin unit.

Kingdom

Organic compounds

Super Class

Phenylpropanoids and polyketides

Class

Tannins

Sub Class

Hydrolyzable tannins

Direct Parent

Hydrolyzable tannins

Alternative Parents

Substituents

Hydrolyzable tannin
Benzodioxole
Coumaran
Alkyl aryl ether
Fatty acid ester
Dicarboxylic acid or derivatives
Fatty acyl
Benzenoid
Vinylogous ester
Alpha,beta-unsaturated carboxylic ester
Enoate ester
Tertiary alcohol
Carboxylic acid ester
Ketone
Acetal
Carboxylic acid derivative
Oxacycle
Ether
Organoheterocyclic compound
Alcohol
Carbonyl group
Hydrocarbon derivative
Organic oxygen compound
Organic oxide
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	3.47	ALOGPS
logP	3.86	ChemAxon
logS	-4.7	ALOGPS
pKa (Strongest Acidic)	13.64	ChemAxon
pKa (Strongest Basic)	-3.4	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	9	ChemAxon
Hydrogen Donor Count	1	ChemAxon
Polar Surface Area	136.05 Å²	ChemAxon
Rotatable Bond Count	8	ChemAxon
Refractivity	156.52 m³·mol⁻¹	ChemAxon
Polarizability	61.71 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	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

138112821

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

LOTUS database [Link]

Showing NP-Card for 14-hydroxy-18,19-dimethoxy-13,14-dimethyl-12-[(2-methylbut-2-enoyl)oxy]-20-oxo-3,6,8-trioxapentacyclo[9.9.1.0¹,¹⁶.0⁴,²¹.0⁵,⁹]henicosa-4(21),5(9),10,16,18-pentaen-15-yl 2-methylbut-2-enoate (NP0153283)

MOL for NP0153283 (14-hydroxy-18,19-dimethoxy-13,14-dimethyl-12-[(2-methylbut-2-enoyl)oxy]-20-oxo-3,6,8-trioxapentacyclo[9.9.1.0¹,¹⁶.0⁴,²¹.0⁵,⁹]henicosa-4(21),5(9),10,16,18-pentaen-15-yl 2-methylbut-2-enoate)

3D MOL for NP0153283 (14-hydroxy-18,19-dimethoxy-13,14-dimethyl-12-[(2-methylbut-2-enoyl)oxy]-20-oxo-3,6,8-trioxapentacyclo[9.9.1.0¹,¹⁶.0⁴,²¹.0⁵,⁹]henicosa-4(21),5(9),10,16,18-pentaen-15-yl 2-methylbut-2-enoate)

3D SDF for NP0153283 (14-hydroxy-18,19-dimethoxy-13,14-dimethyl-12-[(2-methylbut-2-enoyl)oxy]-20-oxo-3,6,8-trioxapentacyclo[9.9.1.0¹,¹⁶.0⁴,²¹.0⁵,⁹]henicosa-4(21),5(9),10,16,18-pentaen-15-yl 2-methylbut-2-enoate)

3D-SDF for NP0153283 (14-hydroxy-18,19-dimethoxy-13,14-dimethyl-12-[(2-methylbut-2-enoyl)oxy]-20-oxo-3,6,8-trioxapentacyclo[9.9.1.0¹,¹⁶.0⁴,²¹.0⁵,⁹]henicosa-4(21),5(9),10,16,18-pentaen-15-yl 2-methylbut-2-enoate)

PDB for NP0153283 (14-hydroxy-18,19-dimethoxy-13,14-dimethyl-12-[(2-methylbut-2-enoyl)oxy]-20-oxo-3,6,8-trioxapentacyclo[9.9.1.0¹,¹⁶.0⁴,²¹.0⁵,⁹]henicosa-4(21),5(9),10,16,18-pentaen-15-yl 2-methylbut-2-enoate)

3D PDB for NP0153283 (14-hydroxy-18,19-dimethoxy-13,14-dimethyl-12-[(2-methylbut-2-enoyl)oxy]-20-oxo-3,6,8-trioxapentacyclo[9.9.1.0¹,¹⁶.0⁴,²¹.0⁵,⁹]henicosa-4(21),5(9),10,16,18-pentaen-15-yl 2-methylbut-2-enoate)

SMILES for NP0153283 (14-hydroxy-18,19-dimethoxy-13,14-dimethyl-12-[(2-methylbut-2-enoyl)oxy]-20-oxo-3,6,8-trioxapentacyclo[9.9.1.0¹,¹⁶.0⁴,²¹.0⁵,⁹]henicosa-4(21),5(9),10,16,18-pentaen-15-yl 2-methylbut-2-enoate)

INCHI for NP0153283 (14-hydroxy-18,19-dimethoxy-13,14-dimethyl-12-[(2-methylbut-2-enoyl)oxy]-20-oxo-3,6,8-trioxapentacyclo[9.9.1.0¹,¹⁶.0⁴,²¹.0⁵,⁹]henicosa-4(21),5(9),10,16,18-pentaen-15-yl 2-methylbut-2-enoate)

Structure for NP0153283 (14-hydroxy-18,19-dimethoxy-13,14-dimethyl-12-[(2-methylbut-2-enoyl)oxy]-20-oxo-3,6,8-trioxapentacyclo[9.9.1.0¹,¹⁶.0⁴,²¹.0⁵,⁹]henicosa-4(21),5(9),10,16,18-pentaen-15-yl 2-methylbut-2-enoate)

3D Structure for NP0153283 (14-hydroxy-18,19-dimethoxy-13,14-dimethyl-12-[(2-methylbut-2-enoyl)oxy]-20-oxo-3,6,8-trioxapentacyclo[9.9.1.0¹,¹⁶.0⁴,²¹.0⁵,⁹]henicosa-4(21),5(9),10,16,18-pentaen-15-yl 2-methylbut-2-enoate)