NP-MRD: Showing NP-Card for (1s,12r,13r,14r)-19,20-dimethoxy-13,14-dimethyl-18-oxo-3,6,8-trioxapentacyclo[9.9.1.0¹,¹⁶.0⁴,²¹.0⁵,⁹]henicosa-4(21),5(9),10,16,19-pentaen-12-yl (2z)-2-methylbut-2-enoate (NP0223167)

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Record Information

Version

2.0

Created at

2022-09-06 01:11:21 UTC

Updated at

2022-09-06 01:11:21 UTC

NP-MRD ID

NP0223167

Secondary Accession Numbers

None

Natural Product Identification

Common Name

(1s,12r,13r,14r)-19,20-dimethoxy-13,14-dimethyl-18-oxo-3,6,8-trioxapentacyclo[9.9.1.0¹,¹⁶.0⁴,²¹.0⁵,⁹]henicosa-4(21),5(9),10,16,19-pentaen-12-yl (2z)-2-methylbut-2-enoate

Description

Interiorin belongs to the class of organic compounds known as benzodioxoles. These are organic compounds containing a benzene ring fused to either isomers of dioxole. Dioxole is a five-membered unsaturated ring of two oxygen atoms and three carbon atoms. (1s,12r,13r,14r)-19,20-dimethoxy-13,14-dimethyl-18-oxo-3,6,8-trioxapentacyclo[9.9.1.0¹,¹⁶.0⁴,²¹.0⁵,⁹]henicosa-4(21),5(9),10,16,19-pentaen-12-yl (2z)-2-methylbut-2-enoate is found in Kadsura heteroclita, Kadsura interior and Schisandra rubriflora. (1s,12r,13r,14r)-19,20-dimethoxy-13,14-dimethyl-18-oxo-3,6,8-trioxapentacyclo[9.9.1.0¹,¹⁶.0⁴,²¹.0⁵,⁹]henicosa-4(21),5(9),10,16,19-pentaen-12-yl (2z)-2-methylbut-2-enoate was first documented in 2006 (PMID: 17135051). Based on a literature review a small amount of articles have been published on Interiorin (PMID: 19023792) (PMID: 35039063).

Structure

MOL SDF PDB SMILES InChI


  Mrv1652309062203112D          

 35 39  0  0  1  0            999 V2000
    5.0676    5.0726    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.9651    5.8912    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.2049    6.2118    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.1023    7.0304    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5472    5.7137    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.7870    6.0342    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.6497    4.8951    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.9920    4.3970    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    3.2005    3.5988    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.0255    3.5936    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.4335    2.8765    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.0165    2.1646    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.1915    2.1699    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.7835    2.8869    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.9853    2.6784    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    1.9369    1.8549    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.7052    1.5543    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.2734    3.0954    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.5068    2.7052    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.4328    1.8613    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3558    1.6190    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.9856    1.1830    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.0095    0.3583    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.7356   -0.0333    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4882    1.8781    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1733    1.4185    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.1178    0.5954    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.0650    3.8937    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4820    4.6055    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    0.9839    5.2632    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.2802    4.8140    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    2.3930    5.6312    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.5646    1.5481    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.3204    1.8789    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.2394    2.6999    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0  0  0  0
  2  3  2  0  0  0  0
  3  4  1  0  0  0  0
  3  5  1  0  0  0  0
  5  6  2  0  0  0  0
  5  7  1  0  0  0  0
  8  7  1  1  0  0  0
  8  9  1  0  0  0  0
  9 10  2  0  0  0  0
 10 11  1  0  0  0  0
 11 12  2  0  0  0  0
 12 13  1  0  0  0  0
 13 14  2  0  0  0  0
  9 14  1  0  0  0  0
 15 14  1  1  0  0  0
 15 16  1  0  0  0  0
 16 17  1  0  0  0  0
 13 17  1  0  0  0  0
 15 18  1  0  0  0  0
 18 19  2  0  0  0  0
 19 20  1  0  0  0  0
 20 21  2  0  0  0  0
 20 22  1  0  0  0  0
 22 23  1  0  0  0  0
 23 24  1  0  0  0  0
 22 25  2  0  0  0  0
 15 25  1  0  0  0  0
 25 26  1  0  0  0  0
 26 27  1  0  0  0  0
 18 28  1  0  0  0  0
 28 29  1  0  0  0  0
 29 30  1  1  0  0  0
 29 31  1  0  0  0  0
  8 31  1  0  0  0  0
 31 32  1  1  0  0  0
 12 33  1  0  0  0  0
 33 34  1  0  0  0  0
 34 35  1  0  0  0  0
 11 35  1  0  0  0  0
M  END


  Mrv1652309062203112D          

 35 39  0  0  1  0            999 V2000
    5.0676    5.0726    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.9651    5.8912    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.2049    6.2118    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.1023    7.0304    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5472    5.7137    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.7870    6.0342    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.6497    4.8951    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.9920    4.3970    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    3.2005    3.5988    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.0255    3.5936    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.4335    2.8765    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.0165    2.1646    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.1915    2.1699    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.7835    2.8869    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.9853    2.6784    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    1.9369    1.8549    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.7052    1.5543    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.2734    3.0954    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.5068    2.7052    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.4328    1.8613    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3558    1.6190    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.9856    1.1830    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.0095    0.3583    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.7356   -0.0333    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4882    1.8781    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1733    1.4185    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.1178    0.5954    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.0650    3.8937    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4820    4.6055    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    0.9839    5.2632    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.2802    4.8140    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    2.3930    5.6312    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.5646    1.5481    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.3204    1.8789    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.2394    2.6999    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0  0  0  0
  2  3  2  0  0  0  0
  3  4  1  0  0  0  0
  3  5  1  0  0  0  0
  5  6  2  0  0  0  0
  5  7  1  0  0  0  0
  8  7  1  1  0  0  0
  8  9  1  0  0  0  0
  9 10  2  0  0  0  0
 10 11  1  0  0  0  0
 11 12  2  0  0  0  0
 12 13  1  0  0  0  0
 13 14  2  0  0  0  0
  9 14  1  0  0  0  0
 15 14  1  1  0  0  0
 15 16  1  0  0  0  0
 16 17  1  0  0  0  0
 13 17  1  0  0  0  0
 15 18  1  0  0  0  0
 18 19  2  0  0  0  0
 19 20  1  0  0  0  0
 20 21  2  0  0  0  0
 20 22  1  0  0  0  0
 22 23  1  0  0  0  0
 23 24  1  0  0  0  0
 22 25  2  0  0  0  0
 15 25  1  0  0  0  0
 25 26  1  0  0  0  0
 26 27  1  0  0  0  0
 18 28  1  0  0  0  0
 28 29  1  0  0  0  0
 29 30  1  1  0  0  0
 29 31  1  0  0  0  0
  8 31  1  0  0  0  0
 31 32  1  1  0  0  0
 12 33  1  0  0  0  0
 33 34  1  0  0  0  0
 34 35  1  0  0  0  0
 11 35  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0223167

> <DATABASE_NAME>
NP-MRD

> <SMILES>
COC1=C(OC)[C@]23COC4=C2C(=CC2=C4OCO2)[C@H](OC(=O)C(\C)=C/C)[C@H](C)[C@H](C)CC3=CC1=O

> <INCHI_IDENTIFIER>
InChI=1S/C27H30O8/c1-7-13(2)26(29)35-21-15(4)14(3)8-16-9-18(28)22(30-5)25(31-6)27(16)11-32-24-20(27)17(21)10-19-23(24)34-12-33-19/h7,9-10,14-15,21H,8,11-12H2,1-6H3/b13-7-/t14-,15-,21-,27+/m1/s1

> <INCHI_KEY>
NACPYYYBTUKNNL-YSKMNHBWSA-N

> <FORMULA>
C27H30O8

> <MOLECULAR_WEIGHT>
482.529

> <EXACT_MASS>
482.194067926

> <JCHEM_ACCEPTOR_COUNT>
7

> <JCHEM_ATOM_COUNT>
65

> <JCHEM_AVERAGE_POLARIZABILITY>
49.717485892120706

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
0

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
0

> <JCHEM_IUPAC>
(1S,12R,13R,14R)-19,20-dimethoxy-13,14-dimethyl-18-oxo-3,6,8-trioxapentacyclo[9.9.1.0^{1,16}.0^{4,21}.0^{5,9}]henicosa-4(21),5(9),10,16,19-pentaen-12-yl (2Z)-2-methylbut-2-enoate

> <JCHEM_LOGP>
3.7605419240000004

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
5

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA_STRONGEST_ACIDIC>
17.773741417379767

> <JCHEM_PKA_STRONGEST_BASIC>
-4.294167321147467

> <JCHEM_POLAR_SURFACE_AREA>
89.52000000000001

> <JCHEM_REFRACTIVITY>
129.74679999999998

> <JCHEM_ROTATABLE_BOND_COUNT>
5

> <JCHEM_RULE_OF_FIVE>
1

> <JCHEM_TRADITIONAL_IUPAC>
(1S,12R,13R,14R)-19,20-dimethoxy-13,14-dimethyl-18-oxo-3,6,8-trioxapentacyclo[9.9.1.0^{1,16}.0^{4,21}.0^{5,9}]henicosa-4(21),5(9),10,16,19-pentaen-12-yl (2Z)-2-methylbut-2-enoate

> <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       9.459   9.469   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0       9.268  10.997   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0       7.849  11.595   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0       7.658  13.123   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0       6.621  10.666   0.000  0.00  0.00           C+0
HETATM    6  O   UNK     0       5.202  11.264   0.000  0.00  0.00           O+0
HETATM    7  O   UNK     0       6.813   9.137   0.000  0.00  0.00           O+0
HETATM    8  C   UNK     0       5.585   8.208   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0       5.974   6.718   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0       7.514   6.708   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0       8.276   5.369   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0       7.497   4.041   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0       5.957   4.050   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0       5.196   5.389   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0       3.706   5.000   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0       3.616   3.462   0.000  0.00  0.00           C+0
HETATM   17  O   UNK     0       5.050   2.901   0.000  0.00  0.00           O+0
HETATM   18  C   UNK     0       2.377   5.778   0.000  0.00  0.00           C+0
HETATM   19  C   UNK     0       0.946   5.050   0.000  0.00  0.00           C+0
HETATM   20  C   UNK     0       0.808   3.475   0.000  0.00  0.00           C+0
HETATM   21  O   UNK     0      -0.664   3.022   0.000  0.00  0.00           O+0
HETATM   22  C   UNK     0       1.840   2.208   0.000  0.00  0.00           C+0
HETATM   23  O   UNK     0       1.884   0.669   0.000  0.00  0.00           O+0
HETATM   24  C   UNK     0       3.240  -0.062   0.000  0.00  0.00           C+0
HETATM   25  C   UNK     0       2.778   3.506   0.000  0.00  0.00           C+0
HETATM   26  O   UNK     0       4.057   2.648   0.000  0.00  0.00           O+0
HETATM   27  C   UNK     0       3.953   1.111   0.000  0.00  0.00           C+0
HETATM   28  C   UNK     0       1.988   7.268   0.000  0.00  0.00           C+0
HETATM   29  C   UNK     0       2.766   8.597   0.000  0.00  0.00           C+0
HETATM   30  C   UNK     0       1.837   9.825   0.000  0.00  0.00           C+0
HETATM   31  C   UNK     0       4.256   8.986   0.000  0.00  0.00           C+0
HETATM   32  C   UNK     0       4.467  10.512   0.000  0.00  0.00           C+0
HETATM   33  O   UNK     0       8.521   2.890   0.000  0.00  0.00           O+0
HETATM   34  C   UNK     0       9.931   3.507   0.000  0.00  0.00           C+0
HETATM   35  O   UNK     0       9.780   5.040   0.000  0.00  0.00           O+0
CONECT    1    2                                                            
CONECT    2    1    3                                                       
CONECT    3    2    4    5                                                  
CONECT    4    3                                                            
CONECT    5    3    6    7                                                  
CONECT    6    5                                                            
CONECT    7    5    8                                                       
CONECT    8    7    9   31                                                  
CONECT    9    8   10   14                                                  
CONECT   10    9   11                                                       
CONECT   11   10   12   35                                                  
CONECT   12   11   13   33                                                  
CONECT   13   12   14   17                                                  
CONECT   14   13    9   15                                                  
CONECT   15   14   16   18   25                                             
CONECT   16   15   17                                                       
CONECT   17   16   13                                                       
CONECT   18   15   19   28                                                  
CONECT   19   18   20                                                       
CONECT   20   19   21   22                                                  
CONECT   21   20                                                            
CONECT   22   20   23   25                                                  
CONECT   23   22   24                                                       
CONECT   24   23                                                            
CONECT   25   22   15   26                                                  
CONECT   26   25   27                                                       
CONECT   27   26                                                            
CONECT   28   18   29                                                       
CONECT   29   28   30   31                                                  
CONECT   30   29                                                            
CONECT   31   29    8   32                                                  
CONECT   32   31                                                            
CONECT   33   12   34                                                       
CONECT   34   33   35                                                       
CONECT   35   34   11                                                       
MASTER        0    0    0    0    0    0    0    0   35    0   78    0
END

View in JSmol

Synonyms

Not Available

Chemical Formula

C₂₇H₃₀O₈

Average Mass

482.5290 Da

Monoisotopic Mass

482.19407 Da

IUPAC Name

(1S,12R,13R,14R)-19,20-dimethoxy-13,14-dimethyl-18-oxo-3,6,8-trioxapentacyclo[9.9.1.0^{1,16}.0^{4,21}.0^{5,9}]henicosa-4(21),5(9),10,16,19-pentaen-12-yl (2Z)-2-methylbut-2-enoate

Traditional Name

(1S,12R,13R,14R)-19,20-dimethoxy-13,14-dimethyl-18-oxo-3,6,8-trioxapentacyclo[9.9.1.0^{1,16}.0^{4,21}.0^{5,9}]henicosa-4(21),5(9),10,16,19-pentaen-12-yl (2Z)-2-methylbut-2-enoate

CAS Registry Number

Not Available

SMILES

COC1=C(OC)[C@]23COC4=C2C(=CC2=C4OCO2)[C@H](OC(=O)C(\C)=C/C)[C@H](C)[C@H](C)CC3=CC1=O

InChI Identifier

InChI=1S/C27H30O8/c1-7-13(2)26(29)35-21-15(4)14(3)8-16-9-18(28)22(30-5)25(31-6)27(16)11-32-24-20(27)17(21)10-19-23(24)34-12-33-19/h7,9-10,14-15,21H,8,11-12H2,1-6H3/b13-7-/t14-,15-,21-,27+/m1/s1

InChI Key

NACPYYYBTUKNNL-YSKMNHBWSA-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 heteroclita	LOTUS Database	35616633
Kadsura interior	LOTUS Database	35616633
Schisandra rubriflora	LOTUS Database	35616633

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as benzodioxoles. These are organic compounds containing a benzene ring fused to either isomers of dioxole. Dioxole is a five-membered unsaturated ring of two oxygen atoms and three carbon atoms.

Kingdom

Organic compounds

Super Class

Organoheterocyclic compounds

Class

Benzodioxoles

Sub Class

Not Available

Direct Parent

Benzodioxoles

Alternative Parents

Substituents

Benzodioxole
Coumaran
Alkyl aryl ether
Fatty acid ester
Fatty acyl
Benzenoid
Vinylogous ester
Alpha,beta-unsaturated carboxylic ester
Enoate ester
Carboxylic acid ester
Cyclic ketone
Ketone
Acetal
Carboxylic acid derivative
Ether
Oxacycle
Monocarboxylic acid or derivatives
Aldehyde
Carbonyl group
Hydrocarbon derivative
Organic oxygen compound
Organooxygen compound
Organic oxide
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	3.76	ChemAxon
pKa (Strongest Acidic)	17.77	ChemAxon
pKa (Strongest Basic)	-4.3	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	7	ChemAxon
Hydrogen Donor Count	0	ChemAxon
Polar Surface Area	89.52 Å²	ChemAxon
Rotatable Bond Count	5	ChemAxon
Refractivity	129.75 m³·mol⁻¹	ChemAxon
Polarizability	49.72 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

C00033952

Chemspider ID

24700551

KEGG Compound ID

Not Available

BioCyc ID

Not Available

BiGG ID

Not Available

Wikipedia Link

Not Available

METLIN ID

Not Available

PubChem Compound

14755542

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

Lu Y, Chen DF: Kadsutherin D, a new dibenzocyclooctadiene lignan from Kadsura species. Nat Prod Res. 2008;22(15):1344-9. doi: 10.1080/14786410601133525. [PubMed:19023792 ]
Xu J, Liu J, Li B, Wei X, Qi Y, Zhang B, Liu H, Xiao P: Comparison of blood tonic efficacy and chemical constituents of Kadsura interior A.C. Smith and its closely related species. Chin Med. 2022 Jan 17;17(1):14. doi: 10.1186/s13020-021-00544-w. [PubMed:35039063 ]
Chen M, Jia ZW, Chen DF: Heteroclitin H, a new lignan from Kadsura heteroclita. J Asian Nat Prod Res. 2006 Oct-Nov;8(7):643-8. doi: 10.1080/10286020500209053. [PubMed:17135051 ]
LOTUS database [Link]

Showing NP-Card for (1s,12r,13r,14r)-19,20-dimethoxy-13,14-dimethyl-18-oxo-3,6,8-trioxapentacyclo[9.9.1.0¹,¹⁶.0⁴,²¹.0⁵,⁹]henicosa-4(21),5(9),10,16,19-pentaen-12-yl (2z)-2-methylbut-2-enoate (NP0223167)

MOL for NP0223167 ((1s,12r,13r,14r)-19,20-dimethoxy-13,14-dimethyl-18-oxo-3,6,8-trioxapentacyclo[9.9.1.0¹,¹⁶.0⁴,²¹.0⁵,⁹]henicosa-4(21),5(9),10,16,19-pentaen-12-yl (2z)-2-methylbut-2-enoate)

3D MOL for NP0223167 ((1s,12r,13r,14r)-19,20-dimethoxy-13,14-dimethyl-18-oxo-3,6,8-trioxapentacyclo[9.9.1.0¹,¹⁶.0⁴,²¹.0⁵,⁹]henicosa-4(21),5(9),10,16,19-pentaen-12-yl (2z)-2-methylbut-2-enoate)

3D SDF for NP0223167 ((1s,12r,13r,14r)-19,20-dimethoxy-13,14-dimethyl-18-oxo-3,6,8-trioxapentacyclo[9.9.1.0¹,¹⁶.0⁴,²¹.0⁵,⁹]henicosa-4(21),5(9),10,16,19-pentaen-12-yl (2z)-2-methylbut-2-enoate)

3D-SDF for NP0223167 ((1s,12r,13r,14r)-19,20-dimethoxy-13,14-dimethyl-18-oxo-3,6,8-trioxapentacyclo[9.9.1.0¹,¹⁶.0⁴,²¹.0⁵,⁹]henicosa-4(21),5(9),10,16,19-pentaen-12-yl (2z)-2-methylbut-2-enoate)

PDB for NP0223167 ((1s,12r,13r,14r)-19,20-dimethoxy-13,14-dimethyl-18-oxo-3,6,8-trioxapentacyclo[9.9.1.0¹,¹⁶.0⁴,²¹.0⁵,⁹]henicosa-4(21),5(9),10,16,19-pentaen-12-yl (2z)-2-methylbut-2-enoate)

3D PDB for NP0223167 ((1s,12r,13r,14r)-19,20-dimethoxy-13,14-dimethyl-18-oxo-3,6,8-trioxapentacyclo[9.9.1.0¹,¹⁶.0⁴,²¹.0⁵,⁹]henicosa-4(21),5(9),10,16,19-pentaen-12-yl (2z)-2-methylbut-2-enoate)

SMILES for NP0223167 ((1s,12r,13r,14r)-19,20-dimethoxy-13,14-dimethyl-18-oxo-3,6,8-trioxapentacyclo[9.9.1.0¹,¹⁶.0⁴,²¹.0⁵,⁹]henicosa-4(21),5(9),10,16,19-pentaen-12-yl (2z)-2-methylbut-2-enoate)

INCHI for NP0223167 ((1s,12r,13r,14r)-19,20-dimethoxy-13,14-dimethyl-18-oxo-3,6,8-trioxapentacyclo[9.9.1.0¹,¹⁶.0⁴,²¹.0⁵,⁹]henicosa-4(21),5(9),10,16,19-pentaen-12-yl (2z)-2-methylbut-2-enoate)

Structure for NP0223167 ((1s,12r,13r,14r)-19,20-dimethoxy-13,14-dimethyl-18-oxo-3,6,8-trioxapentacyclo[9.9.1.0¹,¹⁶.0⁴,²¹.0⁵,⁹]henicosa-4(21),5(9),10,16,19-pentaen-12-yl (2z)-2-methylbut-2-enoate)

3D Structure for NP0223167 ((1s,12r,13r,14r)-19,20-dimethoxy-13,14-dimethyl-18-oxo-3,6,8-trioxapentacyclo[9.9.1.0¹,¹⁶.0⁴,²¹.0⁵,⁹]henicosa-4(21),5(9),10,16,19-pentaen-12-yl (2z)-2-methylbut-2-enoate)