NP-MRD: Showing NP-Card for 7-hydroxy-6,14-dimethoxy-13-[(3,4,5-trihydroxy-6-methyloxan-2-yl)oxy]-2,9-dioxatetracyclo[6.6.2.0⁴,¹⁶.0¹¹,¹⁵]hexadeca-1(15),4(16),5,7,11,13-hexaene-3,10-dione (NP0311946)

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Record Information

Version

2.0

Created at

2022-09-11 08:17:37 UTC

Updated at

2022-09-11 08:17:37 UTC

NP-MRD ID

NP0311946

Secondary Accession Numbers

None

Natural Product Identification

Common Name

7-hydroxy-6,14-dimethoxy-13-[(3,4,5-trihydroxy-6-methyloxan-2-yl)oxy]-2,9-dioxatetracyclo[6.6.2.0⁴,¹⁶.0¹¹,¹⁵]hexadeca-1(15),4(16),5,7,11,13-hexaene-3,10-dione

Description

7-Hydroxy-6,14-dimethoxy-13-[(3,4,5-trihydroxy-6-methyloxan-2-yl)oxy]-2,9-dioxatetracyclo[6.6.2.0⁴,¹⁶.0¹¹,¹⁵]Hexadeca-1(15),4,6,8(16),11,13-hexaene-3,10-dione belongs to the class of organic compounds known as beta carbolines. Beta carbolines are compounds containing a 9H-pyrido[3,4-b]indole moiety. 7-hydroxy-6,14-dimethoxy-13-[(3,4,5-trihydroxy-6-methyloxan-2-yl)oxy]-2,9-dioxatetracyclo[6.6.2.0⁴,¹⁶.0¹¹,¹⁵]hexadeca-1(15),4(16),5,7,11,13-hexaene-3,10-dione is found in Punica granatum. 7-Hydroxy-6,14-dimethoxy-13-[(3,4,5-trihydroxy-6-methyloxan-2-yl)oxy]-2,9-dioxatetracyclo[6.6.2.0⁴,¹⁶.0¹¹,¹⁵]Hexadeca-1(15),4,6,8(16),11,13-hexaene-3,10-dione is an extremely weak basic (essentially neutral) compound (based on its pKa).

Structure

MOL 3D MOL SDF PDB SMILES InChI


  Mrv1533004171505072D          

 34 38  0  0  0  0            999 V2000
    5.9664   -0.1105    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.5539   -0.8250    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.7289   -0.8250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.3164   -1.5395    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.4914   -1.5395    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.0789   -2.2539    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.4914   -2.9684    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.2539   -2.2539    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.8414   -1.5395    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.0164   -1.5395    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.6039   -2.2539    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2211   -2.2539    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.6039   -0.8250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2211   -0.8250    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6336   -0.1105    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4586   -0.1105    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8711    0.6039    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6961    0.6039    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4586    1.3184    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8711    2.0329    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6336    1.3184    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2211    2.0329    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2211    0.6039    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.6039    0.6039    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.0164   -0.1105    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.8414   -0.1105    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.2539    0.6039    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.8414    1.3184    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.0789    0.6039    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.4914   -0.1105    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.3164   -0.1105    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.7289    0.6039    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.0789   -0.8250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.2539   -0.8250    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
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 13 25  2  0  0  0  0
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  3 31  1  0  0  0  0
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  5 33  2  0  0  0  0
 33 34  1  0  0  0  0
  9 34  1  0  0  0  0
 26 34  2  0  0  0  0
M  END

     RDKit          3D

 54 58  0  0  0  0  0  0  0  0999 V2000
    8.4057    0.0588   -0.8433 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.6555    0.2198    0.3294 O   0  0  0  0  0  0  0  0  0  0  0  0
    6.2850    0.2215    0.3850 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.5412    0.0563   -0.7705 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.1586    0.0507   -0.7667 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.4052   -0.1128   -1.9051 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.0064   -0.2660   -3.0167 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.1069   -0.1058   -1.8116 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.4533    0.0521   -0.6665 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0589    0.0515   -0.6272 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5635   -0.1303   -1.8726 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7600   -1.5227   -2.2020 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6505    0.2094    0.5087 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9961    0.2143    0.5662 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.0436    0.1549   -0.3049 C   0  0  2  0  0  0  0  0  0  0  0  0
   -3.9137    1.2128   -0.0040 O   0  0  0  0  0  0  0  0  0  0  0  0
   -5.1656    1.0659   -0.5454 C   0  0  2  0  0  0  0  0  0  0  0  0
   -5.9042    2.3753   -0.3723 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.8983    0.0309    0.3051 C   0  0  1  0  0  0  0  0  0  0  0  0
   -7.0317   -0.3429   -0.3906 O   0  0  0  0  0  0  0  0  0  0  0  0
   -4.9931   -1.1307    0.6248 C   0  0  2  0  0  0  0  0  0  0  0  0
   -4.6531   -1.0582    1.9538 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.7712   -1.1762   -0.2521 C   0  0  1  0  0  0  0  0  0  0  0  0
   -4.0874   -1.6251   -1.5314 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.0999    0.3775    1.6902 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4660    0.3785    1.6612 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.2352    0.5435    2.8151 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.6589    0.6954    3.9192 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.5479    0.5419    2.7600 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.2329    0.3896    1.6493 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.6087    0.3863    1.5825 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.3391    0.5512    2.7364 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.5334    0.2217    0.4727 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1633    0.2176    0.4885 C   0  0  0  0  0  0  0  0  0  0  0  0
    9.4516   -0.1972   -0.5289 H   0  0  0  0  0  0  0  0  0  0  0  0
    8.3953    1.0402   -1.3788 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.9843   -0.7357   -1.4922 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.0577   -0.0763   -1.7329 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6267   -1.5123   -2.9126 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0020   -2.0965   -1.2884 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.1290   -1.9304   -2.7273 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7277    0.2836   -1.3546 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.1681    0.7926   -1.6129 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.9452    2.6283    0.7036 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.3942    3.2121   -0.8870 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.9531    2.2467   -0.7535 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.2234    0.5587    1.2255 H   0  0  0  0  0  0  0  0  0  0  0  0
   -7.2267    0.2547   -1.1587 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.5620   -2.0654    0.4411 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.2259   -1.8819    2.3022 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.0672   -1.9045    0.2004 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.9564   -2.6029   -1.6418 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4417    0.5024    2.5979 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.9726    0.6775    3.6496 H   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0
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  3  4  2  0
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  5 33  2  0
 33 30  1  0
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 31  3  1  0
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 21 49  1  1
 22 50  1  0
 23 51  1  1
 24 52  1  0
 25 53  1  0
 32 54  1  0
M  END


  Mrv1533004171505072D          

 34 38  0  0  0  0            999 V2000
    5.9664   -0.1105    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.5539   -0.8250    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.7289   -0.8250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.3164   -1.5395    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.4914   -1.5395    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.0789   -2.2539    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.4914   -2.9684    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.2539   -2.2539    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.8414   -1.5395    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.0164   -1.5395    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.6039   -2.2539    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2211   -2.2539    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.6039   -0.8250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2211   -0.8250    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6336   -0.1105    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4586   -0.1105    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8711    0.6039    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6961    0.6039    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4586    1.3184    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8711    2.0329    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
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   -0.2211    2.0329    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2211    0.6039    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.6039    0.6039    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
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    1.8414   -0.1105    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
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    1.8414    1.3184    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.0789    0.6039    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.4914   -0.1105    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.3164   -0.1105    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.7289    0.6039    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.0789   -0.8250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.2539   -0.8250    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
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 33 34  1  0  0  0  0
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 26 34  2  0  0  0  0
M  END
> <DATABASE_ID>
NP0311946

> <DATABASE_NAME>
NP-MRD

> <SMILES>
COC1=CC2=C3C(OC(=O)C4=C3C(OC2=O)=C(OC)C(OC2OC(C)C(O)C(O)C2O)=C4)=C1O

> <INCHI_IDENTIFIER>
InChI=1S/C22H20O12/c1-6-13(23)15(25)16(26)22(31-6)32-10-5-8-12-11-7(21(28)34-19(12)17(10)30-3)4-9(29-2)14(24)18(11)33-20(8)27/h4-6,13,15-16,22-26H,1-3H3

> <INCHI_KEY>
PBBNQHBZSUCLLZ-UHFFFAOYSA-N

> <FORMULA>
C22H20O12

> <MOLECULAR_WEIGHT>
476.39

> <EXACT_MASS>
476.095476084

> <JCHEM_ACCEPTOR_COUNT>
10

> <JCHEM_ATOM_COUNT>
54

> <JCHEM_AVERAGE_POLARIZABILITY>
45.114050783995054

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
4

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
1

> <JCHEM_IUPAC>
7-hydroxy-6,14-dimethoxy-13-[(3,4,5-trihydroxy-6-methyloxan-2-yl)oxy]-2,9-dioxatetracyclo[6.6.2.0⁴,¹⁶.0¹¹,¹⁵]hexadeca-1(14),4(16),5,7,11(15),12-hexaene-3,10-dione

> <ALOGPS_LOGP>
1.04

> <JCHEM_LOGP>
0.7365524033333326

> <ALOGPS_LOGS>
-2.65

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
5

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA>
12.214646801368355

> <JCHEM_PKA_STRONGEST_ACIDIC>
9.678468874487715

> <JCHEM_PKA_STRONGEST_BASIC>
-3.6053089967193204

> <JCHEM_POLAR_SURFACE_AREA>
170.44

> <JCHEM_REFRACTIVITY>
110.17289999999998

> <JCHEM_ROTATABLE_BOND_COUNT>
4

> <JCHEM_RULE_OF_FIVE>
1

> <ALOGPS_SOLUBILITY>
1.06e+00 g/l

> <JCHEM_TRADITIONAL_IUPAC>
7-hydroxy-6,14-dimethoxy-13-[(3,4,5-trihydroxy-6-methyloxan-2-yl)oxy]-2,9-dioxatetracyclo[6.6.2.0⁴,¹⁶.0¹¹,¹⁵]hexadeca-1(14),4(16),5,7,11(15),12-hexaene-3,10-dione

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 17-APR-15   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   17-APR-15         0                                  
HETATM    1  C   UNK     0      11.137  -0.206   0.000  0.00  0.00           C+0
HETATM    2  O   UNK     0      10.367  -1.540   0.000  0.00  0.00           O+0
HETATM    3  C   UNK     0       8.827  -1.540   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0       8.057  -2.874   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0       6.517  -2.874   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0       5.747  -4.207   0.000  0.00  0.00           C+0
HETATM    7  O   UNK     0       6.517  -5.541   0.000  0.00  0.00           O+0
HETATM    8  O   UNK     0       4.207  -4.207   0.000  0.00  0.00           O+0
HETATM    9  C   UNK     0       3.437  -2.874   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0       1.897  -2.874   0.000  0.00  0.00           C+0
HETATM   11  O   UNK     0       1.127  -4.207   0.000  0.00  0.00           O+0
HETATM   12  C   UNK     0      -0.413  -4.207   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0       1.127  -1.540   0.000  0.00  0.00           C+0
HETATM   14  O   UNK     0      -0.413  -1.540   0.000  0.00  0.00           O+0
HETATM   15  C   UNK     0      -1.183  -0.206   0.000  0.00  0.00           C+0
HETATM   16  O   UNK     0      -2.723  -0.206   0.000  0.00  0.00           O+0
HETATM   17  C   UNK     0      -3.493   1.127   0.000  0.00  0.00           C+0
HETATM   18  C   UNK     0      -5.033   1.127   0.000  0.00  0.00           C+0
HETATM   19  C   UNK     0      -2.723   2.461   0.000  0.00  0.00           C+0
HETATM   20  O   UNK     0      -3.493   3.795   0.000  0.00  0.00           O+0
HETATM   21  C   UNK     0      -1.183   2.461   0.000  0.00  0.00           C+0
HETATM   22  O   UNK     0      -0.413   3.795   0.000  0.00  0.00           O+0
HETATM   23  C   UNK     0      -0.413   1.127   0.000  0.00  0.00           C+0
HETATM   24  O   UNK     0       1.127   1.127   0.000  0.00  0.00           O+0
HETATM   25  C   UNK     0       1.897  -0.206   0.000  0.00  0.00           C+0
HETATM   26  C   UNK     0       3.437  -0.206   0.000  0.00  0.00           C+0
HETATM   27  C   UNK     0       4.207   1.127   0.000  0.00  0.00           C+0
HETATM   28  O   UNK     0       3.437   2.461   0.000  0.00  0.00           O+0
HETATM   29  O   UNK     0       5.747   1.127   0.000  0.00  0.00           O+0
HETATM   30  C   UNK     0       6.517  -0.206   0.000  0.00  0.00           C+0
HETATM   31  C   UNK     0       8.057  -0.206   0.000  0.00  0.00           C+0
HETATM   32  O   UNK     0       8.827   1.127   0.000  0.00  0.00           O+0
HETATM   33  C   UNK     0       5.747  -1.540   0.000  0.00  0.00           C+0
HETATM   34  C   UNK     0       4.207  -1.540   0.000  0.00  0.00           C+0
CONECT    1    2                                                            
CONECT    2    1    3                                                       
CONECT    3    2    4   31                                                  
CONECT    4    3    5                                                       
CONECT    5    4    6   33                                                  
CONECT    6    5    7    8                                                  
CONECT    7    6                                                            
CONECT    8    6    9                                                       
CONECT    9    8   10   34                                                  
CONECT   10    9   11   13                                                  
CONECT   11   10   12                                                       
CONECT   12   11                                                            
CONECT   13   10   14   25                                                  
CONECT   14   13   15                                                       
CONECT   15   14   16   23                                                  
CONECT   16   15   17                                                       
CONECT   17   16   18   19                                                  
CONECT   18   17                                                            
CONECT   19   17   20   21                                                  
CONECT   20   19                                                            
CONECT   21   19   22   23                                                  
CONECT   22   21                                                            
CONECT   23   21   15   24                                                  
CONECT   24   23                                                            
CONECT   25   13   26                                                       
CONECT   26   25   27   34                                                  
CONECT   27   26   28   29                                                  
CONECT   28   27                                                            
CONECT   29   27   30                                                       
CONECT   30   29   31   33                                                  
CONECT   31   30    3   32                                                  
CONECT   32   31                                                            
CONECT   33   30    5   34                                                  
CONECT   34   33    9   26                                                  
MASTER        0    0    0    0    0    0    0    0   34    0   76    0
END

View in JSmol

Synonyms

Not Available

Chemical Formula

C₂₂H₂₀O₁₂

Average Mass

476.3900 Da

Monoisotopic Mass

476.09548 Da

IUPAC Name

7-hydroxy-6,14-dimethoxy-13-[(3,4,5-trihydroxy-6-methyloxan-2-yl)oxy]-2,9-dioxatetracyclo[6.6.2.0⁴,¹⁶.0¹¹,¹⁵]hexadeca-1(14),4(16),5,7,11(15),12-hexaene-3,10-dione

Traditional Name

7-hydroxy-6,14-dimethoxy-13-[(3,4,5-trihydroxy-6-methyloxan-2-yl)oxy]-2,9-dioxatetracyclo[6.6.2.0⁴,¹⁶.0¹¹,¹⁵]hexadeca-1(14),4(16),5,7,11(15),12-hexaene-3,10-dione

CAS Registry Number

Not Available

SMILES

COC1=CC2=C3C(OC(=O)C4=C3C(OC2=O)=C(OC)C(OC2OC(C)C(O)C(O)C2O)=C4)=C1O

InChI Identifier

InChI=1S/C22H20O12/c1-6-13(23)15(25)16(26)22(31-6)32-10-5-8-12-11-7(21(28)34-19(12)17(10)30-3)4-9(29-2)14(24)18(11)33-20(8)27/h4-6,13,15-16,22-26H,1-3H3

InChI Key

PBBNQHBZSUCLLZ-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
Punica granatum	LOTUS Database	35616633

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as beta carbolines. Beta carbolines are compounds containing a 9H-pyrido[3,4-b]indole moiety.

Kingdom

Organic compounds

Super Class

Organoheterocyclic compounds

Class

Indoles and derivatives

Sub Class

Pyridoindoles

Direct Parent

Beta carbolines

Alternative Parents

Substituents

Beta-carboline
Alpha-amino acid or derivatives
3-alkylindole
Indole
Anisole
Dioxopiperazine
Phenol ether
2,5-dioxopiperazine
Alkyl aryl ether
N-alkylpiperazine
Piperazine
1,4-diazinane
Benzenoid
Tertiary carboxylic acid amide
Pyrrolidine
Pyrrole
Heteroaromatic compound
Carboxamide group
Lactam
Alkanolamine
Azacycle
Carboxylic acid derivative
Dialkyl ether
Ether
Organic nitrogen compound
Carbonyl group
Hydrocarbon derivative
Organic oxygen compound
Organic oxide
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	1.04	ALOGPS
logP	0.74	ChemAxon
logS	-2.6	ALOGPS
pKa (Strongest Acidic)	9.68	ChemAxon
pKa (Strongest Basic)	-3.6	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	10	ChemAxon
Hydrogen Donor Count	4	ChemAxon
Polar Surface Area	170.44 Å²	ChemAxon
Rotatable Bond Count	4	ChemAxon
Refractivity	110.17 m³·mol⁻¹	ChemAxon
Polarizability	45.11 Å³	ChemAxon
Number of Rings	5	ChemAxon
Bioavailability	Yes	ChemAxon
Rule of Five	Yes	ChemAxon
Ghose Filter	Yes	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

Not Available

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

LOTUS database [Link]

Showing NP-Card for 7-hydroxy-6,14-dimethoxy-13-[(3,4,5-trihydroxy-6-methyloxan-2-yl)oxy]-2,9-dioxatetracyclo[6.6.2.0⁴,¹⁶.0¹¹,¹⁵]hexadeca-1(15),4(16),5,7,11,13-hexaene-3,10-dione (NP0311946)

MOL for NP0311946 (7-hydroxy-6,14-dimethoxy-13-[(3,4,5-trihydroxy-6-methyloxan-2-yl)oxy]-2,9-dioxatetracyclo[6.6.2.0⁴,¹⁶.0¹¹,¹⁵]hexadeca-1(15),4(16),5,7,11,13-hexaene-3,10-dione)

3D MOL for NP0311946 (7-hydroxy-6,14-dimethoxy-13-[(3,4,5-trihydroxy-6-methyloxan-2-yl)oxy]-2,9-dioxatetracyclo[6.6.2.0⁴,¹⁶.0¹¹,¹⁵]hexadeca-1(15),4(16),5,7,11,13-hexaene-3,10-dione)

3D SDF for NP0311946 (7-hydroxy-6,14-dimethoxy-13-[(3,4,5-trihydroxy-6-methyloxan-2-yl)oxy]-2,9-dioxatetracyclo[6.6.2.0⁴,¹⁶.0¹¹,¹⁵]hexadeca-1(15),4(16),5,7,11,13-hexaene-3,10-dione)

3D-SDF for NP0311946 (7-hydroxy-6,14-dimethoxy-13-[(3,4,5-trihydroxy-6-methyloxan-2-yl)oxy]-2,9-dioxatetracyclo[6.6.2.0⁴,¹⁶.0¹¹,¹⁵]hexadeca-1(15),4(16),5,7,11,13-hexaene-3,10-dione)

PDB for NP0311946 (7-hydroxy-6,14-dimethoxy-13-[(3,4,5-trihydroxy-6-methyloxan-2-yl)oxy]-2,9-dioxatetracyclo[6.6.2.0⁴,¹⁶.0¹¹,¹⁵]hexadeca-1(15),4(16),5,7,11,13-hexaene-3,10-dione)

3D PDB for NP0311946 (7-hydroxy-6,14-dimethoxy-13-[(3,4,5-trihydroxy-6-methyloxan-2-yl)oxy]-2,9-dioxatetracyclo[6.6.2.0⁴,¹⁶.0¹¹,¹⁵]hexadeca-1(15),4(16),5,7,11,13-hexaene-3,10-dione)

SMILES for NP0311946 (7-hydroxy-6,14-dimethoxy-13-[(3,4,5-trihydroxy-6-methyloxan-2-yl)oxy]-2,9-dioxatetracyclo[6.6.2.0⁴,¹⁶.0¹¹,¹⁵]hexadeca-1(15),4(16),5,7,11,13-hexaene-3,10-dione)

INCHI for NP0311946 (7-hydroxy-6,14-dimethoxy-13-[(3,4,5-trihydroxy-6-methyloxan-2-yl)oxy]-2,9-dioxatetracyclo[6.6.2.0⁴,¹⁶.0¹¹,¹⁵]hexadeca-1(15),4(16),5,7,11,13-hexaene-3,10-dione)

Structure for NP0311946 (7-hydroxy-6,14-dimethoxy-13-[(3,4,5-trihydroxy-6-methyloxan-2-yl)oxy]-2,9-dioxatetracyclo[6.6.2.0⁴,¹⁶.0¹¹,¹⁵]hexadeca-1(15),4(16),5,7,11,13-hexaene-3,10-dione)

3D Structure for NP0311946 (7-hydroxy-6,14-dimethoxy-13-[(3,4,5-trihydroxy-6-methyloxan-2-yl)oxy]-2,9-dioxatetracyclo[6.6.2.0⁴,¹⁶.0¹¹,¹⁵]hexadeca-1(15),4(16),5,7,11,13-hexaene-3,10-dione)