NP-MRD: Showing NP-Card for Scandenin (NP0056817)

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Record Information

Version

2.0

Created at

2022-04-28 02:27:56 UTC

Updated at

2022-04-28 02:27:56 UTC

NP-MRD ID

NP0056817

Secondary Accession Numbers

None

Natural Product Identification

Common Name

Scandenin

Description

Scandenin belongs to the class of organic compounds known as pyranoisoflavonoids. These are isoflavonoids that contain a pyran ring fused to either of the A, B, or C ring of the isoflavonoid skeleton. Thus, scandenin is considered to be a flavonoid lipid molecule. Scandenin is found in Deguelia hatschbachii, Deguelia spruceana and Derris scandens . Scandenin is a very hydrophobic molecule, practically insoluble (in water), and relatively neutral.

Structure

MOL 3D MOL SDF PDB SMILES InChI


  Mrv1533004161513092D          

 32 35  0  0  0  0            999 V2000
    0.3020    2.5559    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.1270    2.5559    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.5395    1.8414    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.3645    1.8414    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.7770    2.5559    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.6020    2.5559    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.0145    3.2704    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.6020    3.9849    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.8395    3.2704    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.7770    1.1270    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.6020    1.1270    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.0145    0.4125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.6465    0.9428    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.6465   -0.1178    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.6020   -0.3020    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.7770   -0.3020    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.3645    0.4125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.5395    0.4125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.1270   -0.3020    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.3020   -0.3020    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1105   -1.0164    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1105    0.4125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.3020    1.1270    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1105    1.8414    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.1270    1.1270    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9355    0.4125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3480   -0.3020    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1730   -0.3020    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5855    0.4125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.4105    0.4125    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1730    1.1270    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3480    1.1270    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
  6  7  2  0  0  0  0
  7  8  1  0  0  0  0
  7  9  1  0  0  0  0
  4 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
 12 14  1  0  0  0  0
 12 15  1  0  0  0  0
 15 16  2  0  0  0  0
 16 17  1  0  0  0  0
 10 17  2  0  0  0  0
 17 18  1  0  0  0  0
 18 19  1  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  2  0  0  0  0
 23 24  1  0  0  0  0
 23 25  1  0  0  0  0
  3 25  1  0  0  0  0
 18 25  2  0  0  0  0
 22 26  1  0  0  0  0
 26 27  2  0  0  0  0
 27 28  1  0  0  0  0
 28 29  2  0  0  0  0
 29 30  1  0  0  0  0
 29 31  1  0  0  0  0
 31 32  2  0  0  0  0
 26 32  1  0  0  0  0
M  END

     RDKit          3D

 58 61  0  0  0  0  0  0  0  0999 V2000
   -0.1203   -2.2188   -2.1942 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3044   -1.8933   -0.8053 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3450   -0.5160   -0.4691 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5520    0.1390   -0.5341 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8032   -0.5978   -0.9013 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.2790   -1.3902    0.2594 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5233   -2.6872    0.2565 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.3706   -3.5868   -0.8969 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.9949   -3.3213    1.5442 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6390    1.4974   -0.2181 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5012    2.1422    0.1546 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7272    1.5156    0.2348 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.8045    2.1890    0.6112 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.9761    1.6060    0.6989 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.0132    2.2283    1.0550 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.1280    0.2522    0.3982 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.4457   -0.3477    0.4971 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.4335   -0.1175   -0.4535 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.6804   -0.7014   -0.3501 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.9946   -1.5366    0.7025 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.2742   -2.1076    0.7648 O   0  0  0  0  0  0  0  0  0  0  0  0
    6.0290   -1.7752    1.6518 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.7892   -1.1929    1.5463 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.0204   -0.4653    0.0036 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1226   -1.8092   -0.2994 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.7903    0.1693   -0.0848 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5694    3.5653    0.4612 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7471    4.1527    0.3565 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.9972    3.4860   -0.0477 C   0  0  1  0  0  0  0  0  0  0  0  0
   -4.0116    3.6534    1.0635 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5582    4.1022   -1.3259 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8753    2.1132   -0.3002 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2578   -1.2943   -2.8015 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.8284   -2.6777   -2.4239 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9320   -2.9448   -2.4485 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5742   -1.2106   -1.7777 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5764    0.1416   -1.1913 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.4211   -0.8098    1.1814 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.2425   -3.1085   -1.8663 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5122   -4.2881   -0.7512 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.2719   -4.2593   -1.0215 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5965   -2.6865    2.3930 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.6116   -4.3496    1.6406 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.0943   -3.2483    1.6213 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.2211    0.5384   -1.2940 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.4539   -0.5062   -1.1137 H   0  0  0  0  0  0  0  0  0  0  0  0
    8.5135   -2.7105    1.5167 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.2661   -2.4262    2.4719 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.9978   -1.3599    2.2879 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.9393   -2.3749   -0.2718 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.3266    4.0621    0.7547 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8080    5.2128    0.5843 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.9272    3.0827    0.8976 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.2288    4.7460    1.1836 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5016    3.2893    2.0045 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8886    3.8124   -2.1577 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.5454    3.6287   -1.4957 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5940    5.1941   -1.3024 H   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0
  2  3  1  0
  3  4  2  0
  4  5  1  0
  5  6  1  0
  6  7  2  3
  7  8  1  0
  7  9  1  0
  4 10  1  0
 10 11  2  0
 11 27  1  0
 27 28  2  0
 28 29  1  0
 29 30  1  1
 29 31  1  0
 29 32  1  0
 11 12  1  0
 12 26  2  0
 26 24  1  0
 24 25  1  0
 24 16  2  0
 16 14  1  0
 14 15  2  0
 14 13  1  0
 16 17  1  0
 17 18  2  0
 18 19  1  0
 19 20  2  0
 20 21  1  0
 20 22  1  0
 22 23  2  0
 26  3  1  0
 23 17  1  0
 32 10  1  0
 13 12  1  0
  1 33  1  0
  1 34  1  0
  1 35  1  0
  5 36  1  0
  5 37  1  0
  6 38  1  0
  8 39  1  0
  8 40  1  0
  8 41  1  0
  9 42  1  0
  9 43  1  0
  9 44  1  0
 27 51  1  0
 28 52  1  0
 30 53  1  0
 30 54  1  0
 30 55  1  0
 31 56  1  0
 31 57  1  0
 31 58  1  0
 25 50  1  0
 18 45  1  0
 19 46  1  0
 21 47  1  0
 22 48  1  0
 23 49  1  0
M  END


  Mrv1533004161513092D          

 32 35  0  0  0  0            999 V2000
    0.3020    2.5559    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.1270    2.5559    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.5395    1.8414    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.3645    1.8414    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.7770    2.5559    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.6020    2.5559    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.0145    3.2704    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.6020    3.9849    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.8395    3.2704    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.7770    1.1270    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.6020    1.1270    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.0145    0.4125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.6465    0.9428    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.6465   -0.1178    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.6020   -0.3020    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.7770   -0.3020    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.3645    0.4125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.5395    0.4125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.1270   -0.3020    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.3020   -0.3020    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1105   -1.0164    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1105    0.4125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.3020    1.1270    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1105    1.8414    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.1270    1.1270    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9355    0.4125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3480   -0.3020    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1730   -0.3020    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5855    0.4125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.4105    0.4125    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1730    1.1270    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3480    1.1270    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
  6  7  2  0  0  0  0
  7  8  1  0  0  0  0
  7  9  1  0  0  0  0
  4 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
 12 14  1  0  0  0  0
 12 15  1  0  0  0  0
 15 16  2  0  0  0  0
 16 17  1  0  0  0  0
 10 17  2  0  0  0  0
 17 18  1  0  0  0  0
 18 19  1  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  2  0  0  0  0
 23 24  1  0  0  0  0
 23 25  1  0  0  0  0
  3 25  1  0  0  0  0
 18 25  2  0  0  0  0
 22 26  1  0  0  0  0
 26 27  2  0  0  0  0
 27 28  1  0  0  0  0
 28 29  2  0  0  0  0
 29 30  1  0  0  0  0
 29 31  1  0  0  0  0
 31 32  2  0  0  0  0
 26 32  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0056817

> <DATABASE_NAME>
NP-MRD

> <SMILES>
COC1=C(CC=C(C)C)C2=C(C=CC(C)(C)O2)C2=C1C(O)=C(C(=O)O2)C1=CC=C(O)C=C1

> <INCHI_IDENTIFIER>
InChI=1S/C26H26O6/c1-14(2)6-11-17-22-18(12-13-26(3,4)32-22)24-20(23(17)30-5)21(28)19(25(29)31-24)15-7-9-16(27)10-8-15/h6-10,12-13,27-28H,11H2,1-5H3

> <INCHI_KEY>
AAKJUGSASOCUFQ-UHFFFAOYSA-N

> <FORMULA>
C26H26O6

> <MOLECULAR_WEIGHT>
434.488

> <EXACT_MASS>
434.172938557

> <JCHEM_ACCEPTOR_COUNT>
5

> <JCHEM_ATOM_COUNT>
58

> <JCHEM_AVERAGE_POLARIZABILITY>
47.07087234214371

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
2

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
1

> <JCHEM_IUPAC>
4-hydroxy-3-(4-hydroxyphenyl)-5-methoxy-8,8-dimethyl-6-(3-methylbut-2-en-1-yl)-2H,8H-pyrano[2,3-f]chromen-2-one

> <ALOGPS_LOGP>
4.50

> <JCHEM_LOGP>
4.865854325666667

> <ALOGPS_LOGS>
-5.12

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
4

> <JCHEM_PHYSIOLOGICAL_CHARGE>
-1

> <JCHEM_PKA>
8.892661550296902

> <JCHEM_PKA_STRONGEST_ACIDIC>
6.366851578799083

> <JCHEM_PKA_STRONGEST_BASIC>
-4.611249637961529

> <JCHEM_POLAR_SURFACE_AREA>
85.22000000000001

> <JCHEM_REFRACTIVITY>
124.97329999999997

> <JCHEM_ROTATABLE_BOND_COUNT>
4

> <JCHEM_RULE_OF_FIVE>
1

> <ALOGPS_SOLUBILITY>
3.30e-03 g/l

> <JCHEM_TRADITIONAL_IUPAC>
scandenin

> <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       0.564   4.771   0.000  0.00  0.00           C+0
HETATM    2  O   UNK     0       2.104   4.771   0.000  0.00  0.00           O+0
HETATM    3  C   UNK     0       2.874   3.437   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0       4.414   3.437   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0       5.184   4.771   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0       6.724   4.771   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0       7.494   6.105   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0       6.724   7.438   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0       9.034   6.105   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0       5.184   2.104   0.000  0.00  0.00           C+0
HETATM   11  O   UNK     0       6.724   2.104   0.000  0.00  0.00           O+0
HETATM   12  C   UNK     0       7.494   0.770   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0       8.673   1.760   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0       8.673  -0.220   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0       6.724  -0.564   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0       5.184  -0.564   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0       4.414   0.770   0.000  0.00  0.00           C+0
HETATM   18  C   UNK     0       2.874   0.770   0.000  0.00  0.00           C+0
HETATM   19  O   UNK     0       2.104  -0.564   0.000  0.00  0.00           O+0
HETATM   20  C   UNK     0       0.564  -0.564   0.000  0.00  0.00           C+0
HETATM   21  O   UNK     0      -0.206  -1.897   0.000  0.00  0.00           O+0
HETATM   22  C   UNK     0      -0.206   0.770   0.000  0.00  0.00           C+0
HETATM   23  C   UNK     0       0.564   2.104   0.000  0.00  0.00           C+0
HETATM   24  O   UNK     0      -0.206   3.437   0.000  0.00  0.00           O+0
HETATM   25  C   UNK     0       2.104   2.104   0.000  0.00  0.00           C+0
HETATM   26  C   UNK     0      -1.746   0.770   0.000  0.00  0.00           C+0
HETATM   27  C   UNK     0      -2.516  -0.564   0.000  0.00  0.00           C+0
HETATM   28  C   UNK     0      -4.056  -0.564   0.000  0.00  0.00           C+0
HETATM   29  C   UNK     0      -4.826   0.770   0.000  0.00  0.00           C+0
HETATM   30  O   UNK     0      -6.366   0.770   0.000  0.00  0.00           O+0
HETATM   31  C   UNK     0      -4.056   2.104   0.000  0.00  0.00           C+0
HETATM   32  C   UNK     0      -2.516   2.104   0.000  0.00  0.00           C+0
CONECT    1    2                                                            
CONECT    2    1    3                                                       
CONECT    3    2    4   25                                                  
CONECT    4    3    5   10                                                  
CONECT    5    4    6                                                       
CONECT    6    5    7                                                       
CONECT    7    6    8    9                                                  
CONECT    8    7                                                            
CONECT    9    7                                                            
CONECT   10    4   11   17                                                  
CONECT   11   10   12                                                       
CONECT   12   11   13   14   15                                             
CONECT   13   12                                                            
CONECT   14   12                                                            
CONECT   15   12   16                                                       
CONECT   16   15   17                                                       
CONECT   17   16   10   18                                                  
CONECT   18   17   19   25                                                  
CONECT   19   18   20                                                       
CONECT   20   19   21   22                                                  
CONECT   21   20                                                            
CONECT   22   20   23   26                                                  
CONECT   23   22   24   25                                                  
CONECT   24   23                                                            
CONECT   25   23    3   18                                                  
CONECT   26   22   27   32                                                  
CONECT   27   26   28                                                       
CONECT   28   27   29                                                       
CONECT   29   28   30   31                                                  
CONECT   30   29                                                            
CONECT   31   29   32                                                       
CONECT   32   31   26                                                       
MASTER        0    0    0    0    0    0    0    0   32    0   70    0
END

View in JSmol

Synonyms

Not Available

Chemical Formula

C₂₆H₂₆O₆

Average Mass

434.4880 Da

Monoisotopic Mass

434.17294 Da

IUPAC Name

4-hydroxy-3-(4-hydroxyphenyl)-5-methoxy-8,8-dimethyl-6-(3-methylbut-2-en-1-yl)-2H,8H-pyrano[2,3-f]chromen-2-one

Traditional Name

scandenin

CAS Registry Number

Not Available

SMILES

COC1=C(CC=C(C)C)C2=C(C=CC(C)(C)O2)C2=C1C(O)=C(C(=O)O2)C1=CC=C(O)C=C1

InChI Identifier

InChI=1S/C26H26O6/c1-14(2)6-11-17-22-18(12-13-26(3,4)32-22)24-20(23(17)30-5)21(28)19(25(29)31-24)15-7-9-16(27)10-8-15/h6-10,12-13,27-28H,11H2,1-5H3

InChI Key

AAKJUGSASOCUFQ-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, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 100 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 252 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 1000 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 50 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 200 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 75 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 300 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 101 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 400 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 126 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 500 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 151 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 600 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 176 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 700 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 201 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 800 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 226 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 900 MHz, D₂O, 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
Deguelia hatschbachii	Plant	KNApSAcK
Deguelia spruceana	LOTUS Database	35616633
Solori scandens	Plant	KNApSAcK

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as pyranoisoflavonoids. These are isoflavonoids that contain a pyran ring fused to either of the A, B, or C ring of the isoflavonoid skeleton.

Kingdom

Organic compounds

Super Class

Phenylpropanoids and polyketides

Class

Isoflavonoids

Sub Class

Pyranoisoflavonoids

Direct Parent

Pyranoisoflavonoids

Alternative Parents

Substituents

Pyranoisoflavonoid
Isoflav-3-enone skeleton
Hydroxyisoflavonoid
Pyranocoumarin
Angular pyranocoumarin
Pyranochromene
2,2-dimethyl-1-benzopyran
Coumarin
Benzopyran
1-benzopyran
Anisole
1-hydroxy-2-unsubstituted benzenoid
Phenol
Pyranone
Alkyl aryl ether
Monocyclic benzene moiety
Benzenoid
Pyran
Vinylogous acid
Heteroaromatic compound
Lactone
Organoheterocyclic compound
Ether
Oxacycle
Organooxygen compound
Organic oxide
Hydrocarbon derivative
Organic oxygen compound
Aromatic heteropolycyclic compound

Molecular Framework

Aromatic heteropolycyclic compounds

External Descriptors

Other Flavonoids (LMPK12160022 )

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	4.5	ALOGPS
logP	4.87	ChemAxon
logS	-5.1	ALOGPS
pKa (Strongest Acidic)	6.37	ChemAxon
pKa (Strongest Basic)	-4.6	ChemAxon
Physiological Charge	-1	ChemAxon
Hydrogen Acceptor Count	5	ChemAxon
Hydrogen Donor Count	2	ChemAxon
Polar Surface Area	85.22 Å²	ChemAxon
Rotatable Bond Count	4	ChemAxon
Refractivity	124.97 m³·mol⁻¹	ChemAxon
Polarizability	47.07 Å³	ChemAxon
Number of Rings	4	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

54676535

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

Not Available

Showing NP-Card for Scandenin (NP0056817)

MOL for NP0056817 (Scandenin)

3D MOL for NP0056817 (Scandenin)

3D SDF for NP0056817 (Scandenin)

3D-SDF for NP0056817 (Scandenin)

PDB for NP0056817 (Scandenin)

3D PDB for NP0056817 (Scandenin)

SMILES for NP0056817 (Scandenin)

INCHI for NP0056817 (Scandenin)

Structure for NP0056817 (Scandenin)

3D Structure for NP0056817 (Scandenin)