NP-MRD: Showing NP-Card for semiglabrin (NP0166563)

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Record Information

Version

2.0

Created at

2022-09-03 01:58:11 UTC

Updated at

2022-09-03 01:58:11 UTC

NP-MRD ID

NP0166563

Secondary Accession Numbers

None

Natural Product Identification

Common Name

semiglabrin

Description

Semiglabrin belongs to the class of organic compounds known as 8-prenylated flavones. These are flavones that features a C5-isoprenoid substituent at the 8-position. Thus, semiglabrin is considered to be a flavonoid lipid molecule. semiglabrin is found in Indigofera tinctoria, Tephrosia nubica and Tephrosia purpurea. Semiglabrin is a very hydrophobic molecule, practically insoluble (in water), and relatively neutral.

Structure

MOL 3D MOL SDF PDB SMILES InChI


  Mrv1533004191514422D          

 29 33  0  0  0  0            999 V2000
    4.3482   -2.9208    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.9474   -2.1997    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.1225   -2.1863    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.3715   -1.4921    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.9707   -0.7710    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.3186   -0.0229    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.7146    0.5391    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.0624    1.2872    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.8814    1.1876    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.5034    1.7295    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.2837    1.4618    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.4421    0.6521    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.2224    0.3844    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.8444    0.9263    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    7.3807   -0.4253    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.7587   -0.9672    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.9784   -0.6995    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.8200    0.1102    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.0397    0.3779    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.9170   -1.7769    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.6974   -2.0446    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.8557   -2.8543    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.2337   -3.3962    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.4533   -3.1285    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.2950   -2.3188    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.9935    0.1383    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.1518   -0.6713    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.3657   -0.9217    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.9587   -1.4734    0.0000 C   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
  2  4  1  0  0  0  0
  4  5  1  0  0  0  0
  5  6  1  0  0  0  0
  6  7  1  0  0  0  0
  7  8  1  0  0  0  0
  8  9  1  0  0  0  0
  9 10  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
 13 15  1  0  0  0  0
 15 16  2  0  0  0  0
 16 17  1  0  0  0  0
 17 18  1  0  0  0  0
 12 18  1  0  0  0  0
 18 19  2  0  0  0  0
  6 19  1  0  0  0  0
  9 19  1  0  0  0  0
 16 20  1  0  0  0  0
 20 21  2  0  0  0  0
 21 22  1  0  0  0  0
 22 23  2  0  0  0  0
 23 24  1  0  0  0  0
 24 25  2  0  0  0  0
 20 25  1  0  0  0  0
  7 26  1  0  0  0  0
 26 27  1  0  0  0  0
  5 27  1  0  0  0  0
 27 28  1  0  0  0  0
 27 29  1  0  0  0  0
M  END

     RDKit          3D

 49 53  0  0  0  0  0  0  0  0999 V2000
   -0.7360    0.0082   -3.4155 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3709    0.2818   -2.1018 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7443    1.4631   -1.8826 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5514   -0.7293   -1.1374 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1582   -0.3596    0.0596 C   0  0  2  0  0  0  0  0  0  0  0  0
   -1.3277   -0.6375    1.2836 C   0  0  1  0  0  0  0  0  0  0  0  0
   -0.6417    0.5779    1.7057 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5093    1.2970    2.5004 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0711    2.4979    3.0159 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.1936    2.9778    2.7536 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.0573    2.2506    1.9561 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.3269    2.6645    1.6530 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.7328    3.7406    2.1093 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.0928    1.8331    0.8364 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.6389    0.6391    0.3316 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.4415   -0.2301   -0.5229 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.7234    0.0571   -0.9055 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.4822   -0.7795   -1.7220 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.9131   -1.9520   -2.1647 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.6228   -2.2742   -1.7990 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.9060   -1.4275   -0.9946 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.3951    0.2959    0.6650 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.6437    1.0469    1.4282 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7129    0.5727    2.5938 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4060   -0.8046    2.3305 C   0  0  1  0  0  0  0  0  0  0  0  0
   -3.4267   -1.4495    1.6872 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.4279   -1.1122    0.3628 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.6505   -0.2832    0.0417 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.4596   -2.3203   -0.5561 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5369    0.0718   -4.1816 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0638    0.8916   -3.6227 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1747   -0.9274   -3.4250 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4330    0.7354    0.0983 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6836   -1.5232    1.1859 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7133    3.0822    3.6345 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.5570    3.9138    3.1460 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.0965    2.1735    0.6046 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.1761    0.9662   -0.5672 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.4770   -0.5248   -2.0003 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.5004   -2.5999   -2.7969 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.2179   -3.2001   -2.1677 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.8988   -1.6560   -0.6957 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0369   -1.3158    3.2192 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.1385    0.1048    0.9708 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.4041   -0.8803   -0.5170 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.3358    0.5670   -0.6187 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5598   -2.9298   -0.3620 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.4160   -1.9282   -1.5885 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.4035   -2.8653   -0.4282 H   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0
  2  3  2  0
  2  4  1  0
  4  5  1  0
  5  6  1  0
  6 25  1  0
 25 24  1  0
 24  8  1  0
  8  9  2  0
  9 10  1  0
 10 11  2  0
 11 12  1  0
 12 13  2  0
 12 14  1  0
 14 15  2  0
 15 22  1  0
 22 23  1  0
 23  7  2  0
 15 16  1  0
 16 17  2  0
 17 18  1  0
 18 19  2  0
 19 20  1  0
 20 21  2  0
 25 26  1  0
 26 27  1  0
 27 28  1  0
 27 29  1  0
 27  5  1  0
  7  6  1  0
 21 16  1  0
  7  8  1  0
 23 11  1  0
  1 30  1  0
  1 31  1  0
  1 32  1  0
  5 33  1  6
  6 34  1  6
 25 43  1  1
  9 35  1  0
 10 36  1  0
 14 37  1  0
 17 38  1  0
 18 39  1  0
 19 40  1  0
 20 41  1  0
 21 42  1  0
 28 44  1  0
 28 45  1  0
 28 46  1  0
 29 47  1  0
 29 48  1  0
 29 49  1  0
M  END


  Mrv1533004191514422D          

 29 33  0  0  0  0            999 V2000
    4.3482   -2.9208    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.9474   -2.1997    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.1225   -2.1863    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.3715   -1.4921    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.9707   -0.7710    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.3186   -0.0229    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.7146    0.5391    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.0624    1.2872    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.8814    1.1876    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.5034    1.7295    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.2837    1.4618    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.4421    0.6521    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.2224    0.3844    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.8444    0.9263    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    7.3807   -0.4253    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.7587   -0.9672    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.9784   -0.6995    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.8200    0.1102    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.0397    0.3779    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.9170   -1.7769    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.6974   -2.0446    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.8557   -2.8543    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.2337   -3.3962    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.4533   -3.1285    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.2950   -2.3188    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.9935    0.1383    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.1518   -0.6713    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.3657   -0.9217    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.9587   -1.4734    0.0000 C   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
  2  4  1  0  0  0  0
  4  5  1  0  0  0  0
  5  6  1  0  0  0  0
  6  7  1  0  0  0  0
  7  8  1  0  0  0  0
  8  9  1  0  0  0  0
  9 10  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
 13 15  1  0  0  0  0
 15 16  2  0  0  0  0
 16 17  1  0  0  0  0
 17 18  1  0  0  0  0
 12 18  1  0  0  0  0
 18 19  2  0  0  0  0
  6 19  1  0  0  0  0
  9 19  1  0  0  0  0
 16 20  1  0  0  0  0
 20 21  2  0  0  0  0
 21 22  1  0  0  0  0
 22 23  2  0  0  0  0
 23 24  1  0  0  0  0
 24 25  2  0  0  0  0
 20 25  1  0  0  0  0
  7 26  1  0  0  0  0
 26 27  1  0  0  0  0
  5 27  1  0  0  0  0
 27 28  1  0  0  0  0
 27 29  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0166563

> <DATABASE_NAME>
NP-MRD

> <SMILES>
CC(=O)OC1C2C(OC3=CC=C4C(=O)C=C(OC4=C23)C2=CC=CC=C2)OC1(C)C

> <INCHI_IDENTIFIER>
InChI=1S/C23H20O6/c1-12(24)26-21-19-18-16(28-22(19)29-23(21,2)3)10-9-14-15(25)11-17(27-20(14)18)13-7-5-4-6-8-13/h4-11,19,21-22H,1-3H3

> <INCHI_KEY>
XTIQPKJOGKMOSY-UHFFFAOYSA-N

> <FORMULA>
C23H20O6

> <MOLECULAR_WEIGHT>
392.407

> <EXACT_MASS>
392.125988364

> <JCHEM_ACCEPTOR_COUNT>
5

> <JCHEM_ATOM_COUNT>
49

> <JCHEM_AVERAGE_POLARIZABILITY>
40.536289982706364

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
0

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
1

> <JCHEM_IUPAC>
14,14-dimethyl-6-oxo-4-phenyl-3,11,13-trioxatetracyclo[8.6.0.0²,⁷.0¹²,¹⁶]hexadeca-1,4,7,9-tetraen-15-yl acetate

> <ALOGPS_LOGP>
3.92

> <JCHEM_LOGP>
3.2300467590000013

> <ALOGPS_LOGS>
-4.76

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
5

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA_STRONGEST_ACIDIC>
15.749052652625576

> <JCHEM_PKA_STRONGEST_BASIC>
-4.259089322321807

> <JCHEM_POLAR_SURFACE_AREA>
71.06

> <JCHEM_REFRACTIVITY>
104.52950000000004

> <JCHEM_ROTATABLE_BOND_COUNT>
3

> <JCHEM_RULE_OF_FIVE>
1

> <ALOGPS_SOLUBILITY>
6.83e-03 g/l

> <JCHEM_TRADITIONAL_IUPAC>
semiglabrin

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 19-APR-15   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   19-APR-15         0                                  
HETATM    1  C   UNK     0       8.117  -5.452   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0       7.368  -4.106   0.000  0.00  0.00           C+0
HETATM    3  O   UNK     0       5.829  -4.081   0.000  0.00  0.00           O+0
HETATM    4  O   UNK     0       8.160  -2.785   0.000  0.00  0.00           O+0
HETATM    5  C   UNK     0       7.412  -1.439   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0       8.061  -0.043   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0       6.934   1.006   0.000  0.00  0.00           C+0
HETATM    8  O   UNK     0       7.583   2.403   0.000  0.00  0.00           O+0
HETATM    9  C   UNK     0       9.112   2.217   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0      10.273   3.228   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0      11.730   2.729   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0      12.025   1.217   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0      13.482   0.718   0.000  0.00  0.00           C+0
HETATM   14  O   UNK     0      14.643   1.729   0.000  0.00  0.00           O+0
HETATM   15  C   UNK     0      13.777  -0.794   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0      12.616  -1.805   0.000  0.00  0.00           C+0
HETATM   17  O   UNK     0      11.160  -1.306   0.000  0.00  0.00           O+0
HETATM   18  C   UNK     0      10.864   0.206   0.000  0.00  0.00           C+0
HETATM   19  C   UNK     0       9.407   0.705   0.000  0.00  0.00           C+0
HETATM   20  C   UNK     0      12.912  -3.317   0.000  0.00  0.00           C+0
HETATM   21  C   UNK     0      14.368  -3.817   0.000  0.00  0.00           C+0
HETATM   22  C   UNK     0      14.664  -5.328   0.000  0.00  0.00           C+0
HETATM   23  C   UNK     0      13.503  -6.340   0.000  0.00  0.00           C+0
HETATM   24  C   UNK     0      12.046  -5.840   0.000  0.00  0.00           C+0
HETATM   25  C   UNK     0      11.751  -4.328   0.000  0.00  0.00           C+0
HETATM   26  O   UNK     0       5.588   0.258   0.000  0.00  0.00           O+0
HETATM   27  C   UNK     0       5.883  -1.253   0.000  0.00  0.00           C+0
HETATM   28  C   UNK     0       4.416  -1.720   0.000  0.00  0.00           C+0
HETATM   29  C   UNK     0       5.523  -2.750   0.000  0.00  0.00           C+0
CONECT    1    2                                                            
CONECT    2    1    3    4                                                  
CONECT    3    2                                                            
CONECT    4    2    5                                                       
CONECT    5    4    6   27                                                  
CONECT    6    5    7   19                                                  
CONECT    7    6    8   26                                                  
CONECT    8    7    9                                                       
CONECT    9    8   10   19                                                  
CONECT   10    9   11                                                       
CONECT   11   10   12                                                       
CONECT   12   11   13   18                                                  
CONECT   13   12   14   15                                                  
CONECT   14   13                                                            
CONECT   15   13   16                                                       
CONECT   16   15   17   20                                                  
CONECT   17   16   18                                                       
CONECT   18   17   12   19                                                  
CONECT   19   18    6    9                                                  
CONECT   20   16   21   25                                                  
CONECT   21   20   22                                                       
CONECT   22   21   23                                                       
CONECT   23   22   24                                                       
CONECT   24   23   25                                                       
CONECT   25   24   20                                                       
CONECT   26    7   27                                                       
CONECT   27   26    5   28   29                                             
CONECT   28   27                                                            
CONECT   29   27                                                            
MASTER        0    0    0    0    0    0    0    0   29    0   66    0
END

View in JSmol

Synonyms

Value	Source
Pseudosemiglabrin, (7aalpha,10alpha,10aalpha)-(-)-isomer	MeSH
Pseudosemiglabrin	MeSH

Chemical Formula

C₂₃H₂₀O₆

Average Mass

392.4070 Da

Monoisotopic Mass

392.12599 Da

IUPAC Name

14,14-dimethyl-6-oxo-4-phenyl-3,11,13-trioxatetracyclo[8.6.0.0²,⁷.0¹²,¹⁶]hexadeca-1,4,7,9-tetraen-15-yl acetate

Traditional Name

semiglabrin

CAS Registry Number

Not Available

SMILES

CC(=O)OC1C2C(OC3=CC=C4C(=O)C=C(OC4=C23)C2=CC=CC=C2)OC1(C)C

InChI Identifier

InChI=1S/C23H20O6/c1-12(24)26-21-19-18-16(28-22(19)29-23(21,2)3)10-9-14-15(25)11-17(27-20(14)18)13-7-5-4-6-8-13/h4-11,19,21-22H,1-3H3

InChI Key

XTIQPKJOGKMOSY-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
Indigofera tinctoria	LOTUS Database	35616633
Tephrosia nubica	LOTUS Database	35616633
Tephrosia purpurea	LOTUS Database	35616633

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as 8-prenylated flavones. These are flavones that features a C5-isoprenoid substituent at the 8-position.

Kingdom

Organic compounds

Super Class

Phenylpropanoids and polyketides

Class

Flavonoids

Sub Class

Flavones

Direct Parent

8-prenylated flavones

Alternative Parents

Substituents

8-prenylated flavone
Chromone
Benzopyran
1-benzopyran
Coumaran
Pyranone
Monocyclic benzene moiety
Monosaccharide
Benzenoid
Pyran
Heteroaromatic compound
Tetrahydrofuran
Carboxylic acid ester
Oxacycle
Monocarboxylic acid or derivatives
Acetal
Carboxylic acid derivative
Organoheterocyclic compound
Organooxygen compound
Hydrocarbon derivative
Carbonyl group
Organic oxide
Organic oxygen compound
Aromatic heteropolycyclic compound

Molecular Framework

Aromatic heteropolycyclic compounds

External Descriptors

Flavones and Flavonols (LMPK12110016 )

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	3.92	ALOGPS
logP	3.23	ChemAxon
logS	-4.8	ALOGPS
pKa (Strongest Acidic)	15.75	ChemAxon
pKa (Strongest Basic)	-4.3	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	5	ChemAxon
Hydrogen Donor Count	0	ChemAxon
Polar Surface Area	71.06 Å²	ChemAxon
Rotatable Bond Count	3	ChemAxon
Refractivity	104.53 m³·mol⁻¹	ChemAxon
Polarizability	40.54 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

353369

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

LOTUS database [Link]

Showing NP-Card for semiglabrin (NP0166563)

MOL for NP0166563 (semiglabrin)

3D MOL for NP0166563 (semiglabrin)

3D SDF for NP0166563 (semiglabrin)

3D-SDF for NP0166563 (semiglabrin)

PDB for NP0166563 (semiglabrin)

3D PDB for NP0166563 (semiglabrin)

SMILES for NP0166563 (semiglabrin)

INCHI for NP0166563 (semiglabrin)

Structure for NP0166563 (semiglabrin)

3D Structure for NP0166563 (semiglabrin)