NP-MRD: Showing NP-Card for Lupinalbin F (NP0057062)

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Record Information

Version

2.0

Created at

2022-04-28 02:37:07 UTC

Updated at

2022-04-28 02:37:07 UTC

NP-MRD ID

NP0057062

Secondary Accession Numbers

None

Natural Product Identification

Common Name

Lupinalbin F

Description

Lupinalbin f belongs to the class of organic compounds known as 6-prenylated isoflavanones. These are isoflavanones featuring a C5-isoprenoid unit at the 6-position. Thus, lupinalbin F is considered to be a flavonoid lipid molecule. Lupinalbin F is found in Lupinus albus . Lupinalbin f is a very hydrophobic molecule, practically insoluble (in water), and relatively neutral.

Structure

MOL 3D MOL SDF PDB SMILES InChI


  Mrv1533004251514272D          

 31 34  0  0  0  0            999 V2000
    1.3558   -3.9816    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.1932   -3.1728    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.8123   -2.6276    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.5941   -2.8912    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.2132   -2.3459    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.0506   -1.5371    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.2688   -1.2735    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.6697   -0.9919    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.4515   -1.2554    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.0706   -0.7102    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.8524   -0.9738    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.5714   -0.5692    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    7.1784   -1.1279    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.9997   -1.0507    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.3436   -0.3008    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.8661    0.3719    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.2099    1.1219    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.7324    1.7946    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    9.0313    1.1990    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.4773   -1.7235    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    9.2987   -1.6463    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    8.1334   -2.4734    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.3120   -2.5506    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.8345   -1.8779    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.0150   -1.7826    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.3959   -2.3278    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.5585   -3.1366    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.6141   -2.0642    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.9950   -2.6095    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.1576   -3.4183    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.4114   -2.9092    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
  3  4  1  0  0  0  0
  4  5  1  0  0  0  0
  5  6  2  0  0  0  0
  6  7  1  0  0  0  0
  6  8  1  0  0  0  0
  8  9  2  0  0  0  0
  9 10  1  0  0  0  0
 10 11  1  0  0  0  0
 11 12  1  0  0  0  0
 12 13  1  0  0  0  0
 13 14  2  0  0  0  0
 14 15  1  0  0  0  0
 15 16  1  0  0  0  0
 16 17  2  0  0  0  0
 17 18  1  0  0  0  0
 17 19  1  0  0  0  0
 14 20  1  0  0  0  0
 20 21  1  0  0  0  0
 20 22  2  0  0  0  0
 22 23  1  0  0  0  0
 23 24  2  0  0  0  0
 13 24  1  0  0  0  0
 24 25  1  0  0  0  0
 11 25  2  0  0  0  0
 25 26  1  0  0  0  0
 26 27  2  0  0  0  0
 26 28  1  0  0  0  0
  9 28  1  0  0  0  0
 28 29  2  0  0  0  0
  5 29  1  0  0  0  0
 29 30  1  0  0  0  0
  2 31  1  0  0  0  0
M  END

     RDKit          3D

 55 58  0  0  0  0  0  0  0  0999 V2000
   -7.2636    1.4268   -0.3762 C   0  0  0  0  0  0  0  0  0  0  0  0
   -7.2391    0.2558    0.5225 C   0  0  0  0  0  0  0  0  0  0  0  0
   -8.2108    0.1608    1.6286 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.3449   -0.6980    0.3464 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.3243   -0.6757   -0.7271 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.9798   -0.6051   -0.1333 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.7712   -0.4440    1.2028 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.8431   -0.3365    2.0760 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4623   -0.3872    1.6688 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3791   -0.4917    0.7875 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1505   -0.4378    1.2407 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.9202   -0.5296    0.4704 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.2108   -0.5053    0.7088 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.9160   -0.6367   -0.3872 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.2639   -0.6762   -0.6699 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.2267   -0.5639    0.4731 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.3951    0.8384    0.9406 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.6014    1.4054    0.9657 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.7725    2.7967    1.4271 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.8206    0.6301    0.5332 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.7288   -0.8303   -1.9728 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.0994   -0.8541   -2.1465 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.8516   -0.9523   -3.0419 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.5057   -0.9140   -2.7606 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.0365   -0.7609   -1.4711 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7917   -0.6904   -0.8960 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4888   -0.7504   -1.4009 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6622   -0.8963   -2.6382 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5957   -0.6514   -0.5590 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8889   -0.7092   -1.0196 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.0814   -0.8742   -2.3839 O   0  0  0  0  0  0  0  0  0  0  0  0
   -8.2181    2.0045   -0.2757 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.4448    2.1111   -0.0214 H   0  0  0  0  0  0  0  0  0  0  0  0
   -7.1818    1.1809   -1.4497 H   0  0  0  0  0  0  0  0  0  0  0  0
   -7.8642    0.8758    2.4242 H   0  0  0  0  0  0  0  0  0  0  0  0
   -9.1985    0.4396    1.2577 H   0  0  0  0  0  0  0  0  0  0  0  0
   -8.2085   -0.8448    2.0941 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.3527   -1.5754    1.0021 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.4344   -1.6532   -1.2997 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.4850    0.0936   -1.4970 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.7697   -0.2197    3.0726 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3071   -0.2594    2.7282 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.7321   -1.0999    1.3371 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.1787   -1.0402    0.1996 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.5395    1.3957    1.2570 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.5139    3.4724    0.5771 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.8611    2.9931    1.6520 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.2206    3.0335    2.3520 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.8754    0.5180   -0.5511 H   0  0  0  0  0  0  0  0  0  0  0  0
    8.7389    1.2063    0.8310 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.8338   -0.3129    1.0968 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.5462   -0.9613   -3.0597 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.2131   -1.0724   -4.0571 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.7784   -1.0063   -3.5465 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.0221   -0.9223   -2.7698 H   0  0  0  0  0  0  0  0  0  0  0  0
 19 18  1  0
 18 20  1  0
 18 17  2  3
 17 16  1  0
 16 15  1  0
 15 14  2  0
 14 13  1  0
 13 12  1  0
 12 26  2  0
 26 25  1  0
 25 24  2  0
 24 23  1  0
 23 21  2  0
 21 22  1  0
 26 27  1  0
 27 28  2  0
 27 29  1  0
 29 30  2  0
 30 31  1  0
 30  6  1  0
  6  5  1  0
  5  4  1  0
  4  2  2  3
  2  1  1  0
  2  3  1  0
  6  7  2  0
  7  8  1  0
  7  9  1  0
  9 10  2  0
 10 11  1  0
 21 15  1  0
 10 29  1  0
 25 14  1  0
 11 12  1  0
 19 46  1  0
 19 47  1  0
 19 48  1  0
 20 49  1  0
 20 50  1  0
 20 51  1  0
 17 45  1  0
 16 43  1  0
 16 44  1  0
 24 54  1  0
 23 53  1  0
 22 52  1  0
 31 55  1  0
  5 39  1  0
  5 40  1  0
  4 38  1  0
  1 32  1  0
  1 33  1  0
  1 34  1  0
  3 35  1  0
  3 36  1  0
  3 37  1  0
  8 41  1  0
  9 42  1  0
M  END


  Mrv1533004251514272D          

 31 34  0  0  0  0            999 V2000
    1.3558   -3.9816    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.1932   -3.1728    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.8123   -2.6276    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.5941   -2.8912    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.2132   -2.3459    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.0506   -1.5371    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.2688   -1.2735    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.6697   -0.9919    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.4515   -1.2554    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.0706   -0.7102    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.8524   -0.9738    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.5714   -0.5692    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    7.1784   -1.1279    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.9997   -1.0507    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.3436   -0.3008    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.8661    0.3719    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.2099    1.1219    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.7324    1.7946    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    9.0313    1.1990    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.4773   -1.7235    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    9.2987   -1.6463    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    8.1334   -2.4734    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.3120   -2.5506    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.8345   -1.8779    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.0150   -1.7826    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.3959   -2.3278    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.5585   -3.1366    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.6141   -2.0642    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.9950   -2.6095    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.1576   -3.4183    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.4114   -2.9092    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
  3  4  1  0  0  0  0
  4  5  1  0  0  0  0
  5  6  2  0  0  0  0
  6  7  1  0  0  0  0
  6  8  1  0  0  0  0
  8  9  2  0  0  0  0
  9 10  1  0  0  0  0
 10 11  1  0  0  0  0
 11 12  1  0  0  0  0
 12 13  1  0  0  0  0
 13 14  2  0  0  0  0
 14 15  1  0  0  0  0
 15 16  1  0  0  0  0
 16 17  2  0  0  0  0
 17 18  1  0  0  0  0
 17 19  1  0  0  0  0
 14 20  1  0  0  0  0
 20 21  1  0  0  0  0
 20 22  2  0  0  0  0
 22 23  1  0  0  0  0
 23 24  2  0  0  0  0
 13 24  1  0  0  0  0
 24 25  1  0  0  0  0
 11 25  2  0  0  0  0
 25 26  1  0  0  0  0
 26 27  2  0  0  0  0
 26 28  1  0  0  0  0
  9 28  1  0  0  0  0
 28 29  2  0  0  0  0
  5 29  1  0  0  0  0
 29 30  1  0  0  0  0
  2 31  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0057062

> <DATABASE_NAME>
NP-MRD

> <SMILES>
CC(C)=CCC1=C2OC3=C(C2=CC=C1O)C(=O)C1=C(O)C(CC=C(C)C)=C(O)C=C1O3

> <INCHI_IDENTIFIER>
InChI=1S/C25H24O6/c1-12(2)5-7-14-18(27)11-19-21(22(14)28)23(29)20-16-9-10-17(26)15(8-6-13(3)4)24(16)31-25(20)30-19/h5-6,9-11,26-28H,7-8H2,1-4H3

> <INCHI_KEY>
WNJJWUYKQKUQED-UHFFFAOYSA-N

> <FORMULA>
C25H24O6

> <MOLECULAR_WEIGHT>
420.461

> <EXACT_MASS>
420.157288493

> <JCHEM_ACCEPTOR_COUNT>
4

> <JCHEM_ATOM_COUNT>
55

> <JCHEM_AVERAGE_POLARIZABILITY>
46.38151318344192

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
3

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
0

> <JCHEM_IUPAC>
5,7,14-trihydroxy-6,15-bis(3-methylbut-2-en-1-yl)-2,17-dioxatetracyclo[8.7.0.0³,⁸.0¹¹,¹⁶]heptadeca-1(10),3,5,7,11,13,15-heptaen-9-one

> <ALOGPS_LOGP>
5.00

> <JCHEM_LOGP>
6.404492663333334

> <ALOGPS_LOGS>
-3.90

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
4

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA>
8.319625914218726

> <JCHEM_PKA_STRONGEST_ACIDIC>
7.244641981501527

> <JCHEM_PKA_STRONGEST_BASIC>
-3.0379044634732635

> <JCHEM_POLAR_SURFACE_AREA>
100.13000000000001

> <JCHEM_REFRACTIVITY>
119.33899999999997

> <JCHEM_ROTATABLE_BOND_COUNT>
4

> <JCHEM_RULE_OF_FIVE>
0

> <ALOGPS_SOLUBILITY>
5.26e-02 g/l

> <JCHEM_TRADITIONAL_IUPAC>
lupinalbin F

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 25-APR-15   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   25-APR-15         0                                  
HETATM    1  C   UNK     0       2.531  -7.432   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0       2.227  -5.923   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0       3.383  -4.905   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0       4.842  -5.397   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0       5.998  -4.379   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0       5.694  -2.869   0.000  0.00  0.00           C+0
HETATM    7  O   UNK     0       4.235  -2.377   0.000  0.00  0.00           O+0
HETATM    8  C   UNK     0       6.850  -1.851   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0       8.309  -2.343   0.000  0.00  0.00           C+0
HETATM   10  O   UNK     0       9.465  -1.326   0.000  0.00  0.00           O+0
HETATM   11  C   UNK     0      10.925  -1.818   0.000  0.00  0.00           C+0
HETATM   12  O   UNK     0      12.267  -1.062   0.000  0.00  0.00           O+0
HETATM   13  C   UNK     0      13.400  -2.105   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0      14.933  -1.961   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0      15.575  -0.562   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0      14.683   0.694   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0      15.325   2.094   0.000  0.00  0.00           C+0
HETATM   18  C   UNK     0      14.434   3.350   0.000  0.00  0.00           C+0
HETATM   19  C   UNK     0      16.858   2.238   0.000  0.00  0.00           C+0
HETATM   20  C   UNK     0      15.824  -3.217   0.000  0.00  0.00           C+0
HETATM   21  O   UNK     0      17.357  -3.073   0.000  0.00  0.00           O+0
HETATM   22  C   UNK     0      15.182  -4.617   0.000  0.00  0.00           C+0
HETATM   23  C   UNK     0      13.649  -4.761   0.000  0.00  0.00           C+0
HETATM   24  C   UNK     0      12.758  -3.505   0.000  0.00  0.00           C+0
HETATM   25  C   UNK     0      11.228  -3.327   0.000  0.00  0.00           C+0
HETATM   26  C   UNK     0      10.072  -4.345   0.000  0.00  0.00           C+0
HETATM   27  O   UNK     0      10.376  -5.855   0.000  0.00  0.00           O+0
HETATM   28  C   UNK     0       8.613  -3.853   0.000  0.00  0.00           C+0
HETATM   29  C   UNK     0       7.457  -4.871   0.000  0.00  0.00           C+0
HETATM   30  O   UNK     0       7.761  -6.381   0.000  0.00  0.00           O+0
HETATM   31  C   UNK     0       0.768  -5.431   0.000  0.00  0.00           C+0
CONECT    1    2                                                            
CONECT    2    1    3   31                                                  
CONECT    3    2    4                                                       
CONECT    4    3    5                                                       
CONECT    5    4    6   29                                                  
CONECT    6    5    7    8                                                  
CONECT    7    6                                                            
CONECT    8    6    9                                                       
CONECT    9    8   10   28                                                  
CONECT   10    9   11                                                       
CONECT   11   10   12   25                                                  
CONECT   12   11   13                                                       
CONECT   13   12   14   24                                                  
CONECT   14   13   15   20                                                  
CONECT   15   14   16                                                       
CONECT   16   15   17                                                       
CONECT   17   16   18   19                                                  
CONECT   18   17                                                            
CONECT   19   17                                                            
CONECT   20   14   21   22                                                  
CONECT   21   20                                                            
CONECT   22   20   23                                                       
CONECT   23   22   24                                                       
CONECT   24   23   13   25                                                  
CONECT   25   24   11   26                                                  
CONECT   26   25   27   28                                                  
CONECT   27   26                                                            
CONECT   28   26    9   29                                                  
CONECT   29   28    5   30                                                  
CONECT   30   29                                                            
CONECT   31    2                                                            
MASTER        0    0    0    0    0    0    0    0   31    0   68    0
END

View in JSmol

Synonyms

Not Available

Chemical Formula

C₂₅H₂₄O₆

Average Mass

420.4610 Da

Monoisotopic Mass

420.15729 Da

IUPAC Name

5,7,14-trihydroxy-6,15-bis(3-methylbut-2-en-1-yl)-2,17-dioxatetracyclo[8.7.0.0³,⁸.0¹¹,¹⁶]heptadeca-1(10),3,5,7,11,13,15-heptaen-9-one

Traditional Name

lupinalbin F

CAS Registry Number

Not Available

SMILES

CC(C)=CCC1=C2OC3=C(C2=CC=C1O)C(=O)C1=C(O)C(CC=C(C)C)=C(O)C=C1O3

InChI Identifier

InChI=1S/C25H24O6/c1-12(2)5-7-14-18(27)11-19-21(22(14)28)23(29)20-16-9-10-17(26)15(8-6-13(3)4)24(16)31-25(20)30-19/h5-6,9-11,26-28H,7-8H2,1-4H3

InChI Key

WNJJWUYKQKUQED-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
Lupinus albus	Plant	KNApSAcK

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as 6-prenylated isoflavanones. These are isoflavanones featuring a C5-isoprenoid unit at the 6-position.

Kingdom

Organic compounds

Super Class

Phenylpropanoids and polyketides

Class

Isoflavonoids

Sub Class

Isoflavans

Direct Parent

6-prenylated isoflavanones

Alternative Parents

Substituents

6-prenylated isoflavanone
Isoflavone
Coumaronochromene
Chromone
Coumarin
Benzopyran
1-benzopyran
Benzofuran
Furopyran
Pyranone
Phenol
1-hydroxy-4-unsubstituted benzenoid
1-hydroxy-2-unsubstituted benzenoid
Benzenoid
Pyran
Heteroaromatic compound
Vinylogous acid
Furan
Oxacycle
Organoheterocyclic compound
Polyol
Hydrocarbon derivative
Organic oxygen compound
Organic oxide
Organooxygen compound
Aromatic heteropolycyclic compound

Molecular Framework

Aromatic heteropolycyclic compounds

External Descriptors

Other Flavonoids (LMPK12160006 )

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	5	ALOGPS
logP	6.4	ChemAxon
logS	-3.9	ALOGPS
pKa (Strongest Acidic)	7.24	ChemAxon
pKa (Strongest Basic)	-3	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	4	ChemAxon
Hydrogen Donor Count	3	ChemAxon
Polar Surface Area	100.13 Å²	ChemAxon
Rotatable Bond Count	4	ChemAxon
Refractivity	119.34 m³·mol⁻¹	ChemAxon
Polarizability	46.38 Å³	ChemAxon
Number of Rings	4	ChemAxon
Bioavailability	Yes	ChemAxon
Rule of Five	No	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

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

44260100

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

Not Available

Showing NP-Card for Lupinalbin F (NP0057062)

MOL for NP0057062 (Lupinalbin F)

3D MOL for NP0057062 (Lupinalbin F)

3D SDF for NP0057062 (Lupinalbin F)

3D-SDF for NP0057062 (Lupinalbin F)

PDB for NP0057062 (Lupinalbin F)

3D PDB for NP0057062 (Lupinalbin F)

SMILES for NP0057062 (Lupinalbin F)

INCHI for NP0057062 (Lupinalbin F)

Structure for NP0057062 (Lupinalbin F)

3D Structure for NP0057062 (Lupinalbin F)