NP-MRD: Showing NP-Card for 5,7,4'-Trihydroxy-5'-methoxycoumaronochromone 7-O-glucoside (NP0062758)

Jump To Section:

Identification Spectra BioTaxonomy ChemoTaxonomy Physical properties Links References XML

Record Information

Version

2.0

Created at

2022-04-28 07:19:55 UTC

Updated at

2022-04-28 07:19:55 UTC

NP-MRD ID

NP0062758

Secondary Accession Numbers

None

Natural Product Identification

Common Name

5,7,4'-Trihydroxy-5'-methoxycoumaronochromone 7-O-glucoside

Description

7,14-Dihydroxy-13-methoxy-5-{[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}-2,17-dioxatetracyclo[8.7.0.0³,⁸.0¹¹,¹⁶]Heptadeca-1(10),3,5,7,11,13,15-heptaen-9-one belongs to the class of organic compounds known as isoflavones. These are polycyclic compounds containing a 2-isoflavene skeleton which bears a ketone group at the C4 carbon atom. 5,7,4'-Trihydroxy-5'-methoxycoumaronochromone 7-O-glucoside is found in Desmodium oxyphyllum and Hylodesmum podocarpum. Based on a literature review very few articles have been published on 7,14-dihydroxy-13-methoxy-5-{[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}-2,17-dioxatetracyclo[8.7.0.0³,⁸.0¹¹,¹⁶]Heptadeca-1(10),3,5,7,11,13,15-heptaen-9-one.

Structure

MOL 3D MOL SDF PDB SMILES InChI


  Mrv1652304282209192D          

 34 38  0  0  1  0            999 V2000
    5.3198    0.1489    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.1571    0.9577    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.3754    1.2213    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.7562    0.6761    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.9189   -0.1327    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.7006   -0.3963    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.2997   -0.6780    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.5180   -0.4144    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.3553    0.3944    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.9745    0.9396    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8119    1.7485    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.5359    0.4897    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.1920   -0.2602    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.7990   -0.8190    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.3706   -0.3374    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1069    0.3353    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.2369    1.0852    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.0583    1.1624    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2406    1.7580    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0620    1.6808    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9283    0.2581    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.2128    2.0301    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    6.1015   -0.1146    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    6.7207    0.4306    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    6.5581    1.2394    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    7.1772    1.7846    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    7.9590    1.5211    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    8.1216    0.7123    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    7.5024    0.1670    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    8.9033    0.4487    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    9.5225    0.9939    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    8.5781    2.0663    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    7.0146    2.5935    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.7763    1.5030    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  2  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  2  0  0  0  0
  1  6  1  0  0  0  0
  5  7  1  0  0  0  0
  7  8  1  0  0  0  0
  8  9  2  0  0  0  0
  9 10  1  0  0  0  0
  4 10  1  0  0  0  0
 10 11  2  0  0  0  0
  9 12  1  0  0  0  0
 12 13  1  0  0  0  0
 13 14  1  0  0  0  0
  8 14  1  0  0  0  0
 13 15  2  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
 12 18  2  0  0  0  0
 17 19  1  0  0  0  0
 19 20  1  0  0  0  0
 16 21  1  0  0  0  0
  3 22  1  0  0  0  0
  1 23  1  0  0  0  0
 24 23  1  1  0  0  0
 24 25  1  0  0  0  0
 25 26  1  0  0  0  0
 26 27  1  0  0  0  0
 27 28  1  0  0  0  0
 28 29  1  0  0  0  0
 24 29  1  0  0  0  0
 28 30  1  1  0  0  0
 30 31  1  0  0  0  0
 27 32  1  6  0  0  0
 26 33  1  1  0  0  0
 25 34  1  6  0  0  0
M  END

     RDKit          3D

 54 58  0  0  0  0  0  0  0  0999 V2000
    8.2112    1.7754    0.4266 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.3265    0.5995   -0.3082 O   0  0  0  0  0  0  0  0  0  0  0  0
    7.2932   -0.1948   -0.7247 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.9781    0.1089   -0.4426 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.9471   -0.7275   -0.8852 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.1901   -1.8736   -1.6106 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.5217   -2.1685   -1.8884 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.5222   -1.3441   -1.4510 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.8436   -1.6636   -1.7433 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.0492   -2.4316   -1.8733 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.0534   -1.7295   -1.3681 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.7507   -1.8638   -1.3575 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.9257   -1.0112   -0.7716 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4332   -1.2571   -0.8259 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3607   -0.3979   -0.2286 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6749   -0.7709   -0.3647 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.7208   -0.0302    0.1677 C   0  0  2  0  0  0  0  0  0  0  0  0
   -4.3883   -0.8817    1.0762 O   0  0  0  0  0  0  0  0  0  0  0  0
   -5.3270   -0.1477    1.8096 C   0  0  2  0  0  0  0  0  0  0  0  0
   -5.8297   -1.0268    2.9227 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.7776   -0.3551    3.7024 O   0  0  0  0  0  0  0  0  0  0  0  0
   -6.4490    0.3450    0.9430 C   0  0  1  0  0  0  0  0  0  0  0  0
   -7.1496    1.3169    1.6746 O   0  0  0  0  0  0  0  0  0  0  0  0
   -5.8838    1.0470   -0.2741 C   0  0  2  0  0  0  0  0  0  0  0  0
   -6.8793    1.3043   -1.2131 O   0  0  0  0  0  0  0  0  0  0  0  0
   -4.7564    0.2761   -0.9136 C   0  0  1  0  0  0  0  0  0  0  0  0
   -4.2256    1.0430   -1.9306 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8852    0.7075    0.4201 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.4935    0.9404    0.4650 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.9418    2.0515    1.1191 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.3955    0.1071   -0.1145 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.7618    0.2993   -0.0939 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.2356    1.2900    0.4840 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.5863   -0.6187   -0.7202 C   0  0  0  0  0  0  0  0  0  0  0  0
    9.0752    2.0258    1.0394 H   0  0  0  0  0  0  0  0  0  0  0  0
    8.0669    2.6206   -0.3044 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.3175    1.8089    1.0810 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.7085    0.9844    0.1177 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.7084   -3.0622   -2.4539 H   0  0  0  0  0  0  0  0  0  0  0  0
    9.1368   -2.4661   -2.2601 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7545   -2.1521   -1.3557 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.4772    0.8766    0.7105 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.7660    0.7219    2.2311 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.2464   -1.9577    2.4905 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.9740   -1.2648    3.5751 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.3982    0.5524    3.8753 H   0  0  0  0  0  0  0  0  0  0  0  0
   -7.0828   -0.5110    0.6823 H   0  0  0  0  0  0  0  0  0  0  0  0
   -7.4558    2.0527    1.0776 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.5057    2.0363    0.0735 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.7186    0.8549   -2.0716 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.1265   -0.7022   -1.2638 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.5399    0.7757   -2.8194 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5732    1.3799    0.8849 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.3197    2.7087    1.5698 H   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0
  2  3  1  0
  3  8  2  0
  8  9  1  0
  8  7  1  0
  7  6  2  0
  6 10  1  0
 10 11  1  0
 11 34  2  0
 34  5  1  0
  5  4  2  0
 34 32  1  0
 32 33  2  0
 32 31  1  0
 31 29  2  0
 29 30  1  0
 29 28  1  0
 28 15  2  0
 15 16  1  0
 16 17  1  0
 17 18  1  0
 18 19  1  0
 19 20  1  0
 20 21  1  0
 19 22  1  0
 22 23  1  0
 22 24  1  0
 24 25  1  0
 24 26  1  0
 26 27  1  0
 15 14  1  0
 14 13  2  0
 13 12  1  0
  4  3  1  0
 13 31  1  0
  5  6  1  0
 26 17  1  0
 12 11  1  0
  1 35  1  0
  1 36  1  0
  1 37  1  0
  9 40  1  0
  7 39  1  0
  4 38  1  0
 30 54  1  0
 28 53  1  0
 17 42  1  1
 19 43  1  1
 20 44  1  0
 20 45  1  0
 21 46  1  0
 22 47  1  6
 23 48  1  0
 24 49  1  1
 25 50  1  0
 26 51  1  6
 27 52  1  0
 14 41  1  0
M  END


  Mrv1652304282209192D          

 34 38  0  0  1  0            999 V2000
    5.3198    0.1489    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.1571    0.9577    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.3754    1.2213    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.7562    0.6761    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.9189   -0.1327    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.7006   -0.3963    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.2997   -0.6780    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.5180   -0.4144    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.3553    0.3944    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.9745    0.9396    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8119    1.7485    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.5359    0.4897    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.1920   -0.2602    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.7990   -0.8190    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.3706   -0.3374    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1069    0.3353    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.2369    1.0852    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.0583    1.1624    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2406    1.7580    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0620    1.6808    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9283    0.2581    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.2128    2.0301    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    6.1015   -0.1146    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    6.7207    0.4306    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    6.5581    1.2394    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    7.1772    1.7846    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    7.9590    1.5211    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    8.1216    0.7123    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    7.5024    0.1670    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    8.9033    0.4487    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    9.5225    0.9939    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    8.5781    2.0663    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    7.0146    2.5935    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.7763    1.5030    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  2  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  2  0  0  0  0
  1  6  1  0  0  0  0
  5  7  1  0  0  0  0
  7  8  1  0  0  0  0
  8  9  2  0  0  0  0
  9 10  1  0  0  0  0
  4 10  1  0  0  0  0
 10 11  2  0  0  0  0
  9 12  1  0  0  0  0
 12 13  1  0  0  0  0
 13 14  1  0  0  0  0
  8 14  1  0  0  0  0
 13 15  2  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
 12 18  2  0  0  0  0
 17 19  1  0  0  0  0
 19 20  1  0  0  0  0
 16 21  1  0  0  0  0
  3 22  1  0  0  0  0
  1 23  1  0  0  0  0
 24 23  1  1  0  0  0
 24 25  1  0  0  0  0
 25 26  1  0  0  0  0
 26 27  1  0  0  0  0
 27 28  1  0  0  0  0
 28 29  1  0  0  0  0
 24 29  1  0  0  0  0
 28 30  1  1  0  0  0
 30 31  1  0  0  0  0
 27 32  1  6  0  0  0
 26 33  1  1  0  0  0
 25 34  1  6  0  0  0
M  END
> <DATABASE_ID>
NP0062758

> <DATABASE_NAME>
NP-MRD

> <SMILES>
COC1=C(O)C=C2OC3=C(C2=C1)C(=O)C1=C(O)C=C(O[C@@H]2O[C@H](CO)[C@@H](O)[C@H](O)[C@H]2O)C=C1O3

> <INCHI_IDENTIFIER>
InChI=1S/C22H20O12/c1-30-12-4-8-11(5-9(12)24)32-21-15(8)18(27)16-10(25)2-7(3-13(16)33-21)31-22-20(29)19(28)17(26)14(6-23)34-22/h2-5,14,17,19-20,22-26,28-29H,6H2,1H3/t14-,17-,19+,20-,22-/m1/s1

> <INCHI_KEY>
VVSJHRJAOJYBFU-UDEBZQQRSA-N

> <FORMULA>
C22H20O12

> <MOLECULAR_WEIGHT>
476.39

> <EXACT_MASS>
476.095476084

> <JCHEM_ACCEPTOR_COUNT>
10

> <JCHEM_ATOM_COUNT>
54

> <JCHEM_AVERAGE_POLARIZABILITY>
46.09458769123104

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
6

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
1

> <JCHEM_IUPAC>
7,14-dihydroxy-13-methoxy-5-{[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}-2,17-dioxatetracyclo[8.7.0.0^{3,8}.0^{11,16}]heptadeca-1(10),3,5,7,11,13,15-heptaen-9-one

> <ALOGPS_LOGP>
0.68

> <JCHEM_LOGP>
0.5216193056666663

> <ALOGPS_LOGS>
-2.16

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
5

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA>
8.921719874047598

> <JCHEM_PKA_STRONGEST_ACIDIC>
8.10589606189724

> <JCHEM_PKA_STRONGEST_BASIC>
-2.981092343758667

> <JCHEM_POLAR_SURFACE_AREA>
188.51

> <JCHEM_REFRACTIVITY>
109.46099999999998

> <JCHEM_ROTATABLE_BOND_COUNT>
4

> <JCHEM_RULE_OF_FIVE>
0

> <ALOGPS_SOLUBILITY>
3.33e+00 g/l

> <JCHEM_TRADITIONAL_IUPAC>
7,14-dihydroxy-13-methoxy-5-{[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}-2,17-dioxatetracyclo[8.7.0.0^{3,8}.0^{11,16}]heptadeca-1(10),3,5,7,11,13,15-heptaen-9-one

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 28-APR-22   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   28-APR-22         0                                  
HETATM    1  C   UNK     0       9.930   0.278   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0       9.627   1.788   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0       8.167   2.280   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0       7.012   1.262   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0       7.315  -0.248   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0       8.774  -0.740   0.000  0.00  0.00           C+0
HETATM    7  O   UNK     0       6.159  -1.266   0.000  0.00  0.00           O+0
HETATM    8  C   UNK     0       4.700  -0.774   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0       4.397   0.736   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0       5.552   1.754   0.000  0.00  0.00           C+0
HETATM   11  O   UNK     0       5.249   3.264   0.000  0.00  0.00           O+0
HETATM   12  C   UNK     0       2.867   0.914   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0       2.225  -0.486   0.000  0.00  0.00           C+0
HETATM   14  O   UNK     0       3.358  -1.529   0.000  0.00  0.00           O+0
HETATM   15  C   UNK     0       0.692  -0.630   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0      -0.200   0.626   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0       0.442   2.026   0.000  0.00  0.00           C+0
HETATM   18  C   UNK     0       1.976   2.170   0.000  0.00  0.00           C+0
HETATM   19  O   UNK     0      -0.449   3.282   0.000  0.00  0.00           O+0
HETATM   20  C   UNK     0      -1.982   3.138   0.000  0.00  0.00           C+0
HETATM   21  O   UNK     0      -1.733   0.482   0.000  0.00  0.00           O+0
HETATM   22  O   UNK     0       7.864   3.790   0.000  0.00  0.00           O+0
HETATM   23  O   UNK     0      11.390  -0.214   0.000  0.00  0.00           O+0
HETATM   24  C   UNK     0      12.545   0.804   0.000  0.00  0.00           C+0
HETATM   25  C   UNK     0      12.242   2.314   0.000  0.00  0.00           C+0
HETATM   26  C   UNK     0      13.397   3.331   0.000  0.00  0.00           C+0
HETATM   27  C   UNK     0      14.857   2.839   0.000  0.00  0.00           C+0
HETATM   28  C   UNK     0      15.160   1.330   0.000  0.00  0.00           C+0
HETATM   29  O   UNK     0      14.005   0.312   0.000  0.00  0.00           O+0
HETATM   30  C   UNK     0      16.620   0.838   0.000  0.00  0.00           C+0
HETATM   31  O   UNK     0      17.775   1.855   0.000  0.00  0.00           O+0
HETATM   32  O   UNK     0      16.012   3.857   0.000  0.00  0.00           O+0
HETATM   33  O   UNK     0      13.094   4.841   0.000  0.00  0.00           O+0
HETATM   34  O   UNK     0      10.782   2.806   0.000  0.00  0.00           O+0
CONECT    1    2    6   23                                                  
CONECT    2    1    3                                                       
CONECT    3    2    4   22                                                  
CONECT    4    3    5   10                                                  
CONECT    5    4    6    7                                                  
CONECT    6    5    1                                                       
CONECT    7    5    8                                                       
CONECT    8    7    9   14                                                  
CONECT    9    8   10   12                                                  
CONECT   10    9    4   11                                                  
CONECT   11   10                                                            
CONECT   12    9   13   18                                                  
CONECT   13   12   14   15                                                  
CONECT   14   13    8                                                       
CONECT   15   13   16                                                       
CONECT   16   15   17   21                                                  
CONECT   17   16   18   19                                                  
CONECT   18   17   12                                                       
CONECT   19   17   20                                                       
CONECT   20   19                                                            
CONECT   21   16                                                            
CONECT   22    3                                                            
CONECT   23    1   24                                                       
CONECT   24   23   25   29                                                  
CONECT   25   24   26   34                                                  
CONECT   26   25   27   33                                                  
CONECT   27   26   28   32                                                  
CONECT   28   27   29   30                                                  
CONECT   29   28   24                                                       
CONECT   30   28   31                                                       
CONECT   31   30                                                            
CONECT   32   27                                                            
CONECT   33   26                                                            
CONECT   34   25                                                            
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

7,14-dihydroxy-13-methoxy-5-{[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}-2,17-dioxatetracyclo[8.7.0.0^{3,8}.0^{11,16}]heptadeca-1(10),3,5,7,11,13,15-heptaen-9-one

Traditional Name

7,14-dihydroxy-13-methoxy-5-{[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}-2,17-dioxatetracyclo[8.7.0.0^{3,8}.0^{11,16}]heptadeca-1(10),3,5,7,11,13,15-heptaen-9-one

CAS Registry Number

Not Available

SMILES

COC1=C(O)C=C2OC3=C(C2=C1)C(=O)C1=C(O)C=C(O[C@@H]2O[C@H](CO)[C@@H](O)[C@H](O)[C@H]2O)C=C1O3

InChI Identifier

InChI=1S/C22H20O12/c1-30-12-4-8-11(5-9(12)24)32-21-15(8)18(27)16-10(25)2-7(3-13(16)33-21)31-22-20(29)19(28)17(26)14(6-23)34-22/h2-5,14,17,19-20,22-26,28-29H,6H2,1H3/t14-,17-,19+,20-,22-/m1/s1

InChI Key

VVSJHRJAOJYBFU-UDEBZQQRSA-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
Desmodium oxyphyllum	Plant	KNApSAcK
Desmodium podocarpum	LOTUS Database	35616633

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as isoflavones. These are polycyclic compounds containing a 2-isoflavene skeleton which bears a ketone group at the C4 carbon atom.

Kingdom

Organic compounds

Super Class

Phenylpropanoids and polyketides

Class

Isoflavonoids

Sub Class

Isoflav-2-enes

Direct Parent

Isoflavones

Alternative Parents

Substituents

Isoflavone
Coumaronochromene
Phenolic glycoside
Hexose monosaccharide
O-glycosyl compound
Chromone
Coumarin
Glycosyl compound
Benzopyran
1-benzopyran
Benzofuran
Furopyran
Anisole
1-hydroxy-4-unsubstituted benzenoid
1-hydroxy-2-unsubstituted benzenoid
Alkyl aryl ether
Pyranone
Oxane
Monosaccharide
Pyran
Benzenoid
Heteroaromatic compound
Furan
Vinylogous acid
Secondary alcohol
Ether
Organoheterocyclic compound
Oxacycle
Acetal
Polyol
Organic oxygen compound
Alcohol
Hydrocarbon derivative
Organic oxide
Primary alcohol
Organooxygen 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	0.68	ALOGPS
logP	0.52	ChemAxon
logS	-2.2	ALOGPS
pKa (Strongest Acidic)	8.11	ChemAxon
pKa (Strongest Basic)	-3	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	10	ChemAxon
Hydrogen Donor Count	6	ChemAxon
Polar Surface Area	188.51 Å²	ChemAxon
Rotatable Bond Count	4	ChemAxon
Refractivity	109.46 m³·mol⁻¹	ChemAxon
Polarizability	46.09 Å³	ChemAxon
Number of Rings	5	ChemAxon
Bioavailability	Yes	ChemAxon
Rule of Five	No	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

15126299

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

Not Available

Showing NP-Card for 5,7,4'-Trihydroxy-5'-methoxycoumaronochromone 7-O-glucoside (NP0062758)

MOL for NP0062758 (5,7,4'-Trihydroxy-5'-methoxycoumaronochromone 7-O-glucoside)

3D MOL for NP0062758 (5,7,4'-Trihydroxy-5'-methoxycoumaronochromone 7-O-glucoside)

3D SDF for NP0062758 (5,7,4'-Trihydroxy-5'-methoxycoumaronochromone 7-O-glucoside)

3D-SDF for NP0062758 (5,7,4'-Trihydroxy-5'-methoxycoumaronochromone 7-O-glucoside)

PDB for NP0062758 (5,7,4'-Trihydroxy-5'-methoxycoumaronochromone 7-O-glucoside)

3D PDB for NP0062758 (5,7,4'-Trihydroxy-5'-methoxycoumaronochromone 7-O-glucoside)

SMILES for NP0062758 (5,7,4'-Trihydroxy-5'-methoxycoumaronochromone 7-O-glucoside)

INCHI for NP0062758 (5,7,4'-Trihydroxy-5'-methoxycoumaronochromone 7-O-glucoside)

Structure for NP0062758 (5,7,4'-Trihydroxy-5'-methoxycoumaronochromone 7-O-glucoside)

3D Structure for NP0062758 (5,7,4'-Trihydroxy-5'-methoxycoumaronochromone 7-O-glucoside)