NP-MRD: Showing NP-Card for Preussochromone E (NP0010644)

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Record Information

Version

2.0

Created at

2021-01-05 20:05:40 UTC

Updated at

2021-07-15 17:06:40 UTC

NP-MRD ID

NP0010644

Secondary Accession Numbers

None

Natural Product Identification

Common Name

Preussochromone E

Provided By

NPAtlas

Description

Preussochromone E belongs to the class of organic compounds known as chromones. Chromones are compounds containing a benzopyran-4-one moiety. Preussochromone E is found in Preussia africana. Based on a literature review very few articles have been published on Preussochromone E.

Structure

MOL 3D MOL SDF 3D SDF PDB SMILES InChI


  Mrv1652306242107393D          

 38 40  0  0  0  0            999 V2000
   -3.8065   -2.5298   -0.4658 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.2076   -1.5166    0.3365 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2045   -0.6931   -0.1288 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8108   -0.8529   -1.3114 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5755    0.3535    0.6774 C   0  0  2  0  0  0  0  0  0  0  0  0
   -2.1188    0.4133    1.9776 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8355    1.7475    0.0855 C   0  0  1  0  0  0  0  0  0  0  0  0
   -2.7515    2.4619    0.8058 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4621    2.3896    0.0380 C   0  0  2  0  0  0  0  0  0  0  0  0
   -0.3720    3.5053   -0.9551 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.3705    1.2026   -0.2986 C   0  0  1  0  0  0  0  0  0  0  0  0
    1.7396    1.3481   -0.1301 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.5046    0.1701   -0.1444 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.8495    0.1947   -0.4527 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.5979   -0.9393   -0.4694 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.0251   -2.1449   -0.1767 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.6579   -2.2043    0.1415 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1748   -3.4474    0.4202 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.9086   -1.0513    0.1555 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.4868   -1.0460    0.4763 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1544   -2.0936    0.4584 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1059    0.2443    0.8087 C   0  0  2  0  0  0  0  0  0  0  0  0
   -3.2882   -3.5079   -0.2954 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.8534   -2.6315   -0.0967 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.7695   -2.2553   -1.5504 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5089   -0.4716    2.1769 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1559    1.6076   -0.9590 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4673    2.5750    1.7369 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1561    2.7252    1.0718 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3240    4.0682   -0.9258 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.4179    4.2160   -0.5889 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0793    3.1767   -1.9515 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.1201    0.7765   -1.2915 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.3369    1.1505   -0.6922 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.6589   -0.8558   -0.7214 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.6349   -3.0439   -0.1936 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.2688   -3.7241    0.6710 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.2548    0.6824    1.7615 H   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
  3  5  1  0  0  0  0
  5  6  1  1  0  0  0
  5  7  1  0  0  0  0
  7  8  1  0  0  0  0
  7  9  1  0  0  0  0
  9 10  1  0  0  0  0
  9 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  2  0  0  0  0
 16 17  1  0  0  0  0
 17 18  1  0  0  0  0
 17 19  2  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  5  1  0  0  0  0
 22 11  1  0  0  0  0
 19 13  1  0  0  0  0
  1 23  1  0  0  0  0
  1 24  1  0  0  0  0
  1 25  1  0  0  0  0
  6 26  1  0  0  0  0
  7 27  1  6  0  0  0
  8 28  1  0  0  0  0
  9 29  1  1  0  0  0
 10 30  1  0  0  0  0
 10 31  1  0  0  0  0
 10 32  1  0  0  0  0
 11 33  1  6  0  0  0
 14 34  1  0  0  0  0
 15 35  1  0  0  0  0
 16 36  1  0  0  0  0
 18 37  1  0  0  0  0
 22 38  1  1  0  0  0
M  END

     RDKit          3D

 38 40  0  0  0  0  0  0  0  0999 V2000
   -3.8065   -2.5298   -0.4658 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.2076   -1.5166    0.3365 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2045   -0.6931   -0.1288 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8108   -0.8529   -1.3114 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5755    0.3535    0.6774 C   0  0  2  0  0  0  0  0  0  0  0  0
   -2.1188    0.4133    1.9776 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8355    1.7475    0.0855 C   0  0  1  0  0  0  0  0  0  0  0  0
   -2.7515    2.4619    0.8058 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4621    2.3896    0.0380 C   0  0  2  0  0  0  0  0  0  0  0  0
   -0.3720    3.5053   -0.9551 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.3705    1.2026   -0.2986 C   0  0  1  0  0  0  0  0  0  0  0  0
    1.7396    1.3481   -0.1301 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.5046    0.1701   -0.1444 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.8495    0.1947   -0.4527 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.5979   -0.9393   -0.4694 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.0251   -2.1449   -0.1767 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.6579   -2.2043    0.1415 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1748   -3.4474    0.4202 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.9086   -1.0513    0.1555 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.4868   -1.0460    0.4763 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1544   -2.0936    0.4584 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1059    0.2443    0.8087 C   0  0  2  0  0  0  0  0  0  0  0  0
   -3.2882   -3.5079   -0.2954 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.8534   -2.6315   -0.0967 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.7695   -2.2553   -1.5504 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5089   -0.4716    2.1769 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1559    1.6076   -0.9590 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4673    2.5750    1.7369 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1561    2.7252    1.0718 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3240    4.0682   -0.9258 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.4179    4.2160   -0.5889 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0793    3.1767   -1.9515 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.1201    0.7765   -1.2915 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.3369    1.1505   -0.6922 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.6589   -0.8558   -0.7214 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.6349   -3.0439   -0.1936 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.2688   -3.7241    0.6710 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.2548    0.6824    1.7615 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
  3  5  1  0
  5  6  1  1
  5  7  1  0
  7  8  1  0
  7  9  1  0
  9 10  1  0
  9 11  1  0
 11 12  1  0
 12 13  1  0
 13 14  2  0
 14 15  1  0
 15 16  2  0
 16 17  1  0
 17 18  1  0
 17 19  2  0
 19 20  1  0
 20 21  2  0
 20 22  1  0
 22  5  1  0
 22 11  1  0
 19 13  1  0
  1 23  1  0
  1 24  1  0
  1 25  1  0
  6 26  1  0
  7 27  1  6
  8 28  1  0
  9 29  1  1
 10 30  1  0
 10 31  1  0
 10 32  1  0
 11 33  1  6
 14 34  1  0
 15 35  1  0
 16 36  1  0
 18 37  1  0
 22 38  1  1
M  END


  Mrv1652306242107393D          

 38 40  0  0  0  0            999 V2000
   -3.8065   -2.5298   -0.4658 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.2076   -1.5166    0.3365 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2045   -0.6931   -0.1288 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8108   -0.8529   -1.3114 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5755    0.3535    0.6774 C   0  0  2  0  0  0  0  0  0  0  0  0
   -2.1188    0.4133    1.9776 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8355    1.7475    0.0855 C   0  0  1  0  0  0  0  0  0  0  0  0
   -2.7515    2.4619    0.8058 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4621    2.3896    0.0380 C   0  0  2  0  0  0  0  0  0  0  0  0
   -0.3720    3.5053   -0.9551 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.3705    1.2026   -0.2986 C   0  0  1  0  0  0  0  0  0  0  0  0
    1.7396    1.3481   -0.1301 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.5046    0.1701   -0.1444 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.8495    0.1947   -0.4527 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.5979   -0.9393   -0.4694 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.0251   -2.1449   -0.1767 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.6579   -2.2043    0.1415 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1748   -3.4474    0.4202 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.9086   -1.0513    0.1555 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.4868   -1.0460    0.4763 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1544   -2.0936    0.4584 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1059    0.2443    0.8087 C   0  0  2  0  0  0  0  0  0  0  0  0
   -3.2882   -3.5079   -0.2954 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.8534   -2.6315   -0.0967 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.7695   -2.2553   -1.5504 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5089   -0.4716    2.1769 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1559    1.6076   -0.9590 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4673    2.5750    1.7369 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1561    2.7252    1.0718 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3240    4.0682   -0.9258 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.4179    4.2160   -0.5889 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0793    3.1767   -1.9515 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.1201    0.7765   -1.2915 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.3369    1.1505   -0.6922 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.6589   -0.8558   -0.7214 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.6349   -3.0439   -0.1936 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.2688   -3.7241    0.6710 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.2548    0.6824    1.7615 H   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
  3  5  1  0  0  0  0
  5  6  1  1  0  0  0
  5  7  1  0  0  0  0
  7  8  1  0  0  0  0
  7  9  1  0  0  0  0
  9 10  1  0  0  0  0
  9 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  2  0  0  0  0
 16 17  1  0  0  0  0
 17 18  1  0  0  0  0
 17 19  2  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  5  1  0  0  0  0
 22 11  1  0  0  0  0
 19 13  1  0  0  0  0
  1 23  1  0  0  0  0
  1 24  1  0  0  0  0
  1 25  1  0  0  0  0
  6 26  1  0  0  0  0
  7 27  1  6  0  0  0
  8 28  1  0  0  0  0
  9 29  1  1  0  0  0
 10 30  1  0  0  0  0
 10 31  1  0  0  0  0
 10 32  1  0  0  0  0
 11 33  1  6  0  0  0
 14 34  1  0  0  0  0
 15 35  1  0  0  0  0
 16 36  1  0  0  0  0
 18 37  1  0  0  0  0
 22 38  1  1  0  0  0
M  END
> <DATABASE_ID>
NP0010644

> <DATABASE_NAME>
NP-MRD

> <SMILES>
[H]OC1=C2C(O[C@@]3([H])[C@]([H])(C2=O)[C@](O[H])(C(=O)OC([H])([H])[H])[C@@]([H])(O[H])[C@]3([H])C([H])([H])[H])=C([H])C([H])=C1[H]

> <INCHI_IDENTIFIER>
InChI=1S/C15H16O7/c1-6-12-10(15(20,13(6)18)14(19)21-2)11(17)9-7(16)4-3-5-8(9)22-12/h3-6,10,12-13,16,18,20H,1-2H3/t6-,10+,12-,13+,15-/m1/s1

> <INCHI_KEY>
FHOZFIROEVROQO-MSFILTLLSA-N

> <FORMULA>
C15H16O7

> <MOLECULAR_WEIGHT>
308.286

> <EXACT_MASS>
308.089602855

> <JCHEM_ACCEPTOR_COUNT>
6

> <JCHEM_ATOM_COUNT>
38

> <JCHEM_AVERAGE_POLARIZABILITY>
29.796973420227616

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
3

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
1

> <JCHEM_IUPAC>
methyl (3R,4S,5S,6R,7S)-5,6,10-trihydroxy-4-methyl-8-oxo-2-oxatricyclo[7.4.0.0^{3,7}]trideca-1(13),9,11-triene-6-carboxylate

> <ALOGPS_LOGP>
0.56

> <JCHEM_LOGP>
0.6291956943333336

> <ALOGPS_LOGS>
-0.93

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
3

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA>
9.937143110329773

> <JCHEM_PKA_STRONGEST_ACIDIC>
7.364041919908248

> <JCHEM_PKA_STRONGEST_BASIC>
-3.4843609873751697

> <JCHEM_POLAR_SURFACE_AREA>
113.29000000000002

> <JCHEM_REFRACTIVITY>
72.9036

> <JCHEM_ROTATABLE_BOND_COUNT>
2

> <JCHEM_RULE_OF_FIVE>
1

> <ALOGPS_SOLUBILITY>
3.59e+01 g/l

> <JCHEM_TRADITIONAL_IUPAC>
methyl (3R,4S,5S,6R,7S)-5,6,10-trihydroxy-4-methyl-8-oxo-2-oxatricyclo[7.4.0.0^{3,7}]trideca-1(13),9,11-triene-6-carboxylate

> <JCHEM_VEBER_RULE>
0

$$$$

     RDKit          3D

 38 40  0  0  0  0  0  0  0  0999 V2000
   -3.8065   -2.5298   -0.4658 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.2076   -1.5166    0.3365 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2045   -0.6931   -0.1288 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8108   -0.8529   -1.3114 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5755    0.3535    0.6774 C   0  0  2  0  0  0  0  0  0  0  0  0
   -2.1188    0.4133    1.9776 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8355    1.7475    0.0855 C   0  0  1  0  0  0  0  0  0  0  0  0
   -2.7515    2.4619    0.8058 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4621    2.3896    0.0380 C   0  0  2  0  0  0  0  0  0  0  0  0
   -0.3720    3.5053   -0.9551 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.3705    1.2026   -0.2986 C   0  0  1  0  0  0  0  0  0  0  0  0
    1.7396    1.3481   -0.1301 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.5046    0.1701   -0.1444 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.8495    0.1947   -0.4527 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.5979   -0.9393   -0.4694 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.0251   -2.1449   -0.1767 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.6579   -2.2043    0.1415 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1748   -3.4474    0.4202 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.9086   -1.0513    0.1555 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.4868   -1.0460    0.4763 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1544   -2.0936    0.4584 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1059    0.2443    0.8087 C   0  0  2  0  0  0  0  0  0  0  0  0
   -3.2882   -3.5079   -0.2954 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.8534   -2.6315   -0.0967 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.7695   -2.2553   -1.5504 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5089   -0.4716    2.1769 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1559    1.6076   -0.9590 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4673    2.5750    1.7369 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1561    2.7252    1.0718 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3240    4.0682   -0.9258 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.4179    4.2160   -0.5889 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0793    3.1767   -1.9515 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.1201    0.7765   -1.2915 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.3369    1.1505   -0.6922 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.6589   -0.8558   -0.7214 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.6349   -3.0439   -0.1936 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.2688   -3.7241    0.6710 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.2548    0.6824    1.7615 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
  3  5  1  0
  5  6  1  1
  5  7  1  0
  7  8  1  0
  7  9  1  0
  9 10  1  0
  9 11  1  0
 11 12  1  0
 12 13  1  0
 13 14  2  0
 14 15  1  0
 15 16  2  0
 16 17  1  0
 17 18  1  0
 17 19  2  0
 19 20  1  0
 20 21  2  0
 20 22  1  0
 22  5  1  0
 22 11  1  0
 19 13  1  0
  1 23  1  0
  1 24  1  0
  1 25  1  0
  6 26  1  0
  7 27  1  6
  8 28  1  0
  9 29  1  1
 10 30  1  0
 10 31  1  0
 10 32  1  0
 11 33  1  6
 14 34  1  0
 15 35  1  0
 16 36  1  0
 18 37  1  0
 22 38  1  1
M  END

HEADER    PROTEIN                                 24-JUN-21   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   24-JUN-21         0                                  
HETATM    1  C   UNK     0      -3.807  -2.530  -0.466  0.00  0.00           C+0
HETATM    2  O   UNK     0      -3.208  -1.517   0.337  0.00  0.00           O+0
HETATM    3  C   UNK     0      -2.204  -0.693  -0.129  0.00  0.00           C+0
HETATM    4  O   UNK     0      -1.811  -0.853  -1.311  0.00  0.00           O+0
HETATM    5  C   UNK     0      -1.575   0.354   0.677  0.00  0.00           C+0
HETATM    6  O   UNK     0      -2.119   0.413   1.978  0.00  0.00           O+0
HETATM    7  C   UNK     0      -1.835   1.748   0.086  0.00  0.00           C+0
HETATM    8  O   UNK     0      -2.752   2.462   0.806  0.00  0.00           O+0
HETATM    9  C   UNK     0      -0.462   2.390   0.038  0.00  0.00           C+0
HETATM   10  C   UNK     0      -0.372   3.505  -0.955  0.00  0.00           C+0
HETATM   11  C   UNK     0       0.371   1.203  -0.299  0.00  0.00           C+0
HETATM   12  O   UNK     0       1.740   1.348  -0.130  0.00  0.00           O+0
HETATM   13  C   UNK     0       2.505   0.170  -0.144  0.00  0.00           C+0
HETATM   14  C   UNK     0       3.849   0.195  -0.453  0.00  0.00           C+0
HETATM   15  C   UNK     0       4.598  -0.939  -0.469  0.00  0.00           C+0
HETATM   16  C   UNK     0       4.025  -2.145  -0.177  0.00  0.00           C+0
HETATM   17  C   UNK     0       2.658  -2.204   0.142  0.00  0.00           C+0
HETATM   18  O   UNK     0       2.175  -3.447   0.420  0.00  0.00           O+0
HETATM   19  C   UNK     0       1.909  -1.051   0.156  0.00  0.00           C+0
HETATM   20  C   UNK     0       0.487  -1.046   0.476  0.00  0.00           C+0
HETATM   21  O   UNK     0      -0.154  -2.094   0.458  0.00  0.00           O+0
HETATM   22  C   UNK     0      -0.106   0.244   0.809  0.00  0.00           C+0
HETATM   23  H   UNK     0      -3.288  -3.508  -0.295  0.00  0.00           H+0
HETATM   24  H   UNK     0      -4.853  -2.632  -0.097  0.00  0.00           H+0
HETATM   25  H   UNK     0      -3.769  -2.255  -1.550  0.00  0.00           H+0
HETATM   26  H   UNK     0      -2.509  -0.472   2.177  0.00  0.00           H+0
HETATM   27  H   UNK     0      -2.156   1.608  -0.959  0.00  0.00           H+0
HETATM   28  H   UNK     0      -2.467   2.575   1.737  0.00  0.00           H+0
HETATM   29  H   UNK     0      -0.156   2.725   1.072  0.00  0.00           H+0
HETATM   30  H   UNK     0      -1.324   4.068  -0.926  0.00  0.00           H+0
HETATM   31  H   UNK     0       0.418   4.216  -0.589  0.00  0.00           H+0
HETATM   32  H   UNK     0      -0.079   3.177  -1.952  0.00  0.00           H+0
HETATM   33  H   UNK     0       0.120   0.777  -1.292  0.00  0.00           H+0
HETATM   34  H   UNK     0       4.337   1.151  -0.692  0.00  0.00           H+0
HETATM   35  H   UNK     0       5.659  -0.856  -0.721  0.00  0.00           H+0
HETATM   36  H   UNK     0       4.635  -3.044  -0.194  0.00  0.00           H+0
HETATM   37  H   UNK     0       1.269  -3.724   0.671  0.00  0.00           H+0
HETATM   38  H   UNK     0       0.255   0.682   1.762  0.00  0.00           H+0
CONECT    1    2   23   24   25                                             
CONECT    2    1    3                                                       
CONECT    3    2    4    5                                                  
CONECT    4    3                                                            
CONECT    5    3    6    7   22                                             
CONECT    6    5   26                                                       
CONECT    7    5    8    9   27                                             
CONECT    8    7   28                                                       
CONECT    9    7   10   11   29                                             
CONECT   10    9   30   31   32                                             
CONECT   11    9   12   22   33                                             
CONECT   12   11   13                                                       
CONECT   13   12   14   19                                                  
CONECT   14   13   15   34                                                  
CONECT   15   14   16   35                                                  
CONECT   16   15   17   36                                                  
CONECT   17   16   18   19                                                  
CONECT   18   17   37                                                       
CONECT   19   17   20   13                                                  
CONECT   20   19   21   22                                                  
CONECT   21   20                                                            
CONECT   22   20    5   11   38                                             
CONECT   23    1                                                            
CONECT   24    1                                                            
CONECT   25    1                                                            
CONECT   26    6                                                            
CONECT   27    7                                                            
CONECT   28    8                                                            
CONECT   29    9                                                            
CONECT   30   10                                                            
CONECT   31   10                                                            
CONECT   32   10                                                            
CONECT   33   11                                                            
CONECT   34   14                                                            
CONECT   35   15                                                            
CONECT   36   16                                                            
CONECT   37   18                                                            
CONECT   38   22                                                            
MASTER        0    0    0    0    0    0    0    0   38    0   80    0
END

RDKit          3D

38 40  0  0  0  0  0  0  0  0999 V2000
   -3.8065   -2.5298   -0.4658 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.2076   -1.5166    0.3365 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2045   -0.6931   -0.1288 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8108   -0.8529   -1.3114 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5755    0.3535    0.6774 C   0  0  2  0  0  0  0  0  0  0  0  0
   -2.1188    0.4133    1.9776 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8355    1.7475    0.0855 C   0  0  1  0  0  0  0  0  0  0  0  0
   -2.7515    2.4619    0.8058 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4621    2.3896    0.0380 C   0  0  2  0  0  0  0  0  0  0  0  0
   -0.3720    3.5053   -0.9551 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.3705    1.2026   -0.2986 C   0  0  1  0  0  0  0  0  0  0  0  0
    1.7396    1.3481   -0.1301 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.5046    0.1701   -0.1444 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.8495    0.1947   -0.4527 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.5979   -0.9393   -0.4694 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.0251   -2.1449   -0.1767 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.6579   -2.2043    0.1415 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1748   -3.4474    0.4202 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.9086   -1.0513    0.1555 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.4868   -1.0460    0.4763 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1544   -2.0936    0.4584 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1059    0.2443    0.8087 C   0  0  2  0  0  0  0  0  0  0  0  0
   -3.2882   -3.5079   -0.2954 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.8534   -2.6315   -0.0967 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.7695   -2.2553   -1.5504 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5089   -0.4716    2.1769 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1559    1.6076   -0.9590 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4673    2.5750    1.7369 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1561    2.7252    1.0718 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3240    4.0682   -0.9258 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.4179    4.2160   -0.5889 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0793    3.1767   -1.9515 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.1201    0.7765   -1.2915 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.3369    1.1505   -0.6922 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.6589   -0.8558   -0.7214 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.6349   -3.0439   -0.1936 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.2688   -3.7241    0.6710 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.2548    0.6824    1.7615 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
  3  5  1  0
  5  6  1  1
  5  7  1  0
  7  8  1  0
  7  9  1  0
  9 10  1  0
  9 11  1  0
 11 12  1  0
 12 13  1  0
 13 14  2  0
 14 15  1  0
 15 16  2  0
 16 17  1  0
 17 18  1  0
 17 19  2  0
 19 20  1  0
 20 21  2  0
 20 22  1  0
 22  5  1  0
 22 11  1  0
 19 13  1  0
  1 23  1  0
  1 24  1  0
  1 25  1  0
  6 26  1  0
  7 27  1  6
  8 28  1  0
  9 29  1  1
 10 30  1  0
 10 31  1  0
 10 32  1  0
 11 33  1  6
 14 34  1  0
 15 35  1  0
 16 36  1  0
 18 37  1  0
 22 38  1  1
M  END

View in JSmol View NMR Assignments

Synonyms

Value	Source
Methyl (3R,4S,5S,6R,7S)-5,6,10-trihydroxy-4-methyl-8-oxo-2-oxatricyclo[7.4.0.0,]trideca-1(13),9,11-triene-6-carboxylic acid	Generator

Chemical Formula

C₁₅H₁₆O₇

Average Mass

308.2860 Da

Monoisotopic Mass

308.08960 Da

IUPAC Name

methyl (3R,4S,5S,6R,7S)-5,6,10-trihydroxy-4-methyl-8-oxo-2-oxatricyclo[7.4.0.0^{3,7}]trideca-1(13),9,11-triene-6-carboxylate

Traditional Name

methyl (3R,4S,5S,6R,7S)-5,6,10-trihydroxy-4-methyl-8-oxo-2-oxatricyclo[7.4.0.0^{3,7}]trideca-1(13),9,11-triene-6-carboxylate

CAS Registry Number

Not Available

SMILES

COC(=O)[C@]1(O)[C@@H](O)[C@H](C)[C@H]2OC3=C(C(O)=CC=C3)C(=O)[C@H]12

InChI Identifier

InChI=1S/C15H16O7/c1-6-12-10(15(20,13(6)18)14(19)21-2)11(17)9-7(16)4-3-5-8(9)22-12/h3-6,10,12-13,16,18,20H,1-2H3/t6-,10+,12-,13+,15-/m1/s1

InChI Key

FHOZFIROEVROQO-MSFILTLLSA-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
Preussia africana	NPAtlas	22324636

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as chromones. Chromones are compounds containing a benzopyran-4-one moiety.

Kingdom

Organic compounds

Super Class

Organoheterocyclic compounds

Class

Benzopyrans

Sub Class

1-benzopyrans

Direct Parent

Chromones

Alternative Parents

Substituents

Chromone
Aryl alkyl ketone
Aryl ketone
1-hydroxy-4-unsubstituted benzenoid
1-hydroxy-2-unsubstituted benzenoid
Alkyl aryl ether
Beta-hydroxy acid
Benzenoid
Hydroxy acid
Cyclic alcohol
Vinylogous acid
Methyl ester
Tertiary alcohol
1,2-diol
Carboxylic acid ester
Secondary alcohol
Ketone
Ether
Oxacycle
Carboxylic acid derivative
Monocarboxylic acid or derivatives
Polyol
Organic oxygen compound
Hydrocarbon derivative
Alcohol
Carbonyl group
Organic oxide
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	0.56	ALOGPS
logP	0.63	ChemAxon
logS	-0.93	ALOGPS
pKa (Strongest Acidic)	7.36	ChemAxon
pKa (Strongest Basic)	-3.5	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	6	ChemAxon
Hydrogen Donor Count	3	ChemAxon
Polar Surface Area	113.29 Å²	ChemAxon
Rotatable Bond Count	2	ChemAxon
Refractivity	72.9 m³·mol⁻¹	ChemAxon
Polarizability	29.8 Å³	ChemAxon
Number of Rings	3	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

NPAtlas ID

NPA003826

HMDB ID

Not Available

DrugBank ID

Not Available

Phenol Explorer Compound ID

Not Available

FoodDB ID

Not Available

KNApSAcK ID

Not Available

Chemspider ID

28503673

KEGG Compound ID

Not Available

BioCyc ID

Not Available

BiGG ID

Not Available

Wikipedia Link

Not Available

METLIN ID

Not Available

PubChem Compound

57333292

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

Showing NP-Card for Preussochromone E (NP0010644)

MOL for NP0010644 (Preussochromone E)

3D MOL for NP0010644 (Preussochromone E)

3D SDF for NP0010644 (Preussochromone E)

3D-SDF for NP0010644 (Preussochromone E)

PDB for NP0010644 (Preussochromone E)

3D PDB for NP0010644 (Preussochromone E)

SMILES for NP0010644 (Preussochromone E)

INCHI for NP0010644 (Preussochromone E)

Structure for NP0010644 (Preussochromone E)

3D Structure for NP0010644 (Preussochromone E)