NP-MRD: Showing NP-Card for Oxyjavanicin (NP0009059)

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Record Information

Version

2.0

Created at

2020-12-09 06:31:28 UTC

Updated at

2021-07-15 17:02:11 UTC

NP-MRD ID

NP0009059

Secondary Accession Numbers

None

Natural Product Identification

Common Name

Oxyjavanicin

Provided By

NPAtlas

Description

3,5,10-Trihydroxy-7-methoxy-3-methyl-1H,3H,4H,6H,9H-naphtho[2,3-c]pyran-6,9-dione belongs to the class of organic compounds known as isochromanequinones. These are polycyclic compounds containing an isochromanequinone, which is structurally characterized by a quinone fused to an isochromane, and forming a naphtho[2,3-c]pyran-6,9-dione skeleton. Oxyjavanicin is found in Fusarium, Fusarium javanicum, Fusarium martii, Fusarium moniliforme and Nectria haematococca. Based on a literature review very few articles have been published on 3,5,10-trihydroxy-7-methoxy-3-methyl-1H,3H,4H,6H,9H-naphtho[2,3-c]pyran-6,9-dione.

Structure

MOL 3D MOL SDF 3D SDF PDB SMILES InChI


  Mrv1652306242106323D          

 36 38  0  0  0  0            999 V2000
    6.0755    0.3777    0.4708 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.8806    1.0865    0.6999 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.6569    0.5323    0.3228 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.6832   -0.5748   -0.4139 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.4615   -1.2263   -0.8559 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.4716   -2.2752   -1.5539 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.1697   -0.6469   -0.4789 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0224   -1.2776   -0.9065 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.1132   -2.4412   -1.6803 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1844   -0.7302   -0.5502 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2371    0.3896    0.1947 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0886    1.0435    0.6376 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1813    2.1736    1.3892 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.1508    0.5222    0.2991 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.3958    1.1409    0.7193 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.4220    2.1729    1.4063 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5351    0.9502    0.5592 C   0  0  1  0  0  0  0  0  0  0  0  0
   -3.6944    0.0486    0.2917 C   0  0  2  0  0  0  0  0  0  0  0  0
   -4.8870    0.9426   -0.0023 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.0198   -0.6367    1.4859 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5750   -0.8442   -0.6977 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4067   -1.4055   -1.0077 C   0  0  2  0  0  0  0  0  0  0  0  0
    6.2719    0.1475   -0.5846 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.0624   -0.5932    1.0346 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.9086    0.9817    0.9151 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.6237   -1.0379   -0.7154 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7619   -2.8602   -1.9651 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.3882    2.8060    1.8139 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5193    1.1844    1.6438 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6350    1.9436    0.0469 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.7827    0.2578    0.0229 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.9884    1.7582    0.7361 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.8134    1.3150   -1.0460 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.7597   -1.2788    1.3325 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3663   -2.4555   -0.6451 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3217   -1.4904   -2.1319 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
  4  5  1  0  0  0  0
  5  6  2  0  0  0  0
  5  7  1  0  0  0  0
  7  8  2  0  0  0  0
  8  9  1  0  0  0  0
  8 10  1  0  0  0  0
 10 11  2  0  0  0  0
 11 12  1  0  0  0  0
 12 13  1  0  0  0  0
 12 14  2  0  0  0  0
 14 15  1  0  0  0  0
 15 16  2  0  0  0  0
 11 17  1  0  0  0  0
 17 18  1  0  0  0  0
 18 19  1  0  0  0  0
 18 20  1  1  0  0  0
 18 21  1  0  0  0  0
 21 22  1  0  0  0  0
 15  3  1  0  0  0  0
 14  7  1  0  0  0  0
 22 10  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
  4 26  1  0  0  0  0
  9 27  1  0  0  0  0
 13 28  1  0  0  0  0
 17 29  1  0  0  0  0
 17 30  1  0  0  0  0
 19 31  1  0  0  0  0
 19 32  1  0  0  0  0
 19 33  1  0  0  0  0
 20 34  1  0  0  0  0
 22 35  1  0  0  0  0
 22 36  1  0  0  0  0
M  END

     RDKit          3D

 36 38  0  0  0  0  0  0  0  0999 V2000
    6.0755    0.3777    0.4708 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.8806    1.0865    0.6999 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.6569    0.5323    0.3228 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.6832   -0.5748   -0.4139 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.4615   -1.2263   -0.8559 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.4716   -2.2752   -1.5539 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.1697   -0.6469   -0.4789 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0224   -1.2776   -0.9065 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.1132   -2.4412   -1.6803 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1844   -0.7302   -0.5502 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2371    0.3896    0.1947 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0886    1.0435    0.6376 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1813    2.1736    1.3892 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.1508    0.5222    0.2991 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.3958    1.1409    0.7193 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.4220    2.1729    1.4063 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5351    0.9502    0.5592 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.6944    0.0486    0.2917 C   0  0  2  0  0  0  0  0  0  0  0  0
   -4.8870    0.9426   -0.0023 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.0198   -0.6367    1.4859 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5750   -0.8442   -0.6977 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4067   -1.4055   -1.0077 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.2719    0.1475   -0.5846 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.0624   -0.5932    1.0346 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.9086    0.9817    0.9151 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.6237   -1.0379   -0.7154 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7619   -2.8602   -1.9651 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.3882    2.8060    1.8139 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5193    1.1844    1.6438 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6350    1.9436    0.0469 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.7827    0.2578    0.0229 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.9884    1.7582    0.7361 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.8134    1.3150   -1.0460 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.7597   -1.2788    1.3325 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3663   -2.4555   -0.6451 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3217   -1.4904   -2.1319 H   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0
  2  3  1  0
  3  4  2  0
  4  5  1  0
  5  6  2  0
  5  7  1  0
  7  8  2  0
  8  9  1  0
  8 10  1  0
 10 11  2  0
 11 12  1  0
 12 13  1  0
 12 14  2  0
 14 15  1  0
 15 16  2  0
 11 17  1  0
 17 18  1  0
 18 19  1  0
 18 20  1  1
 18 21  1  0
 21 22  1  0
 15  3  1  0
 14  7  1  0
 22 10  1  0
  1 23  1  0
  1 24  1  0
  1 25  1  0
  4 26  1  0
  9 27  1  0
 13 28  1  0
 17 29  1  0
 17 30  1  0
 19 31  1  0
 19 32  1  0
 19 33  1  0
 20 34  1  0
 22 35  1  0
 22 36  1  0
M  END


  Mrv1652306242106323D          

 36 38  0  0  0  0            999 V2000
    6.0755    0.3777    0.4708 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.8806    1.0865    0.6999 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.6569    0.5323    0.3228 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.6832   -0.5748   -0.4139 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.4615   -1.2263   -0.8559 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.4716   -2.2752   -1.5539 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.1697   -0.6469   -0.4789 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0224   -1.2776   -0.9065 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.1132   -2.4412   -1.6803 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1844   -0.7302   -0.5502 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2371    0.3896    0.1947 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0886    1.0435    0.6376 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1813    2.1736    1.3892 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.1508    0.5222    0.2991 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.3958    1.1409    0.7193 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.4220    2.1729    1.4063 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5351    0.9502    0.5592 C   0  0  1  0  0  0  0  0  0  0  0  0
   -3.6944    0.0486    0.2917 C   0  0  2  0  0  0  0  0  0  0  0  0
   -4.8870    0.9426   -0.0023 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.0198   -0.6367    1.4859 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5750   -0.8442   -0.6977 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4067   -1.4055   -1.0077 C   0  0  2  0  0  0  0  0  0  0  0  0
    6.2719    0.1475   -0.5846 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.0624   -0.5932    1.0346 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.9086    0.9817    0.9151 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.6237   -1.0379   -0.7154 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7619   -2.8602   -1.9651 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.3882    2.8060    1.8139 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5193    1.1844    1.6438 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6350    1.9436    0.0469 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.7827    0.2578    0.0229 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.9884    1.7582    0.7361 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.8134    1.3150   -1.0460 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.7597   -1.2788    1.3325 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3663   -2.4555   -0.6451 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3217   -1.4904   -2.1319 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
  4  5  1  0  0  0  0
  5  6  2  0  0  0  0
  5  7  1  0  0  0  0
  7  8  2  0  0  0  0
  8  9  1  0  0  0  0
  8 10  1  0  0  0  0
 10 11  2  0  0  0  0
 11 12  1  0  0  0  0
 12 13  1  0  0  0  0
 12 14  2  0  0  0  0
 14 15  1  0  0  0  0
 15 16  2  0  0  0  0
 11 17  1  0  0  0  0
 17 18  1  0  0  0  0
 18 19  1  0  0  0  0
 18 20  1  1  0  0  0
 18 21  1  0  0  0  0
 21 22  1  0  0  0  0
 15  3  1  0  0  0  0
 14  7  1  0  0  0  0
 22 10  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
  4 26  1  0  0  0  0
  9 27  1  0  0  0  0
 13 28  1  0  0  0  0
 17 29  1  0  0  0  0
 17 30  1  0  0  0  0
 19 31  1  0  0  0  0
 19 32  1  0  0  0  0
 19 33  1  0  0  0  0
 20 34  1  0  0  0  0
 22 35  1  0  0  0  0
 22 36  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0009059

> <DATABASE_NAME>
NP-MRD

> <SMILES>
[H]OC1=C2C(=O)C([H])=C(OC([H])([H])[H])C(=O)C2=C(O[H])C2=C1C([H])([H])O[C@](O[H])(C([H])([H])[H])C2([H])[H]

> <INCHI_IDENTIFIER>
InChI=1S/C15H14O7/c1-15(20)4-6-7(5-22-15)13(18)10-8(16)3-9(21-2)14(19)11(10)12(6)17/h3,17-18,20H,4-5H2,1-2H3/t15-/m1/s1

> <INCHI_KEY>
FKJXMYJPOKQPSS-UHFFFAOYSA-N

> <FORMULA>
C15H14O7

> <MOLECULAR_WEIGHT>
306.27

> <EXACT_MASS>
306.073952791

> <JCHEM_ACCEPTOR_COUNT>
7

> <JCHEM_ATOM_COUNT>
36

> <JCHEM_AVERAGE_POLARIZABILITY>
29.940650714026248

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
3

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
1

> <JCHEM_IUPAC>
(3R)-3,5,10-trihydroxy-7-methoxy-3-methyl-1H,3H,4H,6H,9H-naphtho[2,3-c]pyran-6,9-dione

> <ALOGPS_LOGP>
1.46

> <JCHEM_LOGP>
1.352159576

> <ALOGPS_LOGS>
-2.35

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
3

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA>
9.933604315486201

> <JCHEM_PKA_STRONGEST_ACIDIC>
8.14468032090559

> <JCHEM_PKA_STRONGEST_BASIC>
-4.071728203630195

> <JCHEM_POLAR_SURFACE_AREA>
113.29000000000002

> <JCHEM_REFRACTIVITY>
77.90240000000001

> <JCHEM_ROTATABLE_BOND_COUNT>
1

> <JCHEM_RULE_OF_FIVE>
1

> <ALOGPS_SOLUBILITY>
1.36e+00 g/l

> <JCHEM_TRADITIONAL_IUPAC>
(3R)-3,5,10-trihydroxy-7-methoxy-3-methyl-1H,4H-naphtho[2,3-c]pyran-6,9-dione

> <JCHEM_VEBER_RULE>
0

$$$$

     RDKit          3D

 36 38  0  0  0  0  0  0  0  0999 V2000
    6.0755    0.3777    0.4708 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.8806    1.0865    0.6999 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.6569    0.5323    0.3228 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.6832   -0.5748   -0.4139 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.4615   -1.2263   -0.8559 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.4716   -2.2752   -1.5539 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.1697   -0.6469   -0.4789 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0224   -1.2776   -0.9065 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.1132   -2.4412   -1.6803 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1844   -0.7302   -0.5502 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2371    0.3896    0.1947 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0886    1.0435    0.6376 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1813    2.1736    1.3892 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.1508    0.5222    0.2991 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.3958    1.1409    0.7193 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.4220    2.1729    1.4063 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5351    0.9502    0.5592 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.6944    0.0486    0.2917 C   0  0  2  0  0  0  0  0  0  0  0  0
   -4.8870    0.9426   -0.0023 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.0198   -0.6367    1.4859 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5750   -0.8442   -0.6977 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4067   -1.4055   -1.0077 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.2719    0.1475   -0.5846 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.0624   -0.5932    1.0346 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.9086    0.9817    0.9151 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.6237   -1.0379   -0.7154 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7619   -2.8602   -1.9651 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.3882    2.8060    1.8139 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5193    1.1844    1.6438 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6350    1.9436    0.0469 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.7827    0.2578    0.0229 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.9884    1.7582    0.7361 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.8134    1.3150   -1.0460 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.7597   -1.2788    1.3325 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3663   -2.4555   -0.6451 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3217   -1.4904   -2.1319 H   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0
  2  3  1  0
  3  4  2  0
  4  5  1  0
  5  6  2  0
  5  7  1  0
  7  8  2  0
  8  9  1  0
  8 10  1  0
 10 11  2  0
 11 12  1  0
 12 13  1  0
 12 14  2  0
 14 15  1  0
 15 16  2  0
 11 17  1  0
 17 18  1  0
 18 19  1  0
 18 20  1  1
 18 21  1  0
 21 22  1  0
 15  3  1  0
 14  7  1  0
 22 10  1  0
  1 23  1  0
  1 24  1  0
  1 25  1  0
  4 26  1  0
  9 27  1  0
 13 28  1  0
 17 29  1  0
 17 30  1  0
 19 31  1  0
 19 32  1  0
 19 33  1  0
 20 34  1  0
 22 35  1  0
 22 36  1  0
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       6.075   0.378   0.471  0.00  0.00           C+0
HETATM    2  O   UNK     0       4.881   1.087   0.700  0.00  0.00           O+0
HETATM    3  C   UNK     0       3.657   0.532   0.323  0.00  0.00           C+0
HETATM    4  C   UNK     0       3.683  -0.575  -0.414  0.00  0.00           C+0
HETATM    5  C   UNK     0       2.462  -1.226  -0.856  0.00  0.00           C+0
HETATM    6  O   UNK     0       2.472  -2.275  -1.554  0.00  0.00           O+0
HETATM    7  C   UNK     0       1.170  -0.647  -0.479  0.00  0.00           C+0
HETATM    8  C   UNK     0       0.022  -1.278  -0.907  0.00  0.00           C+0
HETATM    9  O   UNK     0       0.113  -2.441  -1.680  0.00  0.00           O+0
HETATM   10  C   UNK     0      -1.184  -0.730  -0.550  0.00  0.00           C+0
HETATM   11  C   UNK     0      -1.237   0.390   0.195  0.00  0.00           C+0
HETATM   12  C   UNK     0      -0.089   1.044   0.638  0.00  0.00           C+0
HETATM   13  O   UNK     0      -0.181   2.174   1.389  0.00  0.00           O+0
HETATM   14  C   UNK     0       1.151   0.522   0.299  0.00  0.00           C+0
HETATM   15  C   UNK     0       2.396   1.141   0.719  0.00  0.00           C+0
HETATM   16  O   UNK     0       2.422   2.173   1.406  0.00  0.00           O+0
HETATM   17  C   UNK     0      -2.535   0.950   0.559  0.00  0.00           C+0
HETATM   18  C   UNK     0      -3.694   0.049   0.292  0.00  0.00           C+0
HETATM   19  C   UNK     0      -4.887   0.943  -0.002  0.00  0.00           C+0
HETATM   20  O   UNK     0      -4.020  -0.637   1.486  0.00  0.00           O+0
HETATM   21  O   UNK     0      -3.575  -0.844  -0.698  0.00  0.00           O+0
HETATM   22  C   UNK     0      -2.407  -1.406  -1.008  0.00  0.00           C+0
HETATM   23  H   UNK     0       6.272   0.148  -0.585  0.00  0.00           H+0
HETATM   24  H   UNK     0       6.062  -0.593   1.035  0.00  0.00           H+0
HETATM   25  H   UNK     0       6.909   0.982   0.915  0.00  0.00           H+0
HETATM   26  H   UNK     0       4.624  -1.038  -0.715  0.00  0.00           H+0
HETATM   27  H   UNK     0      -0.762  -2.860  -1.965  0.00  0.00           H+0
HETATM   28  H   UNK     0       0.388   2.806   1.814  0.00  0.00           H+0
HETATM   29  H   UNK     0      -2.519   1.184   1.644  0.00  0.00           H+0
HETATM   30  H   UNK     0      -2.635   1.944   0.047  0.00  0.00           H+0
HETATM   31  H   UNK     0      -5.783   0.258   0.023  0.00  0.00           H+0
HETATM   32  H   UNK     0      -4.988   1.758   0.736  0.00  0.00           H+0
HETATM   33  H   UNK     0      -4.813   1.315  -1.046  0.00  0.00           H+0
HETATM   34  H   UNK     0      -4.760  -1.279   1.333  0.00  0.00           H+0
HETATM   35  H   UNK     0      -2.366  -2.455  -0.645  0.00  0.00           H+0
HETATM   36  H   UNK     0      -2.322  -1.490  -2.132  0.00  0.00           H+0
CONECT    1    2   23   24   25                                             
CONECT    2    1    3                                                       
CONECT    3    2    4   15                                                  
CONECT    4    3    5   26                                                  
CONECT    5    4    6    7                                                  
CONECT    6    5                                                            
CONECT    7    5    8   14                                                  
CONECT    8    7    9   10                                                  
CONECT    9    8   27                                                       
CONECT   10    8   11   22                                                  
CONECT   11   10   12   17                                                  
CONECT   12   11   13   14                                                  
CONECT   13   12   28                                                       
CONECT   14   12   15    7                                                  
CONECT   15   14   16    3                                                  
CONECT   16   15                                                            
CONECT   17   11   18   29   30                                             
CONECT   18   17   19   20   21                                             
CONECT   19   18   31   32   33                                             
CONECT   20   18   34                                                       
CONECT   21   18   22                                                       
CONECT   22   21   10   35   36                                             
CONECT   23    1                                                            
CONECT   24    1                                                            
CONECT   25    1                                                            
CONECT   26    4                                                            
CONECT   27    9                                                            
CONECT   28   13                                                            
CONECT   29   17                                                            
CONECT   30   17                                                            
CONECT   31   19                                                            
CONECT   32   19                                                            
CONECT   33   19                                                            
CONECT   34   20                                                            
CONECT   35   22                                                            
CONECT   36   22                                                            
MASTER        0    0    0    0    0    0    0    0   36    0   76    0
END

RDKit          3D

36 38  0  0  0  0  0  0  0  0999 V2000
    6.0755    0.3777    0.4708 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.8806    1.0865    0.6999 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.6569    0.5323    0.3228 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.6832   -0.5748   -0.4139 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.4615   -1.2263   -0.8559 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.4716   -2.2752   -1.5539 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.1697   -0.6469   -0.4789 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0224   -1.2776   -0.9065 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.1132   -2.4412   -1.6803 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1844   -0.7302   -0.5502 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2371    0.3896    0.1947 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0886    1.0435    0.6376 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1813    2.1736    1.3892 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.1508    0.5222    0.2991 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.3958    1.1409    0.7193 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.4220    2.1729    1.4063 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5351    0.9502    0.5592 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.6944    0.0486    0.2917 C   0  0  2  0  0  0  0  0  0  0  0  0
   -4.8870    0.9426   -0.0023 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.0198   -0.6367    1.4859 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5750   -0.8442   -0.6977 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4067   -1.4055   -1.0077 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.2719    0.1475   -0.5846 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.0624   -0.5932    1.0346 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.9086    0.9817    0.9151 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.6237   -1.0379   -0.7154 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7619   -2.8602   -1.9651 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.3882    2.8060    1.8139 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5193    1.1844    1.6438 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6350    1.9436    0.0469 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.7827    0.2578    0.0229 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.9884    1.7582    0.7361 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.8134    1.3150   -1.0460 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.7597   -1.2788    1.3325 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3663   -2.4555   -0.6451 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3217   -1.4904   -2.1319 H   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0
  2  3  1  0
  3  4  2  0
  4  5  1  0
  5  6  2  0
  5  7  1  0
  7  8  2  0
  8  9  1  0
  8 10  1  0
 10 11  2  0
 11 12  1  0
 12 13  1  0
 12 14  2  0
 14 15  1  0
 15 16  2  0
 11 17  1  0
 17 18  1  0
 18 19  1  0
 18 20  1  1
 18 21  1  0
 21 22  1  0
 15  3  1  0
 14  7  1  0
 22 10  1  0
  1 23  1  0
  1 24  1  0
  1 25  1  0
  4 26  1  0
  9 27  1  0
 13 28  1  0
 17 29  1  0
 17 30  1  0
 19 31  1  0
 19 32  1  0
 19 33  1  0
 20 34  1  0
 22 35  1  0
 22 36  1  0
M  END

View in JSmol View NMR Assignments

Synonyms

Not Available

Chemical Formula

C₁₅H₁₄O₇

Average Mass

306.2700 Da

Monoisotopic Mass

306.07395 Da

IUPAC Name

(3R)-3,5,10-trihydroxy-7-methoxy-3-methyl-1H,3H,4H,6H,9H-naphtho[2,3-c]pyran-6,9-dione

Traditional Name

(3R)-3,5,10-trihydroxy-7-methoxy-3-methyl-1H,4H-naphtho[2,3-c]pyran-6,9-dione

CAS Registry Number

Not Available

SMILES

COC1=CC(=O)C2=C(C(O)=C3CC(C)(O)OCC3=C2O)C1=O

InChI Identifier

InChI=1S/C15H14O7/c1-15(20)4-6-7(5-22-15)13(18)10-8(16)3-9(21-2)14(19)11(10)12(6)17/h3,17-18,20H,4-5H2,1-2H3

InChI Key

FKJXMYJPOKQPSS-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
Fusarium	NPAtlas	20264584
Fusarium javanicum	Fungi	KNApSAcK
Fusarium martii	LOTUS Database	35616633
Fusarium verticillioides	Fungi	KNApSAcK
Nectria haematococca	Fungi	KNApSAcK

Species Where Detected

Species Name	Source	Reference
Fusarium decemcellulare	KNApSAcK Database	22123792
Fusarium solani	KNApSAcK Database	22123792
Neocosmospora africana	KNApSAcK Database	22123792
Neocosmospora vasinfectum	KNApSAcK Database	22123792

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as isochromanequinones. These are polycyclic compounds containing an isochromanequinone, which is structurally characterized by a quinone fused to an isochromane, and forming a naphtho[2,3-c]pyran-6,9-dione skeleton.

Kingdom

Organic compounds

Super Class

Phenylpropanoids and polyketides

Class

Isochromanequinones

Sub Class

Not Available

Direct Parent

Isochromanequinones

Alternative Parents

Substituents

Isochromanequinone
Naphthopyranone
Naphthopyran
Naphthoquinone
Benzopyran
Isochromane
Naphthalene
2-benzopyran
Aryl ketone
Quinone
Pyranone
Pyran
Benzenoid
Vinylogous acid
Vinylogous ester
Ketone
Hemiacetal
Polyol
Organoheterocyclic compound
Oxacycle
Organooxygen compound
Hydrocarbon derivative
Organic oxide
Organic oxygen 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	1.46	ALOGPS
logP	1.35	ChemAxon
logS	-2.4	ALOGPS
pKa (Strongest Acidic)	8.14	ChemAxon
pKa (Strongest Basic)	-4.1	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	7	ChemAxon
Hydrogen Donor Count	3	ChemAxon
Polar Surface Area	113.29 Å²	ChemAxon
Rotatable Bond Count	1	ChemAxon
Refractivity	77.9 m³·mol⁻¹	ChemAxon
Polarizability	29.94 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

NPA000830

HMDB ID

Not Available

DrugBank ID

Not Available

Phenol Explorer Compound ID

Not Available

FoodDB ID

Not Available

KNApSAcK ID

Not Available

Chemspider ID

66134

KEGG Compound ID

Not Available

BioCyc ID

Not Available

BiGG ID

Not Available

Wikipedia Link

Not Available

METLIN ID

Not Available

PubChem Compound

73421

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

Showing NP-Card for Oxyjavanicin (NP0009059)

MOL for NP0009059 (Oxyjavanicin)

3D MOL for NP0009059 (Oxyjavanicin)

3D SDF for NP0009059 (Oxyjavanicin)

3D-SDF for NP0009059 (Oxyjavanicin)

PDB for NP0009059 (Oxyjavanicin)

3D PDB for NP0009059 (Oxyjavanicin)

SMILES for NP0009059 (Oxyjavanicin)

INCHI for NP0009059 (Oxyjavanicin)

Structure for NP0009059 (Oxyjavanicin)

3D Structure for NP0009059 (Oxyjavanicin)