NP-MRD: Showing NP-Card for 6-O- methyl-2-deprenylrheediaxanthone B (NP0012127)

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Record Information

Version

2.0

Created at

2021-01-05 21:36:14 UTC

Updated at

2021-07-15 17:10:54 UTC

NP-MRD ID

NP0012127

Secondary Accession Numbers

None

Natural Product Identification

Common Name

6-O- methyl-2-deprenylrheediaxanthone B

Provided By

NPAtlas

Description

6-O-Methyl-2-deprenylrheediaxanthone B is a secondary metabolite. Secondary metabolites are metabolically or physiologically non-essential metabolites that may serve a role as defense or signalling molecules. In some cases they are simply molecules that arise from the incomplete metabolism of other secondary metabolites. 6-O- methyl-2-deprenylrheediaxanthone B is found in Phomopsis sp. 6-O- methyl-2-deprenylrheediaxanthone B was first documented in 2004 (PMID: 15104511). Based on a literature review very few articles have been published on 6-O-Methyl-2-deprenylrheediaxanthone B.

Structure

MOL 3D MOL SDF 3D SDF PDB SMILES InChI


  Mrv1652306242117023D          

 43 46  0  0  0  0            999 V2000
    6.2282   -1.5761   -0.2370 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.8246   -1.8050   -0.1414 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.9427   -0.7330   -0.0890 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.4432    0.5571   -0.1306 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5490    1.6007   -0.0771 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.2058    1.3473    0.0146 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.2633    2.3718    0.0714 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.6749    3.5473    0.0365 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0924    2.0900    0.1641 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0357    3.0967    0.2211 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6131    4.4175    0.1845 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3640    2.7415    0.3124 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7738    1.4215    0.3482 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8187    0.4309    0.2903 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4912    0.7806    0.1991 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.4315   -0.1740    0.1431 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.7089    0.0583    0.0560 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.6018   -1.0146    0.0028 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.0817   -2.3042    0.0457 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5471   -0.8484    0.3469 C   0  0  2  0  0  0  0  0  0  0  0  0
   -1.8154   -1.9385    1.0713 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.9095   -1.2481   -1.0691 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.8159   -0.4412    1.0668 C   0  0  2  0  0  0  0  0  0  0  0  0
   -4.9319   -1.4065    0.7833 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.0537    0.8292    0.4377 O   0  0  0  0  0  0  0  0  0  0  0  0
    6.5780   -0.8439    0.5283 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.4144   -1.1711   -1.2481 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.7834   -2.5181   -0.1053 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.5074    0.7304   -0.2031 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.8740    2.6404   -0.1054 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2156    5.2058    0.2200 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.1287    3.5307    0.3588 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.6404   -3.1315    0.0134 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3549   -2.8963    0.8372 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9282   -1.8152    2.1754 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7894   -2.0707    0.7442 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8431   -2.3565   -1.1185 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.9201   -0.8997   -1.3077 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1663   -0.8279   -1.7829 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5981   -0.3347    2.1358 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.8293   -0.9127    0.3615 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.1810   -1.9166    1.7552 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.5362   -2.2130    0.1311 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
  6  7  1  0  0  0  0
  7  8  2  0  0  0  0
  7  9  1  0  0  0  0
  9 10  2  0  0  0  0
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 16 17  1  0  0  0  0
 17 18  2  0  0  0  0
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 14 20  1  0  0  0  0
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 18  3  1  0  0  0  0
 17  6  1  0  0  0  0
 15  9  1  0  0  0  0
 25 13  1  0  0  0  0
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 23 40  1  1  0  0  0
 24 41  1  0  0  0  0
 24 42  1  0  0  0  0
 24 43  1  0  0  0  0
M  END

     RDKit          3D

 43 46  0  0  0  0  0  0  0  0999 V2000
    6.2282   -1.5761   -0.2370 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.8246   -1.8050   -0.1414 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.9427   -0.7330   -0.0890 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.4432    0.5571   -0.1306 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5490    1.6007   -0.0771 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.2058    1.3473    0.0146 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.2633    2.3718    0.0714 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.6749    3.5473    0.0365 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0924    2.0900    0.1641 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0357    3.0967    0.2211 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6131    4.4175    0.1845 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3640    2.7415    0.3124 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7738    1.4215    0.3482 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8187    0.4309    0.2903 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4912    0.7806    0.1991 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.4315   -0.1740    0.1431 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.7089    0.0583    0.0560 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.6018   -1.0146    0.0028 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.0817   -2.3042    0.0457 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5471   -0.8484    0.3469 C   0  0  2  0  0  0  0  0  0  0  0  0
   -1.8154   -1.9385    1.0713 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.9095   -1.2481   -1.0691 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.8159   -0.4412    1.0668 C   0  0  2  0  0  0  0  0  0  0  0  0
   -4.9319   -1.4065    0.7833 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.0537    0.8292    0.4377 O   0  0  0  0  0  0  0  0  0  0  0  0
    6.5780   -0.8439    0.5283 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.4144   -1.1711   -1.2481 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.7834   -2.5181   -0.1053 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.5074    0.7304   -0.2031 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.8740    2.6404   -0.1054 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2156    5.2058    0.2200 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.1287    3.5307    0.3588 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.6404   -3.1315    0.0134 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3549   -2.8963    0.8372 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9282   -1.8152    2.1754 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7894   -2.0707    0.7442 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8431   -2.3565   -1.1185 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.9201   -0.8997   -1.3077 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1663   -0.8279   -1.7829 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5981   -0.3347    2.1358 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.8293   -0.9127    0.3615 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.1810   -1.9166    1.7552 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.5362   -2.2130    0.1311 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
  6  7  1  0
  7  8  2  0
  7  9  1  0
  9 10  2  0
 10 11  1  0
 10 12  1  0
 12 13  2  0
 13 14  1  0
 14 15  2  0
 15 16  1  0
 16 17  1  0
 17 18  2  0
 18 19  1  0
 14 20  1  0
 20 21  1  1
 20 22  1  0
 20 23  1  0
 23 24  1  0
 23 25  1  0
 18  3  1  0
 17  6  1  0
 15  9  1  0
 25 13  1  0
  1 26  1  0
  1 27  1  0
  1 28  1  0
  4 29  1  0
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 19 33  1  0
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 23 40  1  1
 24 41  1  0
 24 42  1  0
 24 43  1  0
M  END


  Mrv1652306242117023D          

 43 46  0  0  0  0            999 V2000
    6.2282   -1.5761   -0.2370 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.8246   -1.8050   -0.1414 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.9427   -0.7330   -0.0890 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.4432    0.5571   -0.1306 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5490    1.6007   -0.0771 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.2058    1.3473    0.0146 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.2633    2.3718    0.0714 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.6749    3.5473    0.0365 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0924    2.0900    0.1641 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0357    3.0967    0.2211 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6131    4.4175    0.1845 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3640    2.7415    0.3124 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7738    1.4215    0.3482 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8187    0.4309    0.2903 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4912    0.7806    0.1991 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.4315   -0.1740    0.1431 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.7089    0.0583    0.0560 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.6018   -1.0146    0.0028 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.0817   -2.3042    0.0457 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5471   -0.8484    0.3469 C   0  0  2  0  0  0  0  0  0  0  0  0
   -1.8154   -1.9385    1.0713 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.9095   -1.2481   -1.0691 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.8159   -0.4412    1.0668 C   0  0  2  0  0  0  0  0  0  0  0  0
   -4.9319   -1.4065    0.7833 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.0537    0.8292    0.4377 O   0  0  0  0  0  0  0  0  0  0  0  0
    6.5780   -0.8439    0.5283 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.4144   -1.1711   -1.2481 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.7834   -2.5181   -0.1053 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.5074    0.7304   -0.2031 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.8740    2.6404   -0.1054 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2156    5.2058    0.2200 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.1287    3.5307    0.3588 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.6404   -3.1315    0.0134 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3549   -2.8963    0.8372 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9282   -1.8152    2.1754 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7894   -2.0707    0.7442 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8431   -2.3565   -1.1185 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.9201   -0.8997   -1.3077 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1663   -0.8279   -1.7829 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5981   -0.3347    2.1358 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.8293   -0.9127    0.3615 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.1810   -1.9166    1.7552 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.5362   -2.2130    0.1311 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
  6  7  1  0  0  0  0
  7  8  2  0  0  0  0
  7  9  1  0  0  0  0
  9 10  2  0  0  0  0
 10 11  1  0  0  0  0
 10 12  1  0  0  0  0
 12 13  2  0  0  0  0
 13 14  1  0  0  0  0
 14 15  2  0  0  0  0
 15 16  1  0  0  0  0
 16 17  1  0  0  0  0
 17 18  2  0  0  0  0
 18 19  1  0  0  0  0
 14 20  1  0  0  0  0
 20 21  1  1  0  0  0
 20 22  1  0  0  0  0
 20 23  1  0  0  0  0
 23 24  1  0  0  0  0
 23 25  1  0  0  0  0
 18  3  1  0  0  0  0
 17  6  1  0  0  0  0
 15  9  1  0  0  0  0
 25 13  1  0  0  0  0
  1 26  1  0  0  0  0
  1 27  1  0  0  0  0
  1 28  1  0  0  0  0
  4 29  1  0  0  0  0
  5 30  1  0  0  0  0
 11 31  1  0  0  0  0
 12 32  1  0  0  0  0
 19 33  1  0  0  0  0
 21 34  1  0  0  0  0
 21 35  1  0  0  0  0
 21 36  1  0  0  0  0
 22 37  1  0  0  0  0
 22 38  1  0  0  0  0
 22 39  1  0  0  0  0
 23 40  1  1  0  0  0
 24 41  1  0  0  0  0
 24 42  1  0  0  0  0
 24 43  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0012127

> <DATABASE_NAME>
NP-MRD

> <SMILES>
[H]OC1=C2C(=O)C3=C([H])C([H])=C(OC([H])([H])[H])C(O[H])=C3OC2=C2C(O[C@@]([H])(C([H])([H])[H])C2(C([H])([H])[H])C([H])([H])[H])=C1[H]

> <INCHI_IDENTIFIER>
InChI=1S/C19H18O6/c1-8-19(2,3)14-12(24-8)7-10(20)13-15(21)9-5-6-11(23-4)16(22)17(9)25-18(13)14/h5-8,20,22H,1-4H3/t8-/m0/s1

> <INCHI_KEY>
DNYSLSNXLMFTTC-UHFFFAOYSA-N

> <FORMULA>
C19H18O6

> <MOLECULAR_WEIGHT>
342.347

> <EXACT_MASS>
342.1103383

> <JCHEM_ACCEPTOR_COUNT>
5

> <JCHEM_ATOM_COUNT>
43

> <JCHEM_AVERAGE_POLARIZABILITY>
35.282897382089956

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
2

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
1

> <JCHEM_IUPAC>
5,10-dihydroxy-9-methoxy-1,1,2-trimethyl-1H,2H,6H-furo[2,3-c]xanthen-6-one

> <ALOGPS_LOGP>
4.06

> <JCHEM_LOGP>
3.886604253

> <ALOGPS_LOGS>
-3.90

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
4

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA>
8.8594371925169

> <JCHEM_PKA_STRONGEST_ACIDIC>
8.238583908566921

> <JCHEM_PKA_STRONGEST_BASIC>
-3.753726534989051

> <JCHEM_POLAR_SURFACE_AREA>
85.22000000000001

> <JCHEM_REFRACTIVITY>
90.30260000000003

> <JCHEM_ROTATABLE_BOND_COUNT>
1

> <JCHEM_RULE_OF_FIVE>
1

> <ALOGPS_SOLUBILITY>
4.34e-02 g/l

> <JCHEM_TRADITIONAL_IUPAC>
5,10-dihydroxy-9-methoxy-1,1,2-trimethyl-2H-furo[2,3-c]xanthen-6-one

> <JCHEM_VEBER_RULE>
0

$$$$

     RDKit          3D

 43 46  0  0  0  0  0  0  0  0999 V2000
    6.2282   -1.5761   -0.2370 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.8246   -1.8050   -0.1414 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.9427   -0.7330   -0.0890 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.4432    0.5571   -0.1306 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5490    1.6007   -0.0771 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.2058    1.3473    0.0146 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.2633    2.3718    0.0714 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.6749    3.5473    0.0365 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0924    2.0900    0.1641 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0357    3.0967    0.2211 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6131    4.4175    0.1845 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3640    2.7415    0.3124 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7738    1.4215    0.3482 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8187    0.4309    0.2903 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4912    0.7806    0.1991 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.4315   -0.1740    0.1431 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.7089    0.0583    0.0560 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.6018   -1.0146    0.0028 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.0817   -2.3042    0.0457 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5471   -0.8484    0.3469 C   0  0  2  0  0  0  0  0  0  0  0  0
   -1.8154   -1.9385    1.0713 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.9095   -1.2481   -1.0691 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.8159   -0.4412    1.0668 C   0  0  2  0  0  0  0  0  0  0  0  0
   -4.9319   -1.4065    0.7833 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.0537    0.8292    0.4377 O   0  0  0  0  0  0  0  0  0  0  0  0
    6.5780   -0.8439    0.5283 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.4144   -1.1711   -1.2481 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.7834   -2.5181   -0.1053 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.5074    0.7304   -0.2031 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.8740    2.6404   -0.1054 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2156    5.2058    0.2200 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.1287    3.5307    0.3588 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.6404   -3.1315    0.0134 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3549   -2.8963    0.8372 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9282   -1.8152    2.1754 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7894   -2.0707    0.7442 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8431   -2.3565   -1.1185 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.9201   -0.8997   -1.3077 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1663   -0.8279   -1.7829 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5981   -0.3347    2.1358 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.8293   -0.9127    0.3615 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.1810   -1.9166    1.7552 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.5362   -2.2130    0.1311 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
  6  7  1  0
  7  8  2  0
  7  9  1  0
  9 10  2  0
 10 11  1  0
 10 12  1  0
 12 13  2  0
 13 14  1  0
 14 15  2  0
 15 16  1  0
 16 17  1  0
 17 18  2  0
 18 19  1  0
 14 20  1  0
 20 21  1  1
 20 22  1  0
 20 23  1  0
 23 24  1  0
 23 25  1  0
 18  3  1  0
 17  6  1  0
 15  9  1  0
 25 13  1  0
  1 26  1  0
  1 27  1  0
  1 28  1  0
  4 29  1  0
  5 30  1  0
 11 31  1  0
 12 32  1  0
 19 33  1  0
 21 34  1  0
 21 35  1  0
 21 36  1  0
 22 37  1  0
 22 38  1  0
 22 39  1  0
 23 40  1  1
 24 41  1  0
 24 42  1  0
 24 43  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       6.228  -1.576  -0.237  0.00  0.00           C+0
HETATM    2  O   UNK     0       4.825  -1.805  -0.141  0.00  0.00           O+0
HETATM    3  C   UNK     0       3.943  -0.733  -0.089  0.00  0.00           C+0
HETATM    4  C   UNK     0       4.443   0.557  -0.131  0.00  0.00           C+0
HETATM    5  C   UNK     0       3.549   1.601  -0.077  0.00  0.00           C+0
HETATM    6  C   UNK     0       2.206   1.347   0.015  0.00  0.00           C+0
HETATM    7  C   UNK     0       1.263   2.372   0.071  0.00  0.00           C+0
HETATM    8  O   UNK     0       1.675   3.547   0.037  0.00  0.00           O+0
HETATM    9  C   UNK     0      -0.092   2.090   0.164  0.00  0.00           C+0
HETATM   10  C   UNK     0      -1.036   3.097   0.221  0.00  0.00           C+0
HETATM   11  O   UNK     0      -0.613   4.418   0.185  0.00  0.00           O+0
HETATM   12  C   UNK     0      -2.364   2.741   0.312  0.00  0.00           C+0
HETATM   13  C   UNK     0      -2.774   1.422   0.348  0.00  0.00           C+0
HETATM   14  C   UNK     0      -1.819   0.431   0.290  0.00  0.00           C+0
HETATM   15  C   UNK     0      -0.491   0.781   0.199  0.00  0.00           C+0
HETATM   16  O   UNK     0       0.432  -0.174   0.143  0.00  0.00           O+0
HETATM   17  C   UNK     0       1.709   0.058   0.056  0.00  0.00           C+0
HETATM   18  C   UNK     0       2.602  -1.015   0.003  0.00  0.00           C+0
HETATM   19  O   UNK     0       2.082  -2.304   0.046  0.00  0.00           O+0
HETATM   20  C   UNK     0      -2.547  -0.848   0.347  0.00  0.00           C+0
HETATM   21  C   UNK     0      -1.815  -1.938   1.071  0.00  0.00           C+0
HETATM   22  C   UNK     0      -2.910  -1.248  -1.069  0.00  0.00           C+0
HETATM   23  C   UNK     0      -3.816  -0.441   1.067  0.00  0.00           C+0
HETATM   24  C   UNK     0      -4.932  -1.407   0.783  0.00  0.00           C+0
HETATM   25  O   UNK     0      -4.054   0.829   0.438  0.00  0.00           O+0
HETATM   26  H   UNK     0       6.578  -0.844   0.528  0.00  0.00           H+0
HETATM   27  H   UNK     0       6.414  -1.171  -1.248  0.00  0.00           H+0
HETATM   28  H   UNK     0       6.783  -2.518  -0.105  0.00  0.00           H+0
HETATM   29  H   UNK     0       5.507   0.730  -0.203  0.00  0.00           H+0
HETATM   30  H   UNK     0       3.874   2.640  -0.105  0.00  0.00           H+0
HETATM   31  H   UNK     0      -1.216   5.206   0.220  0.00  0.00           H+0
HETATM   32  H   UNK     0      -3.129   3.531   0.359  0.00  0.00           H+0
HETATM   33  H   UNK     0       2.640  -3.131   0.013  0.00  0.00           H+0
HETATM   34  H   UNK     0      -2.355  -2.896   0.837  0.00  0.00           H+0
HETATM   35  H   UNK     0      -1.928  -1.815   2.175  0.00  0.00           H+0
HETATM   36  H   UNK     0      -0.789  -2.071   0.744  0.00  0.00           H+0
HETATM   37  H   UNK     0      -2.843  -2.357  -1.119  0.00  0.00           H+0
HETATM   38  H   UNK     0      -3.920  -0.900  -1.308  0.00  0.00           H+0
HETATM   39  H   UNK     0      -2.166  -0.828  -1.783  0.00  0.00           H+0
HETATM   40  H   UNK     0      -3.598  -0.335   2.136  0.00  0.00           H+0
HETATM   41  H   UNK     0      -5.829  -0.913   0.362  0.00  0.00           H+0
HETATM   42  H   UNK     0      -5.181  -1.917   1.755  0.00  0.00           H+0
HETATM   43  H   UNK     0      -4.536  -2.213   0.131  0.00  0.00           H+0
CONECT    1    2   26   27   28                                             
CONECT    2    1    3                                                       
CONECT    3    2    4   18                                                  
CONECT    4    3    5   29                                                  
CONECT    5    4    6   30                                                  
CONECT    6    5    7   17                                                  
CONECT    7    6    8    9                                                  
CONECT    8    7                                                            
CONECT    9    7   10   15                                                  
CONECT   10    9   11   12                                                  
CONECT   11   10   31                                                       
CONECT   12   10   13   32                                                  
CONECT   13   12   14   25                                                  
CONECT   14   13   15   20                                                  
CONECT   15   14   16    9                                                  
CONECT   16   15   17                                                       
CONECT   17   16   18    6                                                  
CONECT   18   17   19    3                                                  
CONECT   19   18   33                                                       
CONECT   20   14   21   22   23                                             
CONECT   21   20   34   35   36                                             
CONECT   22   20   37   38   39                                             
CONECT   23   20   24   25   40                                             
CONECT   24   23   41   42   43                                             
CONECT   25   23   13                                                       
CONECT   26    1                                                            
CONECT   27    1                                                            
CONECT   28    1                                                            
CONECT   29    4                                                            
CONECT   30    5                                                            
CONECT   31   11                                                            
CONECT   32   12                                                            
CONECT   33   19                                                            
CONECT   34   21                                                            
CONECT   35   21                                                            
CONECT   36   21                                                            
CONECT   37   22                                                            
CONECT   38   22                                                            
CONECT   39   22                                                            
CONECT   40   23                                                            
CONECT   41   24                                                            
CONECT   42   24                                                            
CONECT   43   24                                                            
MASTER        0    0    0    0    0    0    0    0   43    0   92    0
END

RDKit          3D

43 46  0  0  0  0  0  0  0  0999 V2000
    6.2282   -1.5761   -0.2370 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.8246   -1.8050   -0.1414 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.9427   -0.7330   -0.0890 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.4432    0.5571   -0.1306 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5490    1.6007   -0.0771 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.2058    1.3473    0.0146 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.2633    2.3718    0.0714 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.6749    3.5473    0.0365 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0924    2.0900    0.1641 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0357    3.0967    0.2211 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6131    4.4175    0.1845 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3640    2.7415    0.3124 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7738    1.4215    0.3482 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8187    0.4309    0.2903 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4912    0.7806    0.1991 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.4315   -0.1740    0.1431 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.7089    0.0583    0.0560 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.6018   -1.0146    0.0028 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.0817   -2.3042    0.0457 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5471   -0.8484    0.3469 C   0  0  2  0  0  0  0  0  0  0  0  0
   -1.8154   -1.9385    1.0713 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.9095   -1.2481   -1.0691 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.8159   -0.4412    1.0668 C   0  0  2  0  0  0  0  0  0  0  0  0
   -4.9319   -1.4065    0.7833 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.0537    0.8292    0.4377 O   0  0  0  0  0  0  0  0  0  0  0  0
    6.5780   -0.8439    0.5283 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.4144   -1.1711   -1.2481 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.7834   -2.5181   -0.1053 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.5074    0.7304   -0.2031 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.8740    2.6404   -0.1054 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2156    5.2058    0.2200 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.1287    3.5307    0.3588 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.6404   -3.1315    0.0134 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3549   -2.8963    0.8372 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9282   -1.8152    2.1754 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7894   -2.0707    0.7442 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8431   -2.3565   -1.1185 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.9201   -0.8997   -1.3077 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1663   -0.8279   -1.7829 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5981   -0.3347    2.1358 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.8293   -0.9127    0.3615 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.1810   -1.9166    1.7552 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.5362   -2.2130    0.1311 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
  6  7  1  0
  7  8  2  0
  7  9  1  0
  9 10  2  0
 10 11  1  0
 10 12  1  0
 12 13  2  0
 13 14  1  0
 14 15  2  0
 15 16  1  0
 16 17  1  0
 17 18  2  0
 18 19  1  0
 14 20  1  0
 20 21  1  1
 20 22  1  0
 20 23  1  0
 23 24  1  0
 23 25  1  0
 18  3  1  0
 17  6  1  0
 15  9  1  0
 25 13  1  0
  1 26  1  0
  1 27  1  0
  1 28  1  0
  4 29  1  0
  5 30  1  0
 11 31  1  0
 12 32  1  0
 19 33  1  0
 21 34  1  0
 21 35  1  0
 21 36  1  0
 22 37  1  0
 22 38  1  0
 22 39  1  0
 23 40  1  1
 24 41  1  0
 24 42  1  0
 24 43  1  0
M  END

View in JSmol View NMR Assignments

Synonyms

Not Available

Chemical Formula

C₁₉H₁₈O₆

Average Mass

342.3470 Da

Monoisotopic Mass

342.11034 Da

IUPAC Name

5,10-dihydroxy-9-methoxy-1,1,2-trimethyl-1H,2H,6H-furo[2,3-c]xanthen-6-one

Traditional Name

5,10-dihydroxy-9-methoxy-1,1,2-trimethyl-2H-furo[2,3-c]xanthen-6-one

CAS Registry Number

Not Available

SMILES

COC1=C(O)C2=C(C=C1)C(=O)C1=C(O)C=C3OC(C)C(C)(C)C3=C1O2

InChI Identifier

InChI=1S/C19H18O6/c1-8-19(2,3)14-12(24-8)7-10(20)13-15(21)9-5-6-11(23-4)16(22)17(9)25-18(13)14/h5-8,20,22H,1-4H3

InChI Key

DNYSLSNXLMFTTC-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
Phomopsis sp.	NPAtlas	24042071

Chemical Taxonomy

Classification

Not classified

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	4.06	ALOGPS
logP	3.89	ChemAxon
logS	-3.9	ALOGPS
pKa (Strongest Acidic)	8.24	ChemAxon
pKa (Strongest Basic)	-3.8	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	5	ChemAxon
Hydrogen Donor Count	2	ChemAxon
Polar Surface Area	85.22 Å²	ChemAxon
Rotatable Bond Count	1	ChemAxon
Refractivity	90.3 m³·mol⁻¹	ChemAxon
Polarizability	35.28 Å³	ChemAxon
Number of Rings	4	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

NPA017249

HMDB ID

Not Available

DrugBank ID

Not Available

Phenol Explorer Compound ID

Not Available

FoodDB ID

Not Available

KNApSAcK ID

Not Available

Chemspider ID

9614146

KEGG Compound ID

Not Available

BioCyc ID

Not Available

BiGG ID

Not Available

Wikipedia Link

Not Available

METLIN ID

Not Available

PubChem Compound

11439282

PDB ID

Not Available

ChEBI ID

66366

Good Scents ID

Not Available

References

General References

Hay AE, Aumond MC, Mallet S, Dumontet V, Litaudon M, Rondeau D, Richomme P: Antioxidant xanthones from Garcinia vieillardii. J Nat Prod. 2004 Apr;67(4):707-9. doi: 10.1021/np0304971. [PubMed:15104511 ]

Showing NP-Card for 6-O- methyl-2-deprenylrheediaxanthone B (NP0012127)

MOL for NP0012127 (6-O- methyl-2-deprenylrheediaxanthone B)

3D MOL for NP0012127 (6-O- methyl-2-deprenylrheediaxanthone B)

3D SDF for NP0012127 (6-O- methyl-2-deprenylrheediaxanthone B)

3D-SDF for NP0012127 (6-O- methyl-2-deprenylrheediaxanthone B)

PDB for NP0012127 (6-O- methyl-2-deprenylrheediaxanthone B)

3D PDB for NP0012127 (6-O- methyl-2-deprenylrheediaxanthone B)

SMILES for NP0012127 (6-O- methyl-2-deprenylrheediaxanthone B)

INCHI for NP0012127 (6-O- methyl-2-deprenylrheediaxanthone B)

Structure for NP0012127 (6-O- methyl-2-deprenylrheediaxanthone B)

3D Structure for NP0012127 (6-O- methyl-2-deprenylrheediaxanthone B)