NP-MRD: Showing NP-Card for Biscopyran (NP0005831)

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Record Information

Version

2.0

Created at

2020-12-09 02:58:43 UTC

Updated at

2021-07-15 16:53:06 UTC

NP-MRD ID

NP0005831

Secondary Accession Numbers

None

Natural Product Identification

Common Name

Biscopyran

Provided By

NPAtlas

Description

Biscopyran belongs to the class of organic compounds known as pyrans. Pyrans are compounds containing a pyran ring, which is a six-member heterocyclic, non-aromatic ring with five carbon atoms, one oxygen atom and two ring double bonds. Biscopyran is found in Biscogniauxia mediterranea. Biscopyran was first documented in 2005 (PMID: 15844950). Based on a literature review very few articles have been published on Biscopyran.

Structure

MOL 3D MOL SDF 3D SDF PDB SMILES InChI


  Mrv1652306242118233D          

 56 57  0  0  0  0            999 V2000
    2.0397    3.7115   -0.0359 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.2479    2.2327    0.1518 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.9559    1.5103   -0.7157 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.4545    2.2881   -1.7719 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.3135    1.7836   -2.7318 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.2267    0.1160   -0.6654 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.9696   -0.3526   -1.6071 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.7778   -0.8422    0.3055 C   0  0  1  0  0  0  0  0  0  0  0  0
    1.7819   -0.3788    1.1591 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.4329   -0.6379    0.9292 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.1148   -1.8765    0.4545 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.1507   -2.6959   -0.1381 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.8831   -4.0405   -0.6346 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.4102   -2.1858   -0.1990 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.4284   -3.0651   -0.7918 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2539   -2.3266    0.5890 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6658   -3.6211    0.0335 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1422   -1.5086    1.1777 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5294   -2.0495    1.2884 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7921   -0.1798    1.6485 C   0  0  2  0  0  0  0  0  0  0  0  0
   -2.8100    0.8666    1.3958 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.9558    0.5836    1.9330 O   0  0  0  0  0  0  0  0  0  0  0  0
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   -1.7583    3.8524   -0.6386 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.8718    2.9100    0.6050 O   0  0  0  0  0  0  0  0  0  0  0  0
   -5.1332    2.6002    1.1355 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5621    0.2745    1.1532 O   0  0  0  0  0  0  0  0  0  0  0  0
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    5.2548    1.4009   -2.3033 H   0  0  0  0  0  0  0  0  0  0  0  0
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    3.6624   -1.0695    1.0136 H   0  0  0  0  0  0  0  0  0  0  0  0
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   -5.1567    2.5277    2.2455 H   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0  0  0  0
  2  3  2  0  0  0  0
  3  4  1  0  0  0  0
  4  5  1  0  0  0  0
  3  6  1  0  0  0  0
  6  7  2  0  0  0  0
  6  8  1  0  0  0  0
  8  9  1  0  0  0  0
  9 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
 11 16  1  0  0  0  0
 16 17  1  0  0  0  0
 16 18  2  0  0  0  0
 18 19  1  0  0  0  0
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 14  8  1  0  0  0  0
 28 10  1  0  0  0  0
  1 29  1  0  0  0  0
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  8 36  1  1  0  0  0
 13 37  1  0  0  0  0
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 27 56  1  0  0  0  0
M  END

     RDKit          3D

 56 57  0  0  0  0  0  0  0  0999 V2000
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    4.3135    1.7836   -2.7318 C   0  0  0  0  0  0  0  0  0  0  0  0
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    1.7819   -0.3788    1.1591 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.4329   -0.6379    0.9292 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.1148   -1.8765    0.4545 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.1507   -2.6959   -0.1381 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.8831   -4.0405   -0.6346 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.4102   -2.1858   -0.1990 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.4284   -3.0651   -0.7918 C   0  0  0  0  0  0  0  0  0  0  0  0
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  2  3  2  0
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M  END


  Mrv1652306242118233D          

 56 57  0  0  0  0            999 V2000
    2.0397    3.7115   -0.0359 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.2479    2.2327    0.1518 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.9559    1.5103   -0.7157 C   0  0  0  0  0  0  0  0  0  0  0  0
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    1.9319   -4.5481   -0.6539 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.6608   -4.1631   -1.7042 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.4217   -4.7527    0.0698 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.7277   -3.8945   -0.0933 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.3679   -2.4787   -0.9085 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.1883   -3.4376   -1.7983 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4106   -3.7856   -1.0394 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8089   -3.4738   -0.1644 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7247   -4.4731    0.6861 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5068   -3.1512    1.5742 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.0408   -1.9584    0.3360 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.0989   -1.5909    2.1345 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7587   -0.2548    2.7868 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7426    2.0427    0.0317 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6800    3.6533   -1.7142 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9179    4.5135   -0.3628 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6960    4.3782   -0.4483 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.7903    3.4821    0.8826 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.5163    1.6943    0.6390 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.1567    2.5277    2.2455 H   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0  0  0  0
  2  3  2  0  0  0  0
  3  4  1  0  0  0  0
  4  5  1  0  0  0  0
  3  6  1  0  0  0  0
  6  7  2  0  0  0  0
  6  8  1  0  0  0  0
  8  9  1  0  0  0  0
  9 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
 11 16  1  0  0  0  0
 16 17  1  0  0  0  0
 16 18  2  0  0  0  0
 18 19  1  0  0  0  0
 18 20  1  0  0  0  0
 20 21  1  0  0  0  0
 21 22  2  0  0  0  0
 21 23  1  0  0  0  0
 23 24  2  0  0  0  0
 24 25  1  0  0  0  0
 23 26  1  0  0  0  0
 26 27  1  0  0  0  0
 20 28  1  0  0  0  0
 14  8  1  0  0  0  0
 28 10  1  0  0  0  0
  1 29  1  0  0  0  0
  1 30  1  0  0  0  0
  1 31  1  0  0  0  0
  2 32  1  0  0  0  0
  5 33  1  0  0  0  0
  5 34  1  0  0  0  0
  5 35  1  0  0  0  0
  8 36  1  1  0  0  0
 13 37  1  0  0  0  0
 13 38  1  0  0  0  0
 13 39  1  0  0  0  0
 15 40  1  0  0  0  0
 15 41  1  0  0  0  0
 15 42  1  0  0  0  0
 17 43  1  0  0  0  0
 17 44  1  0  0  0  0
 17 45  1  0  0  0  0
 19 46  1  0  0  0  0
 19 47  1  0  0  0  0
 19 48  1  0  0  0  0
 20 49  1  1  0  0  0
 24 50  1  0  0  0  0
 25 51  1  0  0  0  0
 25 52  1  0  0  0  0
 25 53  1  0  0  0  0
 27 54  1  0  0  0  0
 27 55  1  0  0  0  0
 27 56  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0005831

> <DATABASE_NAME>
NP-MRD

> <SMILES>
[H]\C(=C(\OC([H])([H])[H])C(=O)[C@]1([H])OC2=C(C(=C1C([H])([H])[H])C([H])([H])[H])C(=C(C([H])([H])[H])[C@]([H])(O2)C(=O)C(\OC([H])([H])[H])=C(/[H])C([H])([H])[H])C([H])([H])[H])C([H])([H])[H]

> <INCHI_IDENTIFIER>
InChI=1S/C22H28O6/c1-9-15(25-7)18(23)20-13(5)11(3)17-12(4)14(6)21(28-22(17)27-20)19(24)16(10-2)26-8/h9-10,20-21H,1-8H3/b15-9-,16-10-/t20-,21+

> <INCHI_KEY>
YPPQLGPCXICENU-NAPRVIBBSA-N

> <FORMULA>
C22H28O6

> <MOLECULAR_WEIGHT>
388.46

> <EXACT_MASS>
388.188588622

> <JCHEM_ACCEPTOR_COUNT>
6

> <JCHEM_ATOM_COUNT>
56

> <JCHEM_AVERAGE_POLARIZABILITY>
42.78699767202458

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
0

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
1

> <JCHEM_IUPAC>
(2Z)-2-methoxy-1-[(2S,7R)-7-[(2Z)-2-methoxybut-2-enoyl]-3,4,5,6-tetramethyl-2H,7H-pyrano[2,3-b]pyran-2-yl]but-2-en-1-one

> <ALOGPS_LOGP>
3.92

> <JCHEM_LOGP>
3.666942972

> <ALOGPS_LOGS>
-4.16

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
2

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA>
16.92245236119776

> <JCHEM_PKA_STRONGEST_ACIDIC>
16.24025467790045

> <JCHEM_PKA_STRONGEST_BASIC>
-4.402550748010693

> <JCHEM_POLAR_SURFACE_AREA>
71.06

> <JCHEM_REFRACTIVITY>
120.3235

> <JCHEM_ROTATABLE_BOND_COUNT>
6

> <JCHEM_RULE_OF_FIVE>
1

> <ALOGPS_SOLUBILITY>
2.70e-02 g/l

> <JCHEM_TRADITIONAL_IUPAC>
(2Z)-2-methoxy-1-[(2S,7R)-7-[(2Z)-2-methoxybut-2-enoyl]-3,4,5,6-tetramethyl-2H,7H-pyrano[2,3-b]pyran-2-yl]but-2-en-1-one

> <JCHEM_VEBER_RULE>
0

$$$$

     RDKit          3D

 56 57  0  0  0  0  0  0  0  0999 V2000
    2.0397    3.7115   -0.0359 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.2479    2.2327    0.1518 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.9559    1.5103   -0.7157 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.4545    2.2881   -1.7719 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.3135    1.7836   -2.7318 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.2267    0.1160   -0.6654 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.9696   -0.3526   -1.6071 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.7778   -0.8422    0.3055 C   0  0  1  0  0  0  0  0  0  0  0  0
    1.7819   -0.3788    1.1591 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.4329   -0.6379    0.9292 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.1148   -1.8765    0.4545 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.1507   -2.6959   -0.1381 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.8831   -4.0405   -0.6346 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.4102   -2.1858   -0.1990 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.4284   -3.0651   -0.7918 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2539   -2.3266    0.5890 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6658   -3.6211    0.0335 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1422   -1.5086    1.1777 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5294   -2.0495    1.2884 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7921   -0.1798    1.6485 C   0  0  2  0  0  0  0  0  0  0  0  0
   -2.8100    0.8666    1.3958 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.9558    0.5836    1.9330 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7497    2.0853    0.6898 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6797    2.5316    0.0773 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7583    3.8524   -0.6386 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.8718    2.9100    0.6050 O   0  0  0  0  0  0  0  0  0  0  0  0
   -5.1332    2.6002    1.1355 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5621    0.2745    1.1532 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.9726    4.2735    0.2537 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.8491    3.9546   -1.0818 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.2248    4.0578    0.6083 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.8317    1.7873    0.9982 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.2548    1.4009   -2.3033 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.8309    1.0333   -3.3961 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.6409    2.6476   -3.3881 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.6624   -1.0695    1.0136 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.9319   -4.5481   -0.6539 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.6608   -4.1631   -1.7042 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.4217   -4.7527    0.0698 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.7277   -3.8945   -0.0933 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.3679   -2.4787   -0.9085 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.1883   -3.4376   -1.7983 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4106   -3.7856   -1.0394 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8089   -3.4738   -0.1644 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7247   -4.4731    0.6861 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5068   -3.1512    1.5742 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.0408   -1.9584    0.3360 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.0989   -1.5909    2.1345 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7587   -0.2548    2.7868 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7426    2.0427    0.0317 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6800    3.6533   -1.7142 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9179    4.5135   -0.3628 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6960    4.3782   -0.4483 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.7903    3.4821    0.8826 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.5163    1.6943    0.6390 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.1567    2.5277    2.2455 H   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0
  2  3  2  0
  3  4  1  0
  4  5  1  0
  3  6  1  0
  6  7  2  0
  6  8  1  0
  8  9  1  0
  9 10  1  0
 10 11  2  0
 11 12  1  0
 12 13  1  0
 12 14  2  0
 14 15  1  0
 11 16  1  0
 16 17  1  0
 16 18  2  0
 18 19  1  0
 18 20  1  0
 20 21  1  0
 21 22  2  0
 21 23  1  0
 23 24  2  0
 24 25  1  0
 23 26  1  0
 26 27  1  0
 20 28  1  0
 14  8  1  0
 28 10  1  0
  1 29  1  0
  1 30  1  0
  1 31  1  0
  2 32  1  0
  5 33  1  0
  5 34  1  0
  5 35  1  0
  8 36  1  1
 13 37  1  0
 13 38  1  0
 13 39  1  0
 15 40  1  0
 15 41  1  0
 15 42  1  0
 17 43  1  0
 17 44  1  0
 17 45  1  0
 19 46  1  0
 19 47  1  0
 19 48  1  0
 20 49  1  1
 24 50  1  0
 25 51  1  0
 25 52  1  0
 25 53  1  0
 27 54  1  0
 27 55  1  0
 27 56  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       2.040   3.712  -0.036  0.00  0.00           C+0
HETATM    2  C   UNK     0       2.248   2.233   0.152  0.00  0.00           C+0
HETATM    3  C   UNK     0       2.956   1.510  -0.716  0.00  0.00           C+0
HETATM    4  O   UNK     0       3.454   2.288  -1.772  0.00  0.00           O+0
HETATM    5  C   UNK     0       4.314   1.784  -2.732  0.00  0.00           C+0
HETATM    6  C   UNK     0       3.227   0.116  -0.665  0.00  0.00           C+0
HETATM    7  O   UNK     0       3.970  -0.353  -1.607  0.00  0.00           O+0
HETATM    8  C   UNK     0       2.778  -0.842   0.306  0.00  0.00           C+0
HETATM    9  O   UNK     0       1.782  -0.379   1.159  0.00  0.00           O+0
HETATM   10  C   UNK     0       0.433  -0.638   0.929  0.00  0.00           C+0
HETATM   11  C   UNK     0       0.115  -1.877   0.455  0.00  0.00           C+0
HETATM   12  C   UNK     0       1.151  -2.696  -0.138  0.00  0.00           C+0
HETATM   13  C   UNK     0       0.883  -4.040  -0.635  0.00  0.00           C+0
HETATM   14  C   UNK     0       2.410  -2.186  -0.199  0.00  0.00           C+0
HETATM   15  C   UNK     0       3.428  -3.065  -0.792  0.00  0.00           C+0
HETATM   16  C   UNK     0      -1.254  -2.327   0.589  0.00  0.00           C+0
HETATM   17  C   UNK     0      -1.666  -3.621   0.034  0.00  0.00           C+0
HETATM   18  C   UNK     0      -2.142  -1.509   1.178  0.00  0.00           C+0
HETATM   19  C   UNK     0      -3.529  -2.050   1.288  0.00  0.00           C+0
HETATM   20  C   UNK     0      -1.792  -0.180   1.649  0.00  0.00           C+0
HETATM   21  C   UNK     0      -2.810   0.867   1.396  0.00  0.00           C+0
HETATM   22  O   UNK     0      -3.956   0.584   1.933  0.00  0.00           O+0
HETATM   23  C   UNK     0      -2.750   2.085   0.690  0.00  0.00           C+0
HETATM   24  C   UNK     0      -1.680   2.532   0.077  0.00  0.00           C+0
HETATM   25  C   UNK     0      -1.758   3.852  -0.639  0.00  0.00           C+0
HETATM   26  O   UNK     0      -3.872   2.910   0.605  0.00  0.00           O+0
HETATM   27  C   UNK     0      -5.133   2.600   1.135  0.00  0.00           C+0
HETATM   28  O   UNK     0      -0.562   0.275   1.153  0.00  0.00           O+0
HETATM   29  H   UNK     0       2.973   4.274   0.254  0.00  0.00           H+0
HETATM   30  H   UNK     0       1.849   3.955  -1.082  0.00  0.00           H+0
HETATM   31  H   UNK     0       1.225   4.058   0.608  0.00  0.00           H+0
HETATM   32  H   UNK     0       1.832   1.787   0.998  0.00  0.00           H+0
HETATM   33  H   UNK     0       5.255   1.401  -2.303  0.00  0.00           H+0
HETATM   34  H   UNK     0       3.831   1.033  -3.396  0.00  0.00           H+0
HETATM   35  H   UNK     0       4.641   2.648  -3.388  0.00  0.00           H+0
HETATM   36  H   UNK     0       3.662  -1.069   1.014  0.00  0.00           H+0
HETATM   37  H   UNK     0       1.932  -4.548  -0.654  0.00  0.00           H+0
HETATM   38  H   UNK     0       0.661  -4.163  -1.704  0.00  0.00           H+0
HETATM   39  H   UNK     0       0.422  -4.753   0.070  0.00  0.00           H+0
HETATM   40  H   UNK     0       3.728  -3.894  -0.093  0.00  0.00           H+0
HETATM   41  H   UNK     0       4.368  -2.479  -0.909  0.00  0.00           H+0
HETATM   42  H   UNK     0       3.188  -3.438  -1.798  0.00  0.00           H+0
HETATM   43  H   UNK     0      -1.411  -3.786  -1.039  0.00  0.00           H+0
HETATM   44  H   UNK     0      -2.809  -3.474  -0.164  0.00  0.00           H+0
HETATM   45  H   UNK     0      -1.725  -4.473   0.686  0.00  0.00           H+0
HETATM   46  H   UNK     0      -3.507  -3.151   1.574  0.00  0.00           H+0
HETATM   47  H   UNK     0      -4.041  -1.958   0.336  0.00  0.00           H+0
HETATM   48  H   UNK     0      -4.099  -1.591   2.135  0.00  0.00           H+0
HETATM   49  H   UNK     0      -1.759  -0.255   2.787  0.00  0.00           H+0
HETATM   50  H   UNK     0      -0.743   2.043   0.032  0.00  0.00           H+0
HETATM   51  H   UNK     0      -1.680   3.653  -1.714  0.00  0.00           H+0
HETATM   52  H   UNK     0      -0.918   4.513  -0.363  0.00  0.00           H+0
HETATM   53  H   UNK     0      -2.696   4.378  -0.448  0.00  0.00           H+0
HETATM   54  H   UNK     0      -5.790   3.482   0.883  0.00  0.00           H+0
HETATM   55  H   UNK     0      -5.516   1.694   0.639  0.00  0.00           H+0
HETATM   56  H   UNK     0      -5.157   2.528   2.245  0.00  0.00           H+0
CONECT    1    2   29   30   31                                             
CONECT    2    1    3   32                                                  
CONECT    3    2    4    6                                                  
CONECT    4    3    5                                                       
CONECT    5    4   33   34   35                                             
CONECT    6    3    7    8                                                  
CONECT    7    6                                                            
CONECT    8    6    9   14   36                                             
CONECT    9    8   10                                                       
CONECT   10    9   11   28                                                  
CONECT   11   10   12   16                                                  
CONECT   12   11   13   14                                                  
CONECT   13   12   37   38   39                                             
CONECT   14   12   15    8                                                  
CONECT   15   14   40   41   42                                             
CONECT   16   11   17   18                                                  
CONECT   17   16   43   44   45                                             
CONECT   18   16   19   20                                                  
CONECT   19   18   46   47   48                                             
CONECT   20   18   21   28   49                                             
CONECT   21   20   22   23                                                  
CONECT   22   21                                                            
CONECT   23   21   24   26                                                  
CONECT   24   23   25   50                                                  
CONECT   25   24   51   52   53                                             
CONECT   26   23   27                                                       
CONECT   27   26   54   55   56                                             
CONECT   28   20   10                                                       
CONECT   29    1                                                            
CONECT   30    1                                                            
CONECT   31    1                                                            
CONECT   32    2                                                            
CONECT   33    5                                                            
CONECT   34    5                                                            
CONECT   35    5                                                            
CONECT   36    8                                                            
CONECT   37   13                                                            
CONECT   38   13                                                            
CONECT   39   13                                                            
CONECT   40   15                                                            
CONECT   41   15                                                            
CONECT   42   15                                                            
CONECT   43   17                                                            
CONECT   44   17                                                            
CONECT   45   17                                                            
CONECT   46   19                                                            
CONECT   47   19                                                            
CONECT   48   19                                                            
CONECT   49   20                                                            
CONECT   50   24                                                            
CONECT   51   25                                                            
CONECT   52   25                                                            
CONECT   53   25                                                            
CONECT   54   27                                                            
CONECT   55   27                                                            
CONECT   56   27                                                            
MASTER        0    0    0    0    0    0    0    0   56    0  114    0
END

RDKit          3D

56 57  0  0  0  0  0  0  0  0999 V2000
    2.0397    3.7115   -0.0359 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.2479    2.2327    0.1518 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.9559    1.5103   -0.7157 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.4545    2.2881   -1.7719 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.3135    1.7836   -2.7318 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.2267    0.1160   -0.6654 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.9696   -0.3526   -1.6071 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.7778   -0.8422    0.3055 C   0  0  1  0  0  0  0  0  0  0  0  0
    1.7819   -0.3788    1.1591 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.4329   -0.6379    0.9292 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.1148   -1.8765    0.4545 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.1507   -2.6959   -0.1381 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.8831   -4.0405   -0.6346 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.4102   -2.1858   -0.1990 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.4284   -3.0651   -0.7918 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2539   -2.3266    0.5890 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6658   -3.6211    0.0335 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1422   -1.5086    1.1777 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5294   -2.0495    1.2884 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7921   -0.1798    1.6485 C   0  0  2  0  0  0  0  0  0  0  0  0
   -2.8100    0.8666    1.3958 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.9558    0.5836    1.9330 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7497    2.0853    0.6898 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6797    2.5316    0.0773 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7583    3.8524   -0.6386 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.8718    2.9100    0.6050 O   0  0  0  0  0  0  0  0  0  0  0  0
   -5.1332    2.6002    1.1355 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5621    0.2745    1.1532 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.9726    4.2735    0.2537 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.8491    3.9546   -1.0818 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.2248    4.0578    0.6083 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.8317    1.7873    0.9982 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.2548    1.4009   -2.3033 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.8309    1.0333   -3.3961 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.6409    2.6476   -3.3881 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.6624   -1.0695    1.0136 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.9319   -4.5481   -0.6539 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.6608   -4.1631   -1.7042 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.4217   -4.7527    0.0698 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.7277   -3.8945   -0.0933 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.3679   -2.4787   -0.9085 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.1883   -3.4376   -1.7983 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4106   -3.7856   -1.0394 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8089   -3.4738   -0.1644 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7247   -4.4731    0.6861 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5068   -3.1512    1.5742 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.0408   -1.9584    0.3360 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.0989   -1.5909    2.1345 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7587   -0.2548    2.7868 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7426    2.0427    0.0317 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6800    3.6533   -1.7142 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9179    4.5135   -0.3628 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6960    4.3782   -0.4483 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.7903    3.4821    0.8826 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.5163    1.6943    0.6390 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.1567    2.5277    2.2455 H   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0
  2  3  2  0
  3  4  1  0
  4  5  1  0
  3  6  1  0
  6  7  2  0
  6  8  1  0
  8  9  1  0
  9 10  1  0
 10 11  2  0
 11 12  1  0
 12 13  1  0
 12 14  2  0
 14 15  1  0
 11 16  1  0
 16 17  1  0
 16 18  2  0
 18 19  1  0
 18 20  1  0
 20 21  1  0
 21 22  2  0
 21 23  1  0
 23 24  2  0
 24 25  1  0
 23 26  1  0
 26 27  1  0
 20 28  1  0
 14  8  1  0
 28 10  1  0
  1 29  1  0
  1 30  1  0
  1 31  1  0
  2 32  1  0
  5 33  1  0
  5 34  1  0
  5 35  1  0
  8 36  1  1
 13 37  1  0
 13 38  1  0
 13 39  1  0
 15 40  1  0
 15 41  1  0
 15 42  1  0
 17 43  1  0
 17 44  1  0
 17 45  1  0
 19 46  1  0
 19 47  1  0
 19 48  1  0
 20 49  1  1
 24 50  1  0
 25 51  1  0
 25 52  1  0
 25 53  1  0
 27 54  1  0
 27 55  1  0
 27 56  1  0
M  END

View in JSmol View NMR Assignments

Synonyms

Not Available

Chemical Formula

C₂₂H₂₈O₆

Average Mass

388.4600 Da

Monoisotopic Mass

388.18859 Da

IUPAC Name

(2Z)-2-methoxy-1-[(2S,7R)-7-[(2Z)-2-methoxybut-2-enoyl]-3,4,5,6-tetramethyl-2H,7H-pyrano[2,3-b]pyran-2-yl]but-2-en-1-one

Traditional Name

(2Z)-2-methoxy-1-[(2S,7R)-7-[(2Z)-2-methoxybut-2-enoyl]-3,4,5,6-tetramethyl-2H,7H-pyrano[2,3-b]pyran-2-yl]but-2-en-1-one

CAS Registry Number

Not Available

SMILES

CO\C(=C/C)C(=O)[C@@H]1OC2=C(C(C)=C1C)C(C)=C(C)[C@H](O2)C(=O)C(\OC)=C\C

InChI Identifier

InChI=1S/C22H28O6/c1-9-15(25-7)18(23)20-13(5)11(3)17-12(4)14(6)21(28-22(17)27-20)19(24)16(10-2)26-8/h9-10,20-21H,1-8H3/b15-9-,16-10-/t20-,21+

InChI Key

YPPQLGPCXICENU-NAPRVIBBSA-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
Biscogniauxia mediterranea	NPAtlas	15844950

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as pyrans. Pyrans are compounds containing a pyran ring, which is a six-member heterocyclic, non-aromatic ring with five carbon atoms, one oxygen atom and two ring double bonds.

Kingdom

Organic compounds

Super Class

Organoheterocyclic compounds

Class

Pyrans

Sub Class

Not Available

Direct Parent

Pyrans

Alternative Parents

Substituents

Alpha-branched alpha,beta-unsaturated-ketone
Pyran
Monosaccharide
Alpha,beta-unsaturated ketone
Enone
Acryloyl-group
Ketone
Ketene acetal or derivatives
Oxacycle
Organic oxygen compound
Organic oxide
Hydrocarbon derivative
Organooxygen compound
Carbonyl group
Aliphatic heteropolycyclic compound

Molecular Framework

Aliphatic 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	3.92	ALOGPS
logP	3.67	ChemAxon
logS	-4.2	ALOGPS
pKa (Strongest Acidic)	16.24	ChemAxon
pKa (Strongest Basic)	-4.4	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	6	ChemAxon
Hydrogen Donor Count	0	ChemAxon
Polar Surface Area	71.06 Å²	ChemAxon
Rotatable Bond Count	6	ChemAxon
Refractivity	120.32 m³·mol⁻¹	ChemAxon
Polarizability	42.79 Å³	ChemAxon
Number of Rings	2	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

NPA007941

HMDB ID

Not Available

DrugBank ID

Not Available

Phenol Explorer Compound ID

Not Available

FoodDB ID

Not Available

KNApSAcK ID

C00042285

Chemspider ID

78437191

KEGG Compound ID

Not Available

BioCyc ID

Not Available

BiGG ID

Not Available

Wikipedia Link

Not Available

METLIN ID

Not Available

PubChem Compound

139585310

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

Evidente A, Andolfi A, Maddau L, Franceschini A, Marras F: Biscopyran, a phytotoxic hexasubstituted pyranopyran produced by Biscogniauxia mediterranea, a fungus pathogen of cork oak. J Nat Prod. 2005 Apr;68(4):568-71. doi: 10.1021/np049621m. [PubMed:15844950 ]

Showing NP-Card for Biscopyran (NP0005831)

MOL for NP0005831 (Biscopyran)

3D MOL for NP0005831 (Biscopyran)

3D SDF for NP0005831 (Biscopyran)

3D-SDF for NP0005831 (Biscopyran)

PDB for NP0005831 (Biscopyran)

3D PDB for NP0005831 (Biscopyran)

SMILES for NP0005831 (Biscopyran)

INCHI for NP0005831 (Biscopyran)

Structure for NP0005831 (Biscopyran)

3D Structure for NP0005831 (Biscopyran)