NP-MRD: Showing NP-Card for Enokipodin C (NP0003769)

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Record Information

Version

2.0

Created at

2020-12-09 00:55:48 UTC

Updated at

2021-07-15 16:47:20 UTC

NP-MRD ID

NP0003769

Secondary Accession Numbers

None

Natural Product Identification

Common Name

Enokipodin C

Provided By

NPAtlas

Description

(1R,9R,11R)-1,5,12,12-tetramethyl-8-oxatricyclo[7.2.1.0²,⁷]Dodeca-2(7),3,5-triene-4,9,11-triol belongs to the class of organic compounds known as 1-benzopyrans. These are organic aromatic compounds that 1-benzopyran, a bicyclic compound made up of a benzene ring fused to a pyran, so that the oxygen atom is at the 1-position. Enokipodin C is found in Flammulina velutipes. It was first documented in 2001 (PMID: 11473426). Based on a literature review very few articles have been published on (1R,9R,11R)-1,5,12,12-tetramethyl-8-oxatricyclo[7.2.1.0²,⁷]Dodeca-2(7),3,5-triene-4,9,11-triol.

Structure

MOL 3D MOL SDF 3D SDF PDB SMILES InChI


  Mrv1652306242117493D          

 39 41  0  0  0  0            999 V2000
    4.3650   -0.1482   -1.8544 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.0504   -0.0714   -1.1641 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.9050    0.3576   -1.7982 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7245    0.3994   -1.0859 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.6703    0.0183    0.2537 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.7950   -0.4034    0.8780 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.9838   -0.4498    0.1751 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.1487   -0.8748    0.7816 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6663    0.1138    0.8959 C   0  0  1  0  0  0  0  0  0  0  0  0
   -0.7256   -0.5121    2.2466 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0608    1.5692    0.9143 C   0  0  2  0  0  0  0  0  0  0  0  0
   -1.5901    1.9675    2.1314 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0676    1.7506   -0.2264 C   0  0  2  0  0  0  0  0  0  0  0  0
   -1.7188    0.5698   -1.1344 C   0  0  1  0  0  0  0  0  0  0  0  0
   -2.6650    0.3304   -2.0902 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4608    0.8266   -1.6852 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6370   -0.5476   -0.0852 C   0  0  1  0  0  0  0  0  0  0  0  0
   -1.0366   -1.7964   -0.6359 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.9966   -0.7436    0.5121 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.0087    0.6820   -1.5023 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.2527   -0.0515   -2.9456 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.8603   -1.0914   -1.5504 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.9329    0.6574   -2.8414 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.7268   -0.6937    1.9175 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.1111   -1.1511    1.7515 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.0413   -0.0768    2.8848 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7141   -0.2054    2.6974 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6325   -1.5955    2.1993 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2020    2.2411    0.6562 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1401    2.8082    2.4558 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9064    2.6923   -0.7662 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.0621    1.6544    0.2077 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5459    0.7068   -1.9217 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5205   -1.6682   -1.5897 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3060   -2.2319    0.0912 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8495   -2.5537   -0.7835 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.0323   -1.7985    0.9073 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.8152   -0.6416   -0.2311 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.2245   -0.0383    1.3345 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  2  0  0  0  0
  5  6  1  0  0  0  0
  6  7  2  0  0  0  0
  7  8  1  0  0  0  0
  5  9  1  0  0  0  0
  9 10  1  1  0  0  0
  9 11  1  0  0  0  0
 11 12  1  0  0  0  0
 11 13  1  0  0  0  0
 13 14  1  0  0  0  0
 14 15  1  6  0  0  0
 14 16  1  0  0  0  0
 14 17  1  0  0  0  0
 17 18  1  6  0  0  0
 17 19  1  0  0  0  0
  7  2  1  0  0  0  0
 17  9  1  0  0  0  0
 16  4  1  0  0  0  0
  1 20  1  0  0  0  0
  1 21  1  0  0  0  0
  1 22  1  0  0  0  0
  3 23  1  0  0  0  0
  6 24  1  0  0  0  0
  8 25  1  0  0  0  0
 10 26  1  0  0  0  0
 10 27  1  0  0  0  0
 10 28  1  0  0  0  0
 11 29  1  6  0  0  0
 12 30  1  0  0  0  0
 13 31  1  0  0  0  0
 13 32  1  0  0  0  0
 15 33  1  0  0  0  0
 18 34  1  0  0  0  0
 18 35  1  0  0  0  0
 18 36  1  0  0  0  0
 19 37  1  0  0  0  0
 19 38  1  0  0  0  0
 19 39  1  0  0  0  0
M  END

     RDKit          3D

 39 41  0  0  0  0  0  0  0  0999 V2000
    4.3650   -0.1482   -1.8544 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.0504   -0.0714   -1.1641 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.9050    0.3576   -1.7982 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7245    0.3994   -1.0859 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.6703    0.0183    0.2537 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.7950   -0.4034    0.8780 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.9838   -0.4498    0.1751 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.1487   -0.8748    0.7816 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6663    0.1138    0.8959 C   0  0  1  0  0  0  0  0  0  0  0  0
   -0.7256   -0.5121    2.2466 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0608    1.5692    0.9143 C   0  0  2  0  0  0  0  0  0  0  0  0
   -1.5901    1.9675    2.1314 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0676    1.7506   -0.2264 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7188    0.5698   -1.1344 C   0  0  1  0  0  0  0  0  0  0  0  0
   -2.6650    0.3304   -2.0902 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4608    0.8266   -1.6852 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6370   -0.5476   -0.0852 C   0  0  1  0  0  0  0  0  0  0  0  0
   -1.0366   -1.7964   -0.6359 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.9966   -0.7436    0.5121 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.0087    0.6820   -1.5023 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.2527   -0.0515   -2.9456 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.8603   -1.0914   -1.5504 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.9329    0.6574   -2.8414 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.7268   -0.6937    1.9175 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.1111   -1.1511    1.7515 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.0413   -0.0768    2.8848 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7141   -0.2054    2.6974 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6325   -1.5955    2.1993 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2020    2.2411    0.6562 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1401    2.8082    2.4558 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9064    2.6923   -0.7662 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.0621    1.6544    0.2077 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5459    0.7068   -1.9217 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5205   -1.6682   -1.5897 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3060   -2.2319    0.0912 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8495   -2.5537   -0.7835 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.0323   -1.7985    0.9073 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.8152   -0.6416   -0.2311 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.2245   -0.0383    1.3345 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  2  0
  5  6  1  0
  6  7  2  0
  7  8  1  0
  5  9  1  0
  9 10  1  1
  9 11  1  0
 11 12  1  0
 11 13  1  0
 13 14  1  0
 14 15  1  6
 14 16  1  0
 14 17  1  0
 17 18  1  6
 17 19  1  0
  7  2  1  0
 17  9  1  0
 16  4  1  0
  1 20  1  0
  1 21  1  0
  1 22  1  0
  3 23  1  0
  6 24  1  0
  8 25  1  0
 10 26  1  0
 10 27  1  0
 10 28  1  0
 11 29  1  6
 12 30  1  0
 13 31  1  0
 13 32  1  0
 15 33  1  0
 18 34  1  0
 18 35  1  0
 18 36  1  0
 19 37  1  0
 19 38  1  0
 19 39  1  0
M  END


  Mrv1652306242117493D          

 39 41  0  0  0  0            999 V2000
    4.3650   -0.1482   -1.8544 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.0504   -0.0714   -1.1641 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.9050    0.3576   -1.7982 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7245    0.3994   -1.0859 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.6703    0.0183    0.2537 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.7950   -0.4034    0.8780 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.9838   -0.4498    0.1751 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.1487   -0.8748    0.7816 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6663    0.1138    0.8959 C   0  0  1  0  0  0  0  0  0  0  0  0
   -0.7256   -0.5121    2.2466 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0608    1.5692    0.9143 C   0  0  2  0  0  0  0  0  0  0  0  0
   -1.5901    1.9675    2.1314 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0676    1.7506   -0.2264 C   0  0  2  0  0  0  0  0  0  0  0  0
   -1.7188    0.5698   -1.1344 C   0  0  1  0  0  0  0  0  0  0  0  0
   -2.6650    0.3304   -2.0902 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4608    0.8266   -1.6852 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6370   -0.5476   -0.0852 C   0  0  1  0  0  0  0  0  0  0  0  0
   -1.0366   -1.7964   -0.6359 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.9966   -0.7436    0.5121 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.0087    0.6820   -1.5023 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.2527   -0.0515   -2.9456 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.8603   -1.0914   -1.5504 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.9329    0.6574   -2.8414 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.7268   -0.6937    1.9175 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.1111   -1.1511    1.7515 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.0413   -0.0768    2.8848 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7141   -0.2054    2.6974 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6325   -1.5955    2.1993 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2020    2.2411    0.6562 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1401    2.8082    2.4558 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9064    2.6923   -0.7662 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.0621    1.6544    0.2077 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5459    0.7068   -1.9217 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5205   -1.6682   -1.5897 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3060   -2.2319    0.0912 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8495   -2.5537   -0.7835 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.0323   -1.7985    0.9073 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.8152   -0.6416   -0.2311 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.2245   -0.0383    1.3345 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  2  0  0  0  0
  5  6  1  0  0  0  0
  6  7  2  0  0  0  0
  7  8  1  0  0  0  0
  5  9  1  0  0  0  0
  9 10  1  1  0  0  0
  9 11  1  0  0  0  0
 11 12  1  0  0  0  0
 11 13  1  0  0  0  0
 13 14  1  0  0  0  0
 14 15  1  6  0  0  0
 14 16  1  0  0  0  0
 14 17  1  0  0  0  0
 17 18  1  6  0  0  0
 17 19  1  0  0  0  0
  7  2  1  0  0  0  0
 17  9  1  0  0  0  0
 16  4  1  0  0  0  0
  1 20  1  0  0  0  0
  1 21  1  0  0  0  0
  1 22  1  0  0  0  0
  3 23  1  0  0  0  0
  6 24  1  0  0  0  0
  8 25  1  0  0  0  0
 10 26  1  0  0  0  0
 10 27  1  0  0  0  0
 10 28  1  0  0  0  0
 11 29  1  6  0  0  0
 12 30  1  0  0  0  0
 13 31  1  0  0  0  0
 13 32  1  0  0  0  0
 15 33  1  0  0  0  0
 18 34  1  0  0  0  0
 18 35  1  0  0  0  0
 18 36  1  0  0  0  0
 19 37  1  0  0  0  0
 19 38  1  0  0  0  0
 19 39  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0003769

> <DATABASE_NAME>
NP-MRD

> <SMILES>
[H]OC1=C([H])C2=C(O[C@]3(O[H])C([H])([H])[C@@]([H])(O[H])[C@@]2(C([H])([H])[H])C3(C([H])([H])[H])C([H])([H])[H])C([H])=C1C([H])([H])[H]

> <INCHI_IDENTIFIER>
InChI=1S/C15H20O4/c1-8-5-11-9(6-10(8)16)14(4)12(17)7-15(18,19-11)13(14,2)3/h5-6,12,16-18H,7H2,1-4H3/t12-,14+,15-/m1/s1

> <INCHI_KEY>
DHKFEYFQGRWJNR-VHDGCEQUSA-N

> <FORMULA>
C15H20O4

> <MOLECULAR_WEIGHT>
264.321

> <EXACT_MASS>
264.136159124

> <JCHEM_ACCEPTOR_COUNT>
4

> <JCHEM_ATOM_COUNT>
39

> <JCHEM_AVERAGE_POLARIZABILITY>
28.095481288653282

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
3

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
1

> <JCHEM_IUPAC>
(1R,9R,11R)-1,5,12,12-tetramethyl-8-oxatricyclo[7.2.1.0^{2,7}]dodeca-2(7),3,5-triene-4,9,11-triol

> <ALOGPS_LOGP>
1.55

> <JCHEM_LOGP>
2.587784801333334

> <ALOGPS_LOGS>
-1.96

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
3

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA>
11.480272427374484

> <JCHEM_PKA_STRONGEST_ACIDIC>
10.144658566615488

> <JCHEM_PKA_STRONGEST_BASIC>
-3.081219148479372

> <JCHEM_POLAR_SURFACE_AREA>
69.92

> <JCHEM_REFRACTIVITY>
70.4125

> <JCHEM_ROTATABLE_BOND_COUNT>
0

> <JCHEM_RULE_OF_FIVE>
1

> <ALOGPS_SOLUBILITY>
2.89e+00 g/l

> <JCHEM_TRADITIONAL_IUPAC>
(1R,9R,11R)-1,5,12,12-tetramethyl-8-oxatricyclo[7.2.1.0^{2,7}]dodeca-2(7),3,5-triene-4,9,11-triol

> <JCHEM_VEBER_RULE>
0

$$$$

     RDKit          3D

 39 41  0  0  0  0  0  0  0  0999 V2000
    4.3650   -0.1482   -1.8544 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.0504   -0.0714   -1.1641 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.9050    0.3576   -1.7982 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7245    0.3994   -1.0859 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.6703    0.0183    0.2537 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.7950   -0.4034    0.8780 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.9838   -0.4498    0.1751 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.1487   -0.8748    0.7816 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6663    0.1138    0.8959 C   0  0  1  0  0  0  0  0  0  0  0  0
   -0.7256   -0.5121    2.2466 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0608    1.5692    0.9143 C   0  0  2  0  0  0  0  0  0  0  0  0
   -1.5901    1.9675    2.1314 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0676    1.7506   -0.2264 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7188    0.5698   -1.1344 C   0  0  1  0  0  0  0  0  0  0  0  0
   -2.6650    0.3304   -2.0902 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4608    0.8266   -1.6852 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6370   -0.5476   -0.0852 C   0  0  1  0  0  0  0  0  0  0  0  0
   -1.0366   -1.7964   -0.6359 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.9966   -0.7436    0.5121 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.0087    0.6820   -1.5023 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.2527   -0.0515   -2.9456 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.8603   -1.0914   -1.5504 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.9329    0.6574   -2.8414 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.7268   -0.6937    1.9175 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.1111   -1.1511    1.7515 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.0413   -0.0768    2.8848 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7141   -0.2054    2.6974 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6325   -1.5955    2.1993 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2020    2.2411    0.6562 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1401    2.8082    2.4558 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9064    2.6923   -0.7662 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.0621    1.6544    0.2077 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5459    0.7068   -1.9217 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5205   -1.6682   -1.5897 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3060   -2.2319    0.0912 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8495   -2.5537   -0.7835 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.0323   -1.7985    0.9073 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.8152   -0.6416   -0.2311 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.2245   -0.0383    1.3345 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  2  0
  5  6  1  0
  6  7  2  0
  7  8  1  0
  5  9  1  0
  9 10  1  1
  9 11  1  0
 11 12  1  0
 11 13  1  0
 13 14  1  0
 14 15  1  6
 14 16  1  0
 14 17  1  0
 17 18  1  6
 17 19  1  0
  7  2  1  0
 17  9  1  0
 16  4  1  0
  1 20  1  0
  1 21  1  0
  1 22  1  0
  3 23  1  0
  6 24  1  0
  8 25  1  0
 10 26  1  0
 10 27  1  0
 10 28  1  0
 11 29  1  6
 12 30  1  0
 13 31  1  0
 13 32  1  0
 15 33  1  0
 18 34  1  0
 18 35  1  0
 18 36  1  0
 19 37  1  0
 19 38  1  0
 19 39  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       4.365  -0.148  -1.854  0.00  0.00           C+0
HETATM    2  C   UNK     0       3.050  -0.071  -1.164  0.00  0.00           C+0
HETATM    3  C   UNK     0       1.905   0.358  -1.798  0.00  0.00           C+0
HETATM    4  C   UNK     0       0.725   0.399  -1.086  0.00  0.00           C+0
HETATM    5  C   UNK     0       0.670   0.018   0.254  0.00  0.00           C+0
HETATM    6  C   UNK     0       1.795  -0.403   0.878  0.00  0.00           C+0
HETATM    7  C   UNK     0       2.984  -0.450   0.175  0.00  0.00           C+0
HETATM    8  O   UNK     0       4.149  -0.875   0.782  0.00  0.00           O+0
HETATM    9  C   UNK     0      -0.666   0.114   0.896  0.00  0.00           C+0
HETATM   10  C   UNK     0      -0.726  -0.512   2.247  0.00  0.00           C+0
HETATM   11  C   UNK     0      -1.061   1.569   0.914  0.00  0.00           C+0
HETATM   12  O   UNK     0      -1.590   1.968   2.131  0.00  0.00           O+0
HETATM   13  C   UNK     0      -2.068   1.751  -0.226  0.00  0.00           C+0
HETATM   14  C   UNK     0      -1.719   0.570  -1.134  0.00  0.00           C+0
HETATM   15  O   UNK     0      -2.665   0.330  -2.090  0.00  0.00           O+0
HETATM   16  O   UNK     0      -0.461   0.827  -1.685  0.00  0.00           O+0
HETATM   17  C   UNK     0      -1.637  -0.548  -0.085  0.00  0.00           C+0
HETATM   18  C   UNK     0      -1.037  -1.796  -0.636  0.00  0.00           C+0
HETATM   19  C   UNK     0      -2.997  -0.744   0.512  0.00  0.00           C+0
HETATM   20  H   UNK     0       5.009   0.682  -1.502  0.00  0.00           H+0
HETATM   21  H   UNK     0       4.253  -0.052  -2.946  0.00  0.00           H+0
HETATM   22  H   UNK     0       4.860  -1.091  -1.550  0.00  0.00           H+0
HETATM   23  H   UNK     0       1.933   0.657  -2.841  0.00  0.00           H+0
HETATM   24  H   UNK     0       1.727  -0.694   1.918  0.00  0.00           H+0
HETATM   25  H   UNK     0       4.111  -1.151   1.752  0.00  0.00           H+0
HETATM   26  H   UNK     0       0.041  -0.077   2.885  0.00  0.00           H+0
HETATM   27  H   UNK     0      -1.714  -0.205   2.697  0.00  0.00           H+0
HETATM   28  H   UNK     0      -0.633  -1.595   2.199  0.00  0.00           H+0
HETATM   29  H   UNK     0      -0.202   2.241   0.656  0.00  0.00           H+0
HETATM   30  H   UNK     0      -1.140   2.808   2.456  0.00  0.00           H+0
HETATM   31  H   UNK     0      -1.906   2.692  -0.766  0.00  0.00           H+0
HETATM   32  H   UNK     0      -3.062   1.654   0.208  0.00  0.00           H+0
HETATM   33  H   UNK     0      -3.546   0.707  -1.922  0.00  0.00           H+0
HETATM   34  H   UNK     0      -0.521  -1.668  -1.590  0.00  0.00           H+0
HETATM   35  H   UNK     0      -0.306  -2.232   0.091  0.00  0.00           H+0
HETATM   36  H   UNK     0      -1.849  -2.554  -0.784  0.00  0.00           H+0
HETATM   37  H   UNK     0      -3.032  -1.799   0.907  0.00  0.00           H+0
HETATM   38  H   UNK     0      -3.815  -0.642  -0.231  0.00  0.00           H+0
HETATM   39  H   UNK     0      -3.224  -0.038   1.335  0.00  0.00           H+0
CONECT    1    2   20   21   22                                             
CONECT    2    1    3    7                                                  
CONECT    3    2    4   23                                                  
CONECT    4    3    5   16                                                  
CONECT    5    4    6    9                                                  
CONECT    6    5    7   24                                                  
CONECT    7    6    8    2                                                  
CONECT    8    7   25                                                       
CONECT    9    5   10   11   17                                             
CONECT   10    9   26   27   28                                             
CONECT   11    9   12   13   29                                             
CONECT   12   11   30                                                       
CONECT   13   11   14   31   32                                             
CONECT   14   13   15   16   17                                             
CONECT   15   14   33                                                       
CONECT   16   14    4                                                       
CONECT   17   14   18   19    9                                             
CONECT   18   17   34   35   36                                             
CONECT   19   17   37   38   39                                             
CONECT   20    1                                                            
CONECT   21    1                                                            
CONECT   22    1                                                            
CONECT   23    3                                                            
CONECT   24    6                                                            
CONECT   25    8                                                            
CONECT   26   10                                                            
CONECT   27   10                                                            
CONECT   28   10                                                            
CONECT   29   11                                                            
CONECT   30   12                                                            
CONECT   31   13                                                            
CONECT   32   13                                                            
CONECT   33   15                                                            
CONECT   34   18                                                            
CONECT   35   18                                                            
CONECT   36   18                                                            
CONECT   37   19                                                            
CONECT   38   19                                                            
CONECT   39   19                                                            
MASTER        0    0    0    0    0    0    0    0   39    0   82    0
END

RDKit          3D

39 41  0  0  0  0  0  0  0  0999 V2000
    4.3650   -0.1482   -1.8544 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.0504   -0.0714   -1.1641 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.9050    0.3576   -1.7982 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7245    0.3994   -1.0859 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.6703    0.0183    0.2537 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.7950   -0.4034    0.8780 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.9838   -0.4498    0.1751 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.1487   -0.8748    0.7816 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6663    0.1138    0.8959 C   0  0  1  0  0  0  0  0  0  0  0  0
   -0.7256   -0.5121    2.2466 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0608    1.5692    0.9143 C   0  0  2  0  0  0  0  0  0  0  0  0
   -1.5901    1.9675    2.1314 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0676    1.7506   -0.2264 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7188    0.5698   -1.1344 C   0  0  1  0  0  0  0  0  0  0  0  0
   -2.6650    0.3304   -2.0902 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4608    0.8266   -1.6852 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6370   -0.5476   -0.0852 C   0  0  1  0  0  0  0  0  0  0  0  0
   -1.0366   -1.7964   -0.6359 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.9966   -0.7436    0.5121 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.0087    0.6820   -1.5023 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.2527   -0.0515   -2.9456 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.8603   -1.0914   -1.5504 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.9329    0.6574   -2.8414 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.7268   -0.6937    1.9175 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.1111   -1.1511    1.7515 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.0413   -0.0768    2.8848 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7141   -0.2054    2.6974 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6325   -1.5955    2.1993 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2020    2.2411    0.6562 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1401    2.8082    2.4558 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9064    2.6923   -0.7662 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.0621    1.6544    0.2077 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5459    0.7068   -1.9217 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5205   -1.6682   -1.5897 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3060   -2.2319    0.0912 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8495   -2.5537   -0.7835 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.0323   -1.7985    0.9073 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.8152   -0.6416   -0.2311 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.2245   -0.0383    1.3345 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  2  0
  5  6  1  0
  6  7  2  0
  7  8  1  0
  5  9  1  0
  9 10  1  1
  9 11  1  0
 11 12  1  0
 11 13  1  0
 13 14  1  0
 14 15  1  6
 14 16  1  0
 14 17  1  0
 17 18  1  6
 17 19  1  0
  7  2  1  0
 17  9  1  0
 16  4  1  0
  1 20  1  0
  1 21  1  0
  1 22  1  0
  3 23  1  0
  6 24  1  0
  8 25  1  0
 10 26  1  0
 10 27  1  0
 10 28  1  0
 11 29  1  6
 12 30  1  0
 13 31  1  0
 13 32  1  0
 15 33  1  0
 18 34  1  0
 18 35  1  0
 18 36  1  0
 19 37  1  0
 19 38  1  0
 19 39  1  0
M  END

View in JSmol View NMR Assignments

Synonyms

Not Available

Chemical Formula

C₁₅H₂₀O₄

Average Mass

264.3210 Da

Monoisotopic Mass

264.13616 Da

IUPAC Name

(1R,9R,11R)-1,5,12,12-tetramethyl-8-oxatricyclo[7.2.1.0^{2,7}]dodeca-2(7),3,5-triene-4,9,11-triol

Traditional Name

(1R,9R,11R)-1,5,12,12-tetramethyl-8-oxatricyclo[7.2.1.0^{2,7}]dodeca-2(7),3,5-triene-4,9,11-triol

CAS Registry Number

Not Available

SMILES

CC1=C(O)C=C2C(O[C@]3(O)C[C@@H](O)[C@@]2(C)C3(C)C)=C1

InChI Identifier

InChI=1S/C15H20O4/c1-8-5-11-9(6-10(8)16)14(4)12(17)7-15(18,19-11)13(14,2)3/h5-6,12,16-18H,7H2,1-4H3/t12-,14+,15-/m1/s1

InChI Key

DHKFEYFQGRWJNR-VHDGCEQUSA-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
Agaricus bisporus	FooDB	Shmuel Yannai Dictionary of Food Compounds with CD-ROM: Additives, Flavors, and Ingredients. Chap...
Flammulina velutipes	NPAtlas	11473426
Pleurotus ostreatus	FooDB	Shmuel Yannai Dictionary of Food Compounds with CD-ROM: Additives, Flavors, and Ingredients. Chap...

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as 1-benzopyrans. These are organic aromatic compounds that 1-benzopyran, a bicyclic compound made up of a benzene ring fused to a pyran, so that the oxygen atom is at the 1-position.

Kingdom

Organic compounds

Super Class

Organoheterocyclic compounds

Class

Benzopyrans

Sub Class

1-benzopyrans

Direct Parent

1-benzopyrans

Alternative Parents

Substituents

1-benzopyran
1-hydroxy-2-unsubstituted benzenoid
Benzenoid
Cyclic alcohol
Secondary alcohol
Hemiacetal
Oxacycle
Polyol
Organic oxygen compound
Hydrocarbon derivative
Organooxygen compound
Alcohol
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	1.55	ALOGPS
logP	2.59	ChemAxon
logS	-2	ALOGPS
pKa (Strongest Acidic)	10.14	ChemAxon
pKa (Strongest Basic)	-3.1	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	4	ChemAxon
Hydrogen Donor Count	3	ChemAxon
Polar Surface Area	69.92 Å²	ChemAxon
Rotatable Bond Count	0	ChemAxon
Refractivity	70.41 m³·mol⁻¹	ChemAxon
Polarizability	28.1 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

NPA017113

HMDB ID

Not Available

DrugBank ID

Not Available

Phenol Explorer Compound ID

Not Available

FoodDB ID

Not Available

KNApSAcK ID

Not Available

Chemspider ID

9218814

KEGG Compound ID

Not Available

BioCyc ID

Not Available

BiGG ID

Not Available

Wikipedia Link

Not Available

METLIN ID

Not Available

PubChem Compound

11043646

PDB ID

Not Available

ChEBI ID

174484

Good Scents ID

Not Available

References

General References

Ishikawa NK, Fukushi Y, Yamaji K, Tahara S, Takahashi K: Antimicrobial cuparene-type sesquiterpenes, enokipodins C and D, from a mycelial culture of Flammulina velutipes. J Nat Prod. 2001 Jul;64(7):932-4. doi: 10.1021/np000593r. [PubMed:11473426 ]

Showing NP-Card for Enokipodin C (NP0003769)

MOL for NP0003769 (Enokipodin C)

3D MOL for NP0003769 (Enokipodin C)

3D SDF for NP0003769 (Enokipodin C)

3D-SDF for NP0003769 (Enokipodin C)

PDB for NP0003769 (Enokipodin C)

3D PDB for NP0003769 (Enokipodin C)

SMILES for NP0003769 (Enokipodin C)

INCHI for NP0003769 (Enokipodin C)

Structure for NP0003769 (Enokipodin C)

3D Structure for NP0003769 (Enokipodin C)