NP-MRD: Showing NP-Card for gloeophyllol D (NP0029449)

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Record Information

Version

2.0

Created at

2021-06-19 21:04:21 UTC

Updated at

2021-06-29 23:56:48 UTC

NP-MRD ID

NP0029449

Secondary Accession Numbers

None

Natural Product Identification

Common Name

gloeophyllol D

Provided By

JEOL Database JEOL Logo

Description

gloeophyllol D is found in Gloeophyllum sp., Gloeophyllum sp.97022 and Gloeophyllum species 97022.. gloeophyllol D was first documented in 2000 (Rasser, F., et al.).

Structure

MOL 3D MOL SDF 3D SDF PDB SMILES InChI


  Mrv1652306192123043D          

 41 42  0  0  0  0            999 V2000
   -3.1098   -0.2068    1.8127 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0081   -0.1328    0.7818 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8347    0.5679    1.0951 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6918    1.1579    2.3188 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.1702    0.6967    0.1543 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0049    0.1924   -1.1407 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1372   -0.5257   -1.5028 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2814   -1.0127   -2.9214 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1641   -0.6912   -0.5278 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.4297   -1.4657   -0.8835 C   0  0  2  0  0  0  0  0  0  0  0  0
   -3.2568   -2.9841   -0.7674 C   0  0  2  0  0  0  0  0  0  0  0  0
   -3.1554   -3.4068    0.5873 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.1989    0.5402   -1.9968 C   0  0  2  0  0  0  0  0  0  0  0  0
    1.8670    1.6677   -1.1731 C   0  0  1  0  0  0  0  0  0  0  0  0
    3.3558    1.7914   -1.4753 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.2822    2.9452   -1.5264 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.5153    1.3587    0.3167 C   0  0  2  0  0  0  0  0  0  0  0  0
    2.4862    0.4271    1.0397 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.3638    2.5542    1.0870 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7638    0.0633    2.8152 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.9174    0.4802    1.5402 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5095   -1.2196    1.8997 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.0504    1.7962    2.2471 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3066   -1.1675   -3.3947 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7926   -1.9760   -2.9778 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8404   -0.2780   -3.5092 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.7291   -1.2071   -1.9062 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.2669   -1.1405   -0.2573 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3751   -3.3494   -1.3016 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.1341   -3.4812   -1.1936 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3493   -2.9976    0.9513 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.8888    0.9006   -2.9825 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.8425   -0.3409   -2.0901 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.5130    2.0833   -2.5201 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.8125    2.5754   -0.8611 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.8938    0.8545   -1.3024 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.3118    2.8492   -1.4603 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.4569    0.9131    1.1866 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.6425   -0.5121    0.4985 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.1185    0.1784    2.0425 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.5747    3.2877    0.4723 H   0  0  0  0  0  0  0  0  0  0  0  0
 17  5  1  0  0  0  0
  7  6  1  0  0  0  0
  9 10  1  0  0  0  0
  5  6  2  0  0  0  0
 10 11  1  0  0  0  0
  3  2  2  0  0  0  0
 11 12  1  0  0  0  0
  5  3  1  0  0  0  0
  2  1  1  0  0  0  0
  2  9  1  0  0  0  0
  3  4  1  0  0  0  0
 17 18  1  0  0  0  0
  9  7  2  0  0  0  0
 14 15  1  0  0  0  0
  6 13  1  0  0  0  0
  7  8  1  0  0  0  0
 13 14  1  0  0  0  0
 14 16  1  0  0  0  0
 14 17  1  0  0  0  0
 17 19  1  0  0  0  0
 13 32  1  0  0  0  0
 13 33  1  0  0  0  0
 10 27  1  0  0  0  0
 10 28  1  0  0  0  0
 11 29  1  0  0  0  0
 11 30  1  0  0  0  0
 12 31  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
  4 23  1  0  0  0  0
 18 38  1  0  0  0  0
 18 39  1  0  0  0  0
 18 40  1  0  0  0  0
 15 34  1  0  0  0  0
 15 35  1  0  0  0  0
 15 36  1  0  0  0  0
  8 24  1  0  0  0  0
  8 25  1  0  0  0  0
  8 26  1  0  0  0  0
 16 37  1  0  0  0  0
 19 41  1  0  0  0  0
M  END

     RDKit          3D

 41 42  0  0  0  0  0  0  0  0999 V2000
   -3.1098   -0.2068    1.8127 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0081   -0.1328    0.7818 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8347    0.5679    1.0951 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6918    1.1579    2.3188 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.1702    0.6967    0.1543 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0049    0.1924   -1.1407 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1372   -0.5257   -1.5028 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2814   -1.0127   -2.9214 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1641   -0.6912   -0.5278 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.4297   -1.4657   -0.8835 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.2568   -2.9841   -0.7674 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.1554   -3.4068    0.5873 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.1989    0.5402   -1.9968 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.8670    1.6677   -1.1731 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.3558    1.7914   -1.4753 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.2822    2.9452   -1.5264 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.5153    1.3587    0.3167 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.4862    0.4271    1.0397 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.3638    2.5542    1.0870 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7638    0.0633    2.8152 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.9174    0.4802    1.5402 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5095   -1.2196    1.8997 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.0504    1.7962    2.2471 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3066   -1.1675   -3.3947 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7926   -1.9760   -2.9778 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8404   -0.2780   -3.5092 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.7291   -1.2071   -1.9062 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.2669   -1.1405   -0.2573 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3751   -3.3494   -1.3016 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.1341   -3.4812   -1.1936 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3493   -2.9976    0.9513 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.8888    0.9006   -2.9825 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.8425   -0.3409   -2.0901 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.5130    2.0833   -2.5201 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.8125    2.5754   -0.8611 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.8938    0.8545   -1.3024 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.3118    2.8492   -1.4603 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.4569    0.9131    1.1866 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.6425   -0.5121    0.4985 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.1185    0.1784    2.0425 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.5747    3.2877    0.4723 H   0  0  0  0  0  0  0  0  0  0  0  0
 17  5  1  0
  7  6  1  0
  9 10  1  0
  5  6  2  0
 10 11  1  0
  3  2  2  0
 11 12  1  0
  5  3  1  0
  2  1  1  0
  2  9  1  0
  3  4  1  0
 17 18  1  0
  9  7  2  0
 14 15  1  0
  6 13  1  0
  7  8  1  0
 13 14  1  0
 14 16  1  0
 14 17  1  0
 17 19  1  0
 13 32  1  0
 13 33  1  0
 10 27  1  0
 10 28  1  0
 11 29  1  0
 11 30  1  0
 12 31  1  0
  1 20  1  0
  1 21  1  0
  1 22  1  0
  4 23  1  0
 18 38  1  0
 18 39  1  0
 18 40  1  0
 15 34  1  0
 15 35  1  0
 15 36  1  0
  8 24  1  0
  8 25  1  0
  8 26  1  0
 16 37  1  0
 19 41  1  0
M  END


  Mrv1652306192123043D          

 41 42  0  0  0  0            999 V2000
   -3.1098   -0.2068    1.8127 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0081   -0.1328    0.7818 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8347    0.5679    1.0951 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6918    1.1579    2.3188 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.1702    0.6967    0.1543 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0049    0.1924   -1.1407 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1372   -0.5257   -1.5028 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2814   -1.0127   -2.9214 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1641   -0.6912   -0.5278 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.4297   -1.4657   -0.8835 C   0  0  2  0  0  0  0  0  0  0  0  0
   -3.2568   -2.9841   -0.7674 C   0  0  2  0  0  0  0  0  0  0  0  0
   -3.1554   -3.4068    0.5873 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.1989    0.5402   -1.9968 C   0  0  2  0  0  0  0  0  0  0  0  0
    1.8670    1.6677   -1.1731 C   0  0  1  0  0  0  0  0  0  0  0  0
    3.3558    1.7914   -1.4753 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.2822    2.9452   -1.5264 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.5153    1.3587    0.3167 C   0  0  2  0  0  0  0  0  0  0  0  0
    2.4862    0.4271    1.0397 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.3638    2.5542    1.0870 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7638    0.0633    2.8152 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.9174    0.4802    1.5402 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5095   -1.2196    1.8997 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.0504    1.7962    2.2471 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3066   -1.1675   -3.3947 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7926   -1.9760   -2.9778 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8404   -0.2780   -3.5092 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.7291   -1.2071   -1.9062 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.2669   -1.1405   -0.2573 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3751   -3.3494   -1.3016 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.1341   -3.4812   -1.1936 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3493   -2.9976    0.9513 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.8888    0.9006   -2.9825 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.8425   -0.3409   -2.0901 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.5130    2.0833   -2.5201 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.8125    2.5754   -0.8611 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.8938    0.8545   -1.3024 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.3118    2.8492   -1.4603 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.4569    0.9131    1.1866 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.6425   -0.5121    0.4985 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.1185    0.1784    2.0425 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.5747    3.2877    0.4723 H   0  0  0  0  0  0  0  0  0  0  0  0
 17  5  1  0  0  0  0
  7  6  1  0  0  0  0
  9 10  1  0  0  0  0
  5  6  2  0  0  0  0
 10 11  1  0  0  0  0
  3  2  2  0  0  0  0
 11 12  1  0  0  0  0
  5  3  1  0  0  0  0
  2  1  1  0  0  0  0
  2  9  1  0  0  0  0
  3  4  1  0  0  0  0
 17 18  1  0  0  0  0
  9  7  2  0  0  0  0
 14 15  1  0  0  0  0
  6 13  1  0  0  0  0
  7  8  1  0  0  0  0
 13 14  1  0  0  0  0
 14 16  1  0  0  0  0
 14 17  1  0  0  0  0
 17 19  1  0  0  0  0
 13 32  1  0  0  0  0
 13 33  1  0  0  0  0
 10 27  1  0  0  0  0
 10 28  1  0  0  0  0
 11 29  1  0  0  0  0
 11 30  1  0  0  0  0
 12 31  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
  4 23  1  0  0  0  0
 18 38  1  0  0  0  0
 18 39  1  0  0  0  0
 18 40  1  0  0  0  0
 15 34  1  0  0  0  0
 15 35  1  0  0  0  0
 15 36  1  0  0  0  0
  8 24  1  0  0  0  0
  8 25  1  0  0  0  0
  8 26  1  0  0  0  0
 16 37  1  0  0  0  0
 19 41  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0029449

> <DATABASE_NAME>
NP-MRD

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

> <INCHI_IDENTIFIER>
InChI=1S/C15H22O4/c1-8-10(5-6-16)9(2)13(17)12-11(8)7-14(3,18)15(12,4)19/h16-19H,5-7H2,1-4H3/t14-,15+/m1/s1

> <INCHI_KEY>
SENBANUKJNFPRG-CABCVRRESA-N

> <FORMULA>
C15H22O4

> <MOLECULAR_WEIGHT>
266.337

> <EXACT_MASS>
266.151809188

> <JCHEM_ACCEPTOR_COUNT>
4

> <JCHEM_ATOM_COUNT>
41

> <JCHEM_AVERAGE_POLARIZABILITY>
29.143587504413563

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
4

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
1

> <JCHEM_IUPAC>
(1S,2R)-5-(2-hydroxyethyl)-1,2,4,6-tetramethyl-2,3-dihydro-1H-indene-1,2,7-triol

> <ALOGPS_LOGP>
0.58

> <JCHEM_LOGP>
1.480958914333333

> <ALOGPS_LOGS>
-2.19

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
2

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA>
13.16441015302976

> <JCHEM_PKA_STRONGEST_ACIDIC>
10.607390798303907

> <JCHEM_PKA_STRONGEST_BASIC>
-2.4134709368149823

> <JCHEM_POLAR_SURFACE_AREA>
80.92

> <JCHEM_REFRACTIVITY>
74.72680000000001

> <JCHEM_ROTATABLE_BOND_COUNT>
2

> <JCHEM_RULE_OF_FIVE>
1

> <ALOGPS_SOLUBILITY>
1.74e+00 g/l

> <JCHEM_TRADITIONAL_IUPAC>
(1S,2R)-5-(2-hydroxyethyl)-1,2,4,6-tetramethyl-3H-indene-1,2,7-triol

> <JCHEM_VEBER_RULE>
0

$$$$

     RDKit          3D

 41 42  0  0  0  0  0  0  0  0999 V2000
   -3.1098   -0.2068    1.8127 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0081   -0.1328    0.7818 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8347    0.5679    1.0951 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6918    1.1579    2.3188 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.1702    0.6967    0.1543 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0049    0.1924   -1.1407 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1372   -0.5257   -1.5028 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2814   -1.0127   -2.9214 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1641   -0.6912   -0.5278 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.4297   -1.4657   -0.8835 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.2568   -2.9841   -0.7674 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.1554   -3.4068    0.5873 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.1989    0.5402   -1.9968 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.8670    1.6677   -1.1731 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.3558    1.7914   -1.4753 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.2822    2.9452   -1.5264 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.5153    1.3587    0.3167 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.4862    0.4271    1.0397 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.3638    2.5542    1.0870 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7638    0.0633    2.8152 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.9174    0.4802    1.5402 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5095   -1.2196    1.8997 H   0  0  0  0  0  0  0  0  0  0  0  0
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   -4.2669   -1.1405   -0.2573 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3751   -3.3494   -1.3016 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.1341   -3.4812   -1.1936 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3493   -2.9976    0.9513 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.8888    0.9006   -2.9825 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.8425   -0.3409   -2.0901 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.5130    2.0833   -2.5201 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.8125    2.5754   -0.8611 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.8938    0.8545   -1.3024 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.3118    2.8492   -1.4603 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.4569    0.9131    1.1866 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.6425   -0.5121    0.4985 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.1185    0.1784    2.0425 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.5747    3.2877    0.4723 H   0  0  0  0  0  0  0  0  0  0  0  0
 17  5  1  0
  7  6  1  0
  9 10  1  0
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 13 32  1  0
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  1 20  1  0
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 19 41  1  0
M  END

HEADER    PROTEIN                                 19-JUN-21   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   19-JUN-21         0                                  
HETATM    1  C   UNK     0      -3.110  -0.207   1.813  0.00  0.00           C+0
HETATM    2  C   UNK     0      -2.008  -0.133   0.782  0.00  0.00           C+0
HETATM    3  C   UNK     0      -0.835   0.568   1.095  0.00  0.00           C+0
HETATM    4  O   UNK     0      -0.692   1.158   2.319  0.00  0.00           O+0
HETATM    5  C   UNK     0       0.170   0.697   0.154  0.00  0.00           C+0
HETATM    6  C   UNK     0       0.005   0.192  -1.141  0.00  0.00           C+0
HETATM    7  C   UNK     0      -1.137  -0.526  -1.503  0.00  0.00           C+0
HETATM    8  C   UNK     0      -1.281  -1.013  -2.921  0.00  0.00           C+0
HETATM    9  C   UNK     0      -2.164  -0.691  -0.528  0.00  0.00           C+0
HETATM   10  C   UNK     0      -3.430  -1.466  -0.884  0.00  0.00           C+0
HETATM   11  C   UNK     0      -3.257  -2.984  -0.767  0.00  0.00           C+0
HETATM   12  O   UNK     0      -3.155  -3.407   0.587  0.00  0.00           O+0
HETATM   13  C   UNK     0       1.199   0.540  -1.997  0.00  0.00           C+0
HETATM   14  C   UNK     0       1.867   1.668  -1.173  0.00  0.00           C+0
HETATM   15  C   UNK     0       3.356   1.791  -1.475  0.00  0.00           C+0
HETATM   16  O   UNK     0       1.282   2.945  -1.526  0.00  0.00           O+0
HETATM   17  C   UNK     0       1.515   1.359   0.317  0.00  0.00           C+0
HETATM   18  C   UNK     0       2.486   0.427   1.040  0.00  0.00           C+0
HETATM   19  O   UNK     0       1.364   2.554   1.087  0.00  0.00           O+0
HETATM   20  H   UNK     0      -2.764   0.063   2.815  0.00  0.00           H+0
HETATM   21  H   UNK     0      -3.917   0.480   1.540  0.00  0.00           H+0
HETATM   22  H   UNK     0      -3.510  -1.220   1.900  0.00  0.00           H+0
HETATM   23  H   UNK     0       0.050   1.796   2.247  0.00  0.00           H+0
HETATM   24  H   UNK     0      -0.307  -1.167  -3.395  0.00  0.00           H+0
HETATM   25  H   UNK     0      -1.793  -1.976  -2.978  0.00  0.00           H+0
HETATM   26  H   UNK     0      -1.840  -0.278  -3.509  0.00  0.00           H+0
HETATM   27  H   UNK     0      -3.729  -1.207  -1.906  0.00  0.00           H+0
HETATM   28  H   UNK     0      -4.267  -1.141  -0.257  0.00  0.00           H+0
HETATM   29  H   UNK     0      -2.375  -3.349  -1.302  0.00  0.00           H+0
HETATM   30  H   UNK     0      -4.134  -3.481  -1.194  0.00  0.00           H+0
HETATM   31  H   UNK     0      -2.349  -2.998   0.951  0.00  0.00           H+0
HETATM   32  H   UNK     0       0.889   0.901  -2.982  0.00  0.00           H+0
HETATM   33  H   UNK     0       1.843  -0.341  -2.090  0.00  0.00           H+0
HETATM   34  H   UNK     0       3.513   2.083  -2.520  0.00  0.00           H+0
HETATM   35  H   UNK     0       3.813   2.575  -0.861  0.00  0.00           H+0
HETATM   36  H   UNK     0       3.894   0.855  -1.302  0.00  0.00           H+0
HETATM   37  H   UNK     0       0.312   2.849  -1.460  0.00  0.00           H+0
HETATM   38  H   UNK     0       3.457   0.913   1.187  0.00  0.00           H+0
HETATM   39  H   UNK     0       2.643  -0.512   0.499  0.00  0.00           H+0
HETATM   40  H   UNK     0       2.119   0.178   2.042  0.00  0.00           H+0
HETATM   41  H   UNK     0       1.575   3.288   0.472  0.00  0.00           H+0
CONECT    1    2   20   21   22                                             
CONECT    2    3    1    9                                                  
CONECT    3    2    5    4                                                  
CONECT    4    3   23                                                       
CONECT    5   17    6    3                                                  
CONECT    6    7    5   13                                                  
CONECT    7    6    9    8                                                  
CONECT    8    7   24   25   26                                             
CONECT    9   10    2    7                                                  
CONECT   10    9   11   27   28                                             
CONECT   11   10   12   29   30                                             
CONECT   12   11   31                                                       
CONECT   13    6   14   32   33                                             
CONECT   14   15   13   16   17                                             
CONECT   15   14   34   35   36                                             
CONECT   16   14   37                                                       
CONECT   17    5   18   14   19                                             
CONECT   18   17   38   39   40                                             
CONECT   19   17   41                                                       
CONECT   20    1                                                            
CONECT   21    1                                                            
CONECT   22    1                                                            
CONECT   23    4                                                            
CONECT   24    8                                                            
CONECT   25    8                                                            
CONECT   26    8                                                            
CONECT   27   10                                                            
CONECT   28   10                                                            
CONECT   29   11                                                            
CONECT   30   11                                                            
CONECT   31   12                                                            
CONECT   32   13                                                            
CONECT   33   13                                                            
CONECT   34   15                                                            
CONECT   35   15                                                            
CONECT   36   15                                                            
CONECT   37   16                                                            
CONECT   38   18                                                            
CONECT   39   18                                                            
CONECT   40   18                                                            
CONECT   41   19                                                            
MASTER        0    0    0    0    0    0    0    0   41    0   84    0
END

RDKit          3D

41 42  0  0  0  0  0  0  0  0999 V2000
   -3.1098   -0.2068    1.8127 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0081   -0.1328    0.7818 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8347    0.5679    1.0951 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6918    1.1579    2.3188 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.1702    0.6967    0.1543 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0049    0.1924   -1.1407 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1372   -0.5257   -1.5028 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2814   -1.0127   -2.9214 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1641   -0.6912   -0.5278 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.4297   -1.4657   -0.8835 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.2568   -2.9841   -0.7674 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.1554   -3.4068    0.5873 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.1989    0.5402   -1.9968 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.8670    1.6677   -1.1731 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.3558    1.7914   -1.4753 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.2822    2.9452   -1.5264 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.5153    1.3587    0.3167 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.4862    0.4271    1.0397 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.3638    2.5542    1.0870 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7638    0.0633    2.8152 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.9174    0.4802    1.5402 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5095   -1.2196    1.8997 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.0504    1.7962    2.2471 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3066   -1.1675   -3.3947 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7926   -1.9760   -2.9778 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8404   -0.2780   -3.5092 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.7291   -1.2071   -1.9062 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.2669   -1.1405   -0.2573 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3751   -3.3494   -1.3016 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.1341   -3.4812   -1.1936 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3493   -2.9976    0.9513 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.8888    0.9006   -2.9825 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.8425   -0.3409   -2.0901 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.5130    2.0833   -2.5201 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.8125    2.5754   -0.8611 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.8938    0.8545   -1.3024 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.3118    2.8492   -1.4603 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.4569    0.9131    1.1866 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.6425   -0.5121    0.4985 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.1185    0.1784    2.0425 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.5747    3.2877    0.4723 H   0  0  0  0  0  0  0  0  0  0  0  0
 17  5  1  0
  7  6  1  0
  9 10  1  0
  5  6  2  0
 10 11  1  0
  3  2  2  0
 11 12  1  0
  5  3  1  0
  2  1  1  0
  2  9  1  0
  3  4  1  0
 17 18  1  0
  9  7  2  0
 14 15  1  0
  6 13  1  0
  7  8  1  0
 13 14  1  0
 14 16  1  0
 14 17  1  0
 17 19  1  0
 13 32  1  0
 13 33  1  0
 10 27  1  0
 10 28  1  0
 11 29  1  0
 11 30  1  0
 12 31  1  0
  1 20  1  0
  1 21  1  0
  1 22  1  0
  4 23  1  0
 18 38  1  0
 18 39  1  0
 18 40  1  0
 15 34  1  0
 15 35  1  0
 15 36  1  0
  8 24  1  0
  8 25  1  0
  8 26  1  0
 16 37  1  0
 19 41  1  0
M  END

View in JSmol

Synonyms

Not Available

Chemical Formula

C₁₅H₂₂O₄

Average Mass

266.3370 Da

Monoisotopic Mass

266.15181 Da

IUPAC Name

(1S,2R)-5-(2-hydroxyethyl)-1,2,4,6-tetramethyl-2,3-dihydro-1H-indene-1,2,7-triol

Traditional Name

(1S,2R)-5-(2-hydroxyethyl)-1,2,4,6-tetramethyl-3H-indene-1,2,7-triol

CAS Registry Number

Not Available

SMILES

[H]OC1=C(C(=C(C2=C1[C@@](O[H])(C([H])([H])[H])[C@@](O[H])(C([H])([H])[H])C2([H])[H])C([H])([H])[H])C([H])([H])C([H])([H])O[H])C([H])([H])[H]

InChI Identifier

InChI=1S/C15H22O4/c1-8-10(5-6-16)9(2)13(17)12-11(8)7-14(3,18)15(12,4)19/h16-19H,5-7H2,1-4H3/t14-,15+/m1/s1

InChI Key

SENBANUKJNFPRG-CABCVRRESA-N

Experimental Spectra

Spectrum Type	Description	Depositor Email	Depositor Organization	Depositor	Deposition Date	View
1D NMR	¹³C NMR Spectrum (1D, 500 MHz, acetone-d6, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 500 MHz, acetone-d6, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 100 MHz, acetone-d6, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 100 MHz, acetone-d6, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 200 MHz, acetone-d6, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 200 MHz, acetone-d6, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 300 MHz, acetone-d6, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 300 MHz, acetone-d6, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 400 MHz, acetone-d6, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 400 MHz, acetone-d6, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 600 MHz, acetone-d6, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 600 MHz, acetone-d6, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 700 MHz, acetone-d6, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 700 MHz, acetone-d6, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 800 MHz, acetone-d6, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 800 MHz, acetone-d6, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 900 MHz, acetone-d6, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 900 MHz, acetone-d6, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 1000 MHz, acetone-d6, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 1000 MHz, acetone-d6, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum

Predicted Spectra

Not Available

Chemical Shift Submissions

Not Available

Species

Species of Origin

Species Name	Source	Reference
Gloeophyllum sp.	Fungi	KNApSAcK
Gloeophyllum sp.97022	Fungi	KNApSAcK
Gloeophyllum species 97022.	JEOL database	Rasser, F., et al, Phytochemistry 54, 511 (2000)

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	0.58	ALOGPS
logP	1.48	ChemAxon
logS	-2.2	ALOGPS
pKa (Strongest Acidic)	10.61	ChemAxon
pKa (Strongest Basic)	-2.4	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	4	ChemAxon
Hydrogen Donor Count	4	ChemAxon
Polar Surface Area	80.92 Å²	ChemAxon
Rotatable Bond Count	2	ChemAxon
Refractivity	74.73 m³·mol⁻¹	ChemAxon
Polarizability	29.14 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

Not Available

References

General References

Rasser, F., et al. (2000). Rasser, F., et al, Phytochemistry 54, 511 (2000). Phytochem..

Showing NP-Card for gloeophyllol D (NP0029449)

MOL for NP0029449 (gloeophyllol D)

3D MOL for NP0029449 (gloeophyllol D)

3D SDF for NP0029449 (gloeophyllol D)

3D-SDF for NP0029449 (gloeophyllol D)

PDB for NP0029449 (gloeophyllol D)

3D PDB for NP0029449 (gloeophyllol D)

SMILES for NP0029449 (gloeophyllol D)

INCHI for NP0029449 (gloeophyllol D)

Structure for NP0029449 (gloeophyllol D)

3D Structure for NP0029449 (gloeophyllol D)