NP-MRD: Showing NP-Card for didehydroconicol (NP0028523)

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Record Information

Version

2.0

Created at

2021-06-19 20:23:27 UTC

Updated at

2021-06-29 23:55:22 UTC

NP-MRD ID

NP0028523

Secondary Accession Numbers

None

Natural Product Identification

Common Name

didehydroconicol

Provided By

JEOL Database JEOL Logo

Description

didehydroconicol is found in Aplidium aff. densum. didehydroconicol was first documented in 2005 (Simon-Levert, A., et al.). Based on a literature review very few articles have been published on 6,6,9-trimethyl-6H-benzo[c]chromen-2-ol.

Structure

MOL 3D MOL SDF 3D SDF PDB SMILES InChI


  Mrv1652306192122233D          

 34 36  0  0  0  0            999 V2000
   -0.8747   -5.3150   -1.2903 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5976   -3.8695   -1.0009 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.4921   -3.2261   -1.5834 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7303   -1.8770   -1.3244 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1199   -1.1399   -0.4785 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2533   -1.7635    0.0801 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4670   -3.1300   -0.1865 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1472   -0.9534    0.9226 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.4301   -1.3629    1.3247 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.2112   -0.5614    2.1574 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.4446   -1.0270    2.5084 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.7465    0.6639    2.6144 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4846    1.0946    2.2163 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7071    0.3018    1.3654 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4855    0.8192    1.0332 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.1110    0.3447   -0.1969 C   0  0  1  0  0  0  0  0  0  0  0  0
    1.6055    0.6746   -0.0198 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4489    1.1916   -1.3534 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3359   -5.8040   -0.4258 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5479   -5.4022   -2.1487 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.0518   -5.8551   -1.5119 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.1657   -3.7698   -2.2420 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.5865   -1.4093   -1.8029 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3173   -3.6474    0.2508 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.8504   -2.3083    0.9964 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.8692   -0.3740    3.0887 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.3433    1.2909    3.2682 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1020    2.0524    2.5584 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.0501    0.0539    0.7675 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.1848    0.5332   -0.9375 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.7381    1.7167    0.2965 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5241    1.0246   -1.4875 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3248    2.2614   -1.1488 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.0452    0.9611   -2.3037 H   0  0  0  0  0  0  0  0  0  0  0  0
 12 10  2  0  0  0  0
  6  7  1  0  0  0  0
  8  9  2  0  0  0  0
 14  8  1  0  0  0  0
 10 11  1  0  0  0  0
 10  9  1  0  0  0  0
 14 13  2  0  0  0  0
  7  2  2  0  0  0  0
  2  3  1  0  0  0  0
 14 15  1  0  0  0  0
  8  6  1  0  0  0  0
  6  5  2  0  0  0  0
  5 16  1  0  0  0  0
 16 15  1  0  0  0  0
  3  4  2  0  0  0  0
  2  1  1  0  0  0  0
  4  5  1  0  0  0  0
 16 17  1  0  0  0  0
 13 12  1  0  0  0  0
 16 18  1  0  0  0  0
 12 27  1  0  0  0  0
 13 28  1  0  0  0  0
 11 26  1  0  0  0  0
  3 22  1  0  0  0  0
  4 23  1  0  0  0  0
  9 25  1  0  0  0  0
  7 24  1  0  0  0  0
  1 19  1  0  0  0  0
  1 20  1  0  0  0  0
  1 21  1  0  0  0  0
 17 29  1  0  0  0  0
 17 30  1  0  0  0  0
 17 31  1  0  0  0  0
 18 32  1  0  0  0  0
 18 33  1  0  0  0  0
 18 34  1  0  0  0  0
M  END

     RDKit          3D

 34 36  0  0  0  0  0  0  0  0999 V2000
   -0.8747   -5.3150   -1.2903 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5976   -3.8695   -1.0009 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.4921   -3.2261   -1.5834 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7303   -1.8770   -1.3244 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1199   -1.1399   -0.4785 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2533   -1.7635    0.0801 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4670   -3.1300   -0.1865 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1472   -0.9534    0.9226 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.4301   -1.3629    1.3247 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.2112   -0.5614    2.1574 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.4446   -1.0270    2.5084 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.7465    0.6639    2.6144 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4846    1.0946    2.2163 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7071    0.3018    1.3654 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4855    0.8192    1.0332 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.1110    0.3447   -0.1969 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.6055    0.6746   -0.0198 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4489    1.1916   -1.3534 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3359   -5.8040   -0.4258 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5479   -5.4022   -2.1487 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.0518   -5.8551   -1.5119 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.1657   -3.7698   -2.2420 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.5865   -1.4093   -1.8029 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3173   -3.6474    0.2508 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.8504   -2.3083    0.9964 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.8692   -0.3740    3.0887 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.3433    1.2909    3.2682 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1020    2.0524    2.5584 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.0501    0.0539    0.7675 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.1848    0.5332   -0.9375 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.7381    1.7167    0.2965 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5241    1.0246   -1.4875 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3248    2.2614   -1.1488 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.0452    0.9611   -2.3037 H   0  0  0  0  0  0  0  0  0  0  0  0
 12 10  2  0
  6  7  1  0
  8  9  2  0
 14  8  1  0
 10 11  1  0
 10  9  1  0
 14 13  2  0
  7  2  2  0
  2  3  1  0
 14 15  1  0
  8  6  1  0
  6  5  2  0
  5 16  1  0
 16 15  1  0
  3  4  2  0
  2  1  1  0
  4  5  1  0
 16 17  1  0
 13 12  1  0
 16 18  1  0
 12 27  1  0
 13 28  1  0
 11 26  1  0
  3 22  1  0
  4 23  1  0
  9 25  1  0
  7 24  1  0
  1 19  1  0
  1 20  1  0
  1 21  1  0
 17 29  1  0
 17 30  1  0
 17 31  1  0
 18 32  1  0
 18 33  1  0
 18 34  1  0
M  END


  Mrv1652306192122233D          

 34 36  0  0  0  0            999 V2000
   -0.8747   -5.3150   -1.2903 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5976   -3.8695   -1.0009 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.4921   -3.2261   -1.5834 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7303   -1.8770   -1.3244 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1199   -1.1399   -0.4785 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2533   -1.7635    0.0801 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4670   -3.1300   -0.1865 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1472   -0.9534    0.9226 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.4301   -1.3629    1.3247 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.2112   -0.5614    2.1574 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.4446   -1.0270    2.5084 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.7465    0.6639    2.6144 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4846    1.0946    2.2163 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7071    0.3018    1.3654 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4855    0.8192    1.0332 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.1110    0.3447   -0.1969 C   0  0  1  0  0  0  0  0  0  0  0  0
    1.6055    0.6746   -0.0198 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4489    1.1916   -1.3534 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3359   -5.8040   -0.4258 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5479   -5.4022   -2.1487 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.0518   -5.8551   -1.5119 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.1657   -3.7698   -2.2420 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.5865   -1.4093   -1.8029 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3173   -3.6474    0.2508 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.8504   -2.3083    0.9964 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.8692   -0.3740    3.0887 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.3433    1.2909    3.2682 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1020    2.0524    2.5584 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.0501    0.0539    0.7675 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.1848    0.5332   -0.9375 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.7381    1.7167    0.2965 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5241    1.0246   -1.4875 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3248    2.2614   -1.1488 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.0452    0.9611   -2.3037 H   0  0  0  0  0  0  0  0  0  0  0  0
 12 10  2  0  0  0  0
  6  7  1  0  0  0  0
  8  9  2  0  0  0  0
 14  8  1  0  0  0  0
 10 11  1  0  0  0  0
 10  9  1  0  0  0  0
 14 13  2  0  0  0  0
  7  2  2  0  0  0  0
  2  3  1  0  0  0  0
 14 15  1  0  0  0  0
  8  6  1  0  0  0  0
  6  5  2  0  0  0  0
  5 16  1  0  0  0  0
 16 15  1  0  0  0  0
  3  4  2  0  0  0  0
  2  1  1  0  0  0  0
  4  5  1  0  0  0  0
 16 17  1  0  0  0  0
 13 12  1  0  0  0  0
 16 18  1  0  0  0  0
 12 27  1  0  0  0  0
 13 28  1  0  0  0  0
 11 26  1  0  0  0  0
  3 22  1  0  0  0  0
  4 23  1  0  0  0  0
  9 25  1  0  0  0  0
  7 24  1  0  0  0  0
  1 19  1  0  0  0  0
  1 20  1  0  0  0  0
  1 21  1  0  0  0  0
 17 29  1  0  0  0  0
 17 30  1  0  0  0  0
 17 31  1  0  0  0  0
 18 32  1  0  0  0  0
 18 33  1  0  0  0  0
 18 34  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0028523

> <DATABASE_NAME>
NP-MRD

> <SMILES>
[H]OC1=C([H])C([H])=C2OC(C3=C(C([H])=C(C([H])=C3[H])C([H])([H])[H])C2=C1[H])(C([H])([H])[H])C([H])([H])[H]

> <INCHI_IDENTIFIER>
InChI=1S/C16H16O2/c1-10-4-6-14-12(8-10)13-9-11(17)5-7-15(13)18-16(14,2)3/h4-9,17H,1-3H3

> <INCHI_KEY>
AXYGIQAHRDDHJD-UHFFFAOYSA-N

> <FORMULA>
C16H16O2

> <MOLECULAR_WEIGHT>
240.302

> <EXACT_MASS>
240.115029755

> <JCHEM_ACCEPTOR_COUNT>
2

> <JCHEM_ATOM_COUNT>
34

> <JCHEM_AVERAGE_POLARIZABILITY>
27.344900026893505

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
1

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
1

> <JCHEM_IUPAC>
6,6,9-trimethyl-6H-benzo[c]chromen-2-ol

> <ALOGPS_LOGP>
4.58

> <JCHEM_LOGP>
4.121034974333334

> <ALOGPS_LOGS>
-4.37

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
3

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA_STRONGEST_ACIDIC>
9.763248142583679

> <JCHEM_PKA_STRONGEST_BASIC>
-4.898197160486751

> <JCHEM_POLAR_SURFACE_AREA>
29.46

> <JCHEM_REFRACTIVITY>
72.2911

> <JCHEM_ROTATABLE_BOND_COUNT>
0

> <JCHEM_RULE_OF_FIVE>
1

> <ALOGPS_SOLUBILITY>
1.02e-02 g/l

> <JCHEM_TRADITIONAL_IUPAC>
6,6,9-trimethylbenzo[c]chromen-2-ol

> <JCHEM_VEBER_RULE>
1

$$$$

     RDKit          3D

 34 36  0  0  0  0  0  0  0  0999 V2000
   -0.8747   -5.3150   -1.2903 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5976   -3.8695   -1.0009 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.4921   -3.2261   -1.5834 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7303   -1.8770   -1.3244 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1199   -1.1399   -0.4785 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2533   -1.7635    0.0801 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4670   -3.1300   -0.1865 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1472   -0.9534    0.9226 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.4301   -1.3629    1.3247 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.2112   -0.5614    2.1574 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.4446   -1.0270    2.5084 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.7465    0.6639    2.6144 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4846    1.0946    2.2163 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7071    0.3018    1.3654 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4855    0.8192    1.0332 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.1110    0.3447   -0.1969 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.6055    0.6746   -0.0198 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4489    1.1916   -1.3534 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3359   -5.8040   -0.4258 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5479   -5.4022   -2.1487 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.0518   -5.8551   -1.5119 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.1657   -3.7698   -2.2420 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.5865   -1.4093   -1.8029 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3173   -3.6474    0.2508 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.8504   -2.3083    0.9964 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.8692   -0.3740    3.0887 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.3433    1.2909    3.2682 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1020    2.0524    2.5584 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.0501    0.0539    0.7675 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.1848    0.5332   -0.9375 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.7381    1.7167    0.2965 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5241    1.0246   -1.4875 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3248    2.2614   -1.1488 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.0452    0.9611   -2.3037 H   0  0  0  0  0  0  0  0  0  0  0  0
 12 10  2  0
  6  7  1  0
  8  9  2  0
 14  8  1  0
 10 11  1  0
 10  9  1  0
 14 13  2  0
  7  2  2  0
  2  3  1  0
 14 15  1  0
  8  6  1  0
  6  5  2  0
  5 16  1  0
 16 15  1  0
  3  4  2  0
  2  1  1  0
  4  5  1  0
 16 17  1  0
 13 12  1  0
 16 18  1  0
 12 27  1  0
 13 28  1  0
 11 26  1  0
  3 22  1  0
  4 23  1  0
  9 25  1  0
  7 24  1  0
  1 19  1  0
  1 20  1  0
  1 21  1  0
 17 29  1  0
 17 30  1  0
 17 31  1  0
 18 32  1  0
 18 33  1  0
 18 34  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      -0.875  -5.315  -1.290  0.00  0.00           C+0
HETATM    2  C   UNK     0      -0.598  -3.869  -1.001  0.00  0.00           C+0
HETATM    3  C   UNK     0       0.492  -3.226  -1.583  0.00  0.00           C+0
HETATM    4  C   UNK     0       0.730  -1.877  -1.324  0.00  0.00           C+0
HETATM    5  C   UNK     0      -0.120  -1.140  -0.479  0.00  0.00           C+0
HETATM    6  C   UNK     0      -1.253  -1.764   0.080  0.00  0.00           C+0
HETATM    7  C   UNK     0      -1.467  -3.130  -0.187  0.00  0.00           C+0
HETATM    8  C   UNK     0      -2.147  -0.953   0.923  0.00  0.00           C+0
HETATM    9  C   UNK     0      -3.430  -1.363   1.325  0.00  0.00           C+0
HETATM   10  C   UNK     0      -4.211  -0.561   2.157  0.00  0.00           C+0
HETATM   11  O   UNK     0      -5.445  -1.027   2.508  0.00  0.00           O+0
HETATM   12  C   UNK     0      -3.747   0.664   2.614  0.00  0.00           C+0
HETATM   13  C   UNK     0      -2.485   1.095   2.216  0.00  0.00           C+0
HETATM   14  C   UNK     0      -1.707   0.302   1.365  0.00  0.00           C+0
HETATM   15  O   UNK     0      -0.486   0.819   1.033  0.00  0.00           O+0
HETATM   16  C   UNK     0       0.111   0.345  -0.197  0.00  0.00           C+0
HETATM   17  C   UNK     0       1.605   0.675  -0.020  0.00  0.00           C+0
HETATM   18  C   UNK     0      -0.449   1.192  -1.353  0.00  0.00           C+0
HETATM   19  H   UNK     0      -1.336  -5.804  -0.426  0.00  0.00           H+0
HETATM   20  H   UNK     0      -1.548  -5.402  -2.149  0.00  0.00           H+0
HETATM   21  H   UNK     0       0.052  -5.855  -1.512  0.00  0.00           H+0
HETATM   22  H   UNK     0       1.166  -3.770  -2.242  0.00  0.00           H+0
HETATM   23  H   UNK     0       1.587  -1.409  -1.803  0.00  0.00           H+0
HETATM   24  H   UNK     0      -2.317  -3.647   0.251  0.00  0.00           H+0
HETATM   25  H   UNK     0      -3.850  -2.308   0.996  0.00  0.00           H+0
HETATM   26  H   UNK     0      -5.869  -0.374   3.089  0.00  0.00           H+0
HETATM   27  H   UNK     0      -4.343   1.291   3.268  0.00  0.00           H+0
HETATM   28  H   UNK     0      -2.102   2.052   2.558  0.00  0.00           H+0
HETATM   29  H   UNK     0       2.050   0.054   0.768  0.00  0.00           H+0
HETATM   30  H   UNK     0       2.185   0.533  -0.938  0.00  0.00           H+0
HETATM   31  H   UNK     0       1.738   1.717   0.297  0.00  0.00           H+0
HETATM   32  H   UNK     0      -1.524   1.025  -1.488  0.00  0.00           H+0
HETATM   33  H   UNK     0      -0.325   2.261  -1.149  0.00  0.00           H+0
HETATM   34  H   UNK     0       0.045   0.961  -2.304  0.00  0.00           H+0
CONECT    1    2   19   20   21                                             
CONECT    2    7    3    1                                                  
CONECT    3    2    4   22                                                  
CONECT    4    3    5   23                                                  
CONECT    5    6   16    4                                                  
CONECT    6    7    8    5                                                  
CONECT    7    6    2   24                                                  
CONECT    8    9   14    6                                                  
CONECT    9    8   10   25                                                  
CONECT   10   12   11    9                                                  
CONECT   11   10   26                                                       
CONECT   12   10   13   27                                                  
CONECT   13   14   12   28                                                  
CONECT   14    8   13   15                                                  
CONECT   15   14   16                                                       
CONECT   16    5   15   17   18                                             
CONECT   17   16   29   30   31                                             
CONECT   18   16   32   33   34                                             
CONECT   19    1                                                            
CONECT   20    1                                                            
CONECT   21    1                                                            
CONECT   22    3                                                            
CONECT   23    4                                                            
CONECT   24    7                                                            
CONECT   25    9                                                            
CONECT   26   11                                                            
CONECT   27   12                                                            
CONECT   28   13                                                            
CONECT   29   17                                                            
CONECT   30   17                                                            
CONECT   31   17                                                            
CONECT   32   18                                                            
CONECT   33   18                                                            
CONECT   34   18                                                            
MASTER        0    0    0    0    0    0    0    0   34    0   72    0
END

RDKit          3D

34 36  0  0  0  0  0  0  0  0999 V2000
   -0.8747   -5.3150   -1.2903 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5976   -3.8695   -1.0009 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.4921   -3.2261   -1.5834 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7303   -1.8770   -1.3244 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1199   -1.1399   -0.4785 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2533   -1.7635    0.0801 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4670   -3.1300   -0.1865 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1472   -0.9534    0.9226 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.4301   -1.3629    1.3247 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.2112   -0.5614    2.1574 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.4446   -1.0270    2.5084 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.7465    0.6639    2.6144 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4846    1.0946    2.2163 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7071    0.3018    1.3654 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4855    0.8192    1.0332 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.1110    0.3447   -0.1969 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.6055    0.6746   -0.0198 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4489    1.1916   -1.3534 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3359   -5.8040   -0.4258 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5479   -5.4022   -2.1487 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.0518   -5.8551   -1.5119 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.1657   -3.7698   -2.2420 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.5865   -1.4093   -1.8029 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3173   -3.6474    0.2508 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.8504   -2.3083    0.9964 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.8692   -0.3740    3.0887 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.3433    1.2909    3.2682 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1020    2.0524    2.5584 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.0501    0.0539    0.7675 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.1848    0.5332   -0.9375 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.7381    1.7167    0.2965 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5241    1.0246   -1.4875 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3248    2.2614   -1.1488 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.0452    0.9611   -2.3037 H   0  0  0  0  0  0  0  0  0  0  0  0
 12 10  2  0
  6  7  1  0
  8  9  2  0
 14  8  1  0
 10 11  1  0
 10  9  1  0
 14 13  2  0
  7  2  2  0
  2  3  1  0
 14 15  1  0
  8  6  1  0
  6  5  2  0
  5 16  1  0
 16 15  1  0
  3  4  2  0
  2  1  1  0
  4  5  1  0
 16 17  1  0
 13 12  1  0
 16 18  1  0
 12 27  1  0
 13 28  1  0
 11 26  1  0
  3 22  1  0
  4 23  1  0
  9 25  1  0
  7 24  1  0
  1 19  1  0
  1 20  1  0
  1 21  1  0
 17 29  1  0
 17 30  1  0
 17 31  1  0
 18 32  1  0
 18 33  1  0
 18 34  1  0
M  END

View in JSmol View DFT Assignments 3D Conformers

Synonyms

Not Available

Chemical Formula

C₁₆H₁₆O₂

Average Mass

240.3020 Da

Monoisotopic Mass

240.11503 Da

IUPAC Name

6,6,9-trimethyl-6H-benzo[c]chromen-2-ol

Traditional Name

6,6,9-trimethylbenzo[c]chromen-2-ol

CAS Registry Number

Not Available

SMILES

[H]OC1=C([H])C([H])=C2OC(C3=C(C([H])=C(C([H])=C3[H])C([H])([H])[H])C2=C1[H])(C([H])([H])[H])C([H])([H])[H]

InChI Identifier

InChI=1S/C16H16O2/c1-10-4-6-14-12(8-10)13-9-11(17)5-7-15(13)18-16(14,2)3/h4-9,17H,1-3H3

InChI Key

AXYGIQAHRDDHJD-UHFFFAOYSA-N

Experimental Spectra

Spectrum Type	Description	Depositor Email	Depositor Organization	Depositor	Deposition Date	View
1D NMR	¹³C NMR Spectrum (1D, 400 MHz, CDCl₃, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 400 MHz, CDCl₃, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 100 MHz, CDCl₃, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 100 MHz, CDCl₃, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 200 MHz, CDCl₃, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 200 MHz, CDCl₃, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 300 MHz, CDCl₃, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 300 MHz, CDCl₃, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 500 MHz, CDCl₃, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 500 MHz, CDCl₃, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 600 MHz, CDCl₃, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 600 MHz, CDCl₃, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 700 MHz, CDCl₃, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 700 MHz, CDCl₃, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 800 MHz, CDCl₃, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 800 MHz, CDCl₃, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 900 MHz, CDCl₃, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 900 MHz, CDCl₃, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 1000 MHz, CDCl₃, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 1000 MHz, CDCl₃, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum

Predicted Spectra

Spectrum Type	Description	Depositor ID	Depositor Organization	Depositor	Deposition Date	View
1D NMR	¹³C NMR Spectrum (1D, 100 MHz, chcl3, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 125 MHz, chcl3, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 150 MHz, chcl3, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 175 MHz, chcl3, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 200 MHz, chcl3, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 225 MHz, chcl3, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 25 MHz, chcl3, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 250 MHz, chcl3, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 50 MHz, chcl3, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 75 MHz, chcl3, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 100 MHz, chcl3, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 1000 MHz, chcl3, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 200 MHz, chcl3, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 300 MHz, chcl3, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 400 MHz, chcl3, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 500 MHz, chcl3, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 600 MHz, chcl3, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 700 MHz, chcl3, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 800 MHz, chcl3, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 900 MHz, chcl3, 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
Aplidium aff. densum	JEOL database	Simon-Levert, A., et al, J. Nat. Prod. 68, 1412 (2005)
Rhynchosia minima	KNApSAcK Database	22123792

Species Where Detected

Species Name	Source	Reference
Aplidium aff.densum	KNApSAcK Database	22123792

Chemical Taxonomy

Description

This compound belongs to the class of organic compounds known as dibenzopyrans. These are organic heterocyclic compounds with a structure containing a dibenzopyran moiety, made up of two benzene rings fused to a central pyran ring.

Kingdom

Organic compounds

Super Class

Organoheterocyclic compounds

Class

Benzopyrans

Sub Class

1-benzopyrans

Direct Parent

Dibenzopyrans

Alternative Parents

Substituents

Dibenzopyran
2-benzopyran
1-hydroxy-2-unsubstituted benzenoid
Phenol
Alkyl aryl ether
Benzenoid
Oxacycle
Ether
Organic oxygen compound
Hydrocarbon derivative
Organooxygen compound
Aromatic heteropolycyclic compound

Molecular Framework

Aromatic heteropolycyclic compounds

External Descriptors

Not Available

Physical Properties

State

Not Available

Experimental Properties

Property	Value	Reference
Melting Point	Not Available	Not Available
Boiling Point	Not Available	Not Available
Water Solubility	Not Available	Not Available
LogP	Not Available	Not Available

Predicted Properties

Property	Value	Source
logP	4.58	ALOGPS
logP	4.12	ChemAxon
logS	-4.4	ALOGPS
pKa (Strongest Acidic)	9.76	ChemAxon
pKa (Strongest Basic)	-4.9	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	2	ChemAxon
Hydrogen Donor Count	1	ChemAxon
Polar Surface Area	29.46 Å²	ChemAxon
Rotatable Bond Count	0	ChemAxon
Refractivity	72.29 m³·mol⁻¹	ChemAxon
Polarizability	27.34 Å³	ChemAxon
Number of Rings	3	ChemAxon
Bioavailability	Yes	ChemAxon
Rule of Five	Yes	ChemAxon
Ghose Filter	Yes	ChemAxon
Veber's Rule	Yes	ChemAxon
MDDR-like Rule	No	ChemAxon

External Links

HMDB ID

Not Available

DrugBank ID

Not Available

Phenol Explorer Compound ID

Not Available

FoodDB ID

Not Available

KNApSAcK ID

C00042471

Chemspider ID

9754365

KEGG Compound ID

Not Available

BioCyc ID

Not Available

BiGG ID

Not Available

Wikipedia Link

Not Available

METLIN ID

Not Available

PubChem Compound

11579599

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

Simon-Levert, A., et al. (2005). Simon-Levert, A., et al, J. Nat. Prod. 68, 1412 (2005). J. Nat. Prod..

Showing NP-Card for didehydroconicol (NP0028523)

MOL for NP0028523 (didehydroconicol)

3D MOL for NP0028523 (didehydroconicol)

3D SDF for NP0028523 (didehydroconicol)

3D-SDF for NP0028523 (didehydroconicol)

PDB for NP0028523 (didehydroconicol)

3D PDB for NP0028523 (didehydroconicol)

SMILES for NP0028523 (didehydroconicol)

INCHI for NP0028523 (didehydroconicol)

Structure for NP0028523 (didehydroconicol)

3D Structure for NP0028523 (didehydroconicol)