NP-MRD: Showing NP-Card for 1,7-dihydroxy-3a,3b,6,6,9a-pentamethyl-4h,5h,5ah,7h,8h,9h,9bh-cyclopenta[a]phenanthrene-2,3-dione (NP0247814)

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Record Information

Version

2.0

Created at

2022-09-07 09:47:40 UTC

Updated at

2022-09-07 09:47:41 UTC

NP-MRD ID

NP0247814

Secondary Accession Numbers

None

Natural Product Identification

Common Name

1,7-dihydroxy-3a,3b,6,6,9a-pentamethyl-4h,5h,5ah,7h,8h,9h,9bh-cyclopenta[a]phenanthrene-2,3-dione

Description

5,14-Dihydroxy-2,6,6,10,11-pentamethyltetracyclo[8.7.0.0²,⁷.0¹¹,¹⁵]Heptadeca-14,16-diene-12,13-dione belongs to the class of organic compounds known as 16-oxosteroids. These are steroid derivatives carrying a C=O group at the 16-position of the steroid skeleton. 1,7-dihydroxy-3a,3b,6,6,9a-pentamethyl-4h,5h,5ah,7h,8h,9h,9bh-cyclopenta[a]phenanthrene-2,3-dione is found in Paeonia lactiflora and Paeonia suffruticosa. 5,14-Dihydroxy-2,6,6,10,11-pentamethyltetracyclo[8.7.0.0²,⁷.0¹¹,¹⁵]Heptadeca-14,16-diene-12,13-dione is an extremely weak basic (essentially neutral) compound (based on its pKa).

Structure

MOL 3D MOL SDF PDB SMILES InChI


  Mrv1533004181502572D          

 26 29  0  0  0  0            999 V2000
    6.6328    1.6026    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.9193    1.1884    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.6353    1.9630    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.4511    0.5577    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.2632    0.7029    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    6.1708   -0.2182    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.3587   -0.3634    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.8269    0.2673    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.5466   -0.5086    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.1072    1.0432    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.5754    1.6739    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.7633    1.5287    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.4830    0.7528    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.9511    1.3835    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.0148    0.1221    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.7345   -0.6539    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.9224   -0.7991    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.3905   -0.1684    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.5660   -0.1416    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.0596   -0.7929    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.3367    0.6509    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.5607    0.9312    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.0195    1.1139    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.0463    1.9385    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.6708    0.6076    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.6113    1.4304    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0  0  0  0
  2  3  1  0  0  0  0
  2  4  1  0  0  0  0
  4  5  1  0  0  0  0
  4  6  1  0  0  0  0
  6  7  1  0  0  0  0
  7  8  1  0  0  0  0
  8  9  1  0  0  0  0
  8 10  1  0  0  0  0
  2 10  1  0  0  0  0
 10 11  1  0  0  0  0
 11 12  1  0  0  0  0
 12 13  1  0  0  0  0
 13 14  1  0  0  0  0
 13 15  1  0  0  0  0
  8 15  1  0  0  0  0
 15 16  1  0  0  0  0
 16 17  2  0  0  0  0
 17 18  1  0  0  0  0
 18 19  2  0  0  0  0
 19 20  1  0  0  0  0
 19 21  1  0  0  0  0
 21 22  2  0  0  0  0
 21 23  1  0  0  0  0
 23 24  2  0  0  0  0
 23 25  1  0  0  0  0
 13 25  1  0  0  0  0
 18 25  1  0  0  0  0
 25 26  1  0  0  0  0
M  END

     RDKit          3D

 56 59  0  0  0  0  0  0  0  0999 V2000
   -3.7148    1.5140    0.3165 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.9436    0.3268   -0.2576 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.4070    0.2505   -1.7261 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.3535   -0.9715    0.3527 C   0  0  1  0  0  0  0  0  0  0  0  0
   -3.7333   -1.9323   -0.6170 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4361   -1.6027    1.3215 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9632   -1.3691    1.0784 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7209    0.0806    0.9158 C   0  0  2  0  0  0  0  0  0  0  0  0
   -1.2328    0.7431    2.2054 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4597    0.5624   -0.2987 C   0  0  1  0  0  0  0  0  0  0  0  0
   -0.9223   -0.1961   -1.4855 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.5327   -0.4005   -1.5279 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.3554    0.3333   -0.5041 C   0  0  1  0  0  0  0  0  0  0  0  0
    1.6458    1.7109   -1.1471 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7307    0.4995    0.8145 C   0  0  2  0  0  0  0  0  0  0  0  0
    1.5036    0.1010    2.0052 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8054   -0.0656    1.9425 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.4679    0.1488    0.6657 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.6108    0.6984    0.3041 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.5136    1.2391    1.2144 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.7347    0.6308   -1.1517 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.6776    1.0476   -1.8422 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.5452   -0.0193   -1.6678 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.2818   -0.2547   -2.8655 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.7025   -0.3524   -0.5219 C   0  0  2  0  0  0  0  0  0  0  0  0
    2.5812   -1.8525   -0.3973 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.0787    2.3577    0.5926 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.3946    1.1504    1.1286 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.4397    1.9480   -0.4351 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.5362    0.2801   -1.6277 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.1528    1.1481   -2.2884 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.1950   -0.7116   -2.1887 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.3241   -0.7650    0.8987 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.5921   -1.6680   -1.0257 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7183   -1.3177    2.3788 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5813   -2.7045    1.2899 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4392   -1.7173    2.0078 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6574   -2.0344    0.2787 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6850    1.6832    2.3723 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3216    0.8224    2.2385 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9670    0.0616    3.0512 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2943    1.6364   -0.4375 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3210    0.2934   -2.3981 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4003   -1.2193   -1.4272 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.9051   -0.0795   -2.5397 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.8254   -1.4922   -1.5113 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.4752    1.6787   -1.8496 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.7399    2.1192   -1.6127 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.9619    2.3516   -0.2836 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.6327    1.6417    0.9621 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.0326   -0.0716    2.9781 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.4198   -0.3404    2.8039 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.4491    0.8810    1.3429 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.6430   -2.3808   -1.3636 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.4878   -2.2139    0.1756 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.7246   -2.2076    0.1660 H   0  0  0  0  0  0  0  0  0  0  0  0
 25 26  1  1
 25 23  1  0
 23 24  2  0
 23 21  1  0
 21 22  2  0
 21 19  1  0
 19 20  1  0
 19 18  2  0
 18 17  1  0
 17 16  2  0
 16 15  1  0
 15  8  1  0
  8  9  1  1
  8  7  1  0
  7  6  1  0
  6  4  1  0
  4  5  1  0
  4  2  1  0
  2  1  1  0
  2  3  1  0
  2 10  1  0
 10 11  1  0
 11 12  1  0
 12 13  1  0
 13 14  1  6
 18 25  1  0
 13 15  1  0
 13 25  1  0
 10  8  1  0
 26 54  1  0
 26 55  1  0
 26 56  1  0
 20 53  1  0
 17 52  1  0
 16 51  1  0
 15 50  1  1
  9 39  1  0
  9 40  1  0
  9 41  1  0
  7 37  1  0
  7 38  1  0
  6 35  1  0
  6 36  1  0
  4 33  1  1
  5 34  1  0
  1 27  1  0
  1 28  1  0
  1 29  1  0
  3 30  1  0
  3 31  1  0
  3 32  1  0
 10 42  1  6
 11 43  1  0
 11 44  1  0
 12 45  1  0
 12 46  1  0
 14 47  1  0
 14 48  1  0
 14 49  1  0
M  END


  Mrv1533004181502572D          

 26 29  0  0  0  0            999 V2000
    6.6328    1.6026    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.9193    1.1884    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.6353    1.9630    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.4511    0.5577    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.2632    0.7029    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    6.1708   -0.2182    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.3587   -0.3634    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.8269    0.2673    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.5466   -0.5086    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.1072    1.0432    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.5754    1.6739    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.7633    1.5287    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.4830    0.7528    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.9511    1.3835    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.0148    0.1221    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.7345   -0.6539    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.9224   -0.7991    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.3905   -0.1684    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.5660   -0.1416    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.0596   -0.7929    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.3367    0.6509    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.5607    0.9312    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.0195    1.1139    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.0463    1.9385    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.6708    0.6076    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.6113    1.4304    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0  0  0  0
  2  3  1  0  0  0  0
  2  4  1  0  0  0  0
  4  5  1  0  0  0  0
  4  6  1  0  0  0  0
  6  7  1  0  0  0  0
  7  8  1  0  0  0  0
  8  9  1  0  0  0  0
  8 10  1  0  0  0  0
  2 10  1  0  0  0  0
 10 11  1  0  0  0  0
 11 12  1  0  0  0  0
 12 13  1  0  0  0  0
 13 14  1  0  0  0  0
 13 15  1  0  0  0  0
  8 15  1  0  0  0  0
 15 16  1  0  0  0  0
 16 17  2  0  0  0  0
 17 18  1  0  0  0  0
 18 19  2  0  0  0  0
 19 20  1  0  0  0  0
 19 21  1  0  0  0  0
 21 22  2  0  0  0  0
 21 23  1  0  0  0  0
 23 24  2  0  0  0  0
 23 25  1  0  0  0  0
 13 25  1  0  0  0  0
 18 25  1  0  0  0  0
 25 26  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0247814

> <DATABASE_NAME>
NP-MRD

> <SMILES>
CC12C(=O)C(=O)C(O)=C1C=CC1C3(C)CCC(O)C(C)(C)C3CCC21C

> <INCHI_IDENTIFIER>
InChI=1S/C22H30O4/c1-19(2)13-8-11-21(4)14(20(13,3)10-9-15(19)23)7-6-12-16(24)17(25)18(26)22(12,21)5/h6-7,13-15,23-24H,8-11H2,1-5H3

> <INCHI_KEY>
KIAKLFLISZCITK-UHFFFAOYSA-N

> <FORMULA>
C22H30O4

> <MOLECULAR_WEIGHT>
358.478

> <EXACT_MASS>
358.214409446

> <JCHEM_ACCEPTOR_COUNT>
4

> <JCHEM_ATOM_COUNT>
56

> <JCHEM_AVERAGE_POLARIZABILITY>
39.6897398660515

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
2

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
1

> <JCHEM_IUPAC>
5,14-dihydroxy-2,6,6,10,11-pentamethyltetracyclo[8.7.0.0²,⁷.0¹¹,¹⁵]heptadeca-14,16-diene-12,13-dione

> <ALOGPS_LOGP>
3.52

> <JCHEM_LOGP>
3.7285426626666665

> <ALOGPS_LOGS>
-4.44

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
4

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA>
19.489420327713596

> <JCHEM_PKA_STRONGEST_ACIDIC>
8.301192154316697

> <JCHEM_PKA_STRONGEST_BASIC>
-0.8351275481131463

> <JCHEM_POLAR_SURFACE_AREA>
74.6

> <JCHEM_REFRACTIVITY>
101.80939999999997

> <JCHEM_ROTATABLE_BOND_COUNT>
0

> <JCHEM_RULE_OF_FIVE>
1

> <ALOGPS_SOLUBILITY>
1.31e-02 g/l

> <JCHEM_TRADITIONAL_IUPAC>
5,14-dihydroxy-2,6,6,10,11-pentamethyltetracyclo[8.7.0.0²,⁷.0¹¹,¹⁵]heptadeca-14,16-diene-12,13-dione

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 18-APR-15   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   18-APR-15         0                                  
HETATM    1  C   UNK     0      12.381   2.992   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0      11.049   2.218   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0      10.519   3.664   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0      12.042   1.041   0.000  0.00  0.00           C+0
HETATM    5  O   UNK     0      13.558   1.312   0.000  0.00  0.00           O+0
HETATM    6  C   UNK     0      11.519  -0.407   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0      10.003  -0.678   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0       9.010   0.499   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0       8.487  -0.949   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0       9.533   1.947   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0       8.541   3.125   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0       7.025   2.854   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0       6.502   1.405   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0       5.509   2.583   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0       7.494   0.228   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0       6.971  -1.221   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0       5.455  -1.492   0.000  0.00  0.00           C+0
HETATM   18  C   UNK     0       4.462  -0.314   0.000  0.00  0.00           C+0
HETATM   19  C   UNK     0       2.923  -0.264   0.000  0.00  0.00           C+0
HETATM   20  O   UNK     0       1.978  -1.480   0.000  0.00  0.00           O+0
HETATM   21  C   UNK     0       2.495   1.215   0.000  0.00  0.00           C+0
HETATM   22  O   UNK     0       1.047   1.738   0.000  0.00  0.00           O+0
HETATM   23  C   UNK     0       3.770   2.079   0.000  0.00  0.00           C+0
HETATM   24  O   UNK     0       3.820   3.618   0.000  0.00  0.00           O+0
HETATM   25  C   UNK     0       4.986   1.134   0.000  0.00  0.00           C+0
HETATM   26  C   UNK     0       4.874   2.670   0.000  0.00  0.00           C+0
CONECT    1    2                                                            
CONECT    2    1    3    4   10                                             
CONECT    3    2                                                            
CONECT    4    2    5    6                                                  
CONECT    5    4                                                            
CONECT    6    4    7                                                       
CONECT    7    6    8                                                       
CONECT    8    7    9   10   15                                             
CONECT    9    8                                                            
CONECT   10    8    2   11                                                  
CONECT   11   10   12                                                       
CONECT   12   11   13                                                       
CONECT   13   12   14   15   25                                             
CONECT   14   13                                                            
CONECT   15   13    8   16                                                  
CONECT   16   15   17                                                       
CONECT   17   16   18                                                       
CONECT   18   17   19   25                                                  
CONECT   19   18   20   21                                                  
CONECT   20   19                                                            
CONECT   21   19   22   23                                                  
CONECT   22   21                                                            
CONECT   23   21   24   25                                                  
CONECT   24   23                                                            
CONECT   25   23   13   18   26                                             
CONECT   26   25                                                            
MASTER        0    0    0    0    0    0    0    0   26    0   58    0
END

View in JSmol

Synonyms

Not Available

Chemical Formula

C₂₂H₃₀O₄

Average Mass

358.4780 Da

Monoisotopic Mass

358.21441 Da

IUPAC Name

5,14-dihydroxy-2,6,6,10,11-pentamethyltetracyclo[8.7.0.0²,⁷.0¹¹,¹⁵]heptadeca-14,16-diene-12,13-dione

Traditional Name

5,14-dihydroxy-2,6,6,10,11-pentamethyltetracyclo[8.7.0.0²,⁷.0¹¹,¹⁵]heptadeca-14,16-diene-12,13-dione

CAS Registry Number

Not Available

SMILES

CC12C(=O)C(=O)C(O)=C1C=CC1C3(C)CCC(O)C(C)(C)C3CCC21C

InChI Identifier

InChI=1S/C22H30O4/c1-19(2)13-8-11-21(4)14(20(13,3)10-9-15(19)23)7-6-12-16(24)17(25)18(26)22(12,21)5/h6-7,13-15,23-24H,8-11H2,1-5H3

InChI Key

KIAKLFLISZCITK-UHFFFAOYSA-N

Experimental Spectra

Not Available

Predicted Spectra

Spectrum Type	Description	Depositor ID	Depositor Organization	Depositor	Deposition Date	View
1D NMR	¹³C NMR Spectrum (1D, 25 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 100 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 252 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 1000 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 50 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 200 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 75 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 300 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 101 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 400 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 126 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 500 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 151 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 600 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 176 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 700 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 201 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 800 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 226 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 900 MHz, H₂O, 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
Paeonia lactiflora	LOTUS Database	35616633
Paeonia suffruticosa	LOTUS Database	35616633

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as 16-oxosteroids. These are steroid derivatives carrying a C=O group at the 16-position of the steroid skeleton.

Kingdom

Organic compounds

Super Class

Lipids and lipid-like molecules

Class

Steroids and steroid derivatives

Sub Class

Oxosteroids

Direct Parent

16-oxosteroids

Alternative Parents

Substituents

3-hydroxysteroid
Hydroxysteroid
16-oxosteroid
17-hydroxysteroid
Cyclic alcohol
Ketone
Cyclic ketone
Secondary alcohol
Enol
Organic oxygen compound
Hydrocarbon derivative
Organic oxide
Carbonyl group
Organooxygen compound
Alcohol
Aliphatic homopolycyclic compound

Molecular Framework

Aliphatic homopolycyclic compounds

External Descriptors

Not Available

Physical Properties

State

Not Available

Experimental Properties

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

Predicted Properties

Property	Value	Source
logP	3.52	ALOGPS
logP	3.73	ChemAxon
logS	-4.4	ALOGPS
pKa (Strongest Acidic)	8.3	ChemAxon
pKa (Strongest Basic)	-0.84	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	4	ChemAxon
Hydrogen Donor Count	2	ChemAxon
Polar Surface Area	74.6 Å²	ChemAxon
Rotatable Bond Count	0	ChemAxon
Refractivity	101.81 m³·mol⁻¹	ChemAxon
Polarizability	39.69 Å³	ChemAxon
Number of Rings	4	ChemAxon
Bioavailability	Yes	ChemAxon
Rule of Five	Yes	ChemAxon
Ghose Filter	Yes	ChemAxon
Veber's Rule	No	ChemAxon
MDDR-like Rule	No	ChemAxon

External Links

HMDB ID

Not Available

DrugBank ID

Not Available

Phenol Explorer Compound ID

Not Available

FoodDB ID

Not Available

KNApSAcK ID

Not Available

Chemspider ID

Not Available

KEGG Compound ID

Not Available

BioCyc ID

Not Available

BiGG ID

Not Available

Wikipedia Link

Not Available

METLIN ID

Not Available

PubChem Compound

53463552

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

LOTUS database [Link]

Showing NP-Card for 1,7-dihydroxy-3a,3b,6,6,9a-pentamethyl-4h,5h,5ah,7h,8h,9h,9bh-cyclopenta[a]phenanthrene-2,3-dione (NP0247814)

MOL for NP0247814 (1,7-dihydroxy-3a,3b,6,6,9a-pentamethyl-4h,5h,5ah,7h,8h,9h,9bh-cyclopenta[a]phenanthrene-2,3-dione)

3D MOL for NP0247814 (1,7-dihydroxy-3a,3b,6,6,9a-pentamethyl-4h,5h,5ah,7h,8h,9h,9bh-cyclopenta[a]phenanthrene-2,3-dione)

3D SDF for NP0247814 (1,7-dihydroxy-3a,3b,6,6,9a-pentamethyl-4h,5h,5ah,7h,8h,9h,9bh-cyclopenta[a]phenanthrene-2,3-dione)

3D-SDF for NP0247814 (1,7-dihydroxy-3a,3b,6,6,9a-pentamethyl-4h,5h,5ah,7h,8h,9h,9bh-cyclopenta[a]phenanthrene-2,3-dione)

PDB for NP0247814 (1,7-dihydroxy-3a,3b,6,6,9a-pentamethyl-4h,5h,5ah,7h,8h,9h,9bh-cyclopenta[a]phenanthrene-2,3-dione)

3D PDB for NP0247814 (1,7-dihydroxy-3a,3b,6,6,9a-pentamethyl-4h,5h,5ah,7h,8h,9h,9bh-cyclopenta[a]phenanthrene-2,3-dione)

SMILES for NP0247814 (1,7-dihydroxy-3a,3b,6,6,9a-pentamethyl-4h,5h,5ah,7h,8h,9h,9bh-cyclopenta[a]phenanthrene-2,3-dione)

INCHI for NP0247814 (1,7-dihydroxy-3a,3b,6,6,9a-pentamethyl-4h,5h,5ah,7h,8h,9h,9bh-cyclopenta[a]phenanthrene-2,3-dione)

Structure for NP0247814 (1,7-dihydroxy-3a,3b,6,6,9a-pentamethyl-4h,5h,5ah,7h,8h,9h,9bh-cyclopenta[a]phenanthrene-2,3-dione)

3D Structure for NP0247814 (1,7-dihydroxy-3a,3b,6,6,9a-pentamethyl-4h,5h,5ah,7h,8h,9h,9bh-cyclopenta[a]phenanthrene-2,3-dione)