NP-MRD: Showing NP-Card for Deacetylcinobufagin (NP0139147)

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Record Information

Version

1.0

Created at

2022-06-29 19:41:19 UTC

Updated at

2022-06-29 19:41:19 UTC

NP-MRD ID

NP0139147

Secondary Accession Numbers

None

Natural Product Identification

Common Name

Deacetylcinobufagin

Description

Deacetylcinobufagin belongs to the class of organic compounds known as bufanolides and derivatives. These are steroid lactones containing a pyran-2-one moiety linked to the C17 atom of a cyclopenta[a]phenanthrene derivative. Deacetylcinobufagin is found in Bufo bufo and Bufo gargarizans. Deacetylcinobufagin is an extremely weak basic (essentially neutral) compound (based on its pKa).

Structure

MOL 3D MOL SDF PDB SMILES InChI


  Mrv1533004201500502D          

 29 34  0  0  0  0            999 V2000
    3.1176   -0.5086    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.3979    0.2673    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.9298   -0.3634    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.7419   -0.2182    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.0222    0.5577    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.8343    0.7029    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.4904    1.1884    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.6782    1.0432    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.1464    1.6739    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.3343    1.5287    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.0540    0.7528    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.5858    0.1221    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.3055   -0.6539    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4934   -0.7991    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.9616   -0.1684    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.6017   -0.9107    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.1370   -0.1416    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0923    0.6509    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8682    0.9312    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.5906    1.1139    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.3547    1.4248    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.2419    0.6076    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3693   -0.7929    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0584   -1.5571    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5648   -2.2084    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3820   -2.0955    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8884   -2.7469    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6929   -1.3314    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1866   -0.6800    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
  3  4  1  0  0  0  0
  4  5  1  0  0  0  0
  5  6  1  0  0  0  0
  5  7  1  0  0  0  0
  7  8  1  0  0  0  0
  2  8  1  0  0  0  0
  8  9  1  0  0  0  0
  9 10  1  0  0  0  0
 10 11  1  0  0  0  0
 11 12  1  0  0  0  0
  2 12  1  0  0  0  0
 12 13  1  0  0  0  0
 13 14  1  0  0  0  0
 14 15  1  0  0  0  0
 15 16  1  0  0  0  0
 15 17  1  0  0  0  0
 17 18  1  0  0  0  0
 18 19  1  0  0  0  0
 18 20  1  0  0  0  0
 20 21  1  0  0  0  0
 21 22  1  0  0  0  0
 11 22  1  0  0  0  0
 15 22  1  0  0  0  0
 20 22  1  0  0  0  0
 17 23  1  0  0  0  0
 23 24  2  0  0  0  0
 24 25  1  0  0  0  0
 25 26  1  0  0  0  0
 26 27  2  0  0  0  0
 26 28  1  0  0  0  0
 28 29  2  0  0  0  0
 23 29  1  0  0  0  0
M  END

     RDKit          3D

 61 66  0  0  0  0  0  0  0  0999 V2000
   -2.8525   -1.5622    1.3967 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4660   -0.5789    0.3249 C   0  0  1  0  0  0  0  0  0  0  0  0
   -3.2667   -0.7903   -0.9302 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.7091   -0.7827   -0.5935 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.1186    0.0364    0.5626 C   0  0  2  0  0  0  0  0  0  0  0  0
   -6.3600    0.6389    0.2373 O   0  0  0  0  0  0  0  0  0  0  0  0
   -4.2014    1.1105    0.9892 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7403    0.8426    0.7687 C   0  0  2  0  0  0  0  0  0  0  0  0
   -2.2219    1.8440   -0.2001 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8614    1.6144   -0.7232 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5173    0.1844   -1.0295 C   0  0  2  0  0  0  0  0  0  0  0  0
   -1.0074   -0.7205    0.0556 C   0  0  1  0  0  0  0  0  0  0  0  0
   -0.1926   -0.3547    1.2939 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.1974   -0.8295    1.0582 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.7982   -0.4916   -0.2482 C   0  0  2  0  0  0  0  0  0  0  0  0
    2.4539   -1.7415   -0.8010 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8160    0.6300   -0.0446 C   0  0  1  0  0  0  0  0  0  0  0  0
    4.0954    0.1884    0.4964 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.4459    0.4706    1.8246 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.6434    0.0676    2.3711 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.4936   -0.6348    1.5433 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.6110   -1.0250    2.0122 O   0  0  0  0  0  0  0  0  0  0  0  0
    6.1874   -0.9055    0.3124 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.0483   -0.5195   -0.1999 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8584    1.4113   -1.3034 C   0  0  1  0  0  0  0  0  0  0  0  0
    3.9433    1.1903   -2.1125 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.5960    1.1014   -2.0671 C   0  0  1  0  0  0  0  0  0  0  0  0
    1.3917   -0.1446   -2.6134 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.9258    0.0701   -1.2894 C   0  0  2  0  0  0  0  0  0  0  0  0
   -3.6656   -2.2652    1.0484 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0047   -2.2620    1.6581 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.1416   -1.0810    2.3533 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.0673    0.0508   -1.6300 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.9804   -1.7204   -1.4709 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.2732   -0.4969   -1.5288 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.0238   -1.8531   -0.4166 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.3707   -0.6256    1.4434 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.8974   -0.0046   -0.3102 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.5171    2.0917    0.5258 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.3629    1.2831    2.0943 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1610    0.9744    1.7282 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2213    2.8439    0.3289 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.9606    2.0002   -1.0411 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7788    2.1709   -1.7043 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0410    2.0736   -0.0971 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0646   -0.1012   -1.9756 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7675   -1.7723   -0.1684 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6047   -0.8707    2.1644 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1545    0.7472    1.4477 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.8314   -0.4186    1.8990 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.2003   -1.9424    1.2571 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.6258   -2.5143   -0.8015 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.7209   -1.6483   -1.8718 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.2233   -2.1652   -0.1538 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.3175    1.2852    0.7340 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.7653    1.0220    2.4553 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.9511    0.2641    3.3875 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.8465   -0.7715   -1.2274 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.8342    2.5226   -1.0965 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.6804    0.9448   -3.0347 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.0719    1.9192   -2.5598 H   0  0  0  0  0  0  0  0  0  0  0  0
 15 16  1  6
 15 14  1  0
 14 13  1  0
 13 12  1  0
 12 11  1  0
 11 10  1  0
 10  9  1  0
  9  8  1  0
  8  7  1  0
  7  5  1  0
  5  6  1  0
  5  4  1  0
  4  3  1  0
  3  2  1  0
  2  1  1  1
 11 29  1  0
 29 28  1  6
 28 27  1  0
 27 25  1  0
 25 26  1  0
 25 17  1  0
 17 18  1  0
 18 24  2  0
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 29 15  1  0
 27 29  1  0
 19 18  1  0
 17 15  1  0
  2 12  1  0
  2  8  1  0
 16 52  1  0
 16 53  1  0
 16 54  1  0
 14 50  1  0
 14 51  1  0
 13 48  1  0
 13 49  1  0
 12 47  1  6
 11 46  1  6
 10 44  1  0
 10 45  1  0
  9 42  1  0
  9 43  1  0
  8 41  1  1
  7 39  1  0
  7 40  1  0
  5 37  1  1
  6 38  1  0
  4 35  1  0
  4 36  1  0
  3 33  1  0
  3 34  1  0
  1 30  1  0
  1 31  1  0
  1 32  1  0
 27 61  1  6
 25 59  1  1
 26 60  1  0
 17 55  1  1
 24 58  1  0
 20 57  1  0
 19 56  1  0
M  END


  Mrv1533004201500502D          

 29 34  0  0  0  0            999 V2000
    3.1176   -0.5086    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.3979    0.2673    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.9298   -0.3634    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.7419   -0.2182    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.0222    0.5577    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.8343    0.7029    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.4904    1.1884    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.6782    1.0432    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.1464    1.6739    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.3343    1.5287    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.0540    0.7528    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.5858    0.1221    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.3055   -0.6539    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4934   -0.7991    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.9616   -0.1684    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.6017   -0.9107    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.1370   -0.1416    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0923    0.6509    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8682    0.9312    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.5906    1.1139    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.3547    1.4248    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.2419    0.6076    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3693   -0.7929    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0584   -1.5571    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5648   -2.2084    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3820   -2.0955    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8884   -2.7469    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6929   -1.3314    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1866   -0.6800    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
  3  4  1  0  0  0  0
  4  5  1  0  0  0  0
  5  6  1  0  0  0  0
  5  7  1  0  0  0  0
  7  8  1  0  0  0  0
  2  8  1  0  0  0  0
  8  9  1  0  0  0  0
  9 10  1  0  0  0  0
 10 11  1  0  0  0  0
 11 12  1  0  0  0  0
  2 12  1  0  0  0  0
 12 13  1  0  0  0  0
 13 14  1  0  0  0  0
 14 15  1  0  0  0  0
 15 16  1  0  0  0  0
 15 17  1  0  0  0  0
 17 18  1  0  0  0  0
 18 19  1  0  0  0  0
 18 20  1  0  0  0  0
 20 21  1  0  0  0  0
 21 22  1  0  0  0  0
 11 22  1  0  0  0  0
 15 22  1  0  0  0  0
 20 22  1  0  0  0  0
 17 23  1  0  0  0  0
 23 24  2  0  0  0  0
 24 25  1  0  0  0  0
 25 26  1  0  0  0  0
 26 27  2  0  0  0  0
 26 28  1  0  0  0  0
 28 29  2  0  0  0  0
 23 29  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0139147

> <DATABASE_NAME>
NP-MRD

> <SMILES>
CC12CCC3C(CCC4CC(O)CCC34C)C11OC1C(O)C2C1=COC(=O)C=C1

> <INCHI_IDENTIFIER>
InChI=1S/C24H32O5/c1-22-9-7-15(25)11-14(22)4-5-17-16(22)8-10-23(2)19(13-3-6-18(26)28-12-13)20(27)21-24(17,23)29-21/h3,6,12,14-17,19-21,25,27H,4-5,7-11H2,1-2H3

> <INCHI_KEY>
IXZHDDUFQVXHIL-UHFFFAOYSA-N

> <FORMULA>
C24H32O5

> <MOLECULAR_WEIGHT>
400.515

> <EXACT_MASS>
400.22497413

> <JCHEM_ACCEPTOR_COUNT>
4

> <JCHEM_ATOM_COUNT>
61

> <JCHEM_AVERAGE_POLARIZABILITY>
44.033326399398916

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
2

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
1

> <JCHEM_IUPAC>
5-{5,14-dihydroxy-7,11-dimethyl-3-oxapentacyclo[8.8.0.0²,⁴.0²,⁷.0¹¹,¹⁶]octadecan-6-yl}-2H-pyran-2-one

> <ALOGPS_LOGP>
2.50

> <JCHEM_LOGP>
2.366611592000001

> <ALOGPS_LOGS>
-3.93

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
6

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA>
18.296396316655187

> <JCHEM_PKA_STRONGEST_ACIDIC>
13.755583150652406

> <JCHEM_PKA_STRONGEST_BASIC>
-1.3564021673643665

> <JCHEM_POLAR_SURFACE_AREA>
79.28999999999999

> <JCHEM_REFRACTIVITY>
107.62459999999999

> <JCHEM_ROTATABLE_BOND_COUNT>
1

> <JCHEM_RULE_OF_FIVE>
1

> <ALOGPS_SOLUBILITY>
4.71e-02 g/l

> <JCHEM_TRADITIONAL_IUPAC>
5-{5,14-dihydroxy-7,11-dimethyl-3-oxapentacyclo[8.8.0.0²,⁴.0²,⁷.0¹¹,¹⁶]octadecan-6-yl}pyran-2-one

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 20-APR-15   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   20-APR-15         0                                  
HETATM    1  C   UNK     0       5.820  -0.949   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0       6.343   0.499   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0       7.336  -0.678   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0       8.852  -0.407   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0       9.375   1.041   0.000  0.00  0.00           C+0
HETATM    6  O   UNK     0      10.891   1.312   0.000  0.00  0.00           O+0
HETATM    7  C   UNK     0       8.382   2.218   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0       6.866   1.947   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0       5.873   3.125   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0       4.357   2.854   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0       3.834   1.405   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0       4.827   0.228   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0       4.304  -1.221   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0       2.788  -1.492   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0       1.795  -0.314   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0       1.123  -1.700   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0       0.256  -0.264   0.000  0.00  0.00           C+0
HETATM   18  C   UNK     0      -0.172   1.215   0.000  0.00  0.00           C+0
HETATM   19  O   UNK     0      -1.621   1.738   0.000  0.00  0.00           O+0
HETATM   20  C   UNK     0       1.102   2.079   0.000  0.00  0.00           C+0
HETATM   21  O   UNK     0       2.529   2.660   0.000  0.00  0.00           O+0
HETATM   22  C   UNK     0       2.318   1.134   0.000  0.00  0.00           C+0
HETATM   23  C   UNK     0      -0.689  -1.480   0.000  0.00  0.00           C+0
HETATM   24  C   UNK     0      -0.109  -2.907   0.000  0.00  0.00           C+0
HETATM   25  O   UNK     0      -1.054  -4.122   0.000  0.00  0.00           O+0
HETATM   26  C   UNK     0      -2.580  -3.912   0.000  0.00  0.00           C+0
HETATM   27  O   UNK     0      -3.525  -5.127   0.000  0.00  0.00           O+0
HETATM   28  C   UNK     0      -3.160  -2.485   0.000  0.00  0.00           C+0
HETATM   29  C   UNK     0      -2.215  -1.269   0.000  0.00  0.00           C+0
CONECT    1    2                                                            
CONECT    2    1    3    8   12                                             
CONECT    3    2    4                                                       
CONECT    4    3    5                                                       
CONECT    5    4    6    7                                                  
CONECT    6    5                                                            
CONECT    7    5    8                                                       
CONECT    8    7    2    9                                                  
CONECT    9    8   10                                                       
CONECT   10    9   11                                                       
CONECT   11   10   12   22                                                  
CONECT   12   11    2   13                                                  
CONECT   13   12   14                                                       
CONECT   14   13   15                                                       
CONECT   15   14   16   17   22                                             
CONECT   16   15                                                            
CONECT   17   15   18   23                                                  
CONECT   18   17   19   20                                                  
CONECT   19   18                                                            
CONECT   20   18   21   22                                                  
CONECT   21   20   22                                                       
CONECT   22   21   11   15   20                                             
CONECT   23   17   24   29                                                  
CONECT   24   23   25                                                       
CONECT   25   24   26                                                       
CONECT   26   25   27   28                                                  
CONECT   27   26                                                            
CONECT   28   26   29                                                       
CONECT   29   28   23                                                       
MASTER        0    0    0    0    0    0    0    0   29    0   68    0
END

View in JSmol

Synonyms

Value	Source
Desacetylcinobufagin	MeSH

Chemical Formula

C₂₄H₃₂O₅

Average Mass

400.5150 Da

Monoisotopic Mass

400.22497 Da

IUPAC Name

5-{5,14-dihydroxy-7,11-dimethyl-3-oxapentacyclo[8.8.0.0²,⁴.0²,⁷.0¹¹,¹⁶]octadecan-6-yl}-2H-pyran-2-one

Traditional Name

5-{5,14-dihydroxy-7,11-dimethyl-3-oxapentacyclo[8.8.0.0²,⁴.0²,⁷.0¹¹,¹⁶]octadecan-6-yl}pyran-2-one

CAS Registry Number

Not Available

SMILES

CC12CCC3C(CCC4CC(O)CCC34C)C11OC1C(O)C2C1=COC(=O)C=C1

InChI Identifier

InChI=1S/C24H32O5/c1-22-9-7-15(25)11-14(22)4-5-17-16(22)8-10-23(2)19(13-3-6-18(26)28-12-13)20(27)21-24(17,23)29-21/h3,6,12,14-17,19-21,25,27H,4-5,7-11H2,1-2H3

InChI Key

IXZHDDUFQVXHIL-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
Bufo bufo	LOTUS Database	35616633
Bufo gargarizans	LOTUS Database	35616633

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as bufanolides and derivatives. These are steroid lactones containing a pyran-2-one moiety linked to the C17 atom of a cyclopenta[a]phenanthrene derivative.

Kingdom

Organic compounds

Super Class

Lipids and lipid-like molecules

Class

Steroids and steroid derivatives

Sub Class

Steroid lactones

Direct Parent

Bufanolides and derivatives

Alternative Parents

Substituents

Bufanolide-skeleton
Naphthopyran
Naphthalene
Pyranone
Pyran
Oxane
Cyclic alcohol
Heteroaromatic compound
Lactone
Secondary alcohol
Dialkyl ether
Oxirane
Ether
Oxacycle
Organoheterocyclic compound
Organic oxygen compound
Hydrocarbon derivative
Organic oxide
Alcohol
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	2.5	ALOGPS
logP	2.37	ChemAxon
logS	-3.9	ALOGPS
pKa (Strongest Acidic)	13.76	ChemAxon
pKa (Strongest Basic)	-1.4	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	4	ChemAxon
Hydrogen Donor Count	2	ChemAxon
Polar Surface Area	79.29 Å²	ChemAxon
Rotatable Bond Count	1	ChemAxon
Refractivity	107.62 m³·mol⁻¹	ChemAxon
Polarizability	44.03 Å³	ChemAxon
Number of Rings	6	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

314718

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

Not Available

Showing NP-Card for Deacetylcinobufagin (NP0139147)

MOL for NP0139147 (Deacetylcinobufagin)

3D MOL for NP0139147 (Deacetylcinobufagin)

3D SDF for NP0139147 (Deacetylcinobufagin)

3D-SDF for NP0139147 (Deacetylcinobufagin)

PDB for NP0139147 (Deacetylcinobufagin)

3D PDB for NP0139147 (Deacetylcinobufagin)

SMILES for NP0139147 (Deacetylcinobufagin)

INCHI for NP0139147 (Deacetylcinobufagin)

Structure for NP0139147 (Deacetylcinobufagin)

3D Structure for NP0139147 (Deacetylcinobufagin)