NP-MRD: Showing NP-Card for (1r,3br,4s,5r,5as,6r,9ar,9bs,11as)-1-(furan-3-yl)-4,5,6-trihydroxy-3b,6,9a,11a-tetramethyl-1h,2h,4h,5h,5ah,9bh,10h,11h-cyclopenta[a]phenanthren-9-one (NP0239499)

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Record Information

Version

2.0

Created at

2022-09-06 23:06:44 UTC

Updated at

2022-09-06 23:06:45 UTC

NP-MRD ID

NP0239499

Secondary Accession Numbers

None

Natural Product Identification

Common Name

(1r,3br,4s,5r,5as,6r,9ar,9bs,11as)-1-(furan-3-yl)-4,5,6-trihydroxy-3b,6,9a,11a-tetramethyl-1h,2h,4h,5h,5ah,9bh,10h,11h-cyclopenta[a]phenanthren-9-one

Description

Ceramicine L belongs to the class of organic compounds known as 17-furanylsteroids and derivatives. These are steroidal compounds having a furanyl group linked to the steroid backbone at the C17 position. (1r,3br,4s,5r,5as,6r,9ar,9bs,11as)-1-(furan-3-yl)-4,5,6-trihydroxy-3b,6,9a,11a-tetramethyl-1h,2h,4h,5h,5ah,9bh,10h,11h-cyclopenta[a]phenanthren-9-one is found in Chisocheton ceramicus. Based on a literature review very few articles have been published on Ceramicine L.

Structure

MOL 3D MOL SDF PDB SMILES InChI


  Mrv1652309072201062D          

 30 34  0  0  1  0            999 V2000
    4.3228    1.7357    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.9629    0.9934    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    3.4311    1.6241    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.6190    1.4789    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.3387    0.7029    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    2.8705    0.0722    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    3.4023   -0.5585    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.6826    0.2174    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.3340   -0.2889    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.0168    0.1741    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.7875    0.9666    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    5.2939    1.6179    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.0646    2.4104    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.7474    2.8734    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.3987    2.3670    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    6.1184    1.5911    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.5902   -0.7037    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    3.1220   -1.3344    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.7781   -0.8489    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    1.4978   -1.6248    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.2463   -0.2182    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    0.4342   -0.3634    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    0.7182   -1.1380    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2793   -0.7776    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0976    0.2673    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.1827    1.0432    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.9948    1.1884    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.2751    1.9643    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.5266    0.5577    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    1.8069    1.3336    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
  2  1  1  6  0  0  0
  2  3  1  0  0  0  0
  3  4  1  0  0  0  0
  5  4  1  1  0  0  0
  5  6  1  0  0  0  0
  6  7  1  1  0  0  0
  6  8  1  0  0  0  0
  2  8  1  0  0  0  0
  8  9  2  0  0  0  0
  9 10  1  0  0  0  0
 10 11  1  0  0  0  0
  2 11  1  0  0  0  0
 11 12  1  6  0  0  0
 12 13  1  0  0  0  0
 13 14  2  0  0  0  0
 14 15  1  0  0  0  0
 15 16  1  0  0  0  0
 12 16  2  0  0  0  0
  6 17  1  0  0  0  0
 17 18  1  6  0  0  0
 17 19  1  0  0  0  0
 19 20  1  6  0  0  0
 21 19  1  1  0  0  0
 21 22  1  0  0  0  0
 22 23  1  1  0  0  0
 22 24  1  6  0  0  0
 22 25  1  0  0  0  0
 25 26  2  0  0  0  0
 26 27  1  0  0  0  0
 27 28  2  0  0  0  0
 27 29  1  0  0  0  0
 21 29  1  0  0  0  0
  5 29  1  0  0  0  0
 29 30  1  1  0  0  0
M  END

     RDKit          3D

 62 66  0  0  0  0  0  0  0  0999 V2000
    2.3774    1.4287   -0.3510 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1577    0.2262    0.4757 C   0  0  1  0  0  0  0  0  0  0  0  0
    1.4792    0.4795    1.7962 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0173    0.8169    1.6383 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6544    0.2093    0.4597 C   0  0  1  0  0  0  0  0  0  0  0  0
   -0.0593   -1.0466   -0.0764 C   0  0  2  0  0  0  0  0  0  0  0  0
   -0.2518   -2.2835    0.7700 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4198   -0.8818   -0.1878 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.3146   -1.6627   -0.8063 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.6972   -1.1371   -0.5933 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.4973   -0.4255    0.7584 C   0  0  1  0  0  0  0  0  0  0  0  0
    4.6147    0.4985    0.9613 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.3275    1.2045    0.0171 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.2918    1.9091    0.7016 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.1583    1.6376    1.9674 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.1869    0.8110    2.1930 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5723   -1.2667   -1.4785 C   0  0  2  0  0  0  0  0  0  0  0  0
    0.0122   -0.3329   -2.3144 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0908   -1.2231   -1.5258 C   0  0  2  0  0  0  0  0  0  0  0  0
   -2.4299   -1.2004   -2.8920 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6051    0.0498   -0.9303 C   0  0  1  0  0  0  0  0  0  0  0  0
   -4.0219    0.3430   -1.2055 C   0  0  2  0  0  0  0  0  0  0  0  0
   -5.0281   -0.6659   -0.7884 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.1571    0.4873   -2.6100 O   0  0  0  0  0  0  0  0  0  0  0  0
   -4.4502    1.6675   -0.6477 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.7806    2.1175    0.3908 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6738    1.4662    1.0517 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1675    1.9949    2.0562 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1673    0.1928    0.5289 C   0  0  2  0  0  0  0  0  0  0  0  0
   -2.7573   -0.8839    1.3922 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.1266    2.1253    0.1049 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.5039    2.0702   -0.5605 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.8007    1.1221   -1.3282 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.0378    1.3033    2.2917 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.6428   -0.4130    2.4390 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.0301    1.9449    1.5164 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4753    0.5059    2.5836 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4882    0.9477   -0.3985 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.5294   -3.0181    0.3808 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1889   -2.8130    0.6214 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.0716   -2.1031    1.7947 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.1209   -2.5543   -1.3880 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.3682   -1.9927   -0.3642 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.0548   -0.4685   -1.3655 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.3721   -1.1497    1.5921 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.1674    1.2107   -1.0746 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.0293    2.5729    0.2471 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.8565    0.4147    3.1693 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2655   -2.2726   -1.8322 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6131    0.2379   -2.7964 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4515   -2.1379   -1.0509 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6725   -1.3670   -3.4772 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9984    0.8687   -1.4383 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.3428   -0.6134    0.2730 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.9785   -0.4449   -1.3623 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.7825   -1.7062   -1.0698 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.7227    1.3666   -2.8044 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.2760    2.1535   -1.1366 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.1278    3.0944    0.7684 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1091   -1.2623    2.1837 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.2493   -1.6720    0.7666 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.6546   -0.4797    1.9640 H   0  0  0  0  0  0  0  0  0  0  0  0
  2  1  1  6
  2  3  1  0
  3  4  1  0
  4  5  1  0
  5  6  1  0
  6  7  1  1
  6 17  1  0
 17 18  1  0
 17 19  1  0
 19 20  1  0
 19 21  1  0
 21 22  1  0
 22 23  1  0
 22 24  1  6
 22 25  1  0
 25 26  2  0
 26 27  1  0
 27 28  2  0
 27 29  1  0
 29 30  1  1
  6  8  1  0
  8  9  2  0
  9 10  1  0
 10 11  1  0
 11 12  1  0
 12 16  2  0
 16 15  1  0
 15 14  1  0
 14 13  2  0
  8  2  1  0
 13 12  1  0
 11  2  1  0
 29  5  1  0
 29 21  1  0
  1 31  1  0
  1 32  1  0
  1 33  1  0
  3 34  1  0
  3 35  1  0
  4 36  1  0
  4 37  1  0
  5 38  1  6
  7 39  1  0
  7 40  1  0
  7 41  1  0
 17 49  1  6
 18 50  1  0
 19 51  1  1
 20 52  1  0
 21 53  1  6
 23 54  1  0
 23 55  1  0
 23 56  1  0
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 25 58  1  0
 26 59  1  0
 30 60  1  0
 30 61  1  0
 30 62  1  0
  9 42  1  0
 10 43  1  0
 10 44  1  0
 11 45  1  1
 16 48  1  0
 14 47  1  0
 13 46  1  0
M  END


  Mrv1652309072201062D          

 30 34  0  0  1  0            999 V2000
    4.3228    1.7357    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.9629    0.9934    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    3.4311    1.6241    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.6190    1.4789    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.3387    0.7029    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    2.8705    0.0722    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    3.4023   -0.5585    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.6826    0.2174    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.3340   -0.2889    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.0168    0.1741    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.7875    0.9666    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    5.2939    1.6179    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.0646    2.4104    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.7474    2.8734    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.3987    2.3670    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    6.1184    1.5911    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.5902   -0.7037    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    3.1220   -1.3344    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.7781   -0.8489    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    1.4978   -1.6248    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.2463   -0.2182    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    0.4342   -0.3634    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    0.7182   -1.1380    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2793   -0.7776    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0976    0.2673    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.1827    1.0432    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.9948    1.1884    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.2751    1.9643    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.5266    0.5577    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    1.8069    1.3336    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
  2  1  1  6  0  0  0
  2  3  1  0  0  0  0
  3  4  1  0  0  0  0
  5  4  1  1  0  0  0
  5  6  1  0  0  0  0
  6  7  1  1  0  0  0
  6  8  1  0  0  0  0
  2  8  1  0  0  0  0
  8  9  2  0  0  0  0
  9 10  1  0  0  0  0
 10 11  1  0  0  0  0
  2 11  1  0  0  0  0
 11 12  1  6  0  0  0
 12 13  1  0  0  0  0
 13 14  2  0  0  0  0
 14 15  1  0  0  0  0
 15 16  1  0  0  0  0
 12 16  2  0  0  0  0
  6 17  1  0  0  0  0
 17 18  1  6  0  0  0
 17 19  1  0  0  0  0
 19 20  1  6  0  0  0
 21 19  1  1  0  0  0
 21 22  1  0  0  0  0
 22 23  1  1  0  0  0
 22 24  1  6  0  0  0
 22 25  1  0  0  0  0
 25 26  2  0  0  0  0
 26 27  1  0  0  0  0
 27 28  2  0  0  0  0
 27 29  1  0  0  0  0
 21 29  1  0  0  0  0
  5 29  1  0  0  0  0
 29 30  1  1  0  0  0
M  END
> <DATABASE_ID>
NP0239499

> <DATABASE_NAME>
NP-MRD

> <SMILES>
C[C@@]12CC[C@H]3[C@@](C)([C@H](O)[C@H](O)[C@H]4[C@](C)(O)C=CC(=O)[C@]34C)C1=CC[C@H]2C1=COC=C1

> <INCHI_IDENTIFIER>
InChI=1S/C25H32O5/c1-22-10-7-17-24(3,16(22)6-5-15(22)14-9-12-30-13-14)21(28)19(27)20-23(2,29)11-8-18(26)25(17,20)4/h6,8-9,11-13,15,17,19-21,27-29H,5,7,10H2,1-4H3/t15-,17-,19+,20-,21+,22-,23+,24-,25-/m0/s1

> <INCHI_KEY>
ZYWHPZZHPATFAR-MIWZOCFRSA-N

> <FORMULA>
C25H32O5

> <MOLECULAR_WEIGHT>
412.526

> <EXACT_MASS>
412.22497413

> <JCHEM_ACCEPTOR_COUNT>
4

> <JCHEM_ATOM_COUNT>
62

> <JCHEM_AVERAGE_POLARIZABILITY>
45.10072972953675

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
3

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
1

> <JCHEM_IUPAC>
(1S,2R,6R,7S,8R,9S,10R,14R,15S)-14-(furan-3-yl)-6,8,9-trihydroxy-2,6,10,15-tetramethyltetracyclo[8.7.0.0^{2,7}.0^{11,15}]heptadeca-4,11-dien-3-one

> <JCHEM_LOGP>
2.4709241656666663

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
5

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA>
14.252904232771627

> <JCHEM_PKA_STRONGEST_ACIDIC>
13.374113219832491

> <JCHEM_PKA_STRONGEST_BASIC>
-2.8042127586717034

> <JCHEM_POLAR_SURFACE_AREA>
90.9

> <JCHEM_REFRACTIVITY>
114.56970000000003

> <JCHEM_ROTATABLE_BOND_COUNT>
1

> <JCHEM_RULE_OF_FIVE>
1

> <JCHEM_TRADITIONAL_IUPAC>
(1S,2R,6R,7S,8R,9S,10R,14R,15S)-14-(furan-3-yl)-6,8,9-trihydroxy-2,6,10,15-tetramethyltetracyclo[8.7.0.0^{2,7}.0^{11,15}]heptadeca-4,11-dien-3-one

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 07-SEP-22   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   07-SEP-22         0                                  
HETATM    1  C   UNK     0       8.069   3.240   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0       7.398   1.854   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0       6.405   3.032   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0       4.889   2.761   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0       4.366   1.312   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0       5.358   0.135   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0       6.351  -1.043   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0       6.874   0.406   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0       8.090  -0.539   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0       9.365   0.325   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0       8.937   1.804   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0       9.882   3.020   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0       9.454   4.499   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0      10.728   5.364   0.000  0.00  0.00           C+0
HETATM   15  O   UNK     0      11.944   4.418   0.000  0.00  0.00           O+0
HETATM   16  C   UNK     0      11.421   2.970   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0       4.835  -1.314   0.000  0.00  0.00           C+0
HETATM   18  O   UNK     0       5.828  -2.491   0.000  0.00  0.00           O+0
HETATM   19  C   UNK     0       3.319  -1.585   0.000  0.00  0.00           C+0
HETATM   20  O   UNK     0       2.796  -3.033   0.000  0.00  0.00           O+0
HETATM   21  C   UNK     0       2.326  -0.407   0.000  0.00  0.00           C+0
HETATM   22  C   UNK     0       0.810  -0.678   0.000  0.00  0.00           C+0
HETATM   23  C   UNK     0       1.341  -2.124   0.000  0.00  0.00           C+0
HETATM   24  O   UNK     0      -0.521  -1.452   0.000  0.00  0.00           O+0
HETATM   25  C   UNK     0      -0.182   0.499   0.000  0.00  0.00           C+0
HETATM   26  C   UNK     0       0.341   1.947   0.000  0.00  0.00           C+0
HETATM   27  C   UNK     0       1.857   2.218   0.000  0.00  0.00           C+0
HETATM   28  O   UNK     0       2.380   3.667   0.000  0.00  0.00           O+0
HETATM   29  C   UNK     0       2.850   1.041   0.000  0.00  0.00           C+0
HETATM   30  C   UNK     0       3.373   2.489   0.000  0.00  0.00           C+0
CONECT    1    2                                                            
CONECT    2    1    3    8   11                                             
CONECT    3    2    4                                                       
CONECT    4    3    5                                                       
CONECT    5    4    6   29                                                  
CONECT    6    5    7    8   17                                             
CONECT    7    6                                                            
CONECT    8    6    2    9                                                  
CONECT    9    8   10                                                       
CONECT   10    9   11                                                       
CONECT   11   10    2   12                                                  
CONECT   12   11   13   16                                                  
CONECT   13   12   14                                                       
CONECT   14   13   15                                                       
CONECT   15   14   16                                                       
CONECT   16   15   12                                                       
CONECT   17    6   18   19                                                  
CONECT   18   17                                                            
CONECT   19   17   20   21                                                  
CONECT   20   19                                                            
CONECT   21   19   22   29                                                  
CONECT   22   21   23   24   25                                             
CONECT   23   22                                                            
CONECT   24   22                                                            
CONECT   25   22   26                                                       
CONECT   26   25   27                                                       
CONECT   27   26   28   29                                                  
CONECT   28   27                                                            
CONECT   29   27   21    5   30                                             
CONECT   30   29                                                            
MASTER        0    0    0    0    0    0    0    0   30    0   68    0
END

View in JSmol

Synonyms

Not Available

Chemical Formula

C₂₅H₃₂O₅

Average Mass

412.5260 Da

Monoisotopic Mass

412.22497 Da

IUPAC Name

(1S,2R,6R,7S,8R,9S,10R,14R,15S)-14-(furan-3-yl)-6,8,9-trihydroxy-2,6,10,15-tetramethyltetracyclo[8.7.0.0^{2,7}.0^{11,15}]heptadeca-4,11-dien-3-one

Traditional Name

(1S,2R,6R,7S,8R,9S,10R,14R,15S)-14-(furan-3-yl)-6,8,9-trihydroxy-2,6,10,15-tetramethyltetracyclo[8.7.0.0^{2,7}.0^{11,15}]heptadeca-4,11-dien-3-one

CAS Registry Number

Not Available

SMILES

C[C@@]12CC[C@H]3[C@@](C)([C@H](O)[C@H](O)[C@H]4[C@](C)(O)C=CC(=O)[C@]34C)C1=CC[C@H]2C1=COC=C1

InChI Identifier

InChI=1S/C25H32O5/c1-22-10-7-17-24(3,16(22)6-5-15(22)14-9-12-30-13-14)21(28)19(27)20-23(2,29)11-8-18(26)25(17,20)4/h6,8-9,11-13,15,17,19-21,27-29H,5,7,10H2,1-4H3/t15-,17-,19+,20-,21+,22-,23+,24-,25-/m0/s1

InChI Key

ZYWHPZZHPATFAR-MIWZOCFRSA-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
Chisocheton ceramicus	LOTUS Database	35616633

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as 17-furanylsteroids and derivatives. These are steroidal compounds having a furanyl group linked to the steroid backbone at the C17 position.

Kingdom

Organic compounds

Super Class

Lipids and lipid-like molecules

Class

Steroids and steroid derivatives

Sub Class

17-furanylsteroids and derivatives

Direct Parent

17-furanylsteroids and derivatives

Alternative Parents

Substituents

17-furanylsteroid skeleton
4-hydroxysteroid
6-hydroxysteroid
Hydroxysteroid
1-oxosteroid
Oxosteroid
7-hydroxysteroid
Cyclohexenone
Furan
Tertiary alcohol
Cyclic alcohol
Heteroaromatic compound
Secondary alcohol
Ketone
Polyol
Oxacycle
Organoheterocyclic compound
Organic oxygen compound
Hydrocarbon derivative
Organic oxide
Carbonyl group
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	2.47	ChemAxon
pKa (Strongest Acidic)	13.37	ChemAxon
pKa (Strongest Basic)	-2.8	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	4	ChemAxon
Hydrogen Donor Count	3	ChemAxon
Polar Surface Area	90.9 Å²	ChemAxon
Rotatable Bond Count	1	ChemAxon
Refractivity	114.57 m³·mol⁻¹	ChemAxon
Polarizability	45.1 Å³	ChemAxon
Number of Rings	5	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

29416310

KEGG Compound ID

Not Available

BioCyc ID

Not Available

BiGG ID

Not Available

Wikipedia Link

Not Available

METLIN ID

Not Available

PubChem Compound

71718852

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

LOTUS database [Link]

Showing NP-Card for (1r,3br,4s,5r,5as,6r,9ar,9bs,11as)-1-(furan-3-yl)-4,5,6-trihydroxy-3b,6,9a,11a-tetramethyl-1h,2h,4h,5h,5ah,9bh,10h,11h-cyclopenta[a]phenanthren-9-one (NP0239499)

MOL for NP0239499 ((1r,3br,4s,5r,5as,6r,9ar,9bs,11as)-1-(furan-3-yl)-4,5,6-trihydroxy-3b,6,9a,11a-tetramethyl-1h,2h,4h,5h,5ah,9bh,10h,11h-cyclopenta[a]phenanthren-9-one)

3D MOL for NP0239499 ((1r,3br,4s,5r,5as,6r,9ar,9bs,11as)-1-(furan-3-yl)-4,5,6-trihydroxy-3b,6,9a,11a-tetramethyl-1h,2h,4h,5h,5ah,9bh,10h,11h-cyclopenta[a]phenanthren-9-one)

3D SDF for NP0239499 ((1r,3br,4s,5r,5as,6r,9ar,9bs,11as)-1-(furan-3-yl)-4,5,6-trihydroxy-3b,6,9a,11a-tetramethyl-1h,2h,4h,5h,5ah,9bh,10h,11h-cyclopenta[a]phenanthren-9-one)

3D-SDF for NP0239499 ((1r,3br,4s,5r,5as,6r,9ar,9bs,11as)-1-(furan-3-yl)-4,5,6-trihydroxy-3b,6,9a,11a-tetramethyl-1h,2h,4h,5h,5ah,9bh,10h,11h-cyclopenta[a]phenanthren-9-one)

PDB for NP0239499 ((1r,3br,4s,5r,5as,6r,9ar,9bs,11as)-1-(furan-3-yl)-4,5,6-trihydroxy-3b,6,9a,11a-tetramethyl-1h,2h,4h,5h,5ah,9bh,10h,11h-cyclopenta[a]phenanthren-9-one)

3D PDB for NP0239499 ((1r,3br,4s,5r,5as,6r,9ar,9bs,11as)-1-(furan-3-yl)-4,5,6-trihydroxy-3b,6,9a,11a-tetramethyl-1h,2h,4h,5h,5ah,9bh,10h,11h-cyclopenta[a]phenanthren-9-one)

SMILES for NP0239499 ((1r,3br,4s,5r,5as,6r,9ar,9bs,11as)-1-(furan-3-yl)-4,5,6-trihydroxy-3b,6,9a,11a-tetramethyl-1h,2h,4h,5h,5ah,9bh,10h,11h-cyclopenta[a]phenanthren-9-one)

INCHI for NP0239499 ((1r,3br,4s,5r,5as,6r,9ar,9bs,11as)-1-(furan-3-yl)-4,5,6-trihydroxy-3b,6,9a,11a-tetramethyl-1h,2h,4h,5h,5ah,9bh,10h,11h-cyclopenta[a]phenanthren-9-one)

Structure for NP0239499 ((1r,3br,4s,5r,5as,6r,9ar,9bs,11as)-1-(furan-3-yl)-4,5,6-trihydroxy-3b,6,9a,11a-tetramethyl-1h,2h,4h,5h,5ah,9bh,10h,11h-cyclopenta[a]phenanthren-9-one)

3D Structure for NP0239499 ((1r,3br,4s,5r,5as,6r,9ar,9bs,11as)-1-(furan-3-yl)-4,5,6-trihydroxy-3b,6,9a,11a-tetramethyl-1h,2h,4h,5h,5ah,9bh,10h,11h-cyclopenta[a]phenanthren-9-one)