NP-MRD: Showing NP-Card for methyl 4,9-bis(acetyloxy)-7-ethenyl-8-hydroxy-1,4a,7-trimethyl-3,4,5,6,8,9,10,10a-octahydro-2h-phenanthrene-1-carboxylate (NP0159502)

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Record Information

Version

1.0

Created at

2022-09-02 17:15:35 UTC

Updated at

2022-09-02 17:15:35 UTC

NP-MRD ID

NP0159502

Secondary Accession Numbers

None

Natural Product Identification

Common Name

methyl 4,9-bis(acetyloxy)-7-ethenyl-8-hydroxy-1,4a,7-trimethyl-3,4,5,6,8,9,10,10a-octahydro-2h-phenanthrene-1-carboxylate

Description

Methyl 4,9-bis(acetyloxy)-7-ethenyl-8-hydroxy-1,4a,7-trimethyl-1,2,3,4,4a,5,6,7,8,9,10,10a-dodecahydrophenanthrene-1-carboxylate belongs to the class of organic compounds known as diterpenoids. These are terpene compounds formed by four isoprene units. methyl 4,9-bis(acetyloxy)-7-ethenyl-8-hydroxy-1,4a,7-trimethyl-3,4,5,6,8,9,10,10a-octahydro-2h-phenanthrene-1-carboxylate is found in Lycopus europaeus. Methyl 4,9-bis(acetyloxy)-7-ethenyl-8-hydroxy-1,4a,7-trimethyl-1,2,3,4,4a,5,6,7,8,9,10,10a-dodecahydrophenanthrene-1-carboxylate is an extremely weak basic (essentially neutral) compound (based on its pKa).

Structure

MOL 3D MOL SDF PDB SMILES InChI


  Mrv1533004161522512D          

 32 34  0  0  0  0            999 V2000
    4.8659    2.1876    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.0907    2.4697    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.4587    1.9394    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.6835    2.2216    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.6020    1.1270    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.3772    1.4091    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.0145    0.4125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.6020   -0.3020    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.7770   -0.3020    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.3645   -1.0164    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.7770   -1.7309    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.6020   -1.7309    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.3645   -2.4454    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.3645    0.4125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.9520   -0.3020    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.7770    1.1270    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.3645    1.8414    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.5395    1.8414    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.1270    2.5559    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.5395    3.2704    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.3645    3.2704    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.1270    3.9849    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.1270    1.1270    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.5395    0.4125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.1270   -0.3020    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.3020   -0.3020    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1105    0.4125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7425   -0.1178    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7425    0.9428    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5178    0.6606    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.3020    1.1270    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1105    1.8414    0.0000 O   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  2  0  0  0  0
  3  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
  8  9  1  0  0  0  0
  9 10  1  0  0  0  0
 10 11  1  0  0  0  0
 11 12  2  0  0  0  0
 11 13  1  0  0  0  0
  9 14  1  0  0  0  0
 14 15  1  0  0  0  0
 14 16  1  0  0  0  0
  5 16  1  0  0  0  0
 16 17  1  0  0  0  0
 17 18  1  0  0  0  0
 18 19  1  0  0  0  0
 19 20  1  0  0  0  0
 20 21  2  0  0  0  0
 20 22  1  0  0  0  0
 18 23  1  0  0  0  0
 23 24  2  0  0  0  0
 14 24  1  0  0  0  0
 24 25  1  0  0  0  0
 25 26  1  0  0  0  0
 26 27  1  0  0  0  0
 27 28  1  0  0  0  0
 27 29  1  0  0  0  0
 29 30  2  0  0  0  0
 27 31  1  0  0  0  0
 23 31  1  0  0  0  0
 31 32  1  0  0  0  0
M  END

     RDKit          3D

 68 70  0  0  0  0  0  0  0  0999 V2000
    5.8332    0.6489    0.4810 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.6364    0.4382    0.9978 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.3681    0.8988    0.3194 C   0  0  2  0  0  0  0  0  0  0  0  0
    3.8141    1.9324   -0.7077 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.5293    1.5233    1.3987 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.1277    1.8426    0.9171 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.4479    0.6287    0.3740 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.2172   -0.3370   -0.1100 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.6930   -1.7138   -0.4193 C   0  0  1  0  0  0  0  0  0  0  0  0
    1.4636   -2.7468    0.0971 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.0486   -3.6981   -0.7369 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8813   -4.8245   -0.2525 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.8507   -3.5826   -1.9699 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7499   -1.8489    0.0195 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4404   -0.6092   -0.4602 C   0  0  1  0  0  0  0  0  0  0  0  0
   -2.8738   -0.8167   -0.7399 C   0  0  1  0  0  0  0  0  0  0  0  0
   -2.9569   -1.5331   -2.1100 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.6046   -1.7017    0.1766 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.0184   -2.2262    1.1314 O   0  0  0  0  0  0  0  0  0  0  0  0
   -4.9411   -1.9453   -0.0309 O   0  0  0  0  0  0  0  0  0  0  0  0
   -5.7176   -2.7822    0.8000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5849    0.4968   -0.9643 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5311    1.5248   -1.3851 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7239    1.7716   -0.1022 C   0  0  2  0  0  0  0  0  0  0  0  0
   -0.9729    2.9336   -0.1746 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2336    4.0965    0.5368 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4110    5.3223    0.4368 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2255    4.0689    1.2926 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0429    0.5419    0.3972 C   0  0  2  0  0  0  0  0  0  0  0  0
   -1.3851    0.3507    1.8762 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.6728   -0.1930   -0.4090 C   0  0  2  0  0  0  0  0  0  0  0  0
    3.3186   -1.3906   -0.0166 O   0  0  0  0  0  0  0  0  0  0  0  0
    6.6823    0.2884    1.0288 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.9337    1.1653   -0.4569 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.4807   -0.0779    1.9414 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.9119    2.4205   -1.1277 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.2301    1.3243   -1.5642 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.5327    2.6382   -0.2937 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.4962    0.8838    2.2940 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.9957    2.4880    1.6821 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.6193    2.2759    1.7997 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.2869    2.5925    0.0885 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.6645   -1.7950   -1.5335 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.6351   -5.0699   -1.0442 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.2565   -5.7534   -0.1365 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.3556   -4.5473    0.7081 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7249   -1.9919    1.1054 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1684   -2.7209   -0.5241 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9630   -0.3907   -1.4734 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.9491   -1.3728   -2.5646 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1365   -1.1732   -2.7315 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8201   -2.6251   -1.9075 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.4619   -3.3760    0.2521 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.2526   -2.1100    1.5092 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.0418   -3.4903    1.3399 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.0168    0.8172   -0.0115 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.3640    0.4394   -1.7378 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.1006    2.4704   -1.5577 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9282    1.2185   -2.2316 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5490    1.9990    0.6450 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9966    6.0556   -0.1801 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.5412    5.1455   -0.0941 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2750    5.8113    1.4204 H   0  0  0  0  0  0  0  0  0  0  0  0
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   -0.7595   -0.4227    2.3598 H   0  0  0  0  0  0  0  0  0  0  0  0
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    2.8416   -0.1491   -1.5221 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.0700   -1.6087   -0.6074 H   0  0  0  0  0  0  0  0  0  0  0  0
 21 20  1  0
 20 18  1  0
 18 19  2  0
 16 18  1  1
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 16 22  1  0
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 14  9  1  0
  9 10  1  0
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  9  8  1  0
  8  7  2  0
  7  6  1  0
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  5  3  1  0
  3  4  1  0
  3  2  1  1
  2  1  2  3
  3 31  1  0
 31 32  1  0
 15 16  1  0
 31  8  1  0
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 21 53  1  0
 21 54  1  0
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 27 61  1  0
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 27 63  1  0
 30 64  1  0
 30 65  1  0
 30 66  1  0
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 14 47  1  0
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  9 43  1  6
 12 44  1  0
 12 45  1  0
 12 46  1  0
  6 41  1  0
  6 42  1  0
  5 39  1  0
  5 40  1  0
  4 36  1  0
  4 37  1  0
  4 38  1  0
  2 35  1  0
  1 33  1  0
  1 34  1  0
 31 67  1  6
 32 68  1  0
M  END


  Mrv1533004161522512D          

 32 34  0  0  0  0            999 V2000
    4.8659    2.1876    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.0907    2.4697    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.4587    1.9394    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.6835    2.2216    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.6020    1.1270    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.3772    1.4091    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.0145    0.4125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.6020   -0.3020    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.7770   -0.3020    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.3645   -1.0164    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.7770   -1.7309    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.6020   -1.7309    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.3645   -2.4454    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.3645    0.4125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.9520   -0.3020    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.7770    1.1270    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.3645    1.8414    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.5395    1.8414    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.1270    2.5559    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.5395    3.2704    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.3645    3.2704    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.1270    3.9849    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.1270    1.1270    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.5395    0.4125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.1270   -0.3020    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.3020   -0.3020    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1105    0.4125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7425   -0.1178    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7425    0.9428    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
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    0.3020    1.1270    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1105    1.8414    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0  0  0  0
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  3  4  2  0  0  0  0
  3  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
  8  9  1  0  0  0  0
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  5 16  1  0  0  0  0
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 20 22  1  0  0  0  0
 18 23  1  0  0  0  0
 23 24  2  0  0  0  0
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 26 27  1  0  0  0  0
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 27 29  1  0  0  0  0
 29 30  2  0  0  0  0
 27 31  1  0  0  0  0
 23 31  1  0  0  0  0
 31 32  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0159502

> <DATABASE_NAME>
NP-MRD

> <SMILES>
COC(=O)C1(C)CCC(OC(C)=O)C2(C)C1CC(OC(C)=O)C1=C2CCC(C)(C=C)C1O

> <INCHI_IDENTIFIER>
InChI=1S/C25H36O7/c1-8-23(4)11-9-16-20(21(23)28)17(31-14(2)26)13-18-24(5,22(29)30-7)12-10-19(25(16,18)6)32-15(3)27/h8,17-19,21,28H,1,9-13H2,2-7H3

> <INCHI_KEY>
BFNKIBKGOSKZTK-UHFFFAOYSA-N

> <FORMULA>
C25H36O7

> <MOLECULAR_WEIGHT>
448.556

> <EXACT_MASS>
448.246103499

> <JCHEM_ACCEPTOR_COUNT>
4

> <JCHEM_ATOM_COUNT>
68

> <JCHEM_AVERAGE_POLARIZABILITY>
48.56935003442115

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
1

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
1

> <JCHEM_IUPAC>
methyl 4,9-bis(acetyloxy)-7-ethenyl-8-hydroxy-1,4a,7-trimethyl-1,2,3,4,4a,5,6,7,8,9,10,10a-dodecahydrophenanthrene-1-carboxylate

> <ALOGPS_LOGP>
3.19

> <JCHEM_LOGP>
2.5151458899999994

> <ALOGPS_LOGS>
-4.68

> <JCHEM_MDDR_LIKE_RULE>
1

> <JCHEM_NUMBER_OF_RINGS>
3

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA_STRONGEST_ACIDIC>
14.010821591751263

> <JCHEM_PKA_STRONGEST_BASIC>
-3.2314666357679975

> <JCHEM_POLAR_SURFACE_AREA>
99.13000000000001

> <JCHEM_REFRACTIVITY>
117.5328

> <JCHEM_ROTATABLE_BOND_COUNT>
7

> <JCHEM_RULE_OF_FIVE>
1

> <ALOGPS_SOLUBILITY>
9.27e-03 g/l

> <JCHEM_TRADITIONAL_IUPAC>
methyl 4,9-bis(acetyloxy)-7-ethenyl-8-hydroxy-1,4a,7-trimethyl-3,4,5,6,8,9,10,10a-octahydro-2H-phenanthrene-1-carboxylate

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 16-APR-15   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   16-APR-15         0                                  
HETATM    1  C   UNK     0       9.083   4.083   0.000  0.00  0.00           C+0
HETATM    2  O   UNK     0       7.636   4.610   0.000  0.00  0.00           O+0
HETATM    3  C   UNK     0       6.456   3.620   0.000  0.00  0.00           C+0
HETATM    4  O   UNK     0       5.009   4.147   0.000  0.00  0.00           O+0
HETATM    5  C   UNK     0       6.724   2.104   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0       8.171   2.630   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0       7.494   0.770   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0       6.724  -0.564   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0       5.184  -0.564   0.000  0.00  0.00           C+0
HETATM   10  O   UNK     0       4.414  -1.897   0.000  0.00  0.00           O+0
HETATM   11  C   UNK     0       5.184  -3.231   0.000  0.00  0.00           C+0
HETATM   12  O   UNK     0       6.724  -3.231   0.000  0.00  0.00           O+0
HETATM   13  C   UNK     0       4.414  -4.565   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0       4.414   0.770   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0       3.644  -0.564   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0       5.184   2.104   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0       4.414   3.437   0.000  0.00  0.00           C+0
HETATM   18  C   UNK     0       2.874   3.437   0.000  0.00  0.00           C+0
HETATM   19  O   UNK     0       2.104   4.771   0.000  0.00  0.00           O+0
HETATM   20  C   UNK     0       2.874   6.105   0.000  0.00  0.00           C+0
HETATM   21  O   UNK     0       4.414   6.105   0.000  0.00  0.00           O+0
HETATM   22  C   UNK     0       2.104   7.438   0.000  0.00  0.00           C+0
HETATM   23  C   UNK     0       2.104   2.104   0.000  0.00  0.00           C+0
HETATM   24  C   UNK     0       2.874   0.770   0.000  0.00  0.00           C+0
HETATM   25  C   UNK     0       2.104  -0.564   0.000  0.00  0.00           C+0
HETATM   26  C   UNK     0       0.564  -0.564   0.000  0.00  0.00           C+0
HETATM   27  C   UNK     0      -0.206   0.770   0.000  0.00  0.00           C+0
HETATM   28  C   UNK     0      -1.386  -0.220   0.000  0.00  0.00           C+0
HETATM   29  C   UNK     0      -1.386   1.760   0.000  0.00  0.00           C+0
HETATM   30  C   UNK     0      -2.833   1.233   0.000  0.00  0.00           C+0
HETATM   31  C   UNK     0       0.564   2.104   0.000  0.00  0.00           C+0
HETATM   32  O   UNK     0      -0.206   3.437   0.000  0.00  0.00           O+0
CONECT    1    2                                                            
CONECT    2    1    3                                                       
CONECT    3    2    4    5                                                  
CONECT    4    3                                                            
CONECT    5    3    6    7   16                                             
CONECT    6    5                                                            
CONECT    7    5    8                                                       
CONECT    8    7    9                                                       
CONECT    9    8   10   14                                                  
CONECT   10    9   11                                                       
CONECT   11   10   12   13                                                  
CONECT   12   11                                                            
CONECT   13   11                                                            
CONECT   14    9   15   16   24                                             
CONECT   15   14                                                            
CONECT   16   14    5   17                                                  
CONECT   17   16   18                                                       
CONECT   18   17   19   23                                                  
CONECT   19   18   20                                                       
CONECT   20   19   21   22                                                  
CONECT   21   20                                                            
CONECT   22   20                                                            
CONECT   23   18   24   31                                                  
CONECT   24   23   14   25                                                  
CONECT   25   24   26                                                       
CONECT   26   25   27                                                       
CONECT   27   26   28   29   31                                             
CONECT   28   27                                                            
CONECT   29   27   30                                                       
CONECT   30   29                                                            
CONECT   31   27   23   32                                                  
CONECT   32   31                                                            
MASTER        0    0    0    0    0    0    0    0   32    0   68    0
END

View in JSmol

Synonyms

Value	Source
Methyl 4,9-bis(acetyloxy)-7-ethenyl-8-hydroxy-1,4a,7-trimethyl-1,2,3,4,4a,5,6,7,8,9,10,10a-dodecahydrophenanthrene-1-carboxylic acid	Generator

Chemical Formula

C₂₅H₃₆O₇

Average Mass

448.5560 Da

Monoisotopic Mass

448.24610 Da

IUPAC Name

methyl 4,9-bis(acetyloxy)-7-ethenyl-8-hydroxy-1,4a,7-trimethyl-1,2,3,4,4a,5,6,7,8,9,10,10a-dodecahydrophenanthrene-1-carboxylate

Traditional Name

methyl 4,9-bis(acetyloxy)-7-ethenyl-8-hydroxy-1,4a,7-trimethyl-3,4,5,6,8,9,10,10a-octahydro-2H-phenanthrene-1-carboxylate

CAS Registry Number

Not Available

SMILES

COC(=O)C1(C)CCC(OC(C)=O)C2(C)C1CC(OC(C)=O)C1=C2CCC(C)(C=C)C1O

InChI Identifier

InChI=1S/C25H36O7/c1-8-23(4)11-9-16-20(21(23)28)17(31-14(2)26)13-18-24(5,22(29)30-7)12-10-19(25(16,18)6)32-15(3)27/h8,17-19,21,28H,1,9-13H2,2-7H3

InChI Key

BFNKIBKGOSKZTK-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
Lycopus europaeus	LOTUS Database	35616633

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as diterpenoids. These are terpene compounds formed by four isoprene units.

Kingdom

Organic compounds

Super Class

Lipids and lipid-like molecules

Class

Prenol lipids

Sub Class

Diterpenoids

Direct Parent

Diterpenoids

Alternative Parents

Substituents

Diterpenoid
Pimarane diterpenoid
Hydrophenanthrene
Phenanthrene
Tricarboxylic acid or derivatives
Methyl ester
Carboxylic acid ester
Secondary alcohol
Carboxylic acid derivative
Hydrocarbon derivative
Organic oxide
Organic oxygen compound
Alcohol
Carbonyl group
Organooxygen compound
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	3.19	ALOGPS
logP	2.52	ChemAxon
logS	-4.7	ALOGPS
pKa (Strongest Acidic)	14.01	ChemAxon
pKa (Strongest Basic)	-3.2	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	4	ChemAxon
Hydrogen Donor Count	1	ChemAxon
Polar Surface Area	99.13 Å²	ChemAxon
Rotatable Bond Count	7	ChemAxon
Refractivity	117.53 m³·mol⁻¹	ChemAxon
Polarizability	48.57 Å³	ChemAxon
Number of Rings	3	ChemAxon
Bioavailability	Yes	ChemAxon
Rule of Five	Yes	ChemAxon
Ghose Filter	Yes	ChemAxon
Veber's Rule	No	ChemAxon
MDDR-like Rule	Yes	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

73813590

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

LOTUS database [Link]

Showing NP-Card for methyl 4,9-bis(acetyloxy)-7-ethenyl-8-hydroxy-1,4a,7-trimethyl-3,4,5,6,8,9,10,10a-octahydro-2h-phenanthrene-1-carboxylate (NP0159502)

MOL for NP0159502 (methyl 4,9-bis(acetyloxy)-7-ethenyl-8-hydroxy-1,4a,7-trimethyl-3,4,5,6,8,9,10,10a-octahydro-2h-phenanthrene-1-carboxylate)

3D MOL for NP0159502 (methyl 4,9-bis(acetyloxy)-7-ethenyl-8-hydroxy-1,4a,7-trimethyl-3,4,5,6,8,9,10,10a-octahydro-2h-phenanthrene-1-carboxylate)

3D SDF for NP0159502 (methyl 4,9-bis(acetyloxy)-7-ethenyl-8-hydroxy-1,4a,7-trimethyl-3,4,5,6,8,9,10,10a-octahydro-2h-phenanthrene-1-carboxylate)

3D-SDF for NP0159502 (methyl 4,9-bis(acetyloxy)-7-ethenyl-8-hydroxy-1,4a,7-trimethyl-3,4,5,6,8,9,10,10a-octahydro-2h-phenanthrene-1-carboxylate)

PDB for NP0159502 (methyl 4,9-bis(acetyloxy)-7-ethenyl-8-hydroxy-1,4a,7-trimethyl-3,4,5,6,8,9,10,10a-octahydro-2h-phenanthrene-1-carboxylate)

3D PDB for NP0159502 (methyl 4,9-bis(acetyloxy)-7-ethenyl-8-hydroxy-1,4a,7-trimethyl-3,4,5,6,8,9,10,10a-octahydro-2h-phenanthrene-1-carboxylate)

SMILES for NP0159502 (methyl 4,9-bis(acetyloxy)-7-ethenyl-8-hydroxy-1,4a,7-trimethyl-3,4,5,6,8,9,10,10a-octahydro-2h-phenanthrene-1-carboxylate)

INCHI for NP0159502 (methyl 4,9-bis(acetyloxy)-7-ethenyl-8-hydroxy-1,4a,7-trimethyl-3,4,5,6,8,9,10,10a-octahydro-2h-phenanthrene-1-carboxylate)

Structure for NP0159502 (methyl 4,9-bis(acetyloxy)-7-ethenyl-8-hydroxy-1,4a,7-trimethyl-3,4,5,6,8,9,10,10a-octahydro-2h-phenanthrene-1-carboxylate)

3D Structure for NP0159502 (methyl 4,9-bis(acetyloxy)-7-ethenyl-8-hydroxy-1,4a,7-trimethyl-3,4,5,6,8,9,10,10a-octahydro-2h-phenanthrene-1-carboxylate)