NP-MRD: Showing NP-Card for methyl (2r,6r)-6-[(1r,3ar,5ar,7r,9ar,9bs,11ar)-7-(acetyloxy)-3a,6,6,9a,11a-pentamethyl-1h,2h,3h,5h,5ah,7h,8h,9h,9bh,10h,11h-cyclopenta[a]phenanthren-1-yl]-2-methyl-4-oxoheptanoate (NP0301443)

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Record Information

Version

2.0

Created at

2022-09-10 14:24:32 UTC

Updated at

2022-09-10 14:24:32 UTC

NP-MRD ID

NP0301443

Secondary Accession Numbers

None

Natural Product Identification

Common Name

methyl (2r,6r)-6-[(1r,3ar,5ar,7r,9ar,9bs,11ar)-7-(acetyloxy)-3a,6,6,9a,11a-pentamethyl-1h,2h,3h,5h,5ah,7h,8h,9h,9bh,10h,11h-cyclopenta[a]phenanthren-1-yl]-2-methyl-4-oxoheptanoate

Description

Methyl (2R,6R)-6-[(1S,2R,5R,7R,11R,14R,15R)-5-(acetyloxy)-2,6,6,11,15-pentamethyltetracyclo[8.7.0.0²,⁷.0¹¹,¹⁵]Heptadec-9-en-14-yl]-2-methyl-4-oxoheptanoate belongs to the class of organic compounds known as triterpenoids. These are terpene molecules containing six isoprene units. methyl (2r,6r)-6-[(1r,3ar,5ar,7r,9ar,9bs,11ar)-7-(acetyloxy)-3a,6,6,9a,11a-pentamethyl-1h,2h,3h,5h,5ah,7h,8h,9h,9bh,10h,11h-cyclopenta[a]phenanthren-1-yl]-2-methyl-4-oxoheptanoate is found in Abies pinsapo. Based on a literature review very few articles have been published on methyl (2R,6R)-6-[(1S,2R,5R,7R,11R,14R,15R)-5-(acetyloxy)-2,6,6,11,15-pentamethyltetracyclo[8.7.0.0²,⁷.0¹¹,¹⁵]Heptadec-9-en-14-yl]-2-methyl-4-oxoheptanoate.

Structure

MOL 3D MOL SDF PDB SMILES InChI


  Mrv1652309102216242D          

 38 41  0  0  1  0            999 V2000
    8.3550   -2.5302    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    9.0694   -2.9427    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    9.7839   -2.5302    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    9.7839   -1.7052    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   10.4984   -2.9427    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
   10.4984   -3.7677    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   11.2128   -2.5302    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   11.9273   -2.9427    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   11.9273   -3.7677    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   12.6418   -2.5302    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   13.3563   -2.9427    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
   13.3563   -3.7677    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   14.0707   -2.5302    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
   14.1570   -1.7097    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   14.9639   -1.5382    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   15.3764   -2.2527    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
   15.8614   -1.5852    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   16.1834   -2.4242    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   16.7354   -1.8111    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   17.5424   -1.9826    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   17.7974   -2.7673    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
   18.6043   -2.9388    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   18.6331   -2.1143    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   19.4213   -2.8240    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   18.8593   -3.7234    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
   19.6662   -3.8949    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   19.9212   -4.6795    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   20.7281   -4.8511    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   19.3691   -5.2926    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   18.3072   -4.3365    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   17.5003   -4.1650    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   17.2453   -3.3803    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
   16.6933   -3.9934    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   16.4383   -3.2088    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
   15.8863   -3.8219    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   15.0793   -3.6504    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   14.8244   -2.8658    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
   14.2113   -3.4178    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  2  0  0  0  0
  3  5  1  0  0  0  0
  5  6  1  1  0  0  0
  5  7  1  0  0  0  0
  7  8  1  0  0  0  0
  8  9  2  0  0  0  0
  8 10  1  0  0  0  0
 10 11  1  0  0  0  0
 11 12  1  6  0  0  0
 13 11  1  1  0  0  0
 13 14  1  0  0  0  0
 14 15  1  0  0  0  0
 15 16  1  0  0  0  0
 16 17  1  6  0  0  0
 16 18  1  0  0  0  0
 18 19  2  0  0  0  0
 19 20  1  0  0  0  0
 21 20  1  1  0  0  0
 21 22  1  0  0  0  0
 22 23  1  0  0  0  0
 22 24  1  0  0  0  0
 22 25  1  0  0  0  0
 25 26  1  6  0  0  0
 26 27  1  0  0  0  0
 27 28  1  0  0  0  0
 27 29  2  0  0  0  0
 25 30  1  0  0  0  0
 30 31  1  0  0  0  0
 31 32  1  0  0  0  0
 21 32  1  0  0  0  0
 32 33  1  1  0  0  0
 32 34  1  0  0  0  0
 34 18  1  6  0  0  0
 34 35  1  0  0  0  0
 35 36  1  0  0  0  0
 36 37  1  0  0  0  0
 13 37  1  0  0  0  0
 16 37  1  0  0  0  0
 37 38  1  1  0  0  0
M  END

     RDKit          3D

 90 93  0  0  0  0  0  0  0  0999 V2000
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    9.7446    1.8989   -0.6773 O   0  0  0  0  0  0  0  0  0  0  0  0
    8.6708    1.0965   -1.0308 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.3888    0.8204   -2.2050 O   0  0  0  0  0  0  0  0  0  0  0  0
    7.8303    0.5516    0.0654 C   0  0  2  0  0  0  0  0  0  0  0  0
    8.5924   -0.3081    1.0239 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.6728   -0.2626   -0.5199 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.8826   -0.7721    0.6292 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.3614   -1.6893    1.2910 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.5785   -0.1734    0.9309 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.4093   -0.9747    0.3328 C   0  0  1  0  0  0  0  0  0  0  0  0
    3.4940   -2.3413    0.9398 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1810   -0.2144    0.6729 C   0  0  1  0  0  0  0  0  0  0  0  0
    2.3279    1.1773    0.0359 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.9157    1.6028   -0.3576 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0460    0.5904    0.3499 C   0  0  1  0  0  0  0  0  0  0  0  0
    0.0118    0.9433    1.7947 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2895    0.4535   -0.2314 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8642    1.4739   -0.8300 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.2247    1.2373   -1.3889 C   0  0  0  0  0  0  0  0  0  0  0  0
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   -6.1659   -0.4393    0.3989 C   0  0  2  0  0  0  0  0  0  0  0  0
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   -8.6004   -0.0690    0.6960 C   0  0  0  0  0  0  0  0  0  0  0  0
   -9.7312    0.6473    1.3301 C   0  0  0  0  0  0  0  0  0  0  0  0
   -8.8468   -0.9775   -0.1367 O   0  0  0  0  0  0  0  0  0  0  0  0
   -5.3996   -1.0783    1.4899 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.9614   -1.3435    1.2831 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.4210   -0.8779   -0.0481 C   0  0  1  0  0  0  0  0  0  0  0  0
   -3.9760   -1.8779   -1.0722 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9491   -0.8663   -0.1298 C   0  0  2  0  0  0  0  0  0  0  0  0
   -1.2626   -1.6757    0.9476 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.2033   -1.8017    0.7333 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.8973   -0.6688    0.0912 C   0  0  2  0  0  0  0  0  0  0  0  0
    1.0817   -0.8406   -1.4007 C   0  0  0  0  0  0  0  0  0  0  0  0
   11.5451    2.6727   -1.2548 H   0  0  0  0  0  0  0  0  0  0  0  0
   10.0570    3.3659   -2.0611 H   0  0  0  0  0  0  0  0  0  0  0  0
   10.6549    1.7207   -2.5536 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.4353    1.4247    0.6251 H   0  0  0  0  0  0  0  0  0  0  0  0
    9.6713    0.0158    1.0620 H   0  0  0  0  0  0  0  0  0  0  0  0
    8.1932   -0.2357    2.0644 H   0  0  0  0  0  0  0  0  0  0  0  0
    8.5997   -1.3733    0.6902 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.0726    0.4475   -1.1069 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.0872   -1.0863   -1.1330 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.4415   -0.0928    2.0285 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.5250    0.8752    0.5251 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.6434   -1.0551   -0.7442 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.4512   -2.7997    0.5482 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.6144   -2.3373    2.0434 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.7066   -3.0436    0.5982 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.1741   -0.0251    1.7629 H   0  0  0  0  0  0  0  0  0  0  0  0
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    0.6519    1.8431    2.0357 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0350    1.3053    2.0192 H   0  0  0  0  0  0  0  0  0  0  0  0
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   -3.7795    2.1689   -1.5583 H   0  0  0  0  0  0  0  0  0  0  0  0
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   -6.7676    1.3081   -1.9720 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.4739   -0.4282   -2.0154 H   0  0  0  0  0  0  0  0  0  0  0  0
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   -1.7246   -2.7059    0.8738 H   0  0  0  0  0  0  0  0  0  0  0  0
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    0.3885   -2.7293    0.1141 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.7204   -2.0181    1.7092 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.0259   -0.3980   -1.7804 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.2804   -0.2820   -1.9695 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.0975   -1.9076   -1.7119 H   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0
  2  3  1  0
  3  4  2  0
  3  5  1  0
  5  6  1  0
  5  7  1  0
  7  8  1  0
  8  9  2  0
  8 10  1  0
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 36 86  1  0
 36 87  1  0
 38 88  1  0
 38 89  1  0
 38 90  1  0
 28 73  1  0
 28 74  1  0
 28 75  1  0
M  END


  Mrv1652309102216242D          

 38 41  0  0  1  0            999 V2000
    8.3550   -2.5302    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    9.0694   -2.9427    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    9.7839   -2.5302    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    9.7839   -1.7052    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   10.4984   -2.9427    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
   10.4984   -3.7677    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   11.2128   -2.5302    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   11.9273   -2.9427    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   11.9273   -3.7677    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   12.6418   -2.5302    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   13.3563   -2.9427    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
   13.3563   -3.7677    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   14.0707   -2.5302    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
   14.1570   -1.7097    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   14.9639   -1.5382    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   15.3764   -2.2527    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
   15.8614   -1.5852    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   16.1834   -2.4242    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   16.7354   -1.8111    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   17.5424   -1.9826    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   17.7974   -2.7673    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
   18.6043   -2.9388    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   18.6331   -2.1143    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   19.4213   -2.8240    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   18.8593   -3.7234    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
   19.6662   -3.8949    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   19.9212   -4.6795    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   20.7281   -4.8511    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   19.3691   -5.2926    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   18.3072   -4.3365    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   17.5003   -4.1650    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   17.2453   -3.3803    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
   16.6933   -3.9934    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   16.4383   -3.2088    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
   15.8863   -3.8219    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   15.0793   -3.6504    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   14.8244   -2.8658    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
   14.2113   -3.4178    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  2  0  0  0  0
  3  5  1  0  0  0  0
  5  6  1  1  0  0  0
  5  7  1  0  0  0  0
  7  8  1  0  0  0  0
  8  9  2  0  0  0  0
  8 10  1  0  0  0  0
 10 11  1  0  0  0  0
 11 12  1  6  0  0  0
 13 11  1  1  0  0  0
 13 14  1  0  0  0  0
 14 15  1  0  0  0  0
 15 16  1  0  0  0  0
 16 17  1  6  0  0  0
 16 18  1  0  0  0  0
 18 19  2  0  0  0  0
 19 20  1  0  0  0  0
 21 20  1  1  0  0  0
 21 22  1  0  0  0  0
 22 23  1  0  0  0  0
 22 24  1  0  0  0  0
 22 25  1  0  0  0  0
 25 26  1  6  0  0  0
 26 27  1  0  0  0  0
 27 28  1  0  0  0  0
 27 29  2  0  0  0  0
 25 30  1  0  0  0  0
 30 31  1  0  0  0  0
 31 32  1  0  0  0  0
 21 32  1  0  0  0  0
 32 33  1  1  0  0  0
 32 34  1  0  0  0  0
 34 18  1  6  0  0  0
 34 35  1  0  0  0  0
 35 36  1  0  0  0  0
 36 37  1  0  0  0  0
 13 37  1  0  0  0  0
 16 37  1  0  0  0  0
 37 38  1  1  0  0  0
M  END
> <DATABASE_ID>
NP0301443

> <DATABASE_NAME>
NP-MRD

> <SMILES>
COC(=O)[C@H](C)CC(=O)C[C@@H](C)[C@H]1CC[C@@]2(C)C3=CC[C@H]4C(C)(C)[C@@H](CC[C@]4(C)[C@@H]3CC[C@]12C)OC(C)=O

> <INCHI_IDENTIFIER>
InChI=1S/C33H52O5/c1-20(18-23(35)19-21(2)29(36)37-9)24-12-16-33(8)26-10-11-27-30(4,5)28(38-22(3)34)14-15-31(27,6)25(26)13-17-32(24,33)7/h10,20-21,24-25,27-28H,11-19H2,1-9H3/t20-,21-,24-,25-,27+,28-,31-,32-,33+/m1/s1

> <INCHI_KEY>
KSABNVUMGNYNHH-YLHGYTFTSA-N

> <FORMULA>
C33H52O5

> <MOLECULAR_WEIGHT>
528.774

> <EXACT_MASS>
528.381474774

> <JCHEM_ACCEPTOR_COUNT>
3

> <JCHEM_ATOM_COUNT>
90

> <JCHEM_AVERAGE_POLARIZABILITY>
62.773695486025375

> <JCHEM_BIOAVAILABILITY>
0

> <JCHEM_DONOR_COUNT>
0

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
0

> <JCHEM_IUPAC>
methyl (2R,6R)-6-[(1S,2R,5R,7R,11R,14R,15R)-5-(acetyloxy)-2,6,6,11,15-pentamethyltetracyclo[8.7.0.0^{2,7}.0^{11,15}]heptadec-9-en-14-yl]-2-methyl-4-oxoheptanoate

> <JCHEM_LOGP>
6.499436984999998

> <JCHEM_MDDR_LIKE_RULE>
1

> <JCHEM_NUMBER_OF_RINGS>
4

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA_STRONGEST_ACIDIC>
17.839206977862343

> <JCHEM_PKA_STRONGEST_BASIC>
-6.641490350721306

> <JCHEM_POLAR_SURFACE_AREA>
69.67000000000002

> <JCHEM_REFRACTIVITY>
150.21460000000002

> <JCHEM_ROTATABLE_BOND_COUNT>
9

> <JCHEM_RULE_OF_FIVE>
0

> <JCHEM_TRADITIONAL_IUPAC>
methyl (2R,6R)-6-[(1S,2R,5R,7R,11R,14R,15R)-5-(acetyloxy)-2,6,6,11,15-pentamethyltetracyclo[8.7.0.0^{2,7}.0^{11,15}]heptadec-9-en-14-yl]-2-methyl-4-oxoheptanoate

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 10-SEP-22   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   10-SEP-22         0                                  
HETATM    1  C   UNK     0      15.596  -4.723   0.000  0.00  0.00           C+0
HETATM    2  O   UNK     0      16.930  -5.493   0.000  0.00  0.00           O+0
HETATM    3  C   UNK     0      18.263  -4.723   0.000  0.00  0.00           C+0
HETATM    4  O   UNK     0      18.263  -3.183   0.000  0.00  0.00           O+0
HETATM    5  C   UNK     0      19.597  -5.493   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0      19.597  -7.033   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0      20.931  -4.723   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0      22.264  -5.493   0.000  0.00  0.00           C+0
HETATM    9  O   UNK     0      22.264  -7.033   0.000  0.00  0.00           O+0
HETATM   10  C   UNK     0      23.598  -4.723   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0      24.932  -5.493   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0      24.932  -7.033   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0      26.265  -4.723   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0      26.426  -3.191   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0      27.933  -2.871   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0      28.703  -4.205   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0      29.608  -2.959   0.000  0.00  0.00           C+0
HETATM   18  C   UNK     0      30.209  -4.525   0.000  0.00  0.00           C+0
HETATM   19  C   UNK     0      31.239  -3.381   0.000  0.00  0.00           C+0
HETATM   20  C   UNK     0      32.746  -3.701   0.000  0.00  0.00           C+0
HETATM   21  C   UNK     0      33.222  -5.166   0.000  0.00  0.00           C+0
HETATM   22  C   UNK     0      34.728  -5.486   0.000  0.00  0.00           C+0
HETATM   23  C   UNK     0      34.782  -3.947   0.000  0.00  0.00           C+0
HETATM   24  C   UNK     0      36.253  -5.271   0.000  0.00  0.00           C+0
HETATM   25  C   UNK     0      35.204  -6.950   0.000  0.00  0.00           C+0
HETATM   26  O   UNK     0      36.710  -7.271   0.000  0.00  0.00           O+0
HETATM   27  C   UNK     0      37.186  -8.735   0.000  0.00  0.00           C+0
HETATM   28  C   UNK     0      38.693  -9.055   0.000  0.00  0.00           C+0
HETATM   29  O   UNK     0      36.156  -9.880   0.000  0.00  0.00           O+0
HETATM   30  C   UNK     0      34.174  -8.095   0.000  0.00  0.00           C+0
HETATM   31  C   UNK     0      32.667  -7.775   0.000  0.00  0.00           C+0
HETATM   32  C   UNK     0      32.191  -6.310   0.000  0.00  0.00           C+0
HETATM   33  C   UNK     0      31.161  -7.454   0.000  0.00  0.00           C+0
HETATM   34  C   UNK     0      30.685  -5.990   0.000  0.00  0.00           C+0
HETATM   35  C   UNK     0      29.654  -7.134   0.000  0.00  0.00           C+0
HETATM   36  C   UNK     0      28.148  -6.814   0.000  0.00  0.00           C+0
HETATM   37  C   UNK     0      27.672  -5.349   0.000  0.00  0.00           C+0
HETATM   38  C   UNK     0      26.528  -6.380   0.000  0.00  0.00           C+0
CONECT    1    2                                                            
CONECT    2    1    3                                                       
CONECT    3    2    4    5                                                  
CONECT    4    3                                                            
CONECT    5    3    6    7                                                  
CONECT    6    5                                                            
CONECT    7    5    8                                                       
CONECT    8    7    9   10                                                  
CONECT    9    8                                                            
CONECT   10    8   11                                                       
CONECT   11   10   12   13                                                  
CONECT   12   11                                                            
CONECT   13   11   14   37                                                  
CONECT   14   13   15                                                       
CONECT   15   14   16                                                       
CONECT   16   15   17   18   37                                             
CONECT   17   16                                                            
CONECT   18   16   19   34                                                  
CONECT   19   18   20                                                       
CONECT   20   19   21                                                       
CONECT   21   20   22   32                                                  
CONECT   22   21   23   24   25                                             
CONECT   23   22                                                            
CONECT   24   22                                                            
CONECT   25   22   26   30                                                  
CONECT   26   25   27                                                       
CONECT   27   26   28   29                                                  
CONECT   28   27                                                            
CONECT   29   27                                                            
CONECT   30   25   31                                                       
CONECT   31   30   32                                                       
CONECT   32   31   21   33   34                                             
CONECT   33   32                                                            
CONECT   34   32   18   35                                                  
CONECT   35   34   36                                                       
CONECT   36   35   37                                                       
CONECT   37   36   13   16   38                                             
CONECT   38   37                                                            
MASTER        0    0    0    0    0    0    0    0   38    0   82    0
END

View in JSmol

Synonyms

Value	Source
Methyl (2R,6R)-6-[(1S,2R,5R,7R,11R,14R,15R)-5-(acetyloxy)-2,6,6,11,15-pentamethyltetracyclo[8.7.0.0,.0,]heptadec-9-en-14-yl]-2-methyl-4-oxoheptanoic acid	Generator

Chemical Formula

C₃₃H₅₂O₅

Average Mass

528.7740 Da

Monoisotopic Mass

528.38147 Da

IUPAC Name

methyl (2R,6R)-6-[(1S,2R,5R,7R,11R,14R,15R)-5-(acetyloxy)-2,6,6,11,15-pentamethyltetracyclo[8.7.0.0^{2,7}.0^{11,15}]heptadec-9-en-14-yl]-2-methyl-4-oxoheptanoate

Traditional Name

methyl (2R,6R)-6-[(1S,2R,5R,7R,11R,14R,15R)-5-(acetyloxy)-2,6,6,11,15-pentamethyltetracyclo[8.7.0.0^{2,7}.0^{11,15}]heptadec-9-en-14-yl]-2-methyl-4-oxoheptanoate

CAS Registry Number

Not Available

SMILES

COC(=O)[C@H](C)CC(=O)C[C@@H](C)[C@H]1CC[C@@]2(C)C3=CC[C@H]4C(C)(C)[C@@H](CC[C@]4(C)[C@@H]3CC[C@]12C)OC(C)=O

InChI Identifier

InChI=1S/C33H52O5/c1-20(18-23(35)19-21(2)29(36)37-9)24-12-16-33(8)26-10-11-27-30(4,5)28(38-22(3)34)14-15-31(27,6)25(26)13-17-32(24,33)7/h10,20-21,24-25,27-28H,11-19H2,1-9H3/t20-,21-,24-,25-,27+,28-,31-,32-,33+/m1/s1

InChI Key

KSABNVUMGNYNHH-YLHGYTFTSA-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
Abies pinsapo	LOTUS Database	35616633

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as triterpenoids. These are terpene molecules containing six isoprene units.

Kingdom

Organic compounds

Super Class

Lipids and lipid-like molecules

Class

Prenol lipids

Sub Class

Triterpenoids

Direct Parent

Triterpenoids

Alternative Parents

Substituents

Triterpenoid
23-oxosteroid
Bile acid, alcohol, or derivatives
Steroid ester
14-alpha-methylsteroid
Oxosteroid
Delta-7-steroid
Steroid
Gamma-keto acid
Keto acid
Dicarboxylic acid or derivatives
Methyl ester
Ketone
Carboxylic acid ester
Carboxylic acid derivative
Hydrocarbon derivative
Organic oxide
Organooxygen compound
Carbonyl group
Organic oxygen 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	6.5	ChemAxon
pKa (Strongest Acidic)	17.84	ChemAxon
pKa (Strongest Basic)	-6.6	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	3	ChemAxon
Hydrogen Donor Count	0	ChemAxon
Polar Surface Area	69.67 Å²	ChemAxon
Rotatable Bond Count	9	ChemAxon
Refractivity	150.21 m³·mol⁻¹	ChemAxon
Polarizability	62.77 Å³	ChemAxon
Number of Rings	4	ChemAxon
Bioavailability	No	ChemAxon
Rule of Five	No	ChemAxon
Ghose Filter	No	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

163008866

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

LOTUS database [Link]

Showing NP-Card for methyl (2r,6r)-6-[(1r,3ar,5ar,7r,9ar,9bs,11ar)-7-(acetyloxy)-3a,6,6,9a,11a-pentamethyl-1h,2h,3h,5h,5ah,7h,8h,9h,9bh,10h,11h-cyclopenta[a]phenanthren-1-yl]-2-methyl-4-oxoheptanoate (NP0301443)

MOL for NP0301443 (methyl (2r,6r)-6-[(1r,3ar,5ar,7r,9ar,9bs,11ar)-7-(acetyloxy)-3a,6,6,9a,11a-pentamethyl-1h,2h,3h,5h,5ah,7h,8h,9h,9bh,10h,11h-cyclopenta[a]phenanthren-1-yl]-2-methyl-4-oxoheptanoate)

3D MOL for NP0301443 (methyl (2r,6r)-6-[(1r,3ar,5ar,7r,9ar,9bs,11ar)-7-(acetyloxy)-3a,6,6,9a,11a-pentamethyl-1h,2h,3h,5h,5ah,7h,8h,9h,9bh,10h,11h-cyclopenta[a]phenanthren-1-yl]-2-methyl-4-oxoheptanoate)

3D SDF for NP0301443 (methyl (2r,6r)-6-[(1r,3ar,5ar,7r,9ar,9bs,11ar)-7-(acetyloxy)-3a,6,6,9a,11a-pentamethyl-1h,2h,3h,5h,5ah,7h,8h,9h,9bh,10h,11h-cyclopenta[a]phenanthren-1-yl]-2-methyl-4-oxoheptanoate)

3D-SDF for NP0301443 (methyl (2r,6r)-6-[(1r,3ar,5ar,7r,9ar,9bs,11ar)-7-(acetyloxy)-3a,6,6,9a,11a-pentamethyl-1h,2h,3h,5h,5ah,7h,8h,9h,9bh,10h,11h-cyclopenta[a]phenanthren-1-yl]-2-methyl-4-oxoheptanoate)

PDB for NP0301443 (methyl (2r,6r)-6-[(1r,3ar,5ar,7r,9ar,9bs,11ar)-7-(acetyloxy)-3a,6,6,9a,11a-pentamethyl-1h,2h,3h,5h,5ah,7h,8h,9h,9bh,10h,11h-cyclopenta[a]phenanthren-1-yl]-2-methyl-4-oxoheptanoate)

3D PDB for NP0301443 (methyl (2r,6r)-6-[(1r,3ar,5ar,7r,9ar,9bs,11ar)-7-(acetyloxy)-3a,6,6,9a,11a-pentamethyl-1h,2h,3h,5h,5ah,7h,8h,9h,9bh,10h,11h-cyclopenta[a]phenanthren-1-yl]-2-methyl-4-oxoheptanoate)

SMILES for NP0301443 (methyl (2r,6r)-6-[(1r,3ar,5ar,7r,9ar,9bs,11ar)-7-(acetyloxy)-3a,6,6,9a,11a-pentamethyl-1h,2h,3h,5h,5ah,7h,8h,9h,9bh,10h,11h-cyclopenta[a]phenanthren-1-yl]-2-methyl-4-oxoheptanoate)

INCHI for NP0301443 (methyl (2r,6r)-6-[(1r,3ar,5ar,7r,9ar,9bs,11ar)-7-(acetyloxy)-3a,6,6,9a,11a-pentamethyl-1h,2h,3h,5h,5ah,7h,8h,9h,9bh,10h,11h-cyclopenta[a]phenanthren-1-yl]-2-methyl-4-oxoheptanoate)

Structure for NP0301443 (methyl (2r,6r)-6-[(1r,3ar,5ar,7r,9ar,9bs,11ar)-7-(acetyloxy)-3a,6,6,9a,11a-pentamethyl-1h,2h,3h,5h,5ah,7h,8h,9h,9bh,10h,11h-cyclopenta[a]phenanthren-1-yl]-2-methyl-4-oxoheptanoate)

3D Structure for NP0301443 (methyl (2r,6r)-6-[(1r,3ar,5ar,7r,9ar,9bs,11ar)-7-(acetyloxy)-3a,6,6,9a,11a-pentamethyl-1h,2h,3h,5h,5ah,7h,8h,9h,9bh,10h,11h-cyclopenta[a]phenanthren-1-yl]-2-methyl-4-oxoheptanoate)