NP-MRD: Showing NP-Card for 2-[(1r,2s,5r)-2-[(2s,6s,8as)-6-hydroxy-8a-methyl-1-oxo-2,3,5,6,7,8-hexahydronaphthalen-2-yl]-5-[(2r,5r)-5,6-dimethylhept-3-en-2-yl]-1-methylcyclopentyl]ethyl acetate (NP0201562)

Jump To Section:

Identification Spectra BioTaxonomy ChemoTaxonomy Physical properties Links References XML

Record Information

Version

2.0

Created at

2022-09-04 20:38:10 UTC

Updated at

2022-09-04 20:38:10 UTC

NP-MRD ID

NP0201562

Secondary Accession Numbers

None

Natural Product Identification

Common Name

2-[(1r,2s,5r)-2-[(2s,6s,8as)-6-hydroxy-8a-methyl-1-oxo-2,3,5,6,7,8-hexahydronaphthalen-2-yl]-5-[(2r,5r)-5,6-dimethylhept-3-en-2-yl]-1-methylcyclopentyl]ethyl acetate

Description

2-[(1R,2S,5R)-2-[(2S,6S,8aS)-6-hydroxy-8a-methyl-1-oxo-1,2,3,5,6,7,8,8a-octahydronaphthalen-2-yl]-5-[(2R,5R)-5,6-dimethylhept-3-en-2-yl]-1-methylcyclopentyl]ethyl acetate belongs to the class of organic compounds known as ergostane steroids. These are steroids with a structure based on the ergostane skeleton, which arises from the methylation of cholestane at the 24-position. 2-[(1r,2s,5r)-2-[(2s,6s,8as)-6-hydroxy-8a-methyl-1-oxo-2,3,5,6,7,8-hexahydronaphthalen-2-yl]-5-[(2r,5r)-5,6-dimethylhept-3-en-2-yl]-1-methylcyclopentyl]ethyl acetate is found in Sinularia leptoclados. Based on a literature review very few articles have been published on 2-[(1R,2S,5R)-2-[(2S,6S,8aS)-6-hydroxy-8a-methyl-1-oxo-1,2,3,5,6,7,8,8a-octahydronaphthalen-2-yl]-5-[(2R,5R)-5,6-dimethylhept-3-en-2-yl]-1-methylcyclopentyl]ethyl acetate.

Structure

MOL 3D MOL SDF PDB SMILES InChI


  Mrv1652309042222382D          

 34 36  0  0  1  0            999 V2000
   -0.5473   -3.1850    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.1671   -3.5975    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.1671   -4.4225    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.8816   -3.1850    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.5961   -3.5975    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.3106   -3.1850    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.0250   -3.5975    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    2.5401   -4.2649    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.3606   -2.8438    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    2.9481   -2.1293    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    2.1231   -2.1293    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.7106   -1.4148    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1231   -0.7004    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.7106    0.0141    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1231    0.7286    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    1.7106    1.4430    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.9481    0.7286    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.3606    0.0141    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.9481   -0.7004    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    3.7731   -0.7004    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.3606   -1.4148    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.1856   -1.4148    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.1811   -2.9300    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.3526   -3.7370    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.6381   -4.1495    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    3.5519   -4.9700    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    2.7982   -5.3055    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.2193   -5.4549    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.1331   -6.2754    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.8005   -6.7603    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    5.5542   -6.4247    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.7143   -7.5808    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.3817   -8.0657    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.9606   -7.9163    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0  0  0  0
  2  3  2  0  0  0  0
  2  4  1  0  0  0  0
  4  5  1  0  0  0  0
  5  6  1  0  0  0  0
  7  6  1  1  0  0  0
  7  8  1  6  0  0  0
  7  9  1  0  0  0  0
  9 10  1  6  0  0  0
 10 11  1  6  0  0  0
 11 12  1  0  0  0  0
 12 13  2  0  0  0  0
 13 14  1  0  0  0  0
 14 15  1  0  0  0  0
 15 16  1  1  0  0  0
 15 17  1  0  0  0  0
 17 18  1  0  0  0  0
 18 19  1  0  0  0  0
 13 19  1  0  0  0  0
 19 20  1  1  0  0  0
 19 21  1  0  0  0  0
 10 21  1  0  0  0  0
 21 22  2  0  0  0  0
  9 23  1  0  0  0  0
 23 24  1  0  0  0  0
 24 25  1  0  0  0  0
  7 25  1  0  0  0  0
 25 26  1  6  0  0  0
 26 27  1  1  0  0  0
 26 28  1  0  0  0  0
 28 29  2  3  0  0  0
 29 30  1  0  0  0  0
 30 31  1  6  0  0  0
 30 32  1  0  0  0  0
 32 33  1  0  0  0  0
 32 34  1  0  0  0  0
M  END

     RDKit          3D

 82 84  0  0  0  0  0  0  0  0999 V2000
    2.0322    5.8494    2.3956 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.0423    5.0933    1.5880 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0784    5.5922    1.3680 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.3368    3.8281    1.0647 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.3475    3.1281    0.2860 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.8955    1.8205   -0.1519 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0027    0.9548   -0.9818 C   0  0  1  0  0  0  0  0  0  0  0  0
   -0.1775    1.4328   -2.3719 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7414   -0.3948   -1.0492 C   0  0  2  0  0  0  0  0  0  0  0  0
    1.6557   -0.5688   -2.1830 C   0  0  2  0  0  0  0  0  0  0  0  0
    1.9619   -2.1009   -2.2340 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.4962   -2.5224   -0.9260 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.4536   -1.8202   -0.3471 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.0116   -2.2134    0.9651 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.3057   -1.5681    1.3133 C   0  0  1  0  0  0  0  0  0  0  0  0
    6.3896   -2.2990    0.7954 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.4489   -0.1330    0.9535 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.4318    0.4057    0.0011 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.9970   -0.6205   -1.0072 C   0  0  1  0  0  0  0  0  0  0  0  0
    5.2556   -1.0689   -1.7608 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.0416    0.0053   -1.9701 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.4191    0.9855   -2.5739 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4751   -1.3169   -1.2345 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2537   -0.8825   -0.0225 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2337    0.6591   -0.1879 C   0  0  2  0  0  0  0  0  0  0  0  0
   -2.5504    0.9924   -0.8262 C   0  0  2  0  0  0  0  0  0  0  0  0
   -2.8130    2.4861   -0.6764 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.6720    0.4226    0.0691 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.5227   -0.4603   -0.3862 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.6043   -1.0271    0.4331 C   0  0  2  0  0  0  0  0  0  0  0  0
   -5.6067   -0.4712    1.8210 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.5664   -2.5390    0.4278 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.7776   -3.0869    1.1494 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.3250   -3.1092    1.0300 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.3787    6.7044    1.7490 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.9404    5.2501    2.6042 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.5964    6.3005    3.2969 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.1014    3.8295   -0.5334 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5189    3.0563    0.9633 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.8779    2.0437   -0.6599 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.2228    1.2822    0.7882 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.8426    1.8120   -2.7032 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8583    2.2272   -2.5941 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4637    0.5892   -3.0638 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.2191   -0.6563   -0.1000 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.3450   -0.2987   -3.1755 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.7944   -2.1766   -2.9768 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.1199   -2.6752   -2.5837 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.1354   -3.4117   -0.3882 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.1785   -3.3241    0.9760 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.2784   -2.0094    1.7813 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.4175   -1.6339    2.4389 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.1606   -1.6810    0.6545 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.4088    0.5294    1.8591 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.4698    0.0455    0.5368 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.5689    0.8626    0.5312 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.9110    1.2437   -0.5670 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.3805   -2.1667   -1.7494 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.1937   -0.7003   -2.8264 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.1732   -0.6156   -1.3586 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0254   -1.1125   -2.1536 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1993   -2.3871   -1.1110 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6449   -1.1479    0.8819 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2602   -1.2827    0.0319 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2161    1.0511    0.8491 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7425    0.6152   -1.8071 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1154    3.1652   -1.0906 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.8822    2.6825   -0.9550 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8156    2.6418    0.4492 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.6840    0.8085    1.0707 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.4456   -0.8107   -1.4267 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.5695   -0.7473   -0.0685 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.5769   -0.7095    2.3491 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.5862    0.6380    1.7632 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.7916   -0.8229    2.4604 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.6094   -2.8995   -0.6395 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.7558   -4.2035    1.1910 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.8395   -2.7183    2.1853 H   0  0  0  0  0  0  0  0  0  0  0  0
   -7.7101   -2.7944    0.6070 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.6007   -3.9685    1.6769 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.6485   -3.5443    0.2528 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.7597   -2.3329    1.5828 H   0  0  0  0  0  0  0  0  0  0  0  0
 33 32  1  0
 32 34  1  0
 32 30  1  0
 30 31  1  0
 30 29  1  0
 29 28  2  0
 28 26  1  0
 26 27  1  0
 26 25  1  0
 25 24  1  0
 24 23  1  0
 23  9  1  0
  9 10  1  0
 10 11  1  0
 11 12  1  0
 12 13  2  0
 13 14  1  0
 14 15  1  0
 15 16  1  0
 15 17  1  0
 17 18  1  0
 18 19  1  0
 19 20  1  6
 19 21  1  0
 21 22  2  0
  9  7  1  0
  7  8  1  6
  7  6  1  0
  6  5  1  0
  5  4  1  0
  4  2  1  0
  2  1  1  0
  2  3  2  0
  7 25  1  0
 21 10  1  0
 19 13  1  0
 33 77  1  0
 33 78  1  0
 33 79  1  0
 32 76  1  0
 34 80  1  0
 34 81  1  0
 34 82  1  0
 30 72  1  6
 31 73  1  0
 31 74  1  0
 31 75  1  0
 29 71  1  0
 28 70  1  0
 26 66  1  6
 27 67  1  0
 27 68  1  0
 27 69  1  0
 25 65  1  1
 24 63  1  0
 24 64  1  0
 23 61  1  0
 23 62  1  0
  9 45  1  1
 10 46  1  6
 11 47  1  0
 11 48  1  0
 12 49  1  0
 14 50  1  0
 14 51  1  0
 15 52  1  1
 16 53  1  0
 17 54  1  0
 17 55  1  0
 18 56  1  0
 18 57  1  0
 20 58  1  0
 20 59  1  0
 20 60  1  0
  8 42  1  0
  8 43  1  0
  8 44  1  0
  6 40  1  0
  6 41  1  0
  5 38  1  0
  5 39  1  0
  1 35  1  0
  1 36  1  0
  1 37  1  0
M  END


  Mrv1652309042222382D          

 34 36  0  0  1  0            999 V2000
   -0.5473   -3.1850    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.1671   -3.5975    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.1671   -4.4225    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.8816   -3.1850    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.5961   -3.5975    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.3106   -3.1850    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.0250   -3.5975    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    2.5401   -4.2649    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.3606   -2.8438    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    2.9481   -2.1293    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    2.1231   -2.1293    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.7106   -1.4148    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1231   -0.7004    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.7106    0.0141    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1231    0.7286    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    1.7106    1.4430    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.9481    0.7286    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.3606    0.0141    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.9481   -0.7004    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    3.7731   -0.7004    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.3606   -1.4148    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.1856   -1.4148    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.1811   -2.9300    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.3526   -3.7370    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.6381   -4.1495    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    3.5519   -4.9700    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    2.7982   -5.3055    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.2193   -5.4549    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.1331   -6.2754    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.8005   -6.7603    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    5.5542   -6.4247    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.7143   -7.5808    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.3817   -8.0657    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.9606   -7.9163    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0  0  0  0
  2  3  2  0  0  0  0
  2  4  1  0  0  0  0
  4  5  1  0  0  0  0
  5  6  1  0  0  0  0
  7  6  1  1  0  0  0
  7  8  1  6  0  0  0
  7  9  1  0  0  0  0
  9 10  1  6  0  0  0
 10 11  1  6  0  0  0
 11 12  1  0  0  0  0
 12 13  2  0  0  0  0
 13 14  1  0  0  0  0
 14 15  1  0  0  0  0
 15 16  1  1  0  0  0
 15 17  1  0  0  0  0
 17 18  1  0  0  0  0
 18 19  1  0  0  0  0
 13 19  1  0  0  0  0
 19 20  1  1  0  0  0
 19 21  1  0  0  0  0
 10 21  1  0  0  0  0
 21 22  2  0  0  0  0
  9 23  1  0  0  0  0
 23 24  1  0  0  0  0
 24 25  1  0  0  0  0
  7 25  1  0  0  0  0
 25 26  1  6  0  0  0
 26 27  1  1  0  0  0
 26 28  1  0  0  0  0
 28 29  2  3  0  0  0
 29 30  1  0  0  0  0
 30 31  1  6  0  0  0
 30 32  1  0  0  0  0
 32 33  1  0  0  0  0
 32 34  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0201562

> <DATABASE_NAME>
NP-MRD

> <SMILES>
CC(C)[C@@H](C)C=C[C@@H](C)[C@H]1CC[C@@H]([C@@H]2CC=C3C[C@@H](O)CC[C@]3(C)C2=O)[C@]1(C)CCOC(C)=O

> <INCHI_IDENTIFIER>
InChI=1S/C30H48O4/c1-19(2)20(3)8-9-21(4)26-12-13-27(30(26,7)16-17-34-22(5)31)25-11-10-23-18-24(32)14-15-29(23,6)28(25)33/h8-10,19-21,24-27,32H,11-18H2,1-7H3/t20-,21+,24-,25-,26+,27-,29-,30+/m0/s1

> <INCHI_KEY>
AXJAPIKLGIZTPC-FPGITTBRSA-N

> <FORMULA>
C30H48O4

> <MOLECULAR_WEIGHT>
472.71

> <EXACT_MASS>
472.355260026

> <JCHEM_ACCEPTOR_COUNT>
3

> <JCHEM_ATOM_COUNT>
82

> <JCHEM_AVERAGE_POLARIZABILITY>
55.76965125797387

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
1

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
0

> <JCHEM_IUPAC>
2-[(1R,2S,5R)-2-[(2S,6S,8aS)-6-hydroxy-8a-methyl-1-oxo-1,2,3,5,6,7,8,8a-octahydronaphthalen-2-yl]-5-[(2R,5R)-5,6-dimethylhept-3-en-2-yl]-1-methylcyclopentyl]ethyl acetate

> <JCHEM_LOGP>
6.252392555999998

> <JCHEM_MDDR_LIKE_RULE>
1

> <JCHEM_NUMBER_OF_RINGS>
3

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA_STRONGEST_ACIDIC>
18.270272808087725

> <JCHEM_PKA_STRONGEST_BASIC>
-1.368381406276487

> <JCHEM_POLAR_SURFACE_AREA>
63.6

> <JCHEM_REFRACTIVITY>
139.9356

> <JCHEM_ROTATABLE_BOND_COUNT>
9

> <JCHEM_RULE_OF_FIVE>
0

> <JCHEM_TRADITIONAL_IUPAC>
2-[(1R,2S,5R)-2-[(2S,6S,8aS)-6-hydroxy-8a-methyl-1-oxo-2,3,5,6,7,8-hexahydronaphthalen-2-yl]-5-[(2R,5R)-5,6-dimethylhept-3-en-2-yl]-1-methylcyclopentyl]ethyl acetate

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 04-SEP-22   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   04-SEP-22         0                                  
HETATM    1  C   UNK     0      -1.022  -5.945   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0       0.312  -6.715   0.000  0.00  0.00           C+0
HETATM    3  O   UNK     0       0.312  -8.255   0.000  0.00  0.00           O+0
HETATM    4  O   UNK     0       1.646  -5.945   0.000  0.00  0.00           O+0
HETATM    5  C   UNK     0       2.979  -6.715   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0       4.313  -5.945   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0       5.647  -6.715   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0       4.742  -7.961   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0       6.273  -5.308   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0       5.503  -3.975   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0       3.963  -3.975   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0       3.193  -2.641   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0       3.963  -1.307   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0       3.193   0.026   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0       3.963   1.360   0.000  0.00  0.00           C+0
HETATM   16  O   UNK     0       3.193   2.694   0.000  0.00  0.00           O+0
HETATM   17  C   UNK     0       5.503   1.360   0.000  0.00  0.00           C+0
HETATM   18  C   UNK     0       6.273   0.026   0.000  0.00  0.00           C+0
HETATM   19  C   UNK     0       5.503  -1.307   0.000  0.00  0.00           C+0
HETATM   20  C   UNK     0       7.043  -1.307   0.000  0.00  0.00           C+0
HETATM   21  C   UNK     0       6.273  -2.641   0.000  0.00  0.00           C+0
HETATM   22  O   UNK     0       7.813  -2.641   0.000  0.00  0.00           O+0
HETATM   23  C   UNK     0       7.805  -5.469   0.000  0.00  0.00           C+0
HETATM   24  C   UNK     0       8.125  -6.976   0.000  0.00  0.00           C+0
HETATM   25  C   UNK     0       6.791  -7.746   0.000  0.00  0.00           C+0
HETATM   26  C   UNK     0       6.630  -9.277   0.000  0.00  0.00           C+0
HETATM   27  C   UNK     0       5.223  -9.904   0.000  0.00  0.00           C+0
HETATM   28  C   UNK     0       7.876 -10.182   0.000  0.00  0.00           C+0
HETATM   29  C   UNK     0       7.715 -11.714   0.000  0.00  0.00           C+0
HETATM   30  C   UNK     0       8.961 -12.619   0.000  0.00  0.00           C+0
HETATM   31  C   UNK     0      10.368 -11.993   0.000  0.00  0.00           C+0
HETATM   32  C   UNK     0       8.800 -14.151   0.000  0.00  0.00           C+0
HETATM   33  C   UNK     0      10.046 -15.056   0.000  0.00  0.00           C+0
HETATM   34  C   UNK     0       7.393 -14.777   0.000  0.00  0.00           C+0
CONECT    1    2                                                            
CONECT    2    1    3    4                                                  
CONECT    3    2                                                            
CONECT    4    2    5                                                       
CONECT    5    4    6                                                       
CONECT    6    5    7                                                       
CONECT    7    6    8    9   25                                             
CONECT    8    7                                                            
CONECT    9    7   10   23                                                  
CONECT   10    9   11   21                                                  
CONECT   11   10   12                                                       
CONECT   12   11   13                                                       
CONECT   13   12   14   19                                                  
CONECT   14   13   15                                                       
CONECT   15   14   16   17                                                  
CONECT   16   15                                                            
CONECT   17   15   18                                                       
CONECT   18   17   19                                                       
CONECT   19   18   13   20   21                                             
CONECT   20   19                                                            
CONECT   21   19   10   22                                                  
CONECT   22   21                                                            
CONECT   23    9   24                                                       
CONECT   24   23   25                                                       
CONECT   25   24    7   26                                                  
CONECT   26   25   27   28                                                  
CONECT   27   26                                                            
CONECT   28   26   29                                                       
CONECT   29   28   30                                                       
CONECT   30   29   31   32                                                  
CONECT   31   30                                                            
CONECT   32   30   33   34                                                  
CONECT   33   32                                                            
CONECT   34   32                                                            
MASTER        0    0    0    0    0    0    0    0   34    0   72    0
END

View in JSmol

Synonyms

Value	Source
2-[(1R,2S,5R)-2-[(2S,6S,8AS)-6-hydroxy-8a-methyl-1-oxo-1,2,3,5,6,7,8,8a-octahydronaphthalen-2-yl]-5-[(2R,5R)-5,6-dimethylhept-3-en-2-yl]-1-methylcyclopentyl]ethyl acetic acid	Generator

Chemical Formula

C₃₀H₄₈O₄

Average Mass

472.7100 Da

Monoisotopic Mass

472.35526 Da

IUPAC Name

2-[(1R,2S,5R)-2-[(2S,6S,8aS)-6-hydroxy-8a-methyl-1-oxo-1,2,3,5,6,7,8,8a-octahydronaphthalen-2-yl]-5-[(2R,5R)-5,6-dimethylhept-3-en-2-yl]-1-methylcyclopentyl]ethyl acetate

Traditional Name

2-[(1R,2S,5R)-2-[(2S,6S,8aS)-6-hydroxy-8a-methyl-1-oxo-2,3,5,6,7,8-hexahydronaphthalen-2-yl]-5-[(2R,5R)-5,6-dimethylhept-3-en-2-yl]-1-methylcyclopentyl]ethyl acetate

CAS Registry Number

Not Available

SMILES

CC(C)[C@@H](C)C=C[C@@H](C)[C@H]1CC[C@@H]([C@@H]2CC=C3C[C@@H](O)CC[C@]3(C)C2=O)[C@]1(C)CCOC(C)=O

InChI Identifier

InChI=1S/C30H48O4/c1-19(2)20(3)8-9-21(4)26-12-13-27(30(26,7)16-17-34-22(5)31)25-11-10-23-18-24(32)14-15-29(23,6)28(25)33/h8-10,19-21,24-27,32H,11-18H2,1-7H3/t20-,21+,24-,25-,26+,27-,29-,30+/m0/s1

InChI Key

AXJAPIKLGIZTPC-FPGITTBRSA-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
Sinularia leptoclados	LOTUS Database	35616633

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as ergostane steroids. These are steroids with a structure based on the ergostane skeleton, which arises from the methylation of cholestane at the 24-position.

Kingdom

Organic compounds

Super Class

Lipids and lipid-like molecules

Class

Steroids and steroid derivatives

Sub Class

Ergostane steroids

Direct Parent

Ergostane steroids

Alternative Parents

Substituents

Ergostane-skeleton
Cyclohexenone
Cyclic alcohol
Secondary alcohol
Ketone
Carboxylic acid ester
Monocarboxylic acid or derivatives
Carboxylic acid derivative
Organic oxygen compound
Organic oxide
Hydrocarbon derivative
Organooxygen compound
Carbonyl group
Alcohol
Aliphatic homopolycyclic compound

Molecular Framework

Aliphatic homopolycyclic compounds

External Descriptors

Not Available

Physical Properties

State

Not Available

Experimental Properties

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

Predicted Properties

Property	Value	Source
logP	6.25	ChemAxon
pKa (Strongest Acidic)	18.27	ChemAxon
pKa (Strongest Basic)	-1.4	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	3	ChemAxon
Hydrogen Donor Count	1	ChemAxon
Polar Surface Area	63.6 Å²	ChemAxon
Rotatable Bond Count	9	ChemAxon
Refractivity	139.94 m³·mol⁻¹	ChemAxon
Polarizability	55.77 Å³	ChemAxon
Number of Rings	3	ChemAxon
Bioavailability	Yes	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

162918764

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

LOTUS database [Link]

Showing NP-Card for 2-[(1r,2s,5r)-2-[(2s,6s,8as)-6-hydroxy-8a-methyl-1-oxo-2,3,5,6,7,8-hexahydronaphthalen-2-yl]-5-[(2r,5r)-5,6-dimethylhept-3-en-2-yl]-1-methylcyclopentyl]ethyl acetate (NP0201562)

MOL for NP0201562 (2-[(1r,2s,5r)-2-[(2s,6s,8as)-6-hydroxy-8a-methyl-1-oxo-2,3,5,6,7,8-hexahydronaphthalen-2-yl]-5-[(2r,5r)-5,6-dimethylhept-3-en-2-yl]-1-methylcyclopentyl]ethyl acetate)

3D MOL for NP0201562 (2-[(1r,2s,5r)-2-[(2s,6s,8as)-6-hydroxy-8a-methyl-1-oxo-2,3,5,6,7,8-hexahydronaphthalen-2-yl]-5-[(2r,5r)-5,6-dimethylhept-3-en-2-yl]-1-methylcyclopentyl]ethyl acetate)

3D SDF for NP0201562 (2-[(1r,2s,5r)-2-[(2s,6s,8as)-6-hydroxy-8a-methyl-1-oxo-2,3,5,6,7,8-hexahydronaphthalen-2-yl]-5-[(2r,5r)-5,6-dimethylhept-3-en-2-yl]-1-methylcyclopentyl]ethyl acetate)

3D-SDF for NP0201562 (2-[(1r,2s,5r)-2-[(2s,6s,8as)-6-hydroxy-8a-methyl-1-oxo-2,3,5,6,7,8-hexahydronaphthalen-2-yl]-5-[(2r,5r)-5,6-dimethylhept-3-en-2-yl]-1-methylcyclopentyl]ethyl acetate)

PDB for NP0201562 (2-[(1r,2s,5r)-2-[(2s,6s,8as)-6-hydroxy-8a-methyl-1-oxo-2,3,5,6,7,8-hexahydronaphthalen-2-yl]-5-[(2r,5r)-5,6-dimethylhept-3-en-2-yl]-1-methylcyclopentyl]ethyl acetate)

3D PDB for NP0201562 (2-[(1r,2s,5r)-2-[(2s,6s,8as)-6-hydroxy-8a-methyl-1-oxo-2,3,5,6,7,8-hexahydronaphthalen-2-yl]-5-[(2r,5r)-5,6-dimethylhept-3-en-2-yl]-1-methylcyclopentyl]ethyl acetate)

SMILES for NP0201562 (2-[(1r,2s,5r)-2-[(2s,6s,8as)-6-hydroxy-8a-methyl-1-oxo-2,3,5,6,7,8-hexahydronaphthalen-2-yl]-5-[(2r,5r)-5,6-dimethylhept-3-en-2-yl]-1-methylcyclopentyl]ethyl acetate)

INCHI for NP0201562 (2-[(1r,2s,5r)-2-[(2s,6s,8as)-6-hydroxy-8a-methyl-1-oxo-2,3,5,6,7,8-hexahydronaphthalen-2-yl]-5-[(2r,5r)-5,6-dimethylhept-3-en-2-yl]-1-methylcyclopentyl]ethyl acetate)

Structure for NP0201562 (2-[(1r,2s,5r)-2-[(2s,6s,8as)-6-hydroxy-8a-methyl-1-oxo-2,3,5,6,7,8-hexahydronaphthalen-2-yl]-5-[(2r,5r)-5,6-dimethylhept-3-en-2-yl]-1-methylcyclopentyl]ethyl acetate)

3D Structure for NP0201562 (2-[(1r,2s,5r)-2-[(2s,6s,8as)-6-hydroxy-8a-methyl-1-oxo-2,3,5,6,7,8-hexahydronaphthalen-2-yl]-5-[(2r,5r)-5,6-dimethylhept-3-en-2-yl]-1-methylcyclopentyl]ethyl acetate)