NP-MRD: Showing NP-Card for 5-Acetoxyoxachamigrene (NP0004214)

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Record Information

Version

2.0

Created at

2020-12-09 01:42:14 UTC

Updated at

2021-07-15 16:48:33 UTC

NP-MRD ID

NP0004214

Secondary Accession Numbers

None

Natural Product Identification

Common Name

5-Acetoxyoxachamigrene

Provided By

NPAtlas

Description

5-Acetoxyoxachamigrene is found in Unknown-fungus sp. 5-Acetoxyoxachamigrene was first documented in 2002 (PMID: 12088448). Based on a literature review very few articles have been published on (2R,3'R,4'R,6'R)-3'-bromo-4'-chloro-1,3,3,4'-tetramethyl-7-oxaspiro[bicyclo[2.2.1]Heptane-2,1'-cyclohexane]-6'-yl acetate.

Structure

MOL 3D MOL SDF 3D SDF PDB SMILES InChI


  Mrv1652306242118053D          

 48 50  0  0  0  0            999 V2000
    1.0367    4.0632    1.2369 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.0066    2.5760    1.4904 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.0777    2.1307    2.6513 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.8997    1.7795    0.3953 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.8564    0.3506    0.4978 C   0  0  2  0  0  0  0  0  0  0  0  0
    2.2221   -0.0807    0.0119 C   0  0  1  0  0  0  0  0  0  0  0  0
    2.3573   -1.5364   -0.2570 C   0  0  1  0  0  0  0  0  0  0  0  0
    3.7479   -1.8768   -0.6628 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.8672   -2.4195    1.2171 Cl  0  0  0  0  0  0  0  0  0  0  0  0
    1.3343   -1.8655   -1.3275 C   0  0  2  0  0  0  0  0  0  0  0  0
    1.6676   -1.0993   -3.0087 Br  0  0  0  0  0  0  0  0  0  0  0  0
    0.0029   -1.6430   -0.7115 C   0  0  1  0  0  0  0  0  0  0  0  0
   -0.2995   -0.2807   -0.1520 C   0  0  2  0  0  0  0  0  0  0  0  0
   -0.9863    0.6355   -1.1285 C   0  0  1  0  0  0  0  0  0  0  0  0
   -0.2468    1.7326   -1.7436 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8796   -0.0804   -2.1171 C   0  0  1  0  0  0  0  0  0  0  0  0
   -2.9658   -0.5891   -1.2250 C   0  0  2  0  0  0  0  0  0  0  0  0
   -2.6530    0.0628    0.0724 C   0  0  2  0  0  0  0  0  0  0  0  0
   -2.0139    1.2539   -0.3551 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4459   -0.5343    0.8001 C   0  0  1  0  0  0  0  0  0  0  0  0
   -1.7865   -1.9707    1.0492 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3933    0.1507    2.1155 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4512    4.5619    2.1386 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0017    4.3595    1.0087 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.6651    4.2162    0.3476 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.8664    0.1155    1.5796 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.5830    0.4626   -0.8796 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.9511    0.1846    0.8130 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.3547   -0.9697   -0.7610 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.2662   -2.5374    0.0895 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.6994   -2.3823   -1.6617 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.4199   -2.9917   -1.4453 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7615   -2.0677   -1.3526 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.0375   -2.3263    0.1975 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4185    2.7425   -1.2564 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7012    1.9159   -2.7697 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.8113    1.6604   -1.9215 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2868    0.7447   -2.7746 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4018   -0.7847   -2.7729 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.1132   -1.6665   -1.2164 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.9464   -0.1559   -1.5632 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.4908    0.2536    0.7322 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7951   -1.9288    1.5730 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1406   -2.4523    1.8396 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9703   -2.5940    0.1782 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4607    1.2527    2.0783 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6445   -0.2417    2.8335 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3783   -0.1303    2.6209 H   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
  6  7  1  0  0  0  0
  7  8  1  0  0  0  0
  7  9  1  1  0  0  0
  7 10  1  0  0  0  0
 10 11  1  0  0  0  0
 10 12  1  0  0  0  0
 13 12  1  6  0  0  0
 13 14  1  0  0  0  0
 14 15  1  6  0  0  0
 14 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
 18 20  1  0  0  0  0
 20 21  1  1  0  0  0
 20 22  1  0  0  0  0
 13  5  1  0  0  0  0
 19 14  1  0  0  0  0
 20 13  1  0  0  0  0
  1 23  1  0  0  0  0
  1 24  1  0  0  0  0
  1 25  1  0  0  0  0
  5 26  1  1  0  0  0
  6 27  1  0  0  0  0
  6 28  1  0  0  0  0
  8 29  1  0  0  0  0
  8 30  1  0  0  0  0
  8 31  1  0  0  0  0
 10 32  1  6  0  0  0
 12 33  1  0  0  0  0
 12 34  1  0  0  0  0
 15 35  1  0  0  0  0
 15 36  1  0  0  0  0
 15 37  1  0  0  0  0
 16 38  1  0  0  0  0
 16 39  1  0  0  0  0
 17 40  1  0  0  0  0
 17 41  1  0  0  0  0
 18 42  1  1  0  0  0
 21 43  1  0  0  0  0
 21 44  1  0  0  0  0
 21 45  1  0  0  0  0
 22 46  1  0  0  0  0
 22 47  1  0  0  0  0
 22 48  1  0  0  0  0
M  END

     RDKit          3D

 48 50  0  0  0  0  0  0  0  0999 V2000
    1.0367    4.0632    1.2369 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.0066    2.5760    1.4904 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.0777    2.1307    2.6513 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.8997    1.7795    0.3953 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.8564    0.3506    0.4978 C   0  0  2  0  0  0  0  0  0  0  0  0
    2.2221   -0.0807    0.0119 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.3573   -1.5364   -0.2570 C   0  0  1  0  0  0  0  0  0  0  0  0
    3.7479   -1.8768   -0.6628 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.8672   -2.4195    1.2171 Cl  0  0  0  0  0  0  0  0  0  0  0  0
    1.3343   -1.8655   -1.3275 C   0  0  2  0  0  0  0  0  0  0  0  0
    1.6676   -1.0993   -3.0087 Br  0  0  0  0  0  0  0  0  0  0  0  0
    0.0029   -1.6430   -0.7115 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2995   -0.2807   -0.1520 C   0  0  2  0  0  0  0  0  0  0  0  0
   -0.9863    0.6355   -1.1285 C   0  0  1  0  0  0  0  0  0  0  0  0
   -0.2468    1.7326   -1.7436 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8796   -0.0804   -2.1171 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.9658   -0.5891   -1.2250 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6530    0.0628    0.0724 C   0  0  2  0  0  0  0  0  0  0  0  0
   -2.0139    1.2539   -0.3551 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4459   -0.5343    0.8001 C   0  0  1  0  0  0  0  0  0  0  0  0
   -1.7865   -1.9707    1.0492 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3933    0.1507    2.1155 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4512    4.5619    2.1386 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0017    4.3595    1.0087 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.6651    4.2162    0.3476 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.8664    0.1155    1.5796 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.5830    0.4626   -0.8796 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.9511    0.1846    0.8130 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.3547   -0.9697   -0.7610 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.2662   -2.5374    0.0895 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.6994   -2.3823   -1.6617 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.4199   -2.9917   -1.4453 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7615   -2.0677   -1.3526 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.0375   -2.3263    0.1975 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4185    2.7425   -1.2564 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7012    1.9159   -2.7697 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.8113    1.6604   -1.9215 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2868    0.7447   -2.7746 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4018   -0.7847   -2.7729 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.1132   -1.6665   -1.2164 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.9464   -0.1559   -1.5632 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.4908    0.2536    0.7322 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7951   -1.9288    1.5730 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1406   -2.4523    1.8396 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9703   -2.5940    0.1782 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4607    1.2527    2.0783 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6445   -0.2417    2.8335 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3783   -0.1303    2.6209 H   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0
  2  3  2  0
  2  4  1  0
  4  5  1  0
  5  6  1  0
  6  7  1  0
  7  8  1  0
  7  9  1  1
  7 10  1  0
 10 11  1  0
 10 12  1  0
 13 12  1  6
 13 14  1  0
 14 15  1  6
 14 16  1  0
 16 17  1  0
 17 18  1  0
 18 19  1  0
 18 20  1  0
 20 21  1  1
 20 22  1  0
 13  5  1  0
 19 14  1  0
 20 13  1  0
  1 23  1  0
  1 24  1  0
  1 25  1  0
  5 26  1  1
  6 27  1  0
  6 28  1  0
  8 29  1  0
  8 30  1  0
  8 31  1  0
 10 32  1  6
 12 33  1  0
 12 34  1  0
 15 35  1  0
 15 36  1  0
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 16 38  1  0
 16 39  1  0
 17 40  1  0
 17 41  1  0
 18 42  1  1
 21 43  1  0
 21 44  1  0
 21 45  1  0
 22 46  1  0
 22 47  1  0
 22 48  1  0
M  END


  Mrv1652306242118053D          

 48 50  0  0  0  0            999 V2000
    1.0367    4.0632    1.2369 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.0066    2.5760    1.4904 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.0777    2.1307    2.6513 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.8997    1.7795    0.3953 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.8564    0.3506    0.4978 C   0  0  2  0  0  0  0  0  0  0  0  0
    2.2221   -0.0807    0.0119 C   0  0  1  0  0  0  0  0  0  0  0  0
    2.3573   -1.5364   -0.2570 C   0  0  1  0  0  0  0  0  0  0  0  0
    3.7479   -1.8768   -0.6628 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.8672   -2.4195    1.2171 Cl  0  0  0  0  0  0  0  0  0  0  0  0
    1.3343   -1.8655   -1.3275 C   0  0  2  0  0  0  0  0  0  0  0  0
    1.6676   -1.0993   -3.0087 Br  0  0  0  0  0  0  0  0  0  0  0  0
    0.0029   -1.6430   -0.7115 C   0  0  1  0  0  0  0  0  0  0  0  0
   -0.2995   -0.2807   -0.1520 C   0  0  2  0  0  0  0  0  0  0  0  0
   -0.9863    0.6355   -1.1285 C   0  0  1  0  0  0  0  0  0  0  0  0
   -0.2468    1.7326   -1.7436 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8796   -0.0804   -2.1171 C   0  0  1  0  0  0  0  0  0  0  0  0
   -2.9658   -0.5891   -1.2250 C   0  0  2  0  0  0  0  0  0  0  0  0
   -2.6530    0.0628    0.0724 C   0  0  2  0  0  0  0  0  0  0  0  0
   -2.0139    1.2539   -0.3551 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4459   -0.5343    0.8001 C   0  0  1  0  0  0  0  0  0  0  0  0
   -1.7865   -1.9707    1.0492 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3933    0.1507    2.1155 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4512    4.5619    2.1386 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0017    4.3595    1.0087 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.6651    4.2162    0.3476 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.8664    0.1155    1.5796 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.5830    0.4626   -0.8796 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.9511    0.1846    0.8130 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.3547   -0.9697   -0.7610 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.2662   -2.5374    0.0895 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.6994   -2.3823   -1.6617 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.4199   -2.9917   -1.4453 H   0  0  0  0  0  0  0  0  0  0  0  0
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    0.0375   -2.3263    0.1975 H   0  0  0  0  0  0  0  0  0  0  0  0
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   -0.7012    1.9159   -2.7697 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.8113    1.6604   -1.9215 H   0  0  0  0  0  0  0  0  0  0  0  0
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   -3.9464   -0.1559   -1.5632 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.4908    0.2536    0.7322 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7951   -1.9288    1.5730 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1406   -2.4523    1.8396 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9703   -2.5940    0.1782 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4607    1.2527    2.0783 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6445   -0.2417    2.8335 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3783   -0.1303    2.6209 H   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
  6  7  1  0  0  0  0
  7  8  1  0  0  0  0
  7  9  1  1  0  0  0
  7 10  1  0  0  0  0
 10 11  1  0  0  0  0
 10 12  1  0  0  0  0
 13 12  1  6  0  0  0
 13 14  1  0  0  0  0
 14 15  1  6  0  0  0
 14 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
 18 20  1  0  0  0  0
 20 21  1  1  0  0  0
 20 22  1  0  0  0  0
 13  5  1  0  0  0  0
 19 14  1  0  0  0  0
 20 13  1  0  0  0  0
  1 23  1  0  0  0  0
  1 24  1  0  0  0  0
  1 25  1  0  0  0  0
  5 26  1  1  0  0  0
  6 27  1  0  0  0  0
  6 28  1  0  0  0  0
  8 29  1  0  0  0  0
  8 30  1  0  0  0  0
  8 31  1  0  0  0  0
 10 32  1  6  0  0  0
 12 33  1  0  0  0  0
 12 34  1  0  0  0  0
 15 35  1  0  0  0  0
 15 36  1  0  0  0  0
 15 37  1  0  0  0  0
 16 38  1  0  0  0  0
 16 39  1  0  0  0  0
 17 40  1  0  0  0  0
 17 41  1  0  0  0  0
 18 42  1  1  0  0  0
 21 43  1  0  0  0  0
 21 44  1  0  0  0  0
 21 45  1  0  0  0  0
 22 46  1  0  0  0  0
 22 47  1  0  0  0  0
 22 48  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0004214

> <DATABASE_NAME>
NP-MRD

> <SMILES>
[H]C([H])([H])C(=O)O[C@]1([H])C([H])([H])[C@](Cl)(C([H])([H])[H])[C@]([H])(Br)C([H])([H])[C@]11[C@@]2(O[C@@]([H])(C([H])([H])C2([H])[H])C1(C([H])([H])[H])C([H])([H])[H])C([H])([H])[H]

> <INCHI_IDENTIFIER>
InChI=1S/C17H26BrClO3/c1-10(20)21-13-9-15(4,19)11(18)8-17(13)14(2,3)12-6-7-16(17,5)22-12/h11-13H,6-9H2,1-5H3/t11-,12+,13-,15-,16-,17+/m1/s1

> <INCHI_KEY>
DVONIFXCMJQOGF-OGOWZMLDSA-N

> <FORMULA>
C17H26BrClO3

> <MOLECULAR_WEIGHT>
393.75

> <EXACT_MASS>
392.075385

> <JCHEM_ACCEPTOR_COUNT>
2

> <JCHEM_ATOM_COUNT>
48

> <JCHEM_AVERAGE_POLARIZABILITY>
36.36661822791931

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
0

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
1

> <JCHEM_IUPAC>
(1R,2R,3'R,4S,4'R,6'R)-3'-bromo-4'-chloro-1,3,3,4'-tetramethyl-7-oxaspiro[bicyclo[2.2.1]heptane-2,1'-cyclohexane]-6'-yl acetate

> <ALOGPS_LOGP>
4.87

> <JCHEM_LOGP>
3.5433364679999997

> <ALOGPS_LOGS>
-5.99

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
3

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA_STRONGEST_BASIC>
-4.194092276241602

> <JCHEM_POLAR_SURFACE_AREA>
35.53

> <JCHEM_REFRACTIVITY>
89.19139999999999

> <JCHEM_ROTATABLE_BOND_COUNT>
2

> <JCHEM_RULE_OF_FIVE>
1

> <ALOGPS_SOLUBILITY>
4.02e-04 g/l

> <JCHEM_TRADITIONAL_IUPAC>
(1R,2R,3'R,4S,4'R,6'R)-3'-bromo-4'-chloro-1,3,3,4'-tetramethyl-7-oxaspiro[bicyclo[2.2.1]heptane-2,1'-cyclohexane]-6'-yl acetate

> <JCHEM_VEBER_RULE>
1

$$$$

     RDKit          3D

 48 50  0  0  0  0  0  0  0  0999 V2000
    1.0367    4.0632    1.2369 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.0066    2.5760    1.4904 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.0777    2.1307    2.6513 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.8997    1.7795    0.3953 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.8564    0.3506    0.4978 C   0  0  2  0  0  0  0  0  0  0  0  0
    2.2221   -0.0807    0.0119 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.3573   -1.5364   -0.2570 C   0  0  1  0  0  0  0  0  0  0  0  0
    3.7479   -1.8768   -0.6628 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.8672   -2.4195    1.2171 Cl  0  0  0  0  0  0  0  0  0  0  0  0
    1.3343   -1.8655   -1.3275 C   0  0  2  0  0  0  0  0  0  0  0  0
    1.6676   -1.0993   -3.0087 Br  0  0  0  0  0  0  0  0  0  0  0  0
    0.0029   -1.6430   -0.7115 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2995   -0.2807   -0.1520 C   0  0  2  0  0  0  0  0  0  0  0  0
   -0.9863    0.6355   -1.1285 C   0  0  1  0  0  0  0  0  0  0  0  0
   -0.2468    1.7326   -1.7436 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8796   -0.0804   -2.1171 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.9658   -0.5891   -1.2250 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6530    0.0628    0.0724 C   0  0  2  0  0  0  0  0  0  0  0  0
   -2.0139    1.2539   -0.3551 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4459   -0.5343    0.8001 C   0  0  1  0  0  0  0  0  0  0  0  0
   -1.7865   -1.9707    1.0492 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3933    0.1507    2.1155 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4512    4.5619    2.1386 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0017    4.3595    1.0087 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.6651    4.2162    0.3476 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.8664    0.1155    1.5796 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.5830    0.4626   -0.8796 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.9511    0.1846    0.8130 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.3547   -0.9697   -0.7610 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.2662   -2.5374    0.0895 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.6994   -2.3823   -1.6617 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.4199   -2.9917   -1.4453 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7615   -2.0677   -1.3526 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.0375   -2.3263    0.1975 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4185    2.7425   -1.2564 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7012    1.9159   -2.7697 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.8113    1.6604   -1.9215 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2868    0.7447   -2.7746 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4018   -0.7847   -2.7729 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.1132   -1.6665   -1.2164 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.9464   -0.1559   -1.5632 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.4908    0.2536    0.7322 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7951   -1.9288    1.5730 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1406   -2.4523    1.8396 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9703   -2.5940    0.1782 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4607    1.2527    2.0783 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6445   -0.2417    2.8335 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3783   -0.1303    2.6209 H   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0
  2  3  2  0
  2  4  1  0
  4  5  1  0
  5  6  1  0
  6  7  1  0
  7  8  1  0
  7  9  1  1
  7 10  1  0
 10 11  1  0
 10 12  1  0
 13 12  1  6
 13 14  1  0
 14 15  1  6
 14 16  1  0
 16 17  1  0
 17 18  1  0
 18 19  1  0
 18 20  1  0
 20 21  1  1
 20 22  1  0
 13  5  1  0
 19 14  1  0
 20 13  1  0
  1 23  1  0
  1 24  1  0
  1 25  1  0
  5 26  1  1
  6 27  1  0
  6 28  1  0
  8 29  1  0
  8 30  1  0
  8 31  1  0
 10 32  1  6
 12 33  1  0
 12 34  1  0
 15 35  1  0
 15 36  1  0
 15 37  1  0
 16 38  1  0
 16 39  1  0
 17 40  1  0
 17 41  1  0
 18 42  1  1
 21 43  1  0
 21 44  1  0
 21 45  1  0
 22 46  1  0
 22 47  1  0
 22 48  1  0
M  END

HEADER    PROTEIN                                 24-JUN-21   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   24-JUN-21         0                                  
HETATM    1  C   UNK     0       1.037   4.063   1.237  0.00  0.00           C+0
HETATM    2  C   UNK     0       1.007   2.576   1.490  0.00  0.00           C+0
HETATM    3  O   UNK     0       1.078   2.131   2.651  0.00  0.00           O+0
HETATM    4  O   UNK     0       0.900   1.780   0.395  0.00  0.00           O+0
HETATM    5  C   UNK     0       0.856   0.351   0.498  0.00  0.00           C+0
HETATM    6  C   UNK     0       2.222  -0.081   0.012  0.00  0.00           C+0
HETATM    7  C   UNK     0       2.357  -1.536  -0.257  0.00  0.00           C+0
HETATM    8  C   UNK     0       3.748  -1.877  -0.663  0.00  0.00           C+0
HETATM    9 Cl   UNK     0       1.867  -2.420   1.217  0.00  0.00          Cl+0
HETATM   10  C   UNK     0       1.334  -1.865  -1.327  0.00  0.00           C+0
HETATM   11 Br   UNK     0       1.668  -1.099  -3.009  0.00  0.00          Br+0
HETATM   12  C   UNK     0       0.003  -1.643  -0.712  0.00  0.00           C+0
HETATM   13  C   UNK     0      -0.300  -0.281  -0.152  0.00  0.00           C+0
HETATM   14  C   UNK     0      -0.986   0.636  -1.129  0.00  0.00           C+0
HETATM   15  C   UNK     0      -0.247   1.733  -1.744  0.00  0.00           C+0
HETATM   16  C   UNK     0      -1.880  -0.080  -2.117  0.00  0.00           C+0
HETATM   17  C   UNK     0      -2.966  -0.589  -1.225  0.00  0.00           C+0
HETATM   18  C   UNK     0      -2.653   0.063   0.072  0.00  0.00           C+0
HETATM   19  O   UNK     0      -2.014   1.254  -0.355  0.00  0.00           O+0
HETATM   20  C   UNK     0      -1.446  -0.534   0.800  0.00  0.00           C+0
HETATM   21  C   UNK     0      -1.787  -1.971   1.049  0.00  0.00           C+0
HETATM   22  C   UNK     0      -1.393   0.151   2.115  0.00  0.00           C+0
HETATM   23  H   UNK     0       1.451   4.562   2.139  0.00  0.00           H+0
HETATM   24  H   UNK     0      -0.002   4.359   1.009  0.00  0.00           H+0
HETATM   25  H   UNK     0       1.665   4.216   0.348  0.00  0.00           H+0
HETATM   26  H   UNK     0       0.866   0.116   1.580  0.00  0.00           H+0
HETATM   27  H   UNK     0       2.583   0.463  -0.880  0.00  0.00           H+0
HETATM   28  H   UNK     0       2.951   0.185   0.813  0.00  0.00           H+0
HETATM   29  H   UNK     0       4.355  -0.970  -0.761  0.00  0.00           H+0
HETATM   30  H   UNK     0       4.266  -2.537   0.090  0.00  0.00           H+0
HETATM   31  H   UNK     0       3.699  -2.382  -1.662  0.00  0.00           H+0
HETATM   32  H   UNK     0       1.420  -2.992  -1.445  0.00  0.00           H+0
HETATM   33  H   UNK     0      -0.762  -2.068  -1.353  0.00  0.00           H+0
HETATM   34  H   UNK     0       0.038  -2.326   0.198  0.00  0.00           H+0
HETATM   35  H   UNK     0      -0.419   2.743  -1.256  0.00  0.00           H+0
HETATM   36  H   UNK     0      -0.701   1.916  -2.770  0.00  0.00           H+0
HETATM   37  H   UNK     0       0.811   1.660  -1.922  0.00  0.00           H+0
HETATM   38  H   UNK     0      -2.287   0.745  -2.775  0.00  0.00           H+0
HETATM   39  H   UNK     0      -1.402  -0.785  -2.773  0.00  0.00           H+0
HETATM   40  H   UNK     0      -3.113  -1.667  -1.216  0.00  0.00           H+0
HETATM   41  H   UNK     0      -3.946  -0.156  -1.563  0.00  0.00           H+0
HETATM   42  H   UNK     0      -3.491   0.254   0.732  0.00  0.00           H+0
HETATM   43  H   UNK     0      -2.795  -1.929   1.573  0.00  0.00           H+0
HETATM   44  H   UNK     0      -1.141  -2.452   1.840  0.00  0.00           H+0
HETATM   45  H   UNK     0      -1.970  -2.594   0.178  0.00  0.00           H+0
HETATM   46  H   UNK     0      -1.461   1.253   2.078  0.00  0.00           H+0
HETATM   47  H   UNK     0      -0.645  -0.242   2.833  0.00  0.00           H+0
HETATM   48  H   UNK     0      -2.378  -0.130   2.621  0.00  0.00           H+0
CONECT    1    2   23   24   25                                             
CONECT    2    1    3    4                                                  
CONECT    3    2                                                            
CONECT    4    2    5                                                       
CONECT    5    4    6   13   26                                             
CONECT    6    5    7   27   28                                             
CONECT    7    6    8    9   10                                             
CONECT    8    7   29   30   31                                             
CONECT    9    7                                                            
CONECT   10    7   11   12   32                                             
CONECT   11   10                                                            
CONECT   12   10   13   33   34                                             
CONECT   13   12   14    5   20                                             
CONECT   14   13   15   16   19                                             
CONECT   15   14   35   36   37                                             
CONECT   16   14   17   38   39                                             
CONECT   17   16   18   40   41                                             
CONECT   18   17   19   20   42                                             
CONECT   19   18   14                                                       
CONECT   20   18   21   22   13                                             
CONECT   21   20   43   44   45                                             
CONECT   22   20   46   47   48                                             
CONECT   23    1                                                            
CONECT   24    1                                                            
CONECT   25    1                                                            
CONECT   26    5                                                            
CONECT   27    6                                                            
CONECT   28    6                                                            
CONECT   29    8                                                            
CONECT   30    8                                                            
CONECT   31    8                                                            
CONECT   32   10                                                            
CONECT   33   12                                                            
CONECT   34   12                                                            
CONECT   35   15                                                            
CONECT   36   15                                                            
CONECT   37   15                                                            
CONECT   38   16                                                            
CONECT   39   16                                                            
CONECT   40   17                                                            
CONECT   41   17                                                            
CONECT   42   18                                                            
CONECT   43   21                                                            
CONECT   44   21                                                            
CONECT   45   21                                                            
CONECT   46   22                                                            
CONECT   47   22                                                            
CONECT   48   22                                                            
MASTER        0    0    0    0    0    0    0    0   48    0  100    0
END

RDKit          3D

48 50  0  0  0  0  0  0  0  0999 V2000
    1.0367    4.0632    1.2369 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.0066    2.5760    1.4904 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.0777    2.1307    2.6513 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.8997    1.7795    0.3953 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.8564    0.3506    0.4978 C   0  0  2  0  0  0  0  0  0  0  0  0
    2.2221   -0.0807    0.0119 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.3573   -1.5364   -0.2570 C   0  0  1  0  0  0  0  0  0  0  0  0
    3.7479   -1.8768   -0.6628 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.8672   -2.4195    1.2171 Cl  0  0  0  0  0  0  0  0  0  0  0  0
    1.3343   -1.8655   -1.3275 C   0  0  2  0  0  0  0  0  0  0  0  0
    1.6676   -1.0993   -3.0087 Br  0  0  0  0  0  0  0  0  0  0  0  0
    0.0029   -1.6430   -0.7115 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2995   -0.2807   -0.1520 C   0  0  2  0  0  0  0  0  0  0  0  0
   -0.9863    0.6355   -1.1285 C   0  0  1  0  0  0  0  0  0  0  0  0
   -0.2468    1.7326   -1.7436 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8796   -0.0804   -2.1171 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.9658   -0.5891   -1.2250 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6530    0.0628    0.0724 C   0  0  2  0  0  0  0  0  0  0  0  0
   -2.0139    1.2539   -0.3551 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4459   -0.5343    0.8001 C   0  0  1  0  0  0  0  0  0  0  0  0
   -1.7865   -1.9707    1.0492 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3933    0.1507    2.1155 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4512    4.5619    2.1386 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0017    4.3595    1.0087 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.6651    4.2162    0.3476 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.8664    0.1155    1.5796 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.5830    0.4626   -0.8796 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.9511    0.1846    0.8130 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.3547   -0.9697   -0.7610 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.2662   -2.5374    0.0895 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.6994   -2.3823   -1.6617 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.4199   -2.9917   -1.4453 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7615   -2.0677   -1.3526 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.0375   -2.3263    0.1975 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4185    2.7425   -1.2564 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7012    1.9159   -2.7697 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.8113    1.6604   -1.9215 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2868    0.7447   -2.7746 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4018   -0.7847   -2.7729 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.1132   -1.6665   -1.2164 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.9464   -0.1559   -1.5632 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.4908    0.2536    0.7322 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7951   -1.9288    1.5730 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1406   -2.4523    1.8396 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9703   -2.5940    0.1782 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4607    1.2527    2.0783 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6445   -0.2417    2.8335 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3783   -0.1303    2.6209 H   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0
  2  3  2  0
  2  4  1  0
  4  5  1  0
  5  6  1  0
  6  7  1  0
  7  8  1  0
  7  9  1  1
  7 10  1  0
 10 11  1  0
 10 12  1  0
 13 12  1  6
 13 14  1  0
 14 15  1  6
 14 16  1  0
 16 17  1  0
 17 18  1  0
 18 19  1  0
 18 20  1  0
 20 21  1  1
 20 22  1  0
 13  5  1  0
 19 14  1  0
 20 13  1  0
  1 23  1  0
  1 24  1  0
  1 25  1  0
  5 26  1  1
  6 27  1  0
  6 28  1  0
  8 29  1  0
  8 30  1  0
  8 31  1  0
 10 32  1  6
 12 33  1  0
 12 34  1  0
 15 35  1  0
 15 36  1  0
 15 37  1  0
 16 38  1  0
 16 39  1  0
 17 40  1  0
 17 41  1  0
 18 42  1  1
 21 43  1  0
 21 44  1  0
 21 45  1  0
 22 46  1  0
 22 47  1  0
 22 48  1  0
M  END

View in JSmol View NMR Assignments

Synonyms

Value	Source
(2R,3'r,4'r,6'r)-3'-Bromo-4'-chloro-1,3,3,4'-tetramethyl-7-oxaspiro[bicyclo[2.2.1]heptane-2,1'-cyclohexane]-6'-yl acetic acid	Generator

Chemical Formula

C₁₇H₂₆BrClO₃

Average Mass

393.7500 Da

Monoisotopic Mass

392.07538 Da

IUPAC Name

(1R,2R,3'R,4S,4'R,6'R)-3'-bromo-4'-chloro-1,3,3,4'-tetramethyl-7-oxaspiro[bicyclo[2.2.1]heptane-2,1'-cyclohexane]-6'-yl acetate

Traditional Name

(1R,2R,3'R,4S,4'R,6'R)-3'-bromo-4'-chloro-1,3,3,4'-tetramethyl-7-oxaspiro[bicyclo[2.2.1]heptane-2,1'-cyclohexane]-6'-yl acetate

CAS Registry Number

Not Available

SMILES

CC(=O)O[C@@H]1C[C@@](C)(Cl)[C@H](Br)C[C@@]11C(C)(C)C2CCC1(C)O2

InChI Identifier

InChI=1S/C17H26BrClO3/c1-10(20)21-13-9-15(4,19)11(18)8-17(13)14(2,3)12-6-7-16(17,5)22-12/h11-13H,6-9H2,1-5H3/t11-,12?,13-,15-,16?,17+/m1/s1

InChI Key

DVONIFXCMJQOGF-OGOWZMLDSA-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, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 100 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 252 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 1000 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 50 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 200 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 75 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 300 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 101 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 400 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 126 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 500 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 151 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 600 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 176 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 700 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 201 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 800 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 226 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 900 MHz, D₂O, 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
Unknown-fungus sp.	NPAtlas	12088448

Chemical Taxonomy

Classification

Not classified

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	4.87	ALOGPS
logP	3.54	ChemAxon
logS	-6	ALOGPS
pKa (Strongest Basic)	-4.2	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	2	ChemAxon
Hydrogen Donor Count	0	ChemAxon
Polar Surface Area	35.53 Å²	ChemAxon
Rotatable Bond Count	2	ChemAxon
Refractivity	89.19 m³·mol⁻¹	ChemAxon
Polarizability	36.37 Å³	ChemAxon
Number of Rings	3	ChemAxon
Bioavailability	Yes	ChemAxon
Rule of Five	Yes	ChemAxon
Ghose Filter	Yes	ChemAxon
Veber's Rule	Yes	ChemAxon
MDDR-like Rule	No	ChemAxon

External Links

NPAtlas ID

NPA006267

HMDB ID

Not Available

DrugBank ID

Not Available

Phenol Explorer Compound ID

Not Available

FoodDB ID

Not Available

KNApSAcK ID

Not Available

Chemspider ID

78442567

KEGG Compound ID

Not Available

BioCyc ID

Not Available

BiGG ID

Not Available

Wikipedia Link

Not Available

METLIN ID

Not Available

PubChem Compound

139584853

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

Brito I, Cueto M, Diaz-Marrero AR, Darias J, San Martin A: Oxachamigrenes, new halogenated sesquiterpenes from Laurencia obtusa. J Nat Prod. 2002 Jun;65(6):946-8. doi: 10.1021/np010580t. [PubMed:12088448 ]

Showing NP-Card for 5-Acetoxyoxachamigrene (NP0004214)

MOL for NP0004214 (5-Acetoxyoxachamigrene)

3D MOL for NP0004214 (5-Acetoxyoxachamigrene)

3D SDF for NP0004214 (5-Acetoxyoxachamigrene)

3D-SDF for NP0004214 (5-Acetoxyoxachamigrene)

PDB for NP0004214 (5-Acetoxyoxachamigrene)

3D PDB for NP0004214 (5-Acetoxyoxachamigrene)

SMILES for NP0004214 (5-Acetoxyoxachamigrene)

INCHI for NP0004214 (5-Acetoxyoxachamigrene)

Structure for NP0004214 (5-Acetoxyoxachamigrene)

3D Structure for NP0004214 (5-Acetoxyoxachamigrene)