NP-MRD: Showing NP-Card for (+)-Isogosterone B (NP0082793)

Jump To Section:

Identification Spectra BioTaxonomy ChemoTaxonomy Physical properties Links References XML

Record Information

Version

2.0

Created at

2022-04-29 03:52:51 UTC

Updated at

2022-04-29 03:52:51 UTC

NP-MRD ID

NP0082793

Secondary Accession Numbers

None

Natural Product Identification

Common Name

(+)-Isogosterone B

Description

(2R,2'S,3'S,4'aS,4'bS,5S,10'aR)-2',5-dihydroxy-2',4'b-dimethyl-5-[(2R)-6-methyl-3-oxoheptan-2-yl]-7'-oxo-3',4',4'a,4'b,7',9',10',10'a-octahydro-2'H-spiro[oxolane-2,1'-phenanthrene]-3'-yl acetate belongs to the class of organic compounds known as phenanthrenes and derivatives. These are polycyclic compounds containing a phenanthrene moiety, which is a tricyclic aromatic compound with three non-linearly fused benzene. (+)-Isogosterone B is found in Dendronephythya sp. Based on a literature review very few articles have been published on (2R,2'S,3'S,4'aS,4'bS,5S,10'aR)-2',5-dihydroxy-2',4'b-dimethyl-5-[(2R)-6-methyl-3-oxoheptan-2-yl]-7'-oxo-3',4',4'a,4'b,7',9',10',10'a-octahydro-2'H-spiro[oxolane-2,1'-phenanthrene]-3'-yl acetate.

Structure

MOL 3D MOL SDF PDB SMILES InChI


  Mrv1652304292205522D          

 36 39  0  0  1  0            999 V2000
    2.4248    0.0335    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.7624   -0.4584    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    1.8573   -1.2779    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    2.6144   -1.6055    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    3.2767   -1.1136    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    3.1819   -0.2941    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    3.8442    0.1978    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.7494    1.0173    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.9923    1.3449    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.4117    1.5092    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.7914   -1.7584    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.0991   -1.0475    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.3332   -2.0105    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.1701   -2.8193    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.3506   -2.9141    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    2.0071   -2.1640    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.3506   -3.7391    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    3.0650   -4.1516    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.0650   -4.9766    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.7795   -3.7391    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.4940   -4.1516    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.2084   -3.7391    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.9229   -4.1516    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.2084   -2.9141    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.6361   -4.1516    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.6449   -3.3414    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.1949   -1.7698    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.4378   -1.4421    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.3430   -0.6226    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4142   -0.2949    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5090    0.5246    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2662    0.8522    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.1533    1.0165    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.9105    0.6888    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.0053   -0.1307    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    1.6676    0.3612    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
  2  1  1  1  0  0  0
  2  3  1  0  0  0  0
  3  4  1  0  0  0  0
  4  5  1  0  0  0  0
  5  6  1  0  0  0  0
  1  6  1  0  0  0  0
  6  7  1  6  0  0  0
  7  8  1  0  0  0  0
  8  9  2  0  0  0  0
  8 10  1  0  0  0  0
  5 11  1  1  0  0  0
  5 12  1  6  0  0  0
  4 13  1  0  0  0  0
 13 14  1  0  0  0  0
 14 15  1  0  0  0  0
 15 16  1  0  0  0  0
  4 16  1  6  0  0  0
 15 17  1  1  0  0  0
 17 18  1  0  0  0  0
 18 19  2  0  0  0  0
 18 20  1  0  0  0  0
 20 21  1  0  0  0  0
 21 22  1  0  0  0  0
 22 23  1  0  0  0  0
 22 24  1  0  0  0  0
 17 25  1  1  0  0  0
 15 26  1  6  0  0  0
  3 27  1  6  0  0  0
 27 28  1  0  0  0  0
 28 29  1  0  0  0  0
 29 30  2  0  0  0  0
 30 31  1  0  0  0  0
 31 32  2  0  0  0  0
 31 33  1  0  0  0  0
 33 34  2  0  0  0  0
 34 35  1  0  0  0  0
  2 35  1  0  0  0  0
 29 35  1  0  0  0  0
 35 36  1  6  0  0  0
M  END

     RDKit          3D

 78 81  0  0  0  0  0  0  0  0999 V2000
   -1.9677    4.5445    3.1532 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4667    3.3193    2.4886 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.7204    3.1341    2.4339 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6322    2.3670    1.9251 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1333    1.1820    1.2860 C   0  0  1  0  0  0  0  0  0  0  0  0
   -1.6350    1.1863   -0.1234 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8015   -0.0686   -0.8790 C   0  0  1  0  0  0  0  0  0  0  0  0
   -1.8736   -1.2567    0.0699 C   0  0  1  0  0  0  0  0  0  0  0  0
   -1.5947   -2.4998   -0.7313 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5119   -2.5734   -1.9437 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5271   -1.4564   -1.7618 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.7740   -1.7673   -1.5229 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.7152   -0.6738   -1.3545 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.9058   -0.9508   -1.1278 O   0  0  0  0  0  0  0  0  0  0  0  0
   -5.2064    0.6844   -1.4619 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.9389    0.9443   -1.7002 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.9490   -0.1013   -1.8712 C   0  0  1  0  0  0  0  0  0  0  0  0
   -2.3122   -0.0486   -3.2682 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9285   -1.0175    1.1861 C   0  0  1  0  0  0  0  0  0  0  0  0
   -0.6187   -2.2404    2.0051 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.8540   -2.4604    1.7807 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.2987   -1.0566    1.4582 C   0  0  1  0  0  0  0  0  0  0  0  0
    1.6077   -0.4088    2.6366 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.5535   -1.0286    0.6076 C   0  0  2  0  0  0  0  0  0  0  0  0
    3.6959   -1.6145    1.4548 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.9261    0.3898    0.3529 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1479    1.2598    0.7028 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.2086    0.7657   -0.3121 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.0729    0.6719   -1.8120 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.3372    1.0431   -2.5284 C   0  0  1  0  0  0  0  0  0  0  0  0
    5.7598    2.4716   -2.2275 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.5042    0.1682   -2.1240 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.2549   -0.4756    0.7702 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6198    0.0130    2.0954 C   0  0  2  0  0  0  0  0  0  0  0  0
   -2.8280   -0.7276    2.6755 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8330    0.4038    3.1483 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4759    4.6979    4.1403 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8741    4.4822    3.3168 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1380    5.4292    2.5059 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.2375    1.2473    1.3634 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5453    1.4965   -0.0590 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1193    2.0228   -0.6424 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8628   -0.2375   -1.4649 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.9399   -1.2983    0.4217 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8104   -3.3889   -0.1091 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5703   -2.5774   -1.0892 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.0417   -3.5196   -1.9234 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9874   -2.4853   -2.8931 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.0654   -2.8089   -1.4572 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.9407    1.5061   -1.3314 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.7101    2.0150   -1.7711 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1048    0.9925   -3.5697 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3427   -0.5698   -3.1852 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.9871   -0.5813   -3.9399 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7277   -1.9756    3.0779 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2492   -3.1009    1.8243 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.0656   -3.0780    0.8851 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.3775   -2.9131    2.6331 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.0153   -1.0137    3.3181 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.4930   -1.6401   -0.2947 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.1568   -0.8153    2.0643 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.3345   -2.4337    2.0868 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.4717   -2.0497    0.7691 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.3813    1.8630   -0.0997 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.0794    0.2533    0.0932 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.2478    1.3108   -2.1718 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.8143   -0.3786   -2.0750 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.2184    0.9561   -3.6233 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.9242    2.6487   -1.1508 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.0473    3.2006   -2.6657 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.7463    2.6664   -2.7377 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.3288   -0.9070   -2.2687 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.8223    0.4056   -1.0746 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.3610    0.4554   -2.7677 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.7742   -0.3065    2.2326 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8725   -0.6469    3.7714 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8368   -1.7996    2.4242 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3995    0.7543    3.8715 H   0  0  0  0  0  0  0  0  0  0  0  0
 31 30  1  0
 30 32  1  0
 30 29  1  0
 29 28  1  0
 28 26  1  0
 26 27  2  0
 26 24  1  0
 24 25  1  0
 24 22  1  0
 22 23  1  1
 22 21  1  0
 21 20  1  0
 20 19  1  0
 19 33  1  6
 19  8  1  0
  8  9  1  0
  9 10  1  0
 10 11  1  0
 11 12  2  0
 12 13  1  0
 13 14  2  0
 13 15  1  0
 15 16  2  0
 16 17  1  0
 17 18  1  6
 17  7  1  0
  7  6  1  0
  6  5  1  0
  5  4  1  0
  4  2  1  0
  2  1  1  0
  2  3  2  0
  5 34  1  0
 34 35  1  0
 34 36  1  1
 33 22  1  0
  7  8  1  0
 34 19  1  0
 17 11  1  0
 31 69  1  0
 31 70  1  0
 31 71  1  0
 30 68  1  6
 32 72  1  0
 32 73  1  0
 32 74  1  0
 29 66  1  0
 29 67  1  0
 28 64  1  0
 28 65  1  0
 24 60  1  6
 25 61  1  0
 25 62  1  0
 25 63  1  0
 23 59  1  0
 21 57  1  0
 21 58  1  0
 20 55  1  0
 20 56  1  0
  8 44  1  1
  9 45  1  0
  9 46  1  0
 10 47  1  0
 10 48  1  0
 12 49  1  0
 15 50  1  0
 16 51  1  0
 18 52  1  0
 18 53  1  0
 18 54  1  0
  7 43  1  6
  6 41  1  0
  6 42  1  0
  5 40  1  6
  1 37  1  0
  1 38  1  0
  1 39  1  0
 35 75  1  0
 35 76  1  0
 35 77  1  0
 36 78  1  0
M  END


  Mrv1652304292205522D          

 36 39  0  0  1  0            999 V2000
    2.4248    0.0335    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.7624   -0.4584    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    1.8573   -1.2779    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    2.6144   -1.6055    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    3.2767   -1.1136    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    3.1819   -0.2941    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    3.8442    0.1978    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.7494    1.0173    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.9923    1.3449    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.4117    1.5092    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.7914   -1.7584    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.0991   -1.0475    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.3332   -2.0105    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.1701   -2.8193    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.3506   -2.9141    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    2.0071   -2.1640    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.3506   -3.7391    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    3.0650   -4.1516    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.0650   -4.9766    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.7795   -3.7391    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.4940   -4.1516    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.2084   -3.7391    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.9229   -4.1516    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.2084   -2.9141    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.6361   -4.1516    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.6449   -3.3414    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.1949   -1.7698    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.4378   -1.4421    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.3430   -0.6226    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4142   -0.2949    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5090    0.5246    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2662    0.8522    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.1533    1.0165    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.9105    0.6888    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.0053   -0.1307    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    1.6676    0.3612    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
  2  1  1  1  0  0  0
  2  3  1  0  0  0  0
  3  4  1  0  0  0  0
  4  5  1  0  0  0  0
  5  6  1  0  0  0  0
  1  6  1  0  0  0  0
  6  7  1  6  0  0  0
  7  8  1  0  0  0  0
  8  9  2  0  0  0  0
  8 10  1  0  0  0  0
  5 11  1  1  0  0  0
  5 12  1  6  0  0  0
  4 13  1  0  0  0  0
 13 14  1  0  0  0  0
 14 15  1  0  0  0  0
 15 16  1  0  0  0  0
  4 16  1  6  0  0  0
 15 17  1  1  0  0  0
 17 18  1  0  0  0  0
 18 19  2  0  0  0  0
 18 20  1  0  0  0  0
 20 21  1  0  0  0  0
 21 22  1  0  0  0  0
 22 23  1  0  0  0  0
 22 24  1  0  0  0  0
 17 25  1  1  0  0  0
 15 26  1  6  0  0  0
  3 27  1  6  0  0  0
 27 28  1  0  0  0  0
 28 29  1  0  0  0  0
 29 30  2  0  0  0  0
 30 31  1  0  0  0  0
 31 32  2  0  0  0  0
 31 33  1  0  0  0  0
 33 34  2  0  0  0  0
 34 35  1  0  0  0  0
  2 35  1  0  0  0  0
 29 35  1  0  0  0  0
 35 36  1  6  0  0  0
M  END
> <DATABASE_ID>
NP0082793

> <DATABASE_NAME>
NP-MRD

> <SMILES>
CC(C)CCC(=O)[C@@H](C)[C@]1(O)CC[C@@]2(O1)[C@@H]1CCC3=CC(=O)C=C[C@@]3(C)[C@H]1C[C@H](OC(C)=O)[C@]2(C)O

> <INCHI_IDENTIFIER>
InChI=1S/C29H42O7/c1-17(2)7-10-24(32)18(3)29(34)14-13-28(36-29)22-9-8-20-15-21(31)11-12-26(20,5)23(22)16-25(27(28,6)33)35-19(4)30/h11-12,15,17-18,22-23,25,33-34H,7-10,13-14,16H2,1-6H3/t18-,22-,23+,25+,26-,27+,28-,29+/m1/s1

> <INCHI_KEY>
UPGQWRBTEVLPHO-YWECBFJXSA-N

> <FORMULA>
C29H42O7

> <MOLECULAR_WEIGHT>
502.648

> <EXACT_MASS>
502.293053692

> <JCHEM_ACCEPTOR_COUNT>
6

> <JCHEM_ATOM_COUNT>
78

> <JCHEM_AVERAGE_POLARIZABILITY>
54.630524566812085

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
2

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
0

> <JCHEM_IUPAC>
(2R,2'S,3'S,4'aS,4'bS,5S,10'aR)-2',5-dihydroxy-2',4'b-dimethyl-5-[(2R)-6-methyl-3-oxoheptan-2-yl]-7'-oxo-3',4',4'a,4'b,7',9',10',10'a-octahydro-2'H-spiro[oxolane-2,1'-phenanthrene]-3'-yl acetate

> <ALOGPS_LOGP>
3.06

> <JCHEM_LOGP>
4.080634212333332

> <ALOGPS_LOGS>
-4.95

> <JCHEM_MDDR_LIKE_RULE>
1

> <JCHEM_NUMBER_OF_RINGS>
4

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA>
12.954820162609895

> <JCHEM_PKA_STRONGEST_ACIDIC>
11.63805389148282

> <JCHEM_PKA_STRONGEST_BASIC>
-3.7068962881386325

> <JCHEM_POLAR_SURFACE_AREA>
110.13000000000002

> <JCHEM_REFRACTIVITY>
136.4585

> <JCHEM_ROTATABLE_BOND_COUNT>
7

> <JCHEM_RULE_OF_FIVE>
0

> <ALOGPS_SOLUBILITY>
5.65e-03 g/l

> <JCHEM_TRADITIONAL_IUPAC>
(2R,2'S,3'S,4'aS,4'bS,5S,10'aR)-2',5-dihydroxy-2',4'b-dimethyl-5-[(2R)-6-methyl-3-oxoheptan-2-yl]-7'-oxo-3',4',4'a,9',10',10'a-hexahydrospiro[oxolane-2,1'-phenanthrene]-3'-yl acetate

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 29-APR-22   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   29-APR-22         0                                  
HETATM    1  C   UNK     0       4.526   0.063   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0       3.290  -0.856   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0       3.467  -2.385   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0       4.880  -2.997   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0       6.117  -2.079   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0       5.940  -0.549   0.000  0.00  0.00           C+0
HETATM    7  O   UNK     0       7.176   0.369   0.000  0.00  0.00           O+0
HETATM    8  C   UNK     0       6.999   1.899   0.000  0.00  0.00           C+0
HETATM    9  O   UNK     0       5.586   2.511   0.000  0.00  0.00           O+0
HETATM   10  C   UNK     0       8.235   2.817   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0       7.077  -3.282   0.000  0.00  0.00           C+0
HETATM   12  O   UNK     0       7.652  -1.955   0.000  0.00  0.00           O+0
HETATM   13  C   UNK     0       6.222  -3.753   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0       5.918  -5.263   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0       4.388  -5.440   0.000  0.00  0.00           C+0
HETATM   16  O   UNK     0       3.747  -4.039   0.000  0.00  0.00           O+0
HETATM   17  C   UNK     0       4.388  -6.980   0.000  0.00  0.00           C+0
HETATM   18  C   UNK     0       5.721  -7.750   0.000  0.00  0.00           C+0
HETATM   19  O   UNK     0       5.721  -9.290   0.000  0.00  0.00           O+0
HETATM   20  C   UNK     0       7.055  -6.980   0.000  0.00  0.00           C+0
HETATM   21  C   UNK     0       8.389  -7.750   0.000  0.00  0.00           C+0
HETATM   22  C   UNK     0       9.722  -6.980   0.000  0.00  0.00           C+0
HETATM   23  C   UNK     0      11.056  -7.750   0.000  0.00  0.00           C+0
HETATM   24  C   UNK     0       9.722  -5.440   0.000  0.00  0.00           C+0
HETATM   25  C   UNK     0       3.054  -7.750   0.000  0.00  0.00           C+0
HETATM   26  O   UNK     0       3.070  -6.237   0.000  0.00  0.00           O+0
HETATM   27  C   UNK     0       2.231  -3.304   0.000  0.00  0.00           C+0
HETATM   28  C   UNK     0       0.817  -2.692   0.000  0.00  0.00           C+0
HETATM   29  C   UNK     0       0.640  -1.162   0.000  0.00  0.00           C+0
HETATM   30  C   UNK     0      -0.773  -0.551   0.000  0.00  0.00           C+0
HETATM   31  C   UNK     0      -0.950   0.979   0.000  0.00  0.00           C+0
HETATM   32  O   UNK     0      -2.363   1.591   0.000  0.00  0.00           O+0
HETATM   33  C   UNK     0       0.286   1.897   0.000  0.00  0.00           C+0
HETATM   34  C   UNK     0       1.700   1.286   0.000  0.00  0.00           C+0
HETATM   35  C   UNK     0       1.877  -0.244   0.000  0.00  0.00           C+0
HETATM   36  C   UNK     0       3.113   0.674   0.000  0.00  0.00           C+0
CONECT    1    2    6                                                       
CONECT    2    1    3   35                                                  
CONECT    3    2    4   27                                                  
CONECT    4    3    5   13   16                                             
CONECT    5    4    6   11   12                                             
CONECT    6    5    1    7                                                  
CONECT    7    6    8                                                       
CONECT    8    7    9   10                                                  
CONECT    9    8                                                            
CONECT   10    8                                                            
CONECT   11    5                                                            
CONECT   12    5                                                            
CONECT   13    4   14                                                       
CONECT   14   13   15                                                       
CONECT   15   14   16   17   26                                             
CONECT   16   15    4                                                       
CONECT   17   15   18   25                                                  
CONECT   18   17   19   20                                                  
CONECT   19   18                                                            
CONECT   20   18   21                                                       
CONECT   21   20   22                                                       
CONECT   22   21   23   24                                                  
CONECT   23   22                                                            
CONECT   24   22                                                            
CONECT   25   17                                                            
CONECT   26   15                                                            
CONECT   27    3   28                                                       
CONECT   28   27   29                                                       
CONECT   29   28   30   35                                                  
CONECT   30   29   31                                                       
CONECT   31   30   32   33                                                  
CONECT   32   31                                                            
CONECT   33   31   34                                                       
CONECT   34   33   35                                                       
CONECT   35   34    2   29   36                                             
CONECT   36   35                                                            
MASTER        0    0    0    0    0    0    0    0   36    0   78    0
END

View in JSmol

Synonyms

Value	Source
(2R,2's,3's,4'AS,4'BS,5S,10'ar)-2',5-dihydroxy-2',4'b-dimethyl-5-[(2R)-6-methyl-3-oxoheptan-2-yl]-7'-oxo-3',4',4'a,4'b,7',9',10',10'a-octahydro-2'H-spiro[oxolane-2,1'-phenanthrene]-3'-yl acetic acid	Generator

Chemical Formula

C₂₉H₄₂O₇

Average Mass

502.6480 Da

Monoisotopic Mass

502.29305 Da

IUPAC Name

(2R,2'S,3'S,4'aS,4'bS,5S,10'aR)-2',5-dihydroxy-2',4'b-dimethyl-5-[(2R)-6-methyl-3-oxoheptan-2-yl]-7'-oxo-3',4',4'a,4'b,7',9',10',10'a-octahydro-2'H-spiro[oxolane-2,1'-phenanthrene]-3'-yl acetate

Traditional Name

(2R,2'S,3'S,4'aS,4'bS,5S,10'aR)-2',5-dihydroxy-2',4'b-dimethyl-5-[(2R)-6-methyl-3-oxoheptan-2-yl]-7'-oxo-3',4',4'a,9',10',10'a-hexahydrospiro[oxolane-2,1'-phenanthrene]-3'-yl acetate

CAS Registry Number

Not Available

SMILES

CC(C)CCC(=O)[C@@H](C)[C@]1(O)CC[C@@]2(O1)[C@@H]1CCC3=CC(=O)C=C[C@@]3(C)[C@H]1C[C@H](OC(C)=O)[C@]2(C)O

InChI Identifier

InChI=1S/C29H42O7/c1-17(2)7-10-24(32)18(3)29(34)14-13-28(36-29)22-9-8-20-15-21(31)11-12-26(20,5)23(22)16-25(27(28,6)33)35-19(4)30/h11-12,15,17-18,22-23,25,33-34H,7-10,13-14,16H2,1-6H3/t18-,22-,23+,25+,26-,27+,28-,29+/m1/s1

InChI Key

UPGQWRBTEVLPHO-YWECBFJXSA-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
Dendronephythya sp.	-	KNApSAcK

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as phenanthrenes and derivatives. These are polycyclic compounds containing a phenanthrene moiety, which is a tricyclic aromatic compound with three non-linearly fused benzene.

Kingdom

Organic compounds

Super Class

Benzenoids

Class

Phenanthrenes and derivatives

Sub Class

Not Available

Direct Parent

Phenanthrenes and derivatives

Alternative Parents

Substituents

Phenanthrene
Beta-hydroxy ketone
Tetrahydrofuran
Tertiary alcohol
Cyclic alcohol
Cyclic ketone
Ketone
Hemiacetal
Carboxylic acid ester
Oxacycle
Organoheterocyclic compound
Monocarboxylic acid or derivatives
Carboxylic acid derivative
Organic oxygen compound
Organic oxide
Hydrocarbon derivative
Organooxygen compound
Carbonyl group
Alcohol
Aliphatic heteropolycyclic compound

Molecular Framework

Aliphatic heteropolycyclic compounds

External Descriptors

Not Available

Physical Properties

State

Not Available

Experimental Properties

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

Predicted Properties

Property	Value	Source
logP	3.06	ALOGPS
logP	4.08	ChemAxon
logS	-5	ALOGPS
pKa (Strongest Acidic)	11.64	ChemAxon
pKa (Strongest Basic)	-3.7	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	6	ChemAxon
Hydrogen Donor Count	2	ChemAxon
Polar Surface Area	110.13 Å²	ChemAxon
Rotatable Bond Count	7	ChemAxon
Refractivity	136.46 m³·mol⁻¹	ChemAxon
Polarizability	54.63 Å³	ChemAxon
Number of Rings	4	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

163091927

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

Not Available

Showing NP-Card for (+)-Isogosterone B (NP0082793)

MOL for NP0082793 ((+)-Isogosterone B)

3D MOL for NP0082793 ((+)-Isogosterone B)

3D SDF for NP0082793 ((+)-Isogosterone B)

3D-SDF for NP0082793 ((+)-Isogosterone B)

PDB for NP0082793 ((+)-Isogosterone B)

3D PDB for NP0082793 ((+)-Isogosterone B)

SMILES for NP0082793 ((+)-Isogosterone B)

INCHI for NP0082793 ((+)-Isogosterone B)

Structure for NP0082793 ((+)-Isogosterone B)

3D Structure for NP0082793 ((+)-Isogosterone B)