NP-MRD: Showing NP-Card for (-)-Telosmoside A6 (NP0073225)

Jump To Section:

Identification Spectra BioTaxonomy ChemoTaxonomy Physical properties Links References XML

Record Information

Version

2.0

Created at

2022-04-28 18:30:14 UTC

Updated at

2022-04-28 18:30:14 UTC

NP-MRD ID

NP0073225

Secondary Accession Numbers

None

Natural Product Identification

Common Name

(-)-Telosmoside A6

Description

(1S)-1-[(1S,2S,5S,7S,10R,11S,14S,15S,16R)-16-(acetyloxy)-11,14-dihydroxy-5-{[(2S,4S,5S,6R)-4-hydroxy-5-{[(2S,4S,5R,6R)-5-{[(2S,4R,5R,6R)-5-hydroxy-4-methoxy-6-methyloxan-2-yl]oxy}-4-methoxy-6-methyloxan-2-yl]oxy}-6-methyloxan-2-yl]oxy}-2,15-dimethyltetracyclo[8.7.0.0²,⁷.0¹¹,¹⁵]Heptadecan-14-yl]ethyl (2S)-2-methylbutanoate belongs to the class of organic compounds known as steroidal glycosides. These are sterol lipids containing a carbohydrate moiety glycosidically linked to the steroid skeleton. (-)-Telosmoside A6 is found in Telosma procumbens . Based on a literature review very few articles have been published on (1S)-1-[(1S,2S,5S,7S,10R,11S,14S,15S,16R)-16-(acetyloxy)-11,14-dihydroxy-5-{[(2S,4S,5S,6R)-4-hydroxy-5-{[(2S,4S,5R,6R)-5-{[(2S,4R,5R,6R)-5-hydroxy-4-methoxy-6-methyloxan-2-yl]oxy}-4-methoxy-6-methyloxan-2-yl]oxy}-6-methyloxan-2-yl]oxy}-2,15-dimethyltetracyclo[8.7.0.0²,⁷.0¹¹,¹⁵]Heptadecan-14-yl]ethyl (2S)-2-methylbutanoate.

Structure

MOL 3D MOL SDF PDB SMILES InChI


  Mrv1652304282220302D          

 64 70  0  0  1  0            999 V2000
    4.2475    2.1537    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.5278    1.3777    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    3.9960    0.7470    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.1838    0.8922    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    2.9035    1.6682    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    3.4354    2.2989    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.0914    1.8134    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    1.5596    1.1827    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    1.8399    0.4067    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.6520    0.2615    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7475    1.3279    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    0.4672    2.1038    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    0.9990    2.7345    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    1.8111    2.5893    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7187    3.5104    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.2505    4.1411    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.9702    4.9171    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.0626    3.9959    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3574    2.0770    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
   -0.5867    1.2845    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0962    0.8215    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1183    2.3959    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
   -1.7749    1.8964    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5357    2.2152    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6400    3.0336    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.1923    1.7157    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
   -3.9532    2.0346    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.6098    1.5351    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.0880    0.8974    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2225    3.2143    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4788    2.8930    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.1073    2.8462    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.9451    0.5269    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.6232    2.4441    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.3399    1.2325    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.8717    1.8632    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    6.6838    1.7180    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    7.2157    2.3487    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    6.9354    3.1246    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    6.1232    3.2699    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    5.5914    2.6391    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.8429    4.0458    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    7.4672    3.7553    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    8.2793    3.6101    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    8.8111    4.2408    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    9.6232    4.0956    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    9.9035    3.3197    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    9.3717    2.6890    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    8.5596    2.8342    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    9.6520    1.9131    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   10.7157    3.1745    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   11.2475    3.8052    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
   12.0596    3.6600    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   12.5914    4.2907    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
   12.3111    5.0666    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
   11.4990    5.2118    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
   10.9672    4.5811    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   11.2187    5.9877    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   11.7505    6.6185    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   12.8429    5.6973    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   13.4035    4.1455    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   10.1551    4.7263    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    9.8748    5.5023    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.0278    2.2035    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0  0  0  0
  2  3  1  0  0  0  0
  4  3  1  6  0  0  0
  4  5  1  0  0  0  0
  5  6  1  0  0  0  0
  1  6  1  0  0  0  0
  5  7  1  0  0  0  0
  7  8  1  0  0  0  0
  8  9  1  1  0  0  0
  9 10  1  0  0  0  0
  4 10  1  0  0  0  0
  8 11  1  0  0  0  0
 11 12  1  0  0  0  0
 12 13  1  0  0  0  0
 13 14  1  0  0  0  0
  7 14  1  6  0  0  0
 13 15  1  6  0  0  0
 15 16  1  0  0  0  0
 16 17  2  0  0  0  0
 16 18  1  0  0  0  0
 12 19  1  0  0  0  0
 19 20  1  0  0  0  0
 20 21  1  0  0  0  0
 11 21  1  0  0  0  0
 19 22  1  1  0  0  0
 22 23  1  0  0  0  0
 23 24  1  0  0  0  0
 24 25  2  0  0  0  0
 24 26  1  0  0  0  0
 26 27  1  0  0  0  0
 27 28  1  0  0  0  0
 26 29  1  1  0  0  0
 22 30  1  1  0  0  0
 19 31  1  6  0  0  0
 12 32  1  6  0  0  0
 11 33  1  6  0  0  0
  5 34  1  6  0  0  0
  2 35  1  6  0  0  0
 36 35  1  6  0  0  0
 36 37  1  0  0  0  0
 37 38  1  0  0  0  0
 38 39  1  0  0  0  0
 39 40  1  0  0  0  0
 40 41  1  0  0  0  0
 36 41  1  0  0  0  0
 40 42  1  6  0  0  0
 39 43  1  6  0  0  0
 44 43  1  1  0  0  0
 44 45  1  0  0  0  0
 45 46  1  0  0  0  0
 46 47  1  0  0  0  0
 47 48  1  0  0  0  0
 48 49  1  0  0  0  0
 44 49  1  0  0  0  0
 48 50  1  1  0  0  0
 47 51  1  6  0  0  0
 52 51  1  1  0  0  0
 52 53  1  0  0  0  0
 53 54  1  0  0  0  0
 54 55  1  0  0  0  0
 55 56  1  0  0  0  0
 56 57  1  0  0  0  0
 52 57  1  0  0  0  0
 56 58  1  1  0  0  0
 58 59  1  0  0  0  0
 55 60  1  6  0  0  0
 54 61  1  1  0  0  0
 46 62  1  6  0  0  0
 62 63  1  0  0  0  0
 38 64  1  1  0  0  0
M  END

     RDKit          3D

144150  0  0  0  0  0  0  0  0999 V2000
  -12.8959    0.1125    1.7132 C   0  0  0  0  0  0  0  0  0  0  0  0
  -13.7434    0.1802    0.4643 C   0  0  0  0  0  0  0  0  0  0  0  0
  -13.1774   -0.7667   -0.5506 C   0  0  2  0  0  0  0  0  0  0  0  0
  -13.1908   -2.1772   -0.0008 C   0  0  0  0  0  0  0  0  0  0  0  0
  -11.8440   -0.3477   -0.9916 C   0  0  0  0  0  0  0  0  0  0  0  0
  -11.6074   -0.0664   -2.2121 O   0  0  0  0  0  0  0  0  0  0  0  0
  -10.7695   -0.2301   -0.1327 O   0  0  0  0  0  0  0  0  0  0  0  0
   -9.4537    0.1912   -0.6096 C   0  0  1  0  0  0  0  0  0  0  0  0
   -9.2262    1.4688    0.1042 C   0  0  0  0  0  0  0  0  0  0  0  0
   -8.5696   -0.9665   -0.2648 C   0  0  2  0  0  0  0  0  0  0  0  0
   -9.1940   -2.0757   -0.9282 O   0  0  0  0  0  0  0  0  0  0  0  0
   -8.5704   -1.3118    1.1816 C   0  0  0  0  0  0  0  0  0  0  0  0
   -7.2073   -0.9571    1.6533 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.3723   -1.3877    0.4559 C   0  0  2  0  0  0  0  0  0  0  0  0
   -6.4391   -2.8053    0.5083 O   0  0  0  0  0  0  0  0  0  0  0  0
   -4.9674   -0.9974    0.5335 C   0  0  2  0  0  0  0  0  0  0  0  0
   -4.5623   -0.6436    1.9737 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.0712   -0.4440    2.0695 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6092    0.5943    1.0465 C   0  0  1  0  0  0  0  0  0  0  0  0
   -1.1640    0.9062    1.2224 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5059    1.6845    0.1669 C   0  0  1  0  0  0  0  0  0  0  0  0
    0.8527    1.5267    0.0241 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.6194    2.6376    0.1913 C   0  0  2  0  0  0  0  0  0  0  0  0
    2.5172    2.9840   -0.9536 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.4527    1.8129   -1.1925 C   0  0  2  0  0  0  0  0  0  0  0  0
    2.7582    0.6020   -1.2459 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.3244    1.7580    0.0739 C   0  0  2  0  0  0  0  0  0  0  0  0
    5.3109    0.8124   -0.0422 O   0  0  0  0  0  0  0  0  0  0  0  0
    6.5989    1.3677    0.0898 C   0  0  1  0  0  0  0  0  0  0  0  0
    7.4136    0.6664    1.1521 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.9015   -0.6369    0.5604 C   0  0  2  0  0  0  0  0  0  0  0  0
    8.2966   -1.5466    1.4989 O   0  0  0  0  0  0  0  0  0  0  0  0
    7.5303   -2.7013    1.3554 C   0  0  0  0  0  0  0  0  0  0  0  0
    9.0321   -0.2611   -0.4030 C   0  0  2  0  0  0  0  0  0  0  0  0
   10.2331   -0.0686    0.2394 O   0  0  0  0  0  0  0  0  0  0  0  0
   11.2525   -0.8731   -0.2117 C   0  0  1  0  0  0  0  0  0  0  0  0
   12.3892   -0.1099   -0.8569 C   0  0  0  0  0  0  0  0  0  0  0  0
   13.5963   -1.0569   -0.8243 C   0  0  1  0  0  0  0  0  0  0  0  0
   14.6598   -0.5642   -1.5573 O   0  0  0  0  0  0  0  0  0  0  0  0
   15.0681   -1.4308   -2.5703 C   0  0  0  0  0  0  0  0  0  0  0  0
   14.0001   -1.1721    0.6238 C   0  0  2  0  0  0  0  0  0  0  0  0
   14.8567   -2.2338    0.8227 O   0  0  0  0  0  0  0  0  0  0  0  0
   12.7529   -1.2582    1.5048 C   0  0  1  0  0  0  0  0  0  0  0  0
   12.5139    0.0125    2.2549 C   0  0  0  0  0  0  0  0  0  0  0  0
   11.6577   -1.7124    0.7945 O   0  0  0  0  0  0  0  0  0  0  0  0
    8.6120    1.0594   -1.0178 C   0  0  1  0  0  0  0  0  0  0  0  0
    9.2064    1.1384   -2.4161 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.2484    1.1782   -1.1528 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.3599    1.4943    1.2095 C   0  0  1  0  0  0  0  0  0  0  0  0
    4.0725    1.1881    2.4996 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.3899    2.4497    1.3287 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0988    1.5333   -1.2167 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5702    1.3516   -1.2363 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.0057    0.2158   -0.3555 C   0  0  1  0  0  0  0  0  0  0  0  0
   -2.4960   -1.1235   -0.7834 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.5376    0.1419   -0.3216 C   0  0  1  0  0  0  0  0  0  0  0  0
   -5.1427    0.0231   -1.6613 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.6717    0.2398   -1.4535 C   0  0  1  0  0  0  0  0  0  0  0  0
   -7.1415    0.2318   -2.8114 O   0  0  0  0  0  0  0  0  0  0  0  0
   -7.5699    1.3520   -3.4846 C   0  0  0  0  0  0  0  0  0  0  0  0
   -8.0575    1.3315   -4.8876 C   0  0  0  0  0  0  0  0  0  0  0  0
   -7.5527    2.4549   -2.8930 O   0  0  0  0  0  0  0  0  0  0  0  0
   -7.1674   -0.9625   -0.7522 C   0  0  2  0  0  0  0  0  0  0  0  0
   -6.9133   -2.0977   -1.7815 C   0  0  0  0  0  0  0  0  0  0  0  0
  -12.0200    0.7912    1.5566 H   0  0  0  0  0  0  0  0  0  0  0  0
  -13.4792    0.5238    2.5731 H   0  0  0  0  0  0  0  0  0  0  0  0
  -12.5880   -0.9242    1.8675 H   0  0  0  0  0  0  0  0  0  0  0  0
  -14.8027   -0.0190    0.6977 H   0  0  0  0  0  0  0  0  0  0  0  0
  -13.6540    1.2310    0.0623 H   0  0  0  0  0  0  0  0  0  0  0  0
  -13.8549   -0.7644   -1.4315 H   0  0  0  0  0  0  0  0  0  0  0  0
  -13.2398   -2.8651   -0.8921 H   0  0  0  0  0  0  0  0  0  0  0  0
  -14.1237   -2.3453    0.5607 H   0  0  0  0  0  0  0  0  0  0  0  0
  -12.2889   -2.4481    0.5476 H   0  0  0  0  0  0  0  0  0  0  0  0
   -9.5721    0.3581   -1.6713 H   0  0  0  0  0  0  0  0  0  0  0  0
   -8.7292    2.2782   -0.4643 H   0  0  0  0  0  0  0  0  0  0  0  0
  -10.2497    1.9273    0.3138 H   0  0  0  0  0  0  0  0  0  0  0  0
   -8.7578    1.4295    1.0836 H   0  0  0  0  0  0  0  0  0  0  0  0
   -9.4810   -1.7736   -1.8330 H   0  0  0  0  0  0  0  0  0  0  0  0
   -9.3925   -0.8652    1.7609 H   0  0  0  0  0  0  0  0  0  0  0  0
   -8.6924   -2.4224    1.3198 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.9512   -1.6504    2.4975 H   0  0  0  0  0  0  0  0  0  0  0  0
   -7.0285    0.0801    1.9362 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.9208   -3.1443    1.2918 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.2906   -1.8658    0.2758 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.0389    0.2821    2.3173 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.8377   -1.5154    2.5887 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8900    0.0391    3.0739 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4846   -1.3570    2.0533 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.2029    1.5057    1.2895 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6340   -0.0847    1.3173 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0380    1.3773    2.2213 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6433    2.7848    0.4079 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.9149    3.4867    0.4375 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.1776    3.8240   -0.6015 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.0217    3.3448   -1.8505 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.1050    1.9571   -2.0566 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.8875    0.1076   -2.0770 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.8028    2.7377    0.2535 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.5527    2.4697    0.2676 H   0  0  0  0  0  0  0  0  0  0  0  0
    8.2870    1.3447    1.3590 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.8819    0.5083    2.0862 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.0901   -1.0308   -0.0672 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.6648   -3.1474    0.3294 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.8316   -3.4938    2.0666 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.4349   -2.4895    1.4378 H   0  0  0  0  0  0  0  0  0  0  0  0
    9.0812   -1.0436   -1.1930 H   0  0  0  0  0  0  0  0  0  0  0  0
   10.8277   -1.5214   -1.0332 H   0  0  0  0  0  0  0  0  0  0  0  0
   12.2012    0.0794   -1.9312 H   0  0  0  0  0  0  0  0  0  0  0  0
   12.6161    0.8274   -0.3428 H   0  0  0  0  0  0  0  0  0  0  0  0
   13.2582   -2.0496   -1.1708 H   0  0  0  0  0  0  0  0  0  0  0  0
   15.9190   -0.9319   -3.0826 H   0  0  0  0  0  0  0  0  0  0  0  0
   15.3264   -2.4364   -2.1981 H   0  0  0  0  0  0  0  0  0  0  0  0
   14.2377   -1.4429   -3.3233 H   0  0  0  0  0  0  0  0  0  0  0  0
   14.5124   -0.2142    0.8933 H   0  0  0  0  0  0  0  0  0  0  0  0
   14.7186   -2.6282    1.7189 H   0  0  0  0  0  0  0  0  0  0  0  0
   12.9919   -2.0471    2.2652 H   0  0  0  0  0  0  0  0  0  0  0  0
   11.4996    0.4227    2.1408 H   0  0  0  0  0  0  0  0  0  0  0  0
   12.6640   -0.1054    3.3671 H   0  0  0  0  0  0  0  0  0  0  0  0
   13.3101    0.7539    1.9598 H   0  0  0  0  0  0  0  0  0  0  0  0
    8.9946    1.9331   -0.4691 H   0  0  0  0  0  0  0  0  0  0  0  0
   10.2730    1.4289   -2.3939 H   0  0  0  0  0  0  0  0  0  0  0  0
    9.1322    0.1394   -2.8784 H   0  0  0  0  0  0  0  0  0  0  0  0
    8.6267    1.8503   -3.0265 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.8222    0.5408    0.9242 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.4475    1.2862    3.3843 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.9640    1.8825    2.5259 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.5099    0.1677    2.5073 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6356    0.6980   -1.7850 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8793    2.4469   -1.8484 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.0611    2.2664   -0.8526 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8671    1.2016   -2.3016 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2632   -1.8003    0.0754 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.2402   -1.5809   -1.4688 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5498   -1.0764   -1.3719 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.8817    1.0896    0.1474 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.8738    0.8593   -2.3576 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.0528   -0.9533   -2.1451 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.7211    1.1999   -0.9679 H   0  0  0  0  0  0  0  0  0  0  0  0
   -7.3332    1.9323   -5.4948 H   0  0  0  0  0  0  0  0  0  0  0  0
   -9.0221    1.8784   -4.9467 H   0  0  0  0  0  0  0  0  0  0  0  0
   -8.1584    0.2996   -5.2818 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.9587   -2.6351   -1.5348 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.9227   -1.7322   -2.8064 H   0  0  0  0  0  0  0  0  0  0  0  0
   -7.6913   -2.8821   -1.7097 H   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0
  2  3  1  0
  3  4  1  0
  3  5  1  0
  5  6  2  0
  5  7  1  0
  7  8  1  0
  8  9  1  0
  8 10  1  0
 10 11  1  6
 10 12  1  0
 12 13  1  0
 13 14  1  0
 14 15  1  6
 14 16  1  0
 16 17  1  0
 17 18  1  0
 18 19  1  0
 19 20  1  0
 20 21  1  0
 21 52  1  0
 52 53  1  0
 53 54  1  0
 54 55  1  6
 54 56  1  0
 56 57  1  0
 57 58  1  0
 58 59  1  0
 59 60  1  0
 60 61  1  0
 60 62  2  0
 58 63  1  0
 63 64  1  6
 21 22  1  0
 22 23  1  0
 23 24  1  0
 24 25  1  0
 25 26  1  0
 25 27  1  0
 27 28  1  0
 28 29  1  0
 29 30  1  0
 30 31  1  0
 31 32  1  0
 32 33  1  0
 31 34  1  0
 34 35  1  0
 35 36  1  0
 36 37  1  0
 37 38  1  0
 38 39  1  0
 39 40  1  0
 38 41  1  0
 41 42  1  0
 41 43  1  0
 43 44  1  0
 43 45  1  0
 34 46  1  0
 46 47  1  0
 46 48  1  0
 27 49  1  0
 49 50  1  0
 49 51  1  0
 63 10  1  0
 51 23  1  0
 63 14  1  0
 48 29  1  0
 56 16  1  0
 45 36  1  0
 54 19  1  0
  1 65  1  0
  1 66  1  0
  1 67  1  0
  2 68  1  0
  2 69  1  0
  3 70  1  6
  4 71  1  0
  4 72  1  0
  4 73  1  0
  8 74  1  6
  9 75  1  0
  9 76  1  0
  9 77  1  0
 11 78  1  0
 12 79  1  0
 12 80  1  0
 13 81  1  0
 13 82  1  0
 15 83  1  0
 16 84  1  6
 17 85  1  0
 17 86  1  0
 18 87  1  0
 18 88  1  0
 19 89  1  1
 20 90  1  0
 20 91  1  0
 21 92  1  1
 52128  1  0
 52129  1  0
 53130  1  0
 53131  1  0
 55132  1  0
 55133  1  0
 55134  1  0
 56135  1  1
 57136  1  0
 57137  1  0
 58138  1  1
 61139  1  0
 61140  1  0
 61141  1  0
 64142  1  0
 64143  1  0
 64144  1  0
 23 93  1  1
 24 94  1  0
 24 95  1  0
 25 96  1  6
 26 97  1  0
 27 98  1  1
 29 99  1  1
 30100  1  0
 30101  1  0
 31102  1  6
 33103  1  0
 33104  1  0
 33105  1  0
 34106  1  6
 36107  1  6
 37108  1  0
 37109  1  0
 38110  1  6
 40111  1  0
 40112  1  0
 40113  1  0
 41114  1  1
 42115  1  0
 43116  1  1
 44117  1  0
 44118  1  0
 44119  1  0
 46120  1  1
 47121  1  0
 47122  1  0
 47123  1  0
 49124  1  6
 50125  1  0
 50126  1  0
 50127  1  0
M  END


  Mrv1652304282220302D          

 64 70  0  0  1  0            999 V2000
    4.2475    2.1537    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.5278    1.3777    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    3.9960    0.7470    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.1838    0.8922    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    2.9035    1.6682    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    3.4354    2.2989    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.0914    1.8134    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    1.5596    1.1827    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    1.8399    0.4067    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.6520    0.2615    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7475    1.3279    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    0.4672    2.1038    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    0.9990    2.7345    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    1.8111    2.5893    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7187    3.5104    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.2505    4.1411    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.9702    4.9171    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.0626    3.9959    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3574    2.0770    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
   -0.5867    1.2845    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0962    0.8215    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1183    2.3959    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
   -1.7749    1.8964    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5357    2.2152    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6400    3.0336    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.1923    1.7157    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
   -3.9532    2.0346    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.6098    1.5351    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.0880    0.8974    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2225    3.2143    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4788    2.8930    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.1073    2.8462    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.9451    0.5269    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.6232    2.4441    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.3399    1.2325    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.8717    1.8632    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    6.6838    1.7180    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    7.2157    2.3487    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    6.9354    3.1246    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    6.1232    3.2699    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    5.5914    2.6391    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.8429    4.0458    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    7.4672    3.7553    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    8.2793    3.6101    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    8.8111    4.2408    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    9.6232    4.0956    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    9.9035    3.3197    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    9.3717    2.6890    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    8.5596    2.8342    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    9.6520    1.9131    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   10.7157    3.1745    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   11.2475    3.8052    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
   12.0596    3.6600    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   12.5914    4.2907    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
   12.3111    5.0666    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
   11.4990    5.2118    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
   10.9672    4.5811    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   11.2187    5.9877    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   11.7505    6.6185    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   12.8429    5.6973    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   13.4035    4.1455    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   10.1551    4.7263    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    9.8748    5.5023    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.0278    2.2035    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0  0  0  0
  2  3  1  0  0  0  0
  4  3  1  6  0  0  0
  4  5  1  0  0  0  0
  5  6  1  0  0  0  0
  1  6  1  0  0  0  0
  5  7  1  0  0  0  0
  7  8  1  0  0  0  0
  8  9  1  1  0  0  0
  9 10  1  0  0  0  0
  4 10  1  0  0  0  0
  8 11  1  0  0  0  0
 11 12  1  0  0  0  0
 12 13  1  0  0  0  0
 13 14  1  0  0  0  0
  7 14  1  6  0  0  0
 13 15  1  6  0  0  0
 15 16  1  0  0  0  0
 16 17  2  0  0  0  0
 16 18  1  0  0  0  0
 12 19  1  0  0  0  0
 19 20  1  0  0  0  0
 20 21  1  0  0  0  0
 11 21  1  0  0  0  0
 19 22  1  1  0  0  0
 22 23  1  0  0  0  0
 23 24  1  0  0  0  0
 24 25  2  0  0  0  0
 24 26  1  0  0  0  0
 26 27  1  0  0  0  0
 27 28  1  0  0  0  0
 26 29  1  1  0  0  0
 22 30  1  1  0  0  0
 19 31  1  6  0  0  0
 12 32  1  6  0  0  0
 11 33  1  6  0  0  0
  5 34  1  6  0  0  0
  2 35  1  6  0  0  0
 36 35  1  6  0  0  0
 36 37  1  0  0  0  0
 37 38  1  0  0  0  0
 38 39  1  0  0  0  0
 39 40  1  0  0  0  0
 40 41  1  0  0  0  0
 36 41  1  0  0  0  0
 40 42  1  6  0  0  0
 39 43  1  6  0  0  0
 44 43  1  1  0  0  0
 44 45  1  0  0  0  0
 45 46  1  0  0  0  0
 46 47  1  0  0  0  0
 47 48  1  0  0  0  0
 48 49  1  0  0  0  0
 44 49  1  0  0  0  0
 48 50  1  1  0  0  0
 47 51  1  6  0  0  0
 52 51  1  1  0  0  0
 52 53  1  0  0  0  0
 53 54  1  0  0  0  0
 54 55  1  0  0  0  0
 55 56  1  0  0  0  0
 56 57  1  0  0  0  0
 52 57  1  0  0  0  0
 56 58  1  1  0  0  0
 58 59  1  0  0  0  0
 55 60  1  6  0  0  0
 54 61  1  1  0  0  0
 46 62  1  6  0  0  0
 62 63  1  0  0  0  0
 38 64  1  1  0  0  0
M  END
> <DATABASE_ID>
NP0073225

> <DATABASE_NAME>
NP-MRD

> <SMILES>
CC[C@H](C)C(=O)O[C@@H](C)[C@]1(O)CC[C@]2(O)[C@@H]3CC[C@H]4C[C@H](CC[C@]4(C)[C@H]3C[C@@H](OC(C)=O)[C@]12C)O[C@@H]1C[C@H](O)[C@H](O[C@H]2C[C@H](OC)[C@H](O[C@H]3C[C@@H](OC)[C@H](O)[C@@H](C)O3)[C@@H](C)O2)[C@@H](C)O1

> <INCHI_IDENTIFIER>
InChI=1S/C48H80O16/c1-12-24(2)44(52)60-28(6)47(53)17-18-48(54)32-14-13-30-19-31(15-16-45(30,8)33(32)20-37(46(47,48)9)61-29(7)49)62-38-21-34(50)42(26(4)58-38)63-40-23-36(56-11)43(27(5)59-40)64-39-22-35(55-10)41(51)25(3)57-39/h24-28,30-43,50-51,53-54H,12-23H2,1-11H3/t24-,25+,26+,27+,28-,30-,31-,32+,33-,34-,35+,36-,37+,38+,39-,40-,41+,42+,43+,45-,46+,47+,48-/m0/s1

> <INCHI_KEY>
YXOYGVIDDCWYNT-DXGBTZFSSA-N

> <FORMULA>
C48H80O16

> <MOLECULAR_WEIGHT>
913.152

> <EXACT_MASS>
912.544636496

> <JCHEM_ACCEPTOR_COUNT>
14

> <JCHEM_ATOM_COUNT>
144

> <JCHEM_AVERAGE_POLARIZABILITY>
101.5227191619777

> <JCHEM_BIOAVAILABILITY>
0

> <JCHEM_DONOR_COUNT>
4

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
0

> <JCHEM_IUPAC>
(1S)-1-[(1S,2S,5S,7S,10R,11S,14S,15S,16R)-16-(acetyloxy)-11,14-dihydroxy-5-{[(2S,4S,5S,6R)-4-hydroxy-5-{[(2S,4S,5R,6R)-5-{[(2S,4R,5R,6R)-5-hydroxy-4-methoxy-6-methyloxan-2-yl]oxy}-4-methoxy-6-methyloxan-2-yl]oxy}-6-methyloxan-2-yl]oxy}-2,15-dimethyltetracyclo[8.7.0.0^{2,7}.0^{11,15}]heptadecan-14-yl]ethyl (2S)-2-methylbutanoate

> <ALOGPS_LOGP>
3.54

> <JCHEM_LOGP>
4.928573225666666

> <ALOGPS_LOGS>
-4.89

> <JCHEM_MDDR_LIKE_RULE>
1

> <JCHEM_NUMBER_OF_RINGS>
7

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA>
13.38454349317406

> <JCHEM_PKA_STRONGEST_ACIDIC>
12.875231343678518

> <JCHEM_PKA_STRONGEST_BASIC>
-3.233537056844188

> <JCHEM_POLAR_SURFACE_AREA>
207.35999999999993

> <JCHEM_REFRACTIVITY>
227.88299999999998

> <JCHEM_ROTATABLE_BOND_COUNT>
15

> <JCHEM_RULE_OF_FIVE>
0

> <ALOGPS_SOLUBILITY>
1.17e-02 g/l

> <JCHEM_TRADITIONAL_IUPAC>
(1S)-1-[(1S,2S,5S,7S,10R,11S,14S,15S,16R)-16-(acetyloxy)-11,14-dihydroxy-5-{[(2S,4S,5S,6R)-4-hydroxy-5-{[(2S,4S,5R,6R)-5-{[(2S,4R,5R,6R)-5-hydroxy-4-methoxy-6-methyloxan-2-yl]oxy}-4-methoxy-6-methyloxan-2-yl]oxy}-6-methyloxan-2-yl]oxy}-2,15-dimethyltetracyclo[8.7.0.0^{2,7}.0^{11,15}]heptadecan-14-yl]ethyl (2S)-2-methylbutanoate

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 28-APR-22   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   28-APR-22         0                                  
HETATM    1  C   UNK     0       7.929   4.020   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0       8.452   2.572   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0       7.459   1.394   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0       5.943   1.666   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0       5.420   3.114   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0       6.413   4.291   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0       3.904   3.385   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0       2.911   2.208   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0       3.434   0.759   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0       4.950   0.488   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0       1.395   2.479   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0       0.872   3.927   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0       1.865   5.104   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0       3.381   4.833   0.000  0.00  0.00           C+0
HETATM   15  O   UNK     0       1.342   6.553   0.000  0.00  0.00           O+0
HETATM   16  C   UNK     0       2.334   7.730   0.000  0.00  0.00           C+0
HETATM   17  O   UNK     0       1.811   9.179   0.000  0.00  0.00           O+0
HETATM   18  C   UNK     0       3.850   7.459   0.000  0.00  0.00           C+0
HETATM   19  C   UNK     0      -0.667   3.877   0.000  0.00  0.00           C+0
HETATM   20  C   UNK     0      -1.095   2.398   0.000  0.00  0.00           C+0
HETATM   21  C   UNK     0       0.179   1.534   0.000  0.00  0.00           C+0
HETATM   22  C   UNK     0      -2.087   4.472   0.000  0.00  0.00           C+0
HETATM   23  O   UNK     0      -3.313   3.540   0.000  0.00  0.00           O+0
HETATM   24  C   UNK     0      -4.733   4.135   0.000  0.00  0.00           C+0
HETATM   25  O   UNK     0      -4.928   5.663   0.000  0.00  0.00           O+0
HETATM   26  C   UNK     0      -5.959   3.203   0.000  0.00  0.00           C+0
HETATM   27  C   UNK     0      -7.379   3.798   0.000  0.00  0.00           C+0
HETATM   28  C   UNK     0      -8.605   2.866   0.000  0.00  0.00           C+0
HETATM   29  C   UNK     0      -5.764   1.675   0.000  0.00  0.00           C+0
HETATM   30  C   UNK     0      -2.282   6.000   0.000  0.00  0.00           C+0
HETATM   31  O   UNK     0      -0.894   5.400   0.000  0.00  0.00           O+0
HETATM   32  C   UNK     0       0.200   5.313   0.000  0.00  0.00           C+0
HETATM   33  O   UNK     0       1.764   0.984   0.000  0.00  0.00           O+0
HETATM   34  C   UNK     0       4.897   4.562   0.000  0.00  0.00           C+0
HETATM   35  O   UNK     0       9.968   2.301   0.000  0.00  0.00           O+0
HETATM   36  C   UNK     0      10.961   3.478   0.000  0.00  0.00           C+0
HETATM   37  O   UNK     0      12.477   3.207   0.000  0.00  0.00           O+0
HETATM   38  C   UNK     0      13.469   4.384   0.000  0.00  0.00           C+0
HETATM   39  C   UNK     0      12.946   5.833   0.000  0.00  0.00           C+0
HETATM   40  C   UNK     0      11.430   6.104   0.000  0.00  0.00           C+0
HETATM   41  C   UNK     0      10.437   4.926   0.000  0.00  0.00           C+0
HETATM   42  O   UNK     0      10.907   7.552   0.000  0.00  0.00           O+0
HETATM   43  O   UNK     0      13.939   7.010   0.000  0.00  0.00           O+0
HETATM   44  C   UNK     0      15.455   6.739   0.000  0.00  0.00           C+0
HETATM   45  C   UNK     0      16.447   7.916   0.000  0.00  0.00           C+0
HETATM   46  C   UNK     0      17.963   7.645   0.000  0.00  0.00           C+0
HETATM   47  C   UNK     0      18.487   6.197   0.000  0.00  0.00           C+0
HETATM   48  C   UNK     0      17.494   5.019   0.000  0.00  0.00           C+0
HETATM   49  O   UNK     0      15.978   5.291   0.000  0.00  0.00           O+0
HETATM   50  C   UNK     0      18.017   3.571   0.000  0.00  0.00           C+0
HETATM   51  O   UNK     0      20.003   5.926   0.000  0.00  0.00           O+0
HETATM   52  C   UNK     0      20.995   7.103   0.000  0.00  0.00           C+0
HETATM   53  O   UNK     0      22.511   6.832   0.000  0.00  0.00           O+0
HETATM   54  C   UNK     0      23.504   8.009   0.000  0.00  0.00           C+0
HETATM   55  C   UNK     0      22.981   9.458   0.000  0.00  0.00           C+0
HETATM   56  C   UNK     0      21.465   9.729   0.000  0.00  0.00           C+0
HETATM   57  C   UNK     0      20.472   8.551   0.000  0.00  0.00           C+0
HETATM   58  O   UNK     0      20.942  11.177   0.000  0.00  0.00           O+0
HETATM   59  C   UNK     0      21.934  12.354   0.000  0.00  0.00           C+0
HETATM   60  O   UNK     0      23.973  10.635   0.000  0.00  0.00           O+0
HETATM   61  C   UNK     0      25.020   7.738   0.000  0.00  0.00           C+0
HETATM   62  O   UNK     0      18.956   8.822   0.000  0.00  0.00           O+0
HETATM   63  C   UNK     0      18.433  10.271   0.000  0.00  0.00           C+0
HETATM   64  C   UNK     0      14.985   4.113   0.000  0.00  0.00           C+0
CONECT    1    2    6                                                       
CONECT    2    1    3   35                                                  
CONECT    3    2    4                                                       
CONECT    4    3    5   10                                                  
CONECT    5    4    6    7   34                                             
CONECT    6    5    1                                                       
CONECT    7    5    8   14                                                  
CONECT    8    7    9   11                                                  
CONECT    9    8   10                                                       
CONECT   10    9    4                                                       
CONECT   11    8   12   21   33                                             
CONECT   12   11   13   19   32                                             
CONECT   13   12   14   15                                                  
CONECT   14   13    7                                                       
CONECT   15   13   16                                                       
CONECT   16   15   17   18                                                  
CONECT   17   16                                                            
CONECT   18   16                                                            
CONECT   19   12   20   22   31                                             
CONECT   20   19   21                                                       
CONECT   21   20   11                                                       
CONECT   22   19   23   30                                                  
CONECT   23   22   24                                                       
CONECT   24   23   25   26                                                  
CONECT   25   24                                                            
CONECT   26   24   27   29                                                  
CONECT   27   26   28                                                       
CONECT   28   27                                                            
CONECT   29   26                                                            
CONECT   30   22                                                            
CONECT   31   19                                                            
CONECT   32   12                                                            
CONECT   33   11                                                            
CONECT   34    5                                                            
CONECT   35    2   36                                                       
CONECT   36   35   37   41                                                  
CONECT   37   36   38                                                       
CONECT   38   37   39   64                                                  
CONECT   39   38   40   43                                                  
CONECT   40   39   41   42                                                  
CONECT   41   40   36                                                       
CONECT   42   40                                                            
CONECT   43   39   44                                                       
CONECT   44   43   45   49                                                  
CONECT   45   44   46                                                       
CONECT   46   45   47   62                                                  
CONECT   47   46   48   51                                                  
CONECT   48   47   49   50                                                  
CONECT   49   48   44                                                       
CONECT   50   48                                                            
CONECT   51   47   52                                                       
CONECT   52   51   53   57                                                  
CONECT   53   52   54                                                       
CONECT   54   53   55   61                                                  
CONECT   55   54   56   60                                                  
CONECT   56   55   57   58                                                  
CONECT   57   56   52                                                       
CONECT   58   56   59                                                       
CONECT   59   58                                                            
CONECT   60   55                                                            
CONECT   61   54                                                            
CONECT   62   46   63                                                       
CONECT   63   62                                                            
CONECT   64   38                                                            
MASTER        0    0    0    0    0    0    0    0   64    0  140    0
END

View in JSmol

Synonyms

Value	Source
(1S)-1-[(1S,2S,5S,7S,10R,11S,14S,15S,16R)-16-(Acetyloxy)-11,14-dihydroxy-5-{[(2S,4S,5S,6R)-4-hydroxy-5-{[(2S,4S,5R,6R)-5-{[(2S,4R,5R,6R)-5-hydroxy-4-methoxy-6-methyloxan-2-yl]oxy}-4-methoxy-6-methyloxan-2-yl]oxy}-6-methyloxan-2-yl]oxy}-2,15-dimethyltetracyclo[8.7.0.0,.0,]heptadecan-14-yl]ethyl (2S)-2-methylbutanoic acid	Generator

Chemical Formula

C₄₈H₈₀O₁₆

Average Mass

913.1520 Da

Monoisotopic Mass

912.54464 Da

IUPAC Name

Traditional Name

CAS Registry Number

Not Available

SMILES

CC[C@H](C)C(=O)O[C@@H](C)[C@]1(O)CC[C@]2(O)[C@@H]3CC[C@H]4C[C@H](CC[C@]4(C)[C@H]3C[C@@H](OC(C)=O)[C@]12C)O[C@@H]1C[C@H](O)[C@H](O[C@H]2C[C@H](OC)[C@H](O[C@H]3C[C@@H](OC)[C@H](O)[C@@H](C)O3)[C@@H](C)O2)[C@@H](C)O1

InChI Identifier

InChI=1S/C48H80O16/c1-12-24(2)44(52)60-28(6)47(53)17-18-48(54)32-14-13-30-19-31(15-16-45(30,8)33(32)20-37(46(47,48)9)61-29(7)49)62-38-21-34(50)42(26(4)58-38)63-40-23-36(56-11)43(27(5)59-40)64-39-22-35(55-10)41(51)25(3)57-39/h24-28,30-43,50-51,53-54H,12-23H2,1-11H3/t24-,25+,26+,27+,28-,30-,31-,32+,33-,34-,35+,36-,37+,38+,39-,40-,41+,42+,43+,45-,46+,47+,48-/m0/s1

InChI Key

YXOYGVIDDCWYNT-DXGBTZFSSA-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
Telosma procumbens	Plant	KNApSAcK

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as steroidal glycosides. These are sterol lipids containing a carbohydrate moiety glycosidically linked to the steroid skeleton.

Kingdom

Organic compounds

Super Class

Lipids and lipid-like molecules

Class

Steroids and steroid derivatives

Sub Class

Steroidal glycosides

Direct Parent

Steroidal glycosides

Alternative Parents

Substituents

Steroidal glycoside
Oligosaccharide
Pregnane-skeleton
Steroid ester
17-hydroxysteroid
Hydroxysteroid
14-hydroxysteroid
O-glycosyl compound
Glycosyl compound
Oxane
Dicarboxylic acid or derivatives
Tertiary alcohol
Cyclic alcohol
Secondary alcohol
Carboxylic acid ester
Oxacycle
Organoheterocyclic compound
Ether
Dialkyl ether
Carboxylic acid derivative
Acetal
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	3.54	ALOGPS
logP	4.93	ChemAxon
logS	-4.9	ALOGPS
pKa (Strongest Acidic)	12.88	ChemAxon
pKa (Strongest Basic)	-3.2	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	14	ChemAxon
Hydrogen Donor Count	4	ChemAxon
Polar Surface Area	207.36 Å²	ChemAxon
Rotatable Bond Count	15	ChemAxon
Refractivity	227.88 m³·mol⁻¹	ChemAxon
Polarizability	101.52 Å³	ChemAxon
Number of Rings	7	ChemAxon
Bioavailability	No	ChemAxon
Rule of Five	No	ChemAxon
Ghose Filter	No	ChemAxon
Veber's Rule	No	ChemAxon
MDDR-like Rule	Yes	ChemAxon

External Links

HMDB ID

Not Available

DrugBank ID

Not Available

Phenol Explorer Compound ID

Not Available

FoodDB ID

Not Available

KNApSAcK ID

Not Available

Chemspider ID

Not Available

KEGG Compound ID

Not Available

BioCyc ID

Not Available

BiGG ID

Not Available

Wikipedia Link

Not Available

METLIN ID

Not Available

PubChem Compound

162844071

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

Not Available

Showing NP-Card for (-)-Telosmoside A6 (NP0073225)

MOL for NP0073225 ((-)-Telosmoside A6)

3D MOL for NP0073225 ((-)-Telosmoside A6)

3D SDF for NP0073225 ((-)-Telosmoside A6)

3D-SDF for NP0073225 ((-)-Telosmoside A6)

PDB for NP0073225 ((-)-Telosmoside A6)

3D PDB for NP0073225 ((-)-Telosmoside A6)

SMILES for NP0073225 ((-)-Telosmoside A6)

INCHI for NP0073225 ((-)-Telosmoside A6)

Structure for NP0073225 ((-)-Telosmoside A6)

3D Structure for NP0073225 ((-)-Telosmoside A6)