NP-MRD: Showing NP-Card for (-)-Asparanin A (NP0073710)

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Record Information

Version

2.0

Created at

2022-04-28 18:55:59 UTC

Updated at

2022-04-28 18:55:59 UTC

NP-MRD ID

NP0073710

Secondary Accession Numbers

None

Natural Product Identification

Common Name

(-)-Asparanin A

Description

(2S,3R,4S,5R,6R)-2-{[(2R,3R,4S,5R,6R)-4,5-dihydroxy-6-(hydroxymethyl)-2-[(1'R,2R,2'S,4'S,5S,7'S,8'R,9'R,12'S,13'S,16'S,18'S)-2',5,7',13'-tetramethyl-5'-oxaspiro[oxane-2,6'-pentacyclo[10.8.0.0²,⁹.0⁴,⁸.0¹³,¹⁸]Icosane]oxy]oxan-3-yl]oxy}-6-(hydroxymethyl)oxane-3,4,5-triol 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. (-)-Asparanin A is found in Asparagus oligoclonos and Asparagus racemosus . Based on a literature review very few articles have been published on (2S,3R,4S,5R,6R)-2-{[(2R,3R,4S,5R,6R)-4,5-dihydroxy-6-(hydroxymethyl)-2-[(1'R,2R,2'S,4'S,5S,7'S,8'R,9'R,12'S,13'S,16'S,18'S)-2',5,7',13'-tetramethyl-5'-oxaspiro[oxane-2,6'-pentacyclo[10.8.0.0²,⁹.0⁴,⁸.0¹³,¹⁸]Icosane]oxy]oxan-3-yl]oxy}-6-(hydroxymethyl)oxane-3,4,5-triol.

Structure

MOL 3D MOL SDF PDB SMILES InChI


  Mrv1652304282220562D          

 52 59  0  0  1  0            999 V2000
    7.0487    4.8600    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.4190    4.1227    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    6.9656    3.4334    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.1420    3.4814    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    5.7717    4.2186    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    6.2251    4.9079    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.9481    4.2665    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    4.4948    3.5773    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    4.8651    2.8400    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.6887    2.7921    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.6712    3.6252    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    3.3009    4.3624    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    3.7543    5.0517    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.5779    5.0038    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.4854    4.2381    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    2.3516    3.4240    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    3.0845    3.0452    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.5360    3.2997    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.1657    4.0369    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    1.7525    4.6169    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    1.6281    5.4324    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.6428    3.3988    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1712    3.5325    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4624    4.3044    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    0.0604    4.9426    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.8745    4.8088    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2765    4.4382    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.9624    2.8533    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.4015    4.9558    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.2426    4.0748    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    8.6959    4.7641    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    8.3256    5.5013    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    8.7789    6.1906    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    9.6025    6.1427    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    9.9728    5.4054    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    9.5195    4.7161    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    9.8898    3.9789    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   10.7134    3.9310    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
   11.0837    3.1937    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
   11.9073    3.1458    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
   12.3606    3.8351    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
   11.9903    4.5723    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
   11.1667    4.6202    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   12.4436    5.2616    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   13.2672    5.2137    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   13.1842    3.7871    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   12.2776    2.4085    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   10.6303    2.5044    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   10.7964    5.3575    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   10.0559    6.8319    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    8.4086    6.9278    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.5850    6.9758    0.0000 O   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  1  0  0  0
 13 14  1  0  0  0  0
  7 14  1  6  0  0  0
 15 12  1  1  0  0  0
 15 16  1  0  0  0  0
 16 17  1  0  0  0  0
 11 17  1  0  0  0  0
 16 18  1  6  0  0  0
 19 18  1  6  0  0  0
 19 20  1  0  0  0  0
 15 20  1  0  0  0  0
 20 21  1  1  0  0  0
 19 22  1  0  0  0  0
 22 23  1  0  0  0  0
 23 24  1  0  0  0  0
 24 25  1  0  0  0  0
 25 26  1  0  0  0  0
 19 26  1  0  0  0  0
 24 27  1  1  0  0  0
 11 28  1  1  0  0  0
  5 29  1  6  0  0  0
  2 30  1  6  0  0  0
 31 30  1  6  0  0  0
 31 32  1  0  0  0  0
 32 33  1  0  0  0  0
 33 34  1  0  0  0  0
 34 35  1  0  0  0  0
 35 36  1  0  0  0  0
 31 36  1  0  0  0  0
 36 37  1  1  0  0  0
 38 37  1  6  0  0  0
 38 39  1  0  0  0  0
 39 40  1  0  0  0  0
 40 41  1  0  0  0  0
 41 42  1  0  0  0  0
 42 43  1  0  0  0  0
 38 43  1  0  0  0  0
 42 44  1  6  0  0  0
 44 45  1  0  0  0  0
 41 46  1  6  0  0  0
 40 47  1  6  0  0  0
 39 48  1  1  0  0  0
 35 49  1  6  0  0  0
 34 50  1  6  0  0  0
 33 51  1  6  0  0  0
 51 52  1  0  0  0  0
M  END

     RDKit          3D

116123  0  0  0  0  0  0  0  0999 V2000
   11.5968    0.4501    1.4530 C   0  0  0  0  0  0  0  0  0  0  0  0
   10.8378    0.3254    0.1329 C   0  0  1  0  0  0  0  0  0  0  0  0
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    7.2598   -0.1748   -1.3963 O   0  0  0  0  0  0  0  0  0  0  0  0
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    4.8467   -0.5825   -1.7248 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.7714    0.1155   -0.8826 C   0  0  1  0  0  0  0  0  0  0  0  0
    3.5685    1.4804   -1.4205 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.4882   -0.5731   -0.7757 C   0  0  2  0  0  0  0  0  0  0  0  0
    1.6568   -0.5769   -2.0326 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.4051   -1.3871   -1.8384 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3373   -0.9158   -0.6219 C   0  0  1  0  0  0  0  0  0  0  0  0
   -1.6548   -1.5737   -0.4209 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3492   -0.9306    0.7604 C   0  0  1  0  0  0  0  0  0  0  0  0
   -3.6162   -1.4657    0.8267 O   0  0  0  0  0  0  0  0  0  0  0  0
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   -5.3291   -0.6065    1.9429 O   0  0  0  0  0  0  0  0  0  0  0  0
   -6.4030   -1.4468    1.9851 C   0  0  2  0  0  0  0  0  0  0  0  0
   -6.6561   -1.8774    3.4001 C   0  0  0  0  0  0  0  0  0  0  0  0
   -7.7467   -2.7361    3.4953 O   0  0  0  0  0  0  0  0  0  0  0  0
   -6.3263   -2.6217    1.0380 C   0  0  2  0  0  0  0  0  0  0  0  0
   -5.2619   -3.4215    1.4374 O   0  0  0  0  0  0  0  0  0  0  0  0
   -6.2008   -2.1775   -0.3984 C   0  0  2  0  0  0  0  0  0  0  0  0
   -5.3836   -3.1071   -1.0420 O   0  0  0  0  0  0  0  0  0  0  0  0
   -5.5633   -0.8020   -0.4609 C   0  0  1  0  0  0  0  0  0  0  0  0
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   -7.5051    0.9668   -3.9317 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5118   -1.2358    1.9815 C   0  0  0  0  0  0  0  0  0  0  0  0
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    0.5572   -0.9347    0.6129 C   0  0  1  0  0  0  0  0  0  0  0  0
    1.1467   -2.3045    0.8617 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.6590    0.0835    0.2955 C   0  0  1  0  0  0  0  0  0  0  0  0
    2.3218    0.5334    1.5141 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.7473    1.0722    1.3220 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.4532    0.0670    0.4941 C   0  0  2  0  0  0  0  0  0  0  0  0
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    0.4969   -2.8296    1.6144 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.1767   -2.9533   -0.0116 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.1268   -2.1877    1.3857 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.0900    0.9588   -0.1424 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.7527    1.3910    1.9590 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.3921   -0.2436    2.3016 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.2140    1.0776    2.3354 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.6292    2.0674    0.9068 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.1115   -0.9302    0.9373 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.2386   -1.0301    0.3782 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.2414    0.6933    1.7187 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.2342    2.6895   -0.5414 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.5065    2.8741    1.1957 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.8591    2.8542    0.5746 H   0  0  0  0  0  0  0  0  0  0  0  0
 52 51  1  0
 51 50  1  0
 50  9  1  0
  9 10  1  0
 10 11  1  0
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 11 49  1  0
 49 48  1  0
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 49111  1  1
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  2 56  1  6
  1 53  1  0
  1 54  1  0
  1 55  1  0
  7 61  1  0
  7 62  1  0
M  END


  Mrv1652304282220562D          

 52 59  0  0  1  0            999 V2000
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    7.4190    4.1227    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    6.9656    3.4334    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.1420    3.4814    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    5.7717    4.2186    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    6.2251    4.9079    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.9481    4.2665    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    4.4948    3.5773    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    4.8651    2.8400    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.6887    2.7921    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.6712    3.6252    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    3.3009    4.3624    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    3.7543    5.0517    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.5779    5.0038    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.4854    4.2381    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    2.3516    3.4240    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    3.0845    3.0452    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
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    1.7525    4.6169    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    1.6281    5.4324    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.6428    3.3988    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1712    3.5325    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4624    4.3044    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    0.0604    4.9426    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.8745    4.8088    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2765    4.4382    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.9624    2.8533    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.4015    4.9558    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.2426    4.0748    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    8.6959    4.7641    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    8.3256    5.5013    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    8.7789    6.1906    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    9.6025    6.1427    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    9.9728    5.4054    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    9.5195    4.7161    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    9.8898    3.9789    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   10.7134    3.9310    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
   11.0837    3.1937    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
   11.9073    3.1458    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
   12.3606    3.8351    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
   11.9903    4.5723    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
   11.1667    4.6202    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   12.4436    5.2616    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   13.2672    5.2137    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   13.1842    3.7871    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   12.2776    2.4085    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   10.6303    2.5044    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   10.7964    5.3575    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   10.0559    6.8319    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    8.4086    6.9278    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.5850    6.9758    0.0000 O   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  1  0  0  0
 13 14  1  0  0  0  0
  7 14  1  6  0  0  0
 15 12  1  1  0  0  0
 15 16  1  0  0  0  0
 16 17  1  0  0  0  0
 11 17  1  0  0  0  0
 16 18  1  6  0  0  0
 19 18  1  6  0  0  0
 19 20  1  0  0  0  0
 15 20  1  0  0  0  0
 20 21  1  1  0  0  0
 19 22  1  0  0  0  0
 22 23  1  0  0  0  0
 23 24  1  0  0  0  0
 24 25  1  0  0  0  0
 25 26  1  0  0  0  0
 19 26  1  0  0  0  0
 24 27  1  1  0  0  0
 11 28  1  1  0  0  0
  5 29  1  6  0  0  0
  2 30  1  6  0  0  0
 31 30  1  6  0  0  0
 31 32  1  0  0  0  0
 32 33  1  0  0  0  0
 33 34  1  0  0  0  0
 34 35  1  0  0  0  0
 35 36  1  0  0  0  0
 31 36  1  0  0  0  0
 36 37  1  1  0  0  0
 38 37  1  6  0  0  0
 38 39  1  0  0  0  0
 39 40  1  0  0  0  0
 40 41  1  0  0  0  0
 41 42  1  0  0  0  0
 42 43  1  0  0  0  0
 38 43  1  0  0  0  0
 42 44  1  6  0  0  0
 44 45  1  0  0  0  0
 41 46  1  6  0  0  0
 40 47  1  6  0  0  0
 39 48  1  1  0  0  0
 35 49  1  6  0  0  0
 34 50  1  6  0  0  0
 33 51  1  6  0  0  0
 51 52  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0073710

> <DATABASE_NAME>
NP-MRD

> <SMILES>
C[C@H]1[C@@H]2[C@H](C[C@]3(C)[C@@H]2CC[C@H]2[C@H]3CC[C@H]3C[C@H](CC[C@]23C)O[C@@H]2O[C@H](CO)[C@H](O)[C@H](O)[C@H]2O[C@@H]2O[C@H](CO)[C@H](O)[C@H](O)[C@H]2O)O[C@]11CC[C@H](C)CO1

> <INCHI_IDENTIFIER>
InChI=1S/C39H64O13/c1-18-9-12-39(47-17-18)19(2)28-24-8-7-22-23(38(24,4)14-25(28)52-39)6-5-20-13-21(10-11-37(20,22)3)48-36-34(32(45)30(43)27(16-41)50-36)51-35-33(46)31(44)29(42)26(15-40)49-35/h18-36,40-46H,5-17H2,1-4H3/t18-,19-,20-,21-,22-,23+,24+,25-,26+,27+,28-,29-,30-,31-,32-,33+,34+,35-,36+,37-,38-,39+/m0/s1

> <INCHI_KEY>
IATIAUOAJIFOSI-XVTUODIHSA-N

> <FORMULA>
C39H64O13

> <MOLECULAR_WEIGHT>
740.928

> <EXACT_MASS>
740.434692121

> <JCHEM_ACCEPTOR_COUNT>
13

> <JCHEM_ATOM_COUNT>
116

> <JCHEM_AVERAGE_POLARIZABILITY>
83.03638488162244

> <JCHEM_BIOAVAILABILITY>
0

> <JCHEM_DONOR_COUNT>
7

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
0

> <JCHEM_IUPAC>
(2S,3R,4S,5R,6R)-2-{[(2R,3R,4S,5R,6R)-4,5-dihydroxy-6-(hydroxymethyl)-2-[(1'R,2R,2'S,4'S,5S,7'S,8'R,9'R,12'S,13'S,16'S,18'S)-2',5,7',13'-tetramethyl-5'-oxaspiro[oxane-2,6'-pentacyclo[10.8.0.0^{2,9}.0^{4,8}.0^{13,18}]icosane]oxy]oxan-3-yl]oxy}-6-(hydroxymethyl)oxane-3,4,5-triol

> <ALOGPS_LOGP>
1.76

> <JCHEM_LOGP>
1.791213643999999

> <ALOGPS_LOGS>
-3.75

> <JCHEM_MDDR_LIKE_RULE>
1

> <JCHEM_NUMBER_OF_RINGS>
8

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA>
12.700613227970958

> <JCHEM_PKA_STRONGEST_ACIDIC>
12.089851426942849

> <JCHEM_PKA_STRONGEST_BASIC>
-2.9810835766873476

> <JCHEM_POLAR_SURFACE_AREA>
196.98999999999998

> <JCHEM_REFRACTIVITY>
184.24250000000004

> <JCHEM_ROTATABLE_BOND_COUNT>
6

> <JCHEM_RULE_OF_FIVE>
0

> <ALOGPS_SOLUBILITY>
1.31e-01 g/l

> <JCHEM_TRADITIONAL_IUPAC>
(2S,3R,4S,5R,6R)-2-{[(2R,3R,4S,5R,6R)-4,5-dihydroxy-6-(hydroxymethyl)-2-[(1'R,2R,2'S,4'S,5S,7'S,8'R,9'R,12'S,13'S,16'S,18'S)-2',5,7',13'-tetramethyl-5'-oxaspiro[oxane-2,6'-pentacyclo[10.8.0.0^{2,9}.0^{4,8}.0^{13,18}]icosane]oxy]oxan-3-yl]oxy}-6-(hydroxymethyl)oxane-3,4,5-triol

> <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      13.158   9.072   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0      13.849   7.696   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0      13.003   6.409   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0      11.465   6.499   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0      10.774   7.875   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0      11.620   9.161   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0       9.237   7.964   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0       8.390   6.678   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0       9.082   5.301   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0      10.619   5.212   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0       6.853   6.767   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0       6.162   8.143   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0       7.008   9.430   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0       8.545   9.340   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0       4.639   7.911   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0       4.390   6.391   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0       5.758   5.684   0.000  0.00  0.00           C+0
HETATM   18  O   UNK     0       2.867   6.159   0.000  0.00  0.00           O+0
HETATM   19  C   UNK     0       2.176   7.536   0.000  0.00  0.00           C+0
HETATM   20  C   UNK     0       3.271   8.618   0.000  0.00  0.00           C+0
HETATM   21  C   UNK     0       3.039  10.141   0.000  0.00  0.00           C+0
HETATM   22  O   UNK     0       1.200   6.344   0.000  0.00  0.00           O+0
HETATM   23  C   UNK     0      -0.320   6.594   0.000  0.00  0.00           C+0
HETATM   24  C   UNK     0      -0.863   8.035   0.000  0.00  0.00           C+0
HETATM   25  C   UNK     0       0.113   9.226   0.000  0.00  0.00           C+0
HETATM   26  C   UNK     0       1.632   8.976   0.000  0.00  0.00           C+0
HETATM   27  C   UNK     0      -2.383   8.285   0.000  0.00  0.00           C+0
HETATM   28  C   UNK     0       7.396   5.326   0.000  0.00  0.00           C+0
HETATM   29  C   UNK     0      10.083   9.251   0.000  0.00  0.00           C+0
HETATM   30  O   UNK     0      15.386   7.606   0.000  0.00  0.00           O+0
HETATM   31  C   UNK     0      16.232   8.893   0.000  0.00  0.00           C+0
HETATM   32  O   UNK     0      15.541  10.269   0.000  0.00  0.00           O+0
HETATM   33  C   UNK     0      16.387  11.556   0.000  0.00  0.00           C+0
HETATM   34  C   UNK     0      17.925  11.466   0.000  0.00  0.00           C+0
HETATM   35  C   UNK     0      18.616  10.090   0.000  0.00  0.00           C+0
HETATM   36  C   UNK     0      17.770   8.803   0.000  0.00  0.00           C+0
HETATM   37  O   UNK     0      18.461   7.427   0.000  0.00  0.00           O+0
HETATM   38  C   UNK     0      19.998   7.338   0.000  0.00  0.00           C+0
HETATM   39  C   UNK     0      20.690   5.962   0.000  0.00  0.00           C+0
HETATM   40  C   UNK     0      22.227   5.872   0.000  0.00  0.00           C+0
HETATM   41  C   UNK     0      23.073   7.159   0.000  0.00  0.00           C+0
HETATM   42  C   UNK     0      22.382   8.535   0.000  0.00  0.00           C+0
HETATM   43  O   UNK     0      20.845   8.624   0.000  0.00  0.00           O+0
HETATM   44  C   UNK     0      23.228   9.822   0.000  0.00  0.00           C+0
HETATM   45  O   UNK     0      24.766   9.732   0.000  0.00  0.00           O+0
HETATM   46  O   UNK     0      24.611   7.069   0.000  0.00  0.00           O+0
HETATM   47  O   UNK     0      22.918   4.496   0.000  0.00  0.00           O+0
HETATM   48  O   UNK     0      19.843   4.675   0.000  0.00  0.00           O+0
HETATM   49  O   UNK     0      20.153  10.001   0.000  0.00  0.00           O+0
HETATM   50  O   UNK     0      18.771  12.753   0.000  0.00  0.00           O+0
HETATM   51  C   UNK     0      15.696  12.932   0.000  0.00  0.00           C+0
HETATM   52  O   UNK     0      14.159  13.021   0.000  0.00  0.00           O+0
CONECT    1    2    6                                                       
CONECT    2    1    3   30                                                  
CONECT    3    2    4                                                       
CONECT    4    3    5   10                                                  
CONECT    5    4    6    7   29                                             
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   17   28                                             
CONECT   12   11   13   15                                                  
CONECT   13   12   14                                                       
CONECT   14   13    7                                                       
CONECT   15   12   16   20                                                  
CONECT   16   15   17   18                                                  
CONECT   17   16   11                                                       
CONECT   18   16   19                                                       
CONECT   19   18   20   22   26                                             
CONECT   20   19   15   21                                                  
CONECT   21   20                                                            
CONECT   22   19   23                                                       
CONECT   23   22   24                                                       
CONECT   24   23   25   27                                                  
CONECT   25   24   26                                                       
CONECT   26   25   19                                                       
CONECT   27   24                                                            
CONECT   28   11                                                            
CONECT   29    5                                                            
CONECT   30    2   31                                                       
CONECT   31   30   32   36                                                  
CONECT   32   31   33                                                       
CONECT   33   32   34   51                                                  
CONECT   34   33   35   50                                                  
CONECT   35   34   36   49                                                  
CONECT   36   35   31   37                                                  
CONECT   37   36   38                                                       
CONECT   38   37   39   43                                                  
CONECT   39   38   40   48                                                  
CONECT   40   39   41   47                                                  
CONECT   41   40   42   46                                                  
CONECT   42   41   43   44                                                  
CONECT   43   42   38                                                       
CONECT   44   42   45                                                       
CONECT   45   44                                                            
CONECT   46   41                                                            
CONECT   47   40                                                            
CONECT   48   39                                                            
CONECT   49   35                                                            
CONECT   50   34                                                            
CONECT   51   33   52                                                       
CONECT   52   51                                                            
MASTER        0    0    0    0    0    0    0    0   52    0  118    0
END

View in JSmol

Synonyms

Not Available

Chemical Formula

C₃₉H₆₄O₁₃

Average Mass

740.9280 Da

Monoisotopic Mass

740.43469 Da

IUPAC Name

Traditional Name

CAS Registry Number

Not Available

SMILES

C[C@H]1[C@@H]2[C@H](C[C@]3(C)[C@@H]2CC[C@H]2[C@H]3CC[C@H]3C[C@H](CC[C@]23C)O[C@@H]2O[C@H](CO)[C@H](O)[C@H](O)[C@H]2O[C@@H]2O[C@H](CO)[C@H](O)[C@H](O)[C@H]2O)O[C@]11CC[C@H](C)CO1

InChI Identifier

InChI=1S/C39H64O13/c1-18-9-12-39(47-17-18)19(2)28-24-8-7-22-23(38(24,4)14-25(28)52-39)6-5-20-13-21(10-11-37(20,22)3)48-36-34(32(45)30(43)27(16-41)50-36)51-35-33(46)31(44)29(42)26(15-40)49-35/h18-36,40-46H,5-17H2,1-4H3/t18-,19-,20-,21-,22-,23+,24+,25-,26+,27+,28-,29-,30-,31-,32-,33+,34+,35-,36+,37-,38-,39+/m0/s1

InChI Key

IATIAUOAJIFOSI-XVTUODIHSA-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
Asparagus oligoclonos	Plant	KNApSAcK
Asparagus racemosus	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

Diterpene glycoside
Steroidal glycoside
Diterpenoid
14-alpha-methylsteroid
Terpene glycoside
O-glycosyl compound
Glycosyl compound
Disaccharide
Ketal
Oxane
Tetrahydrofuran
Secondary alcohol
Oxacycle
Organoheterocyclic compound
Polyol
Acetal
Organic oxygen compound
Hydrocarbon derivative
Primary alcohol
Organooxygen compound
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	1.76	ALOGPS
logP	1.79	ChemAxon
logS	-3.8	ALOGPS
pKa (Strongest Acidic)	12.09	ChemAxon
pKa (Strongest Basic)	-3	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	13	ChemAxon
Hydrogen Donor Count	7	ChemAxon
Polar Surface Area	196.99 Å²	ChemAxon
Rotatable Bond Count	6	ChemAxon
Refractivity	184.24 m³·mol⁻¹	ChemAxon
Polarizability	83.04 Å³	ChemAxon
Number of Rings	8	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

163067719

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

Not Available

Showing NP-Card for (-)-Asparanin A (NP0073710)

MOL for NP0073710 ((-)-Asparanin A)

3D MOL for NP0073710 ((-)-Asparanin A)

3D SDF for NP0073710 ((-)-Asparanin A)

3D-SDF for NP0073710 ((-)-Asparanin A)

PDB for NP0073710 ((-)-Asparanin A)

3D PDB for NP0073710 ((-)-Asparanin A)

SMILES for NP0073710 ((-)-Asparanin A)

INCHI for NP0073710 ((-)-Asparanin A)

Structure for NP0073710 ((-)-Asparanin A)

3D Structure for NP0073710 ((-)-Asparanin A)