NP-MRD: Showing NP-Card for 15-{[4-(dimethylamino)-3-hydroxy-6-methyloxan-2-yl]oxy}-7-ethyl-5',8,9,14-tetrahydroxy-4'-methoxy-4',6',8,10,12,14,16-heptamethyl-decahydrospiro[[1,3]dioxino[5,4-c]oxacyclotetradecane-2,2'-oxane]-5,11-dione (NP0300638)

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Record Information

Version

2.0

Created at

2022-09-10 13:08:44 UTC

Updated at

2022-09-10 13:08:44 UTC

NP-MRD ID

NP0300638

Secondary Accession Numbers

None

Natural Product Identification

Common Name

15-{[4-(dimethylamino)-3-hydroxy-6-methyloxan-2-yl]oxy}-7-ethyl-5',8,9,14-tetrahydroxy-4'-methoxy-4',6',8,10,12,14,16-heptamethyl-decahydrospiro[[1,3]dioxino[5,4-c]oxacyclotetradecane-2,2'-oxane]-5,11-dione

Description

AC1NOXK9 belongs to the class of organic compounds known as aminoglycosides. These are molecules or a portion of a molecule composed of amino-modified sugars. AC1NOXK9 is a very strong basic compound (based on its pKa).

Structure

MOL 3D MOL SDF PDB SMILES InChI


  Mrv1533004161515202D          

 52 55  0  0  0  0            999 V2000
    2.0024    2.4900    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.3105    2.0407    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.3538    1.2168    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.0889    0.8423    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.7807    1.2917    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.7375    2.1156    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.5158    0.9172    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.2077    1.3666    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.9428    0.9921    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.9861    0.1682    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.6779    0.6176    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.4130    0.2431    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.2319    0.1427    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.6542    1.0321    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    7.4580    1.2177    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.4563   -0.5807    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.1914   -0.9552    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.7644   -1.0301    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.8077   -1.8540    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.0293   -0.6556    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.2942   -0.2811    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.5591    0.0933    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8672   -0.3560    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1321    0.0184    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.9105   -1.1799    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.6456   -1.5544    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.6888   -2.3783    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.4239   -2.7527    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.4672   -3.5766    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.2023   -3.9511    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.7753   -4.0260    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.0402   -3.6515    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.9969   -2.8276    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.2618   -2.4532    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.3483   -4.1009    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    2.3916   -4.9248    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.6132   -3.7264    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.2186   -1.6293    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.7813   -2.2326    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.7221   -2.2882    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.4835   -1.2548    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7916   -1.7042    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.8349   -2.5281    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0565   -1.3297    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6354   -1.7791    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.0133   -0.5058    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7218   -0.1314    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7051   -0.0565    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4402   -0.4309    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.6619    0.7674    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1630    0.7529    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.1886    1.4432    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
  3  4  1  0  0  0  0
  4  5  1  0  0  0  0
  5  6  2  0  0  0  0
  5  7  1  0  0  0  0
  7  8  1  0  0  0  0
  8  9  1  0  0  0  0
  9 10  1  0  0  0  0
 10 11  1  0  0  0  0
 11 12  1  0  0  0  0
 12 13  1  0  0  0  0
 12 14  1  0  0  0  0
 14 15  1  0  0  0  0
 12 16  1  0  0  0  0
 16 17  1  0  0  0  0
 16 18  1  0  0  0  0
 18 19  1  0  0  0  0
 18 20  1  0  0  0  0
 10 20  1  0  0  0  0
 10 21  1  0  0  0  0
 21 22  1  0  0  0  0
  7 22  1  0  0  0  0
 22 23  1  0  0  0  0
 23 24  1  0  0  0  0
 23 25  1  0  0  0  0
 25 26  1  0  0  0  0
 26 27  1  0  0  0  0
 27 28  1  0  0  0  0
 28 29  1  0  0  0  0
 29 30  1  0  0  0  0
 29 31  1  0  0  0  0
 31 32  1  0  0  0  0
 32 33  1  0  0  0  0
 27 33  1  0  0  0  0
 33 34  1  0  0  0  0
 32 35  1  0  0  0  0
 35 36  1  0  0  0  0
 35 37  1  0  0  0  0
 25 38  1  0  0  0  0
 38 39  1  0  0  0  0
 38 40  1  0  0  0  0
 38 41  1  0  0  0  0
 41 42  1  0  0  0  0
 42 43  1  0  0  0  0
 42 44  1  0  0  0  0
 44 45  2  0  0  0  0
 44 46  1  0  0  0  0
 46 47  1  0  0  0  0
 46 48  1  0  0  0  0
 48 49  1  0  0  0  0
 48 50  1  0  0  0  0
  3 50  1  0  0  0  0
 50 51  1  0  0  0  0
 50 52  1  0  0  0  0
M  END

     RDKit          3D

117120  0  0  0  0  0  0  0  0999 V2000
   -5.2377    3.7730    0.2679 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.1102    2.7562    0.0981 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8553    3.4411   -0.3606 C   0  0  2  0  0  0  0  0  0  0  0  0
   -1.7498    2.6893   -0.5778 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3072    1.6740   -1.3265 C   0  0  0  0  0  0  0  0  0  0  0  0
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   -1.5664    0.2650   -0.9190 C   0  0  1  0  0  0  0  0  0  0  0  0
   -2.6726   -0.1769   -1.9240 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.1480   -1.3365   -1.3371 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1360   -2.3056   -1.5903 C   0  0  2  0  0  0  0  0  0  0  0  0
   -2.6893   -3.0468   -2.8223 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.9097   -3.8735   -2.3721 C   0  0  2  0  0  0  0  0  0  0  0  0
   -4.5654   -4.3977   -3.6271 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.7260   -3.0544   -1.6210 O   0  0  0  0  0  0  0  0  0  0  0  0
   -5.8577   -3.6493   -1.1330 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.3543   -4.9965   -1.5328 C   0  0  1  0  0  0  0  0  0  0  0  0
   -2.6417   -5.8246   -2.4083 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4526   -4.4017   -0.4865 C   0  0  1  0  0  0  0  0  0  0  0  0
   -1.2422   -5.3243   -0.2652 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1275   -3.1183   -0.5359 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9416   -1.7711   -1.9930 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4451   -0.6958   -1.2245 C   0  0  2  0  0  0  0  0  0  0  0  0
    0.3609   -1.2064   -0.0703 C   0  0  1  0  0  0  0  0  0  0  0  0
    1.1566   -2.3882   -0.6819 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4194   -0.3180    0.4904 C   0  0  2  0  0  0  0  0  0  0  0  0
    2.7260   -0.7515    0.2621 O   0  0  0  0  0  0  0  0  0  0  0  0
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    0.2025    1.1099    2.1959 C   0  0  0  0  0  0  0  0  0  0  0  0
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   -0.6741    4.2781    2.4258 C   0  0  1  0  0  0  0  0  0  0  0  0
   -0.5779    5.6241    3.1333 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0034    4.4865    0.9700 C   0  0  2  0  0  0  0  0  0  0  0  0
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   -2.4972    4.4501    0.7477 C   0  0  1  0  0  0  0  0  0  0  0  0
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   -3.0404   -4.5482    0.4940 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5377   -4.7965    0.3754 H   0  0  0  0  0  0  0  0  0  0  0  0
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   -0.1454   -1.1328    3.1534 H   0  0  0  0  0  0  0  0  0  0  0  0
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   -0.1309    1.5753    1.2555 H   0  0  0  0  0  0  0  0  0  0  0  0
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   -0.1017    3.0180    5.0532 H   0  0  0  0  0  0  0  0  0  0  0  0
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    0.1102    1.2543    5.1025 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4665    3.6896    2.8932 H   0  0  0  0  0  0  0  0  0  0  0  0
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    0.1930    5.5754    3.9384 H   0  0  0  0  0  0  0  0  0  0  0  0
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   -0.6132    5.7940   -0.3780 H   0  0  0  0  0  0  0  0  0  0  0  0
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 38 40  1  1
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 41 42  1  0
 42 43  1  0
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 44 45  2  0
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 50  3  1  0
 22  7  1  0
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 29 83  1  1
 30 84  1  0
 30 85  1  0
 30 86  1  0
 31 87  1  0
 31 88  1  0
 32 89  1  6
 36 96  1  6
 37 97  1  0
 34 90  1  0
 34 91  1  0
 34 92  1  0
 35 93  1  0
 35 94  1  0
 35 95  1  0
 39 98  1  0
 39 99  1  0
 39100  1  0
 40101  1  0
 41102  1  0
 41103  1  0
 42104  1  1
 43105  1  0
 43106  1  0
 43107  1  0
 46108  1  1
 47109  1  0
 47110  1  0
 47111  1  0
 48112  1  6
 49113  1  0
 51114  1  0
 51115  1  0
 51116  1  0
 52117  1  0
M  END


  Mrv1533004161515202D          

 52 55  0  0  0  0            999 V2000
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    1.3538    1.2168    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
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    2.8672   -0.3560    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1321    0.0184    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.9105   -1.1799    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.6456   -1.5544    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
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    4.4239   -2.7527    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.4672   -3.5766    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.2023   -3.9511    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.7753   -4.0260    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.0402   -3.6515    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.9969   -2.8276    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.2618   -2.4532    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.3483   -4.1009    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    2.3916   -4.9248    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.6132   -3.7264    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.2186   -1.6293    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.7813   -2.2326    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.7221   -2.2882    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.4835   -1.2548    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7916   -1.7042    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.8349   -2.5281    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0565   -1.3297    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6354   -1.7791    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.0133   -0.5058    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7218   -0.1314    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7051   -0.0565    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4402   -0.4309    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.6619    0.7674    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1630    0.7529    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.1886    1.4432    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
  3  4  1  0  0  0  0
  4  5  1  0  0  0  0
  5  6  2  0  0  0  0
  5  7  1  0  0  0  0
  7  8  1  0  0  0  0
  8  9  1  0  0  0  0
  9 10  1  0  0  0  0
 10 11  1  0  0  0  0
 11 12  1  0  0  0  0
 12 13  1  0  0  0  0
 12 14  1  0  0  0  0
 14 15  1  0  0  0  0
 12 16  1  0  0  0  0
 16 17  1  0  0  0  0
 16 18  1  0  0  0  0
 18 19  1  0  0  0  0
 18 20  1  0  0  0  0
 10 20  1  0  0  0  0
 10 21  1  0  0  0  0
 21 22  1  0  0  0  0
  7 22  1  0  0  0  0
 22 23  1  0  0  0  0
 23 24  1  0  0  0  0
 23 25  1  0  0  0  0
 25 26  1  0  0  0  0
 26 27  1  0  0  0  0
 27 28  1  0  0  0  0
 28 29  1  0  0  0  0
 29 30  1  0  0  0  0
 29 31  1  0  0  0  0
 31 32  1  0  0  0  0
 32 33  1  0  0  0  0
 27 33  1  0  0  0  0
 33 34  1  0  0  0  0
 32 35  1  0  0  0  0
 35 36  1  0  0  0  0
 35 37  1  0  0  0  0
 25 38  1  0  0  0  0
 38 39  1  0  0  0  0
 38 40  1  0  0  0  0
 38 41  1  0  0  0  0
 41 42  1  0  0  0  0
 42 43  1  0  0  0  0
 42 44  1  0  0  0  0
 44 45  2  0  0  0  0
 44 46  1  0  0  0  0
 46 47  1  0  0  0  0
 46 48  1  0  0  0  0
 48 49  1  0  0  0  0
 48 50  1  0  0  0  0
  3 50  1  0  0  0  0
 50 51  1  0  0  0  0
 50 52  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0300638

> <DATABASE_NAME>
NP-MRD

> <SMILES>
CCC1OC(=O)C2COC3(CC(C)(OC)C(O)C(C)O3)OC2C(C)C(OC2OC(C)CC(C2O)N(C)C)C(C)(O)CC(C)C(=O)C(C)C(O)C1(C)O

> <INCHI_IDENTIFIER>
InChI=1S/C37H65NO14/c1-13-25-36(9,45)29(41)20(4)26(39)18(2)15-34(7,44)31(50-33-27(40)24(38(10)11)14-19(3)48-33)21(5)28-23(32(43)49-25)16-47-37(52-28)17-35(8,46-12)30(42)22(6)51-37/h18-25,27-31,33,40-42,44-45H,13-17H2,1-12H3

> <INCHI_KEY>
PRUSTPADOGZAML-UHFFFAOYSA-N

> <FORMULA>
C37H65NO14

> <MOLECULAR_WEIGHT>
747.92

> <EXACT_MASS>
747.440505777

> <JCHEM_ACCEPTOR_COUNT>
14

> <JCHEM_ATOM_COUNT>
117

> <JCHEM_AVERAGE_POLARIZABILITY>
80.29829749695593

> <JCHEM_BIOAVAILABILITY>
0

> <JCHEM_DONOR_COUNT>
5

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
0

> <JCHEM_IUPAC>
15-{[4-(dimethylamino)-3-hydroxy-6-methyloxan-2-yl]oxy}-7-ethyl-5',8,9,14-tetrahydroxy-4'-methoxy-4',6',8,10,12,14,16-heptamethyl-tetradecahydrospiro[[1,3]dioxino[5,4-c]oxacyclotetradecane-2,2'-oxane]-5,11-dione

> <ALOGPS_LOGP>
1.93

> <JCHEM_LOGP>
1.0681918600000024

> <ALOGPS_LOGS>
-2.88

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
4

> <JCHEM_PHYSIOLOGICAL_CHARGE>
1

> <JCHEM_PKA>
12.905540802891569

> <JCHEM_PKA_STRONGEST_ACIDIC>
12.436358854028885

> <JCHEM_PKA_STRONGEST_BASIC>
8.380974578962906

> <JCHEM_POLAR_SURFACE_AREA>
203.14

> <JCHEM_REFRACTIVITY>
186.65150000000006

> <JCHEM_ROTATABLE_BOND_COUNT>
5

> <JCHEM_RULE_OF_FIVE>
0

> <ALOGPS_SOLUBILITY>
9.80e-01 g/l

> <JCHEM_TRADITIONAL_IUPAC>
15-{[4-(dimethylamino)-3-hydroxy-6-methyloxan-2-yl]oxy}-7-ethyl-5',8,9,14-tetrahydroxy-4'-methoxy-4',6',8,10,12,14,16-heptamethyl-decahydrospiro[[1,3]dioxino[5,4-c]oxacyclotetradecane-2,2'-oxane]-5,11-dione

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 16-APR-15   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   16-APR-15         0                                  
HETATM    1  C   UNK     0       3.738   4.648   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0       2.446   3.809   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0       2.527   2.271   0.000  0.00  0.00           C+0
HETATM    4  O   UNK     0       3.899   1.572   0.000  0.00  0.00           O+0
HETATM    5  C   UNK     0       5.191   2.411   0.000  0.00  0.00           C+0
HETATM    6  O   UNK     0       5.110   3.949   0.000  0.00  0.00           O+0
HETATM    7  C   UNK     0       6.563   1.712   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0       7.854   2.551   0.000  0.00  0.00           C+0
HETATM    9  O   UNK     0       9.227   1.852   0.000  0.00  0.00           O+0
HETATM   10  C   UNK     0       9.307   0.314   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0      10.599   1.153   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0      11.971   0.454   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0      13.500   0.266   0.000  0.00  0.00           C+0
HETATM   14  O   UNK     0      12.421   1.927   0.000  0.00  0.00           O+0
HETATM   15  C   UNK     0      13.922   2.273   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0      12.052  -1.084   0.000  0.00  0.00           C+0
HETATM   17  O   UNK     0      13.424  -1.783   0.000  0.00  0.00           O+0
HETATM   18  C   UNK     0      10.760  -1.923   0.000  0.00  0.00           C+0
HETATM   19  C   UNK     0      10.841  -3.461   0.000  0.00  0.00           C+0
HETATM   20  O   UNK     0       9.388  -1.224   0.000  0.00  0.00           O+0
HETATM   21  O   UNK     0       8.016  -0.525   0.000  0.00  0.00           O+0
HETATM   22  C   UNK     0       6.644   0.174   0.000  0.00  0.00           C+0
HETATM   23  C   UNK     0       5.352  -0.665   0.000  0.00  0.00           C+0
HETATM   24  C   UNK     0       3.980   0.034   0.000  0.00  0.00           C+0
HETATM   25  C   UNK     0       5.433  -2.202   0.000  0.00  0.00           C+0
HETATM   26  O   UNK     0       6.805  -2.902   0.000  0.00  0.00           O+0
HETATM   27  C   UNK     0       6.886  -4.439   0.000  0.00  0.00           C+0
HETATM   28  O   UNK     0       8.258  -5.138   0.000  0.00  0.00           O+0
HETATM   29  C   UNK     0       8.339  -6.676   0.000  0.00  0.00           C+0
HETATM   30  C   UNK     0       9.711  -7.375   0.000  0.00  0.00           C+0
HETATM   31  C   UNK     0       7.047  -7.515   0.000  0.00  0.00           C+0
HETATM   32  C   UNK     0       5.675  -6.816   0.000  0.00  0.00           C+0
HETATM   33  C   UNK     0       5.594  -5.278   0.000  0.00  0.00           C+0
HETATM   34  O   UNK     0       4.222  -4.579   0.000  0.00  0.00           O+0
HETATM   35  N   UNK     0       4.384  -7.655   0.000  0.00  0.00           N+0
HETATM   36  C   UNK     0       4.464  -9.193   0.000  0.00  0.00           C+0
HETATM   37  C   UNK     0       3.011  -6.956   0.000  0.00  0.00           C+0
HETATM   38  C   UNK     0       4.141  -3.041   0.000  0.00  0.00           C+0
HETATM   39  C   UNK     0       5.192  -4.168   0.000  0.00  0.00           C+0
HETATM   40  O   UNK     0       3.215  -4.271   0.000  0.00  0.00           O+0
HETATM   41  C   UNK     0       2.769  -2.342   0.000  0.00  0.00           C+0
HETATM   42  C   UNK     0       1.478  -3.181   0.000  0.00  0.00           C+0
HETATM   43  C   UNK     0       1.558  -4.719   0.000  0.00  0.00           C+0
HETATM   44  C   UNK     0       0.105  -2.482   0.000  0.00  0.00           C+0
HETATM   45  O   UNK     0      -1.186  -3.321   0.000  0.00  0.00           O+0
HETATM   46  C   UNK     0       0.025  -0.944   0.000  0.00  0.00           C+0
HETATM   47  C   UNK     0      -1.347  -0.245   0.000  0.00  0.00           C+0
HETATM   48  C   UNK     0       1.316  -0.105   0.000  0.00  0.00           C+0
HETATM   49  O   UNK     0       2.688  -0.804   0.000  0.00  0.00           O+0
HETATM   50  C   UNK     0       1.236   1.432   0.000  0.00  0.00           C+0
HETATM   51  C   UNK     0      -0.304   1.406   0.000  0.00  0.00           C+0
HETATM   52  O   UNK     0       0.352   2.694   0.000  0.00  0.00           O+0
CONECT    1    2                                                            
CONECT    2    1    3                                                       
CONECT    3    2    4   50                                                  
CONECT    4    3    5                                                       
CONECT    5    4    6    7                                                  
CONECT    6    5                                                            
CONECT    7    5    8   22                                                  
CONECT    8    7    9                                                       
CONECT    9    8   10                                                       
CONECT   10    9   11   20   21                                             
CONECT   11   10   12                                                       
CONECT   12   11   13   14   16                                             
CONECT   13   12                                                            
CONECT   14   12   15                                                       
CONECT   15   14                                                            
CONECT   16   12   17   18                                                  
CONECT   17   16                                                            
CONECT   18   16   19   20                                                  
CONECT   19   18                                                            
CONECT   20   18   10                                                       
CONECT   21   10   22                                                       
CONECT   22   21    7   23                                                  
CONECT   23   22   24   25                                                  
CONECT   24   23                                                            
CONECT   25   23   26   38                                                  
CONECT   26   25   27                                                       
CONECT   27   26   28   33                                                  
CONECT   28   27   29                                                       
CONECT   29   28   30   31                                                  
CONECT   30   29                                                            
CONECT   31   29   32                                                       
CONECT   32   31   33   35                                                  
CONECT   33   32   27   34                                                  
CONECT   34   33                                                            
CONECT   35   32   36   37                                                  
CONECT   36   35                                                            
CONECT   37   35                                                            
CONECT   38   25   39   40   41                                             
CONECT   39   38                                                            
CONECT   40   38                                                            
CONECT   41   38   42                                                       
CONECT   42   41   43   44                                                  
CONECT   43   42                                                            
CONECT   44   42   45   46                                                  
CONECT   45   44                                                            
CONECT   46   44   47   48                                                  
CONECT   47   46                                                            
CONECT   48   46   49   50                                                  
CONECT   49   48                                                            
CONECT   50   48    3   51   52                                             
CONECT   51   50                                                            
CONECT   52   50                                                            
MASTER        0    0    0    0    0    0    0    0   52    0  110    0
END

View in JSmol

Synonyms

Not Available

Chemical Formula

C₃₇H₆₅NO₁₄

Average Mass

747.9200 Da

Monoisotopic Mass

747.44051 Da

IUPAC Name

15-{[4-(dimethylamino)-3-hydroxy-6-methyloxan-2-yl]oxy}-7-ethyl-5',8,9,14-tetrahydroxy-4'-methoxy-4',6',8,10,12,14,16-heptamethyl-tetradecahydrospiro[[1,3]dioxino[5,4-c]oxacyclotetradecane-2,2'-oxane]-5,11-dione

Traditional Name

CAS Registry Number

Not Available

SMILES

CCC1OC(=O)C2COC3(CC(C)(OC)C(O)C(C)O3)OC2C(C)C(OC2OC(C)CC(C2O)N(C)C)C(C)(O)CC(C)C(=O)C(C)C(O)C1(C)O

InChI Identifier

InChI=1S/C37H65NO14/c1-13-25-36(9,45)29(41)20(4)26(39)18(2)15-34(7,44)31(50-33-27(40)24(38(10)11)14-19(3)48-33)21(5)28-23(32(43)49-25)16-47-37(52-28)17-35(8,46-12)30(42)22(6)51-37/h18-25,27-31,33,40-42,44-45H,13-17H2,1-12H3

InChI Key

PRUSTPADOGZAML-UHFFFAOYSA-N

Experimental Spectra

Not Available

Predicted Spectra

Spectrum Type	Description	Depositor ID	Depositor Organization	Depositor	Deposition Date	View
1D NMR	¹³C NMR Spectrum (1D, 25 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 100 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 252 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 1000 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 50 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 200 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 75 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 300 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 101 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 400 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 126 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 500 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 151 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 600 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 176 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 700 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 201 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 800 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 226 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 900 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum

Chemical Shift Submissions

Not Available

Species

Species of Origin

Not Available

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as aminoglycosides. These are molecules or a portion of a molecule composed of amino-modified sugars.

Kingdom

Organic compounds

Super Class

Organic oxygen compounds

Class

Organooxygen compounds

Sub Class

Carbohydrates and carbohydrate conjugates

Direct Parent

Aminoglycosides

Alternative Parents

Substituents

Aminoglycoside core
Carboxylic acid orthoester
Ortho ester
Meta-dioxane
Monosaccharide
Oxane
Tertiary alcohol
Cyclic ketone
Amino acid or derivatives
Carboxylic acid ester
Ketone
Lactone
Orthocarboxylic acid derivative
Secondary alcohol
1,2-aminoalcohol
Tertiary amine
Tertiary aliphatic amine
Polyol
Organoheterocyclic compound
Oxacycle
Carboxylic acid derivative
Acetal
Dialkyl ether
Ether
Monocarboxylic acid or derivatives
Hydrocarbon derivative
Organonitrogen compound
Amine
Carbonyl group
Organic oxide
Organopnictogen compound
Alcohol
Aldehyde
Organic nitrogen compound
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	1.93	ALOGPS
logP	1.07	ChemAxon
logS	-2.9	ALOGPS
pKa (Strongest Acidic)	12.44	ChemAxon
pKa (Strongest Basic)	8.38	ChemAxon
Physiological Charge	1	ChemAxon
Hydrogen Acceptor Count	14	ChemAxon
Hydrogen Donor Count	5	ChemAxon
Polar Surface Area	203.14 Å²	ChemAxon
Rotatable Bond Count	5	ChemAxon
Refractivity	186.65 m³·mol⁻¹	ChemAxon
Polarizability	80.3 Å³	ChemAxon
Number of Rings	4	ChemAxon
Bioavailability	No	ChemAxon
Rule of Five	No	ChemAxon
Ghose Filter	No	ChemAxon
Veber's Rule	No	ChemAxon
MDDR-like Rule	No	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

5120667

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

LOTUS database [Link]

Showing NP-Card for 15-{[4-(dimethylamino)-3-hydroxy-6-methyloxan-2-yl]oxy}-7-ethyl-5',8,9,14-tetrahydroxy-4'-methoxy-4',6',8,10,12,14,16-heptamethyl-decahydrospiro[[1,3]dioxino[5,4-c]oxacyclotetradecane-2,2'-oxane]-5,11-dione (NP0300638)

MOL for NP0300638 (15-{[4-(dimethylamino)-3-hydroxy-6-methyloxan-2-yl]oxy}-7-ethyl-5',8,9,14-tetrahydroxy-4'-methoxy-4',6',8,10,12,14,16-heptamethyl-decahydrospiro[[1,3]dioxino[5,4-c]oxacyclotetradecane-2,2'-oxane]-5,11-dione)

3D MOL for NP0300638 (15-{[4-(dimethylamino)-3-hydroxy-6-methyloxan-2-yl]oxy}-7-ethyl-5',8,9,14-tetrahydroxy-4'-methoxy-4',6',8,10,12,14,16-heptamethyl-decahydrospiro[[1,3]dioxino[5,4-c]oxacyclotetradecane-2,2'-oxane]-5,11-dione)

3D SDF for NP0300638 (15-{[4-(dimethylamino)-3-hydroxy-6-methyloxan-2-yl]oxy}-7-ethyl-5',8,9,14-tetrahydroxy-4'-methoxy-4',6',8,10,12,14,16-heptamethyl-decahydrospiro[[1,3]dioxino[5,4-c]oxacyclotetradecane-2,2'-oxane]-5,11-dione)

3D-SDF for NP0300638 (15-{[4-(dimethylamino)-3-hydroxy-6-methyloxan-2-yl]oxy}-7-ethyl-5',8,9,14-tetrahydroxy-4'-methoxy-4',6',8,10,12,14,16-heptamethyl-decahydrospiro[[1,3]dioxino[5,4-c]oxacyclotetradecane-2,2'-oxane]-5,11-dione)

PDB for NP0300638 (15-{[4-(dimethylamino)-3-hydroxy-6-methyloxan-2-yl]oxy}-7-ethyl-5',8,9,14-tetrahydroxy-4'-methoxy-4',6',8,10,12,14,16-heptamethyl-decahydrospiro[[1,3]dioxino[5,4-c]oxacyclotetradecane-2,2'-oxane]-5,11-dione)

3D PDB for NP0300638 (15-{[4-(dimethylamino)-3-hydroxy-6-methyloxan-2-yl]oxy}-7-ethyl-5',8,9,14-tetrahydroxy-4'-methoxy-4',6',8,10,12,14,16-heptamethyl-decahydrospiro[[1,3]dioxino[5,4-c]oxacyclotetradecane-2,2'-oxane]-5,11-dione)

SMILES for NP0300638 (15-{[4-(dimethylamino)-3-hydroxy-6-methyloxan-2-yl]oxy}-7-ethyl-5',8,9,14-tetrahydroxy-4'-methoxy-4',6',8,10,12,14,16-heptamethyl-decahydrospiro[[1,3]dioxino[5,4-c]oxacyclotetradecane-2,2'-oxane]-5,11-dione)

INCHI for NP0300638 (15-{[4-(dimethylamino)-3-hydroxy-6-methyloxan-2-yl]oxy}-7-ethyl-5',8,9,14-tetrahydroxy-4'-methoxy-4',6',8,10,12,14,16-heptamethyl-decahydrospiro[[1,3]dioxino[5,4-c]oxacyclotetradecane-2,2'-oxane]-5,11-dione)

Structure for NP0300638 (15-{[4-(dimethylamino)-3-hydroxy-6-methyloxan-2-yl]oxy}-7-ethyl-5',8,9,14-tetrahydroxy-4'-methoxy-4',6',8,10,12,14,16-heptamethyl-decahydrospiro[[1,3]dioxino[5,4-c]oxacyclotetradecane-2,2'-oxane]-5,11-dione)

3D Structure for NP0300638 (15-{[4-(dimethylamino)-3-hydroxy-6-methyloxan-2-yl]oxy}-7-ethyl-5',8,9,14-tetrahydroxy-4'-methoxy-4',6',8,10,12,14,16-heptamethyl-decahydrospiro[[1,3]dioxino[5,4-c]oxacyclotetradecane-2,2'-oxane]-5,11-dione)