NP-MRD: Showing NP-Card for (2r,3e,5e,7e,9e)-2-hydroxy-n-[(2s,3r)-3-hydroxy-1-{[(3r,4s,5s,6r)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}tricosan-2-yl]trideca-3,5,7,9-tetraenimidic acid (NP0201864)

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Record Information

Version

2.0

Created at

2022-09-04 20:58:56 UTC

Updated at

2022-09-04 20:58:56 UTC

NP-MRD ID

NP0201864

Secondary Accession Numbers

None

Natural Product Identification

Common Name

(2r,3e,5e,7e,9e)-2-hydroxy-n-[(2s,3r)-3-hydroxy-1-{[(3r,4s,5s,6r)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}tricosan-2-yl]trideca-3,5,7,9-tetraenimidic acid

Description

Asperiamide B belongs to the class of organic compounds known as glycosphingolipids. These are sphingolipids containing a saccharide moiety glycosidically attached to the sphingoid base. Although saccharide moieties are mostly O-glycosidically linked to the ceramide moiety, other sphingolipids with glycosidic bonds of other types (e.G. S-,C-, or N-type) has been reported. Based on a literature review very few articles have been published on Asperiamide B.

Structure

MOL 3D MOL SDF PDB SMILES InChI


  Mrv1652309042222582D          

 52 52  0  0  1  0            999 V2000
    3.0363    8.4919    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.9614    7.6703    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.2124    7.3244    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1375    6.5028    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.3885    6.1568    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.3136    5.3352    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.5647    4.9893    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.4898    4.1677    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2592    3.8218    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3341    3.0002    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0831    2.6543    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1580    1.8327    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
   -1.9069    1.4867    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4839    1.3570    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.2651    1.7029    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5588    0.5354    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    0.1153    0.0598    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    0.0404   -0.7618    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7145   -1.2375    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.6396   -2.0591    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.3136   -2.5348    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.2387   -3.3563    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    1.9128   -3.8320    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.8379   -4.6536    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.4898   -3.7023    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    0.4149   -4.5239    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1843   -3.2266    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
   -0.9333   -3.5726    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1094   -2.4050    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
   -0.7835   -1.9294    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.8643    0.4057    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    0.9392    1.2273    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.5383   -0.0700    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.2873    0.2760    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.9614   -0.1997    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.7103    0.1462    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.3844   -0.3294    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.1334    0.0165    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.8075   -0.4591    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.5564   -0.1132    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.2305   -0.5889    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.9795   -0.2429    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.6535   -0.7186    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    9.4025   -0.3727    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   10.0766   -0.8483    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   10.8256   -0.5024    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   11.4996   -0.9780    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   12.2486   -0.6321    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   12.9227   -1.1078    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   13.6716   -0.7618    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   14.3457   -1.2375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   15.0947   -0.8916    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
  3  4  1  0  0  0  0
  4  5  2  0  0  0  0
  5  6  1  0  0  0  0
  6  7  2  0  0  0  0
  7  8  1  0  0  0  0
  8  9  2  0  0  0  0
  9 10  1  0  0  0  0
 10 11  2  0  0  0  0
 11 12  1  0  0  0  0
 12 13  1  6  0  0  0
 12 14  1  0  0  0  0
 14 15  1  4  0  0  0
 14 16  2  0  0  0  0
 17 16  1  6  0  0  0
 17 18  1  0  0  0  0
 18 19  1  0  0  0  0
 19 20  1  0  0  0  0
 20 21  1  0  0  0  0
 21 22  1  0  0  0  0
 22 23  1  6  0  0  0
 23 24  1  0  0  0  0
 22 25  1  0  0  0  0
 25 26  1  1  0  0  0
 25 27  1  0  0  0  0
 27 28  1  6  0  0  0
 27 29  1  0  0  0  0
 20 29  1  0  0  0  0
 29 30  1  1  0  0  0
 17 31  1  0  0  0  0
 31 32  1  6  0  0  0
 31 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
 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
 41 42  1  0  0  0  0
 42 43  1  0  0  0  0
 43 44  1  0  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
 49 50  1  0  0  0  0
 50 51  1  0  0  0  0
 51 52  1  0  0  0  0
M  END

     RDKit          3D

127127  0  0  0  0  0  0  0  0999 V2000
   -4.2102    5.0424    7.4847 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.1760    3.6176    6.9953 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.1830    2.7752    7.7303 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.2235    1.3787    7.1630 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1378    0.8762    6.6291 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0377   -0.4582    6.0444 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8997   -0.8684    5.5307 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7294   -2.1961    4.9259 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.4240   -2.5361    4.4191 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.6655   -3.8525    3.7980 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.8491   -4.1289    3.2910 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1431   -5.4057    2.6692 C   0  0  1  0  0  0  0  0  0  0  0  0
    1.1571   -6.3494    3.0347 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.3068   -5.4853    1.2259 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.9816   -6.7006    0.7650 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.0011   -4.7512    0.2610 N   0  0  0  0  0  0  0  0  0  0  0  0
    1.3581   -3.4998    0.1177 C   0  0  1  0  0  0  0  0  0  0  0  0
    2.0759   -2.2762    0.4194 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.3104   -2.0427   -0.1947 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.9566   -0.9667    0.4460 C   0  0  1  0  0  0  0  0  0  0  0  0
    4.8946   -1.5851    1.2679 O   0  0  0  0  0  0  0  0  0  0  0  0
    6.0450   -0.9444    1.5406 C   0  0  2  0  0  0  0  0  0  0  0  0
    6.5368   -1.4391    2.9020 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.7283   -0.8223    3.2566 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.7636    0.5354    1.6868 C   0  0  1  0  0  0  0  0  0  0  0  0
    6.8570    1.2557    2.1500 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.4979    0.9941    0.2552 C   0  0  2  0  0  0  0  0  0  0  0  0
    5.1676    2.3433    0.2575 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.4199    0.1292   -0.3746 C   0  0  1  0  0  0  0  0  0  0  0  0
    4.9353   -0.3289   -1.5808 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.2602   -3.4776   -0.9514 C   0  0  2  0  0  0  0  0  0  0  0  0
   -0.6539   -4.5474   -0.4290 O   0  0  0  0  0  0  0  0  0  0  0  0
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    0.4645   -2.0124   -3.5433 C   0  0  0  0  0  0  0  0  0  0  0  0
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   -2.1652    1.6297   -1.2101 C   0  0  0  0  0  0  0  0  0  0  0  0
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   -4.0916    0.1579   -1.8024 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.2530    0.7378   -1.1857 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.1910    1.6985   -1.7279 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.9636    3.0928   -2.0838 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.9710    3.4195   -3.1178 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.9698    4.9266   -3.4435 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.9411    5.2157   -4.5169 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.2183    4.4826   -5.7971 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.1197    4.8636   -6.7975 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.8541    5.6460    6.8118 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.1936    5.5157    7.4304 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.6532    5.1564    8.4936 H   0  0  0  0  0  0  0  0  0  0  0  0
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    1.4417   -1.3823    0.0344 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.1953   -1.9925    1.4900 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.1937   -0.5890    1.1993 H   0  0  0  0  0  0  0  0  0  0  0  0
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    0.2335    0.5624   -1.4422 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5201    0.7667   -3.1198 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4161    2.9076   -0.9584 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1817    3.0305   -2.5616 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7840    2.4199   -0.7318 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9237    0.9206   -0.3848 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.9056    1.3948   -3.1977 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1461   -0.0132   -2.4986 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.4697   -0.4071   -2.7464 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.7218   -0.7595   -1.1993 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.9143   -0.1769   -0.8636 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.0146    1.1136   -0.1066 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.7653    1.1919   -2.6272 H   0  0  0  0  0  0  0  0  0  0  0  0
   -7.1396    1.7429   -1.0164 H   0  0  0  0  0  0  0  0  0  0  0  0
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   -2.9640    4.8013   -4.1191 H   0  0  0  0  0  0  0  0  0  0  0  0
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  1 55  1  0
M  END


  Mrv1652309042222582D          

 52 52  0  0  1  0            999 V2000
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    1.3136   -2.5348    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.2387   -3.3563    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    1.9128   -3.8320    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.8379   -4.6536    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.4898   -3.7023    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    0.4149   -4.5239    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1843   -3.2266    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
   -0.9333   -3.5726    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1094   -2.4050    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
   -0.7835   -1.9294    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.8643    0.4057    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    0.9392    1.2273    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.5383   -0.0700    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.2873    0.2760    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.9614   -0.1997    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.7103    0.1462    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.3844   -0.3294    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
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    5.8075   -0.4591    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.5564   -0.1132    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.2305   -0.5889    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.9795   -0.2429    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.6535   -0.7186    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    9.4025   -0.3727    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   10.0766   -0.8483    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   10.8256   -0.5024    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   11.4996   -0.9780    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   12.2486   -0.6321    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   12.9227   -1.1078    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   13.6716   -0.7618    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   14.3457   -1.2375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   15.0947   -0.8916    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
  3  4  1  0  0  0  0
  4  5  2  0  0  0  0
  5  6  1  0  0  0  0
  6  7  2  0  0  0  0
  7  8  1  0  0  0  0
  8  9  2  0  0  0  0
  9 10  1  0  0  0  0
 10 11  2  0  0  0  0
 11 12  1  0  0  0  0
 12 13  1  6  0  0  0
 12 14  1  0  0  0  0
 14 15  1  4  0  0  0
 14 16  2  0  0  0  0
 17 16  1  6  0  0  0
 17 18  1  0  0  0  0
 18 19  1  0  0  0  0
 19 20  1  0  0  0  0
 20 21  1  0  0  0  0
 21 22  1  0  0  0  0
 22 23  1  6  0  0  0
 23 24  1  0  0  0  0
 22 25  1  0  0  0  0
 25 26  1  1  0  0  0
 25 27  1  0  0  0  0
 27 28  1  6  0  0  0
 27 29  1  0  0  0  0
 20 29  1  0  0  0  0
 29 30  1  1  0  0  0
 17 31  1  0  0  0  0
 31 32  1  6  0  0  0
 31 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
 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
 41 42  1  0  0  0  0
 42 43  1  0  0  0  0
 43 44  1  0  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
 49 50  1  0  0  0  0
 50 51  1  0  0  0  0
 51 52  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0201864

> <DATABASE_NAME>
NP-MRD

> <SMILES>
CCCCCCCCCCCCCCCCCCCC[C@@H](O)[C@H](COC1O[C@H](CO)[C@@H](O)[C@H](O)[C@H]1O)N=C(O)[C@H](O)\C=C\C=C\C=C\C=C\CCC

> <INCHI_IDENTIFIER>
InChI=1S/C42H75NO9/c1-3-5-7-9-11-13-14-15-16-17-18-19-20-21-23-24-26-28-30-35(45)34(33-51-42-40(49)39(48)38(47)37(32-44)52-42)43-41(50)36(46)31-29-27-25-22-12-10-8-6-4-2/h8,10,12,22,25,27,29,31,34-40,42,44-49H,3-7,9,11,13-21,23-24,26,28,30,32-33H2,1-2H3,(H,43,50)/b10-8+,22-12+,27-25+,31-29+/t34-,35+,36+,37+,38+,39-,40+,42?/m0/s1

> <INCHI_KEY>
XYVQIIFHEOOJMH-NZBJCEFGSA-N

> <FORMULA>
C42H75NO9

> <MOLECULAR_WEIGHT>
738.06

> <EXACT_MASS>
737.544182999

> <JCHEM_ACCEPTOR_COUNT>
10

> <JCHEM_ATOM_COUNT>
127

> <JCHEM_AVERAGE_POLARIZABILITY>
92.082925772977

> <JCHEM_BIOAVAILABILITY>
0

> <JCHEM_DONOR_COUNT>
7

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
0

> <JCHEM_IUPAC>
(2R,3E,5E,7E,9E)-2-hydroxy-N-[(2S,3R)-3-hydroxy-1-{[(3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}tricosan-2-yl]trideca-3,5,7,9-tetraenimidic acid

> <JCHEM_LOGP>
8.846430064333335

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
1

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA>
12.202338074080451

> <JCHEM_PKA_STRONGEST_ACIDIC>
3.721538484008968

> <JCHEM_PKA_STRONGEST_BASIC>
1.6199571760359721

> <JCHEM_POLAR_SURFACE_AREA>
172.42999999999998

> <JCHEM_REFRACTIVITY>
212.75470000000004

> <JCHEM_ROTATABLE_BOND_COUNT>
32

> <JCHEM_RULE_OF_FIVE>
0

> <JCHEM_TRADITIONAL_IUPAC>
(2R,3E,5E,7E,9E)-2-hydroxy-N-[(2S,3R)-3-hydroxy-1-{[(3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}tricosan-2-yl]trideca-3,5,7,9-tetraenimidic acid

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 04-SEP-22   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   04-SEP-22         0                                  
HETATM    1  C   UNK     0       5.668  15.852   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0       5.528  14.318   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0       4.130  13.672   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0       3.990  12.139   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0       2.592  11.493   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0       2.452   9.959   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0       1.054   9.313   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0       0.914   7.780   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0      -0.484   7.134   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0      -0.624   5.600   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0      -2.022   4.955   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0      -2.162   3.421   0.000  0.00  0.00           C+0
HETATM   13  O   UNK     0      -3.560   2.775   0.000  0.00  0.00           O+0
HETATM   14  C   UNK     0      -0.903   2.533   0.000  0.00  0.00           C+0
HETATM   15  O   UNK     0       0.495   3.179   0.000  0.00  0.00           O+0
HETATM   16  N   UNK     0      -1.043   0.999   0.000  0.00  0.00           N+0
HETATM   17  C   UNK     0       0.215   0.112   0.000  0.00  0.00           C+0
HETATM   18  C   UNK     0       0.075  -1.422   0.000  0.00  0.00           C+0
HETATM   19  O   UNK     0       1.334  -2.310   0.000  0.00  0.00           O+0
HETATM   20  C   UNK     0       1.194  -3.844   0.000  0.00  0.00           C+0
HETATM   21  O   UNK     0       2.452  -4.732   0.000  0.00  0.00           O+0
HETATM   22  C   UNK     0       2.312  -6.265   0.000  0.00  0.00           C+0
HETATM   23  C   UNK     0       3.571  -7.153   0.000  0.00  0.00           C+0
HETATM   24  O   UNK     0       3.431  -8.687   0.000  0.00  0.00           O+0
HETATM   25  C   UNK     0       0.914  -6.911   0.000  0.00  0.00           C+0
HETATM   26  O   UNK     0       0.774  -8.445   0.000  0.00  0.00           O+0
HETATM   27  C   UNK     0      -0.344  -6.023   0.000  0.00  0.00           C+0
HETATM   28  O   UNK     0      -1.742  -6.669   0.000  0.00  0.00           O+0
HETATM   29  C   UNK     0      -0.204  -4.489   0.000  0.00  0.00           C+0
HETATM   30  O   UNK     0      -1.462  -3.601   0.000  0.00  0.00           O+0
HETATM   31  C   UNK     0       1.613   0.757   0.000  0.00  0.00           C+0
HETATM   32  O   UNK     0       1.753   2.291   0.000  0.00  0.00           O+0
HETATM   33  C   UNK     0       2.872  -0.131   0.000  0.00  0.00           C+0
HETATM   34  C   UNK     0       4.270   0.515   0.000  0.00  0.00           C+0
HETATM   35  C   UNK     0       5.528  -0.373   0.000  0.00  0.00           C+0
HETATM   36  C   UNK     0       6.926   0.273   0.000  0.00  0.00           C+0
HETATM   37  C   UNK     0       8.184  -0.615   0.000  0.00  0.00           C+0
HETATM   38  C   UNK     0       9.582   0.031   0.000  0.00  0.00           C+0
HETATM   39  C   UNK     0      10.841  -0.857   0.000  0.00  0.00           C+0
HETATM   40  C   UNK     0      12.239  -0.211   0.000  0.00  0.00           C+0
HETATM   41  C   UNK     0      13.497  -1.099   0.000  0.00  0.00           C+0
HETATM   42  C   UNK     0      14.895  -0.453   0.000  0.00  0.00           C+0
HETATM   43  C   UNK     0      16.153  -1.341   0.000  0.00  0.00           C+0
HETATM   44  C   UNK     0      17.551  -0.696   0.000  0.00  0.00           C+0
HETATM   45  C   UNK     0      18.810  -1.584   0.000  0.00  0.00           C+0
HETATM   46  C   UNK     0      20.208  -0.938   0.000  0.00  0.00           C+0
HETATM   47  C   UNK     0      21.466  -1.826   0.000  0.00  0.00           C+0
HETATM   48  C   UNK     0      22.864  -1.180   0.000  0.00  0.00           C+0
HETATM   49  C   UNK     0      24.122  -2.068   0.000  0.00  0.00           C+0
HETATM   50  C   UNK     0      25.520  -1.422   0.000  0.00  0.00           C+0
HETATM   51  C   UNK     0      26.779  -2.310   0.000  0.00  0.00           C+0
HETATM   52  C   UNK     0      28.177  -1.664   0.000  0.00  0.00           C+0
CONECT    1    2                                                            
CONECT    2    1    3                                                       
CONECT    3    2    4                                                       
CONECT    4    3    5                                                       
CONECT    5    4    6                                                       
CONECT    6    5    7                                                       
CONECT    7    6    8                                                       
CONECT    8    7    9                                                       
CONECT    9    8   10                                                       
CONECT   10    9   11                                                       
CONECT   11   10   12                                                       
CONECT   12   11   13   14                                                  
CONECT   13   12                                                            
CONECT   14   12   15   16                                                  
CONECT   15   14                                                            
CONECT   16   14   17                                                       
CONECT   17   16   18   31                                                  
CONECT   18   17   19                                                       
CONECT   19   18   20                                                       
CONECT   20   19   21   29                                                  
CONECT   21   20   22                                                       
CONECT   22   21   23   25                                                  
CONECT   23   22   24                                                       
CONECT   24   23                                                            
CONECT   25   22   26   27                                                  
CONECT   26   25                                                            
CONECT   27   25   28   29                                                  
CONECT   28   27                                                            
CONECT   29   27   20   30                                                  
CONECT   30   29                                                            
CONECT   31   17   32   33                                                  
CONECT   32   31                                                            
CONECT   33   31   34                                                       
CONECT   34   33   35                                                       
CONECT   35   34   36                                                       
CONECT   36   35   37                                                       
CONECT   37   36   38                                                       
CONECT   38   37   39                                                       
CONECT   39   38   40                                                       
CONECT   40   39   41                                                       
CONECT   41   40   42                                                       
CONECT   42   41   43                                                       
CONECT   43   42   44                                                       
CONECT   44   43   45                                                       
CONECT   45   44   46                                                       
CONECT   46   45   47                                                       
CONECT   47   46   48                                                       
CONECT   48   47   49                                                       
CONECT   49   48   50                                                       
CONECT   50   49   51                                                       
CONECT   51   50   52                                                       
CONECT   52   51                                                            
MASTER        0    0    0    0    0    0    0    0   52    0  104    0
END

View in JSmol

Synonyms

Not Available

Chemical Formula

C₄₂H₇₅NO₉

Average Mass

738.0600 Da

Monoisotopic Mass

737.54418 Da

IUPAC Name

(2R,3E,5E,7E,9E)-2-hydroxy-N-[(2S,3R)-3-hydroxy-1-{[(3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}tricosan-2-yl]trideca-3,5,7,9-tetraenimidic acid

Traditional Name

(2R,3E,5E,7E,9E)-2-hydroxy-N-[(2S,3R)-3-hydroxy-1-{[(3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}tricosan-2-yl]trideca-3,5,7,9-tetraenimidic acid

CAS Registry Number

Not Available

SMILES

CCCCCCCCCCCCCCCCCCCC[C@@H](O)[C@H](COC1O[C@H](CO)[C@@H](O)[C@H](O)[C@H]1O)N=C(O)[C@H](O)\C=C\C=C\C=C\C=C\CCC

InChI Identifier

InChI=1S/C42H75NO9/c1-3-5-7-9-11-13-14-15-16-17-18-19-20-21-23-24-26-28-30-35(45)34(33-51-42-40(49)39(48)38(47)37(32-44)52-42)43-41(50)36(46)31-29-27-25-22-12-10-8-6-4-2/h8,10,12,22,25,27,29,31,34-40,42,44-49H,3-7,9,11,13-21,23-24,26,28,30,32-33H2,1-2H3,(H,43,50)/b10-8+,22-12+,27-25+,31-29+/t34-,35+,36+,37+,38+,39-,40+,42?/m0/s1

InChI Key

XYVQIIFHEOOJMH-NZBJCEFGSA-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 glycosphingolipids. These are sphingolipids containing a saccharide moiety glycosidically attached to the sphingoid base. Although saccharide moieties are mostly O-glycosidically linked to the ceramide moiety, other sphingolipids with glycosidic bonds of other types (e.G. S-,C-, or N-type) has been reported.

Kingdom

Organic compounds

Super Class

Lipids and lipid-like molecules

Class

Sphingolipids

Sub Class

Glycosphingolipids

Direct Parent

Glycosphingolipids

Alternative Parents

Substituents

Glycosphingolipid
Fatty acyl glycoside
Fatty acyl glycoside of mono- or disaccharide
Alkyl glycoside
Hexose monosaccharide
Glycosyl compound
O-glycosyl compound
Fatty acyl
Monosaccharide
N-acyl-amine
Oxane
Carboxamide group
Secondary carboxylic acid amide
Secondary alcohol
Acetal
Carboxylic acid derivative
Oxacycle
Organoheterocyclic compound
Polyol
Hydrocarbon derivative
Organic oxide
Organopnictogen compound
Alcohol
Organic oxygen compound
Organic nitrogen compound
Primary alcohol
Carbonyl group
Organonitrogen compound
Organooxygen compound
Aliphatic heteromonocyclic compound

Molecular Framework

Aliphatic heteromonocyclic 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	8.85	ChemAxon
pKa (Strongest Acidic)	3.72	ChemAxon
pKa (Strongest Basic)	1.62	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	10	ChemAxon
Hydrogen Donor Count	7	ChemAxon
Polar Surface Area	172.43 Å²	ChemAxon
Rotatable Bond Count	32	ChemAxon
Refractivity	212.75 m³·mol⁻¹	ChemAxon
Polarizability	92.08 Å³	ChemAxon
Number of Rings	1	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

C00048618

Chemspider ID

78441374

KEGG Compound ID

Not Available

BioCyc ID

Not Available

BiGG ID

Not Available

Wikipedia Link

Not Available

METLIN ID

Not Available

PubChem Compound

139587498

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

LOTUS database [Link]

Showing NP-Card for (2r,3e,5e,7e,9e)-2-hydroxy-n-[(2s,3r)-3-hydroxy-1-{[(3r,4s,5s,6r)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}tricosan-2-yl]trideca-3,5,7,9-tetraenimidic acid (NP0201864)

MOL for NP0201864 ((2r,3e,5e,7e,9e)-2-hydroxy-n-[(2s,3r)-3-hydroxy-1-{[(3r,4s,5s,6r)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}tricosan-2-yl]trideca-3,5,7,9-tetraenimidic acid)

3D MOL for NP0201864 ((2r,3e,5e,7e,9e)-2-hydroxy-n-[(2s,3r)-3-hydroxy-1-{[(3r,4s,5s,6r)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}tricosan-2-yl]trideca-3,5,7,9-tetraenimidic acid)

3D SDF for NP0201864 ((2r,3e,5e,7e,9e)-2-hydroxy-n-[(2s,3r)-3-hydroxy-1-{[(3r,4s,5s,6r)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}tricosan-2-yl]trideca-3,5,7,9-tetraenimidic acid)

3D-SDF for NP0201864 ((2r,3e,5e,7e,9e)-2-hydroxy-n-[(2s,3r)-3-hydroxy-1-{[(3r,4s,5s,6r)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}tricosan-2-yl]trideca-3,5,7,9-tetraenimidic acid)

PDB for NP0201864 ((2r,3e,5e,7e,9e)-2-hydroxy-n-[(2s,3r)-3-hydroxy-1-{[(3r,4s,5s,6r)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}tricosan-2-yl]trideca-3,5,7,9-tetraenimidic acid)

3D PDB for NP0201864 ((2r,3e,5e,7e,9e)-2-hydroxy-n-[(2s,3r)-3-hydroxy-1-{[(3r,4s,5s,6r)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}tricosan-2-yl]trideca-3,5,7,9-tetraenimidic acid)

SMILES for NP0201864 ((2r,3e,5e,7e,9e)-2-hydroxy-n-[(2s,3r)-3-hydroxy-1-{[(3r,4s,5s,6r)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}tricosan-2-yl]trideca-3,5,7,9-tetraenimidic acid)

INCHI for NP0201864 ((2r,3e,5e,7e,9e)-2-hydroxy-n-[(2s,3r)-3-hydroxy-1-{[(3r,4s,5s,6r)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}tricosan-2-yl]trideca-3,5,7,9-tetraenimidic acid)

Structure for NP0201864 ((2r,3e,5e,7e,9e)-2-hydroxy-n-[(2s,3r)-3-hydroxy-1-{[(3r,4s,5s,6r)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}tricosan-2-yl]trideca-3,5,7,9-tetraenimidic acid)

3D Structure for NP0201864 ((2r,3e,5e,7e,9e)-2-hydroxy-n-[(2s,3r)-3-hydroxy-1-{[(3r,4s,5s,6r)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}tricosan-2-yl]trideca-3,5,7,9-tetraenimidic acid)