NP-MRD: Showing NP-Card for (2r,3r,5r,6s)-2-[(6-hydroxyhentriacontan-2-yl)oxy]-6-methyloxane-3,5-diol (NP0148232)

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Record Information

Version

2.0

Created at

2022-09-02 03:57:20 UTC

Updated at

2022-09-02 03:57:21 UTC

NP-MRD ID

NP0148232

Secondary Accession Numbers

None

Natural Product Identification

Common Name

(2r,3r,5r,6s)-2-[(6-hydroxyhentriacontan-2-yl)oxy]-6-methyloxane-3,5-diol

Description

Ascaroside B belongs to the class of organic compounds known as hexoses. These are monosaccharides in which the sugar unit is a is a six-carbon containing moeity. (2r,3r,5r,6s)-2-[(6-hydroxyhentriacontan-2-yl)oxy]-6-methyloxane-3,5-diol is found in Ascaris suum. (2r,3r,5r,6s)-2-[(6-hydroxyhentriacontan-2-yl)oxy]-6-methyloxane-3,5-diol was first documented in 2019 (PMID: 31484427). Based on a literature review very few articles have been published on Ascaroside B.

Structure

MOL 3D MOL SDF PDB SMILES InChI


  Mrv1652309022205572D          

 42 42  0  0  1  0            999 V2000
    9.2881  -18.5625    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   10.0026  -18.9750    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   10.7171  -18.5625    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   11.4315  -18.9750    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   12.1460  -18.5625    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   12.8605  -18.9750    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   13.5749  -18.5625    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   14.2894  -18.9750    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   15.0039  -18.5625    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   15.7184  -18.9750    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   16.4328  -18.5625    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   17.1473  -18.9750    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   17.8618  -18.5625    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   18.5762  -18.9750    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   19.2907  -18.5625    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   20.0052  -18.9750    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   20.7197  -18.5625    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   21.4341  -18.9750    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   22.1486  -18.5625    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   22.8631  -18.9750    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   23.5775  -18.5625    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   24.2920  -18.9750    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   25.0065  -18.5625    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   25.7210  -18.9750    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   26.4354  -18.5625    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   27.1499  -18.9750    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   27.1499  -19.8000    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   27.8644  -18.5625    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   28.5788  -18.9750    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   29.2933  -18.5625    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   30.0078  -18.9750    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   30.0078  -19.8000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   30.7223  -18.5625    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   31.4367  -18.9750    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
   32.1512  -18.5625    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   32.8657  -18.9750    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
   33.5801  -18.5625    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   32.8657  -19.8000    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
   33.5801  -20.2125    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   32.1512  -20.2125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   31.4367  -19.8000    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
   30.7223  -20.2125    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  1  0  0  0  0
  6  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
 13 14  1  0  0  0  0
 14 15  1  0  0  0  0
 15 16  1  0  0  0  0
 16 17  1  0  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  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
 26 27  1  0  0  0  0
 26 28  1  0  0  0  0
 28 29  1  0  0  0  0
 29 30  1  0  0  0  0
 30 31  1  0  0  0  0
 31 32  1  0  0  0  0
 31 33  1  0  0  0  0
 34 33  1  6  0  0  0
 34 35  1  0  0  0  0
 35 36  1  0  0  0  0
 36 37  1  1  0  0  0
 36 38  1  0  0  0  0
 38 39  1  6  0  0  0
 38 40  1  0  0  0  0
 40 41  1  0  0  0  0
 34 41  1  0  0  0  0
 41 42  1  1  0  0  0
M  END

     RDKit          3D

116116  0  0  0  0  0  0  0  0999 V2000
   14.2643   -1.6519   -3.5324 C   0  0  0  0  0  0  0  0  0  0  0  0
   13.5713   -0.4208   -2.9299 C   0  0  0  0  0  0  0  0  0  0  0  0
   13.7746   -0.4325   -1.4355 C   0  0  0  0  0  0  0  0  0  0  0  0
   13.1576    0.7244   -0.7225 C   0  0  0  0  0  0  0  0  0  0  0  0
   11.6847    0.8698   -0.8598 C   0  0  0  0  0  0  0  0  0  0  0  0
   10.9531   -0.3527   -0.3305 C   0  0  0  0  0  0  0  0  0  0  0  0
    9.4812   -0.0617   -0.4901 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.5904   -1.1888   -0.0176 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.7764   -1.5561    1.4044 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.5879   -0.5673    2.4539 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.3578    0.1685    2.7215 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.1007   -0.5343    3.0721 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.4245   -1.3487    2.0317 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.9419   -0.4898    0.8728 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.9394    0.5426    1.3317 C   0  0  0  0  0  0  0  0  0  0  0  0
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   -5.4210    2.2283    1.3724 C   0  0  1  0  0  0  0  0  0  0  0  0
   -5.6373    3.5618    0.9794 O   0  0  0  0  0  0  0  0  0  0  0  0
   -6.7351    1.4845    1.4360 C   0  0  0  0  0  0  0  0  0  0  0  0
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   -8.7612    0.7535    0.1545 C   0  0  0  0  0  0  0  0  0  0  0  0
   -9.4632    0.7897   -1.1849 C   0  0  2  0  0  0  0  0  0  0  0  0
   -9.6584    2.2779   -1.4860 C   0  0  0  0  0  0  0  0  0  0  0  0
  -10.6744    0.1328   -1.1700 O   0  0  0  0  0  0  0  0  0  0  0  0
  -10.8631   -0.8234   -2.1281 C   0  0  2  0  0  0  0  0  0  0  0  0
  -12.0337   -0.4355   -2.8305 O   0  0  0  0  0  0  0  0  0  0  0  0
  -13.0040   -0.2790   -1.8321 C   0  0  1  0  0  0  0  0  0  0  0  0
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  -13.5760   -1.6485   -1.5424 C   0  0  2  0  0  0  0  0  0  0  0  0
  -14.1190   -1.7316   -0.2601 O   0  0  0  0  0  0  0  0  0  0  0  0
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  -10.2227   -3.1296   -1.9270 O   0  0  0  0  0  0  0  0  0  0  0  0
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 36 38  1  0
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 38 40  1  0
 40 41  1  0
 41 42  1  0
 41 34  1  0
  1 43  1  0
  1 44  1  0
  1 45  1  0
  2 46  1  0
  2 47  1  0
  3 48  1  0
  3 49  1  0
  4 50  1  0
  4 51  1  0
  5 52  1  0
  5 53  1  0
  6 54  1  0
  6 55  1  0
  7 56  1  0
  7 57  1  0
  8 58  1  0
  8 59  1  0
  9 60  1  0
  9 61  1  0
 10 62  1  0
 10 63  1  0
 11 64  1  0
 11 65  1  0
 12 66  1  0
 12 67  1  0
 13 68  1  0
 13 69  1  0
 14 70  1  0
 14 71  1  0
 15 72  1  0
 15 73  1  0
 16 74  1  0
 16 75  1  0
 17 76  1  0
 17 77  1  0
 18 78  1  0
 18 79  1  0
 19 80  1  0
 19 81  1  0
 20 82  1  0
 20 83  1  0
 21 84  1  0
 21 85  1  0
 22 86  1  0
 22 87  1  0
 23 88  1  0
 23 89  1  0
 24 90  1  0
 24 91  1  0
 25 92  1  0
 25 93  1  0
 26 94  1  1
 27 95  1  0
 28 96  1  0
 28 97  1  0
 29 98  1  0
 29 99  1  0
 30100  1  0
 30101  1  0
 31102  1  6
 32103  1  0
 32104  1  0
 32105  1  0
 34106  1  6
 36107  1  1
 37108  1  0
 37109  1  0
 37110  1  0
 38111  1  6
 39112  1  0
 40113  1  0
 40114  1  0
 41115  1  1
 42116  1  0
M  END


  Mrv1652309022205572D          

 42 42  0  0  1  0            999 V2000
    9.2881  -18.5625    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   10.0026  -18.9750    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   10.7171  -18.5625    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   11.4315  -18.9750    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   12.1460  -18.5625    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   12.8605  -18.9750    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   13.5749  -18.5625    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   14.2894  -18.9750    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   15.0039  -18.5625    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   15.7184  -18.9750    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   16.4328  -18.5625    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   17.1473  -18.9750    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   17.8618  -18.5625    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   18.5762  -18.9750    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   19.2907  -18.5625    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   20.0052  -18.9750    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   20.7197  -18.5625    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   21.4341  -18.9750    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   22.1486  -18.5625    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   22.8631  -18.9750    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   23.5775  -18.5625    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   24.2920  -18.9750    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   25.0065  -18.5625    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   25.7210  -18.9750    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   26.4354  -18.5625    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   27.1499  -18.9750    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   27.1499  -19.8000    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   27.8644  -18.5625    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   28.5788  -18.9750    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   29.2933  -18.5625    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   30.0078  -18.9750    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   30.0078  -19.8000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   30.7223  -18.5625    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   31.4367  -18.9750    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
   32.1512  -18.5625    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   32.8657  -18.9750    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
   33.5801  -18.5625    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   32.8657  -19.8000    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
   33.5801  -20.2125    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   32.1512  -20.2125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   31.4367  -19.8000    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
   30.7223  -20.2125    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  1  0  0  0  0
  6  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
 13 14  1  0  0  0  0
 14 15  1  0  0  0  0
 15 16  1  0  0  0  0
 16 17  1  0  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  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
 26 27  1  0  0  0  0
 26 28  1  0  0  0  0
 28 29  1  0  0  0  0
 29 30  1  0  0  0  0
 30 31  1  0  0  0  0
 31 32  1  0  0  0  0
 31 33  1  0  0  0  0
 34 33  1  6  0  0  0
 34 35  1  0  0  0  0
 35 36  1  0  0  0  0
 36 37  1  1  0  0  0
 36 38  1  0  0  0  0
 38 39  1  6  0  0  0
 38 40  1  0  0  0  0
 40 41  1  0  0  0  0
 34 41  1  0  0  0  0
 41 42  1  1  0  0  0
M  END
> <DATABASE_ID>
NP0148232

> <DATABASE_NAME>
NP-MRD

> <SMILES>
CCCCCCCCCCCCCCCCCCCCCCCCCC(O)CCCC(C)O[C@@H]1O[C@@H](C)[C@H](O)C[C@H]1O

> <INCHI_IDENTIFIER>
InChI=1S/C37H74O5/c1-4-5-6-7-8-9-10-11-12-13-14-15-16-17-18-19-20-21-22-23-24-25-26-29-34(38)30-27-28-32(2)41-37-36(40)31-35(39)33(3)42-37/h32-40H,4-31H2,1-3H3/t32?,33-,34?,35+,36+,37+/m0/s1

> <INCHI_KEY>
ZHQGZAGCRJWKCK-NWNZWMTCSA-N

> <FORMULA>
C37H74O5

> <MOLECULAR_WEIGHT>
598.994

> <EXACT_MASS>
598.553625483

> <JCHEM_ACCEPTOR_COUNT>
5

> <JCHEM_ATOM_COUNT>
116

> <JCHEM_AVERAGE_POLARIZABILITY>
79.94984291458161

> <JCHEM_BIOAVAILABILITY>
0

> <JCHEM_DONOR_COUNT>
3

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
0

> <JCHEM_IUPAC>
(2R,3R,5R,6S)-2-[(6-hydroxyhentriacontan-2-yl)oxy]-6-methyloxane-3,5-diol

> <ALOGPS_LOGP>
9.55

> <JCHEM_LOGP>
11.360332735666665

> <ALOGPS_LOGS>
-6.99

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
1

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA>
14.278534061185468

> <JCHEM_PKA_STRONGEST_ACIDIC>
13.264073045569202

> <JCHEM_PKA_STRONGEST_BASIC>
-1.2741406094878749

> <JCHEM_POLAR_SURFACE_AREA>
79.15

> <JCHEM_REFRACTIVITY>
177.6217

> <JCHEM_ROTATABLE_BOND_COUNT>
30

> <JCHEM_RULE_OF_FIVE>
0

> <ALOGPS_SOLUBILITY>
6.11e-05 g/l

> <JCHEM_TRADITIONAL_IUPAC>
(2R,3R,5R,6S)-2-[(6-hydroxyhentriacontan-2-yl)oxy]-6-methyloxane-3,5-diol

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 02-SEP-22   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   02-SEP-22         0                                  
HETATM    1  C   UNK     0      17.338 -34.650   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0      18.672 -35.420   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0      20.005 -34.650   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0      21.339 -35.420   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0      22.673 -34.650   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0      24.006 -35.420   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0      25.340 -34.650   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0      26.674 -35.420   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0      28.007 -34.650   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0      29.341 -35.420   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0      30.675 -34.650   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0      32.008 -35.420   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0      33.342 -34.650   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0      34.676 -35.420   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0      36.009 -34.650   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0      37.343 -35.420   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0      38.677 -34.650   0.000  0.00  0.00           C+0
HETATM   18  C   UNK     0      40.010 -35.420   0.000  0.00  0.00           C+0
HETATM   19  C   UNK     0      41.344 -34.650   0.000  0.00  0.00           C+0
HETATM   20  C   UNK     0      42.678 -35.420   0.000  0.00  0.00           C+0
HETATM   21  C   UNK     0      44.011 -34.650   0.000  0.00  0.00           C+0
HETATM   22  C   UNK     0      45.345 -35.420   0.000  0.00  0.00           C+0
HETATM   23  C   UNK     0      46.679 -34.650   0.000  0.00  0.00           C+0
HETATM   24  C   UNK     0      48.012 -35.420   0.000  0.00  0.00           C+0
HETATM   25  C   UNK     0      49.346 -34.650   0.000  0.00  0.00           C+0
HETATM   26  C   UNK     0      50.680 -35.420   0.000  0.00  0.00           C+0
HETATM   27  O   UNK     0      50.680 -36.960   0.000  0.00  0.00           O+0
HETATM   28  C   UNK     0      52.013 -34.650   0.000  0.00  0.00           C+0
HETATM   29  C   UNK     0      53.347 -35.420   0.000  0.00  0.00           C+0
HETATM   30  C   UNK     0      54.681 -34.650   0.000  0.00  0.00           C+0
HETATM   31  C   UNK     0      56.015 -35.420   0.000  0.00  0.00           C+0
HETATM   32  C   UNK     0      56.015 -36.960   0.000  0.00  0.00           C+0
HETATM   33  O   UNK     0      57.348 -34.650   0.000  0.00  0.00           O+0
HETATM   34  C   UNK     0      58.682 -35.420   0.000  0.00  0.00           C+0
HETATM   35  O   UNK     0      60.016 -34.650   0.000  0.00  0.00           O+0
HETATM   36  C   UNK     0      61.349 -35.420   0.000  0.00  0.00           C+0
HETATM   37  C   UNK     0      62.683 -34.650   0.000  0.00  0.00           C+0
HETATM   38  C   UNK     0      61.349 -36.960   0.000  0.00  0.00           C+0
HETATM   39  O   UNK     0      62.683 -37.730   0.000  0.00  0.00           O+0
HETATM   40  C   UNK     0      60.016 -37.730   0.000  0.00  0.00           C+0
HETATM   41  C   UNK     0      58.682 -36.960   0.000  0.00  0.00           C+0
HETATM   42  O   UNK     0      57.348 -37.730   0.000  0.00  0.00           O+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                                                       
CONECT   13   12   14                                                       
CONECT   14   13   15                                                       
CONECT   15   14   16                                                       
CONECT   16   15   17                                                       
CONECT   17   16   18                                                       
CONECT   18   17   19                                                       
CONECT   19   18   20                                                       
CONECT   20   19   21                                                       
CONECT   21   20   22                                                       
CONECT   22   21   23                                                       
CONECT   23   22   24                                                       
CONECT   24   23   25                                                       
CONECT   25   24   26                                                       
CONECT   26   25   27   28                                                  
CONECT   27   26                                                            
CONECT   28   26   29                                                       
CONECT   29   28   30                                                       
CONECT   30   29   31                                                       
CONECT   31   30   32   33                                                  
CONECT   32   31                                                            
CONECT   33   31   34                                                       
CONECT   34   33   35   41                                                  
CONECT   35   34   36                                                       
CONECT   36   35   37   38                                                  
CONECT   37   36                                                            
CONECT   38   36   39   40                                                  
CONECT   39   38                                                            
CONECT   40   38   41                                                       
CONECT   41   40   34   42                                                  
CONECT   42   41                                                            
MASTER        0    0    0    0    0    0    0    0   42    0   84    0
END

View in JSmol

Synonyms

Not Available

Chemical Formula

C₃₇H₇₄O₅

Average Mass

598.9940 Da

Monoisotopic Mass

598.55363 Da

IUPAC Name

(2R,3R,5R,6S)-2-[(6-hydroxyhentriacontan-2-yl)oxy]-6-methyloxane-3,5-diol

Traditional Name

(2R,3R,5R,6S)-2-[(6-hydroxyhentriacontan-2-yl)oxy]-6-methyloxane-3,5-diol

CAS Registry Number

Not Available

SMILES

CCCCCCCCCCCCCCCCCCCCCCCCCC(O)CCCC(C)O[C@@H]1O[C@@H](C)[C@H](O)C[C@H]1O

InChI Identifier

InChI=1S/C37H74O5/c1-4-5-6-7-8-9-10-11-12-13-14-15-16-17-18-19-20-21-22-23-24-25-26-29-34(38)30-27-28-32(2)41-37-36(40)31-35(39)33(3)42-37/h32-40H,4-31H2,1-3H3/t32?,33-,34?,35+,36+,37+/m0/s1

InChI Key

ZHQGZAGCRJWKCK-NWNZWMTCSA-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

Species Name	Source	Reference
Ascaris suum	LOTUS Database	35616633

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as hexoses. These are monosaccharides in which the sugar unit is a is a six-carbon containing moeity.

Kingdom

Organic compounds

Super Class

Organic oxygen compounds

Class

Organooxygen compounds

Sub Class

Carbohydrates and carbohydrate conjugates

Direct Parent

Hexoses

Alternative Parents

Substituents

Hexose monosaccharide
Fatty alcohol
Fatty acyl
Oxane
Secondary alcohol
Oxacycle
Organoheterocyclic compound
Acetal
Hydrocarbon derivative
Alcohol
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	9.55	ALOGPS
logP	11.36	ChemAxon
logS	-7	ALOGPS
pKa (Strongest Acidic)	13.26	ChemAxon
pKa (Strongest Basic)	-1.3	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	5	ChemAxon
Hydrogen Donor Count	3	ChemAxon
Polar Surface Area	79.15 Å²	ChemAxon
Rotatable Bond Count	30	ChemAxon
Refractivity	177.62 m³·mol⁻¹	ChemAxon
Polarizability	79.95 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

C00036884

Chemspider ID

57524651

KEGG Compound ID

Not Available

BioCyc ID

Not Available

BiGG ID

Not Available

Wikipedia Link

Not Available

METLIN ID

Not Available

PubChem Compound

44151568

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

Gao M, Li Y, Zhang W, Wei P, Wang X, Feng Y, Zhang X: Bx-daf-22 Contributes to Mate Attraction in the Gonochoristic Nematode Bursaphelenchus xylophilus. Int J Mol Sci. 2019 Sep 3;20(17):4316. doi: 10.3390/ijms20174316. [PubMed:31484427 ]
LOTUS database [Link]

Showing NP-Card for (2r,3r,5r,6s)-2-[(6-hydroxyhentriacontan-2-yl)oxy]-6-methyloxane-3,5-diol (NP0148232)

MOL for NP0148232 ((2r,3r,5r,6s)-2-[(6-hydroxyhentriacontan-2-yl)oxy]-6-methyloxane-3,5-diol)

3D MOL for NP0148232 ((2r,3r,5r,6s)-2-[(6-hydroxyhentriacontan-2-yl)oxy]-6-methyloxane-3,5-diol)

3D SDF for NP0148232 ((2r,3r,5r,6s)-2-[(6-hydroxyhentriacontan-2-yl)oxy]-6-methyloxane-3,5-diol)

3D-SDF for NP0148232 ((2r,3r,5r,6s)-2-[(6-hydroxyhentriacontan-2-yl)oxy]-6-methyloxane-3,5-diol)

PDB for NP0148232 ((2r,3r,5r,6s)-2-[(6-hydroxyhentriacontan-2-yl)oxy]-6-methyloxane-3,5-diol)

3D PDB for NP0148232 ((2r,3r,5r,6s)-2-[(6-hydroxyhentriacontan-2-yl)oxy]-6-methyloxane-3,5-diol)

SMILES for NP0148232 ((2r,3r,5r,6s)-2-[(6-hydroxyhentriacontan-2-yl)oxy]-6-methyloxane-3,5-diol)

INCHI for NP0148232 ((2r,3r,5r,6s)-2-[(6-hydroxyhentriacontan-2-yl)oxy]-6-methyloxane-3,5-diol)

Structure for NP0148232 ((2r,3r,5r,6s)-2-[(6-hydroxyhentriacontan-2-yl)oxy]-6-methyloxane-3,5-diol)

3D Structure for NP0148232 ((2r,3r,5r,6s)-2-[(6-hydroxyhentriacontan-2-yl)oxy]-6-methyloxane-3,5-diol)