NP-MRD: Showing NP-Card for 2,4,5-trihydroxy-3-{[3,4,5-trihydroxy-6-({[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}methyl)oxan-2-yl]oxy}pentanal (NP0293364)

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Record Information

Version

2.0

Created at

2022-09-10 01:20:00 UTC

Updated at

2022-09-10 01:20:01 UTC

NP-MRD ID

NP0293364

Secondary Accession Numbers

None

Natural Product Identification

Common Name

2,4,5-trihydroxy-3-{[3,4,5-trihydroxy-6-({[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}methyl)oxan-2-yl]oxy}pentanal

Description

2,4,5-Trihydroxy-3-{[3,4,5-trihydroxy-6-({[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}methyl)oxan-2-yl]oxy}pentanal belongs to the class of organic compounds known as oligosaccharides. These are carbohydrates made up of 3 to 10 monosaccharide units linked to each other through glycosidic bonds. 2,4,5-trihydroxy-3-{[3,4,5-trihydroxy-6-({[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}methyl)oxan-2-yl]oxy}pentanal is found in Terminalia anogeissiana. 2,4,5-Trihydroxy-3-{[3,4,5-trihydroxy-6-({[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}methyl)oxan-2-yl]oxy}pentanal is an extremely weak basic (essentially neutral) compound (based on its pKa).

Structure

MOL 3D MOL SDF PDB SMILES InChI


  Mrv1533004241513282D          

 32 33  0  0  0  0            999 V2000
   -1.8414   -4.2355    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4289   -4.9500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6039   -4.9500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1914   -4.2355    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1914   -5.6645    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6039   -6.3789    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1914   -7.0934    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.6336   -7.0934    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.0461   -7.8079    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.8711   -7.8079    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.2836   -7.0934    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.1086   -7.0934    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5211   -6.3789    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.3461   -6.3789    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.7586   -5.6645    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.5836   -5.6645    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.7586   -7.0934    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.5836   -7.0934    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.3461   -7.8079    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.7586   -8.5224    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.5211   -7.8079    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.1086   -8.5224    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.6336   -8.5224    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.0461   -9.2368    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1914   -8.5224    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6039   -9.2368    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6039   -7.8079    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4289   -7.8079    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.6336   -5.6645    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.0461   -6.3789    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.0461   -4.9500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.8711   -4.9500    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
  3  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
 14 17  1  0  0  0  0
 17 18  1  0  0  0  0
 17 19  1  0  0  0  0
 19 20  1  0  0  0  0
 19 21  1  0  0  0  0
 12 21  1  0  0  0  0
 21 22  1  0  0  0  0
  9 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
 25 27  1  0  0  0  0
  7 27  1  0  0  0  0
 27 28  1  0  0  0  0
  5 29  1  0  0  0  0
 29 30  1  0  0  0  0
 29 31  1  0  0  0  0
 31 32  2  0  0  0  0
M  END

     RDKit          3D

 62 63  0  0  0  0  0  0  0  0999 V2000
   -0.9384    3.3530   -1.4338 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0826    3.2754   -0.9564 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2904    2.5177    0.2795 C   0  0  2  0  0  0  0  0  0  0  0  0
   -0.9619    2.1513    0.7228 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.0566    1.2437    0.1005 C   0  0  2  0  0  0  0  0  0  0  0  0
   -2.5527    0.4323   -0.8987 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9709   -0.6854   -0.3793 C   0  0  2  0  0  0  0  0  0  0  0  0
   -0.6283   -0.8593   -0.7910 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.0000   -1.6768    0.1356 C   0  0  2  0  0  0  0  0  0  0  0  0
    1.1620   -2.4342   -0.4726 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1556   -1.6605   -0.9886 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.8210   -0.8133   -0.1762 C   0  0  2  0  0  0  0  0  0  0  0  0
    2.6784    0.5279   -0.5422 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.9862    1.3915    0.4778 C   0  0  2  0  0  0  0  0  0  0  0  0
    3.5095    2.7294   -0.0319 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.6676    2.5441   -0.7847 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.8879    0.8495    1.5225 C   0  0  1  0  0  0  0  0  0  0  0  0
    3.1575    0.5382    2.6953 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.7865   -0.2686    1.1216 C   0  0  2  0  0  0  0  0  0  0  0  0
    6.1138    0.1360    0.9474 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.3087   -1.0595   -0.0766 C   0  0  2  0  0  0  0  0  0  0  0  0
    4.9825   -0.5075   -1.1893 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9198   -2.6628    0.7995 C   0  0  2  0  0  0  0  0  0  0  0  0
   -0.1825   -3.8297    1.0971 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1000   -3.0763    0.0020 C   0  0  2  0  0  0  0  0  0  0  0  0
   -1.9143   -4.2165   -0.7584 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6669   -1.9697   -0.8620 C   0  0  2  0  0  0  0  0  0  0  0  0
   -2.2089   -2.2047   -2.1604 O   0  0  0  0  0  0  0  0  0  0  0  0
   -4.5329    1.3271    0.1576 C   0  0  1  0  0  0  0  0  0  0  0  0
   -5.0413    2.2040    1.1107 O   0  0  0  0  0  0  0  0  0  0  0  0
   -5.2149    1.4493   -1.1590 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.1497    2.7147   -1.6521 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8282    3.7912   -1.5167 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7149    3.1563    1.0552 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0629    1.4693    1.4355 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8098    0.6852    1.1179 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0143   -0.7189    0.7199 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.4096   -1.0037    0.9159 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.5104   -3.2334    0.2128 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.7140   -3.0003   -1.3448 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.4244   -0.8918    0.8561 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.0032    1.6536    0.9728 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.7358    3.2140   -0.6819 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.7374    3.4214    0.7774 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.6615    2.9702   -1.6601 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.5654    1.6898    1.8624 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.2501    0.9621    2.6585 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.8215   -0.9847    1.9956 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.7590   -0.5506    1.2870 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.5689   -2.1099    0.0638 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.4400   -1.2190   -1.7046 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2316   -2.2647    1.7986 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5857   -4.6353    0.6969 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.9225   -3.3282    0.7352 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4767   -3.9486   -1.6059 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.7527   -1.8825   -0.8019 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2808   -1.4257   -2.7486 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.9258    0.2967    0.5798 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.7251    1.8710    1.9981 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.7015    0.7289   -1.8522 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.2604    1.0778   -1.0279 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.1126    2.7497   -2.6516 H   0  0  0  0  0  0  0  0  0  0  0  0
 32 31  1  0
 31 29  1  0
 29 30  1  0
 29  5  1  0
  5  6  1  0
  6  7  1  0
  7  8  1  0
  8  9  1  0
  9 10  1  0
 10 11  1  0
 11 12  1  0
 12 13  1  0
 13 14  1  0
 14 15  1  0
 15 16  1  0
 14 17  1  0
 17 18  1  0
 17 19  1  0
 19 20  1  0
 19 21  1  0
 21 22  1  0
  9 23  1  0
 23 24  1  0
 23 25  1  0
 25 26  1  0
 25 27  1  0
 27 28  1  0
  5  3  1  0
  3  4  1  0
  3  2  1  0
  2  1  2  0
 27  7  1  0
 21 12  1  0
 32 62  1  0
 31 60  1  0
 31 61  1  0
 29 58  1  1
 30 59  1  0
  5 36  1  1
  7 37  1  1
  9 38  1  1
 10 39  1  0
 10 40  1  0
 12 41  1  1
 14 42  1  1
 15 43  1  0
 15 44  1  0
 16 45  1  0
 17 46  1  1
 18 47  1  0
 19 48  1  1
 20 49  1  0
 21 50  1  1
 22 51  1  0
 23 52  1  1
 24 53  1  0
 25 54  1  1
 26 55  1  0
 27 56  1  6
 28 57  1  0
  3 34  1  1
  4 35  1  0
  2 33  1  0
M  END


  Mrv1533004241513282D          

 32 33  0  0  0  0            999 V2000
   -1.8414   -4.2355    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4289   -4.9500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6039   -4.9500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1914   -4.2355    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1914   -5.6645    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6039   -6.3789    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1914   -7.0934    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.6336   -7.0934    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.0461   -7.8079    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.8711   -7.8079    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.2836   -7.0934    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.1086   -7.0934    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5211   -6.3789    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.3461   -6.3789    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.7586   -5.6645    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.5836   -5.6645    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.7586   -7.0934    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.5836   -7.0934    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.3461   -7.8079    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.7586   -8.5224    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.5211   -7.8079    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.1086   -8.5224    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.6336   -8.5224    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.0461   -9.2368    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1914   -8.5224    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6039   -9.2368    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6039   -7.8079    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4289   -7.8079    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.6336   -5.6645    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.0461   -6.3789    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.0461   -4.9500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.8711   -4.9500    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
  3  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
 14 17  1  0  0  0  0
 17 18  1  0  0  0  0
 17 19  1  0  0  0  0
 19 20  1  0  0  0  0
 19 21  1  0  0  0  0
 12 21  1  0  0  0  0
 21 22  1  0  0  0  0
  9 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
 25 27  1  0  0  0  0
  7 27  1  0  0  0  0
 27 28  1  0  0  0  0
  5 29  1  0  0  0  0
 29 30  1  0  0  0  0
 29 31  1  0  0  0  0
 31 32  2  0  0  0  0
M  END
> <DATABASE_ID>
NP0293364

> <DATABASE_NAME>
NP-MRD

> <SMILES>
OCC(O)C(OC1OC(COC2OC(CO)C(O)C(O)C2O)C(O)C(O)C1O)C(O)C=O

> <INCHI_IDENTIFIER>
InChI=1S/C17H30O15/c18-1-5(21)15(6(22)2-19)32-17-14(28)12(26)10(24)8(31-17)4-29-16-13(27)11(25)9(23)7(3-20)30-16/h1,5-17,19-28H,2-4H2

> <INCHI_KEY>
QITIYHVQGNHDNI-UHFFFAOYSA-N

> <FORMULA>
C17H30O15

> <MOLECULAR_WEIGHT>
474.412

> <EXACT_MASS>
474.158470266

> <JCHEM_ACCEPTOR_COUNT>
15

> <JCHEM_ATOM_COUNT>
62

> <JCHEM_AVERAGE_POLARIZABILITY>
44.00886510854126

> <JCHEM_BIOAVAILABILITY>
0

> <JCHEM_DONOR_COUNT>
10

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
0

> <JCHEM_IUPAC>
2,4,5-trihydroxy-3-{[3,4,5-trihydroxy-6-({[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}methyl)oxan-2-yl]oxy}pentanal

> <ALOGPS_LOGP>
-2.81

> <JCHEM_LOGP>
-6.479696912333333

> <ALOGPS_LOGS>
-0.21

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
2

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA>
12.241448149317387

> <JCHEM_PKA_STRONGEST_ACIDIC>
11.797156128576546

> <JCHEM_PKA_STRONGEST_BASIC>
-3.52967570192079

> <JCHEM_POLAR_SURFACE_AREA>
256.28999999999996

> <JCHEM_REFRACTIVITY>
96.20970000000001

> <JCHEM_ROTATABLE_BOND_COUNT>
10

> <JCHEM_RULE_OF_FIVE>
0

> <ALOGPS_SOLUBILITY>
2.93e+02 g/l

> <JCHEM_TRADITIONAL_IUPAC>
2,4,5-trihydroxy-3-{[3,4,5-trihydroxy-6-({[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}methyl)oxan-2-yl]oxy}pentanal

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 24-APR-15   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   24-APR-15         0                                  
HETATM    1  O   UNK     0      -3.437  -7.906   0.000  0.00  0.00           O+0
HETATM    2  C   UNK     0      -2.667  -9.240   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0      -1.127  -9.240   0.000  0.00  0.00           C+0
HETATM    4  O   UNK     0      -0.357  -7.906   0.000  0.00  0.00           O+0
HETATM    5  C   UNK     0      -0.357 -10.574   0.000  0.00  0.00           C+0
HETATM    6  O   UNK     0      -1.127 -11.907   0.000  0.00  0.00           O+0
HETATM    7  C   UNK     0      -0.357 -13.241   0.000  0.00  0.00           C+0
HETATM    8  O   UNK     0       1.183 -13.241   0.000  0.00  0.00           O+0
HETATM    9  C   UNK     0       1.953 -14.575   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0       3.493 -14.575   0.000  0.00  0.00           C+0
HETATM   11  O   UNK     0       4.263 -13.241   0.000  0.00  0.00           O+0
HETATM   12  C   UNK     0       5.803 -13.241   0.000  0.00  0.00           C+0
HETATM   13  O   UNK     0       6.573 -11.907   0.000  0.00  0.00           O+0
HETATM   14  C   UNK     0       8.113 -11.907   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0       8.883 -10.574   0.000  0.00  0.00           C+0
HETATM   16  O   UNK     0      10.423 -10.574   0.000  0.00  0.00           O+0
HETATM   17  C   UNK     0       8.883 -13.241   0.000  0.00  0.00           C+0
HETATM   18  O   UNK     0      10.423 -13.241   0.000  0.00  0.00           O+0
HETATM   19  C   UNK     0       8.113 -14.575   0.000  0.00  0.00           C+0
HETATM   20  O   UNK     0       8.883 -15.908   0.000  0.00  0.00           O+0
HETATM   21  C   UNK     0       6.573 -14.575   0.000  0.00  0.00           C+0
HETATM   22  O   UNK     0       5.803 -15.908   0.000  0.00  0.00           O+0
HETATM   23  C   UNK     0       1.183 -15.908   0.000  0.00  0.00           C+0
HETATM   24  O   UNK     0       1.953 -17.242   0.000  0.00  0.00           O+0
HETATM   25  C   UNK     0      -0.357 -15.908   0.000  0.00  0.00           C+0
HETATM   26  O   UNK     0      -1.127 -17.242   0.000  0.00  0.00           O+0
HETATM   27  C   UNK     0      -1.127 -14.575   0.000  0.00  0.00           C+0
HETATM   28  O   UNK     0      -2.667 -14.575   0.000  0.00  0.00           O+0
HETATM   29  C   UNK     0       1.183 -10.574   0.000  0.00  0.00           C+0
HETATM   30  O   UNK     0       1.953 -11.907   0.000  0.00  0.00           O+0
HETATM   31  C   UNK     0       1.953  -9.240   0.000  0.00  0.00           C+0
HETATM   32  O   UNK     0       3.493  -9.240   0.000  0.00  0.00           O+0
CONECT    1    2                                                            
CONECT    2    1    3                                                       
CONECT    3    2    4    5                                                  
CONECT    4    3                                                            
CONECT    5    3    6   29                                                  
CONECT    6    5    7                                                       
CONECT    7    6    8   27                                                  
CONECT    8    7    9                                                       
CONECT    9    8   10   23                                                  
CONECT   10    9   11                                                       
CONECT   11   10   12                                                       
CONECT   12   11   13   21                                                  
CONECT   13   12   14                                                       
CONECT   14   13   15   17                                                  
CONECT   15   14   16                                                       
CONECT   16   15                                                            
CONECT   17   14   18   19                                                  
CONECT   18   17                                                            
CONECT   19   17   20   21                                                  
CONECT   20   19                                                            
CONECT   21   19   12   22                                                  
CONECT   22   21                                                            
CONECT   23    9   24   25                                                  
CONECT   24   23                                                            
CONECT   25   23   26   27                                                  
CONECT   26   25                                                            
CONECT   27   25    7   28                                                  
CONECT   28   27                                                            
CONECT   29    5   30   31                                                  
CONECT   30   29                                                            
CONECT   31   29   32                                                       
CONECT   32   31                                                            
MASTER        0    0    0    0    0    0    0    0   32    0   66    0
END

View in JSmol

Synonyms

Not Available

Chemical Formula

C₁₇H₃₀O₁₅

Average Mass

474.4120 Da

Monoisotopic Mass

474.15847 Da

IUPAC Name

2,4,5-trihydroxy-3-{[3,4,5-trihydroxy-6-({[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}methyl)oxan-2-yl]oxy}pentanal

Traditional Name

2,4,5-trihydroxy-3-{[3,4,5-trihydroxy-6-({[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}methyl)oxan-2-yl]oxy}pentanal

CAS Registry Number

Not Available

SMILES

OCC(O)C(OC1OC(COC2OC(CO)C(O)C(O)C2O)C(O)C(O)C1O)C(O)C=O

InChI Identifier

InChI=1S/C17H30O15/c18-1-5(21)15(6(22)2-19)32-17-14(28)12(26)10(24)8(31-17)4-29-16-13(27)11(25)9(23)7(3-20)30-16/h1,5-17,19-28H,2-4H2

InChI Key

QITIYHVQGNHDNI-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

Species Name	Source	Reference
Anogeissus latifolia	LOTUS Database	35616633

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as oligosaccharides. These are carbohydrates made up of 3 to 10 monosaccharide units linked to each other through glycosidic bonds.

Kingdom

Organic compounds

Super Class

Organic oxygen compounds

Class

Organooxygen compounds

Sub Class

Carbohydrates and carbohydrate conjugates

Direct Parent

Oligosaccharides

Alternative Parents

Substituents

Oligosaccharide
Glycosyl compound
O-glycosyl compound
Oxane
Alpha-hydroxyaldehyde
Secondary alcohol
Polyol
Organoheterocyclic compound
Oxacycle
Acetal
Primary alcohol
Hydrocarbon derivative
Organic oxide
Carbonyl group
Aldehyde
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	-2.8	ALOGPS
logP	-6.5	ChemAxon
logS	-0.21	ALOGPS
pKa (Strongest Acidic)	11.8	ChemAxon
pKa (Strongest Basic)	-3.5	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	15	ChemAxon
Hydrogen Donor Count	10	ChemAxon
Polar Surface Area	256.29 Å²	ChemAxon
Rotatable Bond Count	10	ChemAxon
Refractivity	96.21 m³·mol⁻¹	ChemAxon
Polarizability	44.01 Å³	ChemAxon
Number of Rings	2	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

Not Available

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

LOTUS database [Link]

Showing NP-Card for 2,4,5-trihydroxy-3-{[3,4,5-trihydroxy-6-({[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}methyl)oxan-2-yl]oxy}pentanal (NP0293364)

MOL for NP0293364 (2,4,5-trihydroxy-3-{[3,4,5-trihydroxy-6-({[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}methyl)oxan-2-yl]oxy}pentanal)

3D MOL for NP0293364 (2,4,5-trihydroxy-3-{[3,4,5-trihydroxy-6-({[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}methyl)oxan-2-yl]oxy}pentanal)

3D SDF for NP0293364 (2,4,5-trihydroxy-3-{[3,4,5-trihydroxy-6-({[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}methyl)oxan-2-yl]oxy}pentanal)

3D-SDF for NP0293364 (2,4,5-trihydroxy-3-{[3,4,5-trihydroxy-6-({[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}methyl)oxan-2-yl]oxy}pentanal)

PDB for NP0293364 (2,4,5-trihydroxy-3-{[3,4,5-trihydroxy-6-({[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}methyl)oxan-2-yl]oxy}pentanal)

3D PDB for NP0293364 (2,4,5-trihydroxy-3-{[3,4,5-trihydroxy-6-({[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}methyl)oxan-2-yl]oxy}pentanal)

SMILES for NP0293364 (2,4,5-trihydroxy-3-{[3,4,5-trihydroxy-6-({[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}methyl)oxan-2-yl]oxy}pentanal)

INCHI for NP0293364 (2,4,5-trihydroxy-3-{[3,4,5-trihydroxy-6-({[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}methyl)oxan-2-yl]oxy}pentanal)

Structure for NP0293364 (2,4,5-trihydroxy-3-{[3,4,5-trihydroxy-6-({[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}methyl)oxan-2-yl]oxy}pentanal)

3D Structure for NP0293364 (2,4,5-trihydroxy-3-{[3,4,5-trihydroxy-6-({[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}methyl)oxan-2-yl]oxy}pentanal)