NP-MRD: Showing NP-Card for 3-Fucosyllactose (NP0086871)

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Record Information

Version

2.0

Created at

2022-05-11 16:33:21 UTC

Updated at

2022-05-11 16:33:21 UTC

NP-MRD ID

NP0086871

Secondary Accession Numbers

None

Natural Product Identification

Common Name

3-Fucosyllactose

Description

3-Fucosyllactose 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. 3-Fucosyllactose is an extremely weak basic (essentially neutral) compound (based on its pKa). 3-Fucosyllactose is a milk oligosaccharide isolated in 1958 (PMID: 13546862 ), And that was also isolated for the first time from the urine of a blood group O, nonsecretor, woman during pregnancy and lactation in 1977 (PMID: 838696 ).

Structure

MOL 3D MOL SDF PDB SMILES InChI


  Mrv0541 02231219212D          

 33 35  0  0  1  0            999 V2000
   14.7447   -9.3776    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   13.3159  -11.8524    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   14.7447  -11.8524    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   16.1737   -9.3776    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   14.0304  -13.9150    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   13.3159  -10.2026    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   16.1737  -10.2026    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   11.8869  -12.6774    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   14.7447   -7.7276    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   16.1737   -6.9026    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   11.8869  -14.3276    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   17.6027   -7.7276    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   13.3159  -15.1524    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   16.8613  -11.1787    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   15.4594  -13.0900    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   14.7447  -10.2026    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
   14.0304  -10.6150    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
   15.4594  -10.6150    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
   14.0304  -11.4400    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
   13.3159  -12.6774    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
   15.4594  -11.4400    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
   15.4594   -8.9651    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
   12.6014  -13.0900    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
   14.0304  -13.0900    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
   15.4594   -8.1400    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
   16.1737   -7.7276    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
   12.6014  -13.9150    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
   16.8882   -8.1400    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
   16.8882   -8.9651    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
   13.3159  -14.3276    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   16.1737  -11.8524    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   14.7447  -12.6774    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   17.6027   -9.3776    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
 16  1  1  1  0  0  0
 22  1  1  1  0  0  0
 19  2  1  1  0  0  0
 20  2  1  6  0  0  0
  3 19  1  0  0  0  0
  3 21  1  0  0  0  0
  4 22  1  0  0  0  0
  4 29  1  0  0  0  0
  5 24  1  0  0  0  0
  5 30  1  0  0  0  0
 17  6  1  6  0  0  0
 18  7  1  1  0  0  0
 23  8  1  1  0  0  0
 25  9  1  1  0  0  0
 26 10  1  6  0  0  0
 27 11  1  6  0  0  0
 28 12  1  6  0  0  0
 13 30  1  0  0  0  0
 14 31  1  0  0  0  0
 15 32  1  0  0  0  0
 16 17  1  0  0  0  0
 16 18  1  0  0  0  0
 17 19  1  0  0  0  0
 18 21  1  0  0  0  0
 20 23  1  0  0  0  0
 20 24  1  0  0  0  0
 21 31  1  1  0  0  0
 22 25  1  0  0  0  0
 23 27  1  0  0  0  0
 24 32  1  1  0  0  0
 25 26  1  0  0  0  0
 26 28  1  0  0  0  0
 27 30  1  0  0  0  0
 28 29  1  0  0  0  0
 29 33  1  6  0  0  0
M  END

     RDKit          3D

 65 67  0  0  0  0  0  0  0  0999 V2000
    4.5039   -0.2192    2.6333 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.3133    0.1180    1.3997 C   0  0  2  0  0  0  0  0  0  0  0  0
    4.5121    0.8297    0.5037 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.3672    0.1366    0.1867 C   0  0  1  0  0  0  0  0  0  0  0  0
    2.4940    1.0001   -0.4801 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.2640    1.1134    0.1635 C   0  0  1  0  0  0  0  0  0  0  0  0
    1.0121    2.5656    0.5866 C   0  0  1  0  0  0  0  0  0  0  0  0
    1.0192    3.3769   -0.5692 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3935    2.6237    1.1335 C   0  0  1  0  0  0  0  0  0  0  0  0
   -0.6692    3.9128    1.8629 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9901    3.8620    2.3128 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2528    2.4478    0.0365 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1801    1.0959   -0.2944 C   0  0  1  0  0  0  0  0  0  0  0  0
   -2.1162    0.7368   -1.2527 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.0423   -0.1878   -0.8027 C   0  0  2  0  0  0  0  0  0  0  0  0
   -3.1084   -1.4154   -1.6682 C   0  0  1  0  0  0  0  0  0  0  0  0
   -2.8950   -2.6354   -0.8000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7479   -3.7926   -1.5729 O   0  0  0  0  0  0  0  0  0  0  0  0
   -4.2244   -1.5002   -2.4537 O   0  0  0  0  0  0  0  0  0  0  0  0
   -5.4190   -1.5102   -1.7596 C   0  0  1  0  0  0  0  0  0  0  0  0
   -5.7351   -2.8009   -1.2874 O   0  0  0  0  0  0  0  0  0  0  0  0
   -5.4776   -0.5468   -0.6262 C   0  0  2  0  0  0  0  0  0  0  0  0
   -6.7054    0.1116   -0.6478 O   0  0  0  0  0  0  0  0  0  0  0  0
   -4.4023    0.5016   -0.8196 C   0  0  1  0  0  0  0  0  0  0  0  0
   -4.4831    1.5247    0.1072 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.1890    0.6916   -0.7899 C   0  0  2  0  0  0  0  0  0  0  0  0
    0.1856   -0.7155   -0.8429 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.7275   -1.0378   -0.6867 C   0  0  1  0  0  0  0  0  0  0  0  0
    3.4595   -0.7363   -2.0420 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.1729   -1.3793   -0.5946 C   0  0  2  0  0  0  0  0  0  0  0  0
    5.3660   -2.7386   -0.9275 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.7669   -1.1954    0.7867 C   0  0  2  0  0  0  0  0  0  0  0  0
    5.4786   -2.2861    1.6049 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.6986    0.5061    2.8003 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.1891   -0.2220    3.5142 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.0250   -1.2301    2.5040 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.1645    0.7488    1.7264 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.8813   -0.2838    1.1079 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.1937    0.5054    1.0818 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.7421    2.9046    1.3304 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.1506    3.3948   -1.0185 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5374    1.7592    1.7905 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4849    4.7783    1.2054 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0154    3.9493    2.7399 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1907    2.9259    2.5343 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4108    0.5329    0.6323 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8236   -0.4409    0.2516 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2245   -1.3708   -2.3553 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.7101   -2.8054   -0.0916 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9580   -2.5305   -0.2159 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.4390   -4.4572   -1.4179 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.2159   -1.2631   -2.4900 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.7070   -2.8221   -1.0840 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.4076   -1.0353    0.3668 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.7676    0.8192    0.0242 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.5361    0.8882   -1.8603 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.2598    2.3808   -0.3606 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.3616    1.0263   -1.8318 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.1563   -1.0142    0.1022 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.0589   -1.9138   -0.4650 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.1028    0.1844   -2.1203 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.8109   -0.8138   -1.3035 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.2689   -2.8937   -1.3120 H   0  0  0  0  0  0  0  0  0  0  0  0
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    5.0245   -3.0153    1.1306 H   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0
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 26  6  1  0
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 26 58  1  6
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 29 61  1  0
 30 62  1  6
 31 63  1  0
 32 64  1  6
 33 65  1  0
M  END


  Mrv0541 02231219212D          

 33 35  0  0  1  0            999 V2000
   14.7447   -9.3776    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   13.3159  -11.8524    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   14.7447  -11.8524    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   16.1737   -9.3776    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   14.0304  -13.9150    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   13.3159  -10.2026    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   16.1737  -10.2026    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   11.8869  -12.6774    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   14.7447   -7.7276    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   16.1737   -6.9026    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   11.8869  -14.3276    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   17.6027   -7.7276    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   13.3159  -15.1524    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   16.8613  -11.1787    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   15.4594  -13.0900    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   14.7447  -10.2026    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
   14.0304  -10.6150    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
   15.4594  -10.6150    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
   14.0304  -11.4400    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
   13.3159  -12.6774    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
   15.4594  -11.4400    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
   15.4594   -8.9651    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
   12.6014  -13.0900    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
   14.0304  -13.0900    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
   15.4594   -8.1400    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
   16.1737   -7.7276    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
   12.6014  -13.9150    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
   16.8882   -8.1400    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
   16.8882   -8.9651    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
   13.3159  -14.3276    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   16.1737  -11.8524    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   14.7447  -12.6774    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   17.6027   -9.3776    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
 16  1  1  1  0  0  0
 22  1  1  1  0  0  0
 19  2  1  1  0  0  0
 20  2  1  6  0  0  0
  3 19  1  0  0  0  0
  3 21  1  0  0  0  0
  4 22  1  0  0  0  0
  4 29  1  0  0  0  0
  5 24  1  0  0  0  0
  5 30  1  0  0  0  0
 17  6  1  6  0  0  0
 18  7  1  1  0  0  0
 23  8  1  1  0  0  0
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 28 12  1  6  0  0  0
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 15 32  1  0  0  0  0
 16 17  1  0  0  0  0
 16 18  1  0  0  0  0
 17 19  1  0  0  0  0
 18 21  1  0  0  0  0
 20 23  1  0  0  0  0
 20 24  1  0  0  0  0
 21 31  1  1  0  0  0
 22 25  1  0  0  0  0
 23 27  1  0  0  0  0
 24 32  1  1  0  0  0
 25 26  1  0  0  0  0
 26 28  1  0  0  0  0
 27 30  1  0  0  0  0
 28 29  1  0  0  0  0
 29 33  1  6  0  0  0
M  END
> <DATABASE_ID>
NP0086871

> <DATABASE_NAME>
NP-MRD

> <SMILES>
C[C@@H]1O[C@@H](O[C@H]2[C@@H](O)[C@@H](CO)O[C@@H](O[C@H]3[C@H](O)[C@@H](O)C(O)O[C@@H]3CO)[C@@H]2O)[C@@H](O)[C@H](O)[C@@H]1O

> <INCHI_IDENTIFIER>
InChI=1S/C18H32O15/c1-4-7(21)9(23)12(26)17(29-4)33-15-8(22)5(2-19)31-18(13(15)27)32-14-6(3-20)30-16(28)11(25)10(14)24/h4-28H,2-3H2,1H3/t4-,5+,6+,7+,8-,9+,10+,11+,12-,13+,14+,15-,16?,17-,18-/m0/s1

> <INCHI_KEY>
AUNPEJDACLEKSC-ZAYDSPBTSA-N

> <FORMULA>
C18H32O15

> <MOLECULAR_WEIGHT>
488.4377

> <EXACT_MASS>
488.174120354

> <JCHEM_ACCEPTOR_COUNT>
15

> <JCHEM_AVERAGE_POLARIZABILITY>
46.18914981797366

> <JCHEM_BIOAVAILABILITY>
0

> <JCHEM_DONOR_COUNT>
10

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
0

> <JCHEM_IUPAC>
(2S,3S,4R,5S,6S)-2-{[(2R,3S,4S,5R,6S)-3,5-dihydroxy-2-(hydroxymethyl)-6-{[(2R,3S,4R,5R)-4,5,6-trihydroxy-2-(hydroxymethyl)oxan-3-yl]oxy}oxan-4-yl]oxy}-6-methyloxane-3,4,5-triol

> <ALOGPS_LOGP>
-2.41

> <JCHEM_LOGP>
-5.427300542666666

> <ALOGPS_LOGS>
-0.09

> <JCHEM_MDDR_LIKE_RULE>
1

> <JCHEM_NUMBER_OF_RINGS>
3

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA>
11.965051727670089

> <JCHEM_PKA_STRONGEST_ACIDIC>
11.216464746745071

> <JCHEM_PKA_STRONGEST_BASIC>
-3.6121826089745888

> <JCHEM_POLAR_SURFACE_AREA>
248.44999999999996

> <JCHEM_REFRACTIVITY>
99.20629999999994

> <JCHEM_ROTATABLE_BOND_COUNT>
6

> <JCHEM_RULE_OF_FIVE>
0

> <ALOGPS_SOLUBILITY>
3.98e+02 g/l

> <JCHEM_TRADITIONAL_IUPAC>
3-fucosyllactose

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 23-FEB-12   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   23-FEB-12         0                                  
HETATM    1  O   UNK     0      27.524 -17.505   0.000  0.00  0.00           O+0
HETATM    2  O   UNK     0      24.856 -22.125   0.000  0.00  0.00           O+0
HETATM    3  O   UNK     0      27.524 -22.125   0.000  0.00  0.00           O+0
HETATM    4  O   UNK     0      30.191 -17.505   0.000  0.00  0.00           O+0
HETATM    5  O   UNK     0      26.190 -25.975   0.000  0.00  0.00           O+0
HETATM    6  O   UNK     0      24.856 -19.045   0.000  0.00  0.00           O+0
HETATM    7  O   UNK     0      30.191 -19.045   0.000  0.00  0.00           O+0
HETATM    8  O   UNK     0      22.189 -23.665   0.000  0.00  0.00           O+0
HETATM    9  O   UNK     0      27.524 -14.425   0.000  0.00  0.00           O+0
HETATM   10  O   UNK     0      30.191 -12.885   0.000  0.00  0.00           O+0
HETATM   11  O   UNK     0      22.189 -26.745   0.000  0.00  0.00           O+0
HETATM   12  O   UNK     0      32.858 -14.425   0.000  0.00  0.00           O+0
HETATM   13  O   UNK     0      24.856 -28.285   0.000  0.00  0.00           O+0
HETATM   14  O   UNK     0      31.474 -20.867   0.000  0.00  0.00           O+0
HETATM   15  O   UNK     0      28.858 -24.435   0.000  0.00  0.00           O+0
HETATM   16  C   UNK     0      27.524 -19.045   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0      26.190 -19.815   0.000  0.00  0.00           C+0
HETATM   18  C   UNK     0      28.858 -19.815   0.000  0.00  0.00           C+0
HETATM   19  C   UNK     0      26.190 -21.355   0.000  0.00  0.00           C+0
HETATM   20  C   UNK     0      24.856 -23.665   0.000  0.00  0.00           C+0
HETATM   21  C   UNK     0      28.858 -21.355   0.000  0.00  0.00           C+0
HETATM   22  C   UNK     0      28.858 -16.735   0.000  0.00  0.00           C+0
HETATM   23  C   UNK     0      23.523 -24.435   0.000  0.00  0.00           C+0
HETATM   24  C   UNK     0      26.190 -24.435   0.000  0.00  0.00           C+0
HETATM   25  C   UNK     0      28.858 -15.195   0.000  0.00  0.00           C+0
HETATM   26  C   UNK     0      30.191 -14.425   0.000  0.00  0.00           C+0
HETATM   27  C   UNK     0      23.523 -25.975   0.000  0.00  0.00           C+0
HETATM   28  C   UNK     0      31.525 -15.195   0.000  0.00  0.00           C+0
HETATM   29  C   UNK     0      31.525 -16.735   0.000  0.00  0.00           C+0
HETATM   30  C   UNK     0      24.856 -26.745   0.000  0.00  0.00           C+0
HETATM   31  C   UNK     0      30.191 -22.125   0.000  0.00  0.00           C+0
HETATM   32  C   UNK     0      27.524 -23.665   0.000  0.00  0.00           C+0
HETATM   33  C   UNK     0      32.858 -17.505   0.000  0.00  0.00           C+0
CONECT    1   16   22                                                       
CONECT    2   19   20                                                       
CONECT    3   19   21                                                       
CONECT    4   22   29                                                       
CONECT    5   24   30                                                       
CONECT    6   17                                                            
CONECT    7   18                                                            
CONECT    8   23                                                            
CONECT    9   25                                                            
CONECT   10   26                                                            
CONECT   11   27                                                            
CONECT   12   28                                                            
CONECT   13   30                                                            
CONECT   14   31                                                            
CONECT   15   32                                                            
CONECT   16    1   17   18                                                  
CONECT   17    6   16   19                                                  
CONECT   18    7   16   21                                                  
CONECT   19    2    3   17                                                  
CONECT   20    2   23   24                                                  
CONECT   21    3   18   31                                                  
CONECT   22    1    4   25                                                  
CONECT   23    8   20   27                                                  
CONECT   24    5   20   32                                                  
CONECT   25    9   22   26                                                  
CONECT   26   10   25   28                                                  
CONECT   27   11   23   30                                                  
CONECT   28   12   26   29                                                  
CONECT   29    4   28   33                                                  
CONECT   30    5   13   27                                                  
CONECT   31   14   21                                                       
CONECT   32   15   24                                                       
CONECT   33   29                                                            
MASTER        0    0    0    0    0    0    0    0   33    0   70    0
END

View in JSmol

Synonyms

Value	Source
3'-Fucosyllactose	HMDB
3-O-Fucosyllactose	HMDB
O-6-Deoxy-a-L-galactopyranosyl-(1->3)-O-[b-D-galactopyranosyl-(1->4)]- D-glucose	HMDB
O-6-Deoxy-alpha-L-galactopyranosyl-(1->3)-O-[b-D-galactopyranosyl-(1->4)]- D-glucose	HMDB
O-6-Deoxy-alpha-L-galactopyranosyl-(1->3)-O-[b-delta-galactopyranosyl-(1->4)]- D-glucose	HMDB

Chemical Formula

C₁₈H₃₂O₁₅

Average Mass

488.4377 Da

Monoisotopic Mass

488.17412 Da

IUPAC Name

(2S,3S,4R,5S,6S)-2-{[(2R,3S,4S,5R,6S)-3,5-dihydroxy-2-(hydroxymethyl)-6-{[(2R,3S,4R,5R)-4,5,6-trihydroxy-2-(hydroxymethyl)oxan-3-yl]oxy}oxan-4-yl]oxy}-6-methyloxane-3,4,5-triol

Traditional Name

3-fucosyllactose

CAS Registry Number

Not Available

SMILES

C[C@@H]1O[C@@H](O[C@H]2[C@@H](O)[C@@H](CO)O[C@@H](O[C@H]3[C@H](O)[C@@H](O)C(O)O[C@@H]3CO)[C@@H]2O)[C@@H](O)[C@H](O)[C@@H]1O

InChI Identifier

InChI=1S/C18H32O15/c1-4-7(21)9(23)12(26)17(29-4)33-15-8(22)5(2-19)31-18(13(15)27)32-14-6(3-20)30-16(28)11(25)10(14)24/h4-28H,2-3H2,1H3/t4-,5+,6+,7+,8-,9+,10+,11+,12-,13+,14+,15-,16?,17-,18-/m0/s1

InChI Key

AUNPEJDACLEKSC-ZAYDSPBTSA-N

Experimental Spectra

Not Available

Predicted Spectra

Spectrum Type	Description	Depositor ID	Depositor Organization	Depositor	Deposition Date	View
1D NMR	¹³C NMR Spectrum (1D, 25 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 100 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 252 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 1000 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 50 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 200 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 75 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 300 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 101 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 400 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 126 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 500 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 151 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 600 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 176 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 700 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 201 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 800 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 226 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 900 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum

Chemical Shift Submissions

Not Available

Species

Species of Origin

Species Name	Source	Reference
Anas platyrhynchos	FooDB	FooDB
Anatidae	FooDB	FooDB
Anser anser	FooDB	FooDB
Bison bison	FooDB	FooDB
Bos taurus	FooDB	FooDB
Bos taurus X Bison bison	FooDB	FooDB
Bubalus bubalis	FooDB	FooDB
Capra aegagrus hircus	FooDB	FooDB
Cervidae	FooDB	FooDB
Cervus canadensis	FooDB	FooDB
Columba	FooDB	FooDB
Columbidae	FooDB	FooDB
Dromaius novaehollandiae	FooDB	FooDB
Equus caballus	FooDB	FooDB
Gallus gallus	FooDB	FooDB
Lagopus muta	FooDB	FooDB
Leporidae	FooDB	FooDB
Lepus timidus	FooDB	FooDB
Melanitta fusca	FooDB	FooDB
Meleagris gallopavo	FooDB	FooDB
Numida meleagris	FooDB	FooDB
Odocoileus	FooDB	FooDB
Oryctolagus	FooDB	FooDB
Ovis aries	FooDB	FooDB
Phasianidae	FooDB	FooDB
Phasianus colchicus	FooDB	FooDB
Struthio camelus	FooDB	FooDB
Sus scrofa	FooDB	FooDB
Sus scrofa domestica	FooDB	FooDB

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
O-glycosyl compound
Glycosyl compound
Oxane
Secondary alcohol
Hemiacetal
Oxacycle
Organoheterocyclic compound
Polyol
Acetal
Hydrocarbon derivative
Primary alcohol
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	-2.4	ALOGPS
logP	-5.4	ChemAxon
logS	-0.09	ALOGPS
pKa (Strongest Acidic)	11.22	ChemAxon
pKa (Strongest Basic)	-3.6	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	15	ChemAxon
Hydrogen Donor Count	10	ChemAxon
Polar Surface Area	248.45 Å²	ChemAxon
Rotatable Bond Count	6	ChemAxon
Refractivity	99.21 m³·mol⁻¹	ChemAxon
Polarizability	46.19 Å³	ChemAxon
Number of Rings	3	ChemAxon
Bioavailability	No	ChemAxon
Rule of Five	No	ChemAxon
Ghose Filter	No	ChemAxon
Veber's Rule	No	ChemAxon
MDDR-like Rule	Yes	ChemAxon

External Links

HMDB ID

HMDB0002094

DrugBank ID

Not Available

Phenol Explorer Compound ID

Not Available

FoodDB ID

FDB022842

KNApSAcK ID

Not Available

Chemspider ID

141824

KEGG Compound ID

Not Available

BioCyc ID

Not Available

BiGG ID

Not Available

Wikipedia Link

Not Available

METLIN ID

Not Available

PubChem Compound

161460

PDB ID

Not Available

ChEBI ID

90065

Good Scents ID

Not Available

References

General References

Showing NP-Card for 3-Fucosyllactose (NP0086871)

MOL for NP0086871 (3-Fucosyllactose)

3D MOL for NP0086871 (3-Fucosyllactose)

3D SDF for NP0086871 (3-Fucosyllactose)

3D-SDF for NP0086871 (3-Fucosyllactose)

PDB for NP0086871 (3-Fucosyllactose)

3D PDB for NP0086871 (3-Fucosyllactose)

SMILES for NP0086871 (3-Fucosyllactose)

INCHI for NP0086871 (3-Fucosyllactose)

Structure for NP0086871 (3-Fucosyllactose)

3D Structure for NP0086871 (3-Fucosyllactose)