NP-MRD: Showing NP-Card for Neolloydosin (NP0076899)

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Record Information

Version

2.0

Created at

2022-04-28 22:05:15 UTC

Updated at

2022-04-28 22:05:15 UTC

NP-MRD ID

NP0076899

Secondary Accession Numbers

None

Natural Product Identification

Common Name

Neolloydosin

Description

3'-Methoxy-4'-[6-O-(alpha-L-arabinopyranosyl)-beta-D-glucopyranosyloxy]acetophenone belongs to the class of organic compounds known as phenolic glycosides. These are organic compounds containing a phenolic structure attached to a glycosyl moiety. Some examples of phenolic structures include lignans, and flavonoids. Among the sugar units found in natural glycosides are D-glucose, L-Fructose, and L rhamnose. Neolloydosin is found in Stachys byzantina and Stachys lanata. Based on a literature review very few articles have been published on 3'-Methoxy-4'-[6-O-(alpha-L-arabinopyranosyl)-beta-D-glucopyranosyloxy]acetophenone.

Structure

MOL 3D MOL SDF PDB SMILES InChI


  Mrv1652304292200052D          

 32 34  0  0  1  0            999 V2000
    1.4289   -2.4750    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    2.1434   -2.8875    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    2.1434   -3.7125    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    1.4289   -4.1250    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    0.7145   -3.7125    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.7145   -2.8875    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    0.0000   -2.4750    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.0000   -1.6500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7145   -1.2375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7145   -0.4125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0000    0.0000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7145   -0.4125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7145   -1.2375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0000    0.8250    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
   -0.7145    1.2375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4289   -1.6500    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1434   -1.2375    0.0000 C   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
    2.1434   -5.3625    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.1434   -6.1875    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    2.8579   -6.6000    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.8579   -7.4250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1434   -7.8375    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    1.4289   -7.4250    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    1.4289   -6.6000    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    0.7145   -6.1875    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.7145   -7.8375    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.1434   -8.6625    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.8579   -4.1250    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.8579   -2.4750    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.4289   -1.6500    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
  1  6  1  0  0  0  0
  6  7  1  1  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  2  0  0  0  0
  8 13  1  0  0  0  0
 11 14  1  0  0  0  0
 14 15  2  0  0  0  0
 14 16  1  0  0  0  0
  9 17  1  0  0  0  0
 17 18  1  0  0  0  0
  4 19  1  1  0  0  0
 19 20  1  0  0  0  0
 21 20  1  6  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
 21 26  1  0  0  0  0
 26 27  1  1  0  0  0
 25 28  1  6  0  0  0
 24 29  1  6  0  0  0
  3 30  1  6  0  0  0
  2 31  1  1  0  0  0
  1 32  1  6  0  0  0
M  END

     RDKit          3D

 60 62  0  0  0  0  0  0  0  0999 V2000
    5.0002    1.3080    2.9492 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.9827    0.8874    2.0820 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.3248    0.4038    0.8279 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.6504    0.3481    0.4649 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.0450   -0.1237   -0.7690 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.4375   -0.1887   -1.1654 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.5190    0.2456   -0.2606 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.7106   -0.6278   -2.3098 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.0393   -0.5344   -1.6140 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.6855   -0.4828   -1.2566 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.2980   -0.0124   -0.0269 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.0276    0.0946    0.4538 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.8443   -0.2552   -0.2105 C   0  0  2  0  0  0  0  0  0  0  0  0
    0.0158    0.8308   -0.4416 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2966    0.6436   -0.0095 C   0  0  2  0  0  0  0  0  0  0  0  0
   -2.1152    1.8488   -0.2992 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.4360    1.8056    0.0251 O   0  0  0  0  0  0  0  0  0  0  0  0
   -4.1937    0.8492   -0.6374 C   0  0  2  0  0  0  0  0  0  0  0  0
   -5.1483    1.4442   -1.4671 O   0  0  0  0  0  0  0  0  0  0  0  0
   -5.5100    0.5379   -2.4641 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.9252   -0.7913   -1.8732 C   0  0  2  0  0  0  0  0  0  0  0  0
   -7.0989   -1.1970   -2.4989 O   0  0  0  0  0  0  0  0  0  0  0  0
   -6.1957   -0.5340   -0.4016 C   0  0  2  0  0  0  0  0  0  0  0  0
   -7.1965    0.3838   -0.2129 O   0  0  0  0  0  0  0  0  0  0  0  0
   -4.8722   -0.1463    0.2397 C   0  0  1  0  0  0  0  0  0  0  0  0
   -4.0842   -1.3059    0.3455 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1926    0.3411    1.4715 C   0  0  1  0  0  0  0  0  0  0  0  0
   -2.3651    0.5005    2.1661 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7320   -1.0907    1.5890 C   0  0  2  0  0  0  0  0  0  0  0  0
   -0.1723   -1.3556    2.8376 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.1644   -1.4260    0.4566 C   0  0  1  0  0  0  0  0  0  0  0  0
   -0.4946   -2.1889   -0.5165 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.7371    0.4753    3.1514 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.6400    1.6300    3.9314 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.6281    2.1191    2.5065 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.4490    0.6710    1.1294 H   0  0  0  0  0  0  0  0  0  0  0  0
    9.4877    0.3088   -0.8152 H   0  0  0  0  0  0  0  0  0  0  0  0
    8.2311    1.2400    0.1509 H   0  0  0  0  0  0  0  0  0  0  0  0
    8.6697   -0.4532    0.5679 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.3005   -0.9101   -2.5881 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.9298   -0.8159   -1.9524 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.1253   -0.6243   -1.2280 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7181   -0.2297   -0.5130 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6757    2.7177    0.2742 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0005    2.1620   -1.3695 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5005    0.3003   -1.3190 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.6647    0.3483   -3.1524 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.3473    0.9257   -3.0595 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.1834   -1.5892   -2.0242 H   0  0  0  0  0  0  0  0  0  0  0  0
   -7.9095   -0.9543   -1.9980 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.4881   -1.5131    0.0364 H   0  0  0  0  0  0  0  0  0  0  0  0
   -7.4408    0.8897   -1.0281 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.0392    0.2237    1.2768 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.0584   -1.6288    1.2808 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3937    1.0456    1.8593 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2056    1.1334    2.9217 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6653   -1.7263    1.5603 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8599   -1.1735    3.5150 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.0175   -2.0447    0.8786 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.2189   -2.7398   -0.9520 H   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0
  2  3  1  0
  3 11  2  0
 11 12  1  0
 12 13  1  0
 13 14  1  0
 14 15  1  0
 15 16  1  0
 16 17  1  0
 17 18  1  0
 18 19  1  0
 19 20  1  0
 20 21  1  0
 21 22  1  0
 21 23  1  0
 23 24  1  0
 23 25  1  0
 25 26  1  0
 15 27  1  0
 27 28  1  0
 27 29  1  0
 29 30  1  0
 29 31  1  0
 31 32  1  0
 11 10  1  0
 10  9  2  0
  9  5  1  0
  5  4  2  0
  5  6  1  0
  6  7  1  0
  6  8  2  0
  4  3  1  0
 31 13  1  0
 25 18  1  0
  1 33  1  0
  1 34  1  0
  1 35  1  0
 13 42  1  6
 15 43  1  6
 16 44  1  0
 16 45  1  0
 18 46  1  6
 20 47  1  0
 20 48  1  0
 21 49  1  1
 22 50  1  0
 23 51  1  1
 24 52  1  0
 25 53  1  1
 26 54  1  0
 27 55  1  1
 28 56  1  0
 29 57  1  6
 30 58  1  0
 31 59  1  1
 32 60  1  0
 10 41  1  0
  9 40  1  0
  4 36  1  0
  7 37  1  0
  7 38  1  0
  7 39  1  0
M  END


  Mrv1652304292200052D          

 32 34  0  0  1  0            999 V2000
    1.4289   -2.4750    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    2.1434   -2.8875    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    2.1434   -3.7125    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    1.4289   -4.1250    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    0.7145   -3.7125    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.7145   -2.8875    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    0.0000   -2.4750    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.0000   -1.6500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7145   -1.2375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7145   -0.4125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0000    0.0000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7145   -0.4125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7145   -1.2375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0000    0.8250    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
   -0.7145    1.2375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4289   -1.6500    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1434   -1.2375    0.0000 C   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
    2.1434   -5.3625    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.1434   -6.1875    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    2.8579   -6.6000    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.8579   -7.4250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1434   -7.8375    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    1.4289   -7.4250    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    1.4289   -6.6000    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    0.7145   -6.1875    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.7145   -7.8375    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.1434   -8.6625    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.8579   -4.1250    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.8579   -2.4750    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.4289   -1.6500    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
  1  6  1  0  0  0  0
  6  7  1  1  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  2  0  0  0  0
  8 13  1  0  0  0  0
 11 14  1  0  0  0  0
 14 15  2  0  0  0  0
 14 16  1  0  0  0  0
  9 17  1  0  0  0  0
 17 18  1  0  0  0  0
  4 19  1  1  0  0  0
 19 20  1  0  0  0  0
 21 20  1  6  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
 21 26  1  0  0  0  0
 26 27  1  1  0  0  0
 25 28  1  6  0  0  0
 24 29  1  6  0  0  0
  3 30  1  6  0  0  0
  2 31  1  1  0  0  0
  1 32  1  6  0  0  0
M  END
> <DATABASE_ID>
NP0076899

> <DATABASE_NAME>
NP-MRD

> <SMILES>
COC1=C(O[C@@H]2O[C@H](CO[C@@H]3OC[C@H](O)[C@H](O)[C@H]3O)[C@@H](O)[C@H](O)[C@H]2O)C=CC(=C1)C(C)=O

> <INCHI_IDENTIFIER>
InChI=1S/C20H28O12/c1-8(21)9-3-4-11(12(5-9)28-2)31-20-18(27)16(25)15(24)13(32-20)7-30-19-17(26)14(23)10(22)6-29-19/h3-5,10,13-20,22-27H,6-7H2,1-2H3/t10-,13+,14-,15+,16-,17+,18+,19-,20+/m0/s1

> <INCHI_KEY>
PBILEZBWIBJOSA-FLMFJWNSSA-N

> <FORMULA>
C20H28O12

> <MOLECULAR_WEIGHT>
460.432

> <EXACT_MASS>
460.158076342

> <JCHEM_ACCEPTOR_COUNT>
12

> <JCHEM_ATOM_COUNT>
60

> <JCHEM_AVERAGE_POLARIZABILITY>
44.68471842581446

> <JCHEM_BIOAVAILABILITY>
0

> <JCHEM_DONOR_COUNT>
6

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
0

> <JCHEM_IUPAC>
1-(3-methoxy-4-{[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-({[(2S,3R,4S,5S)-3,4,5-trihydroxyoxan-2-yl]oxy}methyl)oxan-2-yl]oxy}phenyl)ethan-1-one

> <ALOGPS_LOGP>
-1.21

> <JCHEM_LOGP>
-2.338912049666666

> <ALOGPS_LOGS>
-1.66

> <JCHEM_MDDR_LIKE_RULE>
1

> <JCHEM_NUMBER_OF_RINGS>
3

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA>
12.457022040716012

> <JCHEM_PKA_STRONGEST_ACIDIC>
11.922521510522401

> <JCHEM_PKA_STRONGEST_BASIC>
-3.526580404084756

> <JCHEM_POLAR_SURFACE_AREA>
184.6

> <JCHEM_REFRACTIVITY>
103.50009999999997

> <JCHEM_ROTATABLE_BOND_COUNT>
7

> <JCHEM_RULE_OF_FIVE>
0

> <ALOGPS_SOLUBILITY>
1.00e+01 g/l

> <JCHEM_TRADITIONAL_IUPAC>
1-(3-methoxy-4-{[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-({[(2S,3R,4S,5S)-3,4,5-trihydroxyoxan-2-yl]oxy}methyl)oxan-2-yl]oxy}phenyl)ethanone

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 29-APR-22   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   29-APR-22         0                                  
HETATM    1  C   UNK     0       2.667  -4.620   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0       4.001  -5.390   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0       4.001  -6.930   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0       2.667  -7.700   0.000  0.00  0.00           C+0
HETATM    5  O   UNK     0       1.334  -6.930   0.000  0.00  0.00           O+0
HETATM    6  C   UNK     0       1.334  -5.390   0.000  0.00  0.00           C+0
HETATM    7  O   UNK     0       0.000  -4.620   0.000  0.00  0.00           O+0
HETATM    8  C   UNK     0       0.000  -3.080   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0      -1.334  -2.310   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0      -1.334  -0.770   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0       0.000   0.000   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0       1.334  -0.770   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0       1.334  -2.310   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0       0.000   1.540   0.000  0.00  0.00           C+0
HETATM   15  O   UNK     0       1.334   2.310   0.000  0.00  0.00           O+0
HETATM   16  C   UNK     0      -1.334   2.310   0.000  0.00  0.00           C+0
HETATM   17  O   UNK     0      -2.667  -3.080   0.000  0.00  0.00           O+0
HETATM   18  C   UNK     0      -4.001  -2.310   0.000  0.00  0.00           C+0
HETATM   19  C   UNK     0       2.667  -9.240   0.000  0.00  0.00           C+0
HETATM   20  O   UNK     0       4.001 -10.010   0.000  0.00  0.00           O+0
HETATM   21  C   UNK     0       4.001 -11.550   0.000  0.00  0.00           C+0
HETATM   22  O   UNK     0       5.335 -12.320   0.000  0.00  0.00           O+0
HETATM   23  C   UNK     0       5.335 -13.860   0.000  0.00  0.00           C+0
HETATM   24  C   UNK     0       4.001 -14.630   0.000  0.00  0.00           C+0
HETATM   25  C   UNK     0       2.667 -13.860   0.000  0.00  0.00           C+0
HETATM   26  C   UNK     0       2.667 -12.320   0.000  0.00  0.00           C+0
HETATM   27  O   UNK     0       1.334 -11.550   0.000  0.00  0.00           O+0
HETATM   28  O   UNK     0       1.334 -14.630   0.000  0.00  0.00           O+0
HETATM   29  O   UNK     0       4.001 -16.170   0.000  0.00  0.00           O+0
HETATM   30  O   UNK     0       5.335  -7.700   0.000  0.00  0.00           O+0
HETATM   31  O   UNK     0       5.335  -4.620   0.000  0.00  0.00           O+0
HETATM   32  O   UNK     0       2.667  -3.080   0.000  0.00  0.00           O+0
CONECT    1    2    6   32                                                  
CONECT    2    1    3   31                                                  
CONECT    3    2    4   30                                                  
CONECT    4    3    5   19                                                  
CONECT    5    4    6                                                       
CONECT    6    5    1    7                                                  
CONECT    7    6    8                                                       
CONECT    8    7    9   13                                                  
CONECT    9    8   10   17                                                  
CONECT   10    9   11                                                       
CONECT   11   10   12   14                                                  
CONECT   12   11   13                                                       
CONECT   13   12    8                                                       
CONECT   14   11   15   16                                                  
CONECT   15   14                                                            
CONECT   16   14                                                            
CONECT   17    9   18                                                       
CONECT   18   17                                                            
CONECT   19    4   20                                                       
CONECT   20   19   21                                                       
CONECT   21   20   22   26                                                  
CONECT   22   21   23                                                       
CONECT   23   22   24                                                       
CONECT   24   23   25   29                                                  
CONECT   25   24   26   28                                                  
CONECT   26   25   21   27                                                  
CONECT   27   26                                                            
CONECT   28   25                                                            
CONECT   29   24                                                            
CONECT   30    3                                                            
CONECT   31    2                                                            
CONECT   32    1                                                            
MASTER        0    0    0    0    0    0    0    0   32    0   68    0
END

View in JSmol

Synonyms

Value	Source
3'-Methoxy-4'-[6-O-(a-L-arabinopyranosyl)-b-D-glucopyranosyloxy]acetophenone	Generator
3'-Methoxy-4'-[6-O-(α-L-arabinopyranosyl)-β-D-glucopyranosyloxy]acetophenone	Generator

Chemical Formula

C₂₀H₂₈O₁₂

Average Mass

460.4320 Da

Monoisotopic Mass

460.15808 Da

IUPAC Name

1-(3-methoxy-4-{[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-({[(2S,3R,4S,5S)-3,4,5-trihydroxyoxan-2-yl]oxy}methyl)oxan-2-yl]oxy}phenyl)ethan-1-one

Traditional Name

1-(3-methoxy-4-{[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-({[(2S,3R,4S,5S)-3,4,5-trihydroxyoxan-2-yl]oxy}methyl)oxan-2-yl]oxy}phenyl)ethanone

CAS Registry Number

Not Available

SMILES

COC1=C(O[C@@H]2O[C@H](CO[C@@H]3OC[C@H](O)[C@H](O)[C@H]3O)[C@@H](O)[C@H](O)[C@H]2O)C=CC(=C1)C(C)=O

InChI Identifier

InChI=1S/C20H28O12/c1-8(21)9-3-4-11(12(5-9)28-2)31-20-18(27)16(25)15(24)13(32-20)7-30-19-17(26)14(23)10(22)6-29-19/h3-5,10,13-20,22-27H,6-7H2,1-2H3/t10-,13+,14-,15+,16-,17+,18+,19-,20+/m0/s1

InChI Key

PBILEZBWIBJOSA-FLMFJWNSSA-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
Stachys byzantina	LOTUS Database	35616633
Stachys lanata	Plant	KNApSAcK

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as phenolic glycosides. These are organic compounds containing a phenolic structure attached to a glycosyl moiety. Some examples of phenolic structures include lignans, and flavonoids. Among the sugar units found in natural glycosides are D-glucose, L-Fructose, and L rhamnose.

Kingdom

Organic compounds

Super Class

Organic oxygen compounds

Class

Organooxygen compounds

Sub Class

Carbohydrates and carbohydrate conjugates

Direct Parent

Phenolic glycosides

Alternative Parents

Substituents

Phenolic glycoside
Alkyl-phenylketone
Disaccharide
O-glycosyl compound
Acetophenone
Phenylketone
Phenoxy compound
Anisole
Benzoyl
Phenol ether
Aryl ketone
Aryl alkyl ketone
Methoxybenzene
Alkyl aryl ether
Oxane
Monocyclic benzene moiety
Benzenoid
Ketone
Secondary alcohol
Polyol
Ether
Acetal
Organoheterocyclic compound
Oxacycle
Aldehyde
Hydrocarbon derivative
Organic oxide
Alcohol
Aromatic heteromonocyclic compound

Molecular Framework

Aromatic 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	-1.2	ALOGPS
logP	-2.3	ChemAxon
logS	-1.7	ALOGPS
pKa (Strongest Acidic)	11.92	ChemAxon
pKa (Strongest Basic)	-3.5	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	12	ChemAxon
Hydrogen Donor Count	6	ChemAxon
Polar Surface Area	184.6 Å²	ChemAxon
Rotatable Bond Count	7	ChemAxon
Refractivity	103.5 m³·mol⁻¹	ChemAxon
Polarizability	44.68 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

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

101637371

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

Showing NP-Card for Neolloydosin (NP0076899)

MOL for NP0076899 (Neolloydosin)

3D MOL for NP0076899 (Neolloydosin)

3D SDF for NP0076899 (Neolloydosin)

3D-SDF for NP0076899 (Neolloydosin)

PDB for NP0076899 (Neolloydosin)

3D PDB for NP0076899 (Neolloydosin)

SMILES for NP0076899 (Neolloydosin)

INCHI for NP0076899 (Neolloydosin)

Structure for NP0076899 (Neolloydosin)

3D Structure for NP0076899 (Neolloydosin)