NP-MRD: Showing NP-Card for (-)-Markhamioside F (NP0075558)

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Record Information

Version

2.0

Created at

2022-04-28 20:49:38 UTC

Updated at

2022-04-28 20:49:38 UTC

NP-MRD ID

NP0075558

Secondary Accession Numbers

None

Natural Product Identification

Common Name

(-)-Markhamioside F

Description

(2R,3S,4S,5R,6R)-5-{[(2S,3R,4R)-3,4-dihydroxy-4-(hydroxymethyl)oxolan-2-yl]oxy}-6-(4-hydroxy-3-methoxyphenoxy)-2-(hydroxymethyl)oxane-3,4-diol 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. (-)-Markhamioside F is found in Markhamia stipulata . Based on a literature review very few articles have been published on (2R,3S,4S,5R,6R)-5-{[(2S,3R,4R)-3,4-dihydroxy-4-(hydroxymethyl)oxolan-2-yl]oxy}-6-(4-hydroxy-3-methoxyphenoxy)-2-(hydroxymethyl)oxane-3,4-diol.

Structure

MOL 3D MOL SDF PDB SMILES InChI


  Mrv1652304282222492D          

 30 32  0  0  1  0            999 V2000
    2.5986   -4.1130    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    3.0835   -4.7804    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    2.7479   -5.5341    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    1.9275   -5.6203    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    1.4425   -4.9529    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.7781   -4.1992    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    1.2932   -3.5318    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.4727   -3.6180    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.1371   -4.3717    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6833   -4.4579    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1683   -3.7905    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8327   -3.0368    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0122   -2.9506    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9888   -3.8767    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0189   -5.2116    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8394   -5.2978    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.5919   -6.3740    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7714   -6.4602    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.2329   -6.2015    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.9040   -4.6942    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.9341   -3.3593    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.4492   -2.6919    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    1.6242   -2.6919    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.3693   -1.9072    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.0367   -1.4223    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    2.7041   -1.9072    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    3.4888   -1.6523    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.6317   -0.7036    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.8068   -0.6949    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.4417   -0.7036    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  6  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
 10 15  1  0  0  0  0
 15 16  1  0  0  0  0
  4 17  1  1  0  0  0
 17 18  1  0  0  0  0
  3 19  1  6  0  0  0
  2 20  1  1  0  0  0
  1 21  1  6  0  0  0
 22 21  1  6  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
 22 26  1  0  0  0  0
 26 27  1  1  0  0  0
 25 28  1  6  0  0  0
 28 29  1  0  0  0  0
 25 30  1  1  0  0  0
M  END

     RDKit          3D

 56 58  0  0  0  0  0  0  0  0999 V2000
   -4.2743    3.3140   -0.9216 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.3220    3.0358    0.4605 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.6345    1.9655    1.0179 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8842    1.1476    0.2144 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1872    0.0640    0.7735 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4656   -0.6991   -0.0938 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6868   -1.8248    0.1880 C   0  0  1  0  0  0  0  0  0  0  0  0
   -1.2890   -2.9026   -0.4236 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9925   -2.9957   -1.7779 C   0  0  2  0  0  0  0  0  0  0  0  0
   -1.9060   -3.9499   -2.4834 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5578   -3.9964   -3.8319 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.4568   -3.4301   -1.8304 C   0  0  1  0  0  0  0  0  0  0  0  0
    0.8423   -3.9121   -3.0461 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.2171   -2.1656   -1.4359 C   0  0  2  0  0  0  0  0  0  0  0  0
    2.5971   -2.3944   -1.4717 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.7503   -1.6165   -0.1436 C   0  0  1  0  0  0  0  0  0  0  0  0
    0.9917   -0.2360   -0.1422 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.9224    0.1555    0.7868 C   0  0  2  0  0  0  0  0  0  0  0  0
    1.3725    1.1529    1.5689 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.4049    1.8111    2.2080 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.4563    1.9392    1.1332 C   0  0  2  0  0  0  0  0  0  0  0  0
    4.6850    1.6903    1.7157 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.4578    3.3243    0.5188 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.6942    4.2940    1.4622 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.1026    0.8780    0.1338 C   0  0  1  0  0  0  0  0  0  0  0  0
    4.1321   -0.0174   -0.1129 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2738   -0.1538    2.1245 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.0429    0.6875    2.9359 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.7265    1.7529    2.3769 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.4855    2.5767    3.2040 O   0  0  0  0  0  0  0  0  0  0  0  0
   -4.9099    4.2117   -1.1088 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.5926    2.4336   -1.4998 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.2305    3.6378   -1.1607 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8449    1.3551   -0.8367 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7426   -2.0189    1.2745 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1397   -1.9859   -2.2130 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.9754   -3.7004   -2.3510 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7234   -4.9659   -2.0776 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3016   -3.5891   -4.3407 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.6741   -4.1660   -1.0178 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.0909   -4.8663   -2.9507 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.0052   -1.4318   -2.2506 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.8831   -2.5028   -2.4093 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.4268   -2.0298    0.6626 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.3125   -0.7041    1.3679 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.0349    2.8342    2.5007 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.7450    1.2879    3.1032 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.1783    1.0018    1.1943 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.2523    3.3554   -0.2469 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.4423    3.4747    0.0786 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.6589    4.5179    1.5736 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.7651    1.3951   -0.7946 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.4663    0.1041   -1.0395 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7578   -0.9706    2.5966 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.0756    0.4710    3.9869 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.9959    3.3562    2.8509 H   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0
  2  3  1  0
  3 29  2  0
 29 30  1  0
 29 28  1  0
 28 27  2  0
 27  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
  9 12  1  0
 12 13  1  0
 12 14  1  0
 14 15  1  0
 14 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  1
 21 23  1  0
 23 24  1  0
 21 25  1  0
 25 26  1  0
  5  4  2  0
  4  3  1  0
 16  7  1  0
 25 18  1  0
  1 31  1  0
  1 32  1  0
  1 33  1  0
 30 56  1  0
 28 55  1  0
 27 54  1  0
  7 35  1  1
  9 36  1  6
 10 37  1  0
 10 38  1  0
 11 39  1  0
 12 40  1  1
 13 41  1  0
 14 42  1  6
 15 43  1  0
 16 44  1  1
 18 45  1  1
 20 46  1  0
 20 47  1  0
 22 48  1  0
 23 49  1  0
 23 50  1  0
 24 51  1  0
 25 52  1  6
 26 53  1  0
  4 34  1  0
M  END


  Mrv1652304282222492D          

 30 32  0  0  1  0            999 V2000
    2.5986   -4.1130    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    3.0835   -4.7804    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    2.7479   -5.5341    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    1.9275   -5.6203    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    1.4425   -4.9529    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.7781   -4.1992    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    1.2932   -3.5318    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.4727   -3.6180    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.1371   -4.3717    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6833   -4.4579    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1683   -3.7905    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8327   -3.0368    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0122   -2.9506    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9888   -3.8767    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0189   -5.2116    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8394   -5.2978    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.5919   -6.3740    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7714   -6.4602    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.2329   -6.2015    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.9040   -4.6942    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.9341   -3.3593    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.4492   -2.6919    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    1.6242   -2.6919    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.3693   -1.9072    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.0367   -1.4223    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    2.7041   -1.9072    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    3.4888   -1.6523    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.6317   -0.7036    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.8068   -0.6949    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.4417   -0.7036    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  6  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
 10 15  1  0  0  0  0
 15 16  1  0  0  0  0
  4 17  1  1  0  0  0
 17 18  1  0  0  0  0
  3 19  1  6  0  0  0
  2 20  1  1  0  0  0
  1 21  1  6  0  0  0
 22 21  1  6  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
 22 26  1  0  0  0  0
 26 27  1  1  0  0  0
 25 28  1  6  0  0  0
 28 29  1  0  0  0  0
 25 30  1  1  0  0  0
M  END
> <DATABASE_ID>
NP0075558

> <DATABASE_NAME>
NP-MRD

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

> <INCHI_IDENTIFIER>
InChI=1S/C18H26O12/c1-26-10-4-8(2-3-9(10)21)28-16-14(13(23)12(22)11(5-19)29-16)30-17-15(24)18(25,6-20)7-27-17/h2-4,11-17,19-25H,5-7H2,1H3/t11-,12-,13+,14-,15+,16+,17+,18-/m1/s1

> <INCHI_KEY>
PGQMRTLJEMEERX-GGHVOWDZSA-N

> <FORMULA>
C18H26O12

> <MOLECULAR_WEIGHT>
434.394

> <EXACT_MASS>
434.142426277

> <JCHEM_ACCEPTOR_COUNT>
12

> <JCHEM_ATOM_COUNT>
56

> <JCHEM_AVERAGE_POLARIZABILITY>
41.76129318128888

> <JCHEM_BIOAVAILABILITY>
0

> <JCHEM_DONOR_COUNT>
7

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
0

> <JCHEM_IUPAC>
(2R,3S,4S,5R,6R)-5-{[(2S,3R,4R)-3,4-dihydroxy-4-(hydroxymethyl)oxolan-2-yl]oxy}-6-(4-hydroxy-3-methoxyphenoxy)-2-(hydroxymethyl)oxane-3,4-diol

> <ALOGPS_LOGP>
-1.15

> <JCHEM_LOGP>
-2.3361232463333326

> <ALOGPS_LOGS>
-1.28

> <JCHEM_MDDR_LIKE_RULE>
1

> <JCHEM_NUMBER_OF_RINGS>
3

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA>
11.818158127498801

> <JCHEM_PKA_STRONGEST_ACIDIC>
10.25666804457639

> <JCHEM_PKA_STRONGEST_BASIC>
-2.9810925693034376

> <JCHEM_POLAR_SURFACE_AREA>
187.76

> <JCHEM_REFRACTIVITY>
95.29759999999997

> <JCHEM_ROTATABLE_BOND_COUNT>
7

> <JCHEM_RULE_OF_FIVE>
0

> <ALOGPS_SOLUBILITY>
2.27e+01 g/l

> <JCHEM_TRADITIONAL_IUPAC>
(2R,3S,4S,5R,6R)-5-{[(2S,3R,4R)-3,4-dihydroxy-4-(hydroxymethyl)oxolan-2-yl]oxy}-6-(4-hydroxy-3-methoxyphenoxy)-2-(hydroxymethyl)oxane-3,4-diol

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 28-APR-22   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   28-APR-22         0                                  
HETATM    1  C   UNK     0       4.851  -7.678   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0       5.756  -8.923   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0       5.129 -10.330   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0       3.598 -10.491   0.000  0.00  0.00           C+0
HETATM    5  O   UNK     0       2.693  -9.245   0.000  0.00  0.00           O+0
HETATM    6  C   UNK     0       3.319  -7.839   0.000  0.00  0.00           C+0
HETATM    7  O   UNK     0       2.414  -6.593   0.000  0.00  0.00           O+0
HETATM    8  C   UNK     0       0.882  -6.754   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0       0.256  -8.160   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0      -1.276  -8.321   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0      -2.181  -7.076   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0      -1.554  -5.669   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0      -0.023  -5.508   0.000  0.00  0.00           C+0
HETATM   14  O   UNK     0      -3.712  -7.237   0.000  0.00  0.00           O+0
HETATM   15  O   UNK     0      -1.902  -9.728   0.000  0.00  0.00           O+0
HETATM   16  C   UNK     0      -3.434  -9.889   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0       2.972 -11.898   0.000  0.00  0.00           C+0
HETATM   18  O   UNK     0       1.440 -12.059   0.000  0.00  0.00           O+0
HETATM   19  O   UNK     0       6.035 -11.576   0.000  0.00  0.00           O+0
HETATM   20  O   UNK     0       7.287  -8.762   0.000  0.00  0.00           O+0
HETATM   21  O   UNK     0       5.477  -6.271   0.000  0.00  0.00           O+0
HETATM   22  C   UNK     0       4.572  -5.025   0.000  0.00  0.00           C+0
HETATM   23  O   UNK     0       3.032  -5.025   0.000  0.00  0.00           O+0
HETATM   24  C   UNK     0       2.556  -3.560   0.000  0.00  0.00           C+0
HETATM   25  C   UNK     0       3.802  -2.655   0.000  0.00  0.00           C+0
HETATM   26  C   UNK     0       5.048  -3.560   0.000  0.00  0.00           C+0
HETATM   27  O   UNK     0       6.512  -3.084   0.000  0.00  0.00           O+0
HETATM   28  C   UNK     0       3.046  -1.313   0.000  0.00  0.00           C+0
HETATM   29  O   UNK     0       1.506  -1.297   0.000  0.00  0.00           O+0
HETATM   30  O   UNK     0       4.558  -1.313   0.000  0.00  0.00           O+0
CONECT    1    2    6   21                                                  
CONECT    2    1    3   20                                                  
CONECT    3    2    4   19                                                  
CONECT    4    3    5   17                                                  
CONECT    5    4    6                                                       
CONECT    6    5    1    7                                                  
CONECT    7    6    8                                                       
CONECT    8    7    9   13                                                  
CONECT    9    8   10                                                       
CONECT   10    9   11   15                                                  
CONECT   11   10   12   14                                                  
CONECT   12   11   13                                                       
CONECT   13   12    8                                                       
CONECT   14   11                                                            
CONECT   15   10   16                                                       
CONECT   16   15                                                            
CONECT   17    4   18                                                       
CONECT   18   17                                                            
CONECT   19    3                                                            
CONECT   20    2                                                            
CONECT   21    1   22                                                       
CONECT   22   21   23   26                                                  
CONECT   23   22   24                                                       
CONECT   24   23   25                                                       
CONECT   25   24   26   28   30                                             
CONECT   26   25   22   27                                                  
CONECT   27   26                                                            
CONECT   28   25   29                                                       
CONECT   29   28                                                            
CONECT   30   25                                                            
MASTER        0    0    0    0    0    0    0    0   30    0   64    0
END

View in JSmol

Synonyms

Not Available

Chemical Formula

C₁₈H₂₆O₁₂

Average Mass

434.3940 Da

Monoisotopic Mass

434.14243 Da

IUPAC Name

(2R,3S,4S,5R,6R)-5-{[(2S,3R,4R)-3,4-dihydroxy-4-(hydroxymethyl)oxolan-2-yl]oxy}-6-(4-hydroxy-3-methoxyphenoxy)-2-(hydroxymethyl)oxane-3,4-diol

Traditional Name

(2R,3S,4S,5R,6R)-5-{[(2S,3R,4R)-3,4-dihydroxy-4-(hydroxymethyl)oxolan-2-yl]oxy}-6-(4-hydroxy-3-methoxyphenoxy)-2-(hydroxymethyl)oxane-3,4-diol

CAS Registry Number

Not Available

SMILES

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

InChI Identifier

InChI=1S/C18H26O12/c1-26-10-4-8(2-3-9(10)21)28-16-14(13(23)12(22)11(5-19)29-16)30-17-15(24)18(25,6-20)7-27-17/h2-4,11-17,19-25H,5-7H2,1H3/t11-,12-,13+,14-,15+,16+,17+,18-/m1/s1

InChI Key

PGQMRTLJEMEERX-GGHVOWDZSA-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
Markhamia stipulata	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
Disaccharide
O-glycosyl compound
Methoxyphenol
4-alkoxyphenol
Anisole
Phenoxy compound
Phenol ether
Methoxybenzene
1-hydroxy-2-unsubstituted benzenoid
Alkyl aryl ether
Phenol
Oxane
Monocyclic benzene moiety
Benzenoid
Tertiary alcohol
Tetrahydrofuran
Secondary alcohol
Organoheterocyclic compound
Acetal
Oxacycle
Ether
Primary alcohol
Hydrocarbon derivative
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	-1.3	ALOGPS
pKa (Strongest Acidic)	10.26	ChemAxon
pKa (Strongest Basic)	-3	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	12	ChemAxon
Hydrogen Donor Count	7	ChemAxon
Polar Surface Area	187.76 Å²	ChemAxon
Rotatable Bond Count	7	ChemAxon
Refractivity	95.3 m³·mol⁻¹	ChemAxon
Polarizability	41.76 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

163029770

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

Not Available

Showing NP-Card for (-)-Markhamioside F (NP0075558)

MOL for NP0075558 ((-)-Markhamioside F)

3D MOL for NP0075558 ((-)-Markhamioside F)

3D SDF for NP0075558 ((-)-Markhamioside F)

3D-SDF for NP0075558 ((-)-Markhamioside F)

PDB for NP0075558 ((-)-Markhamioside F)

3D PDB for NP0075558 ((-)-Markhamioside F)

SMILES for NP0075558 ((-)-Markhamioside F)

INCHI for NP0075558 ((-)-Markhamioside F)

Structure for NP0075558 ((-)-Markhamioside F)

3D Structure for NP0075558 ((-)-Markhamioside F)