NP-MRD: Showing NP-Card for methyl (1s,2r,4s,5s,6s,10s)-5-hydroxy-2-methyl-10-{[(2s,3r,4s,5s,6r)-3,4,5-trihydroxy-6-({[(2s,3r,4s,5r,6r)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}methyl)oxan-2-yl]oxy}-3,9-dioxatricyclo[4.4.0.0²,⁴]dec-7-ene-7-carboxylate (NP0239251)

Jump To Section:

Identification Spectra BioTaxonomy ChemoTaxonomy Physical properties Links References XML

Record Information

Version

2.0

Created at

2022-09-06 22:48:33 UTC

Updated at

2022-09-06 22:48:33 UTC

NP-MRD ID

NP0239251

Secondary Accession Numbers

None

Natural Product Identification

Common Name

methyl (1s,2r,4s,5s,6s,10s)-5-hydroxy-2-methyl-10-{[(2s,3r,4s,5s,6r)-3,4,5-trihydroxy-6-({[(2s,3r,4s,5r,6r)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}methyl)oxan-2-yl]oxy}-3,9-dioxatricyclo[4.4.0.0²,⁴]dec-7-ene-7-carboxylate

Description

1Alpha-[6-O-(alpha-D-Galactopyranosyl)-beta-D-glucopyranosyloxy]-6alpha,7alpha-epoxy-5alpha-hydroxy-7-methyl-1,4aalpha,5,6,7,7aalpha-hexahydrocyclopenta[c]pyran-4-carboxylic acid methyl ester belongs to the class of organic compounds known as o-glycosyl compounds. These are glycoside in which a sugar group is bonded through one carbon to another group via a O-glycosidic bond. methyl (1s,2r,4s,5s,6s,10s)-5-hydroxy-2-methyl-10-{[(2s,3r,4s,5s,6r)-3,4,5-trihydroxy-6-({[(2s,3r,4s,5r,6r)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}methyl)oxan-2-yl]oxy}-3,9-dioxatricyclo[4.4.0.0²,⁴]dec-7-ene-7-carboxylate is found in Phlomoides rotata. Based on a literature review very few articles have been published on 1alpha-[6-O-(alpha-D-Galactopyranosyl)-beta-D-glucopyranosyloxy]-6alpha,7alpha-epoxy-5alpha-hydroxy-7-methyl-1,4aalpha,5,6,7,7aalpha-hexahydrocyclopenta[c]pyran-4-carboxylic acid methyl ester.

Structure

MOL 3D MOL SDF PDB SMILES InChI


  Mrv1652309072200482D          

 39 43  0  0  1  0            999 V2000
    6.4205    2.1489    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.8247    2.7195    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.0326    2.4888    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.4367    3.0595    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.8363    1.6875    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.4322    1.1169    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.2359    0.3156    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.4438    0.0849    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    4.2476   -0.7164    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.8434   -1.2870    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    5.6355   -1.0563    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    6.2314   -1.6270    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    7.0234   -1.3963    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.2197   -0.5949    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    8.0118   -0.3642    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    8.2080    0.4371    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    9.0001    0.6678    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    9.1964    1.4691    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    9.9884    1.6998    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    9.5959    0.0972    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
   10.3880    0.3279    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    9.3997   -0.7041    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    9.9955   -1.2748    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    8.6076   -0.9348    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    8.4114   -1.7362    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    6.0351   -2.4283    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    6.6309   -2.9989    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.2430   -2.6590    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    5.0468   -3.4603    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.6472   -2.0884    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    3.8551   -2.3191    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.8480    0.6555    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    4.0442    1.4568    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    3.3428    1.8911    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    3.2818    2.7138    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.7130    1.3582    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    2.2078    0.7059    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.0253    0.5945    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    2.9999   -0.2301    0.0000 C   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  2  0  0  0  0
  3  5  1  0  0  0  0
  5  6  2  0  0  0  0
  6  7  1  0  0  0  0
  7  8  1  0  0  0  0
  8  9  1  1  0  0  0
 10  9  1  6  0  0  0
 10 11  1  0  0  0  0
 11 12  1  0  0  0  0
 12 13  1  6  0  0  0
 13 14  1  0  0  0  0
 15 14  1  1  0  0  0
 15 16  1  0  0  0  0
 16 17  1  0  0  0  0
 17 18  1  6  0  0  0
 18 19  1  0  0  0  0
 17 20  1  0  0  0  0
 20 21  1  6  0  0  0
 20 22  1  0  0  0  0
 22 23  1  6  0  0  0
 22 24  1  0  0  0  0
 15 24  1  0  0  0  0
 24 25  1  1  0  0  0
 12 26  1  0  0  0  0
 26 27  1  1  0  0  0
 26 28  1  0  0  0  0
 28 29  1  6  0  0  0
 28 30  1  0  0  0  0
 10 30  1  0  0  0  0
 30 31  1  1  0  0  0
  8 32  1  0  0  0  0
 32 33  1  0  0  0  0
 33  5  1  6  0  0  0
 33 34  1  0  0  0  0
 34 35  1  1  0  0  0
 34 36  1  0  0  0  0
 36 37  1  1  0  0  0
 37 38  1  0  0  0  0
 36 38  1  0  0  0  0
 32 38  1  6  0  0  0
 38 39  1  6  0  0  0
M  END

     RDKit          3D

 73 77  0  0  0  0  0  0  0  0999 V2000
    7.3678    3.2569   -2.2160 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.4666    2.2449   -1.8074 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.9480    1.3468   -2.7063 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.2919    1.4403   -3.9116 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.0273    0.3259   -2.2438 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.5427   -0.5262   -3.1319 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.6514   -1.5339   -2.7545 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.9311   -1.2956   -1.5441 C   0  0  1  0  0  0  0  0  0  0  0  0
    2.0218   -2.2889   -1.2821 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.7111   -1.8744   -1.3069 C   0  0  2  0  0  0  0  0  0  0  0  0
    0.0934   -2.0386   -0.0882 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1265   -1.3185   -0.0838 C   0  0  2  0  0  0  0  0  0  0  0  0
   -1.6350   -1.1276    1.3134 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8167   -0.4234    1.2630 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.4043   -0.1668    2.4778 C   0  0  1  0  0  0  0  0  0  0  0  0
   -3.3554    1.1832    2.7959 O   0  0  0  0  0  0  0  0  0  0  0  0
   -4.0548    1.9591    1.8778 C   0  0  2  0  0  0  0  0  0  0  0  0
   -4.2505    3.3306    2.4883 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.9482    4.1798    1.6300 O   0  0  0  0  0  0  0  0  0  0  0  0
   -5.4258    1.3841    1.5992 C   0  0  2  0  0  0  0  0  0  0  0  0
   -6.4183    2.3463    1.4885 O   0  0  0  0  0  0  0  0  0  0  0  0
   -5.7831    0.3375    2.6499 C   0  0  2  0  0  0  0  0  0  0  0  0
   -5.8136    1.0411    3.8770 O   0  0  0  0  0  0  0  0  0  0  0  0
   -4.7403   -0.7552    2.6908 C   0  0  1  0  0  0  0  0  0  0  0  0
   -5.1194   -1.6750    1.7126 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0466   -2.0519   -0.9986 C   0  0  1  0  0  0  0  0  0  0  0  0
   -3.3579   -1.6231   -0.9444 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4617   -1.8913   -2.4084 C   0  0  2  0  0  0  0  0  0  0  0  0
   -2.2910   -2.3848   -3.3796 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1130   -2.5803   -2.3726 C   0  0  1  0  0  0  0  0  0  0  0  0
    0.5205   -2.5409   -3.6094 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.9461   -1.0477   -0.4790 C   0  0  1  0  0  0  0  0  0  0  0  0
    4.6591    0.2578   -0.8276 C   0  0  2  0  0  0  0  0  0  0  0  0
    3.6715    1.2801   -0.3728 C   0  0  2  0  0  0  0  0  0  0  0  0
    4.3859    2.4540   -0.0415 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.1050    0.6547    0.8980 C   0  0  2  0  0  0  0  0  0  0  0  0
    4.2754    0.1022    1.6511 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.3475   -0.6867    0.8629 C   0  0  2  0  0  0  0  0  0  0  0  0
    2.7992   -1.8127    1.6857 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.2459    3.1788   -1.5385 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.7119    3.0971   -3.2375 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.8426    4.2261   -2.0608 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.8123   -0.4828   -4.1849 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.3484   -0.3577   -1.7174 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.7050   -0.7906   -1.5449 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8750   -0.3421   -0.5581 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6553   -2.0316    1.9123 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8898   -0.4407    1.8183 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7000   -0.6440    3.2316 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5429    2.0980    0.9128 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.6808    3.2919    3.4913 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.2169    3.7726    2.5780 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.8176    3.8731    0.6942 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.3723    0.8499    0.6317 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.6344    2.6993    2.4067 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.8001   -0.0454    2.4993 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.0944    0.7286    4.4683 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.8109   -1.1953    3.7114 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.6829   -1.2693    1.0096 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9984   -3.1314   -0.7598 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.8325   -1.8454   -1.7882 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2599   -0.7927   -2.5201 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5641   -3.2883   -3.1288 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2966   -3.6354   -2.1159 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0773   -2.1066   -4.2813 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.7242   -1.8124   -0.4078 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.5879    0.2801   -0.2190 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.9027    1.5043   -1.1122 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.7950    2.2980    0.8526 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.4657    1.2645    1.5563 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.8844   -1.5680    2.2257 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.5549   -2.6522    0.9715 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.6198   -2.2122    2.3384 H   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0
  2  3  1  0
  3  4  2  0
  3  5  1  0
  5  6  2  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
 16 17  1  0
 17 18  1  0
 18 19  1  0
 17 20  1  0
 20 21  1  0
 20 22  1  0
 22 23  1  0
 22 24  1  0
 24 25  1  0
 12 26  1  0
 26 27  1  0
 26 28  1  0
 28 29  1  0
 28 30  1  0
 30 31  1  0
  8 32  1  0
 32 33  1  0
 33 34  1  0
 34 35  1  0
 34 36  1  0
 36 37  1  0
 37 38  1  0
 38 39  1  1
 33  5  1  0
 38 36  1  0
 30 10  1  0
 38 32  1  0
 24 15  1  0
  1 40  1  0
  1 41  1  0
  1 42  1  0
  6 43  1  0
  8 44  1  6
 10 45  1  6
 12 46  1  6
 13 47  1  0
 13 48  1  0
 15 49  1  1
 17 50  1  6
 18 51  1  0
 18 52  1  0
 19 53  1  0
 20 54  1  6
 21 55  1  0
 22 56  1  6
 23 57  1  0
 24 58  1  1
 25 59  1  0
 26 60  1  1
 27 61  1  0
 28 62  1  6
 29 63  1  0
 30 64  1  1
 31 65  1  0
 32 66  1  1
 33 67  1  1
 34 68  1  6
 35 69  1  0
 36 70  1  1
 39 71  1  0
 39 72  1  0
 39 73  1  0
M  END


  Mrv1652309072200482D          

 39 43  0  0  1  0            999 V2000
    6.4205    2.1489    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.8247    2.7195    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.0326    2.4888    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.4367    3.0595    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.8363    1.6875    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.4322    1.1169    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.2359    0.3156    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.4438    0.0849    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    4.2476   -0.7164    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.8434   -1.2870    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    5.6355   -1.0563    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    6.2314   -1.6270    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    7.0234   -1.3963    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.2197   -0.5949    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    8.0118   -0.3642    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    8.2080    0.4371    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    9.0001    0.6678    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    9.1964    1.4691    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    9.9884    1.6998    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    9.5959    0.0972    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
   10.3880    0.3279    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    9.3997   -0.7041    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    9.9955   -1.2748    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    8.6076   -0.9348    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    8.4114   -1.7362    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    6.0351   -2.4283    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    6.6309   -2.9989    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.2430   -2.6590    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    5.0468   -3.4603    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.6472   -2.0884    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    3.8551   -2.3191    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.8480    0.6555    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    4.0442    1.4568    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    3.3428    1.8911    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    3.2818    2.7138    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.7130    1.3582    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    2.2078    0.7059    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.0253    0.5945    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    2.9999   -0.2301    0.0000 C   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  2  0  0  0  0
  3  5  1  0  0  0  0
  5  6  2  0  0  0  0
  6  7  1  0  0  0  0
  7  8  1  0  0  0  0
  8  9  1  1  0  0  0
 10  9  1  6  0  0  0
 10 11  1  0  0  0  0
 11 12  1  0  0  0  0
 12 13  1  6  0  0  0
 13 14  1  0  0  0  0
 15 14  1  1  0  0  0
 15 16  1  0  0  0  0
 16 17  1  0  0  0  0
 17 18  1  6  0  0  0
 18 19  1  0  0  0  0
 17 20  1  0  0  0  0
 20 21  1  6  0  0  0
 20 22  1  0  0  0  0
 22 23  1  6  0  0  0
 22 24  1  0  0  0  0
 15 24  1  0  0  0  0
 24 25  1  1  0  0  0
 12 26  1  0  0  0  0
 26 27  1  1  0  0  0
 26 28  1  0  0  0  0
 28 29  1  6  0  0  0
 28 30  1  0  0  0  0
 10 30  1  0  0  0  0
 30 31  1  1  0  0  0
  8 32  1  0  0  0  0
 32 33  1  0  0  0  0
 33  5  1  6  0  0  0
 33 34  1  0  0  0  0
 34 35  1  1  0  0  0
 34 36  1  0  0  0  0
 36 37  1  1  0  0  0
 37 38  1  0  0  0  0
 36 38  1  0  0  0  0
 32 38  1  6  0  0  0
 38 39  1  6  0  0  0
M  END
> <DATABASE_ID>
NP0239251

> <DATABASE_NAME>
NP-MRD

> <SMILES>
COC(=O)C1=CO[C@@H](O[C@@H]2O[C@H](CO[C@H]3O[C@H](CO)[C@H](O)[C@H](O)[C@H]3O)[C@@H](O)[C@H](O)[C@H]2O)[C@H]2[C@@H]1[C@H](O)[C@@H]1O[C@]21C

> <INCHI_IDENTIFIER>
InChI=1S/C23H34O16/c1-23-10-9(13(27)18(23)39-23)6(19(32)33-2)4-34-20(10)38-22-17(31)15(29)12(26)8(37-22)5-35-21-16(30)14(28)11(25)7(3-24)36-21/h4,7-18,20-22,24-31H,3,5H2,1-2H3/t7-,8-,9-,10-,11+,12-,13+,14+,15+,16-,17-,18+,20+,21+,22+,23-/m1/s1

> <INCHI_KEY>
WBFTYMQVABCVIU-FVBCGIQZSA-N

> <FORMULA>
C23H34O16

> <MOLECULAR_WEIGHT>
566.509

> <EXACT_MASS>
566.184685015

> <JCHEM_ACCEPTOR_COUNT>
15

> <JCHEM_ATOM_COUNT>
73

> <JCHEM_AVERAGE_POLARIZABILITY>
53.90621516525833

> <JCHEM_BIOAVAILABILITY>
0

> <JCHEM_DONOR_COUNT>
8

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
0

> <JCHEM_IUPAC>
methyl (1S,2R,4S,5S,6S,10S)-5-hydroxy-2-methyl-10-{[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-({[(2S,3R,4S,5R,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}methyl)oxan-2-yl]oxy}-3,9-dioxatricyclo[4.4.0.0^{2,4}]dec-7-ene-7-carboxylate

> <JCHEM_LOGP>
-4.341448028666667

> <JCHEM_MDDR_LIKE_RULE>
1

> <JCHEM_NUMBER_OF_RINGS>
5

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA>
12.41691060790194

> <JCHEM_PKA_STRONGEST_ACIDIC>
11.90249557518959

> <JCHEM_PKA_STRONGEST_BASIC>
-2.981083422322401

> <JCHEM_POLAR_SURFACE_AREA>
246.81999999999996

> <JCHEM_REFRACTIVITY>
118.82940000000005

> <JCHEM_ROTATABLE_BOND_COUNT>
8

> <JCHEM_RULE_OF_FIVE>
0

> <JCHEM_TRADITIONAL_IUPAC>
methyl (1S,2R,4S,5S,6S,10S)-5-hydroxy-2-methyl-10-{[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-({[(2S,3R,4S,5R,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}methyl)oxan-2-yl]oxy}-3,9-dioxatricyclo[4.4.0.0^{2,4}]dec-7-ene-7-carboxylate

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 07-SEP-22   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   07-SEP-22         0                                  
HETATM    1  C   UNK     0      11.985   4.011   0.000  0.00  0.00           C+0
HETATM    2  O   UNK     0      10.873   5.076   0.000  0.00  0.00           O+0
HETATM    3  C   UNK     0       9.394   4.646   0.000  0.00  0.00           C+0
HETATM    4  O   UNK     0       8.282   5.711   0.000  0.00  0.00           O+0
HETATM    5  C   UNK     0       9.028   3.150   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0      10.140   2.085   0.000  0.00  0.00           C+0
HETATM    7  O   UNK     0       9.774   0.589   0.000  0.00  0.00           O+0
HETATM    8  C   UNK     0       8.295   0.158   0.000  0.00  0.00           C+0
HETATM    9  O   UNK     0       7.929  -1.337   0.000  0.00  0.00           O+0
HETATM   10  C   UNK     0       9.041  -2.402   0.000  0.00  0.00           C+0
HETATM   11  O   UNK     0      10.520  -1.972   0.000  0.00  0.00           O+0
HETATM   12  C   UNK     0      11.632  -3.037   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0      13.110  -2.606   0.000  0.00  0.00           C+0
HETATM   14  O   UNK     0      13.477  -1.111   0.000  0.00  0.00           O+0
HETATM   15  C   UNK     0      14.955  -0.680   0.000  0.00  0.00           C+0
HETATM   16  O   UNK     0      15.322   0.816   0.000  0.00  0.00           O+0
HETATM   17  C   UNK     0      16.800   1.247   0.000  0.00  0.00           C+0
HETATM   18  C   UNK     0      17.167   2.742   0.000  0.00  0.00           C+0
HETATM   19  O   UNK     0      18.645   3.173   0.000  0.00  0.00           O+0
HETATM   20  C   UNK     0      17.912   0.181   0.000  0.00  0.00           C+0
HETATM   21  O   UNK     0      19.391   0.612   0.000  0.00  0.00           O+0
HETATM   22  C   UNK     0      17.546  -1.314   0.000  0.00  0.00           C+0
HETATM   23  O   UNK     0      18.658  -2.380   0.000  0.00  0.00           O+0
HETATM   24  C   UNK     0      16.068  -1.745   0.000  0.00  0.00           C+0
HETATM   25  O   UNK     0      15.701  -3.241   0.000  0.00  0.00           O+0
HETATM   26  C   UNK     0      11.266  -4.533   0.000  0.00  0.00           C+0
HETATM   27  O   UNK     0      12.378  -5.598   0.000  0.00  0.00           O+0
HETATM   28  C   UNK     0       9.787  -4.963   0.000  0.00  0.00           C+0
HETATM   29  O   UNK     0       9.421  -6.459   0.000  0.00  0.00           O+0
HETATM   30  C   UNK     0       8.675  -3.898   0.000  0.00  0.00           C+0
HETATM   31  O   UNK     0       7.196  -4.329   0.000  0.00  0.00           O+0
HETATM   32  C   UNK     0       7.183   1.224   0.000  0.00  0.00           C+0
HETATM   33  C   UNK     0       7.549   2.719   0.000  0.00  0.00           C+0
HETATM   34  C   UNK     0       6.240   3.530   0.000  0.00  0.00           C+0
HETATM   35  O   UNK     0       6.126   5.066   0.000  0.00  0.00           O+0
HETATM   36  C   UNK     0       5.064   2.535   0.000  0.00  0.00           C+0
HETATM   37  O   UNK     0       4.121   1.318   0.000  0.00  0.00           O+0
HETATM   38  C   UNK     0       5.647   1.110   0.000  0.00  0.00           C+0
HETATM   39  C   UNK     0       5.600  -0.429   0.000  0.00  0.00           C+0
CONECT    1    2                                                            
CONECT    2    1    3                                                       
CONECT    3    2    4    5                                                  
CONECT    4    3                                                            
CONECT    5    3    6   33                                                  
CONECT    6    5    7                                                       
CONECT    7    6    8                                                       
CONECT    8    7    9   32                                                  
CONECT    9    8   10                                                       
CONECT   10    9   11   30                                                  
CONECT   11   10   12                                                       
CONECT   12   11   13   26                                                  
CONECT   13   12   14                                                       
CONECT   14   13   15                                                       
CONECT   15   14   16   24                                                  
CONECT   16   15   17                                                       
CONECT   17   16   18   20                                                  
CONECT   18   17   19                                                       
CONECT   19   18                                                            
CONECT   20   17   21   22                                                  
CONECT   21   20                                                            
CONECT   22   20   23   24                                                  
CONECT   23   22                                                            
CONECT   24   22   15   25                                                  
CONECT   25   24                                                            
CONECT   26   12   27   28                                                  
CONECT   27   26                                                            
CONECT   28   26   29   30                                                  
CONECT   29   28                                                            
CONECT   30   28   10   31                                                  
CONECT   31   30                                                            
CONECT   32    8   33   38                                                  
CONECT   33   32    5   34                                                  
CONECT   34   33   35   36                                                  
CONECT   35   34                                                            
CONECT   36   34   37   38                                                  
CONECT   37   36   38                                                       
CONECT   38   37   36   32   39                                             
CONECT   39   38                                                            
MASTER        0    0    0    0    0    0    0    0   39    0   86    0
END

View in JSmol

Synonyms

Value	Source
1a-[6-O-(a-D-Galactopyranosyl)-b-D-glucopyranosyloxy]-6a,7a-epoxy-5a-hydroxy-7-methyl-1,4aalpha,5,6,7,7aalpha-hexahydrocyclopenta[c]pyran-4-carboxylate methyl ester	Generator
1a-[6-O-(a-D-Galactopyranosyl)-b-D-glucopyranosyloxy]-6a,7a-epoxy-5a-hydroxy-7-methyl-1,4aalpha,5,6,7,7aalpha-hexahydrocyclopenta[c]pyran-4-carboxylic acid methyl ester	Generator
1alpha-[6-O-(alpha-D-Galactopyranosyl)-beta-D-glucopyranosyloxy]-6alpha,7alpha-epoxy-5alpha-hydroxy-7-methyl-1,4aalpha,5,6,7,7aalpha-hexahydrocyclopenta[c]pyran-4-carboxylate methyl ester	Generator
1Α-[6-O-(α-D-galactopyranosyl)-β-D-glucopyranosyloxy]-6α,7α-epoxy-5α-hydroxy-7-methyl-1,4aalpha,5,6,7,7aalpha-hexahydrocyclopenta[c]pyran-4-carboxylate methyl ester	Generator
1Α-[6-O-(α-D-galactopyranosyl)-β-D-glucopyranosyloxy]-6α,7α-epoxy-5α-hydroxy-7-methyl-1,4aalpha,5,6,7,7aalpha-hexahydrocyclopenta[c]pyran-4-carboxylic acid methyl ester	Generator

Chemical Formula

C₂₃H₃₄O₁₆

Average Mass

566.5090 Da

Monoisotopic Mass

566.18469 Da

IUPAC Name

methyl (1S,2R,4S,5S,6S,10S)-5-hydroxy-2-methyl-10-{[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-({[(2S,3R,4S,5R,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}methyl)oxan-2-yl]oxy}-3,9-dioxatricyclo[4.4.0.0^{2,4}]dec-7-ene-7-carboxylate

Traditional Name

CAS Registry Number

Not Available

SMILES

COC(=O)C1=CO[C@@H](O[C@@H]2O[C@H](CO[C@H]3O[C@H](CO)[C@H](O)[C@H](O)[C@H]3O)[C@@H](O)[C@H](O)[C@H]2O)[C@H]2[C@@H]1[C@H](O)[C@@H]1O[C@]21C

InChI Identifier

InChI=1S/C23H34O16/c1-23-10-9(13(27)18(23)39-23)6(19(32)33-2)4-34-20(10)38-22-17(31)15(29)12(26)8(37-22)5-35-21-16(30)14(28)11(25)7(3-24)36-21/h4,7-18,20-22,24-31H,3,5H2,1-2H3/t7-,8-,9-,10-,11+,12-,13+,14+,15+,16-,17-,18+,20+,21+,22+,23-/m1/s1

InChI Key

WBFTYMQVABCVIU-FVBCGIQZSA-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
Lamiophlomis rotata	LOTUS Database	35616633

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as o-glycosyl compounds. These are glycoside in which a sugar group is bonded through one carbon to another group via a O-glycosidic bond.

Kingdom

Organic compounds

Super Class

Organic oxygen compounds

Class

Organooxygen compounds

Sub Class

Carbohydrates and carbohydrate conjugates

Direct Parent

O-glycosyl compounds

Alternative Parents

Substituents

Disaccharide
O-glycosyl compound
Oxane
Cyclic alcohol
Methyl ester
Enoate ester
Alpha,beta-unsaturated carboxylic ester
Vinylogous ester
Secondary alcohol
Carboxylic acid ester
Organoheterocyclic compound
Polyol
Oxacycle
Carboxylic acid derivative
Monocarboxylic acid or derivatives
Ether
Oxirane
Dialkyl ether
Acetal
Primary alcohol
Organic oxide
Alcohol
Carbonyl group
Hydrocarbon derivative
Aliphatic heteropolycyclic compound

Molecular Framework

Aliphatic heteropolycyclic 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	-4.3	ChemAxon
pKa (Strongest Acidic)	11.9	ChemAxon
pKa (Strongest Basic)	-3	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	15	ChemAxon
Hydrogen Donor Count	8	ChemAxon
Polar Surface Area	246.82 Å²	ChemAxon
Rotatable Bond Count	8	ChemAxon
Refractivity	118.83 m³·mol⁻¹	ChemAxon
Polarizability	53.91 Å³	ChemAxon
Number of Rings	5	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

102588684

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

LOTUS database [Link]

Showing NP-Card for methyl (1s,2r,4s,5s,6s,10s)-5-hydroxy-2-methyl-10-{[(2s,3r,4s,5s,6r)-3,4,5-trihydroxy-6-({[(2s,3r,4s,5r,6r)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}methyl)oxan-2-yl]oxy}-3,9-dioxatricyclo[4.4.0.0²,⁴]dec-7-ene-7-carboxylate (NP0239251)

MOL for NP0239251 (methyl (1s,2r,4s,5s,6s,10s)-5-hydroxy-2-methyl-10-{[(2s,3r,4s,5s,6r)-3,4,5-trihydroxy-6-({[(2s,3r,4s,5r,6r)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}methyl)oxan-2-yl]oxy}-3,9-dioxatricyclo[4.4.0.0²,⁴]dec-7-ene-7-carboxylate)

3D MOL for NP0239251 (methyl (1s,2r,4s,5s,6s,10s)-5-hydroxy-2-methyl-10-{[(2s,3r,4s,5s,6r)-3,4,5-trihydroxy-6-({[(2s,3r,4s,5r,6r)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}methyl)oxan-2-yl]oxy}-3,9-dioxatricyclo[4.4.0.0²,⁴]dec-7-ene-7-carboxylate)

3D SDF for NP0239251 (methyl (1s,2r,4s,5s,6s,10s)-5-hydroxy-2-methyl-10-{[(2s,3r,4s,5s,6r)-3,4,5-trihydroxy-6-({[(2s,3r,4s,5r,6r)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}methyl)oxan-2-yl]oxy}-3,9-dioxatricyclo[4.4.0.0²,⁴]dec-7-ene-7-carboxylate)

3D-SDF for NP0239251 (methyl (1s,2r,4s,5s,6s,10s)-5-hydroxy-2-methyl-10-{[(2s,3r,4s,5s,6r)-3,4,5-trihydroxy-6-({[(2s,3r,4s,5r,6r)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}methyl)oxan-2-yl]oxy}-3,9-dioxatricyclo[4.4.0.0²,⁴]dec-7-ene-7-carboxylate)

PDB for NP0239251 (methyl (1s,2r,4s,5s,6s,10s)-5-hydroxy-2-methyl-10-{[(2s,3r,4s,5s,6r)-3,4,5-trihydroxy-6-({[(2s,3r,4s,5r,6r)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}methyl)oxan-2-yl]oxy}-3,9-dioxatricyclo[4.4.0.0²,⁴]dec-7-ene-7-carboxylate)

3D PDB for NP0239251 (methyl (1s,2r,4s,5s,6s,10s)-5-hydroxy-2-methyl-10-{[(2s,3r,4s,5s,6r)-3,4,5-trihydroxy-6-({[(2s,3r,4s,5r,6r)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}methyl)oxan-2-yl]oxy}-3,9-dioxatricyclo[4.4.0.0²,⁴]dec-7-ene-7-carboxylate)

SMILES for NP0239251 (methyl (1s,2r,4s,5s,6s,10s)-5-hydroxy-2-methyl-10-{[(2s,3r,4s,5s,6r)-3,4,5-trihydroxy-6-({[(2s,3r,4s,5r,6r)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}methyl)oxan-2-yl]oxy}-3,9-dioxatricyclo[4.4.0.0²,⁴]dec-7-ene-7-carboxylate)

INCHI for NP0239251 (methyl (1s,2r,4s,5s,6s,10s)-5-hydroxy-2-methyl-10-{[(2s,3r,4s,5s,6r)-3,4,5-trihydroxy-6-({[(2s,3r,4s,5r,6r)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}methyl)oxan-2-yl]oxy}-3,9-dioxatricyclo[4.4.0.0²,⁴]dec-7-ene-7-carboxylate)

Structure for NP0239251 (methyl (1s,2r,4s,5s,6s,10s)-5-hydroxy-2-methyl-10-{[(2s,3r,4s,5s,6r)-3,4,5-trihydroxy-6-({[(2s,3r,4s,5r,6r)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}methyl)oxan-2-yl]oxy}-3,9-dioxatricyclo[4.4.0.0²,⁴]dec-7-ene-7-carboxylate)

3D Structure for NP0239251 (methyl (1s,2r,4s,5s,6s,10s)-5-hydroxy-2-methyl-10-{[(2s,3r,4s,5s,6r)-3,4,5-trihydroxy-6-({[(2s,3r,4s,5r,6r)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}methyl)oxan-2-yl]oxy}-3,9-dioxatricyclo[4.4.0.0²,⁴]dec-7-ene-7-carboxylate)