NP-MRD: Showing NP-Card for (6e,14e)-12-hydroxy-2-({[(2r,3r,4r,5r,6r)-5-hydroxy-3,4-dimethoxy-6-methyloxan-2-yl]oxy}methyl)-9-{[(2r,3s,4r,6s)-3-hydroxy-4-methoxy-6-methyloxan-2-yl]oxy}-3,8,10,12-tetramethyl-4,17-dioxabicyclo[14.1.0]heptadeca-6,14-diene-5,13-dione (NP0273748)

Jump To Section:

Identification Spectra BioTaxonomy ChemoTaxonomy Physical properties Links References XML

Record Information

Version

1.0

Created at

2022-09-08 20:53:47 UTC

Updated at

2022-09-08 20:53:47 UTC

NP-MRD ID

NP0273748

Secondary Accession Numbers

None

Natural Product Identification

Common Name

(6e,14e)-12-hydroxy-2-({[(2r,3r,4r,5r,6r)-5-hydroxy-3,4-dimethoxy-6-methyloxan-2-yl]oxy}methyl)-9-{[(2r,3s,4r,6s)-3-hydroxy-4-methoxy-6-methyloxan-2-yl]oxy}-3,8,10,12-tetramethyl-4,17-dioxabicyclo[14.1.0]heptadeca-6,14-diene-5,13-dione

Description

Chalcomycin A belongs to the class of organic compounds known as macrolides and analogues. These are organic compounds containing a lactone ring of at least twelve members. (6e,14e)-12-hydroxy-2-({[(2r,3r,4r,5r,6r)-5-hydroxy-3,4-dimethoxy-6-methyloxan-2-yl]oxy}methyl)-9-{[(2r,3s,4r,6s)-3-hydroxy-4-methoxy-6-methyloxan-2-yl]oxy}-3,8,10,12-tetramethyl-4,17-dioxabicyclo[14.1.0]heptadeca-6,14-diene-5,13-dione is found in Streptomyces bikiniensis. Based on a literature review very few articles have been published on Chalcomycin A.

Structure

MOL 3D MOL SDF PDB SMILES InChI


  Mrv1652309082222532D          

 49 52  0  0  1  0            999 V2000
    7.4748    4.1415    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.1142    3.3995    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    6.2913    3.3408    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    5.8290    4.0241    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.0061    3.9654    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    4.5438    4.6487    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.6455    3.2233    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.1078    2.5400    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    4.7472    1.7980    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.9243    1.7393    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.3866    1.0560    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.2095    1.1147    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.0260    0.3140    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.2031    0.2553    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8425   -0.4868    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.3048   -1.1701    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.0196   -0.5455    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.5573    0.1378    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.9179    0.8798    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7344    0.0791    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.3738   -0.6629    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4491   -0.7216    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8097   -1.4637    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
   -1.6326   -1.5224    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9932   -2.2644    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
   -2.8162   -2.3231    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5309   -2.9477    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
   -1.8915   -3.6897    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7080   -2.8890    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
   -0.2457   -3.5723    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.5772   -3.5136    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3474   -2.1470    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    0.4755   -2.0882    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.8361   -1.3462    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.2721    0.7624    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1902    1.4457    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.6327    1.5044    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4556    1.5631    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.8162    2.3052    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.6391    2.3639    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.1014    1.6806    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.9997    3.1059    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.2063    3.3322    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.0847    3.9265    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.8226    3.1646    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.2849    2.4813    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.9161    3.0125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.9307    2.5988    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    6.3930    1.9155    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0  0  0  0
  3  2  1  1  0  0  0
  3  4  1  0  0  0  0
  4  5  1  0  0  0  0
  5  6  1  1  0  0  0
  5  7  1  0  0  0  0
  7  8  1  0  0  0  0
  8  9  1  1  0  0  0
  9 10  1  0  0  0  0
 10 11  1  0  0  0  0
 11 12  1  0  0  0  0
 11 13  1  0  0  0  0
 13 14  2  0  0  0  0
 14 15  1  0  0  0  0
 15 16  2  0  0  0  0
 15 17  1  0  0  0  0
 17 18  1  0  0  0  0
 18 19  1  0  0  0  0
 18 20  1  0  0  0  0
 20 21  1  0  0  0  0
 21 22  1  0  0  0  0
 23 22  1  1  0  0  0
 23 24  1  0  0  0  0
 24 25  1  0  0  0  0
 25 26  1  1  0  0  0
 25 27  1  0  0  0  0
 27 28  1  6  0  0  0
 27 29  1  0  0  0  0
 29 30  1  6  0  0  0
 30 31  1  0  0  0  0
 29 32  1  0  0  0  0
 23 32  1  0  0  0  0
 32 33  1  6  0  0  0
 33 34  1  0  0  0  0
 20 35  1  0  0  0  0
 35 36  1  0  0  0  0
 36 37  1  0  0  0  0
 35 37  1  0  0  0  0
 37 38  1  0  0  0  0
 38 39  2  0  0  0  0
 39 40  1  0  0  0  0
 40 41  2  0  0  0  0
 40 42  1  0  0  0  0
 42 43  1  0  0  0  0
 42 44  1  0  0  0  0
 42 45  1  0  0  0  0
 45 46  1  0  0  0  0
 10 46  1  0  0  0  0
 46 47  1  0  0  0  0
  8 48  1  0  0  0  0
  3 48  1  0  0  0  0
 48 49  1  6  0  0  0
M  END

     RDKit          3D

105108  0  0  0  0  0  0  0  0999 V2000
   -8.5843    0.8370    1.8827 C   0  0  0  0  0  0  0  0  0  0  0  0
   -7.5317    0.1208    1.3145 O   0  0  0  0  0  0  0  0  0  0  0  0
   -7.3776    0.3504   -0.0347 C   0  0  2  0  0  0  0  0  0  0  0  0
   -7.6632   -0.8650   -0.8970 C   0  0  0  0  0  0  0  0  0  0  0  0
   -7.2366   -0.4185   -2.3056 C   0  0  2  0  0  0  0  0  0  0  0  0
   -7.7466   -1.4937   -3.2369 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.8730   -0.4129   -2.3278 O   0  0  0  0  0  0  0  0  0  0  0  0
   -5.2162    0.2534   -1.3420 C   0  0  2  0  0  0  0  0  0  0  0  0
   -4.3338   -0.6677   -0.7309 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.0106   -0.3708   -0.9227 C   0  0  2  0  0  0  0  0  0  0  0  0
   -2.2618   -1.3881   -1.7422 C   0  0  2  0  0  0  0  0  0  0  0  0
   -2.2226   -2.7610   -1.2222 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9884   -0.7938   -2.1913 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.2214   -1.2134   -2.1161 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7819   -2.4305   -1.5595 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4621   -3.1447   -2.4005 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.6959   -2.9167   -0.3079 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.1810   -2.4557    0.9192 C   0  0  2  0  0  0  0  0  0  0  0  0
    0.1666   -2.4644    2.0078 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.9468   -1.1711    0.8787 C   0  0  2  0  0  0  0  0  0  0  0  0
    3.4248   -1.4531    0.5010 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.0543   -0.2122    0.5579 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.4203   -0.2781    0.2993 C   0  0  2  0  0  0  0  0  0  0  0  0
    6.1583    0.0896    1.3936 O   0  0  0  0  0  0  0  0  0  0  0  0
    7.3240    0.7597    1.1601 C   0  0  2  0  0  0  0  0  0  0  0  0
    7.2206    2.2665    1.2714 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.0391    0.3797   -0.0974 C   0  0  1  0  0  0  0  0  0  0  0  0
    8.5956   -0.9055    0.0685 O   0  0  0  0  0  0  0  0  0  0  0  0
    7.2014    0.3879   -1.3317 C   0  0  1  0  0  0  0  0  0  0  0  0
    7.5160   -0.6572   -2.2020 O   0  0  0  0  0  0  0  0  0  0  0  0
    7.9892   -0.2069   -3.4335 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.7466    0.4226   -0.9767 C   0  0  1  0  0  0  0  0  0  0  0  0
    5.0847   -0.2882   -2.0079 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.2154    0.4960   -2.7266 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.0192   -0.5932    2.2550 C   0  0  1  0  0  0  0  0  0  0  0  0
    3.2158   -0.0107    2.6838 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.8988    0.7240    2.5550 C   0  0  1  0  0  0  0  0  0  0  0  0
    2.1152    1.8671    1.7002 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.3377    2.4699    0.8479 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0274    2.2015    0.4602 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2010    1.9483   -0.7975 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2419    2.1734    1.2577 C   0  0  1  0  0  0  0  0  0  0  0  0
   -1.0755    1.7906    2.7072 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6647    3.5494    1.3274 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4066    1.4721    0.6451 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2824    0.0176    0.3741 C   0  0  1  0  0  0  0  0  0  0  0  0
   -3.0680   -0.6930    1.4940 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.0570    0.9630   -0.3257 C   0  0  1  0  0  0  0  0  0  0  0  0
   -6.2853    2.3028   -0.6840 O   0  0  0  0  0  0  0  0  0  0  0  0
   -9.5236    0.5424    1.3779 H   0  0  0  0  0  0  0  0  0  0  0  0
   -8.4692    1.9305    1.7809 H   0  0  0  0  0  0  0  0  0  0  0  0
   -8.6538    0.5811    2.9544 H   0  0  0  0  0  0  0  0  0  0  0  0
   -8.1846    1.0834   -0.3123 H   0  0  0  0  0  0  0  0  0  0  0  0
   -7.0660   -1.7390   -0.6064 H   0  0  0  0  0  0  0  0  0  0  0  0
   -8.7520   -1.0290   -0.8866 H   0  0  0  0  0  0  0  0  0  0  0  0
   -7.6942    0.5761   -2.4993 H   0  0  0  0  0  0  0  0  0  0  0  0
   -7.6125   -2.4753   -2.7037 H   0  0  0  0  0  0  0  0  0  0  0  0
   -7.2383   -1.5098   -4.2150 H   0  0  0  0  0  0  0  0  0  0  0  0
   -8.8656   -1.4111   -3.3646 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.5621    1.0214   -1.8541 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.9832    0.5745   -1.5445 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8797   -1.4439   -2.7108 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.2080   -3.2575   -1.4986 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4855   -3.3437   -1.8168 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1386   -2.8982   -0.1505 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1725    0.2078   -2.6752 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.0097   -0.5509   -2.5545 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.9597   -3.2355    1.2167 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.5774   -2.9610    2.9311 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1464   -1.4516    2.3200 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7221   -3.1060    1.7636 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.6019   -0.4604    0.1122 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.4699   -1.7894   -0.5659 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.8849   -2.1629    1.1852 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.6346   -1.3723    0.1205 H   0  0  0  0  0  0  0  0  0  0  0  0
    8.0215    0.4665    2.0044 H   0  0  0  0  0  0  0  0  0  0  0  0
    8.2421    2.7205    1.1488 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.8772    2.5957    2.2712 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.5834    2.7389    0.5283 H   0  0  0  0  0  0  0  0  0  0  0  0
    8.9066    1.0914   -0.2096 H   0  0  0  0  0  0  0  0  0  0  0  0
    9.3909   -0.8323    0.6665 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.4227    1.3299   -1.9175 H   0  0  0  0  0  0  0  0  0  0  0  0
    8.2065   -1.0960   -4.0551 H   0  0  0  0  0  0  0  0  0  0  0  0
    8.9746    0.3257   -3.3141 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.2400    0.4660   -3.8836 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.3498    1.4533   -1.0526 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.4137    0.9333   -2.1011 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.7289    1.2499   -3.3673 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.6947   -0.1852   -3.4440 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.7099   -1.3532    3.0435 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.5685    1.0343    3.6000 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.1424    2.3185    1.8136 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.8270    3.3436    0.3201 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3220    2.4247    3.2188 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0930    2.0059    3.1701 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9488    0.7062    2.8666 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0616    3.9919    1.9886 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.2851    1.6663    1.3326 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7405    1.9679   -0.3155 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2738   -0.3920    0.3793 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5817   -1.6190    1.8257 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.1319   -0.8737    1.1671 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.1679   -0.0378    2.3940 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.4879    1.0434    0.6476 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.6628    2.6182   -1.3877 H   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0
  2  3  1  0
  3  4  1  0
  4  5  1  0
  5  6  1  0
  5  7  1  0
  7  8  1  0
  8  9  1  0
  9 10  1  0
 10 46  1  0
 46 47  1  0
 46 45  1  0
 45 42  1  0
 42 43  1  0
 42 44  1  1
 42 40  1  0
 40 41  2  0
 40 39  1  0
 39 38  2  0
 38 37  1  0
 37 36  1  0
 36 35  1  0
 35 20  1  0
 20 21  1  0
 21 22  1  0
 22 23  1  0
 23 24  1  0
 24 25  1  0
 25 26  1  0
 25 27  1  0
 27 28  1  0
 27 29  1  0
 29 30  1  0
 30 31  1  0
 29 32  1  0
 32 33  1  0
 33 34  1  0
 20 18  1  0
 18 19  1  0
 18 17  1  0
 17 15  1  0
 15 16  2  0
 15 14  1  0
 14 13  2  0
 13 11  1  0
 11 12  1  0
  8 48  1  0
 48 49  1  0
 48  3  1  0
 11 10  1  0
 35 37  1  0
 32 23  1  0
  1 50  1  0
  1 51  1  0
  1 52  1  0
  3 53  1  6
  4 54  1  0
  4 55  1  0
  5 56  1  6
  6 57  1  0
  6 58  1  0
  6 59  1  0
  8 60  1  6
 10 61  1  6
 46100  1  6
 47101  1  0
 47102  1  0
 47103  1  0
 45 98  1  0
 45 99  1  0
 43 94  1  0
 43 95  1  0
 43 96  1  0
 44 97  1  0
 39 93  1  0
 38 92  1  0
 37 91  1  1
 35 90  1  1
 20 72  1  6
 21 73  1  0
 21 74  1  0
 23 75  1  6
 25 76  1  1
 26 77  1  0
 26 78  1  0
 26 79  1  0
 27 80  1  6
 28 81  1  0
 29 82  1  6
 31 83  1  0
 31 84  1  0
 31 85  1  0
 32 86  1  1
 34 87  1  0
 34 88  1  0
 34 89  1  0
 18 68  1  1
 19 69  1  0
 19 70  1  0
 19 71  1  0
 14 67  1  0
 13 66  1  0
 11 62  1  6
 12 63  1  0
 12 64  1  0
 12 65  1  0
 48104  1  1
 49105  1  0
M  END


  Mrv1652309082222532D          

 49 52  0  0  1  0            999 V2000
    7.4748    4.1415    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.1142    3.3995    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    6.2913    3.3408    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    5.8290    4.0241    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.0061    3.9654    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    4.5438    4.6487    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.6455    3.2233    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.1078    2.5400    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    4.7472    1.7980    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.9243    1.7393    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.3866    1.0560    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.2095    1.1147    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.0260    0.3140    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.2031    0.2553    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8425   -0.4868    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.3048   -1.1701    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.0196   -0.5455    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.5573    0.1378    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.9179    0.8798    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7344    0.0791    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.3738   -0.6629    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4491   -0.7216    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8097   -1.4637    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
   -1.6326   -1.5224    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9932   -2.2644    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
   -2.8162   -2.3231    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5309   -2.9477    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
   -1.8915   -3.6897    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7080   -2.8890    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
   -0.2457   -3.5723    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.5772   -3.5136    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3474   -2.1470    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    0.4755   -2.0882    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.8361   -1.3462    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.2721    0.7624    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1902    1.4457    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.6327    1.5044    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4556    1.5631    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.8162    2.3052    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.6391    2.3639    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.1014    1.6806    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.9997    3.1059    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.2063    3.3322    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.0847    3.9265    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.8226    3.1646    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.2849    2.4813    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.9161    3.0125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.9307    2.5988    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    6.3930    1.9155    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0  0  0  0
  3  2  1  1  0  0  0
  3  4  1  0  0  0  0
  4  5  1  0  0  0  0
  5  6  1  1  0  0  0
  5  7  1  0  0  0  0
  7  8  1  0  0  0  0
  8  9  1  1  0  0  0
  9 10  1  0  0  0  0
 10 11  1  0  0  0  0
 11 12  1  0  0  0  0
 11 13  1  0  0  0  0
 13 14  2  0  0  0  0
 14 15  1  0  0  0  0
 15 16  2  0  0  0  0
 15 17  1  0  0  0  0
 17 18  1  0  0  0  0
 18 19  1  0  0  0  0
 18 20  1  0  0  0  0
 20 21  1  0  0  0  0
 21 22  1  0  0  0  0
 23 22  1  1  0  0  0
 23 24  1  0  0  0  0
 24 25  1  0  0  0  0
 25 26  1  1  0  0  0
 25 27  1  0  0  0  0
 27 28  1  6  0  0  0
 27 29  1  0  0  0  0
 29 30  1  6  0  0  0
 30 31  1  0  0  0  0
 29 32  1  0  0  0  0
 23 32  1  0  0  0  0
 32 33  1  6  0  0  0
 33 34  1  0  0  0  0
 20 35  1  0  0  0  0
 35 36  1  0  0  0  0
 36 37  1  0  0  0  0
 35 37  1  0  0  0  0
 37 38  1  0  0  0  0
 38 39  2  0  0  0  0
 39 40  1  0  0  0  0
 40 41  2  0  0  0  0
 40 42  1  0  0  0  0
 42 43  1  0  0  0  0
 42 44  1  0  0  0  0
 42 45  1  0  0  0  0
 45 46  1  0  0  0  0
 10 46  1  0  0  0  0
 46 47  1  0  0  0  0
  8 48  1  0  0  0  0
  3 48  1  0  0  0  0
 48 49  1  6  0  0  0
M  END
> <DATABASE_ID>
NP0273748

> <DATABASE_NAME>
NP-MRD

> <SMILES>
CO[C@@H]1C[C@H](C)O[C@H](OC2C(C)CC(C)(O)C(=O)\C=C\C3OC3C(CO[C@@H]3O[C@H](C)[C@@H](O)[C@@H](OC)[C@H]3OC)C(C)OC(=O)\C=C\C2C)[C@H]1O

> <INCHI_IDENTIFIER>
InChI=1S/C35H56O14/c1-17-10-13-26(37)46-20(4)22(16-44-34-32(43-9)31(42-8)27(38)21(5)47-34)30-23(48-30)11-12-25(36)35(6,40)15-18(2)29(17)49-33-28(39)24(41-7)14-19(3)45-33/h10-13,17-24,27-34,38-40H,14-16H2,1-9H3/b12-11+,13-10+/t17?,18?,19-,20?,21+,22?,23?,24+,27+,28-,29?,30?,31+,32+,33+,34+,35?/m0/s1

> <INCHI_KEY>
KLGADJPDTCIJLO-JVECKAFRSA-N

> <FORMULA>
C35H56O14

> <MOLECULAR_WEIGHT>
700.819

> <EXACT_MASS>
700.367006483

> <JCHEM_ACCEPTOR_COUNT>
13

> <JCHEM_ATOM_COUNT>
105

> <JCHEM_AVERAGE_POLARIZABILITY>
73.1386545184076

> <JCHEM_BIOAVAILABILITY>
0

> <JCHEM_DONOR_COUNT>
3

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
0

> <JCHEM_IUPAC>
(6E,14E)-12-hydroxy-2-({[(2R,3R,4R,5R,6R)-5-hydroxy-3,4-dimethoxy-6-methyloxan-2-yl]oxy}methyl)-9-{[(2R,3S,4R,6S)-3-hydroxy-4-methoxy-6-methyloxan-2-yl]oxy}-3,8,10,12-tetramethyl-4,17-dioxabicyclo[14.1.0]heptadeca-6,14-diene-5,13-dione

> <JCHEM_LOGP>
2.6698131436666683

> <JCHEM_MDDR_LIKE_RULE>
1

> <JCHEM_NUMBER_OF_RINGS>
4

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA>
12.986775963458786

> <JCHEM_PKA_STRONGEST_ACIDIC>
12.314209169541527

> <JCHEM_PKA_STRONGEST_BASIC>
-3.5601831667877395

> <JCHEM_POLAR_SURFACE_AREA>
181.2

> <JCHEM_REFRACTIVITY>
175.18740000000003

> <JCHEM_ROTATABLE_BOND_COUNT>
8

> <JCHEM_RULE_OF_FIVE>
0

> <JCHEM_TRADITIONAL_IUPAC>
(6E,14E)-12-hydroxy-2-({[(2R,3R,4R,5R,6R)-5-hydroxy-3,4-dimethoxy-6-methyloxan-2-yl]oxy}methyl)-9-{[(2R,3S,4R,6S)-3-hydroxy-4-methoxy-6-methyloxan-2-yl]oxy}-3,8,10,12-tetramethyl-4,17-dioxabicyclo[14.1.0]heptadeca-6,14-diene-5,13-dione

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 08-SEP-22   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   08-SEP-22         0                                  
HETATM    1  C   UNK     0      13.953   7.731   0.000  0.00  0.00           C+0
HETATM    2  O   UNK     0      13.280   6.346   0.000  0.00  0.00           O+0
HETATM    3  C   UNK     0      11.744   6.236   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0      10.881   7.512   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0       9.345   7.402   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0       8.482   8.677   0.000  0.00  0.00           C+0
HETATM    7  O   UNK     0       8.672   6.017   0.000  0.00  0.00           O+0
HETATM    8  C   UNK     0       9.535   4.741   0.000  0.00  0.00           C+0
HETATM    9  O   UNK     0       8.861   3.356   0.000  0.00  0.00           O+0
HETATM   10  C   UNK     0       7.325   3.247   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0       8.188   1.971   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0       9.724   2.081   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0       7.515   0.586   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0       5.979   0.476   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0       5.306  -0.909   0.000  0.00  0.00           C+0
HETATM   16  O   UNK     0       6.169  -2.184   0.000  0.00  0.00           O+0
HETATM   17  O   UNK     0       3.770  -1.018   0.000  0.00  0.00           O+0
HETATM   18  C   UNK     0       2.907   0.257   0.000  0.00  0.00           C+0
HETATM   19  C   UNK     0       3.580   1.642   0.000  0.00  0.00           C+0
HETATM   20  C   UNK     0       1.371   0.148   0.000  0.00  0.00           C+0
HETATM   21  C   UNK     0       0.698  -1.237   0.000  0.00  0.00           C+0
HETATM   22  O   UNK     0      -0.838  -1.347   0.000  0.00  0.00           O+0
HETATM   23  C   UNK     0      -1.512  -2.732   0.000  0.00  0.00           C+0
HETATM   24  O   UNK     0      -3.048  -2.842   0.000  0.00  0.00           O+0
HETATM   25  C   UNK     0      -3.721  -4.227   0.000  0.00  0.00           C+0
HETATM   26  C   UNK     0      -5.257  -4.337   0.000  0.00  0.00           C+0
HETATM   27  C   UNK     0      -2.858  -5.502   0.000  0.00  0.00           C+0
HETATM   28  O   UNK     0      -3.531  -6.887   0.000  0.00  0.00           O+0
HETATM   29  C   UNK     0      -1.322  -5.393   0.000  0.00  0.00           C+0
HETATM   30  O   UNK     0      -0.459  -6.668   0.000  0.00  0.00           O+0
HETATM   31  C   UNK     0       1.077  -6.559   0.000  0.00  0.00           C+0
HETATM   32  C   UNK     0      -0.649  -4.008   0.000  0.00  0.00           C+0
HETATM   33  O   UNK     0       0.888  -3.898   0.000  0.00  0.00           O+0
HETATM   34  C   UNK     0       1.561  -2.513   0.000  0.00  0.00           C+0
HETATM   35  C   UNK     0       0.508   1.423   0.000  0.00  0.00           C+0
HETATM   36  O   UNK     0      -0.355   2.699   0.000  0.00  0.00           O+0
HETATM   37  C   UNK     0       1.181   2.808   0.000  0.00  0.00           C+0
HETATM   38  C   UNK     0       2.717   2.918   0.000  0.00  0.00           C+0
HETATM   39  C   UNK     0       3.390   4.303   0.000  0.00  0.00           C+0
HETATM   40  C   UNK     0       4.926   4.413   0.000  0.00  0.00           C+0
HETATM   41  O   UNK     0       5.789   3.137   0.000  0.00  0.00           O+0
HETATM   42  C   UNK     0       5.599   5.798   0.000  0.00  0.00           C+0
HETATM   43  C   UNK     0       4.118   6.220   0.000  0.00  0.00           C+0
HETATM   44  O   UNK     0       5.758   7.329   0.000  0.00  0.00           O+0
HETATM   45  C   UNK     0       7.135   5.907   0.000  0.00  0.00           C+0
HETATM   46  C   UNK     0       7.998   4.632   0.000  0.00  0.00           C+0
HETATM   47  C   UNK     0       9.177   5.623   0.000  0.00  0.00           C+0
HETATM   48  C   UNK     0      11.071   4.851   0.000  0.00  0.00           C+0
HETATM   49  O   UNK     0      11.934   3.576   0.000  0.00  0.00           O+0
CONECT    1    2                                                            
CONECT    2    1    3                                                       
CONECT    3    2    4   48                                                  
CONECT    4    3    5                                                       
CONECT    5    4    6    7                                                  
CONECT    6    5                                                            
CONECT    7    5    8                                                       
CONECT    8    7    9   48                                                  
CONECT    9    8   10                                                       
CONECT   10    9   11   46                                                  
CONECT   11   10   12   13                                                  
CONECT   12   11                                                            
CONECT   13   11   14                                                       
CONECT   14   13   15                                                       
CONECT   15   14   16   17                                                  
CONECT   16   15                                                            
CONECT   17   15   18                                                       
CONECT   18   17   19   20                                                  
CONECT   19   18                                                            
CONECT   20   18   21   35                                                  
CONECT   21   20   22                                                       
CONECT   22   21   23                                                       
CONECT   23   22   24   32                                                  
CONECT   24   23   25                                                       
CONECT   25   24   26   27                                                  
CONECT   26   25                                                            
CONECT   27   25   28   29                                                  
CONECT   28   27                                                            
CONECT   29   27   30   32                                                  
CONECT   30   29   31                                                       
CONECT   31   30                                                            
CONECT   32   29   23   33                                                  
CONECT   33   32   34                                                       
CONECT   34   33                                                            
CONECT   35   20   36   37                                                  
CONECT   36   35   37                                                       
CONECT   37   36   35   38                                                  
CONECT   38   37   39                                                       
CONECT   39   38   40                                                       
CONECT   40   39   41   42                                                  
CONECT   41   40                                                            
CONECT   42   40   43   44   45                                             
CONECT   43   42                                                            
CONECT   44   42                                                            
CONECT   45   42   46                                                       
CONECT   46   45   10   47                                                  
CONECT   47   46                                                            
CONECT   48    8    3   49                                                  
CONECT   49   48                                                            
MASTER        0    0    0    0    0    0    0    0   49    0  104    0
END

View in JSmol

Synonyms

Not Available

Chemical Formula

C₃₅H₅₆O₁₄

Average Mass

700.8190 Da

Monoisotopic Mass

700.36701 Da

IUPAC Name

(6E,14E)-12-hydroxy-2-({[(2R,3R,4R,5R,6R)-5-hydroxy-3,4-dimethoxy-6-methyloxan-2-yl]oxy}methyl)-9-{[(2R,3S,4R,6S)-3-hydroxy-4-methoxy-6-methyloxan-2-yl]oxy}-3,8,10,12-tetramethyl-4,17-dioxabicyclo[14.1.0]heptadeca-6,14-diene-5,13-dione

Traditional Name

CAS Registry Number

Not Available

SMILES

CO[C@@H]1C[C@H](C)O[C@H](OC2C(C)CC(C)(O)C(=O)\C=C\C3OC3C(CO[C@@H]3O[C@H](C)[C@@H](O)[C@@H](OC)[C@H]3OC)C(C)OC(=O)\C=C\C2C)[C@H]1O

InChI Identifier

InChI=1S/C35H56O14/c1-17-10-13-26(37)46-20(4)22(16-44-34-32(43-9)31(42-8)27(38)21(5)47-34)30-23(48-30)11-12-25(36)35(6,40)15-18(2)29(17)49-33-28(39)24(41-7)14-19(3)45-33/h10-13,17-24,27-34,38-40H,14-16H2,1-9H3/b12-11+,13-10+/t17?,18?,19-,20?,21+,22?,23?,24+,27+,28-,29?,30?,31+,32+,33+,34+,35?/m0/s1

InChI Key

KLGADJPDTCIJLO-JVECKAFRSA-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
Streptomyces bikiniensis	LOTUS Database	35616633

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as macrolides and analogues. These are organic compounds containing a lactone ring of at least twelve members.

Kingdom

Organic compounds

Super Class

Phenylpropanoids and polyketides

Class

Macrolides and analogues

Sub Class

Not Available

Direct Parent

Macrolides and analogues

Alternative Parents

Substituents

Macrolide
Glycosyl compound
O-glycosyl compound
Acyloin
Monosaccharide
Oxane
Alpha,beta-unsaturated carboxylic ester
Enoate ester
Tertiary alcohol
Carboxylic acid ester
Ketone
Lactone
Cyclic ketone
Secondary alcohol
Monocarboxylic acid or derivatives
Ether
Oxirane
Dialkyl ether
Acetal
Carboxylic acid derivative
Oxacycle
Organoheterocyclic compound
Hydrocarbon derivative
Alcohol
Organic oxygen compound
Organic oxide
Carbonyl group
Organooxygen compound
Aldehyde
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	2.67	ChemAxon
pKa (Strongest Acidic)	12.31	ChemAxon
pKa (Strongest Basic)	-3.6	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	13	ChemAxon
Hydrogen Donor Count	3	ChemAxon
Polar Surface Area	181.2 Å²	ChemAxon
Rotatable Bond Count	8	ChemAxon
Refractivity	175.19 m³·mol⁻¹	ChemAxon
Polarizability	73.14 Å³	ChemAxon
Number of Rings	4	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

8970138

KEGG Compound ID

Not Available

BioCyc ID

Not Available

BiGG ID

Not Available

Wikipedia Link

Not Available

METLIN ID

Not Available

PubChem Compound

10794830

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

LOTUS database [Link]

Showing NP-Card for (6e,14e)-12-hydroxy-2-({[(2r,3r,4r,5r,6r)-5-hydroxy-3,4-dimethoxy-6-methyloxan-2-yl]oxy}methyl)-9-{[(2r,3s,4r,6s)-3-hydroxy-4-methoxy-6-methyloxan-2-yl]oxy}-3,8,10,12-tetramethyl-4,17-dioxabicyclo[14.1.0]heptadeca-6,14-diene-5,13-dione (NP0273748)

MOL for NP0273748 ((6e,14e)-12-hydroxy-2-({[(2r,3r,4r,5r,6r)-5-hydroxy-3,4-dimethoxy-6-methyloxan-2-yl]oxy}methyl)-9-{[(2r,3s,4r,6s)-3-hydroxy-4-methoxy-6-methyloxan-2-yl]oxy}-3,8,10,12-tetramethyl-4,17-dioxabicyclo[14.1.0]heptadeca-6,14-diene-5,13-dione)

3D MOL for NP0273748 ((6e,14e)-12-hydroxy-2-({[(2r,3r,4r,5r,6r)-5-hydroxy-3,4-dimethoxy-6-methyloxan-2-yl]oxy}methyl)-9-{[(2r,3s,4r,6s)-3-hydroxy-4-methoxy-6-methyloxan-2-yl]oxy}-3,8,10,12-tetramethyl-4,17-dioxabicyclo[14.1.0]heptadeca-6,14-diene-5,13-dione)

3D SDF for NP0273748 ((6e,14e)-12-hydroxy-2-({[(2r,3r,4r,5r,6r)-5-hydroxy-3,4-dimethoxy-6-methyloxan-2-yl]oxy}methyl)-9-{[(2r,3s,4r,6s)-3-hydroxy-4-methoxy-6-methyloxan-2-yl]oxy}-3,8,10,12-tetramethyl-4,17-dioxabicyclo[14.1.0]heptadeca-6,14-diene-5,13-dione)

3D-SDF for NP0273748 ((6e,14e)-12-hydroxy-2-({[(2r,3r,4r,5r,6r)-5-hydroxy-3,4-dimethoxy-6-methyloxan-2-yl]oxy}methyl)-9-{[(2r,3s,4r,6s)-3-hydroxy-4-methoxy-6-methyloxan-2-yl]oxy}-3,8,10,12-tetramethyl-4,17-dioxabicyclo[14.1.0]heptadeca-6,14-diene-5,13-dione)

PDB for NP0273748 ((6e,14e)-12-hydroxy-2-({[(2r,3r,4r,5r,6r)-5-hydroxy-3,4-dimethoxy-6-methyloxan-2-yl]oxy}methyl)-9-{[(2r,3s,4r,6s)-3-hydroxy-4-methoxy-6-methyloxan-2-yl]oxy}-3,8,10,12-tetramethyl-4,17-dioxabicyclo[14.1.0]heptadeca-6,14-diene-5,13-dione)

3D PDB for NP0273748 ((6e,14e)-12-hydroxy-2-({[(2r,3r,4r,5r,6r)-5-hydroxy-3,4-dimethoxy-6-methyloxan-2-yl]oxy}methyl)-9-{[(2r,3s,4r,6s)-3-hydroxy-4-methoxy-6-methyloxan-2-yl]oxy}-3,8,10,12-tetramethyl-4,17-dioxabicyclo[14.1.0]heptadeca-6,14-diene-5,13-dione)

SMILES for NP0273748 ((6e,14e)-12-hydroxy-2-({[(2r,3r,4r,5r,6r)-5-hydroxy-3,4-dimethoxy-6-methyloxan-2-yl]oxy}methyl)-9-{[(2r,3s,4r,6s)-3-hydroxy-4-methoxy-6-methyloxan-2-yl]oxy}-3,8,10,12-tetramethyl-4,17-dioxabicyclo[14.1.0]heptadeca-6,14-diene-5,13-dione)

INCHI for NP0273748 ((6e,14e)-12-hydroxy-2-({[(2r,3r,4r,5r,6r)-5-hydroxy-3,4-dimethoxy-6-methyloxan-2-yl]oxy}methyl)-9-{[(2r,3s,4r,6s)-3-hydroxy-4-methoxy-6-methyloxan-2-yl]oxy}-3,8,10,12-tetramethyl-4,17-dioxabicyclo[14.1.0]heptadeca-6,14-diene-5,13-dione)

Structure for NP0273748 ((6e,14e)-12-hydroxy-2-({[(2r,3r,4r,5r,6r)-5-hydroxy-3,4-dimethoxy-6-methyloxan-2-yl]oxy}methyl)-9-{[(2r,3s,4r,6s)-3-hydroxy-4-methoxy-6-methyloxan-2-yl]oxy}-3,8,10,12-tetramethyl-4,17-dioxabicyclo[14.1.0]heptadeca-6,14-diene-5,13-dione)

3D Structure for NP0273748 ((6e,14e)-12-hydroxy-2-({[(2r,3r,4r,5r,6r)-5-hydroxy-3,4-dimethoxy-6-methyloxan-2-yl]oxy}methyl)-9-{[(2r,3s,4r,6s)-3-hydroxy-4-methoxy-6-methyloxan-2-yl]oxy}-3,8,10,12-tetramethyl-4,17-dioxabicyclo[14.1.0]heptadeca-6,14-diene-5,13-dione)