NP-MRD: Showing NP-Card for (1r)-1-[(6r,9s,10r,11s,16s)-5,16-dihydroxy-11-{[(2r,5s)-5-hydroxy-6-methyloxan-2-yl]oxy}-4,8,10-trimethyl-3,14-dioxo-2-azatetracyclo[7.6.1.0²,⁶.0¹²,¹⁶]hexadeca-1(15),4,7,12-tetraen-6-yl]ethyl acetate (NP0194780)

Jump To Section:

Identification Spectra BioTaxonomy ChemoTaxonomy Physical properties Links References XML

Record Information

Version

2.0

Created at

2022-09-04 12:30:59 UTC

Updated at

2022-09-04 12:30:59 UTC

NP-MRD ID

NP0194780

Secondary Accession Numbers

None

Natural Product Identification

Common Name

(1r)-1-[(6r,9s,10r,11s,16s)-5,16-dihydroxy-11-{[(2r,5s)-5-hydroxy-6-methyloxan-2-yl]oxy}-4,8,10-trimethyl-3,14-dioxo-2-azatetracyclo[7.6.1.0²,⁶.0¹²,¹⁶]hexadeca-1(15),4,7,12-tetraen-6-yl]ethyl acetate

Description

(1R)-1-[(6R,9S,10R,11S,16S)-5,16-dihydroxy-11-{[(2R,5S)-5-hydroxy-6-methyloxan-2-yl]oxy}-4,8,10-trimethyl-3,14-dioxo-2-azatetracyclo[7.6.1.0²,⁶.0¹²,¹⁶]Hexadeca-1(15),4,7,12-tetraen-6-yl]ethyl acetate belongs to the class of organic compounds known as azepines. These are organic compounds containing an unsaturated seven-member heterocycle with one nitrogen atom replacing a carbon atom. Based on a literature review very few articles have been published on (1R)-1-[(6R,9S,10R,11S,16S)-5,16-dihydroxy-11-{[(2R,5S)-5-hydroxy-6-methyloxan-2-yl]oxy}-4,8,10-trimethyl-3,14-dioxo-2-azatetracyclo[7.6.1.0²,⁶.0¹²,¹⁶]Hexadeca-1(15),4,7,12-tetraen-6-yl]ethyl acetate.

Structure

MOL 3D MOL SDF PDB SMILES InChI


  Mrv1652309042214312D          

 38 42  0  0  1  0            999 V2000
    2.5420   -2.9534    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.0369   -2.2933    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.8560   -2.3918    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.7126   -1.5347    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.2075   -0.8746    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    4.0266   -0.9731    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8832   -0.1160    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    2.3689   -0.7610    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.5439   -0.7610    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.1859   -1.5043    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.0295   -0.1160    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    0.2078   -0.1899    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
   -0.2153   -0.8982    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1164    0.5687    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
   -0.9207    0.7522    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4819    0.1475    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
   -1.2387   -0.6409    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7999   -1.2456    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6042   -1.0621    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
   -3.1653   -1.6668    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8474   -0.2737    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.6517   -0.0901    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2862    0.3311    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.5048    1.1115    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.5172    1.9364    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.2378    2.3381    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.2501    3.1630    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.9460    1.9150    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.9564    1.0463    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.6997    0.6883    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    3.4079    1.1115    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.4818    1.9331    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.0292    0.5687    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.8335    0.7522    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.7049   -0.1899    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.3262   -0.7327    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.2131    0.6883    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    1.8581    0.1739    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0  0  0  0
  2  3  2  0  0  0  0
  2  4  1  0  0  0  0
  4  5  1  0  0  0  0
  5  6  1  1  0  0  0
  7  5  1  1  0  0  0
  7  8  1  0  0  0  0
  8  9  2  0  0  0  0
  9 10  1  0  0  0  0
 11  9  1  6  0  0  0
 11 12  1  0  0  0  0
 12 13  1  1  0  0  0
 12 14  1  0  0  0  0
 14 15  1  6  0  0  0
 16 15  1  1  0  0  0
 16 17  1  0  0  0  0
 17 18  1  0  0  0  0
 18 19  1  0  0  0  0
 19 20  1  6  0  0  0
 19 21  1  0  0  0  0
 21 22  1  0  0  0  0
 21 23  1  0  0  0  0
 16 23  1  0  0  0  0
 14 24  1  0  0  0  0
 24 25  2  0  0  0  0
 25 26  1  0  0  0  0
 26 27  2  0  0  0  0
 26 28  1  0  0  0  0
 28 29  2  0  0  0  0
 29 30  1  0  0  0  0
  7 30  1  0  0  0  0
 30 31  1  0  0  0  0
 31 32  2  0  0  0  0
 31 33  1  0  0  0  0
 33 34  1  0  0  0  0
 33 35  2  0  0  0  0
  7 35  1  0  0  0  0
 35 36  1  0  0  0  0
 29 37  1  0  0  0  0
 24 37  1  0  0  0  0
 11 37  1  0  0  0  0
 37 38  1  1  0  0  0
M  END

     RDKit          3D

 73 77  0  0  0  0  0  0  0  0999 V2000
    6.2745   -2.5372   -1.9606 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.5839   -2.1672   -0.6869 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.2321   -2.3425    0.3771 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.3016   -1.6600   -0.6850 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.6288   -1.2948    0.5148 C   0  0  2  0  0  0  0  0  0  0  0  0
    2.6132   -2.3113    0.7901 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.3209    0.1651    0.5187 C   0  0  1  0  0  0  0  0  0  0  0  0
    2.8277    0.7280   -0.7500 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.5915    0.7083   -1.2395 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4674    1.3837   -2.5583 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.3913    0.1163   -0.6736 C   0  0  2  0  0  0  0  0  0  0  0  0
   -0.9274    0.4863   -1.3599 C   0  0  1  0  0  0  0  0  0  0  0  0
   -1.2946   -0.4377   -2.4761 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9742    0.2721   -0.2376 C   0  0  2  0  0  0  0  0  0  0  0  0
   -3.0874    1.0125   -0.4842 O   0  0  0  0  0  0  0  0  0  0  0  0
   -4.2808    0.3207   -0.4164 C   0  0  1  0  0  0  0  0  0  0  0  0
   -5.2799    0.9190    0.5209 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.5114    1.3722   -0.2216 C   0  0  0  0  0  0  0  0  0  0  0  0
   -7.1351    0.1952   -0.9754 C   0  0  2  0  0  0  0  0  0  0  0  0
   -7.8210   -0.6427   -0.1042 O   0  0  0  0  0  0  0  0  0  0  0  0
   -6.0131   -0.4938   -1.6997 C   0  0  2  0  0  0  0  0  0  0  0  0
   -5.6960   -1.8442   -1.1270 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.8418    0.2799   -1.6977 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1835    0.8869    0.8899 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5759    1.6736    1.8531 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5929    2.1423    2.7926 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8900    2.8862    3.7297 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.8108    1.6952    2.5949 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.1447    0.8756    1.6192 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.5981    0.6596    1.6569 N   0  0  0  0  0  0  0  0  0  0  0  0
    3.4000    1.1700    2.6777 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.2392    1.5479    3.8424 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.7535    1.2052    2.0608 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.0075    1.7416    2.6982 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.7303    0.7040    0.8696 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.7924    0.6336   -0.0186 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.1647    0.2593    0.7674 C   0  0  2  0  0  0  0  0  0  0  0  0
   -0.1422   -1.0642    1.3179 O   0  0  0  0  0  0  0  0  0  0  0  0
    7.3585   -2.5879   -1.8458 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.9322   -1.8174   -2.7234 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.9085   -3.5547   -2.2238 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.4578   -1.4738    1.3172 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.8170   -2.4922    0.0911 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.1760   -2.2100    1.8290 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.1328   -3.3412    0.8998 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.5782    1.2207   -1.3564 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.4117    1.9600   -2.8030 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.6804    2.1650   -2.5828 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.3910    0.6629   -3.4078 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.4377   -1.0083   -0.9004 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0027    1.5137   -1.6725 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9214   -1.2568   -2.0738 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9729    0.1341   -3.1656 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4194   -0.8461   -3.0343 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1342   -0.7671   -0.0139 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.0112   -0.7428   -0.1562 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.6234    0.2063    1.3020 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.8424    1.8258    0.9897 H   0  0  0  0  0  0  0  0  0  0  0  0
   -7.2497    1.8203    0.4576 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.2544    2.1226   -1.0115 H   0  0  0  0  0  0  0  0  0  0  0  0
   -7.8495    0.6112   -1.7065 H   0  0  0  0  0  0  0  0  0  0  0  0
   -8.2398   -0.1481    0.6376 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.2899   -0.6255   -2.7644 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.6999   -2.1916   -1.4173 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.4837   -2.5582   -1.4757 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.7361   -1.8229   -0.0090 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6419    1.9611    1.9284 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.5462    2.0941    3.2728 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.7058    2.3287    3.6053 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.6605    0.9183    3.0534 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.5276    2.4495    2.0345 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.5280    1.3498   -0.0194 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5044   -0.9302    2.2253 H   0  0  0  0  0  0  0  0  0  0  0  0
  6  5  1  0
  5  4  1  0
  4  2  1  0
  2  1  1  0
  2  3  2  0
  5  7  1  0
  7  8  1  6
  8  9  2  0
  9 10  1  0
  9 11  1  0
 11 12  1  0
 12 13  1  0
 12 14  1  0
 14 15  1  0
 15 16  1  0
 16 17  1  0
 17 18  1  0
 18 19  1  0
 19 20  1  0
 19 21  1  0
 21 22  1  0
 21 23  1  0
 14 24  1  0
 24 25  2  0
 25 26  1  0
 26 27  2  0
 26 28  1  0
 28 29  2  0
 29 30  1  0
 30 31  1  0
 31 32  2  0
 31 33  1  0
 33 34  1  0
 33 35  2  0
 35 36  1  0
 29 37  1  0
 37 38  1  1
 30  7  1  0
 35  7  1  0
 37 11  1  0
 23 16  1  0
 37 24  1  0
  6 43  1  0
  6 44  1  0
  6 45  1  0
  5 42  1  1
  1 39  1  0
  1 40  1  0
  1 41  1  0
  8 46  1  0
 10 47  1  0
 10 48  1  0
 10 49  1  0
 11 50  1  1
 12 51  1  6
 13 52  1  0
 13 53  1  0
 13 54  1  0
 14 55  1  1
 16 56  1  1
 17 57  1  0
 17 58  1  0
 18 59  1  0
 18 60  1  0
 19 61  1  6
 20 62  1  0
 21 63  1  6
 22 64  1  0
 22 65  1  0
 22 66  1  0
 25 67  1  0
 28 68  1  0
 34 69  1  0
 34 70  1  0
 34 71  1  0
 36 72  1  0
 38 73  1  0
M  END


  Mrv1652309042214312D          

 38 42  0  0  1  0            999 V2000
    2.5420   -2.9534    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.0369   -2.2933    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.8560   -2.3918    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.7126   -1.5347    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.2075   -0.8746    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    4.0266   -0.9731    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8832   -0.1160    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    2.3689   -0.7610    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.5439   -0.7610    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.1859   -1.5043    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.0295   -0.1160    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    0.2078   -0.1899    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
   -0.2153   -0.8982    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1164    0.5687    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
   -0.9207    0.7522    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4819    0.1475    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
   -1.2387   -0.6409    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7999   -1.2456    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6042   -1.0621    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
   -3.1653   -1.6668    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8474   -0.2737    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.6517   -0.0901    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2862    0.3311    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.5048    1.1115    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.5172    1.9364    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.2378    2.3381    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.2501    3.1630    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.9460    1.9150    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.9564    1.0463    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.6997    0.6883    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    3.4079    1.1115    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.4818    1.9331    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.0292    0.5687    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.8335    0.7522    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.7049   -0.1899    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.3262   -0.7327    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.2131    0.6883    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    1.8581    0.1739    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0  0  0  0
  2  3  2  0  0  0  0
  2  4  1  0  0  0  0
  4  5  1  0  0  0  0
  5  6  1  1  0  0  0
  7  5  1  1  0  0  0
  7  8  1  0  0  0  0
  8  9  2  0  0  0  0
  9 10  1  0  0  0  0
 11  9  1  6  0  0  0
 11 12  1  0  0  0  0
 12 13  1  1  0  0  0
 12 14  1  0  0  0  0
 14 15  1  6  0  0  0
 16 15  1  1  0  0  0
 16 17  1  0  0  0  0
 17 18  1  0  0  0  0
 18 19  1  0  0  0  0
 19 20  1  6  0  0  0
 19 21  1  0  0  0  0
 21 22  1  0  0  0  0
 21 23  1  0  0  0  0
 16 23  1  0  0  0  0
 14 24  1  0  0  0  0
 24 25  2  0  0  0  0
 25 26  1  0  0  0  0
 26 27  2  0  0  0  0
 26 28  1  0  0  0  0
 28 29  2  0  0  0  0
 29 30  1  0  0  0  0
  7 30  1  0  0  0  0
 30 31  1  0  0  0  0
 31 32  2  0  0  0  0
 31 33  1  0  0  0  0
 33 34  1  0  0  0  0
 33 35  2  0  0  0  0
  7 35  1  0  0  0  0
 35 36  1  0  0  0  0
 29 37  1  0  0  0  0
 24 37  1  0  0  0  0
 11 37  1  0  0  0  0
 37 38  1  1  0  0  0
M  END
> <DATABASE_ID>
NP0194780

> <DATABASE_NAME>
NP-MRD

> <SMILES>
C[C@@H](OC(C)=O)[C@@]12C=C(C)[C@@H]3[C@@H](C)[C@H](O[C@H]4CC[C@H](O)C(C)O4)C4=CC(=O)C=C(N1C(=O)C(C)=C2O)[C@]34O

> <INCHI_IDENTIFIER>
InChI=1S/C28H35NO9/c1-12-11-27(16(5)37-17(6)30)25(33)14(3)26(34)29(27)21-10-18(31)9-19-24(13(2)23(12)28(19,21)35)38-22-8-7-20(32)15(4)36-22/h9-11,13,15-16,20,22-24,32-33,35H,7-8H2,1-6H3/t13-,15?,16-,20+,22+,23-,24+,27-,28+/m1/s1

> <INCHI_KEY>
PDESUVPLPIOXLG-BUVHAQBMSA-N

> <FORMULA>
C28H35NO9

> <MOLECULAR_WEIGHT>
529.586

> <EXACT_MASS>
529.231181711

> <JCHEM_ACCEPTOR_COUNT>
8

> <JCHEM_ATOM_COUNT>
73

> <JCHEM_AVERAGE_POLARIZABILITY>
54.32256589591948

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
3

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
0

> <JCHEM_IUPAC>
(1R)-1-[(6R,9S,10R,11S,16S)-5,16-dihydroxy-11-{[(2R,5S)-5-hydroxy-6-methyloxan-2-yl]oxy}-4,8,10-trimethyl-3,14-dioxo-2-azatetracyclo[7.6.1.0^{2,6}.0^{12,16}]hexadeca-1(15),4,7,12-tetraen-6-yl]ethyl acetate

> <JCHEM_LOGP>
0.3756212303333335

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
5

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA>
12.90979488073435

> <JCHEM_PKA_STRONGEST_ACIDIC>
7.211864611428021

> <JCHEM_PKA_STRONGEST_BASIC>
-2.4201765767087084

> <JCHEM_POLAR_SURFACE_AREA>
142.83

> <JCHEM_REFRACTIVITY>
137.9719

> <JCHEM_ROTATABLE_BOND_COUNT>
5

> <JCHEM_RULE_OF_FIVE>
0

> <JCHEM_TRADITIONAL_IUPAC>
(1R)-1-[(6R,9S,10R,11S,16S)-5,16-dihydroxy-11-{[(2R,5S)-5-hydroxy-6-methyloxan-2-yl]oxy}-4,8,10-trimethyl-3,14-dioxo-2-azatetracyclo[7.6.1.0^{2,6}.0^{12,16}]hexadeca-1(15),4,7,12-tetraen-6-yl]ethyl acetate

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 04-SEP-22   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   04-SEP-22         0                                  
HETATM    1  C   UNK     0       4.745  -5.513   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0       5.669  -4.281   0.000  0.00  0.00           C+0
HETATM    3  O   UNK     0       7.198  -4.465   0.000  0.00  0.00           O+0
HETATM    4  O   UNK     0       5.064  -2.865   0.000  0.00  0.00           O+0
HETATM    5  C   UNK     0       5.987  -1.633   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0       7.516  -1.816   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0       5.382  -0.217   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0       4.422  -1.421   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0       2.882  -1.421   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0       2.214  -2.808   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0       1.922  -0.217   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0       0.388  -0.355   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0      -0.402  -1.677   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0      -0.217   1.062   0.000  0.00  0.00           C+0
HETATM   15  O   UNK     0      -1.719   1.404   0.000  0.00  0.00           O+0
HETATM   16  C   UNK     0      -2.766   0.275   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0      -2.312  -1.196   0.000  0.00  0.00           C+0
HETATM   18  C   UNK     0      -3.360  -2.325   0.000  0.00  0.00           C+0
HETATM   19  C   UNK     0      -4.861  -1.983   0.000  0.00  0.00           C+0
HETATM   20  O   UNK     0      -5.909  -3.111   0.000  0.00  0.00           O+0
HETATM   21  C   UNK     0      -5.315  -0.511   0.000  0.00  0.00           C+0
HETATM   22  C   UNK     0      -6.816  -0.168   0.000  0.00  0.00           C+0
HETATM   23  O   UNK     0      -4.268   0.618   0.000  0.00  0.00           O+0
HETATM   24  C   UNK     0       0.942   2.075   0.000  0.00  0.00           C+0
HETATM   25  C   UNK     0       0.965   3.615   0.000  0.00  0.00           C+0
HETATM   26  C   UNK     0       2.310   4.365   0.000  0.00  0.00           C+0
HETATM   27  O   UNK     0       2.334   5.904   0.000  0.00  0.00           O+0
HETATM   28  C   UNK     0       3.632   3.575   0.000  0.00  0.00           C+0
HETATM   29  C   UNK     0       3.652   1.953   0.000  0.00  0.00           C+0
HETATM   30  N   UNK     0       5.039   1.285   0.000  0.00  0.00           N+0
HETATM   31  C   UNK     0       6.361   2.075   0.000  0.00  0.00           C+0
HETATM   32  O   UNK     0       6.499   3.609   0.000  0.00  0.00           O+0
HETATM   33  C   UNK     0       7.521   1.062   0.000  0.00  0.00           C+0
HETATM   34  C   UNK     0       9.023   1.404   0.000  0.00  0.00           C+0
HETATM   35  C   UNK     0       6.916  -0.355   0.000  0.00  0.00           C+0
HETATM   36  O   UNK     0       8.076  -1.368   0.000  0.00  0.00           O+0
HETATM   37  C   UNK     0       2.264   1.285   0.000  0.00  0.00           C+0
HETATM   38  O   UNK     0       3.468   0.325   0.000  0.00  0.00           O+0
CONECT    1    2                                                            
CONECT    2    1    3    4                                                  
CONECT    3    2                                                            
CONECT    4    2    5                                                       
CONECT    5    4    6    7                                                  
CONECT    6    5                                                            
CONECT    7    5    8   30   35                                             
CONECT    8    7    9                                                       
CONECT    9    8   10   11                                                  
CONECT   10    9                                                            
CONECT   11    9   12   37                                                  
CONECT   12   11   13   14                                                  
CONECT   13   12                                                            
CONECT   14   12   15   24                                                  
CONECT   15   14   16                                                       
CONECT   16   15   17   23                                                  
CONECT   17   16   18                                                       
CONECT   18   17   19                                                       
CONECT   19   18   20   21                                                  
CONECT   20   19                                                            
CONECT   21   19   22   23                                                  
CONECT   22   21                                                            
CONECT   23   21   16                                                       
CONECT   24   14   25   37                                                  
CONECT   25   24   26                                                       
CONECT   26   25   27   28                                                  
CONECT   27   26                                                            
CONECT   28   26   29                                                       
CONECT   29   28   30   37                                                  
CONECT   30   29    7   31                                                  
CONECT   31   30   32   33                                                  
CONECT   32   31                                                            
CONECT   33   31   34   35                                                  
CONECT   34   33                                                            
CONECT   35   33    7   36                                                  
CONECT   36   35                                                            
CONECT   37   29   24   11   38                                             
CONECT   38   37                                                            
MASTER        0    0    0    0    0    0    0    0   38    0   84    0
END

View in JSmol

Synonyms

Value	Source
(1R)-1-[(6R,9S,10R,11S,16S)-5,16-Dihydroxy-11-{[(2R,5S)-5-hydroxy-6-methyloxan-2-yl]oxy}-4,8,10-trimethyl-3,14-dioxo-2-azatetracyclo[7.6.1.0,.0,]hexadeca-1(15),4,7,12-tetraen-6-yl]ethyl acetic acid	Generator

Chemical Formula

C₂₈H₃₅NO₉

Average Mass

529.5860 Da

Monoisotopic Mass

529.23118 Da

IUPAC Name

Not Available

Traditional Name

Not Available

CAS Registry Number

Not Available

SMILES

C[C@@H](OC(C)=O)[C@@]12C=C(C)[C@@H]3[C@@H](C)[C@H](O[C@H]4CC[C@H](O)C(C)O4)C4=CC(=O)C=C(N1C(=O)C(C)=C2O)[C@]34O

InChI Identifier

InChI=1S/C28H35NO9/c1-12-11-27(16(5)37-17(6)30)25(33)14(3)26(34)29(27)21-10-18(31)9-19-24(13(2)23(12)28(19,21)35)38-22-8-7-20(32)15(4)36-22/h9-11,13,15-16,20,22-24,32-33,35H,7-8H2,1-6H3/t13-,15?,16-,20+,22+,23-,24+,27-,28+/m1/s1

InChI Key

PDESUVPLPIOXLG-BUVHAQBMSA-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

Not Available

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as azepines. These are organic compounds containing an unsaturated seven-member heterocycle with one nitrogen atom replacing a carbon atom.

Kingdom

Organic compounds

Super Class

Organoheterocyclic compounds

Class

Azepines

Sub Class

Not Available

Direct Parent

Azepines

Alternative Parents

Substituents

Azepine
Oxane
Vinylogous amide
Vinylogous acid
Tertiary carboxylic acid amide
Tertiary alcohol
Pyrroline
Cyclic alcohol
Cyclic ketone
Secondary alcohol
Lactam
Ketone
Carboxylic acid ester
Carboxamide group
Oxacycle
Azacycle
Monocarboxylic acid or derivatives
Enol
Carboxylic acid derivative
Acetal
Organic nitrogen compound
Organic oxygen compound
Organopnictogen compound
Organic oxide
Hydrocarbon derivative
Organooxygen compound
Organonitrogen compound
Carbonyl group
Alcohol
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

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

163195309

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

LOTUS database [Link]

Showing NP-Card for (1r)-1-[(6r,9s,10r,11s,16s)-5,16-dihydroxy-11-{[(2r,5s)-5-hydroxy-6-methyloxan-2-yl]oxy}-4,8,10-trimethyl-3,14-dioxo-2-azatetracyclo[7.6.1.0²,⁶.0¹²,¹⁶]hexadeca-1(15),4,7,12-tetraen-6-yl]ethyl acetate (NP0194780)

MOL for NP0194780 ((1r)-1-[(6r,9s,10r,11s,16s)-5,16-dihydroxy-11-{[(2r,5s)-5-hydroxy-6-methyloxan-2-yl]oxy}-4,8,10-trimethyl-3,14-dioxo-2-azatetracyclo[7.6.1.0²,⁶.0¹²,¹⁶]hexadeca-1(15),4,7,12-tetraen-6-yl]ethyl acetate)

3D MOL for NP0194780 ((1r)-1-[(6r,9s,10r,11s,16s)-5,16-dihydroxy-11-{[(2r,5s)-5-hydroxy-6-methyloxan-2-yl]oxy}-4,8,10-trimethyl-3,14-dioxo-2-azatetracyclo[7.6.1.0²,⁶.0¹²,¹⁶]hexadeca-1(15),4,7,12-tetraen-6-yl]ethyl acetate)

3D SDF for NP0194780 ((1r)-1-[(6r,9s,10r,11s,16s)-5,16-dihydroxy-11-{[(2r,5s)-5-hydroxy-6-methyloxan-2-yl]oxy}-4,8,10-trimethyl-3,14-dioxo-2-azatetracyclo[7.6.1.0²,⁶.0¹²,¹⁶]hexadeca-1(15),4,7,12-tetraen-6-yl]ethyl acetate)

3D-SDF for NP0194780 ((1r)-1-[(6r,9s,10r,11s,16s)-5,16-dihydroxy-11-{[(2r,5s)-5-hydroxy-6-methyloxan-2-yl]oxy}-4,8,10-trimethyl-3,14-dioxo-2-azatetracyclo[7.6.1.0²,⁶.0¹²,¹⁶]hexadeca-1(15),4,7,12-tetraen-6-yl]ethyl acetate)

PDB for NP0194780 ((1r)-1-[(6r,9s,10r,11s,16s)-5,16-dihydroxy-11-{[(2r,5s)-5-hydroxy-6-methyloxan-2-yl]oxy}-4,8,10-trimethyl-3,14-dioxo-2-azatetracyclo[7.6.1.0²,⁶.0¹²,¹⁶]hexadeca-1(15),4,7,12-tetraen-6-yl]ethyl acetate)

3D PDB for NP0194780 ((1r)-1-[(6r,9s,10r,11s,16s)-5,16-dihydroxy-11-{[(2r,5s)-5-hydroxy-6-methyloxan-2-yl]oxy}-4,8,10-trimethyl-3,14-dioxo-2-azatetracyclo[7.6.1.0²,⁶.0¹²,¹⁶]hexadeca-1(15),4,7,12-tetraen-6-yl]ethyl acetate)

SMILES for NP0194780 ((1r)-1-[(6r,9s,10r,11s,16s)-5,16-dihydroxy-11-{[(2r,5s)-5-hydroxy-6-methyloxan-2-yl]oxy}-4,8,10-trimethyl-3,14-dioxo-2-azatetracyclo[7.6.1.0²,⁶.0¹²,¹⁶]hexadeca-1(15),4,7,12-tetraen-6-yl]ethyl acetate)

INCHI for NP0194780 ((1r)-1-[(6r,9s,10r,11s,16s)-5,16-dihydroxy-11-{[(2r,5s)-5-hydroxy-6-methyloxan-2-yl]oxy}-4,8,10-trimethyl-3,14-dioxo-2-azatetracyclo[7.6.1.0²,⁶.0¹²,¹⁶]hexadeca-1(15),4,7,12-tetraen-6-yl]ethyl acetate)

Structure for NP0194780 ((1r)-1-[(6r,9s,10r,11s,16s)-5,16-dihydroxy-11-{[(2r,5s)-5-hydroxy-6-methyloxan-2-yl]oxy}-4,8,10-trimethyl-3,14-dioxo-2-azatetracyclo[7.6.1.0²,⁶.0¹²,¹⁶]hexadeca-1(15),4,7,12-tetraen-6-yl]ethyl acetate)

3D Structure for NP0194780 ((1r)-1-[(6r,9s,10r,11s,16s)-5,16-dihydroxy-11-{[(2r,5s)-5-hydroxy-6-methyloxan-2-yl]oxy}-4,8,10-trimethyl-3,14-dioxo-2-azatetracyclo[7.6.1.0²,⁶.0¹²,¹⁶]hexadeca-1(15),4,7,12-tetraen-6-yl]ethyl acetate)