NP-MRD: Showing NP-Card for 18-benzyl-8,20-dihydroxy-6,8,15,16-tetramethyl-2,14-dioxa-19-azatetracyclo[10.8.0.0¹,¹⁷.0¹³,¹⁵]icosa-10,19-diene-3,7-dione (NP0227674)

Jump To Section:

Identification Spectra BioTaxonomy ChemoTaxonomy Physical properties Links References XML

Record Information

Version

2.0

Created at

2022-09-06 07:04:32 UTC

Updated at

2022-09-06 07:04:32 UTC

NP-MRD ID

NP0227674

Secondary Accession Numbers

None

Natural Product Identification

Common Name

18-benzyl-8,20-dihydroxy-6,8,15,16-tetramethyl-2,14-dioxa-19-azatetracyclo[10.8.0.0¹,¹⁷.0¹³,¹⁵]icosa-10,19-diene-3,7-dione

Description

18-Benzyl-8,20-dihydroxy-6,8,15,16-tetramethyl-2,14-dioxa-19-azatetracyclo[10.8.0.0¹,¹⁷.0¹³,¹⁵]Icosa-10,19-diene-3,7-dione belongs to the class of organic compounds known as macrolide lactams. These are cyclic polyketides containing both a cyclic amide and a cyclic ester group. Based on a literature review very few articles have been published on 18-benzyl-8,20-dihydroxy-6,8,15,16-tetramethyl-2,14-dioxa-19-azatetracyclo[10.8.0.0¹,¹⁷.0¹³,¹⁵]Icosa-10,19-diene-3,7-dione.

Structure

MOL 3D MOL SDF PDB SMILES InChI


  Mrv1652309062209042D          

 35 39  0  0  0  0            999 V2000
    1.4341    0.0027    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.6121    0.0732    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.2622    0.8203    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7343    1.4969    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.5563    1.4264    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.0283    2.1030    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.9266    0.5644    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.7282    0.6088    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.9388    0.8486    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.2808    0.3510    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.9230    1.6735    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    2.7026    1.9434    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.9425    2.7327    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.3789    3.3352    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.5753    3.1482    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.0117    3.7507    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.2516    4.5400    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.0551    4.7269    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.6188    4.1245    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.2002    1.2853    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.0222    1.2148    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.4943    1.8914    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.3721    0.4677    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.1192    0.8176    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.7220   -0.2794    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.9001   -0.2089    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.0781   -0.1384    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.6060   -0.8150    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.7840   -0.7444    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.3119   -1.4210    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.4900   -1.3505    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.5632   -2.1722    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3066   -1.5653    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.1401   -0.6034    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6819   -0.5328    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0  0  0  0
  2  3  1  0  0  0  0
  3  4  1  0  0  0  0
  4  5  1  0  0  0  0
  5  6  2  0  0  0  0
  5  7  1  0  0  0  0
  7  8  1  0  0  0  0
  8  9  1  0  0  0  0
  9 10  1  0  0  0  0
  9 11  2  0  0  0  0
 11 12  1  0  0  0  0
 12 13  1  0  0  0  0
 13 14  1  0  0  0  0
 14 15  2  0  0  0  0
 15 16  1  0  0  0  0
 16 17  2  0  0  0  0
 17 18  1  0  0  0  0
 18 19  2  0  0  0  0
 14 19  1  0  0  0  0
 12 20  1  0  0  0  0
  8 20  1  0  0  0  0
 20 21  1  0  0  0  0
 21 22  1  0  0  0  0
 21 23  1  0  0  0  0
 23 24  1  0  0  0  0
 23 25  1  0  0  0  0
 25 26  1  0  0  0  0
 23 26  1  0  0  0  0
 26 27  1  0  0  0  0
  8 27  1  0  0  0  0
 28 27  1  4  0  0  0
 28 29  2  0  0  0  0
 29 30  1  0  0  0  0
 30 31  1  0  0  0  0
 31 32  1  0  0  0  0
 31 33  1  0  0  0  0
 31 34  1  0  0  0  0
  2 34  1  0  0  0  0
 34 35  2  0  0  0  0
M  END

     RDKit          3D

 70 74  0  0  0  0  0  0  0  0999 V2000
   -4.9638    2.2507    1.8674 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.6663    1.7859    1.1713 C   0  0  1  0  0  0  0  0  0  0  0  0
   -2.6722    1.4923    2.2519 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2704    2.0180    1.9562 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2256    0.9846    2.1811 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3402    0.4135    3.3301 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.7693    0.5977    1.3747 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.8194    0.0073    0.1044 C   0  0  1  0  0  0  0  0  0  0  0  0
    1.4179    1.0294   -0.8025 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.0233    2.3500   -0.9637 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.4018    0.5375   -1.4668 N   0  0  0  0  0  0  0  0  0  0  0  0
    2.6261   -0.8691   -1.1255 C   0  0  1  0  0  0  0  0  0  0  0  0
    4.1070   -1.0225   -0.9701 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.7074   -0.1101    0.0460 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.0812    1.1811   -0.3447 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.6472    2.0432    0.5516 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.8498    1.6314    1.8532 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.4927    0.3671    2.2679 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.9277   -0.4797    1.3532 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.8038   -1.1207    0.0778 C   0  0  2  0  0  0  0  0  0  0  0  0
    1.2254   -2.4969    0.2059 C   0  0  2  0  0  0  0  0  0  0  0  0
    2.2015   -3.5491   -0.3231 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0986   -2.7018   -0.4068 C   0  0  1  0  0  0  0  0  0  0  0  0
   -0.2550   -3.1348   -1.8019 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3293   -2.8351    0.1657 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9240   -1.6169    0.2909 C   0  0  2  0  0  0  0  0  0  0  0  0
   -0.5788   -0.3934   -0.3954 C   0  0  2  0  0  0  0  0  0  0  0  0
   -0.7344   -0.2712   -1.8391 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7143    0.4365   -2.4228 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7600    1.1839   -1.6947 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.8274    0.3694   -1.0594 C   0  0  1  0  0  0  0  0  0  0  0  0
   -5.1463    0.7620   -1.7468 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.6763   -1.0039   -1.3245 O   0  0  0  0  0  0  0  0  0  0  0  0
   -4.0500    0.6205    0.3768 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.6434   -0.2822    0.9878 O   0  0  0  0  0  0  0  0  0  0  0  0
   -5.4645    1.3194    2.1985 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.7317    2.8873    2.7331 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.5586    2.7584    1.0924 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.3212    2.6661    0.6275 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.0604    1.8006    3.2206 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6001    0.3648    2.3063 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1842    2.5769    1.0317 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1076    2.7985    2.7703 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.0195    3.0270   -0.2066 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.3000   -1.4149   -2.0338 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.4051   -2.0564   -0.6927 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.5940   -0.7318   -1.9475 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.9197    1.5064   -1.3779 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.9525    3.0649    0.2776 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.2977    2.3148    2.5610 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.6362    0.0103    3.2784 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.6517   -1.4760    1.6607 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.4674   -0.9733    0.9700 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.1274   -2.7346    1.3043 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.5173   -3.3617   -1.3451 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.0328   -3.6883    0.3905 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.6282   -4.5175   -0.3179 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4186   -4.2640   -1.7525 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2057   -2.8171   -2.3176 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.6326   -3.0699   -2.4596 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7286   -1.4778    1.4132 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2134    0.4138    0.0442 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0107   -0.7762   -2.4746 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7250    0.4490   -3.5025 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3384    1.8311   -0.8929 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.2166    1.9011   -2.4078 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.1987    1.8893   -1.6956 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.0164    0.3574   -1.2334 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.1102    0.5299   -2.8317 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.1968   -1.2825   -2.1165 H   0  0  0  0  0  0  0  0  0  0  0  0
 22 21  1  0
 21 20  1  0
 20 12  1  0
 12 13  1  0
 13 14  1  0
 14 15  2  0
 15 16  1  0
 16 17  2  0
 17 18  1  0
 18 19  2  0
 12 11  1  0
 11  9  2  0
  9 10  1  0
  9  8  1  0
  8  7  1  1
  7  5  1  0
  5  6  2  0
  5  4  1  0
  4  3  1  0
  3  2  1  0
  2  1  1  0
  2 34  1  0
 34 35  2  0
 34 31  1  0
 31 32  1  0
 31 33  1  1
 31 30  1  0
 30 29  1  0
 29 28  2  0
 28 27  1  0
 27 26  1  0
 26 25  1  0
 25 23  1  0
 23 24  1  6
 23 21  1  0
  8 20  1  0
 27  8  1  0
 23 26  1  0
 19 14  1  0
 22 55  1  0
 22 56  1  0
 22 57  1  0
 21 54  1  1
 20 53  1  1
 12 45  1  6
 13 46  1  0
 13 47  1  0
 15 48  1  0
 16 49  1  0
 17 50  1  0
 18 51  1  0
 19 52  1  0
 10 44  1  0
  4 42  1  0
  4 43  1  0
  3 40  1  0
  3 41  1  0
  2 39  1  6
  1 36  1  0
  1 37  1  0
  1 38  1  0
 32 67  1  0
 32 68  1  0
 32 69  1  0
 33 70  1  0
 30 65  1  0
 30 66  1  0
 29 64  1  0
 28 63  1  0
 27 62  1  1
 26 61  1  1
 24 58  1  0
 24 59  1  0
 24 60  1  0
M  END


  Mrv1652309062209042D          

 35 39  0  0  0  0            999 V2000
    1.4341    0.0027    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.6121    0.0732    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.2622    0.8203    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7343    1.4969    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.5563    1.4264    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.0283    2.1030    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.9266    0.5644    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.7282    0.6088    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.9388    0.8486    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.2808    0.3510    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.9230    1.6735    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    2.7026    1.9434    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.9425    2.7327    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.3789    3.3352    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.5753    3.1482    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.0117    3.7507    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.2516    4.5400    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.0551    4.7269    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.6188    4.1245    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.2002    1.2853    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.0222    1.2148    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.4943    1.8914    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.3721    0.4677    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.1192    0.8176    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.7220   -0.2794    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.9001   -0.2089    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.0781   -0.1384    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.6060   -0.8150    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.7840   -0.7444    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.3119   -1.4210    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.4900   -1.3505    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.5632   -2.1722    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3066   -1.5653    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.1401   -0.6034    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6819   -0.5328    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0  0  0  0
  2  3  1  0  0  0  0
  3  4  1  0  0  0  0
  4  5  1  0  0  0  0
  5  6  2  0  0  0  0
  5  7  1  0  0  0  0
  7  8  1  0  0  0  0
  8  9  1  0  0  0  0
  9 10  1  0  0  0  0
  9 11  2  0  0  0  0
 11 12  1  0  0  0  0
 12 13  1  0  0  0  0
 13 14  1  0  0  0  0
 14 15  2  0  0  0  0
 15 16  1  0  0  0  0
 16 17  2  0  0  0  0
 17 18  1  0  0  0  0
 18 19  2  0  0  0  0
 14 19  1  0  0  0  0
 12 20  1  0  0  0  0
  8 20  1  0  0  0  0
 20 21  1  0  0  0  0
 21 22  1  0  0  0  0
 21 23  1  0  0  0  0
 23 24  1  0  0  0  0
 23 25  1  0  0  0  0
 25 26  1  0  0  0  0
 23 26  1  0  0  0  0
 26 27  1  0  0  0  0
  8 27  1  0  0  0  0
 28 27  1  4  0  0  0
 28 29  2  0  0  0  0
 29 30  1  0  0  0  0
 30 31  1  0  0  0  0
 31 32  1  0  0  0  0
 31 33  1  0  0  0  0
 31 34  1  0  0  0  0
  2 34  1  0  0  0  0
 34 35  2  0  0  0  0
M  END
> <DATABASE_ID>
NP0227674

> <DATABASE_NAME>
NP-MRD

> <SMILES>
CC1C2C(CC3=CC=CC=C3)N=C(O)C22OC(=O)CCC(C)C(=O)C(C)(O)CC=CC2C2OC12C

> <INCHI_IDENTIFIER>
InChI=1S/C28H35NO6/c1-16-12-13-21(30)34-28-19(11-8-14-26(3,33)23(16)31)24-27(4,35-24)17(2)22(28)20(29-25(28)32)15-18-9-6-5-7-10-18/h5-11,16-17,19-20,22,24,33H,12-15H2,1-4H3,(H,29,32)

> <INCHI_KEY>
FMJRYCBPDIIEAZ-UHFFFAOYSA-N

> <FORMULA>
C28H35NO6

> <MOLECULAR_WEIGHT>
481.589

> <EXACT_MASS>
481.246437851

> <JCHEM_ACCEPTOR_COUNT>
6

> <JCHEM_ATOM_COUNT>
70

> <JCHEM_AVERAGE_POLARIZABILITY>
52.56655308405847

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
2

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
0

> <JCHEM_IUPAC>
18-benzyl-8,20-dihydroxy-6,8,15,16-tetramethyl-2,14-dioxa-19-azatetracyclo[10.8.0.0^{1,17}.0^{13,15}]icosa-10,19-diene-3,7-dione

> <JCHEM_LOGP>
2.64911061063532

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
5

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA>
13.202383561341392

> <JCHEM_PKA_STRONGEST_ACIDIC>
1.8081646481999405

> <JCHEM_PKA_STRONGEST_BASIC>
4.678926927966006

> <JCHEM_POLAR_SURFACE_AREA>
108.72

> <JCHEM_REFRACTIVITY>
130.24120000000005

> <JCHEM_ROTATABLE_BOND_COUNT>
2

> <JCHEM_RULE_OF_FIVE>
1

> <JCHEM_TRADITIONAL_IUPAC>
18-benzyl-8,20-dihydroxy-6,8,15,16-tetramethyl-2,14-dioxa-19-azatetracyclo[10.8.0.0^{1,17}.0^{13,15}]icosa-10,19-diene-3,7-dione

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 06-SEP-22   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   06-SEP-22         0                                  
HETATM    1  C   UNK     0       2.677   0.005   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0       1.143   0.137   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0       0.489   1.531   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0       1.371   2.794   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0       2.905   2.663   0.000  0.00  0.00           C+0
HETATM    6  O   UNK     0       3.786   3.926   0.000  0.00  0.00           O+0
HETATM    7  O   UNK     0       3.596   1.054   0.000  0.00  0.00           O+0
HETATM    8  C   UNK     0       5.093   1.136   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0       3.619   1.584   0.000  0.00  0.00           C+0
HETATM   10  O   UNK     0       2.391   0.655   0.000  0.00  0.00           O+0
HETATM   11  N   UNK     0       3.590   3.124   0.000  0.00  0.00           N+0
HETATM   12  C   UNK     0       5.045   3.628   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0       5.493   5.101   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0       4.441   6.226   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0       2.941   5.877   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0       1.888   7.001   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0       2.336   8.475   0.000  0.00  0.00           C+0
HETATM   18  C   UNK     0       3.836   8.824   0.000  0.00  0.00           C+0
HETATM   19  C   UNK     0       4.888   7.699   0.000  0.00  0.00           C+0
HETATM   20  C   UNK     0       5.974   2.399   0.000  0.00  0.00           C+0
HETATM   21  C   UNK     0       7.508   2.268   0.000  0.00  0.00           C+0
HETATM   22  C   UNK     0       8.389   3.531   0.000  0.00  0.00           C+0
HETATM   23  C   UNK     0       8.161   0.873   0.000  0.00  0.00           C+0
HETATM   24  C   UNK     0       9.556   1.526   0.000  0.00  0.00           C+0
HETATM   25  O   UNK     0       8.814  -0.522   0.000  0.00  0.00           O+0
HETATM   26  C   UNK     0       7.280  -0.390   0.000  0.00  0.00           C+0
HETATM   27  C   UNK     0       5.746  -0.258   0.000  0.00  0.00           C+0
HETATM   28  C   UNK     0       4.865  -1.521   0.000  0.00  0.00           C+0
HETATM   29  C   UNK     0       3.330  -1.390   0.000  0.00  0.00           C+0
HETATM   30  C   UNK     0       2.449  -2.653   0.000  0.00  0.00           C+0
HETATM   31  C   UNK     0       0.915  -2.521   0.000  0.00  0.00           C+0
HETATM   32  C   UNK     0       1.051  -4.055   0.000  0.00  0.00           C+0
HETATM   33  O   UNK     0      -0.572  -2.922   0.000  0.00  0.00           O+0
HETATM   34  C   UNK     0       0.261  -1.126   0.000  0.00  0.00           C+0
HETATM   35  O   UNK     0      -1.273  -0.995   0.000  0.00  0.00           O+0
CONECT    1    2                                                            
CONECT    2    1    3   34                                                  
CONECT    3    2    4                                                       
CONECT    4    3    5                                                       
CONECT    5    4    6    7                                                  
CONECT    6    5                                                            
CONECT    7    5    8                                                       
CONECT    8    7    9   20   27                                             
CONECT    9    8   10   11                                                  
CONECT   10    9                                                            
CONECT   11    9   12                                                       
CONECT   12   11   13   20                                                  
CONECT   13   12   14                                                       
CONECT   14   13   15   19                                                  
CONECT   15   14   16                                                       
CONECT   16   15   17                                                       
CONECT   17   16   18                                                       
CONECT   18   17   19                                                       
CONECT   19   18   14                                                       
CONECT   20   12    8   21                                                  
CONECT   21   20   22   23                                                  
CONECT   22   21                                                            
CONECT   23   21   24   25   26                                             
CONECT   24   23                                                            
CONECT   25   23   26                                                       
CONECT   26   25   23   27                                                  
CONECT   27   26    8   28                                                  
CONECT   28   27   29                                                       
CONECT   29   28   30                                                       
CONECT   30   29   31                                                       
CONECT   31   30   32   33   34                                             
CONECT   32   31                                                            
CONECT   33   31                                                            
CONECT   34   31    2   35                                                  
CONECT   35   34                                                            
MASTER        0    0    0    0    0    0    0    0   35    0   78    0
END

View in JSmol

Synonyms

Not Available

Chemical Formula

C₂₈H₃₅NO₆

Average Mass

481.5890 Da

Monoisotopic Mass

481.24644 Da

IUPAC Name

18-benzyl-8,20-dihydroxy-6,8,15,16-tetramethyl-2,14-dioxa-19-azatetracyclo[10.8.0.0^{1,17}.0^{13,15}]icosa-10,19-diene-3,7-dione

Traditional Name

18-benzyl-8,20-dihydroxy-6,8,15,16-tetramethyl-2,14-dioxa-19-azatetracyclo[10.8.0.0^{1,17}.0^{13,15}]icosa-10,19-diene-3,7-dione

CAS Registry Number

Not Available

SMILES

CC1C2C(CC3=CC=CC=C3)N=C(O)C22OC(=O)CCC(C)C(=O)C(C)(O)CC=CC2C2OC12C

InChI Identifier

InChI=1S/C28H35NO6/c1-16-12-13-21(30)34-28-19(11-8-14-26(3,33)23(16)31)24-27(4,35-24)17(2)22(28)20(29-25(28)32)15-18-9-6-5-7-10-18/h5-11,16-17,19-20,22,24,33H,12-15H2,1-4H3,(H,29,32)

InChI Key

FMJRYCBPDIIEAZ-UHFFFAOYSA-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 macrolide lactams. These are cyclic polyketides containing both a cyclic amide and a cyclic ester group.

Kingdom

Organic compounds

Super Class

Phenylpropanoids and polyketides

Class

Macrolide lactams

Sub Class

Not Available

Direct Parent

Macrolide lactams

Alternative Parents

Substituents

Macrolide lactam
Macrolactam
Macrolide
Isoindolone
Isoindoline
Isoindole or derivatives
Oxepane
Acyloin
Monocyclic benzene moiety
Benzenoid
Pyrrolidone
2-pyrrolidone
Pyrrolidine
Tertiary alcohol
Secondary carboxylic acid amide
Cyclic ketone
Carboxamide group
Carboxylic acid ester
Ketone
Lactam
Lactone
Carboxylic acid derivative
Dialkyl ether
Oxirane
Ether
Monocarboxylic acid or derivatives
Organoheterocyclic compound
Azacycle
Oxacycle
Alcohol
Organic oxygen compound
Organopnictogen compound
Organic oxide
Hydrocarbon derivative
Carbonyl group
Organooxygen compound
Organic nitrogen compound
Organonitrogen compound
Aromatic heteropolycyclic compound

Molecular Framework

Aromatic 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	2.65	ChemAxon
pKa (Strongest Acidic)	1.81	ChemAxon
pKa (Strongest Basic)	4.68	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	6	ChemAxon
Hydrogen Donor Count	2	ChemAxon
Polar Surface Area	108.72 Å²	ChemAxon
Rotatable Bond Count	2	ChemAxon
Refractivity	130.24 m³·mol⁻¹	ChemAxon
Polarizability	52.57 Å³	ChemAxon
Number of Rings	5	ChemAxon
Bioavailability	Yes	ChemAxon
Rule of Five	Yes	ChemAxon
Ghose Filter	No	ChemAxon
Veber's Rule	No	ChemAxon
MDDR-like Rule	No	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

73814010

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

LOTUS database [Link]

Showing NP-Card for 18-benzyl-8,20-dihydroxy-6,8,15,16-tetramethyl-2,14-dioxa-19-azatetracyclo[10.8.0.0¹,¹⁷.0¹³,¹⁵]icosa-10,19-diene-3,7-dione (NP0227674)

MOL for NP0227674 (18-benzyl-8,20-dihydroxy-6,8,15,16-tetramethyl-2,14-dioxa-19-azatetracyclo[10.8.0.0¹,¹⁷.0¹³,¹⁵]icosa-10,19-diene-3,7-dione)

3D MOL for NP0227674 (18-benzyl-8,20-dihydroxy-6,8,15,16-tetramethyl-2,14-dioxa-19-azatetracyclo[10.8.0.0¹,¹⁷.0¹³,¹⁵]icosa-10,19-diene-3,7-dione)

3D SDF for NP0227674 (18-benzyl-8,20-dihydroxy-6,8,15,16-tetramethyl-2,14-dioxa-19-azatetracyclo[10.8.0.0¹,¹⁷.0¹³,¹⁵]icosa-10,19-diene-3,7-dione)

3D-SDF for NP0227674 (18-benzyl-8,20-dihydroxy-6,8,15,16-tetramethyl-2,14-dioxa-19-azatetracyclo[10.8.0.0¹,¹⁷.0¹³,¹⁵]icosa-10,19-diene-3,7-dione)

PDB for NP0227674 (18-benzyl-8,20-dihydroxy-6,8,15,16-tetramethyl-2,14-dioxa-19-azatetracyclo[10.8.0.0¹,¹⁷.0¹³,¹⁵]icosa-10,19-diene-3,7-dione)

3D PDB for NP0227674 (18-benzyl-8,20-dihydroxy-6,8,15,16-tetramethyl-2,14-dioxa-19-azatetracyclo[10.8.0.0¹,¹⁷.0¹³,¹⁵]icosa-10,19-diene-3,7-dione)

SMILES for NP0227674 (18-benzyl-8,20-dihydroxy-6,8,15,16-tetramethyl-2,14-dioxa-19-azatetracyclo[10.8.0.0¹,¹⁷.0¹³,¹⁵]icosa-10,19-diene-3,7-dione)

INCHI for NP0227674 (18-benzyl-8,20-dihydroxy-6,8,15,16-tetramethyl-2,14-dioxa-19-azatetracyclo[10.8.0.0¹,¹⁷.0¹³,¹⁵]icosa-10,19-diene-3,7-dione)

Structure for NP0227674 (18-benzyl-8,20-dihydroxy-6,8,15,16-tetramethyl-2,14-dioxa-19-azatetracyclo[10.8.0.0¹,¹⁷.0¹³,¹⁵]icosa-10,19-diene-3,7-dione)

3D Structure for NP0227674 (18-benzyl-8,20-dihydroxy-6,8,15,16-tetramethyl-2,14-dioxa-19-azatetracyclo[10.8.0.0¹,¹⁷.0¹³,¹⁵]icosa-10,19-diene-3,7-dione)