NP-MRD: Showing NP-Card for 7-(1,2-dihydroxypropan-2-yl)-11-hydroxy-1,2-dimethyl-6-oxa-23-azahexacyclo[12.10.0.0²,¹¹.0⁵,¹⁰.0¹⁶,²⁴.0¹⁷,²²]tetracosa-9,16(24),17,19,21-pentaen-8-one (NP0280528)

Jump To Section:

Identification Spectra BioTaxonomy ChemoTaxonomy Physical properties Links References XML

Record Information

Version

2.0

Created at

2022-09-09 06:22:15 UTC

Updated at

2022-09-09 06:22:16 UTC

NP-MRD ID

NP0280528

Secondary Accession Numbers

None

Natural Product Identification

Common Name

7-(1,2-dihydroxypropan-2-yl)-11-hydroxy-1,2-dimethyl-6-oxa-23-azahexacyclo[12.10.0.0²,¹¹.0⁵,¹⁰.0¹⁶,²⁴.0¹⁷,²²]tetracosa-9,16(24),17,19,21-pentaen-8-one

Description

7-(1,2-Dihydroxypropan-2-yl)-11-hydroxy-1,2-dimethyl-6-oxa-23-azahexacyclo[12.10.0.0²,¹¹.0⁵,¹⁰.0¹⁶,²⁴.0¹⁷,²²]Tetracosa-9,16(24),17,19,21-pentaen-8-one belongs to the class of organic compounds known as naphthopyrans. Naphthopyrans are compounds containing a pyran ring fused to a naphthalene moiety. Furan is a 6 membered-ring non-aromatic ring with five carbon and one oxygen atoms. Naphthalene is a polycyclic aromatic hydrocarbon made up of two fused benzene rings. Based on a literature review very few articles have been published on 7-(1,2-dihydroxypropan-2-yl)-11-hydroxy-1,2-dimethyl-6-oxa-23-azahexacyclo[12.10.0.0²,¹¹.0⁵,¹⁰.0¹⁶,²⁴.0¹⁷,²²]Tetracosa-9,16(24),17,19,21-pentaen-8-one.

Structure

MOL 3D MOL SDF PDB SMILES InChI


  Mrv1652309092208222D          

 33 38  0  0  0  0            999 V2000
    1.1908   -4.8209    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.5292   -4.0685    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.8676   -3.3161    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.7768   -3.7301    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.1076   -4.2125    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.2816   -4.4069    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.9509   -3.9244    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.7033   -4.2628    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.3725   -3.7804    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.1250   -4.1188    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.2081   -4.9396    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.8774   -4.4572    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.5389   -5.4220    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.8696   -5.9044    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.6220   -6.2428    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.3744   -6.5812    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.0437   -6.0988    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.8500   -6.2733    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.2652   -5.5604    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.7155   -4.9452    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.1306   -4.2323    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    7.9370   -4.4069    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.6062   -3.9244    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    9.3586   -4.2628    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    9.4418   -5.0836    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.7725   -5.5660    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.0201   -5.2277    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.9605   -5.2780    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.2184   -4.4943    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.7865   -5.0836    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.1172   -5.5660    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.3648   -5.2277    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.6955   -5.7101    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
  2  4  1  0  0  0  0
  4  5  1  0  0  0  0
  2  6  1  0  0  0  0
  6  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
 10 11  1  0  0  0  0
 11 12  1  0  0  0  0
 11 13  1  0  0  0  0
 13 14  1  0  0  0  0
 13 15  1  0  0  0  0
 15 16  1  0  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  2  0  0  0  0
 20 21  1  0  0  0  0
 21 22  1  0  0  0  0
 22 23  2  0  0  0  0
 23 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
 19 27  1  0  0  0  0
 22 27  1  0  0  0  0
 20 28  1  0  0  0  0
 17 28  1  0  0  0  0
 11 28  1  0  0  0  0
 28 29  1  0  0  0  0
 13 30  1  0  0  0  0
  8 30  1  0  0  0  0
 30 31  2  0  0  0  0
 31 32  1  0  0  0  0
  6 32  1  0  0  0  0
 32 33  2  0  0  0  0
M  END

     RDKit          3D

 66 71  0  0  0  0  0  0  0  0999 V2000
    4.6281    1.4198    1.9897 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.2660    0.4333    1.0703 C   0  0  2  0  0  0  0  0  0  0  0  0
    6.0095   -0.4716    1.8466 O   0  0  0  0  0  0  0  0  0  0  0  0
    6.1862    1.1911    0.1370 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.8514    0.3131   -0.7175 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.2922   -0.3438    0.2184 C   0  0  2  0  0  0  0  0  0  0  0  0
    3.5281    0.4598   -0.5702 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.2075    0.5514   -0.1475 C   0  0  1  0  0  0  0  0  0  0  0  0
    1.4411    1.5860   -0.9023 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0278    1.3737   -0.5937 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4605    0.1089   -1.2576 C   0  0  1  0  0  0  0  0  0  0  0  0
    0.1013    0.1310   -2.6755 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.1822   -1.0852   -0.5860 C   0  0  2  0  0  0  0  0  0  0  0  0
    0.2848   -2.1519   -1.5140 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6828   -1.6239    0.5337 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0145   -2.1201    0.0083 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3502   -1.4977   -1.3321 C   0  0  1  0  0  0  0  0  0  0  0  0
   -3.8770   -1.2946   -1.2751 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.9142   -0.2058   -0.2400 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7441    0.5470   -0.3117 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8314    1.5000    0.6384 N   0  0  0  0  0  0  0  0  0  0  0  0
   -3.9907    1.3588    1.2753 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.5793    2.0672    2.3291 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.8171    1.7134    2.8192 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.5163    0.6509    2.2883 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.9690   -0.0594    1.2601 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.7216    0.3033    0.7720 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9437   -0.0284   -1.3903 C   0  0  1  0  0  0  0  0  0  0  0  0
   -2.4429    0.5201   -2.7117 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.5111   -0.7534   -0.0893 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.2138   -1.7218    0.4964 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5357   -1.3573    0.9817 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.0133   -1.8749    1.9957 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.8794    0.9855    2.6810 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.1724    2.2664    1.4491 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.4636    1.8682    2.5961 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.8190   -0.0208    2.1671 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.8720    1.7893    0.7571 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.5434    1.8750   -0.4678 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.0611   -0.5518   -0.3059 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.9469   -0.9467   -0.4861 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.2606    0.9263    0.9186 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.6936    2.6229   -0.5299 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.6967    1.5619   -1.9594 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6247    2.2179   -0.9469 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0582    1.1958    0.5042 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5094   -0.5161   -3.3584 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.1083    1.1336   -3.1263 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.1109   -0.3463   -2.6902 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.1444   -2.6016   -1.3412 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7966   -0.8526    1.3217 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1753   -2.5227    0.9366 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0360   -3.2209   -0.1287 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7658   -1.8837    0.7900 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0360   -2.0784   -2.1936 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.2421   -0.9546   -2.2457 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.3881   -2.2047   -0.9273 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1533    2.2482    0.8866 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.0628    2.9107    2.7762 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.2617    2.2808    3.6455 H   0  0  0  0  0  0  0  0  0  0  0  0
   -7.4921    0.3578    2.6613 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.4421   -0.9089    0.7786 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5003    0.8976   -2.5608 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5180   -0.2568   -3.4993 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8744    1.4162   -3.0342 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.7952   -2.7010    0.5866 H   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0
  2  3  1  1
  2  4  1  0
  4  5  1  0
  2  6  1  0
  6  7  1  0
  7  8  1  0
  8  9  1  0
  9 10  1  0
 10 11  1  0
 11 12  1  6
 11 28  1  0
 28 29  1  6
 28 17  1  0
 17 18  1  0
 18 19  1  0
 19 20  2  0
 20 21  1  0
 21 22  1  0
 22 23  2  0
 23 24  1  0
 24 25  2  0
 25 26  1  0
 26 27  2  0
 17 16  1  0
 16 15  1  0
 15 13  1  0
 13 14  1  6
 13 30  1  0
 30 31  2  0
 31 32  1  0
 32 33  2  0
 32  6  1  0
 30  8  1  0
 13 11  1  0
 20 28  1  0
 27 22  1  0
 27 19  1  0
  1 34  1  0
  1 35  1  0
  1 36  1  0
  3 37  1  0
  4 38  1  0
  4 39  1  0
  5 40  1  0
  6 41  1  6
  8 42  1  1
  9 43  1  0
  9 44  1  0
 10 45  1  0
 10 46  1  0
 12 47  1  0
 12 48  1  0
 12 49  1  0
 29 63  1  0
 29 64  1  0
 29 65  1  0
 17 55  1  6
 18 56  1  0
 18 57  1  0
 21 58  1  0
 23 59  1  0
 24 60  1  0
 25 61  1  0
 26 62  1  0
 16 53  1  0
 16 54  1  0
 15 51  1  0
 15 52  1  0
 14 50  1  0
 31 66  1  0
M  END


  Mrv1652309092208222D          

 33 38  0  0  0  0            999 V2000
    1.1908   -4.8209    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.5292   -4.0685    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.8676   -3.3161    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.7768   -3.7301    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.1076   -4.2125    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.2816   -4.4069    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.9509   -3.9244    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.7033   -4.2628    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.3725   -3.7804    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.1250   -4.1188    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.2081   -4.9396    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.8774   -4.4572    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.5389   -5.4220    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.8696   -5.9044    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.6220   -6.2428    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.3744   -6.5812    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.0437   -6.0988    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.8500   -6.2733    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.2652   -5.5604    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.7155   -4.9452    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.1306   -4.2323    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    7.9370   -4.4069    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.6062   -3.9244    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    9.3586   -4.2628    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    9.4418   -5.0836    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.7725   -5.5660    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.0201   -5.2277    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.9605   -5.2780    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.2184   -4.4943    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.7865   -5.0836    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.1172   -5.5660    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.3648   -5.2277    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.6955   -5.7101    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
  2  4  1  0  0  0  0
  4  5  1  0  0  0  0
  2  6  1  0  0  0  0
  6  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
 10 11  1  0  0  0  0
 11 12  1  0  0  0  0
 11 13  1  0  0  0  0
 13 14  1  0  0  0  0
 13 15  1  0  0  0  0
 15 16  1  0  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  2  0  0  0  0
 20 21  1  0  0  0  0
 21 22  1  0  0  0  0
 22 23  2  0  0  0  0
 23 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
 19 27  1  0  0  0  0
 22 27  1  0  0  0  0
 20 28  1  0  0  0  0
 17 28  1  0  0  0  0
 11 28  1  0  0  0  0
 28 29  1  0  0  0  0
 13 30  1  0  0  0  0
  8 30  1  0  0  0  0
 30 31  2  0  0  0  0
 31 32  1  0  0  0  0
  6 32  1  0  0  0  0
 32 33  2  0  0  0  0
M  END
> <DATABASE_ID>
NP0280528

> <DATABASE_NAME>
NP-MRD

> <SMILES>
CC(O)(CO)C1OC2CCC3(C)C4(C)C(CC5=C4NC4=CC=CC=C54)CCC3(O)C2=CC1=O

> <INCHI_IDENTIFIER>
InChI=1S/C27H33NO5/c1-24(31,14-29)23-20(30)13-18-21(33-23)9-10-25(2)26(3)15(8-11-27(18,25)32)12-17-16-6-4-5-7-19(16)28-22(17)26/h4-7,13,15,21,23,28-29,31-32H,8-12,14H2,1-3H3

> <INCHI_KEY>
YCXQGKDLXRHABX-UHFFFAOYSA-N

> <FORMULA>
C27H33NO5

> <MOLECULAR_WEIGHT>
451.563

> <EXACT_MASS>
451.235873167

> <JCHEM_ACCEPTOR_COUNT>
5

> <JCHEM_ATOM_COUNT>
66

> <JCHEM_AVERAGE_POLARIZABILITY>
50.72834059332254

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
4

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
1

> <JCHEM_IUPAC>
7-(1,2-dihydroxypropan-2-yl)-11-hydroxy-1,2-dimethyl-6-oxa-23-azahexacyclo[12.10.0.0^{2,11}.0^{5,10}.0^{16,24}.0^{17,22}]tetracosa-9,16(24),17,19,21-pentaen-8-one

> <JCHEM_LOGP>
2.576173294

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
6

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA>
13.774304959076591

> <JCHEM_PKA_STRONGEST_ACIDIC>
12.986006224221406

> <JCHEM_PKA_STRONGEST_BASIC>
-3.1108100720351812

> <JCHEM_POLAR_SURFACE_AREA>
102.78

> <JCHEM_REFRACTIVITY>
124.76020000000001

> <JCHEM_ROTATABLE_BOND_COUNT>
2

> <JCHEM_RULE_OF_FIVE>
1

> <JCHEM_TRADITIONAL_IUPAC>
7-(1,2-dihydroxypropan-2-yl)-11-hydroxy-1,2-dimethyl-6-oxa-23-azahexacyclo[12.10.0.0^{2,11}.0^{5,10}.0^{16,24}.0^{17,22}]tetracosa-9,16(24),17,19,21-pentaen-8-one

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 09-SEP-22   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   09-SEP-22         0                                  
HETATM    1  C   UNK     0       2.223  -8.999   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0       2.855  -7.594   0.000  0.00  0.00           C+0
HETATM    3  O   UNK     0       3.486  -6.190   0.000  0.00  0.00           O+0
HETATM    4  C   UNK     0       1.450  -6.963   0.000  0.00  0.00           C+0
HETATM    5  O   UNK     0       0.201  -7.863   0.000  0.00  0.00           O+0
HETATM    6  C   UNK     0       4.259  -8.226   0.000  0.00  0.00           C+0
HETATM    7  O   UNK     0       5.508  -7.326   0.000  0.00  0.00           O+0
HETATM    8  C   UNK     0       6.913  -7.957   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0       8.162  -7.057   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0       9.567  -7.688   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0       9.722  -9.221   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0      10.971  -8.320   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0       8.473 -10.121   0.000  0.00  0.00           C+0
HETATM   14  O   UNK     0       7.223 -11.022   0.000  0.00  0.00           O+0
HETATM   15  C   UNK     0       8.628 -11.653   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0      10.032 -12.285   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0      11.282 -11.384   0.000  0.00  0.00           C+0
HETATM   18  C   UNK     0      12.787 -11.710   0.000  0.00  0.00           C+0
HETATM   19  C   UNK     0      13.562 -10.379   0.000  0.00  0.00           C+0
HETATM   20  C   UNK     0      12.536  -9.231   0.000  0.00  0.00           C+0
HETATM   21  N   UNK     0      13.311  -7.900   0.000  0.00  0.00           N+0
HETATM   22  C   UNK     0      14.816  -8.226   0.000  0.00  0.00           C+0
HETATM   23  C   UNK     0      16.065  -7.326   0.000  0.00  0.00           C+0
HETATM   24  C   UNK     0      17.469  -7.957   0.000  0.00  0.00           C+0
HETATM   25  C   UNK     0      17.625  -9.489   0.000  0.00  0.00           C+0
HETATM   26  C   UNK     0      16.375 -10.390   0.000  0.00  0.00           C+0
HETATM   27  C   UNK     0      14.971  -9.758   0.000  0.00  0.00           C+0
HETATM   28  C   UNK     0      11.126  -9.852   0.000  0.00  0.00           C+0
HETATM   29  C   UNK     0      11.608  -8.389   0.000  0.00  0.00           C+0
HETATM   30  C   UNK     0       7.068  -9.489   0.000  0.00  0.00           C+0
HETATM   31  C   UNK     0       5.819 -10.390   0.000  0.00  0.00           C+0
HETATM   32  C   UNK     0       4.414  -9.758   0.000  0.00  0.00           C+0
HETATM   33  O   UNK     0       3.165 -10.659   0.000  0.00  0.00           O+0
CONECT    1    2                                                            
CONECT    2    1    3    4    6                                             
CONECT    3    2                                                            
CONECT    4    2    5                                                       
CONECT    5    4                                                            
CONECT    6    2    7   32                                                  
CONECT    7    6    8                                                       
CONECT    8    7    9   30                                                  
CONECT    9    8   10                                                       
CONECT   10    9   11                                                       
CONECT   11   10   12   13   28                                             
CONECT   12   11                                                            
CONECT   13   11   14   15   30                                             
CONECT   14   13                                                            
CONECT   15   13   16                                                       
CONECT   16   15   17                                                       
CONECT   17   16   18   28                                                  
CONECT   18   17   19                                                       
CONECT   19   18   20   27                                                  
CONECT   20   19   21   28                                                  
CONECT   21   20   22                                                       
CONECT   22   21   23   27                                                  
CONECT   23   22   24                                                       
CONECT   24   23   25                                                       
CONECT   25   24   26                                                       
CONECT   26   25   27                                                       
CONECT   27   26   19   22                                                  
CONECT   28   20   17   11   29                                             
CONECT   29   28                                                            
CONECT   30   13    8   31                                                  
CONECT   31   30   32                                                       
CONECT   32   31    6   33                                                  
CONECT   33   32                                                            
MASTER        0    0    0    0    0    0    0    0   33    0   76    0
END

View in JSmol

Synonyms

Not Available

Chemical Formula

C₂₇H₃₃NO₅

Average Mass

451.5630 Da

Monoisotopic Mass

451.23587 Da

IUPAC Name

7-(1,2-dihydroxypropan-2-yl)-11-hydroxy-1,2-dimethyl-6-oxa-23-azahexacyclo[12.10.0.0^{2,11}.0^{5,10}.0^{16,24}.0^{17,22}]tetracosa-9,16(24),17,19,21-pentaen-8-one

Traditional Name

7-(1,2-dihydroxypropan-2-yl)-11-hydroxy-1,2-dimethyl-6-oxa-23-azahexacyclo[12.10.0.0^{2,11}.0^{5,10}.0^{16,24}.0^{17,22}]tetracosa-9,16(24),17,19,21-pentaen-8-one

CAS Registry Number

Not Available

SMILES

CC(O)(CO)C1OC2CCC3(C)C4(C)C(CC5=C4NC4=CC=CC=C54)CCC3(O)C2=CC1=O

InChI Identifier

InChI=1S/C27H33NO5/c1-24(31,14-29)23-20(30)13-18-21(33-23)9-10-25(2)26(3)15(8-11-27(18,25)32)12-17-16-6-4-5-7-19(16)28-22(17)26/h4-7,13,15,21,23,28-29,31-32H,8-12,14H2,1-3H3

InChI Key

YCXQGKDLXRHABX-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 naphthopyrans. Naphthopyrans are compounds containing a pyran ring fused to a naphthalene moiety. Furan is a 6 membered-ring non-aromatic ring with five carbon and one oxygen atoms. Naphthalene is a polycyclic aromatic hydrocarbon made up of two fused benzene rings.

Kingdom

Organic compounds

Super Class

Organoheterocyclic compounds

Class

Naphthopyrans

Sub Class

Not Available

Direct Parent

Naphthopyrans

Alternative Parents

Substituents

Naphthopyran
Naphthalene
3-alkylindole
Indole
Indole or derivatives
Dihydropyranone
Benzenoid
Pyran
Cyclic alcohol
Heteroaromatic compound
Tertiary alcohol
Pyrrole
Ketone
Cyclic ketone
Dialkyl ether
Ether
Oxacycle
Azacycle
Carbonyl group
Hydrocarbon derivative
Organic oxide
Organopnictogen compound
Organic oxygen compound
Alcohol
Organic nitrogen compound
Organonitrogen compound
Organooxygen compound
Primary alcohol
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	2.58	ChemAxon
pKa (Strongest Acidic)	12.99	ChemAxon
pKa (Strongest Basic)	-3.1	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	5	ChemAxon
Hydrogen Donor Count	4	ChemAxon
Polar Surface Area	102.78 Å²	ChemAxon
Rotatable Bond Count	2	ChemAxon
Refractivity	124.76 m³·mol⁻¹	ChemAxon
Polarizability	50.73 Å³	ChemAxon
Number of Rings	6	ChemAxon
Bioavailability	Yes	ChemAxon
Rule of Five	Yes	ChemAxon
Ghose Filter	Yes	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

78167115

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

LOTUS database [Link]

Showing NP-Card for 7-(1,2-dihydroxypropan-2-yl)-11-hydroxy-1,2-dimethyl-6-oxa-23-azahexacyclo[12.10.0.0²,¹¹.0⁵,¹⁰.0¹⁶,²⁴.0¹⁷,²²]tetracosa-9,16(24),17,19,21-pentaen-8-one (NP0280528)

MOL for NP0280528 (7-(1,2-dihydroxypropan-2-yl)-11-hydroxy-1,2-dimethyl-6-oxa-23-azahexacyclo[12.10.0.0²,¹¹.0⁵,¹⁰.0¹⁶,²⁴.0¹⁷,²²]tetracosa-9,16(24),17,19,21-pentaen-8-one)

3D MOL for NP0280528 (7-(1,2-dihydroxypropan-2-yl)-11-hydroxy-1,2-dimethyl-6-oxa-23-azahexacyclo[12.10.0.0²,¹¹.0⁵,¹⁰.0¹⁶,²⁴.0¹⁷,²²]tetracosa-9,16(24),17,19,21-pentaen-8-one)

3D SDF for NP0280528 (7-(1,2-dihydroxypropan-2-yl)-11-hydroxy-1,2-dimethyl-6-oxa-23-azahexacyclo[12.10.0.0²,¹¹.0⁵,¹⁰.0¹⁶,²⁴.0¹⁷,²²]tetracosa-9,16(24),17,19,21-pentaen-8-one)

3D-SDF for NP0280528 (7-(1,2-dihydroxypropan-2-yl)-11-hydroxy-1,2-dimethyl-6-oxa-23-azahexacyclo[12.10.0.0²,¹¹.0⁵,¹⁰.0¹⁶,²⁴.0¹⁷,²²]tetracosa-9,16(24),17,19,21-pentaen-8-one)

PDB for NP0280528 (7-(1,2-dihydroxypropan-2-yl)-11-hydroxy-1,2-dimethyl-6-oxa-23-azahexacyclo[12.10.0.0²,¹¹.0⁵,¹⁰.0¹⁶,²⁴.0¹⁷,²²]tetracosa-9,16(24),17,19,21-pentaen-8-one)

3D PDB for NP0280528 (7-(1,2-dihydroxypropan-2-yl)-11-hydroxy-1,2-dimethyl-6-oxa-23-azahexacyclo[12.10.0.0²,¹¹.0⁵,¹⁰.0¹⁶,²⁴.0¹⁷,²²]tetracosa-9,16(24),17,19,21-pentaen-8-one)

SMILES for NP0280528 (7-(1,2-dihydroxypropan-2-yl)-11-hydroxy-1,2-dimethyl-6-oxa-23-azahexacyclo[12.10.0.0²,¹¹.0⁵,¹⁰.0¹⁶,²⁴.0¹⁷,²²]tetracosa-9,16(24),17,19,21-pentaen-8-one)

INCHI for NP0280528 (7-(1,2-dihydroxypropan-2-yl)-11-hydroxy-1,2-dimethyl-6-oxa-23-azahexacyclo[12.10.0.0²,¹¹.0⁵,¹⁰.0¹⁶,²⁴.0¹⁷,²²]tetracosa-9,16(24),17,19,21-pentaen-8-one)

Structure for NP0280528 (7-(1,2-dihydroxypropan-2-yl)-11-hydroxy-1,2-dimethyl-6-oxa-23-azahexacyclo[12.10.0.0²,¹¹.0⁵,¹⁰.0¹⁶,²⁴.0¹⁷,²²]tetracosa-9,16(24),17,19,21-pentaen-8-one)

3D Structure for NP0280528 (7-(1,2-dihydroxypropan-2-yl)-11-hydroxy-1,2-dimethyl-6-oxa-23-azahexacyclo[12.10.0.0²,¹¹.0⁵,¹⁰.0¹⁶,²⁴.0¹⁷,²²]tetracosa-9,16(24),17,19,21-pentaen-8-one)