NP-MRD: Showing NP-Card for 6,19-dihydroxy-4,5,24,24-tetramethyl-10,11-bis(3-methylbut-2-en-1-yl)-25,26-dioxa-7-azahexacyclo[21.2.1.0¹,²⁰.0⁴,¹⁹.0⁵,¹⁶.0⁸,¹³]hexacosa-6,8(13),9,11,20-pentaene-14,22-dione (NP0313348)

Jump To Section:

Identification Spectra BioTaxonomy ChemoTaxonomy Physical properties Links References XML

Record Information

Version

2.0

Created at

2022-09-11 10:49:27 UTC

Updated at

2022-09-11 10:49:28 UTC

NP-MRD ID

NP0313348

Secondary Accession Numbers

None

Natural Product Identification

Common Name

6,19-dihydroxy-4,5,24,24-tetramethyl-10,11-bis(3-methylbut-2-en-1-yl)-25,26-dioxa-7-azahexacyclo[21.2.1.0¹,²⁰.0⁴,¹⁹.0⁵,¹⁶.0⁸,¹³]hexacosa-6,8(13),9,11,20-pentaene-14,22-dione

Description

6,19-Dihydroxy-4,5,24,24-tetramethyl-10,11-bis(3-methylbut-2-en-1-yl)-25,26-dioxa-7-azahexacyclo[21.2.1.0¹,²⁰.0⁴,¹⁹.0⁵,¹⁶.0⁸,¹³]Hexacosa-6,8(13),9,11,20-pentaene-14,22-dione 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 6,19-dihydroxy-4,5,24,24-tetramethyl-10,11-bis(3-methylbut-2-en-1-yl)-25,26-dioxa-7-azahexacyclo[21.2.1.0¹,²⁰.0⁴,¹⁹.0⁵,¹⁶.0⁸,¹³]Hexacosa-6,8(13),9,11,20-pentaene-14,22-dione.

Structure

MOL 3D MOL SDF PDB SMILES InChI


  Mrv1652309112212492D          

 44 49  0  0  0  0            999 V2000
    7.5667    4.0273    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.7245    3.2176    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.1021    2.6760    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.5047    2.9494    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.6664    2.1194    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.1514    1.4282    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.3412    1.5837    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.8014    0.9598    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.0718    0.1804    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.8821    0.0249    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.4218    0.6488    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    9.2676    0.4498    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    9.6376   -0.3106    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    9.1756   -0.9942    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    9.5366   -1.7360    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.3527   -0.9359    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.7119   -0.5620    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.1445   -1.3041    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.9325   -0.8324    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.1902   -0.4725    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.6504   -1.0964    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.8402   -0.9409    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5697   -0.1615    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.9797   -0.8799    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.7509   -0.0029    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.2579   -0.7188    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4122   -0.5914    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7815   -1.1805    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.0870    0.2128    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.7777    0.4815    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.4208    0.8149    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.0292    1.4127    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.8475    1.2509    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.1095    0.4624    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.7427    1.1736    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.9197    0.3069    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.2371    0.9445    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.2796    1.0492    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.9524    1.9910    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    6.0590    1.3197    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    1.7745    1.4401    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.9818    1.0720    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.5912    1.8496    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.1233    0.9196    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0  0  0  0
  2  3  1  0  0  0  0
  2  4  2  0  0  0  0
  4  5  1  0  0  0  0
  5  6  1  0  0  0  0
  6  7  2  0  0  0  0
  7  8  1  0  0  0  0
  8  9  2  0  0  0  0
  9 10  1  0  0  0  0
 10 11  2  0  0  0  0
  6 11  1  0  0  0  0
 11 12  1  0  0  0  0
 12 13  1  0  0  0  0
 13 14  2  0  0  0  0
 14 15  1  0  0  0  0
 14 16  1  0  0  0  0
  9 17  1  0  0  0  0
 17 18  2  0  0  0  0
 17 19  1  0  0  0  0
 19 20  1  0  0  0  0
 20 21  1  0  0  0  0
 21 22  1  0  0  0  0
 22 23  1  0  0  0  0
 23 24  1  0  0  0  0
 23 25  1  0  0  0  0
 25 26  2  0  0  0  0
 26 27  1  0  0  0  0
 27 28  2  0  0  0  0
 27 29  1  0  0  0  0
 29 30  1  0  0  0  0
 30 31  1  0  0  0  0
 25 31  1  0  0  0  0
 31 32  1  0  0  0  0
 32 33  1  0  0  0  0
 33 34  1  0  0  0  0
 23 34  1  0  0  0  0
 34 35  1  0  0  0  0
 34 36  1  0  0  0  0
 20 36  1  0  0  0  0
 36 37  1  0  0  0  0
 36 38  1  0  0  0  0
 38 39  1  0  0  0  0
 38 40  2  0  0  0  0
 40  8  1  4  0  0  0
 31 41  1  0  0  0  0
 41 42  1  0  0  0  0
 29 42  1  0  0  0  0
 42 43  1  0  0  0  0
 42 44  1  0  0  0  0
M  END

     RDKit          3D

 91 96  0  0  0  0  0  0  0  0999 V2000
   -7.9496   -1.6423    0.4932 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.6545   -1.6090    1.1965 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.0445   -2.8472    1.7174 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.9839   -0.4506    1.3867 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.7028   -0.4160    2.0818 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.6089    0.0666    1.2127 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7786   -0.8727    0.5833 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7464   -0.5089   -0.2087 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5093    0.8411   -0.3977 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2696    1.7913    0.1778 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.3441    1.3997    1.0009 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.1226    2.4773    1.5854 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.2940    2.9808    0.8856 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.7981    2.7961   -0.2972 C   0  0  0  0  0  0  0  0  0  0  0  0
   -7.0942    3.5564   -0.6167 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.2194    1.9445   -1.3491 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4778    1.5075   -1.1925 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6455    2.7605   -1.0225 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.6295    1.3015   -2.0735 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.1326    0.0178   -2.4897 C   0  0  1  0  0  0  0  0  0  0  0  0
    2.5317    0.3075   -3.0753 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.6783   -0.0210   -2.2229 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.6302   -1.1266   -1.2598 C   0  0  1  0  0  0  0  0  0  0  0  0
    4.0409   -2.3830   -1.7833 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.6801   -0.8950   -0.2063 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.9611   -1.2433   -0.4371 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.9426   -1.1008    0.6250 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.1030   -1.5486    0.5943 O   0  0  0  0  0  0  0  0  0  0  0  0
    6.4872   -0.3573    1.8216 C   0  0  2  0  0  0  0  0  0  0  0  0
    5.2068   -0.8667    2.1183 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.4356   -0.3017    1.1100 C   0  0  2  0  0  0  0  0  0  0  0  0
    3.0029   -0.4022    1.5732 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1449   -0.0989    0.3564 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.2579   -1.2565   -0.6198 C   0  0  2  0  0  0  0  0  0  0  0  0
    2.1748   -2.4986    0.2156 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.2383   -1.2143   -1.7261 C   0  0  2  0  0  0  0  0  0  0  0  0
    1.7707   -2.2403   -2.7747 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0135   -1.9004   -1.2566 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0102   -3.3147   -1.4775 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1163   -1.6913   -0.6913 N   0  0  0  0  0  0  0  0  0  0  0  0
    4.8405    1.0287    1.1350 O   0  0  0  0  0  0  0  0  0  0  0  0
    6.2125    1.0558    1.3529 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.6173    2.0667    2.4068 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.9969    1.3883    0.0995 C   0  0  0  0  0  0  0  0  0  0  0  0
   -7.9767   -2.4355   -0.3058 H   0  0  0  0  0  0  0  0  0  0  0  0
   -8.2018   -0.6967   -0.0095 H   0  0  0  0  0  0  0  0  0  0  0  0
   -8.7937   -1.8885    1.1725 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.7459   -3.6920    1.5300 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.9822   -2.7457    2.8238 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.0419   -3.0474    1.2807 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.4726    0.4176    0.9999 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.4438   -1.4648    2.4030 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.7396    0.1509    3.0454 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.0017   -1.9071    0.7622 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0420    2.8306   -0.0019 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.4051    3.3358    1.8254 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.4744    2.2015    2.6287 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.8972    3.6977    1.5184 H   0  0  0  0  0  0  0  0  0  0  0  0
   -7.5778    3.8901    0.3050 H   0  0  0  0  0  0  0  0  0  0  0  0
   -7.7069    2.8403   -1.1702 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.7914    4.4262   -1.2356 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.2524    2.3321   -1.7433 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.9487    1.8707   -2.2313 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.0678    0.9312   -0.9742 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.4565    2.0058   -1.7294 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.3344    1.8737   -3.0239 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.5286   -0.2901   -3.4143 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.6347    1.4275   -3.2840 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.6045   -0.0316   -4.1536 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.5436   -0.2408   -2.9254 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.0641    0.8904   -1.6673 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.1756   -3.0125   -1.0581 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.2539   -1.6244   -1.4013 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.1709   -0.4176    2.6684 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.8441    0.4789    2.2640 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.7372   -1.2816    2.1318 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.6481    0.8216   -0.0651 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.1391    0.0755    0.7222 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.1934   -2.6169    0.6835 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.3803   -2.4020    0.9782 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.0077   -3.4350   -0.3174 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.9383   -3.2143   -2.3346 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.8624   -2.3841   -3.4437 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.5280   -1.8681   -3.4208 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7703   -3.7417   -1.9406 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.5796    1.6950    2.8347 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.8609    2.1797    3.1968 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.8500    3.0555    1.9664 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.9960    0.8969    0.0919 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.4169    1.1477   -0.8306 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.2056    2.4852    0.0373 H   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0
  2  3  1  0
  2  4  2  3
  4  5  1  0
  5  6  1  0
  6  7  2  0
  7  8  1  0
  8  9  2  0
  9 10  1  0
 10 11  2  0
 11 12  1  0
 12 13  1  0
 13 14  2  3
 14 15  1  0
 14 16  1  0
  9 17  1  0
 17 18  2  0
 17 19  1  0
 19 20  1  0
 20 21  1  0
 21 22  1  0
 22 23  1  0
 23 24  1  6
 23 25  1  0
 25 26  2  0
 26 27  1  0
 27 28  2  0
 27 29  1  0
 29 30  1  0
 30 31  1  0
 31 32  1  0
 32 33  1  0
 33 34  1  0
 34 35  1  1
 34 36  1  0
 36 37  1  6
 36 38  1  0
 38 39  1  0
 38 40  2  0
 31 41  1  6
 41 42  1  0
 42 43  1  0
 42 44  1  0
 11  6  1  0
 36 20  1  0
 40  8  1  0
 34 23  1  0
 31 25  1  0
 42 29  1  0
  1 45  1  0
  1 46  1  0
  1 47  1  0
  3 48  1  0
  3 49  1  0
  3 50  1  0
  4 51  1  0
  5 52  1  0
  5 53  1  0
  7 54  1  0
 10 55  1  0
 12 56  1  0
 12 57  1  0
 13 58  1  0
 15 59  1  0
 15 60  1  0
 15 61  1  0
 16 62  1  0
 16 63  1  0
 16 64  1  0
 19 65  1  0
 19 66  1  0
 20 67  1  6
 21 68  1  0
 21 69  1  0
 22 70  1  0
 22 71  1  0
 24 72  1  0
 26 73  1  0
 29 74  1  1
 32 75  1  0
 32 76  1  0
 33 77  1  0
 33 78  1  0
 35 79  1  0
 35 80  1  0
 35 81  1  0
 37 82  1  0
 37 83  1  0
 37 84  1  0
 39 85  1  0
 43 86  1  0
 43 87  1  0
 43 88  1  0
 44 89  1  0
 44 90  1  0
 44 91  1  0
M  END


  Mrv1652309112212492D          

 44 49  0  0  0  0            999 V2000
    7.5667    4.0273    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.7245    3.2176    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.1021    2.6760    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.5047    2.9494    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.6664    2.1194    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.1514    1.4282    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.3412    1.5837    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.8014    0.9598    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.0718    0.1804    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.8821    0.0249    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.4218    0.6488    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    9.2676    0.4498    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    9.6376   -0.3106    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    9.1756   -0.9942    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    9.5366   -1.7360    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.3527   -0.9359    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.7119   -0.5620    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.1445   -1.3041    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.9325   -0.8324    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.1902   -0.4725    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.6504   -1.0964    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.8402   -0.9409    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5697   -0.1615    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.9797   -0.8799    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.7509   -0.0029    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.2579   -0.7188    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4122   -0.5914    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7815   -1.1805    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.0870    0.2128    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.7777    0.4815    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.4208    0.8149    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.0292    1.4127    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.8475    1.2509    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.1095    0.4624    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.7427    1.1736    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.9197    0.3069    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.2371    0.9445    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.2796    1.0492    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.9524    1.9910    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    6.0590    1.3197    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    1.7745    1.4401    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.9818    1.0720    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.5912    1.8496    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.1233    0.9196    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0  0  0  0
  2  3  1  0  0  0  0
  2  4  2  0  0  0  0
  4  5  1  0  0  0  0
  5  6  1  0  0  0  0
  6  7  2  0  0  0  0
  7  8  1  0  0  0  0
  8  9  2  0  0  0  0
  9 10  1  0  0  0  0
 10 11  2  0  0  0  0
  6 11  1  0  0  0  0
 11 12  1  0  0  0  0
 12 13  1  0  0  0  0
 13 14  2  0  0  0  0
 14 15  1  0  0  0  0
 14 16  1  0  0  0  0
  9 17  1  0  0  0  0
 17 18  2  0  0  0  0
 17 19  1  0  0  0  0
 19 20  1  0  0  0  0
 20 21  1  0  0  0  0
 21 22  1  0  0  0  0
 22 23  1  0  0  0  0
 23 24  1  0  0  0  0
 23 25  1  0  0  0  0
 25 26  2  0  0  0  0
 26 27  1  0  0  0  0
 27 28  2  0  0  0  0
 27 29  1  0  0  0  0
 29 30  1  0  0  0  0
 30 31  1  0  0  0  0
 25 31  1  0  0  0  0
 31 32  1  0  0  0  0
 32 33  1  0  0  0  0
 33 34  1  0  0  0  0
 23 34  1  0  0  0  0
 34 35  1  0  0  0  0
 34 36  1  0  0  0  0
 20 36  1  0  0  0  0
 36 37  1  0  0  0  0
 36 38  1  0  0  0  0
 38 39  1  0  0  0  0
 38 40  2  0  0  0  0
 40  8  1  4  0  0  0
 31 41  1  0  0  0  0
 41 42  1  0  0  0  0
 29 42  1  0  0  0  0
 42 43  1  0  0  0  0
 42 44  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0313348

> <DATABASE_NAME>
NP-MRD

> <SMILES>
CC(C)=CCC1=CC2=C(C=C1CC=C(C)C)C(=O)CC1CCC3(O)C4=CC(=O)C5OC4(CCC3(C)C1(C)C(O)=N2)OC5(C)C

> <INCHI_IDENTIFIER>
InChI=1S/C37H47NO6/c1-21(2)9-11-23-17-26-27(18-24(23)12-10-22(3)4)38-32(41)35(8)25(19-28(26)39)13-14-36(42)30-20-29(40)31-33(5,6)44-37(30,43-31)16-15-34(35,36)7/h9-10,17-18,20,25,31,42H,11-16,19H2,1-8H3,(H,38,41)

> <INCHI_KEY>
NYXKDYYTRGPSCQ-UHFFFAOYSA-N

> <FORMULA>
C37H47NO6

> <MOLECULAR_WEIGHT>
601.784

> <EXACT_MASS>
601.340338237

> <JCHEM_ACCEPTOR_COUNT>
7

> <JCHEM_ATOM_COUNT>
91

> <JCHEM_AVERAGE_POLARIZABILITY>
68.46830195716171

> <JCHEM_BIOAVAILABILITY>
0

> <JCHEM_DONOR_COUNT>
2

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
0

> <JCHEM_IUPAC>
6,19-dihydroxy-4,5,24,24-tetramethyl-10,11-bis(3-methylbut-2-en-1-yl)-25,26-dioxa-7-azahexacyclo[21.2.1.0^{1,20}.0^{4,19}.0^{5,16}.0^{8,13}]hexacosa-6,8(13),9,11,20-pentaene-14,22-dione

> <JCHEM_LOGP>
7.324612713

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
6

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA>
13.63703595552806

> <JCHEM_PKA_STRONGEST_ACIDIC>
4.938414413419511

> <JCHEM_PKA_STRONGEST_BASIC>
1.0568238211161862

> <JCHEM_POLAR_SURFACE_AREA>
105.42

> <JCHEM_REFRACTIVITY>
174.84780000000003

> <JCHEM_ROTATABLE_BOND_COUNT>
4

> <JCHEM_RULE_OF_FIVE>
0

> <JCHEM_TRADITIONAL_IUPAC>
6,19-dihydroxy-4,5,24,24-tetramethyl-10,11-bis(3-methylbut-2-en-1-yl)-25,26-dioxa-7-azahexacyclo[21.2.1.0^{1,20}.0^{4,19}.0^{5,16}.0^{8,13}]hexacosa-6,8(13),9,11,20-pentaene-14,22-dione

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 11-SEP-22   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   11-SEP-22         0                                  
HETATM    1  C   UNK     0      14.124   7.518   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0      14.419   6.006   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0      13.257   4.995   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0      15.875   5.505   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0      16.177   3.956   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0      15.216   2.666   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0      13.704   2.956   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0      12.696   1.792   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0      13.201   0.337   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0      14.713   0.046   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0      15.721   1.211   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0      17.299   0.840   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0      17.990  -0.580   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0      17.128  -1.856   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0      17.802  -3.241   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0      15.592  -1.747   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0      12.529  -1.049   0.000  0.00  0.00           C+0
HETATM   18  O   UNK     0      13.336  -2.434   0.000  0.00  0.00           O+0
HETATM   19  C   UNK     0      11.074  -1.554   0.000  0.00  0.00           C+0
HETATM   20  C   UNK     0       9.688  -0.882   0.000  0.00  0.00           C+0
HETATM   21  C   UNK     0       8.681  -2.047   0.000  0.00  0.00           C+0
HETATM   22  C   UNK     0       7.168  -1.756   0.000  0.00  0.00           C+0
HETATM   23  C   UNK     0       6.664  -0.302   0.000  0.00  0.00           C+0
HETATM   24  O   UNK     0       5.562  -1.642   0.000  0.00  0.00           O+0
HETATM   25  C   UNK     0       5.135  -0.005   0.000  0.00  0.00           C+0
HETATM   26  C   UNK     0       4.215  -1.342   0.000  0.00  0.00           C+0
HETATM   27  C   UNK     0       2.636  -1.104   0.000  0.00  0.00           C+0
HETATM   28  O   UNK     0       1.459  -2.204   0.000  0.00  0.00           O+0
HETATM   29  C   UNK     0       2.029   0.397   0.000  0.00  0.00           C+0
HETATM   30  O   UNK     0       3.318   0.899   0.000  0.00  0.00           O+0
HETATM   31  C   UNK     0       4.519   1.521   0.000  0.00  0.00           C+0
HETATM   32  C   UNK     0       5.655   2.637   0.000  0.00  0.00           C+0
HETATM   33  C   UNK     0       7.182   2.335   0.000  0.00  0.00           C+0
HETATM   34  C   UNK     0       7.671   0.863   0.000  0.00  0.00           C+0
HETATM   35  C   UNK     0       8.853   2.191   0.000  0.00  0.00           C+0
HETATM   36  C   UNK     0       9.183   0.573   0.000  0.00  0.00           C+0
HETATM   37  C   UNK     0       7.909   1.763   0.000  0.00  0.00           C+0
HETATM   38  C   UNK     0       9.855   1.959   0.000  0.00  0.00           C+0
HETATM   39  O   UNK     0       9.245   3.717   0.000  0.00  0.00           O+0
HETATM   40  N   UNK     0      11.310   2.463   0.000  0.00  0.00           N+0
HETATM   41  O   UNK     0       3.312   2.688   0.000  0.00  0.00           O+0
HETATM   42  C   UNK     0       1.833   2.001   0.000  0.00  0.00           C+0
HETATM   43  C   UNK     0       1.104   3.453   0.000  0.00  0.00           C+0
HETATM   44  C   UNK     0       0.230   1.717   0.000  0.00  0.00           C+0
CONECT    1    2                                                            
CONECT    2    1    3    4                                                  
CONECT    3    2                                                            
CONECT    4    2    5                                                       
CONECT    5    4    6                                                       
CONECT    6    5    7   11                                                  
CONECT    7    6    8                                                       
CONECT    8    7    9   40                                                  
CONECT    9    8   10   17                                                  
CONECT   10    9   11                                                       
CONECT   11   10    6   12                                                  
CONECT   12   11   13                                                       
CONECT   13   12   14                                                       
CONECT   14   13   15   16                                                  
CONECT   15   14                                                            
CONECT   16   14                                                            
CONECT   17    9   18   19                                                  
CONECT   18   17                                                            
CONECT   19   17   20                                                       
CONECT   20   19   21   36                                                  
CONECT   21   20   22                                                       
CONECT   22   21   23                                                       
CONECT   23   22   24   25   34                                             
CONECT   24   23                                                            
CONECT   25   23   26   31                                                  
CONECT   26   25   27                                                       
CONECT   27   26   28   29                                                  
CONECT   28   27                                                            
CONECT   29   27   30   42                                                  
CONECT   30   29   31                                                       
CONECT   31   30   25   32   41                                             
CONECT   32   31   33                                                       
CONECT   33   32   34                                                       
CONECT   34   33   23   35   36                                             
CONECT   35   34                                                            
CONECT   36   34   20   37   38                                             
CONECT   37   36                                                            
CONECT   38   36   39   40                                                  
CONECT   39   38                                                            
CONECT   40   38    8                                                       
CONECT   41   31   42                                                       
CONECT   42   41   29   43   44                                             
CONECT   43   42                                                            
CONECT   44   42                                                            
MASTER        0    0    0    0    0    0    0    0   44    0   98    0
END

View in JSmol

Synonyms

Not Available

Chemical Formula

C₃₇H₄₇NO₆

Average Mass

601.7840 Da

Monoisotopic Mass

601.34034 Da

IUPAC Name

6,19-dihydroxy-4,5,24,24-tetramethyl-10,11-bis(3-methylbut-2-en-1-yl)-25,26-dioxa-7-azahexacyclo[21.2.1.0^{1,20}.0^{4,19}.0^{5,16}.0^{8,13}]hexacosa-6,8(13),9,11,20-pentaene-14,22-dione

Traditional Name

6,19-dihydroxy-4,5,24,24-tetramethyl-10,11-bis(3-methylbut-2-en-1-yl)-25,26-dioxa-7-azahexacyclo[21.2.1.0^{1,20}.0^{4,19}.0^{5,16}.0^{8,13}]hexacosa-6,8(13),9,11,20-pentaene-14,22-dione

CAS Registry Number

Not Available

SMILES

CC(C)=CCC1=CC2=C(C=C1CC=C(C)C)C(=O)CC1CCC3(O)C4=CC(=O)C5OC4(CCC3(C)C1(C)C(O)=N2)OC5(C)C

InChI Identifier

InChI=1S/C37H47NO6/c1-21(2)9-11-23-17-26-27(18-24(23)12-10-22(3)4)38-32(41)35(8)25(19-28(26)39)13-14-36(42)30-20-29(40)31-33(5,6)44-37(30,43-31)16-15-34(35,36)7/h9-10,17-18,20,25,31,42H,11-16,19H2,1-8H3,(H,38,41)

InChI Key

NYXKDYYTRGPSCQ-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
Aryl ketone
Aryl alkyl ketone
Dihydropyranone
Ketal
Pyran
Benzenoid
Meta-dioxolane
Cyclic alcohol
Tertiary alcohol
Vinylogous amide
Secondary carboxylic acid amide
Carboxamide group
Ketone
Lactam
Azacycle
Oxacycle
Carboxylic acid derivative
Acetal
Alcohol
Organic oxygen compound
Organic nitrogen compound
Organopnictogen compound
Organonitrogen compound
Organooxygen compound
Carbonyl group
Hydrocarbon derivative
Organic oxide
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	7.32	ChemAxon
pKa (Strongest Acidic)	4.94	ChemAxon
pKa (Strongest Basic)	1.06	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	7	ChemAxon
Hydrogen Donor Count	2	ChemAxon
Polar Surface Area	105.42 Å²	ChemAxon
Rotatable Bond Count	4	ChemAxon
Refractivity	174.85 m³·mol⁻¹	ChemAxon
Polarizability	68.47 Å³	ChemAxon
Number of Rings	6	ChemAxon
Bioavailability	No	ChemAxon
Rule of Five	No	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

163063487

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

LOTUS database [Link]

Showing NP-Card for 6,19-dihydroxy-4,5,24,24-tetramethyl-10,11-bis(3-methylbut-2-en-1-yl)-25,26-dioxa-7-azahexacyclo[21.2.1.0¹,²⁰.0⁴,¹⁹.0⁵,¹⁶.0⁸,¹³]hexacosa-6,8(13),9,11,20-pentaene-14,22-dione (NP0313348)

MOL for NP0313348 (6,19-dihydroxy-4,5,24,24-tetramethyl-10,11-bis(3-methylbut-2-en-1-yl)-25,26-dioxa-7-azahexacyclo[21.2.1.0¹,²⁰.0⁴,¹⁹.0⁵,¹⁶.0⁸,¹³]hexacosa-6,8(13),9,11,20-pentaene-14,22-dione)

3D MOL for NP0313348 (6,19-dihydroxy-4,5,24,24-tetramethyl-10,11-bis(3-methylbut-2-en-1-yl)-25,26-dioxa-7-azahexacyclo[21.2.1.0¹,²⁰.0⁴,¹⁹.0⁵,¹⁶.0⁸,¹³]hexacosa-6,8(13),9,11,20-pentaene-14,22-dione)

3D SDF for NP0313348 (6,19-dihydroxy-4,5,24,24-tetramethyl-10,11-bis(3-methylbut-2-en-1-yl)-25,26-dioxa-7-azahexacyclo[21.2.1.0¹,²⁰.0⁴,¹⁹.0⁵,¹⁶.0⁸,¹³]hexacosa-6,8(13),9,11,20-pentaene-14,22-dione)

3D-SDF for NP0313348 (6,19-dihydroxy-4,5,24,24-tetramethyl-10,11-bis(3-methylbut-2-en-1-yl)-25,26-dioxa-7-azahexacyclo[21.2.1.0¹,²⁰.0⁴,¹⁹.0⁵,¹⁶.0⁸,¹³]hexacosa-6,8(13),9,11,20-pentaene-14,22-dione)

PDB for NP0313348 (6,19-dihydroxy-4,5,24,24-tetramethyl-10,11-bis(3-methylbut-2-en-1-yl)-25,26-dioxa-7-azahexacyclo[21.2.1.0¹,²⁰.0⁴,¹⁹.0⁵,¹⁶.0⁸,¹³]hexacosa-6,8(13),9,11,20-pentaene-14,22-dione)

3D PDB for NP0313348 (6,19-dihydroxy-4,5,24,24-tetramethyl-10,11-bis(3-methylbut-2-en-1-yl)-25,26-dioxa-7-azahexacyclo[21.2.1.0¹,²⁰.0⁴,¹⁹.0⁵,¹⁶.0⁸,¹³]hexacosa-6,8(13),9,11,20-pentaene-14,22-dione)

SMILES for NP0313348 (6,19-dihydroxy-4,5,24,24-tetramethyl-10,11-bis(3-methylbut-2-en-1-yl)-25,26-dioxa-7-azahexacyclo[21.2.1.0¹,²⁰.0⁴,¹⁹.0⁵,¹⁶.0⁸,¹³]hexacosa-6,8(13),9,11,20-pentaene-14,22-dione)

INCHI for NP0313348 (6,19-dihydroxy-4,5,24,24-tetramethyl-10,11-bis(3-methylbut-2-en-1-yl)-25,26-dioxa-7-azahexacyclo[21.2.1.0¹,²⁰.0⁴,¹⁹.0⁵,¹⁶.0⁸,¹³]hexacosa-6,8(13),9,11,20-pentaene-14,22-dione)

Structure for NP0313348 (6,19-dihydroxy-4,5,24,24-tetramethyl-10,11-bis(3-methylbut-2-en-1-yl)-25,26-dioxa-7-azahexacyclo[21.2.1.0¹,²⁰.0⁴,¹⁹.0⁵,¹⁶.0⁸,¹³]hexacosa-6,8(13),9,11,20-pentaene-14,22-dione)

3D Structure for NP0313348 (6,19-dihydroxy-4,5,24,24-tetramethyl-10,11-bis(3-methylbut-2-en-1-yl)-25,26-dioxa-7-azahexacyclo[21.2.1.0¹,²⁰.0⁴,¹⁹.0⁵,¹⁶.0⁸,¹³]hexacosa-6,8(13),9,11,20-pentaene-14,22-dione)