NP-MRD: Showing NP-Card for (1s,4r,7s,10s,13s,16s)-2,5,11-trihydroxy-24-methoxy-10-[(4-methoxyphenyl)methyl]-4,9,13,15,29-pentamethyl-7-(2-methylpropyl)-22-oxa-3,6,9,12,15,29-hexaazatetracyclo[14.12.2.2¹⁸,²¹.1²³,²⁷]tritriaconta-2,5,11,18,20,23(31),24,26,32-nonaene-8,14,30-trione (NP0206560)

Jump To Section:

Identification Spectra BioTaxonomy ChemoTaxonomy Physical properties Links References XML

Record Information

Version

2.0

Created at

2022-09-05 02:50:50 UTC

Updated at

2022-09-05 02:50:50 UTC

NP-MRD ID

NP0206560

Secondary Accession Numbers

None

Natural Product Identification

Common Name

(1s,4r,7s,10s,13s,16s)-2,5,11-trihydroxy-24-methoxy-10-[(4-methoxyphenyl)methyl]-4,9,13,15,29-pentamethyl-7-(2-methylpropyl)-22-oxa-3,6,9,12,15,29-hexaazatetracyclo[14.12.2.2¹⁸,²¹.1²³,²⁷]tritriaconta-2,5,11,18,20,23(31),24,26,32-nonaene-8,14,30-trione

Description

RA-XIX belongs to the class of organic compounds known as oligopeptides. These are organic compounds containing a sequence of between three and ten alpha-amino acids joined by peptide bonds. (1s,4r,7s,10s,13s,16s)-2,5,11-trihydroxy-24-methoxy-10-[(4-methoxyphenyl)methyl]-4,9,13,15,29-pentamethyl-7-(2-methylpropyl)-22-oxa-3,6,9,12,15,29-hexaazatetracyclo[14.12.2.2¹⁸,²¹.1²³,²⁷]tritriaconta-2,5,11,18,20,23(31),24,26,32-nonaene-8,14,30-trione is found in Rubia cordifolia. Based on a literature review very few articles have been published on RA-XIX.

Structure

MOL 3D MOL SDF PDB SMILES InChI


  Mrv1652309052204502D          

 59 63  0  0  1  0            999 V2000
   -4.5521   -5.4573    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.8010   -4.6707    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -4.2443   -4.0618    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.4933   -3.2753    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.9366   -2.6664    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.1309   -2.8441    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5742   -2.2353    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7686   -2.4129    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
   -1.5229   -3.2035    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0841   -3.8082    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7127   -3.3904    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4601   -4.1806    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
   -1.0171   -4.7892    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.3467   -4.3617    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.6013   -5.1464    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.8966   -3.7378    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    0.6397   -2.9538    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.7102   -3.9156    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    2.0527   -4.7008    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.7922   -5.1167    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.0406   -4.3307    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.8323   -4.0840    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.4571   -4.5870    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.2079   -5.3748    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.4580   -5.6698    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.0096   -3.9480    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.2808   -3.0277    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.5351   -2.6595    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.3300   -1.8401    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.9726   -1.3379    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.7580   -1.5889    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.8760   -2.4546    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.6553   -2.7254    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    7.2795   -2.1859    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.4885   -1.6711    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.6704   -1.8917    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    2.3414   -1.1161    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8728   -0.4850    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.5324   -0.9268    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    1.2927   -0.1332    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    1.8520    0.4733    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.4843    0.0410    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.2372    0.8281    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0813   -0.5659    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8946   -0.3915    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
   -1.1455    0.3944    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9515    0.5701    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5067   -0.0402    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2024    1.3560    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4544   -1.0027    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2591   -0.8208    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2113   -1.7970    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4060   -1.9764    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.0789   -2.4605    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    1.2897   -2.2199    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.2561   -3.2794    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.0559   -3.4819    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8820   -3.6307    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.4387   -4.2395    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
  3  4  2  0  0  0  0
  4  5  1  0  0  0  0
  5  6  2  0  0  0  0
  6  7  1  0  0  0  0
  8  7  1  6  0  0  0
  8  9  1  0  0  0  0
  9 10  1  4  0  0  0
  9 11  2  0  0  0  0
 11 12  1  0  0  0  0
 12 13  1  6  0  0  0
 12 14  1  0  0  0  0
 14 15  2  0  0  0  0
 14 16  1  0  0  0  0
 16 17  1  0  0  0  0
 16 18  1  0  0  0  0
 18 19  1  6  0  0  0
 19 20  1  0  0  0  0
 20 21  2  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
 20 25  1  0  0  0  0
 23 26  1  0  0  0  0
 26 27  1  0  0  0  0
 27 28  2  0  0  0  0
 28 29  1  0  0  0  0
 29 30  2  0  0  0  0
 30 31  1  0  0  0  0
 31 32  2  0  0  0  0
 27 32  1  0  0  0  0
 32 33  1  0  0  0  0
 33 34  1  0  0  0  0
 29 35  1  0  0  0  0
 35 36  1  0  0  0  0
 36 37  1  0  0  0  0
 37 38  1  4  0  0  0
 37 39  2  0  0  0  0
 39 40  1  0  0  0  0
 40 41  1  1  0  0  0
 40 42  1  0  0  0  0
 42 43  1  4  0  0  0
 42 44  2  0  0  0  0
 44 45  1  0  0  0  0
 45 46  1  6  0  0  0
 46 47  1  0  0  0  0
 47 48  1  0  0  0  0
 47 49  1  0  0  0  0
 45 50  1  0  0  0  0
 50 51  2  0  0  0  0
 50 52  1  0  0  0  0
  8 52  1  0  0  0  0
 52 53  1  0  0  0  0
 36 54  1  6  0  0  0
 54 55  1  0  0  0  0
 54 56  1  0  0  0  0
 18 56  1  0  0  0  0
 56 57  2  0  0  0  0
  6 58  1  0  0  0  0
 58 59  2  0  0  0  0
  3 59  1  0  0  0  0
M  END

     RDKit          3D

115119  0  0  0  0  0  0  0  0999 V2000
   10.0635    1.1478    0.1196 C   0  0  0  0  0  0  0  0  0  0  0  0
    9.0766    0.9906    1.1403 O   0  0  0  0  0  0  0  0  0  0  0  0
    7.7176    1.1532    0.8179 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.3460    1.4602   -0.4681 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.0001    1.6219   -0.7893 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.0075    1.4851    0.1384 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5712    1.6254   -0.1218 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8120    0.3763   -0.3716 C   0  0  1  0  0  0  0  0  0  0  0  0
    1.3260    0.6386   -0.4636 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.8836    0.9201   -1.7617 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.6151    0.5974    0.5175 N   0  0  0  0  0  0  0  0  0  0  0  0
    0.3923    1.2387    1.7519 C   0  0  1  0  0  0  0  0  0  0  0  0
    1.4942    1.0425    2.7644 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.2962    2.7100    1.4974 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.0970    3.4396    2.1780 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5697    3.3312    0.6043 N   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0548    4.4696   -0.1857 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9879    2.9738    0.3694 C   0  0  1  0  0  0  0  0  0  0  0  0
   -2.7005    4.3612    0.3695 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.1903    4.1666    0.1006 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.6021    4.0420   -1.1977 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.8663    3.4003   -1.3949 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.5768    2.9599   -0.3382 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.2449    3.0909    0.9219 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.9566    3.7390    1.1469 C   0  0  0  0  0  0  0  0  0  0  0  0
   -7.8296    2.1428   -0.6548 O   0  0  0  0  0  0  0  0  0  0  0  0
   -7.2448    0.7287   -0.6001 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.0138    0.4909   -1.1371 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.4988   -0.7907   -0.9425 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.2780   -1.7300   -0.2627 C   0  0  0  0  0  0  0  0  0  0  0  0
   -7.5371   -1.4887    0.2541 C   0  0  0  0  0  0  0  0  0  0  0  0
   -8.0110   -0.1656    0.0554 C   0  0  0  0  0  0  0  0  0  0  0  0
   -9.2700    0.0709    0.5832 O   0  0  0  0  0  0  0  0  0  0  0  0
  -10.0276   -0.8899    1.2534 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.0533   -1.1828   -1.0855 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.0979   -0.2366   -0.3257 C   0  0  1  0  0  0  0  0  0  0  0  0
   -2.1612   -1.1154    0.3995 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3213   -1.0626    1.8189 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3326   -1.8260   -0.0817 N   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2703   -2.3494   -0.7484 C   0  0  2  0  0  0  0  0  0  0  0  0
   -0.5861   -3.6739   -1.4953 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7525   -2.8222    0.2739 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.1697   -3.7967    1.1322 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.9161   -2.4565    0.3933 N   0  0  0  0  0  0  0  0  0  0  0  0
    3.1680   -2.5434   -0.2153 C   0  0  1  0  0  0  0  0  0  0  0  0
    3.7077   -3.9390   -0.4681 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.6028   -4.8679    0.6838 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.2010   -6.2041    0.2212 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.3515   -4.4419    1.9000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.3643   -1.7699   -1.4655 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.6370   -2.3648   -2.5648 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.2626   -0.3535   -1.5148 N   0  0  0  0  0  0  0  0  0  0  0  0
    3.5873    0.3457   -2.7408 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5319    0.8164   -1.0995 N   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2754    0.3550   -2.5223 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2012    2.1442   -0.7967 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0248    2.8755   -1.8939 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.4072    1.1740    1.4365 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.7349    1.0122    1.7661 C   0  0  0  0  0  0  0  0  0  0  0  0
   10.0021    2.1749   -0.3017 H   0  0  0  0  0  0  0  0  0  0  0  0
    9.8939    0.4311   -0.7053 H   0  0  0  0  0  0  0  0  0  0  0  0
   11.0802    1.0099    0.5240 H   0  0  0  0  0  0  0  0  0  0  0  0
    8.1355    1.5684   -1.2048 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.7902    1.8747   -1.7966 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.4976    2.3111   -1.0235 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.1184    2.2540    0.6909 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.9639   -0.3360    0.5076 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.9768    0.3003   -2.5382 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5412    0.8884    2.2687 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.0464    0.1078    2.6548 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.0074    0.9772    3.7763 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.1466    1.9377    2.8395 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.0517    4.4662   -0.2294 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3032    5.4378    0.3011 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3774    4.4049   -1.2486 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3431    2.5041    1.2724 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4031    4.8267    1.2974 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1168    4.8966   -0.3830 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.1914    4.3809   -2.1885 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.0848    3.4021   -2.4924 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.7568    2.8538    1.9053 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.8833    3.7847    2.2628 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.4876    1.1683   -1.8992 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.8934   -2.7624   -0.1100 H   0  0  0  0  0  0  0  0  0  0  0  0
   -8.1105   -2.2222    0.7590 H   0  0  0  0  0  0  0  0  0  0  0  0
  -10.9597   -0.4644    1.6732 H   0  0  0  0  0  0  0  0  0  0  0  0
   -9.4770   -1.3075    2.1464 H   0  0  0  0  0  0  0  0  0  0  0  0
  -10.3103   -1.7687    0.6396 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.6721   -1.4296   -2.0549 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.8824   -2.1523   -0.5084 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.8274    0.2974    0.3663 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6456   -0.2544    2.2951 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.2308   -1.7474   -1.5337 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1218   -3.4519   -2.4333 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.3394   -4.2312   -1.6345 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2569   -4.2345   -0.8140 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.0363   -4.7162    0.6861 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.9164   -2.1227    0.5395 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.1173   -4.3811   -1.3126 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.7455   -3.8372   -0.8242 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.5550   -5.1056    0.9367 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.0056   -7.0178    0.9429 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.2858   -6.1034    0.0168 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.7418   -6.4694   -0.7706 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.3087   -3.9457    1.6908 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.6025   -5.3442    2.5139 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.6764   -3.8219    2.5385 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.0759   -0.1728   -3.5963 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.2792    1.3827   -2.7852 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.6763    0.1576   -2.9402 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8464   -0.6629   -2.4821 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5570    1.0611   -2.9448 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.2276    0.3130   -3.0444 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.6649    1.0567    2.2041 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.0631    0.7669    2.7903 H   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0
  2  3  1  0
  3  4  2  0
  4  5  1  0
  5  6  2  0
  6  7  1  0
  7  8  1  0
  8 52  1  0
 52 53  1  0
 52 50  1  0
 50 51  2  0
 50 45  1  0
 45 46  1  0
 46 47  1  0
 47 48  1  0
 47 49  1  0
 45 44  1  0
 44 42  2  0
 42 43  1  0
 42 40  1  0
 40 41  1  0
 40 39  1  0
 39 37  2  0
 37 38  1  0
 37 36  1  0
 36 35  1  0
 35 29  1  0
 29 30  2  0
 30 31  1  0
 31 32  2  0
 32 33  1  0
 33 34  1  0
 32 27  1  0
 27 26  1  0
 26 23  1  0
 23 22  2  0
 22 21  1  0
 21 20  2  0
 20 19  1  0
 19 18  1  0
 18 16  1  0
 16 17  1  0
 16 14  1  0
 14 15  2  0
 14 12  1  0
 12 13  1  0
 12 11  1  0
 11  9  2  0
  9 10  1  0
 18 56  1  0
 56 57  2  0
 56 54  1  0
 54 55  1  0
 20 25  1  0
 25 24  2  0
 27 28  2  0
  6 58  1  0
 58 59  2  0
 59  3  1  0
  9  8  1  0
 54 36  1  0
 28 29  1  0
 24 23  1  0
  1 60  1  0
  1 61  1  0
  1 62  1  0
  4 63  1  0
  5 64  1  0
  7 65  1  0
  7 66  1  0
  8 67  1  1
 53108  1  0
 53109  1  0
 53110  1  0
 45 98  1  1
 46 99  1  0
 46100  1  0
 47101  1  0
 48102  1  0
 48103  1  0
 48104  1  0
 49105  1  0
 49106  1  0
 49107  1  0
 43 97  1  0
 40 93  1  6
 41 94  1  0
 41 95  1  0
 41 96  1  0
 38 92  1  0
 36 91  1  1
 35 89  1  0
 35 90  1  0
 30 84  1  0
 31 85  1  0
 34 86  1  0
 34 87  1  0
 34 88  1  0
 22 80  1  0
 21 79  1  0
 19 77  1  0
 19 78  1  0
 18 76  1  1
 17 73  1  0
 17 74  1  0
 17 75  1  0
 12 69  1  1
 13 70  1  0
 13 71  1  0
 13 72  1  0
 10 68  1  0
 55111  1  0
 55112  1  0
 55113  1  0
 25 82  1  0
 24 81  1  0
 28 83  1  0
 58114  1  0
 59115  1  0
M  END


  Mrv1652309052204502D          

 59 63  0  0  1  0            999 V2000
   -4.5521   -5.4573    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.8010   -4.6707    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -4.2443   -4.0618    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.4933   -3.2753    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.9366   -2.6664    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.1309   -2.8441    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5742   -2.2353    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7686   -2.4129    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
   -1.5229   -3.2035    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0841   -3.8082    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7127   -3.3904    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4601   -4.1806    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
   -1.0171   -4.7892    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.3467   -4.3617    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.6013   -5.1464    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.8966   -3.7378    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    0.6397   -2.9538    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.7102   -3.9156    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    2.0527   -4.7008    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.7922   -5.1167    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.0406   -4.3307    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.8323   -4.0840    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.4571   -4.5870    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.2079   -5.3748    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.4580   -5.6698    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.0096   -3.9480    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.2808   -3.0277    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.5351   -2.6595    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.3300   -1.8401    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.9726   -1.3379    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.7580   -1.5889    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.8760   -2.4546    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.6553   -2.7254    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    7.2795   -2.1859    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.4885   -1.6711    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.6704   -1.8917    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    2.3414   -1.1161    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8728   -0.4850    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.5324   -0.9268    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    1.2927   -0.1332    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    1.8520    0.4733    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.4843    0.0410    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.2372    0.8281    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0813   -0.5659    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8946   -0.3915    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
   -1.1455    0.3944    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9515    0.5701    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5067   -0.0402    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2024    1.3560    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4544   -1.0027    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2591   -0.8208    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2113   -1.7970    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4060   -1.9764    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.0789   -2.4605    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    1.2897   -2.2199    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.2561   -3.2794    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.0559   -3.4819    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8820   -3.6307    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.4387   -4.2395    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
  3  4  2  0  0  0  0
  4  5  1  0  0  0  0
  5  6  2  0  0  0  0
  6  7  1  0  0  0  0
  8  7  1  6  0  0  0
  8  9  1  0  0  0  0
  9 10  1  4  0  0  0
  9 11  2  0  0  0  0
 11 12  1  0  0  0  0
 12 13  1  6  0  0  0
 12 14  1  0  0  0  0
 14 15  2  0  0  0  0
 14 16  1  0  0  0  0
 16 17  1  0  0  0  0
 16 18  1  0  0  0  0
 18 19  1  6  0  0  0
 19 20  1  0  0  0  0
 20 21  2  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
 20 25  1  0  0  0  0
 23 26  1  0  0  0  0
 26 27  1  0  0  0  0
 27 28  2  0  0  0  0
 28 29  1  0  0  0  0
 29 30  2  0  0  0  0
 30 31  1  0  0  0  0
 31 32  2  0  0  0  0
 27 32  1  0  0  0  0
 32 33  1  0  0  0  0
 33 34  1  0  0  0  0
 29 35  1  0  0  0  0
 35 36  1  0  0  0  0
 36 37  1  0  0  0  0
 37 38  1  4  0  0  0
 37 39  2  0  0  0  0
 39 40  1  0  0  0  0
 40 41  1  1  0  0  0
 40 42  1  0  0  0  0
 42 43  1  4  0  0  0
 42 44  2  0  0  0  0
 44 45  1  0  0  0  0
 45 46  1  6  0  0  0
 46 47  1  0  0  0  0
 47 48  1  0  0  0  0
 47 49  1  0  0  0  0
 45 50  1  0  0  0  0
 50 51  2  0  0  0  0
 50 52  1  0  0  0  0
  8 52  1  0  0  0  0
 52 53  1  0  0  0  0
 36 54  1  6  0  0  0
 54 55  1  0  0  0  0
 54 56  1  0  0  0  0
 18 56  1  0  0  0  0
 56 57  2  0  0  0  0
  6 58  1  0  0  0  0
 58 59  2  0  0  0  0
  3 59  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0206560

> <DATABASE_NAME>
NP-MRD

> <SMILES>
COC1=CC=C(C[C@@H]2N(C)C(=O)[C@H](CC(C)C)N=C(O)[C@@H](C)N=C(O)[C@@H]3CC4=CC=C(OC)C(OC5=CC=C(C[C@H](N(C)C(=O)[C@H](C)N=C2O)C(=O)N3C)C=C5)=C4)C=C1

> <INCHI_IDENTIFIER>
InChI=1S/C44H56N6O9/c1-25(2)20-33-43(55)48(5)34(21-28-10-15-31(57-8)16-11-28)41(53)46-27(4)42(54)50(7)36-22-29-12-17-32(18-13-29)59-38-24-30(14-19-37(38)58-9)23-35(49(6)44(36)56)40(52)45-26(3)39(51)47-33/h10-19,24-27,33-36H,20-23H2,1-9H3,(H,45,52)(H,46,53)(H,47,51)/t26-,27+,33+,34+,35+,36+/m1/s1

> <INCHI_KEY>
AOYAGHJWZVPUFX-SQQYMZSVSA-N

> <FORMULA>
C44H56N6O9

> <MOLECULAR_WEIGHT>
812.965

> <EXACT_MASS>
812.410877407

> <JCHEM_ACCEPTOR_COUNT>
11

> <JCHEM_ATOM_COUNT>
115

> <JCHEM_AVERAGE_POLARIZABILITY>
84.75644383664954

> <JCHEM_BIOAVAILABILITY>
0

> <JCHEM_DONOR_COUNT>
3

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
0

> <JCHEM_IUPAC>
(1S,4R,7S,10S,13S,16S)-2,5,11-trihydroxy-24-methoxy-10-[(4-methoxyphenyl)methyl]-4,9,13,15,29-pentamethyl-7-(2-methylpropyl)-22-oxa-3,6,9,12,15,29-hexaazatetracyclo[14.12.2.2^{18,21}.1^{23,27}]tritriaconta-2,5,11,18,20,23(31),24,26,32-nonaene-8,14,30-trione

> <JCHEM_LOGP>
3.6328832119619796

> <JCHEM_MDDR_LIKE_RULE>
1

> <JCHEM_NUMBER_OF_RINGS>
5

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA>
2.885971518502194

> <JCHEM_PKA_STRONGEST_ACIDIC>
0.4180051151723876

> <JCHEM_PKA_STRONGEST_BASIC>
5.402321270037788

> <JCHEM_POLAR_SURFACE_AREA>
186.39

> <JCHEM_REFRACTIVITY>
220.67940000000007

> <JCHEM_ROTATABLE_BOND_COUNT>
6

> <JCHEM_RULE_OF_FIVE>
0

> <JCHEM_TRADITIONAL_IUPAC>
(1S,4R,7S,10S,13S,16S)-2,5,11-trihydroxy-24-methoxy-10-[(4-methoxyphenyl)methyl]-4,9,13,15,29-pentamethyl-7-(2-methylpropyl)-22-oxa-3,6,9,12,15,29-hexaazatetracyclo[14.12.2.2^{18,21}.1^{23,27}]tritriaconta-2,5,11,18,20,23(31),24,26,32-nonaene-8,14,30-trione

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 05-SEP-22   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   05-SEP-22         0                                  
HETATM    1  C   UNK     0      -8.497 -10.187   0.000  0.00  0.00           C+0
HETATM    2  O   UNK     0      -8.962  -8.719   0.000  0.00  0.00           O+0
HETATM    3  C   UNK     0      -7.923  -7.582   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0      -8.387  -6.114   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0      -7.348  -4.977   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0      -5.844  -5.309   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0      -4.805  -4.172   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0      -3.301  -4.504   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0      -2.843  -5.980   0.000  0.00  0.00           C+0
HETATM   10  O   UNK     0      -3.890  -7.109   0.000  0.00  0.00           O+0
HETATM   11  N   UNK     0      -1.330  -6.329   0.000  0.00  0.00           N+0
HETATM   12  C   UNK     0      -0.859  -7.804   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0      -1.899  -8.940   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0       0.647  -8.142   0.000  0.00  0.00           C+0
HETATM   15  O   UNK     0       1.122  -9.607   0.000  0.00  0.00           O+0
HETATM   16  N   UNK     0       1.674  -6.977   0.000  0.00  0.00           N+0
HETATM   17  C   UNK     0       1.194  -5.514   0.000  0.00  0.00           C+0
HETATM   18  C   UNK     0       3.192  -7.309   0.000  0.00  0.00           C+0
HETATM   19  C   UNK     0       3.832  -8.775   0.000  0.00  0.00           C+0
HETATM   20  C   UNK     0       5.212  -9.551   0.000  0.00  0.00           C+0
HETATM   21  C   UNK     0       5.676  -8.084   0.000  0.00  0.00           C+0
HETATM   22  C   UNK     0       7.154  -7.624   0.000  0.00  0.00           C+0
HETATM   23  C   UNK     0       8.320  -8.562   0.000  0.00  0.00           C+0
HETATM   24  C   UNK     0       7.855 -10.033   0.000  0.00  0.00           C+0
HETATM   25  C   UNK     0       6.455 -10.584   0.000  0.00  0.00           C+0
HETATM   26  O   UNK     0       9.351  -7.370   0.000  0.00  0.00           O+0
HETATM   27  C   UNK     0       9.858  -5.652   0.000  0.00  0.00           C+0
HETATM   28  C   UNK     0       8.465  -4.964   0.000  0.00  0.00           C+0
HETATM   29  C   UNK     0       8.083  -3.435   0.000  0.00  0.00           C+0
HETATM   30  C   UNK     0       9.282  -2.497   0.000  0.00  0.00           C+0
HETATM   31  C   UNK     0      10.748  -2.966   0.000  0.00  0.00           C+0
HETATM   32  C   UNK     0      10.969  -4.582   0.000  0.00  0.00           C+0
HETATM   33  O   UNK     0      12.423  -5.087   0.000  0.00  0.00           O+0
HETATM   34  C   UNK     0      13.588  -4.080   0.000  0.00  0.00           C+0
HETATM   35  C   UNK     0       6.512  -3.119   0.000  0.00  0.00           C+0
HETATM   36  C   UNK     0       4.985  -3.531   0.000  0.00  0.00           C+0
HETATM   37  C   UNK     0       4.371  -2.083   0.000  0.00  0.00           C+0
HETATM   38  O   UNK     0       5.362  -0.905   0.000  0.00  0.00           O+0
HETATM   39  N   UNK     0       2.860  -1.730   0.000  0.00  0.00           N+0
HETATM   40  C   UNK     0       2.413  -0.249   0.000  0.00  0.00           C+0
HETATM   41  C   UNK     0       3.457   0.883   0.000  0.00  0.00           C+0
HETATM   42  C   UNK     0       0.904   0.077   0.000  0.00  0.00           C+0
HETATM   43  O   UNK     0       0.443   1.546   0.000  0.00  0.00           O+0
HETATM   44  N   UNK     0      -0.152  -1.056   0.000  0.00  0.00           N+0
HETATM   45  C   UNK     0      -1.670  -0.731   0.000  0.00  0.00           C+0
HETATM   46  C   UNK     0      -2.138   0.736   0.000  0.00  0.00           C+0
HETATM   47  C   UNK     0      -3.643   1.064   0.000  0.00  0.00           C+0
HETATM   48  C   UNK     0      -4.679  -0.075   0.000  0.00  0.00           C+0
HETATM   49  C   UNK     0      -4.111   2.531   0.000  0.00  0.00           C+0
HETATM   50  C   UNK     0      -2.715  -1.872   0.000  0.00  0.00           C+0
HETATM   51  O   UNK     0      -4.217  -1.532   0.000  0.00  0.00           O+0
HETATM   52  N   UNK     0      -2.261  -3.354   0.000  0.00  0.00           N+0
HETATM   53  C   UNK     0      -0.758  -3.689   0.000  0.00  0.00           C+0
HETATM   54  N   UNK     0       3.881  -4.593   0.000  0.00  0.00           N+0
HETATM   55  C   UNK     0       2.408  -4.144   0.000  0.00  0.00           C+0
HETATM   56  C   UNK     0       4.211  -6.121   0.000  0.00  0.00           C+0
HETATM   57  O   UNK     0       5.704  -6.499   0.000  0.00  0.00           O+0
HETATM   58  C   UNK     0      -5.380  -6.777   0.000  0.00  0.00           C+0
HETATM   59  C   UNK     0      -6.419  -7.914   0.000  0.00  0.00           C+0
CONECT    1    2                                                            
CONECT    2    1    3                                                       
CONECT    3    2    4   59                                                  
CONECT    4    3    5                                                       
CONECT    5    4    6                                                       
CONECT    6    5    7   58                                                  
CONECT    7    6    8                                                       
CONECT    8    7    9   52                                                  
CONECT    9    8   10   11                                                  
CONECT   10    9                                                            
CONECT   11    9   12                                                       
CONECT   12   11   13   14                                                  
CONECT   13   12                                                            
CONECT   14   12   15   16                                                  
CONECT   15   14                                                            
CONECT   16   14   17   18                                                  
CONECT   17   16                                                            
CONECT   18   16   19   56                                                  
CONECT   19   18   20                                                       
CONECT   20   19   21   25                                                  
CONECT   21   20   22                                                       
CONECT   22   21   23                                                       
CONECT   23   22   24   26                                                  
CONECT   24   23   25                                                       
CONECT   25   24   20                                                       
CONECT   26   23   27                                                       
CONECT   27   26   28   32                                                  
CONECT   28   27   29                                                       
CONECT   29   28   30   35                                                  
CONECT   30   29   31                                                       
CONECT   31   30   32                                                       
CONECT   32   31   27   33                                                  
CONECT   33   32   34                                                       
CONECT   34   33                                                            
CONECT   35   29   36                                                       
CONECT   36   35   37   54                                                  
CONECT   37   36   38   39                                                  
CONECT   38   37                                                            
CONECT   39   37   40                                                       
CONECT   40   39   41   42                                                  
CONECT   41   40                                                            
CONECT   42   40   43   44                                                  
CONECT   43   42                                                            
CONECT   44   42   45                                                       
CONECT   45   44   46   50                                                  
CONECT   46   45   47                                                       
CONECT   47   46   48   49                                                  
CONECT   48   47                                                            
CONECT   49   47                                                            
CONECT   50   45   51   52                                                  
CONECT   51   50                                                            
CONECT   52   50    8   53                                                  
CONECT   53   52                                                            
CONECT   54   36   55   56                                                  
CONECT   55   54                                                            
CONECT   56   54   18   57                                                  
CONECT   57   56                                                            
CONECT   58    6   59                                                       
CONECT   59   58    3                                                       
MASTER        0    0    0    0    0    0    0    0   59    0  126    0
END

View in JSmol

Synonyms

Not Available

Chemical Formula

C₄₄H₅₆N₆O₉

Average Mass

812.9650 Da

Monoisotopic Mass

812.41088 Da

IUPAC Name

(1S,4R,7S,10S,13S,16S)-2,5,11-trihydroxy-24-methoxy-10-[(4-methoxyphenyl)methyl]-4,9,13,15,29-pentamethyl-7-(2-methylpropyl)-22-oxa-3,6,9,12,15,29-hexaazatetracyclo[14.12.2.2^{18,21}.1^{23,27}]tritriaconta-2,5,11,18,20,23(31),24,26,32-nonaene-8,14,30-trione

Traditional Name

CAS Registry Number

Not Available

SMILES

COC1=CC=C(C[C@@H]2N(C)C(=O)[C@H](CC(C)C)N=C(O)[C@@H](C)N=C(O)[C@@H]3CC4=CC=C(OC)C(OC5=CC=C(C[C@H](N(C)C(=O)[C@H](C)N=C2O)C(=O)N3C)C=C5)=C4)C=C1

InChI Identifier

InChI=1S/C44H56N6O9/c1-25(2)20-33-43(55)48(5)34(21-28-10-15-31(57-8)16-11-28)41(53)46-27(4)42(54)50(7)36-22-29-12-17-32(18-13-29)59-38-24-30(14-19-37(38)58-9)23-35(49(6)44(36)56)40(52)45-26(3)39(51)47-33/h10-19,24-27,33-36H,20-23H2,1-9H3,(H,45,52)(H,46,53)(H,47,51)/t26-,27+,33+,34+,35+,36+/m1/s1

InChI Key

AOYAGHJWZVPUFX-SQQYMZSVSA-N

Experimental Spectra

Not Available

Predicted Spectra

Spectrum Type	Description	Depositor ID	Depositor Organization	Depositor	Deposition Date	View
1D NMR	¹³C NMR Spectrum (1D, 25 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 100 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 252 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 1000 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 50 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 200 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 75 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 300 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 101 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 400 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 126 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 500 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 151 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 600 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 176 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 700 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 201 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 800 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 226 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 900 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum

Chemical Shift Submissions

Not Available

Species

Species of Origin

Species Name	Source	Reference
Rubia cordifolia	LOTUS Database	35616633

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as oligopeptides. These are organic compounds containing a sequence of between three and ten alpha-amino acids joined by peptide bonds.

Kingdom

Organic compounds

Super Class

Organic acids and derivatives

Class

Carboxylic acids and derivatives

Sub Class

Amino acids, peptides, and analogues

Direct Parent

Oligopeptides

Alternative Parents

Substituents

Alpha-oligopeptide
Oxyneolignan skeleton
Macrolactam
Diaryl ether
Alpha-amino acid or derivatives
Anisole
Phenoxy compound
Phenol ether
Methoxybenzene
Alkyl aryl ether
Monocyclic benzene moiety
Benzenoid
Tertiary carboxylic acid amide
Carboxamide group
Lactam
Secondary carboxylic acid amide
Oxacycle
Ether
Organoheterocyclic compound
Azacycle
Organic oxide
Organic oxygen compound
Organic nitrogen compound
Hydrocarbon derivative
Carbonyl group
Organonitrogen compound
Organooxygen 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	3.63	ChemAxon
pKa (Strongest Acidic)	0.42	ChemAxon
pKa (Strongest Basic)	5.4	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	11	ChemAxon
Hydrogen Donor Count	3	ChemAxon
Polar Surface Area	186.39 Å²	ChemAxon
Rotatable Bond Count	6	ChemAxon
Refractivity	220.68 m³·mol⁻¹	ChemAxon
Polarizability	84.76 Å³	ChemAxon
Number of Rings	5	ChemAxon
Bioavailability	No	ChemAxon
Rule of Five	No	ChemAxon
Ghose Filter	No	ChemAxon
Veber's Rule	No	ChemAxon
MDDR-like Rule	Yes	ChemAxon

External Links

HMDB ID

Not Available

DrugBank ID

Not Available

Phenol Explorer Compound ID

Not Available

FoodDB ID

Not Available

KNApSAcK ID

Not Available

Chemspider ID

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

24829365

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

LOTUS database [Link]

Showing NP-Card for (1s,4r,7s,10s,13s,16s)-2,5,11-trihydroxy-24-methoxy-10-[(4-methoxyphenyl)methyl]-4,9,13,15,29-pentamethyl-7-(2-methylpropyl)-22-oxa-3,6,9,12,15,29-hexaazatetracyclo[14.12.2.2¹⁸,²¹.1²³,²⁷]tritriaconta-2,5,11,18,20,23(31),24,26,32-nonaene-8,14,30-trione (NP0206560)

MOL for NP0206560 ((1s,4r,7s,10s,13s,16s)-2,5,11-trihydroxy-24-methoxy-10-[(4-methoxyphenyl)methyl]-4,9,13,15,29-pentamethyl-7-(2-methylpropyl)-22-oxa-3,6,9,12,15,29-hexaazatetracyclo[14.12.2.2¹⁸,²¹.1²³,²⁷]tritriaconta-2,5,11,18,20,23(31),24,26,32-nonaene-8,14,30-trione)

3D MOL for NP0206560 ((1s,4r,7s,10s,13s,16s)-2,5,11-trihydroxy-24-methoxy-10-[(4-methoxyphenyl)methyl]-4,9,13,15,29-pentamethyl-7-(2-methylpropyl)-22-oxa-3,6,9,12,15,29-hexaazatetracyclo[14.12.2.2¹⁸,²¹.1²³,²⁷]tritriaconta-2,5,11,18,20,23(31),24,26,32-nonaene-8,14,30-trione)

3D SDF for NP0206560 ((1s,4r,7s,10s,13s,16s)-2,5,11-trihydroxy-24-methoxy-10-[(4-methoxyphenyl)methyl]-4,9,13,15,29-pentamethyl-7-(2-methylpropyl)-22-oxa-3,6,9,12,15,29-hexaazatetracyclo[14.12.2.2¹⁸,²¹.1²³,²⁷]tritriaconta-2,5,11,18,20,23(31),24,26,32-nonaene-8,14,30-trione)

3D-SDF for NP0206560 ((1s,4r,7s,10s,13s,16s)-2,5,11-trihydroxy-24-methoxy-10-[(4-methoxyphenyl)methyl]-4,9,13,15,29-pentamethyl-7-(2-methylpropyl)-22-oxa-3,6,9,12,15,29-hexaazatetracyclo[14.12.2.2¹⁸,²¹.1²³,²⁷]tritriaconta-2,5,11,18,20,23(31),24,26,32-nonaene-8,14,30-trione)

PDB for NP0206560 ((1s,4r,7s,10s,13s,16s)-2,5,11-trihydroxy-24-methoxy-10-[(4-methoxyphenyl)methyl]-4,9,13,15,29-pentamethyl-7-(2-methylpropyl)-22-oxa-3,6,9,12,15,29-hexaazatetracyclo[14.12.2.2¹⁸,²¹.1²³,²⁷]tritriaconta-2,5,11,18,20,23(31),24,26,32-nonaene-8,14,30-trione)

3D PDB for NP0206560 ((1s,4r,7s,10s,13s,16s)-2,5,11-trihydroxy-24-methoxy-10-[(4-methoxyphenyl)methyl]-4,9,13,15,29-pentamethyl-7-(2-methylpropyl)-22-oxa-3,6,9,12,15,29-hexaazatetracyclo[14.12.2.2¹⁸,²¹.1²³,²⁷]tritriaconta-2,5,11,18,20,23(31),24,26,32-nonaene-8,14,30-trione)

SMILES for NP0206560 ((1s,4r,7s,10s,13s,16s)-2,5,11-trihydroxy-24-methoxy-10-[(4-methoxyphenyl)methyl]-4,9,13,15,29-pentamethyl-7-(2-methylpropyl)-22-oxa-3,6,9,12,15,29-hexaazatetracyclo[14.12.2.2¹⁸,²¹.1²³,²⁷]tritriaconta-2,5,11,18,20,23(31),24,26,32-nonaene-8,14,30-trione)

INCHI for NP0206560 ((1s,4r,7s,10s,13s,16s)-2,5,11-trihydroxy-24-methoxy-10-[(4-methoxyphenyl)methyl]-4,9,13,15,29-pentamethyl-7-(2-methylpropyl)-22-oxa-3,6,9,12,15,29-hexaazatetracyclo[14.12.2.2¹⁸,²¹.1²³,²⁷]tritriaconta-2,5,11,18,20,23(31),24,26,32-nonaene-8,14,30-trione)

Structure for NP0206560 ((1s,4r,7s,10s,13s,16s)-2,5,11-trihydroxy-24-methoxy-10-[(4-methoxyphenyl)methyl]-4,9,13,15,29-pentamethyl-7-(2-methylpropyl)-22-oxa-3,6,9,12,15,29-hexaazatetracyclo[14.12.2.2¹⁸,²¹.1²³,²⁷]tritriaconta-2,5,11,18,20,23(31),24,26,32-nonaene-8,14,30-trione)

3D Structure for NP0206560 ((1s,4r,7s,10s,13s,16s)-2,5,11-trihydroxy-24-methoxy-10-[(4-methoxyphenyl)methyl]-4,9,13,15,29-pentamethyl-7-(2-methylpropyl)-22-oxa-3,6,9,12,15,29-hexaazatetracyclo[14.12.2.2¹⁸,²¹.1²³,²⁷]tritriaconta-2,5,11,18,20,23(31),24,26,32-nonaene-8,14,30-trione)