NP-MRD: Showing NP-Card for (3s,4ar,5s,6r,6ar,10r,10as,10br)-5-(acetyloxy)-4a,6a,7,10b-tetramethyl-5'-oxo-10-(pyridine-3-carbonyloxy)-2,5,6,9,10,10a-hexahydro-1h-spiro[naphtho[2,1-b]pyran-3,3'-oxolan]-6-yl pyridine-3-carboxylate (NP0274241)

Jump To Section:

Identification Spectra BioTaxonomy ChemoTaxonomy Physical properties Links References XML

Record Information

Version

2.0

Created at

2022-09-08 21:33:55 UTC

Updated at

2022-09-08 21:33:56 UTC

NP-MRD ID

NP0274241

Secondary Accession Numbers

None

Natural Product Identification

Common Name

(3s,4ar,5s,6r,6ar,10r,10as,10br)-5-(acetyloxy)-4a,6a,7,10b-tetramethyl-5'-oxo-10-(pyridine-3-carbonyloxy)-2,5,6,9,10,10a-hexahydro-1h-spiro[naphtho[2,1-b]pyran-3,3'-oxolan]-6-yl pyridine-3-carboxylate

Description

CHEMBL3577083 belongs to the class of organic compounds known as diterpene lactones. These are diterpenoids containing a lactone moiety. (3s,4ar,5s,6r,6ar,10r,10as,10br)-5-(acetyloxy)-4a,6a,7,10b-tetramethyl-5'-oxo-10-(pyridine-3-carbonyloxy)-2,5,6,9,10,10a-hexahydro-1h-spiro[naphtho[2,1-b]pyran-3,3'-oxolan]-6-yl pyridine-3-carboxylate is found in Scutellaria barbata. Based on a literature review very few articles have been published on CHEMBL3577083.

Structure

MOL 3D MOL SDF PDB SMILES InChI


  Mrv1652309082223332D          

 45 50  0  0  1  0            999 V2000
    4.0145   -4.9204    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.6020   -4.2059    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.0145   -3.4914    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.7770   -4.2059    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.3645   -3.4914    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    1.5395   -3.4914    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    1.1270   -4.2059    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.5395   -4.9204    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.3645   -4.9204    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.1270   -5.6349    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.5395   -6.3493    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.1270   -7.0638    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.3020   -7.0638    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1105   -6.3493    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    0.3020   -5.6349    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.1270   -2.7770    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    0.7145   -3.4914    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.3020   -2.7770    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1105   -3.4914    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1105   -2.0625    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.3020   -1.3480    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.1270   -1.3480    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    1.5395   -0.6336    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.1270    0.0809    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.3020    0.0809    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.5395    0.7954    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.1270    1.5099    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.5395    2.2243    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.3645    2.2243    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.7770    1.5099    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    2.3645    0.7954    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.5395   -2.0625    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    2.3645   -2.0625    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    1.9520   -1.3480    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.7770   -1.3480    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.6020   -1.3480    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.0145   -2.0625    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    4.4994   -1.3951    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.2840   -1.6500    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.2840   -2.4750    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.9515   -2.9599    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.4994   -2.7299    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.6020   -2.7770    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.7770   -2.7770    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    3.1895   -3.4914    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0  0  0  0
  2  3  2  0  0  0  0
  2  4  1  0  0  0  0
  5  4  1  1  0  0  0
  5  6  1  0  0  0  0
  6  7  1  6  0  0  0
  7  8  1  0  0  0  0
  8  9  2  0  0  0  0
  8 10  1  0  0  0  0
 10 11  2  0  0  0  0
 11 12  1  0  0  0  0
 12 13  2  0  0  0  0
 13 14  1  0  0  0  0
 14 15  2  0  0  0  0
 10 15  1  0  0  0  0
  6 16  1  0  0  0  0
 16 17  1  6  0  0  0
 16 18  1  0  0  0  0
 18 19  1  0  0  0  0
 18 20  2  0  0  0  0
 20 21  1  0  0  0  0
 21 22  1  0  0  0  0
 22 23  1  1  0  0  0
 23 24  1  0  0  0  0
 24 25  2  0  0  0  0
 24 26  1  0  0  0  0
 26 27  2  0  0  0  0
 27 28  1  0  0  0  0
 28 29  2  0  0  0  0
 29 30  1  0  0  0  0
 30 31  2  0  0  0  0
 26 31  1  0  0  0  0
 32 22  1  6  0  0  0
 16 32  1  0  0  0  0
 32 33  1  0  0  0  0
 33 34  1  6  0  0  0
 33 35  1  0  0  0  0
 35 36  1  0  0  0  0
 36 37  1  0  0  0  0
 37 38  1  6  0  0  0
 38 39  1  0  0  0  0
 39 40  1  0  0  0  0
 40 41  2  0  0  0  0
 40 42  1  0  0  0  0
 37 42  1  0  0  0  0
 37 43  1  0  0  0  0
 43 44  1  0  0  0  0
  5 44  1  0  0  0  0
 33 44  1  0  0  0  0
 44 45  1  6  0  0  0
M  END

     RDKit          3D

 83 88  0  0  0  0  0  0  0  0999 V2000
   -2.9166    3.5505   -2.3380 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.9187    2.4761   -1.3110 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.9072    2.3237   -0.5501 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8511    1.6186   -1.1569 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8353    0.5907   -0.1853 C   0  0  1  0  0  0  0  0  0  0  0  0
   -1.7595   -0.7506   -0.8257 C   0  0  2  0  0  0  0  0  0  0  0  0
   -2.5101   -1.7373   -0.1180 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.6679   -2.3224   -0.4911 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.1804   -1.9926   -1.5630 O   0  0  0  0  0  0  0  0  0  0  0  0
   -4.3649   -3.3424    0.3123 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.5531   -3.9006   -0.1351 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.2299   -4.8565    0.5917 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.7012   -5.2583    1.7912 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.5335   -4.7249    2.2543 N   0  0  0  0  0  0  0  0  0  0  0  0
   -3.8955   -3.7938    1.5230 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3982   -1.2199   -1.2049 C   0  0  1  0  0  0  0  0  0  0  0  0
   -0.1555   -2.5884   -0.5971 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3289   -1.5041   -2.6656 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5295   -2.1078   -3.3557 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7141   -1.2796   -3.4137 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.9629   -0.7071   -2.8733 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.9584   -0.7526   -1.3333 C   0  0  1  0  0  0  0  0  0  0  0  0
    3.1102   -0.0732   -0.9696 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.2341   -0.6909   -0.4572 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.1815   -1.9353   -0.3248 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.4373    0.0312   -0.0785 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.5029   -0.6792    0.4223 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.6883   -0.0434    0.8048 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.7988    1.3217    0.6806 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.7462    1.9972    0.1891 N   0  0  0  0  0  0  0  0  0  0  0  0
    5.5875    1.3948   -0.1871 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.6518   -0.1966   -0.9173 C   0  0  2  0  0  0  0  0  0  0  0  0
    0.6133    0.5043    0.3938 C   0  0  1  0  0  0  0  0  0  0  0  0
    1.4681   -0.2586    1.3668 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.2794    1.8839    0.2524 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.3371    2.4851    1.6173 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1242    2.8633    1.9144 C   0  0  1  0  0  0  0  0  0  0  0  0
   -0.3630    3.0471    3.3801 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0961    4.4045    3.6810 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0205    5.1658    2.5554 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.1940    6.3948    2.5125 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2323    4.3085    1.3935 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9982    2.1412    1.2277 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7625    0.8418    0.8793 C   0  0  1  0  0  0  0  0  0  0  0  0
   -1.1039    0.0366    2.1195 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.9072    3.6469   -2.8300 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7043    4.5222   -1.8153 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1119    3.3262   -3.0826 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8068    0.6806    0.3339 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3328   -0.6479   -1.7621 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.9601   -3.5660   -1.0969 H   0  0  0  0  0  0  0  0  0  0  0  0
   -7.1509   -5.2990    0.2600 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.1988   -6.0031    2.3903 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.9787   -3.3903    1.9101 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0404   -2.6220    0.4715 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0867   -3.1662   -0.9084 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.6443   -3.1495   -1.1096 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2015   -2.5886   -4.3186 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9269   -2.9577   -2.7593 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2729   -1.3631   -3.6513 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.6999   -1.5172   -4.5087 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.8041   -1.3276   -3.2749 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.1055    0.3365   -3.2291 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.1368   -1.8231   -1.1106 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.4244   -1.7451    0.5222 H   0  0  0  0  0  0  0  0  0  0  0  0
    8.5203   -0.5957    1.1956 H   0  0  0  0  0  0  0  0  0  0  0  0
    8.7228    1.8215    0.9783 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.7504    1.9625   -0.5817 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.4178    0.6357   -1.6657 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.4523    0.2522    1.5932 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.0003   -0.4277    2.3442 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.8019   -1.2538    0.9945 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.5427    2.4850   -0.3648 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.1967    1.8986   -0.3019 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.9871    3.3940    1.6468 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.6344    1.8532    2.4402 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.2948    2.4453    4.0273 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4436    2.8898    3.5880 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2304    4.4733    0.9210 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.5149    4.5317    0.6298 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2214    0.1630    2.2479 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6823    0.4900    3.0394 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9216   -1.0299    2.0263 H   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0
  2  3  2  0
  2  4  1  0
  4  5  1  0
  5  6  1  0
  6  7  1  0
  7  8  1  0
  8  9  2  0
  8 10  1  0
 10 11  2  0
 11 12  1  0
 12 13  2  0
 13 14  1  0
 14 15  2  0
  6 16  1  0
 16 17  1  1
 16 32  1  0
 32 22  1  0
 22 21  1  0
 21 20  1  0
 20 18  2  0
 18 19  1  0
 22 23  1  0
 23 24  1  0
 24 25  2  0
 24 26  1  0
 26 27  2  0
 27 28  1  0
 28 29  2  0
 29 30  1  0
 30 31  2  0
 32 33  1  0
 33 34  1  1
 33 35  1  0
 35 36  1  0
 36 37  1  0
 37 38  1  0
 38 39  1  0
 39 40  1  0
 40 41  2  0
 40 42  1  0
 37 43  1  6
 43 44  1  0
 44 45  1  1
 44  5  1  0
 15 10  1  0
 18 16  1  0
 31 26  1  0
 44 33  1  0
 42 37  1  0
  1 46  1  0
  1 47  1  0
  1 48  1  0
  5 49  1  1
  6 50  1  6
 11 51  1  0
 12 52  1  0
 13 53  1  0
 15 54  1  0
 17 55  1  0
 17 56  1  0
 17 57  1  0
 32 69  1  6
 22 64  1  6
 21 62  1  0
 21 63  1  0
 20 61  1  0
 19 58  1  0
 19 59  1  0
 19 60  1  0
 27 65  1  0
 28 66  1  0
 29 67  1  0
 31 68  1  0
 34 70  1  0
 34 71  1  0
 34 72  1  0
 35 73  1  0
 35 74  1  0
 36 75  1  0
 36 76  1  0
 38 77  1  0
 38 78  1  0
 42 79  1  0
 42 80  1  0
 45 81  1  0
 45 82  1  0
 45 83  1  0
M  END


  Mrv1652309082223332D          

 45 50  0  0  1  0            999 V2000
    4.0145   -4.9204    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.6020   -4.2059    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.0145   -3.4914    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.7770   -4.2059    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.3645   -3.4914    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    1.5395   -3.4914    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    1.1270   -4.2059    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.5395   -4.9204    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.3645   -4.9204    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.1270   -5.6349    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.5395   -6.3493    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.1270   -7.0638    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.3020   -7.0638    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1105   -6.3493    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    0.3020   -5.6349    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.1270   -2.7770    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    0.7145   -3.4914    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.3020   -2.7770    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1105   -3.4914    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1105   -2.0625    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.3020   -1.3480    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.1270   -1.3480    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    1.5395   -0.6336    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.1270    0.0809    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.3020    0.0809    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.5395    0.7954    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.1270    1.5099    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.5395    2.2243    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.3645    2.2243    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.7770    1.5099    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    2.3645    0.7954    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.5395   -2.0625    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    2.3645   -2.0625    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    1.9520   -1.3480    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.7770   -1.3480    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.6020   -1.3480    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.0145   -2.0625    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    4.4994   -1.3951    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.2840   -1.6500    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.2840   -2.4750    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.9515   -2.9599    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.4994   -2.7299    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.6020   -2.7770    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.7770   -2.7770    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    3.1895   -3.4914    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0  0  0  0
  2  3  2  0  0  0  0
  2  4  1  0  0  0  0
  5  4  1  1  0  0  0
  5  6  1  0  0  0  0
  6  7  1  6  0  0  0
  7  8  1  0  0  0  0
  8  9  2  0  0  0  0
  8 10  1  0  0  0  0
 10 11  2  0  0  0  0
 11 12  1  0  0  0  0
 12 13  2  0  0  0  0
 13 14  1  0  0  0  0
 14 15  2  0  0  0  0
 10 15  1  0  0  0  0
  6 16  1  0  0  0  0
 16 17  1  6  0  0  0
 16 18  1  0  0  0  0
 18 19  1  0  0  0  0
 18 20  2  0  0  0  0
 20 21  1  0  0  0  0
 21 22  1  0  0  0  0
 22 23  1  1  0  0  0
 23 24  1  0  0  0  0
 24 25  2  0  0  0  0
 24 26  1  0  0  0  0
 26 27  2  0  0  0  0
 27 28  1  0  0  0  0
 28 29  2  0  0  0  0
 29 30  1  0  0  0  0
 30 31  2  0  0  0  0
 26 31  1  0  0  0  0
 32 22  1  6  0  0  0
 16 32  1  0  0  0  0
 32 33  1  0  0  0  0
 33 34  1  6  0  0  0
 33 35  1  0  0  0  0
 35 36  1  0  0  0  0
 36 37  1  0  0  0  0
 37 38  1  6  0  0  0
 38 39  1  0  0  0  0
 39 40  1  0  0  0  0
 40 41  2  0  0  0  0
 40 42  1  0  0  0  0
 37 42  1  0  0  0  0
 37 43  1  0  0  0  0
 43 44  1  0  0  0  0
  5 44  1  0  0  0  0
 33 44  1  0  0  0  0
 44 45  1  6  0  0  0
M  END
> <DATABASE_ID>
NP0274241

> <DATABASE_NAME>
NP-MRD

> <SMILES>
CC(=O)O[C@H]1[C@H](OC(=O)C2=CC=CN=C2)[C@]2(C)[C@H]([C@@H](CC=C2C)OC(=O)C2=CC=CN=C2)[C@@]2(C)CC[C@]3(COC(=O)C3)O[C@@]12C

> <INCHI_IDENTIFIER>
InChI=1S/C34H38N2O9/c1-20-10-11-24(43-29(39)22-8-6-14-35-17-22)26-31(3)12-13-34(16-25(38)41-19-34)45-33(31,5)28(42-21(2)37)27(32(20,26)4)44-30(40)23-9-7-15-36-18-23/h6-10,14-15,17-18,24,26-28H,11-13,16,19H2,1-5H3/t24-,26-,27+,28+,31-,32+,33+,34+/m1/s1

> <INCHI_KEY>
HYHZABLEZGMFII-CCZGNDFLSA-N

> <FORMULA>
C34H38N2O9

> <MOLECULAR_WEIGHT>
618.683

> <EXACT_MASS>
618.257730812

> <JCHEM_ACCEPTOR_COUNT>
7

> <JCHEM_ATOM_COUNT>
83

> <JCHEM_AVERAGE_POLARIZABILITY>
63.37508142107441

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
0

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
0

> <JCHEM_IUPAC>
(3S,4aR,5S,6R,6aR,10R,10aS,10bR)-5-(acetyloxy)-4a,6a,7,10b-tetramethyl-5'-oxo-10-(pyridine-3-carbonyloxy)-1,2,4a,5,6,6a,9,10,10a,10b-decahydrospiro[naphtho[2,1-b]pyran-3,3'-oxolane]-6-yl pyridine-3-carboxylate

> <JCHEM_LOGP>
3.4659590919999976

> <JCHEM_MDDR_LIKE_RULE>
1

> <JCHEM_NUMBER_OF_RINGS>
6

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA_STRONGEST_BASIC>
3.541375853494675

> <JCHEM_POLAR_SURFACE_AREA>
140.21

> <JCHEM_REFRACTIVITY>
158.56180000000003

> <JCHEM_ROTATABLE_BOND_COUNT>
8

> <JCHEM_RULE_OF_FIVE>
0

> <JCHEM_TRADITIONAL_IUPAC>
(3S,4aR,5S,6R,6aR,10R,10aS,10bR)-5-(acetyloxy)-4a,6a,7,10b-tetramethyl-5'-oxo-10-(pyridine-3-carbonyloxy)-2,5,6,9,10,10a-hexahydro-1H-spiro[naphtho[2,1-b]pyran-3,3'-oxolane]-6-yl pyridine-3-carboxylate

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 08-SEP-22   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   08-SEP-22         0                                  
HETATM    1  C   UNK     0       7.494  -9.185   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0       6.724  -7.851   0.000  0.00  0.00           C+0
HETATM    3  O   UNK     0       7.494  -6.517   0.000  0.00  0.00           O+0
HETATM    4  O   UNK     0       5.184  -7.851   0.000  0.00  0.00           O+0
HETATM    5  C   UNK     0       4.414  -6.517   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0       2.874  -6.517   0.000  0.00  0.00           C+0
HETATM    7  O   UNK     0       2.104  -7.851   0.000  0.00  0.00           O+0
HETATM    8  C   UNK     0       2.874  -9.185   0.000  0.00  0.00           C+0
HETATM    9  O   UNK     0       4.414  -9.185   0.000  0.00  0.00           O+0
HETATM   10  C   UNK     0       2.104 -10.518   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0       2.874 -11.852   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0       2.104 -13.186   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0       0.564 -13.186   0.000  0.00  0.00           C+0
HETATM   14  N   UNK     0      -0.206 -11.852   0.000  0.00  0.00           N+0
HETATM   15  C   UNK     0       0.564 -10.518   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0       2.104  -5.184   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0       1.334  -6.517   0.000  0.00  0.00           C+0
HETATM   18  C   UNK     0       0.564  -5.184   0.000  0.00  0.00           C+0
HETATM   19  C   UNK     0      -0.206  -6.517   0.000  0.00  0.00           C+0
HETATM   20  C   UNK     0      -0.206  -3.850   0.000  0.00  0.00           C+0
HETATM   21  C   UNK     0       0.564  -2.516   0.000  0.00  0.00           C+0
HETATM   22  C   UNK     0       2.104  -2.516   0.000  0.00  0.00           C+0
HETATM   23  O   UNK     0       2.874  -1.183   0.000  0.00  0.00           O+0
HETATM   24  C   UNK     0       2.104   0.151   0.000  0.00  0.00           C+0
HETATM   25  O   UNK     0       0.564   0.151   0.000  0.00  0.00           O+0
HETATM   26  C   UNK     0       2.874   1.485   0.000  0.00  0.00           C+0
HETATM   27  C   UNK     0       2.104   2.818   0.000  0.00  0.00           C+0
HETATM   28  C   UNK     0       2.874   4.152   0.000  0.00  0.00           C+0
HETATM   29  C   UNK     0       4.414   4.152   0.000  0.00  0.00           C+0
HETATM   30  N   UNK     0       5.184   2.818   0.000  0.00  0.00           N+0
HETATM   31  C   UNK     0       4.414   1.485   0.000  0.00  0.00           C+0
HETATM   32  C   UNK     0       2.874  -3.850   0.000  0.00  0.00           C+0
HETATM   33  C   UNK     0       4.414  -3.850   0.000  0.00  0.00           C+0
HETATM   34  C   UNK     0       3.644  -2.516   0.000  0.00  0.00           C+0
HETATM   35  C   UNK     0       5.184  -2.516   0.000  0.00  0.00           C+0
HETATM   36  C   UNK     0       6.724  -2.516   0.000  0.00  0.00           C+0
HETATM   37  C   UNK     0       7.494  -3.850   0.000  0.00  0.00           C+0
HETATM   38  C   UNK     0       8.399  -2.604   0.000  0.00  0.00           C+0
HETATM   39  O   UNK     0       9.863  -3.080   0.000  0.00  0.00           O+0
HETATM   40  C   UNK     0       9.863  -4.620   0.000  0.00  0.00           C+0
HETATM   41  O   UNK     0      11.109  -5.525   0.000  0.00  0.00           O+0
HETATM   42  C   UNK     0       8.399  -5.096   0.000  0.00  0.00           C+0
HETATM   43  O   UNK     0       6.724  -5.184   0.000  0.00  0.00           O+0
HETATM   44  C   UNK     0       5.184  -5.184   0.000  0.00  0.00           C+0
HETATM   45  C   UNK     0       5.954  -6.517   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   44                                                  
CONECT    6    5    7   16                                                  
CONECT    7    6    8                                                       
CONECT    8    7    9   10                                                  
CONECT    9    8                                                            
CONECT   10    8   11   15                                                  
CONECT   11   10   12                                                       
CONECT   12   11   13                                                       
CONECT   13   12   14                                                       
CONECT   14   13   15                                                       
CONECT   15   14   10                                                       
CONECT   16    6   17   18   32                                             
CONECT   17   16                                                            
CONECT   18   16   19   20                                                  
CONECT   19   18                                                            
CONECT   20   18   21                                                       
CONECT   21   20   22                                                       
CONECT   22   21   23   32                                                  
CONECT   23   22   24                                                       
CONECT   24   23   25   26                                                  
CONECT   25   24                                                            
CONECT   26   24   27   31                                                  
CONECT   27   26   28                                                       
CONECT   28   27   29                                                       
CONECT   29   28   30                                                       
CONECT   30   29   31                                                       
CONECT   31   30   26                                                       
CONECT   32   22   16   33                                                  
CONECT   33   32   34   35   44                                             
CONECT   34   33                                                            
CONECT   35   33   36                                                       
CONECT   36   35   37                                                       
CONECT   37   36   38   42   43                                             
CONECT   38   37   39                                                       
CONECT   39   38   40                                                       
CONECT   40   39   41   42                                                  
CONECT   41   40                                                            
CONECT   42   40   37                                                       
CONECT   43   37   44                                                       
CONECT   44   43    5   33   45                                             
CONECT   45   44                                                            
MASTER        0    0    0    0    0    0    0    0   45    0  100    0
END

View in JSmol

Synonyms

Not Available

Chemical Formula

C₃₄H₃₈N₂O₉

Average Mass

618.6830 Da

Monoisotopic Mass

618.25773 Da

IUPAC Name

(3S,4aR,5S,6R,6aR,10R,10aS,10bR)-5-(acetyloxy)-4a,6a,7,10b-tetramethyl-5'-oxo-10-(pyridine-3-carbonyloxy)-1,2,4a,5,6,6a,9,10,10a,10b-decahydrospiro[naphtho[2,1-b]pyran-3,3'-oxolane]-6-yl pyridine-3-carboxylate

Traditional Name

(3S,4aR,5S,6R,6aR,10R,10aS,10bR)-5-(acetyloxy)-4a,6a,7,10b-tetramethyl-5'-oxo-10-(pyridine-3-carbonyloxy)-2,5,6,9,10,10a-hexahydro-1H-spiro[naphtho[2,1-b]pyran-3,3'-oxolane]-6-yl pyridine-3-carboxylate

CAS Registry Number

Not Available

SMILES

CC(=O)O[C@H]1[C@H](OC(=O)C2=CC=CN=C2)[C@]2(C)[C@H]([C@@H](CC=C2C)OC(=O)C2=CC=CN=C2)[C@@]2(C)CC[C@]3(COC(=O)C3)O[C@@]12C

InChI Identifier

InChI=1S/C34H38N2O9/c1-20-10-11-24(43-29(39)22-8-6-14-35-17-22)26-31(3)12-13-34(16-25(38)41-19-34)45-33(31,5)28(42-21(2)37)27(32(20,26)4)44-30(40)23-9-7-15-36-18-23/h6-10,14-15,17-18,24,26-28H,11-13,16,19H2,1-5H3/t24-,26-,27+,28+,31-,32+,33+,34+/m1/s1

InChI Key

HYHZABLEZGMFII-CCZGNDFLSA-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
Scutellaria barbata	LOTUS Database	35616633

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as diterpene lactones. These are diterpenoids containing a lactone moiety.

Kingdom

Organic compounds

Super Class

Lipids and lipid-like molecules

Class

Prenol lipids

Sub Class

Terpene lactones

Direct Parent

Diterpene lactones

Alternative Parents

Substituents

Diterpene lactone
Diterpenoid
Clerodane diterpenoid
Naphthopyran
Tetracarboxylic acid or derivatives
Naphthalene
Pyridine carboxylic acid or derivatives
Pyridine carboxylic acid
Gamma butyrolactone
Oxane
Pyridine
Pyran
Heteroaromatic compound
Tetrahydrofuran
Carboxylic acid ester
Lactone
Carboxylic acid derivative
Dialkyl ether
Ether
Oxacycle
Azacycle
Organoheterocyclic compound
Organic oxide
Organopnictogen compound
Hydrocarbon derivative
Organic nitrogen compound
Carbonyl group
Organonitrogen compound
Organooxygen compound
Organic oxygen 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	3.47	ChemAxon
pKa (Strongest Basic)	3.54	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	7	ChemAxon
Hydrogen Donor Count	0	ChemAxon
Polar Surface Area	140.21 Å²	ChemAxon
Rotatable Bond Count	8	ChemAxon
Refractivity	158.56 m³·mol⁻¹	ChemAxon
Polarizability	63.38 Å³	ChemAxon
Number of Rings	6	ChemAxon
Bioavailability	Yes	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

59006189

KEGG Compound ID

Not Available

BioCyc ID

Not Available

BiGG ID

Not Available

Wikipedia Link

Not Available

METLIN ID

Not Available

PubChem Compound

44604898

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

LOTUS database [Link]

Showing NP-Card for (3s,4ar,5s,6r,6ar,10r,10as,10br)-5-(acetyloxy)-4a,6a,7,10b-tetramethyl-5'-oxo-10-(pyridine-3-carbonyloxy)-2,5,6,9,10,10a-hexahydro-1h-spiro[naphtho[2,1-b]pyran-3,3'-oxolan]-6-yl pyridine-3-carboxylate (NP0274241)

MOL for NP0274241 ((3s,4ar,5s,6r,6ar,10r,10as,10br)-5-(acetyloxy)-4a,6a,7,10b-tetramethyl-5'-oxo-10-(pyridine-3-carbonyloxy)-2,5,6,9,10,10a-hexahydro-1h-spiro[naphtho[2,1-b]pyran-3,3'-oxolan]-6-yl pyridine-3-carboxylate)

3D MOL for NP0274241 ((3s,4ar,5s,6r,6ar,10r,10as,10br)-5-(acetyloxy)-4a,6a,7,10b-tetramethyl-5'-oxo-10-(pyridine-3-carbonyloxy)-2,5,6,9,10,10a-hexahydro-1h-spiro[naphtho[2,1-b]pyran-3,3'-oxolan]-6-yl pyridine-3-carboxylate)

3D SDF for NP0274241 ((3s,4ar,5s,6r,6ar,10r,10as,10br)-5-(acetyloxy)-4a,6a,7,10b-tetramethyl-5'-oxo-10-(pyridine-3-carbonyloxy)-2,5,6,9,10,10a-hexahydro-1h-spiro[naphtho[2,1-b]pyran-3,3'-oxolan]-6-yl pyridine-3-carboxylate)

3D-SDF for NP0274241 ((3s,4ar,5s,6r,6ar,10r,10as,10br)-5-(acetyloxy)-4a,6a,7,10b-tetramethyl-5'-oxo-10-(pyridine-3-carbonyloxy)-2,5,6,9,10,10a-hexahydro-1h-spiro[naphtho[2,1-b]pyran-3,3'-oxolan]-6-yl pyridine-3-carboxylate)

PDB for NP0274241 ((3s,4ar,5s,6r,6ar,10r,10as,10br)-5-(acetyloxy)-4a,6a,7,10b-tetramethyl-5'-oxo-10-(pyridine-3-carbonyloxy)-2,5,6,9,10,10a-hexahydro-1h-spiro[naphtho[2,1-b]pyran-3,3'-oxolan]-6-yl pyridine-3-carboxylate)

3D PDB for NP0274241 ((3s,4ar,5s,6r,6ar,10r,10as,10br)-5-(acetyloxy)-4a,6a,7,10b-tetramethyl-5'-oxo-10-(pyridine-3-carbonyloxy)-2,5,6,9,10,10a-hexahydro-1h-spiro[naphtho[2,1-b]pyran-3,3'-oxolan]-6-yl pyridine-3-carboxylate)

SMILES for NP0274241 ((3s,4ar,5s,6r,6ar,10r,10as,10br)-5-(acetyloxy)-4a,6a,7,10b-tetramethyl-5'-oxo-10-(pyridine-3-carbonyloxy)-2,5,6,9,10,10a-hexahydro-1h-spiro[naphtho[2,1-b]pyran-3,3'-oxolan]-6-yl pyridine-3-carboxylate)

INCHI for NP0274241 ((3s,4ar,5s,6r,6ar,10r,10as,10br)-5-(acetyloxy)-4a,6a,7,10b-tetramethyl-5'-oxo-10-(pyridine-3-carbonyloxy)-2,5,6,9,10,10a-hexahydro-1h-spiro[naphtho[2,1-b]pyran-3,3'-oxolan]-6-yl pyridine-3-carboxylate)

Structure for NP0274241 ((3s,4ar,5s,6r,6ar,10r,10as,10br)-5-(acetyloxy)-4a,6a,7,10b-tetramethyl-5'-oxo-10-(pyridine-3-carbonyloxy)-2,5,6,9,10,10a-hexahydro-1h-spiro[naphtho[2,1-b]pyran-3,3'-oxolan]-6-yl pyridine-3-carboxylate)

3D Structure for NP0274241 ((3s,4ar,5s,6r,6ar,10r,10as,10br)-5-(acetyloxy)-4a,6a,7,10b-tetramethyl-5'-oxo-10-(pyridine-3-carbonyloxy)-2,5,6,9,10,10a-hexahydro-1h-spiro[naphtho[2,1-b]pyran-3,3'-oxolan]-6-yl pyridine-3-carboxylate)