NP-MRD: Showing NP-Card for methyl (1r,2z,5r,6s,9r,10s,13e,15s,16s,19s,22r,26s,27e,29s)-5,10-dihydroxy-19-isopropyl-1,5,9,13,22,26-hexamethyl-18,21-dioxo-31,32-dioxapentacyclo[26.2.1.1⁶,⁹.0²,¹⁵.0¹⁶,²⁹]dotriaconta-2,13,27-triene-16-carboxylate (NP0305610)

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Record Information

Version

2.0

Created at

2022-09-10 21:35:35 UTC

Updated at

2022-09-10 21:35:35 UTC

NP-MRD ID

NP0305610

Secondary Accession Numbers

None

Natural Product Identification

Common Name

methyl (1r,2z,5r,6s,9r,10s,13e,15s,16s,19s,22r,26s,27e,29s)-5,10-dihydroxy-19-isopropyl-1,5,9,13,22,26-hexamethyl-18,21-dioxo-31,32-dioxapentacyclo[26.2.1.1⁶,⁹.0²,¹⁵.0¹⁶,²⁹]dotriaconta-2,13,27-triene-16-carboxylate

Description

Methyl (1R,5R,6S,9R,10S,13E,15S,16S,19S,22R,26S,29S)-5,10-dihydroxy-1,5,9,13,22,26-hexamethyl-18,21-dioxo-19-(propan-2-yl)-31,32-dioxapentacyclo[26.2.1.1⁶,⁹.0²,¹⁵.0¹⁶,²⁹]Dotriaconta-2,13,27-triene-16-carboxylate belongs to the class of organic compounds known as sesquaterpenoids. These are terpenoids with at least 7 consecutive isoprene units. methyl (1r,2z,5r,6s,9r,10s,13e,15s,16s,19s,22r,26s,27e,29s)-5,10-dihydroxy-19-isopropyl-1,5,9,13,22,26-hexamethyl-18,21-dioxo-31,32-dioxapentacyclo[26.2.1.1⁶,⁹.0²,¹⁵.0¹⁶,²⁹]dotriaconta-2,13,27-triene-16-carboxylate is found in Sarcophyton tortuosum. Based on a literature review very few articles have been published on methyl (1R,5R,6S,9R,10S,13E,15S,16S,19S,22R,26S,29S)-5,10-dihydroxy-1,5,9,13,22,26-hexamethyl-18,21-dioxo-19-(propan-2-yl)-31,32-dioxapentacyclo[26.2.1.1⁶,⁹.0²,¹⁵.0¹⁶,²⁹]Dotriaconta-2,13,27-triene-16-carboxylate.

Structure

MOL 3D MOL SDF PDB SMILES InChI


  Mrv1652309102223352D          

 49 53  0  0  1  0            999 V2000
    4.3255   -1.5473    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.7958   -0.9148    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.0787   -0.1398    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.6716   -0.7134    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.5490    0.4927    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    3.3180   -0.3645    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.0475   -1.1833    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.6255   -1.7720    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.2370   -1.4348    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    2.1481   -2.2550    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.3933   -2.5882    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8140   -2.7421    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.5033   -1.0179    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.8289   -0.5175    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.2322   -1.0872    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.3596    0.1803    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
   -0.4012   -0.1387    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.1910    1.0036    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.3669    1.8234    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.8244    2.5224    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.5126    2.9963    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    1.4051    3.8143    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.3008    2.7160    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.9305    2.1507    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.6762    2.6065    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.3600    2.0559    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    4.9819    2.5980    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.7909    1.6447    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.1439    1.2898    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    4.8106    1.3062    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.6343    1.3518    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.0067    2.0880    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.8304    2.1336    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    6.6425    2.9369    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.5889    2.4582    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    7.2818    1.4430    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    8.0793    1.2318    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.1249    0.4081    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.3608    0.0163    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    7.9457   -0.5655    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.9094    0.7068    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    6.9884   -0.7199    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    7.4546   -1.4005    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    6.0900   -0.8089    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.5083   -1.3940    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.7722   -1.0216    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.6455   -1.8368    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.8988   -0.2064    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.4382    0.5700    0.0000 C   0  0  2  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
  5  3  1  6  0  0  0
  5  6  1  0  0  0  0
  6  7  1  0  0  0  0
  7  8  2  0  0  0  0
  7  9  1  0  0  0  0
  9 10  1  6  0  0  0
 10 11  1  0  0  0  0
 10 12  1  0  0  0  0
  9 13  1  0  0  0  0
 13 14  1  0  0  0  0
 14 15  2  0  0  0  0
 14 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
 19 20  1  0  0  0  0
 20 21  1  0  0  0  0
 21 22  1  6  0  0  0
 21 23  1  0  0  0  0
 23 24  2  0  0  0  0
 24 25  1  0  0  0  0
 25 26  1  0  0  0  0
 26 27  1  6  0  0  0
 26 28  1  0  0  0  0
 29 28  1  6  0  0  0
 24 29  1  0  0  0  0
  5 29  1  0  0  0  0
 26 30  1  0  0  0  0
 30 31  2  0  0  0  0
 31 32  1  0  0  0  0
 32 33  1  0  0  0  0
 33 34  1  6  0  0  0
 33 35  1  1  0  0  0
 33 36  1  0  0  0  0
 36 37  1  0  0  0  0
 37 38  1  0  0  0  0
 38 39  1  0  0  0  0
 39 40  1  1  0  0  0
 39 41  1  0  0  0  0
 36 41  1  6  0  0  0
 39 42  1  0  0  0  0
 42 43  1  1  0  0  0
 42 44  1  0  0  0  0
 44 45  1  0  0  0  0
 45 46  1  0  0  0  0
 46 47  1  0  0  0  0
 46 48  2  0  0  0  0
 48 49  1  0  0  0  0
 49 30  1  6  0  0  0
  5 49  1  0  0  0  0
M  END

     RDKit          3D

111115  0  0  0  0  0  0  0  0999 V2000
   -0.5489    1.3839   -3.3731 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3612    0.8991   -2.0596 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7405    1.6686   -0.9954 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2450    2.7863   -1.2726 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5795    1.2450    0.4036 C   0  0  2  0  0  0  0  0  0  0  0  0
   -1.1588   -0.1124    0.7370 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1777   -1.0914   -0.3628 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1784   -1.3538   -0.9876 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4465   -1.7971   -0.7355 C   0  0  2  0  0  0  0  0  0  0  0  0
   -2.2338   -3.2968   -0.5579 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8766   -3.6333    0.8830 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.3814   -4.1345   -1.0009 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.9026   -1.5122   -2.1298 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.9786   -0.5066   -2.2513 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.7530    0.5170   -2.8575 O   0  0  0  0  0  0  0  0  0  0  0  0
   -5.3114   -0.7123   -1.6611 C   0  0  2  0  0  0  0  0  0  0  0  0
   -6.4027   -0.4611   -2.6964 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.6355    0.1174   -0.4694 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.5411    1.6030   -0.6860 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.1846    2.0954   -0.1755 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.1941    2.5530    1.2372 C   0  0  2  0  0  0  0  0  0  0  0  0
   -3.9416    4.0547    1.3048 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.4306    1.7931    2.2135 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1165    1.6672    2.2447 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1710    1.0146    3.0573 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.0653    1.7282    3.0183 C   0  0  2  0  0  0  0  0  0  0  0  0
    0.5595    2.1049    4.3692 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2998    2.9613    2.2507 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2568    2.3181    1.2350 C   0  0  1  0  0  0  0  0  0  0  0  0
    1.0906    1.0330    2.1791 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.0715    0.4279    2.8237 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.2813    0.0272    2.0944 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.4334   -1.4884    2.0618 C   0  0  1  0  0  0  0  0  0  0  0  0
    3.8474   -1.9740    3.4485 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.2451   -2.1144    1.7273 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.4920   -1.9250    1.1043 C   0  0  2  0  0  0  0  0  0  0  0  0
    5.7985   -1.2146    1.2265 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.3062   -1.2228   -0.2208 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.1816   -1.7914   -1.0260 C   0  0  1  0  0  0  0  0  0  0  0  0
    5.5434   -3.1738   -1.5667 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.0744   -1.8614   -0.2184 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.8543   -0.9409   -2.2379 C   0  0  1  0  0  0  0  0  0  0  0  0
    4.0833   -1.6152   -3.1594 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.2888    0.3717   -1.8166 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.7756    0.3502   -1.6788 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.3327    1.6781   -1.2149 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.5280    2.8199   -2.1806 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.7981    1.9683   -0.0280 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.9093    1.0828    0.7244 C   0  0  2  0  0  0  0  0  0  0  0  0
    0.4356    1.5709   -3.8910 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1017    0.6307   -3.9495 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1161    2.3376   -3.3793 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1842   -0.0351    1.1602 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5694   -0.5549    1.6144 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.2712   -1.5467   -0.0392 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3462   -3.5548   -1.1721 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8023   -3.8595    1.4510 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2218   -4.5294    0.8514 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2852   -2.8066    1.2798 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.2568   -5.1272   -0.4620 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.3726   -3.7903   -0.7099 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.3075   -4.4505   -2.0838 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0241   -1.2282   -2.7885 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.2216   -2.4992   -2.5883 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.4718   -1.7856   -1.3492 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.0733    0.4229   -3.2845 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.4554   -1.3728   -3.3361 H   0  0  0  0  0  0  0  0  0  0  0  0
   -7.3424   -0.2461   -2.1760 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.0960   -0.1286    0.4562 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.7155   -0.0826   -0.2318 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.7508    1.9092   -1.7136 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.2964    2.1427   -0.0452 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5105    1.2576   -0.2719 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.9351    2.9378   -0.8930 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.2809    2.4537    1.5528 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.6397    4.4592    0.2930 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.2055    4.3397    2.0579 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.8645    4.6390    1.5414 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.9199    1.2376    3.0409 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.5383    2.6070    4.2449 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1302    2.8601    4.7941 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.6036    1.2642    5.0878 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9009    3.5804    2.9491 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.4683    3.5696    1.8484 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7024    3.1100    0.6612 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.0385    0.2022    3.8875 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.1468    0.3669    2.7454 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.4514    0.5077    1.1381 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.9700   -2.2051    4.0709 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.4559   -1.1978    3.9365 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.5119   -2.8727    3.3609 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.4288   -3.0091    1.3160 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.6541   -3.0258    1.3014 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.7281   -0.1862    1.6026 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.5126   -1.7743    1.8853 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.1973   -1.8750   -0.2592 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.5689   -0.1841   -0.5329 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.6521   -3.8282   -1.6166 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.3067   -3.6582   -0.9229 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.9837   -3.1235   -2.5803 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.8519   -0.7263   -2.7225 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.3569   -1.3564   -4.0787 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.7446    0.7093   -0.8698 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.5151    1.1368   -2.5916 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.3937    0.2268   -2.7241 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.4164   -0.5058   -1.1181 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.5269    3.1740   -2.4846 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.0530    2.5195   -3.0907 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.0625    3.6048   -1.6057 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.1079    2.9709    0.3487 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.1784    0.0416    0.3609 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
  5  3  1  6
  5  6  1  0
  6  7  1  0
  7  8  2  0
  7  9  1  0
  9 13  1  0
 13 14  1  0
 14 15  2  0
 14 16  1  0
 16 17  1  0
 16 18  1  0
 18 19  1  0
 19 20  1  0
 20 21  1  0
 21 22  1  0
 21 23  1  0
 23 24  2  0
 24 25  1  0
 25 26  1  0
 26 27  1  1
 26 28  1  0
 28 29  1  0
 26 30  1  0
 30 31  2  0
 31 32  1  0
 32 33  1  0
 33 34  1  0
 33 35  1  6
 33 36  1  0
 36 37  1  0
 37 38  1  0
 38 39  1  0
 39 40  1  6
 39 41  1  0
 39 42  1  0
 42 43  1  0
 42 44  1  0
 44 45  1  0
 45 46  1  0
 46 47  1  0
 46 48  2  0
 48 49  1  0
  9 10  1  0
 10 11  1  0
 10 12  1  0
 29  5  1  0
 49 30  1  0
 49  5  1  0
 29 24  1  0
 41 36  1  0
  1 50  1  0
  1 51  1  0
  1 52  1  0
  6 53  1  0
  6 54  1  0
  9 55  1  1
 13 63  1  0
 13 64  1  0
 16 65  1  1
 17 66  1  0
 17 67  1  0
 17 68  1  0
 18 69  1  0
 18 70  1  0
 19 71  1  0
 19 72  1  0
 20 73  1  0
 20 74  1  0
 21 75  1  1
 22 76  1  0
 22 77  1  0
 22 78  1  0
 23 79  1  0
 27 80  1  0
 27 81  1  0
 27 82  1  0
 28 83  1  0
 28 84  1  0
 29 85  1  6
 31 86  1  0
 32 87  1  0
 32 88  1  0
 34 89  1  0
 34 90  1  0
 34 91  1  0
 35 92  1  0
 36 93  1  1
 37 94  1  0
 37 95  1  0
 38 96  1  0
 38 97  1  0
 40 98  1  0
 40 99  1  0
 40100  1  0
 42101  1  6
 43102  1  0
 44103  1  0
 44104  1  0
 45105  1  0
 45106  1  0
 47107  1  0
 47108  1  0
 47109  1  0
 48110  1  0
 49111  1  6
 10 56  1  0
 11 57  1  0
 11 58  1  0
 11 59  1  0
 12 60  1  0
 12 61  1  0
 12 62  1  0
M  END


  Mrv1652309102223352D          

 49 53  0  0  1  0            999 V2000
    4.3255   -1.5473    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.7958   -0.9148    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.0787   -0.1398    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.6716   -0.7134    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.5490    0.4927    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    3.3180   -0.3645    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.0475   -1.1833    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.6255   -1.7720    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.2370   -1.4348    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    2.1481   -2.2550    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.3933   -2.5882    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8140   -2.7421    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.5033   -1.0179    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.8289   -0.5175    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.2322   -1.0872    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.3596    0.1803    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
   -0.4012   -0.1387    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.1910    1.0036    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.3669    1.8234    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.8244    2.5224    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.5126    2.9963    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    1.4051    3.8143    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.3008    2.7160    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.9305    2.1507    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.6762    2.6065    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.3600    2.0559    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    4.9819    2.5980    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.7909    1.6447    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.1439    1.2898    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    4.8106    1.3062    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.6343    1.3518    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.0067    2.0880    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.8304    2.1336    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    6.6425    2.9369    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.5889    2.4582    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    7.2818    1.4430    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    8.0793    1.2318    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.1249    0.4081    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.3608    0.0163    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    7.9457   -0.5655    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.9094    0.7068    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    6.9884   -0.7199    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    7.4546   -1.4005    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    6.0900   -0.8089    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.5083   -1.3940    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.7722   -1.0216    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.6455   -1.8368    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.8988   -0.2064    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.4382    0.5700    0.0000 C   0  0  2  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
  5  3  1  6  0  0  0
  5  6  1  0  0  0  0
  6  7  1  0  0  0  0
  7  8  2  0  0  0  0
  7  9  1  0  0  0  0
  9 10  1  6  0  0  0
 10 11  1  0  0  0  0
 10 12  1  0  0  0  0
  9 13  1  0  0  0  0
 13 14  1  0  0  0  0
 14 15  2  0  0  0  0
 14 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
 19 20  1  0  0  0  0
 20 21  1  0  0  0  0
 21 22  1  6  0  0  0
 21 23  1  0  0  0  0
 23 24  2  0  0  0  0
 24 25  1  0  0  0  0
 25 26  1  0  0  0  0
 26 27  1  6  0  0  0
 26 28  1  0  0  0  0
 29 28  1  6  0  0  0
 24 29  1  0  0  0  0
  5 29  1  0  0  0  0
 26 30  1  0  0  0  0
 30 31  2  0  0  0  0
 31 32  1  0  0  0  0
 32 33  1  0  0  0  0
 33 34  1  6  0  0  0
 33 35  1  1  0  0  0
 33 36  1  0  0  0  0
 36 37  1  0  0  0  0
 37 38  1  0  0  0  0
 38 39  1  0  0  0  0
 39 40  1  1  0  0  0
 39 41  1  0  0  0  0
 36 41  1  6  0  0  0
 39 42  1  0  0  0  0
 42 43  1  1  0  0  0
 42 44  1  0  0  0  0
 44 45  1  0  0  0  0
 45 46  1  0  0  0  0
 46 47  1  0  0  0  0
 46 48  2  0  0  0  0
 48 49  1  0  0  0  0
 49 30  1  6  0  0  0
  5 49  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0305610

> <DATABASE_NAME>
NP-MRD

> <SMILES>
COC(=O)[C@]12CC(=O)[C@@H](CC(=O)[C@H](C)CCC[C@H](C)\C=C3\O[C@](C)(C[C@@H]13)\C1=C/C[C@@](C)(O)[C@@H]3CC[C@@](C)(O3)[C@@H](O)CCC(C)=C[C@H]21)C(C)C

> <INCHI_IDENTIFIER>
InChI=1S/C41H62O8/c1-24(2)28-21-32(42)27(5)12-10-11-25(3)20-34-31-22-40(8,48-34)29-15-17-38(6,46)36-16-18-39(7,49-36)35(44)14-13-26(4)19-30(29)41(31,23-33(28)43)37(45)47-9/h15,19-20,24-25,27-28,30-31,35-36,44,46H,10-14,16-18,21-23H2,1-9H3/b26-19+,29-15-,34-20+/t25-,27+,28-,30-,31+,35-,36-,38+,39+,40+,41-/m0/s1

> <INCHI_KEY>
UGVMXCQHHHCDCW-VMLNHRRJSA-N

> <FORMULA>
C41H62O8

> <MOLECULAR_WEIGHT>
682.939

> <EXACT_MASS>
682.444468956

> <JCHEM_ACCEPTOR_COUNT>
7

> <JCHEM_ATOM_COUNT>
111

> <JCHEM_AVERAGE_POLARIZABILITY>
77.08566218482919

> <JCHEM_BIOAVAILABILITY>
0

> <JCHEM_DONOR_COUNT>
2

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
0

> <JCHEM_IUPAC>
methyl (1R,5R,6S,9R,10S,13E,15S,16S,19S,22R,26S,27E,29S)-5,10-dihydroxy-1,5,9,13,22,26-hexamethyl-18,21-dioxo-19-(propan-2-yl)-31,32-dioxapentacyclo[26.2.1.1^{6,9}.0^{2,15}.0^{16,29}]dotriaconta-2,13,27-triene-16-carboxylate

> <JCHEM_LOGP>
6.009108157

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
5

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA>
14.287788314281336

> <JCHEM_PKA_STRONGEST_ACIDIC>
13.688117187630468

> <JCHEM_PKA_STRONGEST_BASIC>
-3.239850895613288

> <JCHEM_POLAR_SURFACE_AREA>
119.36000000000001

> <JCHEM_REFRACTIVITY>
193.11380000000003

> <JCHEM_ROTATABLE_BOND_COUNT>
3

> <JCHEM_RULE_OF_FIVE>
0

> <JCHEM_TRADITIONAL_IUPAC>
methyl (1R,5R,6S,9R,10S,13E,15S,16S,19S,22R,26S,27E,29S)-5,10-dihydroxy-19-isopropyl-1,5,9,13,22,26-hexamethyl-18,21-dioxo-31,32-dioxapentacyclo[26.2.1.1^{6,9}.0^{2,15}.0^{16,29}]dotriaconta-2,13,27-triene-16-carboxylate

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 10-SEP-22   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   10-SEP-22         0                                  
HETATM    1  C   UNK     0       8.074  -2.888   0.000  0.00  0.00           C+0
HETATM    2  O   UNK     0       7.086  -1.708   0.000  0.00  0.00           O+0
HETATM    3  C   UNK     0       7.614  -0.261   0.000  0.00  0.00           C+0
HETATM    4  O   UNK     0       8.720  -1.332   0.000  0.00  0.00           O+0
HETATM    5  C   UNK     0       6.625   0.920   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0       6.194  -0.680   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0       5.689  -2.209   0.000  0.00  0.00           C+0
HETATM    8  O   UNK     0       6.768  -3.308   0.000  0.00  0.00           O+0
HETATM    9  C   UNK     0       4.176  -2.678   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0       4.010  -4.209   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0       2.601  -4.831   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0       5.253  -5.119   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0       2.806  -1.900   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0       1.547  -0.966   0.000  0.00  0.00           C+0
HETATM   15  O   UNK     0       0.433  -2.029   0.000  0.00  0.00           O+0
HETATM   16  C   UNK     0       0.671   0.336   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0      -0.749  -0.259   0.000  0.00  0.00           C+0
HETATM   18  C   UNK     0       0.357   1.873   0.000  0.00  0.00           C+0
HETATM   19  C   UNK     0       0.685   3.404   0.000  0.00  0.00           C+0
HETATM   20  C   UNK     0       1.539   4.708   0.000  0.00  0.00           C+0
HETATM   21  C   UNK     0       2.824   5.593   0.000  0.00  0.00           C+0
HETATM   22  C   UNK     0       2.623   7.120   0.000  0.00  0.00           C+0
HETATM   23  C   UNK     0       4.295   5.070   0.000  0.00  0.00           C+0
HETATM   24  C   UNK     0       5.470   4.015   0.000  0.00  0.00           C+0
HETATM   25  O   UNK     0       6.862   4.866   0.000  0.00  0.00           O+0
HETATM   26  C   UNK     0       8.139   3.838   0.000  0.00  0.00           C+0
HETATM   27  C   UNK     0       9.300   4.850   0.000  0.00  0.00           C+0
HETATM   28  C   UNK     0       7.076   3.070   0.000  0.00  0.00           C+0
HETATM   29  C   UNK     0       5.869   2.408   0.000  0.00  0.00           C+0
HETATM   30  C   UNK     0       8.980   2.438   0.000  0.00  0.00           C+0
HETATM   31  C   UNK     0      10.517   2.523   0.000  0.00  0.00           C+0
HETATM   32  C   UNK     0      11.212   3.898   0.000  0.00  0.00           C+0
HETATM   33  C   UNK     0      12.750   3.983   0.000  0.00  0.00           C+0
HETATM   34  C   UNK     0      12.399   5.482   0.000  0.00  0.00           C+0
HETATM   35  O   UNK     0      14.166   4.589   0.000  0.00  0.00           O+0
HETATM   36  C   UNK     0      13.593   2.694   0.000  0.00  0.00           C+0
HETATM   37  C   UNK     0      15.081   2.299   0.000  0.00  0.00           C+0
HETATM   38  C   UNK     0      15.166   0.762   0.000  0.00  0.00           C+0
HETATM   39  C   UNK     0      13.740   0.030   0.000  0.00  0.00           C+0
HETATM   40  C   UNK     0      14.832  -1.056   0.000  0.00  0.00           C+0
HETATM   41  O   UNK     0      12.898   1.319   0.000  0.00  0.00           O+0
HETATM   42  C   UNK     0      13.045  -1.344   0.000  0.00  0.00           C+0
HETATM   43  O   UNK     0      13.915  -2.614   0.000  0.00  0.00           O+0
HETATM   44  C   UNK     0      11.368  -1.510   0.000  0.00  0.00           C+0
HETATM   45  C   UNK     0      10.282  -2.602   0.000  0.00  0.00           C+0
HETATM   46  C   UNK     0       8.908  -1.907   0.000  0.00  0.00           C+0
HETATM   47  C   UNK     0       8.672  -3.429   0.000  0.00  0.00           C+0
HETATM   48  C   UNK     0       9.144  -0.385   0.000  0.00  0.00           C+0
HETATM   49  C   UNK     0       8.285   1.064   0.000  0.00  0.00           C+0
CONECT    1    2                                                            
CONECT    2    1    3                                                       
CONECT    3    2    4    5                                                  
CONECT    4    3                                                            
CONECT    5    3    6   29   49                                             
CONECT    6    5    7                                                       
CONECT    7    6    8    9                                                  
CONECT    8    7                                                            
CONECT    9    7   10   13                                                  
CONECT   10    9   11   12                                                  
CONECT   11   10                                                            
CONECT   12   10                                                            
CONECT   13    9   14                                                       
CONECT   14   13   15   16                                                  
CONECT   15   14                                                            
CONECT   16   14   17   18                                                  
CONECT   17   16                                                            
CONECT   18   16   19                                                       
CONECT   19   18   20                                                       
CONECT   20   19   21                                                       
CONECT   21   20   22   23                                                  
CONECT   22   21                                                            
CONECT   23   21   24                                                       
CONECT   24   23   25   29                                                  
CONECT   25   24   26                                                       
CONECT   26   25   27   28   30                                             
CONECT   27   26                                                            
CONECT   28   26   29                                                       
CONECT   29   28   24    5                                                  
CONECT   30   26   31   49                                                  
CONECT   31   30   32                                                       
CONECT   32   31   33                                                       
CONECT   33   32   34   35   36                                             
CONECT   34   33                                                            
CONECT   35   33                                                            
CONECT   36   33   37   41                                                  
CONECT   37   36   38                                                       
CONECT   38   37   39                                                       
CONECT   39   38   40   41   42                                             
CONECT   40   39                                                            
CONECT   41   39   36                                                       
CONECT   42   39   43   44                                                  
CONECT   43   42                                                            
CONECT   44   42   45                                                       
CONECT   45   44   46                                                       
CONECT   46   45   47   48                                                  
CONECT   47   46                                                            
CONECT   48   46   49                                                       
CONECT   49   48   30    5                                                  
MASTER        0    0    0    0    0    0    0    0   49    0  106    0
END

View in JSmol

Synonyms

Value	Source
Methyl (1R,5R,6S,9R,10S,13E,15S,16S,19S,22R,26S,29S)-5,10-dihydroxy-1,5,9,13,22,26-hexamethyl-18,21-dioxo-19-(propan-2-yl)-31,32-dioxapentacyclo[26.2.1.1,.0,.0,]dotriaconta-2,13,27-triene-16-carboxylic acid	Generator

Chemical Formula

C₄₁H₆₂O₈

Average Mass

682.9390 Da

Monoisotopic Mass

682.44447 Da

IUPAC Name

methyl (1R,5R,6S,9R,10S,13E,15S,16S,19S,22R,26S,27E,29S)-5,10-dihydroxy-1,5,9,13,22,26-hexamethyl-18,21-dioxo-19-(propan-2-yl)-31,32-dioxapentacyclo[26.2.1.1^{6,9}.0^{2,15}.0^{16,29}]dotriaconta-2,13,27-triene-16-carboxylate

Traditional Name

methyl (1R,5R,6S,9R,10S,13E,15S,16S,19S,22R,26S,27E,29S)-5,10-dihydroxy-19-isopropyl-1,5,9,13,22,26-hexamethyl-18,21-dioxo-31,32-dioxapentacyclo[26.2.1.1^{6,9}.0^{2,15}.0^{16,29}]dotriaconta-2,13,27-triene-16-carboxylate

CAS Registry Number

Not Available

SMILES

COC(=O)[C@]12CC(=O)[C@@H](CC(=O)[C@H](C)CCC[C@H](C)\C=C3\O[C@](C)(C[C@@H]13)\C1=C/C[C@@](C)(O)[C@@H]3CC[C@@](C)(O3)[C@@H](O)CCC(C)=C[C@H]21)C(C)C

InChI Identifier

InChI=1S/C41H62O8/c1-24(2)28-21-32(42)27(5)12-10-11-25(3)20-34-31-22-40(8,48-34)29-15-17-38(6,46)36-16-18-39(7,49-36)35(44)14-13-26(4)19-30(29)41(31,23-33(28)43)37(45)47-9/h15,19-20,24-25,27-28,30-31,35-36,44,46H,10-14,16-18,21-23H2,1-9H3/b26-19+,29-15-,34-20+/t25-,27+,28-,30-,31+,35-,36-,38+,39+,40+,41-/m0/s1

InChI Key

UGVMXCQHHHCDCW-VMLNHRRJSA-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
Sarcophyton tortuosum	LOTUS Database	35616633

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as sesquaterpenoids. These are terpenoids with at least 7 consecutive isoprene units.

Kingdom

Organic compounds

Super Class

Lipids and lipid-like molecules

Class

Prenol lipids

Sub Class

Sesquaterpenoids

Direct Parent

Sesquaterpenoids

Alternative Parents

Substituents

Sesquaterpenoid
Oxepane
Tertiary alcohol
Tetrahydrofuran
Methyl ester
Carboxylic acid ester
Ketone
Secondary alcohol
Cyclic ketone
Monocarboxylic acid or derivatives
Ether
Dialkyl ether
Oxacycle
Organoheterocyclic compound
Carboxylic acid derivative
Organic oxide
Carbonyl group
Organic oxygen compound
Organooxygen compound
Alcohol
Hydrocarbon derivative
Aliphatic heteropolycyclic compound

Molecular Framework

Aliphatic 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	6.01	ChemAxon
pKa (Strongest Acidic)	13.69	ChemAxon
pKa (Strongest Basic)	-3.2	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	7	ChemAxon
Hydrogen Donor Count	2	ChemAxon
Polar Surface Area	119.36 Å²	ChemAxon
Rotatable Bond Count	3	ChemAxon
Refractivity	193.11 m³·mol⁻¹	ChemAxon
Polarizability	77.09 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	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

163189450

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

LOTUS database [Link]

Showing NP-Card for methyl (1r,2z,5r,6s,9r,10s,13e,15s,16s,19s,22r,26s,27e,29s)-5,10-dihydroxy-19-isopropyl-1,5,9,13,22,26-hexamethyl-18,21-dioxo-31,32-dioxapentacyclo[26.2.1.1⁶,⁹.0²,¹⁵.0¹⁶,²⁹]dotriaconta-2,13,27-triene-16-carboxylate (NP0305610)

MOL for NP0305610 (methyl (1r,2z,5r,6s,9r,10s,13e,15s,16s,19s,22r,26s,27e,29s)-5,10-dihydroxy-19-isopropyl-1,5,9,13,22,26-hexamethyl-18,21-dioxo-31,32-dioxapentacyclo[26.2.1.1⁶,⁹.0²,¹⁵.0¹⁶,²⁹]dotriaconta-2,13,27-triene-16-carboxylate)

3D MOL for NP0305610 (methyl (1r,2z,5r,6s,9r,10s,13e,15s,16s,19s,22r,26s,27e,29s)-5,10-dihydroxy-19-isopropyl-1,5,9,13,22,26-hexamethyl-18,21-dioxo-31,32-dioxapentacyclo[26.2.1.1⁶,⁹.0²,¹⁵.0¹⁶,²⁹]dotriaconta-2,13,27-triene-16-carboxylate)

3D SDF for NP0305610 (methyl (1r,2z,5r,6s,9r,10s,13e,15s,16s,19s,22r,26s,27e,29s)-5,10-dihydroxy-19-isopropyl-1,5,9,13,22,26-hexamethyl-18,21-dioxo-31,32-dioxapentacyclo[26.2.1.1⁶,⁹.0²,¹⁵.0¹⁶,²⁹]dotriaconta-2,13,27-triene-16-carboxylate)

3D-SDF for NP0305610 (methyl (1r,2z,5r,6s,9r,10s,13e,15s,16s,19s,22r,26s,27e,29s)-5,10-dihydroxy-19-isopropyl-1,5,9,13,22,26-hexamethyl-18,21-dioxo-31,32-dioxapentacyclo[26.2.1.1⁶,⁹.0²,¹⁵.0¹⁶,²⁹]dotriaconta-2,13,27-triene-16-carboxylate)

PDB for NP0305610 (methyl (1r,2z,5r,6s,9r,10s,13e,15s,16s,19s,22r,26s,27e,29s)-5,10-dihydroxy-19-isopropyl-1,5,9,13,22,26-hexamethyl-18,21-dioxo-31,32-dioxapentacyclo[26.2.1.1⁶,⁹.0²,¹⁵.0¹⁶,²⁹]dotriaconta-2,13,27-triene-16-carboxylate)

3D PDB for NP0305610 (methyl (1r,2z,5r,6s,9r,10s,13e,15s,16s,19s,22r,26s,27e,29s)-5,10-dihydroxy-19-isopropyl-1,5,9,13,22,26-hexamethyl-18,21-dioxo-31,32-dioxapentacyclo[26.2.1.1⁶,⁹.0²,¹⁵.0¹⁶,²⁹]dotriaconta-2,13,27-triene-16-carboxylate)

SMILES for NP0305610 (methyl (1r,2z,5r,6s,9r,10s,13e,15s,16s,19s,22r,26s,27e,29s)-5,10-dihydroxy-19-isopropyl-1,5,9,13,22,26-hexamethyl-18,21-dioxo-31,32-dioxapentacyclo[26.2.1.1⁶,⁹.0²,¹⁵.0¹⁶,²⁹]dotriaconta-2,13,27-triene-16-carboxylate)

INCHI for NP0305610 (methyl (1r,2z,5r,6s,9r,10s,13e,15s,16s,19s,22r,26s,27e,29s)-5,10-dihydroxy-19-isopropyl-1,5,9,13,22,26-hexamethyl-18,21-dioxo-31,32-dioxapentacyclo[26.2.1.1⁶,⁹.0²,¹⁵.0¹⁶,²⁹]dotriaconta-2,13,27-triene-16-carboxylate)

Structure for NP0305610 (methyl (1r,2z,5r,6s,9r,10s,13e,15s,16s,19s,22r,26s,27e,29s)-5,10-dihydroxy-19-isopropyl-1,5,9,13,22,26-hexamethyl-18,21-dioxo-31,32-dioxapentacyclo[26.2.1.1⁶,⁹.0²,¹⁵.0¹⁶,²⁹]dotriaconta-2,13,27-triene-16-carboxylate)

3D Structure for NP0305610 (methyl (1r,2z,5r,6s,9r,10s,13e,15s,16s,19s,22r,26s,27e,29s)-5,10-dihydroxy-19-isopropyl-1,5,9,13,22,26-hexamethyl-18,21-dioxo-31,32-dioxapentacyclo[26.2.1.1⁶,⁹.0²,¹⁵.0¹⁶,²⁹]dotriaconta-2,13,27-triene-16-carboxylate)