NP-MRD: Showing NP-Card for 4,7,15,19,19,22-hexamethyl-12-oxo-14-oxapentacyclo[13.9.0.0³,¹³.0⁴,¹¹.0⁵,⁹]tetracosa-3(13),17,21-triene-7-carboxylic acid (NP0243418)

Jump To Section:

Identification Spectra BioTaxonomy ChemoTaxonomy Physical properties Links References XML

Record Information

Version

2.0

Created at

2022-09-07 03:57:42 UTC

Updated at

2022-09-07 03:57:43 UTC

NP-MRD ID

NP0243418

Secondary Accession Numbers

None

Natural Product Identification

Common Name

4,7,15,19,19,22-hexamethyl-12-oxo-14-oxapentacyclo[13.9.0.0³,¹³.0⁴,¹¹.0⁵,⁹]tetracosa-3(13),17,21-triene-7-carboxylic acid

Description

4,7,15,19,19,22-Hexamethyl-12-oxo-14-oxapentacyclo[13.9.0.0³,¹³.0⁴,¹¹.0⁵,⁹]Tetracosa-3(13),17,21-triene-7-carboxylic acid belongs to the class of organic compounds known as sesterterpenoids. These are terpenes composed of five consecutive isoprene units. 4,7,15,19,19,22-hexamethyl-12-oxo-14-oxapentacyclo[13.9.0.0³,¹³.0⁴,¹¹.0⁵,⁹]tetracosa-3(13),17,21-triene-7-carboxylic acid is found in Stereum hirsutum. Based on a literature review very few articles have been published on 4,7,15,19,19,22-hexamethyl-12-oxo-14-oxapentacyclo[13.9.0.0³,¹³.0⁴,¹¹.0⁵,⁹]Tetracosa-3(13),17,21-triene-7-carboxylic acid.

Structure

MOL 3D MOL SDF PDB SMILES InChI


  Mrv1652309072205572D          

 34 38  0  0  0  0            999 V2000
   10.3445    1.0174    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   10.5647    0.2224    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   11.3634    0.0156    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   11.6420   -0.8431    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   12.3377   -1.2866    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   12.7060   -0.5483    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   13.1104   -1.5757    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   12.1309   -2.0852    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   11.3074   -2.1354    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   10.6471   -2.7510    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    9.8485   -2.5443    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   10.0687   -3.3393    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    9.2701   -3.1326    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    8.4714   -2.9258    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.2511   -2.1307    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.8295   -1.5425    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    9.6282   -1.7492    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   10.2066   -1.1609    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    9.9863   -0.3659    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.4269   -2.0946    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.7160   -1.3219    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.1378   -2.8672    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.3136   -2.8310    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.0933   -2.0360    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.4478   -1.5223    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.7369   -0.7496    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.9383   -0.5428    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.8591    0.0663    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.2136    0.5801    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    6.6268    0.3685    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    6.5611   -0.7858    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.7814   -1.5808    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.7833   -3.3810    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.7471   -4.2052    0.0000 O   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
  3  4  1  4  0  0  0
  4  5  1  0  0  0  0
  5  6  1  0  0  0  0
  5  7  1  0  0  0  0
  8  5  1  4  0  0  0
  8  9  2  0  0  0  0
  9 10  1  0  0  0  0
 10 11  1  0  0  0  0
 11 12  1  0  0  0  0
 11 13  1  0  0  0  0
 13 14  1  0  0  0  0
 14 15  2  0  0  0  0
 15 16  1  0  0  0  0
 16 17  1  0  0  0  0
 11 17  1  0  0  0  0
 17 18  1  0  0  0  0
 18 19  1  0  0  0  0
  2 19  1  0  0  0  0
 15 20  1  0  0  0  0
 20 21  1  0  0  0  0
 20 22  1  0  0  0  0
 22 23  1  0  0  0  0
 23 24  1  0  0  0  0
 24 25  1  0  0  0  0
 25 26  1  0  0  0  0
 26 27  1  0  0  0  0
 26 28  1  0  0  0  0
 28 29  2  0  0  0  0
 28 30  1  0  0  0  0
 26 31  1  0  0  0  0
 31 32  1  0  0  0  0
 24 32  1  0  0  0  0
 20 32  1  0  0  0  0
 22 33  1  0  0  0  0
 14 33  1  0  0  0  0
 33 34  2  0  0  0  0
M  END

     RDKit          3D

 76 80  0  0  0  0  0  0  0  0999 V2000
   -2.7569    2.0961    3.2538 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.0097    1.6815    1.8158 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.2198    1.8199    1.3177 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.6745    1.4798   -0.0500 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.3520    0.1288   -0.1401 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.7768    0.2505    0.4386 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.5678   -0.1382   -1.6133 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.6116   -0.9657    0.5101 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.4915   -1.5461    0.1558 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6285   -1.2691   -1.0166 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1605   -1.1220   -0.6675 C   0  0  1  0  0  0  0  0  0  0  0  0
   -0.4485   -2.3451   -1.2809 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5914   -0.0151   -1.3470 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.6416    0.4502   -0.9372 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.2438   -0.0008    0.1763 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.6750   -1.1662    0.9137 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8584   -1.1673    0.7718 C   0  0  1  0  0  0  0  0  0  0  0  0
   -1.4252   -0.1534    1.6548 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8597    1.1351    1.0500 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.4368    0.7938    0.4893 C   0  0  1  0  0  0  0  0  0  0  0  0
    2.3261    1.4029    1.8949 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.7190    0.0494    0.4431 C   0  0  1  0  0  0  0  0  0  0  0  0
    3.7987   -1.0490   -0.5602 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.1948   -1.0135   -1.1512 C   0  0  1  0  0  0  0  0  0  0  0  0
    6.0203   -2.1803   -0.6677 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.1604   -1.0848   -2.6368 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.6388   -0.1637   -3.3752 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.5812   -2.2054   -3.2202 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.7855    0.3156   -0.7617 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.7060    1.0906   -0.0756 C   0  0  1  0  0  0  0  0  0  0  0  0
    3.8901    1.9407   -1.0325 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.4791    1.9072   -0.5239 C   0  0  1  0  0  0  0  0  0  0  0  0
    1.5120    1.4481   -1.5501 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.5010    1.8867   -2.7265 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7900    2.6147    3.3393 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6759    1.1539    3.8362 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5350    2.7716    3.6148 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.9779    2.2372    2.0093 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.4237    2.2969   -0.3187 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.8697    1.6456   -0.7571 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.6001    0.5284    1.5169 H   0  0  0  0  0  0  0  0  0  0  0  0
   -7.2778   -0.7288    0.4286 H   0  0  0  0  0  0  0  0  0  0  0  0
   -7.3297    1.0642   -0.0160 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.2208   -1.1716   -1.8816 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.0387    0.5879   -2.2665 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.6678   -0.1601   -1.8679 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.0721   -1.3614    1.4446 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.0883   -2.3728    0.7828 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7535   -2.1229   -1.7418 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.9830   -0.3975   -1.6263 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5692   -3.2168   -0.6192 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.5865   -2.1222   -1.5515 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9760   -2.6010   -2.2314 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.8479   -1.0627    2.0127 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.1179   -2.1111    0.6045 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1313   -2.1951    1.1578 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6936    0.0943    2.4627 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3063   -0.5776    2.2214 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1200    1.1103    0.0042 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0049    1.8716    1.1316 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.6172    0.6521    2.6675 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.3088    1.7864    2.0888 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.0400    2.2497    1.9532 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.0107   -0.2924    1.4706 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.6387   -2.0404   -0.0603 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.0915   -0.9800   -1.3847 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.9441   -2.3603    0.4135 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.6149   -3.0880   -1.1668 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.0567   -2.0382   -1.0294 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.9560   -2.1646   -4.0158 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.2017    0.8609   -1.6439 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.6560    0.2050   -0.0557 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.1211    1.7066    0.7581 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.9898    1.6123   -2.0779 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.2638    2.9805   -0.9386 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.1644    2.8445   -0.0362 H   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0
  2  3  2  0
  3  4  1  0
  4  5  1  0
  5  6  1  0
  5  7  1  0
  5  8  1  0
  8  9  2  0
  9 10  1  0
 10 11  1  0
 11 12  1  6
 11 13  1  0
 13 14  1  0
 14 15  2  0
 15 16  1  0
 16 17  1  0
 17 18  1  0
 18 19  1  0
 15 20  1  0
 20 21  1  1
 20 22  1  0
 22 23  1  0
 23 24  1  0
 24 25  1  0
 24 29  1  0
 29 30  1  0
 30 31  1  0
 31 32  1  0
 32 33  1  0
 33 34  2  0
 24 26  1  6
 26 28  1  0
 26 27  2  0
 19  2  1  0
 32 20  1  0
 17 11  1  0
 30 22  1  0
 33 14  1  0
  1 35  1  0
  1 36  1  0
  1 37  1  0
  3 38  1  0
  4 39  1  0
  4 40  1  0
  6 41  1  0
  6 42  1  0
  6 43  1  0
  7 44  1  0
  7 45  1  0
  7 46  1  0
  8 47  1  0
  9 48  1  0
 10 49  1  0
 10 50  1  0
 12 51  1  0
 12 52  1  0
 12 53  1  0
 16 54  1  0
 16 55  1  0
 17 56  1  1
 18 57  1  0
 18 58  1  0
 19 59  1  0
 19 60  1  0
 21 61  1  0
 21 62  1  0
 21 63  1  0
 22 64  1  1
 23 65  1  0
 23 66  1  0
 25 67  1  0
 25 68  1  0
 25 69  1  0
 29 71  1  0
 29 72  1  0
 30 73  1  1
 31 74  1  0
 31 75  1  0
 32 76  1  1
 28 70  1  0
M  END


  Mrv1652309072205572D          

 34 38  0  0  0  0            999 V2000
   10.3445    1.0174    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   10.5647    0.2224    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   11.3634    0.0156    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   11.6420   -0.8431    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   12.3377   -1.2866    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   12.7060   -0.5483    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   13.1104   -1.5757    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   12.1309   -2.0852    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   11.3074   -2.1354    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   10.6471   -2.7510    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    9.8485   -2.5443    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   10.0687   -3.3393    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    9.2701   -3.1326    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    8.4714   -2.9258    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.2511   -2.1307    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.8295   -1.5425    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    9.6282   -1.7492    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   10.2066   -1.1609    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    9.9863   -0.3659    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.4269   -2.0946    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.7160   -1.3219    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.1378   -2.8672    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.3136   -2.8310    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.0933   -2.0360    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.4478   -1.5223    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.7369   -0.7496    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.9383   -0.5428    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.8591    0.0663    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.2136    0.5801    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    6.6268    0.3685    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    6.5611   -0.7858    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.7814   -1.5808    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.7833   -3.3810    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.7471   -4.2052    0.0000 O   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
  3  4  1  4  0  0  0
  4  5  1  0  0  0  0
  5  6  1  0  0  0  0
  5  7  1  0  0  0  0
  8  5  1  4  0  0  0
  8  9  2  0  0  0  0
  9 10  1  0  0  0  0
 10 11  1  0  0  0  0
 11 12  1  0  0  0  0
 11 13  1  0  0  0  0
 13 14  1  0  0  0  0
 14 15  2  0  0  0  0
 15 16  1  0  0  0  0
 16 17  1  0  0  0  0
 11 17  1  0  0  0  0
 17 18  1  0  0  0  0
 18 19  1  0  0  0  0
  2 19  1  0  0  0  0
 15 20  1  0  0  0  0
 20 21  1  0  0  0  0
 20 22  1  0  0  0  0
 22 23  1  0  0  0  0
 23 24  1  0  0  0  0
 24 25  1  0  0  0  0
 25 26  1  0  0  0  0
 26 27  1  0  0  0  0
 26 28  1  0  0  0  0
 28 29  2  0  0  0  0
 28 30  1  0  0  0  0
 26 31  1  0  0  0  0
 31 32  1  0  0  0  0
 24 32  1  0  0  0  0
 20 32  1  0  0  0  0
 22 33  1  0  0  0  0
 14 33  1  0  0  0  0
 33 34  2  0  0  0  0
M  END
> <DATABASE_ID>
NP0243418

> <DATABASE_NAME>
NP-MRD

> <SMILES>
CC1=CCC(C)(C)C=CCC2(C)OC3=C(CC2CC1)C1(C)C2CC(C)(CC2CC1C3=O)C(O)=O

> <INCHI_IDENTIFIER>
InChI=1S/C30H42O4/c1-18-8-9-20-15-22-25(34-29(20,5)12-7-11-27(2,3)13-10-18)24(31)21-14-19-16-28(4,26(32)33)17-23(19)30(21,22)6/h7,10-11,19-21,23H,8-9,12-17H2,1-6H3,(H,32,33)

> <INCHI_KEY>
HWSXFPLTMMDVHW-UHFFFAOYSA-N

> <FORMULA>
C30H42O4

> <MOLECULAR_WEIGHT>
466.662

> <EXACT_MASS>
466.308309832

> <JCHEM_ACCEPTOR_COUNT>
4

> <JCHEM_ATOM_COUNT>
76

> <JCHEM_AVERAGE_POLARIZABILITY>
54.1643603387596

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
1

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
0

> <JCHEM_IUPAC>
4,7,15,19,19,22-hexamethyl-12-oxo-14-oxapentacyclo[13.9.0.0^{3,13}.0^{4,11}.0^{5,9}]tetracosa-3(13),17,21-triene-7-carboxylic acid

> <JCHEM_LOGP>
6.189468054666665

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
5

> <JCHEM_PHYSIOLOGICAL_CHARGE>
-1

> <JCHEM_PKA_STRONGEST_ACIDIC>
4.127609983477838

> <JCHEM_PKA_STRONGEST_BASIC>
-4.955285079097261

> <JCHEM_POLAR_SURFACE_AREA>
63.6

> <JCHEM_REFRACTIVITY>
137.03889999999998

> <JCHEM_ROTATABLE_BOND_COUNT>
1

> <JCHEM_RULE_OF_FIVE>
0

> <JCHEM_TRADITIONAL_IUPAC>
4,7,15,19,19,22-hexamethyl-12-oxo-14-oxapentacyclo[13.9.0.0^{3,13}.0^{4,11}.0^{5,9}]tetracosa-3(13),17,21-triene-7-carboxylic acid

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 07-SEP-22   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   07-SEP-22         0                                  
HETATM    1  C   UNK     0      19.310   1.899   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0      19.721   0.415   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0      21.212   0.029   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0      21.732  -1.574   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0      23.030  -2.402   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0      23.718  -1.024   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0      24.473  -2.941   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0      22.644  -3.892   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0      21.107  -3.986   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0      19.875  -5.135   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0      18.384  -4.749   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0      18.795  -6.233   0.000  0.00  0.00           C+0
HETATM   13  O   UNK     0      17.304  -5.847   0.000  0.00  0.00           O+0
HETATM   14  C   UNK     0      15.813  -5.461   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0      15.402  -3.977   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0      16.482  -2.879   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0      17.973  -3.265   0.000  0.00  0.00           C+0
HETATM   18  C   UNK     0      19.052  -2.167   0.000  0.00  0.00           C+0
HETATM   19  C   UNK     0      18.641  -0.683   0.000  0.00  0.00           C+0
HETATM   20  C   UNK     0      13.864  -3.910   0.000  0.00  0.00           C+0
HETATM   21  C   UNK     0      14.403  -2.467   0.000  0.00  0.00           C+0
HETATM   22  C   UNK     0      13.324  -5.352   0.000  0.00  0.00           C+0
HETATM   23  C   UNK     0      11.785  -5.285   0.000  0.00  0.00           C+0
HETATM   24  C   UNK     0      11.374  -3.801   0.000  0.00  0.00           C+0
HETATM   25  C   UNK     0      10.169  -2.842   0.000  0.00  0.00           C+0
HETATM   26  C   UNK     0      10.709  -1.399   0.000  0.00  0.00           C+0
HETATM   27  C   UNK     0       9.218  -1.013   0.000  0.00  0.00           C+0
HETATM   28  C   UNK     0      10.937   0.124   0.000  0.00  0.00           C+0
HETATM   29  O   UNK     0       9.732   1.083   0.000  0.00  0.00           O+0
HETATM   30  O   UNK     0      12.370   0.688   0.000  0.00  0.00           O+0
HETATM   31  C   UNK     0      12.247  -1.467   0.000  0.00  0.00           C+0
HETATM   32  C   UNK     0      12.659  -2.951   0.000  0.00  0.00           C+0
HETATM   33  C   UNK     0      14.529  -6.311   0.000  0.00  0.00           C+0
HETATM   34  O   UNK     0      14.461  -7.850   0.000  0.00  0.00           O+0
CONECT    1    2                                                            
CONECT    2    1    3   19                                                  
CONECT    3    2    4                                                       
CONECT    4    3    5                                                       
CONECT    5    4    6    7    8                                             
CONECT    6    5                                                            
CONECT    7    5                                                            
CONECT    8    5    9                                                       
CONECT    9    8   10                                                       
CONECT   10    9   11                                                       
CONECT   11   10   12   13   17                                             
CONECT   12   11                                                            
CONECT   13   11   14                                                       
CONECT   14   13   15   33                                                  
CONECT   15   14   16   20                                                  
CONECT   16   15   17                                                       
CONECT   17   16   11   18                                                  
CONECT   18   17   19                                                       
CONECT   19   18    2                                                       
CONECT   20   15   21   22   32                                             
CONECT   21   20                                                            
CONECT   22   20   23   33                                                  
CONECT   23   22   24                                                       
CONECT   24   23   25   32                                                  
CONECT   25   24   26                                                       
CONECT   26   25   27   28   31                                             
CONECT   27   26                                                            
CONECT   28   26   29   30                                                  
CONECT   29   28                                                            
CONECT   30   28                                                            
CONECT   31   26   32                                                       
CONECT   32   31   24   20                                                  
CONECT   33   22   14   34                                                  
CONECT   34   33                                                            
MASTER        0    0    0    0    0    0    0    0   34    0   76    0
END

View in JSmol

Synonyms

Value	Source
4,7,15,19,19,22-Hexamethyl-12-oxo-14-oxapentacyclo[13.9.0.0,.0,.0,]tetracosa-3(13),17,21-triene-7-carboxylate	Generator

Chemical Formula

C₃₀H₄₂O₄

Average Mass

466.6620 Da

Monoisotopic Mass

466.30831 Da

IUPAC Name

Not Available

Traditional Name

Not Available

CAS Registry Number

Not Available

SMILES

CC1=CCC(C)(C)C=CCC2(C)OC3=C(CC2CC1)C1(C)C2CC(C)(CC2CC1C3=O)C(O)=O

InChI Identifier

InChI=1S/C30H42O4/c1-18-8-9-20-15-22-25(34-29(20,5)12-7-11-27(2,3)13-10-18)24(31)21-14-19-16-28(4,26(32)33)17-23(19)30(21,22)6/h7,10-11,19-21,23H,8-9,12-17H2,1-6H3,(H,32,33)

InChI Key

HWSXFPLTMMDVHW-UHFFFAOYSA-N

Experimental Spectra

Not Available

Predicted Spectra

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

Chemical Shift Submissions

Not Available

Species

Species of Origin

Species Name	Source	Reference
Stereum hirsutum	LOTUS Database	35616633

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as sesterterpenoids. These are terpenes composed of five consecutive isoprene units.

Kingdom

Organic compounds

Super Class

Lipids and lipid-like molecules

Class

Prenol lipids

Sub Class

Sesterterpenoids

Direct Parent

Sesterterpenoids

Alternative Parents

Substituents

Sesterterpenoid
Ketone
Oxacycle
Organoheterocyclic compound
Monocarboxylic acid or derivatives
Carboxylic acid
Carboxylic acid derivative
Organic oxygen compound
Organic oxide
Hydrocarbon derivative
Organooxygen compound
Carbonyl group
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

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

162885846

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

LOTUS database [Link]

Showing NP-Card for 4,7,15,19,19,22-hexamethyl-12-oxo-14-oxapentacyclo[13.9.0.0³,¹³.0⁴,¹¹.0⁵,⁹]tetracosa-3(13),17,21-triene-7-carboxylic acid (NP0243418)

MOL for NP0243418 (4,7,15,19,19,22-hexamethyl-12-oxo-14-oxapentacyclo[13.9.0.0³,¹³.0⁴,¹¹.0⁵,⁹]tetracosa-3(13),17,21-triene-7-carboxylic acid)

3D MOL for NP0243418 (4,7,15,19,19,22-hexamethyl-12-oxo-14-oxapentacyclo[13.9.0.0³,¹³.0⁴,¹¹.0⁵,⁹]tetracosa-3(13),17,21-triene-7-carboxylic acid)

3D SDF for NP0243418 (4,7,15,19,19,22-hexamethyl-12-oxo-14-oxapentacyclo[13.9.0.0³,¹³.0⁴,¹¹.0⁵,⁹]tetracosa-3(13),17,21-triene-7-carboxylic acid)

3D-SDF for NP0243418 (4,7,15,19,19,22-hexamethyl-12-oxo-14-oxapentacyclo[13.9.0.0³,¹³.0⁴,¹¹.0⁵,⁹]tetracosa-3(13),17,21-triene-7-carboxylic acid)

PDB for NP0243418 (4,7,15,19,19,22-hexamethyl-12-oxo-14-oxapentacyclo[13.9.0.0³,¹³.0⁴,¹¹.0⁵,⁹]tetracosa-3(13),17,21-triene-7-carboxylic acid)

3D PDB for NP0243418 (4,7,15,19,19,22-hexamethyl-12-oxo-14-oxapentacyclo[13.9.0.0³,¹³.0⁴,¹¹.0⁵,⁹]tetracosa-3(13),17,21-triene-7-carboxylic acid)

SMILES for NP0243418 (4,7,15,19,19,22-hexamethyl-12-oxo-14-oxapentacyclo[13.9.0.0³,¹³.0⁴,¹¹.0⁵,⁹]tetracosa-3(13),17,21-triene-7-carboxylic acid)

INCHI for NP0243418 (4,7,15,19,19,22-hexamethyl-12-oxo-14-oxapentacyclo[13.9.0.0³,¹³.0⁴,¹¹.0⁵,⁹]tetracosa-3(13),17,21-triene-7-carboxylic acid)

Structure for NP0243418 (4,7,15,19,19,22-hexamethyl-12-oxo-14-oxapentacyclo[13.9.0.0³,¹³.0⁴,¹¹.0⁵,⁹]tetracosa-3(13),17,21-triene-7-carboxylic acid)

3D Structure for NP0243418 (4,7,15,19,19,22-hexamethyl-12-oxo-14-oxapentacyclo[13.9.0.0³,¹³.0⁴,¹¹.0⁵,⁹]tetracosa-3(13),17,21-triene-7-carboxylic acid)