NP-MRD: Showing NP-Card for 9-[(2-hydroxy-3-methylpent-3-enoyl)oxy]-7-(2-hydroxypropan-2-yl)-6-(3-methoxy-3-oxopropyl)-3a,6,9a-trimethyl-3-[5-(2-methylprop-1-en-1-yl)oxolan-3-yl]-2h,3h,4h,5h,5ah,7h,8h,9h-cyclopenta[a]naphthalen-5-yl 2-hydroxy-3-methylpent-3-enoate (NP0306440)

Jump To Section:

Identification Spectra BioTaxonomy ChemoTaxonomy Physical properties Links References XML

Record Information

Version

2.0

Created at

2022-09-10 22:54:48 UTC

Updated at

2022-09-10 22:54:48 UTC

NP-MRD ID

NP0306440

Secondary Accession Numbers

None

Natural Product Identification

Common Name

9-[(2-hydroxy-3-methylpent-3-enoyl)oxy]-7-(2-hydroxypropan-2-yl)-6-(3-methoxy-3-oxopropyl)-3a,6,9a-trimethyl-3-[5-(2-methylprop-1-en-1-yl)oxolan-3-yl]-2h,3h,4h,5h,5ah,7h,8h,9h-cyclopenta[a]naphthalen-5-yl 2-hydroxy-3-methylpent-3-enoate

Description

9-[(2-Hydroxy-3-methylpent-3-enoyl)oxy]-7-(2-hydroxypropan-2-yl)-6-(3-methoxy-3-oxopropyl)-3a,6,9a-trimethyl-3-[5-(2-methylprop-1-en-1-yl)oxolan-3-yl]-2H,3H,3aH,4H,5H,5aH,6H,7H,8H,9H,9aH-cyclopenta[a]naphthalen-5-yl 2-hydroxy-3-methylpent-3-enoate belongs to the class of organic compounds known as sesquiterpenoids. These are terpenes with three consecutive isoprene units. 9-[(2-hydroxy-3-methylpent-3-enoyl)oxy]-7-(2-hydroxypropan-2-yl)-6-(3-methoxy-3-oxopropyl)-3a,6,9a-trimethyl-3-[5-(2-methylprop-1-en-1-yl)oxolan-3-yl]-2h,3h,4h,5h,5ah,7h,8h,9h-cyclopenta[a]naphthalen-5-yl 2-hydroxy-3-methylpent-3-enoate is found in Aglaia argentea. 9-[(2-Hydroxy-3-methylpent-3-enoyl)oxy]-7-(2-hydroxypropan-2-yl)-6-(3-methoxy-3-oxopropyl)-3a,6,9a-trimethyl-3-[5-(2-methylprop-1-en-1-yl)oxolan-3-yl]-2H,3H,3aH,4H,5H,5aH,6H,7H,8H,9H,9aH-cyclopenta[a]naphthalen-5-yl 2-hydroxy-3-methylpent-3-enoate is an extremely weak basic (essentially neutral) compound (based on its pKa).

Structure

MOL 3D MOL SDF PDB SMILES InChI


  Mrv1533004261504532D          

 53 56  0  0  0  0            999 V2000
    5.4603   -3.8368    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.6289   -3.0293    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.0138   -2.4795    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.2301   -2.7373    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.1823   -1.6719    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.5672   -1.1221    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.7358   -0.3145    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.5018   -0.6207    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.1704    0.3867    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.7804    1.1137    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.9558    1.1395    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5658    1.8665    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.0004    2.5677    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.8250    2.5420    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.6104    3.2948    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.7858    3.3205    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.0450    3.9960    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.6551    4.7230    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.0897    5.4242    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.8696    3.9702    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5212    0.4383    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.1312    1.1653    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.9112   -0.2887    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.4766   -0.9900    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.6520   -0.9642    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.2620   -0.2372    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.7565   -0.8892    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4608   -0.0406    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4002    0.7822    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1640    1.0941    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.6966    0.4640    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.8307   -0.5732    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.8913   -1.3960    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.1275   -1.7078    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4051   -1.0778    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0295   -0.3765    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2279   -1.1384    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6917   -0.4561    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5145   -0.5167    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3328    0.2867    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.8666   -1.7170    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.4319   -2.4182    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.6073   -2.3925    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.8219   -3.1452    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.6465   -3.1710    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.3873   -3.8465    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.7773   -4.5735    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.3427   -5.2747    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.5627   -3.8207    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.9950    0.3610    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.0207    1.1856    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.9692   -0.4636    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.8196    0.3352    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0  0  0  0
  2  3  1  0  0  0  0
  3  4  2  0  0  0  0
  3  5  1  0  0  0  0
  5  6  1  0  0  0  0
  6  7  1  0  0  0  0
  7  8  1  0  0  0  0
  7  9  1  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
 12 13  1  0  0  0  0
 13 14  2  0  0  0  0
 13 15  1  0  0  0  0
 15 16  1  0  0  0  0
 15 17  1  0  0  0  0
 17 18  2  0  0  0  0
 18 19  1  4  0  0  0
 17 20  1  0  0  0  0
 11 21  1  0  0  0  0
 21 22  1  0  0  0  0
 21 23  1  0  0  0  0
  7 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  1  0  0  0  0
 29 30  1  0  0  0  0
 30 31  2  0  0  0  0
 21 31  1  0  0  0  0
 26 31  1  0  0  0  0
 28 32  1  0  0  0  0
 32 33  1  0  0  0  0
 33 34  1  0  0  0  0
 34 35  1  0  0  0  0
 35 36  1  0  0  0  0
 32 36  1  0  0  0  0
 35 37  1  0  0  0  0
 37 38  2  0  0  0  0
 38 39  1  0  0  0  0
 38 40  1  0  0  0  0
 24 41  1  0  0  0  0
 41 42  1  0  0  0  0
 42 43  2  0  0  0  0
 42 44  1  0  0  0  0
 44 45  1  0  0  0  0
 44 46  1  0  0  0  0
 46 47  2  0  0  0  0
 47 48  1  4  0  0  0
 46 49  1  0  0  0  0
  9 50  1  0  0  0  0
 50 51  1  0  0  0  0
 50 52  1  0  0  0  0
 50 53  1  0  0  0  0
M  END

     RDKit          3D

119122  0  0  0  0  0  0  0  0999 V2000
   -2.3579   -6.5595    3.3715 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8565   -6.5386    3.3579 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1870   -5.7297    2.5454 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.2941   -5.7217    2.5388 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9302   -4.8433    1.6471 C   0  0  2  0  0  0  0  0  0  0  0  0
   -0.6170   -5.1958    0.3384 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6456   -3.3937    1.8520 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8269   -2.8198    2.9530 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1684   -2.5768    0.8688 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.1487   -1.2463    0.8664 C   0  0  1  0  0  0  0  0  0  0  0  0
    1.7326   -1.1188    0.9396 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.0099    0.2519    1.4214 C   0  0  2  0  0  0  0  0  0  0  0  0
    1.5633    0.2769    2.9012 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.1941    1.3075    0.7835 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.8925    2.4331    0.8687 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.1866    2.2448    1.5211 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.3843    0.7372    1.3775 C   0  0  2  0  0  0  0  0  0  0  0  0
    4.3039    0.4984    0.2887 C   0  0  2  0  0  0  0  0  0  0  0  0
    3.9401    0.9112   -1.0838 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.2051   -0.1975   -1.9223 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.2951   -0.8475   -1.3380 C   0  0  1  0  0  0  0  0  0  0  0  0
    6.4815    0.0240   -1.4681 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.6711   -0.4375   -1.1316 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.9099    0.3969   -1.2409 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.8531   -1.8178   -0.6252 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.9036   -0.8721    0.1272 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1805    1.0702    0.1875 C   0  0  2  0  0  0  0  0  0  0  0  0
   -1.1160    1.5874    1.2341 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2442   -0.3382   -0.2014 C   0  0  2  0  0  0  0  0  0  0  0  0
   -1.5277   -0.7223   -1.0296 C   0  0  1  0  0  0  0  0  0  0  0  0
   -1.0780   -2.1476   -1.4793 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6132   -0.9669   -0.1001 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.8295   -1.7187   -0.2321 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.9087   -1.4859   -1.1657 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.0010   -2.2653   -2.1870 O   0  0  0  0  0  0  0  0  0  0  0  0
   -5.8677   -0.4847   -1.0520 O   0  0  0  0  0  0  0  0  0  0  0  0
   -6.8549   -0.4136   -2.0608 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5262    0.1257   -2.2187 C   0  0  1  0  0  0  0  0  0  0  0  0
   -2.7245    0.6284   -2.9064 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.7088    1.4955   -2.2807 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1956    1.4683   -4.1107 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.2916   -0.4451   -3.6729 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3984    1.1851   -2.2382 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2789    2.0134   -1.0058 C   0  0  1  0  0  0  0  0  0  0  0  0
   -1.3001    2.9563   -0.8500 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1878    4.3128   -0.9326 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0549    4.7989   -1.1775 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3686    5.1851   -0.7396 C   0  0  2  0  0  0  0  0  0  0  0  0
   -2.0198    6.5398   -0.8935 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.9710    5.0549    0.5906 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2414    5.3434    1.8587 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.2283    4.6637    0.6995 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.9392    4.4983    2.0063 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7842   -6.7749    2.3821 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6913   -7.3310    4.0798 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7653   -5.5974    3.7478 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2913   -7.1869    4.0168 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.7173   -4.6983    2.3817 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.6872   -6.3324    1.6958 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.7247   -6.1208    3.4782 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0278   -4.9461    1.8419 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4113   -5.2870   -0.2479 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1045   -0.8316    1.8655 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.0119   -1.3676   -0.0804 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.0611   -1.8493    1.6971 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.4994   -0.7599    3.3008 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.6141    0.8266    3.0338 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.3270    0.7991    3.5095 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.5602    3.4046    0.5004 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.0361    2.7701    1.0562 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.0669    2.4564    2.5953 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.8911    0.3971    2.3397 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.2262    1.1419    0.5351 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.5331    1.7481   -1.4999 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.8854    1.1587   -1.2487 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.3832   -1.8288   -1.7982 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.3992    1.0363   -1.8357 H   0  0  0  0  0  0  0  0  0  0  0  0
    9.7590   -0.2464   -1.5420 H   0  0  0  0  0  0  0  0  0  0  0  0
    8.7787    1.1796   -2.0175 H   0  0  0  0  0  0  0  0  0  0  0  0
    9.1706    0.8676   -0.2510 H   0  0  0  0  0  0  0  0  0  0  0  0
    8.1106   -1.8420    0.4567 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.0107   -2.4850   -0.7982 H   0  0  0  0  0  0  0  0  0  0  0  0
    8.7138   -2.2434   -1.1981 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.8673   -0.9904    0.6812 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.2855   -1.7090    0.4258 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9651    2.0700    0.7202 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5211    0.8421    1.9283 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6530    2.4567    1.8047 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.5606   -0.4471   -0.9988 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2721   -2.2414   -2.5782 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.0094   -2.1666   -1.4038 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5061   -2.9350   -0.8903 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.0355    0.0533    0.3176 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1080   -1.2638    0.9054 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.6892   -2.8535   -0.2518 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.3747   -1.6480    0.8043 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.3857   -0.5961   -3.0665 H   0  0  0  0  0  0  0  0  0  0  0  0
   -7.5934   -1.2378   -1.8880 H   0  0  0  0  0  0  0  0  0  0  0  0
   -7.3584    0.5713   -2.0152 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0948   -0.5057   -3.1045 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.9429    1.4412   -1.2348 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5583    2.6057   -2.5030 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.6996    1.3334   -2.8156 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1161    2.5246   -3.8645 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.0278    1.4539   -4.9023 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3647    0.9783   -4.6139 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.0242    0.0059   -4.1839 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.5501    0.6656   -2.4184 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5231    1.8569   -3.0980 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.6540    2.6019   -1.1723 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.1317    4.9803   -1.5087 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2179    6.7636   -0.3272 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1492    5.2610    1.7489 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5428    6.3929    2.1471 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5736    4.6972    2.6946 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.8509    4.4270   -0.1823 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.0119    4.7721    1.8943 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.5423    5.2043    2.7750 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.9079    3.4737    2.3773 H   0  0  0  0  0  0  0  0  0  0  0  0
 37 36  1  0
 36 34  1  0
 34 35  2  0
 34 33  1  0
 33 32  1  0
 30 32  1  1
 30 31  1  0
 30 38  1  0
 38 43  1  0
 43 44  1  0
 44 45  1  0
 45 46  1  0
 46 47  2  0
 46 48  1  0
 48 49  1  0
 48 50  1  0
 50 51  1  0
 50 52  2  0
 52 53  1  0
 44 27  1  0
 27 28  1  1
 27 29  1  0
 29 10  1  0
 10 11  1  0
 11 12  1  0
 12 13  1  1
 12 17  1  0
 17 16  1  0
 16 15  1  0
 15 14  2  0
 17 18  1  0
 18 19  1  0
 19 20  1  0
 20 21  1  0
 21 26  1  0
 21 22  1  0
 22 23  2  3
 23 24  1  0
 23 25  1  0
 10  9  1  0
  9  7  1  0
  7  8  2  0
  7  5  1  0
  5  6  1  0
  5  3  1  0
  3  4  1  0
  3  2  2  0
  2  1  1  0
 38 39  1  0
 39 40  1  0
 39 41  1  0
 39 42  1  0
 29 30  1  0
 14 12  1  0
 26 18  1  0
 14 27  1  0
 37 97  1  0
 37 98  1  0
 37 99  1  0
 33 95  1  0
 33 96  1  0
 32 93  1  0
 32 94  1  0
 31 90  1  0
 31 91  1  0
 31 92  1  0
 38100  1  6
 43108  1  0
 43109  1  0
 44110  1  6
 48111  1  6
 49112  1  0
 51113  1  0
 51114  1  0
 51115  1  0
 52116  1  0
 53117  1  0
 53118  1  0
 53119  1  0
 28 86  1  0
 28 87  1  0
 28 88  1  0
 29 89  1  6
 10 63  1  1
 11 64  1  0
 11 65  1  0
 13 66  1  0
 13 67  1  0
 13 68  1  0
 17 72  1  1
 16 70  1  0
 16 71  1  0
 15 69  1  0
 18 73  1  1
 19 74  1  0
 19 75  1  0
 21 76  1  6
 26 84  1  0
 26 85  1  0
 22 77  1  0
 24 78  1  0
 24 79  1  0
 24 80  1  0
 25 81  1  0
 25 82  1  0
 25 83  1  0
  5 61  1  6
  6 62  1  0
  4 58  1  0
  4 59  1  0
  4 60  1  0
  2 57  1  0
  1 54  1  0
  1 55  1  0
  1 56  1  0
 40101  1  0
 40102  1  0
 40103  1  0
 41104  1  0
 41105  1  0
 41106  1  0
 42107  1  0
M  END


  Mrv1533004261504532D          

 53 56  0  0  0  0            999 V2000
    5.4603   -3.8368    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.6289   -3.0293    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.0138   -2.4795    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.2301   -2.7373    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.1823   -1.6719    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.5672   -1.1221    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.7358   -0.3145    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.5018   -0.6207    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.1704    0.3867    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.7804    1.1137    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.9558    1.1395    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5658    1.8665    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.0004    2.5677    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.8250    2.5420    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.6104    3.2948    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.7858    3.3205    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.0450    3.9960    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.6551    4.7230    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.0897    5.4242    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.8696    3.9702    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5212    0.4383    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.1312    1.1653    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.9112   -0.2887    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.4766   -0.9900    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.6520   -0.9642    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.2620   -0.2372    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.7565   -0.8892    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4608   -0.0406    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4002    0.7822    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1640    1.0941    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.6966    0.4640    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.8307   -0.5732    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.8913   -1.3960    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.1275   -1.7078    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4051   -1.0778    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0295   -0.3765    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2279   -1.1384    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6917   -0.4561    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5145   -0.5167    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3328    0.2867    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.8666   -1.7170    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.4319   -2.4182    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.6073   -2.3925    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.8219   -3.1452    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.6465   -3.1710    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.3873   -3.8465    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.7773   -4.5735    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.3427   -5.2747    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.5627   -3.8207    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.9950    0.3610    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.0207    1.1856    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.9692   -0.4636    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.8196    0.3352    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0  0  0  0
  2  3  1  0  0  0  0
  3  4  2  0  0  0  0
  3  5  1  0  0  0  0
  5  6  1  0  0  0  0
  6  7  1  0  0  0  0
  7  8  1  0  0  0  0
  7  9  1  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
 12 13  1  0  0  0  0
 13 14  2  0  0  0  0
 13 15  1  0  0  0  0
 15 16  1  0  0  0  0
 15 17  1  0  0  0  0
 17 18  2  0  0  0  0
 18 19  1  4  0  0  0
 17 20  1  0  0  0  0
 11 21  1  0  0  0  0
 21 22  1  0  0  0  0
 21 23  1  0  0  0  0
  7 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  1  0  0  0  0
 29 30  1  0  0  0  0
 30 31  2  0  0  0  0
 21 31  1  0  0  0  0
 26 31  1  0  0  0  0
 28 32  1  0  0  0  0
 32 33  1  0  0  0  0
 33 34  1  0  0  0  0
 34 35  1  0  0  0  0
 35 36  1  0  0  0  0
 32 36  1  0  0  0  0
 35 37  1  0  0  0  0
 37 38  2  0  0  0  0
 38 39  1  0  0  0  0
 38 40  1  0  0  0  0
 24 41  1  0  0  0  0
 41 42  1  0  0  0  0
 42 43  2  0  0  0  0
 42 44  1  0  0  0  0
 44 45  1  0  0  0  0
 44 46  1  0  0  0  0
 46 47  2  0  0  0  0
 47 48  1  4  0  0  0
 46 49  1  0  0  0  0
  9 50  1  0  0  0  0
 50 51  1  0  0  0  0
 50 52  1  0  0  0  0
 50 53  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0306440

> <DATABASE_NAME>
NP-MRD

> <SMILES>
COC(=O)CCC1(C)C(CC(OC(=O)C(O)C(C)=CC)C2(C)C1C(CC1(C)C(CC=C21)C1COC(C1)C=C(C)C)OC(=O)C(O)C(C)=CC)C(C)(C)O

> <INCHI_IDENTIFIER>
InChI=1S/C43H66O10/c1-13-25(5)35(45)38(47)52-30-22-42(10)29(27-20-28(51-23-27)19-24(3)4)15-16-31(42)43(11)33(53-39(48)36(46)26(6)14-2)21-32(40(7,8)49)41(9,37(30)43)18-17-34(44)50-12/h13-14,16,19,27-30,32-33,35-37,45-46,49H,15,17-18,20-23H2,1-12H3

> <INCHI_KEY>
WPEKKKYUGODPOL-UHFFFAOYSA-N

> <FORMULA>
C43H66O10

> <MOLECULAR_WEIGHT>
742.991

> <EXACT_MASS>
742.465598325

> <JCHEM_ACCEPTOR_COUNT>
7

> <JCHEM_ATOM_COUNT>
119

> <JCHEM_AVERAGE_POLARIZABILITY>
84.27900902445074

> <JCHEM_BIOAVAILABILITY>
0

> <JCHEM_DONOR_COUNT>
3

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
0

> <JCHEM_IUPAC>
9-[(2-hydroxy-3-methylpent-3-enoyl)oxy]-7-(2-hydroxypropan-2-yl)-6-(3-methoxy-3-oxopropyl)-3a,6,9a-trimethyl-3-[5-(2-methylprop-1-en-1-yl)oxolan-3-yl]-2H,3H,3aH,4H,5H,5aH,6H,7H,8H,9H,9aH-cyclopenta[a]naphthalen-5-yl 2-hydroxy-3-methylpent-3-enoate

> <ALOGPS_LOGP>
5.77

> <JCHEM_LOGP>
5.448631434333333

> <ALOGPS_LOGS>
-5.77

> <JCHEM_MDDR_LIKE_RULE>
1

> <JCHEM_NUMBER_OF_RINGS>
4

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA>
12.446243285051281

> <JCHEM_PKA_STRONGEST_ACIDIC>
11.84472805803006

> <JCHEM_PKA_STRONGEST_BASIC>
-2.7783994391364777

> <JCHEM_POLAR_SURFACE_AREA>
148.82

> <JCHEM_REFRACTIVITY>
205.81700000000012

> <JCHEM_ROTATABLE_BOND_COUNT>
15

> <JCHEM_RULE_OF_FIVE>
0

> <ALOGPS_SOLUBILITY>
1.26e-03 g/l

> <JCHEM_TRADITIONAL_IUPAC>
9-[(2-hydroxy-3-methylpent-3-enoyl)oxy]-7-(2-hydroxypropan-2-yl)-6-(3-methoxy-3-oxopropyl)-3a,6,9a-trimethyl-3-[5-(2-methylprop-1-en-1-yl)oxolan-3-yl]-2H,3H,4H,5H,5aH,7H,8H,9H-cyclopenta[a]naphthalen-5-yl 2-hydroxy-3-methylpent-3-enoate

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 26-APR-15   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   26-APR-15         0                                  
HETATM    1  C   UNK     0      10.193  -7.162   0.000  0.00  0.00           C+0
HETATM    2  O   UNK     0      10.507  -5.655   0.000  0.00  0.00           O+0
HETATM    3  C   UNK     0       9.359  -4.628   0.000  0.00  0.00           C+0
HETATM    4  O   UNK     0       7.896  -5.110   0.000  0.00  0.00           O+0
HETATM    5  C   UNK     0       9.674  -3.121   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0       8.525  -2.095   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0       8.840  -0.587   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0      10.270  -1.159   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0       9.651   0.722   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0       8.923   2.079   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0       7.384   2.127   0.000  0.00  0.00           C+0
HETATM   12  O   UNK     0       6.656   3.484   0.000  0.00  0.00           O+0
HETATM   13  C   UNK     0       7.467   4.793   0.000  0.00  0.00           C+0
HETATM   14  O   UNK     0       9.007   4.745   0.000  0.00  0.00           O+0
HETATM   15  C   UNK     0       6.739   6.150   0.000  0.00  0.00           C+0
HETATM   16  O   UNK     0       5.200   6.198   0.000  0.00  0.00           O+0
HETATM   17  C   UNK     0       7.551   7.459   0.000  0.00  0.00           C+0
HETATM   18  C   UNK     0       6.823   8.816   0.000  0.00  0.00           C+0
HETATM   19  C   UNK     0       7.634  10.125   0.000  0.00  0.00           C+0
HETATM   20  C   UNK     0       9.090   7.411   0.000  0.00  0.00           C+0
HETATM   21  C   UNK     0       6.573   0.818   0.000  0.00  0.00           C+0
HETATM   22  C   UNK     0       5.845   2.175   0.000  0.00  0.00           C+0
HETATM   23  C   UNK     0       7.301  -0.539   0.000  0.00  0.00           C+0
HETATM   24  C   UNK     0       6.490  -1.848   0.000  0.00  0.00           C+0
HETATM   25  C   UNK     0       4.950  -1.800   0.000  0.00  0.00           C+0
HETATM   26  C   UNK     0       4.222  -0.443   0.000  0.00  0.00           C+0
HETATM   27  C   UNK     0       3.279  -1.660   0.000  0.00  0.00           C+0
HETATM   28  C   UNK     0       2.727  -0.076   0.000  0.00  0.00           C+0
HETATM   29  C   UNK     0       2.614   1.460   0.000  0.00  0.00           C+0
HETATM   30  C   UNK     0       4.039   2.042   0.000  0.00  0.00           C+0
HETATM   31  C   UNK     0       5.034   0.866   0.000  0.00  0.00           C+0
HETATM   32  C   UNK     0       1.551  -1.070   0.000  0.00  0.00           C+0
HETATM   33  C   UNK     0       1.664  -2.606   0.000  0.00  0.00           C+0
HETATM   34  O   UNK     0       0.238  -3.188   0.000  0.00  0.00           O+0
HETATM   35  C   UNK     0      -0.756  -2.012   0.000  0.00  0.00           C+0
HETATM   36  C   UNK     0       0.055  -0.703   0.000  0.00  0.00           C+0
HETATM   37  C   UNK     0      -2.292  -2.125   0.000  0.00  0.00           C+0
HETATM   38  C   UNK     0      -3.158  -0.851   0.000  0.00  0.00           C+0
HETATM   39  C   UNK     0      -4.694  -0.964   0.000  0.00  0.00           C+0
HETATM   40  C   UNK     0      -2.488   0.535   0.000  0.00  0.00           C+0
HETATM   41  O   UNK     0       7.218  -3.205   0.000  0.00  0.00           O+0
HETATM   42  C   UNK     0       6.406  -4.514   0.000  0.00  0.00           C+0
HETATM   43  O   UNK     0       4.867  -4.466   0.000  0.00  0.00           O+0
HETATM   44  C   UNK     0       7.134  -5.871   0.000  0.00  0.00           C+0
HETATM   45  O   UNK     0       8.674  -5.919   0.000  0.00  0.00           O+0
HETATM   46  C   UNK     0       6.323  -7.180   0.000  0.00  0.00           C+0
HETATM   47  C   UNK     0       7.051  -8.537   0.000  0.00  0.00           C+0
HETATM   48  C   UNK     0       6.240  -9.846   0.000  0.00  0.00           C+0
HETATM   49  C   UNK     0       4.784  -7.132   0.000  0.00  0.00           C+0
HETATM   50  C   UNK     0      11.191   0.674   0.000  0.00  0.00           C+0
HETATM   51  C   UNK     0      11.239   2.213   0.000  0.00  0.00           C+0
HETATM   52  C   UNK     0      11.143  -0.865   0.000  0.00  0.00           C+0
HETATM   53  O   UNK     0      12.730   0.626   0.000  0.00  0.00           O+0
CONECT    1    2                                                            
CONECT    2    1    3                                                       
CONECT    3    2    4    5                                                  
CONECT    4    3                                                            
CONECT    5    3    6                                                       
CONECT    6    5    7                                                       
CONECT    7    6    8    9   23                                             
CONECT    8    7                                                            
CONECT    9    7   10   50                                                  
CONECT   10    9   11                                                       
CONECT   11   10   12   21                                                  
CONECT   12   11   13                                                       
CONECT   13   12   14   15                                                  
CONECT   14   13                                                            
CONECT   15   13   16   17                                                  
CONECT   16   15                                                            
CONECT   17   15   18   20                                                  
CONECT   18   17   19                                                       
CONECT   19   18                                                            
CONECT   20   17                                                            
CONECT   21   11   22   23   31                                             
CONECT   22   21                                                            
CONECT   23   21    7   24                                                  
CONECT   24   23   25   41                                                  
CONECT   25   24   26                                                       
CONECT   26   25   27   28   31                                             
CONECT   27   26                                                            
CONECT   28   26   29   32                                                  
CONECT   29   28   30                                                       
CONECT   30   29   31                                                       
CONECT   31   30   21   26                                                  
CONECT   32   28   33   36                                                  
CONECT   33   32   34                                                       
CONECT   34   33   35                                                       
CONECT   35   34   36   37                                                  
CONECT   36   35   32                                                       
CONECT   37   35   38                                                       
CONECT   38   37   39   40                                                  
CONECT   39   38                                                            
CONECT   40   38                                                            
CONECT   41   24   42                                                       
CONECT   42   41   43   44                                                  
CONECT   43   42                                                            
CONECT   44   42   45   46                                                  
CONECT   45   44                                                            
CONECT   46   44   47   49                                                  
CONECT   47   46   48                                                       
CONECT   48   47                                                            
CONECT   49   46                                                            
CONECT   50    9   51   52   53                                             
CONECT   51   50                                                            
CONECT   52   50                                                            
CONECT   53   50                                                            
MASTER        0    0    0    0    0    0    0    0   53    0  112    0
END

View in JSmol

Synonyms

Value	Source
9-[(2-Hydroxy-3-methylpent-3-enoyl)oxy]-7-(2-hydroxypropan-2-yl)-6-(3-methoxy-3-oxopropyl)-3a,6,9a-trimethyl-3-[5-(2-methylprop-1-en-1-yl)oxolan-3-yl]-2H,3H,3ah,4H,5H,5ah,6H,7H,8H,9H,9ah-cyclopenta[a]naphthalen-5-yl 2-hydroxy-3-methylpent-3-enoic acid	Generator

Chemical Formula

C₄₃H₆₆O₁₀

Average Mass

742.9910 Da

Monoisotopic Mass

742.46560 Da

IUPAC Name

9-[(2-hydroxy-3-methylpent-3-enoyl)oxy]-7-(2-hydroxypropan-2-yl)-6-(3-methoxy-3-oxopropyl)-3a,6,9a-trimethyl-3-[5-(2-methylprop-1-en-1-yl)oxolan-3-yl]-2H,3H,3aH,4H,5H,5aH,6H,7H,8H,9H,9aH-cyclopenta[a]naphthalen-5-yl 2-hydroxy-3-methylpent-3-enoate

Traditional Name

9-[(2-hydroxy-3-methylpent-3-enoyl)oxy]-7-(2-hydroxypropan-2-yl)-6-(3-methoxy-3-oxopropyl)-3a,6,9a-trimethyl-3-[5-(2-methylprop-1-en-1-yl)oxolan-3-yl]-2H,3H,4H,5H,5aH,7H,8H,9H-cyclopenta[a]naphthalen-5-yl 2-hydroxy-3-methylpent-3-enoate

CAS Registry Number

Not Available

SMILES

COC(=O)CCC1(C)C(CC(OC(=O)C(O)C(C)=CC)C2(C)C1C(CC1(C)C(CC=C21)C1COC(C1)C=C(C)C)OC(=O)C(O)C(C)=CC)C(C)(C)O

InChI Identifier

InChI=1S/C43H66O10/c1-13-25(5)35(45)38(47)52-30-22-42(10)29(27-20-28(51-23-27)19-24(3)4)15-16-31(42)43(11)33(53-39(48)36(46)26(6)14-2)21-32(40(7,8)49)41(9,37(30)43)18-17-34(44)50-12/h13-14,16,19,27-30,32-33,35-37,45-46,49H,15,17-18,20-23H2,1-12H3

InChI Key

WPEKKKYUGODPOL-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
Aglaia argentea	LOTUS Database	35616633

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as sesquiterpenoids. These are terpenes with three consecutive isoprene units.

Kingdom

Organic compounds

Super Class

Lipids and lipid-like molecules

Class

Prenol lipids

Sub Class

Sesquiterpenoids

Direct Parent

Sesquiterpenoids

Alternative Parents

Substituents

Sesquiterpenoid
Tricarboxylic acid or derivatives
Fatty acid ester
Fatty acyl
Tertiary alcohol
Methyl ester
Tetrahydrofuran
Carboxylic acid ester
Secondary alcohol
Carboxylic acid derivative
Dialkyl ether
Ether
Oxacycle
Organoheterocyclic compound
Carbonyl group
Organic oxide
Organooxygen compound
Hydrocarbon derivative
Alcohol
Organic oxygen compound
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	5.77	ALOGPS
logP	5.45	ChemAxon
logS	-5.8	ALOGPS
pKa (Strongest Acidic)	11.84	ChemAxon
pKa (Strongest Basic)	-2.8	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	7	ChemAxon
Hydrogen Donor Count	3	ChemAxon
Polar Surface Area	148.82 Å²	ChemAxon
Rotatable Bond Count	15	ChemAxon
Refractivity	205.82 m³·mol⁻¹	ChemAxon
Polarizability	84.28 Å³	ChemAxon
Number of Rings	4	ChemAxon
Bioavailability	No	ChemAxon
Rule of Five	No	ChemAxon
Ghose Filter	No	ChemAxon
Veber's Rule	No	ChemAxon
MDDR-like Rule	Yes	ChemAxon

External Links

HMDB ID

Not Available

DrugBank ID

Not Available

Phenol Explorer Compound ID

Not Available

FoodDB ID

Not Available

KNApSAcK ID

Not Available

Chemspider ID

Not Available

KEGG Compound ID

Not Available

BioCyc ID

Not Available

BiGG ID

Not Available

Wikipedia Link

Not Available

METLIN ID

Not Available

PubChem Compound

73804854

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

LOTUS database [Link]

Showing NP-Card for 9-[(2-hydroxy-3-methylpent-3-enoyl)oxy]-7-(2-hydroxypropan-2-yl)-6-(3-methoxy-3-oxopropyl)-3a,6,9a-trimethyl-3-[5-(2-methylprop-1-en-1-yl)oxolan-3-yl]-2h,3h,4h,5h,5ah,7h,8h,9h-cyclopenta[a]naphthalen-5-yl 2-hydroxy-3-methylpent-3-enoate (NP0306440)

MOL for NP0306440 (9-[(2-hydroxy-3-methylpent-3-enoyl)oxy]-7-(2-hydroxypropan-2-yl)-6-(3-methoxy-3-oxopropyl)-3a,6,9a-trimethyl-3-[5-(2-methylprop-1-en-1-yl)oxolan-3-yl]-2h,3h,4h,5h,5ah,7h,8h,9h-cyclopenta[a]naphthalen-5-yl 2-hydroxy-3-methylpent-3-enoate)

3D MOL for NP0306440 (9-[(2-hydroxy-3-methylpent-3-enoyl)oxy]-7-(2-hydroxypropan-2-yl)-6-(3-methoxy-3-oxopropyl)-3a,6,9a-trimethyl-3-[5-(2-methylprop-1-en-1-yl)oxolan-3-yl]-2h,3h,4h,5h,5ah,7h,8h,9h-cyclopenta[a]naphthalen-5-yl 2-hydroxy-3-methylpent-3-enoate)

3D SDF for NP0306440 (9-[(2-hydroxy-3-methylpent-3-enoyl)oxy]-7-(2-hydroxypropan-2-yl)-6-(3-methoxy-3-oxopropyl)-3a,6,9a-trimethyl-3-[5-(2-methylprop-1-en-1-yl)oxolan-3-yl]-2h,3h,4h,5h,5ah,7h,8h,9h-cyclopenta[a]naphthalen-5-yl 2-hydroxy-3-methylpent-3-enoate)

3D-SDF for NP0306440 (9-[(2-hydroxy-3-methylpent-3-enoyl)oxy]-7-(2-hydroxypropan-2-yl)-6-(3-methoxy-3-oxopropyl)-3a,6,9a-trimethyl-3-[5-(2-methylprop-1-en-1-yl)oxolan-3-yl]-2h,3h,4h,5h,5ah,7h,8h,9h-cyclopenta[a]naphthalen-5-yl 2-hydroxy-3-methylpent-3-enoate)

PDB for NP0306440 (9-[(2-hydroxy-3-methylpent-3-enoyl)oxy]-7-(2-hydroxypropan-2-yl)-6-(3-methoxy-3-oxopropyl)-3a,6,9a-trimethyl-3-[5-(2-methylprop-1-en-1-yl)oxolan-3-yl]-2h,3h,4h,5h,5ah,7h,8h,9h-cyclopenta[a]naphthalen-5-yl 2-hydroxy-3-methylpent-3-enoate)

3D PDB for NP0306440 (9-[(2-hydroxy-3-methylpent-3-enoyl)oxy]-7-(2-hydroxypropan-2-yl)-6-(3-methoxy-3-oxopropyl)-3a,6,9a-trimethyl-3-[5-(2-methylprop-1-en-1-yl)oxolan-3-yl]-2h,3h,4h,5h,5ah,7h,8h,9h-cyclopenta[a]naphthalen-5-yl 2-hydroxy-3-methylpent-3-enoate)

SMILES for NP0306440 (9-[(2-hydroxy-3-methylpent-3-enoyl)oxy]-7-(2-hydroxypropan-2-yl)-6-(3-methoxy-3-oxopropyl)-3a,6,9a-trimethyl-3-[5-(2-methylprop-1-en-1-yl)oxolan-3-yl]-2h,3h,4h,5h,5ah,7h,8h,9h-cyclopenta[a]naphthalen-5-yl 2-hydroxy-3-methylpent-3-enoate)

INCHI for NP0306440 (9-[(2-hydroxy-3-methylpent-3-enoyl)oxy]-7-(2-hydroxypropan-2-yl)-6-(3-methoxy-3-oxopropyl)-3a,6,9a-trimethyl-3-[5-(2-methylprop-1-en-1-yl)oxolan-3-yl]-2h,3h,4h,5h,5ah,7h,8h,9h-cyclopenta[a]naphthalen-5-yl 2-hydroxy-3-methylpent-3-enoate)

Structure for NP0306440 (9-[(2-hydroxy-3-methylpent-3-enoyl)oxy]-7-(2-hydroxypropan-2-yl)-6-(3-methoxy-3-oxopropyl)-3a,6,9a-trimethyl-3-[5-(2-methylprop-1-en-1-yl)oxolan-3-yl]-2h,3h,4h,5h,5ah,7h,8h,9h-cyclopenta[a]naphthalen-5-yl 2-hydroxy-3-methylpent-3-enoate)

3D Structure for NP0306440 (9-[(2-hydroxy-3-methylpent-3-enoyl)oxy]-7-(2-hydroxypropan-2-yl)-6-(3-methoxy-3-oxopropyl)-3a,6,9a-trimethyl-3-[5-(2-methylprop-1-en-1-yl)oxolan-3-yl]-2h,3h,4h,5h,5ah,7h,8h,9h-cyclopenta[a]naphthalen-5-yl 2-hydroxy-3-methylpent-3-enoate)