NP-MRD: Showing NP-Card for (1's,2'r,3r,7'r,9'r,10'r)-2,2,2',10',13',14'-hexamethyl-6'-methylidene-6,12',15'-trioxo-8',11'-dioxaspiro[pyran-3,5'-tetracyclo[7.3.3.0¹,⁹.0²,⁷]pentadecan]-13'-ene-7'-carbaldehyde (NP0321131)

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Record Information

Version

2.0

Created at

2022-09-11 23:10:16 UTC

Updated at

2022-09-11 23:10:16 UTC

NP-MRD ID

NP0321131

Secondary Accession Numbers

None

Natural Product Identification

Common Name

(1's,2'r,3r,7'r,9'r,10'r)-2,2,2',10',13',14'-hexamethyl-6'-methylidene-6,12',15'-trioxo-8',11'-dioxaspiro[pyran-3,5'-tetracyclo[7.3.3.0¹,⁹.0²,⁷]pentadecan]-13'-ene-7'-carbaldehyde

Description

Brasilianoid G belongs to the class of organic compounds known as terpene lactones. These are prenol lipids containing a lactone ring. (1's,2'r,3r,7'r,9'r,10'r)-2,2,2',10',13',14'-hexamethyl-6'-methylidene-6,12',15'-trioxo-8',11'-dioxaspiro[pyran-3,5'-tetracyclo[7.3.3.0¹,⁹.0²,⁷]pentadecan]-13'-ene-7'-carbaldehyde is found in Penicillium brasilianum. Based on a literature review very few articles have been published on Brasilianoid G.

Structure

MOL 3D MOL SDF PDB SMILES InChI


  Mrv1652309122201102D          

 32 36  0  0  1  0            999 V2000
    3.4413   -0.9268    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.1401   -0.1587    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.3244   -0.0355    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    2.5436   -0.8309    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.9645   -1.4184    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.6870   -0.5593    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.9918   -0.1150    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    0.4891   -0.3042    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0448   -0.9993    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2730    0.2831    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9313    0.8117    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.1837    1.2677    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.1346    2.0913    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.1996    0.6834    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    0.5045    1.1277    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.4554    1.9512    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1329    0.6039    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.1683   -0.1642    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
   -0.2760   -0.8593    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.0231    0.7325    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    1.6433    1.4649    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.5377    1.3774    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.3534    1.2542    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.6547    0.4862    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    4.1692    1.1310    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.9850    1.0079    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.2862    0.2398    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.1019    0.1167    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.7716   -0.4050    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.9559   -0.2819    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.8043   -1.0928    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.1988   -0.6097    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  2  0  0  0  0
  2  3  1  0  0  0  0
  3  4  1  6  0  0  0
  4  5  2  0  0  0  0
  3  6  1  0  0  0  0
  7  6  1  1  0  0  0
  7  8  1  0  0  0  0
  8  9  2  0  0  0  0
  8 10  1  0  0  0  0
 10 11  1  0  0  0  0
 10 12  2  0  0  0  0
 12 13  1  0  0  0  0
 14 12  1  6  0  0  0
  7 14  1  0  0  0  0
 14 15  1  0  0  0  0
 15 16  2  0  0  0  0
 15 17  1  0  0  0  0
 17 18  1  0  0  0  0
  7 18  1  0  0  0  0
 18 19  1  1  0  0  0
 14 20  1  0  0  0  0
  3 20  1  0  0  0  0
 20 21  1  6  0  0  0
 20 22  1  0  0  0  0
 22 23  1  0  0  0  0
 24 23  1  6  0  0  0
  2 24  1  0  0  0  0
 24 25  1  0  0  0  0
 25 26  2  0  0  0  0
 26 27  1  0  0  0  0
 27 28  2  0  0  0  0
 27 29  1  0  0  0  0
 29 30  1  0  0  0  0
 24 30  1  0  0  0  0
 30 31  1  0  0  0  0
 30 32  1  0  0  0  0
M  END

     RDKit          3D

 60 64  0  0  0  0  0  0  0  0999 V2000
    1.4598   -1.1555   -2.1738 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.1937   -0.6710   -0.9798 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2194   -0.2350   -0.7879 C   0  0  1  0  0  0  0  0  0  0  0  0
   -0.7815    0.1526   -2.1035 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3873    1.0594   -2.8101 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9413   -1.3609   -0.3343 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0799   -0.8961    0.2671 C   0  0  2  0  0  0  0  0  0  0  0  0
   -3.2270   -0.7872   -0.6577 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.6763   -1.7742   -1.3185 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.6974    0.5593   -0.6593 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.9146    1.0016   -1.4444 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.9349    1.3010    0.1032 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.2170    2.7589    0.2970 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8712    0.5128    0.6814 C   0  0  1  0  0  0  0  0  0  0  0  0
   -2.0452    0.4793    2.1469 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2293    1.4425    2.9604 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9766   -0.8533    2.5606 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4322   -1.6919    1.5098 C   0  0  2  0  0  0  0  0  0  0  0  0
   -1.7441   -3.0383    1.5153 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4740    0.8128    0.2116 C   0  0  2  0  0  0  0  0  0  0  0  0
   -0.3895    2.1742   -0.4551 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.4856    0.8370    1.3606 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.5040   -0.2165    1.4117 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1811   -0.6010    0.0916 C   0  0  1  0  0  0  0  0  0  0  0  0
    2.6458   -1.9989    0.3889 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.7868   -2.2312    0.9560 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.6946   -1.1717    1.3336 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.7903   -1.3583    1.8883 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.2532    0.1240    1.0309 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.3865    0.2025   -0.1604 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.2679    1.6549   -0.4285 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.2272   -0.3742   -1.2745 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.6916   -1.2312   -2.9757 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.4077   -1.5342   -2.4824 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6425   -0.3955   -2.5404 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.7072    0.9310   -2.5299 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.7719    0.3221   -1.2429 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.2359    2.0109   -1.1464 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.2040    2.8855    0.8400 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4927    3.2738    0.9243 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.4128    3.2524   -0.6891 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5231   -1.8258    1.5135 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2446   -3.1731    0.5241 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4906   -3.8736    1.5940 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0452   -3.1625    2.3555 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2114    2.9762    0.3134 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2273    2.3973   -1.1102 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.5288    2.1840   -1.0645 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.9378    1.8587    1.5276 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1094    0.7216    2.3272 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.9883   -1.1552    1.7737 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.2728    0.0319    2.1418 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.0010   -2.8046    0.1177 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.1418   -3.2498    1.1884 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.8257    1.9022   -1.4153 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.9215    2.2811    0.4096 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.3491    2.0124   -0.5625 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.9934    0.0990   -2.2634 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.2774    0.0584   -1.0726 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.3439   -1.4503   -1.2751 H   0  0  0  0  0  0  0  0  0  0  0  0
 19 18  1  0
 18 17  1  0
 17 15  1  0
 15 16  2  0
 14 15  1  1
 14 12  1  0
 12 13  1  0
 12 10  2  0
 10 11  1  0
 10  8  1  0
  8  9  2  0
  8  7  1  0
  7  6  1  6
  6  3  1  0
  3  4  1  6
  4  5  2  0
  3  2  1  0
  2  1  2  3
 24  2  1  6
 24 23  1  0
 23 22  1  0
 22 20  1  0
 20 21  1  6
 24 25  1  0
 25 26  2  0
 26 27  1  0
 27 28  2  0
 27 29  1  0
 29 30  1  0
 30 31  1  0
 30 32  1  0
  7 18  1  0
 20  3  1  0
  7 14  1  0
 30 24  1  0
 20 14  1  0
 19 43  1  0
 19 44  1  0
 19 45  1  0
 18 42  1  1
 13 39  1  0
 13 40  1  0
 13 41  1  0
 11 36  1  0
 11 37  1  0
 11 38  1  0
  4 35  1  0
  1 33  1  0
  1 34  1  0
 23 51  1  0
 23 52  1  0
 22 49  1  0
 22 50  1  0
 21 46  1  0
 21 47  1  0
 21 48  1  0
 25 53  1  0
 26 54  1  0
 31 55  1  0
 31 56  1  0
 31 57  1  0
 32 58  1  0
 32 59  1  0
 32 60  1  0
M  END


  Mrv1652309122201102D          

 32 36  0  0  1  0            999 V2000
    3.4413   -0.9268    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.1401   -0.1587    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.3244   -0.0355    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    2.5436   -0.8309    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.9645   -1.4184    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.6870   -0.5593    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.9918   -0.1150    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    0.4891   -0.3042    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0448   -0.9993    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2730    0.2831    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9313    0.8117    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.1837    1.2677    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.1346    2.0913    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.1996    0.6834    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    0.5045    1.1277    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.4554    1.9512    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1329    0.6039    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.1683   -0.1642    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
   -0.2760   -0.8593    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.0231    0.7325    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    1.6433    1.4649    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.5377    1.3774    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.3534    1.2542    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.6547    0.4862    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    4.1692    1.1310    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.9850    1.0079    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.2862    0.2398    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.1019    0.1167    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.7716   -0.4050    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.9559   -0.2819    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.8043   -1.0928    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.1988   -0.6097    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  2  0  0  0  0
  2  3  1  0  0  0  0
  3  4  1  6  0  0  0
  4  5  2  0  0  0  0
  3  6  1  0  0  0  0
  7  6  1  1  0  0  0
  7  8  1  0  0  0  0
  8  9  2  0  0  0  0
  8 10  1  0  0  0  0
 10 11  1  0  0  0  0
 10 12  2  0  0  0  0
 12 13  1  0  0  0  0
 14 12  1  6  0  0  0
  7 14  1  0  0  0  0
 14 15  1  0  0  0  0
 15 16  2  0  0  0  0
 15 17  1  0  0  0  0
 17 18  1  0  0  0  0
  7 18  1  0  0  0  0
 18 19  1  1  0  0  0
 14 20  1  0  0  0  0
  3 20  1  0  0  0  0
 20 21  1  6  0  0  0
 20 22  1  0  0  0  0
 22 23  1  0  0  0  0
 24 23  1  6  0  0  0
  2 24  1  0  0  0  0
 24 25  1  0  0  0  0
 25 26  2  0  0  0  0
 26 27  1  0  0  0  0
 27 28  2  0  0  0  0
 27 29  1  0  0  0  0
 29 30  1  0  0  0  0
 24 30  1  0  0  0  0
 30 31  1  0  0  0  0
 30 32  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0321131

> <DATABASE_NAME>
NP-MRD

> <SMILES>
C[C@H]1OC(=O)[C@]23C(C)=C(C)C(=O)[C@]12O[C@]1(C=O)C(=C)[C@@]2(CC[C@]31C)C=CC(=O)OC2(C)C

> <INCHI_IDENTIFIER>
InChI=1S/C25H28O7/c1-13-14(2)24-19(29)30-16(4)25(24,18(13)28)32-23(12-26)15(3)22(11-10-21(23,24)7)9-8-17(27)31-20(22,5)6/h8-9,12,16H,3,10-11H2,1-2,4-7H3/t16-,21+,22+,23-,24+,25-/m1/s1

> <INCHI_KEY>
OPASHUVCAOVDEQ-QZIZNRCXSA-N

> <FORMULA>
C25H28O7

> <MOLECULAR_WEIGHT>
440.492

> <EXACT_MASS>
440.183503242

> <JCHEM_ACCEPTOR_COUNT>
5

> <JCHEM_ATOM_COUNT>
60

> <JCHEM_AVERAGE_POLARIZABILITY>
44.38126707146444

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
0

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
1

> <JCHEM_IUPAC>
(1'S,2'R,3R,7'R,9'R,10'R)-2,2,2',10',13',14'-hexamethyl-6'-methylidene-6,12',15'-trioxo-2,6-dihydro-8',11'-dioxaspiro[pyran-3,5'-tetracyclo[7.3.3.0^{1,9}.0^{2,7}]pentadecan]-13'-ene-7'-carbaldehyde

> <JCHEM_LOGP>
3.1541359683333345

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
5

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA_STRONGEST_BASIC>
-4.3735562623753745

> <JCHEM_POLAR_SURFACE_AREA>
95.97000000000001

> <JCHEM_REFRACTIVITY>
113.96739999999994

> <JCHEM_ROTATABLE_BOND_COUNT>
1

> <JCHEM_RULE_OF_FIVE>
1

> <JCHEM_TRADITIONAL_IUPAC>
(1'S,2'R,3R,7'R,9'R,10'R)-2,2,2',10',13',14'-hexamethyl-6'-methylidene-6,12',15'-trioxo-8',11'-dioxaspiro[pyran-3,5'-tetracyclo[7.3.3.0^{1,9}.0^{2,7}]pentadecan]-13'-ene-7'-carbaldehyde

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 12-SEP-22   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   12-SEP-22         0                                  
HETATM    1  C   UNK     0       6.424  -1.730   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0       5.862  -0.296   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0       4.339  -0.066   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0       4.748  -1.551   0.000  0.00  0.00           C+0
HETATM    5  O   UNK     0       3.667  -2.648   0.000  0.00  0.00           O+0
HETATM    6  O   UNK     0       3.149  -1.044   0.000  0.00  0.00           O+0
HETATM    7  C   UNK     0       1.851  -0.215   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0       0.913  -0.568   0.000  0.00  0.00           C+0
HETATM    9  O   UNK     0       0.084  -1.865   0.000  0.00  0.00           O+0
HETATM   10  C   UNK     0      -0.510   0.528   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0      -1.738   1.515   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0       0.343   2.366   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0       0.251   3.904   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0       2.239   1.276   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0       0.942   2.105   0.000  0.00  0.00           C+0
HETATM   16  O   UNK     0       0.850   3.642   0.000  0.00  0.00           O+0
HETATM   17  O   UNK     0      -0.248   1.127   0.000  0.00  0.00           O+0
HETATM   18  C   UNK     0       0.314  -0.306   0.000  0.00  0.00           C+0
HETATM   19  C   UNK     0      -0.515  -1.604   0.000  0.00  0.00           C+0
HETATM   20  C   UNK     0       3.777   1.367   0.000  0.00  0.00           C+0
HETATM   21  C   UNK     0       3.067   2.734   0.000  0.00  0.00           C+0
HETATM   22  C   UNK     0       4.737   2.571   0.000  0.00  0.00           C+0
HETATM   23  C   UNK     0       6.260   2.341   0.000  0.00  0.00           C+0
HETATM   24  C   UNK     0       6.822   0.908   0.000  0.00  0.00           C+0
HETATM   25  C   UNK     0       7.783   2.111   0.000  0.00  0.00           C+0
HETATM   26  C   UNK     0       9.305   1.881   0.000  0.00  0.00           C+0
HETATM   27  C   UNK     0       9.867   0.448   0.000  0.00  0.00           C+0
HETATM   28  O   UNK     0      11.390   0.218   0.000  0.00  0.00           O+0
HETATM   29  O   UNK     0       8.907  -0.756   0.000  0.00  0.00           O+0
HETATM   30  C   UNK     0       7.384  -0.526   0.000  0.00  0.00           C+0
HETATM   31  C   UNK     0       7.101  -2.040   0.000  0.00  0.00           C+0
HETATM   32  C   UNK     0       5.971  -1.138   0.000  0.00  0.00           C+0
CONECT    1    2                                                            
CONECT    2    1    3   24                                                  
CONECT    3    2    4    6   20                                             
CONECT    4    3    5                                                       
CONECT    5    4                                                            
CONECT    6    3    7                                                       
CONECT    7    6    8   14   18                                             
CONECT    8    7    9   10                                                  
CONECT    9    8                                                            
CONECT   10    8   11   12                                                  
CONECT   11   10                                                            
CONECT   12   10   13   14                                                  
CONECT   13   12                                                            
CONECT   14   12    7   15   20                                             
CONECT   15   14   16   17                                                  
CONECT   16   15                                                            
CONECT   17   15   18                                                       
CONECT   18   17    7   19                                                  
CONECT   19   18                                                            
CONECT   20   14    3   21   22                                             
CONECT   21   20                                                            
CONECT   22   20   23                                                       
CONECT   23   22   24                                                       
CONECT   24   23    2   25   30                                             
CONECT   25   24   26                                                       
CONECT   26   25   27                                                       
CONECT   27   26   28   29                                                  
CONECT   28   27                                                            
CONECT   29   27   30                                                       
CONECT   30   29   24   31   32                                             
CONECT   31   30                                                            
CONECT   32   30                                                            
MASTER        0    0    0    0    0    0    0    0   32    0   72    0
END

View in JSmol

Synonyms

Not Available

Chemical Formula

C₂₅H₂₈O₇

Average Mass

440.4920 Da

Monoisotopic Mass

440.18350 Da

IUPAC Name

(1'S,2'R,3R,7'R,9'R,10'R)-2,2,2',10',13',14'-hexamethyl-6'-methylidene-6,12',15'-trioxo-2,6-dihydro-8',11'-dioxaspiro[pyran-3,5'-tetracyclo[7.3.3.0^{1,9}.0^{2,7}]pentadecan]-13'-ene-7'-carbaldehyde

Traditional Name

(1'S,2'R,3R,7'R,9'R,10'R)-2,2,2',10',13',14'-hexamethyl-6'-methylidene-6,12',15'-trioxo-8',11'-dioxaspiro[pyran-3,5'-tetracyclo[7.3.3.0^{1,9}.0^{2,7}]pentadecan]-13'-ene-7'-carbaldehyde

CAS Registry Number

Not Available

SMILES

C[C@H]1OC(=O)[C@]23C(C)=C(C)C(=O)[C@]12O[C@]1(C=O)C(=C)[C@@]2(CC[C@]31C)C=CC(=O)OC2(C)C

InChI Identifier

InChI=1S/C25H28O7/c1-13-14(2)24-19(29)30-16(4)25(24,18(13)28)32-23(12-26)15(3)22(11-10-21(23,24)7)9-8-17(27)31-20(22,5)6/h8-9,12,16H,3,10-11H2,1-2,4-7H3/t16-,21+,22+,23-,24+,25-/m1/s1

InChI Key

OPASHUVCAOVDEQ-QZIZNRCXSA-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
Penicillium brasilianum	LOTUS Database	35616633

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as terpene lactones. These are prenol lipids containing a lactone ring.

Kingdom

Organic compounds

Super Class

Lipids and lipid-like molecules

Class

Prenol lipids

Sub Class

Terpene lactones

Direct Parent

Terpene lactones

Alternative Parents

Substituents

Terpene lactone
Monoterpenoid
Furofuran
Dihydropyranone
Pyran
Gamma butyrolactone
Dicarboxylic acid or derivatives
Alpha,beta-unsaturated carboxylic ester
Enoate ester
Tetrahydrofuran
Lactone
Ketone
Carboxylic acid ester
Oxacycle
Organoheterocyclic compound
Ether
Dialkyl ether
Carboxylic acid derivative
Organic oxygen compound
Organic oxide
Hydrocarbon derivative
Organooxygen compound
Carbonyl group
Aldehyde
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	3.15	ChemAxon
pKa (Strongest Basic)	-4.4	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	5	ChemAxon
Hydrogen Donor Count	0	ChemAxon
Polar Surface Area	95.97 Å²	ChemAxon
Rotatable Bond Count	1	ChemAxon
Refractivity	113.97 m³·mol⁻¹	ChemAxon
Polarizability	44.38 Å³	ChemAxon
Number of Rings	5	ChemAxon
Bioavailability	Yes	ChemAxon
Rule of Five	Yes	ChemAxon
Ghose Filter	Yes	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

71720026

KEGG Compound ID

Not Available

BioCyc ID

Not Available

BiGG ID

Not Available

Wikipedia Link

Not Available

METLIN ID

Not Available

PubChem Compound

146682195

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

LOTUS database [Link]

Showing NP-Card for (1's,2'r,3r,7'r,9'r,10'r)-2,2,2',10',13',14'-hexamethyl-6'-methylidene-6,12',15'-trioxo-8',11'-dioxaspiro[pyran-3,5'-tetracyclo[7.3.3.0¹,⁹.0²,⁷]pentadecan]-13'-ene-7'-carbaldehyde (NP0321131)

MOL for NP0321131 ((1's,2'r,3r,7'r,9'r,10'r)-2,2,2',10',13',14'-hexamethyl-6'-methylidene-6,12',15'-trioxo-8',11'-dioxaspiro[pyran-3,5'-tetracyclo[7.3.3.0¹,⁹.0²,⁷]pentadecan]-13'-ene-7'-carbaldehyde)

3D MOL for NP0321131 ((1's,2'r,3r,7'r,9'r,10'r)-2,2,2',10',13',14'-hexamethyl-6'-methylidene-6,12',15'-trioxo-8',11'-dioxaspiro[pyran-3,5'-tetracyclo[7.3.3.0¹,⁹.0²,⁷]pentadecan]-13'-ene-7'-carbaldehyde)

3D SDF for NP0321131 ((1's,2'r,3r,7'r,9'r,10'r)-2,2,2',10',13',14'-hexamethyl-6'-methylidene-6,12',15'-trioxo-8',11'-dioxaspiro[pyran-3,5'-tetracyclo[7.3.3.0¹,⁹.0²,⁷]pentadecan]-13'-ene-7'-carbaldehyde)

3D-SDF for NP0321131 ((1's,2'r,3r,7'r,9'r,10'r)-2,2,2',10',13',14'-hexamethyl-6'-methylidene-6,12',15'-trioxo-8',11'-dioxaspiro[pyran-3,5'-tetracyclo[7.3.3.0¹,⁹.0²,⁷]pentadecan]-13'-ene-7'-carbaldehyde)

PDB for NP0321131 ((1's,2'r,3r,7'r,9'r,10'r)-2,2,2',10',13',14'-hexamethyl-6'-methylidene-6,12',15'-trioxo-8',11'-dioxaspiro[pyran-3,5'-tetracyclo[7.3.3.0¹,⁹.0²,⁷]pentadecan]-13'-ene-7'-carbaldehyde)

3D PDB for NP0321131 ((1's,2'r,3r,7'r,9'r,10'r)-2,2,2',10',13',14'-hexamethyl-6'-methylidene-6,12',15'-trioxo-8',11'-dioxaspiro[pyran-3,5'-tetracyclo[7.3.3.0¹,⁹.0²,⁷]pentadecan]-13'-ene-7'-carbaldehyde)

SMILES for NP0321131 ((1's,2'r,3r,7'r,9'r,10'r)-2,2,2',10',13',14'-hexamethyl-6'-methylidene-6,12',15'-trioxo-8',11'-dioxaspiro[pyran-3,5'-tetracyclo[7.3.3.0¹,⁹.0²,⁷]pentadecan]-13'-ene-7'-carbaldehyde)

INCHI for NP0321131 ((1's,2'r,3r,7'r,9'r,10'r)-2,2,2',10',13',14'-hexamethyl-6'-methylidene-6,12',15'-trioxo-8',11'-dioxaspiro[pyran-3,5'-tetracyclo[7.3.3.0¹,⁹.0²,⁷]pentadecan]-13'-ene-7'-carbaldehyde)

Structure for NP0321131 ((1's,2'r,3r,7'r,9'r,10'r)-2,2,2',10',13',14'-hexamethyl-6'-methylidene-6,12',15'-trioxo-8',11'-dioxaspiro[pyran-3,5'-tetracyclo[7.3.3.0¹,⁹.0²,⁷]pentadecan]-13'-ene-7'-carbaldehyde)

3D Structure for NP0321131 ((1's,2'r,3r,7'r,9'r,10'r)-2,2,2',10',13',14'-hexamethyl-6'-methylidene-6,12',15'-trioxo-8',11'-dioxaspiro[pyran-3,5'-tetracyclo[7.3.3.0¹,⁹.0²,⁷]pentadecan]-13'-ene-7'-carbaldehyde)