NP-MRD: Showing NP-Card for (-)-epi-presilphiperfolan-1-ol (NP0038332)

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Record Information

Version

2.0

Created at

2021-06-20 21:03:07 UTC

Updated at

2021-06-30 00:11:04 UTC

NP-MRD ID

NP0038332

Secondary Accession Numbers

None

Natural Product Identification

Common Name

(-)-epi-presilphiperfolan-1-ol

Provided By

JEOL Database JEOL Logo

Description

(-)-epi-presilphiperfolan-1-ol is found in Anemia tomentosa var. anthriscifolia (Pteridophyta) and Conocephalum conicum. (-)-epi-presilphiperfolan-1-ol was first documented in 2009 (PMID: 20120105). Based on a literature review a small amount of articles have been published on Presilphiperfolan-1-ol (PMID: 28052485) (PMID: 22915502).

Structure

MOL 3D MOL SDF 3D SDF PDB SMILES InChI


  Mrv1652306202123033D          

 42 44  0  0  0  0            999 V2000
   -0.7870   -2.1252   -4.2231 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5982   -1.7775   -2.7481 C   0  0  2  0  0  0  0  0  0  0  0  0
   -1.7949   -0.8819   -2.2320 C   0  0  2  0  0  0  0  0  0  0  0  0
   -1.6213   -0.2336   -0.8119 C   0  0  2  0  0  0  0  0  0  0  0  0
   -0.2084    0.3324   -0.6588 C   0  0  2  0  0  0  0  0  0  0  0  0
    0.7090   -0.8419   -0.9481 C   0  0  2  0  0  0  0  0  0  0  0  0
    2.1167   -0.5594   -0.4342 C   0  0  1  0  0  0  0  0  0  0  0  0
    2.6186   -1.6192    0.5667 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.9618   -0.6944   -1.7211 C   0  0  1  0  0  0  0  0  0  0  0  0
    2.1213   -1.6553   -2.6275 C   0  0  1  0  0  0  0  0  0  0  0  0
    0.7324   -1.0607   -2.4596 C   0  0  1  0  0  0  0  0  0  0  0  0
    0.7501    0.1683   -3.2041 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.9386    0.8021    0.2725 C   0  0  1  0  0  0  0  0  0  0  0  0
    0.4001    0.9257    0.6159 C   0  0  1  0  0  0  0  0  0  0  0  0
    0.0178    2.4020    0.7914 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0125    0.1704    1.8854 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7080   -2.7010   -4.3641 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.0470   -2.7328   -4.5887 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8588   -1.2303   -4.8493 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6242   -2.7225   -2.1885 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7178   -1.4743   -2.2394 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9492   -0.0632   -2.9477 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8186   -0.9977   -0.0506 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3685    0.5556   -0.6746 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1186    1.1245   -1.4132 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.3567   -1.7512   -0.4363 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.6510   -1.4023    0.8648 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.6037   -2.6246    0.1316 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.0230   -1.6556    1.4808 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.0888    0.2785   -2.2106 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.9622   -1.1023   -1.5428 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.4882   -1.6239   -3.6579 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.1726   -2.6857   -2.2595 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.9059   -0.0478   -4.1389 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.5577    0.8986    1.1713 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.2332    1.6088   -0.4110 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.3058    3.0006   -0.0800 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.5168    2.8334    1.6662 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0635    2.5160    0.9261 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.0525   -0.9145    1.7777 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0535    0.3918    2.1484 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.6130    0.4644    2.7352 H   0  0  0  0  0  0  0  0  0  0  0  0
  6  7  1  0  0  0  0
 11  2  1  0  0  0  0
 11 10  1  0  0  0  0
  5  4  1  0  0  0  0
  2  3  1  0  0  0  0
  4  3  1  0  0  0  0
 10  9  1  0  0  0  0
  7  8  1  1  0  0  0
  9  7  1  0  0  0  0
 14 15  1  1  0  0  0
  6 11  1  0  0  0  0
  6 26  1  1  0  0  0
  7 13  1  0  0  0  0
  2  1  1  0  0  0  0
 13 14  1  0  0  0  0
 11 12  1  6  0  0  0
 14  5  1  0  0  0  0
  5 25  1  6  0  0  0
  5  6  1  0  0  0  0
 14 16  1  0  0  0  0
 10 32  1  0  0  0  0
 10 33  1  0  0  0  0
  9 30  1  0  0  0  0
  9 31  1  0  0  0  0
 13 35  1  0  0  0  0
 13 36  1  0  0  0  0
  2 20  1  1  0  0  0
  4 23  1  0  0  0  0
  4 24  1  0  0  0  0
  3 21  1  0  0  0  0
  3 22  1  0  0  0  0
  8 27  1  0  0  0  0
  8 28  1  0  0  0  0
  8 29  1  0  0  0  0
 15 37  1  0  0  0  0
 15 38  1  0  0  0  0
 15 39  1  0  0  0  0
  1 17  1  0  0  0  0
  1 18  1  0  0  0  0
  1 19  1  0  0  0  0
 12 34  1  0  0  0  0
 16 40  1  0  0  0  0
 16 41  1  0  0  0  0
 16 42  1  0  0  0  0
M  END

     RDKit          3D

 42 44  0  0  0  0  0  0  0  0999 V2000
   -0.7870   -2.1252   -4.2231 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5982   -1.7775   -2.7481 C   0  0  2  0  0  0  0  0  0  0  0  0
   -1.7949   -0.8819   -2.2320 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6213   -0.2336   -0.8119 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2084    0.3324   -0.6588 C   0  0  2  0  0  0  0  0  0  0  0  0
    0.7090   -0.8419   -0.9481 C   0  0  2  0  0  0  0  0  0  0  0  0
    2.1167   -0.5594   -0.4342 C   0  0  1  0  0  0  0  0  0  0  0  0
    2.6186   -1.6192    0.5667 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.9618   -0.6944   -1.7211 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1213   -1.6553   -2.6275 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7324   -1.0607   -2.4596 C   0  0  1  0  0  0  0  0  0  0  0  0
    0.7501    0.1683   -3.2041 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.9386    0.8021    0.2725 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.4001    0.9257    0.6159 C   0  0  1  0  0  0  0  0  0  0  0  0
    0.0178    2.4020    0.7914 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0125    0.1704    1.8854 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7080   -2.7010   -4.3641 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.0470   -2.7328   -4.5887 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8588   -1.2303   -4.8493 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6242   -2.7225   -2.1885 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7178   -1.4743   -2.2394 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9492   -0.0632   -2.9477 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8186   -0.9977   -0.0506 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3685    0.5556   -0.6746 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1186    1.1245   -1.4132 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.3567   -1.7512   -0.4363 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.6510   -1.4023    0.8648 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.6037   -2.6246    0.1316 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.0230   -1.6556    1.4808 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.0888    0.2785   -2.2106 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.9622   -1.1023   -1.5428 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.4882   -1.6239   -3.6579 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.1726   -2.6857   -2.2595 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.9059   -0.0478   -4.1389 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.5577    0.8986    1.1713 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.2332    1.6088   -0.4110 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.3058    3.0006   -0.0800 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.5168    2.8334    1.6662 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0635    2.5160    0.9261 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.0525   -0.9145    1.7777 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0535    0.3918    2.1484 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.6130    0.4644    2.7352 H   0  0  0  0  0  0  0  0  0  0  0  0
  6  7  1  0
 11  2  1  0
 11 10  1  0
  5  4  1  0
  2  3  1  0
  4  3  1  0
 10  9  1  0
  7  8  1  1
  9  7  1  0
 14 15  1  1
  6 11  1  0
  6 26  1  1
  7 13  1  0
  2  1  1  0
 13 14  1  0
 11 12  1  6
 14  5  1  0
  5 25  1  6
  5  6  1  0
 14 16  1  0
 10 32  1  0
 10 33  1  0
  9 30  1  0
  9 31  1  0
 13 35  1  0
 13 36  1  0
  2 20  1  1
  4 23  1  0
  4 24  1  0
  3 21  1  0
  3 22  1  0
  8 27  1  0
  8 28  1  0
  8 29  1  0
 15 37  1  0
 15 38  1  0
 15 39  1  0
  1 17  1  0
  1 18  1  0
  1 19  1  0
 12 34  1  0
 16 40  1  0
 16 41  1  0
 16 42  1  0
M  END


  Mrv1652306202123033D          

 42 44  0  0  0  0            999 V2000
   -0.7870   -2.1252   -4.2231 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5982   -1.7775   -2.7481 C   0  0  2  0  0  0  0  0  0  0  0  0
   -1.7949   -0.8819   -2.2320 C   0  0  2  0  0  0  0  0  0  0  0  0
   -1.6213   -0.2336   -0.8119 C   0  0  2  0  0  0  0  0  0  0  0  0
   -0.2084    0.3324   -0.6588 C   0  0  2  0  0  0  0  0  0  0  0  0
    0.7090   -0.8419   -0.9481 C   0  0  2  0  0  0  0  0  0  0  0  0
    2.1167   -0.5594   -0.4342 C   0  0  1  0  0  0  0  0  0  0  0  0
    2.6186   -1.6192    0.5667 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.9618   -0.6944   -1.7211 C   0  0  1  0  0  0  0  0  0  0  0  0
    2.1213   -1.6553   -2.6275 C   0  0  1  0  0  0  0  0  0  0  0  0
    0.7324   -1.0607   -2.4596 C   0  0  1  0  0  0  0  0  0  0  0  0
    0.7501    0.1683   -3.2041 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.9386    0.8021    0.2725 C   0  0  1  0  0  0  0  0  0  0  0  0
    0.4001    0.9257    0.6159 C   0  0  1  0  0  0  0  0  0  0  0  0
    0.0178    2.4020    0.7914 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0125    0.1704    1.8854 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7080   -2.7010   -4.3641 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.0470   -2.7328   -4.5887 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8588   -1.2303   -4.8493 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6242   -2.7225   -2.1885 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7178   -1.4743   -2.2394 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9492   -0.0632   -2.9477 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8186   -0.9977   -0.0506 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3685    0.5556   -0.6746 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1186    1.1245   -1.4132 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.3567   -1.7512   -0.4363 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.6510   -1.4023    0.8648 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.6037   -2.6246    0.1316 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.0230   -1.6556    1.4808 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.0888    0.2785   -2.2106 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.9622   -1.1023   -1.5428 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.4882   -1.6239   -3.6579 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.1726   -2.6857   -2.2595 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.9059   -0.0478   -4.1389 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.5577    0.8986    1.1713 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.2332    1.6088   -0.4110 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.3058    3.0006   -0.0800 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.5168    2.8334    1.6662 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0635    2.5160    0.9261 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.0525   -0.9145    1.7777 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0535    0.3918    2.1484 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.6130    0.4644    2.7352 H   0  0  0  0  0  0  0  0  0  0  0  0
  6  7  1  0  0  0  0
 11  2  1  0  0  0  0
 11 10  1  0  0  0  0
  5  4  1  0  0  0  0
  2  3  1  0  0  0  0
  4  3  1  0  0  0  0
 10  9  1  0  0  0  0
  7  8  1  1  0  0  0
  9  7  1  0  0  0  0
 14 15  1  1  0  0  0
  6 11  1  0  0  0  0
  6 26  1  1  0  0  0
  7 13  1  0  0  0  0
  2  1  1  0  0  0  0
 13 14  1  0  0  0  0
 11 12  1  6  0  0  0
 14  5  1  0  0  0  0
  5 25  1  6  0  0  0
  5  6  1  0  0  0  0
 14 16  1  0  0  0  0
 10 32  1  0  0  0  0
 10 33  1  0  0  0  0
  9 30  1  0  0  0  0
  9 31  1  0  0  0  0
 13 35  1  0  0  0  0
 13 36  1  0  0  0  0
  2 20  1  1  0  0  0
  4 23  1  0  0  0  0
  4 24  1  0  0  0  0
  3 21  1  0  0  0  0
  3 22  1  0  0  0  0
  8 27  1  0  0  0  0
  8 28  1  0  0  0  0
  8 29  1  0  0  0  0
 15 37  1  0  0  0  0
 15 38  1  0  0  0  0
 15 39  1  0  0  0  0
  1 17  1  0  0  0  0
  1 18  1  0  0  0  0
  1 19  1  0  0  0  0
 12 34  1  0  0  0  0
 16 40  1  0  0  0  0
 16 41  1  0  0  0  0
 16 42  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0038332

> <DATABASE_NAME>
NP-MRD

> <SMILES>
[H]O[C@]12C([H])([H])C([H])([H])[C@@]3(C([H])([H])[H])C([H])([H])C(C([H])([H])[H])(C([H])([H])[H])[C@]([H])(C([H])([H])C([H])([H])[C@@]1([H])C([H])([H])[H])[C@@]23[H]

> <INCHI_IDENTIFIER>
InChI=1S/C15H26O/c1-10-5-6-11-12-14(4,9-13(11,2)3)7-8-15(10,12)16/h10-12,16H,5-9H2,1-4H3/t10-,11-,12-,14+,15-/m1/s1

> <INCHI_KEY>
ABEFZRUFMKMACI-MYYUVRNCSA-N

> <FORMULA>
C15H26O

> <MOLECULAR_WEIGHT>
222.372

> <EXACT_MASS>
222.198365457

> <JCHEM_ACCEPTOR_COUNT>
1

> <JCHEM_ATOM_COUNT>
42

> <JCHEM_AVERAGE_POLARIZABILITY>
27.180966904558403

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
1

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
1

> <JCHEM_IUPAC>
(1R,4S,7R,10R,11R)-4,6,6,10-tetramethyltricyclo[5.3.1.0^{4,11}]undecan-1-ol

> <ALOGPS_LOGP>
3.34

> <JCHEM_LOGP>
3.3474379026666665

> <ALOGPS_LOGS>
-4.14

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
3

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA_STRONGEST_BASIC>
-0.09684055767738009

> <JCHEM_POLAR_SURFACE_AREA>
20.23

> <JCHEM_REFRACTIVITY>
66.3725

> <JCHEM_ROTATABLE_BOND_COUNT>
0

> <JCHEM_RULE_OF_FIVE>
1

> <ALOGPS_SOLUBILITY>
1.63e-02 g/l

> <JCHEM_TRADITIONAL_IUPAC>
(1R,4S,7R,10R,11R)-4,6,6,10-tetramethyltricyclo[5.3.1.0^{4,11}]undecan-1-ol

> <JCHEM_VEBER_RULE>
1

$$$$

     RDKit          3D

 42 44  0  0  0  0  0  0  0  0999 V2000
   -0.7870   -2.1252   -4.2231 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5982   -1.7775   -2.7481 C   0  0  2  0  0  0  0  0  0  0  0  0
   -1.7949   -0.8819   -2.2320 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6213   -0.2336   -0.8119 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2084    0.3324   -0.6588 C   0  0  2  0  0  0  0  0  0  0  0  0
    0.7090   -0.8419   -0.9481 C   0  0  2  0  0  0  0  0  0  0  0  0
    2.1167   -0.5594   -0.4342 C   0  0  1  0  0  0  0  0  0  0  0  0
    2.6186   -1.6192    0.5667 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.9618   -0.6944   -1.7211 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1213   -1.6553   -2.6275 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7324   -1.0607   -2.4596 C   0  0  1  0  0  0  0  0  0  0  0  0
    0.7501    0.1683   -3.2041 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.9386    0.8021    0.2725 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.4001    0.9257    0.6159 C   0  0  1  0  0  0  0  0  0  0  0  0
    0.0178    2.4020    0.7914 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0125    0.1704    1.8854 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7080   -2.7010   -4.3641 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.0470   -2.7328   -4.5887 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8588   -1.2303   -4.8493 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6242   -2.7225   -2.1885 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7178   -1.4743   -2.2394 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9492   -0.0632   -2.9477 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8186   -0.9977   -0.0506 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3685    0.5556   -0.6746 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1186    1.1245   -1.4132 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.3567   -1.7512   -0.4363 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.6510   -1.4023    0.8648 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.6037   -2.6246    0.1316 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.0230   -1.6556    1.4808 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.0888    0.2785   -2.2106 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.9622   -1.1023   -1.5428 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.4882   -1.6239   -3.6579 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.1726   -2.6857   -2.2595 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.9059   -0.0478   -4.1389 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.5577    0.8986    1.1713 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.2332    1.6088   -0.4110 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.3058    3.0006   -0.0800 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.5168    2.8334    1.6662 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0635    2.5160    0.9261 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.0525   -0.9145    1.7777 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0535    0.3918    2.1484 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.6130    0.4644    2.7352 H   0  0  0  0  0  0  0  0  0  0  0  0
  6  7  1  0
 11  2  1  0
 11 10  1  0
  5  4  1  0
  2  3  1  0
  4  3  1  0
 10  9  1  0
  7  8  1  1
  9  7  1  0
 14 15  1  1
  6 11  1  0
  6 26  1  1
  7 13  1  0
  2  1  1  0
 13 14  1  0
 11 12  1  6
 14  5  1  0
  5 25  1  6
  5  6  1  0
 14 16  1  0
 10 32  1  0
 10 33  1  0
  9 30  1  0
  9 31  1  0
 13 35  1  0
 13 36  1  0
  2 20  1  1
  4 23  1  0
  4 24  1  0
  3 21  1  0
  3 22  1  0
  8 27  1  0
  8 28  1  0
  8 29  1  0
 15 37  1  0
 15 38  1  0
 15 39  1  0
  1 17  1  0
  1 18  1  0
  1 19  1  0
 12 34  1  0
 16 40  1  0
 16 41  1  0
 16 42  1  0
M  END

HEADER    PROTEIN                                 20-JUN-21   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   20-JUN-21         0                                  
HETATM    1  C   UNK     0      -0.787  -2.125  -4.223  0.00  0.00           C+0
HETATM    2  C   UNK     0      -0.598  -1.778  -2.748  0.00  0.00           C+0
HETATM    3  C   UNK     0      -1.795  -0.882  -2.232  0.00  0.00           C+0
HETATM    4  C   UNK     0      -1.621  -0.234  -0.812  0.00  0.00           C+0
HETATM    5  C   UNK     0      -0.208   0.332  -0.659  0.00  0.00           C+0
HETATM    6  C   UNK     0       0.709  -0.842  -0.948  0.00  0.00           C+0
HETATM    7  C   UNK     0       2.117  -0.559  -0.434  0.00  0.00           C+0
HETATM    8  C   UNK     0       2.619  -1.619   0.567  0.00  0.00           C+0
HETATM    9  C   UNK     0       2.962  -0.694  -1.721  0.00  0.00           C+0
HETATM   10  C   UNK     0       2.121  -1.655  -2.628  0.00  0.00           C+0
HETATM   11  C   UNK     0       0.732  -1.061  -2.460  0.00  0.00           C+0
HETATM   12  O   UNK     0       0.750   0.168  -3.204  0.00  0.00           O+0
HETATM   13  C   UNK     0       1.939   0.802   0.273  0.00  0.00           C+0
HETATM   14  C   UNK     0       0.400   0.926   0.616  0.00  0.00           C+0
HETATM   15  C   UNK     0       0.018   2.402   0.791  0.00  0.00           C+0
HETATM   16  C   UNK     0      -0.013   0.170   1.885  0.00  0.00           C+0
HETATM   17  H   UNK     0      -1.708  -2.701  -4.364  0.00  0.00           H+0
HETATM   18  H   UNK     0       0.047  -2.733  -4.589  0.00  0.00           H+0
HETATM   19  H   UNK     0      -0.859  -1.230  -4.849  0.00  0.00           H+0
HETATM   20  H   UNK     0      -0.624  -2.723  -2.188  0.00  0.00           H+0
HETATM   21  H   UNK     0      -2.718  -1.474  -2.239  0.00  0.00           H+0
HETATM   22  H   UNK     0      -1.949  -0.063  -2.948  0.00  0.00           H+0
HETATM   23  H   UNK     0      -1.819  -0.998  -0.051  0.00  0.00           H+0
HETATM   24  H   UNK     0      -2.369   0.556  -0.675  0.00  0.00           H+0
HETATM   25  H   UNK     0      -0.119   1.125  -1.413  0.00  0.00           H+0
HETATM   26  H   UNK     0       0.357  -1.751  -0.436  0.00  0.00           H+0
HETATM   27  H   UNK     0       3.651  -1.402   0.865  0.00  0.00           H+0
HETATM   28  H   UNK     0       2.604  -2.625   0.132  0.00  0.00           H+0
HETATM   29  H   UNK     0       2.023  -1.656   1.481  0.00  0.00           H+0
HETATM   30  H   UNK     0       3.089   0.279  -2.211  0.00  0.00           H+0
HETATM   31  H   UNK     0       3.962  -1.102  -1.543  0.00  0.00           H+0
HETATM   32  H   UNK     0       2.488  -1.624  -3.658  0.00  0.00           H+0
HETATM   33  H   UNK     0       2.173  -2.686  -2.260  0.00  0.00           H+0
HETATM   34  H   UNK     0       0.906  -0.048  -4.139  0.00  0.00           H+0
HETATM   35  H   UNK     0       2.558   0.899   1.171  0.00  0.00           H+0
HETATM   36  H   UNK     0       2.233   1.609  -0.411  0.00  0.00           H+0
HETATM   37  H   UNK     0       0.306   3.001  -0.080  0.00  0.00           H+0
HETATM   38  H   UNK     0       0.517   2.833   1.666  0.00  0.00           H+0
HETATM   39  H   UNK     0      -1.063   2.516   0.926  0.00  0.00           H+0
HETATM   40  H   UNK     0       0.053  -0.915   1.778  0.00  0.00           H+0
HETATM   41  H   UNK     0      -1.054   0.392   2.148  0.00  0.00           H+0
HETATM   42  H   UNK     0       0.613   0.464   2.735  0.00  0.00           H+0
CONECT    1    2   17   18   19                                             
CONECT    2   11    3    1   20                                             
CONECT    3    2    4   21   22                                             
CONECT    4    5    3   23   24                                             
CONECT    5    4   14   25    6                                             
CONECT    6    7   11   26    5                                             
CONECT    7    6    8    9   13                                             
CONECT    8    7   27   28   29                                             
CONECT    9   10    7   30   31                                             
CONECT   10   11    9   32   33                                             
CONECT   11    2   10    6   12                                             
CONECT   12   11   34                                                       
CONECT   13    7   14   35   36                                             
CONECT   14   15   13    5   16                                             
CONECT   15   14   37   38   39                                             
CONECT   16   14   40   41   42                                             
CONECT   17    1                                                            
CONECT   18    1                                                            
CONECT   19    1                                                            
CONECT   20    2                                                            
CONECT   21    3                                                            
CONECT   22    3                                                            
CONECT   23    4                                                            
CONECT   24    4                                                            
CONECT   25    5                                                            
CONECT   26    6                                                            
CONECT   27    8                                                            
CONECT   28    8                                                            
CONECT   29    8                                                            
CONECT   30    9                                                            
CONECT   31    9                                                            
CONECT   32   10                                                            
CONECT   33   10                                                            
CONECT   34   12                                                            
CONECT   35   13                                                            
CONECT   36   13                                                            
CONECT   37   15                                                            
CONECT   38   15                                                            
CONECT   39   15                                                            
CONECT   40   16                                                            
CONECT   41   16                                                            
CONECT   42   16                                                            
MASTER        0    0    0    0    0    0    0    0   42    0   88    0
END

RDKit          3D

42 44  0  0  0  0  0  0  0  0999 V2000
   -0.7870   -2.1252   -4.2231 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5982   -1.7775   -2.7481 C   0  0  2  0  0  0  0  0  0  0  0  0
   -1.7949   -0.8819   -2.2320 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6213   -0.2336   -0.8119 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2084    0.3324   -0.6588 C   0  0  2  0  0  0  0  0  0  0  0  0
    0.7090   -0.8419   -0.9481 C   0  0  2  0  0  0  0  0  0  0  0  0
    2.1167   -0.5594   -0.4342 C   0  0  1  0  0  0  0  0  0  0  0  0
    2.6186   -1.6192    0.5667 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.9618   -0.6944   -1.7211 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1213   -1.6553   -2.6275 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7324   -1.0607   -2.4596 C   0  0  1  0  0  0  0  0  0  0  0  0
    0.7501    0.1683   -3.2041 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.9386    0.8021    0.2725 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.4001    0.9257    0.6159 C   0  0  1  0  0  0  0  0  0  0  0  0
    0.0178    2.4020    0.7914 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0125    0.1704    1.8854 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7080   -2.7010   -4.3641 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.0470   -2.7328   -4.5887 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8588   -1.2303   -4.8493 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6242   -2.7225   -2.1885 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7178   -1.4743   -2.2394 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9492   -0.0632   -2.9477 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8186   -0.9977   -0.0506 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3685    0.5556   -0.6746 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1186    1.1245   -1.4132 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.3567   -1.7512   -0.4363 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.6510   -1.4023    0.8648 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.6037   -2.6246    0.1316 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.0230   -1.6556    1.4808 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.0888    0.2785   -2.2106 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.9622   -1.1023   -1.5428 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.4882   -1.6239   -3.6579 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.1726   -2.6857   -2.2595 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.9059   -0.0478   -4.1389 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.5577    0.8986    1.1713 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.2332    1.6088   -0.4110 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.3058    3.0006   -0.0800 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.5168    2.8334    1.6662 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0635    2.5160    0.9261 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.0525   -0.9145    1.7777 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0535    0.3918    2.1484 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.6130    0.4644    2.7352 H   0  0  0  0  0  0  0  0  0  0  0  0
  6  7  1  0
 11  2  1  0
 11 10  1  0
  5  4  1  0
  2  3  1  0
  4  3  1  0
 10  9  1  0
  7  8  1  1
  9  7  1  0
 14 15  1  1
  6 11  1  0
  6 26  1  1
  7 13  1  0
  2  1  1  0
 13 14  1  0
 11 12  1  6
 14  5  1  0
  5 25  1  6
  5  6  1  0
 14 16  1  0
 10 32  1  0
 10 33  1  0
  9 30  1  0
  9 31  1  0
 13 35  1  0
 13 36  1  0
  2 20  1  1
  4 23  1  0
  4 24  1  0
  3 21  1  0
  3 22  1  0
  8 27  1  0
  8 28  1  0
  8 29  1  0
 15 37  1  0
 15 38  1  0
 15 39  1  0
  1 17  1  0
  1 18  1  0
  1 19  1  0
 12 34  1  0
 16 40  1  0
 16 41  1  0
 16 42  1  0
M  END

View in JSmol

Synonyms

Not Available

Chemical Formula

C₁₅H₂₆O

Average Mass

222.3720 Da

Monoisotopic Mass

222.19837 Da

IUPAC Name

(1R,4S,7R,10R,11R)-4,6,6,10-tetramethyltricyclo[5.3.1.0^{4,11}]undecan-1-ol

Traditional Name

(1R,4S,7R,10R,11R)-4,6,6,10-tetramethyltricyclo[5.3.1.0^{4,11}]undecan-1-ol

CAS Registry Number

Not Available

SMILES

[H]O[C@]12C([H])([H])C([H])([H])[C@@]3(C([H])([H])[H])C([H])([H])C(C([H])([H])[H])(C([H])([H])[H])[C@]([H])(C([H])([H])C([H])([H])[C@@]1([H])C([H])([H])[H])[C@@]23[H]

InChI Identifier

InChI=1S/C15H26O/c1-10-5-6-11-12-14(4,9-13(11,2)3)7-8-15(10,12)16/h10-12,16H,5-9H2,1-4H3/t10-,11-,12-,14+,15-/m1/s1

InChI Key

ABEFZRUFMKMACI-MYYUVRNCSA-N

Experimental Spectra

Spectrum Type	Description	Depositor Email	Depositor Organization	Depositor	Deposition Date	View
1D NMR	¹³C NMR Spectrum (1D, 400 MHz, C₆D₆, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 400 MHz, C₆D₆, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 100 MHz, C₆D₆, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 100 MHz, C₆D₆, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 200 MHz, C₆D₆, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 200 MHz, C₆D₆, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 300 MHz, C₆D₆, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 300 MHz, C₆D₆, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 500 MHz, C₆D₆, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 500 MHz, C₆D₆, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 600 MHz, C₆D₆, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 600 MHz, C₆D₆, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 700 MHz, C₆D₆, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 700 MHz, C₆D₆, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 800 MHz, C₆D₆, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 800 MHz, C₆D₆, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 900 MHz, C₆D₆, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 900 MHz, C₆D₆, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 1000 MHz, C₆D₆, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 1000 MHz, C₆D₆, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum

Predicted Spectra

Not Available

Chemical Shift Submissions

Not Available

Species

Species of Origin

Species Name	Source	Reference
Anemia tomentosa var. anthriscifolia (Pteridophyta)	JEOL database	Pinto, S. C., et al, Tetrahedron Lett. 50, 4785 (2009)
Conocephalum conicum	Plant	KNApSAcK

Chemical Taxonomy

Classification

Not classified

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	3.34	ALOGPS
logP	3.35	ChemAxon
logS	-4.1	ALOGPS
pKa (Strongest Basic)	-0.097	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	1	ChemAxon
Hydrogen Donor Count	1	ChemAxon
Polar Surface Area	20.23 Å²	ChemAxon
Rotatable Bond Count	0	ChemAxon
Refractivity	66.37 m³·mol⁻¹	ChemAxon
Polarizability	27.18 Å³	ChemAxon
Number of Rings	3	ChemAxon
Bioavailability	Yes	ChemAxon
Rule of Five	Yes	ChemAxon
Ghose Filter	Yes	ChemAxon
Veber's Rule	Yes	ChemAxon
MDDR-like Rule	No	ChemAxon

External Links

HMDB ID

Not Available

DrugBank ID

Not Available

Phenol Explorer Compound ID

Not Available

FoodDB ID

Not Available

KNApSAcK ID

Not Available

Chemspider ID

Not Available

KEGG Compound ID

Not Available

BioCyc ID

Not Available

BiGG ID

Not Available

Wikipedia Link

Not Available

METLIN ID

Not Available

PubChem Compound

100982161

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

Zhang Z, Li Y, Zhao D, He Y, Gong J, Yang Z: A Concise Synthesis of Presilphiperfolane Core through a Tandem TMTU-Co-Catalyzed Pauson-Khand Reaction and a 6pi Electrocyclization Reaction (TMTU=Tetramethyl Thiourea). Chemistry. 2017 Jan 26;23(6):1258-1262. doi: 10.1002/chem.201605438. Epub 2017 Jan 3. [PubMed:28052485 ]
Hong AY, Stoltz BM: Enantioselective total synthesis of the reported structures of (-)-9-epi-presilphiperfolan-1-ol and (-)-presilphiperfolan-1-ol: structural confirmation and reassignment and biosynthetic insights. Angew Chem Int Ed Engl. 2012 Sep 17;51(38):9674-8. doi: 10.1002/anie.201205276. Epub 2012 Aug 22. [PubMed:22915502 ]
Pinto SC, Leitao GG, de Oliveira DR, Bizzo HR, Ramos DF, Coelho TS, Silva PE, Lourenco MC, Leitao SG: Chemical composition and antimycobacterial activity of the essential oil from Anemia tomentosa var. anthriscifolia. Nat Prod Commun. 2009 Dec;4(12):1675-8. [PubMed:20120105 ]
Pinto, S. C., et al. (2009). Pinto, S. C., et al, Tetrahedron Lett. 50, 4785 (2009). Tetrahedron Lett.

Showing NP-Card for (-)-epi-presilphiperfolan-1-ol (NP0038332)

MOL for NP0038332 ((-)-epi-presilphiperfolan-1-ol)

3D MOL for NP0038332 ((-)-epi-presilphiperfolan-1-ol)

3D SDF for NP0038332 ((-)-epi-presilphiperfolan-1-ol)

3D-SDF for NP0038332 ((-)-epi-presilphiperfolan-1-ol)

PDB for NP0038332 ((-)-epi-presilphiperfolan-1-ol)

3D PDB for NP0038332 ((-)-epi-presilphiperfolan-1-ol)

SMILES for NP0038332 ((-)-epi-presilphiperfolan-1-ol)

INCHI for NP0038332 ((-)-epi-presilphiperfolan-1-ol)

Structure for NP0038332 ((-)-epi-presilphiperfolan-1-ol)

3D Structure for NP0038332 ((-)-epi-presilphiperfolan-1-ol)