NP-MRD: Showing NP-Card for artarborol (NP0038873)

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Record Information

Version

2.0

Created at

2021-06-20 21:27:00 UTC

Updated at

2021-06-30 00:11:53 UTC

NP-MRD ID

NP0038873

Secondary Accession Numbers

None

Natural Product Identification

Common Name

artarborol

Provided By

JEOL Database JEOL Logo

Description

Artarborol belongs to the class of organic compounds known as cyclic alcohols and derivatives. These are organic compounds containing an aliphatic ring substituted with at least one hydroxyl group. artarborol is found in Artemisia arborescen and Artemisia arborescens. artarborol was first documented in 2007 (PMID: 17489600). Based on a literature review very few articles have been published on Artarborol.

Structure

MOL 3D MOL SDF 3D SDF PDB SMILES InChI


  Mrv1652306202123273D          

 40 42  0  0  0  0            999 V2000
    0.9661   -0.0936   -2.0966 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5431   -0.0636   -1.8557 C   0  0  2  0  0  0  0  0  0  0  0  0
   -1.2568   -1.0747   -2.7601 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1624    1.3476   -1.9728 C   0  0  2  0  0  0  0  0  0  0  0  0
   -2.0042    1.0690   -0.6927 C   0  0  2  0  0  0  0  0  0  0  0  0
   -2.2644    2.3839    0.0648 C   0  0  2  0  0  0  0  0  0  0  0  0
   -1.0468    2.9066    0.5807 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.3461    2.2722    1.1501 C   0  0  2  0  0  0  0  0  0  0  0  0
   -2.8766    1.9793    2.5789 C   0  0  2  0  0  0  0  0  0  0  0  0
   -1.9547    0.8212    2.6459 C   0  0  1  0  0  0  0  0  0  0  0  0
   -2.1598   -0.1385    3.6862 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4159   -0.5862    2.3416 C   0  0  1  0  0  0  0  0  0  0  0  0
   -3.8531   -0.9645    2.1451 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3787   -1.4868    1.7446 C   0  0  2  0  0  0  0  0  0  0  0  0
   -1.3511   -1.4062    0.2177 C   0  0  1  0  0  0  0  0  0  0  0  0
   -0.9263   -0.0319   -0.3214 C   0  0  1  0  0  0  0  0  0  0  0  0
    1.4873    0.6577   -1.4932 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.3812   -1.0736   -1.8376 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.1993    0.1072   -3.1478 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3411   -1.0681   -2.6077 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8981   -2.0924   -2.5730 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0725   -0.8474   -3.8161 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7499    1.5471   -2.8753 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4315    2.1599   -1.8700 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.9680    0.6103   -0.9623 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6359    3.1085   -0.6725 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2270    3.8070    0.9021 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.1097    1.5495    0.8422 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.8658    3.2391    1.1984 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.7533    1.8281    3.2198 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3622    2.8608    2.9807 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9281    1.1042    2.4453 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.1460   -0.8517    1.0972 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.0129   -2.0097    2.4303 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.5306   -0.3551    2.7515 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5866   -2.5211    2.0447 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3828   -1.2479    2.1392 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6251   -2.1560   -0.1217 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3219   -1.6983   -0.1978 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1042    0.3797    0.2823 H   0  0  0  0  0  0  0  0  0  0  0  0
  5  4  1  0  0  0  0
  4  2  1  0  0  0  0
  2 16  1  0  0  0  0
 10 11  1  0  0  0  0
 10  9  1  0  0  0  0
  9  8  1  0  0  0  0
  8  6  1  0  0  0  0
 14 15  1  0  0  0  0
  2  1  1  1  0  0  0
 15 16  1  0  0  0  0
 16 40  1  1  0  0  0
 16  5  1  0  0  0  0
  6  7  1  0  0  0  0
 12 14  1  0  0  0  0
 10 32  1  6  0  0  0
  5  6  1  0  0  0  0
 12 13  1  1  0  0  0
 12 10  1  0  0  0  0
  5 25  1  6  0  0  0
 11 12  1  0  0  0  0
  2  3  1  0  0  0  0
 14 36  1  0  0  0  0
 14 37  1  0  0  0  0
 15 38  1  0  0  0  0
 15 39  1  0  0  0  0
  6 26  1  6  0  0  0
  4 23  1  0  0  0  0
  4 24  1  0  0  0  0
  9 30  1  0  0  0  0
  9 31  1  0  0  0  0
  8 28  1  0  0  0  0
  8 29  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
  7 27  1  0  0  0  0
 13 33  1  0  0  0  0
 13 34  1  0  0  0  0
 13 35  1  0  0  0  0
  3 20  1  0  0  0  0
  3 21  1  0  0  0  0
  3 22  1  0  0  0  0
M  END

     RDKit          3D

 40 42  0  0  0  0  0  0  0  0999 V2000
    0.9661   -0.0936   -2.0966 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5431   -0.0636   -1.8557 C   0  0  2  0  0  0  0  0  0  0  0  0
   -1.2568   -1.0747   -2.7601 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1624    1.3476   -1.9728 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0042    1.0690   -0.6927 C   0  0  2  0  0  0  0  0  0  0  0  0
   -2.2644    2.3839    0.0648 C   0  0  2  0  0  0  0  0  0  0  0  0
   -1.0468    2.9066    0.5807 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.3461    2.2722    1.1501 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8766    1.9793    2.5789 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9547    0.8212    2.6459 C   0  0  1  0  0  0  0  0  0  0  0  0
   -2.1598   -0.1385    3.6862 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4159   -0.5862    2.3416 C   0  0  1  0  0  0  0  0  0  0  0  0
   -3.8531   -0.9645    2.1451 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3787   -1.4868    1.7446 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3511   -1.4062    0.2177 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9263   -0.0319   -0.3214 C   0  0  1  0  0  0  0  0  0  0  0  0
    1.4873    0.6577   -1.4932 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.3812   -1.0736   -1.8376 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.1993    0.1072   -3.1478 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3411   -1.0681   -2.6077 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8981   -2.0924   -2.5730 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0725   -0.8474   -3.8161 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7499    1.5471   -2.8753 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4315    2.1599   -1.8700 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.9680    0.6103   -0.9623 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6359    3.1085   -0.6725 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2270    3.8070    0.9021 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.1097    1.5495    0.8422 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.8658    3.2391    1.1984 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.7533    1.8281    3.2198 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3622    2.8608    2.9807 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9281    1.1042    2.4453 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.1460   -0.8517    1.0972 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.0129   -2.0097    2.4303 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.5306   -0.3551    2.7515 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5866   -2.5211    2.0447 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3828   -1.2479    2.1392 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6251   -2.1560   -0.1217 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3219   -1.6983   -0.1978 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1042    0.3797    0.2823 H   0  0  0  0  0  0  0  0  0  0  0  0
  5  4  1  0
  4  2  1  0
  2 16  1  0
 10 11  1  0
 10  9  1  0
  9  8  1  0
  8  6  1  0
 14 15  1  0
  2  1  1  1
 15 16  1  0
 16 40  1  1
 16  5  1  0
  6  7  1  0
 12 14  1  0
 10 32  1  6
  5  6  1  0
 12 13  1  1
 12 10  1  0
  5 25  1  6
 11 12  1  0
  2  3  1  0
 14 36  1  0
 14 37  1  0
 15 38  1  0
 15 39  1  0
  6 26  1  6
  4 23  1  0
  4 24  1  0
  9 30  1  0
  9 31  1  0
  8 28  1  0
  8 29  1  0
  1 17  1  0
  1 18  1  0
  1 19  1  0
  7 27  1  0
 13 33  1  0
 13 34  1  0
 13 35  1  0
  3 20  1  0
  3 21  1  0
  3 22  1  0
M  END


  Mrv1652306202123273D          

 40 42  0  0  0  0            999 V2000
    0.9661   -0.0936   -2.0966 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5431   -0.0636   -1.8557 C   0  0  2  0  0  0  0  0  0  0  0  0
   -1.2568   -1.0747   -2.7601 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1624    1.3476   -1.9728 C   0  0  2  0  0  0  0  0  0  0  0  0
   -2.0042    1.0690   -0.6927 C   0  0  2  0  0  0  0  0  0  0  0  0
   -2.2644    2.3839    0.0648 C   0  0  2  0  0  0  0  0  0  0  0  0
   -1.0468    2.9066    0.5807 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.3461    2.2722    1.1501 C   0  0  2  0  0  0  0  0  0  0  0  0
   -2.8766    1.9793    2.5789 C   0  0  2  0  0  0  0  0  0  0  0  0
   -1.9547    0.8212    2.6459 C   0  0  1  0  0  0  0  0  0  0  0  0
   -2.1598   -0.1385    3.6862 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4159   -0.5862    2.3416 C   0  0  1  0  0  0  0  0  0  0  0  0
   -3.8531   -0.9645    2.1451 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3787   -1.4868    1.7446 C   0  0  2  0  0  0  0  0  0  0  0  0
   -1.3511   -1.4062    0.2177 C   0  0  1  0  0  0  0  0  0  0  0  0
   -0.9263   -0.0319   -0.3214 C   0  0  1  0  0  0  0  0  0  0  0  0
    1.4873    0.6577   -1.4932 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.3812   -1.0736   -1.8376 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.1993    0.1072   -3.1478 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3411   -1.0681   -2.6077 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8981   -2.0924   -2.5730 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0725   -0.8474   -3.8161 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7499    1.5471   -2.8753 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4315    2.1599   -1.8700 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.9680    0.6103   -0.9623 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6359    3.1085   -0.6725 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2270    3.8070    0.9021 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.1097    1.5495    0.8422 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.8658    3.2391    1.1984 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.7533    1.8281    3.2198 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3622    2.8608    2.9807 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9281    1.1042    2.4453 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.1460   -0.8517    1.0972 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.0129   -2.0097    2.4303 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.5306   -0.3551    2.7515 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5866   -2.5211    2.0447 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3828   -1.2479    2.1392 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6251   -2.1560   -0.1217 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3219   -1.6983   -0.1978 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1042    0.3797    0.2823 H   0  0  0  0  0  0  0  0  0  0  0  0
  5  4  1  0  0  0  0
  4  2  1  0  0  0  0
  2 16  1  0  0  0  0
 10 11  1  0  0  0  0
 10  9  1  0  0  0  0
  9  8  1  0  0  0  0
  8  6  1  0  0  0  0
 14 15  1  0  0  0  0
  2  1  1  1  0  0  0
 15 16  1  0  0  0  0
 16 40  1  1  0  0  0
 16  5  1  0  0  0  0
  6  7  1  0  0  0  0
 12 14  1  0  0  0  0
 10 32  1  6  0  0  0
  5  6  1  0  0  0  0
 12 13  1  1  0  0  0
 12 10  1  0  0  0  0
  5 25  1  6  0  0  0
 11 12  1  0  0  0  0
  2  3  1  0  0  0  0
 14 36  1  0  0  0  0
 14 37  1  0  0  0  0
 15 38  1  0  0  0  0
 15 39  1  0  0  0  0
  6 26  1  6  0  0  0
  4 23  1  0  0  0  0
  4 24  1  0  0  0  0
  9 30  1  0  0  0  0
  9 31  1  0  0  0  0
  8 28  1  0  0  0  0
  8 29  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
  7 27  1  0  0  0  0
 13 33  1  0  0  0  0
 13 34  1  0  0  0  0
 13 35  1  0  0  0  0
  3 20  1  0  0  0  0
  3 21  1  0  0  0  0
  3 22  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0038873

> <DATABASE_NAME>
NP-MRD

> <SMILES>
[H]O[C@]1([H])C([H])([H])C([H])([H])[C@@]2([H])O[C@]2(C([H])([H])[H])C([H])([H])C([H])([H])[C@]2([H])[C@]1([H])C([H])([H])C2(C([H])([H])[H])C([H])([H])[H]

> <INCHI_IDENTIFIER>
InChI=1S/C14H24O2/c1-13(2)8-9-10(13)6-7-14(3)12(16-14)5-4-11(9)15/h9-12,15H,4-8H2,1-3H3/t9-,10+,11+,12+,14+/m0/s1

> <INCHI_KEY>
SBEAPGVVWPHQSD-WRYZSIRCSA-N

> <FORMULA>
C14H24O2

> <MOLECULAR_WEIGHT>
224.344

> <EXACT_MASS>
224.177630013

> <JCHEM_ACCEPTOR_COUNT>
2

> <JCHEM_ATOM_COUNT>
40

> <JCHEM_AVERAGE_POLARIZABILITY>
26.11986045890464

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
1

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
1

> <JCHEM_IUPAC>
(1R,4R,6R,9R,10S)-4,12,12-trimethyl-5-oxatricyclo[8.2.0.0^{4,6}]dodecan-9-ol

> <ALOGPS_LOGP>
2.30

> <JCHEM_LOGP>
2.3703898009999995

> <ALOGPS_LOGS>
-3.18

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
3

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA_STRONGEST_ACIDIC>
14.9357752166785

> <JCHEM_PKA_STRONGEST_BASIC>
-2.826891920224824

> <JCHEM_POLAR_SURFACE_AREA>
32.76

> <JCHEM_REFRACTIVITY>
63.4793

> <JCHEM_ROTATABLE_BOND_COUNT>
0

> <JCHEM_RULE_OF_FIVE>
1

> <ALOGPS_SOLUBILITY>
1.48e-01 g/l

> <JCHEM_TRADITIONAL_IUPAC>
(1R,4R,6R,9R,10S)-4,12,12-trimethyl-5-oxatricyclo[8.2.0.0^{4,6}]dodecan-9-ol

> <JCHEM_VEBER_RULE>
1

$$$$

     RDKit          3D

 40 42  0  0  0  0  0  0  0  0999 V2000
    0.9661   -0.0936   -2.0966 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5431   -0.0636   -1.8557 C   0  0  2  0  0  0  0  0  0  0  0  0
   -1.2568   -1.0747   -2.7601 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1624    1.3476   -1.9728 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0042    1.0690   -0.6927 C   0  0  2  0  0  0  0  0  0  0  0  0
   -2.2644    2.3839    0.0648 C   0  0  2  0  0  0  0  0  0  0  0  0
   -1.0468    2.9066    0.5807 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.3461    2.2722    1.1501 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8766    1.9793    2.5789 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9547    0.8212    2.6459 C   0  0  1  0  0  0  0  0  0  0  0  0
   -2.1598   -0.1385    3.6862 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4159   -0.5862    2.3416 C   0  0  1  0  0  0  0  0  0  0  0  0
   -3.8531   -0.9645    2.1451 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3787   -1.4868    1.7446 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3511   -1.4062    0.2177 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9263   -0.0319   -0.3214 C   0  0  1  0  0  0  0  0  0  0  0  0
    1.4873    0.6577   -1.4932 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.3812   -1.0736   -1.8376 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.1993    0.1072   -3.1478 H   0  0  0  0  0  0  0  0  0  0  0  0
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   -4.1097    1.5495    0.8422 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.8658    3.2391    1.1984 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.7533    1.8281    3.2198 H   0  0  0  0  0  0  0  0  0  0  0  0
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   -0.9281    1.1042    2.4453 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.1460   -0.8517    1.0972 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.0129   -2.0097    2.4303 H   0  0  0  0  0  0  0  0  0  0  0  0
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   -1.5866   -2.5211    2.0447 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3828   -1.2479    2.1392 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6251   -2.1560   -0.1217 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3219   -1.6983   -0.1978 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1042    0.3797    0.2823 H   0  0  0  0  0  0  0  0  0  0  0  0
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  4  2  1  0
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 10  9  1  0
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 12 14  1  0
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  3 20  1  0
  3 21  1  0
  3 22  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       0.966  -0.094  -2.097  0.00  0.00           C+0
HETATM    2  C   UNK     0      -0.543  -0.064  -1.856  0.00  0.00           C+0
HETATM    3  C   UNK     0      -1.257  -1.075  -2.760  0.00  0.00           C+0
HETATM    4  C   UNK     0      -1.162   1.348  -1.973  0.00  0.00           C+0
HETATM    5  C   UNK     0      -2.004   1.069  -0.693  0.00  0.00           C+0
HETATM    6  C   UNK     0      -2.264   2.384   0.065  0.00  0.00           C+0
HETATM    7  O   UNK     0      -1.047   2.907   0.581  0.00  0.00           O+0
HETATM    8  C   UNK     0      -3.346   2.272   1.150  0.00  0.00           C+0
HETATM    9  C   UNK     0      -2.877   1.979   2.579  0.00  0.00           C+0
HETATM   10  C   UNK     0      -1.955   0.821   2.646  0.00  0.00           C+0
HETATM   11  O   UNK     0      -2.160  -0.139   3.686  0.00  0.00           O+0
HETATM   12  C   UNK     0      -2.416  -0.586   2.342  0.00  0.00           C+0
HETATM   13  C   UNK     0      -3.853  -0.965   2.145  0.00  0.00           C+0
HETATM   14  C   UNK     0      -1.379  -1.487   1.745  0.00  0.00           C+0
HETATM   15  C   UNK     0      -1.351  -1.406   0.218  0.00  0.00           C+0
HETATM   16  C   UNK     0      -0.926  -0.032  -0.321  0.00  0.00           C+0
HETATM   17  H   UNK     0       1.487   0.658  -1.493  0.00  0.00           H+0
HETATM   18  H   UNK     0       1.381  -1.074  -1.838  0.00  0.00           H+0
HETATM   19  H   UNK     0       1.199   0.107  -3.148  0.00  0.00           H+0
HETATM   20  H   UNK     0      -2.341  -1.068  -2.608  0.00  0.00           H+0
HETATM   21  H   UNK     0      -0.898  -2.092  -2.573  0.00  0.00           H+0
HETATM   22  H   UNK     0      -1.073  -0.847  -3.816  0.00  0.00           H+0
HETATM   23  H   UNK     0      -1.750   1.547  -2.875  0.00  0.00           H+0
HETATM   24  H   UNK     0      -0.432   2.160  -1.870  0.00  0.00           H+0
HETATM   25  H   UNK     0      -2.968   0.610  -0.962  0.00  0.00           H+0
HETATM   26  H   UNK     0      -2.636   3.108  -0.673  0.00  0.00           H+0
HETATM   27  H   UNK     0      -1.227   3.807   0.902  0.00  0.00           H+0
HETATM   28  H   UNK     0      -4.110   1.550   0.842  0.00  0.00           H+0
HETATM   29  H   UNK     0      -3.866   3.239   1.198  0.00  0.00           H+0
HETATM   30  H   UNK     0      -3.753   1.828   3.220  0.00  0.00           H+0
HETATM   31  H   UNK     0      -2.362   2.861   2.981  0.00  0.00           H+0
HETATM   32  H   UNK     0      -0.928   1.104   2.445  0.00  0.00           H+0
HETATM   33  H   UNK     0      -4.146  -0.852   1.097  0.00  0.00           H+0
HETATM   34  H   UNK     0      -4.013  -2.010   2.430  0.00  0.00           H+0
HETATM   35  H   UNK     0      -4.531  -0.355   2.752  0.00  0.00           H+0
HETATM   36  H   UNK     0      -1.587  -2.521   2.045  0.00  0.00           H+0
HETATM   37  H   UNK     0      -0.383  -1.248   2.139  0.00  0.00           H+0
HETATM   38  H   UNK     0      -0.625  -2.156  -0.122  0.00  0.00           H+0
HETATM   39  H   UNK     0      -2.322  -1.698  -0.198  0.00  0.00           H+0
HETATM   40  H   UNK     0      -0.104   0.380   0.282  0.00  0.00           H+0
CONECT    1    2   17   18   19                                             
CONECT    2    4   16    1    3                                             
CONECT    3    2   20   21   22                                             
CONECT    4    5    2   23   24                                             
CONECT    5    4   16    6   25                                             
CONECT    6    8    7    5   26                                             
CONECT    7    6   27                                                       
CONECT    8    9    6   28   29                                             
CONECT    9   10    8   30   31                                             
CONECT   10   11    9   32   12                                             
CONECT   11   10   12                                                       
CONECT   12   14   13   10   11                                             
CONECT   13   12   33   34   35                                             
CONECT   14   15   12   36   37                                             
CONECT   15   14   16   38   39                                             
CONECT   16    2   15   40    5                                             
CONECT   17    1                                                            
CONECT   18    1                                                            
CONECT   19    1                                                            
CONECT   20    3                                                            
CONECT   21    3                                                            
CONECT   22    3                                                            
CONECT   23    4                                                            
CONECT   24    4                                                            
CONECT   25    5                                                            
CONECT   26    6                                                            
CONECT   27    7                                                            
CONECT   28    8                                                            
CONECT   29    8                                                            
CONECT   30    9                                                            
CONECT   31    9                                                            
CONECT   32   10                                                            
CONECT   33   13                                                            
CONECT   34   13                                                            
CONECT   35   13                                                            
CONECT   36   14                                                            
CONECT   37   14                                                            
CONECT   38   15                                                            
CONECT   39   15                                                            
CONECT   40   16                                                            
MASTER        0    0    0    0    0    0    0    0   40    0   84    0
END

RDKit          3D

40 42  0  0  0  0  0  0  0  0999 V2000
    0.9661   -0.0936   -2.0966 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5431   -0.0636   -1.8557 C   0  0  2  0  0  0  0  0  0  0  0  0
   -1.2568   -1.0747   -2.7601 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1624    1.3476   -1.9728 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0042    1.0690   -0.6927 C   0  0  2  0  0  0  0  0  0  0  0  0
   -2.2644    2.3839    0.0648 C   0  0  2  0  0  0  0  0  0  0  0  0
   -1.0468    2.9066    0.5807 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.3461    2.2722    1.1501 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8766    1.9793    2.5789 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9547    0.8212    2.6459 C   0  0  1  0  0  0  0  0  0  0  0  0
   -2.1598   -0.1385    3.6862 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4159   -0.5862    2.3416 C   0  0  1  0  0  0  0  0  0  0  0  0
   -3.8531   -0.9645    2.1451 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3787   -1.4868    1.7446 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3511   -1.4062    0.2177 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9263   -0.0319   -0.3214 C   0  0  1  0  0  0  0  0  0  0  0  0
    1.4873    0.6577   -1.4932 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.3812   -1.0736   -1.8376 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.1993    0.1072   -3.1478 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3411   -1.0681   -2.6077 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8981   -2.0924   -2.5730 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0725   -0.8474   -3.8161 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7499    1.5471   -2.8753 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4315    2.1599   -1.8700 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.9680    0.6103   -0.9623 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6359    3.1085   -0.6725 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2270    3.8070    0.9021 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.1097    1.5495    0.8422 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.8658    3.2391    1.1984 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.7533    1.8281    3.2198 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3622    2.8608    2.9807 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9281    1.1042    2.4453 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.1460   -0.8517    1.0972 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.0129   -2.0097    2.4303 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.5306   -0.3551    2.7515 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5866   -2.5211    2.0447 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3828   -1.2479    2.1392 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6251   -2.1560   -0.1217 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3219   -1.6983   -0.1978 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1042    0.3797    0.2823 H   0  0  0  0  0  0  0  0  0  0  0  0
  5  4  1  0
  4  2  1  0
  2 16  1  0
 10 11  1  0
 10  9  1  0
  9  8  1  0
  8  6  1  0
 14 15  1  0
  2  1  1  1
 15 16  1  0
 16 40  1  1
 16  5  1  0
  6  7  1  0
 12 14  1  0
 10 32  1  6
  5  6  1  0
 12 13  1  1
 12 10  1  0
  5 25  1  6
 11 12  1  0
  2  3  1  0
 14 36  1  0
 14 37  1  0
 15 38  1  0
 15 39  1  0
  6 26  1  6
  4 23  1  0
  4 24  1  0
  9 30  1  0
  9 31  1  0
  8 28  1  0
  8 29  1  0
  1 17  1  0
  1 18  1  0
  1 19  1  0
  7 27  1  0
 13 33  1  0
 13 34  1  0
 13 35  1  0
  3 20  1  0
  3 21  1  0
  3 22  1  0
M  END

View in JSmol

Synonyms

Not Available

Chemical Formula

C₁₄H₂₄O₂

Average Mass

224.3440 Da

Monoisotopic Mass

224.17763 Da

IUPAC Name

(1R,4R,6R,9R,10S)-4,12,12-trimethyl-5-oxatricyclo[8.2.0.0^{4,6}]dodecan-9-ol

Traditional Name

(1R,4R,6R,9R,10S)-4,12,12-trimethyl-5-oxatricyclo[8.2.0.0^{4,6}]dodecan-9-ol

CAS Registry Number

Not Available

SMILES

[H]O[C@]1([H])C([H])([H])C([H])([H])[C@@]2([H])O[C@]2(C([H])([H])[H])C([H])([H])C([H])([H])[C@]2([H])[C@]1([H])C([H])([H])C2(C([H])([H])[H])C([H])([H])[H]

InChI Identifier

InChI=1S/C14H24O2/c1-13(2)8-9-10(13)6-7-14(3)12(16-14)5-4-11(9)15/h9-12,15H,4-8H2,1-3H3/t9-,10+,11+,12+,14+/m0/s1

InChI Key

SBEAPGVVWPHQSD-WRYZSIRCSA-N

Experimental Spectra

Spectrum Type	Description	Depositor Email	Depositor Organization	Depositor	Deposition Date	View
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, 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, 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, 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, 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
Artemisia arborescen	JEOL database	Fattorusso, C., et al, Org. Lett. 9, 2377 (2007)
Artemisia arborescens	LOTUS Database	35616633

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as cyclic alcohols and derivatives. These are organic compounds containing an aliphatic ring substituted with at least one hydroxyl group.

Kingdom

Organic compounds

Super Class

Organic oxygen compounds

Class

Organooxygen compounds

Sub Class

Alcohols and polyols

Direct Parent

Cyclic alcohols and derivatives

Alternative Parents

Substituents

Cyclic alcohol
Secondary alcohol
Oxacycle
Organoheterocyclic compound
Ether
Oxirane
Dialkyl ether
Hydrocarbon derivative
Aliphatic heteropolycyclic compound

Molecular Framework

Aliphatic heteropolycyclic compounds

External Descriptors

Not Available

Physical Properties

State

Not Available

Experimental Properties

Property	Value	Reference
Melting Point	Not Available	Not Available
Boiling Point	Not Available	Not Available
Water Solubility	Not Available	Not Available
LogP	Not Available	Not Available

Predicted Properties

Property	Value	Source
logP	2.3	ALOGPS
logP	2.37	ChemAxon
logS	-3.2	ALOGPS
pKa (Strongest Acidic)	14.94	ChemAxon
pKa (Strongest Basic)	-2.8	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	2	ChemAxon
Hydrogen Donor Count	1	ChemAxon
Polar Surface Area	32.76 Å²	ChemAxon
Rotatable Bond Count	0	ChemAxon
Refractivity	63.48 m³·mol⁻¹	ChemAxon
Polarizability	26.12 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

8998338

KEGG Compound ID

Not Available

BioCyc ID

Not Available

BiGG ID

Not Available

Wikipedia Link

Not Available

METLIN ID

Not Available

PubChem Compound

10823037

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

Fattorusso C, Stendardo E, Appendino G, Fattorusso E, Luciano P, Romano A, Taglialatela-Scafati O: Artarborol, a nor-caryophyllane sesquiterpene alcohol from Artemisia arborescens. stereostructure assignment through concurrence of NMR data and computational analysis. Org Lett. 2007 Jun 7;9(12):2377-80. doi: 10.1021/ol070803s. Epub 2007 May 10. [PubMed:17489600 ]
Fattorusso, C., et al. (2007). Fattorusso, C., et al, Org. Lett. 9, 2377 (2007). Org. Lett..

Showing NP-Card for artarborol (NP0038873)

MOL for NP0038873 (artarborol)

3D MOL for NP0038873 (artarborol)

3D SDF for NP0038873 (artarborol)

3D-SDF for NP0038873 (artarborol)

PDB for NP0038873 (artarborol)

3D PDB for NP0038873 (artarborol)

SMILES for NP0038873 (artarborol)

INCHI for NP0038873 (artarborol)

Structure for NP0038873 (artarborol)

3D Structure for NP0038873 (artarborol)