NP-MRD: Showing NP-Card for (+)-10-(ethylene oxide)-allo-aromadendrane (NP0030320)

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Record Information

Version

2.0

Created at

2021-06-19 21:42:31 UTC

Updated at

2021-06-29 23:58:13 UTC

NP-MRD ID

NP0030320

Secondary Accession Numbers

None

Natural Product Identification

Common Name

(+)-10-(ethylene oxide)-allo-aromadendrane

Provided By

JEOL Database JEOL Logo

Description

Aromadendrene oxide 2 belongs to the class of organic compounds known as 5,10-cycloaromadendrane sesquiterpenoids. These are aromadendrane sesquiterpenoids that arise from the C5-C10 cyclization of the aromadendrane skeleton. (+)-10-(ethylene oxide)-allo-aromadendrane is found in Curcuma kwangsiensis , Curcuma longa , Curcuma phaeocaulis , Curcuma wenyujin , Duguetia glabriuscula and Piper nigrum . (+)-10-(ethylene oxide)-allo-aromadendrane was first documented in 2009 (PMID: 19476010). Based on a literature review a small amount of articles have been published on Aromadendrene oxide 2 (PMID: 30166097) (PMID: 29407546).

Structure

MOL 3D MOL SDF 3D SDF PDB SMILES InChI


  Mrv1652306192123423D          

 40 43  0  0  0  0            999 V2000
   -0.7624    1.7061    2.0659 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9814    0.2571    1.6570 C   0  0  2  0  0  0  0  0  0  0  0  0
   -1.0232   -0.6945    2.8548 C   0  0  2  0  0  0  0  0  0  0  0  0
   -0.7386   -2.0538    2.2330 C   0  0  2  0  0  0  0  0  0  0  0  0
    0.4170   -1.7481    1.2824 C   0  0  2  0  0  0  0  0  0  0  0  0
    0.0406   -0.3695    0.6766 C   0  0  2  0  0  0  0  0  0  0  0  0
    1.2957    0.4244    0.4399 C   0  0  1  0  0  0  0  0  0  0  0  0
    2.2585   -0.0532   -0.6259 C   0  0  1  0  0  0  0  0  0  0  0  0
    1.9501   -1.2712   -1.4534 C   0  0  2  0  0  0  0  0  0  0  0  0
    1.9780   -2.5576   -0.6189 C   0  0  1  0  0  0  0  0  0  0  0  0
    0.7299   -2.7769    0.2165 C   0  0  1  0  0  0  0  0  0  0  0  0
    0.2077   -4.1988    0.3282 C   0  0  1  0  0  0  0  0  0  0  0  0
   -0.4049   -3.2328   -0.5365 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.5583    1.2933   -0.7853 C   0  0  1  0  0  0  0  0  0  0  0  0
    0.4911    1.4993   -1.8312 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.4017    2.5298   -0.5693 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7309    2.3599    1.1887 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.1664    1.8366    2.6298 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5832    2.0481    2.7057 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9656    0.2060    1.1686 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9907   -0.6723    3.3657 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2452   -0.4425    3.5857 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6242   -2.4146    1.6966 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4695   -2.7984    2.9884 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.3210   -1.6443    1.9007 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4935   -0.5317   -0.2659 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.7585    0.7178    1.3791 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.3139   -0.0386   -0.3634 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.7239   -1.3414   -2.2278 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.9956   -1.1954   -1.9813 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.1022   -3.4012   -1.3101 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.8537   -2.5659    0.0413 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.7637   -5.0033   -0.1388 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3439   -4.5096    1.2056 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.9531    1.7612   -2.7892 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1423    0.6278   -2.0049 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1668    2.3241   -1.5364 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.1748    2.3727    0.1907 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.9012    2.8169   -1.5004 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.7744    3.3649   -0.2404 H   0  0  0  0  0  0  0  0  0  0  0  0
  6  7  1  0  0  0  0
 11 10  1  0  0  0  0
  5  4  1  0  0  0  0
  4  3  1  0  0  0  0
  3  2  1  0  0  0  0
  2  6  1  0  0  0  0
  9  8  1  0  0  0  0
 11 12  1  0  0  0  0
  7  8  1  0  0  0  0
  2  1  1  0  0  0  0
  6  5  1  0  0  0  0
 11 13  1  6  0  0  0
  5 11  1  0  0  0  0
  7 14  1  0  0  0  0
  8 14  1  0  0  0  0
 10  9  1  0  0  0  0
 14 15  1  6  0  0  0
 14 16  1  0  0  0  0
 12 13  1  0  0  0  0
 10 31  1  0  0  0  0
 10 32  1  0  0  0  0
  9 29  1  0  0  0  0
  9 30  1  0  0  0  0
  7 27  1  1  0  0  0
  8 28  1  1  0  0  0
  6 26  1  6  0  0  0
  5 25  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
  2 20  1  6  0  0  0
 12 33  1  0  0  0  0
 12 34  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
 15 35  1  0  0  0  0
 15 36  1  0  0  0  0
 15 37  1  0  0  0  0
 16 38  1  0  0  0  0
 16 39  1  0  0  0  0
 16 40  1  0  0  0  0
M  END

     RDKit          3D

 40 43  0  0  0  0  0  0  0  0999 V2000
   -0.7624    1.7061    2.0659 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9814    0.2571    1.6570 C   0  0  2  0  0  0  0  0  0  0  0  0
   -1.0232   -0.6945    2.8548 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7386   -2.0538    2.2330 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.4170   -1.7481    1.2824 C   0  0  2  0  0  0  0  0  0  0  0  0
    0.0406   -0.3695    0.6766 C   0  0  2  0  0  0  0  0  0  0  0  0
    1.2957    0.4244    0.4399 C   0  0  1  0  0  0  0  0  0  0  0  0
    2.2585   -0.0532   -0.6259 C   0  0  1  0  0  0  0  0  0  0  0  0
    1.9501   -1.2712   -1.4534 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.9780   -2.5576   -0.6189 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7299   -2.7769    0.2165 C   0  0  1  0  0  0  0  0  0  0  0  0
    0.2077   -4.1988    0.3282 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4049   -3.2328   -0.5365 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.5583    1.2933   -0.7853 C   0  0  1  0  0  0  0  0  0  0  0  0
    0.4911    1.4993   -1.8312 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.4017    2.5298   -0.5693 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7309    2.3599    1.1887 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.1664    1.8366    2.6298 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5832    2.0481    2.7057 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9656    0.2060    1.1686 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9907   -0.6723    3.3657 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2452   -0.4425    3.5857 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6242   -2.4146    1.6966 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4695   -2.7984    2.9884 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.3210   -1.6443    1.9007 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4935   -0.5317   -0.2659 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.7585    0.7178    1.3791 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.3139   -0.0386   -0.3634 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.7239   -1.3414   -2.2278 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.9956   -1.1954   -1.9813 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.1022   -3.4012   -1.3101 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.8537   -2.5659    0.0413 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.7637   -5.0033   -0.1388 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3439   -4.5096    1.2056 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.9531    1.7612   -2.7892 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1423    0.6278   -2.0049 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1668    2.3241   -1.5364 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.1748    2.3727    0.1907 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.9012    2.8169   -1.5004 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.7744    3.3649   -0.2404 H   0  0  0  0  0  0  0  0  0  0  0  0
  6  7  1  0
 11 10  1  0
  5  4  1  0
  4  3  1  0
  3  2  1  0
  2  6  1  0
  9  8  1  0
 11 12  1  0
  7  8  1  0
  2  1  1  0
  6  5  1  0
 11 13  1  6
  5 11  1  0
  7 14  1  0
  8 14  1  0
 10  9  1  0
 14 15  1  6
 14 16  1  0
 12 13  1  0
 10 31  1  0
 10 32  1  0
  9 29  1  0
  9 30  1  0
  7 27  1  1
  8 28  1  1
  6 26  1  6
  5 25  1  1
  4 23  1  0
  4 24  1  0
  3 21  1  0
  3 22  1  0
  2 20  1  6
 12 33  1  0
 12 34  1  0
  1 17  1  0
  1 18  1  0
  1 19  1  0
 15 35  1  0
 15 36  1  0
 15 37  1  0
 16 38  1  0
 16 39  1  0
 16 40  1  0
M  END


  Mrv1652306192123423D          

 40 43  0  0  0  0            999 V2000
   -0.7624    1.7061    2.0659 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9814    0.2571    1.6570 C   0  0  2  0  0  0  0  0  0  0  0  0
   -1.0232   -0.6945    2.8548 C   0  0  2  0  0  0  0  0  0  0  0  0
   -0.7386   -2.0538    2.2330 C   0  0  2  0  0  0  0  0  0  0  0  0
    0.4170   -1.7481    1.2824 C   0  0  2  0  0  0  0  0  0  0  0  0
    0.0406   -0.3695    0.6766 C   0  0  2  0  0  0  0  0  0  0  0  0
    1.2957    0.4244    0.4399 C   0  0  1  0  0  0  0  0  0  0  0  0
    2.2585   -0.0532   -0.6259 C   0  0  1  0  0  0  0  0  0  0  0  0
    1.9501   -1.2712   -1.4534 C   0  0  2  0  0  0  0  0  0  0  0  0
    1.9780   -2.5576   -0.6189 C   0  0  1  0  0  0  0  0  0  0  0  0
    0.7299   -2.7769    0.2165 C   0  0  1  0  0  0  0  0  0  0  0  0
    0.2077   -4.1988    0.3282 C   0  0  1  0  0  0  0  0  0  0  0  0
   -0.4049   -3.2328   -0.5365 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.5583    1.2933   -0.7853 C   0  0  1  0  0  0  0  0  0  0  0  0
    0.4911    1.4993   -1.8312 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.4017    2.5298   -0.5693 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7309    2.3599    1.1887 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.1664    1.8366    2.6298 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5832    2.0481    2.7057 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9656    0.2060    1.1686 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9907   -0.6723    3.3657 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2452   -0.4425    3.5857 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6242   -2.4146    1.6966 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4695   -2.7984    2.9884 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.3210   -1.6443    1.9007 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4935   -0.5317   -0.2659 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.7585    0.7178    1.3791 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.3139   -0.0386   -0.3634 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.7239   -1.3414   -2.2278 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.9956   -1.1954   -1.9813 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.1022   -3.4012   -1.3101 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.8537   -2.5659    0.0413 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.7637   -5.0033   -0.1388 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3439   -4.5096    1.2056 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.9531    1.7612   -2.7892 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1423    0.6278   -2.0049 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1668    2.3241   -1.5364 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.1748    2.3727    0.1907 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.9012    2.8169   -1.5004 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.7744    3.3649   -0.2404 H   0  0  0  0  0  0  0  0  0  0  0  0
  6  7  1  0  0  0  0
 11 10  1  0  0  0  0
  5  4  1  0  0  0  0
  4  3  1  0  0  0  0
  3  2  1  0  0  0  0
  2  6  1  0  0  0  0
  9  8  1  0  0  0  0
 11 12  1  0  0  0  0
  7  8  1  0  0  0  0
  2  1  1  0  0  0  0
  6  5  1  0  0  0  0
 11 13  1  6  0  0  0
  5 11  1  0  0  0  0
  7 14  1  0  0  0  0
  8 14  1  0  0  0  0
 10  9  1  0  0  0  0
 14 15  1  6  0  0  0
 14 16  1  0  0  0  0
 12 13  1  0  0  0  0
 10 31  1  0  0  0  0
 10 32  1  0  0  0  0
  9 29  1  0  0  0  0
  9 30  1  0  0  0  0
  7 27  1  1  0  0  0
  8 28  1  1  0  0  0
  6 26  1  6  0  0  0
  5 25  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
  2 20  1  6  0  0  0
 12 33  1  0  0  0  0
 12 34  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
 15 35  1  0  0  0  0
 15 36  1  0  0  0  0
 15 37  1  0  0  0  0
 16 38  1  0  0  0  0
 16 39  1  0  0  0  0
 16 40  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0030320

> <DATABASE_NAME>
NP-MRD

> <SMILES>
[H]C([H])([H])[C@]1([H])C([H])([H])C([H])([H])[C@]2([H])[C@]1([H])[C@@]1([H])[C@@]([H])(C([H])([H])C([H])([H])[C@]22OC2([H])[H])C1(C([H])([H])[H])C([H])([H])[H]

> <INCHI_IDENTIFIER>
InChI=1S/C15H24O/c1-9-4-5-10-12(9)13-11(14(13,2)3)6-7-15(10)8-16-15/h9-13H,4-8H2,1-3H3/t9-,10-,11-,12-,13-,15-/m1/s1

> <INCHI_KEY>
XPGWKKLDFXNBPJ-QTPLKFIXSA-N

> <FORMULA>
C15H24O

> <MOLECULAR_WEIGHT>
220.356

> <EXACT_MASS>
220.182715393

> <JCHEM_ACCEPTOR_COUNT>
1

> <JCHEM_ATOM_COUNT>
40

> <JCHEM_AVERAGE_POLARIZABILITY>
26.770739753889472

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
0

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
1

> <JCHEM_IUPAC>
(1aS,1bS,2R,4aR,5S,7aR)-1,1,2-trimethyl-decahydrospiro[cyclopropa[e]azulene-5,2'-oxirane]

> <ALOGPS_LOGP>
2.68

> <JCHEM_LOGP>
3.293296024666666

> <ALOGPS_LOGS>
-5.23

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
4

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA_STRONGEST_BASIC>
-4.204612508483695

> <JCHEM_POLAR_SURFACE_AREA>
12.53

> <JCHEM_REFRACTIVITY>
64.6336

> <JCHEM_ROTATABLE_BOND_COUNT>
0

> <JCHEM_RULE_OF_FIVE>
1

> <ALOGPS_SOLUBILITY>
1.30e-03 g/l

> <JCHEM_TRADITIONAL_IUPAC>
(1aS,1bS,2R,4aR,5S,7aR)-1,1,2-trimethyl-octahydro-1aH-spiro[cyclopropa[e]azulene-5,2'-oxirane]

> <JCHEM_VEBER_RULE>
1

$$$$

     RDKit          3D

 40 43  0  0  0  0  0  0  0  0999 V2000
   -0.7624    1.7061    2.0659 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9814    0.2571    1.6570 C   0  0  2  0  0  0  0  0  0  0  0  0
   -1.0232   -0.6945    2.8548 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7386   -2.0538    2.2330 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.4170   -1.7481    1.2824 C   0  0  2  0  0  0  0  0  0  0  0  0
    0.0406   -0.3695    0.6766 C   0  0  2  0  0  0  0  0  0  0  0  0
    1.2957    0.4244    0.4399 C   0  0  1  0  0  0  0  0  0  0  0  0
    2.2585   -0.0532   -0.6259 C   0  0  1  0  0  0  0  0  0  0  0  0
    1.9501   -1.2712   -1.4534 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.9780   -2.5576   -0.6189 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7299   -2.7769    0.2165 C   0  0  1  0  0  0  0  0  0  0  0  0
    0.2077   -4.1988    0.3282 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4049   -3.2328   -0.5365 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.5583    1.2933   -0.7853 C   0  0  1  0  0  0  0  0  0  0  0  0
    0.4911    1.4993   -1.8312 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.4017    2.5298   -0.5693 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7309    2.3599    1.1887 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.1664    1.8366    2.6298 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5832    2.0481    2.7057 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9656    0.2060    1.1686 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9907   -0.6723    3.3657 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2452   -0.4425    3.5857 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6242   -2.4146    1.6966 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4695   -2.7984    2.9884 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.3210   -1.6443    1.9007 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4935   -0.5317   -0.2659 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.7585    0.7178    1.3791 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.3139   -0.0386   -0.3634 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.7239   -1.3414   -2.2278 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.9956   -1.1954   -1.9813 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.1022   -3.4012   -1.3101 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.8537   -2.5659    0.0413 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.7637   -5.0033   -0.1388 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3439   -4.5096    1.2056 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.9531    1.7612   -2.7892 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1423    0.6278   -2.0049 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1668    2.3241   -1.5364 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.1748    2.3727    0.1907 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.9012    2.8169   -1.5004 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.7744    3.3649   -0.2404 H   0  0  0  0  0  0  0  0  0  0  0  0
  6  7  1  0
 11 10  1  0
  5  4  1  0
  4  3  1  0
  3  2  1  0
  2  6  1  0
  9  8  1  0
 11 12  1  0
  7  8  1  0
  2  1  1  0
  6  5  1  0
 11 13  1  6
  5 11  1  0
  7 14  1  0
  8 14  1  0
 10  9  1  0
 14 15  1  6
 14 16  1  0
 12 13  1  0
 10 31  1  0
 10 32  1  0
  9 29  1  0
  9 30  1  0
  7 27  1  1
  8 28  1  1
  6 26  1  6
  5 25  1  1
  4 23  1  0
  4 24  1  0
  3 21  1  0
  3 22  1  0
  2 20  1  6
 12 33  1  0
 12 34  1  0
  1 17  1  0
  1 18  1  0
  1 19  1  0
 15 35  1  0
 15 36  1  0
 15 37  1  0
 16 38  1  0
 16 39  1  0
 16 40  1  0
M  END

HEADER    PROTEIN                                 19-JUN-21   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   19-JUN-21         0                                  
HETATM    1  C   UNK     0      -0.762   1.706   2.066  0.00  0.00           C+0
HETATM    2  C   UNK     0      -0.981   0.257   1.657  0.00  0.00           C+0
HETATM    3  C   UNK     0      -1.023  -0.695   2.855  0.00  0.00           C+0
HETATM    4  C   UNK     0      -0.739  -2.054   2.233  0.00  0.00           C+0
HETATM    5  C   UNK     0       0.417  -1.748   1.282  0.00  0.00           C+0
HETATM    6  C   UNK     0       0.041  -0.370   0.677  0.00  0.00           C+0
HETATM    7  C   UNK     0       1.296   0.424   0.440  0.00  0.00           C+0
HETATM    8  C   UNK     0       2.259  -0.053  -0.626  0.00  0.00           C+0
HETATM    9  C   UNK     0       1.950  -1.271  -1.453  0.00  0.00           C+0
HETATM   10  C   UNK     0       1.978  -2.558  -0.619  0.00  0.00           C+0
HETATM   11  C   UNK     0       0.730  -2.777   0.217  0.00  0.00           C+0
HETATM   12  C   UNK     0       0.208  -4.199   0.328  0.00  0.00           C+0
HETATM   13  O   UNK     0      -0.405  -3.233  -0.537  0.00  0.00           O+0
HETATM   14  C   UNK     0       1.558   1.293  -0.785  0.00  0.00           C+0
HETATM   15  C   UNK     0       0.491   1.499  -1.831  0.00  0.00           C+0
HETATM   16  C   UNK     0       2.402   2.530  -0.569  0.00  0.00           C+0
HETATM   17  H   UNK     0      -0.731   2.360   1.189  0.00  0.00           H+0
HETATM   18  H   UNK     0       0.166   1.837   2.630  0.00  0.00           H+0
HETATM   19  H   UNK     0      -1.583   2.048   2.706  0.00  0.00           H+0
HETATM   20  H   UNK     0      -1.966   0.206   1.169  0.00  0.00           H+0
HETATM   21  H   UNK     0      -1.991  -0.672   3.366  0.00  0.00           H+0
HETATM   22  H   UNK     0      -0.245  -0.443   3.586  0.00  0.00           H+0
HETATM   23  H   UNK     0      -1.624  -2.415   1.697  0.00  0.00           H+0
HETATM   24  H   UNK     0      -0.470  -2.798   2.988  0.00  0.00           H+0
HETATM   25  H   UNK     0       1.321  -1.644   1.901  0.00  0.00           H+0
HETATM   26  H   UNK     0      -0.494  -0.532  -0.266  0.00  0.00           H+0
HETATM   27  H   UNK     0       1.759   0.718   1.379  0.00  0.00           H+0
HETATM   28  H   UNK     0       3.314  -0.039  -0.363  0.00  0.00           H+0
HETATM   29  H   UNK     0       2.724  -1.341  -2.228  0.00  0.00           H+0
HETATM   30  H   UNK     0       0.996  -1.195  -1.981  0.00  0.00           H+0
HETATM   31  H   UNK     0       2.102  -3.401  -1.310  0.00  0.00           H+0
HETATM   32  H   UNK     0       2.854  -2.566   0.041  0.00  0.00           H+0
HETATM   33  H   UNK     0       0.764  -5.003  -0.139  0.00  0.00           H+0
HETATM   34  H   UNK     0      -0.344  -4.510   1.206  0.00  0.00           H+0
HETATM   35  H   UNK     0       0.953   1.761  -2.789  0.00  0.00           H+0
HETATM   36  H   UNK     0      -0.142   0.628  -2.005  0.00  0.00           H+0
HETATM   37  H   UNK     0      -0.167   2.324  -1.536  0.00  0.00           H+0
HETATM   38  H   UNK     0       3.175   2.373   0.191  0.00  0.00           H+0
HETATM   39  H   UNK     0       2.901   2.817  -1.500  0.00  0.00           H+0
HETATM   40  H   UNK     0       1.774   3.365  -0.240  0.00  0.00           H+0
CONECT    1    2   17   18   19                                             
CONECT    2    3    6    1   20                                             
CONECT    3    4    2   21   22                                             
CONECT    4    5    3   23   24                                             
CONECT    5    4    6   11   25                                             
CONECT    6    7    2    5   26                                             
CONECT    7    6    8   14   27                                             
CONECT    8    9    7   14   28                                             
CONECT    9    8   10   29   30                                             
CONECT   10   11    9   31   32                                             
CONECT   11   10   12   13    5                                             
CONECT   12   11   13   33   34                                             
CONECT   13   11   12                                                       
CONECT   14    7    8   15   16                                             
CONECT   15   14   35   36   37                                             
CONECT   16   14   38   39   40                                             
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    7                                                            
CONECT   28    8                                                            
CONECT   29    9                                                            
CONECT   30    9                                                            
CONECT   31   10                                                            
CONECT   32   10                                                            
CONECT   33   12                                                            
CONECT   34   12                                                            
CONECT   35   15                                                            
CONECT   36   15                                                            
CONECT   37   15                                                            
CONECT   38   16                                                            
CONECT   39   16                                                            
CONECT   40   16                                                            
MASTER        0    0    0    0    0    0    0    0   40    0   86    0
END

RDKit          3D

40 43  0  0  0  0  0  0  0  0999 V2000
   -0.7624    1.7061    2.0659 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9814    0.2571    1.6570 C   0  0  2  0  0  0  0  0  0  0  0  0
   -1.0232   -0.6945    2.8548 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7386   -2.0538    2.2330 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.4170   -1.7481    1.2824 C   0  0  2  0  0  0  0  0  0  0  0  0
    0.0406   -0.3695    0.6766 C   0  0  2  0  0  0  0  0  0  0  0  0
    1.2957    0.4244    0.4399 C   0  0  1  0  0  0  0  0  0  0  0  0
    2.2585   -0.0532   -0.6259 C   0  0  1  0  0  0  0  0  0  0  0  0
    1.9501   -1.2712   -1.4534 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.9780   -2.5576   -0.6189 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7299   -2.7769    0.2165 C   0  0  1  0  0  0  0  0  0  0  0  0
    0.2077   -4.1988    0.3282 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4049   -3.2328   -0.5365 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.5583    1.2933   -0.7853 C   0  0  1  0  0  0  0  0  0  0  0  0
    0.4911    1.4993   -1.8312 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.4017    2.5298   -0.5693 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7309    2.3599    1.1887 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.1664    1.8366    2.6298 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5832    2.0481    2.7057 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9656    0.2060    1.1686 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9907   -0.6723    3.3657 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2452   -0.4425    3.5857 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6242   -2.4146    1.6966 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4695   -2.7984    2.9884 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.3210   -1.6443    1.9007 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4935   -0.5317   -0.2659 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.7585    0.7178    1.3791 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.3139   -0.0386   -0.3634 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.7239   -1.3414   -2.2278 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.9956   -1.1954   -1.9813 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.1022   -3.4012   -1.3101 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.8537   -2.5659    0.0413 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.7637   -5.0033   -0.1388 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3439   -4.5096    1.2056 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.9531    1.7612   -2.7892 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1423    0.6278   -2.0049 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1668    2.3241   -1.5364 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.1748    2.3727    0.1907 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.9012    2.8169   -1.5004 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.7744    3.3649   -0.2404 H   0  0  0  0  0  0  0  0  0  0  0  0
  6  7  1  0
 11 10  1  0
  5  4  1  0
  4  3  1  0
  3  2  1  0
  2  6  1  0
  9  8  1  0
 11 12  1  0
  7  8  1  0
  2  1  1  0
  6  5  1  0
 11 13  1  6
  5 11  1  0
  7 14  1  0
  8 14  1  0
 10  9  1  0
 14 15  1  6
 14 16  1  0
 12 13  1  0
 10 31  1  0
 10 32  1  0
  9 29  1  0
  9 30  1  0
  7 27  1  1
  8 28  1  1
  6 26  1  6
  5 25  1  1
  4 23  1  0
  4 24  1  0
  3 21  1  0
  3 22  1  0
  2 20  1  6
 12 33  1  0
 12 34  1  0
  1 17  1  0
  1 18  1  0
  1 19  1  0
 15 35  1  0
 15 36  1  0
 15 37  1  0
 16 38  1  0
 16 39  1  0
 16 40  1  0
M  END

View in JSmol

Synonyms

Not Available

Chemical Formula

C₁₅H₂₄O

Average Mass

220.3560 Da

Monoisotopic Mass

220.18272 Da

IUPAC Name

(1aS,1bS,2R,4aR,5S,7aR)-1,1,2-trimethyl-decahydrospiro[cyclopropa[e]azulene-5,2'-oxirane]

Traditional Name

(1aS,1bS,2R,4aR,5S,7aR)-1,1,2-trimethyl-octahydro-1aH-spiro[cyclopropa[e]azulene-5,2'-oxirane]

CAS Registry Number

Not Available

SMILES

[H]C([H])([H])[C@]1([H])C([H])([H])C([H])([H])[C@]2([H])[C@]1([H])[C@@]1([H])[C@@]([H])(C([H])([H])C([H])([H])[C@]22OC2([H])[H])C1(C([H])([H])[H])C([H])([H])[H]

InChI Identifier

InChI=1S/C15H24O/c1-9-4-5-10-12(9)13-11(14(13,2)3)6-7-15(10)8-16-15/h9-13H,4-8H2,1-3H3/t9-,10-,11-,12-,13-,15-/m1/s1

InChI Key

XPGWKKLDFXNBPJ-QTPLKFIXSA-N

Experimental Spectra

Spectrum Type	Description	Depositor Email	Depositor Organization	Depositor	Deposition Date	View
1D NMR	¹³C NMR Spectrum (1D, 300 MHz, CDCl₃, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 300 MHz, CDCl₃, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 100 MHz, CDCl₃, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 100 MHz, CDCl₃, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 200 MHz, CDCl₃, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 200 MHz, CDCl₃, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 400 MHz, CDCl₃, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 400 MHz, CDCl₃, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 500 MHz, CDCl₃, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 500 MHz, CDCl₃, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 600 MHz, CDCl₃, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 600 MHz, CDCl₃, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 700 MHz, CDCl₃, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 700 MHz, CDCl₃, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 800 MHz, CDCl₃, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 800 MHz, CDCl₃, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 900 MHz, CDCl₃, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 900 MHz, CDCl₃, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 1000 MHz, CDCl₃, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 1000 MHz, CDCl₃, 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
Curcuma kwangsiensis	Plant	KNApSAcK
Curcuma longa	Plant	KNApSAcK
Curcuma phaeocaulis	Plant	KNApSAcK
Curcuma wenyujin	Plant	KNApSAcK
Duguetia glabriuscula	JEOL database	Vizzotto, L., et al, Magn. Reson. Chem. 41,1034 (2003)
Piper nigrum L.	Plant	KNApSAcK

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as 5,10-cycloaromadendrane sesquiterpenoids. These are aromadendrane sesquiterpenoids that arise from the C5-C10 cyclization of the aromadendrane skeleton.

Kingdom

Organic compounds

Super Class

Lipids and lipid-like molecules

Class

Prenol lipids

Sub Class

Sesquiterpenoids

Direct Parent

5,10-cycloaromadendrane sesquiterpenoids

Alternative Parents

Substituents

5,10-cycloaromadendrane sesquiterpenoid
Oxacycle
Organoheterocyclic compound
Ether
Oxirane
Dialkyl ether
Organic oxygen compound
Hydrocarbon derivative
Organooxygen compound
Aliphatic heteropolycyclic compound

Molecular Framework

Aliphatic heteropolycyclic compounds

External Descriptors

Not Available

Physical Properties

State

Not Available

Experimental Properties

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

Predicted Properties

Property	Value	Source
logP	2.68	ALOGPS
logP	3.29	ChemAxon
logS	-5.2	ALOGPS
pKa (Strongest Basic)	-4.2	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	1	ChemAxon
Hydrogen Donor Count	0	ChemAxon
Polar Surface Area	12.53 Å²	ChemAxon
Rotatable Bond Count	0	ChemAxon
Refractivity	64.63 m³·mol⁻¹	ChemAxon
Polarizability	26.77 Å³	ChemAxon
Number of Rings	4	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

17339238

KEGG Compound ID

Not Available

BioCyc ID

Not Available

BiGG ID

Not Available

Wikipedia Link

Not Available

METLIN ID

Not Available

PubChem Compound

16211192

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

Pavithra PS, Mehta A, Verma RS: Synergistic interaction of beta-caryophyllene with aromadendrene oxide 2 and phytol induces apoptosis on skin epidermoid cancer cells. Phytomedicine. 2018 Aug 1;47:121-134. doi: 10.1016/j.phymed.2018.05.001. Epub 2018 May 9. [PubMed:30166097 ]
Pavithra PS, Mehta A, Verma RS: Aromadendrene oxide 2, induces apoptosis in skin epidermoid cancer cells through ROS mediated mitochondrial pathway. Life Sci. 2018 Mar 15;197:19-29. doi: 10.1016/j.lfs.2018.01.029. Epub 2018 Jan 31. [PubMed:29407546 ]
Ugur A, Sarac N, Duru ME: Antimicrobial activity and chemical composition of Senecio sandrasicus on antibiotic resistant staphylococci. Nat Prod Commun. 2009 Apr;4(4):579-84. [PubMed:19476010 ]
Vizzotto, L., et al. (2003). Vizzotto, L., et al, Magn. Reson. Chem. 41,1034 (2003). Mag. Reson. Chem..

Showing NP-Card for (+)-10-(ethylene oxide)-allo-aromadendrane (NP0030320)

MOL for NP0030320 ((+)-10-(ethylene oxide)-allo-aromadendrane)

3D MOL for NP0030320 ((+)-10-(ethylene oxide)-allo-aromadendrane)

3D SDF for NP0030320 ((+)-10-(ethylene oxide)-allo-aromadendrane)

3D-SDF for NP0030320 ((+)-10-(ethylene oxide)-allo-aromadendrane)

PDB for NP0030320 ((+)-10-(ethylene oxide)-allo-aromadendrane)

3D PDB for NP0030320 ((+)-10-(ethylene oxide)-allo-aromadendrane)

SMILES for NP0030320 ((+)-10-(ethylene oxide)-allo-aromadendrane)

INCHI for NP0030320 ((+)-10-(ethylene oxide)-allo-aromadendrane)

Structure for NP0030320 ((+)-10-(ethylene oxide)-allo-aromadendrane)

3D Structure for NP0030320 ((+)-10-(ethylene oxide)-allo-aromadendrane)