NP-MRD: Showing NP-Card for Pentalenene (NP0022149)

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Record Information

Version

2.0

Created at

2021-01-06 07:22:19 UTC

Updated at

2021-07-15 17:38:16 UTC

NP-MRD ID

NP0022149

Secondary Accession Numbers

None

Natural Product Identification

Common Name

Pentalenene

Provided By

NPAtlas

Description

Pentalenene belongs to the class of organic compounds known as angular triquinanes. These are triquinane with a structure based on a [6.3.0.0^1,5] Undecane carbon skeleton. Thus, pentalenene is considered to be an isoprenoid. Pentalenene is found in Laurencia dendroidea and Streptomyces griseochromogenes. Pentalenene was first documented in 1980 (PMID: 7372558). Based on a literature review very few articles have been published on Pentalenene.

Structure

MOL 3D MOL SDF 3D SDF PDB SMILES InChI


  Mrv1652306242105213D          

 39 41  0  0  0  0            999 V2000
   -2.7631   -2.0945    1.4547 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6580   -1.4862    0.6709 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6031   -2.1128    0.2379 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.2776   -1.1804   -0.5029 C   0  0  2  0  0  0  0  0  0  0  0  0
    1.6540   -1.2868    0.0941 C   0  0  1  0  0  0  0  0  0  0  0  0
    2.0622    0.0596    0.5838 C   0  0  2  0  0  0  0  0  0  0  0  0
    2.8094    0.8358   -0.4777 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8875   -0.0351    1.8486 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7130    0.7304    0.8780 C   0  0  1  0  0  0  0  0  0  0  0  0
   -0.2210    0.1931   -0.1697 C   0  0  2  0  0  0  0  0  0  0  0  0
   -1.6064   -0.0744    0.2678 C   0  0  1  0  0  0  0  0  0  0  0  0
   -2.4630    0.0264   -1.0029 C   0  0  2  0  0  0  0  0  0  0  0  0
   -1.6721    0.8030   -2.0009 C   0  0  2  0  0  0  0  0  0  0  0  0
   -0.3458    1.1130   -1.3307 C   0  0  1  0  0  0  0  0  0  0  0  0
   -0.4837    2.5465   -0.8007 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7125   -3.2155    1.4326 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.7540   -1.8370    1.0106 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8010   -1.7045    2.4987 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3467   -3.1649    0.3671 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.2754   -1.3733   -1.5966 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.6603   -1.9686    0.9934 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.3803   -1.7178   -0.6286 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.5119    1.8804   -0.5581 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.6989    0.2958   -1.4563 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.8969    0.8169   -0.2600 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.3263   -1.0701    1.8680 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.3028    0.0814    2.7608 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.7699    0.6455    1.7811 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.3871    0.5777    1.9024 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.8767    1.8076    0.6689 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9877    0.6170    1.0458 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.4495    0.4851   -0.7681 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6827   -0.9654   -1.4372 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2352    1.7174   -2.2692 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4970    0.2495   -2.9559 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.4905    1.0357   -2.0338 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9595    2.5597    0.2029 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.4632    3.0917   -0.8596 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2021    3.1182   -1.4592 H   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0  0  0  0
  2  3  2  0  0  0  0
  3  4  1  0  0  0  0
  4  5  1  0  0  0  0
  5  6  1  0  0  0  0
  6  7  1  6  0  0  0
  6  8  1  0  0  0  0
  6  9  1  0  0  0  0
 10  9  1  1  0  0  0
 10 11  1  0  0  0  0
 11 12  1  0  0  0  0
 12 13  1  0  0  0  0
 13 14  1  0  0  0  0
 14 15  1  0  0  0  0
 11  2  1  0  0  0  0
 10  4  1  0  0  0  0
 14 10  1  0  0  0  0
  1 16  1  0  0  0  0
  1 17  1  0  0  0  0
  1 18  1  0  0  0  0
  3 19  1  0  0  0  0
  4 20  1  6  0  0  0
  5 21  1  0  0  0  0
  5 22  1  0  0  0  0
  7 23  1  0  0  0  0
  7 24  1  0  0  0  0
  7 25  1  0  0  0  0
  8 26  1  0  0  0  0
  8 27  1  0  0  0  0
  8 28  1  0  0  0  0
  9 29  1  0  0  0  0
  9 30  1  0  0  0  0
 11 31  1  1  0  0  0
 12 32  1  0  0  0  0
 12 33  1  0  0  0  0
 13 34  1  0  0  0  0
 13 35  1  0  0  0  0
 14 36  1  6  0  0  0
 15 37  1  0  0  0  0
 15 38  1  0  0  0  0
 15 39  1  0  0  0  0
M  END

     RDKit          3D

 39 41  0  0  0  0  0  0  0  0999 V2000
   -2.7631   -2.0945    1.4547 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6580   -1.4862    0.6709 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6031   -2.1128    0.2379 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.2776   -1.1804   -0.5029 C   0  0  2  0  0  0  0  0  0  0  0  0
    1.6540   -1.2868    0.0941 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.0622    0.0596    0.5838 C   0  0  2  0  0  0  0  0  0  0  0  0
    2.8094    0.8358   -0.4777 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8875   -0.0351    1.8486 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7130    0.7304    0.8780 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2210    0.1931   -0.1697 C   0  0  2  0  0  0  0  0  0  0  0  0
   -1.6064   -0.0744    0.2678 C   0  0  1  0  0  0  0  0  0  0  0  0
   -2.4630    0.0264   -1.0029 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6721    0.8030   -2.0009 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3458    1.1130   -1.3307 C   0  0  1  0  0  0  0  0  0  0  0  0
   -0.4837    2.5465   -0.8007 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7125   -3.2155    1.4326 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.7540   -1.8370    1.0106 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8010   -1.7045    2.4987 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3467   -3.1649    0.3671 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.2754   -1.3733   -1.5966 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.6603   -1.9686    0.9934 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.3803   -1.7178   -0.6286 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.5119    1.8804   -0.5581 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.6989    0.2958   -1.4563 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.8969    0.8169   -0.2600 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.3263   -1.0701    1.8680 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.3028    0.0814    2.7608 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.7699    0.6455    1.7811 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.3871    0.5777    1.9024 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.8767    1.8076    0.6689 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9877    0.6170    1.0458 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.4495    0.4851   -0.7681 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6827   -0.9654   -1.4372 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2352    1.7174   -2.2692 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4970    0.2495   -2.9559 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.4905    1.0357   -2.0338 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9595    2.5597    0.2029 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.4632    3.0917   -0.8596 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2021    3.1182   -1.4592 H   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0
  2  3  2  0
  3  4  1  0
  4  5  1  0
  5  6  1  0
  6  7  1  6
  6  8  1  0
  6  9  1  0
 10  9  1  1
 10 11  1  0
 11 12  1  0
 12 13  1  0
 13 14  1  0
 14 15  1  0
 11  2  1  0
 10  4  1  0
 14 10  1  0
  1 16  1  0
  1 17  1  0
  1 18  1  0
  3 19  1  0
  4 20  1  6
  5 21  1  0
  5 22  1  0
  7 23  1  0
  7 24  1  0
  7 25  1  0
  8 26  1  0
  8 27  1  0
  8 28  1  0
  9 29  1  0
  9 30  1  0
 11 31  1  1
 12 32  1  0
 12 33  1  0
 13 34  1  0
 13 35  1  0
 14 36  1  6
 15 37  1  0
 15 38  1  0
 15 39  1  0
M  END


  Mrv1652306242105213D          

 39 41  0  0  0  0            999 V2000
   -2.7631   -2.0945    1.4547 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6580   -1.4862    0.6709 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6031   -2.1128    0.2379 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.2776   -1.1804   -0.5029 C   0  0  2  0  0  0  0  0  0  0  0  0
    1.6540   -1.2868    0.0941 C   0  0  1  0  0  0  0  0  0  0  0  0
    2.0622    0.0596    0.5838 C   0  0  2  0  0  0  0  0  0  0  0  0
    2.8094    0.8358   -0.4777 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8875   -0.0351    1.8486 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7130    0.7304    0.8780 C   0  0  1  0  0  0  0  0  0  0  0  0
   -0.2210    0.1931   -0.1697 C   0  0  2  0  0  0  0  0  0  0  0  0
   -1.6064   -0.0744    0.2678 C   0  0  1  0  0  0  0  0  0  0  0  0
   -2.4630    0.0264   -1.0029 C   0  0  2  0  0  0  0  0  0  0  0  0
   -1.6721    0.8030   -2.0009 C   0  0  2  0  0  0  0  0  0  0  0  0
   -0.3458    1.1130   -1.3307 C   0  0  1  0  0  0  0  0  0  0  0  0
   -0.4837    2.5465   -0.8007 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7125   -3.2155    1.4326 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.7540   -1.8370    1.0106 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8010   -1.7045    2.4987 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3467   -3.1649    0.3671 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.2754   -1.3733   -1.5966 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.6603   -1.9686    0.9934 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.3803   -1.7178   -0.6286 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.5119    1.8804   -0.5581 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.6989    0.2958   -1.4563 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.8969    0.8169   -0.2600 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.3263   -1.0701    1.8680 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.3028    0.0814    2.7608 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.7699    0.6455    1.7811 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.3871    0.5777    1.9024 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.8767    1.8076    0.6689 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9877    0.6170    1.0458 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.4495    0.4851   -0.7681 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6827   -0.9654   -1.4372 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2352    1.7174   -2.2692 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4970    0.2495   -2.9559 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.4905    1.0357   -2.0338 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9595    2.5597    0.2029 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.4632    3.0917   -0.8596 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2021    3.1182   -1.4592 H   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0  0  0  0
  2  3  2  0  0  0  0
  3  4  1  0  0  0  0
  4  5  1  0  0  0  0
  5  6  1  0  0  0  0
  6  7  1  6  0  0  0
  6  8  1  0  0  0  0
  6  9  1  0  0  0  0
 10  9  1  1  0  0  0
 10 11  1  0  0  0  0
 11 12  1  0  0  0  0
 12 13  1  0  0  0  0
 13 14  1  0  0  0  0
 14 15  1  0  0  0  0
 11  2  1  0  0  0  0
 10  4  1  0  0  0  0
 14 10  1  0  0  0  0
  1 16  1  0  0  0  0
  1 17  1  0  0  0  0
  1 18  1  0  0  0  0
  3 19  1  0  0  0  0
  4 20  1  6  0  0  0
  5 21  1  0  0  0  0
  5 22  1  0  0  0  0
  7 23  1  0  0  0  0
  7 24  1  0  0  0  0
  7 25  1  0  0  0  0
  8 26  1  0  0  0  0
  8 27  1  0  0  0  0
  8 28  1  0  0  0  0
  9 29  1  0  0  0  0
  9 30  1  0  0  0  0
 11 31  1  1  0  0  0
 12 32  1  0  0  0  0
 12 33  1  0  0  0  0
 13 34  1  0  0  0  0
 13 35  1  0  0  0  0
 14 36  1  6  0  0  0
 15 37  1  0  0  0  0
 15 38  1  0  0  0  0
 15 39  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0022149

> <DATABASE_NAME>
NP-MRD

> <SMILES>
[H]C1=C(C([H])([H])[H])[C@]2([H])C([H])([H])C([H])([H])[C@@]([H])(C([H])([H])[H])[C@@]22C([H])([H])C(C([H])([H])[H])(C([H])([H])[H])C([H])([H])[C@@]12[H]

> <INCHI_IDENTIFIER>
InChI=1S/C15H24/c1-10-7-12-8-14(3,4)9-15(12)11(2)5-6-13(10)15/h7,11-13H,5-6,8-9H2,1-4H3/t11-,12-,13+,15-/m1/s1

> <INCHI_KEY>
YGIVIHRLDOVJLL-GUIRCDHDSA-N

> <FORMULA>
C15H24

> <MOLECULAR_WEIGHT>
204.357

> <EXACT_MASS>
204.187800773

> <JCHEM_ACCEPTOR_COUNT>
0

> <JCHEM_ATOM_COUNT>
39

> <JCHEM_AVERAGE_POLARIZABILITY>
25.856542797494406

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
0

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
1

> <JCHEM_IUPAC>
(1R,2R,5S,8S)-2,6,10,10-tetramethyltricyclo[6.3.0.0^{1,5}]undec-6-ene

> <ALOGPS_LOGP>
4.90

> <JCHEM_LOGP>
4.101158186333333

> <ALOGPS_LOGS>
-5.10

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
3

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_POLAR_SURFACE_AREA>
0.0

> <JCHEM_REFRACTIVITY>
65.6944

> <JCHEM_ROTATABLE_BOND_COUNT>
0

> <JCHEM_RULE_OF_FIVE>
1

> <ALOGPS_SOLUBILITY>
1.63e-03 g/l

> <JCHEM_TRADITIONAL_IUPAC>
(1R,2R,5S,8S)-2,6,10,10-tetramethyltricyclo[6.3.0.0^{1,5}]undec-6-ene

> <JCHEM_VEBER_RULE>
1

$$$$

     RDKit          3D

 39 41  0  0  0  0  0  0  0  0999 V2000
   -2.7631   -2.0945    1.4547 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6580   -1.4862    0.6709 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6031   -2.1128    0.2379 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.2776   -1.1804   -0.5029 C   0  0  2  0  0  0  0  0  0  0  0  0
    1.6540   -1.2868    0.0941 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.0622    0.0596    0.5838 C   0  0  2  0  0  0  0  0  0  0  0  0
    2.8094    0.8358   -0.4777 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8875   -0.0351    1.8486 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7130    0.7304    0.8780 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2210    0.1931   -0.1697 C   0  0  2  0  0  0  0  0  0  0  0  0
   -1.6064   -0.0744    0.2678 C   0  0  1  0  0  0  0  0  0  0  0  0
   -2.4630    0.0264   -1.0029 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6721    0.8030   -2.0009 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3458    1.1130   -1.3307 C   0  0  1  0  0  0  0  0  0  0  0  0
   -0.4837    2.5465   -0.8007 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7125   -3.2155    1.4326 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.7540   -1.8370    1.0106 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8010   -1.7045    2.4987 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3467   -3.1649    0.3671 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.2754   -1.3733   -1.5966 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.6603   -1.9686    0.9934 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.3803   -1.7178   -0.6286 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.5119    1.8804   -0.5581 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.6989    0.2958   -1.4563 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.8969    0.8169   -0.2600 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.3263   -1.0701    1.8680 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.3028    0.0814    2.7608 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.7699    0.6455    1.7811 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.3871    0.5777    1.9024 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.8767    1.8076    0.6689 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9877    0.6170    1.0458 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.4495    0.4851   -0.7681 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6827   -0.9654   -1.4372 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2352    1.7174   -2.2692 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4970    0.2495   -2.9559 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.4905    1.0357   -2.0338 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9595    2.5597    0.2029 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.4632    3.0917   -0.8596 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2021    3.1182   -1.4592 H   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0
  2  3  2  0
  3  4  1  0
  4  5  1  0
  5  6  1  0
  6  7  1  6
  6  8  1  0
  6  9  1  0
 10  9  1  1
 10 11  1  0
 11 12  1  0
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 13 14  1  0
 14 15  1  0
 11  2  1  0
 10  4  1  0
 14 10  1  0
  1 16  1  0
  1 17  1  0
  1 18  1  0
  3 19  1  0
  4 20  1  6
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  5 22  1  0
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  7 24  1  0
  7 25  1  0
  8 26  1  0
  8 27  1  0
  8 28  1  0
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  9 30  1  0
 11 31  1  1
 12 32  1  0
 12 33  1  0
 13 34  1  0
 13 35  1  0
 14 36  1  6
 15 37  1  0
 15 38  1  0
 15 39  1  0
M  END

HEADER    PROTEIN                                 24-JUN-21   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   24-JUN-21         0                                  
HETATM    1  C   UNK     0      -2.763  -2.095   1.455  0.00  0.00           C+0
HETATM    2  C   UNK     0      -1.658  -1.486   0.671  0.00  0.00           C+0
HETATM    3  C   UNK     0      -0.603  -2.113   0.238  0.00  0.00           C+0
HETATM    4  C   UNK     0       0.278  -1.180  -0.503  0.00  0.00           C+0
HETATM    5  C   UNK     0       1.654  -1.287   0.094  0.00  0.00           C+0
HETATM    6  C   UNK     0       2.062   0.060   0.584  0.00  0.00           C+0
HETATM    7  C   UNK     0       2.809   0.836  -0.478  0.00  0.00           C+0
HETATM    8  C   UNK     0       2.888  -0.035   1.849  0.00  0.00           C+0
HETATM    9  C   UNK     0       0.713   0.730   0.878  0.00  0.00           C+0
HETATM   10  C   UNK     0      -0.221   0.193  -0.170  0.00  0.00           C+0
HETATM   11  C   UNK     0      -1.606  -0.074   0.268  0.00  0.00           C+0
HETATM   12  C   UNK     0      -2.463   0.026  -1.003  0.00  0.00           C+0
HETATM   13  C   UNK     0      -1.672   0.803  -2.001  0.00  0.00           C+0
HETATM   14  C   UNK     0      -0.346   1.113  -1.331  0.00  0.00           C+0
HETATM   15  C   UNK     0      -0.484   2.547  -0.801  0.00  0.00           C+0
HETATM   16  H   UNK     0      -2.712  -3.216   1.433  0.00  0.00           H+0
HETATM   17  H   UNK     0      -3.754  -1.837   1.011  0.00  0.00           H+0
HETATM   18  H   UNK     0      -2.801  -1.704   2.499  0.00  0.00           H+0
HETATM   19  H   UNK     0      -0.347  -3.165   0.367  0.00  0.00           H+0
HETATM   20  H   UNK     0       0.275  -1.373  -1.597  0.00  0.00           H+0
HETATM   21  H   UNK     0       1.660  -1.969   0.993  0.00  0.00           H+0
HETATM   22  H   UNK     0       2.380  -1.718  -0.629  0.00  0.00           H+0
HETATM   23  H   UNK     0       2.512   1.880  -0.558  0.00  0.00           H+0
HETATM   24  H   UNK     0       2.699   0.296  -1.456  0.00  0.00           H+0
HETATM   25  H   UNK     0       3.897   0.817  -0.260  0.00  0.00           H+0
HETATM   26  H   UNK     0       3.326  -1.070   1.868  0.00  0.00           H+0
HETATM   27  H   UNK     0       2.303   0.081   2.761  0.00  0.00           H+0
HETATM   28  H   UNK     0       3.770   0.646   1.781  0.00  0.00           H+0
HETATM   29  H   UNK     0       0.387   0.578   1.902  0.00  0.00           H+0
HETATM   30  H   UNK     0       0.877   1.808   0.669  0.00  0.00           H+0
HETATM   31  H   UNK     0      -1.988   0.617   1.046  0.00  0.00           H+0
HETATM   32  H   UNK     0      -3.450   0.485  -0.768  0.00  0.00           H+0
HETATM   33  H   UNK     0      -2.683  -0.965  -1.437  0.00  0.00           H+0
HETATM   34  H   UNK     0      -2.235   1.717  -2.269  0.00  0.00           H+0
HETATM   35  H   UNK     0      -1.497   0.250  -2.956  0.00  0.00           H+0
HETATM   36  H   UNK     0       0.491   1.036  -2.034  0.00  0.00           H+0
HETATM   37  H   UNK     0      -0.960   2.560   0.203  0.00  0.00           H+0
HETATM   38  H   UNK     0       0.463   3.092  -0.860  0.00  0.00           H+0
HETATM   39  H   UNK     0      -1.202   3.118  -1.459  0.00  0.00           H+0
CONECT    1    2   16   17   18                                             
CONECT    2    1    3   11                                                  
CONECT    3    2    4   19                                                  
CONECT    4    3    5   10   20                                             
CONECT    5    4    6   21   22                                             
CONECT    6    5    7    8    9                                             
CONECT    7    6   23   24   25                                             
CONECT    8    6   26   27   28                                             
CONECT    9    6   10   29   30                                             
CONECT   10    9   11    4   14                                             
CONECT   11   10   12    2   31                                             
CONECT   12   11   13   32   33                                             
CONECT   13   12   14   34   35                                             
CONECT   14   13   15   10   36                                             
CONECT   15   14   37   38   39                                             
CONECT   16    1                                                            
CONECT   17    1                                                            
CONECT   18    1                                                            
CONECT   19    3                                                            
CONECT   20    4                                                            
CONECT   21    5                                                            
CONECT   22    5                                                            
CONECT   23    7                                                            
CONECT   24    7                                                            
CONECT   25    7                                                            
CONECT   26    8                                                            
CONECT   27    8                                                            
CONECT   28    8                                                            
CONECT   29    9                                                            
CONECT   30    9                                                            
CONECT   31   11                                                            
CONECT   32   12                                                            
CONECT   33   12                                                            
CONECT   34   13                                                            
CONECT   35   13                                                            
CONECT   36   14                                                            
CONECT   37   15                                                            
CONECT   38   15                                                            
CONECT   39   15                                                            
MASTER        0    0    0    0    0    0    0    0   39    0   82    0
END

RDKit          3D

39 41  0  0  0  0  0  0  0  0999 V2000
   -2.7631   -2.0945    1.4547 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6580   -1.4862    0.6709 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6031   -2.1128    0.2379 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.2776   -1.1804   -0.5029 C   0  0  2  0  0  0  0  0  0  0  0  0
    1.6540   -1.2868    0.0941 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.0622    0.0596    0.5838 C   0  0  2  0  0  0  0  0  0  0  0  0
    2.8094    0.8358   -0.4777 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8875   -0.0351    1.8486 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7130    0.7304    0.8780 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2210    0.1931   -0.1697 C   0  0  2  0  0  0  0  0  0  0  0  0
   -1.6064   -0.0744    0.2678 C   0  0  1  0  0  0  0  0  0  0  0  0
   -2.4630    0.0264   -1.0029 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6721    0.8030   -2.0009 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3458    1.1130   -1.3307 C   0  0  1  0  0  0  0  0  0  0  0  0
   -0.4837    2.5465   -0.8007 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7125   -3.2155    1.4326 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.7540   -1.8370    1.0106 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8010   -1.7045    2.4987 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3467   -3.1649    0.3671 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.2754   -1.3733   -1.5966 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.6603   -1.9686    0.9934 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.3803   -1.7178   -0.6286 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.5119    1.8804   -0.5581 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.6989    0.2958   -1.4563 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.8969    0.8169   -0.2600 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.3263   -1.0701    1.8680 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.3028    0.0814    2.7608 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.7699    0.6455    1.7811 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.3871    0.5777    1.9024 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.8767    1.8076    0.6689 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9877    0.6170    1.0458 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.4495    0.4851   -0.7681 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6827   -0.9654   -1.4372 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2352    1.7174   -2.2692 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4970    0.2495   -2.9559 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.4905    1.0357   -2.0338 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9595    2.5597    0.2029 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.4632    3.0917   -0.8596 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2021    3.1182   -1.4592 H   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0
  2  3  2  0
  3  4  1  0
  4  5  1  0
  5  6  1  0
  6  7  1  6
  6  8  1  0
  6  9  1  0
 10  9  1  1
 10 11  1  0
 11 12  1  0
 12 13  1  0
 13 14  1  0
 14 15  1  0
 11  2  1  0
 10  4  1  0
 14 10  1  0
  1 16  1  0
  1 17  1  0
  1 18  1  0
  3 19  1  0
  4 20  1  6
  5 21  1  0
  5 22  1  0
  7 23  1  0
  7 24  1  0
  7 25  1  0
  8 26  1  0
  8 27  1  0
  8 28  1  0
  9 29  1  0
  9 30  1  0
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 12 33  1  0
 13 34  1  0
 13 35  1  0
 14 36  1  6
 15 37  1  0
 15 38  1  0
 15 39  1  0
M  END

View in JSmol View NMR Assignments

Synonyms

Value	Source
(+)-Pentalenene	ChEBI
(1alpha,3a alpha,5a beta,8AR*)-1,2,3,3a,5a,6,7,8-octahydro-1,4,7,7-tetramethylcyclopenta(c)pentalene	ChEBI
(1R,3AS,5as,8ar)-1,2,3,3a,5a,6,7,8-octahydro-1,4,7,7-tetramethylcyclopenta[c]pentalene	ChEBI
(1a,3a a,5a b,8AR*)-1,2,3,3a,5a,6,7,8-octahydro-1,4,7,7-tetramethylcyclopenta(c)pentalene	Generator
(1Α,3a α,5a β,8ar*)-1,2,3,3a,5a,6,7,8-octahydro-1,4,7,7-tetramethylcyclopenta(c)pentalene	Generator

Chemical Formula

C₁₅H₂₄

Average Mass

204.3570 Da

Monoisotopic Mass

204.18780 Da

IUPAC Name

(1R,2R,5S,8S)-2,6,10,10-tetramethyltricyclo[6.3.0.0^{1,5}]undec-6-ene

Traditional Name

(1R,2R,5S,8S)-2,6,10,10-tetramethyltricyclo[6.3.0.0^{1,5}]undec-6-ene

CAS Registry Number

Not Available

SMILES

C[C@@H]1CC[C@H]2C(C)=C[C@@H]3CC(C)(C)C[C@]123

InChI Identifier

InChI=1S/C15H24/c1-10-7-12-8-14(3,4)9-15(12)11(2)5-6-13(10)15/h7,11-13H,5-6,8-9H2,1-4H3/t11-,12-,13+,15-/m1/s1

InChI Key

YGIVIHRLDOVJLL-GUIRCDHDSA-N

Experimental Spectra

Not Available

Predicted Spectra

Spectrum Type	Description	Depositor ID	Depositor Organization	Depositor	Deposition Date	View
1D NMR	¹³C NMR Spectrum (1D, 25 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 100 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 252 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 1000 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 50 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 200 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 75 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 300 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 101 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 400 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 126 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 500 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 151 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 600 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 176 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 700 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 201 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 800 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 226 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 900 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum

Chemical Shift Submissions

Not Available

Species

Species of Origin

Species Name	Source	Reference
Laurencia dendroidea	-	KNApSAcK
Streptomyces griseochromogenes	NPAtlas	7372558

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as angular triquinanes. These are triquinane with a structure based on a [6.3.0.0^1,5] Undecane carbon skeleton.

Kingdom

Organic compounds

Super Class

Lipids and lipid-like molecules

Class

Prenol lipids

Sub Class

Sesquiterpenoids

Direct Parent

Angular triquinanes

Alternative Parents

Substituents

Angular triquinane sesquiterpenoid
Branched unsaturated hydrocarbon
Polycyclic hydrocarbon
Cyclic olefin
Unsaturated aliphatic hydrocarbon
Unsaturated hydrocarbon
Olefin
Hydrocarbon
Aliphatic homopolycyclic compound

Molecular Framework

Aliphatic homopolycyclic compounds

External Descriptors

sesquiterpene (CHEBI:17251 )
ortho-fused tricyclic hydrocarbon (CHEBI:17251 )

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	4.9	ALOGPS
logP	4.1	ChemAxon
logS	-5.1	ALOGPS
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	0	ChemAxon
Hydrogen Donor Count	0	ChemAxon
Polar Surface Area	0 Å²	ChemAxon
Rotatable Bond Count	0	ChemAxon
Refractivity	65.69 m³·mol⁻¹	ChemAxon
Polarizability	25.86 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

NPAtlas ID

NPA001591

HMDB ID

Not Available

DrugBank ID

Not Available

Phenol Explorer Compound ID

Not Available

FoodDB ID

Not Available

KNApSAcK ID

C00021799

Chemspider ID

9184241

KEGG Compound ID

Not Available

BioCyc ID

Not Available

BiGG ID

Not Available

Wikipedia Link

Not Available

METLIN ID

Not Available

PubChem Compound

11009055

PDB ID

Not Available

ChEBI ID

17251

Good Scents ID

Not Available

References

General References

Seto H, Yonehara H: Studies on the biosynthesis of pentalenolactone. III. Isolation of a biosynthetic intermediate hydrocarbon, pentalenene. J Antibiot (Tokyo). 1980 Jan;33(1):92-3. doi: 10.7164/antibiotics.33.92. [PubMed:7372558 ]

Showing NP-Card for Pentalenene (NP0022149)

MOL for NP0022149 (Pentalenene)

3D MOL for NP0022149 (Pentalenene)

3D SDF for NP0022149 (Pentalenene)

3D-SDF for NP0022149 (Pentalenene)

PDB for NP0022149 (Pentalenene)

3D PDB for NP0022149 (Pentalenene)

SMILES for NP0022149 (Pentalenene)

INCHI for NP0022149 (Pentalenene)

Structure for NP0022149 (Pentalenene)

3D Structure for NP0022149 (Pentalenene)