NP-MRD: Showing NP-Card for (1r,4e,8e,12s,16r)-4,8,12,14,14-pentamethyl-13-oxabicyclo[10.2.2]hexadeca-4,8-dien-16-ol (NP0284450)

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Record Information

Version

2.0

Created at

2022-09-09 12:09:19 UTC

Updated at

2022-09-09 12:09:19 UTC

NP-MRD ID

NP0284450

Secondary Accession Numbers

None

Natural Product Identification

Common Name

(1r,4e,8e,12s,16r)-4,8,12,14,14-pentamethyl-13-oxabicyclo[10.2.2]hexadeca-4,8-dien-16-ol

Description

Decaryiol belongs to the class of organic compounds known as oxanes. Oxanes are compounds containing an oxane (tetrahydropyran) ring, which is a six-member saturated aliphatic heterocycle with one oxygen atom and five carbon atoms. (1r,4e,8e,12s,16r)-4,8,12,14,14-pentamethyl-13-oxabicyclo[10.2.2]hexadeca-4,8-dien-16-ol is found in Sarcophyton trocheliophorum. (1r,4e,8e,12s,16r)-4,8,12,14,14-pentamethyl-13-oxabicyclo[10.2.2]hexadeca-4,8-dien-16-ol was first documented in 2003 (PMID: 12929632). Based on a literature review very few articles have been published on Decaryiol (PMID: 28429730).

Structure

MOL 3D MOL SDF PDB SMILES InChI

     RDKit          3D

 56 57  0  0  0  0  0  0  0  0999 V2000
    3.7892   -0.9970   -2.0966 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.2051   -1.1476   -0.7363 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.4953   -2.1913   -0.4184 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4149   -2.1988    0.6178 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.1458   -2.0556   -0.1133 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1052   -1.7019    0.6381 C   0  0  2  0  0  0  0  0  0  0  0  0
   -1.6060   -3.0577    1.1999 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0171   -1.3958   -0.3491 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5990   -0.2085   -0.3910 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.0537   -0.3642    0.0810 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7277    0.2174   -1.8631 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0027    0.9487    0.3293 C   0  0  2  0  0  0  0  0  0  0  0  0
   -0.9202    1.6111   -0.4373 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0449    2.4346    0.3425 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.2416    2.8094   -0.4557 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.1942    4.0082   -1.3292 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.3879    2.0949   -0.4176 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.3525    0.8899    0.4483 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.4406   -0.0911    0.2593 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7165    0.5209    1.7180 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0042   -0.7709    1.7551 C   0  0  1  0  0  0  0  0  0  0  0  0
   -1.4361   -1.4113    2.9658 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.8405   -1.3906   -2.0389 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.2689   -1.6136   -2.8502 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.8835    0.0684   -2.3975 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.6863   -3.1232   -0.9339 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.6281   -1.5872    1.4720 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.4216   -3.2604    1.0261 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.2514   -1.3208   -0.9694 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1119   -3.0140   -0.6712 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4199   -2.8869    1.9345 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0414   -3.6701    0.3852 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7961   -3.5826    1.7208 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.6015   -0.8645   -0.7452 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.0956   -1.0264    0.9529 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.5330    0.6214    0.2303 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.1705    1.2184   -1.9575 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8019    0.0594   -2.4187 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.4855   -0.5035   -2.2895 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8643    1.7122    0.4139 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4316    2.3570   -1.1365 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4249    0.9271   -1.1890 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5192    3.3571    0.6717 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.4068    1.9897    1.2849 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.0005    4.0137   -2.0895 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.4171    4.8880   -0.6582 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.1944    4.2021   -1.7488 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.2587    2.3827   -0.9755 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.3392    0.4673    0.3220 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.3880    1.2590    1.5080 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.6895   -0.5430    1.2566 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.3676    0.4780   -0.0016 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7254    0.3643    2.2086 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1816    1.2822    2.3263 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.0713   -0.5198    1.9711 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4329   -0.6845    3.6389 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  1
  6  8  1  0
  8  9  1  0
  9 10  1  0
  9 11  1  0
  9 12  1  0
 12 20  1  0
 20 21  1  0
 21 22  1  0
 12 13  1  0
 13 14  1  0
 14 15  1  0
 15 16  1  0
 15 17  2  0
 17 18  1  0
 18 19  1  0
 19  2  1  0
 21  6  1  0
  1 23  1  0
  1 24  1  0
  1 25  1  0
  3 26  1  0
  4 27  1  0
  4 28  1  0
  5 29  1  0
  5 30  1  0
  7 31  1  0
  7 32  1  0
  7 33  1  0
 10 34  1  0
 10 35  1  0
 10 36  1  0
 11 37  1  0
 11 38  1  0
 11 39  1  0
 12 40  1  1
 20 53  1  0
 20 54  1  0
 21 55  1  1
 22 56  1  0
 13 41  1  0
 13 42  1  0
 14 43  1  0
 14 44  1  0
 16 45  1  0
 16 46  1  0
 16 47  1  0
 17 48  1  0
 18 49  1  0
 18 50  1  0
 19 51  1  0
 19 52  1  0
M  END


  Mrv1652309082203422D          

 22 23  0  0  1  0            999 V2000
    5.2153    0.0424    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.6245    0.6183    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.9256    0.1642    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.0919    0.0543    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.2795    0.2941    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.7454    0.9781    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    0.9430    1.1699    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.1004    1.5239    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.2483    2.3395    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.4236    2.3173    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.0576    3.1421    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.0083    2.6969    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    2.5763    3.3516    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.3586    3.7062    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.2077    3.5378    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.5757    4.2762    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.8553    2.9596    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.1493    2.1558    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.0600    1.3275    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.6201    2.1467    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.5006    1.3325    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    3.1629    0.8405    0.0000 O   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  1  0  0  0
  6  8  1  0  0  0  0
  8  9  1  0  0  0  0
  9 10  1  0  0  0  0
  9 11  1  0  0  0  0
  9 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
 15 16  1  0  0  0  0
 15 17  2  0  0  0  0
 17 18  1  0  0  0  0
 18 19  1  0  0  0  0
  2 19  1  0  0  0  0
 12 20  1  6  0  0  0
 20 21  1  0  0  0  0
  6 21  1  0  0  0  0
 21 22  1  1  0  0  0
M  END
> <DATABASE_ID>
NP0284450

> <DATABASE_NAME>
NP-MRD

> <SMILES>
C\C1=C\CC[C@]2(C)OC(C)(C)[C@@H](C[C@H]2O)CC\C(C)=C/CC1

> <INCHI_IDENTIFIER>
InChI=1S/C20H34O2/c1-15-8-6-9-16(2)11-12-17-14-18(21)20(5,13-7-10-15)22-19(17,3)4/h9-10,17-18,21H,6-8,11-14H2,1-5H3/b15-10-,16-9-/t17-,18-,20+/m1/s1

> <INCHI_KEY>
QJAIARJGTZFFBW-HHJIHTTCSA-N

> <FORMULA>
C20H34O2

> <MOLECULAR_WEIGHT>
306.49

> <EXACT_MASS>
306.255880335

> <JCHEM_ACCEPTOR_COUNT>
2

> <JCHEM_ATOM_COUNT>
56

> <JCHEM_AVERAGE_POLARIZABILITY>
37.37300755184991

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
1

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
1

> <JCHEM_IUPAC>
(1R,4Z,8Z,12S,16R)-4,8,12,14,14-pentamethyl-13-oxabicyclo[10.2.2]hexadeca-4,8-dien-16-ol

> <JCHEM_LOGP>
4.592944549333334

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
2

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA_STRONGEST_ACIDIC>
13.987424143085697

> <JCHEM_PKA_STRONGEST_BASIC>
-3.2417006798143158

> <JCHEM_POLAR_SURFACE_AREA>
29.46

> <JCHEM_REFRACTIVITY>
94.8276

> <JCHEM_ROTATABLE_BOND_COUNT>
0

> <JCHEM_RULE_OF_FIVE>
1

> <JCHEM_TRADITIONAL_IUPAC>
(1R,4Z,8Z,12S,16R)-4,8,12,14,14-pentamethyl-13-oxabicyclo[10.2.2]hexadeca-4,8-dien-16-ol

> <JCHEM_VEBER_RULE>
1

$$$$

HEADER    PROTEIN                                 08-SEP-22   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   08-SEP-22         0                                  
HETATM    1  C   UNK     0       9.735   0.079   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0       8.632   1.154   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0       7.328   0.306   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0       5.772   0.101   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0       4.255   0.549   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0       3.258   1.826   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0       1.760   2.184   0.000  0.00  0.00           C+0
HETATM    8  O   UNK     0       2.054   2.845   0.000  0.00  0.00           O+0
HETATM    9  C   UNK     0       2.330   4.367   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0       0.791   4.326   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0       1.974   5.865   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0       3.749   5.034   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0       4.809   6.256   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0       6.269   6.918   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0       7.854   6.604   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0       8.541   7.982   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0       9.063   5.525   0.000  0.00  0.00           C+0
HETATM   18  C   UNK     0       9.612   4.024   0.000  0.00  0.00           C+0
HETATM   19  C   UNK     0       9.445   2.478   0.000  0.00  0.00           C+0
HETATM   20  C   UNK     0       4.891   4.007   0.000  0.00  0.00           C+0
HETATM   21  C   UNK     0       4.668   2.487   0.000  0.00  0.00           C+0
HETATM   22  O   UNK     0       5.904   1.569   0.000  0.00  0.00           O+0
CONECT    1    2                                                            
CONECT    2    1    3   19                                                  
CONECT    3    2    4                                                       
CONECT    4    3    5                                                       
CONECT    5    4    6                                                       
CONECT    6    5    7    8   21                                             
CONECT    7    6                                                            
CONECT    8    6    9                                                       
CONECT    9    8   10   11   12                                             
CONECT   10    9                                                            
CONECT   11    9                                                            
CONECT   12    9   13   20                                                  
CONECT   13   12   14                                                       
CONECT   14   13   15                                                       
CONECT   15   14   16   17                                                  
CONECT   16   15                                                            
CONECT   17   15   18                                                       
CONECT   18   17   19                                                       
CONECT   19   18    2                                                       
CONECT   20   12   21                                                       
CONECT   21   20    6   22                                                  
CONECT   22   21                                                            
MASTER        0    0    0    0    0    0    0    0   22    0   46    0
END

View in JSmol

Synonyms

Not Available

Chemical Formula

C₂₀H₃₄O₂

Average Mass

306.4900 Da

Monoisotopic Mass

306.25588 Da

IUPAC Name

(1R,4Z,8Z,12S,16R)-4,8,12,14,14-pentamethyl-13-oxabicyclo[10.2.2]hexadeca-4,8-dien-16-ol

Traditional Name

(1R,4Z,8Z,12S,16R)-4,8,12,14,14-pentamethyl-13-oxabicyclo[10.2.2]hexadeca-4,8-dien-16-ol

CAS Registry Number

Not Available

SMILES

C\C1=C\CC[C@]2(C)OC(C)(C)[C@@H](C[C@H]2O)CC\C(C)=C/CC1

InChI Identifier

InChI=1S/C20H34O2/c1-15-8-6-9-16(2)11-12-17-14-18(21)20(5,13-7-10-15)22-19(17,3)4/h9-10,17-18,21H,6-8,11-14H2,1-5H3/b15-10-,16-9-/t17-,18-,20+/m1/s1

InChI Key

QJAIARJGTZFFBW-HHJIHTTCSA-N

Experimental Spectra

Not Available

Predicted Spectra

Spectrum Type	Description	Depositor ID	Depositor Organization	Depositor	Deposition Date	View
1D NMR	¹³C NMR Spectrum (1D, 25 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 100 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 252 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 1000 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 50 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 200 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 75 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 300 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 101 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 400 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 126 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 500 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 151 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 600 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 176 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 700 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 201 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 800 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 226 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 900 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum

Chemical Shift Submissions

Not Available

Species

Species of Origin

Species Name	Source	Reference
Sarcophyton trocheliophorum	LOTUS Database	35616633

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as oxanes. Oxanes are compounds containing an oxane (tetrahydropyran) ring, which is a six-member saturated aliphatic heterocycle with one oxygen atom and five carbon atoms.

Kingdom

Organic compounds

Super Class

Organoheterocyclic compounds

Class

Oxanes

Sub Class

Not Available

Direct Parent

Oxanes

Alternative Parents

Substituents

Oxane
Secondary alcohol
Oxacycle
Ether
Dialkyl ether
Organic oxygen compound
Hydrocarbon derivative
Organooxygen compound
Alcohol
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	4.59	ChemAxon
pKa (Strongest Acidic)	13.99	ChemAxon
pKa (Strongest Basic)	-3.2	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	2	ChemAxon
Hydrogen Donor Count	1	ChemAxon
Polar Surface Area	29.46 Å²	ChemAxon
Rotatable Bond Count	0	ChemAxon
Refractivity	94.83 m³·mol⁻¹	ChemAxon
Polarizability	37.37 Å³	ChemAxon
Number of Rings	2	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

C00050052

Chemspider ID

Not Available

KEGG Compound ID

Not Available

BioCyc ID

Not Available

BiGG ID

Not Available

Wikipedia Link

Not Available

METLIN ID

Not Available

PubChem Compound

101658812

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

Gross H, Kehraus S, Nett M, Konig GM, Beil W, Wright AD: New cytotoxic cembrane based diterpenes from the soft corals Sarcophyton cherbonnieri and Nephthea sp. Org Biomol Chem. 2003 Mar 21;1(6):944-9. doi: 10.1039/b210039h. [PubMed:12929632 ]
Liang LF, Chen WT, Li XW, Wang HY, Guo YW: New Bicyclic Cembranoids from the South China Sea Soft Coral Sarcophyton trocheliophorum. Sci Rep. 2017 Apr 21;7:46584. doi: 10.1038/srep46584. [PubMed:28429730 ]
LOTUS database [Link]

Showing NP-Card for (1r,4e,8e,12s,16r)-4,8,12,14,14-pentamethyl-13-oxabicyclo[10.2.2]hexadeca-4,8-dien-16-ol (NP0284450)

MOL for NP0284450 ((1r,4e,8e,12s,16r)-4,8,12,14,14-pentamethyl-13-oxabicyclo[10.2.2]hexadeca-4,8-dien-16-ol)

3D MOL for NP0284450 ((1r,4e,8e,12s,16r)-4,8,12,14,14-pentamethyl-13-oxabicyclo[10.2.2]hexadeca-4,8-dien-16-ol)

3D SDF for NP0284450 ((1r,4e,8e,12s,16r)-4,8,12,14,14-pentamethyl-13-oxabicyclo[10.2.2]hexadeca-4,8-dien-16-ol)

3D-SDF for NP0284450 ((1r,4e,8e,12s,16r)-4,8,12,14,14-pentamethyl-13-oxabicyclo[10.2.2]hexadeca-4,8-dien-16-ol)

PDB for NP0284450 ((1r,4e,8e,12s,16r)-4,8,12,14,14-pentamethyl-13-oxabicyclo[10.2.2]hexadeca-4,8-dien-16-ol)

3D PDB for NP0284450 ((1r,4e,8e,12s,16r)-4,8,12,14,14-pentamethyl-13-oxabicyclo[10.2.2]hexadeca-4,8-dien-16-ol)

SMILES for NP0284450 ((1r,4e,8e,12s,16r)-4,8,12,14,14-pentamethyl-13-oxabicyclo[10.2.2]hexadeca-4,8-dien-16-ol)

INCHI for NP0284450 ((1r,4e,8e,12s,16r)-4,8,12,14,14-pentamethyl-13-oxabicyclo[10.2.2]hexadeca-4,8-dien-16-ol)

Structure for NP0284450 ((1r,4e,8e,12s,16r)-4,8,12,14,14-pentamethyl-13-oxabicyclo[10.2.2]hexadeca-4,8-dien-16-ol)

3D Structure for NP0284450 ((1r,4e,8e,12s,16r)-4,8,12,14,14-pentamethyl-13-oxabicyclo[10.2.2]hexadeca-4,8-dien-16-ol)