NP-MRD: Showing NP-Card for (12s)-5-isopropyl-8-methoxy-6,11,11-trimethyl-10-oxatetracyclo[7.5.1.0²,⁷.0¹²,¹⁵]pentadeca-1(15),2,4,6,8-pentaene (NP0155305)

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Record Information

Version

2.0

Created at

2022-09-02 12:20:17 UTC

Updated at

2022-09-02 12:20:17 UTC

NP-MRD ID

NP0155305

Secondary Accession Numbers

None

Natural Product Identification

Common Name

(12s)-5-isopropyl-8-methoxy-6,11,11-trimethyl-10-oxatetracyclo[7.5.1.0²,⁷.0¹²,¹⁵]pentadeca-1(15),2,4,6,8-pentaene

Description

(12S)-8-methoxy-6,11,11-trimethyl-5-(propan-2-yl)-10-oxatetracyclo[7.5.1.0²,⁷.0¹²,¹⁵]Pentadeca-1,3,5,7,9(15)-pentaene belongs to the class of organic compounds known as naphthofurans. Naphthofurans are compounds containing a furan ring fused to a naphthalene moiety. Furan is a 5 membered- ring aromatic ring with four carbon and one oxygen atoms. Naphthalene is a polycyclic aromatic hydrocarbon made up of two fused benzene rings. (12s)-5-isopropyl-8-methoxy-6,11,11-trimethyl-10-oxatetracyclo[7.5.1.0²,⁷.0¹²,¹⁵]pentadeca-1(15),2,4,6,8-pentaene is found in Salvia prionitis. Based on a literature review very few articles have been published on (12S)-8-methoxy-6,11,11-trimethyl-5-(propan-2-yl)-10-oxatetracyclo[7.5.1.0²,⁷.0¹²,¹⁵]Pentadeca-1,3,5,7,9(15)-pentaene.

Structure

MOL 3D MOL SDF PDB SMILES InChI

     RDKit          3D

 49 52  0  0  0  0  0  0  0  0999 V2000
   -0.3396    3.5512   -0.1372 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2238    2.3486   -0.8929 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3651    1.0880   -0.3810 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7212    0.6980   -0.2065 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8801   -0.5184    0.2961 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9642   -1.4311    0.6577 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.3369   -1.0417    0.4832 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.2979   -1.9588    0.7925 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.6034   -1.6184    0.5755 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.9726   -0.3413    0.0423 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.3797   -0.2453   -0.2983 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.3844   -0.8833    0.6012 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.9463    0.7353   -1.2493 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.9896    0.5615   -0.2503 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.3095    1.9321   -0.6419 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.6626    0.2298   -0.0404 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7923   -2.5854    1.0939 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.1440   -2.3293    0.3273 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.2770   -0.8857    0.5569 C   0  0  2  0  0  0  0  0  0  0  0  0
   -3.9511    0.0817   -0.2551 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.5648   -0.3112   -1.5479 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.0684    0.7357    0.5969 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.9890    1.1611   -0.3853 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.4139    4.2895   -0.4558 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3757    3.9315   -0.3219 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3084    3.2730    0.9310 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.0142   -2.9338    1.2029 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.3384   -2.3659    0.8161 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.3744   -1.1955   -1.1179 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.9919   -1.7505    1.1032 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.7892   -0.2029    1.3794 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.2877   -1.2022    0.0100 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.4846    1.6038   -0.8130 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.3255    0.9591   -2.1440 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.8625    0.2469   -1.8064 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.9092    2.3096   -1.5757 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.9667    2.6292    0.2363 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.3686    2.2339   -0.6240 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0384   -2.4781    2.1619 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3724   -3.5540    0.7984 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.9811   -2.6582   -0.6976 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.9008   -2.8876    0.9064 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5137   -0.7324    1.6481 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.6104   -0.6671   -1.3049 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.7430    0.6013   -2.1801 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.1002   -1.1233   -2.0969 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.8906    0.0309    0.7210 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.3348    1.6744    0.0707 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.5598    0.9952    1.5574 H   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0
  2  3  1  0
  3 16  2  0
 16 14  1  0
 14 15  1  0
 14 10  2  0
 10  9  1  0
  9  8  2  0
  8  7  1  0
  7  6  2  0
  6 17  1  0
 17 18  1  0
 18 19  1  0
 19  5  1  0
  5  4  2  0
  4 23  1  0
 23 20  1  0
 20 21  1  0
 20 22  1  0
 10 11  1  0
 11 12  1  0
 11 13  1  0
  4  3  1  0
  7 16  1  0
  5  6  1  0
 20 19  1  0
  1 24  1  0
  1 25  1  0
  1 26  1  0
 15 36  1  0
 15 37  1  0
 15 38  1  0
  9 28  1  0
  8 27  1  0
 17 39  1  0
 17 40  1  0
 18 41  1  0
 18 42  1  0
 19 43  1  1
 21 44  1  0
 21 45  1  0
 21 46  1  0
 22 47  1  0
 22 48  1  0
 22 49  1  0
 11 29  1  0
 12 30  1  0
 12 31  1  0
 12 32  1  0
 13 33  1  0
 13 34  1  0
 13 35  1  0
M  END


  Mrv1652309022214202D          

 23 26  0  0  1  0            999 V2000
    3.6741    1.8361    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.9250    1.4903    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.8500    0.6687    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1010    0.3229    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.0259   -0.4987    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.6999   -0.9745    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.4490   -0.6287    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.1229   -1.1044    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.8720   -0.7586    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.9470    0.0630    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.6960    0.4088    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.3700   -0.0670    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.7711    1.2303    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.2730    0.5387    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.3481    1.3603    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5240    0.1929    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.4557   -1.7625    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.6308   -1.7737    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.3652   -0.9927    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    0.6912   -0.5169    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.2885   -1.2369    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0670   -0.1917    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.9354    0.2711    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0  0  0  0
  2  3  1  0  0  0  0
  3  4  1  0  0  0  0
  4  5  2  0  0  0  0
  5  6  1  0  0  0  0
  6  7  2  0  0  0  0
  7  8  1  0  0  0  0
  8  9  2  0  0  0  0
  9 10  1  0  0  0  0
 10 11  1  0  0  0  0
 11 12  1  0  0  0  0
 11 13  1  0  0  0  0
 10 14  2  0  0  0  0
 14 15  1  0  0  0  0
 14 16  1  0  0  0  0
  3 16  2  0  0  0  0
  7 16  1  0  0  0  0
  6 17  1  0  0  0  0
 17 18  1  0  0  0  0
 19 18  1  6  0  0  0
  5 19  1  0  0  0  0
 19 20  1  0  0  0  0
 20 21  1  0  0  0  0
 20 22  1  0  0  0  0
 20 23  1  0  0  0  0
  4 23  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0155305

> <DATABASE_NAME>
NP-MRD

> <SMILES>
COC1=C2C(C)=C(C=CC2=C2CC[C@H]3C2=C1OC3(C)C)C(C)C

> <INCHI_IDENTIFIER>
InChI=1S/C21H26O2/c1-11(2)13-7-8-14-15-9-10-16-18(15)20(23-21(16,4)5)19(22-6)17(14)12(13)3/h7-8,11,16H,9-10H2,1-6H3/t16-/m0/s1

> <INCHI_KEY>
KYEPDZAEZNKJIE-INIZCTEOSA-N

> <FORMULA>
C21H26O2

> <MOLECULAR_WEIGHT>
310.437

> <EXACT_MASS>
310.193280077

> <JCHEM_ACCEPTOR_COUNT>
2

> <JCHEM_ATOM_COUNT>
49

> <JCHEM_AVERAGE_POLARIZABILITY>
37.31026299559257

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
0

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
1

> <JCHEM_IUPAC>
(12S)-8-methoxy-6,11,11-trimethyl-5-(propan-2-yl)-10-oxatetracyclo[7.5.1.0^{2,7}.0^{12,15}]pentadeca-1,3,5,7,9(15)-pentaene

> <ALOGPS_LOGP>
6.59

> <JCHEM_LOGP>
5.557519093666666

> <ALOGPS_LOGS>
-6.54

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
4

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA_STRONGEST_BASIC>
-4.627986664991087

> <JCHEM_POLAR_SURFACE_AREA>
18.46

> <JCHEM_REFRACTIVITY>
94.74380000000002

> <JCHEM_ROTATABLE_BOND_COUNT>
2

> <JCHEM_RULE_OF_FIVE>
0

> <ALOGPS_SOLUBILITY>
9.02e-05 g/l

> <JCHEM_TRADITIONAL_IUPAC>
(12S)-5-isopropyl-8-methoxy-6,11,11-trimethyl-10-oxatetracyclo[7.5.1.0^{2,7}.0^{12,15}]pentadeca-1,3,5,7,9(15)-pentaene

> <JCHEM_VEBER_RULE>
1

$$$$

HEADER    PROTEIN                                 02-SEP-22   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   02-SEP-22         0                                  
HETATM    1  C   UNK     0       6.858   3.427   0.000  0.00  0.00           C+0
HETATM    2  O   UNK     0       5.460   2.782   0.000  0.00  0.00           O+0
HETATM    3  C   UNK     0       5.320   1.248   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0       3.922   0.603   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0       3.782  -0.931   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0       5.040  -1.819   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0       6.438  -1.173   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0       7.696  -2.062   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0       9.094  -1.416   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0       9.234   0.118   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0      10.633   0.763   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0      11.891  -0.125   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0      10.773   2.297   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0       7.976   1.006   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0       8.116   2.539   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0       6.578   0.360   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0       4.584  -3.290   0.000  0.00  0.00           C+0
HETATM   18  C   UNK     0       3.044  -3.311   0.000  0.00  0.00           C+0
HETATM   19  C   UNK     0       2.548  -1.853   0.000  0.00  0.00           C+0
HETATM   20  C   UNK     0       1.290  -0.965   0.000  0.00  0.00           C+0
HETATM   21  C   UNK     0       0.538  -2.309   0.000  0.00  0.00           C+0
HETATM   22  C   UNK     0      -0.125  -0.358   0.000  0.00  0.00           C+0
HETATM   23  O   UNK     0       1.746   0.506   0.000  0.00  0.00           O+0
CONECT    1    2                                                            
CONECT    2    1    3                                                       
CONECT    3    2    4   16                                                  
CONECT    4    3    5   23                                                  
CONECT    5    4    6   19                                                  
CONECT    6    5    7   17                                                  
CONECT    7    6    8   16                                                  
CONECT    8    7    9                                                       
CONECT    9    8   10                                                       
CONECT   10    9   11   14                                                  
CONECT   11   10   12   13                                                  
CONECT   12   11                                                            
CONECT   13   11                                                            
CONECT   14   10   15   16                                                  
CONECT   15   14                                                            
CONECT   16   14    3    7                                                  
CONECT   17    6   18                                                       
CONECT   18   17   19                                                       
CONECT   19   18    5   20                                                  
CONECT   20   19   21   22   23                                             
CONECT   21   20                                                            
CONECT   22   20                                                            
CONECT   23   20    4                                                       
MASTER        0    0    0    0    0    0    0    0   23    0   52    0
END

View in JSmol

Synonyms

Not Available

Chemical Formula

C₂₁H₂₆O₂

Average Mass

310.4370 Da

Monoisotopic Mass

310.19328 Da

IUPAC Name

(12S)-8-methoxy-6,11,11-trimethyl-5-(propan-2-yl)-10-oxatetracyclo[7.5.1.0^{2,7}.0^{12,15}]pentadeca-1,3,5,7,9(15)-pentaene

Traditional Name

(12S)-5-isopropyl-8-methoxy-6,11,11-trimethyl-10-oxatetracyclo[7.5.1.0^{2,7}.0^{12,15}]pentadeca-1,3,5,7,9(15)-pentaene

CAS Registry Number

Not Available

SMILES

COC1=C2C(C)=C(C=CC2=C2CC[C@H]3C2=C1OC3(C)C)C(C)C

InChI Identifier

InChI=1S/C21H26O2/c1-11(2)13-7-8-14-15-9-10-16-18(15)20(23-21(16,4)5)19(22-6)17(14)12(13)3/h7-8,11,16H,9-10H2,1-6H3/t16-/m0/s1

InChI Key

KYEPDZAEZNKJIE-INIZCTEOSA-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
Salvia prionitis	LOTUS Database	35616633

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as naphthofurans. Naphthofurans are compounds containing a furan ring fused to a naphthalene moiety. Furan is a 5 membered- ring aromatic ring with four carbon and one oxygen atoms. Naphthalene is a polycyclic aromatic hydrocarbon made up of two fused benzene rings.

Kingdom

Organic compounds

Super Class

Organoheterocyclic compounds

Class

Naphthofurans

Sub Class

Not Available

Direct Parent

Naphthofurans

Alternative Parents

Substituents

Naphthofuran
Naphthalene
Coumaran
Indane
Anisole
Alkyl aryl ether
Benzenoid
Oxacycle
Ether
Organic oxygen compound
Hydrocarbon derivative
Organooxygen compound
Aromatic heteropolycyclic compound

Molecular Framework

Aromatic 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	6.59	ALOGPS
logP	5.56	ChemAxon
logS	-6.5	ALOGPS
pKa (Strongest Basic)	-4.6	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	2	ChemAxon
Hydrogen Donor Count	0	ChemAxon
Polar Surface Area	18.46 Å²	ChemAxon
Rotatable Bond Count	2	ChemAxon
Refractivity	94.74 m³·mol⁻¹	ChemAxon
Polarizability	37.31 Å³	ChemAxon
Number of Rings	4	ChemAxon
Bioavailability	Yes	ChemAxon
Rule of Five	No	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

57579908

KEGG Compound ID

Not Available

BioCyc ID

Not Available

BiGG ID

Not Available

Wikipedia Link

Not Available

METLIN ID

Not Available

PubChem Compound

162886251

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

LOTUS database [Link]

Showing NP-Card for (12s)-5-isopropyl-8-methoxy-6,11,11-trimethyl-10-oxatetracyclo[7.5.1.0²,⁷.0¹²,¹⁵]pentadeca-1(15),2,4,6,8-pentaene (NP0155305)

MOL for NP0155305 ((12s)-5-isopropyl-8-methoxy-6,11,11-trimethyl-10-oxatetracyclo[7.5.1.0²,⁷.0¹²,¹⁵]pentadeca-1(15),2,4,6,8-pentaene)

3D MOL for NP0155305 ((12s)-5-isopropyl-8-methoxy-6,11,11-trimethyl-10-oxatetracyclo[7.5.1.0²,⁷.0¹²,¹⁵]pentadeca-1(15),2,4,6,8-pentaene)

3D SDF for NP0155305 ((12s)-5-isopropyl-8-methoxy-6,11,11-trimethyl-10-oxatetracyclo[7.5.1.0²,⁷.0¹²,¹⁵]pentadeca-1(15),2,4,6,8-pentaene)

3D-SDF for NP0155305 ((12s)-5-isopropyl-8-methoxy-6,11,11-trimethyl-10-oxatetracyclo[7.5.1.0²,⁷.0¹²,¹⁵]pentadeca-1(15),2,4,6,8-pentaene)

PDB for NP0155305 ((12s)-5-isopropyl-8-methoxy-6,11,11-trimethyl-10-oxatetracyclo[7.5.1.0²,⁷.0¹²,¹⁵]pentadeca-1(15),2,4,6,8-pentaene)

3D PDB for NP0155305 ((12s)-5-isopropyl-8-methoxy-6,11,11-trimethyl-10-oxatetracyclo[7.5.1.0²,⁷.0¹²,¹⁵]pentadeca-1(15),2,4,6,8-pentaene)

SMILES for NP0155305 ((12s)-5-isopropyl-8-methoxy-6,11,11-trimethyl-10-oxatetracyclo[7.5.1.0²,⁷.0¹²,¹⁵]pentadeca-1(15),2,4,6,8-pentaene)

INCHI for NP0155305 ((12s)-5-isopropyl-8-methoxy-6,11,11-trimethyl-10-oxatetracyclo[7.5.1.0²,⁷.0¹²,¹⁵]pentadeca-1(15),2,4,6,8-pentaene)

Structure for NP0155305 ((12s)-5-isopropyl-8-methoxy-6,11,11-trimethyl-10-oxatetracyclo[7.5.1.0²,⁷.0¹²,¹⁵]pentadeca-1(15),2,4,6,8-pentaene)

3D Structure for NP0155305 ((12s)-5-isopropyl-8-methoxy-6,11,11-trimethyl-10-oxatetracyclo[7.5.1.0²,⁷.0¹²,¹⁵]pentadeca-1(15),2,4,6,8-pentaene)