NP-MRD: Showing NP-Card for (1s,4s,8r,9s,12r,15r)-4,8,12,15-tetramethyl-14-methylidenetetracyclo[7.6.0.0¹,¹².0⁴,⁹]pentadecane (NP0325768)

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Record Information

Version

2.0

Created at

2022-09-12 06:46:28 UTC

Updated at

2022-09-12 06:46:28 UTC

NP-MRD ID

NP0325768

Secondary Accession Numbers

None

Natural Product Identification

Common Name

(1s,4s,8r,9s,12r,15r)-4,8,12,15-tetramethyl-14-methylidenetetracyclo[7.6.0.0¹,¹².0⁴,⁹]pentadecane

Description

Waihoensene belongs to the class of organic compounds known as branched unsaturated hydrocarbons. These are hydrocarbons that contains one or more unsaturated carbon atoms, and an aliphatic branch. (1s,4s,8r,9s,12r,15r)-4,8,12,15-tetramethyl-14-methylidenetetracyclo[7.6.0.0¹,¹².0⁴,⁹]pentadecane is found in Podocarpus totara. (1s,4s,8r,9s,12r,15r)-4,8,12,15-tetramethyl-14-methylidenetetracyclo[7.6.0.0¹,¹².0⁴,⁹]pentadecane was first documented in 2020 (PMID: 32847075). Based on a literature review a small amount of articles have been published on Waihoensene (PMID: 35484150) (PMID: 33103334) (PMID: 32330370).

Structure

MOL 3D MOL SDF PDB SMILES InChI

     RDKit          3D

 52 55  0  0  0  0  0  0  0  0999 V2000
    4.0057    1.3949   -0.3764 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.0047    0.6849    0.0780 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.0021   -0.7561    0.3049 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.5940   -1.1418   -0.1544 C   0  0  1  0  0  0  0  0  0  0  0  0
    1.7886   -1.8149   -1.4775 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.0231   -1.9955    0.9282 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3007   -1.4383    1.3026 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5646   -0.2331    0.4087 C   0  0  2  0  0  0  0  0  0  0  0  0
   -1.1042    0.8574    1.2886 C   0  0  2  0  0  0  0  0  0  0  0  0
   -1.9794    0.2870    2.4114 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9782    1.8366    0.5418 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.1898    1.2000   -0.0524 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.9512   -0.1755   -0.4859 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5106   -0.6185   -0.6603 C   0  0  2  0  0  0  0  0  0  0  0  0
   -1.6870   -2.0989   -0.8931 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9838    0.0586   -1.9137 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.4039    0.5301   -1.6091 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7726    0.1314   -0.2238 C   0  0  2  0  0  0  0  0  0  0  0  0
    1.6030    1.1033    0.4932 C   0  0  2  0  0  0  0  0  0  0  0  0
    1.5471    2.5378    0.1714 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.9331    0.9373   -0.6228 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.9133    2.4627   -0.5118 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.1535   -0.9655    1.3938 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.7876   -1.2971   -0.2244 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.0524   -2.8902   -1.2492 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.9235   -1.8494   -2.1295 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.6369   -1.3956   -2.0553 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.0163   -3.0956    0.6731 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.6553   -1.9886    1.8700 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3637   -1.1614    2.3897 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1164   -2.2044    1.1768 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3332    1.4611    1.8037 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3428   -0.7152    2.1971 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4132    0.2764    3.3857 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8608    0.9340    2.6050 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2606    2.6300    1.2571 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4147    2.3216   -0.2802 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.0041    1.2192    0.7077 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5523    1.8638   -0.8815 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5358   -0.9237    0.1287 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.4100   -0.2951   -1.5159 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8423   -2.7349   -0.7713 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0658   -2.2092   -1.9500 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5213   -2.5371   -0.2693 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0284   -0.6346   -2.8028 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6642    0.9081   -2.2200 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.1530    0.1624   -2.3586 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.4024    1.6343   -1.7304 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.6116    0.8975    1.6023 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.4077    3.0044    0.7536 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.6927    3.1279    0.4368 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.8950    2.7077   -0.8904 H   0  0  0  0  0  0  0  0  0  0  0  0
 20 19  1  0
 19  2  1  0
  2  1  2  3
  2  3  1  0
  3  4  1  0
  4  5  1  6
  4  6  1  0
  6  7  1  0
  8  7  1  1
  8  9  1  0
  9 10  1  0
  9 11  1  0
 11 12  1  0
 12 13  1  0
 13 14  1  0
 14 15  1  6
 14 16  1  0
 16 17  1  0
 18 17  1  6
 18 19  1  0
 18  4  1  0
 14  8  1  0
 18  8  1  0
 20 50  1  0
 20 51  1  0
 20 52  1  0
 19 49  1  1
  1 21  1  0
  1 22  1  0
  3 23  1  0
  3 24  1  0
  5 25  1  0
  5 26  1  0
  5 27  1  0
  6 28  1  0
  6 29  1  0
  7 30  1  0
  7 31  1  0
  9 32  1  1
 10 33  1  0
 10 34  1  0
 10 35  1  0
 11 36  1  0
 11 37  1  0
 12 38  1  0
 12 39  1  0
 13 40  1  0
 13 41  1  0
 15 42  1  0
 15 43  1  0
 15 44  1  0
 16 45  1  0
 16 46  1  0
 17 47  1  0
 17 48  1  0
M  END


  Mrv1652309122208462D          

 20 23  0  0  1  0            999 V2000
    0.4841    0.1179    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.2153    0.5000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.3360    1.3161    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1495    1.4535    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    1.7674    2.1847    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.7268    2.0428    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.4657    1.6759    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.3450    0.8597    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    3.7872    1.5562    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    3.4052    2.2874    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.6115    1.5215    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.9936    0.7903    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.5513    0.0938    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.7271    0.1285    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    4.0306   -0.6386    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.1497   -0.4608    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.4108   -0.0938    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.5315    0.7223    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    1.9542    0.1330    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    2.0916   -0.6805    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  2  0  0  0  0
  2  3  1  0  0  0  0
  3  4  1  0  0  0  0
  4  5  1  6  0  0  0
  4  6  1  0  0  0  0
  6  7  1  0  0  0  0
  8  7  1  6  0  0  0
  8  9  1  0  0  0  0
  9 10  1  6  0  0  0
  9 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
  8 14  1  0  0  0  0
 14 15  1  6  0  0  0
 14 16  1  0  0  0  0
 16 17  1  0  0  0  0
 18 17  1  6  0  0  0
  8 18  1  0  0  0  0
  4 18  1  0  0  0  0
 18 19  1  0  0  0  0
  2 19  1  0  0  0  0
 19 20  1  6  0  0  0
M  END
> <DATABASE_ID>
NP0325768

> <DATABASE_NAME>
NP-MRD

> <SMILES>
C[C@@H]1C(=C)C[C@@]2(C)CC[C@]34[C@H](C)CCC[C@@]3(C)CC[C@]124

> <INCHI_IDENTIFIER>
InChI=1S/C20H32/c1-14-13-18(5)10-11-19-15(2)7-6-8-17(19,4)9-12-20(18,19)16(14)3/h15-16H,1,6-13H2,2-5H3/t15-,16-,17+,18-,19+,20+/m1/s1

> <INCHI_KEY>
FCMUPMSHXJZJBX-NADOGSGZSA-N

> <FORMULA>
C20H32

> <MOLECULAR_WEIGHT>
272.476

> <EXACT_MASS>
272.25040103

> <JCHEM_ACCEPTOR_COUNT>
0

> <JCHEM_ATOM_COUNT>
52

> <JCHEM_AVERAGE_POLARIZABILITY>
33.68977007825434

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
0

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
1

> <JCHEM_IUPAC>
(1S,4S,8R,9S,12R,15R)-4,8,12,15-tetramethyl-14-methylidenetetracyclo[7.6.0.0^{1,12}.0^{4,9}]pentadecane

> <JCHEM_LOGP>
5.471616620333334

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
4

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_POLAR_SURFACE_AREA>
0.0

> <JCHEM_REFRACTIVITY>
85.5205

> <JCHEM_ROTATABLE_BOND_COUNT>
0

> <JCHEM_RULE_OF_FIVE>
0

> <JCHEM_TRADITIONAL_IUPAC>
(1S,4S,8R,9S,12R,15R)-4,8,12,15-tetramethyl-14-methylidenetetracyclo[7.6.0.0^{1,12}.0^{4,9}]pentadecane

> <JCHEM_VEBER_RULE>
1

$$$$

HEADER    PROTEIN                                 12-SEP-22   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   12-SEP-22         0                                  
HETATM    1  C   UNK     0       0.904   0.220   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0       2.269   0.933   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0       2.494   2.457   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0       4.012   2.713   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0       3.299   4.078   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0       5.090   3.813   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0       6.469   3.128   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0       6.244   1.605   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0       7.069   2.905   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0       6.356   4.270   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0       8.608   2.840   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0       9.321   1.475   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0       8.496   0.175   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0       6.957   0.240   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0       7.524  -1.192   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0       5.879  -0.860   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0       4.500  -0.175   0.000  0.00  0.00           C+0
HETATM   18  C   UNK     0       4.726   1.348   0.000  0.00  0.00           C+0
HETATM   19  C   UNK     0       3.648   0.248   0.000  0.00  0.00           C+0
HETATM   20  C   UNK     0       3.904  -1.270   0.000  0.00  0.00           C+0
CONECT    1    2                                                            
CONECT    2    1    3   19                                                  
CONECT    3    2    4                                                       
CONECT    4    3    5    6   18                                             
CONECT    5    4                                                            
CONECT    6    4    7                                                       
CONECT    7    6    8                                                       
CONECT    8    7    9   14   18                                             
CONECT    9    8   10   11                                                  
CONECT   10    9                                                            
CONECT   11    9   12                                                       
CONECT   12   11   13                                                       
CONECT   13   12   14                                                       
CONECT   14   13    8   15   16                                             
CONECT   15   14                                                            
CONECT   16   14   17                                                       
CONECT   17   16   18                                                       
CONECT   18   17    8    4   19                                             
CONECT   19   18    2   20                                                  
CONECT   20   19                                                            
MASTER        0    0    0    0    0    0    0    0   20    0   46    0
END

View in JSmol

Synonyms

Not Available

Chemical Formula

C₂₀H₃₂

Average Mass

272.4760 Da

Monoisotopic Mass

272.25040 Da

IUPAC Name

(1S,4S,8R,9S,12R,15R)-4,8,12,15-tetramethyl-14-methylidenetetracyclo[7.6.0.0^{1,12}.0^{4,9}]pentadecane

Traditional Name

(1S,4S,8R,9S,12R,15R)-4,8,12,15-tetramethyl-14-methylidenetetracyclo[7.6.0.0^{1,12}.0^{4,9}]pentadecane

CAS Registry Number

Not Available

SMILES

C[C@@H]1C(=C)C[C@@]2(C)CC[C@]34[C@H](C)CCC[C@@]3(C)CC[C@]124

InChI Identifier

InChI=1S/C20H32/c1-14-13-18(5)10-11-19-15(2)7-6-8-17(19,4)9-12-20(18,19)16(14)3/h15-16H,1,6-13H2,2-5H3/t15-,16-,17+,18-,19+,20+/m1/s1

InChI Key

FCMUPMSHXJZJBX-NADOGSGZSA-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
Podocarpus totara	LOTUS Database	35616633

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as branched unsaturated hydrocarbons. These are hydrocarbons that contains one or more unsaturated carbon atoms, and an aliphatic branch.

Kingdom

Organic compounds

Super Class

Hydrocarbons

Class

Unsaturated hydrocarbons

Sub Class

Branched unsaturated hydrocarbons

Direct Parent

Branched unsaturated hydrocarbons

Alternative Parents

Substituents

Branched unsaturated hydrocarbon
Polycyclic hydrocarbon
Cyclic olefin
Unsaturated aliphatic hydrocarbon
Olefin
Aliphatic homopolycyclic compound

Molecular Framework

Aliphatic homopolycyclic 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	5.47	ChemAxon
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	85.52 m³·mol⁻¹	ChemAxon
Polarizability	33.69 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

75583387

KEGG Compound ID

Not Available

BioCyc ID

Not Available

BiGG ID

Not Available

Wikipedia Link

Not Available

METLIN ID

Not Available

PubChem Compound

15818459

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

Wang YP, Fang K, Tu YQ, Yin JJ, Zhao Q, Ke T: An efficient approach to angular tricyclic molecular architecture via Nazarov-like cyclization and double ring-expansion cascade. Nat Commun. 2022 Apr 28;13(1):2335. doi: 10.1038/s41467-022-29947-5. [PubMed:35484150 ]
Rosenbaum LC, Hafner M, Gaich T: Total Synthesis of the Diterpene Waihoensene. Angew Chem Int Ed Engl. 2021 Feb 8;60(6):2939-2942. doi: 10.1002/anie.202011298. Epub 2020 Dec 10. [PubMed:33103334 ]
Eggert A, Etling C, Lubken D, Saxarra M, Kalesse M: Contiguous Quaternary Carbons: A Selection of Total Syntheses. Molecules. 2020 Aug 24;25(17):3841. doi: 10.3390/molecules25173841. [PubMed:32847075 ]
Peng C, Arya P, Zhou Z, Snyder SA: A Concise Total Synthesis of (+)-Waihoensene Guided by Quaternary Center Analysis. Angew Chem Int Ed Engl. 2020 Aug 3;59(32):13521-13525. doi: 10.1002/anie.202004177. Epub 2020 Jun 3. [PubMed:32330370 ]
LOTUS database [Link]

Showing NP-Card for (1s,4s,8r,9s,12r,15r)-4,8,12,15-tetramethyl-14-methylidenetetracyclo[7.6.0.0¹,¹².0⁴,⁹]pentadecane (NP0325768)

MOL for NP0325768 ((1s,4s,8r,9s,12r,15r)-4,8,12,15-tetramethyl-14-methylidenetetracyclo[7.6.0.0¹,¹².0⁴,⁹]pentadecane)

3D MOL for NP0325768 ((1s,4s,8r,9s,12r,15r)-4,8,12,15-tetramethyl-14-methylidenetetracyclo[7.6.0.0¹,¹².0⁴,⁹]pentadecane)

3D SDF for NP0325768 ((1s,4s,8r,9s,12r,15r)-4,8,12,15-tetramethyl-14-methylidenetetracyclo[7.6.0.0¹,¹².0⁴,⁹]pentadecane)

3D-SDF for NP0325768 ((1s,4s,8r,9s,12r,15r)-4,8,12,15-tetramethyl-14-methylidenetetracyclo[7.6.0.0¹,¹².0⁴,⁹]pentadecane)

PDB for NP0325768 ((1s,4s,8r,9s,12r,15r)-4,8,12,15-tetramethyl-14-methylidenetetracyclo[7.6.0.0¹,¹².0⁴,⁹]pentadecane)

3D PDB for NP0325768 ((1s,4s,8r,9s,12r,15r)-4,8,12,15-tetramethyl-14-methylidenetetracyclo[7.6.0.0¹,¹².0⁴,⁹]pentadecane)

SMILES for NP0325768 ((1s,4s,8r,9s,12r,15r)-4,8,12,15-tetramethyl-14-methylidenetetracyclo[7.6.0.0¹,¹².0⁴,⁹]pentadecane)

INCHI for NP0325768 ((1s,4s,8r,9s,12r,15r)-4,8,12,15-tetramethyl-14-methylidenetetracyclo[7.6.0.0¹,¹².0⁴,⁹]pentadecane)

Structure for NP0325768 ((1s,4s,8r,9s,12r,15r)-4,8,12,15-tetramethyl-14-methylidenetetracyclo[7.6.0.0¹,¹².0⁴,⁹]pentadecane)

3D Structure for NP0325768 ((1s,4s,8r,9s,12r,15r)-4,8,12,15-tetramethyl-14-methylidenetetracyclo[7.6.0.0¹,¹².0⁴,⁹]pentadecane)