NP-MRD: Showing NP-Card for methyl (7e,11e)-4-isopropyl-7,11-dimethylcyclotetradeca-1,3,7,11-tetraene-1-carboxylate (NP0239106)

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Record Information

Version

2.0

Created at

2022-09-06 22:37:24 UTC

Updated at

2022-09-06 22:37:24 UTC

NP-MRD ID

NP0239106

Secondary Accession Numbers

None

Natural Product Identification

Common Name

methyl (7e,11e)-4-isopropyl-7,11-dimethylcyclotetradeca-1,3,7,11-tetraene-1-carboxylate

Description

methyl (7e,11e)-4-isopropyl-7,11-dimethylcyclotetradeca-1,3,7,11-tetraene-1-carboxylate is found in Sarcophyton trocheliophorum.

Structure

MOL 3D MOL SDF PDB SMILES InChI

     RDKit          3D

 55 55  0  0  0  0  0  0  0  0999 V2000
   -4.5064    3.6440   -2.3901 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.6071    2.8556   -1.5873 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2988    3.2163   -1.4116 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8808    4.2670   -1.9700 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4123    2.3630   -0.5727 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1429    2.6841   -0.3837 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.9396    2.0844    0.3469 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.8278    1.1411    0.0712 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.9078    0.7725    1.0788 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8732   -0.6200    1.5552 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.2722    1.0191    0.4208 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.9686    0.3779   -1.1612 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.0459   -0.7459   -1.4704 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4419   -2.0754   -1.0140 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.7915   -2.5069   -1.6371 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.9151   -2.9674   -0.2287 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3178   -3.0766    0.5710 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0611   -1.8203    0.5619 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1617   -1.6466    1.5374 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.9036   -2.8188    2.0852 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4271   -0.3921    1.8728 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7155    0.8106    1.3519 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1280    1.1996   -0.0187 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.8587    4.4608   -1.7306 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.3749    3.0147   -2.6255 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.9864    4.0414   -3.2748 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.0505    3.6556   -0.9217 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.1248    2.4971    1.3656 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.8636    1.4449    1.9608 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.5437   -1.3235    1.0251 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.8395   -0.9730    1.6534 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.2674   -0.6521    2.6234 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.1474    1.5542   -0.5434 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.9054    1.6509    1.0691 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.7899    0.0762    0.2273 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.8454    1.1624   -1.9847 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.0014    0.0062   -1.3662 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.0079   -0.7712   -2.6383 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.0503   -0.3662   -1.2509 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.6124   -2.3720   -2.7381 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.6099   -1.9093   -1.2624 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.0001   -3.5555   -1.4624 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.5122   -3.9487   -0.0756 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9606   -3.9338    0.2234 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0515   -3.3229    1.6342 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3272   -1.0525    0.8289 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5525   -1.7645   -0.4222 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6083   -3.7101    1.4857 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5857   -3.0409    3.1391 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.9977   -2.7112    2.0124 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.2556   -0.2675    2.6019 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6305    0.7652    1.5493 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0417    1.6874    2.0093 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1122    0.4506   -0.8041 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.2492    1.4424    0.0844 H   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0
  2  3  1  0
  3  4  2  0
  3  5  1  0
  5  6  2  0
  6  7  1  0
  7  8  2  0
  8 12  1  0
 12 13  1  0
 13 14  1  0
 14 15  1  0
 14 16  2  0
 16 17  1  0
 17 18  1  0
 18 19  1  0
 19 20  1  0
 19 21  2  0
 21 22  1  0
 22 23  1  0
  8  9  1  0
  9 10  1  0
  9 11  1  0
 23  5  1  0
  1 24  1  0
  1 25  1  0
  1 26  1  0
  6 27  1  0
  7 28  1  0
 12 36  1  0
 12 37  1  0
 13 38  1  0
 13 39  1  0
 15 40  1  0
 15 41  1  0
 15 42  1  0
 16 43  1  0
 17 44  1  0
 17 45  1  0
 18 46  1  0
 18 47  1  0
 20 48  1  0
 20 49  1  0
 20 50  1  0
 21 51  1  0
 22 52  1  0
 22 53  1  0
 23 54  1  0
 23 55  1  0
  9 29  1  0
 10 30  1  0
 10 31  1  0
 10 32  1  0
 11 33  1  0
 11 34  1  0
 11 35  1  0
M  END


  Mrv1652309072200372D          

 23 23  0  0  0  0            999 V2000
    0.4360    2.6001    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7060    1.8206    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.5161    1.6647    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.0562    2.2883    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.7862    0.8851    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.3263    1.5088    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.1364    1.3529    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.4064    0.5733    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.2166    0.4174    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.4866   -0.3622    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.7567    1.0410    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8664   -0.0503    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.1364   -0.8299    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.5963   -1.4535    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8664   -2.2331    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.7862   -1.2976    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.2461   -1.9213    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.4360   -1.7654    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.1659   -0.9858    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6442   -0.8299    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7060   -0.3622    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.4360    0.4174    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.9760    1.0410    0.0000 C   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  2  0  0  0  0
  3  5  1  0  0  0  0
  5  6  2  0  0  0  0
  6  7  1  4  0  0  0
  7  8  2  0  0  0  0
  8  9  1  4  0  0  0
  9 10  1  0  0  0  0
  9 11  1  0  0  0  0
  8 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
 14 16  2  0  0  0  0
 16 17  1  0  0  0  0
 17 18  1  0  0  0  0
 18 19  1  0  0  0  0
 19 20  1  0  0  0  0
 19 21  2  0  0  0  0
 21 22  1  0  0  0  0
 22 23  1  0  0  0  0
  5 23  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0239106

> <DATABASE_NAME>
NP-MRD

> <SMILES>
COC(=O)C1=CC=C(CC\C(C)=C\CC\C(C)=C\CC1)C(C)C

> <INCHI_IDENTIFIER>
InChI=1S/C21H32O2/c1-16(2)19-13-12-18(4)9-6-8-17(3)10-7-11-20(15-14-19)21(22)23-5/h9-10,14-16H,6-8,11-13H2,1-5H3/b17-10+,18-9+,19-14?,20-15?

> <INCHI_KEY>
JAXCRQBPGSFOHJ-RVHYQEQOSA-N

> <FORMULA>
C21H32O2

> <MOLECULAR_WEIGHT>
316.485

> <EXACT_MASS>
316.24023027

> <JCHEM_ACCEPTOR_COUNT>
1

> <JCHEM_ATOM_COUNT>
55

> <JCHEM_AVERAGE_POLARIZABILITY>
37.220369820135474

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
0

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
0

> <JCHEM_IUPAC>
methyl (7E,11E)-7,11-dimethyl-4-(propan-2-yl)cyclotetradeca-1,3,7,11-tetraene-1-carboxylate

> <JCHEM_LOGP>
6.052227519666666

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
1

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA_STRONGEST_BASIC>
-6.860135538969323

> <JCHEM_POLAR_SURFACE_AREA>
26.3

> <JCHEM_REFRACTIVITY>
101.64429999999999

> <JCHEM_ROTATABLE_BOND_COUNT>
3

> <JCHEM_RULE_OF_FIVE>
0

> <JCHEM_TRADITIONAL_IUPAC>
methyl (7E,11E)-4-isopropyl-7,11-dimethylcyclotetradeca-1,3,7,11-tetraene-1-carboxylate

> <JCHEM_VEBER_RULE>
1

$$$$

HEADER    PROTEIN                                 07-SEP-22   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   07-SEP-22         0                                  
HETATM    1  C   UNK     0       0.814   4.854   0.000  0.00  0.00           C+0
HETATM    2  O   UNK     0       1.318   3.398   0.000  0.00  0.00           O+0
HETATM    3  C   UNK     0       2.830   3.107   0.000  0.00  0.00           C+0
HETATM    4  O   UNK     0       3.838   4.272   0.000  0.00  0.00           O+0
HETATM    5  C   UNK     0       3.334   1.652   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0       4.342   2.816   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0       5.855   2.525   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0       6.359   1.070   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0       7.871   0.779   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0       8.375  -0.676   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0       8.879   1.943   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0       5.351  -0.094   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0       5.855  -1.549   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0       4.846  -2.713   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0       5.351  -4.168   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0       3.334  -2.422   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0       2.326  -3.586   0.000  0.00  0.00           C+0
HETATM   18  C   UNK     0       0.814  -3.295   0.000  0.00  0.00           C+0
HETATM   19  C   UNK     0       0.310  -1.840   0.000  0.00  0.00           C+0
HETATM   20  C   UNK     0      -1.203  -1.549   0.000  0.00  0.00           C+0
HETATM   21  C   UNK     0       1.318  -0.676   0.000  0.00  0.00           C+0
HETATM   22  C   UNK     0       0.814   0.779   0.000  0.00  0.00           C+0
HETATM   23  C   UNK     0       1.822   1.943   0.000  0.00  0.00           C+0
CONECT    1    2                                                            
CONECT    2    1    3                                                       
CONECT    3    2    4    5                                                  
CONECT    4    3                                                            
CONECT    5    3    6   23                                                  
CONECT    6    5    7                                                       
CONECT    7    6    8                                                       
CONECT    8    7    9   12                                                  
CONECT    9    8   10   11                                                  
CONECT   10    9                                                            
CONECT   11    9                                                            
CONECT   12    8   13                                                       
CONECT   13   12   14                                                       
CONECT   14   13   15   16                                                  
CONECT   15   14                                                            
CONECT   16   14   17                                                       
CONECT   17   16   18                                                       
CONECT   18   17   19                                                       
CONECT   19   18   20   21                                                  
CONECT   20   19                                                            
CONECT   21   19   22                                                       
CONECT   22   21   23                                                       
CONECT   23   22    5                                                       
MASTER        0    0    0    0    0    0    0    0   23    0   46    0
END

View in JSmol

Synonyms

Not Available

Chemical Formula

C₂₁H₃₂O₂

Average Mass

316.4850 Da

Monoisotopic Mass

316.24023 Da

IUPAC Name

Not Available

Traditional Name

Not Available

CAS Registry Number

Not Available

SMILES

COC(=O)C1=CC=C(CC\C(C)=C\CC\C(C)=C\CC1)C(C)C

InChI Identifier

InChI=1S/C21H32O2/c1-16(2)19-13-12-18(4)9-6-8-17(3)10-7-11-20(15-14-19)21(22)23-5/h9-10,14-16H,6-8,11-13H2,1-5H3/b17-10+,18-9+,19-14?,20-15?

InChI Key

JAXCRQBPGSFOHJ-RVHYQEQOSA-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

Classification

Not classified

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

External Links

Not Available

References

General References

LOTUS database [Link]

Showing NP-Card for methyl (7e,11e)-4-isopropyl-7,11-dimethylcyclotetradeca-1,3,7,11-tetraene-1-carboxylate (NP0239106)

MOL for NP0239106 (methyl (7e,11e)-4-isopropyl-7,11-dimethylcyclotetradeca-1,3,7,11-tetraene-1-carboxylate)

3D MOL for NP0239106 (methyl (7e,11e)-4-isopropyl-7,11-dimethylcyclotetradeca-1,3,7,11-tetraene-1-carboxylate)

3D SDF for NP0239106 (methyl (7e,11e)-4-isopropyl-7,11-dimethylcyclotetradeca-1,3,7,11-tetraene-1-carboxylate)

3D-SDF for NP0239106 (methyl (7e,11e)-4-isopropyl-7,11-dimethylcyclotetradeca-1,3,7,11-tetraene-1-carboxylate)

PDB for NP0239106 (methyl (7e,11e)-4-isopropyl-7,11-dimethylcyclotetradeca-1,3,7,11-tetraene-1-carboxylate)

3D PDB for NP0239106 (methyl (7e,11e)-4-isopropyl-7,11-dimethylcyclotetradeca-1,3,7,11-tetraene-1-carboxylate)

SMILES for NP0239106 (methyl (7e,11e)-4-isopropyl-7,11-dimethylcyclotetradeca-1,3,7,11-tetraene-1-carboxylate)

INCHI for NP0239106 (methyl (7e,11e)-4-isopropyl-7,11-dimethylcyclotetradeca-1,3,7,11-tetraene-1-carboxylate)

Structure for NP0239106 (methyl (7e,11e)-4-isopropyl-7,11-dimethylcyclotetradeca-1,3,7,11-tetraene-1-carboxylate)

3D Structure for NP0239106 (methyl (7e,11e)-4-isopropyl-7,11-dimethylcyclotetradeca-1,3,7,11-tetraene-1-carboxylate)