NP-MRD: Showing NP-Card for methyl 4-[5-(12-bromododeca-3,11-dien-1-yn-1-yl)oxolan-2-yl]butanoate (NP0200510)

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Record Information

Version

2.0

Created at

2022-09-04 19:22:14 UTC

Updated at

2022-09-04 19:22:15 UTC

NP-MRD ID

NP0200510

Secondary Accession Numbers

None

Natural Product Identification

Common Name

methyl 4-[5-(12-bromododeca-3,11-dien-1-yn-1-yl)oxolan-2-yl]butanoate

Description

Methyl 4-[5-(12-bromododeca-3,11-dien-1-yn-1-yl)oxolan-2-yl]butanoate belongs to the class of organic compounds known as fatty acid methyl esters. Fatty acid methyl esters are compounds containing a fatty acid that is esterified with a methyl group. They have the general structure RC(=O)OR', where R=fatty aliphatic tail or organyl group and R'=methyl group. methyl 4-[5-(12-bromododeca-3,11-dien-1-yn-1-yl)oxolan-2-yl]butanoate is found in Xestospongia muta. Methyl 4-[5-(12-bromododeca-3,11-dien-1-yn-1-yl)oxolan-2-yl]butanoate is an extremely weak basic (essentially neutral) compound (based on its pKa).

Structure

MOL 3D MOL SDF PDB SMILES InChI

     RDKit          3D

 56 56  0  0  0  0  0  0  0  0999 V2000
   -8.8694    2.4908    0.8946 C   0  0  0  0  0  0  0  0  0  0  0  0
   -7.6923    1.9364    0.3375 O   0  0  0  0  0  0  0  0  0  0  0  0
   -7.2246    0.7174    0.7975 C   0  0  0  0  0  0  0  0  0  0  0  0
   -7.7832    0.0571    1.6919 O   0  0  0  0  0  0  0  0  0  0  0  0
   -5.9536    0.1328    0.1864 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.6408   -1.1601    0.8200 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.4807   -1.9200    0.3224 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.1176   -1.3710    0.3639 C   0  0  1  0  0  0  0  0  0  0  0  0
   -2.8992   -0.1610   -0.4487 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3061    0.8369    0.5156 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8500   -0.0734    1.6499 C   0  0  2  0  0  0  0  0  0  0  0  0
   -0.5663   -0.7207    1.2873 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.4657   -1.2593    0.9800 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.6940   -1.9203    0.5943 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.7448   -1.1885    0.1951 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.6980    0.2695    0.1334 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.9317    0.9583   -1.1205 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.1492    1.1370   -1.8608 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.0986    0.1029   -2.2733 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.9441   -0.4445   -1.1780 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.8141    0.7124   -0.5878 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.6223    0.0747    0.4865 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.9605    0.0815    0.4392 C   0  0  0  0  0  0  0  0  0  0  0  0
    9.9034    0.9067   -1.0037 Br  0  0  0  0  0  0  0  0  0  0  0  0
   -2.8497   -1.0100    1.7041 O   0  0  0  0  0  0  0  0  0  0  0  0
   -8.7700    3.6088    0.9428 H   0  0  0  0  0  0  0  0  0  0  0  0
   -9.7301    2.2025    0.2473 H   0  0  0  0  0  0  0  0  0  0  0  0
   -8.9777    2.0794    1.9168 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.1792    0.8885    0.4584 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.0548    0.0307   -0.8974 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.4784   -0.9362    1.9260 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.5688   -1.8328    0.8367 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.7107   -2.2360   -0.7600 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.5125   -2.9356    0.8393 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4006   -2.1902    0.0613 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0731   -0.4163   -1.2050 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.7063    0.2166   -1.0614 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3769    1.2856    0.0695 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.9906    1.5823    0.8997 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7503    0.4845    2.5744 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.8015   -2.9860    0.6144 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.5983   -1.7473   -0.0817 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.6628    0.5570    0.5062 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.3576    0.7265    0.9511 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.1280    0.6037   -1.8895 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.5305    2.0475   -0.9259 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.7541    2.0523   -1.4427 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.8314    1.6484   -2.8682 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.5696   -0.7100   -2.8439 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.8327    0.4842   -3.0646 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.4768   -0.8422   -0.2929 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.7085   -1.1759   -1.5541 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.4126    1.1855   -1.3586 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.0777    1.3617   -0.0755 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.1754   -0.4163    1.3422 H   0  0  0  0  0  0  0  0  0  0  0  0
    9.5696   -0.3758    1.2088 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  1  0
  6  7  1  0
  7  8  1  0
  8  9  1  0
  9 10  1  0
 10 11  1  0
 11 25  1  0
 11 12  1  0
 12 13  3  0
 13 14  1  0
 14 15  2  0
 15 16  1  0
 16 17  1  0
 17 18  1  0
 18 19  1  0
 19 20  1  0
 20 21  1  0
 21 22  1  0
 22 23  2  0
 23 24  1  0
 25  8  1  0
  1 26  1  0
  1 27  1  0
  1 28  1  0
  5 29  1  0
  5 30  1  0
  6 31  1  0
  6 32  1  0
  7 33  1  0
  7 34  1  0
  8 35  1  6
  9 36  1  0
  9 37  1  0
 10 38  1  0
 10 39  1  0
 11 40  1  1
 14 41  1  0
 15 42  1  0
 16 43  1  0
 16 44  1  0
 17 45  1  0
 17 46  1  0
 18 47  1  0
 18 48  1  0
 19 49  1  0
 19 50  1  0
 20 51  1  0
 20 52  1  0
 21 53  1  0
 21 54  1  0
 22 55  1  0
 23 56  1  0
M  END


  Mrv1533004241509342D          

 25 25  0  0  0  0            999 V2000
   -5.2298    0.2247    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.4093    0.3110    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -4.0738    1.0647    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.5587    1.7321    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.2533    1.1509    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.9178    1.9046    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0973    1.9908    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7617    2.7445    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1742    3.4589    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6222    4.0720    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8685    3.7365    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9547    2.9160    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1540    4.1490    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.5604    4.5615    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.2749    4.9740    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.9894    4.5615    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.7039    4.9740    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.4183    4.5615    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.1328    4.9740    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.8473    4.5615    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.5617    4.9740    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.2762    4.5615    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.9907    4.9740    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.7051    4.5615    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.4196    4.9740    0.0000 Br  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  1  0  0  0  0
  6  7  1  0  0  0  0
  7  8  1  0  0  0  0
  8  9  1  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
  8 12  1  0  0  0  0
 11 13  1  0  0  0  0
 13 14  3  0  0  0  0
 15 14  1  4  0  0  0
 15 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
 20 21  1  0  0  0  0
 21 22  1  0  0  0  0
 22 23  1  0  0  0  0
 23 24  2  0  0  0  0
 24 25  1  4  0  0  0
M  END
> <DATABASE_ID>
NP0200510

> <DATABASE_NAME>
NP-MRD

> <SMILES>
COC(=O)CCCC1CCC(O1)C#CC=CCCCCCCC=CBr

> <INCHI_IDENTIFIER>
InChI=1S/C21H31BrO3/c1-24-21(23)15-12-14-20-17-16-19(25-20)13-10-8-6-4-2-3-5-7-9-11-18-22/h6,8,11,18-20H,2-5,7,9,12,14-17H2,1H3

> <INCHI_KEY>
ATHZZRJFORDQAQ-UHFFFAOYSA-N

> <FORMULA>
C21H31BrO3

> <MOLECULAR_WEIGHT>
411.38

> <EXACT_MASS>
410.145658

> <JCHEM_ACCEPTOR_COUNT>
2

> <JCHEM_ATOM_COUNT>
56

> <JCHEM_AVERAGE_POLARIZABILITY>
45.30475804549501

> <JCHEM_BIOAVAILABILITY>
0

> <JCHEM_DONOR_COUNT>
0

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
0

> <JCHEM_IUPAC>
methyl 4-[5-(12-bromododeca-3,11-dien-1-yn-1-yl)oxolan-2-yl]butanoate

> <ALOGPS_LOGP>
6.20

> <JCHEM_LOGP>
6.125627969666665

> <ALOGPS_LOGS>
-5.80

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
1

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA_STRONGEST_BASIC>
-4.251271944454115

> <JCHEM_POLAR_SURFACE_AREA>
35.53

> <JCHEM_REFRACTIVITY>
108.07330000000002

> <JCHEM_ROTATABLE_BOND_COUNT>
14

> <JCHEM_RULE_OF_FIVE>
0

> <ALOGPS_SOLUBILITY>
6.58e-04 g/l

> <JCHEM_TRADITIONAL_IUPAC>
methyl 4-[5-(12-bromododeca-3,11-dien-1-yn-1-yl)oxolan-2-yl]butanoate

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 24-APR-15   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   24-APR-15         0                                  
HETATM    1  C   UNK     0      -9.762   0.420   0.000  0.00  0.00           C+0
HETATM    2  O   UNK     0      -8.231   0.580   0.000  0.00  0.00           O+0
HETATM    3  C   UNK     0      -7.604   1.987   0.000  0.00  0.00           C+0
HETATM    4  O   UNK     0      -8.510   3.233   0.000  0.00  0.00           O+0
HETATM    5  C   UNK     0      -6.073   2.148   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0      -5.446   3.555   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0      -3.915   3.716   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0      -3.289   5.123   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0      -4.059   6.457   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0      -3.028   7.601   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0      -1.621   6.975   0.000  0.00  0.00           C+0
HETATM   12  O   UNK     0      -1.782   5.443   0.000  0.00  0.00           O+0
HETATM   13  C   UNK     0      -0.288   7.745   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0       1.046   8.515   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0       2.380   9.285   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0       3.714   8.515   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0       5.047   9.285   0.000  0.00  0.00           C+0
HETATM   18  C   UNK     0       6.381   8.515   0.000  0.00  0.00           C+0
HETATM   19  C   UNK     0       7.715   9.285   0.000  0.00  0.00           C+0
HETATM   20  C   UNK     0       9.048   8.515   0.000  0.00  0.00           C+0
HETATM   21  C   UNK     0      10.382   9.285   0.000  0.00  0.00           C+0
HETATM   22  C   UNK     0      11.716   8.515   0.000  0.00  0.00           C+0
HETATM   23  C   UNK     0      13.049   9.285   0.000  0.00  0.00           C+0
HETATM   24  C   UNK     0      14.383   8.515   0.000  0.00  0.00           C+0
HETATM   25 Br   UNK     0      15.717   9.285   0.000  0.00  0.00          Br+0
CONECT    1    2                                                            
CONECT    2    1    3                                                       
CONECT    3    2    4    5                                                  
CONECT    4    3                                                            
CONECT    5    3    6                                                       
CONECT    6    5    7                                                       
CONECT    7    6    8                                                       
CONECT    8    7    9   12                                                  
CONECT    9    8   10                                                       
CONECT   10    9   11                                                       
CONECT   11   10   12   13                                                  
CONECT   12   11    8                                                       
CONECT   13   11   14                                                       
CONECT   14   13   15                                                       
CONECT   15   14   16                                                       
CONECT   16   15   17                                                       
CONECT   17   16   18                                                       
CONECT   18   17   19                                                       
CONECT   19   18   20                                                       
CONECT   20   19   21                                                       
CONECT   21   20   22                                                       
CONECT   22   21   23                                                       
CONECT   23   22   24                                                       
CONECT   24   23   25                                                       
CONECT   25   24                                                            
MASTER        0    0    0    0    0    0    0    0   25    0   50    0
END

View in JSmol

Synonyms

Value	Source
Methyl 4-[5-(12-bromododeca-3,11-dien-1-yn-1-yl)oxolan-2-yl]butanoic acid	Generator

Chemical Formula

C₂₁H₃₁BrO₃

Average Mass

411.3800 Da

Monoisotopic Mass

410.14566 Da

IUPAC Name

methyl 4-[5-(12-bromododeca-3,11-dien-1-yn-1-yl)oxolan-2-yl]butanoate

Traditional Name

methyl 4-[5-(12-bromododeca-3,11-dien-1-yn-1-yl)oxolan-2-yl]butanoate

CAS Registry Number

Not Available

SMILES

COC(=O)CCCC1CCC(O1)C#CC=CCCCCCCC=CBr

InChI Identifier

InChI=1S/C21H31BrO3/c1-24-21(23)15-12-14-20-17-16-19(25-20)13-10-8-6-4-2-3-5-7-9-11-18-22/h6,8,11,18-20H,2-5,7,9,12,14-17H2,1H3

InChI Key

ATHZZRJFORDQAQ-UHFFFAOYSA-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
Xestospongia muta	LOTUS Database	35616633

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as fatty acid methyl esters. Fatty acid methyl esters are compounds containing a fatty acid that is esterified with a methyl group. They have the general structure RC(=O)OR', where R=fatty aliphatic tail or organyl group and R'=methyl group.

Kingdom

Organic compounds

Super Class

Lipids and lipid-like molecules

Class

Fatty Acyls

Sub Class

Fatty acid esters

Direct Parent

Fatty acid methyl esters

Alternative Parents

Substituents

Fatty acid methyl ester
Tetrahydrofuran
Methyl ester
Carboxylic acid ester
Carboxylic acid derivative
Dialkyl ether
Ether
Monocarboxylic acid or derivatives
Vinyl bromide
Vinyl halide
Oxacycle
Organoheterocyclic compound
Bromoalkene
Haloalkene
Organic oxide
Carbonyl group
Hydrocarbon derivative
Organic oxygen compound
Organohalogen compound
Organobromide
Organooxygen compound
Aliphatic heteromonocyclic compound

Molecular Framework

Aliphatic heteromonocyclic 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	6.2	ALOGPS
logP	6.13	ChemAxon
logS	-5.8	ALOGPS
pKa (Strongest Basic)	-4.3	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	2	ChemAxon
Hydrogen Donor Count	0	ChemAxon
Polar Surface Area	35.53 Å²	ChemAxon
Rotatable Bond Count	14	ChemAxon
Refractivity	108.07 m³·mol⁻¹	ChemAxon
Polarizability	45.3 Å³	ChemAxon
Number of Rings	1	ChemAxon
Bioavailability	No	ChemAxon
Rule of Five	No	ChemAxon
Ghose Filter	No	ChemAxon
Veber's Rule	No	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

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

73300751

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

LOTUS database [Link]

Showing NP-Card for methyl 4-[5-(12-bromododeca-3,11-dien-1-yn-1-yl)oxolan-2-yl]butanoate (NP0200510)

MOL for NP0200510 (methyl 4-[5-(12-bromododeca-3,11-dien-1-yn-1-yl)oxolan-2-yl]butanoate)

3D MOL for NP0200510 (methyl 4-[5-(12-bromododeca-3,11-dien-1-yn-1-yl)oxolan-2-yl]butanoate)

3D SDF for NP0200510 (methyl 4-[5-(12-bromododeca-3,11-dien-1-yn-1-yl)oxolan-2-yl]butanoate)

3D-SDF for NP0200510 (methyl 4-[5-(12-bromododeca-3,11-dien-1-yn-1-yl)oxolan-2-yl]butanoate)

PDB for NP0200510 (methyl 4-[5-(12-bromododeca-3,11-dien-1-yn-1-yl)oxolan-2-yl]butanoate)

3D PDB for NP0200510 (methyl 4-[5-(12-bromododeca-3,11-dien-1-yn-1-yl)oxolan-2-yl]butanoate)

SMILES for NP0200510 (methyl 4-[5-(12-bromododeca-3,11-dien-1-yn-1-yl)oxolan-2-yl]butanoate)

INCHI for NP0200510 (methyl 4-[5-(12-bromododeca-3,11-dien-1-yn-1-yl)oxolan-2-yl]butanoate)

Structure for NP0200510 (methyl 4-[5-(12-bromododeca-3,11-dien-1-yn-1-yl)oxolan-2-yl]butanoate)

3D Structure for NP0200510 (methyl 4-[5-(12-bromododeca-3,11-dien-1-yn-1-yl)oxolan-2-yl]butanoate)