NP-MRD: Showing NP-Card for (2r,3r,5r)-5-[(1s,3e)-1-bromohex-3-en-1-yl]-2-[(2e)-pent-2-en-4-yn-1-yl]oxolan-3-yl acetate (NP0168725)

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Record Information

Version

2.0

Created at

2022-09-03 04:34:51 UTC

Updated at

2022-09-03 04:34:51 UTC

NP-MRD ID

NP0168725

Secondary Accession Numbers

None

Natural Product Identification

Common Name

(2r,3r,5r)-5-[(1s,3e)-1-bromohex-3-en-1-yl]-2-[(2e)-pent-2-en-4-yn-1-yl]oxolan-3-yl acetate

Description

(2R)-2alpha-(2-Pentene-4-ynyl)-5alpha-[(S)-1-bromo-3-hexenyl]tetrahydrofuran-3alpha-ol acetate belongs to the class of organic compounds known as c-glycosyl compounds. These are glycoside in which a sugar group is bonded through one carbon to another group via a C-glycosidic bond. (2r,3r,5r)-5-[(1s,3e)-1-bromohex-3-en-1-yl]-2-[(2e)-pent-2-en-4-yn-1-yl]oxolan-3-yl acetate is found in Laurencia nipponica. Based on a literature review very few articles have been published on (2R)-2alpha-(2-Pentene-4-ynyl)-5alpha-[(S)-1-bromo-3-hexenyl]tetrahydrofuran-3alpha-ol acetate.

Structure

MOL 3D MOL SDF PDB SMILES InChI

     RDKit          3D

 44 44  0  0  0  0  0  0  0  0999 V2000
   -7.3303    0.8864    0.0308 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.1909    0.7897    0.4050 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.8269    0.6539    0.8390 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.8536    1.4269    0.3909 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4365    1.3074    0.8229 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5434    1.0143   -0.3314 C   0  0  1  0  0  0  0  0  0  0  0  0
   -0.1925    1.0230    0.0301 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.4914    0.4354   -1.0252 C   0  0  1  0  0  0  0  0  0  0  0  0
    1.7077   -0.2501   -0.4897 C   0  0  1  0  0  0  0  0  0  0  0  0
    2.6533   -1.0988   -1.9383 Br  0  0  0  0  0  0  0  0  0  0  0  0
    2.5724    0.8013    0.1919 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.7680    0.1096    0.7119 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.9616    0.4879    0.2743 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.2192   -0.1342    0.7269 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.1402    0.8756    1.3892 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4535   -0.4971   -1.7278 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8004   -0.2268   -1.0862 C   0  0  1  0  0  0  0  0  0  0  0  0
   -2.2643   -1.3199   -0.3381 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.3838   -2.0594   -0.6009 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.8542   -3.2098    0.2037 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.0533   -1.7099   -1.6207 O   0  0  0  0  0  0  0  0  0  0  0  0
   -8.3339    0.9591   -0.2912 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.5315   -0.1051    1.5686 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.1576    2.1845   -0.3394 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1530    2.3378    1.1902 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3708    0.5720    1.6416 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6466    1.8771   -1.0557 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.8326    1.1839   -1.7750 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.4897   -1.0219    0.2646 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.8304    1.6252   -0.4769 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.0285    1.2275    1.0531 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.6750   -0.6883    1.4339 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.0072    1.2915   -0.4489 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.0288   -0.9656    1.4389 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.8072   -0.5711   -0.1190 H   0  0  0  0  0  0  0  0  0  0  0  0
    8.1161    0.4032    1.5534 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.2336    1.7230    0.6775 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.7052    1.2495    2.3297 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4637   -0.3998   -2.8134 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1525   -1.5385   -1.4589 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5122   -0.0756   -1.9241 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.9476   -3.8004    0.4950 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.4944   -3.8819   -0.3883 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.3205   -2.8913    1.1564 H   0  0  0  0  0  0  0  0  0  0  0  0
 15 14  1  0
 14 13  1  0
 13 12  2  0
 12 11  1  0
 11  9  1  0
  9 10  1  0
  9  8  1  0
  8 16  1  0
 16 17  1  0
 17 18  1  0
 18 19  1  0
 19 20  1  0
 19 21  2  0
 17  6  1  0
  6  5  1  0
  5  4  1  0
  4  3  2  0
  3  2  1  0
  2  1  3  0
  6  7  1  0
  7  8  1  0
 15 36  1  0
 15 37  1  0
 15 38  1  0
 14 34  1  0
 14 35  1  0
 13 33  1  0
 12 32  1  0
 11 30  1  0
 11 31  1  0
  9 29  1  1
  8 28  1  6
 16 39  1  0
 16 40  1  0
 17 41  1  6
 20 42  1  0
 20 43  1  0
 20 44  1  0
  6 27  1  6
  5 25  1  0
  5 26  1  0
  4 24  1  0
  3 23  1  0
  1 22  1  0
M  END


  Mrv1652309032206342D          

 21 21  0  0  1  0            999 V2000
   -1.5757    4.0018    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8612    3.5893    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1467    3.1768    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1467    2.3518    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.5678    1.9393    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.5678    1.1143    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    1.2352    0.6294    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.9803   -0.1553    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    1.4652   -0.8227    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    2.2857   -0.7365    0.0000 Br  0  0  0  0  0  0  0  0  0  0  0  0
    1.1296   -1.5764    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.6145   -2.2438    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.2790   -2.9975    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.7639   -3.6649    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.5844   -3.5787    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.1553   -0.1553    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0997    0.6294    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
   -0.8843    0.8843    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4974    0.3323    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3259   -0.4747    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2820    0.5872    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  3  0  0  0  0
  2  3  1  0  0  0  0
  3  4  2  0  0  0  0
  4  5  1  0  0  0  0
  6  5  1  1  0  0  0
  6  7  1  0  0  0  0
  7  8  1  0  0  0  0
  8  9  1  1  0  0  0
  9 10  1  1  0  0  0
  9 11  1  0  0  0  0
 11 12  1  0  0  0  0
 12 13  2  0  0  0  0
 13 14  1  0  0  0  0
 14 15  1  0  0  0  0
  8 16  1  0  0  0  0
 16 17  1  0  0  0  0
  6 17  1  0  0  0  0
 17 18  1  1  0  0  0
 18 19  1  0  0  0  0
 19 20  1  0  0  0  0
 19 21  2  0  0  0  0
M  END
> <DATABASE_ID>
NP0168725

> <DATABASE_NAME>
NP-MRD

> <SMILES>
CC\C=C\C[C@H](Br)[C@H]1C[C@@H](OC(C)=O)[C@@H](C\C=C\C#C)O1

> <INCHI_IDENTIFIER>
InChI=1S/C17H23BrO3/c1-4-6-8-10-14(18)16-12-17(20-13(3)19)15(21-16)11-9-7-5-2/h2,6-9,14-17H,4,10-12H2,1,3H3/b8-6+,9-7+/t14-,15+,16+,17+/m0/s1

> <INCHI_KEY>
BUFQJMZKMZGEFE-GIGMYMNUSA-N

> <FORMULA>
C17H23BrO3

> <MOLECULAR_WEIGHT>
355.272

> <EXACT_MASS>
354.083058

> <JCHEM_ACCEPTOR_COUNT>
2

> <JCHEM_ATOM_COUNT>
44

> <JCHEM_AVERAGE_POLARIZABILITY>
35.27593910117594

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
0

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
1

> <JCHEM_IUPAC>
(2R,3R,5R)-5-[(1S,3E)-1-bromohex-3-en-1-yl]-2-[(2E)-pent-2-en-4-yn-1-yl]oxolan-3-yl acetate

> <ALOGPS_LOGP>
4.90

> <JCHEM_LOGP>
3.748135627999999

> <ALOGPS_LOGS>
-4.80

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
1

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA_STRONGEST_BASIC>
-4.1946777633426935

> <JCHEM_POLAR_SURFACE_AREA>
35.53

> <JCHEM_REFRACTIVITY>
89.20629999999998

> <JCHEM_ROTATABLE_BOND_COUNT>
8

> <JCHEM_RULE_OF_FIVE>
1

> <ALOGPS_SOLUBILITY>
5.60e-03 g/l

> <JCHEM_TRADITIONAL_IUPAC>
(2R,3R,5R)-5-[(1S,3E)-1-bromohex-3-en-1-yl]-2-[(2E)-pent-2-en-4-yn-1-yl]oxolan-3-yl acetate

> <JCHEM_VEBER_RULE>
1

$$$$

HEADER    PROTEIN                                 03-SEP-22   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   03-SEP-22         0                                  
HETATM    1  C   UNK     0      -2.941   7.470   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0      -1.608   6.700   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0      -0.274   5.930   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0      -0.274   4.390   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0       1.060   3.620   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0       1.060   2.080   0.000  0.00  0.00           C+0
HETATM    7  O   UNK     0       2.306   1.175   0.000  0.00  0.00           O+0
HETATM    8  C   UNK     0       1.830  -0.290   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0       2.735  -1.536   0.000  0.00  0.00           C+0
HETATM   10 Br   UNK     0       4.267  -1.375   0.000  0.00  0.00          Br+0
HETATM   11  C   UNK     0       2.109  -2.943   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0       3.014  -4.188   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0       2.387  -5.595   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0       3.293  -6.841   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0       4.824  -6.680   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0       0.290  -0.290   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0      -0.186   1.175   0.000  0.00  0.00           C+0
HETATM   18  O   UNK     0      -1.651   1.651   0.000  0.00  0.00           O+0
HETATM   19  C   UNK     0      -2.795   0.620   0.000  0.00  0.00           C+0
HETATM   20  C   UNK     0      -2.475  -0.886   0.000  0.00  0.00           C+0
HETATM   21  O   UNK     0      -4.260   1.096   0.000  0.00  0.00           O+0
CONECT    1    2                                                            
CONECT    2    1    3                                                       
CONECT    3    2    4                                                       
CONECT    4    3    5                                                       
CONECT    5    4    6                                                       
CONECT    6    5    7   17                                                  
CONECT    7    6    8                                                       
CONECT    8    7    9   16                                                  
CONECT    9    8   10   11                                                  
CONECT   10    9                                                            
CONECT   11    9   12                                                       
CONECT   12   11   13                                                       
CONECT   13   12   14                                                       
CONECT   14   13   15                                                       
CONECT   15   14                                                            
CONECT   16    8   17                                                       
CONECT   17   16    6   18                                                  
CONECT   18   17   19                                                       
CONECT   19   18   20   21                                                  
CONECT   20   19                                                            
CONECT   21   19                                                            
MASTER        0    0    0    0    0    0    0    0   21    0   42    0
END

View in JSmol

Synonyms

Value	Source
(2R)-2a-(2-Pentene-4-ynyl)-5a-[(S)-1-bromo-3-hexenyl]tetrahydrofuran-3a-ol acetate	Generator
(2R)-2a-(2-Pentene-4-ynyl)-5a-[(S)-1-bromo-3-hexenyl]tetrahydrofuran-3a-ol acetic acid	Generator
(2R)-2alpha-(2-Pentene-4-ynyl)-5alpha-[(S)-1-bromo-3-hexenyl]tetrahydrofuran-3alpha-ol acetic acid	Generator
(2R)-2Α-(2-pentene-4-ynyl)-5α-[(S)-1-bromo-3-hexenyl]tetrahydrofuran-3α-ol acetate	Generator
(2R)-2Α-(2-pentene-4-ynyl)-5α-[(S)-1-bromo-3-hexenyl]tetrahydrofuran-3α-ol acetic acid	Generator

Chemical Formula

C₁₇H₂₃BrO₃

Average Mass

355.2720 Da

Monoisotopic Mass

354.08306 Da

IUPAC Name

Not Available

Traditional Name

Not Available

CAS Registry Number

Not Available

SMILES

CC\C=C\C[C@H](Br)[C@H]1C[C@@H](OC(C)=O)[C@@H](C\C=C\C#C)O1

InChI Identifier

InChI=1S/C17H23BrO3/c1-4-6-8-10-14(18)16-12-17(20-13(3)19)15(21-16)11-9-7-5-2/h2,6-9,14-17H,4,10-12H2,1,3H3/b8-6+,9-7+/t14-,15+,16+,17+/m0/s1

InChI Key

BUFQJMZKMZGEFE-GIGMYMNUSA-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
Laurencia nipponica	LOTUS Database	35616633

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as c-glycosyl compounds. These are glycoside in which a sugar group is bonded through one carbon to another group via a C-glycosidic bond.

Kingdom

Organic compounds

Super Class

Organic oxygen compounds

Class

Organooxygen compounds

Sub Class

Carbohydrates and carbohydrate conjugates

Direct Parent

C-glycosyl compounds

Alternative Parents

Substituents

C-glycosyl compound
Tetrahydrofuran
Carboxylic acid ester
Acetylide
Oxacycle
Organoheterocyclic compound
Monocarboxylic acid or derivatives
Ether
Dialkyl ether
Carboxylic acid derivative
Organic oxide
Hydrocarbon derivative
Organobromide
Organohalogen compound
Carbonyl group
Alkyl halide
Alkyl bromide
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	4.9	ALOGPS
logS	-4.8	ALOGPS

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

9947325

KEGG Compound ID

Not Available

BioCyc ID

Not Available

BiGG ID

Not Available

Wikipedia Link

Not Available

METLIN ID

Not Available

PubChem Compound

11772642

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

LOTUS database [Link]

Showing NP-Card for (2r,3r,5r)-5-[(1s,3e)-1-bromohex-3-en-1-yl]-2-[(2e)-pent-2-en-4-yn-1-yl]oxolan-3-yl acetate (NP0168725)

MOL for NP0168725 ((2r,3r,5r)-5-[(1s,3e)-1-bromohex-3-en-1-yl]-2-[(2e)-pent-2-en-4-yn-1-yl]oxolan-3-yl acetate)

3D MOL for NP0168725 ((2r,3r,5r)-5-[(1s,3e)-1-bromohex-3-en-1-yl]-2-[(2e)-pent-2-en-4-yn-1-yl]oxolan-3-yl acetate)

3D SDF for NP0168725 ((2r,3r,5r)-5-[(1s,3e)-1-bromohex-3-en-1-yl]-2-[(2e)-pent-2-en-4-yn-1-yl]oxolan-3-yl acetate)

3D-SDF for NP0168725 ((2r,3r,5r)-5-[(1s,3e)-1-bromohex-3-en-1-yl]-2-[(2e)-pent-2-en-4-yn-1-yl]oxolan-3-yl acetate)

PDB for NP0168725 ((2r,3r,5r)-5-[(1s,3e)-1-bromohex-3-en-1-yl]-2-[(2e)-pent-2-en-4-yn-1-yl]oxolan-3-yl acetate)

3D PDB for NP0168725 ((2r,3r,5r)-5-[(1s,3e)-1-bromohex-3-en-1-yl]-2-[(2e)-pent-2-en-4-yn-1-yl]oxolan-3-yl acetate)

SMILES for NP0168725 ((2r,3r,5r)-5-[(1s,3e)-1-bromohex-3-en-1-yl]-2-[(2e)-pent-2-en-4-yn-1-yl]oxolan-3-yl acetate)

INCHI for NP0168725 ((2r,3r,5r)-5-[(1s,3e)-1-bromohex-3-en-1-yl]-2-[(2e)-pent-2-en-4-yn-1-yl]oxolan-3-yl acetate)

Structure for NP0168725 ((2r,3r,5r)-5-[(1s,3e)-1-bromohex-3-en-1-yl]-2-[(2e)-pent-2-en-4-yn-1-yl]oxolan-3-yl acetate)

3D Structure for NP0168725 ((2r,3r,5r)-5-[(1s,3e)-1-bromohex-3-en-1-yl]-2-[(2e)-pent-2-en-4-yn-1-yl]oxolan-3-yl acetate)