NP-MRD: Showing NP-Card for (2s,3s,5e)-3-bromo-1-[(2r,3r,5r)-5-[(1r)-1-bromoprop-2-yn-1-yl]-3-hydroxyoxolan-2-yl]oct-5-en-2-yl acetate (NP0162730)

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Record Information

Version

2.0

Created at

2022-09-02 21:11:44 UTC

Updated at

2022-09-02 21:11:44 UTC

NP-MRD ID

NP0162730

Secondary Accession Numbers

None

Natural Product Identification

Common Name

(2s,3s,5e)-3-bromo-1-[(2r,3r,5r)-5-[(1r)-1-bromoprop-2-yn-1-yl]-3-hydroxyoxolan-2-yl]oct-5-en-2-yl acetate

Description

(2S,3S,5E)-3-bromo-1-[(2R,3R,5R)-5-[(1R)-1-bromoprop-2-yn-1-yl]-3-hydroxyoxolan-2-yl]oct-5-en-2-yl 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. (2s,3s,5e)-3-bromo-1-[(2r,3r,5r)-5-[(1r)-1-bromoprop-2-yn-1-yl]-3-hydroxyoxolan-2-yl]oct-5-en-2-yl acetate is found in Laurencia obtusa. Based on a literature review very few articles have been published on (2S,3S,5E)-3-bromo-1-[(2R,3R,5R)-5-[(1R)-1-bromoprop-2-yn-1-yl]-3-hydroxyoxolan-2-yl]oct-5-en-2-yl acetate.

Structure

MOL 3D MOL SDF PDB SMILES InChI

     RDKit          3D

 47 47  0  0  0  0  0  0  0  0999 V2000
   -5.0418   -0.6739   -2.4561 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.0206   -0.4931   -1.2677 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.0288   -0.2635    0.1642 C   0  0  1  0  0  0  0  0  0  0  0  0
   -5.0042   -1.9583    1.1071 Br  0  0  0  0  0  0  0  0  0  0  0  0
   -3.8359    0.5184    0.5783 C   0  0  1  0  0  0  0  0  0  0  0  0
   -3.7825    0.7291    2.0889 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3171    0.9973    2.3178 C   0  0  1  0  0  0  0  0  0  0  0  0
   -1.8194    0.1238    3.2640 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7249    0.7595    0.9411 C   0  0  1  0  0  0  0  0  0  0  0  0
   -0.3081    0.3104    1.0195 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.2824    0.0819   -0.3365 C   0  0  2  0  0  0  0  0  0  0  0  0
   -0.5097   -0.8596   -1.0138 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1152   -0.7230   -2.2239 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9281   -1.8247   -2.8349 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9713    0.3613   -2.8218 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.7332   -0.3561   -0.2542 C   0  0  1  0  0  0  0  0  0  0  0  0
    2.4170   -0.3781   -2.0897 Br  0  0  0  0  0  0  0  0  0  0  0  0
    2.4983    0.7479    0.4413 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.9837    0.4537    0.3999 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.7213    0.3083    1.4698 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.1857    0.0182    1.3081 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.5443   -0.0536   -0.1580 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6074   -0.0807    0.3366 O   0  0  0  0  0  0  0  0  0  0  0  0
   -5.0719   -0.8191   -3.5041 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.9697    0.3029    0.4520 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.7897    1.5234    0.0659 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.3938    1.6218    2.2950 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.1364   -0.1786    2.6022 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1756    2.0636    2.6072 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4916   -0.5457    3.5499 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7333    1.7511    0.4179 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.3023    0.9913    1.6563 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3228   -0.6487    1.6244 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.3103    0.9942   -0.9613 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5941   -2.2635   -2.0541 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5078   -1.3873   -3.6707 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1980   -2.5939   -3.1642 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.9100   -1.2810    0.2768 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.2682    0.8044    1.5412 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.3849    1.7318   -0.0586 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.4176    0.3671   -0.6020 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.2678    0.3988    2.4505 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.3121   -1.0319    1.7022 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.8174    0.7063    1.8707 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.6494   -0.2563   -0.2167 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.3815    0.9067   -0.6850 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.0125   -0.9024   -0.6278 H   0  0  0  0  0  0  0  0  0  0  0  0
 22 21  1  0
 21 20  1  0
 20 19  2  0
 19 18  1  0
 18 16  1  0
 16 17  1  0
 16 11  1  0
 11 10  1  0
 10  9  1  0
  9 23  1  0
 23  5  1  0
  5  6  1  0
  6  7  1  0
  7  8  1  0
  5  3  1  0
  3  4  1  0
  3  2  1  0
  2  1  3  0
 11 12  1  0
 12 13  1  0
 13 14  1  0
 13 15  2  0
  7  9  1  0
 22 45  1  0
 22 46  1  0
 22 47  1  0
 21 43  1  0
 21 44  1  0
 20 42  1  0
 19 41  1  0
 18 39  1  0
 18 40  1  0
 16 38  1  1
 11 34  1  6
 10 32  1  0
 10 33  1  0
  9 31  1  6
  5 26  1  6
  6 27  1  0
  6 28  1  0
  7 29  1  1
  8 30  1  0
  3 25  1  6
  1 24  1  0
 14 35  1  0
 14 36  1  0
 14 37  1  0
M  END


  Mrv1652309022223112D          

 23 23  0  0  1  0            999 V2000
    0.1095    5.5957    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.5944    4.9283    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.0793    4.2608    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    0.7438    3.5071    0.0000 Br  0  0  0  0  0  0  0  0  0  0  0  0
    1.8998    4.3471    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    2.3123    5.0615    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.1193    4.8900    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    3.7324    5.4420    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.2055    4.0695    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    3.9200    3.6570    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.9200    2.8320    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    3.2055    2.4195    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.2055    1.5945    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.9200    1.1820    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.4911    1.1820    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.6345    2.4195    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    5.3489    2.8320    0.0000 Br  0  0  0  0  0  0  0  0  0  0  0  0
    4.6345    1.5945    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.3489    1.1820    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.3489    0.3570    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.0634   -0.0555    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.7779    0.3570    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.4519    3.7340    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  1  6  0  0  0
  5  3  1  1  0  0  0
  5  6  1  0  0  0  0
  6  7  1  0  0  0  0
  7  8  1  1  0  0  0
  7  9  1  0  0  0  0
  9 10  1  1  0  0  0
 10 11  1  0  0  0  0
 11 12  1  1  0  0  0
 12 13  1  0  0  0  0
 13 14  1  0  0  0  0
 13 15  2  0  0  0  0
 11 16  1  0  0  0  0
 16 17  1  1  0  0  0
 16 18  1  0  0  0  0
 18 19  1  0  0  0  0
 19 20  2  0  0  0  0
 20 21  1  0  0  0  0
 21 22  1  0  0  0  0
  9 23  1  0  0  0  0
  5 23  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0162730

> <DATABASE_NAME>
NP-MRD

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

> <INCHI_IDENTIFIER>
InChI=1S/C17H24Br2O4/c1-4-6-7-8-13(19)16(22-11(3)20)10-17-14(21)9-15(23-17)12(18)5-2/h2,6-7,12-17,21H,4,8-10H2,1,3H3/b7-6+/t12-,13+,14-,15-,16+,17-/m1/s1

> <INCHI_KEY>
AHJKPRCXDUDCBX-IQQRUZATSA-N

> <FORMULA>
C17H24Br2O4

> <MOLECULAR_WEIGHT>
452.183

> <EXACT_MASS>
450.004135

> <JCHEM_ACCEPTOR_COUNT>
3

> <JCHEM_ATOM_COUNT>
47

> <JCHEM_AVERAGE_POLARIZABILITY>
39.379432557731214

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
1

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
1

> <JCHEM_IUPAC>
(2S,3S,5E)-3-bromo-1-[(2R,3R,5R)-5-[(1R)-1-bromoprop-2-yn-1-yl]-3-hydroxyoxolan-2-yl]oct-5-en-2-yl acetate

> <ALOGPS_LOGP>
4.12

> <JCHEM_LOGP>
3.271635723333332

> <ALOGPS_LOGS>
-4.54

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
1

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA>
19.258986575846176

> <JCHEM_PKA_STRONGEST_ACIDIC>
14.10725984082163

> <JCHEM_PKA_STRONGEST_BASIC>
-3.1892827069398777

> <JCHEM_POLAR_SURFACE_AREA>
55.760000000000005

> <JCHEM_REFRACTIVITY>
96.9576

> <JCHEM_ROTATABLE_BOND_COUNT>
9

> <JCHEM_RULE_OF_FIVE>
1

> <ALOGPS_SOLUBILITY>
1.30e-02 g/l

> <JCHEM_TRADITIONAL_IUPAC>
(2S,3S,5E)-3-bromo-1-[(2R,3R,5R)-5-[(1R)-1-bromoprop-2-yn-1-yl]-3-hydroxyoxolan-2-yl]oct-5-en-2-yl acetate

> <JCHEM_VEBER_RULE>
0

$$$$

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       0.204  10.445   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0       1.110   9.199   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0       2.015   7.954   0.000  0.00  0.00           C+0
HETATM    4 Br   UNK     0       1.388   6.547   0.000  0.00  0.00          Br+0
HETATM    5  C   UNK     0       3.546   8.115   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0       4.316   9.448   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0       5.823   9.128   0.000  0.00  0.00           C+0
HETATM    8  O   UNK     0       6.967  10.158   0.000  0.00  0.00           O+0
HETATM    9  C   UNK     0       5.984   7.596   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0       7.317   6.826   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0       7.317   5.286   0.000  0.00  0.00           C+0
HETATM   12  O   UNK     0       5.984   4.516   0.000  0.00  0.00           O+0
HETATM   13  C   UNK     0       5.984   2.976   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0       7.317   2.206   0.000  0.00  0.00           C+0
HETATM   15  O   UNK     0       4.650   2.206   0.000  0.00  0.00           O+0
HETATM   16  C   UNK     0       8.651   4.516   0.000  0.00  0.00           C+0
HETATM   17 Br   UNK     0       9.985   5.286   0.000  0.00  0.00          Br+0
HETATM   18  C   UNK     0       8.651   2.976   0.000  0.00  0.00           C+0
HETATM   19  C   UNK     0       9.985   2.206   0.000  0.00  0.00           C+0
HETATM   20  C   UNK     0       9.985   0.666   0.000  0.00  0.00           C+0
HETATM   21  C   UNK     0      11.318  -0.104   0.000  0.00  0.00           C+0
HETATM   22  C   UNK     0      12.652   0.666   0.000  0.00  0.00           C+0
HETATM   23  O   UNK     0       4.577   6.970   0.000  0.00  0.00           O+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    9                                                  
CONECT    8    7                                                            
CONECT    9    7   10   23                                                  
CONECT   10    9   11                                                       
CONECT   11   10   12   16                                                  
CONECT   12   11   13                                                       
CONECT   13   12   14   15                                                  
CONECT   14   13                                                            
CONECT   15   13                                                            
CONECT   16   11   17   18                                                  
CONECT   17   16                                                            
CONECT   18   16   19                                                       
CONECT   19   18   20                                                       
CONECT   20   19   21                                                       
CONECT   21   20   22                                                       
CONECT   22   21                                                            
CONECT   23    9    5                                                       
MASTER        0    0    0    0    0    0    0    0   23    0   46    0
END

View in JSmol

Synonyms

Value	Source
(2S,3S,5E)-3-Bromo-1-[(2R,3R,5R)-5-[(1R)-1-bromoprop-2-yn-1-yl]-3-hydroxyoxolan-2-yl]oct-5-en-2-yl acetic acid	Generator

Chemical Formula

C₁₇H₂₄Br₂O₄

Average Mass

452.1830 Da

Monoisotopic Mass

450.00414 Da

IUPAC Name

(2S,3S,5E)-3-bromo-1-[(2R,3R,5R)-5-[(1R)-1-bromoprop-2-yn-1-yl]-3-hydroxyoxolan-2-yl]oct-5-en-2-yl acetate

Traditional Name

(2S,3S,5E)-3-bromo-1-[(2R,3R,5R)-5-[(1R)-1-bromoprop-2-yn-1-yl]-3-hydroxyoxolan-2-yl]oct-5-en-2-yl acetate

CAS Registry Number

Not Available

SMILES

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

InChI Identifier

InChI=1S/C17H24Br2O4/c1-4-6-7-8-13(19)16(22-11(3)20)10-17-14(21)9-15(23-17)12(18)5-2/h2,6-7,12-17,21H,4,8-10H2,1,3H3/b7-6+/t12-,13+,14-,15-,16+,17-/m1/s1

InChI Key

AHJKPRCXDUDCBX-IQQRUZATSA-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 obtusa	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
Secondary alcohol
Acetylide
Carboxylic acid derivative
Dialkyl ether
Ether
Monocarboxylic acid or derivatives
Oxacycle
Organoheterocyclic compound
Alkyl bromide
Organic oxide
Alkyl halide
Alcohol
Organohalogen compound
Organobromide
Hydrocarbon derivative
Carbonyl group
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	4.12	ALOGPS
logP	3.27	ChemAxon
logS	-4.5	ALOGPS
pKa (Strongest Acidic)	14.11	ChemAxon
pKa (Strongest Basic)	-3.2	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	3	ChemAxon
Hydrogen Donor Count	1	ChemAxon
Polar Surface Area	55.76 Å²	ChemAxon
Rotatable Bond Count	9	ChemAxon
Refractivity	96.96 m³·mol⁻¹	ChemAxon
Polarizability	39.38 Å³	ChemAxon
Number of Rings	1	ChemAxon
Bioavailability	Yes	ChemAxon
Rule of Five	Yes	ChemAxon
Ghose Filter	Yes	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

14412598

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

LOTUS database [Link]

Showing NP-Card for (2s,3s,5e)-3-bromo-1-[(2r,3r,5r)-5-[(1r)-1-bromoprop-2-yn-1-yl]-3-hydroxyoxolan-2-yl]oct-5-en-2-yl acetate (NP0162730)

MOL for NP0162730 ((2s,3s,5e)-3-bromo-1-[(2r,3r,5r)-5-[(1r)-1-bromoprop-2-yn-1-yl]-3-hydroxyoxolan-2-yl]oct-5-en-2-yl acetate)

3D MOL for NP0162730 ((2s,3s,5e)-3-bromo-1-[(2r,3r,5r)-5-[(1r)-1-bromoprop-2-yn-1-yl]-3-hydroxyoxolan-2-yl]oct-5-en-2-yl acetate)

3D SDF for NP0162730 ((2s,3s,5e)-3-bromo-1-[(2r,3r,5r)-5-[(1r)-1-bromoprop-2-yn-1-yl]-3-hydroxyoxolan-2-yl]oct-5-en-2-yl acetate)

3D-SDF for NP0162730 ((2s,3s,5e)-3-bromo-1-[(2r,3r,5r)-5-[(1r)-1-bromoprop-2-yn-1-yl]-3-hydroxyoxolan-2-yl]oct-5-en-2-yl acetate)

PDB for NP0162730 ((2s,3s,5e)-3-bromo-1-[(2r,3r,5r)-5-[(1r)-1-bromoprop-2-yn-1-yl]-3-hydroxyoxolan-2-yl]oct-5-en-2-yl acetate)

3D PDB for NP0162730 ((2s,3s,5e)-3-bromo-1-[(2r,3r,5r)-5-[(1r)-1-bromoprop-2-yn-1-yl]-3-hydroxyoxolan-2-yl]oct-5-en-2-yl acetate)

SMILES for NP0162730 ((2s,3s,5e)-3-bromo-1-[(2r,3r,5r)-5-[(1r)-1-bromoprop-2-yn-1-yl]-3-hydroxyoxolan-2-yl]oct-5-en-2-yl acetate)

INCHI for NP0162730 ((2s,3s,5e)-3-bromo-1-[(2r,3r,5r)-5-[(1r)-1-bromoprop-2-yn-1-yl]-3-hydroxyoxolan-2-yl]oct-5-en-2-yl acetate)

Structure for NP0162730 ((2s,3s,5e)-3-bromo-1-[(2r,3r,5r)-5-[(1r)-1-bromoprop-2-yn-1-yl]-3-hydroxyoxolan-2-yl]oct-5-en-2-yl acetate)

3D Structure for NP0162730 ((2s,3s,5e)-3-bromo-1-[(2r,3r,5r)-5-[(1r)-1-bromoprop-2-yn-1-yl]-3-hydroxyoxolan-2-yl]oct-5-en-2-yl acetate)