NP-MRD: Showing NP-Card for (4s,5s)-5-[(1r,2r,4e,6r,7s)-1,7-dihydroxy-2,6-dimethyloct-4-en-1-yl]-4-hydroxyoxolan-2-one (NP0210048)

Jump To Section:

Identification Spectra BioTaxonomy ChemoTaxonomy Physical properties Links References XML

Record Information

Version

2.0

Created at

2022-09-05 07:42:14 UTC

Updated at

2022-09-05 07:42:14 UTC

NP-MRD ID

NP0210048

Secondary Accession Numbers

None

Natural Product Identification

Common Name

(4s,5s)-5-[(1r,2r,4e,6r,7s)-1,7-dihydroxy-2,6-dimethyloct-4-en-1-yl]-4-hydroxyoxolan-2-one

Description

Mupirocin H belongs to the class of organic compounds known as fatty alcohols. These are aliphatic alcohols consisting of a chain of a least six carbon atoms. (4s,5s)-5-[(1r,2r,4e,6r,7s)-1,7-dihydroxy-2,6-dimethyloct-4-en-1-yl]-4-hydroxyoxolan-2-one is found in Pseudomonas fluorescens. (4s,5s)-5-[(1r,2r,4e,6r,7s)-1,7-dihydroxy-2,6-dimethyloct-4-en-1-yl]-4-hydroxyoxolan-2-one was first documented in 2007 (PMID: 17713071). Based on a literature review a small amount of articles have been published on Mupirocin H (PMID: 22294025) (PMID: 21707103) (PMID: 18465759).

Structure

MOL 3D MOL SDF PDB SMILES InChI

     RDKit          3D

 43 43  0  0  0  0  0  0  0  0999 V2000
    4.8846    0.4532   -0.4198 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.5970   -0.5213    0.6769 C   0  0  2  0  0  0  0  0  0  0  0  0
    5.3758   -1.6825    0.4861 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.1613   -0.9693    0.6989 C   0  0  2  0  0  0  0  0  0  0  0  0
    2.8093   -1.6346   -0.5934 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.2464    0.1438    1.0111 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.2637    0.4217    0.1606 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.3527    1.5282    0.4691 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0593    1.0544    0.6184 C   0  0  1  0  0  0  0  0  0  0  0  0
   -1.9002    2.2839    0.9410 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5918    0.2869   -0.5235 C   0  0  1  0  0  0  0  0  0  0  0  0
   -0.8918   -0.8789   -0.7743 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.0370   -0.1109   -0.3641 C   0  0  1  0  0  0  0  0  0  0  0  0
   -3.9010    0.9544   -0.1050 O   0  0  0  0  0  0  0  0  0  0  0  0
   -5.1776    0.5229   -0.4488 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.2754    1.0300   -0.0594 O   0  0  0  0  0  0  0  0  0  0  0  0
   -5.0837   -0.6551   -1.3672 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5814   -0.6459   -1.6772 C   0  0  2  0  0  0  0  0  0  0  0  0
   -3.0936   -1.9242   -1.8618 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.9738    1.0634   -0.6166 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.1949   -0.0959   -1.3402 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.7541    1.0819   -0.1312 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.8848   -0.0815    1.6606 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.3136   -1.3717    0.4102 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.0530   -1.7190    1.5184 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.8843   -0.9522   -1.4601 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.5076   -2.5040   -0.7607 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.7924   -2.0717   -0.5863 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.3793    0.7343    1.9374 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.1671   -0.1473   -0.7386 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.6965    2.0797    1.3878 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.3936    2.3101   -0.3506 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1419    0.4271    1.5642 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2153    2.8339    0.0539 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7439    2.0056    1.6247 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2577    2.9537    1.5488 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5033    0.9024   -1.4505 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1001   -1.5539   -0.0690 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.1831   -0.8774    0.4114 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.6466   -0.5142   -2.2914 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.3366   -1.6019   -0.8274 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.3921    0.0282   -2.5165 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5721   -2.5867   -1.3195 H   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0
  2  3  1  0
  2  4  1  0
  4  5  1  0
  4  6  1  0
  6  7  2  0
  7  8  1  0
  8  9  1  0
  9 10  1  0
  9 11  1  0
 11 12  1  0
 11 13  1  0
 13 14  1  0
 14 15  1  0
 15 16  2  0
 15 17  1  0
 17 18  1  0
 18 19  1  0
 18 13  1  0
  1 20  1  0
  1 21  1  0
  1 22  1  0
  2 23  1  1
  3 24  1  0
  4 25  1  1
  5 26  1  0
  5 27  1  0
  5 28  1  0
  6 29  1  0
  7 30  1  0
  8 31  1  0
  8 32  1  0
  9 33  1  1
 10 34  1  0
 10 35  1  0
 10 36  1  0
 11 37  1  6
 12 38  1  0
 13 39  1  1
 17 40  1  0
 17 41  1  0
 18 42  1  6
 19 43  1  0
M  END


  Mrv1652309052209422D          

 19 19  0  0  1  0            999 V2000
   -2.2901    6.0643    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5757    5.6518    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
   -0.8612    6.0643    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5757    4.8268    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
   -2.2901    4.4143    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8612    4.4143    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  1  0  0  0  0  0  0  0  0  0
   -0.8612    1.9393    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.5678    1.9393    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    1.2822    2.3518    0.0000 O   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  0  0  0  0  0  0  0  0  0  0
    1.4652   -0.8227    0.0000 O   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  2  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  2  1  0  0  0  0
  2  3  1  6  0  0  0
  2  4  1  0  0  0  0
  4  5  1  1  0  0  0
  4  6  1  0  0  0  0
  6  7  2  0  0  0  0
  7  8  1  0  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  1  0  0  0
 13 11  1  1  0  0  0
 13 14  1  0  0  0  0
 14 15  1  0  0  0  0
 15 16  2  0  0  0  0
 15 17  1  0  0  0  0
 17 18  1  0  0  0  0
 13 18  1  0  0  0  0
 18 19  1  6  0  0  0
M  END
> <DATABASE_ID>
NP0210048

> <DATABASE_NAME>
NP-MRD

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

> <INCHI_IDENTIFIER>
InChI=1S/C14H24O5/c1-8(10(3)15)5-4-6-9(2)13(18)14-11(16)7-12(17)19-14/h4-5,8-11,13-16,18H,6-7H2,1-3H3/b5-4+/t8-,9-,10+,11+,13-,14+/m1/s1

> <INCHI_KEY>
AKVNYEYIRKXNJP-JZTXUPKOSA-N

> <FORMULA>
C14H24O5

> <MOLECULAR_WEIGHT>
272.341

> <EXACT_MASS>
272.162373873

> <JCHEM_ACCEPTOR_COUNT>
4

> <JCHEM_ATOM_COUNT>
43

> <JCHEM_AVERAGE_POLARIZABILITY>
29.463807546111504

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
3

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
1

> <JCHEM_IUPAC>
(4S,5S)-5-[(1R,2R,4E,6R,7S)-1,7-dihydroxy-2,6-dimethyloct-4-en-1-yl]-4-hydroxyoxolan-2-one

> <JCHEM_LOGP>
0.6655127003333338

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
1

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA>
14.237726892137228

> <JCHEM_PKA_STRONGEST_ACIDIC>
13.535869024319972

> <JCHEM_PKA_STRONGEST_BASIC>
-1.401213843898633

> <JCHEM_POLAR_SURFACE_AREA>
86.99

> <JCHEM_REFRACTIVITY>
71.23220000000002

> <JCHEM_ROTATABLE_BOND_COUNT>
6

> <JCHEM_RULE_OF_FIVE>
1

> <JCHEM_TRADITIONAL_IUPAC>
(4S,5S)-5-[(1R,2R,4E,6R,7S)-1,7-dihydroxy-2,6-dimethyloct-4-en-1-yl]-4-hydroxyoxolan-2-one

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 05-SEP-22   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   05-SEP-22         0                                  
HETATM    1  C   UNK     0      -4.275  11.320   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0      -2.941  10.550   0.000  0.00  0.00           C+0
HETATM    3  O   UNK     0      -1.608  11.320   0.000  0.00  0.00           O+0
HETATM    4  C   UNK     0      -2.941   9.010   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0      -4.275   8.240   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0      -1.608   8.240   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0      -1.608   6.700   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0      -0.274   5.930   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0      -0.274   4.390   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0      -1.608   3.620   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0       1.060   3.620   0.000  0.00  0.00           C+0
HETATM   12  O   UNK     0       2.393   4.390   0.000  0.00  0.00           O+0
HETATM   13  C   UNK     0       1.060   2.080   0.000  0.00  0.00           C+0
HETATM   14  O   UNK     0       2.306   1.175   0.000  0.00  0.00           O+0
HETATM   15  C   UNK     0       1.830  -0.290   0.000  0.00  0.00           C+0
HETATM   16  O   UNK     0       2.735  -1.536   0.000  0.00  0.00           O+0
HETATM   17  C   UNK     0       0.290  -0.290   0.000  0.00  0.00           C+0
HETATM   18  C   UNK     0      -0.186   1.175   0.000  0.00  0.00           C+0
HETATM   19  O   UNK     0      -1.651   1.651   0.000  0.00  0.00           O+0
CONECT    1    2                                                            
CONECT    2    1    3    4                                                  
CONECT    3    2                                                            
CONECT    4    2    5    6                                                  
CONECT    5    4                                                            
CONECT    6    4    7                                                       
CONECT    7    6    8                                                       
CONECT    8    7    9                                                       
CONECT    9    8   10   11                                                  
CONECT   10    9                                                            
CONECT   11    9   12   13                                                  
CONECT   12   11                                                            
CONECT   13   11   14   18                                                  
CONECT   14   13   15                                                       
CONECT   15   14   16   17                                                  
CONECT   16   15                                                            
CONECT   17   15   18                                                       
CONECT   18   17   13   19                                                  
CONECT   19   18                                                            
MASTER        0    0    0    0    0    0    0    0   19    0   38    0
END

View in JSmol

Synonyms

Not Available

Chemical Formula

C₁₄H₂₄O₅

Average Mass

272.3410 Da

Monoisotopic Mass

272.16237 Da

IUPAC Name

(4S,5S)-5-[(1R,2R,4E,6R,7S)-1,7-dihydroxy-2,6-dimethyloct-4-en-1-yl]-4-hydroxyoxolan-2-one

Traditional Name

(4S,5S)-5-[(1R,2R,4E,6R,7S)-1,7-dihydroxy-2,6-dimethyloct-4-en-1-yl]-4-hydroxyoxolan-2-one

CAS Registry Number

Not Available

SMILES

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

InChI Identifier

InChI=1S/C14H24O5/c1-8(10(3)15)5-4-6-9(2)13(18)14-11(16)7-12(17)19-14/h4-5,8-11,13-16,18H,6-7H2,1-3H3/b5-4+/t8-,9-,10+,11+,13-,14+/m1/s1

InChI Key

AKVNYEYIRKXNJP-JZTXUPKOSA-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
Pseudomonas fluorescens	LOTUS Database	35616633

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as fatty alcohols. These are aliphatic alcohols consisting of a chain of a least six carbon atoms.

Kingdom

Organic compounds

Super Class

Lipids and lipid-like molecules

Class

Fatty Acyls

Sub Class

Fatty alcohols

Direct Parent

Fatty alcohols

Alternative Parents

Substituents

Fatty alcohol
Gamma butyrolactone
Oxolane
Carboxylic acid ester
Lactone
Secondary alcohol
Carboxylic acid derivative
Oxacycle
Monocarboxylic acid or derivatives
Organoheterocyclic compound
Hydrocarbon derivative
Organic oxide
Organic oxygen compound
Carbonyl group
Organooxygen compound
Alcohol
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	0.67	ChemAxon
pKa (Strongest Acidic)	13.54	ChemAxon
pKa (Strongest Basic)	-1.4	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	4	ChemAxon
Hydrogen Donor Count	3	ChemAxon
Polar Surface Area	86.99 Å²	ChemAxon
Rotatable Bond Count	6	ChemAxon
Refractivity	71.23 m³·mol⁻¹	ChemAxon
Polarizability	29.46 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

28289279

KEGG Compound ID

Not Available

BioCyc ID

Not Available

BiGG ID

Not Available

Wikipedia Link

Not Available

METLIN ID

Not Available

PubChem Compound

53465503

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

Scott RW, Mazzetti C, Simpson TJ, Willis CL: gamma-Lactones from delta-lactones: total synthesis of the biosynthetic derailment product mupirocin H. Chem Commun (Camb). 2012 Mar 7;48(20):2639-41. doi: 10.1039/c2cc17721h. Epub 2012 Feb 1. [PubMed:22294025 ]
Udawant SP, Chakraborty TK: Total synthesis of (+)-mupirocin H from D-glucose. J Org Chem. 2011 Aug 5;76(15):6331-7. doi: 10.1021/jo200396q. Epub 2011 Jul 8. [PubMed:21707103 ]
Wu J, Hothersall J, Mazzetti C, O'Connell Y, Shields JA, Rahman AS, Cox RJ, Crosby J, Simpson TJ, Thomas CM, Willis CL: In vivo mutational analysis of the mupirocin gene cluster reveals labile points in the biosynthetic pathway: the "leaky hosepipe" mechanism. Chembiochem. 2008 Jun 16;9(9):1500-8. doi: 10.1002/cbic.200800085. [PubMed:18465759 ]
Wu J, Cooper SM, Cox RJ, Crosby J, Crump MP, Hothersall J, Simpson TJ, Thomas CM, Willis CL: Mupirocin H, a novel metabolite resulting from mutation of the HMG-CoA synthase analogue, mupH in Pseudomonas fluorescens. Chem Commun (Camb). 2007 May 28;(20):2040-2. doi: 10.1039/b700613f. [PubMed:17713071 ]
LOTUS database [Link]

Showing NP-Card for (4s,5s)-5-[(1r,2r,4e,6r,7s)-1,7-dihydroxy-2,6-dimethyloct-4-en-1-yl]-4-hydroxyoxolan-2-one (NP0210048)

MOL for NP0210048 ((4s,5s)-5-[(1r,2r,4e,6r,7s)-1,7-dihydroxy-2,6-dimethyloct-4-en-1-yl]-4-hydroxyoxolan-2-one)

3D MOL for NP0210048 ((4s,5s)-5-[(1r,2r,4e,6r,7s)-1,7-dihydroxy-2,6-dimethyloct-4-en-1-yl]-4-hydroxyoxolan-2-one)

3D SDF for NP0210048 ((4s,5s)-5-[(1r,2r,4e,6r,7s)-1,7-dihydroxy-2,6-dimethyloct-4-en-1-yl]-4-hydroxyoxolan-2-one)

3D-SDF for NP0210048 ((4s,5s)-5-[(1r,2r,4e,6r,7s)-1,7-dihydroxy-2,6-dimethyloct-4-en-1-yl]-4-hydroxyoxolan-2-one)

PDB for NP0210048 ((4s,5s)-5-[(1r,2r,4e,6r,7s)-1,7-dihydroxy-2,6-dimethyloct-4-en-1-yl]-4-hydroxyoxolan-2-one)

3D PDB for NP0210048 ((4s,5s)-5-[(1r,2r,4e,6r,7s)-1,7-dihydroxy-2,6-dimethyloct-4-en-1-yl]-4-hydroxyoxolan-2-one)

SMILES for NP0210048 ((4s,5s)-5-[(1r,2r,4e,6r,7s)-1,7-dihydroxy-2,6-dimethyloct-4-en-1-yl]-4-hydroxyoxolan-2-one)

INCHI for NP0210048 ((4s,5s)-5-[(1r,2r,4e,6r,7s)-1,7-dihydroxy-2,6-dimethyloct-4-en-1-yl]-4-hydroxyoxolan-2-one)

Structure for NP0210048 ((4s,5s)-5-[(1r,2r,4e,6r,7s)-1,7-dihydroxy-2,6-dimethyloct-4-en-1-yl]-4-hydroxyoxolan-2-one)

3D Structure for NP0210048 ((4s,5s)-5-[(1r,2r,4e,6r,7s)-1,7-dihydroxy-2,6-dimethyloct-4-en-1-yl]-4-hydroxyoxolan-2-one)