NP-MRD: Showing NP-Card for (4r,6r)-6-{2-[(1s,2s,8ar)-2-methyl-1,2,6,7,8,8a-hexahydronaphthalen-1-yl]ethyl}-4-hydroxyoxan-2-one (NP0214481)

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Record Information

Version

2.0

Created at

2022-09-05 13:47:21 UTC

Updated at

2022-09-05 13:47:21 UTC

NP-MRD ID

NP0214481

Secondary Accession Numbers

None

Natural Product Identification

Common Name

(4r,6r)-6-{2-[(1s,2s,8ar)-2-methyl-1,2,6,7,8,8a-hexahydronaphthalen-1-yl]ethyl}-4-hydroxyoxan-2-one

Description

ML-236C, also known as ML 236C, belongs to the class of organic compounds known as delta valerolactones. These are cyclic organic compounds containing an oxan-2- one moiety. ML-236C is a secondary metabolite. Secondary metabolites are metabolically or physiologically non-essential metabolites that may serve a role as defense or signalling molecules. In some cases they are simply molecules that arise from the incomplete metabolism of other secondary metabolites. (4r,6r)-6-{2-[(1s,2s,8ar)-2-methyl-1,2,6,7,8,8a-hexahydronaphthalen-1-yl]ethyl}-4-hydroxyoxan-2-one is found in Penicillium citrinum. (4r,6r)-6-{2-[(1s,2s,8ar)-2-methyl-1,2,6,7,8,8a-hexahydronaphthalen-1-yl]ethyl}-4-hydroxyoxan-2-one was first documented in 1976 (PMID: 1010803). Based on a literature review very few articles have been published on ML-236C (PMID: 7726991).

Structure

MOL 3D MOL SDF PDB SMILES InChI

     RDKit          3D

 47 49  0  0  0  0  0  0  0  0999 V2000
    0.8365   -2.7953    0.0307 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.0490   -1.9042    1.2279 C   0  0  1  0  0  0  0  0  0  0  0  0
    2.3958   -2.1574    1.7588 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.4552   -1.3660    1.4935 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.2794   -0.1996    0.6430 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.2207    0.7131    0.5930 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.1325    1.9365   -0.2437 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.1694    1.6544   -1.3735 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.8327    1.2602   -0.7353 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.0162   -0.1161   -0.1295 C   0  0  2  0  0  0  0  0  0  0  0  0
    0.9106   -0.4805    0.8377 C   0  0  1  0  0  0  0  0  0  0  0  0
   -0.4462   -0.0754    0.3275 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5205   -0.2952    1.3407 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8953    0.0871    0.9133 C   0  0  2  0  0  0  0  0  0  0  0  0
   -3.4429   -0.6055   -0.2680 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.4031    0.3092   -1.4841 C   0  0  1  0  0  0  0  0  0  0  0  0
   -3.7418   -0.3342   -2.6480 O   0  0  0  0  0  0  0  0  0  0  0  0
   -4.4803    1.3738   -1.2280 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.0516    2.0624    0.0286 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.6519    3.0969    0.4103 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.9839    1.4877    0.7048 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.1275   -3.5841    0.3094 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.8016   -3.2541   -0.2998 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.3870   -2.2127   -0.8134 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.3199   -2.1270    2.0449 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.5330   -3.0327    2.3984 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.4124   -1.6253    1.9254 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.1305    0.6019    1.1832 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.7725    2.7685    0.3965 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.1501    2.1587   -0.6491 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.0676    2.4828   -2.0734 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.5351    0.7145   -1.8721 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.1006    1.2392   -1.5541 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.5759    1.9794    0.0550 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.0135   -0.8498   -0.9575 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.0947    0.1657    1.7473 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3813    1.0460    0.1764 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6752   -0.4750   -0.6682 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5046   -1.3834    1.6031 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3011    0.2289    2.2943 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5703   -0.1171    1.7915 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.5432   -0.8234   -0.1136 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.0023   -1.5957   -0.4854 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4511    0.8750   -1.5508 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.2421    0.2843   -3.2225 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.5972    2.0503   -2.0726 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.4343    0.8331   -0.9570 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
  4  5  1  0
  5  6  2  0
  6  7  1  0
  7  8  1  0
  8  9  1  0
  9 10  1  0
 10 11  1  0
 11 12  1  0
 12 13  1  0
 13 14  1  0
 14 15  1  0
 15 16  1  0
 16 17  1  0
 16 18  1  0
 18 19  1  0
 19 20  2  0
 19 21  1  0
 11  2  1  0
 21 14  1  0
 10  5  1  0
  1 22  1  0
  1 23  1  0
  1 24  1  0
  2 25  1  1
  3 26  1  0
  4 27  1  0
  6 28  1  0
  7 29  1  0
  7 30  1  0
  8 31  1  0
  8 32  1  0
  9 33  1  0
  9 34  1  0
 10 35  1  6
 11 36  1  1
 12 37  1  0
 12 38  1  0
 13 39  1  0
 13 40  1  0
 14 41  1  1
 15 42  1  0
 15 43  1  0
 16 44  1  6
 17 45  1  0
 18 46  1  0
 18 47  1  0
M  END


  Mrv1652309052215472D          

 21 23  0  0  1  0            999 V2000
    0.0000   -1.6500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7145   -1.2375    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    0.7145   -0.4125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4289    0.0000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1434   -0.4125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8579    0.0000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5724   -0.4125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5724   -1.2375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8579   -1.6500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1434   -1.2375    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    1.4289   -1.6500    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    1.4289   -2.4750    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1434   -2.8875    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1434   -3.7125    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    2.8579   -4.1250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8579   -4.9500    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    3.5724   -5.3625    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.1434   -5.3625    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4289   -4.9500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7145   -5.3625    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.4289   -4.1250    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
  2  1  1  1  0  0  0
  2  3  1  0  0  0  0
  3  4  2  0  0  0  0
  4  5  1  0  0  0  0
  5  6  2  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
 10  9  1  6  0  0  0
  5 10  1  0  0  0  0
 10 11  1  0  0  0  0
  2 11  1  0  0  0  0
 11 12  1  1  0  0  0
 12 13  1  0  0  0  0
 14 13  1  6  0  0  0
 14 15  1  0  0  0  0
 15 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
 19 21  1  0  0  0  0
 14 21  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0214481

> <DATABASE_NAME>
NP-MRD

> <SMILES>
C[C@H]1C=CC2=CCCC[C@@H]2[C@H]1CC[C@@H]1C[C@@H](O)CC(=O)O1

> <INCHI_IDENTIFIER>
InChI=1S/C18H26O3/c1-12-6-7-13-4-2-3-5-17(13)16(12)9-8-15-10-14(19)11-18(20)21-15/h4,6-7,12,14-17,19H,2-3,5,8-11H2,1H3/t12-,14+,15+,16-,17-/m0/s1

> <INCHI_KEY>
NXIASLUNMKAUTN-WFKFIOEPSA-N

> <FORMULA>
C18H26O3

> <MOLECULAR_WEIGHT>
290.403

> <EXACT_MASS>
290.188194697

> <JCHEM_ACCEPTOR_COUNT>
2

> <JCHEM_ATOM_COUNT>
47

> <JCHEM_AVERAGE_POLARIZABILITY>
33.168546337402596

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
1

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
1

> <JCHEM_IUPAC>
(4R,6R)-6-{2-[(1S,2S,8aR)-2-methyl-1,2,6,7,8,8a-hexahydronaphthalen-1-yl]ethyl}-4-hydroxyoxan-2-one

> <JCHEM_LOGP>
2.7947164143333323

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
3

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA_STRONGEST_ACIDIC>
14.914537666957496

> <JCHEM_PKA_STRONGEST_BASIC>
-2.8361812244727904

> <JCHEM_POLAR_SURFACE_AREA>
46.53

> <JCHEM_REFRACTIVITY>
84.0874

> <JCHEM_ROTATABLE_BOND_COUNT>
3

> <JCHEM_RULE_OF_FIVE>
1

> <JCHEM_TRADITIONAL_IUPAC>
(4R,6R)-6-{2-[(1S,2S,8aR)-2-methyl-1,2,6,7,8,8a-hexahydronaphthalen-1-yl]ethyl}-4-hydroxyoxan-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       0.000  -3.080   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0       1.334  -2.310   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0       1.334  -0.770   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0       2.667   0.000   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0       4.001  -0.770   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0       5.335   0.000   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0       6.668  -0.770   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0       6.668  -2.310   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0       5.335  -3.080   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0       4.001  -2.310   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0       2.667  -3.080   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0       2.667  -4.620   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0       4.001  -5.390   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0       4.001  -6.930   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0       5.335  -7.700   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0       5.335  -9.240   0.000  0.00  0.00           C+0
HETATM   17  O   UNK     0       6.668 -10.010   0.000  0.00  0.00           O+0
HETATM   18  C   UNK     0       4.001 -10.010   0.000  0.00  0.00           C+0
HETATM   19  C   UNK     0       2.667  -9.240   0.000  0.00  0.00           C+0
HETATM   20  O   UNK     0       1.334 -10.010   0.000  0.00  0.00           O+0
HETATM   21  O   UNK     0       2.667  -7.700   0.000  0.00  0.00           O+0
CONECT    1    2                                                            
CONECT    2    1    3   11                                                  
CONECT    3    2    4                                                       
CONECT    4    3    5                                                       
CONECT    5    4    6   10                                                  
CONECT    6    5    7                                                       
CONECT    7    6    8                                                       
CONECT    8    7    9                                                       
CONECT    9    8   10                                                       
CONECT   10    9    5   11                                                  
CONECT   11   10    2   12                                                  
CONECT   12   11   13                                                       
CONECT   13   12   14                                                       
CONECT   14   13   15   21                                                  
CONECT   15   14   16                                                       
CONECT   16   15   17   18                                                  
CONECT   17   16                                                            
CONECT   18   16   19                                                       
CONECT   19   18   20   21                                                  
CONECT   20   19                                                            
CONECT   21   19   14                                                       
MASTER        0    0    0    0    0    0    0    0   21    0   46    0
END

View in JSmol

Synonyms

Value	Source
(4R,6R)-4-Hydroxy-6-{2-[(1S,2S,8ar)-2-methyl-1,2,6,7,8,8a-hexahydronaphthalen-1-yl]ethyl}oxan-2-one	ChEBI
Antibiotic ML 236C	ChEBI
ML 236C	ChEBI

Chemical Formula

C₁₈H₂₆O₃

Average Mass

290.4030 Da

Monoisotopic Mass

290.18819 Da

IUPAC Name

(4R,6R)-6-{2-[(1S,2S,8aR)-2-methyl-1,2,6,7,8,8a-hexahydronaphthalen-1-yl]ethyl}-4-hydroxyoxan-2-one

Traditional Name

(4R,6R)-6-{2-[(1S,2S,8aR)-2-methyl-1,2,6,7,8,8a-hexahydronaphthalen-1-yl]ethyl}-4-hydroxyoxan-2-one

CAS Registry Number

Not Available

SMILES

C[C@H]1C=CC2=CCCC[C@@H]2[C@H]1CC[C@@H]1C[C@@H](O)CC(=O)O1

InChI Identifier

InChI=1S/C18H26O3/c1-12-6-7-13-4-2-3-5-17(13)16(12)9-8-15-10-14(19)11-18(20)21-15/h4,6-7,12,14-17,19H,2-3,5,8-11H2,1H3/t12-,14+,15+,16-,17-/m0/s1

InChI Key

NXIASLUNMKAUTN-WFKFIOEPSA-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
Penicillium citrinum	LOTUS Database	35616633

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as delta valerolactones. These are cyclic organic compounds containing an oxan-2- one moiety.

Kingdom

Organic compounds

Super Class

Organoheterocyclic compounds

Class

Lactones

Sub Class

Delta valerolactones

Direct Parent

Delta valerolactones

Alternative Parents

Substituents

Delta_valerolactone
Delta valerolactone
Oxane
Secondary alcohol
Carboxylic acid ester
Oxacycle
Monocarboxylic acid or derivatives
Carboxylic acid derivative
Organic oxygen compound
Organic oxide
Hydrocarbon derivative
Organooxygen compound
Carbonyl group
Alcohol
Aliphatic heteropolycyclic compound

Molecular Framework

Aliphatic heteropolycyclic compounds

External Descriptors

delta-lactone (CHEBI:34828 )

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	2.79	ChemAxon
pKa (Strongest Acidic)	14.91	ChemAxon
pKa (Strongest Basic)	-2.8	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	2	ChemAxon
Hydrogen Donor Count	1	ChemAxon
Polar Surface Area	46.53 Å²	ChemAxon
Rotatable Bond Count	3	ChemAxon
Refractivity	84.09 m³·mol⁻¹	ChemAxon
Polarizability	33.17 Å³	ChemAxon
Number of Rings	3	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

C00018117

Chemspider ID

151559

KEGG Compound ID

C14043

BioCyc ID

Not Available

BiGG ID

Not Available

Wikipedia Link

Not Available

METLIN ID

Not Available

PubChem Compound

173650

PDB ID

Not Available

ChEBI ID

34828

Good Scents ID

Not Available

References

General References

Endo A, Kuroda M, Tsujita Y: ML-236A, ML-236B, and ML-236C, new inhibitors of cholesterogenesis produced by Penicillium citrinium. J Antibiot (Tokyo). 1976 Dec;29(12):1346-8. doi: 10.7164/antibiotics.29.1346. [PubMed:1010803 ]
Murakawa S, Sakai K, Endo A: Isolation of 3 alpha-hydroxy-3,5-dihydro ML-236C (sodium salt) from paecilomyces viridis L-68. J Antibiot (Tokyo). 1994 Jan;47(1):108-9. doi: 10.7164/antibiotics.47.108. [PubMed:7726991 ]
LOTUS database [Link]

Showing NP-Card for (4r,6r)-6-{2-[(1s,2s,8ar)-2-methyl-1,2,6,7,8,8a-hexahydronaphthalen-1-yl]ethyl}-4-hydroxyoxan-2-one (NP0214481)

MOL for NP0214481 ((4r,6r)-6-{2-[(1s,2s,8ar)-2-methyl-1,2,6,7,8,8a-hexahydronaphthalen-1-yl]ethyl}-4-hydroxyoxan-2-one)

3D MOL for NP0214481 ((4r,6r)-6-{2-[(1s,2s,8ar)-2-methyl-1,2,6,7,8,8a-hexahydronaphthalen-1-yl]ethyl}-4-hydroxyoxan-2-one)

3D SDF for NP0214481 ((4r,6r)-6-{2-[(1s,2s,8ar)-2-methyl-1,2,6,7,8,8a-hexahydronaphthalen-1-yl]ethyl}-4-hydroxyoxan-2-one)

3D-SDF for NP0214481 ((4r,6r)-6-{2-[(1s,2s,8ar)-2-methyl-1,2,6,7,8,8a-hexahydronaphthalen-1-yl]ethyl}-4-hydroxyoxan-2-one)

PDB for NP0214481 ((4r,6r)-6-{2-[(1s,2s,8ar)-2-methyl-1,2,6,7,8,8a-hexahydronaphthalen-1-yl]ethyl}-4-hydroxyoxan-2-one)

3D PDB for NP0214481 ((4r,6r)-6-{2-[(1s,2s,8ar)-2-methyl-1,2,6,7,8,8a-hexahydronaphthalen-1-yl]ethyl}-4-hydroxyoxan-2-one)

SMILES for NP0214481 ((4r,6r)-6-{2-[(1s,2s,8ar)-2-methyl-1,2,6,7,8,8a-hexahydronaphthalen-1-yl]ethyl}-4-hydroxyoxan-2-one)

INCHI for NP0214481 ((4r,6r)-6-{2-[(1s,2s,8ar)-2-methyl-1,2,6,7,8,8a-hexahydronaphthalen-1-yl]ethyl}-4-hydroxyoxan-2-one)

Structure for NP0214481 ((4r,6r)-6-{2-[(1s,2s,8ar)-2-methyl-1,2,6,7,8,8a-hexahydronaphthalen-1-yl]ethyl}-4-hydroxyoxan-2-one)

3D Structure for NP0214481 ((4r,6r)-6-{2-[(1s,2s,8ar)-2-methyl-1,2,6,7,8,8a-hexahydronaphthalen-1-yl]ethyl}-4-hydroxyoxan-2-one)