NP-MRD: Showing NP-Card for (2r,4s,8r)-4,8-dihydroxy-2-[(1r)-1-hydroxyheptyl]-2,3,4,6,7,8-hexahydro-1-benzopyran-5-one (NP0291415)

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Record Information

Version

1.0

Created at

2022-09-09 22:29:45 UTC

Updated at

2022-09-09 22:29:45 UTC

NP-MRD ID

NP0291415

Secondary Accession Numbers

None

Natural Product Identification

Common Name

(2r,4s,8r)-4,8-dihydroxy-2-[(1r)-1-hydroxyheptyl]-2,3,4,6,7,8-hexahydro-1-benzopyran-5-one

Description

Koninginin D belongs to the class of organic compounds known as benzopyrans. These are organic compounds containing a benzene ring fused to a pyran ring. Pyran a six-membered heterocyclic, non-aromatic ring, made up of five carbon atoms and one oxygen atom and containing two double bonds. (2r,4s,8r)-4,8-dihydroxy-2-[(1r)-1-hydroxyheptyl]-2,3,4,6,7,8-hexahydro-1-benzopyran-5-one is found in Trichoderma koningii. It was first documented in 2011 (PMID: 21301186). Based on a literature review a small amount of articles have been published on Koninginin D (PMID: 28535995) (PMID: 24273867) (PMID: 29685076).

Structure

MOL 3D MOL SDF PDB SMILES InChI

     RDKit          3D

 47 48  0  0  0  0  0  0  0  0999 V2000
    6.6518    0.8153    0.1685 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.3434    0.1339    0.5294 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.2860    1.1013    0.9214 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.9889    0.3835    1.2961 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.4755   -0.4141    0.1334 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.2113   -1.1801    0.3824 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0171   -0.4059    0.7556 C   0  0  1  0  0  0  0  0  0  0  0  0
    0.2348    0.2796    1.9422 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4782    0.5403   -0.3193 C   0  0  1  0  0  0  0  0  0  0  0  0
   -0.5661   -0.0407   -1.6774 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8868   -0.6691   -2.0164 C   0  0  2  0  0  0  0  0  0  0  0  0
   -2.3392   -0.2850   -3.2959 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.9687   -0.3885   -1.0759 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.9348    0.6436   -0.2567 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7077    1.1440    0.1019 O   0  0  0  0  0  0  0  0  0  0  0  0
   -4.2226    1.2251    0.2463 C   0  0  2  0  0  0  0  0  0  0  0  0
   -3.9020    2.1044    1.2774 O   0  0  0  0  0  0  0  0  0  0  0  0
   -5.1942    0.1954    0.7060 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.0384   -1.1637    0.1240 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.1289   -1.2609   -1.0273 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.3859   -2.0969   -1.9325 O   0  0  0  0  0  0  0  0  0  0  0  0
    7.2470    0.0705   -0.4020 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.2356    1.1070    1.0462 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.4052    1.6460   -0.5174 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.0249   -0.3603   -0.4367 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.4419   -0.6541    1.2720 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.5430    1.7374    1.7768 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.0698    1.7841    0.0708 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.1631   -0.2319    2.1995 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.2426    1.1702    1.5842 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.3800    0.3041   -0.7135 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.2530   -1.1972   -0.1162 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.4475   -1.8466    1.2784 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.0479   -1.9251   -0.4277 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8657   -1.0768    0.9709 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1760    1.1987    1.9189 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.2513    1.3787   -0.3376 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3941    0.7594   -2.4593 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.2311   -0.7822   -1.8780 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7756   -1.7912   -2.0916 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.9239   -1.0128   -3.6781 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.6687    1.8314   -0.5658 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.6039    2.7839    1.4390 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.2301    0.5554    0.4426 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.1793    0.1922    1.8302 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.0241   -1.6469   -0.1193 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.5980   -1.8202    0.9306 H   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0
  2  3  1  0
  3  4  1  0
  4  5  1  0
  5  6  1  0
  6  7  1  0
  7  8  1  0
  7  9  1  0
  9 10  1  0
 10 11  1  0
 11 12  1  0
 11 13  1  0
 13 14  2  0
 14 15  1  0
 14 16  1  0
 16 17  1  0
 16 18  1  0
 18 19  1  0
 19 20  1  0
 20 21  2  0
 15  9  1  0
 20 13  1  0
  1 22  1  0
  1 23  1  0
  1 24  1  0
  2 25  1  0
  2 26  1  0
  3 27  1  0
  3 28  1  0
  4 29  1  0
  4 30  1  0
  5 31  1  0
  5 32  1  0
  6 33  1  0
  6 34  1  0
  7 35  1  1
  8 36  1  0
  9 37  1  6
 10 38  1  0
 10 39  1  0
 11 40  1  6
 12 41  1  0
 16 42  1  6
 17 43  1  0
 18 44  1  0
 18 45  1  0
 19 46  1  0
 19 47  1  0
M  END


  Mrv1652309102200292D          

 21 22  0  0  1  0            999 V2000
   -4.2868   -4.1250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5724   -4.5375    0.0000 C   0  0  0  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
   -2.1434   -4.5375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4289   -4.1250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7145   -4.5375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0000   -4.1250    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    0.0000   -3.3000    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.7145   -4.5375    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    0.7145   -5.3625    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4289   -5.7750    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    1.4289   -6.6000    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
    2.1434   -4.5375    0.0000 C   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
    2.8579   -4.1250    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    2.8579   -3.3000    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.5724   -4.5375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5724   -5.3625    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8579   -5.7750    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8579   -6.6000    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  0  0  0  0
  3  4  1  0  0  0  0
  4  5  1  0  0  0  0
  5  6  1  0  0  0  0
  6  7  1  0  0  0  0
  7  8  1  1  0  0  0
  9  7  1  6  0  0  0
  9 10  1  0  0  0  0
 10 11  1  0  0  0  0
 11 12  1  1  0  0  0
 11 13  1  0  0  0  0
 13 14  2  0  0  0  0
 14 15  1  0  0  0  0
  9 15  1  0  0  0  0
 14 16  1  0  0  0  0
 16 17  1  6  0  0  0
 16 18  1  0  0  0  0
 18 19  1  0  0  0  0
 19 20  1  0  0  0  0
 13 20  1  0  0  0  0
 20 21  2  0  0  0  0
M  END
> <DATABASE_ID>
NP0291415

> <DATABASE_NAME>
NP-MRD

> <SMILES>
CCCCCC[C@@H](O)[C@H]1C[C@H](O)C2=C(O1)[C@H](O)CCC2=O

> <INCHI_IDENTIFIER>
InChI=1S/C16H26O5/c1-2-3-4-5-6-10(17)14-9-13(20)15-11(18)7-8-12(19)16(15)21-14/h10,12-14,17,19-20H,2-9H2,1H3/t10-,12-,13+,14-/m1/s1

> <INCHI_KEY>
YSFPWLQJKYZZEG-RUZUBIRVSA-N

> <FORMULA>
C16H26O5

> <MOLECULAR_WEIGHT>
298.379

> <EXACT_MASS>
298.178023937

> <JCHEM_ACCEPTOR_COUNT>
5

> <JCHEM_ATOM_COUNT>
47

> <JCHEM_AVERAGE_POLARIZABILITY>
33.04039043148261

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
3

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
1

> <JCHEM_IUPAC>
(2R,4S,8R)-4,8-dihydroxy-2-[(1R)-1-hydroxyheptyl]-3,4,5,6,7,8-hexahydro-2H-1-benzopyran-5-one

> <JCHEM_LOGP>
0.8472055136666663

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
2

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA>
14.092170725323218

> <JCHEM_PKA_STRONGEST_ACIDIC>
13.569959538336665

> <JCHEM_PKA_STRONGEST_BASIC>
-3.141487943024174

> <JCHEM_POLAR_SURFACE_AREA>
86.99000000000001

> <JCHEM_REFRACTIVITY>
79.50739999999999

> <JCHEM_ROTATABLE_BOND_COUNT>
6

> <JCHEM_RULE_OF_FIVE>
1

> <JCHEM_TRADITIONAL_IUPAC>
(2R,4S,8R)-4,8-dihydroxy-2-[(1R)-1-hydroxyheptyl]-2,3,4,6,7,8-hexahydro-1-benzopyran-5-one

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 10-SEP-22   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   10-SEP-22         0                                  
HETATM    1  C   UNK     0      -8.002  -7.700   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0      -6.668  -8.470   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0      -5.335  -7.700   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0      -4.001  -8.470   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0      -2.667  -7.700   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0      -1.334  -8.470   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0       0.000  -7.700   0.000  0.00  0.00           C+0
HETATM    8  O   UNK     0       0.000  -6.160   0.000  0.00  0.00           O+0
HETATM    9  C   UNK     0       1.334  -8.470   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0       1.334 -10.010   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0       2.667 -10.780   0.000  0.00  0.00           C+0
HETATM   12  O   UNK     0       2.667 -12.320   0.000  0.00  0.00           O+0
HETATM   13  C   UNK     0       4.001 -10.010   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0       4.001  -8.470   0.000  0.00  0.00           C+0
HETATM   15  O   UNK     0       2.667  -7.700   0.000  0.00  0.00           O+0
HETATM   16  C   UNK     0       5.335  -7.700   0.000  0.00  0.00           C+0
HETATM   17  O   UNK     0       5.335  -6.160   0.000  0.00  0.00           O+0
HETATM   18  C   UNK     0       6.668  -8.470   0.000  0.00  0.00           C+0
HETATM   19  C   UNK     0       6.668 -10.010   0.000  0.00  0.00           C+0
HETATM   20  C   UNK     0       5.335 -10.780   0.000  0.00  0.00           C+0
HETATM   21  O   UNK     0       5.335 -12.320   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                                                       
CONECT    7    6    8    9                                                  
CONECT    8    7                                                            
CONECT    9    7   10   15                                                  
CONECT   10    9   11                                                       
CONECT   11   10   12   13                                                  
CONECT   12   11                                                            
CONECT   13   11   14   20                                                  
CONECT   14   13   15   16                                                  
CONECT   15   14    9                                                       
CONECT   16   14   17   18                                                  
CONECT   17   16                                                            
CONECT   18   16   19                                                       
CONECT   19   18   20                                                       
CONECT   20   19   13   21                                                  
CONECT   21   20                                                            
MASTER        0    0    0    0    0    0    0    0   21    0   44    0
END

View in JSmol

Synonyms

Not Available

Chemical Formula

C₁₆H₂₆O₅

Average Mass

298.3790 Da

Monoisotopic Mass

298.17802 Da

IUPAC Name

(2R,4S,8R)-4,8-dihydroxy-2-[(1R)-1-hydroxyheptyl]-3,4,5,6,7,8-hexahydro-2H-1-benzopyran-5-one

Traditional Name

(2R,4S,8R)-4,8-dihydroxy-2-[(1R)-1-hydroxyheptyl]-2,3,4,6,7,8-hexahydro-1-benzopyran-5-one

CAS Registry Number

Not Available

SMILES

CCCCCC[C@@H](O)[C@H]1C[C@H](O)C2=C(O1)[C@H](O)CCC2=O

InChI Identifier

InChI=1S/C16H26O5/c1-2-3-4-5-6-10(17)14-9-13(20)15-11(18)7-8-12(19)16(15)21-14/h10,12-14,17,19-20H,2-9H2,1H3/t10-,12-,13+,14-/m1/s1

InChI Key

YSFPWLQJKYZZEG-RUZUBIRVSA-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
Trichoderma koningii	LOTUS Database	35616633

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as benzopyrans. These are organic compounds containing a benzene ring fused to a pyran ring. Pyran a six-membered heterocyclic, non-aromatic ring, made up of five carbon atoms and one oxygen atom and containing two double bonds.

Kingdom

Organic compounds

Super Class

Organoheterocyclic compounds

Class

Benzopyrans

Sub Class

Not Available

Direct Parent

Benzopyrans

Alternative Parents

Substituents

Benzopyran
Fatty alcohol
Cyclohexenone
Fatty acyl
Vinylogous ester
Secondary alcohol
Ketone
Oxacycle
Organic oxygen compound
Organic oxide
Hydrocarbon derivative
Organooxygen compound
Carbonyl group
Alcohol
Aliphatic heteropolycyclic compound

Molecular Framework

Aliphatic heteropolycyclic 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	0.85	ChemAxon
pKa (Strongest Acidic)	13.57	ChemAxon
pKa (Strongest Basic)	-3.1	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	5	ChemAxon
Hydrogen Donor Count	3	ChemAxon
Polar Surface Area	86.99 Å²	ChemAxon
Rotatable Bond Count	6	ChemAxon
Refractivity	79.51 m³·mol⁻¹	ChemAxon
Polarizability	33.04 Å³	ChemAxon
Number of Rings	2	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

C00023954

Chemspider ID

78440032

KEGG Compound ID

Not Available

BioCyc ID

Not Available

BiGG ID

Not Available

Wikipedia Link

Not Available

METLIN ID

Not Available

PubChem Compound

133554334

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

Rand TG, Chang CT, McMullin DR, Miller JD: Inflammation-associated gene expression in RAW 264.7 macrophages induced by toxins from fungi common on damp building materials. Toxicol In Vitro. 2017 Sep;43:16-20. doi: 10.1016/j.tiv.2017.05.015. Epub 2017 May 20. [PubMed:28535995 ]
Tarawneh AH, Leon F, Radwan MM, Rosa LH, Cutler SJ: Secondary metabolites from the fungus Emericella nidulans. Nat Prod Commun. 2013 Sep;8(9):1285-8. [PubMed:24273867 ]
Chen L, Wu GW, Liu D, Zhuang WY, Yin WB: Trichodermatides E and F from fungus Trichoderma applanatum. J Asian Nat Prod Res. 2019 Jul;21(7):659-665. doi: 10.1080/10286020.2018.1465051. Epub 2018 Apr 23. [PubMed:29685076 ]
Kang D, Kim J, Choi JN, Liu KH, Lee CH: Chemotaxonomy of Trichoderma spp. Using mass spectrometry-based metabolite profiling. J Microbiol Biotechnol. 2011 Jan;21(1):5-13. doi: 10.4014/jmb.1008.08018. [PubMed:21301186 ]
LOTUS database [Link]

Showing NP-Card for (2r,4s,8r)-4,8-dihydroxy-2-[(1r)-1-hydroxyheptyl]-2,3,4,6,7,8-hexahydro-1-benzopyran-5-one (NP0291415)

MOL for NP0291415 ((2r,4s,8r)-4,8-dihydroxy-2-[(1r)-1-hydroxyheptyl]-2,3,4,6,7,8-hexahydro-1-benzopyran-5-one)

3D MOL for NP0291415 ((2r,4s,8r)-4,8-dihydroxy-2-[(1r)-1-hydroxyheptyl]-2,3,4,6,7,8-hexahydro-1-benzopyran-5-one)

3D SDF for NP0291415 ((2r,4s,8r)-4,8-dihydroxy-2-[(1r)-1-hydroxyheptyl]-2,3,4,6,7,8-hexahydro-1-benzopyran-5-one)

3D-SDF for NP0291415 ((2r,4s,8r)-4,8-dihydroxy-2-[(1r)-1-hydroxyheptyl]-2,3,4,6,7,8-hexahydro-1-benzopyran-5-one)

PDB for NP0291415 ((2r,4s,8r)-4,8-dihydroxy-2-[(1r)-1-hydroxyheptyl]-2,3,4,6,7,8-hexahydro-1-benzopyran-5-one)

3D PDB for NP0291415 ((2r,4s,8r)-4,8-dihydroxy-2-[(1r)-1-hydroxyheptyl]-2,3,4,6,7,8-hexahydro-1-benzopyran-5-one)

SMILES for NP0291415 ((2r,4s,8r)-4,8-dihydroxy-2-[(1r)-1-hydroxyheptyl]-2,3,4,6,7,8-hexahydro-1-benzopyran-5-one)

INCHI for NP0291415 ((2r,4s,8r)-4,8-dihydroxy-2-[(1r)-1-hydroxyheptyl]-2,3,4,6,7,8-hexahydro-1-benzopyran-5-one)

Structure for NP0291415 ((2r,4s,8r)-4,8-dihydroxy-2-[(1r)-1-hydroxyheptyl]-2,3,4,6,7,8-hexahydro-1-benzopyran-5-one)

3D Structure for NP0291415 ((2r,4s,8r)-4,8-dihydroxy-2-[(1r)-1-hydroxyheptyl]-2,3,4,6,7,8-hexahydro-1-benzopyran-5-one)