NP-MRD: Showing NP-Card for (1r,8r,9s,12r)-8,9-dihydroxy-3-(hydroxymethyl)-8,12-dimethyl-5,14-dioxatricyclo[7.4.1.0²,⁶]tetradeca-2,6-diene-4,11-dione (NP0253773)

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Record Information

Version

2.0

Created at

2022-09-07 17:44:39 UTC

Updated at

2022-09-07 17:44:40 UTC

NP-MRD ID

NP0253773

Secondary Accession Numbers

None

Natural Product Identification

Common Name

(1r,8r,9s,12r)-8,9-dihydroxy-3-(hydroxymethyl)-8,12-dimethyl-5,14-dioxatricyclo[7.4.1.0²,⁶]tetradeca-2,6-diene-4,11-dione

Description

(3S,4R,5E,8R,10R)-3,8-Epoxy-3,4,6,13-tetrahydroxy-1-oxogermacra-5,7(11)-diene-12-oic acid 12,6-lactone belongs to the class of organic compounds known as oxepanes. Oxepanes are compounds containing an oxepane ring, which is a seven-member saturated aliphatic heterocycle with one oxygen and six carbon atoms. Based on a literature review very few articles have been published on (3S,4R,5E,8R,10R)-3,8-Epoxy-3,4,6,13-tetrahydroxy-1-oxogermacra-5,7(11)-diene-12-oic acid 12,6-lactone.

Structure

MOL 3D MOL SDF PDB SMILES InChI

     RDKit          3D

 40 42  0  0  0  0  0  0  0  0999 V2000
   -1.4067    1.8610   -2.1205 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0636    2.2452   -0.6721 C   0  0  2  0  0  0  0  0  0  0  0  0
    0.4226    1.9118   -0.3808 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.4887    0.6854    0.3463 C   0  0  1  0  0  0  0  0  0  0  0  0
   -0.5622   -0.0388   -0.2449 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3414   -0.4724    0.7830 C   0  0  1  0  0  0  0  0  0  0  0  0
   -0.9722   -0.2011    2.0842 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5672    0.3124    0.5137 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0511    1.7233    0.2559 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6037    2.5142    0.9913 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2882   -1.9352    0.6668 C   0  0  2  0  0  0  0  0  0  0  0  0
   -1.8342   -2.4939   -0.6252 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0359   -2.5004    1.7015 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.1247   -2.3488    0.8972 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.2888   -1.7554    0.6193 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.5110   -2.3845    0.5320 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.4887   -1.4779    0.2314 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.7266   -1.6266    0.0625 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.8352   -0.1502    0.1167 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5266    1.1112   -0.1821 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.1200    0.9313   -1.4613 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.5509   -0.3106    0.3418 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6286    2.3465   -2.7601 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3562    2.4140   -2.3376 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4823    0.7834   -2.2555 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1127    3.3523   -0.6673 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.8430    2.7720    0.2326 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.8771    1.8699   -1.3733 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.3000    0.9567    1.4035 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7679    0.0068    2.6361 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.2295    0.2685    1.3702 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.0379   -0.0537   -0.4347 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1831   -2.3337   -1.4892 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9689   -3.6013   -0.4858 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8413   -2.0828   -0.7651 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5840   -2.2231    2.5427 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.2327   -3.3336    1.3891 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.4221    1.2660    0.4750 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.9204    2.0070   -0.2690 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.2398   -0.0146   -1.6682 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  1
  6  8  1  0
  8  9  1  0
  9 10  2  0
  6 11  1  0
 11 12  1  0
 11 13  1  1
 11 14  1  0
 14 15  2  0
 15 16  1  0
 16 17  1  0
 17 18  2  0
 17 19  1  0
 19 20  1  0
 20 21  1  0
 19 22  2  0
  9  2  1  0
 22 15  1  0
 22  4  1  0
  1 23  1  0
  1 24  1  0
  1 25  1  0
  2 26  1  6
  3 27  1  0
  3 28  1  0
  4 29  1  1
  7 30  1  0
  8 31  1  0
  8 32  1  0
 12 33  1  0
 12 34  1  0
 12 35  1  0
 13 36  1  0
 14 37  1  0
 20 38  1  0
 20 39  1  0
 21 40  1  0
M  END


  Mrv1652309072219442D          

 22 24  0  0  1  0            999 V2000
    6.3762    0.7173    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.8851    0.0543    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    5.0446    0.1965    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.3430   -0.3343    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    4.6863   -1.0123    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.0221   -1.6940    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    5.3927   -2.4311    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.8679   -1.4521    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.2592   -0.6947    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.0842   -0.7004    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.3309   -2.2228    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    4.9775   -2.7353    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.9925   -2.9752    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.4911   -2.0742    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.1193   -1.3299    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.3043   -1.2024    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.1736   -0.3878    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4378   -0.0148    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.9079   -0.0119    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.0354    0.8032    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.8050    1.1004    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.4924   -0.5941    0.0000 C   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  1  0  0  0  0
  4  5  1  1  0  0  0
  5  6  1  0  0  0  0
  6  7  1  6  0  0  0
  6  8  1  0  0  0  0
  8  9  1  0  0  0  0
  2  9  1  0  0  0  0
  9 10  2  0  0  0  0
  6 11  1  0  0  0  0
 11 12  1  1  0  0  0
 11 13  1  6  0  0  0
 11 14  1  0  0  0  0
 14 15  2  0  0  0  0
 15 16  1  0  0  0  0
 16 17  1  0  0  0  0
 17 18  2  0  0  0  0
 17 19  1  0  0  0  0
 19 20  1  0  0  0  0
 20 21  1  0  0  0  0
 19 22  2  0  0  0  0
 15 22  1  0  0  0  0
  4 22  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0253773

> <DATABASE_NAME>
NP-MRD

> <SMILES>
C[C@@H]1C[C@H]2O[C@@](O)(CC1=O)[C@](C)(O)C=C1OC(=O)C(CO)=C21

> <INCHI_IDENTIFIER>
InChI=1S/C15H18O7/c1-7-3-10-12-8(6-16)13(18)21-11(12)5-14(2,19)15(20,22-10)4-9(7)17/h5,7,10,16,19-20H,3-4,6H2,1-2H3/t7-,10-,14-,15+/m1/s1

> <INCHI_KEY>
RNIHHDCNVISFGS-QPDJSOBASA-N

> <FORMULA>
C15H18O7

> <MOLECULAR_WEIGHT>
310.302

> <EXACT_MASS>
310.10525292

> <JCHEM_ACCEPTOR_COUNT>
6

> <JCHEM_ATOM_COUNT>
40

> <JCHEM_AVERAGE_POLARIZABILITY>
29.756963983092195

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
3

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
0

> <JCHEM_IUPAC>
(1R,8R,9S,12R)-8,9-dihydroxy-3-(hydroxymethyl)-8,12-dimethyl-5,14-dioxatricyclo[7.4.1.0^{2,6}]tetradeca-2,6-diene-4,11-dione

> <JCHEM_LOGP>
-0.5035390970000001

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
3

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA>
13.233410126189515

> <JCHEM_PKA_STRONGEST_ACIDIC>
10.72012218428822

> <JCHEM_PKA_STRONGEST_BASIC>
-2.8740358658185716

> <JCHEM_POLAR_SURFACE_AREA>
113.29

> <JCHEM_REFRACTIVITY>
75.35

> <JCHEM_ROTATABLE_BOND_COUNT>
1

> <JCHEM_RULE_OF_FIVE>
1

> <JCHEM_TRADITIONAL_IUPAC>
(1R,8R,9S,12R)-8,9-dihydroxy-3-(hydroxymethyl)-8,12-dimethyl-5,14-dioxatricyclo[7.4.1.0^{2,6}]tetradeca-2,6-diene-4,11-dione

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 07-SEP-22   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   07-SEP-22         0                                  
HETATM    1  C   UNK     0      11.902   1.339   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0      10.986   0.101   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0       9.417   0.367   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0       8.107  -0.624   0.000  0.00  0.00           C+0
HETATM    5  O   UNK     0       8.748  -1.890   0.000  0.00  0.00           O+0
HETATM    6  C   UNK     0       9.375  -3.162   0.000  0.00  0.00           C+0
HETATM    7  O   UNK     0      10.066  -4.538   0.000  0.00  0.00           O+0
HETATM    8  C   UNK     0      10.953  -2.711   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0      11.684  -1.297   0.000  0.00  0.00           C+0
HETATM   10  O   UNK     0      13.224  -1.307   0.000  0.00  0.00           O+0
HETATM   11  C   UNK     0       8.084  -4.149   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0       9.291  -5.106   0.000  0.00  0.00           C+0
HETATM   13  O   UNK     0       7.453  -5.554   0.000  0.00  0.00           O+0
HETATM   14  C   UNK     0       6.517  -3.872   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0       5.823  -2.482   0.000  0.00  0.00           C+0
HETATM   16  O   UNK     0       4.301  -2.245   0.000  0.00  0.00           O+0
HETATM   17  C   UNK     0       4.057  -0.724   0.000  0.00  0.00           C+0
HETATM   18  O   UNK     0       2.684  -0.028   0.000  0.00  0.00           O+0
HETATM   19  C   UNK     0       5.428  -0.022   0.000  0.00  0.00           C+0
HETATM   20  C   UNK     0       5.666   1.499   0.000  0.00  0.00           C+0
HETATM   21  O   UNK     0       7.103   2.054   0.000  0.00  0.00           O+0
HETATM   22  C   UNK     0       6.519  -1.109   0.000  0.00  0.00           C+0
CONECT    1    2                                                            
CONECT    2    1    3    9                                                  
CONECT    3    2    4                                                       
CONECT    4    3    5   22                                                  
CONECT    5    4    6                                                       
CONECT    6    5    7    8   11                                             
CONECT    7    6                                                            
CONECT    8    6    9                                                       
CONECT    9    8    2   10                                                  
CONECT   10    9                                                            
CONECT   11    6   12   13   14                                             
CONECT   12   11                                                            
CONECT   13   11                                                            
CONECT   14   11   15                                                       
CONECT   15   14   16   22                                                  
CONECT   16   15   17                                                       
CONECT   17   16   18   19                                                  
CONECT   18   17                                                            
CONECT   19   17   20   22                                                  
CONECT   20   19   21                                                       
CONECT   21   20                                                            
CONECT   22   19   15    4                                                  
MASTER        0    0    0    0    0    0    0    0   22    0   48    0
END

View in JSmol

Synonyms

Value	Source
(3S,4R,5E,8R,10R)-3,8-Epoxy-3,4,6,13-tetrahydroxy-1-oxogermacra-5,7(11)-diene-12-Oate 12,6-lactone	Generator

Chemical Formula

C₁₅H₁₈O₇

Average Mass

310.3020 Da

Monoisotopic Mass

310.10525 Da

IUPAC Name

(1R,8R,9S,12R)-8,9-dihydroxy-3-(hydroxymethyl)-8,12-dimethyl-5,14-dioxatricyclo[7.4.1.0^{2,6}]tetradeca-2,6-diene-4,11-dione

Traditional Name

(1R,8R,9S,12R)-8,9-dihydroxy-3-(hydroxymethyl)-8,12-dimethyl-5,14-dioxatricyclo[7.4.1.0^{2,6}]tetradeca-2,6-diene-4,11-dione

CAS Registry Number

Not Available

SMILES

C[C@@H]1C[C@H]2O[C@@](O)(CC1=O)[C@](C)(O)C=C1OC(=O)C(CO)=C21

InChI Identifier

InChI=1S/C15H18O7/c1-7-3-10-12-8(6-16)13(18)21-11(12)5-14(2,19)15(20,22-10)4-9(7)17/h5,7,10,16,19-20H,3-4,6H2,1-2H3/t7-,10-,14-,15+/m1/s1

InChI Key

RNIHHDCNVISFGS-QPDJSOBASA-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

Not Available

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as oxepanes. Oxepanes are compounds containing an oxepane ring, which is a seven-member saturated aliphatic heterocycle with one oxygen and six carbon atoms.

Kingdom

Organic compounds

Super Class

Organoheterocyclic compounds

Class

Oxepanes

Sub Class

Not Available

Direct Parent

Oxepanes

Alternative Parents

Substituents

Oxepane
2-furanone
Dihydrofuran
Enol ester
Alpha,beta-unsaturated carboxylic ester
Enoate ester
Tertiary alcohol
Carboxylic acid ester
Hemiacetal
Ketone
Lactone
Cyclic ketone
Monocarboxylic acid or derivatives
Oxacycle
Carboxylic acid derivative
Carbonyl group
Organic oxygen compound
Hydrocarbon derivative
Organic oxide
Alcohol
Organooxygen compound
Primary 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	-0.5	ChemAxon
pKa (Strongest Acidic)	10.72	ChemAxon
pKa (Strongest Basic)	-2.9	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	6	ChemAxon
Hydrogen Donor Count	3	ChemAxon
Polar Surface Area	113.29 Å²	ChemAxon
Rotatable Bond Count	1	ChemAxon
Refractivity	75.35 m³·mol⁻¹	ChemAxon
Polarizability	29.76 Å³	ChemAxon
Number of Rings	3	ChemAxon
Bioavailability	Yes	ChemAxon
Rule of Five	Yes	ChemAxon
Ghose Filter	No	ChemAxon
Veber's Rule	No	ChemAxon
MDDR-like Rule	No	ChemAxon

External Links

HMDB ID

Not Available

DrugBank ID

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Phenol Explorer Compound ID

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FoodDB ID

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KNApSAcK ID

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Chemspider ID

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KEGG Compound ID

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BioCyc ID

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BiGG ID

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Wikipedia Link

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METLIN ID

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PubChem Compound

101228643

PDB ID

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ChEBI ID

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Good Scents ID

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References

General References

LOTUS database [Link]

Showing NP-Card for (1r,8r,9s,12r)-8,9-dihydroxy-3-(hydroxymethyl)-8,12-dimethyl-5,14-dioxatricyclo[7.4.1.0²,⁶]tetradeca-2,6-diene-4,11-dione (NP0253773)

MOL for NP0253773 ((1r,8r,9s,12r)-8,9-dihydroxy-3-(hydroxymethyl)-8,12-dimethyl-5,14-dioxatricyclo[7.4.1.0²,⁶]tetradeca-2,6-diene-4,11-dione)

3D MOL for NP0253773 ((1r,8r,9s,12r)-8,9-dihydroxy-3-(hydroxymethyl)-8,12-dimethyl-5,14-dioxatricyclo[7.4.1.0²,⁶]tetradeca-2,6-diene-4,11-dione)

3D SDF for NP0253773 ((1r,8r,9s,12r)-8,9-dihydroxy-3-(hydroxymethyl)-8,12-dimethyl-5,14-dioxatricyclo[7.4.1.0²,⁶]tetradeca-2,6-diene-4,11-dione)

3D-SDF for NP0253773 ((1r,8r,9s,12r)-8,9-dihydroxy-3-(hydroxymethyl)-8,12-dimethyl-5,14-dioxatricyclo[7.4.1.0²,⁶]tetradeca-2,6-diene-4,11-dione)

PDB for NP0253773 ((1r,8r,9s,12r)-8,9-dihydroxy-3-(hydroxymethyl)-8,12-dimethyl-5,14-dioxatricyclo[7.4.1.0²,⁶]tetradeca-2,6-diene-4,11-dione)

3D PDB for NP0253773 ((1r,8r,9s,12r)-8,9-dihydroxy-3-(hydroxymethyl)-8,12-dimethyl-5,14-dioxatricyclo[7.4.1.0²,⁶]tetradeca-2,6-diene-4,11-dione)

SMILES for NP0253773 ((1r,8r,9s,12r)-8,9-dihydroxy-3-(hydroxymethyl)-8,12-dimethyl-5,14-dioxatricyclo[7.4.1.0²,⁶]tetradeca-2,6-diene-4,11-dione)

INCHI for NP0253773 ((1r,8r,9s,12r)-8,9-dihydroxy-3-(hydroxymethyl)-8,12-dimethyl-5,14-dioxatricyclo[7.4.1.0²,⁶]tetradeca-2,6-diene-4,11-dione)

Structure for NP0253773 ((1r,8r,9s,12r)-8,9-dihydroxy-3-(hydroxymethyl)-8,12-dimethyl-5,14-dioxatricyclo[7.4.1.0²,⁶]tetradeca-2,6-diene-4,11-dione)

3D Structure for NP0253773 ((1r,8r,9s,12r)-8,9-dihydroxy-3-(hydroxymethyl)-8,12-dimethyl-5,14-dioxatricyclo[7.4.1.0²,⁶]tetradeca-2,6-diene-4,11-dione)