NP-MRD: Showing NP-Card for 6-Deoxyjacareubin (NP0051690)

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Record Information

Version

2.0

Created at

2022-04-27 22:57:48 UTC

Updated at

2022-04-27 22:57:48 UTC

NP-MRD ID

NP0051690

Secondary Accession Numbers

None

Natural Product Identification

Common Name

6-Deoxyjacareubin

Description

6-Deoxyjacareubin belongs to the class of organic compounds known as pyranoxanthones. These are organic aromatic compounds containing a pyran or a hydrogenated derivative fused to a xanthone ring system. 6-Deoxyjacareubin is found in Calophyllum bracteatum, Calophyllum brasilience, Calophyllum brasiliense, Calophyllum brasiliensis, Calophyllum calaba, Calophyllum cuneifolium, Calophyllum fragrans, Calophyllum inophyllum , Calophyllum neo-ebudicum, Calophyllum scriblitifolium, Calophyllum soulattri, Calophyllum tomentosum, Calophyllum trapezifolium, Calophyllum zeylanicum, Cratoxylum formosum, Garcinia bracteata, Garcinia lancilimba, Garcinia merguensis, Garcinia nigrolineata , Garcinia xanthochymus, Hypericum brasiliense, Kielmeyera coriacea Mart., Kielmeyera ferruginea A.P.Duarte., Kielmeyera pumila, Kielmeyera speciosa, Cudrania cochinchinensis , Maclura pomifera, Mourera fluviatilis and Toxylon pomiferum. 6-Deoxyjacareubin is an extremely weak basic (essentially neutral) compound (based on its pKa).

Structure

MOL 3D MOL SDF PDB SMILES InChI

     RDKit          3D

 37 40  0  0  0  0  0  0  0  0999 V2000
   -4.9278    0.0810   -0.3713 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.8208    0.1129    0.6972 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.3640    0.8568    1.9295 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5382   -1.2980    1.0258 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3369   -1.8094    0.9166 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2347   -0.9829    0.4608 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4445    0.3517    0.1381 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4117    1.1876   -0.3059 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.8622    0.6925   -0.4347 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.8488    1.4765   -0.8549 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.0609    0.9951   -0.9746 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.1037    1.7942   -1.4106 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.8363    3.1149   -1.7175 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.3920    1.3230   -1.5490 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.6915    0.0100   -1.2508 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.6533   -0.8166   -0.8082 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.3748   -0.3148   -0.6803 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.3537   -1.1327   -0.2437 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.5284   -2.3356    0.0502 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.0638   -0.6249   -0.1150 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0533   -1.4741    0.3280 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.3347   -2.7891    0.6304 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7263    0.8528    0.2669 O   0  0  0  0  0  0  0  0  0  0  0  0
   -4.6493   -0.6293   -1.1605 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.8287   -0.3369    0.1601 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.1755    1.0847   -0.7231 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5767    1.4879    2.3909 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.1513    1.5397    1.5575 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.7238    0.1310    2.6802 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.3759   -1.9228    1.3713 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1462   -2.8596    1.1653 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6654    2.2148   -0.5351 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.5477    3.7542   -2.0408 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.1895    1.9851   -1.8964 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.6888   -0.3903   -1.3482 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.8187   -1.8554   -0.5575 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3045   -3.4740    0.9512 H   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0
  2  3  1  0
  2 23  1  0
 23  7  1  0
  7  8  2  0
  8  9  1  0
  9 20  2  0
 20 21  1  0
 21 22  1  0
 21  6  2  0
  6  5  1  0
  5  4  2  0
 20 18  1  0
 18 19  2  0
 18 17  1  0
 17 16  2  0
 16 15  1  0
 15 14  2  0
 14 12  1  0
 12 13  1  0
 12 11  2  0
 11 10  1  0
  4  2  1  0
 11 17  1  0
  6  7  1  0
 10  9  1  0
  1 24  1  0
  1 25  1  0
  1 26  1  0
  3 27  1  0
  3 28  1  0
  3 29  1  0
  8 32  1  0
 22 37  1  0
  5 31  1  0
  4 30  1  0
 16 36  1  0
 15 35  1  0
 14 34  1  0
 13 33  1  0
M  END


  Mrv1533004191519332D          

 23 26  0  0  0  0            999 V2000
    1.8612   -2.1123    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
    1.3309   -3.0308    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8579   -2.4750    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.5724   -2.8875    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.2868   -2.4750    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.0013   -2.8875    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.7158   -2.4750    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    6.4302   -2.8875    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.1447   -2.4750    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.1447   -1.6500    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    7.8592   -2.8875    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.8592   -3.7125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.1447   -4.1250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.4302   -3.7125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.7158   -4.1250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.7158   -4.9500    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.0013   -3.7125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.2868   -4.1250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.2868   -4.9500    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.5724   -3.7125    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   -3.7125    0.0000 C   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
  2  4  1  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
  9 10  2  0  0  0  0
 10 11  1  0  0  0  0
 10 12  1  0  0  0  0
 12 13  2  0  0  0  0
 13 14  1  0  0  0  0
 14 15  2  0  0  0  0
  9 15  1  0  0  0  0
 15 16  1  0  0  0  0
 16 17  2  0  0  0  0
 16 18  1  0  0  0  0
  7 18  2  0  0  0  0
 18 19  1  0  0  0  0
 19 20  1  0  0  0  0
 19 21  2  0  0  0  0
  5 21  1  0  0  0  0
 21 22  1  0  0  0  0
 22 23  2  0  0  0  0
  2 23  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0051690

> <DATABASE_NAME>
NP-MRD

> <SMILES>
CC1(C)OC2=CC3=C(C(O)=C2C=C1)C(=O)C1=CC=CC(O)=C1O3

> <INCHI_IDENTIFIER>
InChI=1S/C18H14O5/c1-18(2)7-6-9-12(23-18)8-13-14(15(9)20)16(21)10-4-3-5-11(19)17(10)22-13/h3-8,19-20H,1-2H3

> <INCHI_KEY>
NHNIESSJWQBRJW-UHFFFAOYSA-N

> <FORMULA>
C18H14O5

> <MOLECULAR_WEIGHT>
310.305

> <EXACT_MASS>
310.084123551

> <JCHEM_ACCEPTOR_COUNT>
4

> <JCHEM_ATOM_COUNT>
37

> <JCHEM_AVERAGE_POLARIZABILITY>
32.09082308285871

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
2

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
1

> <JCHEM_IUPAC>
5,10-dihydroxy-2,2-dimethyl-2,6-dihydro-1,11-dioxatetracen-6-one

> <ALOGPS_LOGP>
3.89

> <JCHEM_LOGP>
3.9031329789999987

> <ALOGPS_LOGS>
-3.81

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
4

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA>
8.408863459698033

> <JCHEM_PKA_STRONGEST_ACIDIC>
7.723830507341112

> <JCHEM_PKA_STRONGEST_BASIC>
-3.773278970188447

> <JCHEM_POLAR_SURFACE_AREA>
75.99

> <JCHEM_REFRACTIVITY>
85.17150000000001

> <JCHEM_ROTATABLE_BOND_COUNT>
0

> <JCHEM_RULE_OF_FIVE>
1

> <ALOGPS_SOLUBILITY>
4.80e-02 g/l

> <JCHEM_TRADITIONAL_IUPAC>
6-deoxyjacareubin

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 19-APR-15   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   19-APR-15         0                                  
HETATM    1  C   UNK     0       3.474  -3.943   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0       4.001  -5.390   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0       2.484  -5.657   0.000  0.00  0.00           C+0
HETATM    4  O   UNK     0       5.335  -4.620   0.000  0.00  0.00           O+0
HETATM    5  C   UNK     0       6.668  -5.390   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0       8.002  -4.620   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0       9.336  -5.390   0.000  0.00  0.00           C+0
HETATM    8  O   UNK     0      10.669  -4.620   0.000  0.00  0.00           O+0
HETATM    9  C   UNK     0      12.003  -5.390   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0      13.337  -4.620   0.000  0.00  0.00           C+0
HETATM   11  O   UNK     0      13.337  -3.080   0.000  0.00  0.00           O+0
HETATM   12  C   UNK     0      14.670  -5.390   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0      14.670  -6.930   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0      13.337  -7.700   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0      12.003  -6.930   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0      10.669  -7.700   0.000  0.00  0.00           C+0
HETATM   17  O   UNK     0      10.669  -9.240   0.000  0.00  0.00           O+0
HETATM   18  C   UNK     0       9.336  -6.930   0.000  0.00  0.00           C+0
HETATM   19  C   UNK     0       8.002  -7.700   0.000  0.00  0.00           C+0
HETATM   20  O   UNK     0       8.002  -9.240   0.000  0.00  0.00           O+0
HETATM   21  C   UNK     0       6.668  -6.930   0.000  0.00  0.00           C+0
HETATM   22  C   UNK     0       5.335  -7.700   0.000  0.00  0.00           C+0
HETATM   23  C   UNK     0       4.001  -6.930   0.000  0.00  0.00           C+0
CONECT    1    2                                                            
CONECT    2    1    3    4   23                                             
CONECT    3    2                                                            
CONECT    4    2    5                                                       
CONECT    5    4    6   21                                                  
CONECT    6    5    7                                                       
CONECT    7    6    8   18                                                  
CONECT    8    7    9                                                       
CONECT    9    8   10   15                                                  
CONECT   10    9   11   12                                                  
CONECT   11   10                                                            
CONECT   12   10   13                                                       
CONECT   13   12   14                                                       
CONECT   14   13   15                                                       
CONECT   15   14    9   16                                                  
CONECT   16   15   17   18                                                  
CONECT   17   16                                                            
CONECT   18   16    7   19                                                  
CONECT   19   18   20   21                                                  
CONECT   20   19                                                            
CONECT   21   19    5   22                                                  
CONECT   22   21   23                                                       
CONECT   23   22    2                                                       
MASTER        0    0    0    0    0    0    0    0   23    0   52    0
END

View in JSmol

Synonyms

Value	Source
5,10-Dihydroxy-2,2-dimethylpyrano(3,2-b)xanthen-6(2H)-one	MeSH

Chemical Formula

C₁₈H₁₄O₅

Average Mass

310.3050 Da

Monoisotopic Mass

310.08412 Da

IUPAC Name

5,10-dihydroxy-2,2-dimethyl-2,6-dihydro-1,11-dioxatetracen-6-one

Traditional Name

6-deoxyjacareubin

CAS Registry Number

Not Available

SMILES

CC1(C)OC2=CC3=C(C(O)=C2C=C1)C(=O)C1=CC=CC(O)=C1O3

InChI Identifier

InChI=1S/C18H14O5/c1-18(2)7-6-9-12(23-18)8-13-14(15(9)20)16(21)10-4-3-5-11(19)17(10)22-13/h3-8,19-20H,1-2H3

InChI Key

NHNIESSJWQBRJW-UHFFFAOYSA-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, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 100 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 252 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 1000 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 50 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 200 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 75 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 300 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 101 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 400 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 126 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 500 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 151 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 600 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 176 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 700 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 201 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 800 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 226 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 900 MHz, D₂O, 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
Calophyllum bracteatum	Plant	KNApSAcK
Calophyllum brasilience	Plant	KNApSAcK
Calophyllum brasiliense	LOTUS Database	35616633
Calophyllum brasiliensis	Plant	KNApSAcK
Calophyllum calaba	Plant	KNApSAcK
Calophyllum cuneifolium	Plant	KNApSAcK
Calophyllum fragrans	Plant	KNApSAcK
Calophyllum inophyllum	Plant	KNApSAcK
Calophyllum neo-ebudicum	Plant	KNApSAcK
Calophyllum scriblitifolium	Plant	KNApSAcK
Calophyllum soulattri	Plant	KNApSAcK
Calophyllum tomentosum	Plant	KNApSAcK
Calophyllum trapezifolium	Plant	KNApSAcK
Calophyllum zeylanicum	Plant	KNApSAcK
Cratoxylum formosum	LOTUS Database	35616633
Garcinia bracteata (nom. inval.)	Plant	KNApSAcK
Garcinia lancilimba	Plant	KNApSAcK
Garcinia merguensis	Plant	KNApSAcK
Garcinia nigrolineata	Plant	KNApSAcK
Garcinia xanthochymus	LOTUS Database	35616633
Hypericum brasiliense	LOTUS Database	35616633
Kielmeyera coriacea Mart.	Plant	KNApSAcK
Kielmeyera ferruginea A.P.Duarte.	Plant	KNApSAcK
Kielmeyera pumila	LOTUS Database	35616633
Kielmeyera speciosa	Plant	KNApSAcK
Maclura cochinchinensis	Plant	KNApSAcK
Maclura pomifera	LOTUS Database	35616633
Mourera fluviatilis	LOTUS Database	35616633
Toxylon pomiferum	-	KNApSAcK

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as pyranoxanthones. These are organic aromatic compounds containing a pyran or a hydrogenated derivative fused to a xanthone ring system.

Kingdom

Organic compounds

Super Class

Organoheterocyclic compounds

Class

Benzopyrans

Sub Class

1-benzopyrans

Direct Parent

Pyranoxanthones

Alternative Parents

Substituents

Pyranoxanthone
Pyranochromene
2,2-dimethyl-1-benzopyran
Chromone
1-hydroxy-4-unsubstituted benzenoid
1-hydroxy-2-unsubstituted benzenoid
Alkyl aryl ether
Pyranone
Pyran
Benzenoid
Heteroaromatic compound
Vinylogous acid
Ether
Oxacycle
Organic oxygen compound
Hydrocarbon derivative
Organooxygen compound
Organic oxide
Aromatic heteropolycyclic compound

Molecular Framework

Aromatic heteropolycyclic compounds

External Descriptors

pyranoxanthones (CHEBI:2183 )
xanthenes (C10059 )

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	3.89	ALOGPS
logP	3.9	ChemAxon
logS	-3.8	ALOGPS
pKa (Strongest Acidic)	7.72	ChemAxon
pKa (Strongest Basic)	-3.8	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	4	ChemAxon
Hydrogen Donor Count	2	ChemAxon
Polar Surface Area	75.99 Å²	ChemAxon
Rotatable Bond Count	0	ChemAxon
Refractivity	85.17 m³·mol⁻¹	ChemAxon
Polarizability	32.09 Å³	ChemAxon
Number of Rings	4	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

C00002947

Chemspider ID

Not Available

KEGG Compound ID

C10059

BioCyc ID

Not Available

BiGG ID

Not Available

Wikipedia Link

Not Available

METLIN ID

Not Available

PubChem Compound

5281629

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

Not Available

Showing NP-Card for 6-Deoxyjacareubin (NP0051690)

MOL for NP0051690 (6-Deoxyjacareubin)

3D MOL for NP0051690 (6-Deoxyjacareubin)

3D SDF for NP0051690 (6-Deoxyjacareubin)

3D-SDF for NP0051690 (6-Deoxyjacareubin)

PDB for NP0051690 (6-Deoxyjacareubin)

3D PDB for NP0051690 (6-Deoxyjacareubin)

SMILES for NP0051690 (6-Deoxyjacareubin)

INCHI for NP0051690 (6-Deoxyjacareubin)

Structure for NP0051690 (6-Deoxyjacareubin)

3D Structure for NP0051690 (6-Deoxyjacareubin)