NP-MRD: Showing NP-Card for (1r,17r,18s)-18-hydroxy-17-methoxy-1-methyl-13-oxapentacyclo[10.6.1.0²,¹⁰.0⁵,⁹.0¹⁵,¹⁹]nonadeca-2,4,9,12(19),14-pentaene-6,11,16-trione (NP0258961)

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Record Information

Version

2.0

Created at

2022-09-08 00:40:03 UTC

Updated at

2022-09-08 00:40:03 UTC

NP-MRD ID

NP0258961

Secondary Accession Numbers

None

Natural Product Identification

Common Name

(1r,17r,18s)-18-hydroxy-17-methoxy-1-methyl-13-oxapentacyclo[10.6.1.0²,¹⁰.0⁵,⁹.0¹⁵,¹⁹]nonadeca-2,4,9,12(19),14-pentaene-6,11,16-trione

Description

Beta-Viridin, also known as β-viridin, belongs to the class of organic compounds known as phenanthrenes and derivatives. These are polycyclic compounds containing a phenanthrene moiety, which is a tricyclic aromatic compound with three non-linearly fused benzene. Based on a literature review very few articles have been published on beta-Viridin.

Structure

MOL 3D MOL SDF PDB SMILES InChI


  Mrv1652309082202402D          

 26 30  0  0  1  0            999 V2000
   -0.4374   -1.1109    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.3366   -1.3964    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.9709   -0.8688    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    0.8311   -0.0557    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0570    0.2298    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.4653    0.4719    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4976    1.2963    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.2916    1.5203    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.7500    0.8344    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.2393    0.1864    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.3791   -0.6266    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    2.6313   -1.4122    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.3616   -0.6981    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.6674   -1.4644    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.4839   -1.5827    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.9945   -0.9347    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.6888   -0.1685    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.8723   -0.0502    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5665    0.7161    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.0772    1.3640    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.3230    0.3591    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.0208   -0.0811    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.8178   -0.8807    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.3454   -1.5149    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.7449   -1.1542    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    1.8847   -1.9673    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0  0  0  0
  3  2  1  1  0  0  0
  3  4  1  0  0  0  0
  4  5  2  0  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  2  0  0  0  0
  6 10  1  0  0  0  0
 10 11  1  0  0  0  0
 11 12  1  6  0  0  0
 11 13  1  0  0  0  0
 13 14  2  0  0  0  0
 14 15  1  0  0  0  0
 15 16  2  0  0  0  0
 16 17  1  0  0  0  0
 17 18  2  0  0  0  0
 13 18  1  0  0  0  0
 18 19  1  0  0  0  0
  9 19  1  0  0  0  0
 19 20  2  0  0  0  0
 17 21  1  0  0  0  0
 21 22  1  0  0  0  0
 22 23  1  0  0  0  0
 16 23  1  0  0  0  0
 23 24  2  0  0  0  0
 11 25  1  0  0  0  0
  3 25  1  0  0  0  0
 25 26  1  6  0  0  0
M  END

     RDKit          3D

 42 46  0  0  0  0  0  0  0  0999 V2000
   -4.9528   -0.9753    1.1166 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.8682   -0.1092    1.1441 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.1886   -0.2333   -0.0703 C   0  0  1  0  0  0  0  0  0  0  0  0
   -3.2654    1.0495   -0.8109 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.2616    1.3919   -1.5281 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1278    1.9551   -0.6979 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9035    3.2944   -0.7088 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5974    3.5023   -0.5094 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.0377    2.3568   -0.3686 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9016    1.3854   -0.4886 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7109   -0.0794   -0.4826 C   0  0  1  0  0  0  0  0  0  0  0  0
   -0.8605   -0.4747   -1.9838 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.6623   -0.4274   -0.1392 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.0529   -1.7347    0.0374 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.3658   -2.1042    0.3229 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.3375   -1.1238    0.4380 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.9927    0.1739    0.2719 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.6846    0.5342   -0.0110 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4330    1.9618   -0.1181 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.3303    2.8115   -0.0074 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.2275    0.9915    0.4506 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.3643    0.0285    0.3900 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.7619   -1.3064    0.7300 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.3747   -2.3071    1.1583 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8198   -0.7690    0.2122 C   0  0  2  0  0  0  0  0  0  0  0  0
   -1.8551   -2.1476   -0.1056 O   0  0  0  0  0  0  0  0  0  0  0  0
   -5.5499   -0.9417    2.0444 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.6542   -0.7344    0.2818 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.6126   -2.0294    0.8963 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.7381   -0.9965   -0.6838 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6941    4.0133   -0.8590 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9377   -1.5610   -2.0376 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6956    0.0833   -2.4300 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.1111   -0.1745   -2.4597 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.3757   -2.5729   -0.0335 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.6407   -3.1493    0.4570 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.1637    1.4974    1.4408 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.3665    1.7299   -0.3653 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.1354    0.2896    1.1506 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.8766   -0.0014   -0.5883 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6058   -0.7655    1.3245 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4936   -2.3316   -0.8304 H   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0
  2  3  1  0
  3 25  1  0
 25 26  1  0
 25 11  1  0
 11 12  1  6
 11 10  1  0
 10  9  2  0
  9  8  1  0
  8  7  1  0
  7  6  2  0
  6  4  1  0
  4  5  2  0
  9 19  1  0
 19 20  2  0
 19 18  1  0
 18 17  2  0
 17 21  1  0
 21 22  1  0
 22 23  1  0
 23 24  2  0
 23 16  1  0
 16 15  2  0
 15 14  1  0
 14 13  2  0
  4  3  1  0
 13 18  1  0
 13 11  1  0
  6 10  1  0
 16 17  1  0
  1 27  1  0
  1 28  1  0
  1 29  1  0
  3 30  1  6
 25 41  1  1
 26 42  1  0
 12 32  1  0
 12 33  1  0
 12 34  1  0
  7 31  1  0
 21 37  1  0
 21 38  1  0
 22 39  1  0
 22 40  1  0
 15 36  1  0
 14 35  1  0
M  END


  Mrv1652309082202402D          

 26 30  0  0  1  0            999 V2000
   -0.4374   -1.1109    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.3366   -1.3964    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.9709   -0.8688    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    0.8311   -0.0557    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0570    0.2298    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.4653    0.4719    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4976    1.2963    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.2916    1.5203    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.7500    0.8344    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.2393    0.1864    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.3791   -0.6266    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    2.6313   -1.4122    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.3616   -0.6981    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.6674   -1.4644    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.4839   -1.5827    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.9945   -0.9347    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.6888   -0.1685    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.8723   -0.0502    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5665    0.7161    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.0772    1.3640    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.3230    0.3591    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.0208   -0.0811    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.8178   -0.8807    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.3454   -1.5149    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.7449   -1.1542    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    1.8847   -1.9673    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0  0  0  0
  3  2  1  1  0  0  0
  3  4  1  0  0  0  0
  4  5  2  0  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  2  0  0  0  0
  6 10  1  0  0  0  0
 10 11  1  0  0  0  0
 11 12  1  6  0  0  0
 11 13  1  0  0  0  0
 13 14  2  0  0  0  0
 14 15  1  0  0  0  0
 15 16  2  0  0  0  0
 16 17  1  0  0  0  0
 17 18  2  0  0  0  0
 13 18  1  0  0  0  0
 18 19  1  0  0  0  0
  9 19  1  0  0  0  0
 19 20  2  0  0  0  0
 17 21  1  0  0  0  0
 21 22  1  0  0  0  0
 22 23  1  0  0  0  0
 16 23  1  0  0  0  0
 23 24  2  0  0  0  0
 11 25  1  0  0  0  0
  3 25  1  0  0  0  0
 25 26  1  6  0  0  0
M  END
> <DATABASE_ID>
NP0258961

> <DATABASE_NAME>
NP-MRD

> <SMILES>
CO[C@@H]1[C@@H](O)[C@@]2(C)C3=C(OC=C3C1=O)C(=O)C1=C3CCC(=O)C3=CC=C21

> <INCHI_IDENTIFIER>
InChI=1S/C20H16O6/c1-20-11-5-3-8-9(4-6-12(8)21)13(11)16(23)17-14(20)10(7-26-17)15(22)18(25-2)19(20)24/h3,5,7,18-19,24H,4,6H2,1-2H3/t18-,19+,20+/m0/s1

> <INCHI_KEY>
YEIGUXGHHKAURB-XUVXKRRUSA-N

> <FORMULA>
C20H16O6

> <MOLECULAR_WEIGHT>
352.342

> <EXACT_MASS>
352.094688235

> <JCHEM_ACCEPTOR_COUNT>
5

> <JCHEM_ATOM_COUNT>
42

> <JCHEM_AVERAGE_POLARIZABILITY>
35.4017839942386

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
1

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
1

> <JCHEM_IUPAC>
(1R,17R,18S)-18-hydroxy-17-methoxy-1-methyl-13-oxapentacyclo[10.6.1.0^{2,10}.0^{5,9}.0^{15,19}]nonadeca-2,4,9,12(19),14-pentaene-6,11,16-trione

> <JCHEM_LOGP>
1.2647233459999998

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
5

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA>
14.805496260307578

> <JCHEM_PKA_STRONGEST_ACIDIC>
13.064521774024634

> <JCHEM_PKA_STRONGEST_BASIC>
-3.16595792725604

> <JCHEM_POLAR_SURFACE_AREA>
93.81

> <JCHEM_REFRACTIVITY>
101.96679999999996

> <JCHEM_ROTATABLE_BOND_COUNT>
1

> <JCHEM_RULE_OF_FIVE>
1

> <JCHEM_TRADITIONAL_IUPAC>
(1R,17R,18S)-18-hydroxy-17-methoxy-1-methyl-13-oxapentacyclo[10.6.1.0^{2,10}.0^{5,9}.0^{15,19}]nonadeca-2,4,9,12(19),14-pentaene-6,11,16-trione

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 08-SEP-22   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   08-SEP-22         0                                  
HETATM    1  C   UNK     0      -0.817  -2.074   0.000  0.00  0.00           C+0
HETATM    2  O   UNK     0       0.628  -2.607   0.000  0.00  0.00           O+0
HETATM    3  C   UNK     0       1.812  -1.622   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0       1.551  -0.104   0.000  0.00  0.00           C+0
HETATM    5  O   UNK     0       0.106   0.429   0.000  0.00  0.00           O+0
HETATM    6  C   UNK     0       2.735   0.881   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0       2.796   2.420   0.000  0.00  0.00           C+0
HETATM    8  O   UNK     0       4.278   2.838   0.000  0.00  0.00           O+0
HETATM    9  C   UNK     0       5.133   1.557   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0       4.180   0.348   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0       4.441  -1.170   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0       4.912  -2.636   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0       6.275  -1.303   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0       6.846  -2.733   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0       8.370  -2.954   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0       9.323  -1.745   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0       8.752  -0.315   0.000  0.00  0.00           C+0
HETATM   18  C   UNK     0       7.228  -0.094   0.000  0.00  0.00           C+0
HETATM   19  C   UNK     0       6.657   1.337   0.000  0.00  0.00           C+0
HETATM   20  O   UNK     0       7.611   2.546   0.000  0.00  0.00           O+0
HETATM   21  C   UNK     0       9.936   0.670   0.000  0.00  0.00           C+0
HETATM   22  C   UNK     0      11.239  -0.151   0.000  0.00  0.00           C+0
HETATM   23  C   UNK     0      10.860  -1.644   0.000  0.00  0.00           C+0
HETATM   24  O   UNK     0      11.845  -2.828   0.000  0.00  0.00           O+0
HETATM   25  C   UNK     0       3.257  -2.155   0.000  0.00  0.00           C+0
HETATM   26  O   UNK     0       3.518  -3.672   0.000  0.00  0.00           O+0
CONECT    1    2                                                            
CONECT    2    1    3                                                       
CONECT    3    2    4   25                                                  
CONECT    4    3    5    6                                                  
CONECT    5    4                                                            
CONECT    6    4    7   10                                                  
CONECT    7    6    8                                                       
CONECT    8    7    9                                                       
CONECT    9    8   10   19                                                  
CONECT   10    9    6   11                                                  
CONECT   11   10   12   13   25                                             
CONECT   12   11                                                            
CONECT   13   11   14   18                                                  
CONECT   14   13   15                                                       
CONECT   15   14   16                                                       
CONECT   16   15   17   23                                                  
CONECT   17   16   18   21                                                  
CONECT   18   17   13   19                                                  
CONECT   19   18    9   20                                                  
CONECT   20   19                                                            
CONECT   21   17   22                                                       
CONECT   22   21   23                                                       
CONECT   23   22   16   24                                                  
CONECT   24   23                                                            
CONECT   25   11    3   26                                                  
CONECT   26   25                                                            
MASTER        0    0    0    0    0    0    0    0   26    0   60    0
END

View in JSmol

Synonyms

Value	Source
b-Viridin	Generator
Β-viridin	Generator

Chemical Formula

C₂₀H₁₆O₆

Average Mass

352.3420 Da

Monoisotopic Mass

352.09469 Da

IUPAC Name

Not Available

Traditional Name

Not Available

CAS Registry Number

Not Available

SMILES

CO[C@@H]1[C@@H](O)[C@@]2(C)C3=C(OC=C3C1=O)C(=O)C1=C3CCC(=O)C3=CC=C21

InChI Identifier

InChI=1S/C20H16O6/c1-20-11-5-3-8-9(4-6-12(8)21)13(11)16(23)17-14(20)10(7-26-17)15(22)18(25-2)19(20)24/h3,5,7,18-19,24H,4,6H2,1-2H3/t18-,19+,20+/m0/s1

InChI Key

YEIGUXGHHKAURB-XUVXKRRUSA-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 phenanthrenes and derivatives. These are polycyclic compounds containing a phenanthrene moiety, which is a tricyclic aromatic compound with three non-linearly fused benzene.

Kingdom

Organic compounds

Super Class

Benzenoids

Class

Phenanthrenes and derivatives

Sub Class

Not Available

Direct Parent

Phenanthrenes and derivatives

Alternative Parents

Substituents

Phenanthrene
Naphthofuran
Indanone
Naphthalene
Indane
Aryl alkyl ketone
Aryl ketone
Furan
Heteroaromatic compound
Ketone
Secondary alcohol
Dialkyl ether
Ether
Oxacycle
Organoheterocyclic compound
Organic oxide
Organic oxygen compound
Hydrocarbon derivative
Alcohol
Organooxygen compound
Aromatic heteropolycyclic compound

Molecular Framework

Aromatic 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

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

Not Available

KEGG Compound ID

Not Available

BioCyc ID

Not Available

BiGG ID

Not Available

Wikipedia Link

Not Available

METLIN ID

Not Available

PubChem Compound

101305711

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

LOTUS database [Link]

Showing NP-Card for (1r,17r,18s)-18-hydroxy-17-methoxy-1-methyl-13-oxapentacyclo[10.6.1.0²,¹⁰.0⁵,⁹.0¹⁵,¹⁹]nonadeca-2,4,9,12(19),14-pentaene-6,11,16-trione (NP0258961)

MOL for NP0258961 ((1r,17r,18s)-18-hydroxy-17-methoxy-1-methyl-13-oxapentacyclo[10.6.1.0²,¹⁰.0⁵,⁹.0¹⁵,¹⁹]nonadeca-2,4,9,12(19),14-pentaene-6,11,16-trione)

3D MOL for NP0258961 ((1r,17r,18s)-18-hydroxy-17-methoxy-1-methyl-13-oxapentacyclo[10.6.1.0²,¹⁰.0⁵,⁹.0¹⁵,¹⁹]nonadeca-2,4,9,12(19),14-pentaene-6,11,16-trione)

3D SDF for NP0258961 ((1r,17r,18s)-18-hydroxy-17-methoxy-1-methyl-13-oxapentacyclo[10.6.1.0²,¹⁰.0⁵,⁹.0¹⁵,¹⁹]nonadeca-2,4,9,12(19),14-pentaene-6,11,16-trione)

3D-SDF for NP0258961 ((1r,17r,18s)-18-hydroxy-17-methoxy-1-methyl-13-oxapentacyclo[10.6.1.0²,¹⁰.0⁵,⁹.0¹⁵,¹⁹]nonadeca-2,4,9,12(19),14-pentaene-6,11,16-trione)

PDB for NP0258961 ((1r,17r,18s)-18-hydroxy-17-methoxy-1-methyl-13-oxapentacyclo[10.6.1.0²,¹⁰.0⁵,⁹.0¹⁵,¹⁹]nonadeca-2,4,9,12(19),14-pentaene-6,11,16-trione)

3D PDB for NP0258961 ((1r,17r,18s)-18-hydroxy-17-methoxy-1-methyl-13-oxapentacyclo[10.6.1.0²,¹⁰.0⁵,⁹.0¹⁵,¹⁹]nonadeca-2,4,9,12(19),14-pentaene-6,11,16-trione)

SMILES for NP0258961 ((1r,17r,18s)-18-hydroxy-17-methoxy-1-methyl-13-oxapentacyclo[10.6.1.0²,¹⁰.0⁵,⁹.0¹⁵,¹⁹]nonadeca-2,4,9,12(19),14-pentaene-6,11,16-trione)

INCHI for NP0258961 ((1r,17r,18s)-18-hydroxy-17-methoxy-1-methyl-13-oxapentacyclo[10.6.1.0²,¹⁰.0⁵,⁹.0¹⁵,¹⁹]nonadeca-2,4,9,12(19),14-pentaene-6,11,16-trione)

Structure for NP0258961 ((1r,17r,18s)-18-hydroxy-17-methoxy-1-methyl-13-oxapentacyclo[10.6.1.0²,¹⁰.0⁵,⁹.0¹⁵,¹⁹]nonadeca-2,4,9,12(19),14-pentaene-6,11,16-trione)

3D Structure for NP0258961 ((1r,17r,18s)-18-hydroxy-17-methoxy-1-methyl-13-oxapentacyclo[10.6.1.0²,¹⁰.0⁵,⁹.0¹⁵,¹⁹]nonadeca-2,4,9,12(19),14-pentaene-6,11,16-trione)