NP-MRD: Showing NP-Card for Rhodomollein LIX (NP0350710)

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Record Information

Version

2.0

Created at

2025-02-05 04:45:59 UTC

Updated at

2026-02-08 06:06:21 UTC

NP-MRD ID

NP0350710

Natural Product DOI

https://doi.org/10.57994/3690

Secondary Accession Numbers

None

Natural Product Identification

Common Name

Rhodomollein LIX

Description

Rhodomollein LIX was first documented in 2025 (PMID: 40067880). Based on a literature review very few articles have been published on Rhodomollein LIX.

Structure

MOL SDF PDB SMILES InChI


  Mrv2104 05052304532D          

 37 41  0  0  1  0            999 V2000
    2.0058   -1.0225    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.8114   -0.2207    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    2.4469    0.3060    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    2.6051   -0.5037    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.2335    0.0573    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.9039   -0.6990    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.9512   -0.3495    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.7132    0.7286    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    4.5381    0.7351    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.2230    1.3921    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    3.4717    2.1788    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.2773    2.3567    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.5260    3.1433    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.0358    3.8069    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.5155    4.4781    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.3021    4.2294    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.3086    3.4044    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.8341    1.7479    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.4404    1.1310    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    1.6981    0.7710    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.7868    1.6548    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    2.4376    2.1619    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.4440    2.4052    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.9575    1.4908    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    1.2674    2.2554    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.5864    0.6866    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
   -0.0328    1.0451    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    0.3260    1.7879    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7287    1.3192    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
   -1.5209    1.5492    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4019    2.1088    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.4527    2.2201    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0945    0.0905    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8762    0.4737    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
   -1.3303   -0.2151    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7003    0.5113    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.0083   -0.0441    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
  2  1  1  6  0  0  0
  3  2  1  0  0  0  0
  3  4  1  6  0  0  0
  3  5  1  0  0  0  0
  5  6  1  0  0  0  0
  5  7  1  0  0  0  0
  8  5  1  0  0  0  0
  8  9  1  6  0  0  0
 10  8  1  0  0  0  0
 10 11  1  1  0  0  0
 11 12  1  0  0  0  0
 12 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
 13 17  1  0  0  0  0
 12 18  2  0  0  0  0
 19 10  1  0  0  0  0
 19  3  1  0  0  0  0
 19 20  1  1  0  0  0
 19 21  1  0  0  0  0
 21 22  1  1  0  0  0
 21 23  1  6  0  0  0
 21 24  1  0  0  0  0
 24 25  1  6  0  0  0
 24 26  1  0  0  0  0
 26 27  1  0  0  0  0
 27 28  1  1  0  0  0
 27 29  1  0  0  0  0
 29 30  1  1  0  0  0
 29 31  1  0  0  0  0
 31 32  1  0  0  0  0
 24 32  1  0  0  0  0
 26 33  1  6  0  0  0
 34 33  1  0  0  0  0
 29 34  1  0  0  0  0
 34 35  1  1  0  0  0
 34 36  1  6  0  0  0
 26 37  1  0  0  0  0
  2 37  1  0  0  0  0
M  END


  Mrv2104 05052304532D          

 37 41  0  0  1  0            999 V2000
    2.0058   -1.0225    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.8114   -0.2207    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    2.4469    0.3060    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    2.6051   -0.5037    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.2335    0.0573    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.9039   -0.6990    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.9512   -0.3495    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.7132    0.7286    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    4.5381    0.7351    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.2230    1.3921    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    3.4717    2.1788    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.2773    2.3567    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.5260    3.1433    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.0358    3.8069    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.5155    4.4781    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.3021    4.2294    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.3086    3.4044    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.8341    1.7479    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.4404    1.1310    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    1.6981    0.7710    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.7868    1.6548    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    2.4376    2.1619    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.4440    2.4052    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.9575    1.4908    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    1.2674    2.2554    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.5864    0.6866    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
   -0.0328    1.0451    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    0.3260    1.7879    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7287    1.3192    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
   -1.5209    1.5492    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4019    2.1088    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.4527    2.2201    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0945    0.0905    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8762    0.4737    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
   -1.3303   -0.2151    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7003    0.5113    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.0083   -0.0441    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
  2  1  1  6  0  0  0
  3  2  1  0  0  0  0
  3  4  1  6  0  0  0
  3  5  1  0  0  0  0
  5  6  1  0  0  0  0
  5  7  1  0  0  0  0
  8  5  1  0  0  0  0
  8  9  1  6  0  0  0
 10  8  1  0  0  0  0
 10 11  1  1  0  0  0
 11 12  1  0  0  0  0
 12 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
 13 17  1  0  0  0  0
 12 18  2  0  0  0  0
 19 10  1  0  0  0  0
 19  3  1  0  0  0  0
 19 20  1  1  0  0  0
 19 21  1  0  0  0  0
 21 22  1  1  0  0  0
 21 23  1  6  0  0  0
 21 24  1  0  0  0  0
 24 25  1  6  0  0  0
 24 26  1  0  0  0  0
 26 27  1  0  0  0  0
 27 28  1  1  0  0  0
 27 29  1  0  0  0  0
 29 30  1  1  0  0  0
 29 31  1  0  0  0  0
 31 32  1  0  0  0  0
 24 32  1  0  0  0  0
 26 33  1  6  0  0  0
 34 33  1  0  0  0  0
 29 34  1  0  0  0  0
 34 35  1  1  0  0  0
 34 36  1  6  0  0  0
 26 37  1  0  0  0  0
  2 37  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0350710

> <DATABASE_NAME>
NP-MRD

> <SMILES>
[H][C@]12CC[C@]3([H])[C@@](C[C@@]1(C)O)(C[C@@H](O)[C@@]1(O)[C@@]([H])([C@@H](OC(=O)C4=CC=CO4)[C@H](O)C1(C)C)[C@]3(C)O)[C@@H]2O

> <INCHI_IDENTIFIER>
InChI=1S/C25H36O9/c1-21(2)19(28)16(34-20(29)13-6-5-9-33-13)17-23(4,31)14-8-7-12-18(27)24(14,11-22(12,3)30)10-15(26)25(17,21)32/h5-6,9,12,14-19,26-28,30-32H,7-8,10-11H2,1-4H3/t12-,14+,15-,16-,17+,18-,19+,22-,23-,24+,25-/m1/s1

> <INCHI_KEY>
MIIVYIOMQRFXRD-WYKIBMHASA-N

> <FORMULA>
C25H36O9

> <MOLECULAR_WEIGHT>
480.554

> <EXACT_MASS>
480.235932739

> <JCHEM_ACCEPTOR_COUNT>
7

> <JCHEM_ATOM_COUNT>
70

> <JCHEM_AVERAGE_POLARIZABILITY>
49.94973513213165

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
6

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
0

> <JCHEM_IUPAC>
(1S,3R,4R,6R,7R,8S,9R,10R,13R,14R,16R)-3,4,6,9,14,16-hexahydroxy-5,5,9,14-tetramethyltetracyclo[11.2.1.0^{1,10}.0^{4,8}]hexadecan-7-yl furan-2-carboxylate

> <JCHEM_LOGP>
-0.47269478266666765

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
5

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA>
13.609142600683487

> <JCHEM_PKA_STRONGEST_ACIDIC>
12.891857568535965

> <JCHEM_PKA_STRONGEST_BASIC>
-2.936582017855547

> <JCHEM_POLAR_SURFACE_AREA>
160.82

> <JCHEM_REFRACTIVITY>
118.16619999999998

> <JCHEM_ROTATABLE_BOND_COUNT>
3

> <JCHEM_RULE_OF_FIVE>
0

> <JCHEM_TRADITIONAL_IUPAC>
(1S,3R,4R,6R,7R,8S,9R,10R,13R,14R,16R)-3,4,6,9,14,16-hexahydroxy-5,5,9,14-tetramethyltetracyclo[11.2.1.0^{1,10}.0^{4,8}]hexadecan-7-yl furan-2-carboxylate

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 05-MAY-23   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   05-MAY-23         0                                  
HETATM    1  O   UNK     0       3.744  -1.909   0.000  0.00  0.00           O+0
HETATM    2  C   UNK     0       3.381  -0.412   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0       4.568   0.571   0.000  0.00  0.00           C+0
HETATM    4  O   UNK     0       4.863  -0.940   0.000  0.00  0.00           O+0
HETATM    5  C   UNK     0       6.036   0.107   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0       5.421  -1.305   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0       7.376  -0.652   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0       6.931   1.360   0.000  0.00  0.00           C+0
HETATM    9  O   UNK     0       8.471   1.372   0.000  0.00  0.00           O+0
HETATM   10  C   UNK     0       6.016   2.599   0.000  0.00  0.00           C+0
HETATM   11  O   UNK     0       6.480   4.067   0.000  0.00  0.00           O+0
HETATM   12  C   UNK     0       7.984   4.399   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0       8.449   5.867   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0       7.534   7.106   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0       8.429   8.359   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0       9.897   7.895   0.000  0.00  0.00           C+0
HETATM   17  O   UNK     0       9.909   6.355   0.000  0.00  0.00           O+0
HETATM   18  O   UNK     0       9.024   3.263   0.000  0.00  0.00           O+0
HETATM   19  C   UNK     0       4.555   2.111   0.000  0.00  0.00           C+0
HETATM   20  H   UNK     0       3.170   1.439   0.000  0.00  0.00           H+0
HETATM   21  C   UNK     0       3.335   3.089   0.000  0.00  0.00           C+0
HETATM   22  O   UNK     0       4.550   4.035   0.000  0.00  0.00           O+0
HETATM   23  C   UNK     0       2.695   4.490   0.000  0.00  0.00           C+0
HETATM   24  C   UNK     0       1.787   2.783   0.000  0.00  0.00           C+0
HETATM   25  H   UNK     0       2.366   4.210   0.000  0.00  0.00           H+0
HETATM   26  C   UNK     0       1.095   1.282   0.000  0.00  0.00           C+0
HETATM   27  C   UNK     0      -0.061   1.951   0.000  0.00  0.00           C+0
HETATM   28  O   UNK     0       0.609   3.337   0.000  0.00  0.00           O+0
HETATM   29  C   UNK     0      -1.360   2.462   0.000  0.00  0.00           C+0
HETATM   30  H   UNK     0      -2.839   2.892   0.000  0.00  0.00           H+0
HETATM   31  C   UNK     0      -0.750   3.936   0.000  0.00  0.00           C+0
HETATM   32  C   UNK     0       0.845   4.144   0.000  0.00  0.00           C+0
HETATM   33  C   UNK     0      -0.176   0.169   0.000  0.00  0.00           C+0
HETATM   34  C   UNK     0      -1.635   0.884   0.000  0.00  0.00           C+0
HETATM   35  O   UNK     0      -2.483  -0.401   0.000  0.00  0.00           O+0
HETATM   36  C   UNK     0      -3.174   0.954   0.000  0.00  0.00           C+0
HETATM   37  C   UNK     0       1.882  -0.082   0.000  0.00  0.00           C+0
CONECT    1    2                                                            
CONECT    2    1    3   37                                                  
CONECT    3    2    4    5   19                                             
CONECT    4    3                                                            
CONECT    5    3    6    7    8                                             
CONECT    6    5                                                            
CONECT    7    5                                                            
CONECT    8    5    9   10                                                  
CONECT    9    8                                                            
CONECT   10    8   11   19                                                  
CONECT   11   10   12                                                       
CONECT   12   11   13   18                                                  
CONECT   13   12   14   17                                                  
CONECT   14   13   15                                                       
CONECT   15   14   16                                                       
CONECT   16   15   17                                                       
CONECT   17   16   13                                                       
CONECT   18   12                                                            
CONECT   19   10    3   20   21                                             
CONECT   20   19                                                            
CONECT   21   19   22   23   24                                             
CONECT   22   21                                                            
CONECT   23   21                                                            
CONECT   24   21   25   26   32                                             
CONECT   25   24                                                            
CONECT   26   24   27   33   37                                             
CONECT   27   26   28   29                                                  
CONECT   28   27                                                            
CONECT   29   27   30   31   34                                             
CONECT   30   29                                                            
CONECT   31   29   32                                                       
CONECT   32   31   24                                                       
CONECT   33   26   34                                                       
CONECT   34   33   29   35   36                                             
CONECT   35   34                                                            
CONECT   36   34                                                            
CONECT   37   26    2                                                       
MASTER        0    0    0    0    0    0    0    0   37    0   82    0
END

View in JSmol

Synonyms

Not Available

Chemical Formula

C₂₅H₃₆O₉

Average Mass

480.5540 Da

Monoisotopic Mass

480.23593 Da

IUPAC Name

(1S,3R,4R,6R,7R,8S,9R,10R,13R,14R,16R)-3,4,6,9,14,16-hexahydroxy-5,5,9,14-tetramethyltetracyclo[11.2.1.0^{1,10}.0^{4,8}]hexadecan-7-yl furan-2-carboxylate

Traditional Name

(1S,3R,4R,6R,7R,8S,9R,10R,13R,14R,16R)-3,4,6,9,14,16-hexahydroxy-5,5,9,14-tetramethyltetracyclo[11.2.1.0^{1,10}.0^{4,8}]hexadecan-7-yl furan-2-carboxylate

CAS Registry Number

Not Available

SMILES

[H][C@]12CC[C@]3([H])[C@@](C[C@@]1(C)O)(C[C@@H](O)[C@@]1(O)[C@@]([H])([C@@H](OC(=O)C4=CC=CO4)[C@H](O)C1(C)C)[C@]3(C)O)[C@@H]2O

InChI Identifier

InChI=1S/C25H36O9/c1-21(2)19(28)16(34-20(29)13-6-5-9-33-13)17-23(4,31)14-8-7-12-18(27)24(14,11-22(12,3)30)10-15(26)25(17,21)32/h5-6,9,12,14-19,26-28,30-32H,7-8,10-11H2,1-4H3/t12-,14+,15-,16-,17+,18-,19+,22-,23-,24+,25-/m1/s1

InChI Key

MIIVYIOMQRFXRD-WYKIBMHASA-N

Experimental Spectra

Spectrum Type	Description	Depositor Email	Depositor Organization	Depositor	Deposition Date	View
HSQC NMR	[¹³C, ¹H] NMR Spectrum (2D, 600 MHz, C5D5N, experimental)	songyang@imm.ac.cn	institute of materia medica Chinese Academy of Medical Science & Peking Union Medical College	Song Yang	2025-02-05	View Spectrum
HMBC NMR	[¹³C, ¹H] NMR Spectrum (2D, 600 MHz, C5D5N, experimental)	songyang@imm.ac.cn	institute of materia medica Chinese Academy of Medical Science & Peking Union Medical College	Song Yang	2025-02-05	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 600 MHz, C5D5N, experimental)	songyang@imm.ac.cn	institute of materia medica Chinese Academy of Medical Science & Peking Union Medical College	Song Yang	2025-02-05	View Spectrum
COSY NMR	[¹H, ¹H] NMR Spectrum (2D, 600 MHz, C5D5N, experimental)	songyang@imm.ac.cn	institute of materia medica Chinese Academy of Medical Science & Peking Union Medical College	Song Yang	2025-02-05	View Spectrum
NOESY NMR	[¹H, ¹H] NMR Spectrum (2D, 600 MHz, C5D5N, experimental)	songyang@imm.ac.cn	institute of materia medica Chinese Academy of Medical Science & Peking Union Medical College	Song Yang	2025-02-05	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 151 MHz, C5D5N, experimental)	songyang@imm.ac.cn	institute of materia medica Chinese Academy of Medical Science & Peking Union Medical College	Song Yang	2025-02-05	View Spectrum
DEPT NMR	¹³C NMR Spectrum (1D, 151 MHz, C5D5N, experimental)	songyang@imm.ac.cn	institute of materia medica Chinese Academy of Medical Science & Peking Union Medical College	Song Yang	2025-02-05	View Spectrum

Predicted Spectra

Not Available

Chemical Shift Submissions

Spectrum Type	Description	Depositor Email	Depositor Organization	Depositor	Deposition Date	View
1D NMR	¹H NMR Spectrum (1D, 600.0, Pyridine-d5, simulated)	epoynton@sfu.ca	Not Available	Not Available	2026-02-08	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 150.0, Pyridine-d5, simulated)	epoynton@sfu.ca	Not Available	Not Available	2026-02-08	View Spectrum

Species

Species of Origin

Species Name	Source	Reference
Rhododendron L. Rhododendron molle (Blume) G.Don		Not Available
Rhododendron L. Rhododendron molle (Blume) G.Don		Not Available

Chemical Taxonomy

Classification

Not classified

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	-0.47	ChemAxon
pKa (Strongest Acidic)	12.89	ChemAxon
pKa (Strongest Basic)	-2.9	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	7	ChemAxon
Hydrogen Donor Count	6	ChemAxon
Polar Surface Area	160.82 Å²	ChemAxon
Rotatable Bond Count	3	ChemAxon
Refractivity	118.17 m³·mol⁻¹	ChemAxon
Polarizability	49.95 Å³	ChemAxon
Number of Rings	5	ChemAxon
Bioavailability	Yes	ChemAxon
Rule of Five	No	ChemAxon
Ghose Filter	No	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

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

Not Available

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

Showing NP-Card for Rhodomollein LIX (NP0350710)

MOL for NP0350710 (Rhodomollein LIX)

3D MOL for NP0350710 (Rhodomollein LIX)

3D SDF for NP0350710 (Rhodomollein LIX)

3D-SDF for NP0350710 (Rhodomollein LIX)

PDB for NP0350710 (Rhodomollein LIX)

3D PDB for NP0350710 (Rhodomollein LIX)

SMILES for NP0350710 (Rhodomollein LIX)

INCHI for NP0350710 (Rhodomollein LIX)

Structure for NP0350710 (Rhodomollein LIX)

3D Structure for NP0350710 (Rhodomollein LIX)