NP-MRD: Showing NP-Card for (9e)-16-chloro-17,19-dihydroxy-4-methyl-3,7-dioxatricyclo[13.4.0.0⁶,⁸]nonadeca-1(19),9,11,15,17-pentaene-2,13-dione (NP0280502)

Jump To Section:

Identification Spectra BioTaxonomy ChemoTaxonomy Physical properties Links References XML

Record Information

Version

2.0

Created at

2022-09-09 06:19:47 UTC

Updated at

2022-09-09 06:19:47 UTC

NP-MRD ID

NP0280502

Secondary Accession Numbers

None

Natural Product Identification

Common Name

(9e)-16-chloro-17,19-dihydroxy-4-methyl-3,7-dioxatricyclo[13.4.0.0⁶,⁸]nonadeca-1(19),9,11,15,17-pentaene-2,13-dione

Description

Radicicol, also known as monorden or KF9-a, belongs to the class of organic compounds known as hydroxybenzoic acid derivatives. Hydroxybenzoic acid derivatives are compounds containing a hydroxybenzoic acid (or a derivative), which is a benzene ring bearing a carboxyl and a hydroxyl groups. (9e)-16-chloro-17,19-dihydroxy-4-methyl-3,7-dioxatricyclo[13.4.0.0⁶,⁸]nonadeca-1(19),9,11,15,17-pentaene-2,13-dione is found in Fusarium tenuicristatum. (9e)-16-chloro-17,19-dihydroxy-4-methyl-3,7-dioxatricyclo[13.4.0.0⁶,⁸]nonadeca-1(19),9,11,15,17-pentaene-2,13-dione was first documented in 2022 (PMID: 35841121). Based on a literature review a small amount of articles have been published on radicicol (PMID: 35421731) (PMID: 35752988) (PMID: 35569376).

Structure

MOL 3D MOL SDF PDB SMILES InChI


  Mrv1652309092208192D          

 25 27  0  0  0  0            999 V2000
    6.7929   -0.4626    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.4184   -1.1977    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.8678   -1.8895    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.6917   -1.8463    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.5156   -1.8030    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    8.1411   -2.5382    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.7666   -3.2733    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.9427   -3.3165    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.5682   -4.0516    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.7444   -4.0949    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.2950   -3.4030    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.6695   -2.6679    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.4711   -3.4462    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.0217   -2.7544    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.1979   -2.7976    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8234   -3.5327    0.0000 Cl  0  0  0  0  0  0  0  0  0  0  0  0
    2.7485   -2.1057    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.9246   -2.1490    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.1230   -1.3706    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.9468   -1.3274    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.3213   -0.5923    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.3962   -2.0193    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.2201   -1.9760    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.9903   -2.2716    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.5946   -1.2409    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
  4  6  1  0  0  0  0
  6  7  1  0  0  0  0
  7  8  2  0  0  0  0
  9  8  1  4  0  0  0
  9 10  2  0  0  0  0
 10 11  1  0  0  0  0
 11 12  2  0  0  0  0
 11 13  1  0  0  0  0
 13 14  1  0  0  0  0
 14 15  2  0  0  0  0
 15 16  1  0  0  0  0
 15 17  1  0  0  0  0
 17 18  1  0  0  0  0
 17 19  2  0  0  0  0
 19 20  1  0  0  0  0
 20 21  1  0  0  0  0
 20 22  2  0  0  0  0
 14 22  1  0  0  0  0
 22 23  1  0  0  0  0
 23 24  2  0  0  0  0
 23 25  1  0  0  0  0
  2 25  1  0  0  0  0
M  END

     RDKit          3D

 42 44  0  0  0  0  0  0  0  0999 V2000
    2.0245   -2.0350    1.4954 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.6538   -1.8527    0.0046 C   0  0  2  0  0  0  0  0  0  0  0  0
    2.0468   -0.5094   -0.4835 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.4449   -0.2433   -0.8649 C   0  0  1  0  0  0  0  0  0  0  0  0
    3.3901    1.0426   -1.6672 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.9509    1.1055   -0.4301 C   0  0  1  0  0  0  0  0  0  0  0  0
    3.2967    1.5240    0.7970 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.3022    2.3368    1.0393 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4767    3.1208    0.1662 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.3626    2.8687   -0.4587 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4690    1.7053   -0.5075 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7934    1.2712   -1.6791 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0237    0.9137    0.6029 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1602    0.0360    0.1737 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.4074    0.5951    0.4766 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5321    2.1657    1.2835 Cl  0  0  0  0  0  0  0  0  0  0  0  0
   -4.5681   -0.0425    0.1647 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.8231    0.5223    0.4706 O   0  0  0  0  0  0  0  0  0  0  0  0
   -4.4850   -1.2595   -0.4603 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.2553   -1.8139   -0.7603 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.3206   -3.0421   -1.3884 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0358   -1.1700   -0.4460 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7847   -1.8566   -0.8210 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8982   -2.2586   -2.0668 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.2993   -2.0609   -0.0616 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.4380   -2.9046    1.8467 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.0847   -2.2753    1.6140 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.7428   -1.1673    2.0850 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.3108   -2.6033   -0.4836 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.3908   -0.2842   -1.3499 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.7978    0.2216    0.3301 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.1086   -0.9728   -1.3257 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.0820    1.1235   -0.3744 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.7442    1.0285    1.7123 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.0681    2.4748    2.1449 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.8431    4.1828    0.0196 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0258    3.7208   -1.0990 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2856    0.2339    1.0389 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3234    1.5721    1.4513 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.6342   -0.0150    0.2056 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.4159   -1.7539   -0.7018 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6179   -3.6445   -1.6930 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  2  0
  8  9  1  0
  9 10  2  0
 10 11  1  0
 11 12  2  0
 11 13  1  0
 13 14  1  0
 14 15  2  0
 15 16  1  0
 15 17  1  0
 17 18  1  0
 17 19  2  0
 19 20  1  0
 20 21  1  0
 20 22  2  0
 22 23  1  0
 23 24  2  0
 23 25  1  0
 25  2  1  0
  6  4  1  0
 22 14  1  0
  1 26  1  0
  1 27  1  0
  1 28  1  0
  2 29  1  6
  3 30  1  0
  3 31  1  0
  4 32  1  6
  6 33  1  6
  7 34  1  0
  8 35  1  0
  9 36  1  0
 10 37  1  0
 13 38  1  0
 13 39  1  0
 18 40  1  0
 19 41  1  0
 21 42  1  0
M  END


  Mrv1652309092208192D          

 25 27  0  0  0  0            999 V2000
    6.7929   -0.4626    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.4184   -1.1977    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.8678   -1.8895    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.6917   -1.8463    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.5156   -1.8030    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    8.1411   -2.5382    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.7666   -3.2733    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.9427   -3.3165    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.5682   -4.0516    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.7444   -4.0949    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.2950   -3.4030    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.6695   -2.6679    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.4711   -3.4462    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.0217   -2.7544    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.1979   -2.7976    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8234   -3.5327    0.0000 Cl  0  0  0  0  0  0  0  0  0  0  0  0
    2.7485   -2.1057    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.9246   -2.1490    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.1230   -1.3706    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.9468   -1.3274    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.3213   -0.5923    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.3962   -2.0193    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.2201   -1.9760    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.9903   -2.2716    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.5946   -1.2409    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
  4  6  1  0  0  0  0
  6  7  1  0  0  0  0
  7  8  2  0  0  0  0
  9  8  1  4  0  0  0
  9 10  2  0  0  0  0
 10 11  1  0  0  0  0
 11 12  2  0  0  0  0
 11 13  1  0  0  0  0
 13 14  1  0  0  0  0
 14 15  2  0  0  0  0
 15 16  1  0  0  0  0
 15 17  1  0  0  0  0
 17 18  1  0  0  0  0
 17 19  2  0  0  0  0
 19 20  1  0  0  0  0
 20 21  1  0  0  0  0
 20 22  2  0  0  0  0
 14 22  1  0  0  0  0
 22 23  1  0  0  0  0
 23 24  2  0  0  0  0
 23 25  1  0  0  0  0
  2 25  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0280502

> <DATABASE_NAME>
NP-MRD

> <SMILES>
CC1CC2OC2\C=C\C=CC(=O)CC2=C(Cl)C(O)=CC(O)=C2C(=O)O1

> <INCHI_IDENTIFIER>
InChI=1S/C18H17ClO6/c1-9-6-15-14(25-15)5-3-2-4-10(20)7-11-16(18(23)24-9)12(21)8-13(22)17(11)19/h2-5,8-9,14-15,21-22H,6-7H2,1H3/b4-2?,5-3+

> <INCHI_KEY>
WYZWZEOGROVVHK-FWXDBXGDSA-N

> <FORMULA>
C18H17ClO6

> <MOLECULAR_WEIGHT>
364.78

> <EXACT_MASS>
364.071366

> <JCHEM_ACCEPTOR_COUNT>
5

> <JCHEM_ATOM_COUNT>
42

> <JCHEM_AVERAGE_POLARIZABILITY>
34.82077652173881

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
2

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
1

> <JCHEM_IUPAC>
(9E)-16-chloro-17,19-dihydroxy-4-methyl-3,7-dioxatricyclo[13.4.0.0^{6,8}]nonadeca-1(19),9,11,15,17-pentaene-2,13-dione

> <JCHEM_LOGP>
3.6765286639999997

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
3

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA>
9.843043106370928

> <JCHEM_PKA_STRONGEST_ACIDIC>
7.02260474290897

> <JCHEM_PKA_STRONGEST_BASIC>
-4.124046059412492

> <JCHEM_POLAR_SURFACE_AREA>
96.36

> <JCHEM_REFRACTIVITY>
93.56089999999998

> <JCHEM_ROTATABLE_BOND_COUNT>
0

> <JCHEM_RULE_OF_FIVE>
1

> <JCHEM_TRADITIONAL_IUPAC>
(9E)-16-chloro-17,19-dihydroxy-4-methyl-3,7-dioxatricyclo[13.4.0.0^{6,8}]nonadeca-1(19),9,11,15,17-pentaene-2,13-dione

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 09-SEP-22   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   09-SEP-22         0                                  
HETATM    1  C   UNK     0      12.680  -0.863   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0      11.981  -2.236   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0      12.820  -3.527   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0      14.358  -3.446   0.000  0.00  0.00           C+0
HETATM    5  O   UNK     0      15.896  -3.366   0.000  0.00  0.00           O+0
HETATM    6  C   UNK     0      15.197  -4.738   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0      14.498  -6.110   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0      12.960  -6.191   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0      12.261  -7.563   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0      10.723  -7.644   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0       9.884  -6.352   0.000  0.00  0.00           C+0
HETATM   12  O   UNK     0      10.583  -4.980   0.000  0.00  0.00           O+0
HETATM   13  C   UNK     0       8.346  -6.433   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0       7.507  -5.141   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0       5.969  -5.222   0.000  0.00  0.00           C+0
HETATM   16 Cl   UNK     0       5.270  -6.594   0.000  0.00  0.00          Cl+0
HETATM   17  C   UNK     0       5.131  -3.931   0.000  0.00  0.00           C+0
HETATM   18  O   UNK     0       3.593  -4.011   0.000  0.00  0.00           O+0
HETATM   19  C   UNK     0       5.830  -2.559   0.000  0.00  0.00           C+0
HETATM   20  C   UNK     0       7.367  -2.478   0.000  0.00  0.00           C+0
HETATM   21  O   UNK     0       8.066  -1.106   0.000  0.00  0.00           O+0
HETATM   22  C   UNK     0       8.206  -3.769   0.000  0.00  0.00           C+0
HETATM   23  C   UNK     0       9.744  -3.689   0.000  0.00  0.00           C+0
HETATM   24  O   UNK     0      11.182  -4.240   0.000  0.00  0.00           O+0
HETATM   25  O   UNK     0      10.443  -2.316   0.000  0.00  0.00           O+0
CONECT    1    2                                                            
CONECT    2    1    3   25                                                  
CONECT    3    2    4                                                       
CONECT    4    3    5    6                                                  
CONECT    5    4    6                                                       
CONECT    6    5    4    7                                                  
CONECT    7    6    8                                                       
CONECT    8    7    9                                                       
CONECT    9    8   10                                                       
CONECT   10    9   11                                                       
CONECT   11   10   12   13                                                  
CONECT   12   11                                                            
CONECT   13   11   14                                                       
CONECT   14   13   15   22                                                  
CONECT   15   14   16   17                                                  
CONECT   16   15                                                            
CONECT   17   15   18   19                                                  
CONECT   18   17                                                            
CONECT   19   17   20                                                       
CONECT   20   19   21   22                                                  
CONECT   21   20                                                            
CONECT   22   20   14   23                                                  
CONECT   23   22   24   25                                                  
CONECT   24   23                                                            
CONECT   25   23    2                                                       
MASTER        0    0    0    0    0    0    0    0   25    0   54    0
END

View in JSmol

Synonyms

Value	Source
5-Chloro-6-(7,8-epoxy-10-hydroxy-2-oxo-3,5-undecadienyl)-beta-resorcylic acid mu-lactone	MeSH
KF9-a	MeSH
Monorden	MeSH
Monordene	MeSH

Chemical Formula

C₁₈H₁₇ClO₆

Average Mass

364.7800 Da

Monoisotopic Mass

364.07137 Da

IUPAC Name

(9E)-16-chloro-17,19-dihydroxy-4-methyl-3,7-dioxatricyclo[13.4.0.0^{6,8}]nonadeca-1(19),9,11,15,17-pentaene-2,13-dione

Traditional Name

(9E)-16-chloro-17,19-dihydroxy-4-methyl-3,7-dioxatricyclo[13.4.0.0^{6,8}]nonadeca-1(19),9,11,15,17-pentaene-2,13-dione

CAS Registry Number

Not Available

SMILES

CC1CC2OC2\C=C\C=CC(=O)CC2=C(Cl)C(O)=CC(O)=C2C(=O)O1

InChI Identifier

InChI=1S/C18H17ClO6/c1-9-6-15-14(25-15)5-3-2-4-10(20)7-11-16(18(23)24-9)12(21)8-13(22)17(11)19/h2-5,8-9,14-15,21-22H,6-7H2,1H3/b4-2?,5-3+

InChI Key

WYZWZEOGROVVHK-FWXDBXGDSA-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
Fusarium tenuicristatum	LOTUS Database	35616633

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as hydroxybenzoic acid derivatives. Hydroxybenzoic acid derivatives are compounds containing a hydroxybenzoic acid (or a derivative), which is a benzene ring bearing a carboxyl and a hydroxyl groups.

Kingdom

Organic compounds

Super Class

Benzenoids

Class

Benzene and substituted derivatives

Sub Class

Benzoic acids and derivatives

Direct Parent

Hydroxybenzoic acid derivatives

Alternative Parents

Substituents

Dihydroxybenzoic acid
1-hydroxy-2-unsubstituted benzenoid
Aryl halide
Aryl chloride
Vinylogous acid
Cyclic ketone
Lactone
Ketone
Carboxylic acid ester
Oxacycle
Organoheterocyclic compound
Monocarboxylic acid or derivatives
Ether
Oxirane
Dialkyl ether
Carboxylic acid derivative
Organic oxygen compound
Organic oxide
Hydrocarbon derivative
Organooxygen compound
Organochloride
Organohalogen compound
Carbonyl group
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
logP	3.68	ChemAxon
pKa (Strongest Acidic)	7.02	ChemAxon
pKa (Strongest Basic)	-4.1	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	5	ChemAxon
Hydrogen Donor Count	2	ChemAxon
Polar Surface Area	96.36 Å²	ChemAxon
Rotatable Bond Count	0	ChemAxon
Refractivity	93.56 m³·mol⁻¹	ChemAxon
Polarizability	34.82 Å³	ChemAxon
Number of Rings	3	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

C00040142

Chemspider ID

78431120

KEGG Compound ID

Not Available

BioCyc ID

Not Available

BiGG ID

Not Available

Wikipedia Link

Radicicol

METLIN ID

Not Available

PubChem Compound

135121972

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

Xu Y, Zeng P, Wang H, Han K, Qiu G, Wei Y, Chen R, Wang L, Liu X: Novel matrinic acid derivatives bearing 2-anilinothiazole structure for non-small cell lung cancer treatment with improved Hsp90 targeting effect. Drug Dev Res. 2022 Sep;83(6):1434-1454. doi: 10.1002/ddr.21974. Epub 2022 Jul 15. [PubMed:35841121 ]
Gao Y, Zhou J, Meng X, Ouyang Q, Gan Y, Ruan H: Ilyomycins A - K, radicicol-type resorcylic acid lactones as potential immunosuppressants from a soil-derived Ilyonectria sp. Bioorg Chem. 2022 Jun;123:105796. doi: 10.1016/j.bioorg.2022.105796. Epub 2022 Apr 8. [PubMed:35421731 ]
Zenke K, Okinaka Y: Multiple isoforms of HSP70 and HSP90 required for betanodavirus multiplication in medaka cells. Arch Virol. 2022 Oct;167(10):1961-1975. doi: 10.1007/s00705-022-05489-5. Epub 2022 Jun 26. [PubMed:35752988 ]
Polosak K, Papierniak-Wygladala A, Nalecz KA: Regulation of SLC6A14 trafficking in breast cancer cells by heat shock protein HSP90beta. Biochem Biophys Res Commun. 2022 Jul 23;614:41-46. doi: 10.1016/j.bbrc.2022.05.011. Epub 2022 May 6. [PubMed:35569376 ]
LOTUS database [Link]

Showing NP-Card for (9e)-16-chloro-17,19-dihydroxy-4-methyl-3,7-dioxatricyclo[13.4.0.0⁶,⁸]nonadeca-1(19),9,11,15,17-pentaene-2,13-dione (NP0280502)

MOL for NP0280502 ((9e)-16-chloro-17,19-dihydroxy-4-methyl-3,7-dioxatricyclo[13.4.0.0⁶,⁸]nonadeca-1(19),9,11,15,17-pentaene-2,13-dione)

3D MOL for NP0280502 ((9e)-16-chloro-17,19-dihydroxy-4-methyl-3,7-dioxatricyclo[13.4.0.0⁶,⁸]nonadeca-1(19),9,11,15,17-pentaene-2,13-dione)

3D SDF for NP0280502 ((9e)-16-chloro-17,19-dihydroxy-4-methyl-3,7-dioxatricyclo[13.4.0.0⁶,⁸]nonadeca-1(19),9,11,15,17-pentaene-2,13-dione)

3D-SDF for NP0280502 ((9e)-16-chloro-17,19-dihydroxy-4-methyl-3,7-dioxatricyclo[13.4.0.0⁶,⁸]nonadeca-1(19),9,11,15,17-pentaene-2,13-dione)

PDB for NP0280502 ((9e)-16-chloro-17,19-dihydroxy-4-methyl-3,7-dioxatricyclo[13.4.0.0⁶,⁸]nonadeca-1(19),9,11,15,17-pentaene-2,13-dione)

3D PDB for NP0280502 ((9e)-16-chloro-17,19-dihydroxy-4-methyl-3,7-dioxatricyclo[13.4.0.0⁶,⁸]nonadeca-1(19),9,11,15,17-pentaene-2,13-dione)

SMILES for NP0280502 ((9e)-16-chloro-17,19-dihydroxy-4-methyl-3,7-dioxatricyclo[13.4.0.0⁶,⁸]nonadeca-1(19),9,11,15,17-pentaene-2,13-dione)

INCHI for NP0280502 ((9e)-16-chloro-17,19-dihydroxy-4-methyl-3,7-dioxatricyclo[13.4.0.0⁶,⁸]nonadeca-1(19),9,11,15,17-pentaene-2,13-dione)

Structure for NP0280502 ((9e)-16-chloro-17,19-dihydroxy-4-methyl-3,7-dioxatricyclo[13.4.0.0⁶,⁸]nonadeca-1(19),9,11,15,17-pentaene-2,13-dione)

3D Structure for NP0280502 ((9e)-16-chloro-17,19-dihydroxy-4-methyl-3,7-dioxatricyclo[13.4.0.0⁶,⁸]nonadeca-1(19),9,11,15,17-pentaene-2,13-dione)