NP-MRD: Showing NP-Card for 4-{11-hydroxy-3-methyl-2-oxatricyclo[7.3.1.0⁵,¹³]trideca-1(13),3,5,7,9,11-hexaene-10-carbonyl}-5-methylbenzene-1,3-diol (NP0177125)

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Record Information

Version

2.0

Created at

2022-09-03 14:55:12 UTC

Updated at

2022-09-03 14:55:12 UTC

NP-MRD ID

NP0177125

Secondary Accession Numbers

None

Natural Product Identification

Common Name

4-{11-hydroxy-3-methyl-2-oxatricyclo[7.3.1.0⁵,¹³]trideca-1(13),3,5,7,9,11-hexaene-10-carbonyl}-5-methylbenzene-1,3-diol

Description

4-{11-hydroxy-3-methyl-2-oxatricyclo[7.3.1.0⁵,¹³]trideca-1(13),3,5,7,9,11-hexaene-10-carbonyl}-5-methylbenzene-1,3-diol is found in Streptomyces coelicolor.

Structure

MOL 3D MOL SDF PDB SMILES InChI


  Mrv1652309032216552D          

 26 29  0  0  0  0            999 V2000
    2.1434   -3.7125    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
    1.4289   -2.4750    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4289   -1.6500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7145   -1.2375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7145   -0.4125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4289   -0.0000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1434   -0.4125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8579    0.0000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8579    0.8250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1434    1.2375    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.5724    1.2375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.2868    0.8250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.2868   -0.0000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.0013    1.2375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.0013    2.0625    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
    4.2868    2.4750    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5724    2.0625    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   -0.4125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.3928   -0.4987    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.5724   -1.2375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8579   -1.6500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1434   -1.2375    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
  1  2  1  0  0  0  0
  2  3  2  0  0  0  0
  3  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  2  0  0  0  0
  8  9  1  0  0  0  0
  9 10  1  0  0  0  0
 10 11  2  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
 13 15  1  0  0  0  0
 15 16  2  0  0  0  0
 16 17  1  0  0  0  0
 16 18  1  0  0  0  0
 18 19  2  0  0  0  0
 12 19  1  0  0  0  0
 19 20  1  0  0  0  0
  9 21  2  0  0  0  0
 21 22  1  0  0  0  0
 21 23  1  0  0  0  0
 23 24  2  0  0  0  0
 24 25  1  0  0  0  0
  4 25  2  0  0  0  0
  8 25  1  0  0  0  0
 24 26  1  0  0  0  0
  2 26  1  0  0  0  0
M  END

     RDKit          3D

 42 45  0  0  0  0  0  0  0  0999 V2000
   -5.9891    1.8994    0.6023 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.6097    1.3583    0.3949 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.0647    0.5988    1.3192 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7301    0.0528    1.1614 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2214   -0.7583    2.1569 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9616   -1.2638    1.9461 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2364   -0.9809    0.8145 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7309   -0.1698   -0.1833 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0108    0.0815   -1.3062 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.2807   -0.4629   -1.6048 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4109   -0.7898   -2.8796 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.4553   -0.7347   -0.8395 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8877    0.0503    0.2088 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1414    1.2633    0.6942 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.1062   -0.2180    0.8356 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.9356   -1.2512    0.4604 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.1413   -1.4948    1.1013 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.4921   -2.0355   -0.5996 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.2958   -1.7820   -1.2225 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.9267   -2.6258   -2.2851 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6212    0.8919   -2.2597 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.1036    1.1606   -3.4104 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8873    1.3943   -2.0699 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5968    1.1214   -0.9284 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0198    0.3291    0.0341 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.8967    1.6428   -0.7543 O   0  0  0  0  0  0  0  0  0  0  0  0
   -5.9363    2.8452    1.1929 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.5991    1.1997    1.2070 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.4712    2.0446   -0.3877 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.6182    0.3635    2.2358 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8159   -0.9617    3.0429 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5435   -1.9144    2.7262 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.7131   -1.4335    0.7150 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.9393    2.0385    0.8736 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.4634    1.6392   -0.0663 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.6198    1.0229    1.6187 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.3989    0.4369    1.6647 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.2290   -2.1010    1.8959 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.1483   -2.8454   -0.8909 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.4848   -3.3811   -2.5959 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2783    1.7405   -4.1556 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3561    2.0291   -2.8373 H   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0
  2  3  2  0
  3  4  1  0
  4 25  1  0
 25 24  2  0
 24 26  1  0
 24 23  1  0
 23 21  2  0
 21 22  1  0
 21  9  1  0
  9 10  1  0
 10 11  2  0
 10 12  1  0
 12 13  2  0
 13 14  1  0
 13 15  1  0
 15 16  2  0
 16 17  1  0
 16 18  1  0
 18 19  2  0
 19 20  1  0
  9  8  2  0
  8  7  1  0
  7  6  2  0
  6  5  1  0
 26  2  1  0
 19 12  1  0
  5  4  2  0
  8 25  1  0
  1 27  1  0
  1 28  1  0
  1 29  1  0
  3 30  1  0
 23 42  1  0
 22 41  1  0
 14 34  1  0
 14 35  1  0
 14 36  1  0
 15 37  1  0
 17 38  1  0
 18 39  1  0
 20 40  1  0
  7 33  1  0
  6 32  1  0
  5 31  1  0
M  END


  Mrv1652309032216552D          

 26 29  0  0  0  0            999 V2000
    2.1434   -3.7125    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
    1.4289   -2.4750    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4289   -1.6500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7145   -1.2375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7145   -0.4125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4289   -0.0000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1434   -0.4125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8579    0.0000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8579    0.8250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1434    1.2375    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.5724    1.2375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.2868    0.8250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.2868   -0.0000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.0013    1.2375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.0013    2.0625    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
    4.2868    2.4750    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5724    2.0625    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   -0.4125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.3928   -0.4987    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.5724   -1.2375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8579   -1.6500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1434   -1.2375    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
  1  2  1  0  0  0  0
  2  3  2  0  0  0  0
  3  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  2  0  0  0  0
  8  9  1  0  0  0  0
  9 10  1  0  0  0  0
 10 11  2  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
 13 15  1  0  0  0  0
 15 16  2  0  0  0  0
 16 17  1  0  0  0  0
 16 18  1  0  0  0  0
 18 19  2  0  0  0  0
 12 19  1  0  0  0  0
 19 20  1  0  0  0  0
  9 21  2  0  0  0  0
 21 22  1  0  0  0  0
 21 23  1  0  0  0  0
 23 24  2  0  0  0  0
 24 25  1  0  0  0  0
  4 25  2  0  0  0  0
  8 25  1  0  0  0  0
 24 26  1  0  0  0  0
  2 26  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0177125

> <DATABASE_NAME>
NP-MRD

> <SMILES>
CC1=CC2=C3C(O1)=CC(O)=C(C(=O)C1=C(C)C=C(O)C=C1O)C3=CC=C2

> <INCHI_IDENTIFIER>
InChI=1S/C21H16O5/c1-10-6-13(22)8-15(23)18(10)21(25)20-14-5-3-4-12-7-11(2)26-17(19(12)14)9-16(20)24/h3-9,22-24H,1-2H3

> <INCHI_KEY>
SESGNSJZWSCLAT-UHFFFAOYSA-N

> <FORMULA>
C21H16O5

> <MOLECULAR_WEIGHT>
348.354

> <EXACT_MASS>
348.099773615

> <JCHEM_ACCEPTOR_COUNT>
5

> <JCHEM_ATOM_COUNT>
42

> <JCHEM_AVERAGE_POLARIZABILITY>
36.30862555404745

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
3

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
1

> <JCHEM_IUPAC>
4-{11-hydroxy-3-methyl-2-oxatricyclo[7.3.1.0^{5,13}]trideca-1(12),3,5(13),6,8,10-hexaene-10-carbonyl}-5-methylbenzene-1,3-diol

> <JCHEM_LOGP>
5.374036696666667

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
4

> <JCHEM_PHYSIOLOGICAL_CHARGE>
-1

> <JCHEM_PKA>
7.359167536400507

> <JCHEM_PKA_STRONGEST_ACIDIC>
6.625201388340427

> <JCHEM_PKA_STRONGEST_BASIC>
-5.309996834338082

> <JCHEM_POLAR_SURFACE_AREA>
86.99000000000001

> <JCHEM_REFRACTIVITY>
99.75259999999999

> <JCHEM_ROTATABLE_BOND_COUNT>
2

> <JCHEM_RULE_OF_FIVE>
0

> <JCHEM_TRADITIONAL_IUPAC>
4-{11-hydroxy-3-methyl-2-oxatricyclo[7.3.1.0^{5,13}]trideca-1(12),3,5(13),6,8,10-hexaene-10-carbonyl}-5-methylbenzene-1,3-diol

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 03-SEP-22   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   03-SEP-22         0                                  
HETATM    1  C   UNK     0       4.001  -6.930   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       2.667  -4.620   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0       2.667  -3.080   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0       1.334  -2.310   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0       1.334  -0.770   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0       2.667  -0.000   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0       4.001  -0.770   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0       5.335   0.000   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0       5.335   1.540   0.000  0.00  0.00           C+0
HETATM   11  O   UNK     0       4.001   2.310   0.000  0.00  0.00           O+0
HETATM   12  C   UNK     0       6.668   2.310   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0       8.002   1.540   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0       8.002  -0.000   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0       9.336   2.310   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0       9.336   3.850   0.000  0.00  0.00           C+0
HETATM   17  O   UNK     0      10.669   4.620   0.000  0.00  0.00           O+0
HETATM   18  C   UNK     0       8.002   4.620   0.000  0.00  0.00           C+0
HETATM   19  C   UNK     0       6.668   3.850   0.000  0.00  0.00           C+0
HETATM   20  O   UNK     0       5.335   4.620   0.000  0.00  0.00           O+0
HETATM   21  C   UNK     0       6.668  -0.770   0.000  0.00  0.00           C+0
HETATM   22  O   UNK     0       8.200  -0.931   0.000  0.00  0.00           O+0
HETATM   23  C   UNK     0       6.668  -2.310   0.000  0.00  0.00           C+0
HETATM   24  C   UNK     0       5.335  -3.080   0.000  0.00  0.00           C+0
HETATM   25  C   UNK     0       4.001  -2.310   0.000  0.00  0.00           C+0
HETATM   26  O   UNK     0       5.335  -4.620   0.000  0.00  0.00           O+0
CONECT    1    2                                                            
CONECT    2    1    3   26                                                  
CONECT    3    2    4                                                       
CONECT    4    3    5   25                                                  
CONECT    5    4    6                                                       
CONECT    6    5    7                                                       
CONECT    7    6    8                                                       
CONECT    8    7    9   25                                                  
CONECT    9    8   10   21                                                  
CONECT   10    9   11   12                                                  
CONECT   11   10                                                            
CONECT   12   10   13   19                                                  
CONECT   13   12   14   15                                                  
CONECT   14   13                                                            
CONECT   15   13   16                                                       
CONECT   16   15   17   18                                                  
CONECT   17   16                                                            
CONECT   18   16   19                                                       
CONECT   19   18   12   20                                                  
CONECT   20   19                                                            
CONECT   21    9   22   23                                                  
CONECT   22   21                                                            
CONECT   23   21   24                                                       
CONECT   24   23   25   26                                                  
CONECT   25   24    4    8                                                  
CONECT   26   24    2                                                       
MASTER        0    0    0    0    0    0    0    0   26    0   58    0
END

View in JSmol

Synonyms

Not Available

Chemical Formula

C₂₁H₁₆O₅

Average Mass

348.3540 Da

Monoisotopic Mass

348.09977 Da

IUPAC Name

Not Available

Traditional Name

Not Available

CAS Registry Number

Not Available

SMILES

CC1=CC2=C3C(O1)=CC(O)=C(C(=O)C1=C(C)C=C(O)C=C1O)C3=CC=C2

InChI Identifier

InChI=1S/C21H16O5/c1-10-6-13(22)8-15(23)18(10)21(25)20-14-5-3-4-12-7-11(2)26-17(19(12)14)9-16(20)24/h3-9,22-24H,1-2H3

InChI Key

SESGNSJZWSCLAT-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, 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
Streptomyces coelicolor	LOTUS Database	35616633

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

External Links

Not Available

References

General References

LOTUS database [Link]

Showing NP-Card for 4-{11-hydroxy-3-methyl-2-oxatricyclo[7.3.1.0⁵,¹³]trideca-1(13),3,5,7,9,11-hexaene-10-carbonyl}-5-methylbenzene-1,3-diol (NP0177125)

MOL for NP0177125 (4-{11-hydroxy-3-methyl-2-oxatricyclo[7.3.1.0⁵,¹³]trideca-1(13),3,5,7,9,11-hexaene-10-carbonyl}-5-methylbenzene-1,3-diol)

3D MOL for NP0177125 (4-{11-hydroxy-3-methyl-2-oxatricyclo[7.3.1.0⁵,¹³]trideca-1(13),3,5,7,9,11-hexaene-10-carbonyl}-5-methylbenzene-1,3-diol)

3D SDF for NP0177125 (4-{11-hydroxy-3-methyl-2-oxatricyclo[7.3.1.0⁵,¹³]trideca-1(13),3,5,7,9,11-hexaene-10-carbonyl}-5-methylbenzene-1,3-diol)

3D-SDF for NP0177125 (4-{11-hydroxy-3-methyl-2-oxatricyclo[7.3.1.0⁵,¹³]trideca-1(13),3,5,7,9,11-hexaene-10-carbonyl}-5-methylbenzene-1,3-diol)

PDB for NP0177125 (4-{11-hydroxy-3-methyl-2-oxatricyclo[7.3.1.0⁵,¹³]trideca-1(13),3,5,7,9,11-hexaene-10-carbonyl}-5-methylbenzene-1,3-diol)

3D PDB for NP0177125 (4-{11-hydroxy-3-methyl-2-oxatricyclo[7.3.1.0⁵,¹³]trideca-1(13),3,5,7,9,11-hexaene-10-carbonyl}-5-methylbenzene-1,3-diol)

SMILES for NP0177125 (4-{11-hydroxy-3-methyl-2-oxatricyclo[7.3.1.0⁵,¹³]trideca-1(13),3,5,7,9,11-hexaene-10-carbonyl}-5-methylbenzene-1,3-diol)

INCHI for NP0177125 (4-{11-hydroxy-3-methyl-2-oxatricyclo[7.3.1.0⁵,¹³]trideca-1(13),3,5,7,9,11-hexaene-10-carbonyl}-5-methylbenzene-1,3-diol)

Structure for NP0177125 (4-{11-hydroxy-3-methyl-2-oxatricyclo[7.3.1.0⁵,¹³]trideca-1(13),3,5,7,9,11-hexaene-10-carbonyl}-5-methylbenzene-1,3-diol)

3D Structure for NP0177125 (4-{11-hydroxy-3-methyl-2-oxatricyclo[7.3.1.0⁵,¹³]trideca-1(13),3,5,7,9,11-hexaene-10-carbonyl}-5-methylbenzene-1,3-diol)