NP-MRD: Showing NP-Card for 2,4-dihydroxy-3-({1-hydroxy-3-[9-(hydroxymethyl)-5-methyl-4-oxo-8-oxatetracyclo[7.2.1.1⁷,¹⁰.0¹,⁶]tridec-2-en-5-yl]propylidene}amino)benzoic acid (NP0303490)

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Record Information

Version

2.0

Created at

2022-09-10 17:52:27 UTC

Updated at

2022-09-10 17:52:28 UTC

NP-MRD ID

NP0303490

Secondary Accession Numbers

None

Natural Product Identification

Common Name

2,4-dihydroxy-3-({1-hydroxy-3-[9-(hydroxymethyl)-5-methyl-4-oxo-8-oxatetracyclo[7.2.1.1⁷,¹⁰.0¹,⁶]tridec-2-en-5-yl]propylidene}amino)benzoic acid

Description

2,4-Dihydroxy-3-({1-hydroxy-3-[9-(hydroxymethyl)-5-methyl-4-oxo-8-oxatetracyclo[7.2.1.1⁷,¹⁰.0¹,⁶]Tridec-2-en-5-yl]propylidene}amino)benzoic acid belongs to the class of organic compounds known as acylaminobenzoic acid and derivatives. These are derivatives of amino benzoic acid derivatives where the amine group is N-acylated. 2,4-dihydroxy-3-({1-hydroxy-3-[9-(hydroxymethyl)-5-methyl-4-oxo-8-oxatetracyclo[7.2.1.1⁷,¹⁰.0¹,⁶]tridec-2-en-5-yl]propylidene}amino)benzoic acid is found in Streptomyces platensis. Based on a literature review very few articles have been published on 2,4-dihydroxy-3-({1-hydroxy-3-[9-(hydroxymethyl)-5-methyl-4-oxo-8-oxatetracyclo[7.2.1.1⁷,¹⁰.0¹,⁶]Tridec-2-en-5-yl]propylidene}amino)benzoic acid.

Structure

MOL 3D MOL SDF PDB SMILES InChI


  Mrv1652309102219522D          

 33 37  0  0  0  0            999 V2000
    0.2850   -0.6026    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7214    0.0976    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.3120   -0.4784    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.1084   -1.2779    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.6990   -1.8540    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.4932   -1.6305    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.4955   -2.6535    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    2.0861   -3.2295    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8803   -3.0060    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.0838   -2.2065    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.4709   -3.5820    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.2674   -4.3815    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.4732   -4.6050    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.2697   -5.4045    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8603   -5.9805    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.4755   -5.6280    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.8826   -4.0290    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.0884   -4.2525    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0721    0.3798    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7184   -0.1329    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1664    1.2165    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.5494    1.6632    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.3836    1.4555    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.8833    2.1725    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.6957    1.8629    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.5370    0.9476    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.2210    0.1847    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.0786    0.3097    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.1153    1.1781    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.9139    1.3852    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.1338    2.1803    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.2200    1.4368    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4342    0.5670    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
  3  4  1  0  0  0  0
  4  5  1  0  0  0  0
  5  6  1  0  0  0  0
  5  7  2  0  0  0  0
  7  8  1  4  0  0  0
  8  9  2  0  0  0  0
  9 10  1  0  0  0  0
  9 11  1  0  0  0  0
 11 12  2  0  0  0  0
 12 13  1  0  0  0  0
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 13 17  2  0  0  0  0
  8 17  1  0  0  0  0
 17 18  1  0  0  0  0
  2 19  1  0  0  0  0
 19 20  2  0  0  0  0
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 23 32  1  0  0  0  0
 27 33  1  0  0  0  0
 23 33  1  0  0  0  0
  2 33  1  0  0  0  0
M  END

     RDKit          3D

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   -1.1022   -1.6054   -0.1647 C   0  0  2  0  0  0  0  0  0  0  0  0
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    2.2672    1.1505    0.7452 O   0  0  0  0  0  0  0  0  0  0  0  0
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    6.7283   -0.2549    0.5469 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.1674    1.0279    0.2967 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.2935    1.8884   -0.3328 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.7041    3.2505   -0.6204 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.9253    4.0601   -1.1955 O   0  0  0  0  0  0  0  0  0  0  0  0
    7.9788    3.6874   -0.2611 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.0145    1.4858   -0.7051 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.1924    2.4196   -1.3383 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6065   -2.6360    0.8500 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0456   -2.8123    1.9506 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7785   -3.3940    0.4441 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.7866   -2.6918   -0.0519 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.6053   -1.2453   -0.1211 C   0  0  2  0  0  0  0  0  0  0  0  0
   -4.1375   -0.7319    1.2298 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.1798    0.7483    0.9424 C   0  0  1  0  0  0  0  0  0  0  0  0
   -2.7180    1.1642    1.1568 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1487    0.7183   -0.1656 C   0  0  2  0  0  0  0  0  0  0  0  0
   -3.1014    1.3372   -1.0281 O   0  0  0  0  0  0  0  0  0  0  0  0
   -4.3334    0.9078   -0.5375 C   0  0  2  0  0  0  0  0  0  0  0  0
   -5.4575    1.8148   -0.9298 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.1784    3.0759   -0.4092 O   0  0  0  0  0  0  0  0  0  0  0  0
   -4.5858   -0.5302   -1.0273 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2428   -0.7445   -0.4719 C   0  0  1  0  0  0  0  0  0  0  0  0
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    0.1136   -3.1817   -1.0687 H   0  0  0  0  0  0  0  0  0  0  0  0
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    0.1347   -0.3503    1.1328 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.8090   -1.9087    0.6653 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.2591   -1.1600   -1.5681 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.4900    0.4189   -1.3820 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.2611    0.8308    1.7161 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.6604   -2.6022    0.9002 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.4313   -0.9171    1.0433 H   0  0  0  0  0  0  0  0  0  0  0  0
    8.1800    1.3426    0.5928 H   0  0  0  0  0  0  0  0  0  0  0  0
    8.1206    4.3492    0.4921 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.2633    2.1757   -1.6247 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8424   -4.4948    0.5790 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.6733   -3.2242   -0.3737 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.1252   -1.1851    1.3498 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.4404   -0.9811    2.0511 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.8717    1.3074    1.5526 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3395    0.6477    2.0300 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6148    2.2505    1.2008 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1867    1.1879   -0.2648 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.4046    1.4043   -0.5717 H   0  0  0  0  0  0  0  0  0  0  0  0
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  2  1  1  6
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 29 25  1  0
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 18 46  1  0
 33 60  1  6
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 32 58  1  0
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 22 48  1  0
 21 47  1  0
M  END


  Mrv1652309102219522D          

 33 37  0  0  0  0            999 V2000
    0.2850   -0.6026    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7214    0.0976    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.3120   -0.4784    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.1084   -1.2779    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.6990   -1.8540    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.4932   -1.6305    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.4955   -2.6535    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    2.0861   -3.2295    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
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    1.3836    1.4555    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.8833    2.1725    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.6957    1.8629    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.5370    0.9476    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.2210    0.1847    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.0786    0.3097    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.1153    1.1781    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.9139    1.3852    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.1338    2.1803    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.2200    1.4368    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4342    0.5670    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
  3  4  1  0  0  0  0
  4  5  1  0  0  0  0
  5  6  1  0  0  0  0
  5  7  2  0  0  0  0
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 27 33  1  0  0  0  0
 23 33  1  0  0  0  0
  2 33  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0303490

> <DATABASE_NAME>
NP-MRD

> <SMILES>
CC1(CCC(O)=NC2=C(O)C=CC(C(O)=O)=C2O)C2C3CC4CC2(CC4(CO)O3)C=CC1=O

> <INCHI_IDENTIFIER>
InChI=1S/C24H27NO8/c1-22(6-5-17(29)25-18-14(27)3-2-13(19(18)30)21(31)32)16(28)4-7-23-9-12-8-15(20(22)23)33-24(12,10-23)11-26/h2-4,7,12,15,20,26-27,30H,5-6,8-11H2,1H3,(H,25,29)(H,31,32)

> <INCHI_KEY>
NNGABSPACJBNCJ-UHFFFAOYSA-N

> <FORMULA>
C24H27NO8

> <MOLECULAR_WEIGHT>
457.479

> <EXACT_MASS>
457.173666833

> <JCHEM_ACCEPTOR_COUNT>
9

> <JCHEM_ATOM_COUNT>
60

> <JCHEM_AVERAGE_POLARIZABILITY>
46.386891874534555

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
5

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
1

> <JCHEM_IUPAC>
2,4-dihydroxy-3-({1-hydroxy-3-[9-(hydroxymethyl)-5-methyl-4-oxo-8-oxatetracyclo[7.2.1.1^{7,10}.0^{1,6}]tridec-2-en-5-yl]propylidene}amino)benzoic acid

> <JCHEM_LOGP>
4.216755346000001

> <JCHEM_MDDR_LIKE_RULE>
1

> <JCHEM_NUMBER_OF_RINGS>
5

> <JCHEM_PHYSIOLOGICAL_CHARGE>
-1

> <JCHEM_PKA>
5.167196731357651

> <JCHEM_PKA_STRONGEST_ACIDIC>
3.608882937182524

> <JCHEM_PKA_STRONGEST_BASIC>
-1.2448521955714589

> <JCHEM_POLAR_SURFACE_AREA>
156.88

> <JCHEM_REFRACTIVITY>
119.10929999999998

> <JCHEM_ROTATABLE_BOND_COUNT>
6

> <JCHEM_RULE_OF_FIVE>
1

> <JCHEM_TRADITIONAL_IUPAC>
2,4-dihydroxy-3-({1-hydroxy-3-[9-(hydroxymethyl)-5-methyl-4-oxo-8-oxatetracyclo[7.2.1.1^{7,10}.0^{1,6}]tridec-2-en-5-yl]propylidene}amino)benzoic acid

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 10-SEP-22   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   10-SEP-22         0                                  
HETATM    1  C   UNK     0       0.532  -1.125   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0       1.347   0.182   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0       2.449  -0.893   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0       2.069  -2.386   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0       3.172  -3.461   0.000  0.00  0.00           C+0
HETATM    6  O   UNK     0       4.654  -3.044   0.000  0.00  0.00           O+0
HETATM    7  N   UNK     0       2.792  -4.953   0.000  0.00  0.00           N+0
HETATM    8  C   UNK     0       3.894  -6.028   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0       5.377  -5.611   0.000  0.00  0.00           C+0
HETATM   10  O   UNK     0       5.756  -4.119   0.000  0.00  0.00           O+0
HETATM   11  C   UNK     0       6.479  -6.686   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0       6.099  -8.179   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0       4.617  -8.596   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0       4.237 -10.088   0.000  0.00  0.00           C+0
HETATM   15  O   UNK     0       5.339 -11.164   0.000  0.00  0.00           O+0
HETATM   16  O   UNK     0       2.754 -10.506   0.000  0.00  0.00           O+0
HETATM   17  C   UNK     0       3.514  -7.521   0.000  0.00  0.00           C+0
HETATM   18  O   UNK     0       2.032  -7.938   0.000  0.00  0.00           O+0
HETATM   19  C   UNK     0      -0.135   0.709   0.000  0.00  0.00           C+0
HETATM   20  O   UNK     0      -1.341  -0.248   0.000  0.00  0.00           O+0
HETATM   21  C   UNK     0      -0.311   2.271   0.000  0.00  0.00           C+0
HETATM   22  C   UNK     0       1.026   3.105   0.000  0.00  0.00           C+0
HETATM   23  C   UNK     0       2.583   2.717   0.000  0.00  0.00           C+0
HETATM   24  C   UNK     0       3.515   4.055   0.000  0.00  0.00           C+0
HETATM   25  C   UNK     0       5.032   3.478   0.000  0.00  0.00           C+0
HETATM   26  C   UNK     0       4.736   1.769   0.000  0.00  0.00           C+0
HETATM   27  C   UNK     0       4.146   0.345   0.000  0.00  0.00           C+0
HETATM   28  O   UNK     0       5.747   0.578   0.000  0.00  0.00           O+0
HETATM   29  C   UNK     0       5.815   2.199   0.000  0.00  0.00           C+0
HETATM   30  C   UNK     0       7.306   2.586   0.000  0.00  0.00           C+0
HETATM   31  O   UNK     0       7.717   4.070   0.000  0.00  0.00           O+0
HETATM   32  C   UNK     0       4.144   2.682   0.000  0.00  0.00           C+0
HETATM   33  C   UNK     0       2.677   1.058   0.000  0.00  0.00           C+0
CONECT    1    2                                                            
CONECT    2    1    3   19   33                                             
CONECT    3    2    4                                                       
CONECT    4    3    5                                                       
CONECT    5    4    6    7                                                  
CONECT    6    5                                                            
CONECT    7    5    8                                                       
CONECT    8    7    9   17                                                  
CONECT    9    8   10   11                                                  
CONECT   10    9                                                            
CONECT   11    9   12                                                       
CONECT   12   11   13                                                       
CONECT   13   12   14   17                                                  
CONECT   14   13   15   16                                                  
CONECT   15   14                                                            
CONECT   16   14                                                            
CONECT   17   13    8   18                                                  
CONECT   18   17                                                            
CONECT   19    2   20   21                                                  
CONECT   20   19                                                            
CONECT   21   19   22                                                       
CONECT   22   21   23                                                       
CONECT   23   22   24   32   33                                             
CONECT   24   23   25                                                       
CONECT   25   24   26   29                                                  
CONECT   26   25   27                                                       
CONECT   27   26   28   33                                                  
CONECT   28   27   29                                                       
CONECT   29   28   25   30   32                                             
CONECT   30   29   31                                                       
CONECT   31   30                                                            
CONECT   32   29   23                                                       
CONECT   33   27   23    2                                                  
MASTER        0    0    0    0    0    0    0    0   33    0   74    0
END

View in JSmol

Synonyms

Value	Source
2,4-Dihydroxy-3-({1-hydroxy-3-[9-(hydroxymethyl)-5-methyl-4-oxo-8-oxatetracyclo[7.2.1.1,.0,]tridec-2-en-5-yl]propylidene}amino)benzoate	Generator

Chemical Formula

C₂₄H₂₇NO₈

Average Mass

457.4790 Da

Monoisotopic Mass

457.17367 Da

IUPAC Name

Not Available

Traditional Name

Not Available

CAS Registry Number

Not Available

SMILES

CC1(CCC(O)=NC2=C(O)C=CC(C(O)=O)=C2O)C2C3CC4CC2(CC4(CO)O3)C=CC1=O

InChI Identifier

InChI=1S/C24H27NO8/c1-22(6-5-17(29)25-18-14(27)3-2-13(19(18)30)21(31)32)16(28)4-7-23-9-12-8-15(20(22)23)33-24(12,10-23)11-26/h2-4,7,12,15,20,26-27,30H,5-6,8-11H2,1H3,(H,25,29)(H,31,32)

InChI Key

NNGABSPACJBNCJ-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 platensis	LOTUS Database	35616633

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as acylaminobenzoic acid and derivatives. These are derivatives of amino benzoic acid derivatives where the amine group is N-acylated.

Kingdom

Organic compounds

Super Class

Benzenoids

Class

Benzene and substituted derivatives

Sub Class

Benzoic acids and derivatives

Direct Parent

Acylaminobenzoic acid and derivatives

Alternative Parents

Substituents

Acylaminobenzoic acid or derivatives
Dihydroxybenzoic acid
Hydroxybenzoic acid
Salicylic acid or derivatives
Salicylic acid
Benzoic acid
Anilide
Benzoyl
Resorcinol
N-arylamide
Cyclohexenone
1-hydroxy-4-unsubstituted benzenoid
1-hydroxy-2-unsubstituted benzenoid
Phenol
Oxepane
Fatty acyl
Fatty amide
Oxane
Vinylogous acid
Tetrahydrofuran
Carboxamide group
Cyclic ketone
Secondary carboxylic acid amide
Ketone
Oxacycle
Organoheterocyclic compound
Carboxylic acid derivative
Carboxylic acid
Dialkyl ether
Ether
Monocarboxylic acid or derivatives
Organic nitrogen compound
Hydrocarbon derivative
Carbonyl group
Alcohol
Organopnictogen compound
Organic oxygen compound
Organic oxide
Organonitrogen compound
Organooxygen compound
Primary alcohol
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

76154467

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

LOTUS database [Link]

Showing NP-Card for 2,4-dihydroxy-3-({1-hydroxy-3-[9-(hydroxymethyl)-5-methyl-4-oxo-8-oxatetracyclo[7.2.1.1⁷,¹⁰.0¹,⁶]tridec-2-en-5-yl]propylidene}amino)benzoic acid (NP0303490)

MOL for NP0303490 (2,4-dihydroxy-3-({1-hydroxy-3-[9-(hydroxymethyl)-5-methyl-4-oxo-8-oxatetracyclo[7.2.1.1⁷,¹⁰.0¹,⁶]tridec-2-en-5-yl]propylidene}amino)benzoic acid)

3D MOL for NP0303490 (2,4-dihydroxy-3-({1-hydroxy-3-[9-(hydroxymethyl)-5-methyl-4-oxo-8-oxatetracyclo[7.2.1.1⁷,¹⁰.0¹,⁶]tridec-2-en-5-yl]propylidene}amino)benzoic acid)

3D SDF for NP0303490 (2,4-dihydroxy-3-({1-hydroxy-3-[9-(hydroxymethyl)-5-methyl-4-oxo-8-oxatetracyclo[7.2.1.1⁷,¹⁰.0¹,⁶]tridec-2-en-5-yl]propylidene}amino)benzoic acid)

3D-SDF for NP0303490 (2,4-dihydroxy-3-({1-hydroxy-3-[9-(hydroxymethyl)-5-methyl-4-oxo-8-oxatetracyclo[7.2.1.1⁷,¹⁰.0¹,⁶]tridec-2-en-5-yl]propylidene}amino)benzoic acid)

PDB for NP0303490 (2,4-dihydroxy-3-({1-hydroxy-3-[9-(hydroxymethyl)-5-methyl-4-oxo-8-oxatetracyclo[7.2.1.1⁷,¹⁰.0¹,⁶]tridec-2-en-5-yl]propylidene}amino)benzoic acid)

3D PDB for NP0303490 (2,4-dihydroxy-3-({1-hydroxy-3-[9-(hydroxymethyl)-5-methyl-4-oxo-8-oxatetracyclo[7.2.1.1⁷,¹⁰.0¹,⁶]tridec-2-en-5-yl]propylidene}amino)benzoic acid)

SMILES for NP0303490 (2,4-dihydroxy-3-({1-hydroxy-3-[9-(hydroxymethyl)-5-methyl-4-oxo-8-oxatetracyclo[7.2.1.1⁷,¹⁰.0¹,⁶]tridec-2-en-5-yl]propylidene}amino)benzoic acid)

INCHI for NP0303490 (2,4-dihydroxy-3-({1-hydroxy-3-[9-(hydroxymethyl)-5-methyl-4-oxo-8-oxatetracyclo[7.2.1.1⁷,¹⁰.0¹,⁶]tridec-2-en-5-yl]propylidene}amino)benzoic acid)

Structure for NP0303490 (2,4-dihydroxy-3-({1-hydroxy-3-[9-(hydroxymethyl)-5-methyl-4-oxo-8-oxatetracyclo[7.2.1.1⁷,¹⁰.0¹,⁶]tridec-2-en-5-yl]propylidene}amino)benzoic acid)

3D Structure for NP0303490 (2,4-dihydroxy-3-({1-hydroxy-3-[9-(hydroxymethyl)-5-methyl-4-oxo-8-oxatetracyclo[7.2.1.1⁷,¹⁰.0¹,⁶]tridec-2-en-5-yl]propylidene}amino)benzoic acid)