NP-MRD: Showing NP-Card for n-(2,6-dihydroxyphenyl)-3-{5,9-dimethyl-4-oxo-8-oxatetracyclo[7.2.1.1⁷,¹⁰.0¹,⁶]tridec-2-en-5-yl}propanimidic acid (NP0330513)

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Record Information

Version

1.0

Created at

2022-09-12 15:56:29 UTC

Updated at

2022-09-12 15:56:29 UTC

NP-MRD ID

NP0330513

Secondary Accession Numbers

None

Natural Product Identification

Common Name

n-(2,6-dihydroxyphenyl)-3-{5,9-dimethyl-4-oxo-8-oxatetracyclo[7.2.1.1⁷,¹⁰.0¹,⁶]tridec-2-en-5-yl}propanimidic acid

Description

N-(2,6-dihydroxyphenyl)-3-{5,9-dimethyl-4-oxo-8-oxatetracyclo[7.2.1.1⁷,¹⁰.0¹,⁶]Tridec-2-en-5-yl}propanimidic acid belongs to the class of organic compounds known as resorcinols. Resorcinols are compounds containing a resorcinol moiety, which is a benzene ring bearing two hydroxyl groups at positions 1 and 3. n-(2,6-dihydroxyphenyl)-3-{5,9-dimethyl-4-oxo-8-oxatetracyclo[7.2.1.1⁷,¹⁰.0¹,⁶]tridec-2-en-5-yl}propanimidic acid is found in Streptomyces platensis. Based on a literature review very few articles have been published on N-(2,6-dihydroxyphenyl)-3-{5,9-dimethyl-4-oxo-8-oxatetracyclo[7.2.1.1⁷,¹⁰.0¹,⁶]Tridec-2-en-5-yl}propanimidic acid.

Structure

MOL 3D MOL SDF PDB SMILES InChI


  Mrv1652309122217562D          

 29 33  0  0  0  0            999 V2000
    4.5815   -0.5093    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.0547    0.1257    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.2423   -0.1839    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.7427    0.5331    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.9084    0.3254    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.1926    0.7721    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.2869    1.6088    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.6406    2.1215    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.0804    1.8910    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.6440    2.5912    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.6710    2.4671    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.4675    3.2666    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.0581    3.8426    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.8522    3.6191    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.8545    4.6421    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    3.4451    5.2181    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.2416    6.0176    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.4475    6.2411    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.8322    6.5936    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.6264    6.3701    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.8299    5.5706    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.2393    4.9946    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.4428    4.1951    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.7933    1.4216    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5800    1.8039    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.4376    1.6790    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.4743    0.8105    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5790    0.5518    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.8961    1.0410    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  2  0  0  0  0
  6  7  1  0  0  0  0
  7  8  2  0  0  0  0
  7  9  1  0  0  0  0
  9 10  1  0  0  0  0
  9 11  1  0  0  0  0
 11 12  1  0  0  0  0
 12 13  1  0  0  0  0
 13 14  1  0  0  0  0
 13 15  2  0  0  0  0
 15 16  1  4  0  0  0
 16 17  2  0  0  0  0
 17 18  1  0  0  0  0
 17 19  1  0  0  0  0
 19 20  2  0  0  0  0
 20 21  1  0  0  0  0
 21 22  2  0  0  0  0
 16 22  1  0  0  0  0
 22 23  1  0  0  0  0
  9 24  1  0  0  0  0
  4 24  1  0  0  0  0
 24 25  1  0  0  0  0
 25 26  1  0  0  0  0
 26 27  1  0  0  0  0
  2 27  1  0  0  0  0
 27 28  1  0  0  0  0
  4 28  1  0  0  0  0
 25 29  1  0  0  0  0
  2 29  1  0  0  0  0
M  END

     RDKit          3D

 56 60  0  0  0  0  0  0  0  0999 V2000
   -0.8844   -1.2602    1.8988 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6207   -0.8180    0.5262 C   0  0  1  0  0  0  0  0  0  0  0  0
    0.3356    0.3450    0.5625 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.5717    0.0969    1.3906 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.4621    1.3244    1.3697 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.8469    2.4857    1.9032 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.5730    1.3811    0.9625 N   0  0  0  0  0  0  0  0  0  0  0  0
    4.8013    1.4287    0.5084 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.0753    1.1180   -0.8364 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.0058    0.7679   -1.6245 O   0  0  0  0  0  0  0  0  0  0  0  0
    6.3579    1.1613   -1.3457 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.4086    1.5148   -0.5344 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.1574    1.8204    0.7789 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.8987    1.7826    1.2973 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.6325    2.0898    2.6260 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.0435   -1.9254   -0.2436 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.2426   -1.9709   -0.5604 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8031   -3.0589   -0.6617 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0995   -2.8633   -0.8367 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7327   -1.5625   -0.6316 C   0  0  1  0  0  0  0  0  0  0  0  0
   -3.4914   -1.0831   -1.8922 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.2939    0.0619   -1.2566 C   0  0  2  0  0  0  0  0  0  0  0  0
   -3.3354    1.2294   -1.1303 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5714    0.7617    0.1304 C   0  0  1  0  0  0  0  0  0  0  0  0
   -3.6581    0.4916    0.9598 O   0  0  0  0  0  0  0  0  0  0  0  0
   -4.5041   -0.3052    0.1891 C   0  0  1  0  0  0  0  0  0  0  0  0
   -5.9231   -0.1889    0.6307 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.9470   -1.6929    0.2462 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8065   -0.4353   -0.3056 C   0  0  1  0  0  0  0  0  0  0  0  0
   -1.1328   -0.4029    2.5779 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6095   -2.0388    2.0783 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.0898   -1.6553    2.3164 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.6978    0.5570   -0.4698 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1150    1.2720    0.9771 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.1817   -0.7602    1.0899 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.3274   -0.0440    2.4655 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.9186    2.6777    2.8928 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.0627    0.7310   -1.2691 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.5198    0.9137   -2.3868 H   0  0  0  0  0  0  0  0  0  0  0  0
    8.3865    1.5421   -0.9456 H   0  0  0  0  0  0  0  0  0  0  0  0
    8.0266    2.0985    1.3953 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.4081    2.3504    3.2085 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3822   -4.0367   -0.8253 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7144   -3.6851   -1.1402 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8004   -0.7278   -2.6574 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.1861   -1.8638   -2.2029 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.2002    0.2864   -1.8003 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.8436    2.1776   -0.9631 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6589    1.2063   -1.9915 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0025    1.6359    0.4342 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.2783   -1.0013    1.2801 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.0261    0.8020    1.1574 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.5688   -0.1133   -0.2794 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.6695   -2.3454   -0.3303 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.8281   -2.1343    1.2089 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3442   -0.1382   -1.3028 H   0  0  0  0  0  0  0  0  0  0  0  0
 26 27  1  1
 26 28  1  0
 28 20  1  0
 20 21  1  0
 21 22  1  0
 22 23  1  0
 23 24  1  0
 24 25  1  0
 24 29  1  0
 29  2  1  0
  2  1  1  1
  2  3  1  0
  3  4  1  0
  4  5  1  0
  5  6  1  0
  5  7  2  3
  7  8  1  0
  8  9  2  0
  9 10  1  0
  9 11  1  0
 11 12  2  0
 12 13  1  0
 13 14  2  0
 14 15  1  0
  2 16  1  0
 16 17  2  0
 16 18  1  0
 18 19  2  0
 22 26  1  0
 14  8  1  0
 25 26  1  0
 29 20  1  0
 20 19  1  6
 27 51  1  0
 27 52  1  0
 27 53  1  0
 28 54  1  0
 28 55  1  0
 21 45  1  0
 21 46  1  0
 22 47  1  6
 23 48  1  0
 23 49  1  0
 24 50  1  1
 29 56  1  6
  1 30  1  0
  1 31  1  0
  1 32  1  0
  3 33  1  0
  3 34  1  0
  4 35  1  0
  4 36  1  0
  6 37  1  0
 10 38  1  0
 11 39  1  0
 12 40  1  0
 13 41  1  0
 15 42  1  0
 18 43  1  0
 19 44  1  0
M  END


  Mrv1652309122217562D          

 29 33  0  0  0  0            999 V2000
    4.5815   -0.5093    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.0547    0.1257    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.2423   -0.1839    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.7427    0.5331    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.9084    0.3254    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.1926    0.7721    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.2869    1.6088    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.6406    2.1215    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.0804    1.8910    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.6440    2.5912    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.6710    2.4671    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.4675    3.2666    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.0581    3.8426    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.8522    3.6191    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.8545    4.6421    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    3.4451    5.2181    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.2416    6.0176    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.4475    6.2411    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.8322    6.5936    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.6264    6.3701    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.8299    5.5706    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.2393    4.9946    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.4428    4.1951    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.7933    1.4216    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5800    1.8039    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.4376    1.6790    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.4743    0.8105    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5790    0.5518    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.8961    1.0410    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  2  0  0  0  0
  6  7  1  0  0  0  0
  7  8  2  0  0  0  0
  7  9  1  0  0  0  0
  9 10  1  0  0  0  0
  9 11  1  0  0  0  0
 11 12  1  0  0  0  0
 12 13  1  0  0  0  0
 13 14  1  0  0  0  0
 13 15  2  0  0  0  0
 15 16  1  4  0  0  0
 16 17  2  0  0  0  0
 17 18  1  0  0  0  0
 17 19  1  0  0  0  0
 19 20  2  0  0  0  0
 20 21  1  0  0  0  0
 21 22  2  0  0  0  0
 16 22  1  0  0  0  0
 22 23  1  0  0  0  0
  9 24  1  0  0  0  0
  4 24  1  0  0  0  0
 24 25  1  0  0  0  0
 25 26  1  0  0  0  0
 26 27  1  0  0  0  0
  2 27  1  0  0  0  0
 27 28  1  0  0  0  0
  4 28  1  0  0  0  0
 25 29  1  0  0  0  0
  2 29  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0330513

> <DATABASE_NAME>
NP-MRD

> <SMILES>
CC12CC34CC1CC(O2)C3C(C)(CCC(O)=NC1=C(O)C=CC=C1O)C(=O)C=C4

> <INCHI_IDENTIFIER>
InChI=1S/C23H27NO5/c1-21(8-7-18(28)24-19-14(25)4-3-5-15(19)26)17(27)6-9-23-11-13-10-16(20(21)23)29-22(13,2)12-23/h3-6,9,13,16,20,25-26H,7-8,10-12H2,1-2H3,(H,24,28)

> <INCHI_KEY>
VAXBYZCUDVPKHJ-UHFFFAOYSA-N

> <FORMULA>
C23H27NO5

> <MOLECULAR_WEIGHT>
397.471

> <EXACT_MASS>
397.188922973

> <JCHEM_ACCEPTOR_COUNT>
6

> <JCHEM_ATOM_COUNT>
56

> <JCHEM_AVERAGE_POLARIZABILITY>
42.09001006801087

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
3

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
1

> <JCHEM_IUPAC>
N-(2,6-dihydroxyphenyl)-3-{5,9-dimethyl-4-oxo-8-oxatetracyclo[7.2.1.1^{7,10}.0^{1,6}]tridec-2-en-5-yl}propanimidic acid

> <JCHEM_LOGP>
4.956082404666668

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
5

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA>
9.258588664315305

> <JCHEM_PKA_STRONGEST_ACIDIC>
5.305629263908251

> <JCHEM_PKA_STRONGEST_BASIC>
-0.9924592108484395

> <JCHEM_POLAR_SURFACE_AREA>
99.35000000000001

> <JCHEM_REFRACTIVITY>
110.30940000000001

> <JCHEM_ROTATABLE_BOND_COUNT>
4

> <JCHEM_RULE_OF_FIVE>
1

> <JCHEM_TRADITIONAL_IUPAC>
N-(2,6-dihydroxyphenyl)-3-{5,9-dimethyl-4-oxo-8-oxatetracyclo[7.2.1.1^{7,10}.0^{1,6}]tridec-2-en-5-yl}propanimidic acid

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 12-SEP-22   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   12-SEP-22         0                                  
HETATM    1  C   UNK     0       8.552  -0.951   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0       7.569   0.235   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0       6.052  -0.343   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0       5.120   0.995   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0       3.562   0.607   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0       2.226   1.441   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0       2.402   3.003   0.000  0.00  0.00           C+0
HETATM    8  O   UNK     0       1.196   3.960   0.000  0.00  0.00           O+0
HETATM    9  C   UNK     0       3.883   3.530   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0       3.069   4.837   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0       4.986   4.605   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0       4.606   6.098   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0       5.708   7.173   0.000  0.00  0.00           C+0
HETATM   14  O   UNK     0       7.191   6.756   0.000  0.00  0.00           O+0
HETATM   15  N   UNK     0       5.328   8.665   0.000  0.00  0.00           N+0
HETATM   16  C   UNK     0       6.431   9.740   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0       6.051  11.233   0.000  0.00  0.00           C+0
HETATM   18  O   UNK     0       4.569  11.650   0.000  0.00  0.00           O+0
HETATM   19  C   UNK     0       7.153  12.308   0.000  0.00  0.00           C+0
HETATM   20  C   UNK     0       8.636  11.891   0.000  0.00  0.00           C+0
HETATM   21  C   UNK     0       9.016  10.399   0.000  0.00  0.00           C+0
HETATM   22  C   UNK     0       7.913   9.323   0.000  0.00  0.00           C+0
HETATM   23  O   UNK     0       8.293   7.831   0.000  0.00  0.00           O+0
HETATM   24  C   UNK     0       5.214   2.654   0.000  0.00  0.00           C+0
HETATM   25  C   UNK     0       6.683   3.367   0.000  0.00  0.00           C+0
HETATM   26  C   UNK     0       8.283   3.134   0.000  0.00  0.00           C+0
HETATM   27  C   UNK     0       8.352   1.513   0.000  0.00  0.00           C+0
HETATM   28  C   UNK     0       6.681   1.030   0.000  0.00  0.00           C+0
HETATM   29  O   UNK     0       7.273   1.943   0.000  0.00  0.00           O+0
CONECT    1    2                                                            
CONECT    2    1    3   27   29                                             
CONECT    3    2    4                                                       
CONECT    4    3    5   24   28                                             
CONECT    5    4    6                                                       
CONECT    6    5    7                                                       
CONECT    7    6    8    9                                                  
CONECT    8    7                                                            
CONECT    9    7   10   11   24                                             
CONECT   10    9                                                            
CONECT   11    9   12                                                       
CONECT   12   11   13                                                       
CONECT   13   12   14   15                                                  
CONECT   14   13                                                            
CONECT   15   13   16                                                       
CONECT   16   15   17   22                                                  
CONECT   17   16   18   19                                                  
CONECT   18   17                                                            
CONECT   19   17   20                                                       
CONECT   20   19   21                                                       
CONECT   21   20   22                                                       
CONECT   22   21   16   23                                                  
CONECT   23   22                                                            
CONECT   24    9    4   25                                                  
CONECT   25   24   26   29                                                  
CONECT   26   25   27                                                       
CONECT   27   26    2   28                                                  
CONECT   28   27    4                                                       
CONECT   29   25    2                                                       
MASTER        0    0    0    0    0    0    0    0   29    0   66    0
END

View in JSmol

Synonyms

Value	Source
N-(2,6-Dihydroxyphenyl)-3-{5,9-dimethyl-4-oxo-8-oxatetracyclo[7.2.1.1,.0,]tridec-2-en-5-yl}propanimidate	Generator

Chemical Formula

C₂₃H₂₇NO₅

Average Mass

397.4710 Da

Monoisotopic Mass

397.18892 Da

IUPAC Name

N-(2,6-dihydroxyphenyl)-3-{5,9-dimethyl-4-oxo-8-oxatetracyclo[7.2.1.1^{7,10}.0^{1,6}]tridec-2-en-5-yl}propanimidic acid

Traditional Name

N-(2,6-dihydroxyphenyl)-3-{5,9-dimethyl-4-oxo-8-oxatetracyclo[7.2.1.1^{7,10}.0^{1,6}]tridec-2-en-5-yl}propanimidic acid

CAS Registry Number

Not Available

SMILES

CC12CC34CC1CC(O2)C3C(C)(CCC(O)=NC1=C(O)C=CC=C1O)C(=O)C=C4

InChI Identifier

InChI=1S/C23H27NO5/c1-21(8-7-18(28)24-19-14(25)4-3-5-15(19)26)17(27)6-9-23-11-13-10-16(20(21)23)29-22(13,2)12-23/h3-6,9,13,16,20,25-26H,7-8,10-12H2,1-2H3,(H,24,28)

InChI Key

VAXBYZCUDVPKHJ-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 resorcinols. Resorcinols are compounds containing a resorcinol moiety, which is a benzene ring bearing two hydroxyl groups at positions 1 and 3.

Kingdom

Super Class

Class

Sub Class

Direct Parent

Alternative Parents

Substituents

Resorcinol
1-hydroxy-4-unsubstituted benzenoid
1-hydroxy-2-unsubstituted benzenoid
Cyclohexenone
Oxepane
Monocyclic benzene moiety
Oxane
Oxolane
Ketone
Cyclic ketone
Carboximidic acid
Carboximidic acid derivative
Dialkyl ether
Ether
Oxacycle
Organoheterocyclic compound
Organic 1,3-dipolar compound
Propargyl-type 1,3-dipolar organic compound
Organonitrogen compound
Organooxygen compound
Organic oxide
Hydrocarbon derivative
Organic nitrogen compound
Carbonyl group
Organic oxygen 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
logP	4.96	ChemAxon
pKa (Strongest Acidic)	5.31	ChemAxon
pKa (Strongest Basic)	-0.99	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	6	ChemAxon
Hydrogen Donor Count	3	ChemAxon
Polar Surface Area	99.35 Å²	ChemAxon
Rotatable Bond Count	4	ChemAxon
Refractivity	110.31 m³·mol⁻¹	ChemAxon
Polarizability	42.09 Å³	ChemAxon
Number of Rings	5	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

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

163068932

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

LOTUS database [Link]

Showing NP-Card for n-(2,6-dihydroxyphenyl)-3-{5,9-dimethyl-4-oxo-8-oxatetracyclo[7.2.1.1⁷,¹⁰.0¹,⁶]tridec-2-en-5-yl}propanimidic acid (NP0330513)

MOL for NP0330513 (n-(2,6-dihydroxyphenyl)-3-{5,9-dimethyl-4-oxo-8-oxatetracyclo[7.2.1.1⁷,¹⁰.0¹,⁶]tridec-2-en-5-yl}propanimidic acid)

3D MOL for NP0330513 (n-(2,6-dihydroxyphenyl)-3-{5,9-dimethyl-4-oxo-8-oxatetracyclo[7.2.1.1⁷,¹⁰.0¹,⁶]tridec-2-en-5-yl}propanimidic acid)

3D SDF for NP0330513 (n-(2,6-dihydroxyphenyl)-3-{5,9-dimethyl-4-oxo-8-oxatetracyclo[7.2.1.1⁷,¹⁰.0¹,⁶]tridec-2-en-5-yl}propanimidic acid)

3D-SDF for NP0330513 (n-(2,6-dihydroxyphenyl)-3-{5,9-dimethyl-4-oxo-8-oxatetracyclo[7.2.1.1⁷,¹⁰.0¹,⁶]tridec-2-en-5-yl}propanimidic acid)

PDB for NP0330513 (n-(2,6-dihydroxyphenyl)-3-{5,9-dimethyl-4-oxo-8-oxatetracyclo[7.2.1.1⁷,¹⁰.0¹,⁶]tridec-2-en-5-yl}propanimidic acid)

3D PDB for NP0330513 (n-(2,6-dihydroxyphenyl)-3-{5,9-dimethyl-4-oxo-8-oxatetracyclo[7.2.1.1⁷,¹⁰.0¹,⁶]tridec-2-en-5-yl}propanimidic acid)

SMILES for NP0330513 (n-(2,6-dihydroxyphenyl)-3-{5,9-dimethyl-4-oxo-8-oxatetracyclo[7.2.1.1⁷,¹⁰.0¹,⁶]tridec-2-en-5-yl}propanimidic acid)

INCHI for NP0330513 (n-(2,6-dihydroxyphenyl)-3-{5,9-dimethyl-4-oxo-8-oxatetracyclo[7.2.1.1⁷,¹⁰.0¹,⁶]tridec-2-en-5-yl}propanimidic acid)

Structure for NP0330513 (n-(2,6-dihydroxyphenyl)-3-{5,9-dimethyl-4-oxo-8-oxatetracyclo[7.2.1.1⁷,¹⁰.0¹,⁶]tridec-2-en-5-yl}propanimidic acid)

3D Structure for NP0330513 (n-(2,6-dihydroxyphenyl)-3-{5,9-dimethyl-4-oxo-8-oxatetracyclo[7.2.1.1⁷,¹⁰.0¹,⁶]tridec-2-en-5-yl}propanimidic acid)