NP-MRD: Showing NP-Card for campyrone B (NP0042513)

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Record Information

Version

2.0

Created at

2021-06-21 00:09:22 UTC

Updated at

2021-06-30 00:17:38 UTC

NP-MRD ID

NP0042513

Secondary Accession Numbers

None

Natural Product Identification

Common Name

campyrone B

Provided By

JEOL Database JEOL Logo

Description

N-[(1S)-1-(4-methoxy-2-oxo-2H-pyran-6-yl)-3-methylbutyl]ethanimidic acid belongs to the class of organic compounds known as pyranones and derivatives. Pyranones and derivatives are compounds containing a pyran ring which bears a ketone. campyrone B is found in Aspergillus niger. campyrone B was first documented in 2013 (Talontsi, F. M., et al.). Based on a literature review very few articles have been published on N-[(1S)-1-(4-methoxy-2-oxo-2H-pyran-6-yl)-3-methylbutyl]ethanimidic acid.

Structure

MOL 3D MOL SDF 3D SDF PDB SMILES InChI


  Mrv1652306212102093D          

 37 37  0  0  0  0            999 V2000
   -5.8043    1.2774   -2.3587 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.4671    0.7926   -2.3034 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5788    1.4632   -1.5005 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2630    0.8852   -1.5221 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2821    1.4161   -0.7801 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.1297    0.8801   -0.7351 C   0  0  2  0  0  0  0  0  0  0  0  0
    0.5432    0.3914    0.6678 C   0  0  1  0  0  0  0  0  0  0  0  0
   -0.3139   -0.7522    1.2484 C   0  0  1  0  0  0  0  0  0  0  0  0
   -0.2486   -2.0189    0.3942 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.1467   -1.0686    2.6743 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.0060    1.9573   -1.1707 N   0  0  0  0  0  0  0  0  0  0  0  0
    2.2080    1.7136   -1.7889 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.9840    2.9591   -2.1190 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.6347    0.5900   -2.0308 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5159    2.5626    0.0237 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7490    3.1483    0.0647 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.9763    4.1457    0.7407 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.8194    2.5429   -0.7444 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.8344    2.2967   -2.7575 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.2789    1.2287   -1.3733 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.3687    0.6319   -3.0381 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0936    0.0141   -2.1485 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.2429    0.0568   -1.4503 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.5930    0.0687    0.6361 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.5200    1.2409    1.3649 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3601   -0.4286    1.3066 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6866   -1.8577   -0.5950 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8078   -2.8342    0.8661 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.7855   -2.3534    0.2591 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.0695   -0.1828    3.3136 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.1876   -1.4094    2.6901 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4739   -1.8541    3.1185 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.7439    2.9074   -0.9399 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.6292    2.7680   -2.9809 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.5977    3.2384   -1.2586 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.3111    3.7851   -2.3665 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.7796    3.0332   -0.6763 H   0  0  0  0  0  0  0  0  0  0  0  0
 16 15  1  0  0  0  0
  7  8  1  0  0  0  0
 15  5  1  0  0  0  0
 11 12  1  0  0  0  0
  5  4  2  0  0  0  0
 12 13  1  0  0  0  0
  4  3  1  0  0  0  0
 12 14  2  0  0  0  0
  3  2  1  0  0  0  0
  5  6  1  0  0  0  0
  2  1  1  0  0  0  0
 18 16  1  0  0  0  0
 16 17  2  0  0  0  0
  6  7  1  0  0  0  0
  6 23  1  6  0  0  0
 18  3  2  0  0  0  0
  8  9  1  0  0  0  0
  6 11  1  0  0  0  0
  8 10  1  0  0  0  0
 18 37  1  0  0  0  0
  4 22  1  0  0  0  0
  7 24  1  0  0  0  0
  7 25  1  0  0  0  0
 11 33  1  0  0  0  0
  8 26  1  1  0  0  0
 13 34  1  0  0  0  0
 13 35  1  0  0  0  0
 13 36  1  0  0  0  0
  1 19  1  0  0  0  0
  1 20  1  0  0  0  0
  1 21  1  0  0  0  0
  9 27  1  0  0  0  0
  9 28  1  0  0  0  0
  9 29  1  0  0  0  0
 10 30  1  0  0  0  0
 10 31  1  0  0  0  0
 10 32  1  0  0  0  0
M  END

     RDKit          3D

 37 37  0  0  0  0  0  0  0  0999 V2000
   -5.8043    1.2774   -2.3587 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.4671    0.7926   -2.3034 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5788    1.4632   -1.5005 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2630    0.8852   -1.5221 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2821    1.4161   -0.7801 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.1297    0.8801   -0.7351 C   0  0  2  0  0  0  0  0  0  0  0  0
    0.5432    0.3914    0.6678 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3139   -0.7522    1.2484 C   0  0  1  0  0  0  0  0  0  0  0  0
   -0.2486   -2.0189    0.3942 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.1467   -1.0686    2.6743 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.0060    1.9573   -1.1707 N   0  0  0  0  0  0  0  0  0  0  0  0
    2.2080    1.7136   -1.7889 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.9840    2.9591   -2.1190 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.6347    0.5900   -2.0308 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5159    2.5626    0.0237 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7490    3.1483    0.0647 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.9763    4.1457    0.7407 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.8194    2.5429   -0.7444 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.8344    2.2967   -2.7575 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.2789    1.2287   -1.3733 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.3687    0.6319   -3.0381 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0936    0.0141   -2.1485 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.2429    0.0568   -1.4503 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.5930    0.0687    0.6361 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.5200    1.2409    1.3649 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3601   -0.4286    1.3066 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6866   -1.8577   -0.5950 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8078   -2.8342    0.8661 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.7855   -2.3534    0.2591 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.0695   -0.1828    3.3136 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.1876   -1.4094    2.6901 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4739   -1.8541    3.1185 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.7439    2.9074   -0.9399 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.6292    2.7680   -2.9809 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.5977    3.2384   -1.2586 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.3111    3.7851   -2.3665 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.7796    3.0332   -0.6763 H   0  0  0  0  0  0  0  0  0  0  0  0
 16 15  1  0
  7  8  1  0
 15  5  1  0
 11 12  1  0
  5  4  2  0
 12 13  1  0
  4  3  1  0
 12 14  2  0
  3  2  1  0
  5  6  1  0
  2  1  1  0
 18 16  1  0
 16 17  2  0
  6  7  1  0
  6 23  1  6
 18  3  2  0
  8  9  1  0
  6 11  1  0
  8 10  1  0
 18 37  1  0
  4 22  1  0
  7 24  1  0
  7 25  1  0
 11 33  1  0
  8 26  1  1
 13 34  1  0
 13 35  1  0
 13 36  1  0
  1 19  1  0
  1 20  1  0
  1 21  1  0
  9 27  1  0
  9 28  1  0
  9 29  1  0
 10 30  1  0
 10 31  1  0
 10 32  1  0
M  END


  Mrv1652306212102093D          

 37 37  0  0  0  0            999 V2000
   -5.8043    1.2774   -2.3587 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.4671    0.7926   -2.3034 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5788    1.4632   -1.5005 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2630    0.8852   -1.5221 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2821    1.4161   -0.7801 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.1297    0.8801   -0.7351 C   0  0  2  0  0  0  0  0  0  0  0  0
    0.5432    0.3914    0.6678 C   0  0  1  0  0  0  0  0  0  0  0  0
   -0.3139   -0.7522    1.2484 C   0  0  1  0  0  0  0  0  0  0  0  0
   -0.2486   -2.0189    0.3942 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.1467   -1.0686    2.6743 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.0060    1.9573   -1.1707 N   0  0  0  0  0  0  0  0  0  0  0  0
    2.2080    1.7136   -1.7889 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.9840    2.9591   -2.1190 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.6347    0.5900   -2.0308 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5159    2.5626    0.0237 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7490    3.1483    0.0647 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.9763    4.1457    0.7407 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.8194    2.5429   -0.7444 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.8344    2.2967   -2.7575 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.2789    1.2287   -1.3733 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.3687    0.6319   -3.0381 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0936    0.0141   -2.1485 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.2429    0.0568   -1.4503 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.5930    0.0687    0.6361 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.5200    1.2409    1.3649 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3601   -0.4286    1.3066 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6866   -1.8577   -0.5950 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8078   -2.8342    0.8661 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.7855   -2.3534    0.2591 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.0695   -0.1828    3.3136 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.1876   -1.4094    2.6901 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4739   -1.8541    3.1185 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.7439    2.9074   -0.9399 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.6292    2.7680   -2.9809 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.5977    3.2384   -1.2586 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.3111    3.7851   -2.3665 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.7796    3.0332   -0.6763 H   0  0  0  0  0  0  0  0  0  0  0  0
 16 15  1  0  0  0  0
  7  8  1  0  0  0  0
 15  5  1  0  0  0  0
 11 12  1  0  0  0  0
  5  4  2  0  0  0  0
 12 13  1  0  0  0  0
  4  3  1  0  0  0  0
 12 14  2  0  0  0  0
  3  2  1  0  0  0  0
  5  6  1  0  0  0  0
  2  1  1  0  0  0  0
 18 16  1  0  0  0  0
 16 17  2  0  0  0  0
  6  7  1  0  0  0  0
  6 23  1  6  0  0  0
 18  3  2  0  0  0  0
  8  9  1  0  0  0  0
  6 11  1  0  0  0  0
  8 10  1  0  0  0  0
 18 37  1  0  0  0  0
  4 22  1  0  0  0  0
  7 24  1  0  0  0  0
  7 25  1  0  0  0  0
 11 33  1  0  0  0  0
  8 26  1  1  0  0  0
 13 34  1  0  0  0  0
 13 35  1  0  0  0  0
 13 36  1  0  0  0  0
  1 19  1  0  0  0  0
  1 20  1  0  0  0  0
  1 21  1  0  0  0  0
  9 27  1  0  0  0  0
  9 28  1  0  0  0  0
  9 29  1  0  0  0  0
 10 30  1  0  0  0  0
 10 31  1  0  0  0  0
 10 32  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0042513

> <DATABASE_NAME>
NP-MRD

> <SMILES>
[H]N(C(=O)C([H])([H])[H])[C@]([H])(C1=C([H])C(OC([H])([H])[H])=C([H])C(=O)O1)C([H])([H])C([H])(C([H])([H])[H])C([H])([H])[H]

> <INCHI_IDENTIFIER>
InChI=1S/C13H19NO4/c1-8(2)5-11(14-9(3)15)12-6-10(17-4)7-13(16)18-12/h6-8,11H,5H2,1-4H3,(H,14,15)/t11-/m0/s1

> <INCHI_KEY>
PFIUOLPDUMSADF-NSHDSACASA-N

> <FORMULA>
C13H19NO4

> <MOLECULAR_WEIGHT>
253.298

> <EXACT_MASS>
253.131408096

> <JCHEM_ACCEPTOR_COUNT>
3

> <JCHEM_ATOM_COUNT>
37

> <JCHEM_AVERAGE_POLARIZABILITY>
27.07886358722888

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
1

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
1

> <JCHEM_IUPAC>
N-[(1S)-1-(4-methoxy-2-oxo-2H-pyran-6-yl)-3-methylbutyl]acetamide

> <ALOGPS_LOGP>
1.82

> <JCHEM_LOGP>
0.9976490596666678

> <ALOGPS_LOGS>
-2.70

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
1

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA_STRONGEST_ACIDIC>
13.6624818775866

> <JCHEM_PKA_STRONGEST_BASIC>
-1.3683292693422868

> <JCHEM_POLAR_SURFACE_AREA>
64.63

> <JCHEM_REFRACTIVITY>
69.29549999999999

> <JCHEM_ROTATABLE_BOND_COUNT>
5

> <JCHEM_RULE_OF_FIVE>
1

> <ALOGPS_SOLUBILITY>
5.04e-01 g/l

> <JCHEM_TRADITIONAL_IUPAC>
N-[(1S)-1-(4-methoxy-6-oxopyran-2-yl)-3-methylbutyl]acetamide

> <JCHEM_VEBER_RULE>
0

$$$$

     RDKit          3D

 37 37  0  0  0  0  0  0  0  0999 V2000
   -5.8043    1.2774   -2.3587 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.4671    0.7926   -2.3034 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5788    1.4632   -1.5005 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2630    0.8852   -1.5221 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2821    1.4161   -0.7801 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.1297    0.8801   -0.7351 C   0  0  2  0  0  0  0  0  0  0  0  0
    0.5432    0.3914    0.6678 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3139   -0.7522    1.2484 C   0  0  1  0  0  0  0  0  0  0  0  0
   -0.2486   -2.0189    0.3942 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.1467   -1.0686    2.6743 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.0060    1.9573   -1.1707 N   0  0  0  0  0  0  0  0  0  0  0  0
    2.2080    1.7136   -1.7889 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.9840    2.9591   -2.1190 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.6347    0.5900   -2.0308 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5159    2.5626    0.0237 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7490    3.1483    0.0647 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.9763    4.1457    0.7407 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.8194    2.5429   -0.7444 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.8344    2.2967   -2.7575 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.2789    1.2287   -1.3733 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.3687    0.6319   -3.0381 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0936    0.0141   -2.1485 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.2429    0.0568   -1.4503 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.5930    0.0687    0.6361 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.5200    1.2409    1.3649 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3601   -0.4286    1.3066 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6866   -1.8577   -0.5950 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8078   -2.8342    0.8661 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.7855   -2.3534    0.2591 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.0695   -0.1828    3.3136 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.1876   -1.4094    2.6901 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4739   -1.8541    3.1185 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.7439    2.9074   -0.9399 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.6292    2.7680   -2.9809 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.5977    3.2384   -1.2586 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.3111    3.7851   -2.3665 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.7796    3.0332   -0.6763 H   0  0  0  0  0  0  0  0  0  0  0  0
 16 15  1  0
  7  8  1  0
 15  5  1  0
 11 12  1  0
  5  4  2  0
 12 13  1  0
  4  3  1  0
 12 14  2  0
  3  2  1  0
  5  6  1  0
  2  1  1  0
 18 16  1  0
 16 17  2  0
  6  7  1  0
  6 23  1  6
 18  3  2  0
  8  9  1  0
  6 11  1  0
  8 10  1  0
 18 37  1  0
  4 22  1  0
  7 24  1  0
  7 25  1  0
 11 33  1  0
  8 26  1  1
 13 34  1  0
 13 35  1  0
 13 36  1  0
  1 19  1  0
  1 20  1  0
  1 21  1  0
  9 27  1  0
  9 28  1  0
  9 29  1  0
 10 30  1  0
 10 31  1  0
 10 32  1  0
M  END

HEADER    PROTEIN                                 21-JUN-21   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   21-JUN-21         0                                  
HETATM    1  C   UNK     0      -5.804   1.277  -2.359  0.00  0.00           C+0
HETATM    2  O   UNK     0      -4.467   0.793  -2.303  0.00  0.00           O+0
HETATM    3  C   UNK     0      -3.579   1.463  -1.500  0.00  0.00           C+0
HETATM    4  C   UNK     0      -2.263   0.885  -1.522  0.00  0.00           C+0
HETATM    5  C   UNK     0      -1.282   1.416  -0.780  0.00  0.00           C+0
HETATM    6  C   UNK     0       0.130   0.880  -0.735  0.00  0.00           C+0
HETATM    7  C   UNK     0       0.543   0.391   0.668  0.00  0.00           C+0
HETATM    8  C   UNK     0      -0.314  -0.752   1.248  0.00  0.00           C+0
HETATM    9  C   UNK     0      -0.249  -2.019   0.394  0.00  0.00           C+0
HETATM   10  C   UNK     0       0.147  -1.069   2.674  0.00  0.00           C+0
HETATM   11  N   UNK     0       1.006   1.957  -1.171  0.00  0.00           N+0
HETATM   12  C   UNK     0       2.208   1.714  -1.789  0.00  0.00           C+0
HETATM   13  C   UNK     0       2.984   2.959  -2.119  0.00  0.00           C+0
HETATM   14  O   UNK     0       2.635   0.590  -2.031  0.00  0.00           O+0
HETATM   15  O   UNK     0      -1.516   2.563   0.024  0.00  0.00           O+0
HETATM   16  C   UNK     0      -2.749   3.148   0.065  0.00  0.00           C+0
HETATM   17  O   UNK     0      -2.976   4.146   0.741  0.00  0.00           O+0
HETATM   18  C   UNK     0      -3.819   2.543  -0.744  0.00  0.00           C+0
HETATM   19  H   UNK     0      -5.834   2.297  -2.757  0.00  0.00           H+0
HETATM   20  H   UNK     0      -6.279   1.229  -1.373  0.00  0.00           H+0
HETATM   21  H   UNK     0      -6.369   0.632  -3.038  0.00  0.00           H+0
HETATM   22  H   UNK     0      -2.094   0.014  -2.148  0.00  0.00           H+0
HETATM   23  H   UNK     0       0.243   0.057  -1.450  0.00  0.00           H+0
HETATM   24  H   UNK     0       1.593   0.069   0.636  0.00  0.00           H+0
HETATM   25  H   UNK     0       0.520   1.241   1.365  0.00  0.00           H+0
HETATM   26  H   UNK     0      -1.360  -0.429   1.307  0.00  0.00           H+0
HETATM   27  H   UNK     0      -0.687  -1.858  -0.595  0.00  0.00           H+0
HETATM   28  H   UNK     0      -0.808  -2.834   0.866  0.00  0.00           H+0
HETATM   29  H   UNK     0       0.786  -2.353   0.259  0.00  0.00           H+0
HETATM   30  H   UNK     0       0.070  -0.183   3.314  0.00  0.00           H+0
HETATM   31  H   UNK     0       1.188  -1.409   2.690  0.00  0.00           H+0
HETATM   32  H   UNK     0      -0.474  -1.854   3.119  0.00  0.00           H+0
HETATM   33  H   UNK     0       0.744   2.907  -0.940  0.00  0.00           H+0
HETATM   34  H   UNK     0       3.629   2.768  -2.981  0.00  0.00           H+0
HETATM   35  H   UNK     0       3.598   3.238  -1.259  0.00  0.00           H+0
HETATM   36  H   UNK     0       2.311   3.785  -2.366  0.00  0.00           H+0
HETATM   37  H   UNK     0      -4.780   3.033  -0.676  0.00  0.00           H+0
CONECT    1    2   19   20   21                                             
CONECT    2    3    1                                                       
CONECT    3    4    2   18                                                  
CONECT    4    5    3   22                                                  
CONECT    5   15    4    6                                                  
CONECT    6    5    7   23   11                                             
CONECT    7    8    6   24   25                                             
CONECT    8    7    9   10   26                                             
CONECT    9    8   27   28   29                                             
CONECT   10    8   30   31   32                                             
CONECT   11   12    6   33                                                  
CONECT   12   11   13   14                                                  
CONECT   13   12   34   35   36                                             
CONECT   14   12                                                            
CONECT   15   16    5                                                       
CONECT   16   15   18   17                                                  
CONECT   17   16                                                            
CONECT   18   16    3   37                                                  
CONECT   19    1                                                            
CONECT   20    1                                                            
CONECT   21    1                                                            
CONECT   22    4                                                            
CONECT   23    6                                                            
CONECT   24    7                                                            
CONECT   25    7                                                            
CONECT   26    8                                                            
CONECT   27    9                                                            
CONECT   28    9                                                            
CONECT   29    9                                                            
CONECT   30   10                                                            
CONECT   31   10                                                            
CONECT   32   10                                                            
CONECT   33   11                                                            
CONECT   34   13                                                            
CONECT   35   13                                                            
CONECT   36   13                                                            
CONECT   37   18                                                            
MASTER        0    0    0    0    0    0    0    0   37    0   74    0
END

RDKit          3D

37 37  0  0  0  0  0  0  0  0999 V2000
   -5.8043    1.2774   -2.3587 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.4671    0.7926   -2.3034 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5788    1.4632   -1.5005 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2630    0.8852   -1.5221 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2821    1.4161   -0.7801 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.1297    0.8801   -0.7351 C   0  0  2  0  0  0  0  0  0  0  0  0
    0.5432    0.3914    0.6678 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3139   -0.7522    1.2484 C   0  0  1  0  0  0  0  0  0  0  0  0
   -0.2486   -2.0189    0.3942 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.1467   -1.0686    2.6743 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.0060    1.9573   -1.1707 N   0  0  0  0  0  0  0  0  0  0  0  0
    2.2080    1.7136   -1.7889 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.9840    2.9591   -2.1190 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.6347    0.5900   -2.0308 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5159    2.5626    0.0237 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7490    3.1483    0.0647 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.9763    4.1457    0.7407 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.8194    2.5429   -0.7444 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.8344    2.2967   -2.7575 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.2789    1.2287   -1.3733 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.3687    0.6319   -3.0381 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0936    0.0141   -2.1485 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.2429    0.0568   -1.4503 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.5930    0.0687    0.6361 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.5200    1.2409    1.3649 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3601   -0.4286    1.3066 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6866   -1.8577   -0.5950 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8078   -2.8342    0.8661 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.7855   -2.3534    0.2591 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.0695   -0.1828    3.3136 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.1876   -1.4094    2.6901 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4739   -1.8541    3.1185 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.7439    2.9074   -0.9399 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.6292    2.7680   -2.9809 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.5977    3.2384   -1.2586 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.3111    3.7851   -2.3665 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.7796    3.0332   -0.6763 H   0  0  0  0  0  0  0  0  0  0  0  0
 16 15  1  0
  7  8  1  0
 15  5  1  0
 11 12  1  0
  5  4  2  0
 12 13  1  0
  4  3  1  0
 12 14  2  0
  3  2  1  0
  5  6  1  0
  2  1  1  0
 18 16  1  0
 16 17  2  0
  6  7  1  0
  6 23  1  6
 18  3  2  0
  8  9  1  0
  6 11  1  0
  8 10  1  0
 18 37  1  0
  4 22  1  0
  7 24  1  0
  7 25  1  0
 11 33  1  0
  8 26  1  1
 13 34  1  0
 13 35  1  0
 13 36  1  0
  1 19  1  0
  1 20  1  0
  1 21  1  0
  9 27  1  0
  9 28  1  0
  9 29  1  0
 10 30  1  0
 10 31  1  0
 10 32  1  0
M  END

View in JSmol

Synonyms

Value	Source
N-[(1S)-1-(4-Methoxy-2-oxo-2H-pyran-6-yl)-3-methylbutyl]ethanimidate	Generator

Chemical Formula

C₁₃H₁₉NO₄

Average Mass

253.2980 Da

Monoisotopic Mass

253.13141 Da

IUPAC Name

N-[(1S)-1-(4-methoxy-2-oxo-2H-pyran-6-yl)-3-methylbutyl]acetamide

Traditional Name

N-[(1S)-1-(4-methoxy-6-oxopyran-2-yl)-3-methylbutyl]acetamide

CAS Registry Number

Not Available

SMILES

[H]N(C(=O)C([H])([H])[H])[C@]([H])(C1=C([H])C(OC([H])([H])[H])=C([H])C(=O)O1)C([H])([H])C([H])(C([H])([H])[H])C([H])([H])[H]

InChI Identifier

InChI=1S/C13H19NO4/c1-8(2)5-11(14-9(3)15)12-6-10(17-4)7-13(16)18-12/h6-8,11H,5H2,1-4H3,(H,14,15)/t11-/m0/s1

InChI Key

PFIUOLPDUMSADF-NSHDSACASA-N

Experimental Spectra

Spectrum Type	Description	Depositor Email	Depositor Organization	Depositor	Deposition Date	View
1D NMR	¹³C NMR Spectrum (1D, 300 MHz, CD₃OD, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 300 MHz, CD₃OD, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 100 MHz, CD₃OD, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 100 MHz, CD₃OD, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 200 MHz, CD₃OD, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 200 MHz, CD₃OD, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 400 MHz, CD₃OD, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 400 MHz, CD₃OD, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 500 MHz, CD₃OD, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 500 MHz, CD₃OD, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 600 MHz, CD₃OD, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 600 MHz, CD₃OD, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 700 MHz, CD₃OD, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 700 MHz, CD₃OD, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 800 MHz, CD₃OD, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 800 MHz, CD₃OD, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 900 MHz, CD₃OD, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 900 MHz, CD₃OD, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 1000 MHz, CD₃OD, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 1000 MHz, CD₃OD, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum

Predicted Spectra

Not Available

Chemical Shift Submissions

Not Available

Species

Species of Origin

Species Name	Source	Reference
Aspergillus niger	JEOL database	Talontsi, F. M., et al, Tetrahedron 69, 7147 (2013)

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as pyranones and derivatives. Pyranones and derivatives are compounds containing a pyran ring which bears a ketone.

Kingdom

Organic compounds

Super Class

Organoheterocyclic compounds

Class

Pyrans

Sub Class

Pyranones and derivatives

Direct Parent

Pyranones and derivatives

Alternative Parents

Substituents

Alkyl aryl ether
Pyranone
Heteroaromatic compound
Acetamide
Vinylogous ester
Carboxamide group
Lactone
Secondary carboxylic acid amide
Carboxylic acid derivative
Ether
Oxacycle
Organonitrogen compound
Organic oxide
Organic nitrogen compound
Organic oxygen compound
Organooxygen compound
Hydrocarbon derivative
Carbonyl group
Aromatic heteromonocyclic compound

Molecular Framework

Aromatic heteromonocyclic 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	1.82	ALOGPS
logP	1	ChemAxon
logS	-2.7	ALOGPS
pKa (Strongest Acidic)	13.66	ChemAxon
pKa (Strongest Basic)	-1.4	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	3	ChemAxon
Hydrogen Donor Count	1	ChemAxon
Polar Surface Area	64.63 Å²	ChemAxon
Rotatable Bond Count	5	ChemAxon
Refractivity	69.3 m³·mol⁻¹	ChemAxon
Polarizability	27.08 Å³	ChemAxon
Number of Rings	1	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

78438171

KEGG Compound ID

Not Available

BioCyc ID

Not Available

BiGG ID

Not Available

Wikipedia Link

Not Available

METLIN ID

Not Available

PubChem Compound

72197063

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

Talontsi, F. M., et al. (2013). Talontsi, F. M., et al, Tetrahedron 69, 7147 (2013). Tetrahedron.

Showing NP-Card for campyrone B (NP0042513)

MOL for NP0042513 (campyrone B)

3D MOL for NP0042513 (campyrone B)

3D SDF for NP0042513 (campyrone B)

3D-SDF for NP0042513 (campyrone B)

PDB for NP0042513 (campyrone B)

3D PDB for NP0042513 (campyrone B)

SMILES for NP0042513 (campyrone B)

INCHI for NP0042513 (campyrone B)

Structure for NP0042513 (campyrone B)

3D Structure for NP0042513 (campyrone B)