NP-MRD: Showing NP-Card for Asenjonamide B (NP0017511)

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Record Information

Version

2.0

Created at

2021-01-06 02:12:26 UTC

Updated at

2021-07-15 17:25:41 UTC

NP-MRD ID

NP0017511

Secondary Accession Numbers

None

Natural Product Identification

Common Name

Asenjonamide B

Provided By

NPAtlas

Description

Asenjonamide B belongs to the class of organic compounds known as b'-hydroxy-alpha,beta-unsaturated ketones. These are alpha,beta-unsaturated ketones that carry a hydroxyl group at the beta'-position. Asenjonamide B is found in Streptomyces and Streptomyces asenjonii. Based on a literature review very few articles have been published on Asenjonamide B.

Structure

MOL 3D MOL SDF 3D SDF PDB SMILES InChI


  Mrv1652306242104253D          

 33 32  0  0  0  0            999 V2000
   -5.0048   -0.8304    1.2536 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.1931   -0.0984    0.1784 C   0  0  2  0  0  0  0  0  0  0  0  0
   -2.7863   -0.6428    0.2749 C   0  0  2  0  0  0  0  0  0  0  0  0
   -1.8637   -0.0018   -0.7404 C   0  0  1  0  0  0  0  0  0  0  0  0
   -0.5233   -0.6100   -0.5519 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.5170    0.1415   -0.2332 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.2893    1.5969   -0.0746 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.8343   -0.4498   -0.0456 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.9866   -1.6878   -0.1853 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.0266    0.3708    0.3109 C   0  0  2  0  0  0  0  0  0  0  0  0
    3.2715    1.3987   -0.7967 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.2127   -0.4497    0.5606 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.7538   -1.3121   -0.4617 N   0  0  0  0  0  0  0  0  0  0  0  0
    4.7734   -0.4055    1.6848 O   0  0  0  0  0  0  0  0  0  0  0  0
   -5.0025   -1.9180    0.9999 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.4234   -0.7404    2.2058 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.9994   -0.4062    1.3869 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.2501    0.9801    0.3232 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.6450   -0.4018   -0.7857 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7837   -1.7271    0.1065 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3531   -0.4646    1.2801 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2348   -0.2939   -1.7603 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8601    1.0812   -0.6347 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3887   -1.6752   -0.6744 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.2080    2.0934    0.3557 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.0758    2.0688   -1.0493 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5002    1.8098    0.6897 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.7875    0.9521    1.2239 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.2180    1.0955   -1.2983 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.4822    1.4025   -1.5516 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.4800    2.3919   -0.3501 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.3537   -2.2551   -0.5948 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.5417   -1.0127   -1.0756 H   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
  6  8  1  0  0  0  0
  8  9  2  0  0  0  0
  8 10  1  0  0  0  0
 10 11  1  0  0  0  0
 10 12  1  0  0  0  0
 12 13  1  0  0  0  0
 12 14  2  0  0  0  0
  1 15  1  0  0  0  0
  1 16  1  0  0  0  0
  1 17  1  0  0  0  0
  2 18  1  0  0  0  0
  2 19  1  0  0  0  0
  3 20  1  0  0  0  0
  3 21  1  0  0  0  0
  4 22  1  0  0  0  0
  4 23  1  0  0  0  0
  5 24  1  0  0  0  0
  7 25  1  0  0  0  0
  7 26  1  0  0  0  0
  7 27  1  0  0  0  0
 10 28  1  1  0  0  0
 11 29  1  0  0  0  0
 11 30  1  0  0  0  0
 11 31  1  0  0  0  0
 13 32  1  0  0  0  0
 13 33  1  0  0  0  0
M  END

     RDKit          3D

 33 32  0  0  0  0  0  0  0  0999 V2000
   -5.0048   -0.8304    1.2536 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.1931   -0.0984    0.1784 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7863   -0.6428    0.2749 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8637   -0.0018   -0.7404 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5233   -0.6100   -0.5519 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.5170    0.1415   -0.2332 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.2893    1.5969   -0.0746 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.8343   -0.4498   -0.0456 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.9866   -1.6878   -0.1853 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.0266    0.3708    0.3109 C   0  0  2  0  0  0  0  0  0  0  0  0
    3.2715    1.3987   -0.7967 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.2127   -0.4497    0.5606 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.7538   -1.3121   -0.4617 N   0  0  0  0  0  0  0  0  0  0  0  0
    4.7734   -0.4055    1.6848 O   0  0  0  0  0  0  0  0  0  0  0  0
   -5.0025   -1.9180    0.9999 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.4234   -0.7404    2.2058 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.9994   -0.4062    1.3869 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.2501    0.9801    0.3232 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.6450   -0.4018   -0.7857 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7837   -1.7271    0.1065 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3531   -0.4646    1.2801 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2348   -0.2939   -1.7603 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8601    1.0812   -0.6347 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3887   -1.6752   -0.6744 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.2080    2.0934    0.3557 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.0758    2.0688   -1.0493 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5002    1.8098    0.6897 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.7875    0.9521    1.2239 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.2180    1.0955   -1.2983 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.4822    1.4025   -1.5516 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.4800    2.3919   -0.3501 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.3537   -2.2551   -0.5948 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.5417   -1.0127   -1.0756 H   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0
  2  3  1  0
  3  4  1  0
  4  5  1  0
  5  6  2  0
  6  7  1  0
  6  8  1  0
  8  9  2  0
  8 10  1  0
 10 11  1  0
 10 12  1  0
 12 13  1  0
 12 14  2  0
  1 15  1  0
  1 16  1  0
  1 17  1  0
  2 18  1  0
  2 19  1  0
  3 20  1  0
  3 21  1  0
  4 22  1  0
  4 23  1  0
  5 24  1  0
  7 25  1  0
  7 26  1  0
  7 27  1  0
 10 28  1  1
 11 29  1  0
 11 30  1  0
 11 31  1  0
 13 32  1  0
 13 33  1  0
M  END


  Mrv1652306242104253D          

 33 32  0  0  0  0            999 V2000
   -5.0048   -0.8304    1.2536 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.1931   -0.0984    0.1784 C   0  0  2  0  0  0  0  0  0  0  0  0
   -2.7863   -0.6428    0.2749 C   0  0  2  0  0  0  0  0  0  0  0  0
   -1.8637   -0.0018   -0.7404 C   0  0  1  0  0  0  0  0  0  0  0  0
   -0.5233   -0.6100   -0.5519 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.5170    0.1415   -0.2332 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.2893    1.5969   -0.0746 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.8343   -0.4498   -0.0456 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.9866   -1.6878   -0.1853 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.0266    0.3708    0.3109 C   0  0  2  0  0  0  0  0  0  0  0  0
    3.2715    1.3987   -0.7967 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.2127   -0.4497    0.5606 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.7538   -1.3121   -0.4617 N   0  0  0  0  0  0  0  0  0  0  0  0
    4.7734   -0.4055    1.6848 O   0  0  0  0  0  0  0  0  0  0  0  0
   -5.0025   -1.9180    0.9999 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.4234   -0.7404    2.2058 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.9994   -0.4062    1.3869 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.2501    0.9801    0.3232 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.6450   -0.4018   -0.7857 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7837   -1.7271    0.1065 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3531   -0.4646    1.2801 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2348   -0.2939   -1.7603 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8601    1.0812   -0.6347 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3887   -1.6752   -0.6744 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.2080    2.0934    0.3557 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.0758    2.0688   -1.0493 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5002    1.8098    0.6897 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.7875    0.9521    1.2239 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.2180    1.0955   -1.2983 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.4822    1.4025   -1.5516 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.4800    2.3919   -0.3501 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.3537   -2.2551   -0.5948 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.5417   -1.0127   -1.0756 H   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
  6  8  1  0  0  0  0
  8  9  2  0  0  0  0
  8 10  1  0  0  0  0
 10 11  1  0  0  0  0
 10 12  1  0  0  0  0
 12 13  1  0  0  0  0
 12 14  2  0  0  0  0
  1 15  1  0  0  0  0
  1 16  1  0  0  0  0
  1 17  1  0  0  0  0
  2 18  1  0  0  0  0
  2 19  1  0  0  0  0
  3 20  1  0  0  0  0
  3 21  1  0  0  0  0
  4 22  1  0  0  0  0
  4 23  1  0  0  0  0
  5 24  1  0  0  0  0
  7 25  1  0  0  0  0
  7 26  1  0  0  0  0
  7 27  1  0  0  0  0
 10 28  1  1  0  0  0
 11 29  1  0  0  0  0
 11 30  1  0  0  0  0
 11 31  1  0  0  0  0
 13 32  1  0  0  0  0
 13 33  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0017511

> <DATABASE_NAME>
NP-MRD

> <SMILES>
[H]N([H])C(=O)[C@]([H])(C(=O)C(=C(/[H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])[H])\C([H])([H])[H])C([H])([H])[H]

> <INCHI_IDENTIFIER>
InChI=1S/C11H19NO2/c1-4-5-6-7-8(2)10(13)9(3)11(12)14/h7,9H,4-6H2,1-3H3,(H2,12,14)/b8-7+/t9-/m0/s1

> <INCHI_KEY>
JZDUBTRQFFMDRN-BQYQJAHWSA-N

> <FORMULA>
C11H19NO2

> <MOLECULAR_WEIGHT>
197.278

> <EXACT_MASS>
197.141578856

> <JCHEM_ACCEPTOR_COUNT>
2

> <JCHEM_ATOM_COUNT>
33

> <JCHEM_AVERAGE_POLARIZABILITY>
23.029862408743316

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
1

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
1

> <JCHEM_IUPAC>
(2S,4E)-2,4-dimethyl-3-oxonon-4-enamide

> <ALOGPS_LOGP>
1.81

> <JCHEM_LOGP>
2.6067364049999995

> <ALOGPS_LOGS>
-2.42

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
0

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA>
19.850281381802954

> <JCHEM_PKA_STRONGEST_ACIDIC>
11.909711330299283

> <JCHEM_PKA_STRONGEST_BASIC>
-3.6396458949218142

> <JCHEM_POLAR_SURFACE_AREA>
60.160000000000004

> <JCHEM_REFRACTIVITY>
57.416900000000005

> <JCHEM_ROTATABLE_BOND_COUNT>
6

> <JCHEM_RULE_OF_FIVE>
1

> <ALOGPS_SOLUBILITY>
7.47e-01 g/l

> <JCHEM_TRADITIONAL_IUPAC>
(2S,4E)-2,4-dimethyl-3-oxonon-4-enamide

> <JCHEM_VEBER_RULE>
0

$$$$

     RDKit          3D

 33 32  0  0  0  0  0  0  0  0999 V2000
   -5.0048   -0.8304    1.2536 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.1931   -0.0984    0.1784 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7863   -0.6428    0.2749 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8637   -0.0018   -0.7404 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5233   -0.6100   -0.5519 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.5170    0.1415   -0.2332 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.2893    1.5969   -0.0746 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.8343   -0.4498   -0.0456 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.9866   -1.6878   -0.1853 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.0266    0.3708    0.3109 C   0  0  2  0  0  0  0  0  0  0  0  0
    3.2715    1.3987   -0.7967 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.2127   -0.4497    0.5606 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.7538   -1.3121   -0.4617 N   0  0  0  0  0  0  0  0  0  0  0  0
    4.7734   -0.4055    1.6848 O   0  0  0  0  0  0  0  0  0  0  0  0
   -5.0025   -1.9180    0.9999 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.4234   -0.7404    2.2058 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.9994   -0.4062    1.3869 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.2501    0.9801    0.3232 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.6450   -0.4018   -0.7857 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7837   -1.7271    0.1065 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3531   -0.4646    1.2801 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2348   -0.2939   -1.7603 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8601    1.0812   -0.6347 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3887   -1.6752   -0.6744 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.2080    2.0934    0.3557 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.0758    2.0688   -1.0493 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5002    1.8098    0.6897 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.7875    0.9521    1.2239 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.2180    1.0955   -1.2983 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.4822    1.4025   -1.5516 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.4800    2.3919   -0.3501 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.3537   -2.2551   -0.5948 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.5417   -1.0127   -1.0756 H   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0
  2  3  1  0
  3  4  1  0
  4  5  1  0
  5  6  2  0
  6  7  1  0
  6  8  1  0
  8  9  2  0
  8 10  1  0
 10 11  1  0
 10 12  1  0
 12 13  1  0
 12 14  2  0
  1 15  1  0
  1 16  1  0
  1 17  1  0
  2 18  1  0
  2 19  1  0
  3 20  1  0
  3 21  1  0
  4 22  1  0
  4 23  1  0
  5 24  1  0
  7 25  1  0
  7 26  1  0
  7 27  1  0
 10 28  1  1
 11 29  1  0
 11 30  1  0
 11 31  1  0
 13 32  1  0
 13 33  1  0
M  END

HEADER    PROTEIN                                 24-JUN-21   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   24-JUN-21         0                                  
HETATM    1  C   UNK     0      -5.005  -0.830   1.254  0.00  0.00           C+0
HETATM    2  C   UNK     0      -4.193  -0.098   0.178  0.00  0.00           C+0
HETATM    3  C   UNK     0      -2.786  -0.643   0.275  0.00  0.00           C+0
HETATM    4  C   UNK     0      -1.864  -0.002  -0.740  0.00  0.00           C+0
HETATM    5  C   UNK     0      -0.523  -0.610  -0.552  0.00  0.00           C+0
HETATM    6  C   UNK     0       0.517   0.142  -0.233  0.00  0.00           C+0
HETATM    7  C   UNK     0       0.289   1.597  -0.075  0.00  0.00           C+0
HETATM    8  C   UNK     0       1.834  -0.450  -0.046  0.00  0.00           C+0
HETATM    9  O   UNK     0       1.987  -1.688  -0.185  0.00  0.00           O+0
HETATM   10  C   UNK     0       3.027   0.371   0.311  0.00  0.00           C+0
HETATM   11  C   UNK     0       3.272   1.399  -0.797  0.00  0.00           C+0
HETATM   12  C   UNK     0       4.213  -0.450   0.561  0.00  0.00           C+0
HETATM   13  N   UNK     0       4.754  -1.312  -0.462  0.00  0.00           N+0
HETATM   14  O   UNK     0       4.773  -0.406   1.685  0.00  0.00           O+0
HETATM   15  H   UNK     0      -5.003  -1.918   1.000  0.00  0.00           H+0
HETATM   16  H   UNK     0      -4.423  -0.740   2.206  0.00  0.00           H+0
HETATM   17  H   UNK     0      -5.999  -0.406   1.387  0.00  0.00           H+0
HETATM   18  H   UNK     0      -4.250   0.980   0.323  0.00  0.00           H+0
HETATM   19  H   UNK     0      -4.645  -0.402  -0.786  0.00  0.00           H+0
HETATM   20  H   UNK     0      -2.784  -1.727   0.107  0.00  0.00           H+0
HETATM   21  H   UNK     0      -2.353  -0.465   1.280  0.00  0.00           H+0
HETATM   22  H   UNK     0      -2.235  -0.294  -1.760  0.00  0.00           H+0
HETATM   23  H   UNK     0      -1.860   1.081  -0.635  0.00  0.00           H+0
HETATM   24  H   UNK     0      -0.389  -1.675  -0.674  0.00  0.00           H+0
HETATM   25  H   UNK     0       1.208   2.093   0.356  0.00  0.00           H+0
HETATM   26  H   UNK     0       0.076   2.069  -1.049  0.00  0.00           H+0
HETATM   27  H   UNK     0      -0.500   1.810   0.690  0.00  0.00           H+0
HETATM   28  H   UNK     0       2.788   0.952   1.224  0.00  0.00           H+0
HETATM   29  H   UNK     0       4.218   1.095  -1.298  0.00  0.00           H+0
HETATM   30  H   UNK     0       2.482   1.403  -1.552  0.00  0.00           H+0
HETATM   31  H   UNK     0       3.480   2.392  -0.350  0.00  0.00           H+0
HETATM   32  H   UNK     0       4.354  -2.255  -0.595  0.00  0.00           H+0
HETATM   33  H   UNK     0       5.542  -1.013  -1.076  0.00  0.00           H+0
CONECT    1    2   15   16   17                                             
CONECT    2    1    3   18   19                                             
CONECT    3    2    4   20   21                                             
CONECT    4    3    5   22   23                                             
CONECT    5    4    6   24                                                  
CONECT    6    5    7    8                                                  
CONECT    7    6   25   26   27                                             
CONECT    8    6    9   10                                                  
CONECT    9    8                                                            
CONECT   10    8   11   12   28                                             
CONECT   11   10   29   30   31                                             
CONECT   12   10   13   14                                                  
CONECT   13   12   32   33                                                  
CONECT   14   12                                                            
CONECT   15    1                                                            
CONECT   16    1                                                            
CONECT   17    1                                                            
CONECT   18    2                                                            
CONECT   19    2                                                            
CONECT   20    3                                                            
CONECT   21    3                                                            
CONECT   22    4                                                            
CONECT   23    4                                                            
CONECT   24    5                                                            
CONECT   25    7                                                            
CONECT   26    7                                                            
CONECT   27    7                                                            
CONECT   28   10                                                            
CONECT   29   11                                                            
CONECT   30   11                                                            
CONECT   31   11                                                            
CONECT   32   13                                                            
CONECT   33   13                                                            
MASTER        0    0    0    0    0    0    0    0   33    0   64    0
END

RDKit          3D

33 32  0  0  0  0  0  0  0  0999 V2000
   -5.0048   -0.8304    1.2536 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.1931   -0.0984    0.1784 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7863   -0.6428    0.2749 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8637   -0.0018   -0.7404 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5233   -0.6100   -0.5519 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.5170    0.1415   -0.2332 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.2893    1.5969   -0.0746 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.8343   -0.4498   -0.0456 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.9866   -1.6878   -0.1853 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.0266    0.3708    0.3109 C   0  0  2  0  0  0  0  0  0  0  0  0
    3.2715    1.3987   -0.7967 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.2127   -0.4497    0.5606 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.7538   -1.3121   -0.4617 N   0  0  0  0  0  0  0  0  0  0  0  0
    4.7734   -0.4055    1.6848 O   0  0  0  0  0  0  0  0  0  0  0  0
   -5.0025   -1.9180    0.9999 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.4234   -0.7404    2.2058 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.9994   -0.4062    1.3869 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.2501    0.9801    0.3232 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.6450   -0.4018   -0.7857 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7837   -1.7271    0.1065 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3531   -0.4646    1.2801 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2348   -0.2939   -1.7603 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8601    1.0812   -0.6347 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3887   -1.6752   -0.6744 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.2080    2.0934    0.3557 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.0758    2.0688   -1.0493 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5002    1.8098    0.6897 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.7875    0.9521    1.2239 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.2180    1.0955   -1.2983 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.4822    1.4025   -1.5516 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.4800    2.3919   -0.3501 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.3537   -2.2551   -0.5948 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.5417   -1.0127   -1.0756 H   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0
  2  3  1  0
  3  4  1  0
  4  5  1  0
  5  6  2  0
  6  7  1  0
  6  8  1  0
  8  9  2  0
  8 10  1  0
 10 11  1  0
 10 12  1  0
 12 13  1  0
 12 14  2  0
  1 15  1  0
  1 16  1  0
  1 17  1  0
  2 18  1  0
  2 19  1  0
  3 20  1  0
  3 21  1  0
  4 22  1  0
  4 23  1  0
  5 24  1  0
  7 25  1  0
  7 26  1  0
  7 27  1  0
 10 28  1  1
 11 29  1  0
 11 30  1  0
 11 31  1  0
 13 32  1  0
 13 33  1  0
M  END

View in JSmol View NMR Assignments

Synonyms

Not Available

Chemical Formula

C₁₁H₁₉NO₂

Average Mass

197.2780 Da

Monoisotopic Mass

197.14158 Da

IUPAC Name

(2S,4E)-2,4-dimethyl-3-oxonon-4-enamide

Traditional Name

(2S,4E)-2,4-dimethyl-3-oxonon-4-enamide

CAS Registry Number

Not Available

SMILES

CCCC\C=C(/C)C(=O)C(C)C(N)=O

InChI Identifier

InChI=1S/C11H19NO2/c1-4-5-6-7-8(2)10(13)9(3)11(12)14/h7,9H,4-6H2,1-3H3,(H2,12,14)/b8-7+

InChI Key

JZDUBTRQFFMDRN-BQYQJAHWSA-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, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 100 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 252 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 1000 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 50 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 200 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 75 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 300 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 101 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 400 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 126 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 500 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 151 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 600 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 176 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 700 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 201 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 800 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 226 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 900 MHz, D₂O, 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	NPAtlas	29362461
Streptomyces asenjonii	LOTUS Database	35616633

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as b'-hydroxy-alpha,beta-unsaturated ketones. These are alpha,beta-unsaturated ketones that carry a hydroxyl group at the beta'-position.

Kingdom

Organic compounds

Super Class

Organic oxygen compounds

Class

Organooxygen compounds

Sub Class

Carbonyl compounds

Direct Parent

b'-hydroxy-alpha,beta-unsaturated ketones

Alternative Parents

Substituents

B'-hydroxy-alpha,beta-unsaturated-ketone
Alpha-branched alpha,beta-unsaturated-ketone
Beta-hydroxy ketone
Enone
Acryloyl-group
Ketone
Carboximidic acid derivative
Carboximidic acid
Organic nitrogen compound
Organopnictogen compound
Organic oxide
Hydrocarbon derivative
Organonitrogen compound
Aliphatic acyclic compound

Molecular Framework

Aliphatic acyclic 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	1.81	ALOGPS
logP	2.61	ChemAxon
logS	-2.4	ALOGPS
pKa (Strongest Acidic)	11.91	ChemAxon
pKa (Strongest Basic)	-3.6	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	2	ChemAxon
Hydrogen Donor Count	1	ChemAxon
Polar Surface Area	60.16 Å²	ChemAxon
Rotatable Bond Count	6	ChemAxon
Refractivity	57.42 m³·mol⁻¹	ChemAxon
Polarizability	23.03 Å³	ChemAxon
Number of Rings	0	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

NPAtlas ID

NPA021730

HMDB ID

Not Available

DrugBank ID

Not Available

Phenol Explorer Compound ID

Not Available

FoodDB ID

Not Available

KNApSAcK ID

Not Available

Chemspider ID

78435545

KEGG Compound ID

Not Available

BioCyc ID

Not Available

BiGG ID

Not Available

Wikipedia Link

Not Available

METLIN ID

Not Available

PubChem Compound

139589508

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

Showing NP-Card for Asenjonamide B (NP0017511)

MOL for NP0017511 (Asenjonamide B)

3D MOL for NP0017511 (Asenjonamide B)

3D SDF for NP0017511 (Asenjonamide B)

3D-SDF for NP0017511 (Asenjonamide B)

PDB for NP0017511 (Asenjonamide B)

3D PDB for NP0017511 (Asenjonamide B)

SMILES for NP0017511 (Asenjonamide B)

INCHI for NP0017511 (Asenjonamide B)

Structure for NP0017511 (Asenjonamide B)

3D Structure for NP0017511 (Asenjonamide B)