NP-MRD: Showing NP-Card for oxepinamide D (NP0040956)

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Record Information

Version

2.0

Created at

2021-06-20 22:59:16 UTC

Updated at

2021-06-30 00:15:11 UTC

NP-MRD ID

NP0040956

Secondary Accession Numbers

None

Natural Product Identification

Common Name

oxepinamide D

Provided By

JEOL Database JEOL Logo

Description

oxepinamide D is found in Aspergillus puniceus and Aspergillus puniceus F02Z-1744. oxepinamide D was first documented in 2011 (Lu, X.-H., et al.). Based on a literature review very few articles have been published on (4S,7R)-4-benzyl-4,6-dihydroxy-7-methyl-15-oxa-2,5,8-triazatricyclo[8.5.0.0³,⁸]Pentadeca-1(10),2,5,11,13-pentaen-9-one.

Structure

MOL 3D MOL SDF 3D SDF PDB SMILES InChI


  Mrv1652306212100593D          

 43 46  0  0  0  0            999 V2000
   -0.3522    1.5663    2.3253 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5883    1.1259    0.8841 C   0  0  2  0  0  0  0  0  0  0  0  0
   -1.9571    0.4494    0.7049 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.0191    1.0571    0.8066 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9510   -0.8986    0.4868 N   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8299   -1.7372    0.8098 C   0  0  2  0  0  0  0  0  0  0  0  0
   -1.0762   -2.9168    0.0576 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7865   -2.0968    2.3094 C   0  0  1  0  0  0  0  0  0  0  0  0
    0.4393   -2.8687    2.7437 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.5015   -4.2577    2.5649 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.6417   -4.9692    2.9396 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.7297   -4.3010    3.4969 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.6777   -2.9212    3.6827 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.5380   -2.2070    3.3100 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.4530   -1.0425    0.2750 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.3917   -1.7863   -0.2135 N   0  0  0  0  0  0  0  0  0  0  0  0
    2.5418   -1.1899   -0.6633 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.7532    0.1428   -0.6479 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.6462    0.9850   -0.1003 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.7608    2.2100   -0.0479 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.5208    0.3260    0.3430 N   0  0  0  0  0  0  0  0  0  0  0  0
    3.9244    0.8276   -1.1773 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.1700    0.3398   -1.2529 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.5772   -0.9719   -0.8223 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.7812   -2.0470   -0.8207 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.4596   -2.0985   -1.1859 O   0  0  0  0  0  0  0  0  0  0  0  0
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   -0.6523    2.0364    0.2719 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8411   -1.3512    0.3319 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1850   -3.2752   -0.1377 H   0  0  0  0  0  0  0  0  0  0  0  0
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   -1.6687   -2.7035    2.5596 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3385   -4.7964    2.1300 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.6815   -6.0459    2.7952 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.6179   -4.8561    3.7871 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.5270   -2.4009    4.1181 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.5224   -1.1313    3.4656 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.7551    1.8485   -1.5191 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.9605    0.9761   -1.6464 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.6213   -1.0871   -0.5423 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.1299   -3.0395   -0.5640 H   0  0  0  0  0  0  0  0  0  0  0  0
 21 19  1  0  0  0  0
 26 25  1  0  0  0  0
 21 15  1  0  0  0  0
 22 23  2  0  0  0  0
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 25 24  2  0  0  0  0
 23 24  1  0  0  0  0
 15  6  1  0  0  0  0
  3  4  2  0  0  0  0
  6  5  1  0  0  0  0
 19 20  2  0  0  0  0
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  6  8  1  0  0  0  0
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  8  9  1  0  0  0  0
 18 17  2  0  0  0  0
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 18 22  1  0  0  0  0
 13 14  2  0  0  0  0
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  5 31  1  0  0  0  0
  2 30  1  6  0  0  0
 22 40  1  0  0  0  0
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  7 32  1  0  0  0  0
  1 27  1  0  0  0  0
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  8 33  1  0  0  0  0
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 10 35  1  0  0  0  0
 11 36  1  0  0  0  0
 12 37  1  0  0  0  0
 13 38  1  0  0  0  0
 14 39  1  0  0  0  0
M  END

     RDKit          3D

 43 46  0  0  0  0  0  0  0  0999 V2000
   -0.3522    1.5663    2.3253 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5883    1.1259    0.8841 C   0  0  2  0  0  0  0  0  0  0  0  0
   -1.9571    0.4494    0.7049 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.0191    1.0571    0.8066 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9510   -0.8986    0.4868 N   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8299   -1.7372    0.8098 C   0  0  2  0  0  0  0  0  0  0  0  0
   -1.0762   -2.9168    0.0576 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7865   -2.0968    2.3094 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.4393   -2.8687    2.7437 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.5015   -4.2577    2.5649 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.6417   -4.9692    2.9396 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.7297   -4.3010    3.4969 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.6777   -2.9212    3.6827 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.5380   -2.2070    3.3100 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.4530   -1.0425    0.2750 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.3917   -1.7863   -0.2135 N   0  0  0  0  0  0  0  0  0  0  0  0
    2.5418   -1.1899   -0.6633 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.7532    0.1428   -0.6479 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.6462    0.9850   -0.1003 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.7608    2.2100   -0.0479 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.5208    0.3260    0.3430 N   0  0  0  0  0  0  0  0  0  0  0  0
    3.9244    0.8276   -1.1773 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.1700    0.3398   -1.2529 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.5772   -0.9719   -0.8223 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.7812   -2.0470   -0.8207 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.4596   -2.0985   -1.1859 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2362    2.0640    2.7374 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.4853    2.2699    2.3822 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1029    0.7304    2.9802 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6523    2.0364    0.2719 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8411   -1.3512    0.3319 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1850   -3.2752   -0.1377 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8791   -1.2054    2.9351 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6687   -2.7035    2.5596 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3385   -4.7964    2.1300 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.6815   -6.0459    2.7952 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.6179   -4.8561    3.7871 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.5270   -2.4009    4.1181 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.5224   -1.1313    3.4656 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.7551    1.8485   -1.5191 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.9605    0.9761   -1.6464 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.6213   -1.0871   -0.5423 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.1299   -3.0395   -0.5640 H   0  0  0  0  0  0  0  0  0  0  0  0
 21 19  1  0
 26 25  1  0
 21 15  1  0
 22 23  2  0
 21  2  1  0
 25 24  2  0
 23 24  1  0
 15  6  1  0
  3  4  2  0
  6  5  1  0
 19 20  2  0
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  6  7  1  6
  3  2  1  0
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  6  8  1  0
 18 19  1  0
  8  9  1  0
 18 17  2  0
  9 10  2  0
 17 16  1  0
 10 11  1  0
 17 26  1  0
 11 12  2  0
 16 15  2  0
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 18 22  1  0
 13 14  2  0
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  5 31  1  0
  2 30  1  6
 22 40  1  0
 25 43  1  0
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  7 32  1  0
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  8 33  1  0
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 10 35  1  0
 11 36  1  0
 12 37  1  0
 13 38  1  0
 14 39  1  0
M  END


  Mrv1652306212100593D          

 43 46  0  0  0  0            999 V2000
   -0.3522    1.5663    2.3253 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5883    1.1259    0.8841 C   0  0  2  0  0  0  0  0  0  0  0  0
   -1.9571    0.4494    0.7049 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.0191    1.0571    0.8066 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9510   -0.8986    0.4868 N   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8299   -1.7372    0.8098 C   0  0  2  0  0  0  0  0  0  0  0  0
   -1.0762   -2.9168    0.0576 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7865   -2.0968    2.3094 C   0  0  1  0  0  0  0  0  0  0  0  0
    0.4393   -2.8687    2.7437 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.5015   -4.2577    2.5649 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.6417   -4.9692    2.9396 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.7297   -4.3010    3.4969 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.6777   -2.9212    3.6827 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.5380   -2.2070    3.3100 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.4530   -1.0425    0.2750 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.3917   -1.7863   -0.2135 N   0  0  0  0  0  0  0  0  0  0  0  0
    2.5418   -1.1899   -0.6633 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.7532    0.1428   -0.6479 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.6462    0.9850   -0.1003 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.7608    2.2100   -0.0479 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.5208    0.3260    0.3430 N   0  0  0  0  0  0  0  0  0  0  0  0
    3.9244    0.8276   -1.1773 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.1700    0.3398   -1.2529 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.5772   -0.9719   -0.8223 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.7812   -2.0470   -0.8207 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.4596   -2.0985   -1.1859 O   0  0  0  0  0  0  0  0  0  0  0  0
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    0.4853    2.2699    2.3822 H   0  0  0  0  0  0  0  0  0  0  0  0
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   -0.6523    2.0364    0.2719 H   0  0  0  0  0  0  0  0  0  0  0  0
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   -0.8791   -1.2054    2.9351 H   0  0  0  0  0  0  0  0  0  0  0  0
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    1.6815   -6.0459    2.7952 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.6179   -4.8561    3.7871 H   0  0  0  0  0  0  0  0  0  0  0  0
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    1.5224   -1.1313    3.4656 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.7551    1.8485   -1.5191 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.9605    0.9761   -1.6464 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.6213   -1.0871   -0.5423 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.1299   -3.0395   -0.5640 H   0  0  0  0  0  0  0  0  0  0  0  0
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 26 25  1  0  0  0  0
 21 15  1  0  0  0  0
 22 23  2  0  0  0  0
 21  2  1  0  0  0  0
 25 24  2  0  0  0  0
 23 24  1  0  0  0  0
 15  6  1  0  0  0  0
  3  4  2  0  0  0  0
  6  5  1  0  0  0  0
 19 20  2  0  0  0  0
  5  3  1  0  0  0  0
  6  7  1  6  0  0  0
  3  2  1  0  0  0  0
  2  1  1  0  0  0  0
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 13 14  2  0  0  0  0
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  2 30  1  6  0  0  0
 22 40  1  0  0  0  0
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  7 32  1  0  0  0  0
  1 27  1  0  0  0  0
  1 28  1  0  0  0  0
  1 29  1  0  0  0  0
  8 33  1  0  0  0  0
  8 34  1  0  0  0  0
 10 35  1  0  0  0  0
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 12 37  1  0  0  0  0
 13 38  1  0  0  0  0
 14 39  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0040956

> <DATABASE_NAME>
NP-MRD

> <SMILES>
[H]O[C@@]1(N([H])C(=O)[C@]([H])(N2C(=O)C3=C(OC([H])=C([H])C([H])=C3[H])N=C12)C([H])([H])[H])C([H])([H])C1=C([H])C([H])=C([H])C([H])=C1[H]

> <INCHI_IDENTIFIER>
InChI=1S/C19H17N3O4/c1-12-15(23)21-19(25,11-13-7-3-2-4-8-13)18-20-16-14(17(24)22(12)18)9-5-6-10-26-16/h2-10,12,25H,11H2,1H3,(H,21,23)/t12-,19+/m1/s1

> <INCHI_KEY>
LTIOSJQYEGEEHY-BLVKFPJESA-N

> <FORMULA>
C19H17N3O4

> <MOLECULAR_WEIGHT>
351.362

> <EXACT_MASS>
351.121906039

> <JCHEM_ACCEPTOR_COUNT>
5

> <JCHEM_ATOM_COUNT>
43

> <JCHEM_AVERAGE_POLARIZABILITY>
34.76541694953625

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
2

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
1

> <JCHEM_IUPAC>
(4S,7R)-4-benzyl-4-hydroxy-7-methyl-15-oxa-2,5,8-triazatricyclo[8.5.0.0^{3,8}]pentadeca-1(10),2,11,13-tetraene-6,9-dione

> <ALOGPS_LOGP>
1.40

> <JCHEM_LOGP>
1.5483177393333334

> <ALOGPS_LOGS>
-3.24

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
4

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA>
11.302693852347108

> <JCHEM_PKA_STRONGEST_ACIDIC>
10.211558506934884

> <JCHEM_PKA_STRONGEST_BASIC>
-2.8432422384142932

> <JCHEM_POLAR_SURFACE_AREA>
91.22999999999999

> <JCHEM_REFRACTIVITY>
104.81730000000002

> <JCHEM_ROTATABLE_BOND_COUNT>
2

> <JCHEM_RULE_OF_FIVE>
1

> <ALOGPS_SOLUBILITY>
2.03e-01 g/l

> <JCHEM_TRADITIONAL_IUPAC>
(4S,7R)-4-benzyl-4-hydroxy-7-methyl-15-oxa-2,5,8-triazatricyclo[8.5.0.0^{3,8}]pentadeca-1(10),2,11,13-tetraene-6,9-dione

> <JCHEM_VEBER_RULE>
0

$$$$

     RDKit          3D

 43 46  0  0  0  0  0  0  0  0999 V2000
   -0.3522    1.5663    2.3253 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5883    1.1259    0.8841 C   0  0  2  0  0  0  0  0  0  0  0  0
   -1.9571    0.4494    0.7049 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.0191    1.0571    0.8066 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9510   -0.8986    0.4868 N   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8299   -1.7372    0.8098 C   0  0  2  0  0  0  0  0  0  0  0  0
   -1.0762   -2.9168    0.0576 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7865   -2.0968    2.3094 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.4393   -2.8687    2.7437 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.5015   -4.2577    2.5649 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.6417   -4.9692    2.9396 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.7297   -4.3010    3.4969 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.6777   -2.9212    3.6827 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.5380   -2.2070    3.3100 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.4530   -1.0425    0.2750 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.3917   -1.7863   -0.2135 N   0  0  0  0  0  0  0  0  0  0  0  0
    2.5418   -1.1899   -0.6633 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.7532    0.1428   -0.6479 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.6462    0.9850   -0.1003 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.7608    2.2100   -0.0479 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.5208    0.3260    0.3430 N   0  0  0  0  0  0  0  0  0  0  0  0
    3.9244    0.8276   -1.1773 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.1700    0.3398   -1.2529 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.5772   -0.9719   -0.8223 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.7812   -2.0470   -0.8207 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.4596   -2.0985   -1.1859 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2362    2.0640    2.7374 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.4853    2.2699    2.3822 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1029    0.7304    2.9802 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6523    2.0364    0.2719 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8411   -1.3512    0.3319 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1850   -3.2752   -0.1377 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8791   -1.2054    2.9351 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6687   -2.7035    2.5596 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3385   -4.7964    2.1300 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.6815   -6.0459    2.7952 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.6179   -4.8561    3.7871 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.5270   -2.4009    4.1181 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.5224   -1.1313    3.4656 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.7551    1.8485   -1.5191 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.9605    0.9761   -1.6464 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.6213   -1.0871   -0.5423 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.1299   -3.0395   -0.5640 H   0  0  0  0  0  0  0  0  0  0  0  0
 21 19  1  0
 26 25  1  0
 21 15  1  0
 22 23  2  0
 21  2  1  0
 25 24  2  0
 23 24  1  0
 15  6  1  0
  3  4  2  0
  6  5  1  0
 19 20  2  0
  5  3  1  0
  6  7  1  6
  3  2  1  0
  2  1  1  0
  6  8  1  0
 18 19  1  0
  8  9  1  0
 18 17  2  0
  9 10  2  0
 17 16  1  0
 10 11  1  0
 17 26  1  0
 11 12  2  0
 16 15  2  0
 12 13  1  0
 18 22  1  0
 13 14  2  0
 14  9  1  0
  5 31  1  0
  2 30  1  6
 22 40  1  0
 25 43  1  0
 23 41  1  0
 24 42  1  0
  7 32  1  0
  1 27  1  0
  1 28  1  0
  1 29  1  0
  8 33  1  0
  8 34  1  0
 10 35  1  0
 11 36  1  0
 12 37  1  0
 13 38  1  0
 14 39  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      -0.352   1.566   2.325  0.00  0.00           C+0
HETATM    2  C   UNK     0      -0.588   1.126   0.884  0.00  0.00           C+0
HETATM    3  C   UNK     0      -1.957   0.449   0.705  0.00  0.00           C+0
HETATM    4  O   UNK     0      -3.019   1.057   0.807  0.00  0.00           O+0
HETATM    5  N   UNK     0      -1.951  -0.899   0.487  0.00  0.00           N+0
HETATM    6  C   UNK     0      -0.830  -1.737   0.810  0.00  0.00           C+0
HETATM    7  O   UNK     0      -1.076  -2.917   0.058  0.00  0.00           O+0
HETATM    8  C   UNK     0      -0.787  -2.097   2.309  0.00  0.00           C+0
HETATM    9  C   UNK     0       0.439  -2.869   2.744  0.00  0.00           C+0
HETATM   10  C   UNK     0       0.501  -4.258   2.565  0.00  0.00           C+0
HETATM   11  C   UNK     0       1.642  -4.969   2.940  0.00  0.00           C+0
HETATM   12  C   UNK     0       2.730  -4.301   3.497  0.00  0.00           C+0
HETATM   13  C   UNK     0       2.678  -2.921   3.683  0.00  0.00           C+0
HETATM   14  C   UNK     0       1.538  -2.207   3.310  0.00  0.00           C+0
HETATM   15  C   UNK     0       0.453  -1.042   0.275  0.00  0.00           C+0
HETATM   16  N   UNK     0       1.392  -1.786  -0.214  0.00  0.00           N+0
HETATM   17  C   UNK     0       2.542  -1.190  -0.663  0.00  0.00           C+0
HETATM   18  C   UNK     0       2.753   0.143  -0.648  0.00  0.00           C+0
HETATM   19  C   UNK     0       1.646   0.985  -0.100  0.00  0.00           C+0
HETATM   20  O   UNK     0       1.761   2.210  -0.048  0.00  0.00           O+0
HETATM   21  N   UNK     0       0.521   0.326   0.343  0.00  0.00           N+0
HETATM   22  C   UNK     0       3.924   0.828  -1.177  0.00  0.00           C+0
HETATM   23  C   UNK     0       5.170   0.340  -1.253  0.00  0.00           C+0
HETATM   24  C   UNK     0       5.577  -0.972  -0.822  0.00  0.00           C+0
HETATM   25  C   UNK     0       4.781  -2.047  -0.821  0.00  0.00           C+0
HETATM   26  O   UNK     0       3.460  -2.099  -1.186  0.00  0.00           O+0
HETATM   27  H   UNK     0      -1.236   2.064   2.737  0.00  0.00           H+0
HETATM   28  H   UNK     0       0.485   2.270   2.382  0.00  0.00           H+0
HETATM   29  H   UNK     0      -0.103   0.730   2.980  0.00  0.00           H+0
HETATM   30  H   UNK     0      -0.652   2.036   0.272  0.00  0.00           H+0
HETATM   31  H   UNK     0      -2.841  -1.351   0.332  0.00  0.00           H+0
HETATM   32  H   UNK     0      -0.185  -3.275  -0.138  0.00  0.00           H+0
HETATM   33  H   UNK     0      -0.879  -1.205   2.935  0.00  0.00           H+0
HETATM   34  H   UNK     0      -1.669  -2.704   2.560  0.00  0.00           H+0
HETATM   35  H   UNK     0      -0.339  -4.796   2.130  0.00  0.00           H+0
HETATM   36  H   UNK     0       1.682  -6.046   2.795  0.00  0.00           H+0
HETATM   37  H   UNK     0       3.618  -4.856   3.787  0.00  0.00           H+0
HETATM   38  H   UNK     0       3.527  -2.401   4.118  0.00  0.00           H+0
HETATM   39  H   UNK     0       1.522  -1.131   3.466  0.00  0.00           H+0
HETATM   40  H   UNK     0       3.755   1.849  -1.519  0.00  0.00           H+0
HETATM   41  H   UNK     0       5.960   0.976  -1.646  0.00  0.00           H+0
HETATM   42  H   UNK     0       6.621  -1.087  -0.542  0.00  0.00           H+0
HETATM   43  H   UNK     0       5.130  -3.039  -0.564  0.00  0.00           H+0
CONECT    1    2   27   28   29                                             
CONECT    2   21    3    1   30                                             
CONECT    3    4    5    2                                                  
CONECT    4    3                                                            
CONECT    5    6    3   31                                                  
CONECT    6   15    5    7    8                                             
CONECT    7    6   32                                                       
CONECT    8    6    9   33   34                                             
CONECT    9    8   10   14                                                  
CONECT   10    9   11   35                                                  
CONECT   11   10   12   36                                                  
CONECT   12   11   13   37                                                  
CONECT   13   12   14   38                                                  
CONECT   14   13    9   39                                                  
CONECT   15   21    6   16                                                  
CONECT   16   17   15                                                       
CONECT   17   18   16   26                                                  
CONECT   18   19   17   22                                                  
CONECT   19   21   20   18                                                  
CONECT   20   19                                                            
CONECT   21   19   15    2                                                  
CONECT   22   23   18   40                                                  
CONECT   23   22   24   41                                                  
CONECT   24   25   23   42                                                  
CONECT   25   26   24   43                                                  
CONECT   26   25   17                                                       
CONECT   27    1                                                            
CONECT   28    1                                                            
CONECT   29    1                                                            
CONECT   30    2                                                            
CONECT   31    5                                                            
CONECT   32    7                                                            
CONECT   33    8                                                            
CONECT   34    8                                                            
CONECT   35   10                                                            
CONECT   36   11                                                            
CONECT   37   12                                                            
CONECT   38   13                                                            
CONECT   39   14                                                            
CONECT   40   22                                                            
CONECT   41   23                                                            
CONECT   42   24                                                            
CONECT   43   25                                                            
MASTER        0    0    0    0    0    0    0    0   43    0   92    0
END

RDKit          3D

43 46  0  0  0  0  0  0  0  0999 V2000
   -0.3522    1.5663    2.3253 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5883    1.1259    0.8841 C   0  0  2  0  0  0  0  0  0  0  0  0
   -1.9571    0.4494    0.7049 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.0191    1.0571    0.8066 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9510   -0.8986    0.4868 N   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8299   -1.7372    0.8098 C   0  0  2  0  0  0  0  0  0  0  0  0
   -1.0762   -2.9168    0.0576 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7865   -2.0968    2.3094 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.4393   -2.8687    2.7437 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.5015   -4.2577    2.5649 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.6417   -4.9692    2.9396 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.7297   -4.3010    3.4969 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.6777   -2.9212    3.6827 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.5380   -2.2070    3.3100 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.4530   -1.0425    0.2750 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.3917   -1.7863   -0.2135 N   0  0  0  0  0  0  0  0  0  0  0  0
    2.5418   -1.1899   -0.6633 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.7532    0.1428   -0.6479 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.6462    0.9850   -0.1003 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.7608    2.2100   -0.0479 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.5208    0.3260    0.3430 N   0  0  0  0  0  0  0  0  0  0  0  0
    3.9244    0.8276   -1.1773 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.1700    0.3398   -1.2529 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.5772   -0.9719   -0.8223 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.7812   -2.0470   -0.8207 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.4596   -2.0985   -1.1859 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2362    2.0640    2.7374 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.4853    2.2699    2.3822 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1029    0.7304    2.9802 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6523    2.0364    0.2719 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8411   -1.3512    0.3319 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1850   -3.2752   -0.1377 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8791   -1.2054    2.9351 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6687   -2.7035    2.5596 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3385   -4.7964    2.1300 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.6815   -6.0459    2.7952 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.6179   -4.8561    3.7871 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.5270   -2.4009    4.1181 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.5224   -1.1313    3.4656 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.7551    1.8485   -1.5191 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.9605    0.9761   -1.6464 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.6213   -1.0871   -0.5423 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.1299   -3.0395   -0.5640 H   0  0  0  0  0  0  0  0  0  0  0  0
 21 19  1  0
 26 25  1  0
 21 15  1  0
 22 23  2  0
 21  2  1  0
 25 24  2  0
 23 24  1  0
 15  6  1  0
  3  4  2  0
  6  5  1  0
 19 20  2  0
  5  3  1  0
  6  7  1  6
  3  2  1  0
  2  1  1  0
  6  8  1  0
 18 19  1  0
  8  9  1  0
 18 17  2  0
  9 10  2  0
 17 16  1  0
 10 11  1  0
 17 26  1  0
 11 12  2  0
 16 15  2  0
 12 13  1  0
 18 22  1  0
 13 14  2  0
 14  9  1  0
  5 31  1  0
  2 30  1  6
 22 40  1  0
 25 43  1  0
 23 41  1  0
 24 42  1  0
  7 32  1  0
  1 27  1  0
  1 28  1  0
  1 29  1  0
  8 33  1  0
  8 34  1  0
 10 35  1  0
 11 36  1  0
 12 37  1  0
 13 38  1  0
 14 39  1  0
M  END

View in JSmol

Synonyms

Not Available

Chemical Formula

C₁₉H₁₇N₃O₄

Average Mass

351.3620 Da

Monoisotopic Mass

351.12191 Da

IUPAC Name

(4S,7R)-4-benzyl-4-hydroxy-7-methyl-15-oxa-2,5,8-triazatricyclo[8.5.0.0^{3,8}]pentadeca-1(10),2,11,13-tetraene-6,9-dione

Traditional Name

(4S,7R)-4-benzyl-4-hydroxy-7-methyl-15-oxa-2,5,8-triazatricyclo[8.5.0.0^{3,8}]pentadeca-1(10),2,11,13-tetraene-6,9-dione

CAS Registry Number

Not Available

SMILES

[H]O[C@@]1(N([H])C(=O)[C@]([H])(N2C(=O)C3=C(OC([H])=C([H])C([H])=C3[H])N=C12)C([H])([H])[H])C([H])([H])C1=C([H])C([H])=C([H])C([H])=C1[H]

InChI Identifier

InChI=1S/C19H17N3O4/c1-12-15(23)21-19(25,11-13-7-3-2-4-8-13)18-20-16-14(17(24)22(12)18)9-5-6-10-26-16/h2-10,12,25H,11H2,1H3,(H,21,23)/t12-,19+/m1/s1

InChI Key

LTIOSJQYEGEEHY-BLVKFPJESA-N

Experimental Spectra

Spectrum Type	Description	Depositor Email	Depositor Organization	Depositor	Deposition Date	View
1D NMR	¹³C NMR Spectrum (1D, 500 MHz, DMSO-d6, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 500 MHz, DMSO-d6, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 100 MHz, DMSO-d6, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 100 MHz, DMSO-d6, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 200 MHz, DMSO-d6, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 200 MHz, DMSO-d6, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 300 MHz, DMSO-d6, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 300 MHz, DMSO-d6, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 400 MHz, DMSO-d6, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 400 MHz, DMSO-d6, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 600 MHz, DMSO-d6, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 600 MHz, DMSO-d6, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 700 MHz, DMSO-d6, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 700 MHz, DMSO-d6, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 800 MHz, DMSO-d6, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 800 MHz, DMSO-d6, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 900 MHz, DMSO-d6, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 900 MHz, DMSO-d6, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 1000 MHz, DMSO-d6, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 1000 MHz, DMSO-d6, 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 puniceus	LOTUS Database	35616633
Aspergillus puniceus F02Z-1744	JEOL database	Lu, X.-H., et al, Eur. J. Org. Chem. 2011, 802.

Chemical Taxonomy

Classification

Not classified

Physical Properties

State

Not Available

Experimental Properties

Property	Value	Reference
Melting Point	Not Available	Not Available
Boiling Point	Not Available	Not Available
Water Solubility	Not Available	Not Available
LogP	Not Available	Not Available

Predicted Properties

Property	Value	Source
logP	1.4	ALOGPS
logP	1.55	ChemAxon
logS	-3.2	ALOGPS
pKa (Strongest Acidic)	10.21	ChemAxon
pKa (Strongest Basic)	-2.8	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	5	ChemAxon
Hydrogen Donor Count	2	ChemAxon
Polar Surface Area	91.23 Å²	ChemAxon
Rotatable Bond Count	2	ChemAxon
Refractivity	104.82 m³·mol⁻¹	ChemAxon
Polarizability	34.77 Å³	ChemAxon
Number of Rings	4	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

28288329

KEGG Compound ID

Not Available

BioCyc ID

Not Available

BiGG ID

Not Available

Wikipedia Link

Not Available

METLIN ID

Not Available

PubChem Compound

44156271

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

Lu, X.-H., et al. (2011). Lu, X.-H., et al, Eur. J. Org. Chem. 2011, 802.. Eur. J. Org. Chem..

Showing NP-Card for oxepinamide D (NP0040956)

MOL for NP0040956 (oxepinamide D)

3D MOL for NP0040956 (oxepinamide D)

3D SDF for NP0040956 (oxepinamide D)

3D-SDF for NP0040956 (oxepinamide D)

PDB for NP0040956 (oxepinamide D)

3D PDB for NP0040956 (oxepinamide D)

SMILES for NP0040956 (oxepinamide D)

INCHI for NP0040956 (oxepinamide D)

Structure for NP0040956 (oxepinamide D)

3D Structure for NP0040956 (oxepinamide D)