NP-MRD: Showing NP-Card for Epoxykinamycin (NP0022661)

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Record Information

Version

2.0

Created at

2021-01-06 07:51:17 UTC

Updated at

2021-07-15 17:39:38 UTC

NP-MRD ID

NP0022661

Secondary Accession Numbers

None

Natural Product Identification

Common Name

Epoxykinamycin

Provided By

NPAtlas

Description

Epoxykinamycin is found in Streptomyces chattanoogensis and Streptomyces chattanoogensis subsp. taitungensis subsp. nov. IY2-13. Based on a literature review very few articles have been published on (3S,4S,6R,7R)-3,13-dihydroxy-6-methyl-11,18-dioxo-9-(λ⁵-diazynylidene)-5-oxapentacyclo[8.8.0.0²,⁸.0⁴,⁶.0¹²,¹⁷]Octadeca-1(10),2(8),12(17),13,15-pentaen-7-yl acetate.

Structure

MOL 3D MOL SDF 3D SDF PDB SMILES InChI


  Mrv1652306242105363D          

 43 47  0  0  0  0            999 V2000
   -4.7349    2.5087   -0.5673 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.0484    1.4054    0.1508 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.3431    1.1914    1.3615 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.1027    0.5940   -0.4250 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4394   -0.4616    0.2460 C   0  0  2  0  0  0  0  0  0  0  0  0
   -0.9833   -0.1644    0.1985 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0335   -1.1542    0.0465 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.1853   -0.5031    0.0519 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.4698   -0.9778   -0.0619 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.6472   -2.2152   -0.1992 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.5871   -0.1535   -0.0323 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.8589   -0.6954   -0.1526 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.9336    0.1513   -0.1185 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.7455    1.5173    0.0332 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.4697    2.0163    0.1493 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.2880    3.3987    0.3023 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.3791    1.1957    0.1187 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.0780    1.6556    0.2320 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.9480    2.9079    0.3690 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.9961    0.8030    0.1977 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3634    1.0601    0.2942 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8571    2.2035    0.4387 N   0  3  0  0  0  4  0  0  0  0  0  0
   -1.3517    3.2197    0.9744 N   0  5  0  0  0  2  0  0  0  0  0  0
   -0.4705   -2.5351   -0.0738 C   0  0  2  0  0  0  0  0  0  0  0  0
    0.4060   -3.3994   -0.7119 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7959   -2.6493   -0.7830 C   0  0  2  0  0  0  0  0  0  0  0  0
   -2.1605   -1.7678   -1.7692 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7830   -1.7243   -0.4900 C   0  0  2  0  0  0  0  0  0  0  0  0
   -4.2528   -2.0812   -0.4452 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.0516    2.1825   -1.5819 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.6681    2.7731   -0.0247 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.1226    3.4336   -0.6143 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8347   -0.4833    1.2837 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.9273   -1.7591   -0.2668 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.9181   -0.2703   -0.2119 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.5941    2.2126    0.0629 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.0426    4.0499    0.3321 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6435   -2.9748    0.9536 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.5209   -4.2612   -0.2393 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0808   -3.7284   -0.9633 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.8873   -1.3395   -0.9796 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.5526   -2.0606    0.6186 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.4340   -3.1206   -0.8175 H   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0  0  0  0
  2  3  2  0  0  0  0
  2  4  1  0  0  0  0
  4  5  1  0  0  0  0
  5  6  1  0  0  0  0
  6  7  2  0  0  0  0
  7  8  1  0  0  0  0
  8  9  1  0  0  0  0
  9 10  2  0  0  0  0
  9 11  1  0  0  0  0
 11 12  2  0  0  0  0
 12 13  1  0  0  0  0
 13 14  2  0  0  0  0
 14 15  1  0  0  0  0
 15 16  1  0  0  0  0
 15 17  2  0  0  0  0
 17 18  1  0  0  0  0
 18 19  2  0  0  0  0
 18 20  1  0  0  0  0
 20 21  1  0  0  0  0
 21 22  2  0  0  0  0
 22 23  2  0  0  0  0
  7 24  1  0  0  0  0
 24 25  1  0  0  0  0
 24 26  1  0  0  0  0
 26 27  1  0  0  0  0
 27 28  1  0  0  0  0
 28 29  1  6  0  0  0
 28  5  1  0  0  0  0
 21  6  1  0  0  0  0
 28 26  1  0  0  0  0
 20  8  2  0  0  0  0
 17 11  1  0  0  0  0
  1 30  1  0  0  0  0
  1 31  1  0  0  0  0
  1 32  1  0  0  0  0
  5 33  1  1  0  0  0
 12 34  1  0  0  0  0
 13 35  1  0  0  0  0
 14 36  1  0  0  0  0
 16 37  1  0  0  0  0
 24 38  1  1  0  0  0
 25 39  1  0  0  0  0
 26 40  1  6  0  0  0
 29 41  1  0  0  0  0
 29 42  1  0  0  0  0
 29 43  1  0  0  0  0
M  CHG  2  22   1  23  -1
M  END

     RDKit          3D

 43 47  0  0  0  0  0  0  0  0999 V2000
   -4.7349    2.5087   -0.5673 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.0484    1.4054    0.1508 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.3431    1.1914    1.3615 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.1027    0.5940   -0.4250 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4394   -0.4616    0.2460 C   0  0  2  0  0  0  0  0  0  0  0  0
   -0.9833   -0.1644    0.1985 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0335   -1.1542    0.0465 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.1853   -0.5031    0.0519 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.4698   -0.9778   -0.0619 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.6472   -2.2152   -0.1992 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.5871   -0.1535   -0.0323 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.8589   -0.6954   -0.1526 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.9336    0.1513   -0.1185 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.7455    1.5173    0.0332 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.4697    2.0163    0.1493 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.2880    3.3987    0.3023 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.3791    1.1957    0.1187 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.0780    1.6556    0.2320 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.9480    2.9079    0.3690 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.9961    0.8030    0.1977 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3634    1.0601    0.2942 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8571    2.2035    0.4387 N   0  0  0  0  0  4  0  0  0  0  0  0
   -1.3517    3.2197    0.9744 N   0  0  0  0  0  2  0  0  0  0  0  0
   -0.4705   -2.5351   -0.0738 C   0  0  2  0  0  0  0  0  0  0  0  0
    0.4060   -3.3994   -0.7119 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7959   -2.6493   -0.7830 C   0  0  2  0  0  0  0  0  0  0  0  0
   -2.1605   -1.7678   -1.7692 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7830   -1.7243   -0.4900 C   0  0  2  0  0  0  0  0  0  0  0  0
   -4.2528   -2.0812   -0.4452 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.0516    2.1825   -1.5819 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.6681    2.7731   -0.0247 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.1226    3.4336   -0.6143 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8347   -0.4833    1.2837 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.9273   -1.7591   -0.2668 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.9181   -0.2703   -0.2119 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.5941    2.2126    0.0629 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.0426    4.0499    0.3321 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6435   -2.9748    0.9536 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.5209   -4.2612   -0.2393 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0808   -3.7284   -0.9633 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.8873   -1.3395   -0.9796 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.5526   -2.0606    0.6186 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.4340   -3.1206   -0.8175 H   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0
  2  3  2  0
  2  4  1  0
  4  5  1  0
  5  6  1  0
  6  7  2  0
  7  8  1  0
  8  9  1  0
  9 10  2  0
  9 11  1  0
 11 12  2  0
 12 13  1  0
 13 14  2  0
 14 15  1  0
 15 16  1  0
 15 17  2  0
 17 18  1  0
 18 19  2  0
 18 20  1  0
 20 21  1  0
 21 22  2  0
 22 23  2  0
  7 24  1  0
 24 25  1  0
 24 26  1  0
 26 27  1  0
 27 28  1  0
 28 29  1  6
 28  5  1  0
 21  6  1  0
 28 26  1  0
 20  8  2  0
 17 11  1  0
  1 30  1  0
  1 31  1  0
  1 32  1  0
  5 33  1  1
 12 34  1  0
 13 35  1  0
 14 36  1  0
 16 37  1  0
 24 38  1  1
 25 39  1  0
 26 40  1  6
 29 41  1  0
 29 42  1  0
 29 43  1  0
M  CHG  2  22   1  23  -1
M  END


  Mrv1652306242105363D          

 43 47  0  0  0  0            999 V2000
   -4.7349    2.5087   -0.5673 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.0484    1.4054    0.1508 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.3431    1.1914    1.3615 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.1027    0.5940   -0.4250 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4394   -0.4616    0.2460 C   0  0  2  0  0  0  0  0  0  0  0  0
   -0.9833   -0.1644    0.1985 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0335   -1.1542    0.0465 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.1853   -0.5031    0.0519 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.4698   -0.9778   -0.0619 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.6472   -2.2152   -0.1992 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.5871   -0.1535   -0.0323 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.8589   -0.6954   -0.1526 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.9336    0.1513   -0.1185 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.7455    1.5173    0.0332 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.4697    2.0163    0.1493 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.2880    3.3987    0.3023 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.3791    1.1957    0.1187 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.0780    1.6556    0.2320 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.9480    2.9079    0.3690 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.9961    0.8030    0.1977 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3634    1.0601    0.2942 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8571    2.2035    0.4387 N   0  3  0  0  0  4  0  0  0  0  0  0
   -1.3517    3.2197    0.9744 N   0  5  0  0  0  2  0  0  0  0  0  0
   -0.4705   -2.5351   -0.0738 C   0  0  2  0  0  0  0  0  0  0  0  0
    0.4060   -3.3994   -0.7119 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7959   -2.6493   -0.7830 C   0  0  2  0  0  0  0  0  0  0  0  0
   -2.1605   -1.7678   -1.7692 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7830   -1.7243   -0.4900 C   0  0  2  0  0  0  0  0  0  0  0  0
   -4.2528   -2.0812   -0.4452 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.0516    2.1825   -1.5819 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.6681    2.7731   -0.0247 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.1226    3.4336   -0.6143 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8347   -0.4833    1.2837 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.9273   -1.7591   -0.2668 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.9181   -0.2703   -0.2119 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.5941    2.2126    0.0629 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.0426    4.0499    0.3321 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6435   -2.9748    0.9536 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.5209   -4.2612   -0.2393 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0808   -3.7284   -0.9633 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.8873   -1.3395   -0.9796 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.5526   -2.0606    0.6186 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.4340   -3.1206   -0.8175 H   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0  0  0  0
  2  3  2  0  0  0  0
  2  4  1  0  0  0  0
  4  5  1  0  0  0  0
  5  6  1  0  0  0  0
  6  7  2  0  0  0  0
  7  8  1  0  0  0  0
  8  9  1  0  0  0  0
  9 10  2  0  0  0  0
  9 11  1  0  0  0  0
 11 12  2  0  0  0  0
 12 13  1  0  0  0  0
 13 14  2  0  0  0  0
 14 15  1  0  0  0  0
 15 16  1  0  0  0  0
 15 17  2  0  0  0  0
 17 18  1  0  0  0  0
 18 19  2  0  0  0  0
 18 20  1  0  0  0  0
 20 21  1  0  0  0  0
 21 22  2  0  0  0  0
 22 23  2  0  0  0  0
  7 24  1  0  0  0  0
 24 25  1  0  0  0  0
 24 26  1  0  0  0  0
 26 27  1  0  0  0  0
 27 28  1  0  0  0  0
 28 29  1  6  0  0  0
 28  5  1  0  0  0  0
 21  6  1  0  0  0  0
 28 26  1  0  0  0  0
 20  8  2  0  0  0  0
 17 11  1  0  0  0  0
  1 30  1  0  0  0  0
  1 31  1  0  0  0  0
  1 32  1  0  0  0  0
  5 33  1  1  0  0  0
 12 34  1  0  0  0  0
 13 35  1  0  0  0  0
 14 36  1  0  0  0  0
 16 37  1  0  0  0  0
 24 38  1  1  0  0  0
 25 39  1  0  0  0  0
 26 40  1  6  0  0  0
 29 41  1  0  0  0  0
 29 42  1  0  0  0  0
 29 43  1  0  0  0  0
M  CHG  2  22   1  23  -1
M  END
> <DATABASE_ID>
NP0022661

> <DATABASE_NAME>
NP-MRD

> <SMILES>
[H]OC1=C2C(=O)C3=C(C4=C(C3=[N+]=[N-])[C@@]([H])(OC(=O)C([H])([H])[H])[C@]3(O[C@@]3([H])[C@@]4([H])O[H])C([H])([H])[H])C(=O)C2=C([H])C([H])=C1[H]

> <INCHI_IDENTIFIER>
InChI=1S/C20H14N2O7/c1-6(23)28-18-13-11(17(27)19-20(18,2)29-19)10-12(14(13)22-21)16(26)9-7(15(10)25)4-3-5-8(9)24/h3-5,17-19,24,27H,1-2H3/t17-,18+,19-,20+/m0/s1

> <INCHI_KEY>
ATRXXFLMCRBZNH-ZGXWSNOMSA-N

> <FORMULA>
C20H14N2O7

> <MOLECULAR_WEIGHT>
394.339

> <EXACT_MASS>
394.080100799

> <JCHEM_ACCEPTOR_COUNT>
7

> <JCHEM_ATOM_COUNT>
43

> <JCHEM_AVERAGE_POLARIZABILITY>
38.6299425120269

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
2

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
0

> <JCHEM_IUPAC>
(3S,4S,6R,7R)-3,13-dihydroxy-9-(-lambda4,-lambda2-diazynylidene)-6-methyl-11,18-dioxo-5-oxapentacyclo[8.8.0.0^{2,8}.0^{4,6}.0^{12,17}]octadeca-1(10),2(8),12,14,16-pentaen-7-yl acetate

> <ALOGPS_LOGP>
1.97

> <JCHEM_LOGP>
-0.9169897225426125

> <ALOGPS_LOGS>
-2.66

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
5

> <JCHEM_PHYSIOLOGICAL_CHARGE>
1

> <JCHEM_PKA>
8.991944341691779

> <JCHEM_PKA_STRONGEST_ACIDIC>
8.05964160892315

> <JCHEM_PKA_STRONGEST_BASIC>
-3.530836628731824

> <JCHEM_POLAR_SURFACE_AREA>
130.5

> <JCHEM_REFRACTIVITY>
95.92810000000003

> <JCHEM_ROTATABLE_BOND_COUNT>
2

> <JCHEM_RULE_OF_FIVE>
1

> <ALOGPS_SOLUBILITY>
8.70e-01 g/l

> <JCHEM_TRADITIONAL_IUPAC>
(3S,4S,6R,7R)-3,13-dihydroxy-9-(-lambda4,-lambda2-diazynylidene)-6-methyl-11,18-dioxo-5-oxapentacyclo[8.8.0.0^{2,8}.0^{4,6}.0^{12,17}]octadeca-1(10),2(8),12,14,16-pentaen-7-yl acetate

> <JCHEM_VEBER_RULE>
0

$$$$

     RDKit          3D

 43 47  0  0  0  0  0  0  0  0999 V2000
   -4.7349    2.5087   -0.5673 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.0484    1.4054    0.1508 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.3431    1.1914    1.3615 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.1027    0.5940   -0.4250 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4394   -0.4616    0.2460 C   0  0  2  0  0  0  0  0  0  0  0  0
   -0.9833   -0.1644    0.1985 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0335   -1.1542    0.0465 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.1853   -0.5031    0.0519 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.4698   -0.9778   -0.0619 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.6472   -2.2152   -0.1992 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.5871   -0.1535   -0.0323 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.8589   -0.6954   -0.1526 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.9336    0.1513   -0.1185 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.7455    1.5173    0.0332 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.4697    2.0163    0.1493 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.2880    3.3987    0.3023 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.3791    1.1957    0.1187 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.0780    1.6556    0.2320 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.9480    2.9079    0.3690 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.9961    0.8030    0.1977 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3634    1.0601    0.2942 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8571    2.2035    0.4387 N   0  0  0  0  0  4  0  0  0  0  0  0
   -1.3517    3.2197    0.9744 N   0  0  0  0  0  2  0  0  0  0  0  0
   -0.4705   -2.5351   -0.0738 C   0  0  2  0  0  0  0  0  0  0  0  0
    0.4060   -3.3994   -0.7119 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7959   -2.6493   -0.7830 C   0  0  2  0  0  0  0  0  0  0  0  0
   -2.1605   -1.7678   -1.7692 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7830   -1.7243   -0.4900 C   0  0  2  0  0  0  0  0  0  0  0  0
   -4.2528   -2.0812   -0.4452 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.0516    2.1825   -1.5819 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.6681    2.7731   -0.0247 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.1226    3.4336   -0.6143 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8347   -0.4833    1.2837 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.9273   -1.7591   -0.2668 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.9181   -0.2703   -0.2119 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.5941    2.2126    0.0629 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.0426    4.0499    0.3321 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6435   -2.9748    0.9536 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.5209   -4.2612   -0.2393 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0808   -3.7284   -0.9633 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.8873   -1.3395   -0.9796 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.5526   -2.0606    0.6186 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.4340   -3.1206   -0.8175 H   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0
  2  3  2  0
  2  4  1  0
  4  5  1  0
  5  6  1  0
  6  7  2  0
  7  8  1  0
  8  9  1  0
  9 10  2  0
  9 11  1  0
 11 12  2  0
 12 13  1  0
 13 14  2  0
 14 15  1  0
 15 16  1  0
 15 17  2  0
 17 18  1  0
 18 19  2  0
 18 20  1  0
 20 21  1  0
 21 22  2  0
 22 23  2  0
  7 24  1  0
 24 25  1  0
 24 26  1  0
 26 27  1  0
 27 28  1  0
 28 29  1  6
 28  5  1  0
 21  6  1  0
 28 26  1  0
 20  8  2  0
 17 11  1  0
  1 30  1  0
  1 31  1  0
  1 32  1  0
  5 33  1  1
 12 34  1  0
 13 35  1  0
 14 36  1  0
 16 37  1  0
 24 38  1  1
 25 39  1  0
 26 40  1  6
 29 41  1  0
 29 42  1  0
 29 43  1  0
M  CHG  2  22   1  23  -1
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      -4.735   2.509  -0.567  0.00  0.00           C+0
HETATM    2  C   UNK     0      -4.048   1.405   0.151  0.00  0.00           C+0
HETATM    3  O   UNK     0      -4.343   1.191   1.361  0.00  0.00           O+0
HETATM    4  O   UNK     0      -3.103   0.594  -0.425  0.00  0.00           O+0
HETATM    5  C   UNK     0      -2.439  -0.462   0.246  0.00  0.00           C+0
HETATM    6  C   UNK     0      -0.983  -0.164   0.199  0.00  0.00           C+0
HETATM    7  C   UNK     0      -0.034  -1.154   0.047  0.00  0.00           C+0
HETATM    8  C   UNK     0       1.185  -0.503   0.052  0.00  0.00           C+0
HETATM    9  C   UNK     0       2.470  -0.978  -0.062  0.00  0.00           C+0
HETATM   10  O   UNK     0       2.647  -2.215  -0.199  0.00  0.00           O+0
HETATM   11  C   UNK     0       3.587  -0.154  -0.032  0.00  0.00           C+0
HETATM   12  C   UNK     0       4.859  -0.695  -0.153  0.00  0.00           C+0
HETATM   13  C   UNK     0       5.934   0.151  -0.119  0.00  0.00           C+0
HETATM   14  C   UNK     0       5.745   1.517   0.033  0.00  0.00           C+0
HETATM   15  C   UNK     0       4.470   2.016   0.149  0.00  0.00           C+0
HETATM   16  O   UNK     0       4.288   3.399   0.302  0.00  0.00           O+0
HETATM   17  C   UNK     0       3.379   1.196   0.119  0.00  0.00           C+0
HETATM   18  C   UNK     0       2.078   1.656   0.232  0.00  0.00           C+0
HETATM   19  O   UNK     0       1.948   2.908   0.369  0.00  0.00           O+0
HETATM   20  C   UNK     0       0.996   0.803   0.198  0.00  0.00           C+0
HETATM   21  C   UNK     0      -0.363   1.060   0.294  0.00  0.00           C+0
HETATM   22  N   UNK     0      -0.857   2.204   0.439  0.00  0.00           N+1
HETATM   23  N   UNK     0      -1.352   3.220   0.974  0.00  0.00           N-1
HETATM   24  C   UNK     0      -0.471  -2.535  -0.074  0.00  0.00           C+0
HETATM   25  O   UNK     0       0.406  -3.399  -0.712  0.00  0.00           O+0
HETATM   26  C   UNK     0      -1.796  -2.649  -0.783  0.00  0.00           C+0
HETATM   27  O   UNK     0      -2.160  -1.768  -1.769  0.00  0.00           O+0
HETATM   28  C   UNK     0      -2.783  -1.724  -0.490  0.00  0.00           C+0
HETATM   29  C   UNK     0      -4.253  -2.081  -0.445  0.00  0.00           C+0
HETATM   30  H   UNK     0      -5.052   2.183  -1.582  0.00  0.00           H+0
HETATM   31  H   UNK     0      -5.668   2.773  -0.025  0.00  0.00           H+0
HETATM   32  H   UNK     0      -4.123   3.434  -0.614  0.00  0.00           H+0
HETATM   33  H   UNK     0      -2.835  -0.483   1.284  0.00  0.00           H+0
HETATM   34  H   UNK     0       4.927  -1.759  -0.267  0.00  0.00           H+0
HETATM   35  H   UNK     0       6.918  -0.270  -0.212  0.00  0.00           H+0
HETATM   36  H   UNK     0       6.594   2.213   0.063  0.00  0.00           H+0
HETATM   37  H   UNK     0       5.043   4.050   0.332  0.00  0.00           H+0
HETATM   38  H   UNK     0      -0.644  -2.975   0.954  0.00  0.00           H+0
HETATM   39  H   UNK     0       0.521  -4.261  -0.239  0.00  0.00           H+0
HETATM   40  H   UNK     0      -2.081  -3.728  -0.963  0.00  0.00           H+0
HETATM   41  H   UNK     0      -4.887  -1.339  -0.980  0.00  0.00           H+0
HETATM   42  H   UNK     0      -4.553  -2.061   0.619  0.00  0.00           H+0
HETATM   43  H   UNK     0      -4.434  -3.121  -0.818  0.00  0.00           H+0
CONECT    1    2   30   31   32                                             
CONECT    2    1    3    4                                                  
CONECT    3    2                                                            
CONECT    4    2    5                                                       
CONECT    5    4    6   28   33                                             
CONECT    6    5    7   21                                                  
CONECT    7    6    8   24                                                  
CONECT    8    7    9   20                                                  
CONECT    9    8   10   11                                                  
CONECT   10    9                                                            
CONECT   11    9   12   17                                                  
CONECT   12   11   13   34                                                  
CONECT   13   12   14   35                                                  
CONECT   14   13   15   36                                                  
CONECT   15   14   16   17                                                  
CONECT   16   15   37                                                       
CONECT   17   15   18   11                                                  
CONECT   18   17   19   20                                                  
CONECT   19   18                                                            
CONECT   20   18   21    8                                                  
CONECT   21   20   22    6                                                  
CONECT   22   21   23                                                       
CONECT   23   22                                                            
CONECT   24    7   25   26   38                                             
CONECT   25   24   39                                                       
CONECT   26   24   27   28   40                                             
CONECT   27   26   28                                                       
CONECT   28   27   29    5   26                                             
CONECT   29   28   41   42   43                                             
CONECT   30    1                                                            
CONECT   31    1                                                            
CONECT   32    1                                                            
CONECT   33    5                                                            
CONECT   34   12                                                            
CONECT   35   13                                                            
CONECT   36   14                                                            
CONECT   37   16                                                            
CONECT   38   24                                                            
CONECT   39   25                                                            
CONECT   40   26                                                            
CONECT   41   29                                                            
CONECT   42   29                                                            
CONECT   43   29                                                            
MASTER        0    0    0    0    0    0    0    0   43    0   94    0
END

RDKit          3D

43 47  0  0  0  0  0  0  0  0999 V2000
   -4.7349    2.5087   -0.5673 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.0484    1.4054    0.1508 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.3431    1.1914    1.3615 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.1027    0.5940   -0.4250 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4394   -0.4616    0.2460 C   0  0  2  0  0  0  0  0  0  0  0  0
   -0.9833   -0.1644    0.1985 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0335   -1.1542    0.0465 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.1853   -0.5031    0.0519 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.4698   -0.9778   -0.0619 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.6472   -2.2152   -0.1992 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.5871   -0.1535   -0.0323 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.8589   -0.6954   -0.1526 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.9336    0.1513   -0.1185 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.7455    1.5173    0.0332 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.4697    2.0163    0.1493 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.2880    3.3987    0.3023 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.3791    1.1957    0.1187 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.0780    1.6556    0.2320 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.9480    2.9079    0.3690 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.9961    0.8030    0.1977 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3634    1.0601    0.2942 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8571    2.2035    0.4387 N   0  0  0  0  0  4  0  0  0  0  0  0
   -1.3517    3.2197    0.9744 N   0  0  0  0  0  2  0  0  0  0  0  0
   -0.4705   -2.5351   -0.0738 C   0  0  2  0  0  0  0  0  0  0  0  0
    0.4060   -3.3994   -0.7119 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7959   -2.6493   -0.7830 C   0  0  2  0  0  0  0  0  0  0  0  0
   -2.1605   -1.7678   -1.7692 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7830   -1.7243   -0.4900 C   0  0  2  0  0  0  0  0  0  0  0  0
   -4.2528   -2.0812   -0.4452 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.0516    2.1825   -1.5819 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.6681    2.7731   -0.0247 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.1226    3.4336   -0.6143 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8347   -0.4833    1.2837 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.9273   -1.7591   -0.2668 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.9181   -0.2703   -0.2119 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.5941    2.2126    0.0629 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.0426    4.0499    0.3321 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6435   -2.9748    0.9536 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.5209   -4.2612   -0.2393 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0808   -3.7284   -0.9633 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.8873   -1.3395   -0.9796 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.5526   -2.0606    0.6186 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.4340   -3.1206   -0.8175 H   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0
  2  3  2  0
  2  4  1  0
  4  5  1  0
  5  6  1  0
  6  7  2  0
  7  8  1  0
  8  9  1  0
  9 10  2  0
  9 11  1  0
 11 12  2  0
 12 13  1  0
 13 14  2  0
 14 15  1  0
 15 16  1  0
 15 17  2  0
 17 18  1  0
 18 19  2  0
 18 20  1  0
 20 21  1  0
 21 22  2  0
 22 23  2  0
  7 24  1  0
 24 25  1  0
 24 26  1  0
 26 27  1  0
 27 28  1  0
 28 29  1  6
 28  5  1  0
 21  6  1  0
 28 26  1  0
 20  8  2  0
 17 11  1  0
  1 30  1  0
  1 31  1  0
  1 32  1  0
  5 33  1  1
 12 34  1  0
 13 35  1  0
 14 36  1  0
 16 37  1  0
 24 38  1  1
 25 39  1  0
 26 40  1  6
 29 41  1  0
 29 42  1  0
 29 43  1  0
M  CHG  2  22   1  23  -1
M  END

View in JSmol View NMR Assignments

Synonyms

Value	Source
(3S,4S,6R,7R)-3,13-Dihydroxy-6-methyl-11,18-dioxo-9-(-diazynylidene)-5-oxapentacyclo[8.8.0.0,.0,.0,]octadeca-1(10),2(8),12(17),13,15-pentaen-7-yl acetic acid	Generator

Chemical Formula

C₂₀H₁₄N₂O₇

Average Mass

394.3390 Da

Monoisotopic Mass

394.08010 Da

IUPAC Name

(3S,4S,6R,7R)-3,13-dihydroxy-9-(-lambda4,-lambda2-diazynylidene)-6-methyl-11,18-dioxo-5-oxapentacyclo[8.8.0.0^{2,8}.0^{4,6}.0^{12,17}]octadeca-1(10),2(8),12,14,16-pentaen-7-yl acetate

Traditional Name

(3S,4S,6R,7R)-3,13-dihydroxy-9-(-lambda4,-lambda2-diazynylidene)-6-methyl-11,18-dioxo-5-oxapentacyclo[8.8.0.0^{2,8}.0^{4,6}.0^{12,17}]octadeca-1(10),2(8),12,14,16-pentaen-7-yl acetate

CAS Registry Number

Not Available

SMILES

CC(=O)O[C@@H]1C2=C([C@H](O)[C@@H]3O[C@]13C)C1=C(C2=[N+]=[N-])C(=O)C2=C(C=CC=C2O)C1=O

InChI Identifier

InChI=1S/C20H14N2O7/c1-6(23)28-18-13-11(17(27)19-20(18,2)29-19)10-12(14(13)22-21)16(26)9-7(15(10)25)4-3-5-8(9)24/h3-5,17-19,24,27H,1-2H3/t17-,18+,19-,20+/m0/s1

InChI Key

ATRXXFLMCRBZNH-ZGXWSNOMSA-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 chattanoogensis	NPAtlas	8040072
Streptomyces chattanoogensis subsp. taitungensis subsp. nov. IY2-13	Bacteria	KNApSAcK

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	1.97	ALOGPS
logP	-0.92	ChemAxon
logS	-2.7	ALOGPS
pKa (Strongest Acidic)	8.06	ChemAxon
pKa (Strongest Basic)	-3.5	ChemAxon
Physiological Charge	1	ChemAxon
Hydrogen Acceptor Count	7	ChemAxon
Hydrogen Donor Count	2	ChemAxon
Polar Surface Area	130.5 Å²	ChemAxon
Rotatable Bond Count	2	ChemAxon
Refractivity	95.93 m³·mol⁻¹	ChemAxon
Polarizability	38.63 Å³	ChemAxon
Number of Rings	5	ChemAxon
Bioavailability	Yes	ChemAxon
Rule of Five	Yes	ChemAxon
Ghose Filter	No	ChemAxon
Veber's Rule	No	ChemAxon
MDDR-like Rule	No	ChemAxon

External Links

NPAtlas ID

NPA012808

HMDB ID

Not Available

DrugBank ID

Not Available

Phenol Explorer Compound ID

Not Available

FoodDB ID

Not Available

KNApSAcK ID

Not Available

Chemspider ID

26233556

KEGG Compound ID

Not Available

BioCyc ID

Not Available

BiGG ID

Not Available

Wikipedia Link

Not Available

METLIN ID

Not Available

PubChem Compound

136199620

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

Showing NP-Card for Epoxykinamycin (NP0022661)

MOL for NP0022661 (Epoxykinamycin)

3D MOL for NP0022661 (Epoxykinamycin)

3D SDF for NP0022661 (Epoxykinamycin)

3D-SDF for NP0022661 (Epoxykinamycin)

PDB for NP0022661 (Epoxykinamycin)

3D PDB for NP0022661 (Epoxykinamycin)

SMILES for NP0022661 (Epoxykinamycin)

INCHI for NP0022661 (Epoxykinamycin)

Structure for NP0022661 (Epoxykinamycin)

3D Structure for NP0022661 (Epoxykinamycin)