NP-MRD: Showing NP-Card for Mycemycin E (NP0014775)

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Record Information

Version

2.0

Created at

2021-01-05 23:51:07 UTC

Updated at

2021-07-15 17:18:11 UTC

NP-MRD ID

NP0014775

Secondary Accession Numbers

None

Natural Product Identification

Common Name

Mycemycin E

Provided By

NPAtlas

Description

Mycemycin E is found in Streptomyces sp. FXJ1.235. Based on a literature review very few articles have been published on 5,13-dichloro-10-hydroxy-4-methyl-2-oxa-9-azatricyclo[9.4.0.0³,⁸]Pentadeca-1(11),3(8),4,6,9,12,14-heptaene-7-carboximidic acid.

Structure

MOL 3D MOL SDF 3D SDF PDB SMILES InChI


  Mrv1652306242120063D          

 32 34  0  0  0  0            999 V2000
   -0.9122    3.1698   -0.4232 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3703    1.7967   -0.1637 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7212    1.5271   -0.3001 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.8445    2.8073   -0.7706 Cl  0  0  0  0  0  0  0  0  0  0  0  0
   -3.1543    0.2473   -0.0606 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2573   -0.7708    0.3144 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7875   -2.0981    0.4627 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.2030   -2.3438    0.4033 N   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0765   -3.1014    0.6496 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9378   -0.4549    0.4384 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4574    0.8381    0.2007 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.8708    1.2960    0.2862 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.0476    0.5512    0.0465 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.1178    1.3168   -0.3608 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.3470    0.7547   -0.6397 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.5583   -0.6026   -0.5224 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.1341   -1.3079   -0.8820 Cl  0  0  0  0  0  0  0  0  0  0  0  0
    3.4958   -1.3818   -0.1156 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.2560   -0.8137    0.1656 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.2579   -1.7884    0.5807 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.6515   -2.9644    0.6808 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1209   -1.5382    0.8848 N   0  0  0  0  0  0  0  0  0  0  0  0
    0.0352    3.1112   -0.9997 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6159    3.7551   -1.0366 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7625    3.7452    0.5175 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.2147    0.0367   -0.1682 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.9146   -1.8128    0.9350 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.5143   -3.1096   -0.2206 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.9261    2.3909   -0.4466 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.1632    1.3828   -0.9561 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.6354   -2.4502   -0.0156 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6316   -2.1882    1.5159 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
  3  4  1  0  0  0  0
  3  5  1  0  0  0  0
  5  6  2  0  0  0  0
  6  7  1  0  0  0  0
  7  8  1  0  0  0  0
  7  9  2  0  0  0  0
  6 10  1  0  0  0  0
 10 11  2  0  0  0  0
 11 12  1  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  2  0  0  0  0
 16 17  1  0  0  0  0
 16 18  1  0  0  0  0
 18 19  2  0  0  0  0
 19 20  1  0  0  0  0
 20 21  2  0  0  0  0
 20 22  1  0  0  0  0
 11  2  1  0  0  0  0
 19 13  1  0  0  0  0
 22 10  1  0  0  0  0
  1 23  1  0  0  0  0
  1 24  1  0  0  0  0
  1 25  1  0  0  0  0
  5 26  1  0  0  0  0
  8 27  1  0  0  0  0
  8 28  1  0  0  0  0
 14 29  1  0  0  0  0
 15 30  1  0  0  0  0
 18 31  1  0  0  0  0
 22 32  1  0  0  0  0
M  END

     RDKit          3D

 32 34  0  0  0  0  0  0  0  0999 V2000
   -0.9122    3.1698   -0.4232 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3703    1.7967   -0.1637 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7212    1.5271   -0.3001 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.8445    2.8073   -0.7706 Cl  0  0  0  0  0  0  0  0  0  0  0  0
   -3.1543    0.2473   -0.0606 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2573   -0.7708    0.3144 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7875   -2.0981    0.4627 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.2030   -2.3438    0.4033 N   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0765   -3.1014    0.6496 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9378   -0.4549    0.4384 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4574    0.8381    0.2007 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.8708    1.2960    0.2862 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.0476    0.5512    0.0465 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.1178    1.3168   -0.3608 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.3470    0.7547   -0.6397 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.5583   -0.6026   -0.5224 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.1341   -1.3079   -0.8820 Cl  0  0  0  0  0  0  0  0  0  0  0  0
    3.4958   -1.3818   -0.1156 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.2560   -0.8137    0.1656 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.2579   -1.7884    0.5807 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.6515   -2.9644    0.6808 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1209   -1.5382    0.8848 N   0  0  0  0  0  0  0  0  0  0  0  0
    0.0352    3.1112   -0.9997 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6159    3.7551   -1.0366 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7625    3.7452    0.5175 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.2147    0.0367   -0.1682 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.9146   -1.8128    0.9350 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.5143   -3.1096   -0.2206 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.9261    2.3909   -0.4466 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.1632    1.3828   -0.9561 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.6354   -2.4502   -0.0156 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6316   -2.1882    1.5159 H   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0
  2  3  2  0
  3  4  1  0
  3  5  1  0
  5  6  2  0
  6  7  1  0
  7  8  1  0
  7  9  2  0
  6 10  1  0
 10 11  2  0
 11 12  1  0
 12 13  1  0
 13 14  2  0
 14 15  1  0
 15 16  2  0
 16 17  1  0
 16 18  1  0
 18 19  2  0
 19 20  1  0
 20 21  2  0
 20 22  1  0
 11  2  1  0
 19 13  1  0
 22 10  1  0
  1 23  1  0
  1 24  1  0
  1 25  1  0
  5 26  1  0
  8 27  1  0
  8 28  1  0
 14 29  1  0
 15 30  1  0
 18 31  1  0
 22 32  1  0
M  END


  Mrv1652306242120063D          

 32 34  0  0  0  0            999 V2000
   -0.9122    3.1698   -0.4232 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3703    1.7967   -0.1637 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7212    1.5271   -0.3001 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.8445    2.8073   -0.7706 Cl  0  0  0  0  0  0  0  0  0  0  0  0
   -3.1543    0.2473   -0.0606 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2573   -0.7708    0.3144 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7875   -2.0981    0.4627 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.2030   -2.3438    0.4033 N   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0765   -3.1014    0.6496 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9378   -0.4549    0.4384 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4574    0.8381    0.2007 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.8708    1.2960    0.2862 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.0476    0.5512    0.0465 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.1178    1.3168   -0.3608 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.3470    0.7547   -0.6397 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.5583   -0.6026   -0.5224 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.1341   -1.3079   -0.8820 Cl  0  0  0  0  0  0  0  0  0  0  0  0
    3.4958   -1.3818   -0.1156 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.2560   -0.8137    0.1656 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.2579   -1.7884    0.5807 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.6515   -2.9644    0.6808 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1209   -1.5382    0.8848 N   0  0  0  0  0  0  0  0  0  0  0  0
    0.0352    3.1112   -0.9997 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6159    3.7551   -1.0366 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7625    3.7452    0.5175 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.2147    0.0367   -0.1682 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.9146   -1.8128    0.9350 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.5143   -3.1096   -0.2206 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.9261    2.3909   -0.4466 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.1632    1.3828   -0.9561 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.6354   -2.4502   -0.0156 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6316   -2.1882    1.5159 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
  3  4  1  0  0  0  0
  3  5  1  0  0  0  0
  5  6  2  0  0  0  0
  6  7  1  0  0  0  0
  7  8  1  0  0  0  0
  7  9  2  0  0  0  0
  6 10  1  0  0  0  0
 10 11  2  0  0  0  0
 11 12  1  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  2  0  0  0  0
 16 17  1  0  0  0  0
 16 18  1  0  0  0  0
 18 19  2  0  0  0  0
 19 20  1  0  0  0  0
 20 21  2  0  0  0  0
 20 22  1  0  0  0  0
 11  2  1  0  0  0  0
 19 13  1  0  0  0  0
 22 10  1  0  0  0  0
  1 23  1  0  0  0  0
  1 24  1  0  0  0  0
  1 25  1  0  0  0  0
  5 26  1  0  0  0  0
  8 27  1  0  0  0  0
  8 28  1  0  0  0  0
 14 29  1  0  0  0  0
 15 30  1  0  0  0  0
 18 31  1  0  0  0  0
 22 32  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0014775

> <DATABASE_NAME>
NP-MRD

> <SMILES>
[H]N([H])C(=O)C1=C([H])C(Cl)=C(C2=C1N([H])C(=O)C1=C([H])C(Cl)=C([H])C([H])=C1O2)C([H])([H])[H]

> <INCHI_IDENTIFIER>
InChI=1S/C15H10Cl2N2O3/c1-6-10(17)5-9(14(18)20)12-13(6)22-11-3-2-7(16)4-8(11)15(21)19-12/h2-5H,1H3,(H2,18,20)(H,19,21)

> <INCHI_KEY>
LKTXNDBBKSMZRJ-UHFFFAOYSA-N

> <FORMULA>
C15H10Cl2N2O3

> <MOLECULAR_WEIGHT>
337.16

> <EXACT_MASS>
336.0068476

> <JCHEM_ACCEPTOR_COUNT>
2

> <JCHEM_ATOM_COUNT>
32

> <JCHEM_AVERAGE_POLARIZABILITY>
32.51958982484473

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
2

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
1

> <JCHEM_IUPAC>
5,13-dichloro-4-methyl-10-oxo-2-oxa-9-azatricyclo[9.4.0.0^{3,8}]pentadeca-1(15),3(8),4,6,11,13-hexaene-7-carboxamide

> <ALOGPS_LOGP>
3.15

> <JCHEM_LOGP>
3.8143230249999998

> <ALOGPS_LOGS>
-4.47

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
3

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA>
13.673974098664882

> <JCHEM_PKA_STRONGEST_ACIDIC>
10.909160130023213

> <JCHEM_PKA_STRONGEST_BASIC>
-0.8848273868868998

> <JCHEM_POLAR_SURFACE_AREA>
81.42000000000002

> <JCHEM_REFRACTIVITY>
85.5035

> <JCHEM_ROTATABLE_BOND_COUNT>
1

> <JCHEM_RULE_OF_FIVE>
1

> <ALOGPS_SOLUBILITY>
1.15e-02 g/l

> <JCHEM_TRADITIONAL_IUPAC>
5,13-dichloro-4-methyl-10-oxo-2-oxa-9-azatricyclo[9.4.0.0^{3,8}]pentadeca-1(15),3(8),4,6,11,13-hexaene-7-carboxamide

> <JCHEM_VEBER_RULE>
0

$$$$

     RDKit          3D

 32 34  0  0  0  0  0  0  0  0999 V2000
   -0.9122    3.1698   -0.4232 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3703    1.7967   -0.1637 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7212    1.5271   -0.3001 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.8445    2.8073   -0.7706 Cl  0  0  0  0  0  0  0  0  0  0  0  0
   -3.1543    0.2473   -0.0606 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2573   -0.7708    0.3144 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7875   -2.0981    0.4627 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.2030   -2.3438    0.4033 N   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0765   -3.1014    0.6496 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9378   -0.4549    0.4384 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4574    0.8381    0.2007 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.8708    1.2960    0.2862 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.0476    0.5512    0.0465 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.1178    1.3168   -0.3608 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.3470    0.7547   -0.6397 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.5583   -0.6026   -0.5224 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.1341   -1.3079   -0.8820 Cl  0  0  0  0  0  0  0  0  0  0  0  0
    3.4958   -1.3818   -0.1156 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.2560   -0.8137    0.1656 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.2579   -1.7884    0.5807 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.6515   -2.9644    0.6808 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1209   -1.5382    0.8848 N   0  0  0  0  0  0  0  0  0  0  0  0
    0.0352    3.1112   -0.9997 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6159    3.7551   -1.0366 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7625    3.7452    0.5175 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.2147    0.0367   -0.1682 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.9146   -1.8128    0.9350 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.5143   -3.1096   -0.2206 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.9261    2.3909   -0.4466 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.1632    1.3828   -0.9561 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.6354   -2.4502   -0.0156 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6316   -2.1882    1.5159 H   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0
  2  3  2  0
  3  4  1  0
  3  5  1  0
  5  6  2  0
  6  7  1  0
  7  8  1  0
  7  9  2  0
  6 10  1  0
 10 11  2  0
 11 12  1  0
 12 13  1  0
 13 14  2  0
 14 15  1  0
 15 16  2  0
 16 17  1  0
 16 18  1  0
 18 19  2  0
 19 20  1  0
 20 21  2  0
 20 22  1  0
 11  2  1  0
 19 13  1  0
 22 10  1  0
  1 23  1  0
  1 24  1  0
  1 25  1  0
  5 26  1  0
  8 27  1  0
  8 28  1  0
 14 29  1  0
 15 30  1  0
 18 31  1  0
 22 32  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      -0.912   3.170  -0.423  0.00  0.00           C+0
HETATM    2  C   UNK     0      -1.370   1.797  -0.164  0.00  0.00           C+0
HETATM    3  C   UNK     0      -2.721   1.527  -0.300  0.00  0.00           C+0
HETATM    4 Cl   UNK     0      -3.845   2.807  -0.771  0.00  0.00          Cl+0
HETATM    5  C   UNK     0      -3.154   0.247  -0.061  0.00  0.00           C+0
HETATM    6  C   UNK     0      -2.257  -0.771   0.314  0.00  0.00           C+0
HETATM    7  C   UNK     0      -2.788  -2.098   0.463  0.00  0.00           C+0
HETATM    8  N   UNK     0      -4.203  -2.344   0.403  0.00  0.00           N+0
HETATM    9  O   UNK     0      -2.076  -3.101   0.650  0.00  0.00           O+0
HETATM   10  C   UNK     0      -0.938  -0.455   0.438  0.00  0.00           C+0
HETATM   11  C   UNK     0      -0.457   0.838   0.201  0.00  0.00           C+0
HETATM   12  O   UNK     0       0.871   1.296   0.286  0.00  0.00           O+0
HETATM   13  C   UNK     0       2.048   0.551   0.047  0.00  0.00           C+0
HETATM   14  C   UNK     0       3.118   1.317  -0.361  0.00  0.00           C+0
HETATM   15  C   UNK     0       4.347   0.755  -0.640  0.00  0.00           C+0
HETATM   16  C   UNK     0       4.558  -0.603  -0.522  0.00  0.00           C+0
HETATM   17 Cl   UNK     0       6.134  -1.308  -0.882  0.00  0.00          Cl+0
HETATM   18  C   UNK     0       3.496  -1.382  -0.116  0.00  0.00           C+0
HETATM   19  C   UNK     0       2.256  -0.814   0.166  0.00  0.00           C+0
HETATM   20  C   UNK     0       1.258  -1.788   0.581  0.00  0.00           C+0
HETATM   21  O   UNK     0       1.652  -2.964   0.681  0.00  0.00           O+0
HETATM   22  N   UNK     0      -0.121  -1.538   0.885  0.00  0.00           N+0
HETATM   23  H   UNK     0       0.035   3.111  -1.000  0.00  0.00           H+0
HETATM   24  H   UNK     0      -1.616   3.755  -1.037  0.00  0.00           H+0
HETATM   25  H   UNK     0      -0.763   3.745   0.518  0.00  0.00           H+0
HETATM   26  H   UNK     0      -4.215   0.037  -0.168  0.00  0.00           H+0
HETATM   27  H   UNK     0      -4.915  -1.813   0.935  0.00  0.00           H+0
HETATM   28  H   UNK     0      -4.514  -3.110  -0.221  0.00  0.00           H+0
HETATM   29  H   UNK     0       2.926   2.391  -0.447  0.00  0.00           H+0
HETATM   30  H   UNK     0       5.163   1.383  -0.956  0.00  0.00           H+0
HETATM   31  H   UNK     0       3.635  -2.450  -0.016  0.00  0.00           H+0
HETATM   32  H   UNK     0      -0.632  -2.188   1.516  0.00  0.00           H+0
CONECT    1    2   23   24   25                                             
CONECT    2    1    3   11                                                  
CONECT    3    2    4    5                                                  
CONECT    4    3                                                            
CONECT    5    3    6   26                                                  
CONECT    6    5    7   10                                                  
CONECT    7    6    8    9                                                  
CONECT    8    7   27   28                                                  
CONECT    9    7                                                            
CONECT   10    6   11   22                                                  
CONECT   11   10   12    2                                                  
CONECT   12   11   13                                                       
CONECT   13   12   14   19                                                  
CONECT   14   13   15   29                                                  
CONECT   15   14   16   30                                                  
CONECT   16   15   17   18                                                  
CONECT   17   16                                                            
CONECT   18   16   19   31                                                  
CONECT   19   18   20   13                                                  
CONECT   20   19   21   22                                                  
CONECT   21   20                                                            
CONECT   22   20   10   32                                                  
CONECT   23    1                                                            
CONECT   24    1                                                            
CONECT   25    1                                                            
CONECT   26    5                                                            
CONECT   27    8                                                            
CONECT   28    8                                                            
CONECT   29   14                                                            
CONECT   30   15                                                            
CONECT   31   18                                                            
CONECT   32   22                                                            
MASTER        0    0    0    0    0    0    0    0   32    0   68    0
END

RDKit          3D

32 34  0  0  0  0  0  0  0  0999 V2000
   -0.9122    3.1698   -0.4232 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3703    1.7967   -0.1637 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7212    1.5271   -0.3001 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.8445    2.8073   -0.7706 Cl  0  0  0  0  0  0  0  0  0  0  0  0
   -3.1543    0.2473   -0.0606 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2573   -0.7708    0.3144 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7875   -2.0981    0.4627 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.2030   -2.3438    0.4033 N   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0765   -3.1014    0.6496 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9378   -0.4549    0.4384 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4574    0.8381    0.2007 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.8708    1.2960    0.2862 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.0476    0.5512    0.0465 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.1178    1.3168   -0.3608 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.3470    0.7547   -0.6397 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.5583   -0.6026   -0.5224 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.1341   -1.3079   -0.8820 Cl  0  0  0  0  0  0  0  0  0  0  0  0
    3.4958   -1.3818   -0.1156 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.2560   -0.8137    0.1656 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.2579   -1.7884    0.5807 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.6515   -2.9644    0.6808 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1209   -1.5382    0.8848 N   0  0  0  0  0  0  0  0  0  0  0  0
    0.0352    3.1112   -0.9997 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6159    3.7551   -1.0366 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7625    3.7452    0.5175 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.2147    0.0367   -0.1682 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.9146   -1.8128    0.9350 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.5143   -3.1096   -0.2206 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.9261    2.3909   -0.4466 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.1632    1.3828   -0.9561 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.6354   -2.4502   -0.0156 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6316   -2.1882    1.5159 H   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0
  2  3  2  0
  3  4  1  0
  3  5  1  0
  5  6  2  0
  6  7  1  0
  7  8  1  0
  7  9  2  0
  6 10  1  0
 10 11  2  0
 11 12  1  0
 12 13  1  0
 13 14  2  0
 14 15  1  0
 15 16  2  0
 16 17  1  0
 16 18  1  0
 18 19  2  0
 19 20  1  0
 20 21  2  0
 20 22  1  0
 11  2  1  0
 19 13  1  0
 22 10  1  0
  1 23  1  0
  1 24  1  0
  1 25  1  0
  5 26  1  0
  8 27  1  0
  8 28  1  0
 14 29  1  0
 15 30  1  0
 18 31  1  0
 22 32  1  0
M  END

View in JSmol View NMR Assignments

Synonyms

Value	Source
5,13-Dichloro-10-hydroxy-4-methyl-2-oxa-9-azatricyclo[9.4.0.0,]pentadeca-1(11),3(8),4,6,9,12,14-heptaene-7-carboximidate	Generator

Chemical Formula

C₁₅H₁₀Cl₂N₂O₃

Average Mass

337.1600 Da

Monoisotopic Mass

336.00685 Da

IUPAC Name

5,13-dichloro-4-methyl-10-oxo-2-oxa-9-azatricyclo[9.4.0.0^{3,8}]pentadeca-1(15),3(8),4,6,11,13-hexaene-7-carboxamide

Traditional Name

5,13-dichloro-4-methyl-10-oxo-2-oxa-9-azatricyclo[9.4.0.0^{3,8}]pentadeca-1(15),3(8),4,6,11,13-hexaene-7-carboxamide

CAS Registry Number

Not Available

SMILES

CC1=C(Cl)C=C(C(N)=O)C2=C1OC1=C(C=C(Cl)C=C1)C(=O)N2

InChI Identifier

InChI=1S/C15H10Cl2N2O3/c1-6-10(17)5-9(14(18)20)12-13(6)22-11-3-2-7(16)4-8(11)15(21)19-12/h2-5H,1H3,(H2,18,20)(H,19,21)

InChI Key

LKTXNDBBKSMZRJ-UHFFFAOYSA-N

Experimental Spectra

Not Available

Predicted Spectra

Spectrum Type	Description	Depositor ID	Depositor Organization	Depositor	Deposition Date	View
1D NMR	¹³C NMR Spectrum (1D, 25 MHz, 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 sp. FXJ1.235	NPAtlas	26437421

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	3.15	ALOGPS
logP	3.81	ChemAxon
logS	-4.5	ALOGPS
pKa (Strongest Acidic)	10.91	ChemAxon
pKa (Strongest Basic)	-0.88	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	2	ChemAxon
Hydrogen Donor Count	2	ChemAxon
Polar Surface Area	81.42 Å²	ChemAxon
Rotatable Bond Count	1	ChemAxon
Refractivity	85.5 m³·mol⁻¹	ChemAxon
Polarizability	32.52 Å³	ChemAxon
Number of Rings	3	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

NPA007305

HMDB ID

Not Available

DrugBank ID

Not Available

Phenol Explorer Compound ID

Not Available

FoodDB ID

Not Available

KNApSAcK ID

Not Available

Chemspider ID

40256671

KEGG Compound ID

Not Available

BioCyc ID

Not Available

BiGG ID

Not Available

Wikipedia Link

Not Available

METLIN ID

Not Available

PubChem Compound

139585143

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

Showing NP-Card for Mycemycin E (NP0014775)

MOL for NP0014775 (Mycemycin E)

3D MOL for NP0014775 (Mycemycin E)

3D SDF for NP0014775 (Mycemycin E)

3D-SDF for NP0014775 (Mycemycin E)

PDB for NP0014775 (Mycemycin E)

3D PDB for NP0014775 (Mycemycin E)

SMILES for NP0014775 (Mycemycin E)

INCHI for NP0014775 (Mycemycin E)

Structure for NP0014775 (Mycemycin E)

3D Structure for NP0014775 (Mycemycin E)