NP-MRD: Showing NP-Card for (1r,3r,6s,13s,15s,16s,18s)-5-(2-hydroxyethyl)-13-(hydroxymethyl)-10-methoxy-9,17-dimethyl-8,11-dioxo-5,14,17-triazapentacyclo[12.3.1.0³,¹⁶.0⁶,¹⁵.0⁷,¹²]octadeca-7(12),9-diene-4,18-dicarbonitrile (NP0324285)

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Record Information

Version

2.0

Created at

2022-09-12 04:16:25 UTC

Updated at

2022-09-12 04:16:25 UTC

NP-MRD ID

NP0324285

Secondary Accession Numbers

None

Natural Product Identification

Common Name

(1r,3r,6s,13s,15s,16s,18s)-5-(2-hydroxyethyl)-13-(hydroxymethyl)-10-methoxy-9,17-dimethyl-8,11-dioxo-5,14,17-triazapentacyclo[12.3.1.0³,¹⁶.0⁶,¹⁵.0⁷,¹²]octadeca-7(12),9-diene-4,18-dicarbonitrile

Description

Cyanocycline D belongs to the class of organic compounds known as isoquinoline quinones. These are isoquinoline derivative with a structure containing a 5,8-dihydroisoquinoline-5,8-dione skeleton. (1r,3r,6s,13s,15s,16s,18s)-5-(2-hydroxyethyl)-13-(hydroxymethyl)-10-methoxy-9,17-dimethyl-8,11-dioxo-5,14,17-triazapentacyclo[12.3.1.0³,¹⁶.0⁶,¹⁵.0⁷,¹²]octadeca-7(12),9-diene-4,18-dicarbonitrile is found in Streptomyces lusitanus. Based on a literature review very few articles have been published on Cyanocycline D.

Structure

MOL 3D MOL SDF PDB SMILES InChI


  Mrv1652309122206162D          

 33 37  0  0  1  0            999 V2000
    7.2199    1.3014    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.0317    0.4982    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    6.2419    0.2596    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.0537   -0.5437    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.6552   -1.1083    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.2640   -0.7823    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.0757   -1.5855    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.6624   -0.2176    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.8507    0.5856    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.6404    0.8242    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.8287    1.6274    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.2353    1.1618    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    4.4379    1.9615    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.8467    2.5369    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.4000    0.9431    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    3.2819    0.1283    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    3.8672   -0.4734    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    3.6108   -1.2722    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    4.1560   -1.8914    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.8924   -2.6732    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.4376   -3.2923    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.7772   -1.4271    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.5224   -2.2117    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.2676   -2.9964    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    2.1621   -0.7788    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    1.4880   -0.1841    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.9275    0.8210    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    2.6485    1.3628    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    2.5928    2.1859    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.5371    3.0090    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    1.6340    0.3479    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    0.8383    0.1303    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.4924   -0.1011    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
  1  2  1  0  0  0  0
  2  3  1  0  0  0  0
  3  4  2  0  0  0  0
  4  5  1  0  0  0  0
  4  6  1  0  0  0  0
  6  7  2  0  0  0  0
  6  8  1  0  0  0  0
  8  9  2  0  0  0  0
  9 10  1  0  0  0  0
  3 10  1  0  0  0  0
 10 11  2  0  0  0  0
  9 12  1  0  0  0  0
 12 13  1  6  0  0  0
 13 14  1  0  0  0  0
 12 15  1  0  0  0  0
 16 15  1  6  0  0  0
 16 17  1  0  0  0  0
  8 17  1  0  0  0  0
 17 18  1  6  0  0  0
 18 19  1  0  0  0  0
 19 20  1  0  0  0  0
 20 21  1  0  0  0  0
 18 22  1  0  0  0  0
 22 23  1  0  0  0  0
 23 24  3  0  0  0  0
 22 25  1  0  0  0  0
 25 26  1  6  0  0  0
 26 27  1  0  0  0  0
 27 28  1  0  0  0  0
 15 28  1  0  0  0  0
 28 29  1  1  0  0  0
 29 30  3  0  0  0  0
 27 31  1  1  0  0  0
 31 32  1  0  0  0  0
 33 31  1  6  0  0  0
 16 33  1  0  0  0  0
 25 33  1  0  0  0  0
M  END

     RDKit          3D

 60 64  0  0  0  0  0  0  0  0999 V2000
    5.3772   -1.9765    0.4217 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.7152   -0.9219    1.0476 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.4916   -0.3959    0.6623 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.9595    0.6097    1.2908 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.6730    1.2147    2.4478 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.6576    1.2053    0.9259 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.2139    2.1789    1.5887 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.9364    0.6375   -0.1961 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4699   -0.4003   -0.8698 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.7320   -0.9477   -0.4777 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.2209   -1.9049   -1.0855 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.6378   -0.8320   -2.0170 C   0  0  1  0  0  0  0  0  0  0  0  0
    1.1962   -1.8451   -2.9188 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.4451   -1.4692   -3.4040 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6692   -1.0609   -1.5067 N   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3287    0.1745   -1.1731 C   0  0  1  0  0  0  0  0  0  0  0  0
   -2.5827   -0.0016   -0.3994 C   0  0  2  0  0  0  0  0  0  0  0  0
   -2.4285   -0.0342    1.0716 C   0  0  1  0  0  0  0  0  0  0  0  0
   -2.1053   -1.4820    1.4048 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1824   -2.1493    0.0753 C   0  0  2  0  0  0  0  0  0  0  0  0
   -0.8809   -2.1786   -0.6926 C   0  0  1  0  0  0  0  0  0  0  0  0
   -1.0109   -3.3693   -1.5804 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1348   -4.3060   -2.2720 N   0  0  0  0  0  0  0  0  0  0  0  0
   -3.0854   -1.3523   -0.7396 N   0  0  0  0  0  0  0  0  0  0  0  0
   -4.4660   -1.5007   -0.3678 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3770    0.8907    1.6295 C   0  0  2  0  0  0  0  0  0  0  0  0
   -1.8281    1.6357    2.7917 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1887    2.2403    3.7159 N   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9280    1.7968    0.6246 N   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7242    2.9415    0.4780 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1231    4.2062    0.0105 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1248    4.7479    0.8046 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4080    1.1958   -0.5539 C   0  0  1  0  0  0  0  0  0  0  0  0
    6.3302   -2.1402    0.9880 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.8119   -2.9285    0.5329 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.6155   -1.7233   -0.6223 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.2524    0.4723    3.0331 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.0056    1.8390    3.0497 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.4288    1.9185    2.0061 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.5412    0.1181   -2.6426 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.5328   -1.9042   -3.8178 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.2334   -2.8772   -2.5142 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.3471   -0.6685   -3.9776 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6412    0.6080   -2.1662 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.4021    0.6941   -0.7120 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.3913    0.2397    1.5491 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8699   -1.9006    2.0712 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0741   -1.5444    1.8228 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5836   -3.1864    0.1977 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0545   -2.4060    0.0102 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.1050   -1.3821   -1.2681 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.7721   -0.7790    0.4210 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.6741   -2.5308    0.0113 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5164    0.2305    1.9207 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6620    2.7928   -0.1363 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1607    3.1633    1.5052 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9551    4.9766    0.0413 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8363    4.1979   -1.0693 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.6176    5.1321    0.2960 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1674    2.0417   -1.2669 H   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0
  2  3  1  0
  3  4  2  0
  4  5  1  0
  4  6  1  0
  6  7  2  0
  6  8  1  0
  8  9  2  0
  9 12  1  0
 12 13  1  0
 13 14  1  0
 12 15  1  0
 15 21  1  0
 21 22  1  0
 22 23  3  0
 21 20  1  0
 20 19  1  0
 19 18  1  0
 18 17  1  0
 17 16  1  0
 16 33  1  0
 33 29  1  0
 29 30  1  0
 30 31  1  0
 31 32  1  0
 29 26  1  0
 26 27  1  0
 27 28  3  0
 17 24  1  0
 24 25  1  0
  9 10  1  0
 10 11  2  0
 10  3  1  0
 33  8  1  0
 16 15  1  0
 24 20  1  0
 26 18  1  0
  1 34  1  0
  1 35  1  0
  1 36  1  0
  5 37  1  0
  5 38  1  0
  5 39  1  0
 12 40  1  6
 13 41  1  0
 13 42  1  0
 14 43  1  0
 21 50  1  1
 20 49  1  1
 19 47  1  0
 19 48  1  0
 18 46  1  1
 17 45  1  1
 16 44  1  6
 33 60  1  6
 30 55  1  0
 30 56  1  0
 31 57  1  0
 31 58  1  0
 32 59  1  0
 26 54  1  1
 25 51  1  0
 25 52  1  0
 25 53  1  0
M  END


  Mrv1652309122206162D          

 33 37  0  0  1  0            999 V2000
    7.2199    1.3014    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.0317    0.4982    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    6.2419    0.2596    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.0537   -0.5437    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.6552   -1.1083    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.2640   -0.7823    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.0757   -1.5855    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.6624   -0.2176    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.8507    0.5856    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.6404    0.8242    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.8287    1.6274    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.2353    1.1618    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    4.4379    1.9615    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.8467    2.5369    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.4000    0.9431    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    3.2819    0.1283    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    3.8672   -0.4734    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    3.6108   -1.2722    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    4.1560   -1.8914    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.8924   -2.6732    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.4376   -3.2923    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.7772   -1.4271    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.5224   -2.2117    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.2676   -2.9964    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    2.1621   -0.7788    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    1.4880   -0.1841    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.9275    0.8210    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    2.6485    1.3628    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    2.5928    2.1859    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.5371    3.0090    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    1.6340    0.3479    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    0.8383    0.1303    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.4924   -0.1011    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
  1  2  1  0  0  0  0
  2  3  1  0  0  0  0
  3  4  2  0  0  0  0
  4  5  1  0  0  0  0
  4  6  1  0  0  0  0
  6  7  2  0  0  0  0
  6  8  1  0  0  0  0
  8  9  2  0  0  0  0
  9 10  1  0  0  0  0
  3 10  1  0  0  0  0
 10 11  2  0  0  0  0
  9 12  1  0  0  0  0
 12 13  1  6  0  0  0
 13 14  1  0  0  0  0
 12 15  1  0  0  0  0
 16 15  1  6  0  0  0
 16 17  1  0  0  0  0
  8 17  1  0  0  0  0
 17 18  1  6  0  0  0
 18 19  1  0  0  0  0
 19 20  1  0  0  0  0
 20 21  1  0  0  0  0
 18 22  1  0  0  0  0
 22 23  1  0  0  0  0
 23 24  3  0  0  0  0
 22 25  1  0  0  0  0
 25 26  1  6  0  0  0
 26 27  1  0  0  0  0
 27 28  1  0  0  0  0
 15 28  1  0  0  0  0
 28 29  1  1  0  0  0
 29 30  3  0  0  0  0
 27 31  1  1  0  0  0
 31 32  1  0  0  0  0
 33 31  1  6  0  0  0
 16 33  1  0  0  0  0
 25 33  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0324285

> <DATABASE_NAME>
NP-MRD

> <SMILES>
COC1=C(C)C(=O)C2=C([C@@H](CO)N3[C@H](C#N)[C@H]4C[C@@H]5[C@@H]([C@H]3[C@H]2N(CCO)C5C#N)N4C)C1=O

> <INCHI_IDENTIFIER>
InChI=1S/C23H27N5O5/c1-10-21(31)17-16(22(32)23(10)33-3)15(9-30)28-14(8-25)12-6-11-13(7-24)27(4-5-29)19(17)20(28)18(11)26(12)2/h11-15,18-20,29-30H,4-6,9H2,1-3H3/t11-,12+,13?,14+,15+,18-,19-,20-/m0/s1

> <INCHI_KEY>
WTMKTMCADOSNBQ-ANMJZIKASA-N

> <FORMULA>
C23H27N5O5

> <MOLECULAR_WEIGHT>
453.499

> <EXACT_MASS>
453.201218989

> <JCHEM_ACCEPTOR_COUNT>
10

> <JCHEM_ATOM_COUNT>
60

> <JCHEM_AVERAGE_POLARIZABILITY>
46.092785154901065

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
2

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
0

> <JCHEM_IUPAC>
(1R,3R,6S,13S,15S,16S,18S)-5-(2-hydroxyethyl)-13-(hydroxymethyl)-10-methoxy-9,17-dimethyl-8,11-dioxo-5,14,17-triazapentacyclo[12.3.1.0^{3,16}.0^{6,15}.0^{7,12}]octadeca-7(12),9-diene-4,18-dicarbonitrile

> <JCHEM_LOGP>
-1.3548858983333327

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
5

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA>
15.697478493064356

> <JCHEM_PKA_STRONGEST_ACIDIC>
14.931698295336407

> <JCHEM_PKA_STRONGEST_BASIC>
3.90478574548435

> <JCHEM_POLAR_SURFACE_AREA>
141.13

> <JCHEM_REFRACTIVITY>
118.03799999999998

> <JCHEM_ROTATABLE_BOND_COUNT>
4

> <JCHEM_RULE_OF_FIVE>
1

> <JCHEM_TRADITIONAL_IUPAC>
(1R,3R,6S,13S,15S,16S,18S)-5-(2-hydroxyethyl)-13-(hydroxymethyl)-10-methoxy-9,17-dimethyl-8,11-dioxo-5,14,17-triazapentacyclo[12.3.1.0^{3,16}.0^{6,15}.0^{7,12}]octadeca-7(12),9-diene-4,18-dicarbonitrile

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 12-SEP-22   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   12-SEP-22         0                                  
HETATM    1  C   UNK     0      13.477   2.429   0.000  0.00  0.00           C+0
HETATM    2  O   UNK     0      13.126   0.930   0.000  0.00  0.00           O+0
HETATM    3  C   UNK     0      11.652   0.485   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0      11.300  -1.015   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0      12.423  -2.069   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0       9.826  -1.460   0.000  0.00  0.00           C+0
HETATM    7  O   UNK     0       9.475  -2.960   0.000  0.00  0.00           O+0
HETATM    8  C   UNK     0       8.703  -0.406   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0       9.055   1.093   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0      10.529   1.539   0.000  0.00  0.00           C+0
HETATM   11  O   UNK     0      10.880   3.038   0.000  0.00  0.00           O+0
HETATM   12  C   UNK     0       7.906   2.169   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0       8.284   3.662   0.000  0.00  0.00           C+0
HETATM   14  O   UNK     0       7.180   4.736   0.000  0.00  0.00           O+0
HETATM   15  N   UNK     0       6.347   1.760   0.000  0.00  0.00           N+0
HETATM   16  C   UNK     0       6.126   0.239   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0       7.219  -0.884   0.000  0.00  0.00           C+0
HETATM   18  N   UNK     0       6.740  -2.375   0.000  0.00  0.00           N+0
HETATM   19  C   UNK     0       7.758  -3.531   0.000  0.00  0.00           C+0
HETATM   20  C   UNK     0       7.266  -4.990   0.000  0.00  0.00           C+0
HETATM   21  O   UNK     0       8.284  -6.146   0.000  0.00  0.00           O+0
HETATM   22  C   UNK     0       5.184  -2.664   0.000  0.00  0.00           C+0
HETATM   23  C   UNK     0       4.708  -4.129   0.000  0.00  0.00           C+0
HETATM   24  N   UNK     0       4.233  -5.593   0.000  0.00  0.00           N+0
HETATM   25  C   UNK     0       4.036  -1.454   0.000  0.00  0.00           C+0
HETATM   26  C   UNK     0       2.778  -0.344   0.000  0.00  0.00           C+0
HETATM   27  C   UNK     0       3.598   1.533   0.000  0.00  0.00           C+0
HETATM   28  C   UNK     0       4.944   2.544   0.000  0.00  0.00           C+0
HETATM   29  C   UNK     0       4.840   4.080   0.000  0.00  0.00           C+0
HETATM   30  N   UNK     0       4.736   5.617   0.000  0.00  0.00           N+0
HETATM   31  N   UNK     0       3.050   0.649   0.000  0.00  0.00           N+0
HETATM   32  C   UNK     0       1.565   0.243   0.000  0.00  0.00           C+0
HETATM   33  C   UNK     0       4.653  -0.189   0.000  0.00  0.00           C+0
CONECT    1    2                                                            
CONECT    2    1    3                                                       
CONECT    3    2    4   10                                                  
CONECT    4    3    5    6                                                  
CONECT    5    4                                                            
CONECT    6    4    7    8                                                  
CONECT    7    6                                                            
CONECT    8    6    9   17                                                  
CONECT    9    8   10   12                                                  
CONECT   10    9    3   11                                                  
CONECT   11   10                                                            
CONECT   12    9   13   15                                                  
CONECT   13   12   14                                                       
CONECT   14   13                                                            
CONECT   15   12   16   28                                                  
CONECT   16   15   17   33                                                  
CONECT   17   16    8   18                                                  
CONECT   18   17   19   22                                                  
CONECT   19   18   20                                                       
CONECT   20   19   21                                                       
CONECT   21   20                                                            
CONECT   22   18   23   25                                                  
CONECT   23   22   24                                                       
CONECT   24   23                                                            
CONECT   25   22   26   33                                                  
CONECT   26   25   27                                                       
CONECT   27   26   28   31                                                  
CONECT   28   27   15   29                                                  
CONECT   29   28   30                                                       
CONECT   30   29                                                            
CONECT   31   27   32   33                                                  
CONECT   32   31                                                            
CONECT   33   31   16   25                                                  
MASTER        0    0    0    0    0    0    0    0   33    0   74    0
END

View in JSmol

Synonyms

Not Available

Chemical Formula

C₂₃H₂₇N₅O₅

Average Mass

453.4990 Da

Monoisotopic Mass

453.20122 Da

IUPAC Name

(1R,3R,6S,13S,15S,16S,18S)-5-(2-hydroxyethyl)-13-(hydroxymethyl)-10-methoxy-9,17-dimethyl-8,11-dioxo-5,14,17-triazapentacyclo[12.3.1.0^{3,16}.0^{6,15}.0^{7,12}]octadeca-7(12),9-diene-4,18-dicarbonitrile

Traditional Name

CAS Registry Number

Not Available

SMILES

COC1=C(C)C(=O)C2=C([C@@H](CO)N3[C@H](C#N)[C@H]4C[C@@H]5[C@@H]([C@H]3[C@H]2N(CCO)C5C#N)N4C)C1=O

InChI Identifier

InChI=1S/C23H27N5O5/c1-10-21(31)17-16(22(32)23(10)33-3)15(9-30)28-14(8-25)12-6-11-13(7-24)27(4-5-29)19(17)20(28)18(11)26(12)2/h11-15,18-20,29-30H,4-6,9H2,1-3H3/t11-,12+,13?,14+,15+,18-,19-,20-/m0/s1

InChI Key

WTMKTMCADOSNBQ-ANMJZIKASA-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, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 100 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 252 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 1000 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 50 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 200 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 75 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 300 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 101 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 400 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 126 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 500 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 151 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 600 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 176 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 700 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 201 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 800 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 226 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 900 MHz, H₂O, 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 lusitanus	LOTUS Database	35616633

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as isoquinoline quinones. These are isoquinoline derivative with a structure containing a 5,8-dihydroisoquinoline-5,8-dione skeleton.

Kingdom

Organic compounds

Super Class

Organoheterocyclic compounds

Class

Isoquinolines and derivatives

Sub Class

Isoquinoline quinones

Direct Parent

Isoquinoline quinones

Alternative Parents

Substituents

Isoquinoline quinone
Isoquinolone
Diazanaphthalene
Naphthyridine
Piperazino-3,4-b-piperidine
Azepane
N-alkylpiperazine
N-methylpiperazine
1,4-diazinane
Piperazine
N-alkylpyrrolidine
Piperidine
Vinylogous ester
Pyrrolidine
Alpha-aminonitrile
1,2-aminoalcohol
Ketone
Tertiary aliphatic amine
Tertiary amine
Nitrile
Carbonitrile
Azacycle
Alkanolamine
Organooxygen compound
Organonitrogen compound
Alcohol
Organic oxygen compound
Organic nitrogen compound
Organopnictogen compound
Hydrocarbon derivative
Carbonyl group
Organic oxide
Primary alcohol
Amine
Aliphatic heteropolycyclic compound

Molecular Framework

Aliphatic heteropolycyclic compounds

External Descriptors

Not Available

Physical Properties

State

Not Available

Experimental Properties

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

Predicted Properties

Property	Value	Source
logP	-1.4	ChemAxon
pKa (Strongest Acidic)	14.93	ChemAxon
pKa (Strongest Basic)	3.9	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	10	ChemAxon
Hydrogen Donor Count	2	ChemAxon
Polar Surface Area	141.13 Å²	ChemAxon
Rotatable Bond Count	4	ChemAxon
Refractivity	118.04 m³·mol⁻¹	ChemAxon
Polarizability	46.09 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

HMDB ID

Not Available

DrugBank ID

Not Available

Phenol Explorer Compound ID

Not Available

FoodDB ID

Not Available

KNApSAcK ID

Not Available

Chemspider ID

Not Available

KEGG Compound ID

Not Available

BioCyc ID

Not Available

BiGG ID

Not Available

Wikipedia Link

Not Available

METLIN ID

Not Available

PubChem Compound

139586670

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

LOTUS database [Link]

Showing NP-Card for (1r,3r,6s,13s,15s,16s,18s)-5-(2-hydroxyethyl)-13-(hydroxymethyl)-10-methoxy-9,17-dimethyl-8,11-dioxo-5,14,17-triazapentacyclo[12.3.1.0³,¹⁶.0⁶,¹⁵.0⁷,¹²]octadeca-7(12),9-diene-4,18-dicarbonitrile (NP0324285)

MOL for NP0324285 ((1r,3r,6s,13s,15s,16s,18s)-5-(2-hydroxyethyl)-13-(hydroxymethyl)-10-methoxy-9,17-dimethyl-8,11-dioxo-5,14,17-triazapentacyclo[12.3.1.0³,¹⁶.0⁶,¹⁵.0⁷,¹²]octadeca-7(12),9-diene-4,18-dicarbonitrile)

3D MOL for NP0324285 ((1r,3r,6s,13s,15s,16s,18s)-5-(2-hydroxyethyl)-13-(hydroxymethyl)-10-methoxy-9,17-dimethyl-8,11-dioxo-5,14,17-triazapentacyclo[12.3.1.0³,¹⁶.0⁶,¹⁵.0⁷,¹²]octadeca-7(12),9-diene-4,18-dicarbonitrile)

3D SDF for NP0324285 ((1r,3r,6s,13s,15s,16s,18s)-5-(2-hydroxyethyl)-13-(hydroxymethyl)-10-methoxy-9,17-dimethyl-8,11-dioxo-5,14,17-triazapentacyclo[12.3.1.0³,¹⁶.0⁶,¹⁵.0⁷,¹²]octadeca-7(12),9-diene-4,18-dicarbonitrile)

3D-SDF for NP0324285 ((1r,3r,6s,13s,15s,16s,18s)-5-(2-hydroxyethyl)-13-(hydroxymethyl)-10-methoxy-9,17-dimethyl-8,11-dioxo-5,14,17-triazapentacyclo[12.3.1.0³,¹⁶.0⁶,¹⁵.0⁷,¹²]octadeca-7(12),9-diene-4,18-dicarbonitrile)

PDB for NP0324285 ((1r,3r,6s,13s,15s,16s,18s)-5-(2-hydroxyethyl)-13-(hydroxymethyl)-10-methoxy-9,17-dimethyl-8,11-dioxo-5,14,17-triazapentacyclo[12.3.1.0³,¹⁶.0⁶,¹⁵.0⁷,¹²]octadeca-7(12),9-diene-4,18-dicarbonitrile)

3D PDB for NP0324285 ((1r,3r,6s,13s,15s,16s,18s)-5-(2-hydroxyethyl)-13-(hydroxymethyl)-10-methoxy-9,17-dimethyl-8,11-dioxo-5,14,17-triazapentacyclo[12.3.1.0³,¹⁶.0⁶,¹⁵.0⁷,¹²]octadeca-7(12),9-diene-4,18-dicarbonitrile)

SMILES for NP0324285 ((1r,3r,6s,13s,15s,16s,18s)-5-(2-hydroxyethyl)-13-(hydroxymethyl)-10-methoxy-9,17-dimethyl-8,11-dioxo-5,14,17-triazapentacyclo[12.3.1.0³,¹⁶.0⁶,¹⁵.0⁷,¹²]octadeca-7(12),9-diene-4,18-dicarbonitrile)

INCHI for NP0324285 ((1r,3r,6s,13s,15s,16s,18s)-5-(2-hydroxyethyl)-13-(hydroxymethyl)-10-methoxy-9,17-dimethyl-8,11-dioxo-5,14,17-triazapentacyclo[12.3.1.0³,¹⁶.0⁶,¹⁵.0⁷,¹²]octadeca-7(12),9-diene-4,18-dicarbonitrile)

Structure for NP0324285 ((1r,3r,6s,13s,15s,16s,18s)-5-(2-hydroxyethyl)-13-(hydroxymethyl)-10-methoxy-9,17-dimethyl-8,11-dioxo-5,14,17-triazapentacyclo[12.3.1.0³,¹⁶.0⁶,¹⁵.0⁷,¹²]octadeca-7(12),9-diene-4,18-dicarbonitrile)

3D Structure for NP0324285 ((1r,3r,6s,13s,15s,16s,18s)-5-(2-hydroxyethyl)-13-(hydroxymethyl)-10-methoxy-9,17-dimethyl-8,11-dioxo-5,14,17-triazapentacyclo[12.3.1.0³,¹⁶.0⁶,¹⁵.0⁷,¹²]octadeca-7(12),9-diene-4,18-dicarbonitrile)