NP-MRD: Showing NP-Card for 12-hydroxy-9-methoxy-10,22-dimethyl-4,17-dioxa-2,14,22-triazaheptacyclo[11.10.0.0²,⁶.0³,²¹.0⁷,¹².0¹⁴,¹⁸.0¹⁹,²³]tricosa-6,9-diene-8,11-dione (NP0320713)

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Record Information

Version

2.0

Created at

2022-09-11 22:31:46 UTC

Updated at

2022-09-11 22:31:46 UTC

NP-MRD ID

NP0320713

Secondary Accession Numbers

None

Natural Product Identification

Common Name

12-hydroxy-9-methoxy-10,22-dimethyl-4,17-dioxa-2,14,22-triazaheptacyclo[11.10.0.0²,⁶.0³,²¹.0⁷,¹².0¹⁴,¹⁸.0¹⁹,²³]tricosa-6,9-diene-8,11-dione

Description

12-Hydroxy-9-methoxy-10,22-dimethyl-4,17-dioxa-2,14,22-triazaheptacyclo[11.10.0.0²,⁶.0³,²¹.0⁷,¹².0¹⁴,¹⁸.0¹⁹,²³]Tricosa-6,9-diene-8,11-dione 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. 12-hydroxy-9-methoxy-10,22-dimethyl-4,17-dioxa-2,14,22-triazaheptacyclo[11.10.0.0²,⁶.0³,²¹.0⁷,¹².0¹⁴,¹⁸.0¹⁹,²³]tricosa-6,9-diene-8,11-dione is found in Streptomyces halstedii. 12-Hydroxy-9-methoxy-10,22-dimethyl-4,17-dioxa-2,14,22-triazaheptacyclo[11.10.0.0²,⁶.0³,²¹.0⁷,¹².0¹⁴,¹⁸.0¹⁹,²³]Tricosa-6,9-diene-8,11-dione is a very strong basic compound (based on its pKa).

Structure

MOL 3D MOL SDF PDB SMILES InChI


  Mrv1533004151514082D          

 30 36  0  0  0  0            999 V2000
    0.5081   -3.3788    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.6582   -2.5676    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.4358   -2.2919    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.5858   -1.4807    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.9583   -0.9451    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.3634   -1.2050    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.5134   -0.3938    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.9909   -1.7406    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.1405   -0.9293    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.7861   -1.4577    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.3841   -2.0441    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.1729   -1.8623    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.5343   -1.2075    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.2023   -1.8351    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.7093   -2.8245    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.9201   -3.3515    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.4572   -4.0895    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.6218   -3.9704    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.4748   -3.1380    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8409   -2.5518    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.0633   -2.8275    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.9132   -3.6387    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.2635   -2.8345    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    6.0017   -2.3520    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    6.8028   -2.1546    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.9160   -0.5465    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.0566    0.2664    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.3269    0.6513    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.7353    0.0763    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.0994   -0.6640    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0  0  0  0
  2  3  1  0  0  0  0
  3  4  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  1  0  0  0  0
  8 10  1  0  0  0  0
 10 11  1  0  0  0  0
 11 12  1  0  0  0  0
 12 13  1  0  0  0  0
 13 14  1  0  0  0  0
 14 15  1  0  0  0  0
 15 16  1  0  0  0  0
 16 17  1  0  0  0  0
 17 18  1  0  0  0  0
 18 19  1  0  0  0  0
 19 20  2  0  0  0  0
  8 20  1  0  0  0  0
 20 21  1  0  0  0  0
  3 21  1  0  0  0  0
 21 22  2  0  0  0  0
 19 23  1  0  0  0  0
 11 23  1  0  0  0  0
 16 23  1  0  0  0  0
 15 24  1  0  0  0  0
 12 24  1  0  0  0  0
 24 25  1  0  0  0  0
 13 26  1  0  0  0  0
 26 27  1  0  0  0  0
 27 28  1  0  0  0  0
 28 29  1  0  0  0  0
 29 30  1  0  0  0  0
 10 30  1  0  0  0  0
 26 30  1  0  0  0  0
M  END

     RDKit          3D

 55 61  0  0  0  0  0  0  0  0999 V2000
    5.4694    2.3089   -0.0069 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.8567    1.2578    0.7210 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.6176    0.7539    0.3732 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.4770   -0.3466   -0.3524 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.7332   -1.0527   -0.8031 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1587   -0.8987   -0.7223 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.0163   -1.6093   -1.7206 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.0248   -0.5502    0.1720 C   0  0  1  0  0  0  0  0  0  0  0  0
    1.4012   -1.1359    1.4301 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.1063    0.8843    0.4195 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.1208    1.7142    0.2734 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1776    3.1701    0.4260 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5327    3.0437    0.8836 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0934    2.1955   -0.0314 C   0  0  2  0  0  0  0  0  0  0  0  0
   -3.2859    1.3838    0.4302 C   0  0  2  0  0  0  0  0  0  0  0  0
   -2.7537    0.3218    1.4094 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.0439   -0.9510    0.6998 C   0  0  2  0  0  0  0  0  0  0  0  0
   -2.2011   -2.1126    0.9150 C   0  0  2  0  0  0  0  0  0  0  0  0
   -2.3218   -2.8066    2.1069 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3181   -3.7940    1.9607 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3251   -3.2251    0.9360 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8151   -1.8366    0.8724 N   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2982   -1.1133   -0.2466 C   0  0  1  0  0  0  0  0  0  0  0  0
   -1.2513   -0.0894   -0.8142 C   0  0  1  0  0  0  0  0  0  0  0  0
   -2.7073   -0.4920   -0.7384 C   0  0  2  0  0  0  0  0  0  0  0  0
   -3.6338    0.6139   -0.7779 N   0  0  0  0  0  0  0  0  0  0  0  0
   -3.6057    1.3804   -1.9716 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0772    1.1905   -0.2329 N   0  0  0  0  0  0  0  0  0  0  0  0
    2.3995    1.4585    0.8172 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.4191    2.5113    1.5067 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.6368    2.0320   -1.0776 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.8355    3.2358   -0.0122 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.4690    2.4902    0.4296 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.5559   -1.5851   -1.7572 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.9270   -1.8290   -0.0305 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.5762   -0.3570   -0.8431 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.6989   -0.8099    2.0479 H   0  0  0  0  0  0  0  0  0  0  0  0
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    0.4448    3.6958    1.1363 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2538    2.7352   -0.9632 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.0896    1.9805    0.8233 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6774    0.4253    1.5764 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.3518    0.4398    2.3508 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.1208   -1.2152    0.6830 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4233   -2.8658    0.1014 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7890   -4.7169    1.6054 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7477   -3.9205    2.8909 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5560   -3.7340   -0.0147 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.6995   -3.3209    1.2689 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0913   -1.8685   -1.0480 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0199    0.0006   -1.8946 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.9823   -1.2751   -1.4725 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.2832    0.8624   -2.7134 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6232    1.4276   -2.4812 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.0727    2.3635   -1.8020 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  1  1
  8 23  1  0
 23 24  1  0
 24 25  1  0
 25 17  1  0
 17 16  1  0
 16 15  1  0
 15 14  1  0
 14 13  1  0
 13 12  1  0
 12 11  1  0
 11 28  1  0
 11 10  2  0
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 29 30  2  0
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 26 27  1  0
 17 18  1  0
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 21 22  1  0
 29  3  1  0
 22 18  1  0
 10  8  1  0
 22 23  1  0
 28 24  1  0
 26 25  1  0
 28 14  1  0
  1 31  1  0
  1 32  1  0
  1 33  1  0
  5 34  1  0
  5 35  1  0
  5 36  1  0
  9 37  1  0
 23 50  1  6
 24 51  1  6
 25 52  1  6
 17 44  1  6
 16 42  1  0
 16 43  1  0
 15 41  1  1
 14 40  1  6
 12 38  1  0
 12 39  1  0
 27 53  1  0
 27 54  1  0
 27 55  1  0
 18 45  1  6
 20 46  1  0
 20 47  1  0
 21 48  1  0
 21 49  1  0
M  END


  Mrv1533004151514082D          

 30 36  0  0  0  0            999 V2000
    0.5081   -3.3788    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.6582   -2.5676    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.4358   -2.2919    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.5858   -1.4807    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.9583   -0.9451    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.3634   -1.2050    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.5134   -0.3938    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.9909   -1.7406    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.1405   -0.9293    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.7861   -1.4577    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.3841   -2.0441    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.1729   -1.8623    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.5343   -1.2075    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.2023   -1.8351    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.7093   -2.8245    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.9201   -3.3515    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.4572   -4.0895    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.6218   -3.9704    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.4748   -3.1380    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8409   -2.5518    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.0633   -2.8275    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.9132   -3.6387    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.2635   -2.8345    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    6.0017   -2.3520    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    6.8028   -2.1546    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.9160   -0.5465    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.0566    0.2664    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.3269    0.6513    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.7353    0.0763    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.0994   -0.6640    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0  0  0  0
  2  3  1  0  0  0  0
  3  4  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  1  0  0  0  0
  8 10  1  0  0  0  0
 10 11  1  0  0  0  0
 11 12  1  0  0  0  0
 12 13  1  0  0  0  0
 13 14  1  0  0  0  0
 14 15  1  0  0  0  0
 15 16  1  0  0  0  0
 16 17  1  0  0  0  0
 17 18  1  0  0  0  0
 18 19  1  0  0  0  0
 19 20  2  0  0  0  0
  8 20  1  0  0  0  0
 20 21  1  0  0  0  0
  3 21  1  0  0  0  0
 21 22  2  0  0  0  0
 19 23  1  0  0  0  0
 11 23  1  0  0  0  0
 16 23  1  0  0  0  0
 15 24  1  0  0  0  0
 12 24  1  0  0  0  0
 24 25  1  0  0  0  0
 13 26  1  0  0  0  0
 26 27  1  0  0  0  0
 27 28  1  0  0  0  0
 28 29  1  0  0  0  0
 29 30  1  0  0  0  0
 10 30  1  0  0  0  0
 26 30  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0320713

> <DATABASE_NAME>
NP-MRD

> <SMILES>
COC1=C(C)C(=O)C2(O)C3C4C5C(CC(C6OCC(N46)=C2C1=O)N5C)C1OCCN31

> <INCHI_IDENTIFIER>
InChI=1S/C21H25N3O6/c1-8-16(28-3)15(25)12-11-7-30-20-10-6-9-13(22(10)2)14(24(11)20)17(21(12,27)18(8)26)23-4-5-29-19(9)23/h9-10,13-14,17,19-20,27H,4-7H2,1-3H3

> <INCHI_KEY>
MXQLXPOMPYTJAB-UHFFFAOYSA-N

> <FORMULA>
C21H25N3O6

> <MOLECULAR_WEIGHT>
415.446

> <EXACT_MASS>
415.174335537

> <JCHEM_ACCEPTOR_COUNT>
9

> <JCHEM_ATOM_COUNT>
55

> <JCHEM_AVERAGE_POLARIZABILITY>
41.3125356644238

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
1

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
1

> <JCHEM_IUPAC>
12-hydroxy-9-methoxy-10,22-dimethyl-4,17-dioxa-2,14,22-triazaheptacyclo[11.10.0.0²,⁶.0³,²¹.0⁷,¹².0¹⁴,¹⁸.0¹⁹,²³]tricosa-6,9-diene-8,11-dione

> <ALOGPS_LOGP>
-0.15

> <JCHEM_LOGP>
-0.08060129799999922

> <ALOGPS_LOGS>
-1.00

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
7

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA_STRONGEST_ACIDIC>
11.603360611959438

> <JCHEM_PKA_STRONGEST_BASIC>
6.371830503378809

> <JCHEM_POLAR_SURFACE_AREA>
91.78

> <JCHEM_REFRACTIVITY>
105.26989999999996

> <JCHEM_ROTATABLE_BOND_COUNT>
1

> <JCHEM_RULE_OF_FIVE>
1

> <ALOGPS_SOLUBILITY>
4.19e+01 g/l

> <JCHEM_TRADITIONAL_IUPAC>
12-hydroxy-9-methoxy-10,22-dimethyl-4,17-dioxa-2,14,22-triazaheptacyclo[11.10.0.0²,⁶.0³,²¹.0⁷,¹².0¹⁴,¹⁸.0¹⁹,²³]tricosa-6,9-diene-8,11-dione

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 15-APR-15   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   15-APR-15         0                                  
HETATM    1  C   UNK     0       0.948  -6.307   0.000  0.00  0.00           C+0
HETATM    2  O   UNK     0       1.229  -4.793   0.000  0.00  0.00           O+0
HETATM    3  C   UNK     0       2.680  -4.278   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0       2.960  -2.764   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0       1.789  -1.764   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0       4.412  -2.249   0.000  0.00  0.00           C+0
HETATM    7  O   UNK     0       4.692  -0.735   0.000  0.00  0.00           O+0
HETATM    8  C   UNK     0       5.583  -3.249   0.000  0.00  0.00           C+0
HETATM    9  O   UNK     0       5.862  -1.735   0.000  0.00  0.00           O+0
HETATM   10  C   UNK     0       7.067  -2.721   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0       8.184  -3.816   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0       9.656  -3.476   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0      10.331  -2.254   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0      11.578  -3.425   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0      10.657  -5.272   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0       9.184  -6.256   0.000  0.00  0.00           C+0
HETATM   17  O   UNK     0       8.320  -7.634   0.000  0.00  0.00           O+0
HETATM   18  C   UNK     0       6.761  -7.411   0.000  0.00  0.00           C+0
HETATM   19  C   UNK     0       6.486  -5.858   0.000  0.00  0.00           C+0
HETATM   20  C   UNK     0       5.303  -4.763   0.000  0.00  0.00           C+0
HETATM   21  C   UNK     0       3.851  -5.278   0.000  0.00  0.00           C+0
HETATM   22  O   UNK     0       3.571  -6.792   0.000  0.00  0.00           O+0
HETATM   23  N   UNK     0       7.959  -5.291   0.000  0.00  0.00           N+0
HETATM   24  N   UNK     0      11.203  -4.390   0.000  0.00  0.00           N+0
HETATM   25  C   UNK     0      12.699  -4.022   0.000  0.00  0.00           C+0
HETATM   26  C   UNK     0       9.177  -1.020   0.000  0.00  0.00           C+0
HETATM   27  O   UNK     0       9.439   0.497   0.000  0.00  0.00           O+0
HETATM   28  C   UNK     0       8.077   1.216   0.000  0.00  0.00           C+0
HETATM   29  C   UNK     0       6.973   0.142   0.000  0.00  0.00           C+0
HETATM   30  N   UNK     0       7.652  -1.239   0.000  0.00  0.00           N+0
CONECT    1    2                                                            
CONECT    2    1    3                                                       
CONECT    3    2    4   21                                                  
CONECT    4    3    5    6                                                  
CONECT    5    4                                                            
CONECT    6    4    7    8                                                  
CONECT    7    6                                                            
CONECT    8    6    9   10   20                                             
CONECT    9    8                                                            
CONECT   10    8   11   30                                                  
CONECT   11   10   12   23                                                  
CONECT   12   11   13   24                                                  
CONECT   13   12   14   26                                                  
CONECT   14   13   15                                                       
CONECT   15   14   16   24                                                  
CONECT   16   15   17   23                                                  
CONECT   17   16   18                                                       
CONECT   18   17   19                                                       
CONECT   19   18   20   23                                                  
CONECT   20   19    8   21                                                  
CONECT   21   20    3   22                                                  
CONECT   22   21                                                            
CONECT   23   19   11   16                                                  
CONECT   24   15   12   25                                                  
CONECT   25   24                                                            
CONECT   26   13   27   30                                                  
CONECT   27   26   28                                                       
CONECT   28   27   29                                                       
CONECT   29   28   30                                                       
CONECT   30   29   10   26                                                  
MASTER        0    0    0    0    0    0    0    0   30    0   72    0
END

View in JSmol

Synonyms

Not Available

Chemical Formula

C₂₁H₂₅N₃O₆

Average Mass

415.4460 Da

Monoisotopic Mass

415.17434 Da

IUPAC Name

12-hydroxy-9-methoxy-10,22-dimethyl-4,17-dioxa-2,14,22-triazaheptacyclo[11.10.0.0²,⁶.0³,²¹.0⁷,¹².0¹⁴,¹⁸.0¹⁹,²³]tricosa-6,9-diene-8,11-dione

Traditional Name

12-hydroxy-9-methoxy-10,22-dimethyl-4,17-dioxa-2,14,22-triazaheptacyclo[11.10.0.0²,⁶.0³,²¹.0⁷,¹².0¹⁴,¹⁸.0¹⁹,²³]tricosa-6,9-diene-8,11-dione

CAS Registry Number

Not Available

SMILES

COC1=C(C)C(=O)C2(O)C3C4C5C(CC(C6OCC(N46)=C2C1=O)N5C)C1OCCN31

InChI Identifier

InChI=1S/C21H25N3O6/c1-8-16(28-3)15(25)12-11-7-30-20-10-6-9-13(22(10)2)14(24(11)20)17(21(12,27)18(8)26)23-4-5-29-19(9)23/h9-10,13-14,17,19-20,27H,4-7H2,1-3H3

InChI Key

MXQLXPOMPYTJAB-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, 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 halstedii	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
Naphthyridine
Piperazino-3,4-b-piperidine
Azepane
Cyclohexenone
Tetrahydropyridine
N-alkylpiperazine
N-methylpiperazine
1,4-diazinane
Piperazine
Piperidine
N-alkylpyrrolidine
Oxazolidine
Vinylogous ester
Pyrrolidine
Tertiary alcohol
Vinylogous amide
Tertiary aliphatic amine
Tertiary amine
Hemiaminal
Ketone
Azacycle
Oxacycle
Enamine
Carbonyl group
Hydrocarbon derivative
Organic oxide
Organonitrogen compound
Organooxygen compound
Organic oxygen compound
Amine
Organic nitrogen compound
Alcohol
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	-0.15	ALOGPS
logP	-0.081	ChemAxon
logS	-1	ALOGPS
pKa (Strongest Acidic)	11.6	ChemAxon
pKa (Strongest Basic)	6.37	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	9	ChemAxon
Hydrogen Donor Count	1	ChemAxon
Polar Surface Area	91.78 Å²	ChemAxon
Rotatable Bond Count	1	ChemAxon
Refractivity	105.27 m³·mol⁻¹	ChemAxon
Polarizability	41.31 Å³	ChemAxon
Number of Rings	7	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

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

74369269

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

LOTUS database [Link]

Showing NP-Card for 12-hydroxy-9-methoxy-10,22-dimethyl-4,17-dioxa-2,14,22-triazaheptacyclo[11.10.0.0²,⁶.0³,²¹.0⁷,¹².0¹⁴,¹⁸.0¹⁹,²³]tricosa-6,9-diene-8,11-dione (NP0320713)

MOL for NP0320713 (12-hydroxy-9-methoxy-10,22-dimethyl-4,17-dioxa-2,14,22-triazaheptacyclo[11.10.0.0²,⁶.0³,²¹.0⁷,¹².0¹⁴,¹⁸.0¹⁹,²³]tricosa-6,9-diene-8,11-dione)

3D MOL for NP0320713 (12-hydroxy-9-methoxy-10,22-dimethyl-4,17-dioxa-2,14,22-triazaheptacyclo[11.10.0.0²,⁶.0³,²¹.0⁷,¹².0¹⁴,¹⁸.0¹⁹,²³]tricosa-6,9-diene-8,11-dione)

3D SDF for NP0320713 (12-hydroxy-9-methoxy-10,22-dimethyl-4,17-dioxa-2,14,22-triazaheptacyclo[11.10.0.0²,⁶.0³,²¹.0⁷,¹².0¹⁴,¹⁸.0¹⁹,²³]tricosa-6,9-diene-8,11-dione)

3D-SDF for NP0320713 (12-hydroxy-9-methoxy-10,22-dimethyl-4,17-dioxa-2,14,22-triazaheptacyclo[11.10.0.0²,⁶.0³,²¹.0⁷,¹².0¹⁴,¹⁸.0¹⁹,²³]tricosa-6,9-diene-8,11-dione)

PDB for NP0320713 (12-hydroxy-9-methoxy-10,22-dimethyl-4,17-dioxa-2,14,22-triazaheptacyclo[11.10.0.0²,⁶.0³,²¹.0⁷,¹².0¹⁴,¹⁸.0¹⁹,²³]tricosa-6,9-diene-8,11-dione)

3D PDB for NP0320713 (12-hydroxy-9-methoxy-10,22-dimethyl-4,17-dioxa-2,14,22-triazaheptacyclo[11.10.0.0²,⁶.0³,²¹.0⁷,¹².0¹⁴,¹⁸.0¹⁹,²³]tricosa-6,9-diene-8,11-dione)

SMILES for NP0320713 (12-hydroxy-9-methoxy-10,22-dimethyl-4,17-dioxa-2,14,22-triazaheptacyclo[11.10.0.0²,⁶.0³,²¹.0⁷,¹².0¹⁴,¹⁸.0¹⁹,²³]tricosa-6,9-diene-8,11-dione)

INCHI for NP0320713 (12-hydroxy-9-methoxy-10,22-dimethyl-4,17-dioxa-2,14,22-triazaheptacyclo[11.10.0.0²,⁶.0³,²¹.0⁷,¹².0¹⁴,¹⁸.0¹⁹,²³]tricosa-6,9-diene-8,11-dione)

Structure for NP0320713 (12-hydroxy-9-methoxy-10,22-dimethyl-4,17-dioxa-2,14,22-triazaheptacyclo[11.10.0.0²,⁶.0³,²¹.0⁷,¹².0¹⁴,¹⁸.0¹⁹,²³]tricosa-6,9-diene-8,11-dione)

3D Structure for NP0320713 (12-hydroxy-9-methoxy-10,22-dimethyl-4,17-dioxa-2,14,22-triazaheptacyclo[11.10.0.0²,⁶.0³,²¹.0⁷,¹².0¹⁴,¹⁸.0¹⁹,²³]tricosa-6,9-diene-8,11-dione)