NP-MRD: Showing NP-Card for 3-benzyl-5,11-dihydroxy-6,9,12-triisopropyl-1,7-dioxa-4,10-diazacyclododeca-4,10-diene-2,8-dione (NP0154945)

Jump To Section:

Identification Spectra BioTaxonomy ChemoTaxonomy Physical properties Links References XML

Record Information

Version

2.0

Created at

2022-09-02 11:55:51 UTC

Updated at

2022-09-02 11:55:51 UTC

NP-MRD ID

NP0154945

Secondary Accession Numbers

None

Natural Product Identification

Common Name

3-benzyl-5,11-dihydroxy-6,9,12-triisopropyl-1,7-dioxa-4,10-diazacyclododeca-4,10-diene-2,8-dione

Description

3-Benzyl-5,11-dihydroxy-6,9,12-tris(propan-2-yl)-1,7-dioxa-4,10-diazacyclododeca-4,10-diene-2,8-dione belongs to the class of organic compounds known as cyclic depsipeptides. These are natural or synthetic compounds having sequences of amino and hydroxy carboxylic acid residues (usually α-amino and α-hydroxy acids) connected in a ring. The residues are commonly but not necessarily regularly alternating. 3-benzyl-5,11-dihydroxy-6,9,12-triisopropyl-1,7-dioxa-4,10-diazacyclododeca-4,10-diene-2,8-dione is found in Arthothelium galapagoense. 3-Benzyl-5,11-dihydroxy-6,9,12-tris(propan-2-yl)-1,7-dioxa-4,10-diazacyclododeca-4,10-diene-2,8-dione is an extremely weak basic (essentially neutral) compound (based on its pKa).

Structure

MOL 3D MOL SDF PDB SMILES InChI


  Mrv1533004201502442D          

 32 33  0  0  0  0            999 V2000
   -2.1434    2.2836    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1434    1.4586    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8579    1.0461    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4289    1.0461    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4289    0.2211    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8414   -0.4934    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6664   -0.4934    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4289   -1.2079    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6039   -1.2079    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.1105   -1.6204    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.1105   -2.4454    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.8250   -1.2079    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.5395   -1.6204    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.5395   -2.4454    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.2539   -2.8579    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.2539   -3.6829    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.5395   -4.0954    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.8250   -3.6829    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.8250   -2.8579    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.8250   -0.3829    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    1.2375    0.3316    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.0625    0.3316    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.8250    1.0461    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0000    1.0461    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7145    1.4586    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7145    2.2836    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.2375    1.7605    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.8250    2.4750    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.0625    1.7605    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8414   -1.9224    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4289   -2.6368    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6664   -1.9224    0.0000 C   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
  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
  6  8  1  0  0  0  0
  8  9  1  0  0  0  0
  9 10  1  0  0  0  0
 10 11  2  0  0  0  0
 10 12  1  0  0  0  0
 12 13  1  0  0  0  0
 13 14  1  0  0  0  0
 14 15  2  0  0  0  0
 15 16  1  0  0  0  0
 16 17  2  0  0  0  0
 17 18  1  0  0  0  0
 18 19  2  0  0  0  0
 14 19  1  0  0  0  0
 12 20  1  0  0  0  0
 20 21  1  0  0  0  0
 21 22  2  0  0  0  0
 21 23  1  0  0  0  0
 23 24  1  0  0  0  0
 24 25  1  0  0  0  0
  4 25  1  0  0  0  0
 25 26  2  0  0  0  0
 23 27  1  0  0  0  0
 27 28  1  0  0  0  0
 27 29  1  0  0  0  0
  8 30  1  0  0  0  0
 30 31  1  0  0  0  0
 30 32  1  0  0  0  0
M  END

     RDKit          3D

 66 67  0  0  0  0  0  0  0  0999 V2000
    4.5742   -1.2066   -0.1340 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.2830    0.0915   -0.8195 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.0570    1.2442   -0.2850 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.7671    0.3211   -0.7864 C   0  0  2  0  0  0  0  0  0  0  0  0
    2.2731    0.3819    0.5478 N   0  0  0  0  0  0  0  0  0  0  0  0
    1.4913    1.4477    1.0488 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.6846    1.9077    2.2106 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.4095    2.0902    0.2640 C   0  0  1  0  0  0  0  0  0  0  0  0
    0.5918    3.5770    0.1765 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5341    4.1873   -0.6319 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.8831    3.9825   -0.4828 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.2610    1.5854   -1.0330 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9061    1.0978   -1.5803 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1550    1.3633   -2.7845 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9010    0.2757   -0.8513 C   0  0  1  0  0  0  0  0  0  0  0  0
   -3.2398    0.9567   -1.0125 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.3487    0.2577   -0.3353 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.6583    0.5266    0.9791 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.7114   -0.1301    1.6175 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.4322   -1.0484    0.9108 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.1593   -1.3464   -0.3966 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.1023   -0.6740   -1.0054 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9205   -1.0917   -1.2790 N   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1065   -2.1146   -0.7455 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5376   -3.2731   -0.5435 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.3391   -1.8877   -0.3805 C   0  0  1  0  0  0  0  0  0  0  0  0
    1.0061   -3.1460    0.0618 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.9957   -4.2154   -1.0034 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.4469   -3.7468    1.3169 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.0067   -1.3841   -1.4823 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.1705   -0.7284   -1.6412 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8736   -1.0327   -2.6583 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.0641   -2.0083   -0.7186 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.6719   -1.3958   -0.2210 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.3401   -1.2379    0.9313 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.5174   -0.0658   -1.9097 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.4754    0.9873    0.7264 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.5584    2.2107   -0.3106 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.9758    1.3494   -0.9345 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.6137    1.3005   -1.3265 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.5045   -0.4039    1.1971 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5158    1.9361    0.8875 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.5628    4.0656    1.1761 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5019    3.8878   -0.1983 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4775    5.3065   -0.5401 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4122    3.8807   -1.6936 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.9326    5.1056   -0.5262 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.7208    3.6771    0.1545 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.0116    3.6111   -1.4986 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6465    0.3813    0.2385 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.2121    1.9871   -0.6062 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.4856    1.0594   -2.0927 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.0693    1.2560    1.5052 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.9550    0.0793    2.6460 H   0  0  0  0  0  0  0  0  0  0  0  0
   -7.2524   -1.5482    1.4367 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.7561   -2.0862   -0.9311 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.9091   -0.9216   -2.0351 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5788   -1.3653   -2.0427 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.3660   -1.1580    0.4721 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.0698   -2.9040    0.2616 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.0219   -4.3994   -1.4262 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.3494   -3.8516   -1.8252 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.5859   -5.1737   -0.6346 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.1865   -2.9926    2.0875 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.2447   -4.3791    1.7636 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4021   -4.4586    1.1203 H   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0
  2  3  1  0
  2  4  1  0
  4  5  1  0
  5  6  1  0
  6  7  2  0
  6  8  1  0
  8 12  1  0
 12 13  1  0
 13 14  2  0
 13 15  1  0
 15 16  1  0
 16 17  1  0
 17 18  2  0
 18 19  1  0
 19 20  2  0
 20 21  1  0
 21 22  2  0
 15 23  1  0
 23 24  1  0
 24 25  2  0
 24 26  1  0
 26 30  1  0
 30 31  1  0
 31 32  2  0
 26 27  1  0
 27 28  1  0
 27 29  1  0
  8  9  1  0
  9 10  1  0
  9 11  1  0
 31  4  1  0
 22 17  1  0
  1 33  1  0
  1 34  1  0
  1 35  1  0
  2 36  1  0
  3 37  1  0
  3 38  1  0
  3 39  1  0
  4 40  1  6
  5 41  1  0
  8 42  1  1
 15 50  1  1
 16 51  1  0
 16 52  1  0
 18 53  1  0
 19 54  1  0
 20 55  1  0
 21 56  1  0
 22 57  1  0
 23 58  1  0
 26 59  1  1
 27 60  1  0
 28 61  1  0
 28 62  1  0
 28 63  1  0
 29 64  1  0
 29 65  1  0
 29 66  1  0
  9 43  1  0
 10 44  1  0
 10 45  1  0
 10 46  1  0
 11 47  1  0
 11 48  1  0
 11 49  1  0
M  END


  Mrv1533004201502442D          

 32 33  0  0  0  0            999 V2000
   -2.1434    2.2836    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1434    1.4586    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8579    1.0461    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4289    1.0461    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4289    0.2211    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8414   -0.4934    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6664   -0.4934    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4289   -1.2079    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6039   -1.2079    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.1105   -1.6204    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.1105   -2.4454    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.8250   -1.2079    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.5395   -1.6204    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.5395   -2.4454    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.2539   -2.8579    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.2539   -3.6829    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.5395   -4.0954    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.8250   -3.6829    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.8250   -2.8579    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.8250   -0.3829    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    1.2375    0.3316    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.0625    0.3316    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.8250    1.0461    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0000    1.0461    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7145    1.4586    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7145    2.2836    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.2375    1.7605    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.8250    2.4750    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.0625    1.7605    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8414   -1.9224    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4289   -2.6368    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6664   -1.9224    0.0000 C   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
  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
  6  8  1  0  0  0  0
  8  9  1  0  0  0  0
  9 10  1  0  0  0  0
 10 11  2  0  0  0  0
 10 12  1  0  0  0  0
 12 13  1  0  0  0  0
 13 14  1  0  0  0  0
 14 15  2  0  0  0  0
 15 16  1  0  0  0  0
 16 17  2  0  0  0  0
 17 18  1  0  0  0  0
 18 19  2  0  0  0  0
 14 19  1  0  0  0  0
 12 20  1  0  0  0  0
 20 21  1  0  0  0  0
 21 22  2  0  0  0  0
 21 23  1  0  0  0  0
 23 24  1  0  0  0  0
 24 25  1  0  0  0  0
  4 25  1  0  0  0  0
 25 26  2  0  0  0  0
 23 27  1  0  0  0  0
 27 28  1  0  0  0  0
 27 29  1  0  0  0  0
  8 30  1  0  0  0  0
 30 31  1  0  0  0  0
 30 32  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0154945

> <DATABASE_NAME>
NP-MRD

> <SMILES>
CC(C)C1NC(=O)C(OC(=O)C(CC2=CC=CC=C2)NC(=O)C(OC1=O)C(C)C)C(C)C

> <INCHI_IDENTIFIER>
InChI=1S/C24H34N2O6/c1-13(2)18-24(30)32-19(14(3)4)21(27)25-17(12-16-10-8-7-9-11-16)23(29)31-20(15(5)6)22(28)26-18/h7-11,13-15,17-20H,12H2,1-6H3,(H,25,27)(H,26,28)

> <INCHI_KEY>
DITDIPISKFIWSR-UHFFFAOYSA-N

> <FORMULA>
C24H34N2O6

> <MOLECULAR_WEIGHT>
446.544

> <EXACT_MASS>
446.241686823

> <JCHEM_ACCEPTOR_COUNT>
4

> <JCHEM_ATOM_COUNT>
66

> <JCHEM_AVERAGE_POLARIZABILITY>
46.91697601341682

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
2

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
1

> <JCHEM_IUPAC>
3-benzyl-6,9,12-tris(propan-2-yl)-1,7-dioxa-4,10-diazacyclododecane-2,5,8,11-tetrone

> <ALOGPS_LOGP>
2.49

> <JCHEM_LOGP>
3.6310572503333334

> <ALOGPS_LOGS>
-4.09

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
2

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA>
11.211051094934273

> <JCHEM_PKA_STRONGEST_ACIDIC>
10.674426511269411

> <JCHEM_PKA_STRONGEST_BASIC>
-5.934509946573558

> <JCHEM_POLAR_SURFACE_AREA>
110.80000000000001

> <JCHEM_REFRACTIVITY>
116.89580000000001

> <JCHEM_ROTATABLE_BOND_COUNT>
5

> <JCHEM_RULE_OF_FIVE>
1

> <ALOGPS_SOLUBILITY>
3.66e-02 g/l

> <JCHEM_TRADITIONAL_IUPAC>
3-benzyl-6,9,12-triisopropyl-1,7-dioxa-4,10-diazacyclododecane-2,5,8,11-tetrone

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 20-APR-15   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   20-APR-15         0                                  
HETATM    1  C   UNK     0      -4.001   4.263   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0      -4.001   2.723   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0      -5.335   1.953   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0      -2.667   1.953   0.000  0.00  0.00           C+0
HETATM    5  N   UNK     0      -2.667   0.413   0.000  0.00  0.00           N+0
HETATM    6  C   UNK     0      -3.437  -0.921   0.000  0.00  0.00           C+0
HETATM    7  O   UNK     0      -4.977  -0.921   0.000  0.00  0.00           O+0
HETATM    8  C   UNK     0      -2.667  -2.255   0.000  0.00  0.00           C+0
HETATM    9  O   UNK     0      -1.127  -2.255   0.000  0.00  0.00           O+0
HETATM   10  C   UNK     0       0.206  -3.025   0.000  0.00  0.00           C+0
HETATM   11  O   UNK     0       0.206  -4.565   0.000  0.00  0.00           O+0
HETATM   12  C   UNK     0       1.540  -2.255   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0       2.874  -3.025   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0       2.874  -4.565   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0       4.207  -5.335   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0       4.207  -6.875   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0       2.874  -7.645   0.000  0.00  0.00           C+0
HETATM   18  C   UNK     0       1.540  -6.875   0.000  0.00  0.00           C+0
HETATM   19  C   UNK     0       1.540  -5.335   0.000  0.00  0.00           C+0
HETATM   20  N   UNK     0       1.540  -0.715   0.000  0.00  0.00           N+0
HETATM   21  C   UNK     0       2.310   0.619   0.000  0.00  0.00           C+0
HETATM   22  O   UNK     0       3.850   0.619   0.000  0.00  0.00           O+0
HETATM   23  C   UNK     0       1.540   1.953   0.000  0.00  0.00           C+0
HETATM   24  O   UNK     0       0.000   1.953   0.000  0.00  0.00           O+0
HETATM   25  C   UNK     0      -1.334   2.723   0.000  0.00  0.00           C+0
HETATM   26  O   UNK     0      -1.334   4.263   0.000  0.00  0.00           O+0
HETATM   27  C   UNK     0       2.310   3.286   0.000  0.00  0.00           C+0
HETATM   28  C   UNK     0       1.540   4.620   0.000  0.00  0.00           C+0
HETATM   29  C   UNK     0       3.850   3.286   0.000  0.00  0.00           C+0
HETATM   30  C   UNK     0      -3.437  -3.588   0.000  0.00  0.00           C+0
HETATM   31  C   UNK     0      -2.667  -4.922   0.000  0.00  0.00           C+0
HETATM   32  C   UNK     0      -4.977  -3.588   0.000  0.00  0.00           C+0
CONECT    1    2                                                            
CONECT    2    1    3    4                                                  
CONECT    3    2                                                            
CONECT    4    2    5   25                                                  
CONECT    5    4    6                                                       
CONECT    6    5    7    8                                                  
CONECT    7    6                                                            
CONECT    8    6    9   30                                                  
CONECT    9    8   10                                                       
CONECT   10    9   11   12                                                  
CONECT   11   10                                                            
CONECT   12   10   13   20                                                  
CONECT   13   12   14                                                       
CONECT   14   13   15   19                                                  
CONECT   15   14   16                                                       
CONECT   16   15   17                                                       
CONECT   17   16   18                                                       
CONECT   18   17   19                                                       
CONECT   19   18   14                                                       
CONECT   20   12   21                                                       
CONECT   21   20   22   23                                                  
CONECT   22   21                                                            
CONECT   23   21   24   27                                                  
CONECT   24   23   25                                                       
CONECT   25   24    4   26                                                  
CONECT   26   25                                                            
CONECT   27   23   28   29                                                  
CONECT   28   27                                                            
CONECT   29   27                                                            
CONECT   30    8   31   32                                                  
CONECT   31   30                                                            
CONECT   32   30                                                            
MASTER        0    0    0    0    0    0    0    0   32    0   66    0
END

View in JSmol

Synonyms

Not Available

Chemical Formula

C₂₄H₃₄N₂O₆

Average Mass

446.5440 Da

Monoisotopic Mass

446.24169 Da

IUPAC Name

3-benzyl-6,9,12-tris(propan-2-yl)-1,7-dioxa-4,10-diazacyclododecane-2,5,8,11-tetrone

Traditional Name

3-benzyl-6,9,12-triisopropyl-1,7-dioxa-4,10-diazacyclododecane-2,5,8,11-tetrone

CAS Registry Number

Not Available

SMILES

CC(C)C1NC(=O)C(OC(=O)C(CC2=CC=CC=C2)NC(=O)C(OC1=O)C(C)C)C(C)C

InChI Identifier

InChI=1S/C24H34N2O6/c1-13(2)18-24(30)32-19(14(3)4)21(27)25-17(12-16-10-8-7-9-11-16)23(29)31-20(15(5)6)22(28)26-18/h7-11,13-15,17-20H,12H2,1-6H3,(H,25,27)(H,26,28)

InChI Key

DITDIPISKFIWSR-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
Arthothelium galapagoense	LOTUS Database	35616633

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as cyclic depsipeptides. These are natural or synthetic compounds having sequences of amino and hydroxy carboxylic acid residues (usually α-amino and α-hydroxy acids) connected in a ring. The residues are commonly but not necessarily regularly alternating.

Kingdom

Organic compounds

Super Class

Organic acids and derivatives

Class

Peptidomimetics

Sub Class

Depsipeptides

Direct Parent

Cyclic depsipeptides

Alternative Parents

Substituents

Cyclic depsipeptide
Macrolide lactam
Alpha-amino acid ester
Macrolactam
Macrolide
Alpha-amino acid or derivatives
Monocyclic benzene moiety
Dicarboxylic acid or derivatives
Benzenoid
Carboxamide group
Carboxylic acid ester
Lactam
Secondary carboxylic acid amide
Lactone
Carboxylic acid derivative
Oxacycle
Azacycle
Organoheterocyclic compound
Organic oxygen compound
Hydrocarbon derivative
Organic nitrogen compound
Organic oxide
Carbonyl group
Organopnictogen compound
Organooxygen compound
Organonitrogen compound
Aromatic heteromonocyclic compound

Molecular Framework

Aromatic heteromonocyclic 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	2.49	ALOGPS
logP	3.63	ChemAxon
logS	-4.1	ALOGPS
pKa (Strongest Acidic)	10.67	ChemAxon
pKa (Strongest Basic)	-5.9	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	4	ChemAxon
Hydrogen Donor Count	2	ChemAxon
Polar Surface Area	110.8 Å²	ChemAxon
Rotatable Bond Count	5	ChemAxon
Refractivity	116.9 m³·mol⁻¹	ChemAxon
Polarizability	46.92 Å³	ChemAxon
Number of Rings	2	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

Not Available

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

LOTUS database [Link]

Showing NP-Card for 3-benzyl-5,11-dihydroxy-6,9,12-triisopropyl-1,7-dioxa-4,10-diazacyclododeca-4,10-diene-2,8-dione (NP0154945)

MOL for NP0154945 (3-benzyl-5,11-dihydroxy-6,9,12-triisopropyl-1,7-dioxa-4,10-diazacyclododeca-4,10-diene-2,8-dione)

3D MOL for NP0154945 (3-benzyl-5,11-dihydroxy-6,9,12-triisopropyl-1,7-dioxa-4,10-diazacyclododeca-4,10-diene-2,8-dione)

3D SDF for NP0154945 (3-benzyl-5,11-dihydroxy-6,9,12-triisopropyl-1,7-dioxa-4,10-diazacyclododeca-4,10-diene-2,8-dione)

3D-SDF for NP0154945 (3-benzyl-5,11-dihydroxy-6,9,12-triisopropyl-1,7-dioxa-4,10-diazacyclododeca-4,10-diene-2,8-dione)

PDB for NP0154945 (3-benzyl-5,11-dihydroxy-6,9,12-triisopropyl-1,7-dioxa-4,10-diazacyclododeca-4,10-diene-2,8-dione)

3D PDB for NP0154945 (3-benzyl-5,11-dihydroxy-6,9,12-triisopropyl-1,7-dioxa-4,10-diazacyclododeca-4,10-diene-2,8-dione)

SMILES for NP0154945 (3-benzyl-5,11-dihydroxy-6,9,12-triisopropyl-1,7-dioxa-4,10-diazacyclododeca-4,10-diene-2,8-dione)

INCHI for NP0154945 (3-benzyl-5,11-dihydroxy-6,9,12-triisopropyl-1,7-dioxa-4,10-diazacyclododeca-4,10-diene-2,8-dione)

Structure for NP0154945 (3-benzyl-5,11-dihydroxy-6,9,12-triisopropyl-1,7-dioxa-4,10-diazacyclododeca-4,10-diene-2,8-dione)

3D Structure for NP0154945 (3-benzyl-5,11-dihydroxy-6,9,12-triisopropyl-1,7-dioxa-4,10-diazacyclododeca-4,10-diene-2,8-dione)