MiMeDB: Showing metabocard for (-)-Ternatin (MMDBc0001398)

Record Information

Version

1.0

Status

Detected and Quantified

Creation Date

2021-05-14 19:37:09 UTC

Update Date

2025-10-07 16:04:28 UTC

Metabolite ID

MMDBc0001398

Metabolite Identification

Common Name

(-)-Ternatin

Description

(-)-Ternatin is a natural product belonging to the class of alkaloids, specifically a type of indole alkaloid. It has garnered interest due to its potential biological activities, including antimicrobial and cytotoxic properties. Studies have explored its effects on various biological systems, suggesting that (-)-ternatin may interact with cellular pathways, although the precise mechanisms remain to be fully elucidated. The compound's unique structure, characterized by its indole framework, contributes to its biological activity and potential therapeutic applications. Research has indicated that (-)-ternatin exhibits significant activity against certain pathogens, making it a candidate for further investigation in drug development. However, the current understanding of its pharmacological effects is limited, necessitating more comprehensive studies to explore its full potential and underlying mechanisms of action. For further details on its biological activities and potential applications, refer to the literature, including studies indexed under PMID: 28742094 and PMID: 33046994 .

Structure

MOL SDF PDB SMILES InChI


  Mrv1652305221920452D          

 61 61  0  0  1  0            999 V2000
    3.1391   -6.1880    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.6756   -0.2226    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3455    0.2994    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.8603   -4.2491    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.4391   -2.8836    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.0806   -3.6879    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.0525   -2.6404    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.2624   -4.5426    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.3547    0.1765    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4125    0.7145    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2075   -5.6165    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.8795   -1.4578    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0545   -1.4578    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.4125   -3.5040    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4291   -3.0987    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.4574   -5.7232    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5584   -1.1136    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4672   -3.9311    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8599   -0.3456    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.2556   -3.6879    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.2641   -2.8836    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.5191   -4.9006    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    2.0533   -0.5915    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    0.0000    0.0000    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
   -0.2691   -4.7938    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
   -1.7427   -1.2365    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
   -1.8624   -3.3700    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    1.8374   -4.4358    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    2.8710   -2.5656    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    3.6594   -2.3225    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    2.5677   -1.2365    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0460   -2.5656    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.6874   -3.3700    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.8250    0.0000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0124   -4.4358    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2283   -0.5915    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.0941   -4.7938    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4413   -2.0045    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    1.8991   -3.6131    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    2.2663   -2.0045    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    1.2375   -0.7145    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4125   -0.7145    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    0.4125   -4.3290    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0741   -3.6131    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    3.8430   -1.5181    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.3834   -1.1136    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8344   -2.3225    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.2922   -3.9311    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.2375    0.7145    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6941   -4.9006    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5297    0.1765    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.0325   -5.6165    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.2007   -5.3653    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.8691   -0.4686    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8250   -0.0000    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.4742   -5.1517    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2570   -1.8815    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6789   -4.1743    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.5807   -4.0779    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.0546   -1.7613    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.4758   -3.1268    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
 16  1  1  0  0  0  0
 19  2  1  0  0  0  0
 19  3  1  0  0  0  0
 19 17  1  0  0  0  0
 20  4  1  0  0  0  0
 20  5  1  0  0  0  0
 20 18  1  0  0  0  0
 21  6  1  0  0  0  0
 21  7  1  0  0  0  0
 22  8  1  1  0  0  0
 22 16  1  0  0  0  0
 23  9  1  6  0  0  0
 24 10  1  1  0  0  0
 25 11  1  1  0  0  0
 26 17  1  1  0  0  0
 27 18  1  1  0  0  0
 28 22  1  6  0  0  0
 30 21  1  0  0  0  0
 29 30  1  6  0  0  0
 31 23  1  0  0  0  0
 32 27  1  0  0  0  0
 33 29  1  0  0  0  0
 34 24  1  0  0  0  0
 35 25  1  0  0  0  0
 36 26  1  0  0  0  0
 37 28  1  0  0  0  0
 38 26  1  0  0  0  0
 38 32  2  0  0  0  0
 39 28  1  0  0  0  0
 39 33  2  0  0  0  0
 40 29  1  0  0  0  0
 40 31  2  0  0  0  0
 41 12  1  0  0  0  0
 41 23  1  0  0  0  0
 41 34  1  0  0  0  0
 42 13  1  0  0  0  0
 42 24  1  0  0  0  0
 42 36  1  0  0  0  0
 43 14  1  0  0  0  0
 43 25  1  0  0  0  0
 43 37  1  0  0  0  0
 44 15  1  0  0  0  0
 44 27  1  0  0  0  0
 44 35  1  0  0  0  0
 30 45  1  1  0  0  0
 31 46  1  4  0  0  0
 32 47  1  4  0  0  0
 33 48  1  4  0  0  0
 49 34  2  0  0  0  0
 50 35  2  0  0  0  0
 51 36  2  0  0  0  0
 52 37  2  0  0  0  0
 22 53  1  6  0  0  0
 23 54  1  1  0  0  0
 24 55  1  6  0  0  0
 25 56  1  6  0  0  0
 26 57  1  6  0  0  0
 27 58  1  6  0  0  0
 28 59  1  1  0  0  0
 29 60  1  1  0  0  0
 30 61  1  1  0  0  0
M  END


  Mrv1652305221920452D          

 61 61  0  0  1  0            999 V2000
    3.1391   -6.1880    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.6756   -0.2226    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3455    0.2994    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.8603   -4.2491    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.4391   -2.8836    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.0806   -3.6879    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.0525   -2.6404    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.2624   -4.5426    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.3547    0.1765    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4125    0.7145    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2075   -5.6165    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.8795   -1.4578    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0545   -1.4578    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.4125   -3.5040    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4291   -3.0987    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.4574   -5.7232    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5584   -1.1136    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4672   -3.9311    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8599   -0.3456    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.2556   -3.6879    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.2641   -2.8836    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.5191   -4.9006    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    2.0533   -0.5915    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    0.0000    0.0000    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
   -0.2691   -4.7938    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
   -1.7427   -1.2365    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
   -1.8624   -3.3700    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    1.8374   -4.4358    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    2.8710   -2.5656    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    3.6594   -2.3225    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    2.5677   -1.2365    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0460   -2.5656    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.6874   -3.3700    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.8250    0.0000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0124   -4.4358    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2283   -0.5915    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.0941   -4.7938    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4413   -2.0045    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    1.8991   -3.6131    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    2.2663   -2.0045    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    1.2375   -0.7145    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4125   -0.7145    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    0.4125   -4.3290    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0741   -3.6131    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    3.8430   -1.5181    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.3834   -1.1136    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8344   -2.3225    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.2922   -3.9311    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.2375    0.7145    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6941   -4.9006    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5297    0.1765    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.0325   -5.6165    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.2007   -5.3653    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.8691   -0.4686    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8250   -0.0000    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.4742   -5.1517    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2570   -1.8815    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6789   -4.1743    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.5807   -4.0779    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.0546   -1.7613    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.4758   -3.1268    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
 16  1  1  0  0  0  0
 19  2  1  0  0  0  0
 19  3  1  0  0  0  0
 19 17  1  0  0  0  0
 20  4  1  0  0  0  0
 20  5  1  0  0  0  0
 20 18  1  0  0  0  0
 21  6  1  0  0  0  0
 21  7  1  0  0  0  0
 22  8  1  1  0  0  0
 22 16  1  0  0  0  0
 23  9  1  6  0  0  0
 24 10  1  1  0  0  0
 25 11  1  1  0  0  0
 26 17  1  1  0  0  0
 27 18  1  1  0  0  0
 28 22  1  6  0  0  0
 30 21  1  0  0  0  0
 29 30  1  6  0  0  0
 31 23  1  0  0  0  0
 32 27  1  0  0  0  0
 33 29  1  0  0  0  0
 34 24  1  0  0  0  0
 35 25  1  0  0  0  0
 36 26  1  0  0  0  0
 37 28  1  0  0  0  0
 38 26  1  0  0  0  0
 38 32  2  0  0  0  0
 39 28  1  0  0  0  0
 39 33  2  0  0  0  0
 40 29  1  0  0  0  0
 40 31  2  0  0  0  0
 41 12  1  0  0  0  0
 41 23  1  0  0  0  0
 41 34  1  0  0  0  0
 42 13  1  0  0  0  0
 42 24  1  0  0  0  0
 42 36  1  0  0  0  0
 43 14  1  0  0  0  0
 43 25  1  0  0  0  0
 43 37  1  0  0  0  0
 44 15  1  0  0  0  0
 44 27  1  0  0  0  0
 44 35  1  0  0  0  0
 30 45  1  1  0  0  0
 31 46  1  4  0  0  0
 32 47  1  4  0  0  0
 33 48  1  4  0  0  0
 49 34  2  0  0  0  0
 50 35  2  0  0  0  0
 51 36  2  0  0  0  0
 52 37  2  0  0  0  0
 22 53  1  6  0  0  0
 23 54  1  1  0  0  0
 24 55  1  6  0  0  0
 25 56  1  6  0  0  0
 26 57  1  6  0  0  0
 27 58  1  6  0  0  0
 28 59  1  1  0  0  0
 29 60  1  1  0  0  0
 30 61  1  1  0  0  0
M  END
> <DATABASE_ID>
MMDBc0001398

> <DATABASE_NAME>
MIME

> <SMILES>
[H][C@](C)(CC)[C@@]1([H])N=C(O)[C@]([H])(N=C(O)[C@@]([H])(C)N(C)C(=O)[C@]([H])(C)N(C)C(=O)[C@]([H])(CC(C)C)N=C(O)[C@]([H])(CC(C)C)N(C)C(=O)[C@]([H])(C)N(C)C1=O)[C@]([H])(O)C(C)C

> <INCHI_IDENTIFIER>
InChI=1S/C37H67N7O8/c1-16-22(8)28-37(52)43(14)25(11)35(50)44(15)27(18-20(4)5)32(47)38-26(17-19(2)3)36(51)42(13)24(10)34(49)41(12)23(9)31(46)40-29(33(48)39-28)30(45)21(6)7/h19-30,45H,16-18H2,1-15H3,(H,38,47)(H,39,48)(H,40,46)/t22-,23+,24-,25-,26-,27-,28+,29+,30+/m0/s1

> <INCHI_KEY>
ZMFVAIFXJWEOMH-PTPSPKLBSA-N

> <FORMULA>
C37H67N7O8

> <MOLECULAR_WEIGHT>
737.97

> <EXACT_MASS>
737.505112155

> <JCHEM_ACCEPTOR_COUNT>
11

> <JCHEM_ATOM_COUNT>
119

> <JCHEM_AVERAGE_POLARIZABILITY>
80.81118814021863

> <JCHEM_BIOAVAILABILITY>
0

> <JCHEM_DONOR_COUNT>
4

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
0

> <JCHEM_IUPAC>
(3S,6S,9S,12S,15R,18R,21R)-15-[(2S)-butan-2-yl]-8,17,20-trihydroxy-18-[(1R)-1-hydroxy-2-methylpropyl]-1,3,4,10,12,13,21-heptamethyl-6,9-bis(2-methylpropyl)-1,4,7,10,13,16,19-heptaazacyclohenicosa-7,16,19-triene-2,5,11,14-tetrone

> <ALOGPS_LOGP>
3.16

> <JCHEM_LOGP>
3.6953281406666667

> <ALOGPS_LOGS>
-4.33

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
1

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA>
4.393545025837686

> <JCHEM_PKA_STRONGEST_ACIDIC>
3.5080688794015473

> <JCHEM_PKA_STRONGEST_BASIC>
1.5354063469188666

> <JCHEM_POLAR_SURFACE_AREA>
199.23999999999998

> <JCHEM_REFRACTIVITY>
198.1356000000001

> <JCHEM_ROTATABLE_BOND_COUNT>
8

> <JCHEM_RULE_OF_FIVE>
0

> <ALOGPS_SOLUBILITY>
3.45e-02 g/l

> <JCHEM_TRADITIONAL_IUPAC>
(3S,6S,9S,12S,15R,18R,21R)-15-[(2S)-butan-2-yl]-8,17,20-trihydroxy-18-[(1R)-1-hydroxy-2-methylpropyl]-1,3,4,10,12,13,21-heptamethyl-6,9-bis(2-methylpropyl)-1,4,7,10,13,16,19-heptaazacyclohenicosa-7,16,19-triene-2,5,11,14-tetrone

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 22-MAY-19   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   22-MAY-19         0                                  
HETATM    1  C   UNK     0       5.860 -11.551   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0      -6.861  -0.416   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0      -4.378   0.559   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0      -7.206  -7.932   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0      -6.420  -5.383   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0       7.617  -6.884   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0       9.431  -4.929   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0       6.090  -8.480   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0       4.395   0.329   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0      -0.770   1.334   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0      -0.387 -10.484   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0       1.642  -2.721   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0      -0.102  -2.721   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0       0.770  -6.541   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0      -0.801  -5.784   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0       4.587 -10.683   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0      -4.776  -2.079   0.000  0.00  0.00           C+0
HETATM   18  C   UNK     0      -4.605  -7.338   0.000  0.00  0.00           C+0
HETATM   19  C   UNK     0      -5.338  -0.645   0.000  0.00  0.00           C+0
HETATM   20  C   UNK     0      -6.077  -6.884   0.000  0.00  0.00           C+0
HETATM   21  C   UNK     0       7.960  -5.383   0.000  0.00  0.00           C+0
HETATM   22  C   UNK     0       4.702  -9.148   0.000  0.00  0.00           C+0
HETATM   23  C   UNK     0       3.833  -1.104   0.000  0.00  0.00           C+0
HETATM   24  C   UNK     0       0.000   0.000   0.000  0.00  0.00           C+0
HETATM   25  C   UNK     0      -0.502  -8.948   0.000  0.00  0.00           C+0
HETATM   26  C   UNK     0      -3.253  -2.308   0.000  0.00  0.00           C+0
HETATM   27  C   UNK     0      -3.477  -6.291   0.000  0.00  0.00           C+0
HETATM   28  C   UNK     0       3.430  -8.280   0.000  0.00  0.00           C+0
HETATM   29  C   UNK     0       5.359  -4.789   0.000  0.00  0.00           C+0
HETATM   30  C   UNK     0       6.831  -4.335   0.000  0.00  0.00           C+0
HETATM   31  C   UNK     0       4.793  -2.308   0.000  0.00  0.00           C+0
HETATM   32  C   UNK     0      -3.819  -4.789   0.000  0.00  0.00           C+0
HETATM   33  C   UNK     0       5.017  -6.291   0.000  0.00  0.00           C+0
HETATM   34  C   UNK     0       1.540   0.000   0.000  0.00  0.00           C+0
HETATM   35  C   UNK     0      -1.890  -8.280   0.000  0.00  0.00           C+0
HETATM   36  C   UNK     0      -2.293  -1.104   0.000  0.00  0.00           C+0
HETATM   37  C   UNK     0       2.042  -8.948   0.000  0.00  0.00           C+0
HETATM   38  N   UNK     0      -2.690  -3.742   0.000  0.00  0.00           N+0
HETATM   39  N   UNK     0       3.545  -6.744   0.000  0.00  0.00           N+0
HETATM   40  N   UNK     0       4.230  -3.742   0.000  0.00  0.00           N+0
HETATM   41  N   UNK     0       2.310  -1.334   0.000  0.00  0.00           N+0
HETATM   42  N   UNK     0      -0.770  -1.334   0.000  0.00  0.00           N+0
HETATM   43  N   UNK     0       0.770  -8.081   0.000  0.00  0.00           N+0
HETATM   44  N   UNK     0      -2.005  -6.744   0.000  0.00  0.00           N+0
HETATM   45  O   UNK     0       7.174  -2.834   0.000  0.00  0.00           O+0
HETATM   46  O   UNK     0       6.316  -2.079   0.000  0.00  0.00           O+0
HETATM   47  O   UNK     0      -5.291  -4.335   0.000  0.00  0.00           O+0
HETATM   48  O   UNK     0       6.145  -7.338   0.000  0.00  0.00           O+0
HETATM   49  O   UNK     0       2.310   1.334   0.000  0.00  0.00           O+0
HETATM   50  O   UNK     0      -3.162  -9.148   0.000  0.00  0.00           O+0
HETATM   51  O   UNK     0      -2.855   0.329   0.000  0.00  0.00           O+0
HETATM   52  O   UNK     0       1.927 -10.484   0.000  0.00  0.00           O+0
HETATM   53  H   UNK     0       5.975 -10.015   0.000  0.00  0.00           H+0
HETATM   54  H   UNK     0       5.356  -0.875   0.000  0.00  0.00           H+0
HETATM   55  H   UNK     0      -1.540  -0.000   0.000  0.00  0.00           H+0
HETATM   56  H   UNK     0       0.885  -9.617   0.000  0.00  0.00           H+0
HETATM   57  H   UNK     0      -4.213  -3.512   0.000  0.00  0.00           H+0
HETATM   58  H   UNK     0      -3.134  -7.792   0.000  0.00  0.00           H+0
HETATM   59  H   UNK     0       4.817  -7.612   0.000  0.00  0.00           H+0
HETATM   60  H   UNK     0       5.702  -3.288   0.000  0.00  0.00           H+0
HETATM   61  H   UNK     0       6.488  -5.837   0.000  0.00  0.00           H+0
CONECT    1   16                                                            
CONECT    2   19                                                            
CONECT    3   19                                                            
CONECT    4   20                                                            
CONECT    5   20                                                            
CONECT    6   21                                                            
CONECT    7   21                                                            
CONECT    8   22                                                            
CONECT    9   23                                                            
CONECT   10   24                                                            
CONECT   11   25                                                            
CONECT   12   41                                                            
CONECT   13   42                                                            
CONECT   14   43                                                            
CONECT   15   44                                                            
CONECT   16    1   22                                                       
CONECT   17   19   26                                                       
CONECT   18   20   27                                                       
CONECT   19    2    3   17                                                  
CONECT   20    4    5   18                                                  
CONECT   21    6    7   30                                                  
CONECT   22    8   16   28   53                                             
CONECT   23    9   31   41   54                                             
CONECT   24   10   34   42   55                                             
CONECT   25   11   35   43   56                                             
CONECT   26   17   36   38   57                                             
CONECT   27   18   32   44   58                                             
CONECT   28   22   37   39   59                                             
CONECT   29   30   33   40   60                                             
CONECT   30   21   29   45   61                                             
CONECT   31   23   40   46                                                  
CONECT   32   27   38   47                                                  
CONECT   33   29   39   48                                                  
CONECT   34   24   41   49                                                  
CONECT   35   25   44   50                                                  
CONECT   36   26   42   51                                                  
CONECT   37   28   43   52                                                  
CONECT   38   26   32                                                       
CONECT   39   28   33                                                       
CONECT   40   29   31                                                       
CONECT   41   12   23   34                                                  
CONECT   42   13   24   36                                                  
CONECT   43   14   25   37                                                  
CONECT   44   15   27   35                                                  
CONECT   45   30                                                            
CONECT   46   31                                                            
CONECT   47   32                                                            
CONECT   48   33                                                            
CONECT   49   34                                                            
CONECT   50   35                                                            
CONECT   51   36                                                            
CONECT   52   37                                                            
CONECT   53   22                                                            
CONECT   54   23                                                            
CONECT   55   24                                                            
CONECT   56   25                                                            
CONECT   57   26                                                            
CONECT   58   27                                                            
CONECT   59   28                                                            
CONECT   60   29                                                            
CONECT   61   30                                                            
MASTER        0    0    0    0    0    0    0    0   61    0  122    0
END

Synonyms

Not Available

Molecular Formula

C₃₇H₆₇N₇O₈

Average Mass

737.97

Monoisotopic Mass

737.505112155

IUPAC Name

(3S,6S,9S,12S,15R,18R,21R)-15-[(2S)-butan-2-yl]-8,17,20-trihydroxy-18-[(1R)-1-hydroxy-2-methylpropyl]-1,3,4,10,12,13,21-heptamethyl-6,9-bis(2-methylpropyl)-1,4,7,10,13,16,19-heptaazacyclohenicosa-7,16,19-triene-2,5,11,14-tetrone

Traditional Name

CAS Registry Number

Not Available

SMILES

[H][C@](C)(CC)[C@@]1([H])N=C(O)[C@]([H])(N=C(O)[C@@]([H])(C)N(C)C(=O)[C@]([H])(C)N(C)C(=O)[C@]([H])(CC(C)C)N=C(O)[C@]([H])(CC(C)C)N(C)C(=O)[C@]([H])(C)N(C)C1=O)[C@]([H])(O)C(C)C

InChI Identifier

InChI=1S/C37H67N7O8/c1-16-22(8)28-37(52)43(14)25(11)35(50)44(15)27(18-20(4)5)32(47)38-26(17-19(2)3)36(51)42(13)24(10)34(49)41(12)23(9)31(46)40-29(33(48)39-28)30(45)21(6)7/h19-30,45H,16-18H2,1-15H3,(H,38,47)(H,39,48)(H,40,46)/t22-,23+,24-,25-,26-,27-,28+,29+,30+/m0/s1

InChI Key

ZMFVAIFXJWEOMH-PTPSPKLBSA-N

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as oligopeptides. These are organic compounds containing a sequence of between three and ten alpha-amino acids joined by peptide bonds.

Kingdom

Organic compounds

Super Class

Organic acids and derivatives

Class

Carboxylic acids and derivatives

Sub Class

Amino acids, peptides, and analogues

Direct Parent

Oligopeptides

Alternative Parents

Substituents

Alpha-oligopeptide
Macrolactam
Alpha-amino acid or derivatives
Tertiary carboxylic acid amide
Carboxamide group
Lactam
Secondary alcohol
Secondary carboxylic acid amide
Organoheterocyclic compound
Azacycle
Organopnictogen compound
Carbonyl group
Organic nitrogen compound
Organooxygen compound
Organonitrogen compound
Organic oxygen compound
Alcohol
Hydrocarbon derivative
Organic oxide
Aliphatic heteromonocyclic compound

Molecular Framework

Aliphatic heteromonocyclic compounds

External Descriptors

Not Available

Functional Ontology

Not Available

Physical Properties

State

Expected Solid

Predicted Properties

Property	Value	Source
Water Solubility	0.034 g/L	ALOGPS
logP	3.16	ALOGPS
logP	3.7	ChemAxon
logS	-4.3	ALOGPS
pKa (Strongest Acidic)	3.51	ChemAxon
pKa (Strongest Basic)	1.54	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	11	ChemAxon
Hydrogen Donor Count	4	ChemAxon
Polar Surface Area	199.24 Å²	ChemAxon
Rotatable Bond Count	8	ChemAxon
Refractivity	198.14 m³·mol⁻¹	ChemAxon
Polarizability	80.81 Å³	ChemAxon
Number of Rings	1	ChemAxon
Bioavailability	No	ChemAxon
Rule of Five	No	ChemAxon
Ghose Filter	No	ChemAxon
Veber's Rule	No	ChemAxon
MDDR-like Rule	No	ChemAxon

Spectra

Spectrum Type	Description	Splash Key	Deposition Date	View
Predicted GC-MS	Predicted GC-MS Spectrum - GC-MS (TMS_1_3) - 70eV, Positive	Not Available	2022-08-08	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - 10V, Positive	Not Available	2022-08-10	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - 20V, Positive	Not Available	2022-08-10	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - 40V, Positive	Not Available	2022-08-10	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - 10V, Negative	Not Available	2022-08-10	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - 20V, Negative	Not Available	2022-08-10	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - 40V, Negative	Not Available	2022-08-10	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 100 MHz, H₂O, predicted)		2022-08-17	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 100 MHz, H₂O, predicted)		2022-08-17	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 1000 MHz, H₂O, predicted)		2022-08-17	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 1000 MHz, H₂O, predicted)		2022-08-17	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 200 MHz, H₂O, predicted)		2022-08-17	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 200 MHz, H₂O, predicted)		2022-08-17	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 300 MHz, H₂O, predicted)		2022-08-17	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 300 MHz, H₂O, predicted)		2022-08-17	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 400 MHz, H₂O, predicted)		2022-08-17	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 400 MHz, H₂O, predicted)		2022-08-17	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 500 MHz, H₂O, predicted)		2022-08-17	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 500 MHz, H₂O, predicted)		2022-08-17	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 600 MHz, H₂O, predicted)		2022-08-17	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 600 MHz, H₂O, predicted)		2022-08-17	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 700 MHz, H₂O, predicted)		2022-08-17	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 700 MHz, H₂O, predicted)		2022-08-17	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 800 MHz, H₂O, predicted)		2022-08-17	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 800 MHz, H₂O, predicted)		2022-08-17	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 900 MHz, H₂O, predicted)		2022-08-17	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 900 MHz, H₂O, predicted)		2022-08-17	View Spectrum

Biological Properties

Cellular Locations

Not Available

Biospecimen Locations

Not Available

Tissue Locations

Not Available

Associated OMIM IDs

114500 (Colorectal cancer)
610247 (Eosinophilic esophagitis)

Human Proteins and Enzymes

Protein ID	Protein Name	Protein Type	Uniprot ID	Species

Human Pathways

Pathways

Name	SMPDB/PathBank

Microbial Pathways

Pathways

This table shows at most 5 pathways. For the full list of associated pathways:

See All Associated Bacterial Pathways

Name	SMPDB/PathBank

Metabolic Reactions

Reactions

This table shows at most 20 reactions. For the full list of associated reactions:

See All Associated Reactions

Reaction ID	Precursor	Product	Enzyme	Reaction Type	Data Source	Reference

Health Effects and Bioactivity

Health Outcome/Bioactivity	Metabolite Response/Effect	Evidence Type	Host and Biospecimen	Data Source	Reference

Microbial Sources

Superkingdom/Kingdom	Phylum	Total species	Hosts and Body Sites	Microbial Links
Eukaryota/Fungi	Basidiomycota	1	Human feces	Metabolic reconstruction

Exposure Sources

Other Exposures

Source Type	Data Source	Reference

Host Biospecimen and Location

Host and Biospecimen	Status	Mean	Std	Min	Max	Units	Age	Sex	Health Condition	Data Source	Reference

External Links

HMDB ID

Not Available

DrugBank ID

Not Available

Phenol Explorer Compound ID

Not Available

FooDB ID

FDB020851

KNApSAcK ID

Not Available

Chemspider ID

Not Available

KEGG Compound ID

Not Available

BioCyc ID

Not Available

BiGG ID

Not Available

Wikipedia Link

Ternatin heptapeptide

METLIN ID

Not Available

PubChem Compound

11707536

PDB ID

Not Available

ChEBI ID

Not Available

CMMC Knowledgebase

Not Available

Food Biomarker Ontology

Not Available

References

Synthesis Reference

Not Available

General References

van Santen JA, Poynton EF, Iskakova D, McMann E, Alsup TA, Clark TN, Fergusson CH, Fewer DP, Hughes AH, McCadden CA, Parra J, Soldatou S, Rudolf JD, Janssen EM, Duncan KR, Linington RG: The Natural Products Atlas 2.0: a database of microbially-derived natural products. Nucleic Acids Res. 2022 Jan 7;50(D1):D1317-D1323. doi: 10.1093/nar/gkab941. [PubMed:34718710 ]

Showing metabocard for (-)-Ternatin (MMDBc0001398)

MOL for #<Metabolite:0x00007fd42e338c40>

3D MOL for #<Metabolite:0x00007fd42e338c40>

3D SDF for #<Metabolite:0x00007fd42e338c40>

3D-SDF for #<Metabolite:0x00007fd42e338c40>

PDB for #<Metabolite:0x00007fd42e338c40>

3D PDB for #<Metabolite:0x00007fd42e338c40>

SMILES for #<Metabolite:0x00007fd42e338c40>

INCHI for #<Metabolite:0x00007fd42e338c40>

Structure for #<Metabolite:0x00007fd42e338c40>

3D Structure for #<Metabolite:0x00007fd42e338c40>